Enzymes
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GO Molecular Function help_outline |
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Reaction participants Show >> << Hide
- Name help_outline 4-aminoimidazole Identifier CHEBI:16607 (CAS: 4919-03-3) help_outline Charge 0 Formula C3H5N3 InChIKeyhelp_outline QRZMXADUXZADTF-UHFFFAOYSA-N SMILEShelp_outline Nc1c[nH]cn1 2D coordinates Mol file for the small molecule Search links Involved in 2 reaction(s) Find molecules that contain or resemble this structure Find proteins in UniProtKB for this molecule
- Name help_outline H+ Identifier CHEBI:15378 Charge 1 Formula H InChIKeyhelp_outline GPRLSGONYQIRFK-UHFFFAOYSA-N SMILEShelp_outline [H+] 2D coordinates Mol file for the small molecule Search links Involved in 9,176 reaction(s) Find molecules that contain or resemble this structure Find proteins in UniProtKB for this molecule
- Name help_outline H2O Identifier CHEBI:15377 (Beilstein: 3587155; CAS: 7732-18-5) help_outline Charge 0 Formula H2O InChIKeyhelp_outline XLYOFNOQVPJJNP-UHFFFAOYSA-N SMILEShelp_outline [H]O[H] 2D coordinates Mol file for the small molecule Search links Involved in 6,048 reaction(s) Find molecules that contain or resemble this structure Find proteins in UniProtKB for this molecule
- Name help_outline imidazol-4-one Identifier CHEBI:28470 (Beilstein: 105893) help_outline Charge 0 Formula C3H4N2O InChIKeyhelp_outline CAAMSDWKXXPUJR-UHFFFAOYSA-N SMILEShelp_outline O=C1CN=CN1 2D coordinates Mol file for the small molecule Search links Involved in 2 reaction(s) Find molecules that contain or resemble this structure Find proteins in UniProtKB for this molecule
- Name help_outline NH4+ Identifier CHEBI:28938 (CAS: 14798-03-9) help_outline Charge 1 Formula H4N InChIKeyhelp_outline QGZKDVFQNNGYKY-UHFFFAOYSA-O SMILEShelp_outline [H][N+]([H])([H])[H] 2D coordinates Mol file for the small molecule Search links Involved in 518 reaction(s) Find molecules that contain or resemble this structure Find proteins in UniProtKB for this molecule
Cross-references
RHEA:22348 | RHEA:22349 | RHEA:22350 | RHEA:22351 | |
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Reaction direction help_outline | undefined | left-to-right | right-to-left | bidirectional |
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Publications
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Purine fermentation by Clostridium cylindrosporum. V. Formiminoglycine.
PRICER W.E. Jr., RABINOWITZ J.C.
J Biol Chem 222:537-554(1956) [PubMed] [EuropePMC]
This publication is cited by 2 other entries.
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Degradation of purines and pyrimidines by microorganisms.
Vogels G.D., Van der Drift C.
Bacteriol Rev 40:403-468(1976) [PubMed] [EuropePMC]
This publication is cited by 2 other entries.
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Purine metabolism in Methanococcus vannielii.
DeMoll E., Auffenberg T.
Methanococcus vannielii is capable of degrading purines to the extent that each of these purines may serve as the sole nitrogen source for growth. Results presented here demonstrate that purine degradation by M. vannielii is accomplished by a route similar to that described for clostridia. Various ... >> More
Methanococcus vannielii is capable of degrading purines to the extent that each of these purines may serve as the sole nitrogen source for growth. Results presented here demonstrate that purine degradation by M. vannielii is accomplished by a route similar to that described for clostridia. Various characteristics of the purine-degrading pathway of M. vannielii are described. Additionally, it is shown that M. vannielii does not extensively degrade exogenously supplied guanine if that compound is present at levels near or lower than those required to supply the cellular guanine requirement. Under those conditions, M. vannielii incorporates the intact guanine molecule into its guanine nucleotide pool. The benefits of a purine-degrading pathway to methanogens are discussed. << Less
J Bacteriol 175:5754-5761(1993) [PubMed] [EuropePMC]
This publication is cited by 2 other entries.
Comments
RHEA:22348 part of RHEA:33259