Insight into structural and biochemical determinants of substrate specificity of PFI1625c: Correlation analysis of protein-peptide molecular models
| Autor: | Vishal Trivedi, Kimjolly Lhouvum, Vibin Ramakrishnan |
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| Rok vydání: | 2013 |
| Předmět: |
Models
Molecular Plasmodium Molecular model Stereochemistry Molecular Sequence Data Sequence alignment Peptide Molecular Dynamics Simulation Substrate Specificity Residue (chemistry) Peptide Library Materials Chemistry Amino Acid Sequence Physical and Theoretical Chemistry Binding site Peptide library Peptide sequence Spectroscopy chemistry.chemical_classification Binding Sites biology Active site Computer Graphics and Computer-Aided Design Protein Structure Tertiary chemistry Metalloproteases biology.protein Hydrophobic and Hydrophilic Interactions Sequence Alignment Protein Binding |
| Zdroj: | Journal of Molecular Graphics and Modelling. 43:21-30 |
| ISSN: | 1093-3263 |
| DOI: | 10.1016/j.jmgm.2013.03.008 |
| Popis: | Bioinformatics and sequence comparison indicate PFI1625c as a putative metalloprotease present in plasmodium genome. The structure of PFI1625c consists of two domains with nearly identical folding topology. The active site of PFI1625c is located in a large central cavity between the two domains. Substrate binding regions of PFI1625c are lined by E-136, D-140 which provides negatively charged patches whereas F-53 facilitates binding of bulky hydrophobic residues of substrates. Probing PFI1625c active site with 199 different peptides from a combinatorial peptide library indicates preference of PFI1626c toward hydrophobic residue substituted peptides. Correlation analysis of each position of the peptide indicates that Ser 2 is the most crucial residue and no significant improvement was observed until it is mutated to a hydrophobic residue. The peptide P550 (LVIVAKRA) exhibits significantly better interaction within the active site than a template peptide (LSRVAKRA). The molecular dynamic's simulation studies confirms integrity of the complex, with all structures well within the qualitative limit of compactness and stability during the simulation time. There are structural and biochemical differences between PFI1625c with human metalloprotease and these are sufficient enough to allow us to exploit PFI1625c as drug targets. These computationally obtained insights provided clues about substrate selectivity in PFI1625c and it can be used to exploit PFI1625c as a target for future anti-malarial development. |
| Databáze: | OpenAIRE |
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