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Tryptophan indole-lyase

Analyse Tryptophan indole-lyase in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5W1B
Type
protein
Length
1,864 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Tryptophanase
EC
4.1.99.1
UniProt
P28796
Ligands
K
Pockets
20 · best druggability 0.77

Structure

x-ray diffraction · 1 distinct chain · 44% helix, 16% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, DTryptophanase (EC 4.1.99.1)protein46644% helix, 16% strandP28796

Ligands and binding sites

  • K · Potassium ion · metal · 4 copies · chains A, B, C, D

Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.

Pockets

20 pockets found on a 1 Å grid, 15 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
18410.770.8078empty
28300.770.8074empty
37350.760.8166empty
47860.750.7961empty
5800.730.9725empty

Interfaces

6 interfaces between chains.

  • A–B · 2268 Ų buried · 27 hydrogen bonds · protein-protein
  • C–D · 2231 Ų buried · 28 hydrogen bonds · protein-protein
  • B–D · 1818 Ų buried · 41 hydrogen bonds · protein-protein
  • A–C · 1717 Ų buried · 40 hydrogen bonds · protein-protein
  • A–D · 391 Ų buried · 4 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 modified (cofactor).

Compared structures

  • 5W1B · Tryptophan indole-lyase · the same entry in another collection · chain A against A, TM-score 1.00
  • P28796 · AlphaFold monomer V2.0 prediction for tryptophanase (P28796) · a predicted model of the same protein · chain A against A, TM-score 1.00

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