Entity Details

Primary name FBX11_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ86XK2
EntryNameFBX11_HUMAN
FullNameF-box only protein 11
TaxID9606
Evidenceevidence at protein level
Length927
SequenceStatuscomplete
DateCreated2003-11-07
DateModified2021-06-02

Ontological Relatives

GenesFBXO11

GO terms

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GOName
GO:0000151 ubiquitin ligase complex
GO:0000209 protein polyubiquitination
GO:0004842 ubiquitin-protein transferase activity
GO:0005634 nucleus
GO:0005654 nucleoplasm
GO:0005694 chromosome
GO:0005730 nucleolus
GO:0005737 cytoplasm
GO:0005829 cytosol
GO:0006464 cellular protein modification process
GO:0006511 ubiquitin-dependent protein catabolic process
GO:0007605 sensory perception of sound
GO:0008270 zinc ion binding
GO:0016274 protein-arginine N-methyltransferase activity
GO:0016567 protein ubiquitination
GO:0042981 regulation of apoptotic process
GO:0043687 post-translational protein modification

Subcellular Location

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Subcellular Location
Chromosome
Nucleus

Domains

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DomainNameCategoryType
IPR001810 F-box domainDomainDomain
IPR003126 Zinc finger, UBR-typeDomainDomain
IPR006626 Parallel beta-helix repeatRepeatRepeat
IPR006633 Carbohydrate-binding/sugar hydrolysis domainDomainDomain
IPR007742 Periplasmic copper-binding protein NosD, beta helix domainDomainDomain
IPR011050 Pectin lyase fold/virulence factorFamilyHomologous superfamily
IPR012334 Pectin lyase foldFamilyHomologous superfamily
IPR022441 Parallel beta-helix repeat-2RepeatRepeat
IPR029799 F-box only protein 11FamilyFamily
IPR036047 F-box-like domain superfamilyFamilyHomologous superfamily
IPR039448 Right handed beta helix domainDomainDomain

Diseases

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Disease IDSourceNameDescription
618089 OMIMIntellectual developmental disorder with dysmorphic facies and behavioral abnormalities (IDDFBA)An autosomal dominant developmental disorder with variable manifestations and onset in infancy or first years of life. Clinical features include intellectual disability, speech delay, hyperkinetic disorder, hyperactivity, seizures, pre- and postnatal growth retardation, microcephaly, and facial dysmorphism. The disease is caused by variants affecting the gene represented in this entry.