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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot P43080: Variant p.Ile107Thr

Guanylyl cyclase-activating protein 1
Gene: GUCA1A
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Variant information Variant position: help 107 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 Isoleucine (I) to Threonine (T) at position 107 (I107T, p.Ile107Thr). 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 hydrophobic (I) to medium size and polar (T) 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 CORD14; affects guanylate cyclase regulator activity resulting in constitutive activation of GUCY2D at physiologic calcium concentrations; 10-fold lower affinity for calcium ions. Any additional useful information about the variant.
Other resources: help Links to websites of interest for the variant.


Sequence information Variant position: help 107 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 201 The length of the canonical sequence.
Location on the sequence: help KVEQKLRWYFKLYDVDGNGC I DRDELLTIIQAIRAINPCSD 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                         KVEQKLRWYFKLYDVDGNGCIDRDELLTIIQAIRAINPCSD

Mouse                         KVEQKLRWYFKLYDVDGNGCIDRDELLTIIRAIRTINPWSD

Bovine                        KVEQKLRWYFKLYDVDGNGCIDRDELLTIIRAIRAINPCSD

Chicken                       KVDQKLRWYFKLYDVDGNGCIDRGELLNIIKAIRAINRCNE
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 – 201 Guanylyl cyclase-activating protein 1
Domain 87 – 122 EF-hand 3
Binding site 100 – 100
Binding site 102 – 102
Binding site 104 – 104
Binding site 106 – 106
Binding site 111 – 111



Literature citations
Novel GUCA1A mutations suggesting possible mechanisms of pathogenesis in cone, cone-rod, and macular dystrophy patients.
Kamenarova K.; Corton M.; Garcia-Sandoval B.; Fernandez-San Jose P.; Panchev V.; Avila-Fernandez A.; Lopez-Molina M.I.; Chakarova C.; Ayuso C.; Bhattacharya S.S.;
Biomed. Res. Int. 2013:517570-517570(2013)
Cited for: VARIANTS CORD14 PHE-84 AND THR-107; Two retinal dystrophy-associated missense mutations in GUCA1A with distinct molecular properties result in a similar aberrant regulation of the retinal guanylate cyclase.
Marino V.; Scholten A.; Koch K.W.; Dell'Orco D.;
Hum. Mol. Genet. 24:6653-6666(2015)
Cited for: CHARACTERIZATION OF VARIANTS CORD14 PHE-84 AND THR-107;
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.