UniProtKB/Swiss-Prot P24752: Variant p.Ala333Pro

Acetyl-CoA acetyltransferase, mitochondrial
Gene: ACAT1
Chromosomal location: 11q22.3-q23.1
Variant information

Variant position:  333
The position of the amino-acid change on the UniProtKB canonical protein sequence.

Type of variant:  Disease [Disclaimer]
The variants are classified into three categories: Disease, Polymorphism and Unclassified.
  • Disease: Variants have been found in patients and disease-association is reported in literature. However, this classification is not a definitive assessment of variant pathogenicity.
  • Polymorphism: No disease-association has been reported.
  • Unclassified: Variants have been found in patients but disease-association remains unclear.

Residue change:  From Alanine (A) to Proline (P) at position 333 (A333P, p.Ala333Pro).
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 small size and hydrophobic (A) to medium size and hydrophobic (P)
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

Variant description:  In 3KTD; no activity.
Any additional useful information about the variant.



Sequence information

Variant position:  333
The position of the amino-acid change on the UniProtKB canonical protein sequence.

Protein sequence length:  427
The length of the canonical sequence.

Location on the sequence:   VAFADAAVEPIDFPIAPVYA  A SMVLKDVGLKKEDIAMWEVN
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                         VAFADAAVEPIDFPIAPVYAASMVLKDVGLKK-EDIAMWEVN

Mouse                         AAFADAAVDPIDFPLAPAYAVPKVLKYAGLKK-EDIAMWEV

Rat                           AAFADAAVDPIDFPLAPAYAVPKVLKYAGLKK-EDIAMWEV

Bovine                        AAFADAAVEPIDFPLAPAYAVPKVLKDAGLKK-EDITMWEV

Xenopus tropicalis            VAFADAAVDPIDFPIAPAYAVPKLLSEAGLKK-EDIAMWEI

Zebrafish                     VAFADAAVAPIDFPIAPAFAVPKVLKAAGIKK-EDIAMWEI

Baker's yeast                 KGWGEAAHQPADFTWAPSLAVPKALKHAGIEDINSVDYFEF

Fission yeast                 IGWGEAAQDPERFTTSPSLAIPKALKHAGIEA-SQVDYYEI

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.

TypePositionsDescription
Chain 34 – 427 Acetyl-CoA acetyltransferase, mitochondrial
Modified residue 338 – 338 N6-acetyllysine
Alternative sequence 163 – 427 Missing. In isoform 2.
Helix 328 – 340


Literature citations

Characterization of N93S, I312T, and A333P missense mutations in two Japanese families with mitochondrial acetoacetyl-CoA thiolase deficiency.
Fukao T.; Nakamura H.; Song X.-Q.; Nakamura K.; Orii K.E.; Kohno Y.; Kano M.; Yamaguchi S.; Hashimoto T.; Orii T.; Kondo N.;
Hum. Mutat. 12:245-254(1998)
Cited for: VARIANTS 3KTD SER-93; THR-312 AND PRO-333;

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.