UBR5 - ubiquitin protein ligase E3 component n-recognin 5 Gene

Also Known as DD5; EDD; HYD; EDD1

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 51366

About UBR5

Cytogenetic location: 8q22.3 Genomic coordinates (GRCh38): 8:102,252,273-102,412,700 (from NCBI)

This gene has 13 transcripts (splice variants), 209 orthologues, 24 paralogues and is associated with 104 phenotypes. Ubiquitous expression in testis (RPKM 18.7), lymph node (RPKM 11.2) and 25 other tissues.

Summary

This gene encodes a progestin-induced protein, which belongs to the HECT (homology to E6-AP carboxyl terminus) family. The HECT family proteins function as E3 ubiquitin-protein ligases, targeting specific proteins for ubiquitin-mediated proteolysis. This gene is localized to chromosome 8q22 which is disrupted in a variety of cancers. This gene potentially has a role in regulation of cell proliferation or differentiation. [provided by RefSeq, Jul 2008]

UBR5 Products (2)

mRNA Protein Name
NM_001282873.2 NP_001269802.1 E3 ubiquitin-protein ligase UBR5 isoform 2
NM_015902.6 NP_056986.2 E3 ubiquitin-protein ligase UBR5 isoform 1
Molecular Function GO Annotation Evidence References Source
enables protein binding IPI
IPI: Inferred from physical interaction
12011095 GOA
enables ubiquitin binding IDA
IDA: Inferred from direct assay
17897937 GOA
enables ubiquitin protein ligase activity IDA
IDA: Inferred from direct assay
28689657 GOA
enables ubiquitin-ubiquitin ligase activity IDA
IDA: Inferred from direct assay
21118991 GOA
Biological Process GO Annotation Evidence References Source
involved in DNA damage response IDA
IDA: Inferred from direct assay
12011095 GOA
involved in DNA repair-dependent chromatin remodeling IMP
IMP: Inferred from mutant phenotype
22884692 GOA
involved in cytoplasm protein quality control IDA
IDA: Inferred from direct assay
29033132 GOA
involved in cytoplasm protein quality control by the ubiquitin-proteasome system IDA
IDA: Inferred from direct assay
29033132 GOA
involved in heterochromatin boundary formation IMP
IMP: Inferred from mutant phenotype
22884692 GOA
involved in nuclear protein quality control by the ubiquitin-proteasome system IDA
IDA: Inferred from direct assay
37478846 GOA
involved in positive regulation of canonical Wnt signaling pathway IMP
IMP: Inferred from mutant phenotype
21118991 GOA
acts upstream of or within positive regulation of gene expression IDA
IDA: Inferred from direct assay
18076571 GOA
involved in positive regulation of protein import into nucleus IMP
IMP: Inferred from mutant phenotype
21118991 GOA
involved in progesterone receptor signaling pathway IDA
IDA: Inferred from direct assay
12011095 GOA
involved in proteasome-mediated ubiquitin-dependent protein catabolic process IDA
IDA: Inferred from direct assay
29378950 GOA
involved in protein K11-linked ubiquitination IDA
IDA: Inferred from direct assay
21118991 GOA
involved in protein K29-linked ubiquitination IDA
IDA: Inferred from direct assay
21118991 GOA
involved in protein K48-linked ubiquitination IDA
IDA: Inferred from direct assay
28689657 GOA
involved in protein branched polyubiquitination IDA
IDA: Inferred from direct assay
29033132 GOA
involved in protein polyubiquitination IDA
IDA: Inferred from direct assay
21118991 GOA
Cellular Component GO Annotation Evidence References Source
located in chromatin IDA
IDA: Inferred from direct assay
37478846 GOA
is active in cytoplasm IDA
IDA: Inferred from direct assay
29033132 GOA
is active in nucleus IDA
IDA: Inferred from direct assay
37478846 GOA
located in nucleus IDA
IDA: Inferred from direct assay
12011095 GOA
located in perinuclear region of cytoplasm IDA
IDA: Inferred from direct assay
18076571 GOA
part of protein-containing complex IDA
IDA: Inferred from direct assay
18076571 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

UBR5 Protein Structure

E3_UbLigase_EDD

E3_UbLigase_EDD: E3 ubiquitin ligase EDD (178 - 230)

zf-UBR

zf-UBR: Putative zinc finger in N-recognin (UBR box) (1178 - 1240)

PABP

PABP: Poly-adenylate binding protein, unique domain (2392 - 2448)

HECT

HECT: HECT-domain (ubiquitin-transferase) (2503 - 2798)

  • 0
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  • 2000
  • 2500
  • 2799 a.a.
Protein Preferred Names Protein Names

E3 ubiquitin-protein ligase UBR5

  • E3 identified by differential display

UBR5 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
UBR5 O95071 PAIP2 Homo sapiens Q9BPZ3
SPR
16601676
Intra
UBR5 O95071 PAIP2 Homo sapiens Q9BPZ3
ITC
16601676
Intra
UBR5 O95071 GSK3B Homo sapiens P49841 21118991
Intra
UBR5 O95071 GSK3B Homo sapiens P49841 21118991
Intra
UBR5 O95071 CTNNB1 Homo sapiens P35222 21118991
Intra
UBR5 O95071 CTNNB1 Homo sapiens P35222 21118991
Cross: Cross-species interaction Intra: Intraspecies interaction

UBR5 Antibodies

Cat. No. 상품명 신청 Reactivity
HY-P82885 EDD Antibody (YA2630) WB Human, Mouse

Related Diseases

Diseases Alias
Hypogonadotropic Hypogonadism 16 With Or Without Anosmia
  • HH16

  • Hypogonadism, Hypogonadotropic, Type 16 With/Without Anosmia

Johanson-Blizzard Syndrome
  • JBS

  • Nasal Alar Hypoplasia, Hypothyroidism, Pancreatic Achylia, And Congenital Deafness

  • Nasal Alar Hypoplasia, Hypothyroidism, Pancreatic Achylia And Congenital Deafness

  • Johanson Blizzard Syndrome

Familial Adult Myoclonic Epilepsy
  • Benign Adult Familial Myoclonus Epilepsy

  • Bafme

  • Benign Adult Familial Myoclonic Epilepsy

  • Fame

  • Familial Cortical Myoclonic Tremor And Epilepsy

  • Fcmte

  • Adcme

  • Autosomal Dominant Cortical Myoclonus And Epilepsy

  • Fam

  • Epilepsy, Myoclonic, Familial Adult

  • Epilepsy, Myoclonic, Benign Adult Familial, Type 2

Autism Spectrum Disorder
  • Asd

  • Autism Spectrum Disorders

  • Autistic Continuum

  • Pervasive Developmental Disorder

  • Pervasive Development Disorder

  • Autistic Behavior

  • Autistic Disorder

  • Autistic

  • Autistic Disorder Of Childhood Onset

  • Infantile Autism

  • Childhood Autism

  • Kanner Syndrome

  • Pervasive Developmental Delay Nos

  • Pervasive Developmental Disorder, Not Otherwise Specified

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Rattus norvegicus UBR5 RGD RGD:621236
Felis catus UBR5 VGNC VGNC:66788
Mus musculus UBR5 MGD MGI:1918040
Bos taurus UBR5 VGNC VGNC:36619
Canis familiaris UBR5 VGNC VGNC:48092
Macaca mulatta UBR5 VGNC VGNC:79050
Others UBR5 NCBI