UniProtKB/Swiss-Prot P16435: Variant p.Pro225Leu

NADPH--cytochrome P450 reductase
Gene: POR
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Variant information Variant position:

225 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 Proline (P) to Leucine (L) at position 225 (P225L, p.Pro225Leu). 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
Other resources:

Links to websites of interest for the variant.

Variant rs17853284 [ dbSNP | Ensembl ]

Sequence information Variant position:

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

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

LGDDDGNLEEDFITWREQFW P AVCEHFGVEATGEESSIRQY 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                         LGDD-DGNLEEDFITWREQFWPAVCEHFG--VEATGEESSIRQY

Mouse                         LGDD-DGNLEEDFITWREQFWPAVCEFFG--VEATGEESSI

Rat                           LGDD-DGNLEEDFITWREQFWPAVCEFFG--VEATGEESSI

Pig                           LGDD-DGNLEEDFITWREQFWPAVCEHFG--VEATGEESSI

Bovine                        LGDD-DGNLEEDFITWREQFWPAVCEHFG--VEATGEESSI

Rabbit                        MGDD-DANLEEDFITWREQFWPAVCEHFG--VEATGEESSI

Drosophila                    LGDD-DANIEDDFITWKDRFWPAVCDHFG--IEGGGEEVLI

Slime mold                    EGDD-DATLEEDFNRWKKDMWPVVCKFLGYELKSTEDDKFV

Baker's yeast                 EADDGAGTTDEDYMAWKDSILEVLKDELH--LDEQ-EAKFT

Fission yeast                 LGDDAAGMLEEDYLQWKDDTLPEIGKLFH--LQEVHKEYNP

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	2 – 677	NADPH--cytochrome P450 reductase
Topological domain	43 – 677	Cytoplasmic
Binding site	208 – 208
Helix	212 – 231

Literature citations
Submission
NIEHS SNPs program;
Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA]; VARIANTS LEU-225; ASN-252 AND VAL-500; The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).
The MGC Project Team;
Genome Res. 14:2121-2127(2004)
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA]; VARIANTS LEU-225 AND VAL-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.