Homo sapiens Protein: SLC5A11
Summary
InnateDB Protein IDBP-754127.3
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol SLC5A11
Protein Name
Synonyms
Species Homo sapiens
Ensembl Protein ENSP00000454401
InnateDB Gene IDBG-21339 (SLC5A11)
Protein Structure
UniProt Annotation
Function Involved in the sodium-dependent cotransport of myo- inositol (MI) with a Na(+):MI stoichiometry of 2:1. Exclusively responsible for apical MI transport and absorption in intestine. Also can transport D-chiro-inositol (DCI) but not L-fructose. Exhibits stereospecific cotransport of both D-glucose and D- xylose. May induce apoptosis through the TNF-alpha, PDCD1 pathway. May play a role in the regulation of MI concentration in serum, involving reabsorption in at least the proximal tubule of the kidney. {ECO:0000269PubMed:15172003}.
Subcellular Localization Membrane {ECO:0000250UniProtKB:Q28728}; Multi-pass membrane protein {ECO:0000250UniProtKB:Q28728}.
Disease Associations
Tissue Specificity Highest expression in heart, skeletal muscle, kidney, liver and placenta. Weaker expression in brain, colon, spleen, lung and peripheral blood leukocytes. {ECO:0000269PubMed:12039040}.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
Gene Ontology

Molecular Function
Accession GO Term
GO:0005215 transporter activity
GO:0015293 symporter activity
Biological Process
GO:0006810 transport
GO:0006814 sodium ion transport
GO:0006915 apoptotic process
GO:0008643 carbohydrate transport
GO:0055085 transmembrane transport
Cellular Component
GO:0005886 plasma membrane
GO:0016020 membrane
GO:0016021 integral component of membrane
Protein Structure and Domains
PDB ID
InterPro IPR001734 Sodium/solute symporter
IPR019900 Sodium/solute symporter, subgroup
PFAM PF00474
PRINTS
PIRSF
SMART
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q8WWX8
PhosphoSite PhosphoSite-Q8WWX8
TrEMBL H3BN85
UniProt Splice Variant
Entrez Gene 115584
UniGene Hs.741965
RefSeq XP_006721078
HUGO HGNC:23091
OMIM 610238
CCDS CCDS58437
HPRD
IMGT
EMBL AC008731 AF292385 AJ305237 AK125267 AK295427 AY044906 BC049385 BC057780 CH471145
GenPept AAH49385 AAH57780 AAK97053 AAK97784 BAC86105 BAH12065 CAC83728 EAW55781