MMDBr0013009 | Fe2+ | Iron(3+) | Cbb3-type cytochrome c oxidase subunit CcoN1 | Oxidation | RHEA | 34755880 |
MMDBr0013010 | Fe2+ | Iron(3+) | Cytochrome c oxidase subunit 1 | Oxidation | RHEA | 34755880 |
MMDBr0013170 | Adenosine monophosphate | ADP | Adenylate kinase | Phosphorylation | RHEA | 34755880 |
MMDBr0013172 | Water | formate | Kynurenine formamidase | Amide hydrolysis | RHEA | 34755880 |
MMDBr0013179 | Adenosine triphosphate | ADP | Replicase large subunit | Synthesis of a primer | RHEA | 34755880 |
MMDBr0013339 | aldehydo-D-ribose 5-phosphate | D-Ribulose 5-phosphate | Bifunctional ribokinase/ribose-5-phosphate isomerase A | Isomerization | RHEA | 34755880 |
MMDBr0013416 | L-Glutamic acid | Ornithine | Arginine biosynthesis bifunctional protein ArgJ | Acetylation; Synthesis | RHEA | 34755880 |
MMDBr0013437 | 5-Methylthioribulose 1-phosphate | 5-(methylsulfanyl)-2,3-dioxopentyl phosphate | Probable bifunctional methylthioribose-1-phosphate isomerase/methylthioribulose-1-phosphate dehydratase | Dehydration and isomerisation | RHEA | 34755880 |
MMDBr0013458 | Guanosine triphosphate | Guanosine diphosphate | Adenylosuccinate synthetase | Synthesis | RHEA | 34755880 |
MMDBr0013570 | Water | 2-Aminobenzoic acid | Kynureninase | Cleavage of kynurenine | RHEA | 34755880 |
MMDBr0013908 | Guanosine triphosphate | Guanosine diphosphate | GTPase ArgK | Dephosphorylation; Hydrolysis; Nucleic acid synthesis and/or repair | RHEA | 34755880 |
MMDBr0013941 | S-Methyl-5-thio-alpha-D-ribose 1-phosphate | 5-Methylthioribulose 1-phosphate | 5-deoxyribose 1-phosphate isomerase | Isomerization | RHEA | 34755880 |
MMDBr0014134 | 5-(methylsulfanyl)-2,3-dioxopentyl phosphate | 1,2-dihydroxy-5-(methylsulfanyl)pent-1-en-3-one | Enolase-phosphatase E1 | Enolization | RHEA | 34755880 |
MMDBr0014436 | Acetyl-CoA | CoA | Amino-acid acetyltransferase | Acetylation; Synthesis | RHEA | 34755880 |
MMDBr0014507 | ADP-D-ribose 1''-phosphate | ADP-D-ribose | ADP-ribose 1''-phosphate phosphatase | Dephosphorylation | RHEA | 34755880 |
MMDBr0014517 | L-3-Hydroxykynurenine | 3-Hydroxyanthranilic acid | Kynureninase | Cleavage of kynurenine | RHEA | 34755880 |
MMDBr0016254 | Iron(3+) | Fe2+ | NADH-cytochrome b5 reductase 2 | Reduction | RHEA | 34755880 |
MMDBr0024370 | S-Adenosylmethionine | Hydrogen Ion | Phosphatidylethanolamine N-methyltransferase | Methylation | RHEA | 34755880 |
MMDBr0024568 | Water | Hydrogen Ion | Aspartyl/glutamyl-tRNA(Asn/Gln) amidotransferase subunit C | Amide group addition | RHEA | 34755880 |
MMDBr0024586 | L-Serine | Hydrogen Ion | Probable bifunctional tRNA threonylcarbamoyladenosine biosynthesis protein | Phosphorylation; Synthesis | RHEA | 34755880 |
MMDBr0024720 | Uridine diphosphate glucose | Hydrogen Ion | Sterol 3-beta-glucosyltransferase | Transfer of a glucosyl group | RHEA | 34755880 |
MMDBr0024897 | S-Adenosylmethionine | Hydrogen Ion | tRNA:m(4)X modification enzyme TRM13 | Not Available | RHEA | 34755880 |
MMDBr0025071 | S-Adenosylmethionine | S-Adenosylhomocysteine | tRNA (guanine-N(7)-)-methyltransferase | Methylation | RHEA | 34755880 |
MMDBr0025137 | S-Adenosylmethionine | Hydrogen Ion | tRNA:m(4)X modification enzyme TRM13 | Not Available | RHEA | 34755880 |
MMDBr0025138 | S-Adenosylmethionine | Hydrogen Ion | tRNA:m(4)X modification enzyme TRM13 | Not Available | RHEA | 34755880 |
MMDBr0025237 | L-Threonine | Hydrogen Ion | Probable bifunctional tRNA threonylcarbamoyladenosine biosynthesis protein | Phosphorylation; Synthesis | RHEA | 34755880 |
MMDBr0025305 | NADP(+) | Hydrogen Ion | Very-long-chain 3-oxoacyl-CoA reductase | Reduction | RHEA | 34755880 |
MMDBr0025452 | NADP(+) | Hydrogen Ion | tRNA-dihydrouridine(47) synthase [NAD(P)(+)] | Synthesis | RHEA | 34755880 |
MMDBr0025453 | Hydrogen Ion | NADP(+) | tRNA-dihydrouridine(47) synthase [NAD(P)(+)] | Synthesis | RHEA | 34755880 |
MMDBr0025454 | NAD | Hydrogen Ion | tRNA-dihydrouridine(47) synthase [NAD(P)(+)] | Synthesis | RHEA | 34755880 |
MMDBr0025455 | Hydrogen Ion | NAD | tRNA-dihydrouridine(47) synthase [NAD(P)(+)] | Synthesis | RHEA | 34755880 |