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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot P60891: Variant p.Leu129Ile

Ribose-phosphate pyrophosphokinase 1
Gene: PRPS1
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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 Leucine (L) to Isoleucine (I) at position 129 (L129I, p.Leu129Ile). 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 Similar physico-chemical property. Both residues are medium size and hydrophobic. The physico-chemical property of the reference and variant residues and the change implicated.
BLOSUM score: help 2 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 PRPS1 superactivity; no effect on Km; resistant to inhibition by ADP and GDP. 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 318 The length of the canonical sequence.
Location on the sequence: help AKLVANMLSVAGADHIITMD L HASQIQGFFDIPVDNLYAEP 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                         AKLVANMLSVAGADHIITMDLHASQIQGFFDIPVDNLYAEP

Mouse                         AKLVANMLSVAGADHIITMDLHASQIQGFFDIPVDNLYAEP

Rat                           AKLVANMLSVAGADHIITMDLHASQIQGFFDIPVDNLYAEP

Bovine                        AKLVANMLSVAGADHIITMDLHASQIQGFFDIPVDNLYAEP

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 – 318 Ribose-phosphate pyrophosphokinase 1
Binding site 128 – 128
Binding site 130 – 130
Binding site 130 – 130
Binding site 139 – 139
Binding site 143 – 143
Mutagenesis 132 – 132 S -> A. Reduces catalytic activity.
Mutagenesis 132 – 132 S -> F. No effect on catalytic activity.
Mutagenesis 144 – 144 N -> H. No effect on catalytic activity.
Mutagenesis 146 – 146 Y -> F. No effect on catalytic activity.
Mutagenesis 146 – 146 Y -> M. Reduces catalytic activity.



Literature citations
The genetic and functional basis of purine nucleotide feedback-resistant phosphoribosylpyrophosphate synthetase superactivity.
Becker M.A.; Smith P.R.; Taylor W.; Mustafi R.; Switzer R.L.;
J. Clin. Invest. 96:2133-2141(1995)
Cited for: VARIANTS PRPS1 SUPERACTIVITY HIS-52; SER-114; ILE-129; HIS-183; VAL-190 AND GLN-193; FUNCTION; CATALYTIC ACTIVITY; BIOPHYSICOCHEMICAL PROPERTIES; ACTIVITY REGULATION; CHARACTERIZATION OF VARIANTS PRPS1 SUPERACTIVITY HIS-52; SER-114; ILE-129; HIS-183; VAL-190 AND GLN-193;
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.