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KMO (gene)

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AliasesKMO, dJ317G22.1, kynurenine 3-monooxygenase (kynurenine 3-hydroxylase), kynurenine 3-monooxygenase
End241,595,642 bp[1]
KMO
Identifiers
AliasesKMO, dJ317G22.1, kynurenine 3-monooxygenase (kynurenine 3-hydroxylase), kynurenine 3-monooxygenase
External IDsOMIM: 603538; MGI: 2138151; HomoloGene: 2729; GeneCards: KMO; OMA:KMO - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
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[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Kynurenine 3-monooxygenase is an enzyme that in humans is encoded by the KMO gene.[5][6]

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][6] 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.[7] The KMO gene is upregulated in the lung parenchyma of smokers. [8]

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