MolNFT v1 · #72029 · protein
Crystal structure of NMB1681 from neisseria meningitidis MC58, a fino- like RNA chaperone
3MW6 · Uncharacterized protein NMB1681: “Crystal structure of NMB1681 from neisseria meningitidis MC58, a fino- like RNA chaperone”. X-ray diffraction, 10 pockets (best druggability 0.60). MolNFT v1 #72029 on GenesisL1: 3D structure…
- PDB
- 3MW6
- Type
- protein
- Length
- 681 residues
- Chains
- 6
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Uncharacterized protein NMB1681
- UniProt
- Q9JY98
- Pockets
- 10 · best druggability 0.60
Structure
x-ray diffraction · 6 distinct chains · 63% helix, 7% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Uncharacterized protein NMB1681 | protein | 122 | 66% helix, 7% strand | Q9JY98 |
| B | Uncharacterized protein NMB1681 | protein | 94 | 59% helix, 9% strand | Q9JY98 |
| C | Uncharacterized protein NMB1681 | protein | 112 | 63% helix, 9% strand | Q9JY98 |
| D | Uncharacterized protein NMB1681 | protein | 118 | 59% helix, 7% strand | Q9JY98 |
| E | Uncharacterized protein NMB1681 | protein | 119 | 63% helix, 7% strand | Q9JY98 |
| F | Uncharacterized protein NMB1681 | protein | 116 | 69% helix, 7% strand | Q9JY98 |
Ligands and binding sites
- GOL · Glycerol · additive · chains C
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
10 pockets found on a 1 Å grid, 4 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 268 | 0.60 | 0.79 | 23 | empty |
| 2 | 288 | 0.59 | 0.78 | 25 | empty |
| 3 | 306 | 0.58 | 0.77 | 50 | empty |
| 4 | 216 | 0.51 | 0.76 | 31 | empty |
| 5 | 148 | 0.48 | 0.77 | 21 | empty |
Interfaces
6 interfaces between chains.
- D–E · 728 Ų buried · 6 hydrogen bonds · protein-protein
- A–B · 653 Ų buried · 10 hydrogen bonds · protein-protein
- E–F · 624 Ų buried · 7 hydrogen bonds · protein-protein
- C–D · 601 Ų buried · 6 hydrogen bonds · protein-protein
- B–C · 579 Ų buried · 4 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 14 modified (engineered).
Compared structures
- 3MW6 · Crystal structure of NMB1681 from Neisseria meningitidis MC58, a FinO-like RNA chaperone · 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 Q9JY98
- Elsewhere: RCSB PDB 3MW6 · PDBe 3MW6 · UniProt Q9JY98
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