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Crystal structure of coelenteramide-bound renilla reniformis luciferase RLUC8-D162A variant

Analyse Crystal structure of coelenteramide-bound renilla reniformis luciferase… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7OMR
Type
protein
Length
309 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Coelenterazine H 2-monooxygenase
EC
1.13.12.5
UniProt
P27652
Ligands
CEI
Pockets
1 · best druggability 0.78

Structure

x-ray diffraction · 1 distinct chain · 45% helix, 18% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ACoelenterazine H 2-monooxygenase (EC 1.13.12.5)protein30945% helix, 18% strandP27652

Ligands and binding sites

  • CEI · N-[3-benzyl-5-(4-hydroxyphenyl)pyrazin-2-yl]-2-(4-hydroxyphenyl)acetamide · ligand · chains A
  • GOL · Glycerol · additive · 4 copies · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16240.780.8341CEI

Compared structures

  • 7OMR · Crystal structure of coelenteramide-bound Renilla reniformis luciferase RLuc8-D162A… · the same entry in another collection · chain A against A, TM-score 1.00
  • P27652 · AlphaFold monomer V2.0 prediction for coelenterazine H 2-monooxygenase (P27652) · a predicted model of the same protein · chain A against A, TM-score 0.98

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