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Crystal structure of a putative carveol dehydrogenase from mycobacterium avium bound to NAD

Analyse Crystal structure of a putative carveol dehydrogenase from mycobacterium avium… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4RGB
Type
protein
Length
548 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Carveol dehydrogenase
EC
1.1.1.275
UniProt
A0QDP5
Ligands
NAD
Pockets
6 · best druggability 0.86

Structure

x-ray diffraction · 1 distinct chain · 48% helix, 15% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BCarveol dehydrogenase (EC 1.1.1.275)protein27448% helix, 15% strandA0QDP5

Ligands and binding sites

  • NAD · Nicotinamide-adenine-dinucleotide · ligand · 2 copies · chains A, B

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

Pockets

6 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13900.860.9455NAD
23490.850.9456NAD
32160.510.7625empty
41450.430.7525empty
51140.430.7721empty

Interfaces

1 interface between chains.

  • A–B · 1624 Ų buried · 30 hydrogen bonds · protein-protein

Compared structures

  • 4RGB · Crystal structure of a putative carveol dehydrogenase from Mycobacterium avium bound to… · the same entry in another collection · chain A against A, TM-score 1.00

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