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The structure of dszs acyltransferase with carrier protein

Analyse The structure of dszs acyltransferase with carrier protein in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5ZK4
Type
protein
Length
720 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Disd protein; Disa protein
UniProt
Q4U443, Q4U447
Ligands
9EF, SO4
Pockets
12 · best druggability 0.73

Structure

x-ray diffraction · 2 distinct chains · 54% helix, 12% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BDisd proteinprotein28751% helix, 15% strandQ4U443
C, DDisa proteinprotein7364% helix, 0% strandQ4U447

Ligands and binding sites

  • 9EF · N-[2-(acetylamino)ethyl]-N~3~-[(2R)-2-hydroxy-3,3-dimethyl-4-(phosphonooxy)butanoyl]-beta-alaninamide · ligand · 2 copies · chains A, C, B, D
  • SO4 · Sulfate ion · ion · 10 copies · chains A, B, C, D

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14740.730.8257SO4, 9EF
25020.710.8156SO4, 9EF
3620.580.9017empty
43830.570.7546SO4
51360.490.7819empty

Interfaces

5 interfaces between chains.

  • A–B · 792 Ų buried · 5 hydrogen bonds · protein-protein
  • B–D · 670 Ų buried · 5 hydrogen bonds · protein-protein
  • A–C · 654 Ų buried · 5 hydrogen bonds · protein-protein
  • B–C · 603 Ų buried · 11 hydrogen bonds · protein-protein
  • A–D · 602 Ų buried · 12 hydrogen bonds · protein-protein

Modifications

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

Compared structures

  • 5ZK4 · The structure of DSZS acyltransferase with carrier protein · the same entry in another collection · chain A against A, TM-score 1.00

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