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Crystal structure of the ketone reductase ChKRED20 from the genome of Chryseobacterium sp. CA49 complexed with NAD

Analyse Crystal structure of the ketone reductase ChKRED20 from the genome of… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6IXM
Type
protein
Length
982 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
1.601
Source
Chryseobacterium sp. CA49
Molecule
Short-chain dehydrogenase reductase
UniProt
X2D0L0
Ligands
NAD
Pockets
10 · best druggability 0.86

Structure

x-ray diffraction · resolution 1.601 · 2 distinct chains · 50% helix, 17% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, C, DShort-chain dehydrogenase reductaseprotein24851% helix, 17% strandX2D0L0
BShort-chain dehydrogenase reductaseprotein23849% helix, 18% strandX2D0L0

Ligands and binding sites

  • NAD · Nicotinamide-adenine-dinucleotide · ligand · 3 copies · chains B, C, D

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

Pockets

10 pockets found on a 1 Å grid, 4 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
18360.860.8957empty
210450.800.81101NAD
37550.730.7869NAD
42720.550.7635NAD
51190.450.7824empty

Interfaces

6 interfaces between chains.

  • C–D · 1597 Ų buried · 29 hydrogen bonds · protein-protein
  • A–B · 1587 Ų buried · 25 hydrogen bonds · protein-protein
  • A–C · 1382 Ų buried · 9 hydrogen bonds · protein-protein
  • B–D · 1380 Ų buried · 9 hydrogen bonds · protein-protein
  • A–D · 247 Ų buried · 2 hydrogen bonds · protein-protein

Compared structures

  • 6IXM · Crystal structure of the ketone reductase CHKRED20 from the genome of chryseobacterium… · the same entry in another collection · chain A against A, TM-score 1.00

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