Entity Details

Primary name PMVK_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ15126
EntryNamePMVK_HUMAN
FullNamePhosphomevalonate kinase
TaxID9606
Evidenceevidence at protein level
Length192
SequenceStatuscomplete
DateCreated1998-07-15
DateModified2021-06-02

Ontological Relatives

GenesPMVK

GO terms

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GOName
GO:0004631 phosphomevalonate kinase activity
GO:0005524 ATP binding
GO:0005777 peroxisome
GO:0005829 cytosol
GO:0006695 cholesterol biosynthetic process
GO:0016020 membrane
GO:0016126 sterol biosynthetic process
GO:0019216 regulation of lipid metabolic process
GO:0019287 isopentenyl diphosphate biosynthetic process, mevalonate pathway
GO:0070062 extracellular exosome
GO:0070723 response to cholesterol

Subcellular Location

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Subcellular Location
Cytoplasm

Domains

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DomainNameCategoryType
IPR005919 Higher eukaryotic phosphomevalonate kinaseFamilyFamily
IPR027417 P-loop containing nucleoside triphosphate hydrolaseFamilyHomologous superfamily

Diseases

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Disease IDSourceNameDescription
175800 OMIMPorokeratosis 1, multiple types (POROK1)A form of porokeratosis, a disorder of faulty keratinization characterized by one or more atrophic patches surrounded by a distinctive hyperkeratotic ridgelike border called the cornoid lamella. The keratotic lesions can progress to overt cutaneous neoplasms, typically squamous cell carcinomas. Multiple clinical variants of porokeratosis are recognized, including porokeratosis of Mibelli, linear porokeratosis, disseminated superficial actinic porokeratosis, palmoplantar porokeratosis, and punctate porokeratosis. Different clinical presentations can be observed among members of the same family. Individuals expressing more than one variant have also been reported. The disease is caused by variants affecting the gene represented in this entry.

Interactions

3 interactions

InteractorPartnerSourcesPublicationsLink
PMVK_HUMANDDT4L_HUMANBioGRID, IntAct32296183 details
PMVK_HUMANZN177_HUMANBioGRID, IntAct32296183 details
PMVK_HUMANMCPH1_HUMANBioGRID29150431 details