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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot O75078: Variant p.Ser693Arg

Disintegrin and metalloproteinase domain-containing protein 11
Gene: ADAM11
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Variant information Variant position: help 693 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 Serine (S) to Arginine (R) at position 693 (S693R, p.Ser693Arg). 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 Change from small size and polar (S) to large size and basic (R) 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 a pancreatic ductal adenocarcinoma sample; somatic mutation. Any additional useful information about the variant.


Sequence information Variant position: help 693 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 769 The length of the canonical sequence.
Location on the sequence: help NFSTCPGSGERRICSHHGVC S NEGKCICQPDWTGKDCSIHN 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                         NFSTCPGSGERRICSHHGVCSNEGKCICQPDWTGKDCSIHN

Mouse                         NFSTCPGSGERRICSHHGVCSNEGKCICQPDWTGKDCSIHN

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 226 – 769 Disintegrin and metalloproteinase domain-containing protein 11
Topological domain 226 – 734 Extracellular
Domain 677 – 709 EGF-like
Region 332 – 769 Required for localization to cerebellar cortex basket cell terminals. Also required for localization of KCNA1, KCNA2, DLG4 and ADAM22 to cerebellar cortex basket cell terminal perisomatic axons and pinceaux
Glycosylation 673 – 673 N-linked (GlcNAc...) asparagine
Disulfide bond 686 – 698
Alternative sequence 624 – 769 Missing. In isoform Short.



Literature citations
Core signaling pathways in human pancreatic cancers revealed by global genomic analyses.
Jones S.; Zhang X.; Parsons D.W.; Lin J.C.; Leary R.J.; Angenendt P.; Mankoo P.; Carter H.; Kamiyama H.; Jimeno A.; Hong S.M.; Fu B.; Lin M.T.; Calhoun E.S.; Kamiyama M.; Walter K.; Nikolskaya T.; Nikolsky Y.; Hartigan J.; Smith D.R.; Hidalgo M.; Leach S.D.; Klein A.P.; Jaffee E.M.; Goggins M.; Maitra A.; Iacobuzio-Donahue C.; Eshleman J.R.; Kern S.E.; Hruban R.H.; Karchin R.; Papadopoulos N.; Parmigiani G.; Vogelstein B.; Velculescu V.E.; Kinzler K.W.;
Science 321:1801-1806(2008)
Cited for: VARIANT [LARGE SCALE ANALYSIS] ARG-693;
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.