UniProtKB/Swiss-Prot P05181: Variant p.Val179Ile

Cytochrome P450 2E1
Gene: CYP2E1
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Variant information Variant position:

179 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 Valine (V) to Isoleucine (I) at position 179 (V179I, p.Val179Ile). 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 medium size and hydrophobic. The physico-chemical property of the reference and variant residues and the change implicated.
BLOSUM score:

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:

In allele CYP2E1*4. Any additional useful information about the variant.
Other resources:

Links to websites of interest for the variant.

Variant rs6413419 [ dbSNP | Ensembl ]

Sequence information Variant position:

179 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length:

493 The length of the canonical sequence.
Location on the sequence:

RKTQGQPFDPTFLIGCAPCN V IADILFRKHFDYNDEKFLRL 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                         RKTQGQPFDPTFLIGCAPCNVIADILFRKHFDYNDEKFLRL

                              RGTRGQPFDPTFLLGFAPFNVIADILFHKHFDYSDQTGLRI

Rhesus macaque                RKTQGQPFDPTFLIGCAPCNVIADILFRKHFDYNDEKFLRL

Mouse                         KKTKGQPFDPTFLIGCAPCNVIADILFNKRFDYDDKKCLEL

Rat                           KKTKGQPFDPTFLIGCAPCNVIADILFNKRFDYNDKKCLRL

Pig                           RKTHGQPFDPTFLIGCAPCNVISDILFRQHFDYNDKTCLRL

Bovine                        RKTQGQPFDPTFVVGFAPYNVISDILFHKRFDYKDQTSLRL

Rabbit                        RKTQGQPFDPTFVIGCTPFNVIAKILFNDRFDYKDKQALRL

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 – 493	Cytochrome P450 2E1
Helix	174 – 185

Literature citations
Detection and characterization of novel polymorphisms in the CYP2E1 gene.
Fairbrother K.S.; Grove J.; de Waziers I.; Steimel D.T.; Day C.P.; Crespi C.L.; Daly A.K.;
Pharmacogenetics 8:543-552(1998)
Cited for: VARIANT ILE-179; Genetic variation in eleven phase I drug metabolism genes in an ethnically diverse population.
Solus J.F.; Arietta B.J.; Harris J.R.; Sexton D.P.; Steward J.Q.; McMunn C.; Ihrie P.; Mehall J.M.; Edwards T.L.; Dawson E.P.;
Pharmacogenomics 5:895-931(2004)
Cited for: VARIANTS ILE-179 AND LEU-457;

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.