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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot O43683: Variant p.His265Asn

Mitotic checkpoint serine/threonine-protein kinase BUB1
Gene: BUB1
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Variant information Variant position: help 265 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Type of variant: help US The variants are classified into three categories: LP/P, LB/B and US.
  • LP/P: likely pathogenic or pathogenic.
  • LB/B: likely benign or benign.
  • US: uncertain significance

Residue change: help From Histidine (H) to Asparagine (N) at position 265 (H265N, p.His265Asn). Indicates the amino acid change of the variant. The one-letter and three-letter codes for amino acids used in UniProtKB/Swiss-Prot are those adopted by the commission on Biochemical Nomenclature of the IUPAC-IUB.
Physico-chemical properties: help Similar physico-chemical property. Both residues are medium size and polar. The physico-chemical property of the reference and variant residues and the change implicated.
BLOSUM score: help 1 The score within a Blosum matrix for the corresponding wild-type to variant amino acid change. The log-odds score measures the logarithm for the ratio of the likelihood of two amino acids appearing by chance. The Blosum62 substitution matrix is used. This substitution matrix contains scores for all possible exchanges of one amino acid with another:
  • Lowest score: -4 (low probability of substitution).
  • Highest score: 11 (high probability of substitution).
More information can be found on the following page

Variant description: help In pancreatic cancer; associated with C-259; complete rescue of the spindle-assembly checkpoint activity; increased rate of chromosome congression errors. Any additional useful information about the variant.


Sequence information Variant position: help 265 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 1085 The length of the canonical sequence.
Location on the sequence: help GESEFSFEELRAQKYNQRRK H EQWVNEDRHYMKRKEANAFE 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: help The multiple alignment of the region surrounding the variant against various orthologous sequences.
Human                         GESEFSFEELRAQKYN---------QRRKHEQWVNEDRHYMKRKEANAFE

Mouse                         GDSEFSFEELRAQKYN---------QRKKHEQWVSEDRNYM

Caenorhabditis elegans        AKWKDTFGEDVDDDYR---------KRKDSGVVFVKHQVID

Slime mold                    FGSSRKAAALMAAGQT---------QQTSQMKWDELEPELN

Baker's yeast                 GNKKTSIYADQKQSNNPVYKLINTPGRKPERIVFNFNLIYP

Fission yeast                 SEANTPNLPLLYDKSS---------GKRVEYSAFNFLALYE

Sequence annotation in neighborhood: help 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.
TypePositionsDescription
Chain 1 – 1085 Mitotic checkpoint serine/threonine-protein kinase BUB1



Literature citations
Bub1 regulates chromosome segregation in a kinetochore-independent manner.
Klebig C.; Korinth D.; Meraldi P.;
J. Cell Biol. 185:841-858(2009)
Cited for: FUNCTION; MUTAGENESIS OF ALA-130; CHARACTERIZATION OF VARIANTS CYS-259 AND ASN-265; A double missense variation of the BUB1 gene and a defective mitotic spindle checkpoint in the pancreatic cancer cell line Hs766T.
Hempen P.M.; Kurpad H.; Calhoun E.S.; Abraham S.; Kern S.E.;
Hum. Mutat. 21:445-445(2003)
Cited for: VARIANTS PANCREATIC CANCER CYS-259 AND ASN-265;
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.