Variant position: 202 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 392 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 VDSVASLGGTPLYMDRQGID ILYSGSQKALNAPPGTSLISF
Mouse VDSVASLGGVPIYMDQQGID IMYSSSQKVLNAPPGISLISF
Rat VDSVASLGGVPIYMDQQGID ILYSGSQKVLNAPPGISLISF
Rabbit VDSVASLGGAPIYMDQQGID VLYSGSQKALNAPPGTSLISF
Cat VDSVASLCGTPIYMDQQGID VLYSGSQKVLNSPPGTSLISF
Slime mold VDCVAALGGVPVFVDDWKID ACYTGTQKCLSGPPGISPLTF
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 – 392 Serine--pyruvate aminotransferase
209 – 209 N6-(pyridoxal phosphate)lysine
209 – 209 K -> R. Affects pyridoxal phosphate binding; loss of alanine--glyoxylate aminotransferase activity.
201 – 209
Mutational analysis of AGXT in two Chinese families with primary hyperoxaluria type 1.
Li G.M.; Xu H.; Shen Q.; Gong Y.N.; Fang X.Y.; Sun L.; Liu H.M.; An Y.;
BMC Nephrol. 15:92-92(2014)
Cited for: VARIANT HP1 ASN-202;
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.