UniProtKB/Swiss-Prot P07737: Variant p.Glu117Gly

Profilin-1
Gene: PFN1
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Variant information Variant position:

117 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Type of variant:

US 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 Glutamate (E) to Glycine (G) at position 117 (E117G, p.Glu117Gly). 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:

Change from medium size and acidic (E) to glycine (G) The physico-chemical property of the reference and variant residues and the change implicated.
BLOSUM score:

-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:

In ALS18; uncertain significance; like the wild-type the mutant protein is detected in the soluble fraction of cells. Any additional useful information about the variant.
Other resources:

Links to websites of interest for the variant.

Variant rs140547520 [ dbSNP | Ensembl ]

Sequence information Variant position:

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

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

PTFNVTVTKTDKTLVLLMGK E GVHGGLINKKCYEMASHLRR 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                         PTFNVTVTKTDKTLVLLMGKEGVHGGLINKKCYEMASHLRR

Mouse                         PTFNVTVTMTAKTLVLLMGKEGVHGGLINKKCYEMASHLRR

Rat                           PTFNVTVTMTAKTLVLLMGKEGVHGGLINKKCYEMASHLRR

Bovine                        PTFNITVTMTAKTLVLLMGKEGVHGGMINKKCYEMASHLRR

Caenorhabditis elegans        --FFAVKTKSAVLIAVYEGPNEV-AAQVRKAVESMQTYLNN

Slime mold                    ----CVLVRTGQAIIVGIYDDKVQPGSAALIVEKLGDYLRD

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 – 140	Profilin-1
Modified residue	105 – 105	N6-acetyllysine
Modified residue	108 – 108	N6-acetyllysine
Modified residue	129 – 129	Phosphotyrosine

Literature citations
Mutations in the profilin 1 gene cause familial amyotrophic lateral sclerosis.
Wu C.H.; Fallini C.; Ticozzi N.; Keagle P.J.; Sapp P.C.; Piotrowska K.; Lowe P.; Koppers M.; McKenna-Yasek D.; Baron D.M.; Kost J.E.; Gonzalez-Perez P.; Fox A.D.; Adams J.; Taroni F.; Tiloca C.; Leclerc A.L.; Chafe S.C.; Mangroo D.; Moore M.J.; Zitzewitz J.A.; Xu Z.S.; van den Berg L.H.; Glass J.D.; Siciliano G.; Cirulli E.T.; Goldstein D.B.; Salachas F.; Meininger V.; Rossoll W.; Ratti A.; Gellera C.; Bosco D.A.; Bassell G.J.; Silani V.; Drory V.E.; Brown R.H. Jr.; Landers J.E.;
Nature 488:499-503(2012)
Cited for: VARIANTS ALS18 GLY-71; THR-114; GLY-117 AND VAL-118; CHARACTERIZATION OF VARIANTS ALS18 GLY-71; THR-114; GLY-117 AND VAL-118;

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.