PIM2
Serine/threonine-protein kinase pim-2
Also known as: PIM2_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9P1W9
- Gene
- PIM2
- Ensembl
- ENSG00000102096
- Chromosome
- X
- Canonical length
- 311 aa
- Protein class
- Cancer-related genes, Enzymes, Predicted intracellular proteins, Predicted membrane proteins
- Subcellular location
- Cytosol
OverviewNCBI Gene
This gene encodes a protooncogene that acts as a serine/threonine protein kinase. Studies determined the encoded protein functions to prevent apoptosis and to promote cell survival.[provided by RefSeq, Nov 2009]
Canonical amino-acid sequenceUniProt
311 residues, UniProt reviewed canonical sequence.
>Q9P1W9|PIM2
1 MLTKPLQGPP APPGTPTPPP GGKDREAFEA EYRLGPLLGK GGFGTVFAGH RLTDRLQVAI
61 KVIPRNRVLG WSPLSDSVTC PLEVALLWKV GAGGGHPGVI RLLDWFETQE GFMLVLERPL
121 PAQDLFDYIT EKGPLGEGPS RCFFGQVVAA IQHCHSRGVV HRDIKDENIL IDLRRGCAKL
181 IDFGSGALLH DEPYTDFDGT RVYSPPEWIS RHQYHALPAT VWSLGILLYD MVCGDIPFER
241 DQEILEAELH FPAHVSPDCC ALIRRCLAPK PSSRPSLEEI LLDPWMQTPA EDVPLNPSKG
301 GPAPLAWSLL PLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PIM2 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)
- 0.3
- Highest tissue expression
- 153 nTPM
Expression across tissuesHPA
Tissue
- spleen: 153 nTPM
- lymph node: 107 nTPM
- tonsil: 98 nTPM
- bone marrow: 97 nTPM
- duodenum: 82 nTPM
- appendix: 81 nTPM
Single-cell type
- plasma cells: 421 nCPM
- mast cells: 82 nCPM
- innate lymphoid cells: 78 nCPM
- neutrophils: 69 nCPM
- t-cells: 58 nCPM
- cdc: 53 nCPM
Immune cell
- T-reg: 333 nTPM
- basophil: 281 nTPM
- neutrophil: 196 nTPM
- naive CD4 T-cell: 173 nTPM
- memory CD4 T-cell: 166 nTPM
- memory B-cell: 125 nTPM
Brain region
- hippocampal formation: 30 nTPM
- hypothalamus: 26 nTPM
- cerebral cortex: 23 nTPM
- pons: 23 nTPM
- choroid plexus: 21 nTPM
- basal ganglia: 21 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)
- 0.32
- gnomAD pLI
- 0.95
- gnomAD missense Z
- 1.34
- DepMap mean gene effect
- -0.16
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- apoptotic mitochondrial changes
- G1/S transition of mitotic cell cycle
- macroautophagy
- negative regulation of apoptotic process
- negative regulation of cell population proliferation
- positive regulation of autophagy
- positive regulation of canonical NF-kappaB signal transduction
- positive regulation of DNA-templated transcription
- positive regulation of macroautophagy
- protein phosphorylation
- protein stabilization
- regulation of mitotic cell cycle
- response to virus
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of PIM2 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 PIM2 as an antibody target. Whether an autoantibody or antibody against PIM2 could matter depends on whether native PIM2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PIM2 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 PIM2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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