Variant position: 411 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 461 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 YNNMFCAGFHEGGRDSCQGD SGGPHVTEVEGTSFLTGIISW
Chimpanzee YNNMFCAGFHEGGRDSCQGD SGGPHVTEVEGTSFLTGIISW
Mouse YNNMFCAGYREGGKDSCEGD SGGPHVTEVEGTSFLTGIISW
Rat YNNMFCAGYREGGKDSCEGD SGGPHVTEVEGTSFLTGIISW
Bovine YSHMFCAGYHEGGKDSCQGD SGGPHVTEVEGTSFLTGIISW
Cat YNNMFCAGFHEGGKDSCQGD SGGPHVTEVEGINFLTGIISW
Chicken LHSMFCAGYTAGGKDTCGGD SGGPYTNSIGETWFLTGVTSW
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
47 – 461 Coagulation factor IX
227 – 461 Coagulation factor IXa heavy chain
227 – 459 Peptidase S1
411 – 411 Charge relay system
407 – 435
391 – 391 Y -> T. Strongly increases enzyme activity with a synthetic peptide substrate; when associated with F-305; T-311 and A-365.
Hemophilia B caused by five different nondeletion mutations in the protease domain of factor IX.
Ludwig M.; Sabharwal A.K.; Brackmann H.H.; Olek K.; Smith K.J.; Birktoft J.J.; Bajaj S.P.;
Cited for: VARIANTS HEMB VAL-291; GLN-294; HIS-410; GLY-411 AND ILE-411;
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