Research workbench
SARS-cov-2-NSP1-40S complex, focused on body
Analyse SARS-cov-2-NSP1-40S complex, focused on body in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 6ZOK
- Type
- protein + RNA
- Length
- 4,202 residues
- Chains
- 22
- Method
- electron microscopy
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- 18S ribosomal RNA; 40S ribosomal protein sa; 40S ribosomal protein S3A; 40S ribosomal…
- EC
- 3.4.19.12, 3.4.22.-, 3.4.22.69, 2.7.7.48, 3.6.4.12, 3.6.4.13, 3.1.13.-, 3.1.-.-, 2.1.1.-
- UniProt
- P08865, P61247, P15880, P62701, P62753, P62081, P62241, P46781, P62280, P62277, P62263, P08708, P63220, P62244, P62266, P62847, P62854, P42677, P62861, P0DTD1, P62945
- Ligands
- MG, ZN
- Pockets
- 20 · best druggability 0.88
Structure
electron microscopy · 22 distinct chains · 31% helix, 23% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| 2 | 18S ribosomal RNA | rna | 1232 | — | — |
| A | 40S ribosomal protein sa | protein | 216 | 39% helix, 14% strand | P08865 |
| B | 40S ribosomal protein S3A | protein | 213 | 29% helix, 35% strand | P61247 |
| C | 40S ribosomal protein S2 | protein | 218 | 33% helix, 27% strand | P15880 |
| E | 40S ribosomal protein S4, X isoform | protein | 262 | 18% helix, 33% strand | P62701 |
| G | 40S ribosomal protein S6 | protein | 230 | 28% helix, 24% strand | P62753 |
| H | 40S ribosomal protein S7 | protein | 186 | 41% helix, 23% strand | P62081 |
| I | 40S ribosomal protein S8 | protein | 205 | 31% helix, 25% strand | P62241 |
| J | 40S ribosomal protein S9 | protein | 180 | 51% helix, 6% strand | P46781 |
| L | 40S ribosomal protein S11 | protein | 151 | 7% helix, 32% strand | P62280 |
| N | 40S ribosomal protein S13 | protein | 149 | 58% helix, 0% strand | P62277 |
| O | 40S ribosomal protein S14 | protein | 135 | 25% helix, 25% strand | P62263 |
| R | 40S ribosomal protein S17 | protein | 51 | 18% helix, 12% strand | P08708 |
| V | 40S ribosomal protein S21 | protein | 83 | 20% helix, 27% strand | P63220 |
| W | 40S ribosomal protein S15A | protein | 129 | 32% helix, 27% strand | P62244 |
| X | 40S ribosomal protein S23 | protein | 141 | 26% helix, 29% strand | P62266 |
| Y | 40S ribosomal protein S24 | protein | 124 | 35% helix, 29% strand | P62847 |
| a | 40S ribosomal protein S26 | protein | 101 | 16% helix, 23% strand | P62854 |
| b | 40S ribosomal protein S27 | protein | 82 | 7% helix, 27% strand | P42677 |
| e | 40S ribosomal protein S30 | protein | 56 | 23% helix, 0% strand | P62861 |
| j | Non-structural protein 1 (EC 3.4.19.12, 3.4.22.-, 3.4.22.69, 2.7.7.48, 3.6.4.12, 3.6.4.13, 3.1.13.-, 3.1.-.-, 2.1.1.-) | protein | 33 | 64% helix, 0% strand | P0DTD1 |
| h | 60S ribosomal protein L41 | protein | 25 | 72% helix, 0% strand | P62945 |
Ligands and binding sites
- MG · Magnesium ion · metal · 109 copies · chains 2, a, h, j, N, E, X, I, G, O, L
- ZN · Zinc ion · metal · chains a
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
20 pockets found on a 1 Å grid, 20 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 1146 | 0.88 | 0.90 | 126 | MG |
| 2 | 924 | 0.87 | 0.90 | 72 | empty |
| 3 | 914 | 0.86 | 0.88 | 107 | MG |
| 4 | 1051 | 0.85 | 0.87 | 82 | MG |
| 5 | 1089 | 0.85 | 0.87 | 83 | MG |
Interfaces
56 interfaces between chains.
- 2–G · 5130 Ų buried · 116 hydrogen bonds · protein-nucleic
- 2–I · 4240 Ų buried · 92 hydrogen bonds · protein-nucleic
- 2–E · 3724 Ų buried · 65 hydrogen bonds · protein-nucleic
- 2–J · 3568 Ų buried · 66 hydrogen bonds · protein-nucleic
- 2–X · 3307 Ų buried · 73 hydrogen bonds · protein-nucleic
Modifications
Observed in the structure: 1 disulfide (disulfide).
Compared structures
- 6ZOK · SARS-CoV-2-Nsp1-40S complex, focused on body · the same entry in another collection · chain I against I, TM-score 1.00
Analyse
- Open in the research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides and crosslinks on the 3D structure
- Every structure of UniProt P08865
- Every structure of UniProt P61247
- Every structure of UniProt P15880
- Every structure of UniProt P62701
- Every structure of UniProt P62753
- Every structure of UniProt P62081
- Every structure of UniProt P62241
- Every structure of UniProt P46781
- Every structure of UniProt P62280
- Every structure of UniProt P62277
- Every structure of UniProt P62263
- Every structure of UniProt P08708
- Every structure of UniProt P63220
- Every structure of UniProt P62244
- Every structure of UniProt P62266
- Every structure of UniProt P62847
- Every structure of UniProt P62854
- Every structure of UniProt P42677
- Every structure of UniProt P62861
- Every structure of UniProt P0DTD1
- Every structure of UniProt P62945
- Elsewhere: RCSB PDB 6ZOK · PDBe 6ZOK · UniProt P08865 · UniProt P61247 · UniProt P15880 · UniProt P62701 · UniProt P62753 · UniProt P62081 · UniProt P62241 · UniProt P46781 · UniProt P62280 · UniProt P62277 · UniProt P62263 · UniProt P08708 · UniProt P63220 · UniProt P62244 · UniProt P62266 · UniProt P62847 · UniProt P62854 · UniProt P42677 · UniProt P62861 · UniProt P0DTD1 · UniProt P62945
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