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Crystal structure of the acyltransferase domain from the third module of the ansamitocin polyketide synthase

Analyse Crystal structure of the acyltransferase domain from the third module of the… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6L3N
Type
protein
Length
1,678 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Polyketide synthase
Ligands
DXX, PO4
Pockets
18 · best druggability 0.64

Structure

x-ray diffraction · 2 distinct chains · 46% helix, 16% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, CPolyketide synthaseprotein41946% helix, 16% strand—
B, DPolyketide synthaseprotein42046% helix, 16% strand—

Ligands and binding sites

  • DXX · Methylmalonic acid · ligand · 4 copies · chains A, B, C, D
  • PO4 · Phosphate ion · ion · 6 copies · chains A, B, C, D
  • GOL · Glycerol · additive · 4 copies · chains A, B, C, D

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

Pockets

18 pockets found on a 1 Å grid, 6 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11190.640.8836DXX, GOL
21240.630.8738DXX, GOL
31040.590.8628GOL
4950.590.8729GOL
51330.520.8131empty

Interfaces

3 interfaces between chains.

  • A–B · 505 Ų buried · 10 hydrogen bonds · protein-protein
  • B–D · 498 Ų buried · 8 hydrogen bonds · protein-protein
  • A–C · 435 Ų buried · 5 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 covalent (covalent ligand).

Compared structures

  • 6L3N · Crystal Structure of the acyltransferase domain from the third module of the ansamitocin… · the same entry in another collection · chain A against A, TM-score 1.00

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