PANK1
Pantothenate kinase 1
Also known as: MGC24596, PANK, PANK1_HUMAN, PANK1a, PANK1b
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8TE04
- Gene
- PANK1
- Ensembl
- ENSG00000152782
- Chromosome
- 10
- Canonical length
- 598 aa
- Protein class
- Enzymes, Metabolic proteins, Predicted intracellular proteins
- Quaternary structure
- Homodimer
OverviewNCBI Gene
This gene encodes a member of the pantothenate kinase family. Pantothenate kinases are key regulatory enzymes in the biosynthesis of coenzyme A (CoA). The encoded protein catalyzes the first and rate-limiting enzymatic reaction in CoA biosynthesis and is regulated by CoA through feedback inhibition. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. This gene and an intronic miRNA on the same strand are co-regulated by the tumor suppressor p53 (see PMID 20833636). [provided by RefSeq, Apr 2011]
Canonical amino-acid sequenceUniProt
598 residues, UniProt reviewed canonical sequence.
>Q8TE04|PANK1
1 MLKLVGGGGG QDWACSVAGT SLGGEEAAFE VARPGDQGKA GGGSPGWGCA GIPDSAPGAG
61 VLQAGAVGPA RGGQGAEEVG ESAGGGEERR VRHPQAPALR LLNRKPQGGS GEIKTPENDL
121 QRGRLSRGPR TAPPAPGMGD RSGQQERSVP HSPGAPVGTS AAAVNGLLHN GFHPPPVQPP
181 HVCSRGPVGG SDAAPQRLPL LPELQPQPLL PQHDSPAKKC RLRRRMDSGR KNRPPFPWFG
241 MDIGGTLVKL VYFEPKDITA EEEQEEVENL KSIRKYLTSN TAYGKTGIRD VHLELKNLTM
301 CGRKGNLHFI RFPSCAMHRF IQMGSEKNFS SLHTTLCATG GGAFKFEEDF RMIADLQLHK
361 LDELDCLIQG LLYVDSVGFN GKPECYYFEN PTNPELCQKK PYCLDNPYPM LLVNMGSGVS
421 ILAVYSKDNY KRVTGTSLGG GTFLGLCCLL TGCETFEEAL EMAAKGDSTN VDKLVKDIYG
481 GDYERFGLQG SAVASSFGNM MSKEKRDSIS KEDLARATLV TITNNIGSIA RMCALNENID
541 RVVFVGNFLR INMVSMKLLA YAMDFWSKGQ LKALFLEHEG YFGAVGALLE LFKMTDDKLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PANK1 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)
- 0.43
- Highest tissue expression
- 103 nTPM
Expression across tissuesHPA
Tissue
- liver: 103 nTPM
- kidney: 43 nTPM
- tongue: 26 nTPM
- duodenum: 19 nTPM
- rectum: 16 nTPM
- small intestine: 16 nTPM
Single-cell type
- hepatocytes: 251 nCPM
- myonuclei: 131 nCPM
- choroid plexus epithelial cells: 127 nCPM
- proximal tubule cells: 96 nCPM
- cardiomyocytes: 96 nCPM
- distal convoluted tubule cells: 62 nCPM
Immune cell
- plasmacytoid DC: 0.4 nTPM
- memory CD8 T-cell: 0.3 nTPM
- MAIT T-cell: 0.2 nTPM
- memory B-cell: 0.2 nTPM
- memory CD4 T-cell: 0.2 nTPM
- T-reg: 0.2 nTPM
Brain region
- choroid plexus: 25 nTPM
- cerebellum: 18 nTPM
- cerebral cortex: 12 nTPM
- thalamus: 10 nTPM
- pons: 10 nTPM
- midbrain: 8.8 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)
- 0.69
- gnomAD pLI
- 0
- gnomAD missense Z
- 1.59
- DepMap mean gene effect
- 0.04
- 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
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads PANK1 as an antibody target. Whether an autoantibody or antibody against PANK1 could matter depends on whether native PANK1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PANK1 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 PANK1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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