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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot Q9UHD9: Variant p.Pro509Ser

Ubiquilin-2
Gene: UBQLN2
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Variant information Variant position: help 509 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 Proline (P) to Serine (S) at position 509 (P509S, p.Pro509Ser). 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 medium size and hydrophobic (P) to small size and polar (S) The physico-chemical property of the reference and variant residues and the change implicated.
BLOSUM score: help -1 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 ALS15; reduces binding to HNRNPA1; increases translocation of HNRNPA1 to the cytoplasm. Any additional useful information about the variant.
Other resources: help Links to websites of interest for the variant.


Sequence information Variant position: help 509 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 624 The length of the canonical sequence.
Location on the sequence: help IGPVGPVTPIGPIGPIVPFT P IGPIGPIGPTGPAAPPGSTG 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                         IGPVGPVTPIGPIGPIVPFTPIGPIGPIGPTGPAAPPGSTG

Mouse                         ITPVGPVTPIGPIGPIVPFTPIGPIGPIGPTGPASSPGSTG
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 – 624 Ubiquilin-2
Repeat 509 – 511 7
Region 491 – 526 12 X 3 AA tandem repeats of P-X-X



Literature citations
Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia.
Deng H.X.; Chen W.; Hong S.T.; Boycott K.M.; Gorrie G.H.; Siddique N.; Yang Y.; Fecto F.; Shi Y.; Zhai H.; Jiang H.; Hirano M.; Rampersaud E.; Jansen G.H.; Donkervoort S.; Bigio E.H.; Brooks B.R.; Ajroud K.; Sufit R.L.; Haines J.L.; Mugnaini E.; Pericak-Vance M.A.; Siddique T.;
Nature 477:211-215(2011)
Cited for: VARIANTS ALS15 HIS-497; SER-497; THR-506; SER-509 AND SER-525; CHARACTERIZATION OF VARIANTS ALS15 HIS-497 AND THR-506; ALS-linked mutations in ubiquilin-2 or hnRNPA1 reduce interaction between ubiquilin-2 and hnRNPA1.
Gilpin K.M.; Chang L.; Monteiro M.J.;
Hum. Mol. Genet. 24:2565-2577(2015)
Cited for: INTERACTION WITH HNRNPA1 AND HNRNPU; CHARACTERIZATION OF VARIANTS ALS15 HIS-497; SER-497; THR-506; SER-509 AND SER-525;
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.