GL1X · GenesisL1 explorer

Research workbench

Crystal structure of mhud R26S mutant in complex with biliverdin

Analyse Crystal structure of mhud R26S mutant in complex with biliverdin in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6PLE
Type
protein
Length
192 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Heme oxygenase (mycobilin-producing)
EC
1.14.99.57
UniProt
P9WKH3
Ligands
BLA
Pockets
2 · best druggability 0.72

Structure

x-ray diffraction · 1 distinct chain · 27% helix, 29% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BHeme oxygenase (mycobilin-producing) (EC 1.14.99.57)protein9627% helix, 29% strandP9WKH3

Ligands and binding sites

  • BLA · Biliverdine IX alpha · ligand · 5 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15500.720.8037BLA
25360.710.8035BLA

Interfaces

1 interface between chains.

  • A–B · 278 Ų buried · 1 hydrogen bond · protein-protein

Compared structures

  • 6PLE · Crystal structure of MhuD R26S mutant in complex with biliverdin · the same entry in another collection · chain A against A, TM-score 1.00
  • P9WKH3 · AlphaFold monomer V2.0 prediction for heme oxygenase (mycobilin- producing) (P9WKH3) · a predicted model of the same protein · chain A against A, TM-score 0.92

Analyse

GL1X is a live explorer of the GenesisL1 blockchain. Turn on JavaScript for search, charts and interactive views.