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Crystal structure of a putative 3-oxoacyl-[acyl-carrier PROTEIN]REDUCTASE from escherichia COLI strain CFT073 complexed with NADP+ at 2.5 a resolution

Analyse Crystal structure of a putative 3-oxoacyl-[acyl-carrier PROTEIN]REDUCTASE from… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4IIV
Type
protein
Length
964 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
3-oxoacyl-[acyl-carrier protein] reductase
EC
1.1.1.100
UniProt
Q8FJ14
Ligands
NAP
Pockets
3 · best druggability 0.84

Structure

x-ray diffraction · 2 distinct chains · 51% helix, 16% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, C, D3-oxoacyl-[acyl-carrier protein] reductase (EC 1.1.1.100)protein24251% helix, 16% strandQ8FJ14
B3-oxoacyl-[acyl-carrier protein] reductase (EC 1.1.1.100)protein23852% helix, 16% strandQ8FJ14

Ligands and binding sites

  • NAP · Nadp nicotinamide-adenine-dinucleotide phosphate · ligand · 4 copies · chains A, B, C, D

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

Pockets

3 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15910.840.8951empty
26480.830.8894NAP
32160.750.8939NAP

Interfaces

6 interfaces between chains.

  • A–C · 1745 Ų buried · 32 hydrogen bonds · protein-protein
  • B–D · 1734 Ų buried · 33 hydrogen bonds · protein-protein
  • B–C · 1390 Ų buried · 9 hydrogen bonds · protein-protein
  • A–D · 1357 Ų buried · 12 hydrogen bonds · protein-protein
  • C–D · 95 Ų buried · 0 hydrogen bonds · protein-protein

Compared structures

  • 4IIV · Crystal structure of a putative 3-oxoacyl-[acyl-carrier protein]reductase from… · the same entry in another collection · chain A against A, TM-score 1.00

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