PIM3
Serine/threonine-protein kinase pim-3
Also known as: PIM3_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q86V86
- Gene
- PIM3
- Ensembl
- ENSG00000198355
- Chromosome
- 22
- Canonical length
- 326 aa
- Protein class
- Cancer-related genes, Enzymes, Plasma proteins, Predicted intracellular proteins
- Subcellular location
- Cytosol
OverviewNCBI Gene
The protein encoded by this gene belongs to the Ser/Thr protein kinase family, and PIM subfamily. This gene is overexpressed in hematological and epithelial tumors and is associated with MYC coexpression. It plays a role in the regulation of signal transduction cascades, contributing to both cell proliferation and survival, and provides a selective advantage in tumorigenesis. [provided by RefSeq, Jun 2012]
Canonical amino-acid sequenceUniProt
326 residues, UniProt reviewed canonical sequence.
>Q86V86|PIM3
1 MLLSKFGSLA HLCGPGGVDH LPVKILQPAK ADKESFEKAY QVGAVLGSGG FGTVYAGSRI
61 ADGLPVAVKH VVKERVTEWG SLGGATVPLE VVLLRKVGAA GGARGVIRLL DWFERPDGFL
121 LVLERPEPAQ DLFDFITERG ALDEPLARRF FAQVLAAVRH CHSCGVVHRD IKDENLLVDL
181 RSGELKLIDF GSGALLKDTV YTDFDGTRVY SPPEWIRYHR YHGRSATVWS LGVLLYDMVC
241 GDIPFEQDEE ILRGRLLFRR RVSPECQQLI RWCLSLRPSE RPSLDQIAAH PWMLGADGGV
301 PESCDLRLCT LDPDDVASTT SSSESLLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PIM3 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)
- 0.34
- Highest tissue expression
- 129 nTPM
Expression across tissuesHPA
Tissue
- stomach: 129 nTPM
- skin: 127 nTPM
- skeletal muscle: 122 nTPM
- kidney: 120 nTPM
- lung: 118 nTPM
- bone marrow: 108 nTPM
Single-cell type
- extravillous trophoblasts: 461 nCPM
- syncytiotrophoblasts: 458 nCPM
- prostatic club cells: 352 nCPM
- esophageal apical cells: 318 nCPM
- urothelial cells: 298 nCPM
- prostatic hillock cells: 246 nCPM
Immune cell
- neutrophil: 21 nTPM
- naive B-cell: 7.5 nTPM
- plasmacytoid DC: 7 nTPM
- T-reg: 5.8 nTPM
- non-classical monocyte: 5.2 nTPM
- memory CD4 T-cell: 5 nTPM
Brain region
- medulla oblongata: 71 nTPM
- white matter: 68 nTPM
- cerebral cortex: 66 nTPM
- pons: 64 nTPM
- thalamus: 61 nTPM
- midbrain: 60 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)
- 0.24
- gnomAD pLI
- 0.98
- gnomAD missense Z
- 0.92
- DepMap mean gene effect
- -0.12
- 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 process
- cellular response to forskolin
- negative regulation of apoptotic process
- negative regulation of insulin secretion involved in cellular response to glucose stimulus
- protein phosphorylation
- regulation of mitotic cell cycle
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of PIM3 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 PIM3 as an antibody target. Whether an autoantibody or antibody against PIM3 could matter depends on whether native PIM3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PIM3 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 PIM3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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