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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot Q9UBP0: Variant p.Ala551Tyr

Spastin
Gene: SPAST
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Variant information Variant position: help 551 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 Alanine (A) to Tyrosine (Y) at position 551 (A551Y, p.Ala551Tyr). 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 small size and hydrophobic (A) to large size and aromatic (Y) 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 SPG4; requires 2 nucleotide substitutions. Any additional useful information about the variant.


Sequence information Variant position: help 551 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 616 The length of the canonical sequence.
Location on the sequence: help QKELAQLARMTDGYSGSDLT A LAKDAALGPIRELKPEQVKN 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                         QKELAQLARMTDGYSGSDLTALAKDAALGPIRELKPEQVKN

Mouse                         QKELAQLARMTDGYSGSDLTALAKDAALGPIRELKPEQVKN

Rat                           QKELAQLARMTDGYSGSDLTALAKDAALGPIRELKPEQVKN

Pig                           QKELAQLARLTDGYSGSDLTALAKDAALGPIRELKPEQVKN

Bovine                        QKELAQLARMTNGYSGSDLTALAKDAALGPIRELKPEQVKN

Chicken                       QKELAQLARMTDGYSGSDLTALAKDAALGPIRELKPEQVKN

Xenopus laevis                EKELTQLSRLTEGYSGSDITALAKDAALGPIRELKPEQVKN

Xenopus tropicalis            EKELTQLSRLTEGYSGSDITALAKDAALGPIRELKPEQVKN

Zebrafish                     QKELSQLARLTDGYSGSDLTSLAKDAALGPIRELKPEQVRN

Caenorhabditis elegans        SSDIRYIASNTSGFSNSDLVALCKEAAMVPIREIDRSKLSM

Drosophila                    TEALRRLAKITDGYSGSDLTALAKDAALEPIRELNVEQVKC

Slime mold                    KQQINSLAEVTQGYSGFDLAALCKDAAYEPIRRLGIG-IKD
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 1 – 616 Spastin
Topological domain 78 – 616 Cytoplasmic
Region 228 – 616 Sufficient for microtubule severing
Helix 546 – 557



Literature citations
Mutation analysis of the spastin gene (SPG4) in patients in Germany with autosomal dominant hereditary spastic paraplegia.
Sauter S.M.; Miterski B.; Klimpe S.; Boensch D.; Schoels L.; Visbeck A.; Papke T.; Hopf H.C.; Engel W.; Deufel T.; Epplen J.T.; Neesen J.;
Hum. Mutat. 20:127-132(2002)
Cited for: VARIANTS SPG4 ARG-407; TYR-551 AND ILE-615;
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.