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UniProtKB/Swiss-Prot Q16558: Variant p.Glu65Lys

Calcium-activated potassium channel subunit beta-1
Gene: KCNMB1
Variant information

Variant position:  65
The position of the amino-acid change on the UniProtKB canonical protein sequence.

Type of variant:  LB/B
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:  From Glutamate (E) to Lysine (K) at position 65 (E65K, p.Glu65Lys).
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:  Change from medium size and acidic (E) to large size and basic (K)
The physico-chemical property of the reference and variant residues and the change implicated.

BLOSUM score:  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

Polymorphism:  Genetic variation in KCNMB1 can influence the severity of diastolic hypertension (PubMed:15057310).
Additional information on the polymorphism described.

Variant description:  Has a protective effect against diastolic hypertension.
Any additional useful information about the variant.

Other resources:  
Links to websites of interest for the variant.



Sequence information

Variant position:  65
The position of the amino-acid change on the UniProtKB canonical protein sequence.

Protein sequence length:  191
The length of the canonical sequence.

Location on the sequence:   SVWTQESKCHLIETNIRDQE  E LKGKKVPQYPCLWVNVSAAG
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                         SVWTQESKCHLIETNIRDQEELKGKKVPQYPCLWVNVSAAG

                              SVWTQKSTCHLIETNIREQEELEGKKVPQYPCLWVNVSAVG

Mouse                         SVWTQESICHLIETNIKDQEELEGKKVPQYPCLWVNVSAVG

Rat                           SVWTQESTCHLVETNIKDQEELEGRKVPQYPCLWVNVSAVG

Bovine                        SVWTQESTCHLIETNIRDQEELEGKRVPQYPCLWVNVSSVG

Rabbit                        SVWTQESLCRLIETNIRDQEELEGKKVPQYPCLWVNVSAVG

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.

TypePositionsDescription
Chain 1 – 191 Calcium-activated potassium channel subunit beta-1
Topological domain 40 – 157 Extracellular
Glycosylation 80 – 80 N-linked (GlcNAc...) asparagine


Literature citations

Gain-of-function mutation in the KCNMB1 potassium channel subunit is associated with low prevalence of diastolic hypertension.
Fernandez-Fernandez J.M.; Tomas M.; Vazquez E.; Orio P.; Latorre R.; Senti M.; Marrugat J.; Valverde M.A.;
J. Clin. Invest. 113:1032-1039(2004)
Cited for: VARIANT LYS-65; POLYMORPHISM;

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.