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The complex structure of vink with vinl

Analyse The complex structure of vink with vinl in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5CZD
Type
protein
Length
378 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Malonyl-CoA-[acyl-carrier-protein] transacylase; Acyl-carrier-protein
UniProt
Q76KY5, Q76KY4
Ligands
PNS, 1N2
Pockets
2 · best druggability 0.81

Structure

x-ray diffraction · 2 distinct chains · 50% helix, 14% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AMalonyl-CoA-[acyl-carrier-protein] transacylaseprotein30150% helix, 18% strandQ76KY5
BAcyl-carrier-proteinprotein7752% helix, 0% strandQ76KY4

Ligands and binding sites

  • PNS · 4'-phosphopantetheine · ligand · chains A, B
  • 1N2 · 1,1'-ethane-1,2-diyldipyrrolidine-2,5-dione · ligand · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
18220.810.8481PNS, 1N2
2790.360.7617empty

Interfaces

1 interface between chains.

  • A–B · 702 Ų buried · 7 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 1 cofactor, 1 covalent (phosphopantetheinylation, covalent ligand).

Compared structures

  • 5CZD · The complex structure of VinK with VinL · the same entry in another collection · chain A against A, TM-score 1.00

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