Home  |  Contact

UniProtKB/Swiss-Prot P34913: Variant p.Lys55Arg

Bifunctional epoxide hydrolase 2
Gene: EPHX2
Variant information

Variant position:  55
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 Lysine (K) to Arginine (R) at position 55 (K55R, p.Lys55Arg).
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:  Similar physico-chemical property. Both residues are large size and basic.
The physico-chemical property of the reference and variant residues and the change implicated.

BLOSUM score:  2
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:  Decreased phosphatase activity; no effect on epoxyde hydrolase activity.
Any additional useful information about the variant.

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



Sequence information

Variant position:  55
The position of the amino-acid change on the UniProtKB canonical protein sequence.

Protein sequence length:  555
The length of the canonical sequence.

Location on the sequence:   GLLNDAFQKGGPEGATTRLM  K GEITLSQWIPLMEENCRKCS
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                         GLLNDAFQKGGPEGATTRLMKGEITLSQWIPLMEENCRKCS

Mouse                         DFLLGAYQTEFPEGPTEQLMKGKITFSQWVPLMDESYRKSS

Rat                           DFLLGAFQMKFPEGPTEQLMKGKITFSQWVPLMDESCRKSS

Pig                           GFLNEAFKKGGQDGSVARVMTGEITFSQWVPFMEEDCRKCA

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 – 555 Bifunctional epoxide hydrolase 2
Region 1 – 224 Phosphatase
Modified residue 43 – 43 N6-acetyllysine
Modified residue 55 – 55 N6-succinyllysine
Alternative sequence 1 – 66 Missing. In isoform 3.


Literature citations

Submission
NIEHS SNPs program;
Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA]; VARIANTS ALA-21; GLN-52; ARG-55; CYS-103; TYR-154; LEU-225; GLN-287; VAL-369 AND GLY-470;

Polymorphisms in human soluble epoxide hydrolase.
Przybyla-Zawislak B.D.; Srivastava P.K.; Vazquez-Matias J.; Mohrenweiser H.W.; Maxwell J.E.; Hammock B.D.; Bradbury J.A.; Enayetallah A.E.; Zeldin D.C.; Grant D.F.;
Mol. Pharmacol. 64:482-490(2003)
Cited for: FUNCTION; CATALYTIC ACTIVITY; CHARACTERIZATION OF VARIANTS ARG-55; CYS-103; TYR-154; GLN-287 AND GLY-470;

Polymorphisms in human soluble epoxide hydrolase: effects on enzyme activity, enzyme stability, and quaternary structure.
Srivastava P.K.; Sharma V.K.; Kalonia D.S.; Grant D.F.;
Arch. Biochem. Biophys. 427:164-169(2004)
Cited for: CATALYTIC ACTIVITY; BIOPHYSICOCHEMICAL PROPERTIES; CHARACTERIZATION OF VARIANTS ARG-55; CYS-103; TYR-154; GLN-287 AND GLY-470;

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.