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Contents

   



(Top)
 


1 Function  





2 References  





3 External links  





4 Further reading  














ACY1






Cymraeg
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From Wikipedia, the free encyclopedia
 


ACY1
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesACY1, ACY-1, ACY1D, HEL-S-5, aminoacylase 1
External IDsOMIM: 104620; MGI: 87913; HomoloGene: 110440; GeneCards: ACY1; OMA:ACY1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001198898
NM_000666
NM_001198895
NM_001198896
NM_001198897

NM_001276442
NM_025371

RefSeq (protein)

NP_000657
NP_001185824
NP_001185825
NP_001185826
NP_001185827

NP_001263371
NP_079647

Location (UCSC)Chr 3: 51.98 – 51.99 MbChr 9: 106.31 – 106.32 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Aminoacylase-1 is an enzyme that in humans is encoded by the ACY1 gene.[5][6][7]

Function

[edit]

Aminoacylase-1 is a cytosolic, homodimeric, zinc-binding enzyme that catalyzes the hydrolysis of acylated L-amino acids to L-amino acids and acyl group, and has been postulated to function in the catabolism and salvage of acylated amino acids. ACY1 has been assigned to chromosome 3p21.1, a region reduced to homozygosityinsmall-cell lung cancer (SCLC), and its expression has been reported to be reduced or undetectable in SCLC cell lines and tumors. The amino acid sequence of human aminoacylase-1 is highly homologous to the porcine counterpart, and ACY1 is the first member of a new family of zinc-binding enzymes.[7]

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.
  • ^ Miller YE, Drabkin H, Jones C, Fisher JH (Sep 1990). "Human aminoacylase-1: cloning, regional assignment to distal chromosome 3p21.1, and identification of a cross-hybridizing sequence on chromosome 18". Genomics. 8 (1): 149–154. doi:10.1016/0888-7543(90)90237-O. PMID 1707030.
  • ^ Voss R, Lerer I, Povey S, Solomon E, Bobrow M (Jul 1980). "Confirmation and further regional assignment of aminoacylase 1 (acy-1) on human chromosome 3 using a simplified detection method". Annals of Human Genetics. 44 (Pt 1): 1–9. doi:10.1111/j.1469-1809.1980.tb00940.x. PMID 6948533. S2CID 21566170.
  • ^ a b "Entrez Gene: ACY1 aminoacylase 1".
  • [edit]

    Further reading

    [edit]
  • Mitta M, Kato I, Tsunasawa S (Aug 1993). "The nucleotide sequence of human aminoacylase-1". Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression. 1174 (2): 201–3. doi:10.1016/0167-4781(93)90116-u. PMID 8357837.
  • Cook RM, Burke BJ, Buchhagen DL, Minna JD, Miller YE (Aug 1993). "Human aminoacylase-1. Cloning, sequence, and expression analysis of a chromosome 3p21 gene inactivated in small cell lung cancer". The Journal of Biological Chemistry. 268 (23): 17010–7. doi:10.1016/S0021-9258(19)85294-8. PMID 8394326.
  • Lindner HA, Lunin VV, Alary A, Hecker R, Cygler M, Ménard R (Nov 2003). "Essential roles of zinc ligation and enzyme dimerization for catalysis in the aminoacylase-1/M20 family". The Journal of Biological Chemistry. 278 (45): 44496–44504. doi:10.1074/jbc.M304233200. PMID 12933810.
  • Rual JF, Venkatesan K, Hao T, Hirozane-Kishikawa T, Dricot A, Li N, Berriz GF, Gibbons FD, Dreze M, Ayivi-Guedehoussou N, Klitgord N, Simon C, Boxem M, Milstein S, Rosenberg J, Goldberg DS, Zhang LV, Wong SL, Franklin G, Li S, Albala JS, Lim J, Fraughton C, Llamosas E, Cevik S, Bex C, Lamesch P, Sikorski RS, Vandenhaute J, Zoghbi HY, Smolyar A, Bosak S, Sequerra R, Doucette-Stamm L, Cusick ME, Hill DE, Roth FP, Vidal M (Oct 2005). "Towards a proteome-scale map of the human protein-protein interaction network". Nature. 437 (7062): 1173–1178. Bibcode:2005Natur.437.1173R. doi:10.1038/nature04209. PMID 16189514. S2CID 4427026.
  • Van Coster RN, Gerlo EA, Giardina TG, Engelke UF, Smet JE, De Praeter CM, Meersschaut VA, De Meirleir LJ, Seneca SH, Devreese B, Leroy JG, Herga S, Perrier JP, Wevers RA, Lissens W (Dec 2005). "Aminoacylase I deficiency: a novel inborn error of metabolism". Biochemical and Biophysical Research Communications. 338 (3): 1322–1326. doi:10.1016/j.bbrc.2005.10.126. PMID 16274666.
  • Sass JO, Mohr V, Olbrich H, Engelke U, Horvath J, Fliegauf M, Loges NT, Schweitzer-Krantz S, Moebus R, Weiler P, Kispert A, Superti-Furga A, Wevers RA, Omran H (Mar 2006). "Mutations in ACY1, the gene encoding aminoacylase 1, cause a novel inborn error of metabolism". American Journal of Human Genetics. 78 (3): 401–409. doi:10.1086/500563. PMC 1380284. PMID 16465618.
  • Figueiredo EL, Garcia Leão FV, De Oliveira LV, Moreira Mda C, De Souza Figueiredo AF (Oct 2006). "The amidase activity of human tissue kallikrein is significantly lower in the urine of patients with systolic heart failure". Journal of Cardiac Failure. 12 (8): 653–658. doi:10.1016/j.cardfail.2006.06.004. PMID 17045186.

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    This page was last edited on 22 July 2023, at 13:55 (UTC).

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