Research workbench
Crystal structure of HPV58/33/52 chimeric L1 pentamer
Analyse Crystal structure of HPV58/33/52 chimeric L1 pentamer in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 6IGC
- Type
- protein
- Length
- 16,652 residues
- Chains
- 40
- Method
- x-ray diffraction
- Collection
- MolNFT v2 / PDB Bank
- Contract
- 0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
- Owner
- 0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
- Resolution
- 3.5
- Source
- Human papillomavirus type 58
- Molecule
- Major capsid protein L1
- UniProt
- P26535
- Pockets
- 20 · best druggability 0.83
Structure
x-ray diffraction · resolution 3.5 · 13 distinct chains · 15% helix, 39% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Major capsid protein L1 | protein | 420 | 15% helix, 39% strand | P26535 |
| B | Major capsid protein L1 | protein | 413 | 15% helix, 40% strand | P26535 |
| C | Major capsid protein L1 | protein | 416 | 15% helix, 39% strand | P26535 |
| D | Major capsid protein L1 | protein | 416 | 15% helix, 40% strand | P26535 |
| E | Major capsid protein L1 | protein | 414 | 14% helix, 38% strand | P26535 |
| F, e | Major capsid protein L1 | protein | 416 | 15% helix, 40% strand | P26535 |
| G, L, Q, V, a, f, k | Major capsid protein L1 | protein | 414 | 14% helix, 40% strand | P26535 |
| H, M, R, W, b, g, l | Major capsid protein L1 | protein | 415 | 14% helix, 39% strand | P26535 |
| I, S, X, c, h, m | Major capsid protein L1 | protein | 418 | 15% helix, 39% strand | P26535 |
| J, O, T, Y, d, i, n | Major capsid protein L1 | protein | 420 | 15% helix, 39% strand | P26535 |
| K, P, Z, j | Major capsid protein L1 | protein | 415 | 14% helix, 40% strand | P26535 |
| N | Major capsid protein L1 | protein | 416 | 15% helix, 39% strand | P26535 |
| U | Major capsid protein L1 | protein | 414 | 15% helix, 39% strand | P26535 |
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 | 1001 | 0.83 | 0.84 | 93 | empty |
| 2 | 796 | 0.80 | 0.83 | 87 | empty |
| 3 | 1072 | 0.78 | 0.80 | 114 | empty |
| 4 | 297 | 0.78 | 0.89 | 65 | empty |
| 5 | 939 | 0.76 | 0.79 | 83 | empty |
Interfaces
156 interfaces between chains.
- W–X · 3927 Ų buried · 91 hydrogen bonds · protein-protein
- a–d · 3784 Ų buried · 71 hydrogen bonds · protein-protein
- e–g · 3728 Ų buried · 72 hydrogen bonds · protein-protein
- X–Y · 3718 Ų buried · 61 hydrogen bonds · protein-protein
- I–J · 3713 Ų buried · 63 hydrogen bonds · protein-protein
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 P26535
- Elsewhere: RCSB PDB 6IGC · PDBe 6IGC · UniProt P26535
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