Kisela alfa-glukozidaza
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Lizozomalna alfa-glukozidaza je enzim koji je kod ljudi kodiran GAA genom.[1]
Kisela alfa glukozidaza | |||||||||||
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Identifikatori | |||||||||||
Simboli | GAA; LYAG | ||||||||||
Vanjski ID | OMIM: 606800 MGI: 95609 HomoloGene: 37268 GeneCards: GAA Gene | ||||||||||
EC broj | 3.2.1.20 | ||||||||||
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Pregled RNK izražavanja | |||||||||||
podaci | |||||||||||
Ortolozi | |||||||||||
Vrsta | Čovek | Miš | |||||||||
Entrez | 2548 | 14387 | |||||||||
Ensembl | ENSG00000171298 | ENSMUSG00000025579 | |||||||||
UniProt | P10253 | P70699 | |||||||||
RefSeq (mRNA) | NM_000152.3 | NM_001159324.1 | |||||||||
RefSeq (protein) | NP_000143.2 | NP_001152796.1 | |||||||||
Lokacija (UCSC) | Chr 17: 78.08 - 78.09 Mb | Chr 11: 119.27 - 119.29 Mb | |||||||||
PubMed pretraga | [1] | [2] |
Kisela alfa-glukozidaza je esencijalna za degradaciju glikogena do glukoze u lizozomima. Različite forme kisele alfa-glukozidaze nastaju putem proteolitičke obrade. Tri transkriptne varijante koje kodiraju isti protein su poznate.[1]
Mutacije ovog gena uzrokuju glikogenozu tipa II (Pompeovu bolest). To je autozomno recesivno oboljenje sa širokim kliničkim spektrom.
Reference
urediLiteratura
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- Zhong N, Martiniuk F, Tzall S, Hirschhorn R (1991). „Identification of a missense mutation in one allele of a patient with Pompe disease, and use of endonuclease digestion of PCR-amplified RNA to demonstrate lack of mRNA expression from the second allele.”. Am. J. Hum. Genet. 49 (3): 635–45. PMC 1683123. PMID 1652892.
- Fenouillet E, Gluckman JC (1991). „Effect of a glucosidase inhibitor on the bioactivity and immunoreactivity of human immunodeficiency virus type 1 envelope glycoprotein.”. J. Gen. Virol. 72 ( Pt 8) (8): 1919–26. DOI:10.1099/0022-1317-72-8-1919. PMID 1678778.
- Martiniuk F, Mehler M, Bodkin M, et al. (1992). „Identification of a missense mutation in an adult-onset patient with glycogenosis type II expressing only one allele”. DNA Cell Biol. 10 (9): 681–7. DOI:10.1089/dna.1991.10.681. PMID 1684505.
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- Hermans MM, Kroos MA, van Beeumen J, et al. (1991). „Human lysosomal alpha-glucosidase. Characterization of the catalytic site”. J. Biol. Chem. 266 (21): 13507–12. PMID 1856189.
- Hermans MM, de Graaff E, Kroos MA, et al. (1991). „Identification of a point mutation in the human lysosomal alpha-glucosidase gene causing infantile glycogenosis type II”. Biochem. Biophys. Res. Commun. 179 (2): 919–26. DOI:10.1016/0006-291X(91)91906-S. PMID 1898413.
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- Martiniuk F, Mehler M, Tzall S, et al. (1990). „Sequence of the cDNA and 5'-flanking region for human acid alpha-glucosidase, detection of an intron in the 5' untranslated leader sequence, definition of 18-bp polymorphisms, and differences with previous cDNA and amino acid sequences”. DNA Cell Biol. 9 (2): 85–94. DOI:10.1089/dna.1990.9.85. PMID 2111708.
- Kalyanaraman VS, Rodriguez V, Veronese F, et al. (1990). „Characterization of the secreted, native gp120 and gp160 of the human immunodeficiency virus type 1”. AIDS Res. Hum. Retroviruses 6 (3): 371–80. DOI:10.1089/aid.1990.6.371. PMID 2187500.
- Martiniuk F, Bodkin M, Tzall S, Hirschhorn R (1990). „Identification of the base-pair substitution responsible for a human acid alpha glucosidase allele with lower "affinity" for glycogen (GAA 2) and transient gene expression in deficient cells”. Am. J. Hum. Genet. 47 (3): 440–5. PMC 1683879. PMID 2203258.
- Hoefsloot LH, Hoogeveen-Westerveld M, Reuser AJ, Oostra BA (1991). „Characterization of the human lysosomal alpha-glucosidase gene”. Biochem. J. 272 (2): 493–7. PMC 1149727. PMID 2268276.
- Shimizu H, Tsuchie H, Honma H, et al. (1991). „Effect of N-(3-phenyl-2-propenyl)-1-deoxynojirimycin on the lectin binding to HIV-1 glycoproteins”. Jpn. J. Med. Sci. Biol. 43 (3): 75–87. PMID 2283726.
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