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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot P25189: Variant p.Pro132Leu

Myelin protein P0
Gene: MPZ
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Variant information Variant position: help 132 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 Proline (P) to Leucine (L) at position 132 (P132L, p.Pro132Leu). 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 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: 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 CMT1B; moderate. Any additional useful information about the variant.


Sequence information Variant position: help 132 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 248 The length of the canonical sequence.
Location on the sequence: help IVIHNLDYSDNGTFTCDVKN P PDIVGKTSQVTLYVFEKVPT 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                         IVIHNLDYSDNGTFTCDVKNPPDIVGKTSQVTLYVFEKVPT

Mouse                         IVIHNLDYSDNGTFTCDVKNPPDIVGKTSQVTLYVFEKVPT

Rat                           IVIHNLDYSDNGTFTCDVKNPPDIVGKTSQVTLYVFEKVPT

Bovine                        IVIHNLDYGDNGTFTCDVKNPPDIVGKTSQVTLYVFEKVPT

Horse                         IVIHNLDYSDNGTFTCDVKNPPDIVGKTSQVTLYVFEKVPT

Chicken                       IVIHNLDYTDNGTFTCDVKNPPDIVGKSSQVTLYVLEKVPT

Xenopus laevis                IVVHNLELTDNGTFTCDVKNPPDVVGKSSYVHLQVQEKGPA

Xenopus tropicalis            IVLHNLELIDNGTFTCDVKNPPDVVGKSSYVHLQVQEKGAA
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 30 – 248 Myelin protein P0
Topological domain 30 – 153 Extracellular
Domain 30 – 143 Ig-like V-type
Glycosylation 122 – 122 N-linked (GlcNAc...) (complex) asparagine



Literature citations
Mutation analysis in Charcot-Marie-Tooth disease type 1 (CMT1).
Sorour E.; Upadhyaya M.;
Hum. Mutat. Suppl. 1:S242-S247(1998)
Cited for: VARIANTS CMT1B PHE-58; CYS-68; THR-112; LEU-132 AND ALA-167;
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.