Entity Details

Primary name MIB1_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ86YT6
EntryNameMIB1_HUMAN
FullNameE3 ubiquitin-protein ligase MIB1
TaxID9606
Evidenceevidence at protein level
Length1006
SequenceStatuscomplete
DateCreated2005-07-05
DateModified2021-06-02

Ontological Relatives

GenesMIB1

GO terms

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GOName
GO:0001568 blood vessel development
GO:0001701 in utero embryonic development
GO:0001756 somitogenesis
GO:0001841 neural tube formation
GO:0001947 heart looping
GO:0004842 ubiquitin-protein transferase activity
GO:0005737 cytoplasm
GO:0005813 centrosome
GO:0005829 cytosol
GO:0005886 plasma membrane
GO:0006511 ubiquitin-dependent protein catabolic process
GO:0006897 endocytosis
GO:0007219 Notch signaling pathway
GO:0008270 zinc ion binding
GO:0014069 postsynaptic density
GO:0016567 protein ubiquitination
GO:0031410 cytoplasmic vesicle
GO:0045665 negative regulation of neuron differentiation
GO:0045807 positive regulation of endocytosis

Subcellular Location

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Subcellular Location
Cell membrane
Cytoplasm

Domains

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DomainNameCategoryType
IPR000433 Zinc finger, ZZ-typeDomainDomain
IPR001841 Zinc finger, RING-typeDomainDomain
IPR002110 Ankyrin repeatRepeatRepeat
IPR010606 Mib-herc2DomainDomain
IPR013083 Zinc finger, RING/FYVE/PHD-typeFamilyHomologous superfamily
IPR020683 Ankyrin repeat-containing domainDomainDomain
IPR036770 Ankyrin repeat-containing domain superfamilyFamilyHomologous superfamily
IPR037252 Mib/herc2 domain superfamilyFamilyHomologous superfamily
IPR040847 Mind bomb, SH3 repeat domainDomainDomain
IPR042056 E3 ubiquitin-protein ligase MIB1/2, zinc finger, ZZ-typeDomainDomain
IPR043145 Zinc finger, ZZ-type superfamilyFamilyHomologous superfamily

Diseases

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Disease IDSourceNameDescription
615092 OMIMLeft ventricular non-compaction 7 (LVNC7)A form of left ventricular non-compaction, a cardiomyopathy due to myocardial morphogenesis arrest and characterized by a hypertrophic left ventricle, a severely thickened 2-layered myocardium, numerous prominent trabeculations, deep intertrabecular recesses, and poor systolic function. Clinical manifestations are variable. Some affected individuals experience no symptoms at all, others develop heart failure. In some cases, left ventricular non-compaction is associated with other congenital heart anomalies. LVNC7 is an autosomal dominant condition. The disease is caused by variants affecting the gene represented in this entry.

Interactions

45 interactions

InteractorPartnerSourcesPublicationsLink
MIB1_HUMANSNX5_HUMANBioGRID, HPRD, MINT16857196 details
MIB1_HUMANUB2D1_HUMANBioGRID, IntAct19690564 details
MIB1_HUMANUB2D2_HUMANBioGRID, IntAct19690564 25747658 details
MIB1_HUMANUB2D3_HUMANBioGRID, IntAct19690564 24239288 details
MIB1_HUMANUB2D4_HUMANBioGRID, IntAct19690564 details
MIB1_HUMANUBE2N_HUMANBioGRID, IntAct19690564 21903422 details
MIB1_HUMANUBE2U_HUMANBioGRID, IntAct19690564 details
MIB1_HUMANUBE2W_HUMANBioGRID, IntAct19690564 details
MIB1_HUMANTBK1_HUMANBioGRID, IntAct21903422 31462741 details
MIB1_HUMANGBRAP_HUMANBioGRID, IntAct28712572 details
MIB1_HUMANJAG1_HUMANBioGRID20720151 25747658 details
MIB1_HUMANAZI2_HUMANBioGRID21903422 details
MIB1_HUMANDAPK1_HUMANBioGRID, HPRD12351649 15048887 details
MIB1_HUMANCP131_HUMANBioGRID24121310 31462741 details
MIB1_HUMANBLM_HUMANBioGRID24239288 30044990 details
MIB1_HUMANE41LA_HUMANBioGRID27510968 details
MIB1_HUMANE41L5_HUMANBioGRID27510968 31462741 details
MIB1_HUMANWRN_HUMANBioGRID32652764 details
MIB1_HUMANDAB2_HUMANHPRD11812785 details
MIB1_HUMANPCM1_HUMANBioGRID, IntAct21956701 24121310 25795303 26638075 31462741 34079125 details
MIB1_HUMANRYK_HUMANBioGRID21875946 details
MIB1_HUMANDLL1_HUMANBioGRID21985982 27510968 details
MIB1_HUMANCMIP_HUMANBioGRID20018188 details
MIB1_HUMANSMN_HUMANBioGRID23615451 details
MIB1_HUMANMIB1_HUMANBioGRID24239288 details
MIB1_HUMANUSP9X_HUMANBioGRID24239288 31462741 details
MIB1_HUMANZC3H1_HUMANBioGRID24239288 details
MIB1_HUMANRAGP1_HUMANBioGRID24239288 details
MIB1_HUMANZBT10_HUMANBioGRID24239288 details
MIB1_HUMANGEMI4_HUMANBioGRID24239288 details
MIB1_HUMANMCM3_HUMANBioGRID24239288 details
MIB1_HUMANTOP3A_HUMANBioGRID24239288 details
MIB1_HUMANDDB1_HUMANBioGRID24239288 details
MIB1_HUMANTOP3B_HUMANBioGRID24239288 31462741 details
MIB1_HUMANRBBP4_HUMANBioGRID24239288 details
MIB1_HUMANMCM7_HUMANBioGRID24239288 details
MIB1_HUMANCDC27_HUMANBioGRID24239288 details
MIB1_HUMANPLK4_HUMANBioGRID25795303 details
MIB1_HUMANCYLD_HUMANBioGRID31067453 31462741 details
MIB1_HUMANST7_HUMANBioGRID29395067 31462741 details
MIB1_HUMANTNR6A_HUMANBioGRID29395067 31462741 details
MIB1_HUMANZO1_HUMANBioGRID31462741 details
MIB1_HUMANCRUM1_HUMANBioGRID31462741 details
MIB1_HUMANCRUM3_HUMANBioGRID31462741 details
MIB1_HUMANF120C_HUMANBioGRID29395067 details