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| | A0A2I2FJU6 | RNA polymerase II transcription elongation factor-domain-containing protein. (443 aa) |
| | A0A2I2FIR6 | Uncharacterized protein. (106 aa) |
| | A0A2I2FHY6 | ATP synthase oligomycin sensitivity conferral protein. (227 aa) |
| | A0A2I2FHB2 | Kynurenine formamidase; Catalyzes the hydrolysis of N-formyl-L-kynurenine to L- kynurenine, the second step in the kynurenine pathway of tryptophan degradation. Kynurenine may be further oxidized to nicotinic acid, NAD(H) and NADP(H). Required for elimination of toxic metabolites. (294 aa) |
| | A0A2I2FGZ5 | ATP-synt_C domain-containing protein; Belongs to the ATPase C chain family. (158 aa) |
| | A0A2I2F5K1 | SAICAR_synt domain-containing protein. (307 aa) |
| | A0A2I2F5W9 | Thymidylate kinase. (220 aa) |
| | A0A2I2F658 | Uracil phosphoribosyltransferase. (239 aa) |
| | A0A2I2F688 | Probable acetate kinase. (421 aa) |
| | A0A2I2F694 | Phosphoribosyltransferase-like protein. (316 aa) |
| | A0A2I2F6A5 | ATP synthase complex subunit H-domain-containing protein. (123 aa) |
| | A0A2I2F6B2 | Putative phosphoribosyl transferase. (202 aa) |
| | A0A2I2F7T9 | Uridylate kinase; Catalyzes the phosphorylation of pyrimidine nucleoside monophosphates at the expense of ATP. Plays an important role in de novo pyrimidine nucleotide biosynthesis. Has preference for UMP and dUMP as phosphate acceptors, but can also use CMP, dCMP and AMP. Belongs to the adenylate kinase family. UMP-CMP kinase subfamily. (212 aa) |
| | A0A2I2F7W8 | AMP deaminase. (1016 aa) |
| | A0A2I2F8P8 | Xanthine phosphoribosyltransferase 1. (204 aa) |
| | A0A2I2F973 | ATP synthase subunit 4 mitochondrial. (243 aa) |
| | A0A2I2F974 | ATP synthase subunit alpha; Produces ATP from ADP in the presence of a proton gradient across the membrane. (556 aa) |
| | A0A2I2F988 | HCP-like protein. (350 aa) |
| | A0A2I2F9B8 | Orotidine 5'-phosphate decarboxylase; Belongs to the OMP decarboxylase family. (277 aa) |
| | A0A2I2F9L2 | PRTase-like protein. (232 aa) |
| | BNA4-2 | Kynurenine 3-monooxygenase; Catalyzes the hydroxylation of L-kynurenine (L-Kyn) to form 3-hydroxy-L-kynurenine (L-3OHKyn). Required for synthesis of quinolinic acid. (504 aa) |
| | A0A2I2F9S9 | Adenylosuccinate synthetase; Plays an important role in the de novo pathway and in the salvage pathway of purine nucleotide biosynthesis. Catalyzes the first commited step in the biosynthesis of AMP from IMP. (425 aa) |
| | A0A2I2FAM8 | Nicotinate phosphoribosyltransferase. (454 aa) |
| | A0A2I2FAT1 | Uncharacterized protein. (959 aa) |
| | A0A2I2FB52 | 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. (546 aa) |
| | A0A2I2FB69 | Putative isochorismatase family hydrolase. (236 aa) |
| | A0A2I2FB70 | Indoleamine 2,3-dioxygenase. (428 aa) |
| | BNA5 | Kynureninase; Catalyzes the cleavage of L-kynurenine (L-Kyn) and L-3- hydroxykynurenine (L-3OHKyn) into anthranilic acid (AA) and 3- hydroxyanthranilic acid (3-OHAA), respectively; Belongs to the kynureninase family. (458 aa) |
| | A0A2I2FBT5 | Putative NAD+ kinase. (498 aa) |
| | A0A2I2FBX2 | Ribonucleoside-diphosphate reductase small chain. (401 aa) |
| | A0A2I2FBZ6 | C6 finger domain protein. (664 aa) |
| | A0A2I2FCD8 | Phosphoribosyl pyrophosphokinase. (320 aa) |
| | A0A2I2FCV8 | Ribose-phosphate pyrophosphokinase 4. (431 aa) |
| | A0A2I2FDE0 | CTP synthase; Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen. (582 aa) |
| | A0A2I2FDG9 | Uncharacterized protein. (460 aa) |
| | A0A2I2FDQ9 | Phosphoribosylaminoimidazole carboxylase; In the C-terminal section; belongs to the AIR carboxylase family. Class I subfamily. (572 aa) |
| | A0A2I2FEH1 | Uracil phosphoribosyltransferase. (225 aa) |
| | A0A2I2FET9 | Pyruvate dehydrogenase E1 component alpha subunit mitochondrial. (405 aa) |
| | ADK1 | Adenylate kinase; Catalyzes the reversible transfer of the terminal phosphate group between ATP and AMP. Plays an important role in cellular energy homeostasis and in adenine nucleotide metabolism. Adenylate kinase activity is critical for regulation of the phosphate utilization and the AMP de novo biosynthesis pathways. (257 aa) |
| | A0A2I2FF82 | Phosphoribosylamidoimidazole-succinocarboxamidesynthase. (671 aa) |
| | A0A2I2FFA9 | Acyl-CoA dehydrogenase NM domain-like protein. (425 aa) |
| | A0A2I2FFG9 | Nicotinate-nucleotide pyrophosphorylase [carboxylating]; Involved in the catabolism of quinolinic acid (QA). Belongs to the NadC/ModD family. (323 aa) |
| | A0A2I2FFQ3 | Mitochondrial ATP synthase epsilon chain-domain-containing protein. (74 aa) |
| | A0A2I2FFX4 | Cullin repeat-like-containing domain protein. (1099 aa) |
| | A0A2I2FNQ4 | Uncharacterized protein. (336 aa) |
| | A0A2I2FMZ0 | Putative inosine-uridine preferring nucleoside hydrolase. (373 aa) |
| | A0A2I2FMF6 | ATP-NAD kinase. (444 aa) |
| | A0A2I2FLZ5 | 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. (527 aa) |
| | A0A2I2FLW4 | DFP-domain-containing protein. (397 aa) |
| | A0A2I2FLF0 | Deoxyuridine 5'-triphosphate nucleotidohydrolase. (203 aa) |
| | A0A2I2FLE4 | ATP synthase. (165 aa) |
| | A0A2I2FGJ3 | Pyruvate dehydrogenase E1 component subunit beta; The pyruvate dehydrogenase complex catalyzes the overall conversion of pyruvate to acetyl-CoA and CO2. (377 aa) |
| | A0A2I2FGF4 | Putative mitochondrial F1F0 ATP synthase subunit F. (101 aa) |
| | A0A2I2FGE8 | Uridine kinase; Belongs to the uridine kinase family. (452 aa) |
| | A0A2I2FG87 | Flavoprotein domain-containing protein. (627 aa) |
| | A0A2I2FG68 | Nicotinamide-nucleotide adenylyltransferase; Belongs to the eukaryotic NMN adenylyltransferase family. (285 aa) |
| | A0A2I2FG15 | Serine/threonine phosphatase. (2138 aa) |
| | A0A2I2EYK5 | Putative dihydroorotate reductase pyre. (507 aa) |
| | A0A2I2EYH7 | Dihydroorotase. (356 aa) |
| | A0A2I2EY71 | Uncharacterized protein. (607 aa) |
| | A0A2I2F4X2 | ATP citrate lyase subunit, putatibe. (484 aa) |
| | A0A2I2F4W1 | Putative pyruvate dehydrogenase complex component Pdx1. (290 aa) |
| | A0A2I2F4J7 | Riboflavin kinase. (208 aa) |
| | A0A2I2F4H8 | Uncharacterized protein. (506 aa) |
| | A0A2I2F4E3 | Putative deoxycytidylate deaminase. (343 aa) |
| | A0A2I2F3K9 | CoaE-domain-containing protein. (277 aa) |
| | A0A2I2F3B3 | Acetyl-coenzyme A synthetase. (669 aa) |
| | A0A2I2F2V6 | Carbamoyl-phosphate synthase mitochondrial. (1172 aa) |
| | A0A2I2F2J1 | Pantothenate kinase pank. (424 aa) |
| | A0A2I2F2E4 | Indoleamine 2,3-dioxygenase subfamily. (483 aa) |
| | BNA4 | Kynurenine 3-monooxygenase; Catalyzes the hydroxylation of L-kynurenine (L-Kyn) to form 3-hydroxy-L-kynurenine (L-3OHKyn). Required for synthesis of quinolinic acid. (500 aa) |
| | A0A2I2F272 | Indoleamine 2,3-dioxygenase. (405 aa) |
| | A0A2I2F1Z6 | ATP synthase subunit beta; Produces ATP from ADP in the presence of a proton gradient across the membrane. (517 aa) |
| | A0A2I2F1I6 | Purine nucleoside phosphorylase; The purine nucleoside phosphorylases catalyze the phosphorolytic breakdown of the N-glycosidic bond in the beta- (deoxy)ribonucleoside molecules, with the formation of the corresponding free purine bases and pentose-1-phosphate. (312 aa) |
| | A0A2I2F1F4 | Cytidylyltransferase family protein. (295 aa) |
| | A0A2I2F1D5 | Phosphoribosylglycinamide synthetase. (819 aa) |
| | A0A2I2F192 | Bifunctional purine biosynthesis protein ADE16. (594 aa) |
| | A0A2I2F0U1 | Pyruvate dehydrogenase E1 component subunit alpha; The pyruvate dehydrogenase complex catalyzes the overall conversion of pyruvate to acetyl-CoA and CO(2). (398 aa) |
| | A0A2I2F0P9 | Orotate phosphoribosyltransferase. (247 aa) |
| | A0A2I2F0K9 | PLAC8-domain-containing protein. (135 aa) |
| | A0A2I2F0A9 | ATP synthase E chain-domain-containing protein. (94 aa) |
| | BNA1 | 3-hydroxyanthranilate 3,4-dioxygenase; Catalyzes the oxidative ring opening of 3-hydroxyanthranilate to 2-amino-3-carboxymuconate semialdehyde, which spontaneously cyclizes to quinolinate. (195 aa) |
| | A0A2I2F075 | Flavo protein. (241 aa) |
| | A0A2I2F026 | Uncharacterized protein. (353 aa) |
| | A0A2I2EZZ7 | Isochorismatase hydrolase. (390 aa) |
| | A0A2I2EZZ2 | Acetyl-CoA carboxylase. (2292 aa) |
| | A0A2I2EZW1 | GMP synthase. (540 aa) |
| | A0A2I2EZU0 | FAD synthetase. (319 aa) |
| | A0A2I2EZR8 | Formyltetrahydrofolate deformylase. (287 aa) |
| | A0A2I2EZL9 | Putative adenosine kinase. (351 aa) |
| | A0A2I2EZ56 | Putative bifunctional pyrimidine biosynthesis protein. (2249 aa) |
| | A0A2I2EZ23 | Mitochondrial ATP synthase g subunit-domain-containing protein. (219 aa) |
| | A0A2I2EYY9 | Adenine phosphoribosyltransferase 1. (216 aa) |
| | A0A2I2EYT3 | Adenylate kinase isoenzyme 6 homolog; Broad-specificity nucleoside monophosphate (NMP) kinase that catalyzes the reversible transfer of the terminal phosphate group between nucleoside triphosphates and monophosphates. Has also ATPase activity. May be involved in rRNA maturation and transcription regulation. (592 aa) |
| | A0A2I2EYQ9 | Cytosine deaminase-uracil phosphoribosyltransferase fusion protein. (242 aa) |
| | A0A2I2FNR1 | Phosphoribosylformylglycinamidine synthase. (1360 aa) |
| | A0A2I2FNZ4 | Glutamine-dependent NAD(+) synthetase; In the C-terminal section; belongs to the NAD synthetase family. (717 aa) |
| | A0A2I2FP14 | Nucleoside diphosphate kinase. (155 aa) |
| | A0A2I2FP73 | Acyl-coenzyme A synthetase. (694 aa) |
| | A0A2I2FPR9 | Putative sugar kinase. (651 aa) |
| | A0A2I2FPY2 | Ribose-phosphate pyrophosphokinase 1. (492 aa) |
| | A0A2I2FQ19 | Dihydrolipoamide acetyltransferase component of pyruvate dehydrogenase complex. (815 aa) |
| | A0A2I2EYP6 | Ribonucleoside-diphosphate reductase; Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides. (857 aa) |
| | A0A2I2EYM2 | OMPdecase domain-containing protein. (457 aa) |
| | A0A2I2FLD8 | ATP synthase subunit gamma. (297 aa) |
| | ADK2 | GTP:AMP phosphotransferase, mitochondrial; Involved in maintaining the homeostasis of cellular nucleotides by catalyzing the interconversion of nucleoside phosphates. Has GTP:AMP phosphotransferase and ITP:AMP phosphotransferase activities. (234 aa) |
| | A0A2I2FKS9 | Guanylate kinase. (247 aa) |
| | A0A2I2FKK1 | RED_N domain-containing protein. (532 aa) |
| | A0A2I2FKE3 | Amidophosphoribosyltransferase. (1017 aa) |
| | A0A2I2FKD5 | ATP synthase subunit d, mitochondrial; Mitochondrial membrane ATP synthase (F(1)F(0) ATP synthase or Complex V) produces ATP from ADP in the presence of a proton gradient across the membrane which is generated by electron transport complexes of the respiratory chain. F-type ATPases consist of two structural domains, F(1) - containing the extramembraneous catalytic core, and F(0) - containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the cent [...] (173 aa) |
| | A0A2I2FKC0 | Acetyl-coenzyme A synthetase. (689 aa) |
| | A0A2I2FJX7 | Cytidine deaminase-like protein. (169 aa) |
| | A0A2I2FJX4 | Putative mitochondrial F1F0 ATP synthase subunit Atp18. (57 aa) |
