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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot P00966: Variant p.Thr119Ile

Argininosuccinate synthase
Gene: ASS1
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Variant information Variant position: help 119 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 Threonine (T) to Isoleucine (I) at position 119 (T119I, p.Thr119Ile). 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 (T) to medium size and hydrophobic (I) 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 CTLN1; decreased thermal stability; loss of argininosuccinate synthase activity. Any additional useful information about the variant.


Sequence information Variant position: help 119 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 412 The length of the canonical sequence.
Location on the sequence: help ARKQVEIAQREGAKYVSHGA T GKGNDQVRFELSCYSLAPQI 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                         ARKQVEIAQREGAKYVSHGATGKGNDQVRFELSCYSLAPQI

Mouse                         ARRQVEIAQREGAKYVSHGATGKGNDQVRFELTCYSLAPQI

Rat                           ARKQVEIAQREGAKYVSHGATGKGNDQVRFELTCYSLAPQI

Bovine                        ARKQVEIAQREGAKYVSHGATGKGNDQIRFELTCYSLAPQI

Chicken                       ARHLVLIAQEEGARYIAHGATGKGNDQVRFELGCYALCPSI

Xenopus laevis                AKKQVEIAKKEAAEYVSHGATGKGNDQIRFELTCYSLYPEV

Xenopus tropicalis            AKKQVEIAKKEAAEYVSHGATGKGNDQIRFELTCYALYPEV

Zebrafish                     ARRQVQIAQREGAQYVSHGATGKGNDQVRFELTCYALYPQV

Drosophila                    SVALMEVAREYGAKYLAHGATGKGNDQVRFELCAYALKPDL

Baker's yeast                 AKAQIDVAKQEGCFAVSHGCTGKGNDQIRFELSFYALKPDV

Fission yeast                 ARRQIQIAEKENCIAVSHGCTGKGNDQVRFELAYYALKPDV
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 1 – 412 Argininosuccinate synthase
Binding site 115 – 123
Binding site 119 – 119
Binding site 123 – 123
Binding site 123 – 123
Binding site 124 – 124
Binding site 127 – 127
Modified residue 112 – 112 N6-acetyllysine
Modified residue 113 – 113 Phosphotyrosine



Literature citations
Phenotype and genotype heterogeneity in Mediterranean citrullinemia.
Vilaseca M.A.; Kobayashi K.; Briones P.; Lambruschini N.; Campistol J.; Tabata A.; Alomar A.; Rodes M.; Lluch M.; Saheki T.;
Mol. Genet. Metab. 74:396-398(2001)
Cited for: VARIANTS CTLN1 ALA-69; LEU-108; ASP-117; ILE-119; GLN-270 AND ARG-390; Kinetic mutations in argininosuccinate synthetase deficiency: characterisation and in vitro correction by substrate supplementation.
Diez-Fernandez C.; Wellauer O.; Gemperle C.; Ruefenacht V.; Fingerhut R.; Haeberle J.;
J. Med. Genet. 53:710-719(2016)
Cited for: VARIANTS CTLN1 PRO-91; LEU-96; SER-117; THR-118; ILE-119; ASN-124; CYS-157; HIS-157; CYS-272; HIS-272 AND LEU-272; CHARACTERIZATION OF VARIANTS CTLN1 PRO-91; SER-95; HIS-96; LEU-96; SER-96; SER-117; THR-118; ILE-119; ASN-124; GLN-127; TRP-127; CYS-157; HIS-157; ASN-180; ILE-180; GLN-191; GLN-270; CYS-272; HIS-272 AND LEU-272; CHARACTERIZATION OF VARIANT LEU-127; CATALYTIC ACTIVITY; PATHWAY; FUNCTION; SUBCELLULAR LOCATION;
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.