1-hydroxy-2-naphthoate 1,2-dioxygenase

In today's world, 1-hydroxy-2-naphthoate 1,2-dioxygenase has become increasingly relevant in people's lives. Whether on a personal, professional or social level, 1-hydroxy-2-naphthoate 1,2-dioxygenase has significantly impacted the way we function every day. Its implications are so broad and diverse that it is impossible to ignore its influence on our lives. In this article, we will explore the different facets of 1-hydroxy-2-naphthoate 1,2-dioxygenase, analyzing its impact on society, its evolution over time, and its role in the future. Without a doubt, 1-hydroxy-2-naphthoate 1,2-dioxygenase is a topic that deserves our attention and reflection, since its presence is undeniable in the reality we inhabit.

1-hydroxy-2-naphthoate 1,2-dioxygenase
Identifiers
EC no.1.13.11.38
CAS no.85941-64-6
Databases
IntEnzIntEnz view
BRENDABRENDA entry
ExPASyNiceZyme view
KEGGKEGG entry
MetaCycmetabolic pathway
PRIAMprofile
PDB structuresRCSB PDB PDBe PDBsum
Gene OntologyAmiGO / QuickGO
Search
PMCarticles
PubMedarticles
NCBIproteins

In enzymology, a 1-hydroxy-2-naphthoate 1,2-dioxygenase (EC 1.13.11.38) is an enzyme that catalyzes the chemical reaction

1-hydroxy-2-naphthoate + O2 (3Z)-4-(2-carboxyphenyl)-2-oxobut-3-enoate

Thus, the two substrates of this enzyme are 1-hydroxy-2-naphthoate and O2, whereas its product is (3Z)-4-(2-carboxyphenyl)-2-oxobut-3-enoate.

This enzyme participates in naphthalene and anthracene degradation. It employs one cofactor, iron.

Nomenclature

This enzyme belongs to the family of oxidoreductases, specifically those acting on single donors with O2 as oxidant and incorporation of two atoms of oxygen into the substrate (oxygenases). The oxygen incorporated need not be derived from O2. The systematic name of this enzyme class is 1-hydroxy-2-naphthoate:oxygen 1,2-oxidoreductase (decyclizing). Other names in common use include 1-hydroxy-2-naphthoate dioxygenase, 1-hydroxy-2-naphthoate-degrading enzyme, and 1-hydroxy-2-naphthoic acid dioxygenase.

References

  • Barnsley EA (April 1983). "Phthalate pathway of phenanthrene metabolism: formation of 2'-carboxybenzalpyruvate". Journal of Bacteriology. 154 (1): 113–7. PMC 217437. PMID 6833175.