Structural Basis for Substrate Recognition by the Ankyrin Repeat Domain of Human DHHC17 Palmitoyltransferase. 2017

Raffaello Verardi, and Jin-Sik Kim, and Rodolfo Ghirlando, and Anirban Banerjee
Unit on Structural and Chemical Biology of Membrane Proteins, Cell Biology and Neurobiology Branch, National Institute of Child Health and Human Development, National Institutes of Health, 35A Convent Drive, Bethesda, MD 20892, USA.

DHHC enzymes catalyze palmitoylation, a major post-translational modification that regulates a number of key cellular processes. There are up to 24 DHHCs in mammals and hundreds of substrate proteins that get palmitoylated. However, how DHHC enzymes engage with their substrates is still poorly understood. There is currently no structural information about the interaction between any DHHC enzyme and protein substrates. In this study we have investigated the structural and thermodynamic bases of interaction between the ankyrin repeat domain of human DHHC17 (ANK17) and Snap25b. We solved a high-resolution crystal structure of the complex between ANK17 and a peptide fragment of Snap25b. Through structure-guided mutagenesis, we discovered key residues in DHHC17 that are critically important for interaction with Snap25b. We further extended our finding by showing that the same residues are also crucial for the interaction of DHHC17 with Huntingtin, one of its most physiologically relevant substrates.

UI MeSH Term Description Entries
D008958 Models, Molecular Models used experimentally or theoretically to study molecular shape, electronic properties, or interactions; includes analogous molecules, computer-generated graphics, and mechanical structures. Molecular Models,Model, Molecular,Molecular Model
D009154 Mutation Any detectable and heritable change in the genetic material that causes a change in the GENOTYPE and which is transmitted to daughter cells and to succeeding generations. Mutations
D009419 Nerve Tissue Proteins Proteins, Nerve Tissue,Tissue Proteins, Nerve
D010168 Palmitates Salts and esters of the 16-carbon saturated monocarboxylic acid--palmitic acid. Hexadecanoates,Palmitate
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000071058 Huntingtin Protein A protein that is highly expressed in the nervous system as well as other tissues; its size and structure vary due to polymorphisms. Expanded CAG TRINUCLEOTIDE REPEATS have been identified in the Huntingtin (HD) Gene of patients with HUNTINGTON DISEASE and are associated with abnormal PROTEIN AGGREGATES. Huntingtin interacts with proteins involved in a variety of gene expression and cellular processes; it is also essential for embryonic development. Huntington Disease Protein,IT15 Protein
D000072417 Protein Domains Discrete protein structural units that may fold independently of the rest of the protein and have their own functions. Peptide Domain,Protein Domain,Domain, Peptide,Domain, Protein,Domains, Peptide,Domains, Protein,Peptide Domains
D000217 Acyltransferases Enzymes from the transferase class that catalyze the transfer of acyl groups from donor to acceptor, forming either esters or amides. (From Enzyme Nomenclature 1992) EC 2.3. Acyltransferase
D001665 Binding Sites The parts of a macromolecule that directly participate in its specific combination with another molecule. Combining Site,Binding Site,Combining Sites,Site, Binding,Site, Combining,Sites, Binding,Sites, Combining
D013379 Substrate Specificity A characteristic feature of enzyme activity in relation to the kind of substrate on which the enzyme or catalytic molecule reacts. Specificities, Substrate,Specificity, Substrate,Substrate Specificities

Related Publications

Raffaello Verardi, and Jin-Sik Kim, and Rodolfo Ghirlando, and Anirban Banerjee
May 2010, Blood,
Raffaello Verardi, and Jin-Sik Kim, and Rodolfo Ghirlando, and Anirban Banerjee
January 2005, Nucleic acids symposium series (2004),
Raffaello Verardi, and Jin-Sik Kim, and Rodolfo Ghirlando, and Anirban Banerjee
November 2016, Genes & development,
Raffaello Verardi, and Jin-Sik Kim, and Rodolfo Ghirlando, and Anirban Banerjee
June 2006, Journal of molecular biology,
Raffaello Verardi, and Jin-Sik Kim, and Rodolfo Ghirlando, and Anirban Banerjee
October 2007, Molecular cell,
Raffaello Verardi, and Jin-Sik Kim, and Rodolfo Ghirlando, and Anirban Banerjee
May 2024, Journal of the American Chemical Society,
Raffaello Verardi, and Jin-Sik Kim, and Rodolfo Ghirlando, and Anirban Banerjee
November 2015, Genes & development,
Raffaello Verardi, and Jin-Sik Kim, and Rodolfo Ghirlando, and Anirban Banerjee
January 2022, Biochemical and biophysical research communications,
Raffaello Verardi, and Jin-Sik Kim, and Rodolfo Ghirlando, and Anirban Banerjee
June 2021, Nature communications,
Raffaello Verardi, and Jin-Sik Kim, and Rodolfo Ghirlando, and Anirban Banerjee
June 2023, Nature structural & molecular biology,
Copied contents to your clipboard!