Biology:Neutral amino acid transporter B(0)
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Short description: Protein-coding gene in the species Homo sapiens
 Generic protein structure example |
Neutral amino acid transporter B(0) is a protein that in humans is encoded by the SLC1A5 gene.[1][2][3]
See also
References
- ↑ "Cloning of the sodium-dependent, broad-scope, neutral amino acid transporter Bo from a human placental choriocarcinoma cell line". The Journal of Biological Chemistry 271 (31): 18657–61. August 1996. doi:10.1074/jbc.271.31.18657. PMID 8702519.
- ↑ "The RD114/simian type D retrovirus receptor is a neutral amino acid transporter". Proceedings of the National Academy of Sciences of the United States of America 96 (5): 2129–34. March 1999. doi:10.1073/pnas.96.5.2129. PMID 10051606. Bibcode: 1999PNAS...96.2129R.
- ↑ "Entrez Gene: SLC1A5 solute carrier family 1 (neutral amino acid transporter), member 5". https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=6510.
Further reading
- "A sodium-dependent neutral-amino-acid transporter mediates infections of feline and baboon endogenous retroviruses and simian type D retroviruses". Journal of Virology 73 (5): 4470–4. May 1999. doi:10.1128/JVI.73.5.4470-4474.1999. PMID 10196349.
- "Truncated forms of the dual function human ASCT2 neutral amino acid transporter/retroviral receptor are translationally initiated at multiple alternative CUG and GUG codons". The Journal of Biological Chemistry 276 (29): 27221–30. July 2001. doi:10.1074/jbc.M100737200. PMID 11350958.
- "The envelope glycoprotein of human endogenous retrovirus type W uses a divergent family of amino acid transporters/cell surface receptors". Journal of Virology 76 (13): 6442–52. July 2002. doi:10.1128/JVI.76.13.6442-6452.2002. PMID 12050356.
- "Changes in expression and function of syncytin and its receptor, amino acid transport system B(0) (ASCT2), in human placental choriocarcinoma BeWo cells during syncytialization". Placenta 23 (7): 536–41. August 2002. doi:10.1053/plac.2002.0839. PMID 12175968.
- "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proceedings of the National Academy of Sciences of the United States of America 99 (26): 16899–903. December 2002. doi:10.1073/pnas.242603899. PMID 12477932. Bibcode: 2002PNAS...9916899M.
- "Hartnup disorder: polymorphisms identified in the neutral amino acid transporter SLC1A5". Journal of Inherited Metabolic Disease 25 (6): 437–48. October 2002. doi:10.1023/A:1021286714582. PMID 12555937.
- "N-linked glycosylation and sequence changes in a critical negative control region of the ASCT1 and ASCT2 neutral amino acid transporters determine their retroviral receptor functions". Journal of Virology 77 (5): 2936–45. March 2003. doi:10.1128/JVI.77.5.2936-2945.2003. PMID 12584318.
- "Hypoxia alters expression and function of syncytin and its receptor during trophoblast cell fusion of human placental BeWo cells: implications for impaired trophoblast syncytialisation in pre-eclampsia". Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease 1638 (1): 63–71. May 2003. doi:10.1016/s0925-4439(03)00043-7. PMID 12757936.
- "Transcriptional effects of hypoxia on fusiogenic syncytin and its receptor ASCT2 in human cytotrophoblast BeWo cells and in ex vivo perfused placental cotyledons". American Journal of Obstetrics and Gynecology 189 (2): 583–8. August 2003. doi:10.1067/S0002-9378(03)00538-6. PMID 14520239.
- "The serine/threonine kinases SGK1, 3 and PKB stimulate the amino acid transporter ASCT2". Biochemical and Biophysical Research Communications 331 (1): 272–7. May 2005. doi:10.1016/j.bbrc.2005.03.159. PMID 15845389.
- "Functional regulation of Na+-dependent neutral amino acid transporter ASCT2 by S-nitrosothiols and nitric oxide in Caco-2 cells". FEBS Letters 579 (11): 2499–506. April 2005. doi:10.1016/j.febslet.2005.03.065. PMID 15848195.
- "Identification of the promoter elements involved in the stimulation of ASCT2 expression by glutamine availability in HepG2 cells and the probable involvement of FXR/RXR dimers". Archives of Biochemistry and Biophysics 443 (1–2): 53–9. November 2005. doi:10.1016/j.abb.2005.08.016. PMID 16197915.
- "Search for mutations in SLC1A5 (19q13) in cystinuria patients". Journal of Inherited Metabolic Disease 28 (6): 1169–71. 2006. doi:10.1007/s10545-005-0094-x. PMID 16435221.
- "High-affinity glutamate transporter GLAST/EAAT1 regulates cell surface expression of glutamine/neutral amino acid transporter ASCT2 in human fetal astrocytes". Neurochemistry International 48 (6–7): 611–5. 2006. doi:10.1016/j.neuint.2005.12.033. PMID 16516348.
- "Identification of the hASCT2-binding domain of the Env ERVWE1/syncytin-1 fusogenic glycoprotein". Retrovirology 3: 41. July 2006. doi:10.1186/1742-4690-3-41. PMID 16820059.
- "Proteomic and bioinformatic characterization of the biogenesis and function of melanosomes". Journal of Proteome Research 5 (11): 3135–44. November 2006. doi:10.1021/pr060363j. PMID 17081065.
This article incorporates text from the United States National Library of Medicine, which is in the public domain.
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