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Theoretical Model: The protein structure described on this page was determined theoretically, and hence should be interpreted with caution.

MOLECULAR DOCKING MODEL OF SARS CORONAVIRUS SPIKE PROTEIN S1 SUBUNIT WITH ITS RECEPTOR, ACE2

spinqualitylabelsall models 1xjp Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image   Print3D Structural highlights For a guided tour on the structure components use FirstGlance. Resources: FirstGlance, PDBsum Publication Abstract from PubMed The exact residues within severe acute respiratory syndrome coronavirus (SARS-CoV) S1 protein and its receptor, human ACE2, involved in their interaction still remain largely undetermined. Identification of exact amino acid residues that are crucial for the interaction of S1 with ACE2 could provide working hypotheses for experimental studies and might be helpful for the development of antiviral inhibitor. In this paper, a molecular docking model of SARS-CoV S1 protein in complex with human ACE2 was constructed. The interacting residue pairs within this complex model and their contact types were also identified. Our model, supported by significant biochemical evidence, suggested receptor-binding residues were concentrated in two segments of S1 protein. In contrast, the interfacial residues in ACE2, though close to each other in tertiary structure, were found to be widely scattered in the primary sequence. In particular, the S1 residue ARG453 and ACE2 residue LYS341 might be the key residues in the complex formation. A molecular docking model of SARS-CoV S1 protein in complex with its receptor, human ACE2.,Zhang Y, Zheng N, Hao P, Cao Y, Zhong Y Comput Biol Chem. 2005 Jun;29(3):254-7. PMID:15979045 From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

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