CHST6

CHST6
Identifikatori
Alijasi	CHST6
Spoljašnji ID	OMIM: 605294 MGI: 1931825 HomoloGene: 56927 GeneCards: CHST6
Genska lokacija (miš)
Hr.	Chromosome 8 (mouse)
Kraj	112,637,079 bp
Genska ontologija
Molecular function	• sulfotransferase activity; • transferase activity; • N-acetylglucosamine 6-O-sulfotransferase activity;
Cellular component	• Голџијев апарат; • Golgi membrane; • мембрана; • саставни део мембране; • trans-Golgi network;
Biological process	• sulfur compound metabolic process; • keratan sulfate biosynthetic process; • N-acetylglucosamine metabolic process; • Метаболизам угљених хидрата;
	Sources:Amigo / QuickGO
Ortolozi
	4166
	56773
	ENSG00000183196
	ENSMUSG00000031952
	Q9GZX3
	Q9QUP4
	NM_021615
	NM_019950
	NP_067628
	NP_064334
	Wikidata
View/Edit Human	View/Edit Mouse

Ugljeno hidratna sulfotransferaza 6 (eng. Carbohydrate sulfotransferase 6) je enzim koji je kod ljudi kodiran istoimenim genom CHST6^[4]^[5]^[6] , nalazi se na kratkom kraku 16 hromozoma.^[7] Dužina polipeptidnog lanca je 395 aminokiselina, a molekulska težina 44.099.^[8]

Reference

^ ^а ^б ^в GRCm38: Ensembl release 89: ENSMUSG00000031952 - 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.
^ Vance JM, Jonasson F, Lennon F, Sarrica J, Damji KF, Stauffer J, Pericak-Vance MA, Klintworth GK (јул 1996). „Linkage of a gene for macular corneal dystrophy to chromosome 16”. Am J Hum Genet. 58 (4): 757—62. PMC 1914688  . PMID 8644739.
^ Akama TO, Nishida K, Nakayama J, Watanabe H, Ozaki K, Nakamura T, Dota A, Kawasaki S, Inoue Y, Maeda N, Yamamoto S, Fujiwara T, Thonar EJ, Shimomura Y, Kinoshita S, Tanigami A, Fukuda MN (новембар 2000). „Macular corneal dystrophy type I and type II are caused by distinct mutations in a new sulphotransferase gene”. Nat Genet. 26 (2): 237—41. PMID 11017086. S2CID 25547752. doi:10.1038/79987.
^ „Entrez Gene: CHST6 carbohydrate (N-acetylglucosamine 6-O) sulfotransferase 6”.
^ „HUGO Gene Nomenclature Commitee, HGNC:6938” (на језику: англ.). Приступљено 11. 09. 2017.
^ „UniProt, Q9GZX3” (на језику: англ.). Архивирано из оригинала 17. 01. 2016. г. Приступљено 07. 06. 2024.

Literatura

Bernstein HB, Compans RW (1992). „Sulfation of the human immunodeficiency virus envelope glycoprotein.”. J. Virol. 66 (12): 6953—9. PMC 240329  . PMID 1433500. doi:10.1128/JVI.66.12.6953-6959.1992.
Shilatifard A, Merkle RK, Helland DE, et al. (1993). „Complex-type N-linked oligosaccharides of gp120 from human immunodeficiency virus type 1 contain sulfated N-acetylglucosamine.”. J. Virol. 67 (2): 943—52. PMC 237448  . PMID 8419650. doi:10.1128/JVI.67.2.943-952.1993.
Uchimura K, Fasakhany F, Kadomatsu K, et al. (2000). „Diversity of N-acetylglucosamine-6-O-sulfotransferases: molecular cloning of a novel enzyme with different distribution and specificities.”. Biochem. Biophys. Res. Commun. 274 (2): 291—6. PMID 10913333. doi:10.1006/bbrc.2000.3141.
Spiro MJ, Spiro RG (2001). „Sulfation of the N-linked oligosaccharides of influenza virus hemagglutinin: temporal relationships and localization of sulfotransferases.”. Glycobiology. 10 (11): 1235—42. PMID 11087716. doi:10.1093/glycob/10.11.1235  .
Liu NP, Dew-Knight S, Rayner M, et al. (2001). „Mutations in corneal carbohydrate sulfotransferase 6 gene (CHST6) cause macular corneal dystrophy in Iceland.”. Mol. Vis. 6: 261—4. PMID 11139648.
Hemmerich S, Lee JK, Bhakta S, et al. (2001). „Chromosomal localization and genomic organization for the galactose/ N-acetylgalactosamine/N-acetylglucosamine 6-O-sulfotransferase gene family.”. Glycobiology. 11 (1): 75—87. PMID 11181564. doi:10.1093/glycob/11.1.75  .
Akama TO, Nakayama J, Nishida K, et al. (2001). „Human corneal GlcNac 6-O-sulfotransferase and mouse intestinal GlcNac 6-O-sulfotransferase both produce keratan sulfate.”. J. Biol. Chem. 276 (19): 16271—8. PMID 11278593. doi:10.1074/jbc.M009995200  .
Bartes A, Bhakta S, Hemmerich S (2001). „Sulfation of endothelial mucin by corneal keratan N-acetylglucosamine 6-O-sulfotransferase (GST-4beta).”. Biochem. Biophys. Res. Commun. 282 (4): 928—33. PMID 11352640. doi:10.1006/bbrc.2001.4668.
El-Ashry MF, Abd El-Aziz MM, Wilkins S, et al. (2002). „Identification of novel mutations in the carbohydrate sulfotransferase gene (CHST6) causing macular corneal dystrophy.”. Invest. Ophthalmol. Vis. Sci. 43 (2): 377—82. PMID 11818380.
Akama TO, Misra AK, Hindsgaul O, Fukuda MN (2003). „Enzymatic synthesis in vitro of the disulfated disaccharide unit of corneal keratan sulfate.”. J. Biol. Chem. 277 (45): 42505—13. PMID 12218059. doi:10.1074/jbc.M207412200  .
Strausberg RL, Feingold EA, Grouse LH, et al. (2003). „Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.”. Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899—903. Bibcode:2002PNAS...9916899M. PMC 139241  . PMID 12477932. doi:10.1073/pnas.242603899  .
Niel F, Ellies P, Dighiero P, et al. (2003). „Truncating mutations in the carbohydrate sulfotransferase 6 gene (CHST6) result in macular corneal dystrophy.”. Invest. Ophthalmol. Vis. Sci. 44 (7): 2949—53. PMID 12824236. doi:10.1167/iovs.02-0740.
Iida-Hasegawa N, Furuhata A, Hayatsu H, et al. (2003). „Mutations in the CHST6 gene in patients with macular corneal dystrophy: immunohistochemical evidence of heterogeneity.”. Invest. Ophthalmol. Vis. Sci. 44 (8): 3272—7. PMID 12882769. doi:10.1167/iovs.02-0910.
Ha NT, Chau HM, Cung le X, et al. (2003). „Mutation analysis of the carbohydrate sulfotransferase gene in Vietnamese with macular corneal dystrophy.”. Invest. Ophthalmol. Vis. Sci. 44 (8): 3310—6. PMID 12882775. doi:10.1167/iovs.03-0031.
Ha NT, Chau HM, Cung le X, et al. (2003). „Identification of novel mutations of the CHST6 gene in Vietnamese families affected with macular corneal dystrophy in two generations.”. Cornea. 22 (6): 508—11. PMID 12883341. S2CID 25039164. doi:10.1097/00003226-200308000-00004.
Warren JF, Aldave AJ, Srinivasan M, et al. (2003). „Novel mutations in the CHST6 gene associated with macular corneal dystrophy in southern India.”. Arch. Ophthalmol. 121 (11): 1608—12. PMID 14609920. doi:10.1001/archopht.121.11.1608.
Sultana A, Sridhar MS, Jagannathan A, et al. (2004). „Novel mutations of the carbohydrate sulfotransferase-6 (CHST6) gene causing macular corneal dystrophy in India.”. Mol. Vis. 9: 730—4. PMID 14735064.
Abbruzzese C, Kuhn U, Molina F, et al. (2004). „Novel mutations in the CHST6 gene causing macular corneal dystrophy.”. Clin. Genet. 65 (2): 120—5. PMID 14984470. S2CID 32667901. doi:10.1111/j.0009-9163.2004.00191.x.

[refGRCm38Ensembl-1] а ^б ^в GRCm38: Ensembl release 89: ENSMUSG00000031952 - Ensembl, May 2017

[2] „Human PubMed Reference:”. National Center for Biotechnology Information, U.S. National Library of Medicine.

[3] „Mouse PubMed Reference:”. National Center for Biotechnology Information, U.S. National Library of Medicine.

[pmid8644739-4] Vance JM, Jonasson F, Lennon F, Sarrica J, Damji KF, Stauffer J, Pericak-Vance MA, Klintworth GK (јул 1996). „Linkage of a gene for macular corneal dystrophy to chromosome 16”. Am J Hum Genet. 58 (4): 757—62. PMC 1914688  . PMID 8644739.

[pmid11017086-5] Akama TO, Nishida K, Nakayama J, Watanabe H, Ozaki K, Nakamura T, Dota A, Kawasaki S, Inoue Y, Maeda N, Yamamoto S, Fujiwara T, Thonar EJ, Shimomura Y, Kinoshita S, Tanigami A, Fukuda MN (новембар 2000). „Macular corneal dystrophy type I and type II are caused by distinct mutations in a new sulphotransferase gene”. Nat Genet. 26 (2): 237—41. PMID 11017086. S2CID 25547752. doi:10.1038/79987.

[entrez-6] „Entrez Gene: CHST6 carbohydrate (N-acetylglucosamine 6-O) sulfotransferase 6”.

[HGNC-7] „HUGO Gene Nomenclature Commitee, HGNC:6938” (на језику: англ.). Приступљено 11. 09. 2017.

[UniProt-8] „UniProt, Q9GZX3” (на језику: англ.). Архивирано из оригинала 17. 01. 2016. г. Приступљено 07. 06. 2024.

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