MolNFT v1 · #93827 · protein
The crystal structure of maf protein of bacillus subtilis
4HEB · Septum formation protein maf: “The crystal structure of maf protein of bacillus subtilis”. X-ray diffraction, 1 ligand (UNX), 4 pockets (best druggability 0.54). MolNFT v1 #93827 on GenesisL1: 3D structure, binding sites and pockets…
- PDB
- 4HEB
- Type
- protein
- Length
- 365 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Septum formation protein maf
- UniProt
- Q02169
- Ligands
- UNX
- Pockets
- 4 · best druggability 0.54
Structure
x-ray diffraction · 2 distinct chains · 38% helix, 27% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Septum formation protein maf | protein | 182 | 36% helix, 27% strand | Q02169 |
| B | Septum formation protein maf | protein | 183 | 39% helix, 27% strand | Q02169 |
Ligands and binding sites
- UNX · Unknown atom or ion · ion · 31 copies · chains A, B
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
4 pockets found on a 1 Å grid, 1 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 199 | 0.54 | 0.79 | 33 | UNX |
| 2 | 151 | 0.48 | 0.78 | 31 | UNX |
| 3 | 76 | 0.42 | 0.79 | 17 | empty |
| 4 | 68 | 0.36 | 0.77 | 12 | empty |
Interfaces
1 interface between chains.
- A–B · 1176 Ų buried · 21 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 2 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 Q02169
- Elsewhere: RCSB PDB 4HEB · PDBe 4HEB · UniProt Q02169
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