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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot P06744: Variant p.Gln343Arg

Glucose-6-phosphate isomerase
Gene: GPI
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Variant information Variant position: help 343 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 Arginine (R) at position 343 (Q343R, p.Gln343Arg). 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 large size and basic (R) 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 HA-GPID; GPI Narita and Morcone. Any additional useful information about the variant.
Other resources: help Links to websites of interest for the variant.


Sequence information Variant position: help 343 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 558 The length of the canonical sequence.
Location on the sequence: help LGIWYINCFGCETHAMLPYD Q YLHRFAAYFQQGDMESNGKY 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                         LGIWYINCFGCETHAMLPYDQYLHRFAAYFQQGDMESNGKY

Mouse                         LGIWYINCYGCETHALLPYDQYMHRFAAYFQQGDMESNGKY

Rat                           LGIWYINFYGCETHAMLPYDQYMHRFAAYFQQGDMESNGKY

Pig                           LGIWYINFFGCETHAMLPYDQYLHRFAAYFQQGDMESNGKY

Bovine                        LGIWYINCFGCETHAMLPYDQYLHRFAAYFQQGDMESNGKY

Rabbit                        LGIWYINCFGCETQAVLPYDQYLHRFAAYFQQGDMESNGKY

Drosophila                    LGVWYSNFFKAETHALLPYDQYLHRFAAYFQQGDMESNGKF

Slime mold                    LGVWYNNFFGCQTQAILPYDQYLSRFPAYFQQGDMESNGKS

Baker's yeast                 LSVWYNNFFGAQTHLVAPFDQYLHRFPAYLQQLSMESNGKS

Fission yeast                 ISIWYSDFFGAQTHLVAPYDQYLHRFPAYLQQLSMESNGKA
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 – 558 Glucose-6-phosphate isomerase
Active site 358 – 358 Proton donor
Binding site 354 – 354
Binding site 358 – 358
Helix 343 – 345



Literature citations
Study of the molecular defects in glucose phosphate isomerase-deficient patients affected by chronic hemolytic anemia.
Baronciani L.; Zanella A.; Bianchi P.; Zappa M.; Alfinito F.; Iolascon A.; Tannoia N.; Beutler E.; Sirchia G.;
Blood 88:2306-2310(1996)
Cited for: VARIANTS HA-GPID MET-101; ILE-195; ARG-343 AND THR-525; Molecular analysis of glucose phosphate isomerase deficiency associated with hereditary hemolytic anemia.
Kanno H.; Fujii H.; Hirono A.; Ishida Y.; Ohga S.; Fukumoto Y.; Matsuzawa K.; Ogawa S.; Miwa S.;
Blood 88:2321-2325(1996)
Cited for: VARIANTS HA-GPID ILE-5; MET-224; ARG-343; ARG-375 AND ASN-539;
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.