1. Gene
  2. WWP2 - WW domain containing E3 ubiquitin protein ligase 2 Gene

WWP2 - WW domain containing E3 ubiquitin protein ligase 2 Gene

Homo sapiens

Also known as AIP2; WWp2-like

Gene ID: 11060 | Gene type: protein coding

About WWP2

Cytogenetic location: 16q22.1 Genomic coordinates (GRCh38): 16:69,762,332-69,941,739 (from NCBI)

This gene has 20 transcripts (splice variants), 132 orthologues and 24 paralogues. Ubiquitous expression in lung (RPKM 8.8), spleen (RPKM 8.4) and 25 other tissues.

Summary

This gene encodes a member of the Nedd4 family of E3 Ligases, which play an important role in protein ubiquitination. The encoded protein contains four WW domains and may play a role in multiple processes including chondrogenesis and the regulation of oncogenic signaling pathways via interactions with Smad proteins and the tumor suppressor PTEN. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene, and a pseudogene of this gene is located on the long arm of chromosome 10. [provided by RefSeq, Jul 2012]

WWP2 Products(5)

mRNA Protein Name
NM_001270453.2 NP_001257382.1 NEDD4-like E3 ubiquitin-protein ligase WWP2 isoform 4
NM_001270454.2 NP_001257383.1 NEDD4-like E3 ubiquitin-protein ligase WWP2 isoform WWP2-FL
NM_001270455.2 NP_001257384.1 NEDD4-like E3 ubiquitin-protein ligase WWP2 isoform WWP2-N
NM_007014.5 NP_008945.2 NEDD4-like E3 ubiquitin-protein ligase WWP2 isoform WWP2-FL
NM_199424.3 NP_955456.1 NEDD4-like E3 ubiquitin-protein ligase WWP2 isoform WWP2-C
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables RNA polymerase II-specific DNA-binding transcription factor binding IPI
IPI: Inferred from physical interaction
19274063 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
9647693 GOA
enables transcription factor binding IPI
IPI: Inferred from physical interaction
19651900 GOA
enables ubiquitin-protein transferase activity IDA
IDA: Inferred from direct assay
19274063 GOA
enables ubiquitin-protein transferase activity IMP
IMP: Inferred from mutant phenotype
18776082 GOA
Biological Process GO Annotation Evidence Reference Source
involved in extracellular transport IMP
IMP: Inferred from mutant phenotype
22315426 GOA
involved in negative regulation of gene expression IMP
IMP: Inferred from mutant phenotype
18776082 GOA
involved in negative regulation of protein transport IMP
IMP: Inferred from mutant phenotype
18776082 GOA
involved in negative regulation of transcription by RNA polymerase II IMP
IMP: Inferred from mutant phenotype
19274063 GOA
involved in negative regulation of transporter activity IDA
IDA: Inferred from direct assay
18776082 GOA
involved in proteasome-mediated ubiquitin-dependent protein catabolic process IMP
IMP: Inferred from mutant phenotype
19274063 GOA
involved in protein autoubiquitination IDA
IDA: Inferred from direct assay
24105792 GOA
acts upstream of or within protein ubiquitination IDA
IDA: Inferred from direct assay
26280536 GOA
involved in protein ubiquitination IDA
IDA: Inferred from direct assay
18776082 GOA
involved in protein ubiquitination IMP
IMP: Inferred from mutant phenotype
22315426 GOA
involved in regulation of membrane potential IDA
IDA: Inferred from direct assay
17289006 GOA
involved in regulation of monoatomic ion transmembrane transport IDA
IDA: Inferred from direct assay
17289006 GOA
involved in regulation of potassium ion transmembrane transporter activity IDA
IDA: Inferred from direct assay
17289006 GOA
Cellular Component GO Annotation Evidence Reference Source
located in nucleus IDA
IDA: Inferred from direct assay
19274063 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

WWP2 Protein Structure

WW

WW: WW domain (302 - 331)

WW

WW: WW domain (332 - 361)

WW

WW: WW domain (407 - 435)

WW

WW: WW domain (446 - 475)

HECT

HECT: HECT-domain (ubiquitin-transferase) (566 - 868)

  • 0
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  • 800
  • 870 a.a.
Protein Preferred Names Protein Names

NEDD4-like E3 ubiquitin-protein ligase WWP2

HECT-type E3 ubiquitin transferase WWP2

WWP2 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
WWP2 O00308 HNRNPUL1 Homo sapiens Q9BUJ2 25416956
Intra
WWP2 O00308 HNRNPUL1 Homo sapiens Q9BUJ2 32296183
Intra
WWP2 O00308 LGALS9B Homo sapiens Q3B8N2 25416956
Intra
WWP2 O00308 LGALS9B Homo sapiens Q3B8N2 25416956
Intra
WWP2 O00308 SNRPC Homo sapiens Q5TAL4 25416956
Intra
WWP2 O00308 GGN Homo sapiens Q86UU5 32296183
Intra
WWP2 O00308 SMAD2 Homo sapiens Q15796 21258410
Intra
WWP2 O00308 JPH3 Homo sapiens Q8WXH2 32814053
Intra
WWP2 O00308 JPH3 Homo sapiens Q8WXH2 32814053
Intra
WWP2 O00308 JPH3 Homo sapiens Q8WXH2 32814053
Intra
WWP2 O00308 DNM2 Homo sapiens P50570-2 32814053
Intra
WWP2 O00308 DNM2 Homo sapiens P50570-2 32814053
Intra
WWP2 O00308 DNM2 Homo sapiens P50570-2 32814053
Intra
WWP2 O00308 DMWD Homo sapiens G5E9A7 32814053
Intra
WWP2 O00308 DMWD Homo sapiens G5E9A7 32814053
Intra
WWP2 O00308 DMWD Homo sapiens G5E9A7 32814053
Intra
WWP2 O00308 PATZ1 Homo sapiens Q9HBE1-4 32296183
Intra
WWP2 O00308 NHERF2 Homo sapiens Q15599 32296183
Intra
WWP2 O00308 ATN1 Homo sapiens Q86V38 32814053
Intra
WWP2 O00308 ATN1 Homo sapiens Q86V38 32814053
Intra
WWP2 O00308 ATN1 Homo sapiens Q86V38 32814053
Intra
WWP2 O00308 EFCAB3 Homo sapiens Q8N7B9-2 32296183
Intra
WWP2 O00308 SMR3A Homo sapiens Q99954 32296183
Intra
WWP2 O00308 ANKRD44 Homo sapiens Q8N8A2 31515488
Intra
WWP2 O00308 ANKRD44 Homo sapiens Q8N8A2 25416956
Intra
WWP2 O00308 PRKAA2 Homo sapiens P54646 32296183
Intra
WWP2 O00308 CTSD Homo sapiens P07339 32814053
Intra
WWP2 O00308 CTSD Homo sapiens P07339 32814053
Intra
WWP2 O00308 CTSD Homo sapiens P07339 32814053
Intra
WWP2 O00308 UBE2E2 Homo sapiens Q96LR5 32296183
Intra
WWP2 O00308 ARRDC1 Homo sapiens Q8N5I2
Y2H
23236378
Intra
WWP2 O00308 ARRDC1 Homo sapiens Q8N5I2 32296183
Intra
WWP2 O00308 ARRDC1 Homo sapiens Q8N5I2 33961781
Intra
WWP2 O00308 ARRDC1 Homo sapiens Q8N5I2 28514442
Intra
WWP2 O00308 KLK6 Homo sapiens Q92876 32814053
Intra
WWP2 O00308 KLK6 Homo sapiens Q92876 32814053
Intra
WWP2 O00308 KLK6 Homo sapiens Q92876 32814053
Intra
WWP2 O00308 DCTN1 Homo sapiens Q14203-5 32814053
Intra
WWP2 O00308 DCTN1 Homo sapiens Q14203-5 32814053
Intra
WWP2 O00308 DCTN1 Homo sapiens Q14203-5 32814053
Intra
WWP2 O00308 TPP1 Homo sapiens O14773 32814053
Intra
WWP2 O00308 TPP1 Homo sapiens O14773 32814053
Intra
WWP2 O00308 TPP1 Homo sapiens O14773 32814053
Intra
WWP2 O00308 ARRDC3 Homo sapiens Q96B67
Y2H
23236378
Intra
WWP2 O00308 ARRDC3 Homo sapiens Q96B67 32296183
Intra
WWP2 O00308 ADARB1 Homo sapiens P78563 21847096
Intra
WWP2 O00308 WIPF1 Homo sapiens O43516 25416956
Intra
WWP2 O00308 WIPF1 Homo sapiens O43516 25416956
Intra
WWP2 O00308 WIPF1 Homo sapiens O43516
Y2H
21516116
Intra
WWP2 O00308 SMAD3 Homo sapiens P84022 21258410
Intra
WWP2 O00308 UBE2E3 Homo sapiens Q969T4 32296183
Intra
WWP2 O00308 CFTR Homo sapiens P13569 35156780
Intra
WWP2 O00308 PDLIM7 Homo sapiens Q9NR12 25416956
Intra
WWP2 O00308 PDLIM7 Homo sapiens Q9NR12 25416956
Intra
WWP2 O00308 CCT5 Homo sapiens P48643 32814053
Intra
WWP2 O00308 CCT5 Homo sapiens P48643 32814053
Intra
WWP2 O00308 CCT5 Homo sapiens P48643 32814053
Intra
WWP2 O00308 YWHAE Homo sapiens P62258 36931259
Intra
WWP2 O00308 CPSF6 Homo sapiens Q16630 33961781
Intra
WWP2 O00308 SMARCD1 Homo sapiens Q96GM5 32296183
Intra
WWP2 O00308 SMARCD1 Homo sapiens Q96GM5 33961781
Intra
WWP2 O00308 TRAF4 Homo sapiens Q9BUZ4 25416956
Intra
WWP2 O00308 TRAF4 Homo sapiens Q9BUZ4
Y2H
21516116
Intra
WWP2 O00308 TRAF4 Homo sapiens Q9BUZ4 25416956
Intra
WWP2 O00308 TRAF4 Homo sapiens Q9BUZ4 32296183
Intra
WWP2 O00308 SNRPB Homo sapiens P14678-2 32296183
Intra
WWP2 O00308 GADD45GIP1 Homo sapiens Q8TAE8 32296183
Intra
WWP2 O00308 TARDBP Homo sapiens Q13148 32814053
Intra
WWP2 O00308 TARDBP Homo sapiens Q13148 32814053
Intra
WWP2 O00308 TARDBP Homo sapiens Q13148 32814053
Intra
WWP2 O00308 SMAD7 Homo sapiens O15105 21258410
Intra
WWP2 O00308 MED25 Homo sapiens Q71SY5 32296183
Intra
WWP2 O00308 RNF11 Homo sapiens Q9Y3C5 32814053
Intra
WWP2 O00308 RNF11 Homo sapiens Q9Y3C5 32814053
Intra
WWP2 O00308 RNF11 Homo sapiens Q9Y3C5
Y2H
15231748
Intra
WWP2 O00308 RNF11 Homo sapiens Q9Y3C5 32814053
Intra
WWP2 O00308 HTT Homo sapiens P42858 32814053
Intra
WWP2 O00308 HTT Homo sapiens P42858 32814053
Intra
WWP2 O00308 HTT Homo sapiens P42858 32814053
Intra
WWP2 O00308 POU5F1 Homo sapiens Q01860 19274063
Intra
WWP2 O00308 POU5F1 Homo sapiens Q01860 19274063
Intra
WWP2 O00308 HTRA2 Homo sapiens O43464 32814053
Intra
WWP2 O00308 HTRA2 Homo sapiens O43464 32814053
Intra
WWP2 O00308 HTRA2 Homo sapiens O43464 32814053
Intra
WWP2 O00308 WDR5 Homo sapiens P61964 32296183
Intra
WWP2 O00308 CLN6 Homo sapiens Q9NWW5 32814053
Intra
WWP2 O00308 CLN6 Homo sapiens Q9NWW5 32814053
Intra
WWP2 O00308 CLN6 Homo sapiens Q9NWW5 32814053
Intra
WWP2 O00308 RUSC1 Homo sapiens Q9BVN2 25416956
Intra
WWP2 O00308 RUSC1 Homo sapiens Q9BVN2 25416956
Intra
WWP2 O00308 RUSC1 Homo sapiens Q9BVN2 25416956
Intra
WWP2 O00308 UBA1 Homo sapiens P22314 32814053
Intra
WWP2 O00308 UBA1 Homo sapiens P22314 32814053
Intra
WWP2 O00308 UBA1 Homo sapiens P22314 32814053
Intra
WWP2 O00308 HEXB Homo sapiens P07686 32814053
Intra
WWP2 O00308 HEXB Homo sapiens P07686 32814053
Intra
WWP2 O00308 HEXB Homo sapiens P07686 32814053
Intra
WWP2 O00308 WFS1 Homo sapiens O76024 32814053
Intra
WWP2 O00308 WFS1 Homo sapiens O76024 32814053
Intra
WWP2 O00308 WFS1 Homo sapiens O76024 32814053
Intra
WWP2 O00308 LITAF Homo sapiens Q99732 32814053
Intra
WWP2 O00308 LITAF Homo sapiens Q99732 32814053
Intra
WWP2 O00308 LITAF Homo sapiens Q99732 32814053
Intra
WWP2 O00308 RASD1 Homo sapiens Q9Y272 32296183
Intra
WWP2 O00308 FBXL18 Homo sapiens Q96D16 25416956
Intra
WWP2 O00308 ATOSB Homo sapiens Q7L5A3 32296183
Intra
WWP2 O00308 UBTD1 Homo sapiens Q9HAC8 32296183
Intra
WWP2 O00308 IFIT2 Homo sapiens Q8IZ03 32296183
Intra
WWP2 O00308 q8wu02_human Homo sapiens Q8WU02 25416956
Intra
WWP2 O00308 PRPS1 Homo sapiens P60891 32814053
Intra
WWP2 O00308 PRPS1 Homo sapiens P60891 32814053
Intra
WWP2 O00308 PRPS1 Homo sapiens P60891 32814053
Intra
WWP2 O00308 SNRPC Homo sapiens P09234 32296183
Intra
WWP2 O00308 GAS2L2 Homo sapiens Q8NHY3 32296183
Intra
WWP2 O00308 ENTREP1 Homo sapiens Q15884
Y2H
34927784
Intra
WWP2 O00308 SNCA Homo sapiens P37840 32814053
Intra
WWP2 O00308 SNCA Homo sapiens P37840 32814053
Intra
WWP2 O00308 SNCA Homo sapiens P37840 32814053
Intra
WWP2 O00308 PEX1 Homo sapiens O43933 32814053
Intra
WWP2 O00308 PEX1 Homo sapiens O43933 32814053
Intra
WWP2 O00308 PEX1 Homo sapiens O43933 32814053
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant WWP2 Proteins

Cat. No. Product Name Accession Purity
HY-P77507 WWP2 Protein, Human (sf9, His-GST) O00308-1 (M1-E870) ≥95%

Related Diseases

Diseases Alias
Spondyloepiphyseal Dysplasia, Nishimura Type

SEDN

Spondyloepiphyseal Dysplasia Nishimura Type

Cowden Syndrome 1

Bannayan-Riley-Ruvalcaba Syndrome

Pten Hamartoma Tumor Syndrome

Lhermitte-Duclos Disease

Bannayan-Zonana Syndrome

Phts

Riley-Smith Syndrome

Bzs

Ruvalcaba-Myhre-Smith Syndrome

Multiple Hamartoma Syndrome

Rmss

Brrs

Dysplastic Gangliocytoma Of The Cerebellum

CWS1

Cs

Cd

Mham

Pten Hamartoma Tumor Syndrome With Granular Cell Tumor

Macrocephaly Multiple Lipomas And Hemangiomata

Bannayan-Ruvalcaba-Riley Syndrome

Myhre-Riley-Smith Syndrome

LDD

Cerebelloparenchymal Disorder Vi

Hamartoma Syndrome, Multiple

Bbrs

Macrocephaly, Pseudopapilledema, And Multiple Hemangiomata

Macrocephaly, Multiple Lipomas, And Hemangiomata

Macrocephaly Pseudopapilledema And Multiple Hemangiomas

Ruvalcaba -Myhre-Smith Syndrome

Ruvalcaba-Myhre Syndrome

Cowden Disease

Macrocephaly Pseudopapilledema And Multiple Hemangiomata

Cerebellar Granule Cell Hypertrophy And Megalencephaly

Cpd6

Pten Hamartoma Tumor Syndromes

Cowden Syndrome, Type 1

Lung Cancer

Lung Carcinoma

Non-Small Cell Lung Carcinoma

Lung Cancer, Susceptibility To

Lung Cancer, Protection Against

Adenocarcinoma Of Lung, Somatic

Adenocarcinoma Of Lung, Response To Tyrosine Kinase Inhibitor In

Nonsmall Cell Lung Cancer

Lung Neoplasm

Carcinoma Of Lung

Lung Non-Small Cell Carcinoma

Non-Small Cell Lung Cancer

Nsclc

Lung Neoplasms

Malignant Neoplasm Of Lung

Alveolar Cell Carcinoma

Nonsmall Cell Lung Cancer, Somatic

Nonsmall Cell Lung Cancer, Response To Tyrosine Kinase Inhibitor In

Nonsmall Cell Lung Cancer, Susceptibility To

Lung Cancer, Somatic

Lung Cancer, Resistance To

Cancer Of Lung

Cancer Of Bronchus

Cancer Of The Lung

Lung Malignancies

Lung Malignant Tumors

Malignant Lung Tumor

Malignant Tumor Of Lung

Pulmonary Cancer

Pulmonary Carcinoma

Pulmonary Neoplasms

Respiratory Carcinoma

LNCR

Adenocarcinoma Of Lung

Neoplasm Of Lung

Cancer Lung

Carcinoma Non-Small Cell Lung

Carcinoma, Non-Small-Cell Lung

Lung Cancers

Lung Carcinomas

Cancer, Lung

Cancer, Lung, Non-Small Cell

Primary Malignant Neoplasm Of Lung

Bronchioloalveolar Adenocarcinoma

Cowden Syndrome

Cowden Disease

Multiple Hamartoma Syndrome

Cowden'S Disease

Lhermitte-Duclos Disease

Cd

Cs

Mham

Dysplastic Gangliocytoma Of Cerebellum

Cowden'S Syndrome

Hamartoma Syndrome, Multiple

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
Felis catus WWP2 VGNC VGNC:67100
Rattus norvegicus WWP2 RGD RGD:1310091
Mus musculus WWP2 MGD MGI:1914144
Macaca mulatta WWP2 VGNC VGNC:103887
Canis familiaris WWP2 VGNC VGNC:48444
Bos taurus WWP2 VGNC VGNC:36979
Others WWP2 NCBI