MolNFT v1 · #51123 · protein
Crystal structure of the P pilus rod subunit papa
2UY7 · Periplasmid chaperone papd protein: “Crystal structure of the P pilus rod subunit papa”. X-ray diffraction, 1 ligand (SO4), 11 pockets (best druggability 0.66). MolNFT v1 #51123 on GenesisL1: 3D structure, binding sites and pockets…
- PDB
- 2UY7
- Type
- protein
- Length
- 1,484 residues
- Chains
- 8
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Periplasmid chaperone papd protein; Pap fimbrial major pilin protein
- UniProt
- Q1R2W9, P04127
- Ligands
- SO4
- Pockets
- 11 · best druggability 0.66
Structure
x-ray diffraction · 3 distinct chains · 6% helix, 42% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, C, E, G | Periplasmid chaperone papd protein | protein | 216 | 8% helix, 51% strand | Q1R2W9 |
| B, F | Pap fimbrial major pilin protein | protein | 156 | 3% helix, 37% strand | P04127 |
| D, H | Pap fimbrial major pilin protein | protein | 154 | 5% helix, 33% strand | P04127 |
Ligands and binding sites
- SO4 · Sulfate ion · ion · 13 copies · chains A, C, E, G, H
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
11 pockets found on a 1 Å grid, 5 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 276 | 0.66 | 0.82 | 31 | empty |
| 2 | 254 | 0.63 | 0.81 | 27 | empty |
| 3 | 232 | 0.60 | 0.80 | 28 | empty |
| 4 | 306 | 0.60 | 0.78 | 26 | empty |
| 5 | 83 | 0.60 | 0.88 | 20 | empty |
Interfaces
4 interfaces between chains.
- G–H · 2149 Ų buried · 43 hydrogen bonds · protein-protein
- C–D · 2098 Ų buried · 44 hydrogen bonds · protein-protein
- A–B · 2083 Ų buried · 49 hydrogen bonds · protein-protein
- E–F · 2025 Ų buried · 48 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 8 disulfide (disulfide).
Compared structures
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 Q1R2W9
- Every structure of UniProt P04127
- Elsewhere: RCSB PDB 2UY7 · PDBe 2UY7 · UniProt Q1R2W9 · UniProt P04127
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