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Crystal structure of acyl-[acyl-carrier-protein]--udp-N- acetylglucosamine O-acyltransferase from burkholderia thailandensis
Analyse Crystal structure of acyl-[acyl-carrier-protein]--udp-N- acetylglucosamine… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 4EQY
- Type
- protein
- Length
- 1,566 residues
- Chains
- 7
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Acyl-[acyl-carrier-protein]--udp-N-acetylglucosamine O- acyltransferase; His-his-his…
- EC
- 2.3.1.129
- UniProt
- Q2SWY6
- Pockets
- 18 · best druggability 0.71
Structure
x-ray diffraction · 3 distinct chains · 17% helix, 29% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, B, E | Acyl-[acyl-carrier-protein]--udp-N-acetylglucosamine O- acyltransferase (EC 2.3.1.129) | protein | 261 | 17% helix, 29% strand | Q2SWY6 |
| C, F, G | Acyl-[acyl-carrier-protein]--udp-N-acetylglucosamine O- acyltransferase (EC 2.3.1.129) | protein | 260 | 18% helix, 29% strand | Q2SWY6 |
| X | His-his-his peptide | protein | 3 | 0% helix, 0% strand | — |
Pockets
18 pockets found on a 1 Å grid, 16 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 438 | 0.71 | 0.82 | 56 | empty |
| 2 | 67 | 0.68 | 0.95 | 21 | empty |
| 3 | 72 | 0.68 | 0.94 | 22 | empty |
| 4 | 476 | 0.68 | 0.79 | 46 | empty |
| 5 | 444 | 0.67 | 0.79 | 50 | empty |
Interfaces
8 interfaces between chains.
- E–F · 1142 Ų buried · 17 hydrogen bonds · protein-protein
- F–G · 1133 Ų buried · 18 hydrogen bonds · protein-protein
- A–B · 1126 Ų buried · 18 hydrogen bonds · protein-protein
- E–G · 1123 Ų buried · 17 hydrogen bonds · protein-protein
- B–C · 1118 Ų buried · 18 hydrogen bonds · protein-protein
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 Q2SWY6
- Elsewhere: RCSB PDB 4EQY · PDBe 4EQY · UniProt Q2SWY6
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