PDPK1
3-phosphoinositide-dependent protein kinase 1
Also known as: PDK1, PDPK1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O15530
- Gene
- PDPK1
- Ensembl
- ENSG00000140992
- Chromosome
- 16
- Canonical length
- 556 aa
- Protein class
- Enzymes, Plasma proteins, Predicted intracellular proteins
- Subcellular location
- Primary cilium tip,Cytosol
- Quaternary structure
- Homodimer
OverviewNCBI Gene
Enables 3-phosphoinositide-dependent protein kinase activity; phospholipase activator activity; and phospholipase binding activity. Involved in several processes, including cell surface receptor signaling pathway; intracellular signaling cassette; and regulation of signal transduction. Acts upstream of or within intracellular signal transduction. Located in cell projection; cytosol; and plasma membrane. Implicated in prostate cancer. Biomarker of lung non-small cell carcinoma. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
556 residues, UniProt reviewed canonical sequence.
>O15530|PDPK1
1 MARTTSQLYD AVPIQSSVVL CSCPSPSMVR TQTESSTPPG IPGGSRQGPA MDGTAAEPRP
61 GAGSLQHAQP PPQPRKKRPE DFKFGKILGE GSFSTVVLAR ELATSREYAI KILEKRHIIK
121 ENKVPYVTRE RDVMSRLDHP FFVKLYFTFQ DDEKLYFGLS YAKNGELLKY IRKIGSFDET
181 CTRFYTAEIV SALEYLHGKG IIHRDLKPEN ILLNEDMHIQ ITDFGTAKVL SPESKQARAN
241 SFVGTAQYVS PELLTEKSAC KSSDLWALGC IIYQLVAGLP PFRAGNEYLI FQKIIKLEYD
301 FPEKFFPKAR DLVEKLLVLD ATKRLGCEEM EGYGPLKAHP FFESVTWENL HQQTPPKLTA
361 YLPAMSEDDE DCYGNYDNLL SQFGCMQVSS SSSSHSLSAS DTGLPQRSGS NIEQYIHDLD
421 SNSFELDLQF SEDEKRLLLE KQAGGNPWHQ FVENNLILKM GPVDKRKGLF ARRRQLLLTE
481 GPHLYYVDPV NKVLKGEIPW SQELRPEAKN FKTFFVHTPN RTYYLMDPSG NAHKWCRKIQ
541 EVWRQRYQSH PDAAVQLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PDPK1 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
- Cell surface
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.34
- Highest tissue expression
- 26 nTPM
Expression across tissuesHPA
Tissue
- parathyroid gland: 26 nTPM
- cerebellum: 24 nTPM
- basal ganglia: 21 nTPM
- cerebral cortex: 19 nTPM
- small intestine: 18 nTPM
- pancreas: 18 nTPM
Single-cell type
- oocytes: 184 nCPM
- proximal tubule cells: 157 nCPM
- syncytiotrophoblasts: 140 nCPM
- neutrophils: 112 nCPM
- renal collecting duct intercalated cells: 102 nCPM
- renal connecting tubule cells: 93 nCPM
Immune cell
- neutrophil: 13 nTPM
- non-classical monocyte: 8.8 nTPM
- intermediate monocyte: 8.3 nTPM
- eosinophil: 8.2 nTPM
- plasmacytoid DC: 7.8 nTPM
- classical monocyte: 7 nTPM
Brain region
- basal ganglia: 88 nTPM
- cerebral cortex: 78 nTPM
- hippocampal formation: 77 nTPM
- amygdala: 68 nTPM
- white matter: 61 nTPM
- pons: 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)
- 0.29
- gnomAD pLI
- 0.98
- gnomAD missense Z
- 2.01
- DepMap mean gene effect
- -1.04
- DepMap dependency class
- common
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- actin cytoskeleton organization
- calcium-mediated signaling
- cell migration
- cellular response to epidermal growth factor stimulus
- cellular response to insulin stimulus
- epidermal growth factor receptor signaling pathway
- extrinsic apoptotic signaling pathway
- hyperosmotic response
- insulin receptor signaling pathway
- insulin-like growth factor receptor signaling pathway
- intracellular signal transduction
- negative regulation of cardiac muscle cell apoptotic process
- negative regulation of endothelial cell apoptotic process
- negative regulation of toll-like receptor signaling pathway
- negative regulation of transforming growth factor beta receptor signaling pathway
- phosphatidylinositol 3-kinase/protein kinase B signal transduction
- positive regulation of angiogenesis
- positive regulation of blood vessel endothelial cell migration
- positive regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction
- positive regulation of protein localization to plasma membrane
- positive regulation of release of sequestered calcium ion into cytosol
- positive regulation of sprouting angiogenesis
- positive regulation of vascular endothelial cell proliferation
- protein autophosphorylation
- protein phosphorylation
- regulation of canonical NF-kappaB signal transduction
- regulation of mast cell degranulation
- T cell costimulation
- type B pancreatic cell development
- vascular endothelial cell response to laminar fluid shear stress
- intracellular signaling cassette
Molecular functions
- ATP binding
- phospholipase activator activity
- phospholipase binding
- protein serine kinase activity
- protein serine/threonine kinase activity
- 3-phosphoinositide-dependent protein kinase activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of PDPK1 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 PDPK1 as an antibody target. Whether an autoantibody or antibody against PDPK1 could matter depends on whether native PDPK1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PDPK1 is annotated at the cell surface, where native PDPK1 is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label PDPK1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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