Solute carrier family 2, facilitated glucose transporter member 11 (SLC2A11) also known as glucose transporter type 10/11 (GLUT-10/11) is a protein that in humans is encoded by the SLC2A11 gene.[3]
SLC2A11 belongs to a family of plasma membrane proteins that mediate transport of sugars across the membrane by facilitative diffusion.[3][4]
References
- ^ a b c ENSG00000133460 GRCh38: Ensembl release 89: ENSG00000275744, ENSG00000133460 – Ensembl, May 2017
- ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ a b "Entrez Gene: Solute carrier family 2 (facilitated glucose transporter), member 11".
- ^ Sasaki T, Minoshima S, Shiohama A, Shintani A, Shimizu A, Asakawa S, Kawasaki K, Shimizu N (December 2001). "Molecular cloning of a member of the facilitative glucose transporter gene family GLUT11 (SLC2A11) and identification of transcription variants". Biochemical and Biophysical Research Communications. 289 (5): 1218–24. doi:10.1006/bbrc.2001.6101. PMID 11741323.
Further reading
- Doege H, Bocianski A, Scheepers A, Axer H, Eckel J, Joost HG, Schürmann A (October 2001). "Characterization of human glucose transporter (GLUT) 11 (encoded by SLC2A11), a novel sugar-transport facilitator specifically expressed in heart and skeletal muscle". The Biochemical Journal. 359 (Pt 2): 443–9. doi:10.1042/0264-6021:3590443. PMC 1222165. PMID 11583593.
- Wu X, Li W, Sharma V, Godzik A, Freeze HH (May 2002). "Cloning and characterization of glucose transporter 11, a novel sugar transporter that is alternatively spliced in various tissues". Molecular Genetics and Metabolism. 76 (1): 37–45. doi:10.1016/s1096-7192(02)00018-5. PMID 12175779.
- Manolescu AR, Augustin R, Moley K, Cheeseman C (2007). "A highly conserved hydrophobic motif in the exofacial vestibule of fructose transporting SLC2A proteins acts as a critical determinant of their substrate selectivity". Molecular Membrane Biology. 24 (5–6): 455–63. doi:10.1080/09687680701298143. PMID 17710649. S2CID 35331716.
This article incorporates text from the United States National Library of Medicine, which is in the public domain.
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By group |
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SLC1–10 |
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(1): | |
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(2): | |
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(3): | |
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(4): | |
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(5): | |
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(6): | |
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(7): | |
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(8): | |
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(9): | |
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(10): | |
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| SLC11–20 |
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(11): |
- proton coupled metal ion transporter
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(12): | |
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(13): |
- human Na+-sulfate/carboxylate cotransporter
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(14): | |
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(15): |
- proton oligopeptide cotransporter
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(16): |
- monocarboxylate transporter
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(17): | |
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(18): | |
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(19): | |
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(20): | |
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| SLC21–30 |
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(21): | |
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(22): | |
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(23): |
- Na+-dependent ascorbic acid transporter
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(24): | |
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(25): | |
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(26): |
- multifunctional anion exchanger
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(27): | |
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(28): |
- Na+-coupled nucleoside transport (SLC28A1
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(29): |
- facilitative nucleoside transporter
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(30): | |
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| SLC31–40 |
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(31): | |
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(32): | |
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(33): | |
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(34): |
- type II Na+-phosphate cotransporter
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(35): |
- nucleoside-sugar transporter
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- SLC35E1
- SLC35E2
- SLC35E3
- SLC35E4
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(36): | |
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(37): |
- sugar-phosphate/phosphate exchanger
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(38): |
- System A & N, sodium-coupled neutral amino-acid transporter
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(39): | |
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(40): |
- basolateral iron transporter
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| SLC41–48 |
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(41): | |
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(42): | |
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(43): |
- Na+-independent, system-L like amino-acid transporter
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(44): | |
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(45): |
- Putative sugar transporter
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(46): | |
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(47): | |
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(48): | |
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see also solute carrier disorders |