Entity Details

Primary name TR10B_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionO14763
EntryNameTR10B_HUMAN
FullNameTumor necrosis factor receptor superfamily member 10B
TaxID9606
Evidenceevidence at protein level
Length440
SequenceStatuscomplete
DateCreated2001-09-26
DateModified2021-06-02

Ontological Relatives

GenesTNFRSF10B

GO terms

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GOName
GO:0005886 plasma membrane
GO:0006915 apoptotic process
GO:0006919 activation of cysteine-type endopeptidase activity involved in apoptotic process
GO:0007166 cell surface receptor signaling pathway
GO:0007250 activation of NF-kappaB-inducing kinase activity
GO:0008625 extrinsic apoptotic signaling pathway via death domain receptors
GO:0009986 cell surface
GO:0016021 integral component of membrane
GO:0034976 response to endoplasmic reticulum stress
GO:0036462 TRAIL-activated apoptotic signaling pathway
GO:0036463 TRAIL receptor activity
GO:0038023 signaling receptor activity
GO:0042981 regulation of apoptotic process
GO:0043065 positive regulation of apoptotic process
GO:0043123 positive regulation of I-kappaB kinase/NF-kappaB signaling
GO:0045569 TRAIL binding
GO:0050900 leukocyte migration
GO:0070059 intrinsic apoptotic signaling pathway in response to endoplasmic reticulum stress
GO:0071260 cellular response to mechanical stimulus
GO:1902041 regulation of extrinsic apoptotic signaling pathway via death domain receptors
GO:1902042 negative regulation of extrinsic apoptotic signaling pathway via death domain receptors

Subcellular Location

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Subcellular Location
Membrane

Domains

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DomainNameCategoryType
IPR000488 Death domainDomainDomain
IPR001368 TNFR/NGFR cysteine-rich regionDomainDomain
IPR011029 Death-like domain superfamilyFamilyHomologous superfamily
IPR020465 Tumour necrosis factor receptor 10FamilyFamily
IPR034024 Tumor necrosis factor receptor 10, N-terminalDomainDomain
IPR034029 Tumour necrosis factor receptor 10A/B, death domainDomainDomain

Diseases

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Drugs

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DrugNameSourceType
DB05895 HGS-TR2JDrugbankbiotech
DB06599 LexatumumabDrugbankbiotech

Interactions

0 interactions

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