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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot P15289: Variant p.Arg84Gln

Arylsulfatase A
Gene: ARSA
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Variant information Variant position: help 84 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 Arginine (R) to Glutamine (Q) at position 84 (R84Q, p.Arg84Gln). 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 basic (R) to medium size and polar (Q) 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 MLD; mild. Any additional useful information about the variant.
Other resources: help Links to websites of interest for the variant.


Sequence information Variant position: help 84 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 507 The length of the canonical sequence.
Location on the sequence: help VPVSLCTPSRAALLTGRLPV R MGMYPGVLVPSSRGGLPLEE 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.
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 19 – 507 Arylsulfatase A
Chain 19 – 444 Arylsulfatase A component B
Active site 69 – 69 Nucleophile
Binding site 69 – 69 via 3-oxoalanine
Modified residue 69 – 69 3-oxoalanine (Cys)
Alternative sequence 1 – 84 Missing. In isoform 2.
Mutagenesis 69 – 69 C -> A. Abolishes enzyme activity.
Mutagenesis 69 – 69 C -> S. Abolishes formation of 3-oxoalanine (also known as C-formylglycine, FGly). Strongly decreases enzyme activity.
Helix 82 – 85



Literature citations
Late-onset metachromatic leukodystrophy: molecular pathology in two siblings.
Kappler J.; von Figura K.; Gieselmann V.;
Ann. Neurol. 31:256-261(1992)
Cited for: VARIANT MLD GLN-84; Molecular analysis of ARSA and PSAP genes in twenty-one Italian patients with metachromatic leukodystrophy: identification and functional characterization of 11 novel ARSA alleles.
Grossi S.; Regis S.; Rosano C.; Corsolini F.; Uziel G.; Sessa M.; Di Rocco M.; Parenti G.; Deodato F.; Leuzzi V.; Biancheri R.; Filocamo M.;
Hum. Mutat. 29:E220-E230(2008)
Cited for: VARIANTS MLD ASP-18; HIS-30; GLN-84; PRO-137 DEL; ASP-154; SER-179; CYS-201; PRO-212; HIS-217; LYS-253; SER-282; ASN-302; TRP-370; ASN-376; TRP-390 AND PRO-428; CHARACTERIZATION OF VARIANTS MLD ASP-18; HIS-30; PRO-212; HIS-217; SER-282; ASN-302; TRP-370 AND ASN-376;
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.