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UniProtKB/Swiss-Prot O14773: Variant p.Gly473Arg

Tripeptidyl-peptidase 1
Gene: TPP1
Variant information

Variant position:  473
The position of the amino-acid change on the UniProtKB canonical protein sequence.

Type of variant:  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:  From Glycine (G) to Arginine (R) at position 473 (G473R, p.Gly473Arg).
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:  Change from glycine (G) to large size and basic (R)
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

Variant description:  In CLN2.
Any additional useful information about the variant.

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

Sequence information

Variant position:  473
The position of the amino-acid change on the UniProtKB canonical protein sequence.

Protein sequence length:  563
The length of the canonical sequence.

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                         AALSDGYWVVSNRVPIPWVSGTSASTPV-----------------------------FGGILSLINEHRI


Chimpanzee                    AALSDGYWVVSNRVPIPWVSGTSASTPV-------------

Mouse                         AALSDGYWVVSNMVPIPWVSGTSASTPV-------------

Rat                           AALSDGYWVVSNMVPIPWVSGTSASTPV-------------

Bovine                        AALSDGYWVVSNHVPIPWVSGTSASTPV-------------

Zebrafish                     AALSDNYWVVSNRVPIPWVSGTSASTPV-------------

Slime mold                    SSFSENVVILYKDKLMP-IGGTSASAPI-------------

Baker's yeast                 KDFSDSDIKFAENLHVEF-----------------------


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.

Chain 196 – 563 Tripeptidyl-peptidase 1
Domain 199 – 563 Peptidase S53
Active site 475 – 475 Charge relay system
Disulfide bond 365 – 526
Mutagenesis 475 – 475 S -> A. Inactive. Impaired processing.

Literature citations

Heterogeneity of late-infantile neuronal ceroid lipofuscinosis.
Zhong N.; Moroziewicz D.N.; Ju W.; Jurkiewicz A.; Johnston L.; Wisniewski K.E.; Brown W.T.;
Genet. Med. 2:312-318(2000)
Cited for: VARIANTS CLN2 GLN-127; VAL-284; ASN-428 AND ARG-473;

Two novel CLN2 gene mutations in a Chinese patient with classical late-infantile neuronal ceroid lipofuscinosis.
Lam C.W.; Poon P.M.; Tong S.F.; Ko C.H.;
Am. J. Med. Genet. 99:161-163(2001)
Cited for: VARIANT CLN2 ARG-473;

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.