Entity Details

Primary name CUL7_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ14999
EntryNameCUL7_HUMAN
FullNameCullin-7
TaxID9606
Evidenceevidence at protein level
Length1698
SequenceStatuscomplete
DateCreated1997-11-01
DateModified2021-06-02

Ontological Relatives

GenesCUL7

GO terms

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GOName
GO:0000226 microtubule cytoskeleton organization
GO:0000281 mitotic cytokinesis
GO:0001570 vasculogenesis
GO:0001837 epithelial to mesenchymal transition
GO:0001890 placenta development
GO:0005680 anaphase-promoting complex
GO:0005737 cytoplasm
GO:0005794 Golgi apparatus
GO:0005813 centrosome
GO:0005829 cytosol
GO:0006508 proteolysis
GO:0006511 ubiquitin-dependent protein catabolic process
GO:0007030 Golgi organization
GO:0007088 regulation of mitotic nuclear division
GO:0016032 viral process
GO:0016567 protein ubiquitination
GO:0031461 cullin-RING ubiquitin ligase complex
GO:0031467 Cul7-RING ubiquitin ligase complex
GO:0031625 ubiquitin protein ligase binding
GO:0036498 IRE1-mediated unfolded protein response
GO:0043687 post-translational protein modification
GO:0048471 perinuclear region of cytoplasm
GO:0050775 positive regulation of dendrite morphogenesis
GO:1990393 3M complex

Subcellular Location

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Subcellular Location
Cytoplasm
Golgi apparatus

Domains

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DomainNameCategoryType
IPR001373 Cullin, N-terminalDomainDomain
IPR004939 APC10/DOC domainDomainDomain
IPR008979 Galactose-binding-like domain superfamilyFamilyHomologous superfamily
IPR014722 Ribosomal protein L2, domain 2FamilyHomologous superfamily
IPR016024 Armadillo-type foldFamilyHomologous superfamily
IPR016158 Cullin homology domainDomainDomain
IPR019559 Cullin protein, neddylation domainDomainDomain
IPR021097 CPH domainDomainDomain
IPR031223 Cullin-7FamilyFamily
IPR036317 Cullin homology domain superfamilyFamilyHomologous superfamily

Diseases

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Disease IDSourceNameDescription
273750 OMIM3M syndrome 1 (3M1)An autosomal recessive disorder characterized by severe pre- and postnatal growth retardation, facial dysmorphism, large head circumference, and normal intelligence and endocrine function. Skeletal changes include long slender tubular bones and tall vertebral bodies. The disease is caused by variants affecting the gene represented in this entry.

Interactions

37 interactions

InteractorPartnerSourcesPublicationsLink
CUL7_HUMANPLXB3_HUMANBioGRID, HPRD, IntAct12421765 details
CUL7_HUMANMEG10_HUMANHPRD, IntAct12421765 unassigned5 details
CUL7_HUMANABL1_HUMANIntAct17474147 details
CUL7_HUMANP53_HUMANBioGRID, IntAct, MINT16547496 16875676 17229476 17298945 17332328 17942889 22653443 23443559 24711643 25003318 25609649 26186194 28514442 31152661 31343991 31570706 details
CUL7_HUMANSKP1_HUMANBioGRID, HPRD, IntAct10531037 12481031 17998335 23045529 27705803 31343991 details
CUL7_HUMANMTR1A_HUMANBioGRID, IntAct26514267 details
CUL7_HUMANFBXW8_HUMANBioGRID, DIP, HPRD10531037 12481031 16142236 17205132 17332328 17998335 18498745 21572988 21946088 23029530 23045529 31343991 details
CUL7_HUMANOBSL1_HUMANBioGRID, DIP21572988 21737058 25752541 31343991 details
CUL7_HUMANRBX1_HUMANBioGRID, HPRD10531037 12481031 16142236 16547496 23045529 25752541 31343991 details
CUL7_HUMANCOMD1_HUMANBioGRID21778237 details
CUL7_HUMANUBC12_HUMANBioGRID21946088 details
CUL7_HUMANGLMN_HUMANBioGRID, IntAct12904573 28514442 31343991 details
CUL7_HUMANCCND1_HUMANBioGRID17205132 details
CUL7_HUMANASB2_HUMANBioGRID21119685 details
CUL7_HUMANCUL9_HUMANBioGRID15964813 17229476 17332328 31343991 details
CUL7_HUMANFBX2_HUMANBioGRID21135578 details
CUL7_HUMANERPG3_HUMANBioGRID22032989 details
CUL7_HUMANERCC6_HUMANBioGRID22032989 details
CUL7_HUMANTBC3C_HUMANBioGRID23029530 details
CUL7_HUMANTBC3A_HUMANBioGRID23029530 details
CUL7_HUMANCUL7_HUMANBioGRID23045529 24711643 31343991 details
CUL7_HUMANM4K1_HUMANBioGRID24362026 details
CUL7_HUMANTCPB_HUMANBioGRID24711643 details
CUL7_HUMANCDK1_HUMANBioGRID24711643 details
CUL7_HUMANH2B2E_HUMANBioGRID24711643 29507117 details
CUL7_HUMANHNRPU_HUMANBioGRID24711643 details
CUL7_HUMANRPB1_HUMANBioGRID24711643 30349055 details
CUL7_HUMANSMU1_HUMANBioGRID24711643 29507117 details
CUL7_HUMANXRCC5_HUMANBioGRID24711643 details
CUL7_HUMANCCDC8_HUMANBioGRID24711643 25752541 31343991 details
CUL7_HUMANAMRA1_HUMANBioGRID25499913 details
CUL7_HUMANFBXW7_HUMANBioGRID12904573 details
CUL7_HUMANHDAC4_HUMANBioGRID25752541 details
CUL7_HUMANHDAC5_HUMANBioGRID25752541 details
CUL7_HUMANIRS1_HUMANBioGRID18498745 29269414 details
CUL7_HUMANSTK4_HUMANBioGRID29632206 32252802 details
CUL7_HUMANTULP3_HUMANBioGRID33187986 details