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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot Q13608: Variant p.Arg812Trp

Peroxisomal ATPase PEX6
Gene: PEX6
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Variant information Variant position: help 812 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Type of variant: help LP/P [Disclaimer] 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 Arginine (R) to Tryptophan (W) at position 812 (R812W, p.Arg812Trp). 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 large size and basic (R) to large size and aromatic (W) 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

Variant description: help In PBD4A; atypical. Any additional useful information about the variant.
Other resources: help Links to websites of interest for the variant.


Sequence information Variant position: help 812 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 980 The length of the canonical sequence.
Location on the sequence: help ARAAAPCIIFFDELDSLAPS R GRSGDSGGVMDRVVSQLLAE 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                         ARAAAPCIIFFDELDSLAPSRGRSGDSGGVMDRVVSQLLAE

Mouse                         ARAAAPCIIFFDELDSLAPSRGRSGDSGGVMDRVVSQLLAE

Rat                           ARAAAPCIIFFDELDSLAPSRGRSGDSGGVMDRVVSQLLAE

Slime mold                    ARQAKPCVIFFDELDSLAPSRGNGADSGGVMDRVVSQLLAE

Baker's yeast                 AREAKPCVIFFDEIDSVAPKRGNQGDSGGVMDRIVSQLLAE

Fission yeast                 ARNSSPCVIFFDELDSIAPHRGNSSDSGNVMDRVVSQLLAE

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 – 980 Peroxisomal ATPase PEX6
Alternative sequence 739 – 980 Missing. In isoform 2.
Mutagenesis 803 – 803 D -> N. In B2 mutant; does not affect interaction with PEX6 or PEX26.



Literature citations
Genomic structure and identification of 11 novel mutations of the PEX6 'peroxisome assembly factor-2' gene in patients with peroxisome biogenesis disorders.
Zhang Z.; Suzuki Y.; Shimozawa N.; Fukuda S.; Imamura A.; Tsukamoto T.; Osumi T.; Fujiki Y.; Orii T.; Wanders R.J.A.; Barth P.G.; Moser H.W.; Paton B.C.; Besley G.T.; Kondo N.;
Hum. Mutat. 13:487-496(1999)
Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA]; VARIANTS PBD4A GLN-812 AND TRP-812;
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.