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Crystal structure of TTHA0137 from thermus thermophilus HB8

Analyse Crystal structure of TTHA0137 from thermus thermophilus HB8 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2CSL
Type
protein
Length
744 residues
Chains
6
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Protein translation initiation inhibitor
UniProt
Q5SM06
Pockets
11 · best druggability 0.82

Structure

x-ray diffraction · 1 distinct chain · 31% helix, 32% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, D, E, FProtein translation initiation inhibitorprotein12431% helix, 32% strandQ5SM06

Pockets

11 pockets found on a 1 Å grid, 9 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11560.820.9845empty
21500.810.9745empty
31970.600.8228empty
42180.600.8126empty
51870.590.8122empty

Interfaces

8 interfaces between chains.

  • A–B · 991 Ų buried · 11 hydrogen bonds · protein-protein
  • D–E · 987 Ų buried · 9 hydrogen bonds · protein-protein
  • E–F · 974 Ų buried · 8 hydrogen bonds · protein-protein
  • D–F · 971 Ų buried · 10 hydrogen bonds · protein-protein
  • A–C · 969 Ų buried · 10 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 18 modified (engineered).

Compared structures

  • 2CSL · Crystal structure of TTHA0137 from Thermus Thermophilus HB8 · the same entry in another collection · chain A against A, TM-score 1.00

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