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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot Q9BYJ1: Variant p.Val500Phe

Hydroperoxide isomerase ALOXE3
Gene: ALOXE3
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Variant information Variant position: help 500 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 Valine (V) to Phenylalanine (F) at position 500 (V500F, p.Val500Phe). 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 medium size and hydrophobic (V) to large size and aromatic (F) 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 ARCI3; complete loss of the enzyme activity. Any additional useful information about the variant.
Other resources: help Links to websites of interest for the variant.


Sequence information Variant position: help 500 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 711 The length of the canonical sequence.
Location on the sequence: help GLAHFTYTNFCLPDSLRARG V LAIPNYHYRDDGLKIWAAIE 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                         GLAHFTYTNFCLPDSLRARGVLAIPNYHYRDDGLKIWAAIE

Mouse                         GLAHFTYTDFCLPDSIRARGVLTIPNYHYRDDGLKIWAAIE

Rat                           GLAHFTYTDFCLPDSLRARGVLTIPNYHYRDDGLKIWAAIE

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 – 711 Hydroperoxide isomerase ALOXE3
Domain 120 – 711 Lipoxygenase



Literature citations
Lipoxygenase-3 (ALOXE3) and 12(R)-lipoxygenase (ALOX12B) are mutated in non-bullous congenital ichthyosiform erythroderma (NCIE) linked to chromosome 17p13.1.
Jobard F.; Lefevre C.; Karaduman A.; Blanchet-Bardon C.; Emre S.; Weissenbach J.; Ozguc M.; Lathrop M.; Prud'homme J.-F.; Fischer J.;
Hum. Mol. Genet. 11:107-113(2002)
Cited for: VARIANTS ARCI3 SER-396 AND PHE-500; Mutations associated with a congenital form of ichthyosis (NCIE) inactivate the epidermal lipoxygenases 12R-LOX and eLOX3.
Yu Z.; Schneider C.; Boeglin W.E.; Brash A.R.;
Biochim. Biophys. Acta 1686:238-247(2005)
Cited for: CHARACTERIZATION OF VARIANTS ARCI3 SER-396 AND PHE-500;
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.