Enzymes
| UniProtKB help_outline | 1 proteins |
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- Name help_outline 1-hydroxy-2-naphthoate Identifier CHEBI:15992 (Beilstein: 3906464) help_outline Charge -1 Formula C11H7O3 InChIKeyhelp_outline SJJCQDRGABAVBB-UHFFFAOYSA-M SMILEShelp_outline Oc1c(ccc2ccccc12)C([O-])=O 2D coordinates Mol file for the small molecule Search links Involved in 3 reaction(s) Find molecules that contain or resemble this structure Find proteins in UniProtKB for this molecule
- Name help_outline O2 Identifier CHEBI:15379 (CAS: 7782-44-7) help_outline Charge 0 Formula O2 InChIKeyhelp_outline MYMOFIZGZYHOMD-UHFFFAOYSA-N SMILEShelp_outline O=O 2D coordinates Mol file for the small molecule Search links Involved in 2,648 reaction(s) Find molecules that contain or resemble this structure Find proteins in UniProtKB for this molecule
- Name help_outline (3Z)-4-(2-carboxyphenyl)-2-oxobut-3-enoate Identifier CHEBI:58794 Charge -2 Formula C11H6O5 InChIKeyhelp_outline APKXMKWCGDBYNV-WAYWQWQTSA-L SMILEShelp_outline [O-]C(=O)C(=O)\C=C/c1ccccc1C([O-])=O 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
Cross-references
| RHEA:14749 | RHEA:14750 | RHEA:14751 | RHEA:14752 | |
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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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Phthalate pathway of phenanthrene metabolism: formation of 2'-carboxybenzalpyruvate.
Barnsley E.A.
The metabolism of phenanthrene by a gram-negative organism able to use this compound as a sole source of carbon and energy has been examined. 1-Hydroxy-2-naphthoic acid was oxidized by oxygen in a reaction catalyzed by a dioxygenase which was activated by ferrous ions. The stoichiometry of the oxi ... >> More
The metabolism of phenanthrene by a gram-negative organism able to use this compound as a sole source of carbon and energy has been examined. 1-Hydroxy-2-naphthoic acid was oxidized by oxygen in a reaction catalyzed by a dioxygenase which was activated by ferrous ions. The stoichiometry of the oxidation and the UV spectrum of the product were consistent with the identification of the product as 2'-carboxybenzalpyruvate. This was confirmed by cleaving the product with a partially purified aldolase to yield 2-carboxybenzaldehyde and pyruvate. A number of enzymes for the metabolism of 1-hydroxy-2-naphthoic acid were induced by growth on phthalate or (less well) by growth on protocatechuate. The latter supported only a slow rate of growth, and this and poor induction may have been due to a slow rate of entry into the cell. << Less
J Bacteriol 154:113-117(1983) [PubMed] [EuropePMC]
This publication is cited by 1 other entry.