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Crystal structure of a T1-like thiolase from mycobacterium smegmatis

Analyse Crystal structure of a T1-like thiolase from mycobacterium smegmatis in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5CBQ
Type
protein
Length
2,385 residues
Chains
6
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Beta-ketothiolase
UniProt
A0QUH3
Pockets
20 · best druggability 0.79

Structure

x-ray diffraction · 6 distinct chains · 40% helix, 21% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ABeta-ketothiolaseprotein39941% helix, 22% strandA0QUH3
BBeta-ketothiolaseprotein39840% helix, 22% strandA0QUH3
CBeta-ketothiolaseprotein39740% helix, 21% strandA0QUH3
DBeta-ketothiolaseprotein39840% helix, 21% strandA0QUH3
EBeta-ketothiolaseprotein40040% helix, 22% strandA0QUH3
FBeta-ketothiolaseprotein39341% helix, 21% strandA0QUH3

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11150.790.9834empty
21200.790.9737empty
31180.790.9734empty
43190.690.8350empty
52660.690.8437empty

Interfaces

9 interfaces between chains.

  • E–F · 2991 Ų buried · 77 hydrogen bonds · protein-protein
  • A–B · 2978 Ų buried · 70 hydrogen bonds · protein-protein
  • C–D · 2962 Ų buried · 65 hydrogen bonds · protein-protein
  • B–C · 355 Ų buried · 2 hydrogen bonds · protein-protein
  • A–D · 305 Ų buried · 0 hydrogen bonds · protein-protein

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