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Accession Number: | P13866 |
Protein Name: | SL51 aka SGLT aka SLC5A1 aka SGLT1 |
Length: | 664 |
Molecular Weight: | 73498.00 |
Species: | Homo sapiens (Human) [9606] |
Number of TMSs: | 14 |
Location1 / Topology2 / Orientation3: | Membrane1 / Multi-pass membrane protein2 |
Substrate | water, resveratrol, fucose, D-glucopyranose, D-galactopyranose |
Cross database links:
RefSeq: | NP_000334.1 |
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Entrez Gene ID: | 6523 |
Pfam: | PF00474 |
OMIM: |
182380 gene 606824 phenotype |
KEGG: | hsa:6523 hsa:6523 |
Gene Ontology
GO:0005887
C:integral to plasma membrane
GO:0005412
F:glucose:sodium symporter activity
GO:0005515
F:protein binding
GO:0015758
P:glucose transport
GO:0006814
P:sodium ion transport
GO:0055085
P:transmembrane transport
GO:0016324
C:apical plasma membrane
GO:0031526
C:brush border membrane
GO:0005911
C:cell-cell junction
GO:0005975
P:carbohydrate metabolic process
GO:0050892
P:intestinal absorption
GO:0044281
P:small molecule metabolic process
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References (18)[1] “Homology of the human intestinal Na+/glucose and Escherichia coli Na+/proline cotransporters.” Hediger M.A.et.al. 2490366 [2] “Structure of the human Na+/glucose cotransporter gene SGLT1.” Turk E.et.al. 8195156 [3] “A genome annotation-driven approach to cloning the human ORFeome.” Collins J.E.et.al. 15461802 [4] “Complete sequencing and characterization of 21,243 full-length human cDNAs.” Ota T.et.al. 14702039 [5] “The DNA sequence of human chromosome 22.” Dunham I.et.al. 10591208 [6] “Membrane topology of the human Na+/glucose cotransporter SGLT1.” Turk E.et.al. 8567640 [7] “Glucose/galactose malabsorption caused by a defect in the Na+/glucose cotransporter.” Turk E.et.al. 2008213 [8] “Missense mutations in SGLT1 cause glucose-galactose malabsorption by trafficking defects.” Lam J.T.et.al. 10036327 [9] “A missense mutation in the Na(+)/glucose cotransporter gene SGLT1 in a patient with congenital glucose-galactose malabsorption: normal trafficking but inactivation of the mutant protein.” Kasahara M.et.al. 11406349 [10] “Homology of the human intestinal Na+/glucose and Escherichia coli Na+/proline cotransporters.” Hediger M.A.et.al. 2490366 [11] “Structure of the human Na+/glucose cotransporter gene SGLT1.” Turk E.et.al. 8195156 [12] “A genome annotation-driven approach to cloning the human ORFeome.” Collins J.E.et.al. 15461802 [13] “Complete sequencing and characterization of 21,243 full-length human cDNAs.” Ota T.et.al. 14702039 [14] “The DNA sequence of human chromosome 22.” Dunham I.et.al. 10591208 [15] “Membrane topology of the human Na+/glucose cotransporter SGLT1.” Turk E.et.al. 8567640 [16] “Glucose/galactose malabsorption caused by a defect in the Na+/glucose cotransporter.” Turk E.et.al. 2008213 [17] “Missense mutations in SGLT1 cause glucose-galactose malabsorption by trafficking defects.” Lam J.T.et.al. 10036327 [18] “A missense mutation in the Na(+)/glucose cotransporter gene SGLT1 in a patient with congenital glucose-galactose malabsorption: normal trafficking but inactivation of the mutant protein.” Kasahara M.et.al. 11406349
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External Searches:
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Analyze:
Predict TMSs (Predict number of transmembrane segments) | ||||
FASTA formatted sequence |
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1: MDSSTWSPKT TAVTRPVETH ELIRNAADIS IIVIYFVVVM AVGLWAMFST NRGTVGGFFL 61: AGRSMVWWPI GASLFASNIG SGHFVGLAGT GAASGIAIGG FEWNALVLVV VLGWLFVPIY 121: IKAGVVTMPE YLRKRFGGQR IQVYLSLLSL LLYIFTKISA DIFSGAIFIN LALGLNLYLA 181: IFLLLAITAL YTITGGLAAV IYTDTLQTVI MLVGSLILTG FAFHEVGGYD AFMEKYMKAI 241: PTIVSDGNTT FQEKCYTPRA DSFHIFRDPL TGDLPWPGFI FGMSILTLWY WCTDQVIVQR 301: CLSAKNMSHV KGGCILCGYL KLMPMFIMVM PGMISRILYT EKIACVVPSE CEKYCGTKVG 361: CTNIAYPTLV VELMPNGLRG LMLSVMLASL MSSLTSIFNS ASTLFTMDIY AKVRKRASEK 421: ELMIAGRLFI LVLIGISIAW VPIVQSAQSG QLFDYIQSIT SYLGPPIAAV FLLAIFWKRV 481: NEPGAFWGLI LGLLIGISRM ITEFAYGTGS CMEPSNCPTI ICGVHYLYFA IILFAISFIT 541: IVVISLLTKP IPDVHLYRLC WSLRNSKEER IDLDAEEENI QEGPKETIEI ETQVPEKKKG 601: IFRRAYDLFC GLEQHGAPKM TEEEEKAMKM KMTDTSEKPL WRTVLNVNGI ILVTVAVFCH 661: AYFA