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. 2020 Aug 3;886:173430. doi: 10.1016/j.ejphar.2020.173430

Table 1.

Structure of viral proteins which were used as a targets for molecular docking with PDB ID (4-character unique identifier of every entry in the Protein Data Bank) and source organism.

Name of the protein and description Source PDB ID Structure of protein
Mpro/3CLpro (Main protease of SARS CoV 2) SARS CoV 2 6Y84 Image 1
The crystal structure of COVID-19 main protease SARS CoV 2 6LU7 Image 2
The crystal structure of COVID-19 main protease in apo form SARS CoV 2 6M03 Image 3
Nsp10 (Plays a crucial role in viral transcription by stimulating both nsp14 3′-5′ exoribonuclease and nsp16 2′-O-methyltransferase activities.)
Nsp 16 (S-adenosylmethionine-dependent (nucleoside-2′-O)-methyltransferase only active in the presence of its activating partner nsp10)
SARS CoV 2 6W75 B
6W75D
6W75 A
6W75D
Image 4
Spike glycoprotein SARS CoV 2 6VSBA
6VSBB
6VSBC
Image 5
SARS protein receptor binding domain SARS CoV 2GHV Image 6
Nsp9 (RNA binding protein of SARS CoV 2) and SARS CoV 2 helicase SARS CoV 2 6W4B Image 7
ADP ribose phosphatase of NSP3 from SARS CoV-2 SARS CoV 2 6VXS Image 8
Angiotensin-converting enzyme 2 (ACE2) receptor (Receptor through which virus enters the cell) Human 6M18B
6M18D
Image 9