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Crystal structure of the complex between the mycobacterium beta-ketoacyl-acyl carrier protein synthase III (fabh) and ss-(2-hydroxyethyl)-O-decyl ester CARBONO(DITHIOPEROXOIC) acid

Analyse Crystal structure of the complex between the mycobacterium beta-ketoacyl-acyl… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2QNZ
Type
protein
Length
659 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
3-oxoacyl-[acyl-carrier-protein] synthase 3
EC
2.3.1.41
UniProt
P0A574
Ligands
DFD
Pockets
7 · best druggability 0.77

Structure

x-ray diffraction · 2 distinct chains · 38% helix, 25% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A3-oxoacyl-[acyl-carrier-protein] synthase 3 (EC 2.3.1.41)protein33038% helix, 25% strandP0A574
B3-oxoacyl-[acyl-carrier-protein] synthase 3 (EC 2.3.1.41)protein32939% helix, 25% strandP0A574

Ligands and binding sites

  • DFD · Decyl formate · ligand · 2 copies · chains A, B
  • BME · Beta-mercaptoethanol · additive · 2 copies · chains A, B

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

Pockets

7 pockets found on a 1 Å grid, 4 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1980.770.9824empty
21910.730.8940DFD
32070.730.8941DFD
41660.510.7939empty
51310.420.7529empty

Interfaces

1 interface between chains.

  • A–B · 3190 Ų buried · 44 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 covalent (additive adduct, covalent ligand).

Compared structures

  • 2QNZ · Crystal structure of the complex between the mycobacterium beta-ketoacyl-acyl carrier… · the same entry in another collection · chain B against B, TM-score 1.00

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