Solute carrier family 35 (CMP-sialic acid transporter), member A1
CMP-sialic acid transporter is a protein that in humans is encoded by the SLC35A1 gene.[3][4][5]
See also
References
Further reading
- Wahlberg JE (1976). "Sensitization and testing of guinea pigs with nickel sulfate.". Dermatologica. 152 (6): 321–30. doi:10.1159/000251278. PMID 964426.
- Harvey BE, Thomas P (1993). "Inhibition of CMP-sialic acid transport in human liver and colorectal cancer cell lines by a sialic acid nucleoside conjugate (KI-8110).". Biochem. Biophys. Res. Commun. 190 (2): 571–5. doi:10.1006/bbrc.1993.1086. PMID 8427599.
- Lennon G, Auffray C, Polymeropoulos M, Soares MB (1996). "The I.M.A.G.E. Consortium: an integrated molecular analysis of genomes and their expression.". Genomics. 33 (1): 151–2. doi:10.1006/geno.1996.0177. PMID 8617505.
- 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. doi:10.1073/pnas.242603899. PMC 139241
. PMID 12477932.
- Aoki K, Ishida N, Kawakita M (2003). "Substrate recognition by nucleotide sugar transporters: further characterization of substrate recognition regions by analyses of UDP-galactose/CMP-sialic acid transporter chimeras and biochemical analysis of the substrate specificity of parental and chimeric transporters.". J. Biol. Chem. 278 (25): 22887–93. doi:10.1074/jbc.M302620200. PMID 12682060.
- Mungall AJ, Palmer SA, Sims SK, et al. (2003). "The DNA sequence and analysis of human chromosome 6.". Nature. 425 (6960): 805–11. doi:10.1038/nature02055. PMID 14574404.
- Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs.". Nat. Genet. 36 (1): 40–5. doi:10.1038/ng1285. PMID 14702039.
- Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMC 528928. PMID 15489334.
- Martinez-Duncker I, Dupré T, Piller V, et al. (2005). "Genetic complementation reveals a novel human congenital disorder of glycosylation of type II, due to inactivation of the Golgi CMP-sialic acid transporter.". Blood. 105 (7): 2671–6. doi:10.1182/blood-2004-09-3509. PMID 15576474.
- Misaki R, Fujiyama K, Seki T (2006). "Expression of human CMP-N-acetylneuraminic acid synthetase and CMP-sialic acid transporter in tobacco suspension-cultured cell.". Biochem. Biophys. Res. Commun. 339 (4): 1184–9. doi:10.1016/j.bbrc.2005.11.130. PMID 16343442.
- Zhao W, Chen TL, Vertel BM, Colley KJ (2006). "The CMP-sialic acid transporter is localized in the medial-trans Golgi and possesses two specific endoplasmic reticulum export motifs in its carboxyl-terminal cytoplasmic tail.". J. Biol. Chem. 281 (41): 31106–18. doi:10.1074/jbc.M605564200. PMID 16923816.
External links
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- proton coupled metal ion transporter
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- human Na+-sulfate/carboxylate cotransporter
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- Na+-dependent ascorbic acid transporter
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- multifunctional anion exchanger
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- Na+-coupled nucleoside transport (SLC28A1
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- facilitative nucleoside transporter
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- type II Na+-phosphate cotransporter
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- nucleoside-sugar transporter
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- SLC35E1
- SLC35E2
- SLC35E3
- SLC35E4
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- proton-coupled amino-acid transporter
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- sugar-phosphate/phosphate exchanger
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- basolateral iron transporter
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- Na+-independent, system-L like amino-acid transporter
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- Putative sugar transporter
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see also solute carrier disorders |