Gene list
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COG category: Posttranslational modification, protein turnover, chaperones
Organism: Dictyostelium discoideum AX4, AX4
Number of genes found: 440
Show UniProt / TrEMBL protein name | View in Fasta format (DNA) | View in Fasta format (Protein) | ||||
Dictyostelium discoideum AX4, AX4 | ||||||||
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Name | Locus tag | Product / Description | Genomic element | Type | Begin | Length | Strand | GC-content |
DDB_G0267448 | DDB_G0267448 | DDB0232428 | CDS | 481685 | 1146 | - | 0.286213 | |
DDB_G0267492 | DDB_G0267492 | putative metalloprotease of the peptidase M41 family which belong to a larger family of zinc metalloproteases includes the cell division protein FtsH | DDB0232428 | CDS | 215251 | 2163 | - | 0.314378 |
DDB_G0267512 | DDB_G0267512 | DDB0232428 | CDS | 257711 | 1011 | - | 0.338279 | |
DDB_G0267526 | DDB_G0267526 | DDB0232428 | CDS | 272779 | 981 | + | 0.282365 | |
DDB_G0267952 | DDB_G0267952 | DDB0232428 | CDS | 1173990 | 831 | - | 0.247894 | |
DDB_G0267994 | DDB_G0267994 | DDB0232428 | CDS | 1246116 | 1227 | - | 0.326813 | |
DDB_G0268034 | DDB_G0268034 | homolog of mammalian Rab GDP dissociation inhibitor alpha forms a soluble complex with Rab proteins thereby preventing exchange of GDP for GTP | DDB0232428 | CDS | 1340557 | 1365 | + | 0.347985 |
DDB_G0268066 | DDB_G0268066 | DDB0232428 | CDS | 1394864 | 2595 | + | 0.210019 | |
DDB_G0268138 | DDB_G0268138 | catalyzes the reaction RX glutathione HX R-S-glutathione | DDB0232428 | CDS | 1528262 | 609 | + | 0.302135 |
DDB_G0268156 | DDB_G0268156 | DDB0232428 | CDS | 1548695 | 1461 | - | 0.216975 | |
DDB_G0268192 | DDB_G0268192 | highly conserved protein containing an alkyl hydroperoxide reductasethiol specific antioxidantmal allergen domain | DDB0232428 | CDS | 1640028 | 465 | - | 0.275269 |
DDB_G0268334 | DDB_G0268334 | DDB0232428 | CDS | 714031 | 2337 | - | 0.273427 | |
DDB_G0268358 | DDB_G0268358 | ortholog of the human SDCCAG10 (Serologically Defined Colon Cancer Antigen 10) PPIase is an enzyme that accelerates protein folding by catalyzing the cis-trans isomerization of proline imidic peptide bonds in oligopeptides | DDB0232428 | CDS | 936052 | 1482 | + | 0.262483 |
DDB_G0268850 | DDB_G0268850 | similar though smaller than H. sapiens SACS a very large protein. The SACS defect causes autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) a neurodegenerative disease D. discoideum contains three nearly identical genes located next to each other contains two putative ATP binding domains. | DDB0232428 | CDS | 2235139 | 7986 | + | 0.262334 |
DDB_G0268856 | DDB_G0268856 | DDB0232428 | CDS | 2261646 | 1941 | + | 0.267388 | |
DDB_G0268872 | DDB_G0268872 | similar to members of the ubiquitin specific peptidase (USP) family including USP44 and USP3 | DDB0232428 | CDS | 2287976 | 6378 | + | 0.298056 |
DDB_G0268884 | DDB_G0268884 | ortholog of E. coli OsmC a stress-inducible protein there is another member of this family in Dictyostelium | DDB0232428 | CDS | 2309454 | 471 | + | 0.314225 |
DDB_G0268902 | DDB_G0268902 | DDB0232428 | CDS | 2346148 | 1926 | + | 0.20405 | |
DDB_G0269018 | DDB_G0269018 | DDB0232428 | CDS | 2258756 | 1953 | + | 0.273938 | |
DDB_G0269256 | DDB_G0269256 | highly conserved protein containing an alkyl hydroperoxide reductasethiol specific antioxidantmal allergen domain identical to | DDB0232428 | CDS | 2408349 | 465 | + | 0.27957 |
DDB_G0269260 | DDB_G0269260 | highly conserved protein containing an alkyl hydroperoxide reductasethiol specific antioxidantmal allergen domain | DDB0232428 | CDS | 2415581 | 465 | + | 0.273118 |
DDB_G0269270 | DDB_G0269270 | highly conserved protein containing an alkyl hydroperoxide reductasethiol specific antioxidantmal allergen domain identical to | DDB0232428 | CDS | 2428475 | 465 | - | 0.27957 |
DDB_G0269282 | DDB_G0269282 | DDB0232428 | CDS | 2445906 | 975 | - | 0.324103 | |
DDB_G0269350 | DDB_G0269350 | DDB0232428 | CDS | 2573853 | 2109 | - | 0.245614 | |
DDB_G0269392 | DDB_G0269392 | highly conserved protein containing an alkyl hydroperoxide reductasethiol specific antioxidantmal allergen domain | DDB0232428 | CDS | 2689530 | 429 | - | 0.275058 |
DDB_G0269418 | DDB_G0269418 | similar to E. coli OsmC a stress-inducible protein and down-regulated by hyperosmotic shock there is another member of this gene family in Dictyostelium | DDB0232428 | CDS | 2728317 | 489 | - | 0.280164 |
DDB_G0269736 | DDB_G0269736 | DDB0232428 | CDS | 3451792 | 2052 | - | 0.207602 | |
DDB_G0269782 | DDB_G0269782 | DDB0232428 | CDS | 3553343 | 840 | - | 0.263095 | |
DDB_G0269808 | DDB_G0269808 | DDB0232428 | CDS | 3646239 | 465 | - | 0.255914 | |
DDB_G0269860 | DDB_G0269860 | similar to importin-7 and importin-8 from numerous eukaryotes involved in nuclear protein import | DDB0232428 | CDS | 3747132 | 3198 | + | 0.288618 |
DDB_G0270088 | DDB_G0270088 | DDB0232428 | CDS | 4195432 | 1680 | - | 0.325 | |
DDB_G0270252 | DDB_G0270252 | DDB0232428 | CDS | 4519307 | 2043 | - | 0.256975 | |
DDB_G0270268 | DDB_G0270268 | DDB0232428 | CDS | 4540670 | 1617 | + | 0.222016 | |
DDB_G0270416 | DDB_G0270416 | DDB0232428 | CDS | 4823455 | 2646 | + | 0.228647 | |
DDB_G0270420 | DDB_G0270420 | DDB0232428 | CDS | 4840357 | 966 | - | 0.308489 | |
DDB_G0270694 | DDB_G0270694 | belongs to the band 7 proteins integral membrane proteins that ares thought to regulate cation conductance stomatin is an erythrocyte membrane protein contains one predicted transmembrane domain | DDB0232428 | CDS | 3908437 | 1125 | - | 0.310222 |
DDB_G0270776 | DDB_G0270776 | conserved eukaryotic protein of unknown function ortholog of human SPATA20 (spermatogenesis associated 20) | DDB0232428 | CDS | 4646538 | 2475 | + | 0.273939 |
DDB_G0271084 | DDB_G0271084 | DDB0232428 | CDS | 4795072 | 495 | + | 0.240404 | |
DDB_G0271296 | DDB_G0271296 | DDB0232429 | CDS | 141746 | 1875 | + | 0.2304 | |
DDB_G0271348 | DDB_G0271348 | DDB0232429 | CDS | 62552 | 3114 | + | 0.221901 | |
DDB_G0271700 | DDB_G0271700 | contains a thioredoxin domain which functions as a general disulfide isomerase enriched in gametes | DDB0232429 | CDS | 730777 | 900 | - | 0.26 |
DDB_G0271726 | DDB_G0271726 | DDB0232429 | CDS | 858649 | 516 | + | 0.333333 | |
DDB_G0271798 | DDB_G0271798 | DDB0232429 | CDS | 755175 | 2511 | + | 0.240143 | |
DDB_G0271892 | DDB_G0271892 | similar to bacterial glutathione S-transferase catalyzes the reaction RX glutathione HX R-S-glutathione | DDB0232429 | CDS | 1035063 | 684 | - | 0.302632 |
DDB_G0271958 | DDB_G0271958 | catalyzes the reaction RX glutathione HX R-S-glutathione | DDB0232429 | CDS | 1074422 | 717 | - | 0.1841 |
DDB_G0272230 | DDB_G0272230 | DDB0232429 | CDS | 1716242 | 675 | - | 0.245926 | |
DDB_G0272280 | DDB_G0272280 | highly conserved protein containing an alkyl hydroperoxide reductasethiol specific antioxidantmal allergen domain | DDB0232429 | CDS | 1570828 | 546 | + | 0.287546 |
DDB_G0272298 | DDB_G0272298 | DDB0232429 | CDS | 1664020 | 918 | - | 0.310458 | |
DDB_G0272342 | DDB_G0272342 | DDB0232429 | CDS | 1338747 | 1281 | + | 0.330211 | |
DDB_G0272418 | DDB_G0272418 | DDB0232429 | CDS | 1503629 | 399 | - | 0.285714 | |
DDB_G0272632 | DDB_G0272632 | catalyzes the reaction RX glutathione HX R-S-glutathione there is a second copy of this gene | DDB0232429 | CDS | 2282062 | 597 | + | 0.309883 |
DDB_G0272700 | DDB_G0272700 | DDB0232429 | CDS | 1921731 | 621 | - | 0.330113 | |
DDB_G0272777 | DDB_G0272777 | member of the same super family as valosin-containing protein (VCP) and CDC48brbr bCommunity annotation:b DDB G0272777 appears to be the Dicty-specific AAA-ATPase related cdc48 (cdcD) in Dicty and other organisms. When | DDB0232429 | CDS | 2164739 | 2217 | + | 0.249436 |
DDB_G0272983 | DDB_G0272983 | contains one DnaJ N-terminal domain and one MYND-type zinc finger domain contains 8 putative transmembrane domains | DDB0232429 | CDS | 2010405 | 1719 | - | 0.268179 |
DDB_G0273093 | DDB_G0273093 | similar to the mammalian Hypoxia up-regulated protein 1 (HYOU1) a protein that plays a role in cytoprotective cellular mechanisms triggered by oxygen deprivation there is a second copy of this gene | DDB0232429 | CDS | 2591482 | 2781 | - | 0.280834 |
DDB_G0273813 | DDB_G0273813 | similar to the mammalian Hypoxia up-regulated protein 1 (HYOU1) a protein that plays a role in cytoprotective cellular mechanisms triggered by oxygen deprivation there is a second copy of this gene | DDB0232429 | CDS | 3437085 | 2781 | + | 0.280834 |
DDB_G0274081 | DDB_G0274081 | catalyzes the reaction RX glutathione HX R-S-glutathione there is a second copy of this gene | DDB0232429 | CDS | 3748941 | 597 | - | 0.309883 |
DDB_G0274207 | DDB_G0274207 | DDB0232429 | CDS | 4778748 | 3777 | - | 0.243315 | |
DDB_G0274223 | DDB_G0274223 | catalyzes the reaction RX glutathione HX R-S-glutathione | DDB0232429 | CDS | 4720551 | 783 | + | 0.273308 |
DDB_G0274329 | DDB_G0274329 | DDB0232429 | CDS | 3880324 | 609 | - | 0.269294 | |
DDB_G0274345 | DDB_G0274345 | belongs to the band 7 proteins integral membrane proteins that ares thought to regulate cation conductance stomatin is an erythrocyte membrane protein contains an N-terminal transmembrane domain that might be a signal sequence | DDB0232429 | CDS | 3908527 | 1005 | + | 0.271642 |
DDB_G0274385 | DDB_G0274385 | DDB0232429 | CDS | 4876346 | 1077 | + | 0.311978 | |
DDB_G0274657 | DDB_G0274657 | related to glutaredoxin which functions as an electron carrier in the glutathione-dependent synthesis of deoxyribonucleotides | DDB0232429 | CDS | 4453801 | 432 | + | 0.305556 |
DDB_G0274705 | DDB_G0274705 | catalyzes the reaction RX glutathione HX R-S-glutathione | DDB0232429 | CDS | 4155932 | 780 | + | 0.261538 |
DDB_G0274795 | DDB_G0274795 | very similar to mammalian USP48 ubiquitin-specific protease catalyzes the hydrolysis of various forms of polymeric ubiquitin sequences and removes ubiquitin from larger groups | DDB0232429 | CDS | 3857138 | 4074 | - | 0.241041 |
DDB_G0274827 | DDB_G0274827 | DDB0232429 | CDS | 4039593 | 2760 | - | 0.267391 | |
DDB_G0274887 | DDB_G0274887 | DDB0232429 | CDS | 4345083 | 1044 | + | 0.251916 | |
DDB_G0274897 | DDB_G0274897 | DDB0232429 | CDS | 4364366 | 2733 | - | 0.312477 | |
DDB_G0275025 | DDB_G0275025 | contains one thioredoxin domain similar to human PDIA6 (protein disulfide isomerase A6) | DDB0232429 | CDS | 5326205 | 1230 | + | 0.264228 |
DDB_G0275109 | DDB_G0275109 | DDB0232429 | CDS | 5033896 | 1845 | - | 0.197832 | |
DDB_G0275227 | DDB_G0275227 | similar to FKBP-type peptidyl-prolyl isomerase which functions as a receptor for immunosuppressants in vertebrates | DDB0232429 | CDS | 4935740 | 324 | - | 0.361111 |
DDB_G0275415 | DDB_G0275415 | DDB0232429 | CDS | 5440439 | 8976 | + | 0.29434 | |
DDB_G0275555 | DDB_G0275555 | DDB0232429 | CDS | 5684935 | 723 | + | 0.271093 | |
DDB_G0275595 | DDB_G0275595 | DDB0232429 | CDS | 5571932 | 2052 | - | 0.220273 | |
DDB_G0275693 | DDB_G0275693 | DDB0232429 | CDS | 5531426 | 2103 | + | 0.300048 | |
DDB_G0275755 | DDB_G0275755 | highly conserved protein containing an alkyl hydroperoxide reductasethiol specific antioxidantmal allergen domain | DDB0232429 | CDS | 5846616 | 597 | - | 0.274707 |
DDB_G0276057 | DDB_G0276057 | DDB0232429 | CDS | 6469384 | 1623 | - | 0.32902 | |
DDB_G0276111 | DDB_G0276111 | DDB0232429 | CDS | 6270826 | 1248 | + | 0.308494 | |
DDB_G0276169 | DDB_G0276169 | similar to S. cerevisiae MSP1 a mitochondrial protein involved in sorting of proteins in the mitochondria | DDB0232429 | CDS | 6497773 | 993 | + | 0.286002 |
DDB_G0276351 | DDB_G0276351 | similar to bacterial glutathione S-transferase catalyzes the reaction RX glutathione HX R-S-glutathione | DDB0232429 | CDS | 6703448 | 693 | + | 0.292929 |
DDB_G0276445 | DDB_G0276445 | highly similar to human HSPA5 (78 kDa glucose-regulated protein precursor GRP78) contains a predicted endoplasmic reticulum targeting sequence | DDB0232429 | CDS | 6984336 | 1977 | - | 0.373293 |
DDB_G0276527 | DDB_G0276527 | contains 3 major domains: one RCC1 domain one protein kinase domain and one HECT domain N-terminal region beongs to the SerThr protein kinase family C-terminal region belongs to the CAMK SerThr protein kinase family. | DDB0232429 | CDS | 6772155 | 5664 | - | 0.240643 |
DDB_G0276625 | DDB_G0276625 | belongs to the drugmetabolite transporter superfamily similar to human SLC35D1 (UDP-glucuronic acidUDP-N-acetylgalactosamine transporter) and S. cerevisiae VRG4 (GDP-mannose transporter 1) contains 8 putative transmembrane domains | DDB0232429 | CDS | 7055459 | 945 | - | 0.271958 |
DDB_G0277039 | DDB_G0277039 | DDB0232429 | CDS | 7313618 | 1260 | + | 0.246825 | |
DDB_G0277307 | DDB_G0277307 | highly similar to H. sapiens LONP1 and S. cerevisiae PIM1 Lon protease family members are often located in the mitochondria there is a second Lon protease in Dictyostelium | DDB0232429 | CDS | 7634314 | 2511 | - | 0.322979 |
DDB_G0277625 | DDB_G0277625 | DDB0232429 | CDS | 8269607 | 1263 | - | 0.278702 | |
DDB_G0277695 | DDB_G0277695 | DDB0232429 | CDS | 8344683 | 1074 | + | 0.297952 | |
DDB_G0277775 | DDB_G0277775 | DDB0232429 | CDS | 8465643 | 375 | - | 0.333333 | |
DDB_G0278063 | DDB_G0278063 | highly similar to H. sapiens LONP1 and S. cerevisiae PIM1 Lon protease family members are often located in the mitochondria there is a second Lon protease in Dictyostelium | DDB0232430 | CDS | 211823 | 2871 | + | 0.290143 |
DDB_G0278075 | DDB_G0278075 | DDB0232430 | CDS | 233703 | 699 | + | 0.271817 | |
DDB_G0278123 | DDB_G0278123 | DDB0232430 | CDS | 326427 | 222 | - | 0.405405 | |
DDB_G0278179 | DDB_G0278179 | contains two myb domains similar to Arabidopsis thaliana DNAJ heat shock N-terminal domain-containing protein (NP_187752.1) and Mus musculus zuotin related factor 2 (NP_033610.1) | DDB0232430 | CDS | 400484 | 1905 | - | 0.371129 |
DDB_G0278233 | DDB_G0278233 | DDB0232430 | CDS | 516517 | 915 | + | 0.269945 | |
DDB_G0278333 | DDB_G0278333 | DDB0232430 | CDS | 713907 | 1950 | - | 0.315385 | |
DDB_G0278435 | DDB_G0278435 | DDB0232430 | CDS | 877848 | 2661 | - | 0.269823 | |
DDB_G0278455 | DDB_G0278455 | DDB0232430 | CDS | 904324 | 1101 | - | 0.229791 | |
DDB_G0278501 | DDB_G0278501 | weakly similar to yeast transmembrane ubiquitin ligase E3 (TUL1) protein involved in ubiquitinating and sorting certain membrane proteins contains 6 predicted transmembrane domains and one additional signal sequence | DDB0232430 | CDS | 976180 | 2001 | + | 0.246877 |
DDB_G0278631 | DDB_G0278631 | putative ortholog of H. sapiens SLC35D2 UDP-N-acetylglucosamineUDP-glucoseGDP-mannose transporter contains 10 putative transmembrane domains | DDB0232430 | CDS | 462648 | 1149 | + | 0.222802 |
DDB_G0278789 | DDB_G0278789 | similar to DNAJA3 DnaJ homolog subfamily A member 3 | DDB0232430 | CDS | 1182227 | 1383 | + | 0.336226 |
DDB_G0278997 | DDB_G0278997 | conserved in bacteria and plants there is an almost identical gene | DDB0232430 | CDS | 1499624 | 876 | + | 0.270548 |
DDB_G0278999 | DDB_G0278999 | conserved in bacteria and plants there is an almost identical gene | DDB0232430 | CDS | 1501033 | 876 | + | 0.270548 |
DDB_G0279011 | DDB_G0279011 | DDB0232430 | CDS | 1513004 | 270 | - | 0.296296 | |
DDB_G0279049 | DDB_G0279049 | conserved in dictyostelids contains a predicted peroxisomal targeting signal | DDB0232430 | CDS | 1554715 | 2550 | + | 0.236863 |
DDB_G0279111 | DDB_G0279111 | DDB0232430 | CDS | 1646736 | 1122 | + | 0.251337 | |
DDB_G0279271 | DDB_G0279271 | belongs to the band 7 proteins integral membrane proteins that ares thought to regulate cation conductance stomatin is an erythrocyte membrane protein contains an N-terminal transmembrane domain that might be a signal sequence | DDB0232430 | CDS | 1870767 | 1029 | + | 0.276968 |
DDB_G0279375 | DDB_G0279375 | related to the Ovarian Tumour (OTU) gene of Drosophila function is unknown but conserved cysteine and histidine and possibly the aspartate residues suggests that those not yet recognized as peptidases could possess cysteine protease activity | DDB0232430 | CDS | 2006606 | 1023 | - | 0.250244 |
DDB_G0279491 | DDB_G0279491 | DDB0232430 | CDS | 2147617 | 1725 | - | 0.277681 | |
DDB_G0279949 | DDB_G0279949 | highly conserved protein containing an alkyl hydroperoxide reductasethiol specific antioxidantmal allergen domain | DDB0232430 | CDS | 2741741 | 456 | - | 0.307018 |
DDB_G0279951 | DDB_G0279951 | highly conserved protein containing an alkyl hydroperoxide reductasethiol specific antioxidantmal allergen domain | DDB0232430 | CDS | 2743413 | 459 | - | 0.276688 |
DDB_G0279973 | DDB_G0279973 | highly conserved protein containing an alkyl hydroperoxide reductasethiol specific antioxidantmal allergen domain | DDB0232430 | CDS | 2800822 | 459 | - | 0.296296 |
DDB_G0280089 | DDB_G0280089 | DDB0232430 | CDS | 2915769 | 1374 | - | 0.342795 | |
DDB_G0280091 | DDB_G0280091 | homolog of human UBE2H (ubiquitin-conjugating enzyme E2 H) and S. pombe ubc8 catalyzes the covalent attachment of ubiquitin to other proteins | DDB0232430 | CDS | 2919337 | 558 | - | 0.310036 |
DDB_G0280143 | DDB_G0280143 | DDB0232430 | CDS | 3004846 | 1986 | - | 0.270896 | |
DDB_G0280187 | DDB_G0280187 | similar to cathepsin Z a papain cysteine protease family protein | DDB0232430 | CDS | 3078456 | 876 | + | 0.374429 |
DDB_G0280215 | DDB_G0280215 | DDB0232430 | CDS | 3121269 | 1251 | + | 0.343725 | |
DDB_G0280227 | DDB_G0280227 | DDB0232430 | CDS | 3139657 | 1737 | - | 0.176166 | |
DDB_G0280317 | DDB_G0280317 | catalyzes the reaction RX glutathione HX R-S-glutathione | DDB0232430 | CDS | 3248423 | 615 | - | 0.284553 |
DDB_G0280347 | DDB_G0280347 | DDB0232430 | CDS | 3287782 | 378 | + | 0.306878 | |
DDB_G0280773 | DDB_G0280773 | DDB0232430 | CDS | 3724009 | 2985 | + | 0.236181 | |
DDB_G0280877 | DDB_G0280877 | DDB0232430 | CDS | 3825256 | 2100 | + | 0.261429 | |
DDB_G0280881 | DDB_G0280881 | catalyzes the reaction RX glutathione HX R-S-glutathione | DDB0232430 | CDS | 3830874 | 783 | - | 0.274585 |
DDB_G0280889 | DDB_G0280889 | DDB0232430 | CDS | 3835530 | 897 | - | 0.238573 | |
DDB_G0281081 | DDB_G0281081 | DDB0232430 | CDS | 4027472 | 1944 | + | 0.288066 | |
DDB_G0281369 | DDB_G0281369 | DDB0232430 | CDS | 4370772 | 1206 | - | 0.308458 | |
DDB_G0281521 | DDB_G0281521 | member of the bromo-AAAATPase (BRAT) class of chromatin assembly proteins | DDB0232430 | CDS | 4480305 | 5403 | - | 0.277624 |
DDB_G0281527 | DDB_G0281527 | DDB0232430 | CDS | 4520387 | 1878 | + | 0.205005 | |
DDB_G0281679 | DDB_G0281679 | DDB0232430 | CDS | 4804047 | 1176 | + | 0.244898 | |
DDB_G0281775 | DDB_G0281775 | DDB0232430 | CDS | 4948067 | 1248 | + | 0.306891 | |
DDB_G0281833 | DDB_G0281833 | DDB0232430 | CDS | 4994441 | 456 | - | 0.313596 | |
DDB_G0282215 | DDB_G0282215 | DDB0232430 | CDS | 5528630 | 1605 | - | 0.261682 | |
DDB_G0282241 | DDB_G0282241 | DDB0232430 | CDS | 5561439 | 2478 | + | 0.24778 | |
DDB_G0282267 | DDB_G0282267 | similar to FKBP-type peptidyl-prolyl isomerase which functions as a receptor for immunosuppressants in vertebrates | DDB0232430 | CDS | 5592466 | 402 | + | 0.310945 |
DDB_G0282313 | DDB_G0282313 | DDB0232430 | CDS | 5624970 | 1092 | - | 0.320513 | |
DDB_G0282463 | DDB_G0282463 | DDB0232430 | CDS | 5792759 | 2337 | + | 0.286264 | |
DDB_G0282517 | DDB_G0282517 | highly conserved protein containing an alkyl hydroperoxide reductasethiol specific antioxidantmal allergen domain | DDB0232430 | CDS | 5877016 | 726 | - | 0.316804 |
DDB_G0282783 | DDB_G0282783 | similar to a D. purpureum protein | DDB0232430 | CDS | 5921147 | 9054 | + | 0.230175 |
DDB_G0282845 | DDB_G0282845 | DDB0232430 | CDS | 6289243 | 1224 | - | 0.258987 | |
DDB_G0283033 | DDB_G0283033 | DDB0232431 | CDS | 178285 | 2304 | - | 0.268229 | |
DDB_G0283471 | DDB_G0283471 | DDB0232431 | CDS | 738038 | 6009 | - | 0.192045 | |
DDB_G0283575 | DDB_G0283575 | catalyzes the reaction RX glutathione HX R-S-glutathione enriched in prespore cells | DDB0232431 | CDS | 855359 | 597 | + | 0.303183 |
DDB_G0283655 | DDB_G0283655 | DDB0232431 | CDS | 925419 | 1524 | - | 0.224409 | |
DDB_G0283815 | DDB_G0283815 | DDB0232431 | CDS | 1148242 | 1332 | - | 0.231982 | |
DDB_G0283979 | DDB_G0283979 | DDB0232431 | CDS | 1413537 | 3600 | + | 0.265833 | |
DDB_G0284247 | DDB_G0284247 | DDB0232431 | CDS | 1749570 | 1854 | + | 0.228695 | |
DDB_G0284249 | DDB_G0284249 | putative metalloprotease of the peptidase M41 family which belong to a larger family of zinc metalloproteases includes the cell division protein FtsH and the yeast mitochondrial respiratory chain complexes assembly protein | DDB0232431 | CDS | 1751734 | 2295 | - | 0.31329 |
DDB_G0284263 | DDB_G0284263 | conserved protein ortholog of human DNAJC11 | DDB0232431 | CDS | 1795281 | 1728 | - | 0.284144 |
DDB_G0284381 | DDB_G0284381 | DDB0232431 | CDS | 1916862 | 3270 | + | 0.307951 | |
DDB_G0284627 | DDB_G0284627 | belongs to the band 7 proteins integral membrane proteins that ares thought to regulate cation conductance stomatin is an erythrocyte membrane protein contains an N-terminal transmembrane domain that might be a signal sequence | DDB0232431 | CDS | 2260399 | 1161 | - | 0.274763 |
DDB_G0284847 | DDB_G0284847 | homolog of human SDF2 (stromal cell-derived factor 2) contains 3 MIR domains | DDB0232431 | CDS | 2556090 | 639 | - | 0.317684 |
DDB_G0284939 | DDB_G0284939 | DDB0232431 | CDS | 2667885 | 396 | + | 0.282828 | |
DDB_G0284941 | DDB_G0284941 | DDB0232431 | CDS | 2668956 | 381 | + | 0.230971 | |
DDB_G0285063 | DDB_G0285063 | similar to the H. sapiens HUWE1 an E3 ubiquitin-protein ligase that mediates ubiquitination and subsequent proteasomal degradation of target proteins. | DDB0232431 | CDS | 2707152 | 11379 | - | 0.321997 |
DDB_G0285145 | DDB_G0285145 | DDB0232431 | CDS | 2915991 | 1305 | + | 0.2659 | |
DDB_G0285273 | DDB_G0285273 | highly conserved protein containing an alkyl hydroperoxide reductasethiol specific antioxidantmal allergen domain | DDB0232431 | CDS | 3047069 | 474 | + | 0.308017 |
DDB_G0285333 | DDB_G0285333 | DDB0232431 | CDS | 3097865 | 816 | - | 0.310049 | |
DDB_G0285357 | DDB_G0285357 | similar to FKBP-type peptidyl-prolyl isomerase which functions as a receptor for immunosuppressants in vertebrates | DDB0232431 | CDS | 3165268 | 1095 | - | 0.36895 |
DDB_G0285389 | DDB_G0285389 | putative ortholog of H. sapiens UXT (ubiquitously-expressed transcript) related to prefoldin alpha | DDB0232431 | CDS | 3107718 | 486 | - | 0.201646 |
DDB_G0285471 | DDB_G0285471 | belongs to the DUF836 family similar to S. cerevisiae glutaredoxin-like protein YDR286C | DDB0232431 | CDS | 3274352 | 327 | + | 0.217125 |
DDB_G0285611 | DDB_G0285611 | DDB0232431 | CDS | 3459087 | 1167 | + | 0.24593 | |
DDB_G0285613 | DDB_G0285613 | DDB0232431 | CDS | 3463966 | 1338 | + | 0.254111 | |
DDB_G0285709 | DDB_G0285709 | DDB0232431 | CDS | 3622848 | 1554 | + | 0.341055 | |
DDB_G0285765 | DDB_G0285765 | DDB0232431 | CDS | 3445107 | 2346 | - | 0.252771 | |
DDB_G0286165 | DDB_G0286165 | DDB0232431 | CDS | 4105304 | 1455 | + | 0.181443 | |
DDB_G0286341 | DDB_G0286341 | highly similar to bacterial glutathione S-transferase catalyzes the reaction RX glutathione HX R-S-glutathione | DDB0232431 | CDS | 4285901 | 975 | + | 0.300513 |
DDB_G0286401 | DDB_G0286401 | DDB0232431 | CDS | 4410583 | 1149 | - | 0.238468 | |
DDB_G0286511 | DDB_G0286511 | similar to human ubiquitin-conjugating enzyme E2 J2 (UBE2J2) and yeast ubiquitin-conjugating 6 (UBC6) | DDB0232431 | CDS | 4575968 | 726 | - | 0.311295 |
DDB_G0286765 | DDB_G0286765 | similar to BCS1 a mitochondrial chaperone required for assembly of cytochrome BC(1) complex expressed in pstA and pstO cells and in the upper and lower cups during culmination | DDB0232431 | CDS | 4940455 | 1725 | + | 0.276522 |
DDB_G0286931 | DDB_G0286931 | DDB0232431 | CDS | 5091515 | 15669 | + | 0.264535 | |
DDB_G0286955 | DDB_G0286955 | DDB0232431 | CDS | 5145533 | 1125 | - | 0.277333 | |
DDB_G0286977 | DDB_G0286977 | DDB0232431 | CDS | 5148727 | 1143 | - | 0.276465 | |
DDB_G0287077 | DDB_G0287077 | DDB0232431 | CDS | 5299968 | 1221 | + | 0.22932 | |
DDB_G0287153 | DDB_G0287153 | DDB0232431 | CDS | 5400400 | 480 | + | 0.308333 | |
DDB_G0287165 | DDB_G0287165 | similar to spastin (spastic paraplegia 4 protein) a mammalian ATP-dependent microtubule severing protein | DDB0232431 | CDS | 5420537 | 1968 | + | 0.269817 |
DDB_G0287215 | DDB_G0287215 | DDB0232432 | CDS | 3070 | 1113 | - | 0.28841 | |
DDB_G0287221 | DDB_G0287221 | similar to TRIP12 (thyroid hormone receptor interactor 12) a component of PA700 an ATP-dependent multisubunit protein that activates the proteolytic activities of the 20S proteasome | DDB0232432 | CDS | 10149 | 6294 | - | 0.317445 |
DDB_G0287225 | DDB_G0287225 | DDB0232432 | CDS | 21182 | 2106 | + | 0.195632 | |
DDB_G0287257 | DDB_G0287257 | DDB0232432 | CDS | 49910 | 1513 | - | 0.356907 | |
DDB_G0287559 | DDB_G0287559 | DDB0232432 | CDS | 419276 | 579 | - | 0.262522 | |
DDB_G0287759 | DDB_G0287759 | DDB0232432 | CDS | 662849 | 1140 | - | 0.261404 | |
DDB_G0287793 | DDB_G0287793 | similar to human GSTT2 (glutathione S-transferase theta-2) glutathione transferases participate in the detoxification of reactive electrophilic compounds by catalysing their conjugation to glutathione contains a predicted peroxisomal targeting signal | DDB0232432 | CDS | 710171 | 669 | + | 0.246637 |
DDB_G0287811 | DDB_G0287811 | DDB0232432 | CDS | 748966 | 309 | + | 0.326861 | |
DDB_G0287847 | DDB_G0287847 | DDB0232432 | CDS | 813389 | 2040 | + | 0.260294 | |
DDB_G0287851 | DDB_G0287851 | DDB0232432 | CDS | 822730 | 2889 | + | 0.317411 | |
DDB_G0288153 | DDB_G0288153 | belongs to the thioredoxin family lacks redox-active cysteines compared with many homologs so may be catalytically inactive | DDB0232432 | CDS | 1158956 | 327 | - | 0.235474 |
DDB_G0288221 | DDB_G0288221 | DDB0232432 | CDS | 1272181 | 1188 | + | 0.313131 | |
DDB_G0288265 | DDB_G0288265 | very similar to S. cerevisiae HSP10 A. thaliana CPN10 and human HSPE1 (HSP10)mitochondrial chaperonins | DDB0232432 | CDS | 1314543 | 309 | + | 0.291262 |
DDB_G0288345 | DDB_G0288345 | DDB0232432 | CDS | 1413915 | 1554 | + | 0.261261 | |
DDB_G0288363 | DDB_G0288363 | belongs to the peptidase S8 family contains a predicted signal peptide contains one EGF-like domain | DDB0232432 | CDS | 1391586 | 2037 | + | 0.311733 |
DDB_G0288381 | DDB_G0288381 | DDB0232432 | CDS | 1460823 | 1650 | - | 0.270303 | |
DDB_G0288593 | DDB_G0288593 | DDB0232432 | CDS | 1728286 | 2085 | - | 0.313669 | |
DDB_G0288595 | DDB_G0288595 | DDB0232432 | CDS | 1730911 | 1224 | + | 0.227124 | |
DDB_G0288639 | DDB_G0288639 | conserved protein DnaJ homolog subfamily C member 7 (DNAJC7) | DDB0232432 | CDS | 1756684 | 1620 | + | 0.334568 |
DDB_G0288697 | DDB_G0288697 | DDB0232432 | CDS | 1839851 | 1758 | - | 0.303185 | |
DDB_G0288849 | DDB_G0288849 | contains a predicted signal peptide and a putative C-terminal transmembrane domain similar to S. cerevisiae ERO1 (endoplasmic oxidoreductin-1) which is required for the formation of disulfide bonds in the proteins in the endoplasmic reticulum | DDB0232432 | CDS | 2057527 | 1662 | - | 0.253309 |
DDB_G0288861 | DDB_G0288861 | DDB0232432 | CDS | 1954614 | 2169 | + | 0.319963 | |
DDB_G0288999_ps | DDB_G0288999 | putative pseudogene highly conserved family containing an alkyl hydroperoxide reductasethiol specific antioxidantmal allergen domain | DDB0232432 | CDS | 2216611 | 453 | - | 0.267108 |
DDB_G0289047 | DDB_G0289047 | highly similar to bacterial ClpB expressed in prespore cells | DDB0232432 | CDS | 2299492 | 2388 | - | 0.348827 |
DDB_G0289557 | DDB_G0289557 | DDB0232432 | CDS | 2946489 | 2328 | - | 0.226804 | |
DDB_G0289991 | DDB_G0289991 | DDB0232432 | CDS | 3521273 | 1203 | - | 0.284289 | |
DDB_G0290017 | DDB_G0290017 | DDB0232432 | CDS | 3543307 | 531 | - | 0.271186 | |
DDB_G0290333 | DDB_G0290333 | belongs to the peptidase S53 family similar to P. polycephalum physarolisin contains a predicted signal peptide | DDB0232432 | CDS | 3973178 | 1797 | + | 0.413467 |
DDB_G0290433 | DDB_G0290433 | DDB0232432 | CDS | 4118281 | 4869 | - | 0.326556 | |
DDB_G0290545 | DDB_G0290545 | DDB0232432 | CDS | 4245577 | 2238 | + | 0.224754 | |
DDB_G0290547 | DDB_G0290547 | DDB0232432 | CDS | 4248317 | 444 | - | 0.34009 | |
DDB_G0290629 | DDB_G0290629 | DDB0232432 | CDS | 4394537 | 2913 | - | 0.252317 | |
DDB_G0290995 | DDB_G0290995 | DDB0232432 | CDS | 4867138 | 909 | - | 0.246425 | |
DDB_G0291191 | DDB_G0291191 | DDB0232432 | CDS | 5086072 | 1059 | - | 0.367328 | |
DDB_G0291281 | DDB_G0291281 | DDB0232433 | CDS | 48286 | 372 | + | 0.282258 | |
DDB_G0291299 | DDB_G0291299 | DDB0232433 | CDS | 80308 | 1407 | - | 0.294243 | |
DDB_G0291314 | DDB_G0291314 | highly similar to plant HSP101 expressed in prespore cells | DDB0232433 | CDS | 116087 | 2661 | + | 0.34611 |
DDB_G0291366 | DDB_G0291366 | belongs to the thioredoxin family similar to A. thaliana PRXIIF (peroxiredoxin IIF) lacks redox-active cysteine compared with many homologs so may be catalytically inactive | DDB0232433 | CDS | 184226 | 549 | - | 0.275046 |
DDB_G0292030 | DDB_G0292030 | DDB0232433 | CDS | 1049058 | 1038 | - | 0.226397 | |
DDB_G0292046 | DDB_G0292046 | DDB0232433 | CDS | 1071921 | 9723 | + | 0.246735 | |
DDB_G0292282 | DDB_G0292282 | DDB0232433 | CDS | 1385822 | 1779 | + | 0.226532 | |
DDB_G0292290 | DDB_G0292290 | DDB0232433 | CDS | 1396696 | 2310 | + | 0.237662 | |
DDB_G0292334 | DDB_G0292334 | DDB0232433 | CDS | 1502579 | 2331 | - | 0.277134 | |
DDB_G0292462 | DDB_G0292462 | DDB0232433 | CDS | 1678244 | 972 | + | 0.322016 | |
DDB_G0292710 | DDB_G0292710 | contains one PPIase cyclophilin-type domain and one RRM (RNA recognition motif) domain homolog of human PPIL4 and S. pombe cyp6 PPIase is an enzyme that accelerates protein folding by catalyzing the cis-trans isomerization of proline imidic peptide bonds in oligopeptides | DDB0232433 | CDS | 1995447 | 1470 | - | 0.278912 |
DDB_G0293122 | DDB_G0293122 | similar to human GSTT2 (glutathione S-transferase theta-2) glutathione transferases participate in the detoxification of reactive electrophilic compounds by catalysing their conjugation to glutathione | DDB0232433 | CDS | 2554630 | 660 | - | 0.237879 |
DDB_G0293154 | DDB_G0293154 | this gene belongs to the trx family of genes and is located next to | DDB0232433 | CDS | 2334087 | 153 | - | 0.30719 |
DDB_G0293328 | DDB_G0293328 | DDB0232433 | CDS | 2760211 | 396 | + | 0.39899 | |
DDB_G0293378 | DDB_G0293378 | DDB0232433 | CDS | 2818966 | 1650 | + | 0.287273 | |
DDB_G0293388 | DDB_G0293388 | putative ATP-dependent metalloprotease FtsH similar to S. cerevisiae YME1 that plays a role in mitochondrial protein metabolism | DDB0232433 | CDS | 2798298 | 2304 | - | 0.327691 |
DDB_G0293448 | DDB_G0293448 | DDB0232433 | CDS | 2875111 | 1431 | - | 0.245982 | |
DDB_G0293508 | DDB_G0293508 | DDB0232433 | CDS | 2972530 | 3108 | + | 0.287323 | |
DDB_G0293672 | DDB_G0293672 | DDB0232433 | CDS | 3242621 | 285 | + | 0.249123 | |
DDB_G0293674 | DDB_G0293674 | DDB0232433 | CDS | 3243242 | 1893 | + | 0.310618 | |
DDB_G0293678 | DDB_G0293678 | DDB0232433 | CDS | 3246808 | 1710 | + | 0.293567 | |
DDB_G0293770 | DDB_G0293770 | DDB0232433 | CDS | 3303029 | 6324 | - | 0.306293 | |
DDB_G0294635 | DDB_G0294635 | DDB0232430 | CDS | 2232590 | 2457 | + | 0.265364 | |
DDB_G0295681 | DDB_G0295681 | DDB0232430 | CDS | 32370 | 336 | + | 0.357143 | |
DDB_G0295803 | DDB_G0295803 | DDB0232433 | CDS | 1775198 | 486 | + | 0.162551 | |
DDB_G0295811 | DDB_G0295811 | DDB0232430 | CDS | 1753571 | 912 | - | 0.288377 | |
DDB_G0304475 | DDB_G0304475 | DDB0232430 | CDS | 168687 | 1329 | + | 0.320542 | |
abcB5 | DDB_G0292554 | half transporter consisting of one ABC domain and one transmembrane domain | DDB0232433 | CDS | 1786504 | 2094 | - | 0.294651 |
abcB6 | DDB_G0282931 | half transporter consisting of one ABC domain and one transmembrane domain | DDB0232431 | CDS | 9046 | 2037 | - | 0.300442 |
adprh | DDB_G0289675 | conserved enzyme catalyzes the reaction: N(omega)-(ADP-D-ribosyl)-L-arginine H(2)O ADP-ribose L-arginine reverses the reaction of mono-ADP-ribosylation | DDB0232432 | CDS | 3077727 | 1179 | - | 0.31637 |
ahsa | DDB_G0269712 | DDB0232428 | CDS | 3388870 | 1152 | - | 0.332465 | |
amfr | DDB_G0279345 | ortholog of the long isoform (isoform 2) of the human autocrine motility factor receptor a RING finger-dependent ubiquitin protein ligase (E3) of the endoplasmic reticulum that is involved in tumor invasion and metastasis contains four putative transmembrane domains and an additional signal sequence | DDB0232430 | CDS | 1961529 | 2040 | - | 0.258824 |
anapc10 | DDB_G0268992 | component of the anaphase-promoting complexcyclosome (APCC) a cell cycle-regulated ubiquitin ligase that controls progression through the cell cycle | DDB0232428 | CDS | 2080758 | 567 | + | 0.257496 |
anapc11 | DDB_G0286909 | component of the anaphase-promoting complexcyclosome (APCC) a cell cycle-regulated ubiquitin ligase that controls progression through the cell cycle | DDB0232431 | CDS | 5059870 | 264 | - | 0.348485 |
ate1 | DDB_G0269024 | ortholog of the conserved arginine-tRNA-protein transferase ATE1 involved in the post-translational conjugation of arginine to the amino termini of acceptor proteins which are then subject to degradation via the ubiquitin pathway catalyzes rhe reaction L-arginyl-tRNA protein tRNA L-arginyl-protein | DDB0232428 | CDS | 2333199 | 1890 | + | 0.230688 |
atg4-1 | DDB_G0273443 | ortholog of the conserved ATG4 cysteine protease involved in autophagy there is a second copy of this gene | DDB0232429 | CDS | 2936962 | 2238 | - | 0.272118 |
atg4-2 | DDB_G0273553 | ortholog of the conserved ATG4 cysteine protease involved in autophagy there is a second copy of this gene | DDB0232429 | CDS | 3092131 | 2238 | + | 0.272118 |
atp12 | DDB_G0292678 | DDB0232433 | CDS | 1937753 | 993 | - | 0.257805 | |
bcs1lA | DDB_G0289135 | conserved mitochondrial chaperone necessary for the assembly of mitochondrial respiratory chain complex III Dictyostelium has a second BCS1-like protein | DDB0232432 | CDS | 2391473 | 1266 | + | 0.304897 |
bcs1lB | DDB_G0291910 | conserved mitochondrial chaperone necessary for the assembly of mitochondrial respiratory chain complex III Dictyostelium has a second BCS1-like protein | DDB0232433 | CDS | 923283 | 1377 | + | 0.304285 |
cct2 | DDB_G0291358 | DDB0232433 | CDS | 177191 | 1599 | - | 0.358349 | |
cct3 | DDB_G0281741 | DDB0232430 | CDS | 4903167 | 1593 | + | 0.37602 | |
cct4 | DDB_G0292872 | DDB0232433 | CDS | 2188382 | 1602 | - | 0.373908 | |
cct5 | DDB_G0281849 | DDB0232430 | CDS | 5012149 | 1617 | + | 0.343847 | |
cct6 | DDB_G0277493 | DDB0232429 | CDS | 8001157 | 1620 | - | 0.340741 | |
cct7 | DDB_G0291225 | DDB0232433 | CDS | 201367 | 1668 | + | 0.41307 | |
cct8 | DDB_G0276233 | DDB0232429 | CDS | 6265977 | 1614 | - | 0.366791 | |
cdc6 | DDB_G0275983 | bCommunity annotation:b ortholog of cdc6 long known to be a critical member of the DNA pre-replication complex and more recently implicated in control of mitosis (see | DDB0232429 | CDS | 6146641 | 1317 | + | 0.247532 |
cdcD | DDB_G0288065 | highly conserved protein CDC48 in yeasts | DDB0232432 | CDS | 1118593 | 2382 | + | 0.398825 |
cfaD | DDB_G0281605 | related to cysteine protease C1A but has no detectable peptidase activity autocrine secreted factor that slows cell proliferation and thus has the properties of a chalone generates two products a 65 kDa and a 27 kDa peptide | DDB0232430 | CDS | 4701100 | 1596 | - | 0.379073 |
copZa | DDB_G0289523 | zeta subunit of the coatomer complex essential for the secretory pathway there is another gene encoding a zeta subunit | DDB0232432 | CDS | 2913451 | 528 | - | 0.242424 |
copZb | DDB_G0293086 | zeta subunit of the coatomer complex involved in intracellular protein transport there is another gene encoding a zeta subunit | DDB0232433 | CDS | 2460151 | 537 | + | 0.266294 |
cox10 | DDB_G0288169 | ortholog of COX10 which catalyzes the first step in the conversion of protoheme to the heme A prosthetic group required for cytochrome c oxidase activity contains seven transmembrane domains | DDB0232432 | CDS | 1175200 | 1350 | - | 0.302222 |
cox11 | DDB_G0289353 | ortholog of COX11 the mitochondrial inner membrane protein required for delivering copper to subunit 1 of cytochrome c oxidase. | DDB0232432 | CDS | 2677137 | 939 | + | 0.27263 |
coxA | DDB_G0281549 | ortholog of COX15 required for the hydroxylation of heme O to form heme A a component of cytochrome c oxidase | DDB0232430 | CDS | 4977091 | 1449 | - | 0.31539 |
cprA | DDB_G0290957 | DDB0232432 | CDS | 4812963 | 1032 | + | 0.312984 | |
cprB | DDB_G0279799 | DDB0232430 | CDS | 2569081 | 1131 | - | 0.322723 | |
cprC | DDB_G0283867 | DDB0232431 | CDS | 1092858 | 1014 | + | 0.302761 | |
cprE | DDB_G0272815 | DDB0232429 | CDS | 2212329 | 1035 | - | 0.357488 | |
cprH | DDB_G0278401 | belongs to the peptidase family C1 sub-family C1A (papain family clan CA) repressed after Legionella pneumophila infection | DDB0232430 | CDS | 822687 | 1014 | + | 0.309665 |
csn1 | DDB_G0283587 | subunit of the COP9 signalosome (CSN) a complex of the ubiquitin-proteasome pathway composed of eight subunits (CSN1-8) | DDB0232431 | CDS | 822737 | 1377 | - | 0.284677 |
csn2 | DDB_G0289361 | subunit of the COP9 signalosome (CSN) a complex of the ubiquitin-proteasome pathway composed of eight subunits (CSN1-8) | DDB0232432 | CDS | 2705143 | 1350 | + | 0.28 |
culA | DDB_G0291972 | very similar to mammalian cullin 1 (CUL1) involved in ubiquitin-mediated protein degradation which in Dictyostelium controls PKA function and regulates cell differentiation | DDB0232433 | CDS | 977829 | 2313 | - | 0.285776 |
culB | DDB_G0267384 | similar to mammalian cullin 1 and 2 (CUL1 CUL2) involved in ubiquitin-mediated protein degradation regulates prestalk cell differentiation in Dictyostelium | DDB0232428 | CDS | 551012 | 2316 | - | 0.255613 |
culC | DDB_G0284903 | very similar to mammalian cullin 3 (CUL3) acts as scaffold for ubiquitin ligases (E3) involved in ubiquitin-mediated protein degradation | DDB0232431 | CDS | 2621558 | 2310 | - | 0.290476 |
culD | DDB_G0292794 | very similar to mammalian cullin 4 (CUL4A and CUL4B) acts as scaffold for ubiquitin ligases (E3) involved in ubiquitin-mediated protein degradation | DDB0232433 | CDS | 2047275 | 2409 | - | 0.28352 |
culE | DDB_G0278991 | similar to mammalian cullin 1 2 and 5 (CUL1 CUL2 CUL5) acts as scaffold for ubiquitin ligases (E3) involved in ubiquitin-mediated protein degradation | DDB0232430 | CDS | 1485914 | 2253 | - | 0.316467 |
cypB | DDB_G0269120 | DDB0232428 | CDS | 3371521 | 594 | - | 0.33165 | |
cypD | DDB_G0280401 | DDB0232430 | CDS | 3316821 | 525 | - | 0.321905 | |
cypE | DDB_G0269216 | cyclosporin A-sensitive peptidylprolyl cis-trans isomerase binds the SKIP ortholog snwA in a cyclosporin-independent manner | DDB0232428 | CDS | 3461467 | 471 | - | 0.295117 |
ddj1 | DDB_G0280037 | DDB0232430 | CDS | 3103912 | 1236 | - | 0.394013 | |
dhps | DDB_G0285725 | catalyzes the first step in the formation of deoxyhypusine: [eIF5A]-lysine spermidine [eIF5A]-deoxyhypusine propane-13-diamine an essential post-translational modification only found in mature eIF5A factor the second reaction is catalyzed by Dohh | DDB0232431 | CDS | 3636502 | 1131 | + | 0.318302 |
dnaja1 | DDB_G0291568 | conserved molecular chaperone DnaJ homolog subfamily A member 1 | DDB0232433 | CDS | 558877 | 1380 | + | 0.365942 |
dnaja5 | DDB_G0286579 | conserved eukaryotic protein of unknown function contains DNAJ domain and two C2H2-like Zinc finger domains | DDB0232431 | CDS | 4649529 | 1902 | - | 0.268665 |
dnajc13 | DDB_G0286293 | very similar to the mammalian DnaJ homolog subfamily C member 13 required in D. melanogaster (Rme-8) for receptor-mediated endocytosis 8 | DDB0232431 | CDS | 4307439 | 7779 | - | 0.331919 |
dnajc19 | DDB_G0283735 | putative component of the PAM complex required for the ATP-dependent translocation of transit peptide-containing proteins from the inner membrane into the mitochondrial matrix defects in DNAJC19 in human cause dilated cardiomyopathy with ataxia (DCMA) contains one putative N-terminal signal sequence | DDB0232431 | CDS | 1046052 | 342 | + | 0.304094 |
dnajc3 | DDB_G0286251 | DnaJ (Hsp40) homolog subfamily C member 3 which in H. sapiens is a interferon-induced double-stranded RNA-activated protein kinase inhibitor | DDB0232431 | CDS | 4252375 | 1509 | + | 0.319417 |
dph4 | DDB_G0292980 | DDB0232433 | CDS | 2253222 | 513 | + | 0.224172 | |
drcA | DDB_G0293840 | belongs to the glutathione S-transferase superfamily catalzyes the first step in the breakdown of differentiation-inducing factor 1 | DDB0232433 | CDS | 3374878 | 828 | + | 0.270531 |
efa1G | DDB_G0282979 | component of the eukaryotic translation elongation factor EF-1 which plays a role in attaching aminoacyl-tRNAs to the ribosome | DDB0232431 | CDS | 88701 | 1233 | + | 0.400649 |
espl1 | DDB_G0290325 | caspase-like protease also called separin (ESP1) which plays a central role in sister chromosome segregation in yeastbrbr bCommunity annotation:b espl1 is highly similar to separase (aka separin) a widely-conserved peptidase which cleaves the rad21ssc1 non-SMC subunit of cohesin rings remaining at the centromere at metaphase allowing the sister chromatids to separate. Consistent with this homology espl1 is overexpressed fourfold (p6e-14) in a Dicty strain in which the retinoblastoma-like gene rblA has been disrupted. Most genes with roles in S-phase or mitosis are overexpressed in this strain and most of the overexpressed genes have identifiable cell cycle functions. espl1 also shows the developmental time course most typical of cell cycle genes.br The separase inhibitor securin conserved between yeast and humans which is broken down at the metaphaseanaphase junction under control of the spindle checkpoint is not recognizable in Dicty. Securin is also unrecognizable plants however whle | DDB0232432 | CDS | 3958340 | 7284 | - | 0.240527 |
fntA | DDB_G0283053 | catalyzes the transfer of a farnesyl group or a geranylgeranyl group via a thioether linkage (-C-S-C-) to a cysteine at or near the carboxyl terminus of the protein forms a heterodimer with the | DDB0232431 | CDS | 15565 | 969 | - | 0.28483 |
fntB | DDB_G0270948 | catalyzes the transfer of a farnesyl group or a geranylgeranyl group via a thioether linkage (-C-S-C-) to a cysteine at or near the carboxyl terminus of the protein forms a heterodimer with the | DDB0232428 | CDS | 3561059 | 1503 | + | 0.27811 |
fpaA | DDB_G0269230 | component of the SCF ubiquitin ligase complex the fpaA gene encodes a protein almost identical to that of fpaB differing in one amino acid only series of glycosylation reactions attaches a pentasaccharide chain to HyPro143 | DDB0232428 | CDS | 3989908 | 489 | - | 0.329243 |
fpaB-1 | DDB_G0273251 | component of the SCF ubiquitin ligase complex the fpaB gene encodes a protein almost identical to that of fpaA differing in one amino acid only series of glycosylation reactions attaches a pentasaccharide chain to HyPro143 there is a second copy of this gene | DDB0232429 | CDS | 2857157 | 489 | - | 0.331288 |
fpaB-2 | DDB_G0273615 | component of the SCF ubiquitin ligase complex the fpaB gene encodes a protein almost identical to that of fpaA differing in one amino acid only series of glycosylation reactions attaches a pentasaccharide chain to HyPro143 there is a second copy of this gene | DDB0232429 | CDS | 3173987 | 489 | + | 0.331288 |
gmsA | DDB_G0286015 | homologous to the Chlamydomonas reinhardtii a2gene enriched in gametes | DDB0232431 | CDS | 3951359 | 1347 | - | 0.368226 |
grp94 | DDB_G0280057 | DDB0232430 | CDS | 3124645 | 2304 | - | 0.320312 | |
grpE | DDB_G0283763 | similar to S. cerevisiae MGE1 and H. sapiens GrpE involved in protein import into mitochondria | DDB0232431 | CDS | 1238328 | 642 | - | 0.302181 |
grxA | DDB_G0290015 | DDB0232432 | CDS | 3542247 | 303 | - | 0.290429 | |
hfnA | DDB_G0283983 | contains an N-terminal filaminABP280 repeat and a C-terminal HECT (Homologous to the E6-AP Carboxyl Terminus) domain the latter common in ubiquitin ligases | DDB0232431 | CDS | 1259472 | 3363 | + | 0.223313 |
hspA | DDB_G0288181 | involved in phototaxis growth and morphogenesis and implicated in mitochondrial disease | DDB0232432 | CDS | 1238068 | 1671 | + | 0.36146 |
hspB | DDB_G0269144 | DDB0232428 | CDS | 4410084 | 1923 | - | 0.334893 | |
hspD | DDB_G0267400 | DDB0232428 | CDS | 1280990 | 2103 | - | 0.336662 | |
hspE-1 | DDB_G0273249 | there is a second copy of this gene | DDB0232429 | CDS | 2848730 | 1899 | - | 0.410742 |
hspE-2 | DDB_G0273623 | there is a second copy of this gene | DDB0232429 | CDS | 3181158 | 1899 | + | 0.410742 |
hspF-1 | DDB_G0273409 | there is a second copy of this gene | DDB0232429 | CDS | 2921093 | 702 | - | 0.237892 |
hspF-2 | DDB_G0273561 | there is a second copy of this gene | DDB0232429 | CDS | 3109992 | 702 | + | 0.237892 |
hspG1 | DDB_G0275079 | DDB0232429 | CDS | 5147676 | 549 | - | 0.20765 | |
hspG10 | DDB_G0277123 | DDB0232429 | CDS | 7585241 | 225 | + | 0.24 | |
hspG11 | DDB_G0277125 | DDB0232429 | CDS | 7588267 | 333 | + | 0.252252 | |
hspG12 | DDB_G0277491 | DDB0232429 | CDS | 7996971 | 618 | - | 0.223301 | |
hspG2 | DDB_G0276003 | DDB0232429 | CDS | 6164176 | 603 | + | 0.215589 | |
hspG3 | DDB_G0276607 | DDB0232429 | CDS | 7032092 | 684 | + | 0.238304 | |
hspG4 | DDB_G0276587 | DDB0232429 | CDS | 7028602 | 600 | + | 0.218333 | |
hspG5 | DDB_G0276875 | DDB0232429 | CDS | 7572576 | 609 | + | 0.231527 | |
hspG6 | DDB_G0276949 | DDB0232429 | CDS | 7574080 | 633 | + | 0.227488 | |
hspG7 | DDB_G0276951 | DDB0232429 | CDS | 7575967 | 624 | + | 0.24359 | |
hspG8 | DDB_G0277119 | DDB0232429 | CDS | 7578926 | 636 | + | 0.243711 | |
hspG9 | DDB_G0276953 | DDB0232429 | CDS | 7581914 | 606 | + | 0.234323 | |
hspH | DDB_G0290187 | DDB0232432 | CDS | 3818443 | 2319 | + | 0.378611 | |
hspI | DDB_G0288921 | DDB0232432 | CDS | 2124478 | 672 | - | 0.258929 | |
hspJ | DDB_G0279447 | DDB0232430 | CDS | 2061353 | 486 | - | 0.17284 | |
hspK | DDB_G0275525 | DDB0232429 | CDS | 5922492 | 540 | - | 0.3 | |
hspL | DDB_G0267668 | DDB0232428 | CDS | 537016 | 399 | + | 0.263158 | |
hspM | DDB_G0280013 | DDB0232430 | CDS | 2706627 | 480 | + | 0.1875 | |
hsp_ps | DDB_G0281581 | putative pseudogene similar to a gene family in Dictyostelium including | DDB0232430 | CDS | 4662931 | 357 | + | 0.291317 |
icmA-1 | DDB_G0272799 | prenylcysteine methyltransferase carries out carboyxl methylation of cleaved eukaryotic proteins that terminate in a CaaX motif such as NE81 (lmnB) there is a second copy of this gene | DDB0232429 | CDS | 2383418 | 714 | - | 0.303922 |
icmA-2 | DDB_G0273995 | carries out carboyxl methylation of cleaved eukaryotic proteins that terminate in a CaaX motif such as NE81 (lmnB) there is a second copy of this gene | DDB0232429 | CDS | 3647566 | 714 | + | 0.303922 |
impA | DDB_G0285455 | highly similar to FKBP-type peptidyl-prolyl isomerase which functions as a receptor for immunosuppressants in vertebrates the impA promoter is shared with and inversely regulated with dia1 during the growth-development transition | DDB0232431 | CDS | 3249271 | 585 | + | 0.324786 |
limB | DDB_G0284863 | DDB0232431 | CDS | 2691906 | 1662 | + | 0.353791 | |
maf1 | DDB_G0278673 | negative regulator of RNA polymerase III homolog of H. sapiens and S. cerevisiae MAF1 | DDB0232430 | CDS | 788140 | 837 | - | 0.259259 |
mai | DDB_G0278155 | catalyzes the reaction 4-maleylacetoacetate 4-fumarylacetoacetate | DDB0232430 | CDS | 376116 | 660 | + | 0.319697 |
mbtps1 | DDB_G0282397 | ortholog of H. sapiens MBTPS1 which catalyzes the first step in the proteolytic activation of sterol regulatory element-binding proteins (SREBPs) | DDB0232430 | CDS | 5699822 | 3996 | - | 0.287788 |
mhsp70 | DDB_G0293298 | DDB0232433 | CDS | 2761673 | 1977 | + | 0.376834 | |
msrA | DDB_G0276579 | catalyzes the reaction L-methionine thioredoxin disulfide H2O L-methionine (S)-S-oxide thioredoxin functions as a repair enzyme for proteins that have been inactivated by oxidation | DDB0232429 | CDS | 7002973 | 492 | - | 0.325203 |
msrB | DDB_G0291145 | catalyzes the reaction L-methionine oxidized thioredoxin L-methionine R-oxide reduced thioredoxin | DDB0232432 | CDS | 5047547 | 573 | + | 0.267016 |
nfu1 | DDB_G0285593 | ortholog of S. cerevisiae NFU1 involved in iron metabolism in mitochondria | DDB0232431 | CDS | 3425659 | 945 | - | 0.238095 |
nosA | DDB_G0292264 | DDB0232433 | CDS | 1472850 | 3270 | - | 0.284404 | |
nsfA | DDB_G0276153 | ATPase required for endocytosis membrane trafficking and cell motility acts as a SNAP receptor (SNARE) chaperone which binds through soluble NSF attachment proteins (SNAPs) to SNARE complexes and utilizes the energy of ATP hydrolysis to promote SNARE recycling | DDB0232429 | CDS | 6318754 | 2217 | + | 0.345963 |
nup160 | DDB_G0269502 | component of the nuclear pore complex which plays a role in RNA export | DDB0232428 | CDS | 2888658 | 5376 | + | 0.232887 |
nvl | DDB_G0282181 | DDB0232430 | CDS | 5443128 | 2604 | - | 0.300307 | |
orcA | DDB_G0283073 | DNA replication initiation is driven by a conserved six protein complex the origin recognition complex (ORC) has a role in both chromosomal replication and mating type transcriptional silencing | DDB0232431 | CDS | 182130 | 1896 | - | 0.2827 |
orcD | DDB_G0271562 | DNA replication initiation is driven by a conserved six protein complex the origin recognition complex (ORC) has a role in both chromosomal replication and mating type transcriptional silencing | DDB0232429 | CDS | 681736 | 1323 | + | 0.226757 |
pcmA | DDB_G0280979 | similar to PIMT or PCMT (L-isoaspartylD-aspartyl protein carboxyl methyltransferase or protein-L-isoaspartate (D-aspartate) O-methyltransferase) | DDB0232430 | CDS | 4356442 | 951 | + | 0.287066 |
pdi1 | DDB_G0276141 | DDB0232429 | CDS | 6548168 | 1092 | + | 0.369048 | |
pdi2 | DDB_G0291434 | DDB0232433 | CDS | 299936 | 1542 | - | 0.33463 | |
pex1 | DDB_G0289867 | ortholog of peroxin 1 AAA-family ATPase peroxin required for peroxisome biogenesis mutations in human homolog cause a variety of peroxisomal disorders | DDB0232432 | CDS | 3340420 | 3684 | + | 0.253529 |
pex4 | DDB_G0274313 | ortholog of peroxin 4 a peroxisomal ubiquitin conjugating enzyme required for peroxisomal matrix protein import and peroxisome biogenesis | DDB0232429 | CDS | 3939967 | 450 | - | 0.291111 |
pex6 | DDB_G0292788 | ortholog of peroxin 6 required for peroxisome biogenesis mutations in human homolog cause a variety of peroxisomal disorders | DDB0232433 | CDS | 2034271 | 3606 | - | 0.22518 |
pfdn1 | DDB_G0287827 | DDB0232432 | CDS | 772980 | 348 | - | 0.238506 | |
pfdn5 | DDB_G0280607 | DDB0232430 | CDS | 3564619 | 483 | + | 0.287785 | |
pfdn6 | DDB_G0286147 | DDB0232431 | CDS | 4132037 | 423 | + | 0.255319 | |
pggt1b | DDB_G0269726 | catalyzes the reaction geranylgeranyl diphosphate protein-cysteine S-geranylgeranyl-protein diphosphate | DDB0232428 | CDS | 3425762 | 1059 | - | 0.316336 |
pgpep | DDB_G0267498 | DDB0232428 | CDS | 226283 | 624 | + | 0.241987 | |
phbA | DDB_G0290123 | ortholog of the yeast Phb1p and other prohibitins that are inner mitochondrial membrane chaperones that stabilize newly synthesized proteins also suggested to play a role in cell senescence | DDB0232432 | CDS | 3692217 | 816 | - | 0.300245 |
phbB | DDB_G0284117 | ortholog of the yeast Phb2p and other prohibitins that are inner mitochondrial membrane chaperones that stabilize newly synthesized proteins also suggested to play a role in cell senescence | DDB0232431 | CDS | 1608856 | 882 | + | 0.290249 |
phlp2 | DDB_G0285433 | DDB0232431 | CDS | 3253005 | 720 | + | 0.297222 | |
phlp3 | DDB_G0293848 | DDB0232433 | CDS | 3411418 | 555 | - | 0.257658 | |
phyA | DDB_G0277759 | catalyzes the hydroxylation of Proline 143 of the Skp1 protein (FpaAFpaB) | DDB0232429 | CDS | 8457984 | 855 | + | 0.211696 |
pigK | DDB_G0285461 | DDB0232431 | CDS | 3257355 | 1341 | - | 0.266219 | |
pinA | DDB_G0268618 | DDB0232428 | CDS | 1957162 | 807 | - | 0.313507 | |
ppiA | DDB_G0282359 | DDB0232430 | CDS | 5684660 | 540 | + | 0.409259 | |
ppiD | DDB_G0283663 | ortholog of the mammalian PPID peptidyl-prolyl cis-trans isomerase (PPIase) accelerates protein folding by catalyzing the cis-trans isomerization of proline imidic peptide bonds in oligopeptides | DDB0232431 | CDS | 943186 | 1065 | + | 0.293897 |
ppiH | DDB_G0274281 | highly similar to human PPIH a snRNP-associated protein which interacts with PRP4 | DDB0232429 | CDS | 4043724 | 606 | + | 0.30198 |
ppil2 | DDB_G0284323 | DDB0232431 | CDS | 1783122 | 1845 | + | 0.266125 | |
ppil3 | DDB_G0291734 | DDB0232433 | CDS | 672553 | 486 | - | 0.281893 | |
ppwd1 | DDB_G0269054 | conserved peptidyl-prolyl isomerase and WD repeat-containing protein that might be involved in pre-mRNA processing peptidyl-prolyl cis-trans isomerase (PPIase) accelerates protein folding by catalyzing the cis-trans isomerization of proline imidic peptide bonds in oligopeptides | DDB0232428 | CDS | 1931476 | 1908 | + | 0.28826 |
prdx4 | DDB_G0274859 | expressed in prespore cells ortholog of peroxiredoxin 4 catalyzes the reaction reduced thioredoxin Hsub2subOsub2sub oxidized thioredoxin Hsub2subO | DDB0232429 | CDS | 4213176 | 1398 | + | 0.360515 |
prdx5 | DDB_G0285741 | DDB0232431 | CDS | 3255042 | 519 | + | 0.358382 | |
prtA | DDB_G0271696 | DDB0232429 | CDS | 741000 | 1536 | - | 0.288411 | |
psmA1 | DDB_G0282363 | subunit of the 20S proteasome (macropain) the endopeptidase complex involved in an ATPubiquitin-dependent nonlysosomal proteolytic pathway in eukaryotes composed of up to 28 subunits which form a highly ordered ring-shaped structure (20S ring) suppressor of tagB-stb10 | DDB0232430 | CDS | 5739737 | 747 | - | 0.309237 |
psmA2 | DDB_G0292122 | subunit of an endopeptidase complex involved in an ATPubiquitin-dependent nonlysosomal proteolytic pathway in eukaryotes composed of up to 28 subunits which form a highly ordered ring-shaped structure (20S ring) | DDB0232433 | CDS | 1227398 | 699 | + | 0.317597 |
psmA3 | DDB_G0267408 | subunit of the 20S proteasome (macropain) the endopeptidase complex involved in an ATPubiquitin-dependent nonlysosomal proteolytic pathway in eukaryotes composed of up to 28 subunits which form a highly ordered ring-shaped structure (20S ring) | DDB0232428 | CDS | 277655 | 747 | - | 0.323963 |
psmA4 | DDB_G0280969 | subunit of the 20S proteasome (macropain) the endopeptidase complex involved in an ATPubiquitin-dependent nonlysosomal proteolytic pathway in eukaryotes composed of up to 28 subunits which form a highly ordered ring-shaped structure (20S ring) | DDB0232430 | CDS | 4147505 | 753 | - | 0.335989 |
psmA5 | DDB_G0268538 | subunit of the 20S proteasome (macropain) the endopeptidase complex involved in an ATPubiquitin-dependent nonlysosomal proteolytic pathway in eukaryotes composed of up to 28 subunits which form a highly ordered ring-shaped structure (20S ring) | DDB0232428 | CDS | 1022895 | 726 | + | 0.331956 |
psmA6 | DDB_G0278847 | subunit of the 20S proteasome (macropain) the endopeptidase complex involved in an ATPubiquitin-dependent nonlysosomal proteolytic pathway in eukaryotes composed of up to 28 subunits which form a highly ordered ring-shaped structure (20S ring) | DDB0232430 | CDS | 1274786 | 753 | + | 0.330677 |
psmA7 | DDB_G0272831 | subunit of the 20S proteasome (macropain) the endopeptidase complex involved in an ATPubiquitin-dependent nonlysosomal proteolytic pathway in eukaryotes composed of up to 28 subunits which form a highly ordered ring-shaped structure (20S ring) | DDB0232429 | CDS | 2102038 | 753 | - | 0.321381 |
psmB1 | DDB_G0272969 | subunit of the 20S proteasome (macropain) the endopeptidase complex involved in an ATPubiquitin-dependent nonlysosomal proteolytic pathway in eukaryotes composed of up to 28 subunits which form a highly ordered ring-shaped structure (20S ring) | DDB0232429 | CDS | 1952612 | 711 | - | 0.322082 |
psmB2 | DDB_G0269472 | subunit of the 20S proteasome (macropain) the endopeptidase complex involved in an ATPubiquitin-dependent nonlysosomal proteolytic pathway in eukaryotes composed of up to 28 subunits which form a highly ordered ring-shaped structure (20S ring) | DDB0232428 | CDS | 2839118 | 597 | + | 0.304858 |
psmB3 | DDB_G0269772 | subunit of the 20S proteasome (macropain) the endopeptidase complex involved in an ATPubiquitin-dependent nonlysosomal proteolytic pathway in eukaryotes composed of up to 28 subunits which form a highly ordered ring-shaped structure (20S ring) | DDB0232428 | CDS | 3525818 | 618 | + | 0.317152 |
psmB4-1 | DDB_G0273163 | subunit of the 20S proteasome (macropain) the endopeptidase complex involved in an ATPubiquitin-dependent nonlysosomal proteolytic pathway in eukaryotes composed of up to 28 subunits which form a highly ordered ring-shaped structure (20S ring) there is a second copy of this gene | DDB0232429 | CDS | 2482779 | 780 | + | 0.303846 |
psmB4-2 | DDB_G0273909 | subunit of the 20S proteasome (macropain) the endopeptidase complex involved in an ATPubiquitin-dependent nonlysosomal proteolytic pathway in eukaryotes composed of up to 28 subunits which form a highly ordered ring-shaped structure (20S ring) there is a second copy of this gene | DDB0232429 | CDS | 3547766 | 780 | - | 0.303846 |
psmB5 | DDB_G0293784 | subunit of the 20S proteasome (macropain) the endopeptidase complex involved in an ATPubiquitin-dependent nonlysosomal proteolytic pathway in eukaryotes composed of up to 28 subunits which form a highly ordered ring-shaped structure (20S ring) | DDB0232433 | CDS | 3275662 | 819 | - | 0.328449 |
psmB6 | DDB_G0267390 | subunit of the 20S proteasome (macropain) the endopeptidase complex involved in an ATPubiquitin-dependent nonlysosomal proteolytic pathway in eukaryotes composed of up to 28 subunits which form a highly ordered ring-shaped structure (20S ring) shift of Dictyostelium cells from the proliferative to differentiated state highly expressed during the early stage of differentiation | DDB0232428 | CDS | 487456 | 645 | - | 0.339535 |
psmB7 | DDB_G0283679 | subunit of the 20S proteasome (macropain) the endopeptidase complex involved in an ATPubiquitin-dependent nonlysosomal proteolytic pathway in eukaryotes composed of up to 28 subunits which form a highly ordered ring-shaped structure (20S ring) | DDB0232431 | CDS | 967091 | 801 | - | 0.340824 |
psmC1 | DDB_G0270784 | ATPase subunit and regulatory subcomplex of the 26S proteasome TAT binding protein homolog involved in growth and morphogenesis | DDB0232428 | CDS | 4684536 | 1320 | - | 0.37197 |
psmC2 | DDB_G0276917 | DDB0232429 | CDS | 7234040 | 1287 | - | 0.367521 | |
psmC3 | DDB_G0284415 | DDB0232431 | CDS | 1968066 | 1266 | + | 0.347551 | |
psmC4 | DDB_G0289003 | ATPase subunit and regulatory subcomplex of the 26S proteasome developmentally regulated TAT binding protein homolog | DDB0232432 | CDS | 2227887 | 1212 | + | 0.326733 |
psmC5 | DDB_G0292382 | ATPase subunit and regulatory subcomplex of the 26S proteasome developmentally regulated TAT binding protein homolog | DDB0232433 | CDS | 1673522 | 1212 | - | 0.334158 |
psmC6 | DDB_G0284517 | DDB0232431 | CDS | 2090141 | 1182 | + | 0.335871 | |
psmD1 | DDB_G0287953 | DDB0232432 | CDS | 881632 | 2928 | - | 0.35929 | |
psmD11 | DDB_G0281315 | DDB0232430 | CDS | 4153223 | 1242 | + | 0.274557 | |
psmD12 | DDB_G0281051 | DDB0232430 | CDS | 3979792 | 1344 | + | 0.284226 | |
psmD2 | DDB_G0293752 | DDB0232433 | CDS | 3279468 | 2682 | + | 0.346383 | |
psmD4 | DDB_G0275775 | contains one von Willebrand factor type A (VWFA) domain and two ubiquitin interacting motifs | DDB0232429 | CDS | 5689186 | 1050 | + | 0.32381 |
psmD6 | DDB_G0270188 | DDB0232428 | CDS | 4382128 | 1149 | + | 0.278503 | |
rabggta | DDB_G0269570 | catalyzes the transfer of a geranyl-geranyl moiety from geranyl-geranyl pyrophosphate to both cysteines in Rab proteins with an -XXCC -XCXC and -CCXX C-terminal forms a hetero-dimer with the | DDB0232428 | CDS | 3019090 | 936 | + | 0.244658 |
rabggtb | DDB_G0290671 | catalyzes the transfer of a geranyl-geranyl moiety from geranyl-geranyl pyrophosphate to both cysteines in Rab proteins with an -XXCC -XCXC and -CCXX C-terminal forms a hetero-dimer with the | DDB0232432 | CDS | 4317912 | 1020 | + | 0.281373 |
rad6 | DDB_G0275787 | RAD6 homolog an E2 ubiquitin-conjugating enzyme involved in postreplication repair forms a heterodimer with RAD18 | DDB0232429 | CDS | 5646909 | 456 | + | 0.350877 |
rbx1 | DDB_G0287629 | DDB0232432 | CDS | 496993 | 315 | + | 0.342857 | |
rcaA | DDB_G0272120 | DDB0232429 | CDS | 1622396 | 2535 | - | 0.341617 | |
spyA | DDB_G0285263 | CAZy family GT41 contains 7 TPRs (Tetratrico Peptide Repeats) | DDB0232431 | CDS | 3029506 | 2595 | - | 0.246243 |
sumo | DDB_G0286189 | sumoylates the MAP kinase kinase Mek1 (mekA) sumoylation is involved in cellular translocation after cAMP stimulation and activation of the kinase | DDB0232431 | CDS | 4217038 | 297 | + | 0.356902 |
tbcD | DDB_G0268516 | DDB0232428 | CDS | 802089 | 4443 | + | 0.238352 | |
tcp1 | DDB_G0269190 | DDB0232428 | CDS | 4885046 | 1647 | + | 0.364299 | |
timm22 | DDB_G0283865 | DDB0232431 | CDS | 1077530 | 537 | - | 0.340782 | |
tpp1 | DDB_G0269914 | ortholog of CLN2TPP1 contains a predicted signal peptide enriched in prespore cells | DDB0232428 | CDS | 3852049 | 1803 | - | 0.32335 |
trap1 | DDB_G0276947 | similar to metazoan TRAP1 member of the HSP90 family translocates to mitochondria during the prestarvation response | DDB0232429 | CDS | 7541980 | 2136 | + | 0.309457 |
trrA | DDB_G0280815 | catalyzes the reaction thioredoxin NADP thioredoxin disulfide NADPH H | DDB0232430 | CDS | 3775563 | 960 | - | 0.377083 |
trxC | DDB_G0294489 | small disulphide-containing redox protein that serves as a general protein disulphide oxidoreductase up-regulated at 6 hr developmental stage | DDB0232433 | CDS | 2335005 | 315 | - | 0.32381 |
trxD | DDB_G0287849 | DDB0232432 | CDS | 820586 | 315 | - | 0.260317 | |
trxE | DDB_G0287227 | DDB0232432 | CDS | 23737 | 318 | + | 0.393082 | |
txnl4a | DDB_G0275407 | DDB0232429 | CDS | 5420626 | 426 | - | 0.300469 | |
ubc9 | DDB_G0287693 | DDB0232432 | CDS | 688286 | 480 | - | 0.33125 | |
ubcB | DDB_G0284865 | high similarity to E2ubiquitin-conjugating enzymes from yeast metazoans and plants ubiquitin-conjugating enzymes (EC: 6.3.2.19) (UBC or E2 enzymes) catalyze the covalent attachment of ubiquitin to target proteins | DDB0232431 | CDS | 2571519 | 447 | - | 0.340045 |
ubcC | DDB_G0284009 | DDB0232431 | CDS | 1428069 | 708 | + | 0.310734 | |
ube2c | DDB_G0278775 | putative ortholog of S. pombe ubc11 and H. sapiens UBE2C involved in the destruction of cyclins during mitosisbrbr bCommunity annotation:b A role of this gene in cell cycle progression is supported by its sevenfold overexpression in a Dicty strain lacking the Dicty retinoblastoma like gene | DDB0232430 | CDS | 1152307 | 462 | + | 0.30303 |
ube2m | DDB_G0281725 | DDB0232430 | CDS | 4883727 | 693 | + | 0.314574 | |
ube2n | DDB_G0277267 | DDB0232429 | CDS | 7854255 | 465 | + | 0.344086 | |
ube2s | DDB_G0289021 | DDB0232432 | CDS | 2250572 | 648 | + | 0.290123 | |
ube2t | DDB_G0291199 | interacts with the Fanconi anaemia complex involved DNA cross-link repair null mutant is sensitive to DNA damaging agents brbr the mammalian Fanconi anaemia nuclear complex includes FANC A B C E F G L and M the FA complex interacts with ube2t a E2 ubiquitin-conjugating enzyme to monoubiquitinate FANCD2 and FANCI. Ubiquinated FANCD2 and FANCI form a complex that colocalizes at sites of DNA damage with the FANCJ helicase as well as FANCN and FANCD1 Dictyostelium has orthologs for | DDB0232432 | CDS | 5123925 | 879 | - | 0.246871 |
ube2v | DDB_G0292596 | DDB0232433 | CDS | 1823383 | 417 | - | 0.290168 | |
ube2w | DDB_G0268938 | conserved E2 ubiquitin-conjugating protein which catalyzes the covalent attachment of ubiquitin to other proteins | DDB0232428 | CDS | 1961102 | 450 | + | 0.317778 |
ube3a | DDB_G0290179 | DDB0232432 | CDS | 3742663 | 2163 | - | 0.273694 | |
ubpA | DDB_G0291239 | DDB0232433 | CDS | 283328 | 2514 | + | 0.333731 | |
ubpB | DDB_G0275021 | ubiquitin carboxyl-terminal hydrolase shown to deubiquinate mkkA putative ortholog of H. sapiens USP10 | DDB0232429 | CDS | 5178139 | 1356 | + | 0.286136 |
uduE | DDB_G0277099 | upregulated in the uninfected | DDB0232429 | CDS | 7502309 | 294 | - | 0.227891 |
ufd1 | DDB_G0271122 | similar to S. cerevisiae UDF1 together with npl4 and cdcD involved in recognition of polyubiquitinated proteins and their presentation to the 26S proteasome for degradation | DDB0232429 | CDS | 33552 | 993 | - | 0.288016 |
urm1 | DDB_G0283737 | homolog of human and S. cerevisiae URM1 yeast URM1 is involved in tRNA modification and is alsoindirectly involved in oxidative stress response and regulation of budding and haploid invasive growth | DDB0232431 | CDS | 1046828 | 291 | - | 0.261168 |
usp12 | DDB_G0290453 | DDB0232432 | CDS | 4071585 | 1428 | - | 0.226891 | |
usp14 | DDB_G0271264 | DDB0232429 | CDS | 183660 | 1539 | + | 0.302794 | |
usp39 | DDB_G0278929 | similar to Arabidopsis thaliana ubiquitin carboxyl-terminal hydrolase family protein ortholog of yeast SAD1 which plays a role in pre-mRNA splicing | DDB0232430 | CDS | 1417023 | 2157 | + | 0.236439 |
usp40 | DDB_G0289611 | DDB0232432 | CDS | 3021100 | 5034 | - | 0.283472 | |
usp7 | DDB_G0276443 | DDB0232429 | CDS | 6959828 | 3921 | - | 0.263453 | |
v4-7 | DDB_G0281823 | DDB0232430 | CDS | 5023432 | 2109 | - | 0.373637 | |
vacA | DDB_G0289485 | DDB0232432 | CDS | 2888908 | 1797 | + | 0.341681 | |
vacB | DDB_G0279191 | marker of the post-lysosomal vacuole plays a role late in the endocytic pathway may target the vacuole for exocytosis | DDB0232430 | CDS | 1911215 | 1779 | + | 0.323215 |
vacC | DDB_G0279307 | very similar to Dictyostelium vacuolin A and B | DDB0232430 | CDS | 1908644 | 1761 | + | 0.319137 |
vps4 | DDB_G0284347 | DDB0232431 | CDS | 1865073 | 1335 | + | 0.326592 | |
yod1 | DDB_G0271346 | DDB0232429 | CDS | 66274 | 978 | + | 0.284254 | |
zmpste24 | DDB_G0290849 | proteolytically removes the C-terminal three residues of farnesylated proteins contains 6 putative transmembrane domains and an additional signal peptide | DDB0232432 | CDS | 4673270 | 1281 | - | 0.251366 |