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Crystal structure of beta-ketoacyl-acp synthase III + degraded form of acetyl-CoA

Analyse Crystal structure of beta-ketoacyl-acp synthase III + degraded form of… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1HNH
Type
protein
Length
317 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Beta-ketoacyl-acyl carrier protein synthase III
EC
2.3.1.41
UniProt
P0A6R0
Ligands
COA
Pockets
1 · best druggability 0.65

Structure

x-ray diffraction · 1 distinct chain · 39% helix, 26% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ABeta-ketoacyl-acyl carrier protein synthase III (EC 2.3.1.41)protein31739% helix, 26% strandP0A6R0

Ligands and binding sites

  • COA · Coenzyme A · ligand · chains A

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

Pockets

1 pocket found on a 1 Å grid, 1 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11630.650.8627empty

Modifications

Observed in the structure: 9 modified (engineered, acetylation).

Compared structures

  • 1HNH · Crystal structure of beta-ketoacyl-acp synthase III + degraded form of acetyl-CoA · the same entry in another collection · chain A against A, TM-score 1.00
  • P0A6R0 · AlphaFold monomer V2.0 prediction for 3-oxoacyl-[acyl-carrier- protein] synthase 3… · a predicted model of the same protein · chain A against A, TM-score 0.99

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