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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot Q8WTS1: Variant p.Gln130Pro

1-acylglycerol-3-phosphate O-acyltransferase ABHD5
Gene: ABHD5
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Variant information Variant position: help 130 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 Glutamine (Q) to Proline (P) at position 130 (Q130P, p.Gln130Pro). 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 polar (Q) to medium size and hydrophobic (P) 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 CDS; loss of PNPLA2-dependent triacylclycerol hydrolysis but no effect on LPA acyltransferase activity. Any additional useful information about the variant.
Other resources: help Links to websites of interest for the variant.


Sequence information Variant position: help 130 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 349 The length of the canonical sequence.
Location on the sequence: help LGFGRSSRPRFDSDAEEVEN Q FVESIEEWRCALGLDKMILL 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                         LGFGRSSRPRFDSDAEEVENQFVESIEEWRCALGLDKMILL

Mouse                         LGFGRSSRPRFDSDAEEVENQFVESIEEWRCALRLDKMILL

Rat                           LGFGRSSRPRFDSDAEEVENQFVESIEEWRCALRLDKMILL

Pig                           LGFGRSSRPRFDTDAEEVENQFVESIEEWRCALGLDKVILL
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 – 349 1-acylglycerol-3-phosphate O-acyltransferase ABHD5
Domain 77 – 184 AB hydrolase-1
Modified residue 122 – 122 Phosphoserine



Literature citations
Mutations in CGI-58, the gene encoding a new protein of the esterase/lipase/thioesterase subfamily, in Chanarin-Dorfman syndrome.
Lefevre C.; Jobard F.; Caux F.; Bouadjar B.; Karaduman A.; Heilig R.; Lakhdar H.; Wollenberg A.; Verret J.-L.; Weissenbach J.; Oezguec M.; Lathrop M.; Prud'homme J.-F.; Fischer J.;
Am. J. Hum. Genet. 69:1002-1012(2001)
Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA]; TISSUE SPECIFICITY; VARIANTS CDS LYS-7; PRO-130 AND LYS-260; Adipose triglyceride lipase-mediated lipolysis of cellular fat stores is activated by CGI-58 and defective in Chanarin-Dorfman Syndrome.
Lass A.; Zimmermann R.; Haemmerle G.; Riederer M.; Schoiswohl G.; Schweiger M.; Kienesberger P.; Strauss J.G.; Gorkiewicz G.; Zechner R.;
Cell Metab. 3:309-319(2006)
Cited for: FUNCTION; CHARACTERIZATION OF VARIANTS CDS PRO-130 AND LYS-260; CGI-58, the causative gene for Chanarin-Dorfman syndrome, mediates acylation of lysophosphatidic acid.
Ghosh A.K.; Ramakrishnan G.; Chandramohan C.; Rajasekharan R.;
J. Biol. Chem. 283:24525-24533(2008)
Cited for: FUNCTION; CATALYTIC ACTIVITY; CHARACTERIZATION OF VARIANTS CDS PRO-130 AND LYS-260;
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.