Gene list
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COG category: Inorganic ion transport and metabolism
Organism: Dictyostelium discoideum AX4, AX4
Number of genes found: 155
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_G0267698 | DDB_G0267698 | DDB0232428 | CDS | 623530 | 372 | - | 0.284946 | |
DDB_G0267824 | DDB_G0267824 | DDB0232428 | CDS | 922136 | 1509 | - | 0.266402 | |
DDB_G0267924 | DDB_G0267924 | catalyzes the reaction ATP Hsub2subO Nasupsupn Ksupsupout ADP phosphate Nasupsupout Ksupsupn br contains 10 transmembrane domains | DDB0232428 | CDS | 1128799 | 3330 | + | 0.331231 |
DDB_G0268060 | DDB_G0268060 | DDB0232428 | CDS | 1380972 | 2445 | - | 0.312883 | |
DDB_G0268074 | DDB_G0268074 | DDB0232428 | CDS | 1408319 | 2991 | - | 0.251755 | |
DDB_G0268230 | DDB_G0268230 | DDB0232428 | CDS | 1727069 | 1764 | + | 0.265306 | |
DDB_G0268810 | DDB_G0268810 | ortholog of bacterial Mgsup2sup transporter mgtA contains eight transmembrane domains | DDB0232428 | CDS | 2146485 | 2865 | + | 0.339965 |
DDB_G0269332 | DDB_G0269332 | belongs to a family of zinc transporters that are integral membrane proteins which are found to increase tolerance to divalent metal ions contains 6 putative transmembrane domains | DDB0232428 | CDS | 2554441 | 1845 | + | 0.280217 |
DDB_G0269380 | DDB_G0269380 | P-type ATPase (E1-E2) highly similar to human ATP8A1 believed to be involved in the transport of aminophospholipids | DDB0232428 | CDS | 2645714 | 3942 | - | 0.348554 |
DDB_G0269590 | DDB_G0269590 | DDB0232428 | CDS | 3078895 | 4161 | - | 0.280221 | |
DDB_G0269964 | DDB_G0269964 | DDB0232428 | CDS | 3938864 | 1998 | + | 0.285285 | |
DDB_G0270284 | DDB_G0270284 | contains an N-terminal DOMON domain as it occurs in dopamine beta-monooxygenases the Dictyostelium protein is followed by a cytochrome b561 domain which contains 5 putative transmembrane regions in addition the protein contains a putative signal peptide | DDB0232428 | CDS | 4579488 | 1173 | + | 0.277067 |
DDB_G0270304 | DDB_G0270304 | DDB0232428 | CDS | 4607306 | 630 | - | 0.284127 | |
DDB_G0270720 | DDB_G0270720 | DDB0232428 | CDS | 4125800 | 1560 | + | 0.239744 | |
DDB_G0272192 | DDB_G0272192 | DDB0232429 | CDS | 1412468 | 1497 | + | 0.329993 | |
DDB_G0273083 | DDB_G0273083 | member of the Dyp-type peroxidase family lacking a typical heme-binding region does not appear to be present in higher organisms there is a second copy of this gene | DDB0232429 | CDS | 2623576 | 921 | - | 0.334419 |
DDB_G0273195 | DDB_G0273195 | member of the major facilitator superfamily (MFS) expressed in upper cup during culmination there is a second copy of this gene | DDB0232429 | CDS | 2690707 | 1764 | - | 0.294218 |
DDB_G0273235 | DDB_G0273235 | contains 8 transmembrane domains there is a second copy of this gene | DDB0232429 | CDS | 2765356 | 3843 | - | 0.284934 |
DDB_G0273675 | DDB_G0273675 | contains eight transmembrane domains there is a second copy of this gene | DDB0232429 | CDS | 3262518 | 3843 | + | 0.284934 |
DDB_G0273735 | DDB_G0273735 | member of the major facilitator superfamily (MFS) expressed in upper cup during culmination there is a second copy of this gene | DDB0232429 | CDS | 3339316 | 1764 | + | 0.294218 |
DDB_G0273789 | DDB_G0273789 | member of the Dyp-type peroxidase family lacking a typical heme-binding region does not appear to be present in higher organisms there is a second copy of this gene | DDB0232429 | CDS | 3407290 | 921 | + | 0.334419 |
DDB_G0274547 | DDB_G0274547 | DDB0232429 | CDS | 4197500 | 1554 | + | 0.279923 | |
DDB_G0274643 | DDB_G0274643 | DDB0232429 | CDS | 4531583 | 855 | + | 0.352047 | |
DDB_G0274807 | DDB_G0274807 | DDB0232429 | CDS | 3946871 | 1851 | - | 0.222582 | |
DDB_G0275169 | DDB_G0275169 | DDB0232429 | CDS | 5084018 | 3873 | + | 0.268009 | |
DDB_G0275343 | DDB_G0275343 | DDB0232429 | CDS | 5393905 | 1638 | - | 0.234432 | |
DDB_G0275535 | DDB_G0275535 | DDB0232429 | CDS | 5868742 | 3477 | + | 0.300546 | |
DDB_G0275871 | DDB_G0275871 | DDB0232429 | CDS | 5796327 | 3492 | - | 0.286655 | |
DDB_G0276293 | DDB_G0276293 | DDB0232429 | CDS | 6559102 | 1473 | - | 0.304141 | |
DDB_G0276375 | DDB_G0276375 | DDB0232429 | CDS | 6671139 | 3804 | - | 0.226078 | |
DDB_G0276429 | DDB_G0276429 | DDB0232429 | CDS | 6932540 | 1422 | - | 0.270042 | |
DDB_G0276541 | DDB_G0276541 | DDB0232429 | CDS | 6819663 | 5490 | - | 0.298725 | |
DDB_G0276663 | DDB_G0276663 | DDB0232429 | CDS | 7094813 | 2835 | - | 0.292064 | |
DDB_G0277167 | DDB_G0277167 | DDB0232429 | CDS | 7668593 | 1392 | + | 0.257902 | |
DDB_G0277349 | DDB_G0277349 | DDB0232429 | CDS | 7803232 | 759 | - | 0.310935 | |
DDB_G0278047 | DDB_G0278047 | DDB0232430 | CDS | 191972 | 1164 | - | 0.285223 | |
DDB_G0278059 | DDB_G0278059 | similar to the human acetyl-coenzyme A transporter 1 contains 10 putative transmembrane domains | DDB0232430 | CDS | 207407 | 1857 | - | 0.234787 |
DDB_G0278265 | DDB_G0278265 | DDB0232430 | CDS | 581627 | 1983 | + | 0.252647 | |
DDB_G0278369 | DDB_G0278369 | DDB0232430 | CDS | 768975 | 1170 | + | 0.22735 | |
DDB_G0278675 | DDB_G0278675 | DDB0232430 | CDS | 789665 | 1752 | - | 0.261986 | |
DDB_G0279275 | DDB_G0279275 | DDB0232430 | CDS | 1874332 | 1704 | + | 0.286385 | |
DDB_G0279943 | DDB_G0279943 | belongs to the major facilitator superefamily contains 12 putative transmembrane domains | DDB0232430 | CDS | 2721717 | 1488 | - | 0.309812 |
DDB_G0281155 | DDB_G0281155 | putative sugar transporter contains 12 putative transmembrane domains | DDB0232430 | CDS | 4113808 | 1614 | + | 0.29368 |
DDB_G0281401 | DDB_G0281401 | DDB0232430 | CDS | 4429232 | 3771 | + | 0.307611 | |
DDB_G0281643 | DDB_G0281643 | DDB0232430 | CDS | 4751182 | 2787 | + | 0.22605 | |
DDB_G0282067 | DDB_G0282067 | belongs to a family of zinc transporters that are integral membrane proteins which are found to increase tolerance to divalent metal ions contains 6 putative transmembrane domains | DDB0232430 | CDS | 5363274 | 1722 | - | 0.349013 |
DDB_G0282285 | DDB_G0282285 | DDB0232430 | CDS | 5511594 | 1578 | - | 0.247148 | |
DDB_G0282311 | DDB_G0282311 | DDB0232430 | CDS | 5621318 | 1992 | + | 0.314759 | |
DDB_G0282945 | DDB_G0282945 | DDB0232431 | CDS | 31559 | 2010 | - | 0.280597 | |
DDB_G0282959 | DDB_G0282959 | DDB0232431 | CDS | 52235 | 4611 | + | 0.25591 | |
DDB_G0283191 | DDB_G0283191 | DDB0232431 | CDS | 394762 | 1695 | + | 0.277286 | |
DDB_G0283629 | DDB_G0283629 | belongs to a family of zinc transporters that are integral membrane proteins which are found to increase tolerance to divalent metal ions contains 6 putative transmembrane domains | DDB0232431 | CDS | 885727 | 1632 | - | 0.321691 |
DDB_G0283985 | DDB_G0283985 | DDB0232431 | CDS | 1263489 | 1608 | + | 0.250622 | |
DDB_G0284605 | DDB_G0284605 | conserved plasma membrane calcium ATPases (PMCA) similar to Dictyostelium PAT1 contains 10 predicted transmembrane domains | DDB0232431 | CDS | 2214347 | 2784 | + | 0.354526 |
DDB_G0284849 | DDB_G0284849 | DDB0232431 | CDS | 2557758 | 3561 | + | 0.298512 | |
DDB_G0284955 | DDB_G0284955 | DDB0232431 | CDS | 2684549 | 4602 | - | 0.27488 | |
DDB_G0285079 | DDB_G0285079 | DDB0232431 | CDS | 2802048 | 603 | + | 0.296849 | |
DDB_G0285511 | DDB_G0285511 | DDB0232431 | CDS | 3331170 | 1683 | - | 0.322638 | |
DDB_G0285541 | DDB_G0285541 | putative family member of integral membrane proteins that are found to increase tolerance to divalent metal ions such as cadmium zinc and cobalt contains 5 predicted transmembrane domains | DDB0232431 | CDS | 3356593 | 1305 | - | 0.314176 |
DDB_G0286043 | DDB_G0286043 | DDB0232431 | CDS | 3989629 | 1887 | + | 0.225755 | |
DDB_G0286611 | DDB_G0286611 | DDB0232431 | CDS | 4704484 | 3666 | - | 0.267321 | |
DDB_G0286639 | DDB_G0286639 | DDB0232431 | CDS | 4771485 | 1107 | - | 0.307136 | |
DDB_G0286727 | DDB_G0286727 | similar to ChaC proteins thought to be associated with the putative ChaA calciumhydrogen cation transport protein in E. coli but with a PUA RNA binding domain fused at the carboxyl terminus | DDB0232431 | CDS | 4900621 | 969 | - | 0.330237 |
DDB_G0286763 | DDB_G0286763 | DDB0232431 | CDS | 4937865 | 1977 | - | 0.195245 | |
DDB_G0286891 | DDB_G0286891 | DDB0232431 | CDS | 5031762 | 3546 | + | 0.227862 | |
DDB_G0286979 | DDB_G0286979 | DDB0232431 | CDS | 5150412 | 1884 | - | 0.277601 | |
DDB_G0287843 | DDB_G0287843 | DDB0232432 | CDS | 806278 | 1923 | - | 0.333853 | |
DDB_G0288055 | DDB_G0288055 | belongs to a family of conserved potassium transporters in bacteria yeast and plants overexpressed in | DDB0232432 | CDS | 929613 | 2151 | - | 0.317992 |
DDB_G0288535 | DDB_G0288535 | DDB0232432 | CDS | 1660756 | 1395 | - | 0.235842 | |
DDB_G0289143 | DDB_G0289143 | contains 11 putative transmembrane domains similar to D. purpureum protein | DDB0232432 | CDS | 2407681 | 1719 | + | 0.285049 |
DDB_G0289473 | DDB_G0289473 | ortholog of the conserved plasma membrane calcium ATPases (PMCA) such as Dictyostelium PAT1 contains at least 8 predicted transmembrane domains | DDB0232432 | CDS | 2830601 | 3234 | - | 0.310761 |
DDB_G0289621 | DDB_G0289621 | DDB0232432 | CDS | 3043521 | 714 | + | 0.317927 | |
DDB_G0289703 | DDB_G0289703 | DDB0232432 | CDS | 3127157 | 2931 | + | 0.247015 | |
DDB_G0289985 | DDB_G0289985 | similar to human protein KIAA0195 a transmembrane protein contains 8 putative transmembrane domains | DDB0232432 | CDS | 3471284 | 5832 | - | 0.290123 |
DDB_G0290423 | DDB_G0290423 | DDB0232432 | CDS | 4067949 | 1743 | + | 0.242111 | |
DDB_G0291029 | DDB_G0291029 | catalyzes the reaction SOsub4subsup2-sup ATP APS pyrophosphate | DDB0232432 | CDS | 4928744 | 1767 | - | 0.367289 |
DDB_G0291141 | DDB_G0291141 | belongs to a family of zinc transporters that are integral membrane proteins which are found to increase tolerance to divalent metal ions contains 15 putative transmembrane domains | DDB0232432 | CDS | 5043001 | 2313 | + | 0.278859 |
DDB_G0291384 | DDB_G0291384 | DDB0232433 | CDS | 226725 | 1878 | + | 0.256124 | |
DDB_G0291720 | DDB_G0291720 | DDB0232433 | CDS | 721305 | 1278 | - | 0.311424 | |
DDB_G0291722 | DDB_G0291722 | DDB0232433 | CDS | 719367 | 1344 | - | 0.233631 | |
DDB_G0291758 | DDB_G0291758 | DDB0232433 | CDS | 697440 | 1194 | + | 0.273869 | |
DDB_G0291816 | DDB_G0291816 | DDB0232433 | CDS | 805833 | 1002 | - | 0.313373 | |
DDB_G0291824 | DDB_G0291824 | DDB0232433 | CDS | 827281 | 1878 | - | 0.300319 | |
DDB_G0292412 | DDB_G0292412 | similar to S. cerevisiae and S. pombe TRK1 and TRK2 potassium transporters contains 9 predicted transmembrane domains | DDB0232433 | CDS | 1563103 | 1947 | - | 0.260401 |
DDB_G0292432 | DDB_G0292432 | DDB0232433 | CDS | 1610862 | 1815 | - | 0.293113 | |
alg9 | DDB_G0279349 | CAZy family GT22 catalyzes N-linked mannosylation | DDB0232430 | CDS | 1972184 | 1950 | + | 0.232308 |
alp | DDB_G0278495 | catalyzes the reaction a phosphate monoester Hsub2subO an alcohol phosphate exhibits a punctate pattern in immunoflourescence that most likely represents vesicles enzymatic activity is developmentally regulated in a cell type-specific manner | DDB0232430 | CDS | 968065 | 1680 | - | 0.380952 |
amtA | DDB_G0277503 | DDB0232429 | CDS | 8112427 | 1392 | - | 0.35704 | |
amtB | DDB_G0277889 | similar to Arabidopsis AMT1 involved in transporting ammonia in the environment into the cell contains 11 transmembrane domains | DDB0232430 | CDS | 276805 | 1296 | + | 0.364198 |
amtC | DDB_G0267424 | similar to Arabidopsis AMT1 involved in transporting ammonia in the environment into the cell contains 11 transmembrane domains | DDB0232428 | CDS | 1034624 | 1296 | + | 0.350309 |
arsA | DDB_G0293528 | homologous to bacterial genes that are involved in the transport of arsenate selenate and other anionic compounds outside the cell | DDB0232433 | CDS | 3193289 | 990 | - | 0.285859 |
arsB | DDB_G0289879 | has two putative transmembrane domains bacterial homolog associates with ArsA to transport arsenate selenate and other anionic compounds outside the cell | DDB0232432 | CDS | 3431951 | 1692 | + | 0.253546 |
atox1 | DDB_G0284221 | DDB0232431 | CDS | 1705613 | 204 | - | 0.289216 | |
atp7a | DDB_G0284141 | DDB0232431 | CDS | 1486936 | 2958 | - | 0.315416 | |
atp9b | DDB_G0270870 | P-type ATPase (E1-E2) ortholog of human ATP9B and yeast NEO1 which is involved in transport from the Golgi to the ER | DDB0232428 | CDS | 2777615 | 3588 | + | 0.298495 |
cahA | DDB_G0269106 | DDB0232428 | CDS | 4712273 | 831 | + | 0.34657 | |
catA | DDB_G0274595 | catalyzes the reaction 2Hsub2subOsub2sub catalase 2Hsub2subO Osub2sub expressed throughout development expression restricted to prestalk cells during post-aggregationbr bNomenclature conflict:b Do not confuse the acrA gene encoding the late development adenylate cyclase ACR with the genetic locus acrA corresponding to the catA catalase that confers resistance to acriflavin ( | DDB0232429 | CDS | 3823148 | 1491 | + | 0.380952 |
cax1 | DDB_G0279301 | contains 13 transmembrane domains transports Ca2 or other cations using the gradient of H or Na generated by energy-coupled primary transporters | DDB0232430 | CDS | 1901303 | 2340 | + | 0.29188 |
clcA | DDB_G0294096 | CLC chloride channels are conserved from prokaryotes to mammals where they play broad physiological roles they assemble to form homo-dimers br bNomenclature conflict:b Do not confuse this gene with clc also known as clcA encoding the clathrin light chain | DDB0232429 | CDS | 435997 | 2592 | + | 0.328318 |
clcB | DDB_G0276865 | CLC chloride channels are conserved from prokaryotes to mammals where they play broad physiological roles they assemble to form homo-dimers | DDB0232429 | CDS | 7525349 | 2448 | - | 0.280637 |
clcC | DDB_G0276229 | CLC chloride channels are conserved from prokaryotes to mammals where they play broad physiological roles they assemble to form homo-dimers | DDB0232429 | CDS | 6228081 | 2274 | + | 0.311785 |
clcD | DDB_G0278639 | CLC chloride channels are conserved from prokaryotes to mammals where they play broad physiological roles they assemble to form homo-dimers | DDB0232430 | CDS | 535599 | 3003 | - | 0.360972 |
clcE | DDB_G0286491 | CLC chloride channels are conserved from prokaryotes to mammals where they play broad physiological roles they assemble to form homo-dimers | DDB0232431 | CDS | 4560350 | 2985 | + | 0.283417 |
clcF | DDB_G0293130 | CLC chloride channels are conserved from prokaryotes to mammals where they play broad physiological roles they assemble to form homo-dimers | DDB0232433 | CDS | 2574912 | 2430 | + | 0.295885 |
cln3 | DDB_G0291157 | ortholog of Cln3 responsible for Batten's disease a juvenile neurological disorder | DDB0232432 | CDS | 5060161 | 1266 | - | 0.313586 |
comD | DDB_G0283345 | similar to drug resistance transporters contains 14 transmembrane domains | DDB0232431 | CDS | 539820 | 3528 | + | 0.291667 |
ctaA | DDB_G0293004 | DDB0232433 | CDS | 2385585 | 3897 | - | 0.308442 | |
cutc | DDB_G0287539 | DDB0232432 | CDS | 396188 | 843 | - | 0.269276 | |
fmoA | DDB_G0289779 | belongs to the fmo family similar to flavin-containing monooxygenases from a variety of eukaryotes involved in the metabolism of xenobiotic compounds | DDB0232432 | CDS | 3265452 | 1578 | - | 0.255387 |
fmoB | DDB_G0271660 | belongs to the fmo family similar to flavin-containing monooxygenases from a variety of eukaryotes involved in the metabolism of xenobiotic compounds | DDB0232429 | CDS | 685414 | 1539 | - | 0.237167 |
fmoC | DDB_G0289605 | belongs to the fmo family similar to flavin-containing monooxygenases from a variety of eukaryotes involved in the metabolism of xenobiotic compounds | DDB0232432 | CDS | 3016817 | 1566 | - | 0.244572 |
fmoD | DDB_G0289929 | belongs to the fmo family similar to flavin-containing monooxygenases from a variety of eukaryotes involved in the metabolism of xenobiotic compounds | DDB0232432 | CDS | 3451742 | 1683 | + | 0.250743 |
fmoE | DDB_G0289931 | belongs to the fmo family similar to flavin-containing monooxygenases from a variety of eukaryotes involved in the metabolism of xenobiotic compounds | DDB0232432 | CDS | 3453668 | 1614 | + | 0.245973 |
fmoF | DDB_G0289927 | belongs to the fmo family similar to flavin-containing monooxygenases from a variety of eukaryotes involved in the metabolism of xenobiotic compounds | DDB0232432 | CDS | 3449477 | 1590 | + | 0.255346 |
fmoG | DDB_G0289925 | DDB0232432 | CDS | 3446671 | 1611 | + | 0.248293 | |
fslB | DDB_G0270730 | similar to the G-protein coupled receptors contains 7 putative transmembrane domains and a potential signal sequence | DDB0232428 | CDS | 4235323 | 1929 | - | 0.258683 |
fxn | DDB_G0293246 | yeast and human orthologs regulates mitochondrial iron accumulation mutations in human homolog cause Friedrich's ataxia | DDB0232433 | CDS | 2633195 | 582 | - | 0.261168 |
hatA | DDB_G0282141 | histidine-rich pH-dependent actin binding protein N-terminal myristoylation | DDB0232430 | CDS | 5481850 | 357 | + | 0.420168 |
ionA | DDB_G0277269 | expressed in pstAB cells and in pstA cells and upper cup during culmination transports ions across membranes using ATP hydrolysis for energy contains 8 transmembrane domains | DDB0232429 | CDS | 7864423 | 3699 | + | 0.326304 |
ippA | DDB_G0275663 | converts 1D-myo-inositol 14-bisphosphate H2O to 1D-myo-inositol 4-phosphate phosphate | DDB0232429 | CDS | 5791228 | 936 | + | 0.314103 |
ippB | DDB_G0268652 | very similar to A. thaliana AHL and SAL1 phosphatases and S. pombe tol1 (halotolerance protein) all related to the S. cerevisiae HAL2 these proteins are 3'-phosphoadenosine-5'-phosphate (PAP) phosphatases that also act as inositol polyphosphate 1-phosphatases. | DDB0232428 | CDS | 1844690 | 999 | + | 0.274274 |
kcnma1 | DDB_G0269896 | ortholog of the human KCNMA1 a potassium channel activated by both membrane depolarization and increase in cytosolic Ca(2) that mediates export of K() defects in the gene cause generalized epilepsy and paroxysmal dyskinesia (GEPD) | DDB0232428 | CDS | 3812473 | 3735 | - | 0.274431 |
kil2 | DDB_G0279183 | DDB0232430 | CDS | 1731085 | 3477 | + | 0.33132 | |
mfsd1 | DDB_G0289201 | ortholog of the human MSFD1 also knon as SMAP-4 (Smooth Muscle cell-Associated Protein 4) contains 10 putative transmembrane domains and an additional potential signal peptide | DDB0232432 | CDS | 2461603 | 1521 | - | 0.336621 |
nhe1 | DDB_G0275711 | required for cell polarity mediates both Ksupsup facilitation of cell motility and KsupsupNasupsup requirement in chemotactic orientation the genetic interaction between aip1 and nhe1 suggest that defective chemotaxis in nhe1- mutants may be determined by loss of cofilin-dependent actin dynamics | DDB0232429 | CDS | 6042281 | 2025 | - | 0.281481 |
nhe2 | DDB_G0281877 | DDB0232430 | CDS | 5057597 | 2064 | + | 0.228682 | |
nhe3 | DDB_G0292830 | DDB0232433 | CDS | 2111344 | 2361 | - | 0.345616 | |
nhe4 | DDB_G0290253 | DDB0232432 | CDS | 3840207 | 3027 | - | 0.327387 | |
noxB | DDB_G0287101 | homolog of the mammalian flavocytochrome b large subunit gp91phox essential for spore formation | DDB0232431 | CDS | 5216605 | 2097 | - | 0.244158 |
noxC | DDB_G0291117 | homolog of the mammalian flavocytochrome b large subunit gp91phox essential for spore formation contains calcium-binding EF hand | DDB0232432 | CDS | 5017189 | 3429 | - | 0.222514 |
nramp1 | DDB_G0276973 | ortholog of the mammalian SLC11a1 transports iron across the phagolysosomal membrane contains 12 transmembrane domains | DDB0232429 | CDS | 7564058 | 1602 | + | 0.314607 |
nramp2 | DDB_G0275815 | NRAMP family protein similar to bacterial manganese transport protein mntH contains 12 transmembrane domains involved in iron homeostasis and resistance to pathogenic bacteria | DDB0232429 | CDS | 5536603 | 1890 | + | 0.292593 |
patA | DDB_G0277861 | P-type ATPase that is up-regulated in calcium-adapted cells contains 10 predicted transmembrane domains | DDB0232430 | CDS | 364618 | 3348 | + | 0.373059 |
patB | DDB_G0282817 | plasma membrane P-type Hsupsup-ATPase that is necessary for survival in acidic environments | DDB0232430 | CDS | 6309404 | 3177 | + | 0.36481 |
potA | DDB_G0282291 | DDB0232430 | CDS | 5660926 | 2934 | + | 0.273347 | |
ppk1 | DDB_G0293524 | similar to bacterial PPK (PPK1 family) which synthesizes poly P a polymer of up to hundreds of phosphate residues | DDB0232433 | CDS | 3029753 | 3162 | - | 0.328906 |
redA | DDB_G0293904 | catalyzes the reaction NADPH n oxidized hemoprotein NADP() n reduced hemoprotein involved in the metabolism of compounds that control Dictyostelium cell differentiation | DDB0232433 | CDS | 3580985 | 1896 | - | 0.339135 |
redB | DDB_G0269912 | catalyzes the reaction NADPH n oxidized hemoprotein NADP() n reduced hemoprotein similar to the H. sapiens POR protein that is defect in adrenal hyperplasia variant type (AHV) a syndrome with disordered steroidogenesis | DDB0232428 | CDS | 3848909 | 2004 | - | 0.335329 |
redC | DDB_G0287983 | similar to the H. sapiens NDOR1 an oxidoreductase that catalyzes the NADP-dependent reduction of cytochrome c and one-electron acceptors | DDB0232432 | CDS | 927535 | 1902 | + | 0.244479 |
rhgA | DDB_G0283389 | similar to human Rh50 protein a glycoprotein present on the surface of red blood cells contains 10 transmembrane domains | DDB0232431 | CDS | 634252 | 1584 | - | 0.33649 |
rhgB | DDB_G0280059 | DDB0232430 | CDS | 3188254 | 1803 | + | 0.345535 | |
rliA | DDB_G0272783 | twelve transmembrane domain protein that may act as a transporter repressed after Legionella pneumophila infection | DDB0232429 | CDS | 2172067 | 1416 | + | 0.267655 |
slc4 | DDB_G0270422 | DDB0232428 | CDS | 4842234 | 2307 | - | 0.229736 | |
sod2 | DDB_G0271106 | ortholog of the human SOD2 the mitochondrial superoxide dismutase belongs to the ironmanganese superoxide dismutase family | DDB0232429 | CDS | 35093 | 681 | + | 0.325991 |
sodA | DDB_G0267420 | superoxide dismutase of the SOD1 family expressed at constant levels throughout the life cycle and upregulated upon oxidative stress enriched in prespore cells | DDB0232428 | CDS | 338107 | 462 | + | 0.391775 |
sodB | DDB_G0283021 | DDB0232431 | CDS | 167774 | 1284 | - | 0.351246 | |
sodC | DDB_G0282993 | GPI-anchored plasma membrane superoxide dismutase upregulated upon oxidative stress mutants have defects in cytokinesis chemotaxis and localization of several protein during aggregation | DDB0232431 | CDS | 110200 | 1224 | - | 0.332516 |
sodD | DDB_G0281493 | DDB0232430 | CDS | 4612258 | 456 | - | 0.361842 | |
sodE | DDB_G0290343 | very similar to human SOD1 defects in which cause familial amyotrophic lateral sclerosis (ALS) belongs to the Cu-Zn superoxide dismutase family | DDB0232432 | CDS | 3992463 | 459 | + | 0.294118 |
sodF | DDB_G0281461 | DDB0232430 | CDS | 4537876 | 456 | + | 0.346491 | |
symA | DDB_G0292814 | DDB0232433 | CDS | 2158906 | 1371 | - | 0.33698 | |
zntA | DDB_G0268426 | ZIP family zinc transporter LZT subfamily member contains 8 transmembrane domains expressed in pstAB cells | DDB0232428 | CDS | 1375259 | 1524 | + | 0.256562 |
zntB | DDB_G0286345 | ZIP family zinc transporter LZT subfamily member contains 7 transmembrane domains expressed in pstAB cells | DDB0232431 | CDS | 4327628 | 1119 | + | 0.314567 |
zntC | DDB_G0286049 | ZIP family zinc transporter LZT subfamily member contains 7 transmembrane domains expressed in pstAB cells | DDB0232431 | CDS | 3998261 | 1206 | + | 0.333333 |
zntD | DDB_G0269326 | ZIP family zinc transporter LZT subfamily member contains 8 transmembrane domains expressed in pstAB cells | DDB0232428 | CDS | 2544681 | 2052 | - | 0.273879 |