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Crystal structure of holo-[acyl-carrier-protein] synthase (acps) from neisseria meningitidis in complex with coenzyme a

Analyse Crystal structure of holo-[acyl-carrier-protein] synthase (acps) from neisseria… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5SUV
Type
protein
Length
377 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Holo-[acyl-carrier-protein] synthase
EC
2.7.8.7
UniProt
A1KVH5
Ligands
COA
Pockets
4 · best druggability 0.51

Structure

x-ray diffraction · 2 distinct chains · 44% helix, 32% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BHolo-[acyl-carrier-protein] synthase (EC 2.7.8.7)protein12646% helix, 32% strandA1KVH5
CHolo-[acyl-carrier-protein] synthase (EC 2.7.8.7)protein12542% helix, 32% strandA1KVH5

Ligands and binding sites

  • COA · Coenzyme A · ligand · 3 copies · chains A, B, C

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11230.510.8024empty
21470.430.7532COA
31420.410.7427COA
41470.400.7428COA

Interfaces

3 interfaces between chains.

  • A–B · 854 Ų buried · 7 hydrogen bonds · protein-protein
  • B–C · 815 Ų buried · 10 hydrogen bonds · protein-protein
  • A–C · 764 Ų buried · 10 hydrogen bonds · protein-protein

Compared structures

  • 5SUV · Crystal structure of holo-[acyl-carrier-protein] synthase (AcpS) from Neisseria… · the same entry in another collection · chain A against A, TM-score 1.00
  • A1KVH5 · AlphaFold monomer V2.0 prediction for holo-[acyl-carrier-protein] synthase (A1KVH5) · a predicted model of the same protein · chain C against A, TM-score 0.98

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