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Crystal structure of TT0143 from thermus thermophilus HB8

Analyse Crystal structure of TT0143 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
1ULU
Type
protein
Length
995 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Enoyl-acyl carrier protein reductase
EC
1.3.1.10
UniProt
Q5SLI9
Pockets
8 · best druggability 0.86

Structure

x-ray diffraction · 4 distinct chains · 49% helix, 19% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AEnoyl-acyl carrier protein reductase (EC 1.3.1.10)protein24650% helix, 20% strandQ5SLI9
BEnoyl-acyl carrier protein reductase (EC 1.3.1.10)protein25749% helix, 19% strandQ5SLI9
CEnoyl-acyl carrier protein reductase (EC 1.3.1.10)protein24448% helix, 20% strandQ5SLI9
DEnoyl-acyl carrier protein reductase (EC 1.3.1.10)protein24848% helix, 19% strandQ5SLI9

Pockets

8 pockets found on a 1 Å grid, 5 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110040.860.8756empty
24320.790.8758empty
36490.700.7866empty
44090.590.7535empty
51360.530.8021empty

Interfaces

6 interfaces between chains.

  • B–D · 1857 Ų buried · 38 hydrogen bonds · protein-protein
  • A–C · 1853 Ų buried · 36 hydrogen bonds · protein-protein
  • C–D · 1773 Ų buried · 28 hydrogen bonds · protein-protein
  • A–B · 1753 Ų buried · 24 hydrogen bonds · protein-protein
  • B–C · 710 Ų buried · 9 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 26 modified (engineered).

Compared structures

  • 1ULU · Crystal structure of tt0143 from Thermus thermophilus HB8 · the same entry in another collection · chain A against A, TM-score 1.00

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