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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot Q96HY7: Variant p.Tyr272Asp

2-oxoadipate dehydrogenase complex component E1
Gene: DHTKD1
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Variant information Variant position: help 272 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Type of variant: help 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: help From Tyrosine (Y) to Aspartate (D) at position 272 (Y272D, p.Tyr272Asp). 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 large size and aromatic (Y) to medium size and acidic (D) The physico-chemical property of the reference and variant residues and the change implicated.
BLOSUM score: help -3 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: help Links to websites of interest for the variant.


Sequence information Variant position: help 272 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 919 The length of the canonical sequence.
Location on the sequence: help PENFSATGDVLSHLTSSVDL Y FGAHHPLHVTMLPNPSHLEA 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                         PENFSATGDVLSHLTSSVDLYF-GAHHPLHVTMLPNPSHLEA

Mouse                         PENVATIGDVLSHLTSSVDLDF-GAHQPLHVTMLPNPSHLE

Rat                           PENVAAIGDVLSHLTSSVDLDF-GAHRPLHVTMLPNPSHLE

Xenopus laevis                PENSPSIGDVLSHLTSSVDLDF-GSHRPLHVTMLPNPSHLE

Zebrafish                     PEHSPSIGDVLSHLTSTVELDF-GAGHPLHVTMLPNPSHLE

Caenorhabditis elegans        PESADAAGDVLSHLVSSFDYK--GSEGNVHVTMLPNPSHLE

Drosophila                    SEDIEAMSDVISHFHVSEQLKILGKK--LSFSMVRNPSHLE

Slime mold                    SEGILGVGDVTSHIAVSTDLQFNNNKESVHVSLIHNPSHLE

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
Beta strand 268 – 283



Literature citations
The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).
The MGC Project Team;
Genome Res. 14:2121-2127(2004)
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA]; VARIANTS LEU-20; ASP-272; LEU-308 AND MET-607; Prediction of the coding sequences of unidentified human genes. XVIII. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro.
Nagase T.; Kikuno R.; Nakayama M.; Hirosawa M.; Ohara O.;
DNA Res. 7:273-281(2000)
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] OF 1-886; VARIANTS LEU-20; ASP-272 AND MET-607;
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.