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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot P08473: Variant p.Tyr347Cys

Neprilysin
Gene: MME
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Variant information Variant position: help 347 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 Tyrosine (Y) to Cysteine (C) at position 347 (Y347C, p.Tyr347Cys). 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 large size and aromatic (Y) to medium size and polar (C) The physico-chemical property of the reference and variant residues and the change implicated.
BLOSUM score: help -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: help In CMT2T; results in reduction of neprilysin activity. Any additional useful information about the variant.
Other resources: help Links to websites of interest for the variant.


Sequence information Variant position: help 347 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 750 The length of the canonical sequence.
Location on the sequence: help TNEIMSTVNISITNEEDVVV Y APEYLTKLKPILTKYSARDL 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                         TNEIMSTVNISITNEEDVVVYAPEYLTKLKPILTKYSARDL

Mouse                         TNEIMSTVNINIQNEEEVVVYAPEYLTKLKPILTKYSPRDL

Rat                           TNEIMSTVNINIQNEEEVVVYAPEYLTKLKPILTKYSPRDL

Rabbit                        TNEIMSTVNINIPNEEDVVVYAPEYLIKLKPILTKYFPRDF

Drosophila                    LQAALGP-GIPLQEDEPLVTYGLHYLTEMGKILAHTDRRVV

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 2 – 750 Neprilysin
Topological domain 52 – 750 Extracellular
Domain 56 – 750 Peptidase M13
Disulfide bond 80 – 735
Disulfide bond 88 – 695
Disulfide bond 143 – 411
Beta strand 343 – 347



Literature citations
Rare variants in MME, encoding metalloprotease neprilysin, are linked to late-onset autosomal-dominant axonal polyneuropathies.
Auer-Grumbach M.; Toegel S.; Schabhuettl M.; Weinmann D.; Chiari C.; Bennett D.L.; Beetz C.; Klein D.; Andersen P.M.; Boehme I.; Fink-Puches R.; Gonzalez M.; Harms M.B.; Motley W.; Reilly M.M.; Renner W.; Rudnik-Schoeneborn S.; Schlotter-Weigel B.; Themistocleous A.C.; Weishaupt J.H.; Ludolph A.C.; Wieland T.; Tao F.; Abreu L.; Windhager R.; Zitzelsberger M.; Strom T.M.; Walther T.; Scherer S.S.; Zuechner S.; Martini R.; Senderek J.;
Am. J. Hum. Genet. 99:607-623(2016)
Cited for: FUNCTION; CATALYTIC ACTIVITY; INVOLVEMENT IN CMT2T; VARIANTS CMT2T ALA-12; CYS-347; PRO-348 AND ASP-422; CHARACTERIZATION OF VARIANTS CMT2T CYS-347 AND ASP-422;
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.