Homo sapiens Protein: SLC35A1
Summary
InnateDB Protein IDBP-94140.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol SLC35A1
Protein Name solute carrier family 35 (CMP-sialic acid transporter), member A1
Synonyms CDG2F; CMPST; CST; hCST;
Species Homo sapiens
Ensembl Protein ENSP00000358565
InnateDB Gene IDBG-94128 (SLC35A1)
Protein Structure
UniProt Annotation
Function Transports CMP-sialic acid from the cytosol into Golgi vesicles where glycosyltransferases function.
Subcellular Localization Golgi apparatus membrane; Multi-pass membrane protein.
Disease Associations Congenital disorder of glycosylation 2F (CDG2F) [MIM:603585]: CDGs are a family of severe inherited diseases caused by a defect in protein N-glycosylation. They are characterized by under-glycosylated serum proteins. These multisystem disorders present with a wide variety of clinical features, such as disorders of the nervous system development, psychomotor retardation, dysmorphic features, hypotonia, coagulation disorders, and immunodeficiency. The broad spectrum of features reflects the critical role of N-glycoproteins during embryonic development, differentiation, and maintenance of cell functions. {ECO:0000269PubMed:15576474}. Note=The disease is caused by mutations affecting the gene represented in this entry.
Tissue Specificity
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 2 experimentally validated interaction(s) in this database.
Experimentally validated
Total 2 [view]
Protein-Protein 1 [view]
Protein-DNA 1 [view]
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0005338 nucleotide-sugar transmembrane transporter activity
GO:0005351 sugar:proton symporter activity
GO:0005456 CMP-N-acetylneuraminate transmembrane transporter activity
Biological Process
GO:0005975 carbohydrate metabolic process
GO:0006464 cellular protein modification process
GO:0008643 carbohydrate transport
GO:0015780 nucleotide-sugar transport
GO:0015782 CMP-N-acetylneuraminate transport
GO:0015992 proton transport
GO:0055085 transmembrane transport
GO:1901679 nucleotide transmembrane transport
Cellular Component
GO:0000139 Golgi membrane
GO:0005794 Golgi apparatus
GO:0005887 integral component of plasma membrane
GO:0016021 integral component of membrane
Protein Structure and Domains
PDB ID
InterPro IPR004689 UDP-galactose transporter
IPR007271 Nucleotide-sugar transporter
IPR013657 UAA transporter
IPR021189 UDP/CMP-sugar transporter
PFAM PF04142
PF08449
PRINTS
PIRSF PIRSF005799
SMART
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt P78382
PhosphoSite PhosphoSite-
TrEMBL Q5W1L6
UniProt Splice Variant
Entrez Gene 10559
UniGene Hs.713287
RefSeq NP_006407
HUGO HGNC:11021
OMIM 605634
CCDS CCDS5010
HPRD 09290
IMGT
EMBL AJ851888 AJ851890 AK293696 AL049697 BC017807 D87969
GenPept AAH17807 BAA13522 BAG57132 CAB76857 CAH65468 CAH65470