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PH0679 | 105aa long hypothetical ferredoxin oxidoreductase delta subunit; Similar to owl:PFPORVOR6 percent identity: 86.667 in 105aa; owl:PFPORVOR9 percent identity: 65.333 in 75aa; PIR:E64333 percent identity: 61.333 in 75aa. motif=4Fe-4S ferredoxins, iron-sulfur binding region signature. (105 aa) | ||||
PH0678 | 185aa long hypothetical ferredoxin oxidoreductase gamma subunit; Similar to owl:PFPORVOR5 percent identity: 90.270 in 185aa; PIR:F64333 percent identity: 65.698 in 179aa; owl:TMPMRFDNA2 percent identity: 44.000 in 177aa. (185 aa) | ||||
PH0655 | 348aa long hypothetical dehydrogenase; Catalyzes the NAD(+)-dependent oxidation of L-threonine to 2- amino-3-ketobutyrate. Is much less efficient when using NADP(+) instead of NAD(+). To a lesser extent, also catalyzes the oxidation of L-serine and DL-threo-3- phenylserine, but not that of L-allo-threonine, D-threonine and D-allo- threonine and many other L-amino acids. (348 aa) | ||||
PH0597 | 376aa long hypothetical dehydrogenase; Similar to owl:BSZ9404317 percent identity: 49.821 in 287aa; Swiss_Prot:P37666 percent identity: 43.750 in 327aa; PIR:A64427 percent identity: 42.633 in 330aa. motif=ATP/GTP-binding site motif A (P-loop); D-isomer specific 2-hydroxyacid dehydrogenases s. (376 aa) | ||||
PH0572 | 445aa long hypothetical NADH oxidase; Acts as a coenzyme A disulfide reductase. Specific for CoA disulfide. Shows a slow NAD(P)H oxidase activity in the presence of high concentrations of substrate-level FAD. This demonstrates that it is not likely to act as an NADH oxidase in vivo. (445 aa) | ||||
PH1217 | 216aa long hypothetical alkyl hydroperoxide reductase; Thiol-specific peroxidase that catalyzes the reduction of hydrogen peroxide and organic hydroperoxides to water and alcohols, respectively. Plays a role in cell protection against oxidative stress by detoxifying peroxides. (216 aa) | ||||
PH1277 | 360aa long hypothetical malate dehydrogenase; Similar to Swiss_Prot:P16142 percent identity: 45.231 in 340aa; PIR:H64477 percent identity: 47.038 in 296aa; owl:ECAE00015710 percent identity: 35.780 in 341aa. (360 aa) | ||||
PH1387 | 307aa long hypothetical phosphoglycerate dehydrogenase; Similar to PIR:A64427 percent identity: 55.960 in 305aa; owl:S75016 percent identity: 43.709 in 304aa; owl:CEC31C91 percent identity: 41.391 in 304aa. motif=ATP/GTP-binding site motif A (P-loop); D-isomer specific 2-hydroxyacid dehydrogenases signatures. (307 aa) | ||||
PH1390 | 301aa long hypothetical thiamin biosynthesis protein; Catalyzes the NAD(P)H-dependent reduction of ketopantoate into pantoic acid. (301 aa) | ||||
PH1475 | 351aa long hypothetical glycerol 1-phaphate dehydrogenase; Catalyzes the NAD(P)H-dependent reduction of dihydroxyacetonephosphate (DHAP or glycerone phosphate) to glycerol 1- phosphate (G1P). The G1P thus generated is used as the glycerophosphate backbone of phospholipids in the cellular membranes of Archaea. Belongs to the glycerol-1-phosphate dehydrogenase family. (351 aa) | ||||
PH1516 | 303aa long hypothetical dihydroorotate dehydrogenase; Catalyzes the conversion of dihydroorotate to orotate with NAD(+) as electron acceptor; Belongs to the dihydroorotate dehydrogenase family. Type 1 subfamily. (303 aa) | ||||
PH1593 | 422aa long hypothetical glutamate dehydrogenase; Similar to owl:A47410 percent identity: 96.429 in 420aa; Swiss_Prot:P80319 percent identity: 95.952 in 420aa; owl:THCGLUDEHY percent identity: 87.799 in 419aa. motif=glu / Leu / Phe / Val dehydrogenases active site; Belongs to the Glu/Leu/Phe/Val dehydrogenases family. (422 aa) | ||||
PH1618 | 418aa long hypothetical UDP-N-acetyl-D-mannosaminuronic acid dehydrogenase; Catalyzes the four-electron oxidation of UDP-N-acetyl-D- mannosamine (UDP-ManNAc), reducing NAD(+) and releasing UDP-N- acetylmannosaminuronic acid (UDP-ManNAcA). Belongs to the UDP-glucose/GDP-mannose dehydrogenase family. (418 aa) | ||||
PH1720 | 330aa long hypothetical N-acetyl-gamma-glutamyl-phosphate reductase; Involved in both the arginine and lysine biosynthetic pathways; Belongs to the NAGSA dehydrogenase family. Type 1 subfamily. LysY sub-subfamily. (330 aa) | ||||
PH1722 | 323aa long hypothetical 3-isopropylmalate dehydrogenase; May play a dual role in glutamate and lysine biosynthesis in vivo. Uses isocitrate and homoisocitrate at near equal efficiency and preferentially uses NAD over NADP. (323 aa) | ||||
PH1138 | 618aa long hypothetical indolepyruvate ferredoxin oxidoreductase alpha subunit; Catalyzes the ferredoxin-dependent oxidative decarboxylation of arylpyruvates. (618 aa) | ||||
PH0520 | 333aa long hypothetical dehydrogenase; Similar to PIR:A64427 percent identity: 38.636 in 317aa; owl:BSZ9404317 percent identity: 36.122 in 268aa; Swiss_Prot:P37666 percent identity: 32.384 in 288aa; Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family. (333 aa) | ||||
PH0363 | 1291aa long hypothetical ribonucleoside-diphosphate reductase; Catalyzes the reduction of ribonucleotides to deoxyribonucleotides. May function to provide a pool of deoxyribonucleotide precursors for DNA repair during oxygen limitation and/or for immediate growth after restoration of oxygen. (1291 aa) | ||||
PH0307 | 486aa long hypothetical inosine-5'-monophosphate dehydrogenase; Catalyzes the conversion of inosine 5'-phosphate (IMP) to xanthosine 5'-phosphate (XMP), the first committed and rate-limiting step in the de novo synthesis of guanine nucleotides, and therefore plays an important role in the regulation of cell growth. Belongs to the IMPDH/GMPR family. (486 aa) | ||||
PH1994 | 502aa long hypothetical glycine dehydrogenase subunit 2; The glycine cleavage system catalyzes the degradation of glycine. The P protein binds the alpha-amino group of glycine through its pyridoxal phosphate cofactor; CO(2) is released and the remaining methylamine moiety is then transferred to the lipoamide cofactor of the H protein; Belongs to the GcvP family. C-terminal subunit subfamily. (502 aa) | ||||
PH1995 | 449aa long hypothetical glycine dehydrogenase subunit 1; The glycine cleavage system catalyzes the degradation of glycine. The P protein binds the alpha-amino group of glycine through its pyridoxal phosphate cofactor; CO(2) is released and the remaining methylamine moiety is then transferred to the lipoamide cofactor of the H protein. (449 aa) | ||||
PH0015 | 464aa long hypothetical L-aspartate oxidase; Catalyzes the oxidation of L-aspartate to iminoaspartate. (464 aa) | ||||
PH0181 | 393aa long hypothetical protein; Is involved in the reduction of 2,3- digeranylgeranylglycerophospholipids (unsaturated archaeols) into 2,3- diphytanylglycerophospholipids (saturated archaeols) in the biosynthesis of archaeal membrane lipids. Catalyzes the formation of archaetidic acid (2,3-di-O-phytanyl-sn-glyceryl phosphate) from 2,3-di- O-geranylgeranylglyceryl phosphate (DGGGP) via the hydrogenation of each double bond of the isoprenoid chains. (393 aa) | ||||
PH1805 | 341aa long hypothetical 3-hydroxy-3-methylglutaryl coenzyme A reductase; Converts HMG-CoA to mevalonate. (341 aa) | ||||
PH1830 | 334aa long hypothetical glyceraldehyde-3-phosphate dehydrogenase; Similar to Swiss_Prot:P20286 percent identity: 90.719 in 334aa; Swiss_Prot:P10618 percent identity: 56.061 in 334aa; Swiss_Prot:P19315 percent identity: 57.751 in 335aa. motif=glyceraldehyde 3-phosphate dehydrogenase active site. (334 aa) | ||||
PH1083 | 137aa long hypothetical protein; Uses electrons from reduced NADP, by way of rubredoxin and an oxidoreductase, to catalyze the reduction of superoxide to hydrogen peroxide; Belongs to the desulfoferrodoxin family. (137 aa) | ||||
PH1019 | 607aa long hypothetical aldehyde:ferredoxin oxidoreductase; Similar to owl:PFAOR1 percent identity: 80.629 in 606aa; owl:TLFORPKPF2 percent identity: 39.527 in 620aa; Belongs to the AOR/FOR family. (607 aa) | ||||
PH0939 | 430aa long hypothetical ribulose 1,5-bisphosphate carboxylase large subunit; Catalyzes the addition of molecular CO(2) and H(2)O to ribulose 1,5-bisphosphate (RuBP), generating two molecules of 3- phosphoglycerate (3-PGA). Functions in an archaeal AMP degradation pathway, together with AMP phosphorylase and R15P isomerase. Belongs to the RuBisCO large chain family. Type III subfamily. (430 aa) | ||||
PH0765 | 648aa long hypothetical indolepyruvate ferredoxin oxidoreductase alpha subunit; Catalyzes the ferredoxin-dependent oxidative decarboxylation of arylpyruvates. (648 aa) | ||||
PH0764 | 202aa long hypothetical indolepyruvate ferredoxin oxidoreductase beta subunit; Catalyzes the ferredoxin-dependent oxidative decarboxylation of arylpyruvates. (202 aa) | ||||
PH0685 | 334aa long hypothetical ferredoxin oxidoreductase beta subunit; Similar to owl:PFPORVOR11 percent identity: 92.145 in 331aa; PIR:C64333 percent identity: 62.821 in 252aa; owl:PFPORVOR8 percent identity: 55.187 in 257aa. motif=prokaryotic membrane lipoprotein lipid attachment site. (334 aa) | ||||
PH0684 | 398aa long hypothetical ferredoxin oxidoreductase alpha-2 subunit; Similar to owl:PFPORVOR10 percent identity:88.101 in 395aa; PIR:D64333 percent identity:57.377 in 373aa; owl:PFPORVOR7 percent identity:51.399 in 396aa. (398 aa) | ||||
PH0681 | 314aa long hypothetical ferredoxin oxidoreductase beta subunit; Similar to owl:PFPORVOR8 percent identity: 93.569 in 311aa; PIR:C64333 percent identity: 51.203 in 295aa; owl:PFPORVOR11 percent identity: 56.118 in 253aa. (314 aa) | ||||
PH0680 | 397aa long hypothetical ferredoxin oxidoreductase alpha subunit; Similar to owl:PFPORVOR7 percent identity: 90.609 in 394aa; owl:PFPORVOR10 percent identity: 53.093 in 391aa; PIR:D64333 percent identity: 50.806 in 380aa. (397 aa) |