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Lovastatin esterase pcest in complex with monacolin J

Analyse Lovastatin esterase pcest in complex with monacolin J in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6KJE
Type
protein
Length
800 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
UniProt
B6H6L7
Ligands
MJA

Structure

x-ray diffraction · 1 distinct chain.

ChainMoleculeTypeResiduesSecondary structureUniProt
B, A—protein400—B6H6L7

Ligands and binding sites

  • MJA · (3R,5R)-3,5-dihydroxy-7-[(1s,2s,6r,8s,8ar)-8-hydroxy-2, 6-dimethyl-1,2,6,7,8,8A-hexahydronaphthalen-1-yl]heptanoic acid · ligand · 2 copies · chains B, A
  • 144 · Tris-hydroxymethyl-methyl-ammonium · additive · 2 copies · chains B
  • ACT · Acetate ion · additive · 2 copies · chains B, A

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

Compared structures

  • 6KJE · lovastatin esterase PcEST in complex with monacolin J · the same entry in another collection · chain B against B, TM-score 1.00
  • B6H6L7 · AlphaFold monomer V2.0 prediction for lovastatin esterase (B6H6L7) · a predicted model of the same protein · chain B against A, TM-score 0.99

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