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Identification
HMDB Protein ID HMDBP02114
Secondary Accession Numbers
  • 7596
Name Solute carrier family 2, facilitated glucose transporter member 1
Synonyms
  1. GLUT-1
  2. Glucose transporter type 1, erythrocyte/brain
  3. HepG2 glucose transporter
Gene Name SLC2A1
Protein Type Enzyme
Biological Properties
General Function Involved in glucose transmembrane transporter activity
Specific Function Facilitative glucose transporter. This isoform may be responsible for constitutive or basal glucose uptake. Has a very broad substrate specificity; can transport a wide range of aldoses including both pentoses and hexoses.
Pathways
  • Adipocytokine signaling pathway
  • Bile secretion
  • Congenital disorder of glycosylation CDG-IId
  • GLUT-1 deficiency syndrome
  • HIF-1 signaling pathway
  • Human T-cell leukemia virus 1 infection
  • Insulin secretion
  • Lactose Synthesis
  • Renal cell carcinoma
Reactions Not Available
GO Classification
Biological Process
cellular response to glucose starvation
L-ascorbic acid metabolic process
energy reserve metabolic process
regulation of insulin secretion
response to osmotic stress
Cellular Component
plasma membrane
cell-cell junction
female pronucleus
basolateral plasma membrane
melanosome
caveola
midbody
integral to membrane
Component
membrane
cell part
membrane part
intrinsic to membrane
integral to membrane
Function
glucose transmembrane transporter activity
carbohydrate transmembrane transporter activity
sugar transmembrane transporter activity
monosaccharide transmembrane transporter activity
hexose transmembrane transporter activity
transmembrane transporter activity
substrate-specific transmembrane transporter activity
transporter activity
Molecular Function
glucose transmembrane transporter activity
D-glucose transmembrane transporter activity
dehydroascorbic acid transporter activity
xenobiotic transporter activity
Process
establishment of localization
transport
transmembrane transport
Cellular Location
  1. Cell membrane
  2. Melanosome
  3. Multi-pass membrane protein
Gene Properties
Chromosome Location 1
Locus 1p34.2
SNPs SLC2A1
Gene Sequence
>1479 bp
ATGGAGCCCAGCAGCAAGAAGCTGACGGGTCGCCTCATGCTGGCCGTGGGAGGAGCAGTG
CTTGGCTCCCTGCAGTTTGGCTACAACACTGGAGTCATCAATGCCCCCCAGAAGGTGATC
GAGGAGTTCTACAACCAGACATGGGTCCACCGCTATGGGGAGAGCATCCTGCCCACCACG
CTCACCACGCTCTGGTCCCTCTCAGTGGCCATCTTTTCTGTTGGGGGCATGATTGGCTCC
TTCTCTGTGGGCCTTTTCGTTAACCGCTTTGGCCGGCGGAATTCAATGCTGATGATGAAC
CTGCTGGCCTTCGTGTCCGCCGTGCTCATGGGCTTCTCGAAACTGGGCAAGTCCTTTGAG
ATGCTGATCCTGGGCCGCTTCATCATCGGTGTGTACTGCGGCCTGACCACAGGCTTCGTG
CCCATGTATGTGGGTGAAGTGTCACCCACAGCCCTTCGTGGGGCCCTGGGCACCCTGCAC
CAGCTGGGCATCGTCGTCGGCATCCTCATCGCCCAGGTGTTCGGCCTGGACTCCATCATG
GGCAACAAGGACCTGTGGCCCCTGCTGCTGAGCATCATCTTCATCCCGGCCCTGCTGCAG
TGCATCGTGCTGCCCTTCTGCCCCGAGAGTCCCCGCTTCCTGCTCATCAACCGCAACGAG
GAGAACCGGGCCAAGAGTGTGCTAAAGAAGCTGCGCGGGACAGCTGACGTGACCCATGAC
CTGCAGGAGATGAAGGAAGAGAGTCGGCAGATGATGCGGGAGAAGAAGGTCACCATCCTG
GAGCTGTTCCGCTCCCCCGCCTACCGCCAGCCCATCCTCATCGCTGTGGTGCTGCAGCTG
TCCCAGCAGCTGTCTGGCATCAACGCTGTCTTCTATTACTCCACGAGCATCTTCGAGAAG
GCGGGGGTGCAGCAGCCTGTGTATGCCACCATTGGCTCCGGTATCGTCAACACGGCCTTC
ACTGTCGTGTCGCTGTTTGTGGTGGAGCGAGCAGGCCGGCGGACCCTGCACCTCATAGGC
CTCGCTGGCATGGCGGGTTGTGCCATACTCATGACCATCGCGCTAGCACTGCTGGAGCAG
CTACCCTGGATGTCCTATCTGAGCATCGTGGCCATCTTTGGCTTTGTGGCCTTCTTTGAA
GTGGGTCCTGGCCCCATCCCATGGTTCATCGTGGCTGAACTCTTCAGCCAGGGTCCACGT
CCAGCTGCCATTGCCGTTGCAGGCTTCTCCAACTGGACCTCAAATTTCATTGTGGGCATG
TGCTTCCAGTATGTGGAGCAACTGTGTGGTCCCTACGTCTTCATCATCTTCACTGTGCTC
CTGGTTCTGTTCTTCATCTTCACCTACTTCAAAGTTCCTGAGACTAAAGGCCGGACCTTC
GATGAGATCGCTTCCGGCTTCCGGCAGGGGGGAGCCAGCCAAAGTGACAAGACACCCGAG
GAGCTGTTCCATCCCCTGGGGGCTGATTCCCAAGTGTGA
Protein Properties
Number of Residues 492
Molecular Weight 54083.325
Theoretical pI 8.719
Pfam Domain Function
Signals Not Available
Transmembrane Regions Not Available
Protein Sequence
>Solute carrier family 2, facilitated glucose transporter member 1
MEPSSKKLTGRLMLAVGGAVLGSLQFGYNTGVINAPQKVIEEFYNQTWVHRYGESILPTT
LTTLWSLSVAIFSVGGMIGSFSVGLFVNRFGRRNSMLMMNLLAFVSAVLMGFSKLGKSFE
MLILGRFIIGVYCGLTTGFVPMYVGEVSPTALRGALGTLHQLGIVVGILIAQVFGLDSIM
GNKDLWPLLLSIIFIPALLQCIVLPFCPESPRFLLINRNEENRAKSVLKKLRGTADVTHD
LQEMKEESRQMMREKKVTILELFRSPAYRQPILIAVVLQLSQQLSGINAVFYYSTSIFEK
AGVQQPVYATIGSGIVNTAFTVVSLFVVERAGRRTLHLIGLAGMAGCAILMTIALALLEQ
LPWMSYLSIVAIFGFVAFFEVGPGPIPWFIVAELFSQGPRPAAIAVAGFSNWTSNFIVGM
CFQYVEQLCGPYVFIIFTVLLVLFFIFTYFKVPETKGRTFDEIASGFRQGGASQSDKTPE
ELFHPLGADSQV
GenBank ID Protein 166795299
UniProtKB/Swiss-Prot ID P11166
UniProtKB/Swiss-Prot Entry Name GTR1_HUMAN
PDB IDs
GenBank Gene ID NM_006516.2
GeneCard ID SLC2A1
GenAtlas ID SLC2A1
HGNC ID HGNC:11005
References
General References
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  7. Fukumoto H, Seino S, Imura H, Seino Y, Bell GI: Characterization and expression of human HepG2/erythrocyte glucose-transporter gene. Diabetes. 1988 May;37(5):657-61. [PubMed:2834252 ]
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  9. Wang D, Kranz-Eble P, De Vivo DC: Mutational analysis of GLUT1 (SLC2A1) in Glut-1 deficiency syndrome. Hum Mutat. 2000 Sep;16(3):224-31. [PubMed:10980529 ]
  10. Brockmann K, Wang D, Korenke CG, von Moers A, Ho YY, Pascual JM, Kuang K, Yang H, Ma L, Kranz-Eble P, Fischbarg J, Hanefeld F, De Vivo DC: Autosomal dominant glut-1 deficiency syndrome and familial epilepsy. Ann Neurol. 2001 Oct;50(4):476-85. [PubMed:11603379 ]
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