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| | PH0857 | 394aa long hypothetical threonine synthase; Catalyzes the gamma-elimination of phosphate from L- phosphohomoserine and the beta-addition of water to produce L- threonine. (394 aa) |
| | PH0858 | 359aa long hypothetical protein; Similar to PIR:C64371 percent identity:43.558 in 169aa. motif=aspartokinase signature; Belongs to the aspartokinase family. (359 aa) |
| | PH0926 | 243aa long hypothetical protein; Hydrolyzes mannosyl-3-phosphoglycerate (MPG) to form the osmolyte mannosylglycerate (MG). The enzyme is absolutely specific for MPG. (243 aa) |
| | PH0927 | 394aa long hypothetical protein; Transfers a mannosyl group from GDP-mannose to phosphoglycerate to form mannosyl-3-phosphoglycerate (MPG). The enzyme is absolutely specific for GDP-mannose and 3-phosphoglycerate, and transfers the mannosyl group with retention of configuration. (394 aa) |
| | PH0937 | 383aa long hypothetical protein; Catalyzes the decarboxylation of L-aspartate to produce beta- alanine, and the decarboxylation of L-glutamate to produce 4- aminobutanoate. Can also use cysteate and cysteine sulfite, but not L- tyrosine. Specific activities toward L-aspartate and cysteate are higher than toward L-glutamate. (383 aa) |
| | PH0951 | 283aa long hypothetical 3-methyl-2-oxobutanoate hydroxymethyltransferase; Catalyzes the reversible reaction in which hydroxymethyl group from 5,10-methylenetetrahydrofolate is transferred onto alpha- ketoisovalerate to form ketopantoate; Belongs to the PanB family. (283 aa) |
| | PH0965 | 967aa long hypothetical leucyl-tRNA synthetase; Similar to PIR:A64379 percent identity: 53.987 in 980aa; owl:F21M12 percent identity: 36.017 in 737aa; Swiss_Prot:Q09996 percent identity: 34.910 in 766aa. motif=aminoacyl-transfer RNA synthetases class-I signature. (967 aa) |
| | PH0993 | 723aa long hypothetical methionyl-tRNA synthetase; Is required not only for elongation of protein synthesis but also for the initiation of all mRNA translation through initiator tRNA(fMet) aminoacylation. (723 aa) |
| | PH1006 | 480aa long hypothetical prolyl-tRNA synthetase; Catalyzes the attachment of proline to tRNA(Pro) in a two- step reaction: proline is first activated by ATP to form Pro-AMP and then transferred to the acceptor end of tRNA(Pro). (480 aa) |
| | PH1011 | 375aa long hypothetical tyrosyl-tRNA synthetase; Catalyzes the attachment of tyrosine to tRNA(Tyr) in a two- step reaction: tyrosine is first activated by ATP to form Tyr-AMP and then transferred to the acceptor end of tRNA(Tyr); Belongs to the class-I aminoacyl-tRNA synthetase family. TyrS type 4 subfamily. (375 aa) |
| | PH1020 | 438aa long hypothetical aspartyl-tRNA synthetase; Catalyzes the attachment of L-aspartate to tRNA(Asp) in a two-step reaction: L-aspartate is first activated by ATP to form Asp- AMP and then transferred to the acceptor end of tRNA(Asp). (438 aa) |
| | PH1065 | 1066aa long hypothetical isoleucyl-tRNA synthetase; Catalyzes the attachment of isoleucine to tRNA(Ile). As IleRS can inadvertently accommodate and process structurally similar amino acids such as valine, to avoid such errors it has two additional distinct tRNA(Ile)-dependent editing activities. One activity is designated as 'pretransfer' editing and involves the hydrolysis of activated Val-AMP. The other activity is designated 'posttransfer' editing and involves deacylation of mischarged Val-tRNA(Ile). Belongs to the class-I aminoacyl-tRNA synthetase family. IleS type 2 subfamily. (1066 aa) |
| | PH1075 | 319aa long hypothetical homoserine dehydrogenase; Similar to PIR:A64500 percent identity: 34.967 in 329aa. (319 aa) |
| | PH1086 | 346aa long hypothetical aspartokinase; Similar to Swiss_Prot:P26512 percent identity:34.375 in 130aa; PIR:C64371 percent identity:35.948 in 157aa; OWL:TTHASKAB percent identity:32.308 in 131aa. motif=aspartokinase signature. (346 aa) |
| | PH1087 | 271aa long hypothetical homoserine kinase; Catalyzes the ATP-dependent phosphorylation of L-homoserine to L-homoserine phosphate; Belongs to the GHMP kinase family. Homoserine kinase subfamily. (271 aa) |
| | PH1088 | 334aa long hypothetical aspartate-semialdehyde dehydrogenase; Similar to PIR:F64325 percent identity: 50.000 in 343aa; Swiss_Prot:P41394 percent identity: 45.092 in 345aa; owl:D89129 percent identity: 43.844 in 353aa. (334 aa) |
| | PH1089 | 338aa long hypothetical 5-methyltetrahydropteroyltriglutamate--homocysteine S-methyltransferase; Catalyzes the transfer of a methyl group to L-homocysteine resulting in methionine formation. The physiological methyl donor is unknown (By similarity). (338 aa) |
| | PH1090 | 309aa long hypothetical protein. (309 aa) |
| | PH1091 | 336aa long hypothetical protein. (336 aa) |
| | PH1093 | 371aa long hypothetical cystathionine gamma-lyase; Similar to owl:HPAE0005325 percent identity: 40.774 in 341aa; owl:BSU938741 percent identity: 40.237 in 343aa; Swiss_Prot:P31373 percent identity: 41.791 in 343aa. (371 aa) |
| | PH1102 | 480aa long hypothetical asparagine synthetase; Similar to PIR:C64439 percent identity: 45.304 in 190aa. (480 aa) |
| | PH1138 | 618aa long hypothetical indolepyruvate ferredoxin oxidoreductase alpha subunit; Catalyzes the ferredoxin-dependent oxidative decarboxylation of arylpyruvates. (618 aa) |
| | PH1146 | 401aa long hypothetical aminomethyltransferase; The glycine cleavage system catalyzes the degradation of glycine. (401 aa) |
| | PH1218 | 410aa long hypothetical phosphoglycerate kinase; Similar to Swiss_Prot:P50316 percent identity: 77.995 in 409aa; PIR:A64380 percent identity: 50.125 in 413aa; Swiss_Prot:P20971 percent identity: 44.275 in 401aa. motif=phosphoglycerate kinase signature. (410 aa) |
| | PH1282 | 314aa long hypothetical carbamate kinase (fucoxanthin chlorophyll a/c binding protein); Similar to owl:PFCPA percent identity: 89.103 in 312aa; owl:CPARCABDC3 percent identity: 51.780 in 311aa; owl:ECAE0003708 percent identity: 49.673 in 314aa. (314 aa) |
| | PH1317 | 138aa long hypothetical glycine cleavage system H protein; The glycine cleavage system catalyzes the degradation of glycine. The H protein shuttles the methylamine group of glycine from the P protein to the T protein. (138 aa) |
| | PH1346 | 189aa long hypothetical GMP synthase; Catalyzes the synthesis of GMP from XMP. (189 aa) |
| | PH1353 | 679aa long hypothetical formate dehydrogenase; Similar to owl:MTU526812 percent identity: 48.550 in 677aa; Swiss_Prot:P06131 percent identity: 44.104 in 681aa; owl:MTU738071 percent identity: 43.381 in 646aa. (679 aa) |
| | PH1354 | 196aa long hypothetical protein; Catalyzes the hydrolysis of glutamine to glutamate and ammonia as part of the biosynthesis of pyridoxal 5'-phosphate. The resulting ammonia molecule is channeled to the active site of PdxS. (196 aa) |
| | PH1390 | 301aa long hypothetical thiamin biosynthesis protein; Catalyzes the NAD(P)H-dependent reduction of ketopantoate into pantoic acid. (301 aa) |
| | PH1444 | 401aa long hypothetical protein DFP; Similar to PIR:A64414 percent identity: 42.159 in 405aa; Swiss_Prot:P44953 percent identity: 36.579 in 400aa; Swiss_Prot:P24285 percent identity: 33.509 in 403aa. (401 aa) |
| | PH1463 | 438aa long hypothetical L-asparaginase; Allows the formation of correctly charged Gln-tRNA(Gln) through the transamidation of misacylated Glu-tRNA(Gln) in organisms which lack glutaminyl-tRNA synthetase. The reaction takes place in the presence of glutamine and ATP through an activated gamma-phospho-Glu- tRNA(Gln). The GatDE system is specific for glutamate and does not act on aspartate. (438 aa) |
| | PH1478 | 629aa long hypothetical arginyl-tRNA synthetase; Similar to PIR:F64329 percent identity: 40.975 in 639aa; Swiss_Prot:P43832 percent identity: 40.000 in 192aa. motif=aminoacyl-transfer RNA synthetases class-I signature. (629 aa) |
| | PH1583 | 459aa long hypothetical tryptophan synthase beta chain; The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine. (459 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) |
| | PH1609 | 158aa long hypothetical protein; Similar to PIR:E64339 percent identity: 46.980 in 152aa; Belongs to the PdaD family. (158 aa) |
| | PH1614 | 570aa long hypothetical glycyl-tRNA synthetase; Catalyzes the attachment of glycine to tRNA(Gly). (570 aa) |
| | PH1630 | 341aa long hypothetical protein. (341 aa) |
| | PH1645 | 450aa long hypothetical protein; Catalyzes the phosphorylation of fructose 6-phosphate to fructose 1,6-bisphosphate using ADP as the phosphate donor. (450 aa) |
| | PH1654 | 427aa long hypothetical serine hydroxymethyltransferase; Catalyzes the reversible interconversion of serine and glycine with a modified folate serving as the one-carbon carrier. Also exhibits a pteridine-independent aldolase activity toward beta- hydroxyamino acids, producing glycine and aldehydes, via a retro-aldol mechanism. (427 aa) |
| | PH1661 | 281aa long hypothetical ferredoxin oxidoreductase beta subunit; Similar to PIR:A64367 percent identity: 54.373 in 263aa; owl:HPAE0005725 percent identity: 44.697 in 265aa; PIR:S22397 percent identity: 43.011 in 186aa. (281 aa) |
| | PH1662 | 385aa long hypothetical ferredoxin oxidoreductase alpha subunit; Similar to PIR:E64334 percent identity: 57.939 in 368aa; owl:HPAE0005724 percent identity: 40.947 in 366aa; PIR:S22396 percent identity: 46.108 in 167aa. (385 aa) |
| | PH1665 | 284aa long hypothetical ferredoxin oxidoreductase beta subunit; Similar to PIR:A64367 percent identity: 57.303 in 268aa; owl:HPAE0005725 percent identity: 45.643 in 242aa; PIR:JC4920 percent identity: 45.161 in 187aa. (284 aa) |
| | PH1666 | 408aa long hypothetical ferredoxin oxidoreductase alpha subunit; Similar to PIR:E64334 percent identity: 56.630 in 371aa; owl:HPAE0005724 percent identity: 42.486 in 351aa; PIR:S22396 percent identity: 34.848 in 343aa. motif=prokaryotic membrane lipoprotein lipid attachment site. (408 aa) |
| | PH1686 | 570aa long hypothetical glutaminyl-tRNA synthetase; Catalyzes the attachment of glutamate to tRNA(Glu) in a two- step reaction: glutamate is first activated by ATP to form Glu-AMP and then transferred to the acceptor end of tRNA(Glu). (570 aa) |
| | PH1715 | 325aa long hypothetical protein; Catalyzes the release of L-lysine from [LysW]-gamma-L-lysine and the release of L-ornithine from [LysW]-L-ornithine. (325 aa) |
| | PH1716 | 366aa long hypothetical acetylornithine aminotransferase; Involved in both the arginine and lysine biosynthetic pathways; Belongs to the class-III pyridoxal-phosphate-dependent aminotransferase family. LysJ subfamily. (366 aa) |
| | PH1718 | 249aa long hypothetical protein; Involved in both the arginine and lysine biosynthetic pathways. Phosphorylates the LysW-bound precursors glutamate (for arginine biosynthesis), respectively alpha-aminoadipate (for lysine biosynthesis); Belongs to the acetylglutamate kinase family. LysZ subfamily. (249 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) |
| | PH1721 | 273aa long hypothetical ribosomal protein S6 modification protein; Similar to PIR:D64377 percent identity:31.441 in 238aa. (273 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) |
| | PH1724 | 163aa long hypothetical 3-isopropylmalate dehydratase; Catalyzes the isomerization between 2-isopropylmalate and 3- isopropylmalate, via the formation of 2-isopropylmaleate. Belongs to the LeuD family. LeuD type 2 subfamily. (163 aa) |
| | PH1726 | 380aa long hypothetical isomerase; Catalyzes the isomerization between 2-isopropylmalate and 3- isopropylmalate, via the formation of 2-isopropylmaleate. (380 aa) |
| | PH1727 | 361aa long hypothetical 2-isopropylmalate synthase; Catalyzes the aldol-type condensation of 2-oxoglutarate with acetyl-CoA to yield homocitrate. Carries out the first step of the alpha-aminoadipate (AAA) lysine biosynthesis pathway. Belongs to the alpha-IPM synthase/homocitrate synthase family. Homocitrate synthase LYS20/LYS21 subfamily. (361 aa) |
| | PH1792 | 557aa long hypothetical CTP synthase; Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen. Regulates intracellular CTP levels through interactions with the four ribonucleotide triphosphates. (557 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) |
| | PH1884 | 231aa long hypothetical triosephosphate isomerase; Involved in the gluconeogenesis. Catalyzes stereospecifically the conversion of dihydroxyacetone phosphate (DHAP) to D- glyceraldehyde-3-phosphate (G3P); Belongs to the triosephosphate isomerase family. (231 aa) |
| | PH1921 | 301aa long hypothetical tryptophanyl-tRNA synthetase; Similar to owl:S51901 percent identity: 49.296 in 298aa; Swiss_Prot:Q09692 percent identity: 48.352 in 286aa; Swiss_Prot:P23381 percent identity: 46.831 in 301aa; Belongs to the class-I aminoacyl-tRNA synthetase family. (301 aa) |
| | PH1942 | 428aa long hypothetical phosphoglycerate dehydratase; Catalyzes the reversible conversion of 2-phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis; Belongs to the enolase family. (428 aa) |
| | PH1955 | 227aa long hypothetical phosphoribosylformylglycinamidine synthase I; Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP- dependent manner. PurS interacts with PurQ and PurL an [...] (227 aa) |
| | PH1956 | 192aa long hypothetical protein. (192 aa) |
| | PH1969 | 404aa long hypothetical alanyl-tRNA synthetase; Functions in trans to edit the amino acid moiety from mischarged charged tRNA(Ala). (404 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) |
| | PH0589 | 457aa long hypothetical protein; Catalyzes the ADP-dependent phosphorylation of D-glucose to D-glucose 6-phosphate and glucosamine to glucosamine 6-phosphate. (457 aa) |
| | PH0570 | 478aa long hypothetical pyruvate kinase; Similar to PIR:A57418 percent identity:76.037 in 217aa; PIR:S76677 percent identity:42.128 in 484aa; Swiss_Prot:Q02499 percent identity:43.991 in 475aa. motif=eukaryotic thiol (cysteine) proteases active sites; Belongs to the pyruvate kinase family. (478 aa) |
| | PH0359 | 443aa long hypothetical glutamine synthetase; Probably involved in nitrogen metabolism via ammonium assimilation. Catalyzes the ATP-dependent biosynthesis of glutamine from glutamate and ammonia. (443 aa) |
| | PH0314 | 896aa long hypothetical valyl-tRNA synthetase; Catalyzes the attachment of valine to tRNA(Val). As ValRS can inadvertently accommodate and process structurally similar amino acids such as threonine, to avoid such errors, it has a 'posttransfer' editing activity that hydrolyzes mischarged Thr-tRNA(Val) in a tRNA- dependent manner; Belongs to the class-I aminoacyl-tRNA synthetase family. ValS type 2 subfamily. (896 aa) |
| | PH0297 | 915aa long hypothetical alanyl-tRNA synthetase; Catalyzes the attachment of alanine to tRNA(Ala) in a two- step reaction: alanine is first activated by ATP to form Ala-AMP and then transferred to the acceptor end of tRNA(Ala). Edits incorrectly charged Ser-tRNA(Ala). Incorrectly charged amino acids occur because the of inherent physicochemical limitations on discrimination between closely related amino acids (Gly and Ser) in the charging step. Belongs to the class-II aminoacyl-tRNA synthetase family. (915 aa) |
| | PH0292 | 398aa long hypothetical 5-aminolevulinic acid synthase (8 amino-7-oxonenanoate synthase); Catalyzes the decarboxylative condensation of pimeloyl-[acyl- carrier protein] and L-alanine to produce 8-amino-7-oxononanoate (AON), [acyl-carrier protein], and carbon dioxide. (398 aa) |
| | PH0290 | 431aa long hypothetical histidyl-tRNA synthetase; Similar to PIR:G64424 percent identity: 45.854 in 425aa; owl:HPAE0006251 percent identity: 33.577 in 418aa; Swiss_Prot:P46220 percent identity: 46.617 in 133aa; Belongs to the class-II aminoacyl-tRNA synthetase family. (431 aa) |
| | PH0285 | 112aa long hypothetical methionyl-tRNA synthetase; Similar to PIR:F64457 percent identity:45.370 in 108aa; Swiss_Prot:P23395 percent identity:48.485 in 100aa. (112 aa) |
| | PH0276 | 206aa long hypothetical protein; Similar to PIR:B64386 percent identity: 52.284 in 200aa. (206 aa) |
| | PH0270 | 294aa long hypothetical asparaginyl-tRNA synthetase; Similar to owl:STOMPS3GN percent identity:32.500 in 81aa; Swiss_Prot:P54263 percent identity:39.130 in 93aa. (294 aa) |
| | PH0243 | 601aa long hypothetical glutamine--fructose-6-phosphate aminotransferase; Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source. (601 aa) |
| | PH0241 | 434aa long hypothetical asparaginyl-tRNA synthetase; Similar to Swiss_Prot:P39772 percent identity: 47.242 in 420aa; Swiss_Prot:P54262 percent identity: 44.712 in 419aa; Swiss_Prot:P54263 percent identity: 45.455 in 439aa. motif=aminoacyl-transfer RNA synthetases class-II signatures. (434 aa) |
| | PH0240 | 449aa long hypothetical amidophosphoribosyltransferase; Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine. (449 aa) |
| | PH0224 | 523aa long hypothetical lysyl-tRNA synthetase; Similar to PIR:C64367 percent identity: 40.971 in 535aa. motif=aminoacyl-transfer RNA synthetases class-I signature. (523 aa) |
| | PH0150 | 435aa long hypothetical protein; Catalyzes the formation of cyclic 2,3-diphosphoglycerate (cDPG) by formation of an intramolecular phosphoanhydride bond at the expense of ATP. (435 aa) |
| | PH0125 | 260aa long hypothetical 5'-methylthioadenosine phosphorylase; Catalyzes the reversible phosphorylation of S-methyl-5'- thioadenosine (MTA) to adenine and 5-methylthioribose-1-phosphate. Involved in the breakdown of MTA, a major by-product of polyamine biosynthesis. Responsible for the first step in the methionine salvage pathway after MTA has been generated from S-adenosylmethionine. Has broad substrate specificity with 6-aminopurine nucleosides as preferred substrates; Belongs to the PNP/MTAP phosphorylase family. MTAP subfamily. (260 aa) |
| | PH0108 | 216aa long hypothetical alanyl-tRNA synthetase; Functions in trans to edit the amino acid moiety from mischarged charged Gly-tRNA(Ala) and Ser-tRNA(Ala). Belongs to the class-II aminoacyl-tRNA synthetase family. Editing domain AlaX-M subfamily. (216 aa) |
| | PH0092 | 821aa long hypothetical phosphoenolpyruvate synthase; Catalyzes the phosphorylation of pyruvate to phosphoenolpyruvate; Belongs to the PEP-utilizing enzyme family. (821 aa) |
| | PH0083 | 283aa long hypothetical agmatinase; Catalyzes the formation of putrescine from agmatine. Cannot use arginine. (283 aa) |
| | PH0082 | 281aa long hypothetical protein; Similar to PIR:H64349 percent identity: 36.782 in 274aa; Belongs to the DeoC/FbaB aldolase family. (281 aa) |
| | PH0066 | 328aa long hypothetical L-asparaginase; Similar to Swiss_Prot:P26900 percent identity: 40.373 in 326aa; Swiss_Prot:P18840 percent identity: 38.768 in 278aa; PIR:D64302 percent identity: 39.502 in 297aa. motif=asparaginase / glutaminase active sites signatures. (328 aa) |
| | PH0037 | 412aa long hypothetical phosphonopyruvate decarboxylase; Catalyzes the interconversion of 2-phosphoglycerate and 3- phosphoglycerate. (412 aa) |
| | PH0016 | 475aa long hypothetical protein; Catalyzes the irreversible beta-carboxylation of phosphoenolpyruvate (PEP) to form oxaloacetate (OAA), a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle. Belongs to the PEPCase type 2 family. (475 aa) |
| | PH0013 | 300aa long hypothetical quinolinate synthetase; Catalyzes the condensation of iminoaspartate with dihydroxyacetone phosphate to form quinolinate. (300 aa) |
| | PH0006 | 274aa long hypothetical protein; D-aminoacyl-tRNA deacylase with broad substrate specificity. By recycling D-aminoacyl-tRNA to D-amino acids and free tRNA molecules, this enzyme counteracts the toxicity associated with the formation of D-aminoacyl-tRNA entities in vivo. (274 aa) |
| | PH0726 | 317aa long hypothetical ornithine carbamoyltransferase; Reversibly catalyzes the transfer of the carbamoyl group from carbamoyl phosphate (CP) to the N(epsilon) atom of ornithine (ORN) to produce L-citrulline. (317 aa) |
| | PH0720 | 308aa long hypothetical aspartate carbamoyltransferase catalytic chain; Similar to owl:PAU61765 percent identity: 92.532 in 308aa; PIR:D64497 percent identity: 58.503 in 297aa; owl:VSPYRBI1 percent identity: 55.593 in 302aa. motif=aspartate and ornithine carbamoyltransferases signature. (308 aa) |
| | PH0710 | 460aa long hypothetical seryl-tRNA synthetase; Catalyzes the attachment of serine to tRNA(Ser). Is also able to aminoacylate tRNA(Sec) with serine, to form the misacylated tRNA L- seryl-tRNA(Sec), which will be further converted into selenocysteinyl- tRNA(Sec). (460 aa) |
| | PH0702 | 364aa long hypothetical translation initiation factor eIF-2 beta chain; Catalyzes the interconversion of methylthioribose-1-phosphate (MTR-1-P) into methylthioribulose-1-phosphate (MTRu-1-P). Belongs to the eIF-2B alpha/beta/delta subunits family. MtnA subfamily. (364 aa) |
| | PH0699 | 625aa long hypothetical threonyl-tRNA synthetase; Catalyzes the attachment of threonine to tRNA(Thr) in a two- step reaction: L-threonine is first activated by ATP to form Thr-AMP and then transferred to the acceptor end of tRNA(Thr). Also edits incorrectly charged L-seryl-tRNA(Thr); Belongs to the class-II aminoacyl-tRNA synthetase family. (625 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) |
| | 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) |
| | PH0677 | 350aa long hypothetical acyl carrier protein synthetase; Similar to owl:PFPORVOR4 percent identity: 90.857 in 350aa; PIR:A64493 percent identity: 63.772 in 342aa; owl:PFU418184 percent identity: 38.507 in 351aa; Belongs to the thiolase-like superfamily. UPF0219 family. (350 aa) |
| | PH0658 | 499aa long hypothetical phenylalanyl-tRNA synthetase subunit alpha chain; Similar to PIR:G64360 percent identity: 41.837 in 411aa; owl:SS56KBFR21 percent identity: 38.829 in 495aa; owl:CH19HHR234 percent identity: 42.907 in 297aa. motif=aminoacyl-transfer RNA synthetases class-II signatures; Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 2 subfamily. (499 aa) |
| | PH0657 | 556aa long hypothetical phenylalanyl-tRNA synthetase subunit beta chain; Similar to PIR:C64438 percent identity:44.751 in 550aa; owl:BBU829781 percent identity:34.120 in 564aa; OWL:SS56KBFR20 percent identity:36.420 in 501aa. (556 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) |
| | PH0765 | 648aa long hypothetical indolepyruvate ferredoxin oxidoreductase alpha subunit; Catalyzes the ferredoxin-dependent oxidative decarboxylation of arylpyruvates. (648 aa) |
| | PH0636 | 476aa long hypothetical cysteinyl-tRNA synthetase; Similar to Swiss_Prot:Q06752 percent identity: 48.707 in 473aa; Swiss_Prot:P43816 percent identity: 50.000 in 472aa; Swiss_Prot:P21888 percent identity: 48.904 in 474aa. (476 aa) |
