PWWP3B
PWWP domain-containing DNA repair factor 3B
Also known as: FLJ33516, MUM1L1, PWP3B_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q5H9M0
- Gene
- PWWP3B
- Ensembl
- ENSG00000157502
- Chromosome
- X
- Canonical length
- 696 aa
- Protein class
- Predicted intracellular proteins
OverviewNCBI Gene
This gene encodes a protein which contains a mutated melanoma-associated antigen 1 domain. Proteins which contain mutated antigens are expressed at high levels on certain types of cancers. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Sep 2011]
Canonical amino-acid sequenceUniProt
696 residues, UniProt reviewed canonical sequence.
>Q5H9M0|PWWP3B
1 MESEYVLCNW KDQLWPAKVL SRSETSSNSK RKKAFSLEVQ ILSLDEKIKL DSTETKILNK
61 SQIEAIAASL GLQSEDSAPP TEETAYGRSL KVALGILNER TNLSQASTSD EEEITMLSQN
121 VPQKQSDSPP HKKYRKDEGD LPGCLEEREN SACLLASSES DDSLYDDKSQ APTMVDTIPS
181 EVETKSLQNS SWCETFPSLS EDNDEKENKN KIDISAVMSV HSAVKEESAC VKDEKFAPPL
241 SPLSSDMLIM PKALKEESED TCLETLAVPS ECSAFSENIE DPGEGPSNPC LDTSQNQPSM
301 ESEMGAAACP GSCSRECEVS FSASNPVWDY SHLMSSERNF QRLDFEELEE EGQASDKSLL
361 PSRINLSLLD DDEEDEELPR FILHYETHPF ETGMIVWFKY QKYPFWPAVI KSIRRKERKA
421 SVLFVEANMN SEKKGIRVNF RRLKKFDCKE KQMLVDKARE DYSESIDWCI SLICDYRVRI
481 GCGSFTGSLL EYYAADISYP VRKETKQDTF RNKFPKLHNE DAREPMAVTS QTKKMSFQKI
541 LPDRMKAARD RANKNLVDFI VNAKGTENHL LAIVNGTKGS RWLKSFLNAN RFTPCIETYF
601 EDEDQLDEVV KYLQEVCNQI DQIMPTWIKD DKIKFILEVL LPEAIICSIS AVDGLDYEAA
661 EAKYLKGPCL GYRERELFDA KIIYEKRRKA PTNEAHLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PWWP3B can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Unknown
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.5
- Highest tissue expression
- 104 nTPM
Expression across tissuesHPA
Tissue
- ovary: 104 nTPM
- pancreas: 27 nTPM
- testis: 17 nTPM
- endometrium: 15 nTPM
- cervix: 14 nTPM
- skeletal muscle: 10 nTPM
Single-cell type
- ovarian stromal cells: 292 nCPM
- sertoli cells: 265 nCPM
- peritubular myoid cells: 128 nCPM
- leydig cells: 113 nCPM
- gonadotrophs: 78 nCPM
- epicardial cells: 73 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- hypothalamus: 27 nTPM
- midbrain: 18 nTPM
- pons: 12 nTPM
- cerebral cortex: 10 nTPM
- amygdala: 9.5 nTPM
- basal ganglia: 8.8 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.53
- gnomAD pLI
- 0.48
- DepMap mean gene effect
- 0.11
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Cellular components
Protein domainsUniProt · Pfam · InterPro
- MUM1-like, PWWP domain
- PWWP domain-containing DNA repair factor 3A/3B/4
- PWWP domain-containing DNA repair factor 3A/3B/4, N-terminal
- PWWP domain-containing DNA repair factor 3A/3B/4, C-terminal
- MUM1-like, PWWP domain
- PWWP domain-containing DNA repair factor 3A/B, C-terminal
- PWWP domain-containing DNA repair factor 3A/B, N-terminal
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads PWWP3B as an antibody target. Whether an autoantibody or antibody against PWWP3B could matter depends on whether native PWWP3B is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PWWP3B is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label PWWP3B as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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