PIP5KL1
Phosphatidylinositol 4-phosphate 5-kinase-like protein 1
Also known as: bA203J24.5, MGC46424, PI5L1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q5T9C9
- Gene
- PIP5KL1
- Ensembl
- ENSG00000167103
- Chromosome
- 9
- Canonical length
- 394 aa
- Protein class
- Enzymes, Metabolic proteins, Predicted intracellular proteins
- Subcellular location
- Cytosol
OverviewNCBI Gene
PIP5KL1 is a phosphoinositide kinase-like protein that lacks intrinsic lipid kinase activity but associates with type I PIPKs (see PIP5K1A; MIM 603275) and may play a role in localization of PIPK activity (Chang et al., 2004 [PubMed 14701839]).[supplied by OMIM, Jun 2009]
Canonical amino-acid sequenceUniProt
394 residues, UniProt reviewed canonical sequence.
>Q5T9C9|PIP5KL1
1 MAAPSPGPRE VLAPSPEAGC RAVTSSRRGL LWRLRDKQSR LGLFEISPGH ELHGMTCMMQ
61 AGLWAATQVS MDHPPTGPPS RDDFSEVLTQ VHEGFELGTL AGPAFAWLRR SLGLAEEDYQ
121 AALGPGGPYL QFLSTSKSKA SFFLSHDQRF FLKTQGRREV QALLAHLPRY VQHLQRHPHS
181 LLARLLGVHS LRVDRGKKTY FIVMQSVFYP AGRISERYDI KGCEVSRWVD PAPEGSPLVL
241 VLKDLNFQGK TINLGPQRSW FLRQMELDTT FLRELNVLDY SLLIAFQRLH EDERGPGSSL
301 IFRTARSVQG AQSPEESRAQ NRRLLPDAPN ALHILDGPEQ RYFLGVVDLA TVYGLRKRLE
361 HLWKTLRYPG RTFSTVSPAR YARRLCQWVE AHTELocalizationUniProt · AlphaFold · HPA
Whether an antibody against PIP5KL1 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
- 3.7 nTPM
Expression across tissuesHPA
Tissue
- skin: 3.7 nTPM
- pituitary gland: 3.6 nTPM
- vagina: 3.4 nTPM
- cervix: 3 nTPM
- esophagus: 3 nTPM
- salivary gland: 3 nTPM
Single-cell type
- late spermatids: 40 nCPM
- conjunctival goblet cells: 36 nCPM
- early spermatids: 25 nCPM
- foveolar cells: 19 nCPM
- endometrial glandular cells: 13 nCPM
- endometrial secretory cells: 11 nCPM
Immune cell
- naive B-cell: 0.4 nTPM
- intermediate monocyte: 0.2 nTPM
- MAIT T-cell: 0.2 nTPM
- memory B-cell: 0.2 nTPM
- myeloid DC: 0.2 nTPM
- plasmacytoid DC: 0.2 nTPM
Brain region
- pons: 5.9 nTPM
- cerebral cortex: 4.5 nTPM
- medulla oblongata: 4.5 nTPM
- cerebellum: 4.2 nTPM
- thalamus: 3.6 nTPM
- hypothalamus: 3.1 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)
- 0.95
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.79
- DepMap mean gene effect
- -0.11
- DepMap dependency class
- selective
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
- negative regulation of cell migration
- negative regulation of mitochondrial membrane potential
- negative regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction
- phosphatidylinositol phosphate biosynthetic process
- positive regulation of apoptotic process
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads PIP5KL1 as an antibody target. Whether an autoantibody or antibody against PIP5KL1 could matter depends on whether native PIP5KL1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PIP5KL1 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 PIP5KL1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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