Carbonic anhydrase 5A, mitochondrial

CA5A
Available structures
PDB	Ortholog search: PDBe RCSB
List of PDB id codes
	1DMX, 1DMY, 1KEQ, 1URT
Identifiers
Aliases	CA5A, CA5, CA5AD, CAV, CAVA, GS1-21A4.1, carbonic anhydrase 5A
External IDs	OMIM: 114761 MGI: 101946 HomoloGene: 68200 GeneCards: CA5A
Gene location (Human)
Chr.	Chromosome 16 (human)[1]
End	87,936,580 bp[1]
Gene location (Mouse)
Chr.	Chromosome 8 (mouse)[2]
End	121,944,904 bp[2]
Gene ontology
Molecular function	• carbonate dehydratase activity; • zinc ion binding; • metal ion binding; • lyase activity; • Carbonic anhydrase;
Cellular component	• mitochondrial matrix; • mitochondrion;
Biological process	• bicarbonate transport;
	Sources:Amigo / QuickGO
Orthologs
	763
	12352
	ENSG00000174990
	ENSMUSG00000025317
	P35218
	P23589
	NM_001739; NM_001367225
	NM_007608
	NP_001730
	NP_031634
	Wikidata
View/Edit Human	View/Edit Mouse

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

Function

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

GRCh38: Ensembl release 89: ENSG00000174990 - Ensembl, May 2017
GRCm38: Ensembl release 89: ENSMUSG00000025317 - Ensembl, May 2017
"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.

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.

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

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[refGRCh38Ensembl-1] GRCh38: Ensembl release 89: ENSG00000174990 - Ensembl, May 2017

[refGRCm38Ensembl-2] GRCm38: Ensembl release 89: ENSMUSG00000025317 - Ensembl, May 2017

[3] "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[4] "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[entrez-5] "Entrez Gene: Carbonic anhydrase 5A". Retrieved 2019-12-31.

Carbonic anhydrase 5A, mitochondrial

Function

References

Further reading