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Crystal structure of myo-inositol dehydrogenase from lactobacillus casei with bound cofactor NAD

Analyse Crystal structure of myo-inositol dehydrogenase from lactobacillus casei with… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4MIN
Type
protein
Length
1,356 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Inositol 2-DEHYDROGENASE/D-chiro-inositol 3-dehydrogenase
EC
1.1.1.18
UniProt
B3W8L3
Ligands
NAD, SO4
Pockets
18 · best druggability 0.88

Structure

x-ray diffraction · 1 distinct chain · 37% helix, 23% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, DInositol 2-DEHYDROGENASE/D-chiro-inositol 3-dehydrogenase (EC 1.1.1.18)protein33937% helix, 23% strandB3W8L3

Ligands and binding sites

  • NAD · Nicotinamide-adenine-dinucleotide · ligand · 4 copies · chains A, B, C, D
  • SO4 · Sulfate ion · ion · 6 copies · chains A, D, C, B
  • GOL · Glycerol · additive · 5 copies · chains A, B, C, D

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

Pockets

18 pockets found on a 1 Å grid, 9 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
18330.880.91108GOL
23580.670.8134NAD
34460.650.7856NAD
4690.640.9322empty
53430.640.7948NAD

Interfaces

6 interfaces between chains.

  • B–D · 1454 Ų buried · 17 hydrogen bonds · protein-protein
  • A–C · 1432 Ų buried · 20 hydrogen bonds · protein-protein
  • B–C · 1086 Ų buried · 8 hydrogen bonds · protein-protein
  • A–D · 1082 Ų buried · 9 hydrogen bonds · protein-protein
  • C–D · 710 Ų buried · 24 hydrogen bonds · protein-protein

Compared structures

  • 4MIN · Crystal Structure of myo-inositol dehydrogenase from Lactobacillus casei with bound… · the same entry in another collection · chain A against A, TM-score 1.00

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