Entity Details

Primary name TMLH_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ9NVH6
EntryNameTMLH_HUMAN
FullNameTrimethyllysine dioxygenase, mitochondrial
TaxID9606
Evidenceevidence at protein level
Length421
SequenceStatuscomplete
DateCreated2002-06-20
DateModified2021-06-02

Ontological Relatives

GenesTMLHE

GO terms

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GOName
GO:0005506 iron ion binding
GO:0005739 mitochondrion
GO:0005759 mitochondrial matrix
GO:0045329 carnitine biosynthetic process
GO:0050353 trimethyllysine dioxygenase activity
GO:0051354 negative regulation of oxidoreductase activity

Subcellular Location

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Subcellular Location
Mitochondrion matrix

Domains

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DomainNameCategoryType
IPR003819 TauD/TfdA-like domainDomainDomain
IPR010376 Gamma-butyrobetaine hydroxylase-like, N-terminalDomainDomain
IPR012776 Trimethyllysine dioxygenaseFamilyFamily
IPR038492 GBBH-like, N-terminal domain superfamilyFamilyHomologous superfamily
IPR042098 Taurine dioxygenase TauD-like superfamilyFamilyHomologous superfamily

Diseases

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Disease IDSourceNameDescription
300872 OMIMAutism, X-linked 6 (AUTSX6)A form of autism, a complex multifactorial, pervasive developmental disorder characterized by impairments in reciprocal social interaction and communication, restricted and stereotyped patterns of interests and activities, and the presence of developmental abnormalities by 3 years of age. Most individuals with autism also manifest moderate mental retardation. AUTSX6 patients may respond favorably to carnitine supplementation. The disease is caused by variants affecting the gene represented in this entry.

Drugs

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DrugNameSourceType
DB00126 Ascorbic acidDrugbanksmall molecule

Interactions

2 interactions

InteractorPartnerSourcesPublicationsLink
TMLH_HUMANTMLH_HUMANBioGRID, HPRD11431483 details
TMLH_HUMANTULP3_HUMANBioGRID33187986 details