Research workbench
Crystal structure of the complex of bacterial tryptophan synthase with the transition state analogue inhibitor 4-(2-hydroxyphenylsulfinyl)- butylphosphonic acid
Analyse Crystal structure of the complex of bacterial tryptophan synthase with the… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 1CW2
- Type
- protein
- Length
- 651 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Tryptophan synthase (alpha chain); Tryptophan synthase (beta chain)
- EC
- 4.2.1.20
- UniProt
- P00929, P0A2K1
- Ligands
- HSP, PLP, NA
- Pockets
- 9 · best druggability 0.80
Structure
x-ray diffraction · 2 distinct chains · 47% helix, 19% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Tryptophan synthase (alpha chain) (EC 4.2.1.20) | protein | 264 | 51% helix, 14% strand | P00929 |
| B | Tryptophan synthase (beta chain) (EC 4.2.1.20) | protein | 387 | 45% helix, 22% strand | P0A2K1 |
Ligands and binding sites
- HSP · 4-(2-hydroxyphenylsulfinyl)-butylphosphonic acid · ligand · chains A
- PLP · Pyridoxal-5'-phosphate · ligand · chains B
- NA · Sodium ion · metal · chains B
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
9 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 131 | 0.80 | 0.98 | 35 | HSP |
| 2 | 236 | 0.74 | 0.89 | 42 | PLP |
| 3 | 88 | 0.43 | 0.79 | 22 | empty |
| 4 | 71 | 0.42 | 0.80 | 16 | empty |
| 5 | 77 | 0.40 | 0.79 | 24 | empty |
Interfaces
1 interface between chains.
- A–B · 1386 Ų buried · 28 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 1 cofactor (pyridoxal phosphate Schiff base).
Compared structures
- 1CW2 · Crystal structure of the complex of bacterial tryptophan synthase with the transition… · the same entry in another collection · chain A against A, TM-score 1.00
- P00929 · AlphaFold monomer V2.0 prediction for tryptophan synthase alpha chain (P00929) · a predicted model of the same protein · chain A 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 P00929
- Every structure of UniProt P0A2K1
- Elsewhere: RCSB PDB 1CW2 · PDBe 1CW2 · UniProt P00929 · UniProt P0A2K1
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