UniProtKB/Swiss-Prot P36957: Variant p.Pro213Ala

Dihydrolipoyllysine-residue succinyltransferase component of 2-oxoglutarate dehydrogenase complex, mitochondrial
Gene: DLST
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Variant information Variant position:

213 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Type of variant:

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:

From Proline (P) to Alanine (A) at position 213 (P213A, p.Pro213Ala). 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 medium size and hydrophobic (P) to small size and hydrophobic (A) The physico-chemical property of the reference and variant residues and the change implicated.
BLOSUM score:

-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

Sequence information Variant position:

213 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length:

453 The length of the canonical sequence.
Location on the sequence:

PPSGKPVSAVKPTVAPPLAE P GAGKGLRSEHREKMNRMRQR 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                         P----PSGKPVSAVKPTVAPPLAEPGAGK--GLRSEHREKMNRMRQR

Mouse                         P----PSSKPVSAIKPTAAPPLAEAGAAK--GLRSEHREKM

Rat                           P----PSSKPVSAIKPTAAPPLAEAGAAK--GLRSEHREKM

Pig                           P----LTSKPVSAVKPTAAPPVAEPGAVK--GLRAEHREKM

Bovine                        P----LTSKPVSAVKPTAAPPRAEAGAGV--GLRSEHREKM

Slime mold                    ---------PKSTTTTTSTGP-------------SETRVKM

Baker's yeast                 --------QPKKTVSKAQEPPVASNSFTP--FPRTETRVKM

Fission yeast                 PEFSSPKPKPAKSEPVKQSKPKATETARPSSFSRNEDRVKM

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.

Type	Positions	Description
Chain	68 – 453	Dihydrolipoyllysine-residue succinyltransferase component of 2-oxoglutarate dehydrogenase complex, mitochondrial
Region	152 – 225	Disordered

Literature citations
Human dihydrolipoamide succinyltransferase: cDNA cloning and localization on chromosome 14q24.2-q24.3.
Nakano K.; Matsuda S.; Sakamoto T.; Takase C.; Nakagawa S.; Ohta S.; Ariyama T.; Inazawa J.; Abe T.; Miyata T.;
Biochim. Biophys. Acta 1216:360-368(1993)
Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 1); VARIANT ALA-213; Isolation, characterization and structural organization of the gene and pseudogene for the dihydrolipoamide succinyltransferase component of the human 2-oxoglutarate dehydrogenase complex.
Nakano K.; Takase C.; Sakamoto T.; Nakagawa S.; Inazawa J.; Ohta S.; Matuda S.;
Eur. J. Biochem. 224:179-189(1994)
Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA]; VARIANT ALA-213;

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.