Entity Details

Primary name MVD1_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionP53602
EntryNameMVD1_HUMAN
FullNameDiphosphomevalonate decarboxylase
TaxID9606
Evidenceevidence at protein level
Length400
SequenceStatuscomplete
DateCreated1996-10-01
DateModified2021-06-02

Ontological Relatives

GenesMVD

GO terms

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GOName
GO:0004163 diphosphomevalonate decarboxylase activity
GO:0005524 ATP binding
GO:0005829 cytosol
GO:0006489 dolichyl diphosphate biosynthetic process
GO:0006695 cholesterol biosynthetic process
GO:0008284 positive regulation of cell population proliferation
GO:0008299 isoprenoid biosynthetic process
GO:0019216 regulation of lipid metabolic process
GO:0019287 isopentenyl diphosphate biosynthetic process, mevalonate pathway
GO:0030544 Hsp70 protein binding
GO:0042803 protein homodimerization activity

Subcellular Location

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Subcellular Location
Cytoplasm

Domains

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DomainNameCategoryType
IPR005935 Diphosphomevalonate/phosphomevalonate decarboxylaseFamilyFamily
IPR006204 GHMP kinase N-terminal domainDomainDomain
IPR014721 Ribosomal protein S5 domain 2-type fold, subgroupFamilyHomologous superfamily
IPR020568 Ribosomal protein S5 domain 2-type foldFamilyHomologous superfamily
IPR029765 Diphosphomevalonate decarboxylaseFamilyFamily
IPR036554 GHMP kinase, C-terminal domain superfamilyFamilyHomologous superfamily
IPR041431 Mvd1, C-terminalDomainDomain

Diseases

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Disease IDSourceNameDescription
614714 OMIMPorokeratosis 7, multiple types (POROK7)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

6 interactions

InteractorPartnerSourcesPublicationsLink
MVD1_HUMANGNB5_HUMANBioGRID, HPRD, IntAct16169070 details
MVD1_HUMANEF1G_HUMANBioGRID, HPRD, IntAct16169070 details
MVD1_HUMAN4EBP1_HUMANHPRD, IntAct16169070 details
MVD1_HUMANBTAF1_HUMANBioGRID, HPRD12646231 details
MVD1_HUMANGRP75_HUMANBioGRID, HPRD12646231 details
MVD1_HUMANMVD1_HUMANBioGRID, HPRD8626466 details