MolNFT v1 · #77468 · protein
Crystal structure of the fimd usher bound to its cognate FIMC:FIMH substrate
3RFZ · Type 1 fimbrial adhesin: “Crystal structure of the fimd usher bound to its cognate FIMC:FIMH substrate”. X-ray diffraction, 1 ligand (SO4), 20 pockets (best druggability 0.90). MolNFT v1 #77468 on GenesisL1: 3D structure, binding…
- PDB
- 3RFZ
- Type
- protein
- Length
- 2,516 residues
- Chains
- 6
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Type 1 fimbrial adhesin; Outer membrane usher protein, type 1 fimbrial synthesis…
- UniProt
- Q5D223, C6UL88, P59590
- Ligands
- SO4
- Pockets
- 20 · best druggability 0.90
Structure
x-ray diffraction · 4 distinct chains · 6% helix, 54% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, D | Type 1 fimbrial adhesin | protein | 279 | 2% helix, 51% strand | Q5D223 |
| B | Outer membrane usher protein, type 1 fimbrial synthesis | protein | 778 | 6% helix, 55% strand | C6UL88 |
| C, F | Chaperone protein fimc | protein | 201 | 3% helix, 52% strand | P59590 |
| E | Outer membrane usher protein, type 1 fimbrial synthesis | protein | 778 | 7% helix, 54% strand | C6UL88 |
Ligands and binding sites
- SO4 · Sulfate ion · ion · 2 copies · chains B
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
20 pockets found on a 1 Å grid, 17 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 1029 | 0.90 | 0.92 | 125 | empty |
| 2 | 766 | 0.89 | 0.93 | 110 | empty |
| 3 | 726 | 0.87 | 0.90 | 125 | empty |
| 4 | 389 | 0.82 | 0.90 | 65 | empty |
| 5 | 814 | 0.81 | 0.84 | 98 | empty |
Interfaces
7 interfaces between chains.
- D–E · 3051 Ų buried · 43 hydrogen bonds · protein-protein
- A–B · 2979 Ų buried · 48 hydrogen bonds · protein-protein
- D–F · 1749 Ų buried · 32 hydrogen bonds · protein-protein
- A–C · 1747 Ų buried · 32 hydrogen bonds · protein-protein
- E–F · 1193 Ų buried · 18 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 7 disulfide (disulfide).
Compared structures
- 3RFZ · Crystal structure of the FimD usher bound to its cognate FimC:FimH substrate · the same entry in another collection · chain F against F, TM-score 1.00
- P59590 · AlphaFold monomer V2.0 prediction for chaperone protein fimc (P59590) · a predicted model of the same protein · chain C against A, TM-score 0.99
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 Q5D223
- Every structure of UniProt C6UL88
- Every structure of UniProt P59590
- Elsewhere: RCSB PDB 3RFZ · PDBe 3RFZ · UniProt Q5D223 · UniProt C6UL88 · UniProt P59590
GL1X is a live explorer of the GenesisL1 blockchain. Turn on JavaScript for search, charts and interactive views.