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Crystal structure of the mycobacterum abscessus esxef (MAB_3112- MAB_3113) complex
Analyse Crystal structure of the mycobacterum abscessus esxef (MAB_3112- MAB_3113)… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 4I0X
- Type
- protein
- Length
- 923 residues
- Chains
- 12
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Esat-6-like protein MAB_3112; Esat-6-like protein MAB_3113
- UniProt
- B1MD68, B1MD69
- Ligands
- SO4
- Pockets
- 8 · best druggability 0.60
Structure
x-ray diffraction · 11 distinct chains · 88% helix, 0% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, C | Esat-6-like protein MAB_3112 | protein | 75 | 91% helix, 0% strand | B1MD68 |
| B | Esat-6-like protein MAB_3113 | protein | 83 | 88% helix, 0% strand | B1MD69 |
| D | Esat-6-like protein MAB_3113 | protein | 83 | 84% helix, 0% strand | B1MD69 |
| E | Esat-6-like protein MAB_3112 | protein | 67 | 88% helix, 0% strand | B1MD68 |
| F | Esat-6-like protein MAB_3113 | protein | 85 | 84% helix, 0% strand | B1MD69 |
| G | Esat-6-like protein MAB_3112 | protein | 68 | 91% helix, 0% strand | B1MD68 |
| H | Esat-6-like protein MAB_3113 | protein | 76 | 89% helix, 0% strand | B1MD69 |
| I | Esat-6-like protein MAB_3112 | protein | 76 | 87% helix, 0% strand | B1MD68 |
| J | Esat-6-like protein MAB_3113 | protein | 76 | 91% helix, 0% strand | B1MD69 |
| K | Esat-6-like protein MAB_3112 | protein | 77 | 86% helix, 0% strand | B1MD68 |
| L | Esat-6-like protein MAB_3113 | protein | 82 | 88% helix, 0% strand | B1MD69 |
Ligands and binding sites
- SO4 · Sulfate ion · ion · chains B, D
- BME · Beta-mercaptoethanol · additive · chains B, H
- GOL · Glycerol · additive · chains C, J
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
8 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 230 | 0.60 | 0.81 | 37 | empty |
| 2 | 275 | 0.59 | 0.79 | 36 | empty |
| 3 | 189 | 0.46 | 0.75 | 34 | GOL |
| 4 | 68 | 0.38 | 0.79 | 17 | empty |
| 5 | 90 | 0.35 | 0.75 | 16 | empty |
Interfaces
20 interfaces between chains.
- K–L · 1799 Ų buried · 10 hydrogen bonds · protein-protein
- A–B · 1752 Ų buried · 12 hydrogen bonds · protein-protein
- C–D · 1740 Ų buried · 9 hydrogen bonds · protein-protein
- I–J · 1694 Ų buried · 7 hydrogen bonds · protein-protein
- G–H · 1662 Ų buried · 10 hydrogen bonds · protein-protein
Compared structures
- 4I0X · Crystal structure of the Mycobacterum abscessus EsxEF (Mab_3112-Mab_3113) complex · 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 B1MD68
- Every structure of UniProt B1MD69
- Elsewhere: RCSB PDB 4I0X · PDBe 4I0X · UniProt B1MD68 · UniProt B1MD69
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