Research workbench
X-ray structure of the entire lipid-containing bacteriophage PM2
Analyse X-ray structure of the entire lipid-containing bacteriophage PM2 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 2W0C
- Type
- protein
- Length
- 3,424 residues
- Chains
- 16
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Major capsid protein P2; Protein 2; Protein P3; Protein P6
- UniProt
- P15794, Q9XJR3, Q9XJR6, Q9XJR1
- Ligands
- CA
- Pockets
- 20 · best druggability 0.85
Structure
x-ray diffraction · 7 distinct chains · 28% helix, 28% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, B, C, D, E, F, G, H, I, J | Major capsid protein P2 | protein | 269 | 12% helix, 47% strand | P15794 |
| L | Protein 2 | protein | 335 | 9% helix, 43% strand | Q9XJR3 |
| P | Protein P3 | protein | 65 | 42% helix, 2% strand | Q9XJR6 |
| Q | Protein P3 | protein | 60 | 47% helix, 3% strand | Q9XJR6 |
| R | Protein P3 | protein | 63 | 44% helix, 6% strand | Q9XJR6 |
| S | Protein P3 | protein | 84 | 70% helix, 5% strand | Q9XJR6 |
| T | Protein P6 | protein | 127 | 63% helix, 0% strand | Q9XJR1 |
Ligands and binding sites
- CA · Calcium ion · metal · 11 copies · chains A, B, C, Q, D, E, R, F, G, P, H, I, S, J, L
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 | 615 | 0.85 | 0.90 | 96 | empty |
| 2 | 990 | 0.85 | 0.86 | 93 | empty |
| 3 | 757 | 0.78 | 0.82 | 54 | empty |
| 4 | 194 | 0.74 | 0.91 | 28 | empty |
| 5 | 213 | 0.74 | 0.90 | 30 | empty |
Interfaces
41 interfaces between chains.
- E–R · 1449 Ų buried · 21 hydrogen bonds · protein-protein
- C–Q · 1286 Ų buried · 12 hydrogen bonds · protein-protein
- D–E · 1223 Ų buried · 20 hydrogen bonds · protein-protein
- I–J · 1220 Ų buried · 20 hydrogen bonds · protein-protein
- D–F · 1218 Ų buried · 20 hydrogen bonds · protein-protein
Compared structures
- 2W0C · X-ray structure of the entire lipid-containing bacteriophage PM2 · the same entry in another collection · chain A against A, 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 P15794
- Every structure of UniProt Q9XJR3
- Every structure of UniProt Q9XJR6
- Every structure of UniProt Q9XJR1
- Elsewhere: RCSB PDB 2W0C · PDBe 2W0C · UniProt P15794 · UniProt Q9XJR3 · UniProt Q9XJR6 · UniProt Q9XJR1
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