Variant position: 751 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 810 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 RYEFLNGRVQSTELCAGHLA GGTDSCQGDSGGPLVCFEKDK
Rhesus macaque RYEFLNGTVKTTELCAGHLA GGTDSCQGDSGGPLVCFEKDK
Mouse RVEYLNNRVKSTELCAGQLA GGVDSCQGDSGGPLVCFEKDK
Rat RAEYLNNRVKSTELCAGHLA GGIDSCQGDSGGPLVCFEKDK
Pig RYEYLGGKVSPNELCAGHLA GGIDSCQGDSGGPLVCFEKDK
Bovine RNEYLDGRVKPTELCAGHLI GGTDSCQGDSGGPLVCFEKDK
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
20 – 810 Plasminogen
581 – 810 Plasmin light chain B
581 – 808 Peptidase S1
760 – 760 Charge relay system
699 – 766
741 – 741 S -> A. Proteolytically cleaved, but abolishes plasmin activity and cell detachment.
749 – 751
Plasminogen Kanagawa-I, a novel missense mutation, is caused by the amino acid substitution G732R.
Higuchi Y.; Furihata K.; Ueno I.; Ishikawa S.; Okumura N.; Tozuka M.; Sakurai N.;
Br. J. Haematol. 103:867-870(1998)
Cited for: VARIANT PLGD ARG-751;
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