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Burg (holo) in complex with (Z)-2,3-dihydroxy-6-methyl-hept-2-enoate (13): biosynthesis of cyclopropanol rings in bacterial toxins

Analyse Burg (holo) in complex with (Z)-2,3-dihydroxy-6-methyl-hept-2-enoate (13)… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7PCM
Type
protein
Length
681 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Ketol-acid reductoisomerase
EC
1.1.1.86
UniProt
Q2T3G7
Ligands
NAI, 7I3, MG, NA
Pockets
4 · best druggability 0.78

Structure

x-ray diffraction · 2 distinct chains · 57% helix, 11% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AKetol-acid reductoisomerase (EC 1.1.1.86)protein34057% helix, 11% strandQ2T3G7
BKetol-acid reductoisomerase (EC 1.1.1.86)protein34157% helix, 11% strandQ2T3G7

Ligands and binding sites

  • NAI · 1,4-dihydronicotinamide adenine dinucleotide · ligand · 2 copies · chains A, B
  • 7I3 · (Z)-6-methyl-2,3-bis(oxidanyl)hept-2-enoic acid · ligand · 2 copies · chains A, B
  • MG · Magnesium ion · metal · 4 copies · chains A, B
  • NA · Sodium ion · metal · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15550.780.8464NAI, MG, 7I3
25720.770.84667I3, NAI, MG
36240.710.7942empty
4510.280.7516empty

Interfaces

1 interface between chains.

  • A–B · 6561 Ų buried · 83 hydrogen bonds · protein-protein

Compared structures

  • 7PCM · BurG (holo) in complex with (Z)-2,3-dihydroxy-6-methyl-hept-2-enoate (13): Biosynthesis… · the same entry in another collection · chain A against A, TM-score 1.00

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