UniProtKB/Swiss-Prot Q12809: Variant p.Ala558Pro

• Variant information
• Sequence information
• Literature citations
• All

Variant information

Variant position: 558 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Type of variant: LP/P [Disclaimer: Variants classification is intended for research purposes only, not for clinical and diagnostic use. The label disease variant is assigned according to literature reports on probable disease-association that can be based on theoretical reasons. This label must not be considered as a definitive proof for the pathogenic role of a variant.] 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 Alanine (A) to Proline (P) at position 558 (A558P, p.Ala558Pro). 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 small size and hydrophobic (A) to medium size and hydrophobic (P) 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
Variant description: In LQT2. Any additional useful information about the variant.
Other resources: Links to websites of interest for the variant.

• Variant rs121912516 [ dbSNP | Ensembl ]

Sequence information

Variant position: 558 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 1159 The length of the canonical sequence.
Location on the sequence: KLDRYSEYGAAVLFLLMCTF A LIAHWLACIWYAIGNMEQPH 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.
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
Chain	1 – 1159	Voltage-gated inwardly rectifying potassium channel KCNH2
Transmembrane	548 – 568	Helical; Name=Segment S5
Mutagenesis	540 – 540	D -> A. Does not affect steady-state activation. Significantly slow the activation rate at the most depolarised potentials. Accelerates the activation rate at less positive voltages.
Mutagenesis	543 – 543	S -> A. Increases the activation rate more rapidly at high voltages.
Mutagenesis	546 – 546	G -> A. Slows the activation rate.
Mutagenesis	548 – 548	A -> V. Perturbs steady-state activation. Accelerates the activation rate at the most depolarised potentials. Affects modestly the activation rate at less positive voltages.
Mutagenesis	550 – 550	L -> A. Slows the activation rate at low voltage gradients. Increases the activation rate more rapidly at high voltages.
Helix	546 – 573

Literature citations

Novel KCNQ1 and HERG missense mutations in Dutch long-QT families.
Jongbloed R.J.E.; Wilde A.A.M.; Geelen J.L.M.C.; Doevendans P.; Schaap C.; van Langen I.; van Tintelen J.P.; Cobben J.M.; Beaufort-Krol G.C.M.; Geraedts J.P.M.; Smeets H.J.M.;
Hum. Mutat. 13:301-310(1999)
Cited for: VARIANTS LQT2 PRO-558; CYS-582; SER-604; MET-613 AND LEU-640;