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Crystal structure of ALPHAT183V mutant of tryptophan synthase from salmonella typhimurium with indole glycerol phosphate

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
1KFB
Type
protein
Length
649 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Tryptophan synthase alpha chain; Tryptophan synthase beta chain
UniProt
P00929, P0A2K1
Ligands
IGP, PLP
Pockets
4 · best druggability 0.81

Structure

x-ray diffraction · 2 distinct chains · 50% helix, 19% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ATryptophan synthase alpha chainprotein25553% helix, 15% strandP00929
BTryptophan synthase beta chainprotein39448% helix, 21% strandP0A2K1

Ligands and binding sites

  • IGP · Indole-3-glycerol phosphate · ligand · chains A
  • PLP · Pyridoxal-5'-phosphate · ligand · chains 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, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
17520.810.8482PLP
23800.710.8344IGP
3790.390.7714empty
4720.360.7718empty

Interfaces

1 interface between chains.

  • A–B · 1402 Ų buried · 27 hydrogen bonds · protein-protein

Modifications

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

Compared structures

  • 1KFB · 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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