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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot P05787: Variant p.Ile63Val

Keratin, type II cytoskeletal 8
Gene: KRT8
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Variant information Variant position: help 63 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Type of variant: help 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: help From Isoleucine (I) to Valine (V) at position 63 (I63V, p.Ile63Val). 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 hydrophobic. The physico-chemical property of the reference and variant residues and the change implicated.
BLOSUM score: help 3 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

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


Sequence information Variant position: help 63 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 483 The length of the canonical sequence.
Location on the sequence: help SSNFRGGLGGGYGGASGMGG I TAVTVNQSLLSPLVLEVDPN 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                         SSN--FRGGLGGG---------YGGASGMG---------GITAVTVNQSLLSPLVLEVDPN

Mouse                         SSSSSFRGSMGTGVGL----GGFGGA-GVG---------GI

Rat                           SSSSSFRGSLGG----------FGGA-GVG---------GI

Bovine                        SSSS-FRGGLGTG---MSMAGSYGGAPGLG---------GI

Xenopus laevis                GASR-FGSGYRSG---------FGGA-GVGS-------AGI

Zebrafish                     GVNRGMGAGMGGGSGFISSSSAYGLGMGMGTGMGAGVVAPI

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 – 483 Keratin, type II cytoskeletal 8
Region 1 – 90 Head
Modified residue 43 – 43 Phosphoserine
Modified residue 44 – 44 Phosphoserine
Modified residue 47 – 47 Asymmetric dimethylarginine; alternate
Modified residue 47 – 47 Omega-N-methylarginine; alternate
Modified residue 74 – 74 Phosphoserine; by MAPK
Mutagenesis 72 – 72 L -> P. Increases phosphorylation.
Mutagenesis 74 – 74 S -> A. Generates normal-appearing filaments, that remain stable after okadaic acid treatment.
Mutagenesis 74 – 74 S -> D. Generates normal-appearing filaments, that are destabilized by okadaic acid.
Beta strand 59 – 63



Literature citations
Keratin 8 and 18 mutations are risk factors for developing liver disease of multiple etiologies.
Ku N.-O.; Darling J.M.; Krams S.M.; Esquivel C.O.; Keeffe E.B.; Sibley R.K.; Lee Y.M.; Wright T.L.; Omary M.B.;
Proc. Natl. Acad. Sci. U.S.A. 100:6063-6068(2003)
Cited for: VARIANTS CIRRH VAL-53; CYS-54 AND CYS-62; VARIANT VAL-63;
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.