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Structure of E. COLI undecaprenyl diphosphate synthase in complex with bph-1354

Analyse Structure of E. COLI undecaprenyl diphosphate synthase in complex with bph-1354 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4H2J
Type
protein
Length
428 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Undecaprenyl pyrophosphate synthase
EC
2.5.1.31
UniProt
P60472
Ligands
0YU
Pockets
5 · best druggability 0.62

Structure

x-ray diffraction · 2 distinct chains · 46% helix, 14% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AUndecaprenyl pyrophosphate synthase (EC 2.5.1.31)protein21746% helix, 14% strandP60472
BUndecaprenyl pyrophosphate synthase (EC 2.5.1.31)protein21147% helix, 14% strandP60472

Ligands and binding sites

  • 0YU · N~4~-[4-(4,5-dihydro-1H-imidazol-2-yl)phenyl]-N~1~-[4-(1H-imidazol-2-yl)phenyl]-2-nitrobenzene-1,4-dicarboxamide · ligand · 2 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12360.620.81290YU
22510.610.80320YU
3620.400.8016empty
4550.350.7916empty
5620.270.7320empty

Interfaces

1 interface between chains.

  • A–B · 1852 Ų buried · 28 hydrogen bonds · protein-protein

Compared structures

  • 4H2J · Structure of E. coli undecaprenyl diphosphate synthase in complex with BPH-1354 · the same entry in another collection · chain A against A, TM-score 1.00
  • P60472 · AlphaFold monomer V2.0 prediction for DITRANS,POLYCIS-undecaprenyl- diphosphate synthase… · a predicted model of the same protein · chain B against A, TM-score 0.96

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