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UniProtKB/Swiss-Prot P48634: Variant p.Asp742Glu

Protein PRRC2A
Gene: PRRC2A
Variant information

Variant position:  742
The position of the amino-acid change on the UniProtKB canonical protein sequence.

Type of variant:  LB/B
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:  From Aspartate (D) to Glutamate (E) at position 742 (D742E, p.Asp742Glu).
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:  Similar physico-chemical property. Both residues are medium size and acidic.
The physico-chemical property of the reference and variant residues and the change implicated.

BLOSUM score:  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

Other resources:  
Links to websites of interest for the variant.



Sequence information

Variant position:  742
The position of the amino-acid change on the UniProtKB canonical protein sequence.

Protein sequence length:  2157
The length of the canonical sequence.

Location on the sequence:   RWMMIPPYVDPRLLQGRPPL  D FYPPGVHPSGLVPRERSDSG
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: 
The multiple alignment of the region surrounding the variant against various orthologous sequences.

Human                         RWMMIPPYVDPRLLQGRPPLDFYPPGVHPSGLVPRERSDSG

Rhesus macaque                RWMMIPPYVDPRLLQGRPPLDFYPPGVHPSGLVPRERSDSG

Mouse                         RWMMIPPYVDPRLLQGRPPLDFYPPGVHPSGLVPRERSDSG

Rat                           RWMMIPPYVDPRLLQGRPPLDFYPPGVHPSGLVPRERSDSG

Sequence annotation in neighborhood:  
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 1 – 2157 Protein PRRC2A
Region 41 – 1812 4 X 57 AA type A repeats
Region 740 – 1775 Disordered
Modified residue 759 – 759 Phosphoserine
Modified residue 761 – 761 Phosphoserine


Literature citations

A gene pair from the human major histocompatibility complex encodes large proline-rich proteins with multiple repeated motifs and a single ubiquitin-like domain.
Banerji J.; Sands J.; Strominger J.L.; Spies T.;
Proc. Natl. Acad. Sci. U.S.A. 87:2374-2378(1990)
Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA / MRNA] (ISOFORM 2); VARIANTS ARG-57; GLU-742; PRO-1503 AND VAL-1895;

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.