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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot Q05066: Variant p.Pro108Arg

Sex-determining region Y protein
Gene: SRY
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Variant information Variant position: help 108 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 Proline (P) to Arginine (R) at position 108 (P108R, p.Pro108Arg). 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 (P) to large size and basic (R) 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 SRXY1. Any additional useful information about the variant.


Sequence information Variant position: help 108 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 204 The length of the canonical sequence.
Location on the sequence: help SEISKQLGYQWKMLTEAEKW P FFQEAQKLQAMHREKYPNYK 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                         SEISKQLGYQWKMLTEAEKWPFFQEAQKLQAMHREKYPNYK

Gorilla                       SEISKQLGYQWKMLTEAEKWPFFQEAQKLQAMHREKYPNYK

                              SEISKQLGYQWKMLTEAEKWPFFEEAQRLQAMHREKYPDYK

Rhesus macaque                SEISKQLGYQWKMLTEADKWPFFQEAQKLQAMHREKYPNYK

Chimpanzee                    SEISKQLGYQWKMLTEAEKWPFFQEAQKLQAMHREKYPNYK

Mouse                         TEISKQLGCRWKSLTEAEKRPFFQEAQRLKILHREKYPNYK

Rat                           SEISKHLGYQWKSLTEAEKRPFFQEAQRLKTLHREKYPNYK

Pig                           SEISKWLGCKWKMLTEAEKRPFFEEAQRLQAVHRDKYPGYK

Bovine                        SDISKQLGYEWKRLTDAEKRPFFEEAQRLLAIHRDKYPGYK

Goat                          SEISKQLGYEWKRLTDAEKRPFFEEAQRLLAIHRDKYPGYK

Sheep                         SEISKQLGYEWKRLTDAEKRPFFEEAQRLLAIHRDKYPGYK

Cat                           SEISKQLGYQWKMLTQAEKWPFFEEAQRLQALHREKYPGYR

Horse                         SEISKRLGCQWKMLTEAEKLPFFEEAQRLRAMHQEKYPDYK
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 – 204 Sex-determining region Y protein
DNA binding 60 – 128 HMG box
Region 59 – 136 Sufficient for interaction with KPNB1
Region 107 – 139 Sufficient for interaction with EP300
Mutagenesis 115 – 115 K -> R. Does not abolish acetylation activity.
Mutagenesis 123 – 123 K -> R. Does not abolish acetylation.
Mutagenesis 128 – 128 K -> R. Does not abolish acetylation.
Helix 103 – 118



Literature citations
Another mutation within the HMG-box of the SRY gene associated with Swyer syndrome.
Jakubiczka S.; Bettecken T.; Stumm M.; Neulen J.; Wieacker P.;
Cited for: VARIANT SRXY1 ARG-108;
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.