Variant position: 411 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 492 The length of the canonical sequence.
Location on the sequence:
The residue change on the sequence. Unless the variant is located at the beginning or at the end of the protein sequence, both residues upstream (20) and downstream (20) of the variant will be shown.
Residue conservation: The multiple alignment of the region surrounding the variant against various orthologous sequences.
Human VAELFSQGPRPAAIAVAGFS NWTSNFIVGM-----CFQYVEQLCGP
Mouse VAELFSQGPRPAAIAVAGFS NWTSNFIVGM-----CFQYVE
Rat VAELFSQGPRPAAVAVAGFS NWTSNFIVGM-----CFQYVE
Pig VAELFSQGPRPAAIAVAGFS NWTSNFIVGM-----CFQYVE
Bovine VAELFSQGPRPAAIAVAGFS NWTSNFIVGM-----CFQYVE
Rabbit VAELFSQGPRPAAVAVAGFS NWTSNFIVGM-----CFQYVE
Sheep VAELFSQGPRPAAIAVAGFS NWTSNFIVGM-----CFQYVE
Chicken VAELFSQGPRPAAFAVAGLS NWTSNFIVGM-----GFQYIA
Drosophila TAELFSQGPRPSAMAIAVLV NWMANFVVGI-----GFPSMK
Baker's yeast HDSSDNNNVLLDPKRFEKIS NIMKNFKQSCTKLKSGFKTLI
Fission yeast ----SESNPATDAHRFEKIS NIVKQFKLSCSKMQAQFTTFE
Sequence annotation in neighborhood: The regions or sites of interest surrounding the variant. In general the features listed are posttranslational modifications, binding sites, enzyme active sites, local secondary structure or other characteristics reported in the cited references. The "Sequence annotation in neighborhood" lines have a fixed format:
Type: the type of sequence feature. Positions: endpoints of the sequence feature. Description: contains additional information about the feature.
Type Positions Description
1 – 492 Solute carrier family 2, facilitated glucose transporter member 1
402 – 422 Helical; Name=11
411 – 411 Cytochalasin B; inhibitor
411 – 411 Not glycosylated
400 – 429
Glucose transporter 1 deficiency in the idiopathic generalized epilepsies.
Arsov T.; Mullen S.A.; Rogers S.; Phillips A.M.; Lawrence K.M.; Damiano J.A.; Goldberg-Stern H.; Afawi Z.; Kivity S.; Trager C.; Petrou S.; Berkovic S.F.; Scheffer I.E.;
Ann. Neurol. 72:807-815(2012)
Cited for: VARIANTS EIG12 HIS-51; MET-60; THR-77; ALA-149; SER-218; GLN-223; VAL-243; SER-411 AND TRP-458; CHARACTERIZATION OF VARIANTS EIG12 MET-60; THR-77; SER-218; GLN-223; VAL-243; SER-411 AND TRP-458;
Any medical or genetic information present in this entry is provided for research, educational and informational purposes only. They are not in any way intended to be used as a substitute for professional medical advice, diagnostic, treatment or care.