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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot P60484: Variant p.Phe241Ser

Phosphatidylinositol 3,4,5-trisphosphate 3-phosphatase and dual-specificity protein phosphatase PTEN
Gene: PTEN
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Variant information Variant position: help 241 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 Phenylalanine (F) to Serine (S) at position 241 (F241S, p.Phe241Ser). 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 (F) to small size and polar (S) 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 MCEPHAS. Any additional useful information about the variant.
Other resources: help Links to websites of interest for the variant.


Sequence information Variant position: help 241 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 KVKIYSSNSGPTRREDKFMY F EFPQPLPVCGDIKVEFFHKQ 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                         KVKIYSSNSGPTRR-----------EDKFM-----------------------------------------------------------------YFEFP-QPL-----------PVCGDIKVEFFHKQ

                              KVKIYSSNSGPTRR-----------EDKFM-----------

Mouse                         KVKIYSSNSGPTRR-----------EDKFM-----------

Rat                           KVKIYSSNSGPTRR-----------EDKLM-----------

Xenopus laevis                KVKIFTSTAGP-KR-----------AEKLM-----------

Caenorhabditis elegans        DRALKSKDLNNGMKLHVVLRCVDTRDSKMMEKSEVFGNLAF

Slime mold                    KKTVVDKNKKDPKKKLTKENSEKNIDSQQQQQSQSSLSQSQ

Fission yeast                 ILSLHAFSKGRNIN---------------------------

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 190 – 350 C2 tensin-type
Alternative sequence 191 – 403 Missing. In isoform 3.
Mutagenesis 229 – 229 S -> A. No effect on interaction with DLC1 or p85.
Mutagenesis 232 – 232 T -> A. No effect on interaction with DLC1 or p85.
Beta strand 238 – 259



Literature citations
Subset of individuals with autism spectrum disorders and extreme macrocephaly associated with germline PTEN tumour suppressor gene mutations.
Butler M.G.; Dasouki M.J.; Zhou X.-P.; Talebizadeh Z.; Brown M.; Takahashi T.N.; Miles J.H.; Wang C.H.; Stratton R.; Pilarski R.; Eng C.;
J. Med. Genet. 42:318-321(2005)
Cited for: VARIANTS MCEPHAS ARG-93; SER-241 AND GLY-252;
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.