PDE10A

From Wikipedia, the free encyclopedia
Phosphodiesterase 10A

PDB rendering based on 2o8h.
Available structures
PDB Ortholog search: PDBe, RCSB
Identifiers
SymbolsPDE10A; HSPDE10A
External IDsOMIM: 610652 MGI: 1345143 HomoloGene: 4852 ChEMBL: 4409 GeneCards: PDE10A Gene
EC number3.1.4.17, 3.1.4.35
RNA expression pattern
More reference expression data
Orthologs
SpeciesHumanMouse
Entrez1084623984
EnsemblENSG00000112541ENSMUSG00000023868
UniProtQ9Y233Q8CA95
RefSeq (mRNA)NM_001130690NM_011866
RefSeq (protein)NP_001124162NP_035996
Location (UCSC)Chr 6:
165.74 – 166.08 Mb
Chr 17:
8.53 – 8.99 Mb
PubMed search

cAMP and cAMP-inhibited cGMP 3',5'-cyclic phosphodiesterase 10A is an enzyme that in humans is encoded by the PDE10A gene.[2][3]

Various cellular responses are regulated by the second messengers cAMP and cGMP. Phosphodiesterases, such as PDE10A, eliminate cAMP- and cGMP-mediated intracellular signaling by hydrolyzing the cyclic nucleotide to the corresponding nucleoside 5-prime monophosphate.[3][4]

Inhibitors

3d model of compound 96 (Malamas, 2011)[1]
  • Compound 96: IC50 = 700 pM, high selectivity against all other members of the PDE family[1]
  • Papaverine[5]
  • PF-2545920[6]

References

  1. 1.0 1.1 Malamas MS et al (2011): "Highly potent, selective, and orally active phosphodiesterase 10A inhibitors", J. Med. Chem. 54 (21): 7621. PMID 21988093
  2. Fujishige K, Kotera J, Michibata H, Yuasa K, Takebayashi S, Okumura K, Omori K (Jul 1999). "Cloning and characterization of a novel human phosphodiesterase that hydrolyzes both cAMP and cGMP (PDE10A)". J Biol Chem 274 (26): 18438–45. doi:10.1074/jbc.274.26.18438. PMID 10373451. 
  3. 3.0 3.1 "Entrez Gene: PDE10A phosphodiesterase 10A". 
  4. Fujishige K, Kotera J, Yuasa K, Omori K (October 2000). "The human phosphodiesterase PDE10A gene genomic organization and evolutionary relatedness with other PDEs containing GAF domains". Eur. J. Biochem. 267 (19): 5943–51. doi:10.1046/j.1432-1327.2000.01661.x. PMID 10998054. 
  5. Siuciak JA, Chapin DS, Harms JF, et al. (August 2006). "Inhibition of the striatum-enriched phosphodiesterase PDE10A: a novel approach to the treatment of psychosis". Neuropharmacology 51 (2): 386–96. doi:10.1016/j.neuropharm.2006.04.013. PMID 16780899. 
  6. Verhoest PR, Chapin DS, Corman M, et al. (August 2009). "Discovery of a novel class of phosphodiesterase 10A inhibitors and identification of clinical candidate 2-[4-(1-methyl-4-pyridin-4-yl-1H-pyrazol-3-yl)-phenoxymethyl]-quinoline (PF-2545920) for the treatment of schizophrenia". J. Med. Chem. 52 (16): 5188–96. doi:10.1021/jm900521k. PMID 19630403. 

Further reading

This article incorporates text from the United States National Library of Medicine, which is in the public domain.


This article is issued from Wikipedia. The text is available under the Creative Commons Attribution/Share Alike; additional terms may apply for the media files.