Your Input: | |||||
A0A2I1C5Y4 | Phosphoribosylaminoimidazolecarboxamide formyltransferase/IMP cyclohydrolase. (595 aa) | ||||
A0A2I1BSN6 | Fungal_trans domain-containing protein. (542 aa) | ||||
A0A2I1BSU5 | ATP synthase subunit beta; Produces ATP from ADP in the presence of a proton gradient across the membrane. (511 aa) | ||||
A0A2I1BTB2 | Ribose-phosphate pyrophosphokinase. (436 aa) | ||||
A0A2I1BTR5 | Indoleamine 2,3-dioxygenase subfamily. (497 aa) | ||||
A0A2I1BUJ7 | Indoleamine 2,3-dioxygenase. (449 aa) | ||||
A0A2I1BV83 | GMP synthase. (543 aa) | ||||
A0A2I1BW43 | ATP synthase subunit gamma. (287 aa) | ||||
A0A2I1BWA3 | Putative ATP synthase delta chain mitochondrial. (165 aa) | ||||
A0A2I1BWC9 | dUTP diphosphatase. (175 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. (247 aa) | ||||
A0A2I1BX75 | Putative acetate-CoA ligase. (719 aa) | ||||
A0A2I1BXB9 | Dihydroorotase, homodimeric type. (360 aa) | ||||
A0A2I1BY00 | Putative AMP deaminase; Belongs to the metallo-dependent hydrolases superfamily. Adenosine and AMP deaminases family. (937 aa) | ||||
A0A2I1BY40 | Adenine phosphoribosyltransferase 1. (217 aa) | ||||
A0A2I1BY93 | Nicotinate phosphoribosyltransferase. (490 aa) | ||||
A0A2I1BZ41 | Putative ribose phosphate diphosphokinase Prs1. (483 aa) | ||||
A0A2I1BZ60 | Acetyltransferase component of pyruvate dehydrogenase complex; The pyruvate dehydrogenase complex catalyzes the overall conversion of pyruvate to acetyl-CoA and CO(2). (851 aa) | ||||
A0A2I1BZ95 | CTP synthase; Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen. (569 aa) | ||||
A0A2I1BZQ5 | 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. (235 aa) | ||||
A0A2I1BZV5 | Uncharacterized protein. (353 aa) | ||||
A0A2I1C005 | Uncharacterized protein. (92 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. (192 aa) | ||||
A0A2I1C080 | ATP synthase subunit alpha; Produces ATP from ADP in the presence of a proton gradient across the membrane. (467 aa) | ||||
A0A2I1C0A1 | HCP-like protein. (420 aa) | ||||
A0A2I1C0C3 | CBD9-like protein. (408 aa) | ||||
A0A2I1C0D5 | Putative mitochondrial ATPase subunit ATP4. (283 aa) | ||||
A0A2I1C1P7 | Pyruvate dehydrogenase E1 component subunit beta; The pyruvate dehydrogenase complex catalyzes the overall conversion of pyruvate to acetyl-CoA and CO2. (377 aa) | ||||
A0A2I1C1S8 | Nicotinate-nucleotide pyrophosphorylase [carboxylating]; Involved in the catabolism of quinolinic acid (QA). Belongs to the NadC/ModD family. (313 aa) | ||||
A0A2I1C1X2 | Putative glutaryl-CoA dehydrogenase. (432 aa) | ||||
A0A2I1C1Y1 | Phosphoribosyl-aminoimidazole-succinocarboxamide synthase. (302 aa) | ||||
A0A2I1C2A8 | Putative pantothenate kinase. (456 aa) | ||||
A0A2I1C2C2 | Putative phosphopantothenate-cysteine ligase. (395 aa) | ||||
A0A2I1C2J9 | Putative pyruvate dehydrogenase complex component Pdx1. (291 aa) | ||||
A0A2I1C361 | Uncharacterized protein. (101 aa) | ||||
A0A2I1C393 | Probable acetate kinase. (423 aa) | ||||
A0A2I1C4H5 | Phosphoribosylaminoimidazole carboxylase; In the C-terminal section; belongs to the AIR carboxylase family. Class I subfamily. (555 aa) | ||||
A0A2I1C4W9 | Acetyl-coenzyme A synthetase. (670 aa) | ||||
A0A2I1C4Y1 | Phosphoribosyl diphosphate synthase. (320 aa) | ||||
A0A2I1C4Y3 | P-loop containing nucleoside triphosphate hydrolase protein. (331 aa) | ||||
A0A2I1C5A5 | Indoleamine 2,3-dioxygenase. (430 aa) | ||||
A0A2I1C5E1 | ATP-synt_C domain-containing protein; Belongs to the ATPase C chain family. (144 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. (464 aa) | ||||
A0A2I1C5I8 | Pantetheine-phosphate adenylyltransferase family protein. (404 aa) | ||||
A0A2I1C624 | Putative cytidylyltransferase. (279 aa) | ||||
A0A2I1C6C5 | Uncharacterized protein. (253 aa) | ||||
A0A2I1C6E1 | Ribonucleoside-diphosphate reductase; Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides. (859 aa) | ||||
A0A2I1C6H3 | Putative flavo protein. (243 aa) | ||||
A0A2I1C6Q5 | Putative xanthine-guanine phosphoribosyl transferase Xpt1. (173 aa) | ||||
A0A2I1C6Q9 | Uncharacterized protein. (65 aa) | ||||
A0A2I1C7U4 | Putative mitochondrial F1F0-ATP synthase g subunit. (196 aa) | ||||
A0A2I1C7X3 | OMPdecase domain-containing protein. (451 aa) | ||||
A0A2I1C871 | 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. (424 aa) | ||||
A0A2I1C8D3 | PLAC8 family protein. (142 aa) | ||||
A0A2I1C9F2 | Uncharacterized protein. (144 aa) | ||||
A0A2I1C9R1 | 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. (295 aa) | ||||
A0A2I1CA30 | Guanylate kinase. (191 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. (255 aa) | ||||
A0A2I1CAC8 | Pyruvate dehydrogenase E1 component subunit alpha; The pyruvate dehydrogenase complex catalyzes the overall conversion of pyruvate to acetyl-CoA and CO(2). (405 aa) | ||||
A0A2I1CAR5 | Putative uridine nucleosidase Urh1. (396 aa) | ||||
A0A2I1CC26 | Putative formyltetrahydrofolate deformylase. (292 aa) | ||||
A0A2I1CC80 | Putative bifunctional pyrimidine biosynthesis protein. (2255 aa) | ||||
A0A2I1CC89 | Putative FAD synthetase. (309 aa) | ||||
A0A2I1CCE8 | ATP citrate lyase subunit, putatibe. (486 aa) | ||||
A0A2I1CCW2 | Flavoprotein domain-containing protein. (627 aa) | ||||
A0A2I1CD00 | Nicotinamide-nucleotide adenylyltransferase; Belongs to the eukaryotic NMN adenylyltransferase family. (288 aa) | ||||
A0A2I1CD17 | Adenylate cyclase AcyA. (2117 aa) | ||||
A0A2I1CD39 | RED_N domain-containing protein. (536 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. (512 aa) | ||||
A0A2I1CDR4 | 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. (320 aa) | ||||
A0A2I1CDY6 | Putative bifunctional purine Ade1. (822 aa) | ||||
A0A2I1CE78 | 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) | ||||
A0A2I1CE79 | Amidophosphoribosyltransferase. (583 aa) | ||||
A0A2I1CFI0 | PLAC8 family protein. (156 aa) | ||||
A0A2I1CFT1 | Putative dephospho-CoA kinase. (262 aa) | ||||
A0A2I1CFW8 | V-type proton ATPase catalytic subunit A. (606 aa) | ||||
A0A2I1CFZ7 | Uncharacterized protein. (367 aa) | ||||
A0A2I1CG01 | Phosphoribosylformylglycinamidine synthase. (1362 aa) | ||||
A0A2I1CG78 | Thymidylate kinase. (221 aa) | ||||
A0A2I1CG84 | Glutamine-dependent NAD(+) synthetase; In the C-terminal section; belongs to the NAD synthetase family. (717 aa) | ||||
A0A2I1CGA3 | P-loop containing nucleoside triphosphate hydrolase protein. (322 aa) | ||||
A0A2I1CGA8 | Nucleoside diphosphate kinase. (153 aa) | ||||
A0A2I1CGI8 | Cytosine deaminase-uracil phosphoribosyltransferase fusion protein. (242 aa) | ||||
A0A2I1CGK4 | 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. (177 aa) | ||||
A0A2I1CGM3 | Poly(P)/ATP NAD kinase. (436 aa) | ||||
A0A2I1CGS5 | Putative adenosine kinase. (351 aa) | ||||
A0A2I1CI78 | ATP synthase subunit beta; Produces ATP from ADP in the presence of a proton gradient across the membrane. (504 aa) | ||||
A0A2I1CIS0 | Putative ribonucleotide reductase small subunit RnrA. (405 aa) | ||||
A0A2I1CIY1 | Putative NAD+ kinase. (501 aa) | ||||
A0A2I1CK84 | Putative NAD+ kinase Utr1. (657 aa) | ||||
A0A2I1CKZ0 | 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) | ||||
A0A2I1CKZ2 | Putative isochorismatase family hydrolase. (235 aa) | ||||
A0A2I1CLA4 | Pyruvate dehydrogenase. (388 aa) | ||||
A0A2I1CLI1 | Putative mitochondrial F1F0 ATP synthase subunit F. (101 aa) | ||||
A0A2I1CLI3 | Uridine kinase; Belongs to the uridine kinase family. (453 aa) | ||||
A0A2I1CLK8 | Dienelactone hydrolase. (453 aa) | ||||
A0A2I1CLL0 | Riboflavin kinase. (217 aa) | ||||
A0A2I1CLQ7 | Deoxycytidylate deaminase. (379 aa) | ||||
A0A2I1CLX4 | Putative acyl-CoA synthetase. (659 aa) | ||||
A0A2I1CM15 | Orotidine 5'-phosphate decarboxylase; Belongs to the OMP decarboxylase family. (286 aa) | ||||
A0A2I1CM44 | Acetyl-CoA carboxylase. (2249 aa) | ||||
A0A2I1CM53 | Putative isochorismatase family hydrolase. (410 aa) | ||||
A0A2I1CM91 | Mitochondrial ATP synthase epsilon chain domain-containing protein. (71 aa) | ||||
A0A2I1CMG3 | Large subunit of carbamoyl-phosphate synthase. (1175 aa) | ||||
BNA5-2 | 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. (487 aa) | ||||
A0A2I1CMQ0 | RING-type domain-containing protein. (1033 aa) | ||||
A0A2I1CMR3 | Putative dihydroorotate reductase pyre. (515 aa) | ||||
A0A2I1CMT8 | Orotate phosphoribosyltransferase. (246 aa) | ||||
A0A2I1CMY6 | Adenylosuccinate lyase; Belongs to the lyase 1 family. Adenylosuccinate lyase subfamily. (483 aa) | ||||
A0A2I1CN40 | Putative ATP synthase oligomycin sensitivity conferral protein. (227 aa) | ||||
A0A2I1CPA7 | Uracil phosphoribosyltransferase. (227 aa) | ||||
BNA1-2 | 3-hydroxyanthranilate 3,4-dioxygenase; Catalyzes the oxidative ring opening of 3-hydroxyanthranilate to 2-amino-3-carboxymuconate semialdehyde, which spontaneously cyclizes to quinolinate. (174 aa) | ||||
A0A2I1CPV7 | Zn(2)-C6 fungal-type domain-containing protein. (655 aa) |