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Crystal structure of escherichia COLI tryptophanase purified from alkaline stressed bacterial culture.

Analyse Crystal structure of escherichia COLI tryptophanase purified from alkaline… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4UP2
Type
protein
Length
1,629 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Tryptophanase
EC
4.1.99.1
UniProt
C3SLI7
Ligands
SO4
Pockets
20 · best druggability 0.84

Structure

x-ray diffraction · 4 distinct chains · 44% helix, 15% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ATryptophanase (EC 4.1.99.1)protein42042% helix, 14% strandC3SLI7
BTryptophanase (EC 4.1.99.1)protein40844% helix, 15% strandC3SLI7
CTryptophanase (EC 4.1.99.1)protein40445% helix, 15% strandC3SLI7
DTryptophanase (EC 4.1.99.1)protein39745% helix, 14% strandC3SLI7

Ligands and binding sites

  • SO4 · Sulfate ion · ion · 28 copies · chains A, B, D, C
  • BME · Beta-mercaptoethanol · additive · chains B

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

Pockets

20 pockets found on a 1 Å grid, 12 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12300.840.9739empty
22320.840.9742empty
38390.760.7995SO4, BME
45840.670.7768SO4
53750.640.7842SO4

Interfaces

6 interfaces between chains.

  • B–D · 2312 Ų buried · 48 hydrogen bonds · protein-protein
  • A–C · 2305 Ų buried · 41 hydrogen bonds · protein-protein
  • A–B · 1966 Ų buried · 21 hydrogen bonds · protein-protein
  • C–D · 1310 Ų buried · 19 hydrogen bonds · protein-protein
  • B–C · 459 Ų buried · 5 hydrogen bonds · protein-protein

Compared structures

  • 4UP2 · Crystal structure of Escherichia coli tryptophanase purified from alkaline stressed… · the same entry in another collection · chain A against A, TM-score 1.00

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