PAK2
Serine/threonine-protein kinase PAK 2
Also known as: PAK2_HUMAN, PAK65, PAKgamma
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q13177
- Gene
- PAK2
- Ensembl
- ENSG00000180370
- Chromosome
- 3
- Canonical length
- 524 aa
- Protein class
- Disease related genes, Enzymes, Plasma proteins, Potential drug targets, Predicted intracellular proteins, RAS pathway related proteins
- Subcellular location
- Nucleoplasm,Nuclear speckles,Focal adhesion sites,Cytosol
OverviewNCBI Gene
The p21 activated kinases (PAK) are critical effectors that link Rho GTPases to cytoskeleton reorganization and nuclear signaling. The PAK proteins are a family of serine/threonine kinases that serve as targets for the small GTP binding proteins, CDC42 and RAC1, and have been implicated in a wide range of biological activities. The protein encoded by this gene is activated by proteolytic cleavage during caspase-mediated apoptosis, and may play a role in regulating the apoptotic events in the dying cell. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
524 residues, UniProt reviewed canonical sequence.
>Q13177|PAK2
1 MSDNGELEDK PPAPPVRMSS TIFSTGGKDP LSANHSLKPL PSVPEEKKPR HKIISIFSGT
61 EKGSKKKEKE RPEISPPSDF EHTIHVGFDA VTGEFTGMPE QWARLLQTSN ITKLEQKKNP
121 QAVLDVLKFY DSNTVKQKYL SFTPPEKDGF PSGTPALNAK GTEAPAVVTE EEDDDEETAP
181 PVIAPRPDHT KSIYTRSVID PVPAPVGDSH VDGAAKSLDK QKKKTKMTDE EIMEKLRTIV
241 SIGDPKKKYT RYEKIGQGAS GTVFTATDVA LGQEVAIKQI NLQKQPKKEL IINEILVMKE
301 LKNPNIVNFL DSYLVGDELF VVMEYLAGGS LTDVVTETCM DEAQIAAVCR ECLQALEFLH
361 ANQVIHRDIK SDNVLLGMEG SVKLTDFGFC AQITPEQSKR STMVGTPYWM APEVVTRKAY
421 GPKVDIWSLG IMAIEMVEGE PPYLNENPLR ALYLIATNGT PELQNPEKLS PIFRDFLNRC
481 LEMDVEKRGS AKELLQHPFL KLAKPLSSLT PLIMAAKEAM KSNRLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PAK2 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
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.4
- Highest tissue expression
- 42 nTPM
Expression across tissuesHPA
Tissue
- thymus: 42 nTPM
- spleen: 41 nTPM
- lymph node: 38 nTPM
- tonsil: 37 nTPM
- appendix: 33 nTPM
- urinary bladder: 32 nTPM
Single-cell type
- neutrophils: 826 nCPM
- neutrophil progenitors: 418 nCPM
- monocytes: 351 nCPM
- monocyte progenitors: 304 nCPM
- innate lymphoid cells: 269 nCPM
- kupffer cells: 254 nCPM
Immune cell
- eosinophil: 48 nTPM
- neutrophil: 48 nTPM
- basophil: 38 nTPM
- myeloid DC: 26 nTPM
- intermediate monocyte: 23 nTPM
- non-classical monocyte: 21 nTPM
Brain region
- white matter: 64 nTPM
- medulla oblongata: 53 nTPM
- cerebellum: 47 nTPM
- hypothalamus: 47 nTPM
- spinal cord: 47 nTPM
- basal ganglia: 46 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about PAK2.
Disease | AllUniProt
Conditions PAK2 is implicated in, by any mechanism.
- Knobloch syndrome 2 (KNO2) MIM:618458
Disease | GeneticClinVar
3 pathogenic / likely-pathogenic of 79 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- Knobloch syndrome 2
- Knobloch syndrome
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)
- 0.32
- gnomAD pLI
- 0.97
- gnomAD missense Z
- 3.4
- DepMap mean gene effect
- -0.26
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 15% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- adherens junction assembly
- apoptotic process
- bicellular tight junction assembly
- cardiac muscle hypertrophy
- cell migration
- cellular response to starvation
- cellular response to transforming growth factor beta stimulus
- dendritic spine development
- intracellular signal transduction
- negative regulation of apoptotic process
- negative regulation of protein kinase activity
- negative regulation of stress fiber assembly
- positive regulation of extrinsic apoptotic signaling pathway
- protein autophosphorylation
- protein localization to cell-cell junction
- protein phosphorylation
- regulation of axonogenesis
- regulation of cytoskeleton organization
- regulation of MAPK cascade
- signal transduction
- stimulatory C-type lectin receptor signaling pathway
- vascular endothelial growth factor receptor signaling pathway
Molecular functions
- ATP binding
- cadherin binding
- identical protein binding
- protein kinase activity
- protein kinase binding
- protein serine kinase activity
- protein serine/threonine kinase activity
- protein tyrosine kinase activator activity
- small GTPase binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
- CRIB domain
- Protein kinase domain
- Serine/threonine-protein kinase, active site
- Protein kinase-like domain superfamily
- Protein kinase, ATP binding site
- p21 activated kinase binding domain
- CRIB domain superfamily
- Serine/threonine-protein kinase PAK 3-like
- Protein kinase domain
- P21-Rho-binding domain
- p21-activated kinase 2, catalytic domain
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of PAK2 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads PAK2 as an antibody target. Whether an autoantibody or antibody against PAK2 could matter depends on whether native PAK2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PAK2 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 PAK2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
Loading the interactive Seroatlas protein explorer...