Entity Details

Primary name CHKB_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ9Y259
EntryNameCHKB_HUMAN
FullNameCholine/ethanolamine kinase
TaxID9606
Evidenceevidence at protein level
Length395
SequenceStatuscomplete
DateCreated2000-05-30
DateModified2021-06-02

Ontological Relatives

GenesCHKB

GO terms

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GOName
GO:0004103 choline kinase activity
GO:0004305 ethanolamine kinase activity
GO:0005524 ATP binding
GO:0005829 cytosol
GO:0006646 phosphatidylethanolamine biosynthetic process
GO:0006656 phosphatidylcholine biosynthetic process

Subcellular Location

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Domains

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DomainNameCategoryType
IPR011009 Protein kinase-like domain superfamilyFamilyHomologous superfamily
IPR026712 Choline/Ethanolamine kinaseFamilyFamily

Diseases

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Disease IDSourceNameDescription
602541 OMIMMuscular dystrophy, congenital, megaconial type (MDCMC)An autosomal recessive, congenital muscular dystrophy characterized by early-onset muscle wasting, mental retardation, and dilated cardiomyopathy in half of affected individuals. Some patients may die from cardiomyopathy in the first or second decade of life. Muscle biopsy shows peculiar enlarged mitochondria that are prevalent toward the periphery of the fibers but are sparse in the center. The disease is caused by variants affecting the gene represented in this entry.

Drugs

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DrugNameSourceType
DB00122 CholineDrugbanksmall molecule
DB14006 Choline salicylateDrugbanksmall molecule

Interactions

0 interactions

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