Entity Details

Primary name KAD7_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ96M32
EntryNameKAD7_HUMAN
FullNameAdenylate kinase 7
TaxID9606
Evidenceevidence at protein level
Length723
SequenceStatuscomplete
DateCreated2003-10-03
DateModified2021-06-02

Ontological Relatives

GenesAK7

GO terms

Show/Hide Table
GOName
GO:0004017 adenylate kinase activity
GO:0004127 cytidylate kinase activity
GO:0004550 nucleoside diphosphate kinase activity
GO:0005524 ATP binding
GO:0005737 cytoplasm
GO:0005829 cytosol
GO:0006165 nucleoside diphosphate phosphorylation
GO:0009142 nucleoside triphosphate biosynthetic process
GO:0015949 nucleobase-containing small molecule interconversion
GO:0030030 cell projection organization
GO:0031514 motile cilium

Subcellular Location

Show/Hide Table
Subcellular Location
Cell projection
Cytoplasm

Domains

Show/Hide Table
DomainNameCategoryType
IPR000850 Adenylate kinase/UMP-CMP kinaseFamilyFamily
IPR007858 Dpy-30 motifSiteConserved site
IPR026867 Adenylate kinase 7FamilyFamily
IPR027417 P-loop containing nucleoside triphosphate hydrolaseFamilyHomologous superfamily
IPR036291 NAD(P)-binding domain superfamilyFamilyHomologous superfamily

Diseases

Show/Hide Table
Disease IDSourceNameDescription
617965 OMIMSpermatogenic failure 27 (SPGF27)An autosomal recessive infertility disorder caused by spermatogenesis defects that result in multiple morphologic abnormalities of the sperm flagella, including short, irregular, coiled, or absent flagella. The disease is caused by variants affecting the gene represented in this entry.

Interactions

0 interactions

InteractorPartnerSourcesPublicationsLink