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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot P49419: Variant p.Pro106Leu

Alpha-aminoadipic semialdehyde dehydrogenase
Gene: ALDH7A1
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Variant information Variant position: help 106 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 106 (P106L, p.Pro106Leu). 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 EPEO4; decreased alpha-aminoadipic semialdehyde dehydrogenase activity. Any additional useful information about the variant.


Sequence information Variant position: help 106 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 539 The length of the canonical sequence.
Location on the sequence: help ADYEETVKKAREAWKIWADI P APKRGEIVRQIGDALREKIQ 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                         ADYEETVKKAREAWKIWADIPAPKRGEIVRQIGDALREKIQ

Mouse                         KDYEETIGKAKKAWNIWADIPAPKRGEIVRKIGDAFREKIQ

Rat                           KDYEETIGKAKKAWNIWADIPAPKRGEIVRKIGDALREKIQ

Bovine                        ADYEETVEKAREAWSIWADVPAPKRGEVVRQIGDALREKIQ

Zebrafish                     AEYEETIQKALDAWKVWADVPAPKRGEIVRQIGEALRRKIK

Caenorhabditis elegans        QDYEIAISEAKKAYNDWCEVPAPRRGEIVRQIGDKLRTQLQ

Slime mold                    EEYETCIQAMLAAKVKWALTPAPRRGEIVRLIGQAMREKIE

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 27 – 539 Alpha-aminoadipic semialdehyde dehydrogenase
Modified residue 94 – 94 N6-acetyllysine; alternate
Modified residue 94 – 94 N6-succinyllysine; alternate



Literature citations
Genotypic and phenotypic spectrum of pyridoxine-dependent epilepsy (ALDH7A1 deficiency).
Mills P.B.; Footitt E.J.; Mills K.A.; Tuschl K.; Aylett S.; Varadkar S.; Hemingway C.; Marlow N.; Rennie J.; Baxter P.; Dulac O.; Nabbout R.; Craigen W.J.; Schmitt B.; Feillet F.; Christensen E.; De Lonlay P.; Pike M.G.; Hughes M.I.; Struys E.A.; Jakobs C.; Zuberi S.M.; Clayton P.T.;
Brain 133:2148-2159(2010)
Cited for: VARIANTS EPEO4 LEU-106; SER-197; GLY-203; LEU-317; ARG-328 AND LEU-476; CHARACTERIZATION OF VARIANTS EPEO4 LEU-106; SER-197; GLY-203; LEU-317; ARG-328 AND LEU-476; FUNCTION; 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.