1.65 A resolution structure of SARS-CoV 3CL protease in complex with inhibitor 7j. Determined by X-ray diffraction at 1.65 Å resolution. Released 12 Aug 2020.
Explore 6W2A in 3D Show helices and sheets RCSB PDB PDBe
6W2A contains 34 α-helices and 40 β-strands across 2 chains. Residue ranges use author residue numbering, as in the PDB file, from PDBe. To see them in 3D, choose the Cartoon representation with Secondary structure coloring: helices, sheets and coils get different colors.
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 7 | 1 | 1 |
| α-helix | 8-9 | 2 | |
| α-helix | 11-14 | 4 | |
| β-strand | 17-22 | 6 | 2 |
| β-strand | 25-32 | 8 | 2 |
| β-strand | 35-39 | 5 | 2 |
| α-helix | 40-43 | 4 | |
| α-helix | 46-50 | 5 | |
| α-helix | 54-59 | 6 | |
| α-helix | 63-65 | 3 | |
| β-strand | 66-70 | 5 | 2 |
| β-strand | 73-75 | 3 | 2 |
| α-helix | 76 | 1 | |
| β-strand | 77-83 | 7 | 2 |
| β-strand | 86-91 | 6 | 2 |
| α-helix | 98-99 | 2 | |
| β-strand | 100-103 | 4 | 3 |
| α-helix | 106-107 | 2 | |
| β-strand | 111-118 | 8 | 3 |
| β-strand | 121-129 | 9 | 3 |
| β-strand | 136 | 1 | 3 |
| β-strand | 148-153 | 6 | 3 |
| β-strand | 156-166 | 11 | 3 |
| β-strand | 172-175 | 4 | 3 |
| α-helix | 180 | 1 | |
| β-strand | 181 | 1 | 3 |
| α-helix | 193-197 | 5 | |
| β-strand | 199 | 1 | 4 |
| α-helix | 201-213 | 13 | |
| α-helix | 227-236 | 10 | |
| β-strand | 239 | 1 | 4 |
| α-helix | 240-243 | 4 | |
| α-helix | 244-249 | 6 | |
| α-helix | 251-257 | 7 | |
| α-helix | 261-274 | 14 | |
| β-strand | 281 | 1 | 5 |
| β-strand | 284 | 1 | 5 |
| α-helix | 293-300 | 8 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 7 | 1 | 3 |
| α-helix | 8-9 | 2 | |
| α-helix | 11-14 | 4 | |
| β-strand | 17-22 | 6 | 6 |
| β-strand | 25-32 | 8 | 6 |
| β-strand | 35-39 | 5 | 6 |
| α-helix | 40-43 | 4 | |
| α-helix | 46-48 | 3 | |
| α-helix | 54-59 | 6 | |
| α-helix | 63-65 | 3 | |
| β-strand | 67-70 | 4 | 6 |
| β-strand | 73-75 | 3 | 6 |
| β-strand | 77-83 | 7 | 6 |
| β-strand | 86-91 | 6 | 6 |
| α-helix | 98-99 | 2 | |
| β-strand | 100-103 | 4 | 1 |
| β-strand | 111-118 | 8 | 1 |
| β-strand | 121-130 | 10 | 1 |
| β-strand | 136 | 1 | 1 |
| β-strand | 148-153 | 6 | 1 |
| β-strand | 156-166 | 11 | 1 |
| β-strand | 172-175 | 4 | 1 |
| α-helix | 180 | 1 | |
| β-strand | 181 | 1 | 1 |
| α-helix | 193-197 | 5 | |
| β-strand | 199 | 1 | 7 |
| α-helix | 201-213 | 13 | |
| α-helix | 227-236 | 10 | |
| β-strand | 239 | 1 | 7 |
| α-helix | 240-243 | 4 | |
| α-helix | 244-249 | 6 | |
| α-helix | 251-257 | 7 | |
| α-helix | 261-274 | 14 | |
| β-strand | 281 | 1 | 8 |
| β-strand | 284 | 1 | 8 |
| α-helix | 293-298 | 6 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Replicase polyprotein 1a | A, B | protein | 310 | Human SARS coronavirus | P0C6U8 |
>6W2A_1 Replicase polyprotein 1a (chains A, B) MHHHHHHSGFRKMAFPSGKVEGCMVQVTCGTTTLNGLWLDDTVYCPRHVICTAEDMLNPN YEDLLIRKSNHSFLVQAGNVQLRVIGHSMQNCLLRLKVDTSNPKTPKYKFVRIQPGQTFS VLACYNGSPSGVYQCAMRPNHTIKGSFLNGSCGSVGFNIDYDCVSFCYMHHMELPTGVHA GTDLEGKFYGPFVDRQTAQAAGTDTTITLNVLAWLYAAVINGDRWFLNRFTTTLNDFNLV AMKYNYEPLTQDHVDILGPLSAQTGIAVLDMCAALKELLQNGMNGRTILGSTILEDEFTP FDVVRQCSGV
| ID | Name | Formula | Copies |
|---|---|---|---|
| VDJ | [4,4-bis(fluoranyl)cyclohexyl]methyl ~{N}-[(2~{S})-1-[[(1~{R},2~{S})-1-[bis(oxi… | C21 H35 F2 N3 O8 S | 2 |
| QYS | (1S,2S)-2-[(N-{[(4,4-difluorocyclohexyl)methoxy]carbonyl}-L-leucyl)amino]-1-hyd… | C21 H35 F2 N3 O8 S | 2 |
3C-like protease inhibitors block coronavirus replication in vitro and improve survival in MERS-CoV-infected mice. Rathnayake, A.D., Zheng, J., Kim, Y. et al. Sci Transl Med (2020) 12. DOI 10.1126/scitranslmed.abc5332 · PubMed
Other PDB entries of the same protein (UniProt P0C6U8), best resolution first:
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