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Crystal structure of ALPHAT183V mutant of tryptophan synthase from salmonella typhimurium

Analyse Crystal structure of ALPHAT183V mutant of tryptophan synthase from salmonella… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1K8X
Type
protein
Length
640 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Tryptophan synthase, alpha protein; Tryptophan synthase, beta protein
EC
4.2.1.20
UniProt
P00929, P0A2K1
Ligands
PLP, NA
Pockets
6 · best druggability 0.73

Structure

x-ray diffraction · 2 distinct chains · 48% helix, 19% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ATryptophan synthase, alpha protein (EC 4.2.1.20)protein24951% helix, 14% strandP00929
BTryptophan synthase, beta protein (EC 4.2.1.20)protein39146% helix, 22% strandP0A2K1

Ligands and binding sites

  • 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

6 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13180.730.8660PLP
22890.640.8137empty
3880.400.7715empty
4670.370.7821empty
5560.370.8019empty

Interfaces

1 interface between chains.

  • A–B · 1341 Ų buried · 27 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 1 cofactor (pyridoxal phosphate Schiff base).

Compared structures

  • 1K8X · Crystal Structure Of AlphaT183V Mutant Of Tryptophan Synthase From Salmonella Typhimurium · 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

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