Expasy logo

UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot P60484: Variant p.Gly165Glu

Phosphatidylinositol 3,4,5-trisphosphate 3-phosphatase and dual-specificity protein phosphatase PTEN
Gene: PTEN
Feedback?
Variant information Variant position: help 165 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 Glycine (G) to Glutamate (E) at position 165 (G165E, p.Gly165Glu). 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 glycine (G) to medium size and acidic (E) 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 CWS1. Any additional useful information about the variant.


Sequence information Variant position: help 165 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 403 The length of the canonical sequence.
Location on the sequence: help FLKAQEALDFYGEVRTRDKK G VTIPSQRRYVYYYSYLLKNH 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                         FLKAQEALDFYGEVRTRDKKGVTIPSQRRYVYYYSYLLKNH

                              FLKAQEALDFYGEVRTRDKKGVTIPSQRRYVYYYSYLLKNH

Mouse                         FLKAQEALDFYGEVRTRDKKGVTIPSQRRYVYYYSYLLKNH

Rat                           FLKAQEALDFYGEVRTRDKKGVTIPSQRRYVYYYSYLLKNH

Xenopus laevis                FPRAQEALDFYGEVRTRDKKGVTIPSQRRYVYYYSYLLKNS

Caenorhabditis elegans        YPSPRQILDYYSIIRTKNNKGVTIPSQRRYIYYYHKLRERE

Slime mold                    WKNTEDSLRFYAALRTYNQKGVTIPSQIRYVGYFGRSIRES

Fission yeast                 -LTAKQSLELYTEKRMVRGHGLTISSQIRYVYYIE-ILKQF

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 – 403 Phosphatidylinositol 3,4,5-trisphosphate 3-phosphatase and dual-specificity protein phosphatase PTEN
Domain 14 – 185 Phosphatase tensin-type
Alternative sequence 165 – 190 GVTIPSQRRYVYYYSYLLKNHLDYRP -> ADPTGGIPDKGIIVIGDGSSMDVIAP. In isoform 3.
Mutagenesis 167 – 167 T -> AD. 60% reduction in phosphatase activity towards PtdIns(3,4,5)P3.
Mutagenesis 171 – 171 Q -> AE. 75% reduction in phosphatase activity towards PtdIns(3,4,5)P3.



Literature citations
Novel PTEN mutations in patients with Cowden disease: absence of clear genotype-phenotype correlations.
Nelen M.R.; Kremer H.; Konings I.B.M.; Schoute F.; van Essen A.J.; Koch R.; Woods C.G.; Fryns J.-P.; Hamel B.C.J.; Hoefsloot L.H.; Peeters E.A.J.; Padberg G.W.;
Eur. J. Hum. Genet. 7:267-273(1999)
Cited for: VARIANTS CWS1 ILE-33 DEL; ARG-123; ARG-124 AND GLU-165;
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.