Sequence information
Variant position: 412 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 1441 The length of the canonical sequence.
Location on the sequence:
NVEIVDIRARQLTLQWEPFG
Y AVTRCHSYNLTVQYQYVFNQ
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 NVEIVDIRARQLTLQWEPFGY AVTRCHSYNLTVQYQYVFNQ
Mouse NVEIVDIRARQLTLQWEPFGY AVTRCHSYNLTVQYQYVFNQ
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
Chain
26 – 1441
Receptor-type tyrosine-protein phosphatase T
Topological domain
26 – 747
Extracellular
Domain
389 – 483
Fibronectin type-III 2
Glycosylation
421 – 421
N-linked (GlcNAc...) asparagine
Literature citations
Mutational analysis of the tyrosine phosphatome in colorectal cancers.
Wang Z.; Shen D.; Parsons D.W.; Bardelli A.; Sager J.; Szabo S.; Ptak J.; Silliman N.; Peters B.A.; van der Heijden M.S.; Parmigiani G.; Yan H.; Wang T.-L.; Riggins G.; Powell S.M.; Willson J.K.V.; Markowitz S.; Kinzler K.W.; Vogelstein B.; Velculescu V.E.;
Science 304:1164-1166(2004)
Cited for: VARIANTS SER-74; THR-209; THR-218; SER-248; HIS-280; VAL-395; PHE-412; CYS-453; LYS-510; MET-605; GLY-648; THR-707; VAL-707; PRO-708; ILE-771; GLY-905; LYS-965; PRO-1096; ILE-1106; TRP-1190; LEU-1237; MET-1247; LEU-1324; PHE-1329 AND MET-1346; TISSUE SPECIFICITY;
Disclaimer:
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.