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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot P40926: Variant p.Pro207Leu

Malate dehydrogenase, mitochondrial
Gene: MDH2
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Variant information Variant position: help 207 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 Leucine (L) at position 207 (P207L, p.Pro207Leu). 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 Similar physico-chemical property. Both residues are medium size and hydrophobic. 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
Variant description: help In DEE51; decreased protein abundance; strong decrease in malate dehydrogenase activity; severe defects in aerobic respiration, when assayed in a heterologous system. Any additional useful information about the variant.
Other resources: help Links to websites of interest for the variant.


Sequence information Variant position: help 207 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 338 The length of the canonical sequence.
Location on the sequence: help LDPARVNVPVIGGHAGKTII P LISQCTPKVDFPQDQLTALT 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                         LDPARVNVPVIGGHAGKTIIPLISQCTPKVDFPQDQLTALT

Mouse                         LDPARVNVPVIGGHAGKTIIPLISQCTPKVDFPQDQLATLT

Rat                           LDPARVNVPVIGGHAGKTIIPLISQCTPKVDFPQDQLATLT

Pig                           LDPARVSVPVIGGHAGKTIIPLISQCTPKVDFPQDQLSTLT

Bovine                        LDPARVNVPVIGGHAGKTIIPLISQCTPKVEFPQDQLTTLT

Cat                           LDPARVNVPVIGGHAGKTIIPLISQCTPKVDLPQDQLTAVT

Caenorhabditis elegans        HDASKTVVPVVGGHAGITIIPLLSQVKPSTKFSEEEISKLT

Baker's yeast                 TDPTQERVNVIGGHSGITIIPLISQTNHKL-MSDDKRHELI

Fission yeast                 GKAELLHIPVVGGHSGATIVPLLSQGG--VELTGEKRDALI
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 25 – 338 Malate dehydrogenase, mitochondrial
Active site 200 – 200 Proton acceptor
Modified residue 203 – 203 N6-succinyllysine
Modified residue 215 – 215 N6-acetyllysine; alternate
Modified residue 215 – 215 N6-succinyllysine; alternate
Beta strand 205 – 207



Literature citations
Mutations in MDH2, encoding a Krebs cycle enzyme, cause early-onset severe encephalopathy.
Ait-El-Mkadem S.; Dayem-Quere M.; Gusic M.; Chaussenot A.; Bannwarth S.; Francois B.; Genin E.C.; Fragaki K.; Volker-Touw C.L.; Vasnier C.; Serre V.; van Gassen K.L.; Lespinasse F.; Richter S.; Eisenhofer G.; Rouzier C.; Mochel F.; De Saint-Martin A.; Abi Warde M.T.; de Sain-van der Velde M.G.; Jans J.J.; Amiel J.; Avsec Z.; Mertes C.; Haack T.B.; Strom T.; Meitinger T.; Bonnen P.E.; Taylor R.W.; Gagneur J.; van Hasselt P.M.; Roetig A.; Delahodde A.; Prokisch H.; Fuchs S.A.; Paquis-Flucklinger V.;
Am. J. Hum. Genet. 100:151-159(2017)
Cited for: INVOLVEMENT IN DEE51; VARIANTS DEE51 ARG-37; LEU-133 AND LEU-207; CHARACTERIZATION OF VARIANTS DEE51 LEU-133 AND LEU-207; CATALYTIC ACTIVITY;
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.