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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot P04075: Variant p.Asp129Gly

Fructose-bisphosphate aldolase A
Gene: ALDOA
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Variant information Variant position: help 129 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 Aspartate (D) to Glycine (G) at position 129 (D129G, p.Asp129Gly). 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 acidic (D) to glycine (G) 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 GSD12; thermolabile. Any additional useful information about the variant.
Other resources: help Links to websites of interest for the variant.


Sequence information Variant position: help 129 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 364 The length of the canonical sequence.
Location on the sequence: help VDKGVVPLAGTNGETTTQGL D GLSERCAQYKKDGADFAKWR 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                         VDKGVVPLAGTNGETTTQGLDGLSERCAQYKKDGADFAKWR

Chimpanzee                    VDKGVVPLAGTNGETTTQGLDGLSERCAQYKKDGADFAKWR

Mouse                         VDKGVVPLAGTNGETTTQGLDGLSERCAQYKKDGADFAKWR

Rat                           VDKGVVPLAGTNGETTTQGLDGLSERCAQYKKDGADFAKWR

Rabbit                        VDKGVVPLAGTNGETTTQGLDGLSERCAQYKKDGADFAKWR
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 – 364 Fructose-bisphosphate aldolase A
Binding site 147 – 147
Modified residue 111 – 111 N6-acetyllysine; alternate
Modified residue 111 – 111 N6-malonyllysine; alternate
Modified residue 132 – 132 Phosphoserine
Modified residue 147 – 147 N6-(2-hydroxyisobutyryl)lysine



Literature citations
Human aldolase A deficiency associated with a hemolytic anemia: thermolabile aldolase due to a single base mutation.
Kishi H.; Mukai T.; Hirono A.; Fujii H.; Miwa S.; Hori K.;
Proc. Natl. Acad. Sci. U.S.A. 84:8623-8627(1987)
Cited for: VARIANT GSD12 GLY-129; CHARACTERIZATION OF VARIANT GSD12 GLY-129; Human aldolase A of a hemolytic anemia patient with Asp-128-->Gly substitution: characteristics of an enzyme generated in E. coli transfected with the expression plasmid pHAAD128G.
Takasaki Y.; Takahashi I.; Mukai T.; Hori K.;
J. Biochem. 108:153-157(1990)
Cited for: CHARACTERIZATION OF VARIANT GSD12 GLY-129;
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.