Molecular Docking Performance of Selective Organic Compounds with Target Protein | Zendy

Jacquline Pushparaj | Zendy; Murugan Moorthiraman | Zendy; S. Bharanidharan | Zendy; Rajaram Rajamohan | Zendy

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Molecular Docking Performance of Selective Organic Compounds with Target Protein

Author(s) -

Jacquline Pushparaj,

Murugan Moorthiraman,

S. Bharanidharan,

Rajaram Rajamohan

Publication year - 2021

Publication title -

biointerface research in applied chemistry

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.216

H-Index - 11

ISSN - 2069-5837

DOI - 10.33263/briac114.1241412424

Subject(s) - docking (animal) , chemistry , calmodulin , hydrogen bond , binding site , biochemistry , phenoxazine , receptor , protein–protein interaction , acetylcholinesterase , target protein , enzyme , pharmacology , biology , molecule , gene , medicine , nursing , organic chemistry , phenothiazine

In this article, the docking analysis has been carried out to know some selective compounds' interaction to bind with a targeted protein. There are three approaches have been analyzed here with three different kinds of protein as the target species. They are 2-aminobenzimidazole (2ABZ) with Acetylcholinesterase receptor (AChE), Phenoxazine (POZ) with Penicillin-binding proteins (PBPs) receptor, and Phenothiazines with Calcium/calmodulin-dependent protein kinase IV (CAMK IV) receptor. All three studies showed that the binding is perfect at the binding site and explained with hydrogen bonding interaction via donor-acceptor interactions.

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