Research workbench
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.
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| B, A | — | protein | 400 | — | 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
Analyse
- Open in the research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides and crosslinks on the 3D structure
- Every structure of UniProt B6H6L7
- Elsewhere: RCSB PDB 6KJE · PDBe 6KJE · UniProt B6H6L7
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