Variant position: 228 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 465 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 ATMISCYYEDHQCEVGMIVG TGCNACYMEEMQNVELVEGDE
Mouse ATMISCYYEDRQCEVGMIVG TGCNACYMEEMQNVELVEGDE
Rat ATMISCYYEDRQCEVGMIVG TGCNACYMEEMQNVELVEGDE
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 – 465 Glucokinase
10 – 454 Hexokinase
204 – 443 Hexokinase large subdomain
228 – 228 ATP
231 – 231 Substrate
217 – 217 D -> N. Mildly increases glucokinase activity.
225 – 225 I -> M. Highly decreases glucokinase activity.
248 – 248 E -> K. Highly decreases glucokinase activity.
220 – 237
Human glucokinase gene: isolation, characterization, and identification of two missense mutations linked to early-onset non-insulin-dependent (type 2) diabetes mellitus.
Stoffel M.; Froguel P.; Takeda J.; Zouali H.; Vionnet N.; Nishi S.; Weber I.T.; Harrison R.W.; Pilkis S.J.; Lesage S.; Vaxillaire M.; Velho G.; Sun F.; Iris F.; Passa P.; Cohen D.; Bell G.I.;
Proc. Natl. Acad. Sci. U.S.A. 89:7698-7702(1992)
Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA]; VARIANTS MODY2 MET-228 AND ARG-261;
Neonatal diabetes mellitus due to complete glucokinase deficiency.
Njoelstad P.R.; Soevik O.; Cuesta-Munoz A.; Bjoerkhaug L.; Massa O.; Barbetti F.; Undlien D.E.; Shiota C.; Magnuson M.A.; Molven A.; Matschinsky F.M.; Bell G.I.;
N. Engl. J. Med. 344:1588-1592(2001)
Cited for: VARIANTS MODY2 LYS-210 AND MET-228;
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.