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Contents

   



(Top)
 


1 Function  





2 References  





3 Further reading  














Carbonic anhydrase 5A, mitochondrial






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From Wikipedia, the free encyclopedia
 

(Redirected from Carbonic anhydrase 5A)

CA5A
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesCA5A, CA5, CA5AD, CAV, CAVA, GS1-21A4.1, carbonic anhydrase 5A
External IDsOMIM: 114761; MGI: 101946; HomoloGene: 68200; GeneCards: CA5A; OMA:CA5A - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001739
NM_001367225

NM_007608

RefSeq (protein)

NP_001730

NP_031634

Location (UCSC)Chr 16: 87.88 – 87.94 MbChr 8: 122.64 – 122.67 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Carbonic anhydrase 5A, mitochondrial is a protein that in humans is encoded by the CA5A gene.[5]

Function[edit]

Carbonic anhydrases (CAs) are a family of zinc metalloenzymes that catalyze the reversible hydration of carbon dioxide. They participate in a variety of biological processes, including respiration, calcification, acid-base balance, bone resorption, and the formation of aqueous humor, cerebrospinal fluid, saliva, and gastric acid. They show extensive diversity in tissue distribution and in their subcellular localization. CA5A is localized in the mitochondria and expressed primarily in the liver. It may play an important role in ureagenesis and gluconeogenesis. CA5A gene maps to chromosome 16q24.3 and an unprocessed pseudogene has been assigned to 16p12-p11.2. [provided by RefSeq, Jul 2008].

References[edit]

  • ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  • ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  • ^ "Entrez Gene: Carbonic anhydrase 5A". Retrieved 2019-12-31.
  • Further reading[edit]

    • Vullo D, Nishimori I, Innocenti A, Scozzafava A, Supuran CT (March 2007). "Carbonic anhydrase activators: an activation study of the human mitochondrial isoforms VA and VB with amino acids and amines". Bioorganic & Medicinal Chemistry Letters. 17 (5): 1336–40. doi:10.1016/j.bmcl.2006.11.075. PMID 17174092.
  • Hendrickson SL, Lautenberger JA, Chinn LW, Malasky M, Sezgin E, Kingsley LA, et al. (September 2010). "Genetic variants in nuclear-encoded mitochondrial genes influence AIDS progression". PLOS ONE. 5 (9): e12862. Bibcode:2010PLoSO...512862H. doi:10.1371/journal.pone.0012862. PMC 2943476. PMID 20877624.
  • van Karnebeek CD, Sly WS, Ross CJ, Salvarinova R, Yaplito-Lee J, Santra S, et al. (March 2014). "Mitochondrial carbonic anhydrase VA deficiency resulting from CA5A alterations presents with hyperammonemia in early childhood". American Journal of Human Genetics. 94 (3): 453–61. doi:10.1016/j.ajhg.2014.01.006. PMC 3951944. PMID 24530203.
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  • This article incorporates text from the United States National Library of Medicine, which is in the public domain.


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