KMO (gene)

Kynurenine 3-monooxygenase is an enzyme that in humans is encoded by the KMO gene.

KMO
Identifiers
AliasesKMO, dJ317G22.1, kynurenine 3-monooxygenase (kynurenine 3-hydroxylase), kynurenine 3-monooxygenase
External IDsOMIM: 603538 MGI: 2138151 HomoloGene: 2729 GeneCards: KMO
Orthologs
SpeciesHumanMouse
Entrez

8564

98256

Ensembl

ENSG00000117009

ENSMUSG00000039783

UniProt

O15229

Q91WN4

RefSeq (mRNA)

NM_003679

NM_133809

RefSeq (protein)

NP_003670

NP_598570

Location (UCSC)Chr 1: 241.53 – 241.6 MbChr 1: 175.45 – 175.49 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

Kynurenine 3-monooxygenase (KMO; EC 1.14.13.9) is an NADPH-dependent flavin monooxygenase that catalyzes the hydroxylation of the L-tryptophan metabolite L-kynurenine to form L-3-hydroxykynurenine.[supplied by OMIM] This is the first step in the degradation of Kyneurinine to Quinolinic acid. This pathway is involved in the activation of cytokine mediated changes in behavior due to inflammatory stimuli such as infections. The KMO gene is upregulated in the lung parenchyma of smokers.

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