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Chitinase B from serratia marcescens wildtype in complex with catalytic intermediate

Analyse Chitinase B from serratia marcescens wildtype in complex with catalytic… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1E6Z
Type
protein
Length
995 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Chitinase B
EC
3.2.1.14
UniProt
Q54276
Ligands
NGO, NAG, SO4
Pockets
4 · best druggability 0.79

Structure

x-ray diffraction · 2 distinct chains · 32% helix, 20% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AChitinase B (EC 3.2.1.14)protein49732% helix, 20% strandQ54276
BChitinase B (EC 3.2.1.14)protein49832% helix, 20% strandQ54276

Ligands and binding sites

  • NGO · 2-methyl-4,5-dihydro-(1,2-dideoxy-alpha-D-glucopyranoso)[2,1-D]-1,3-oxazole · ligand · 2 copies · chains A, B
  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 3 copies · chains A, B
  • SO4 · Sulfate ion · ion · 4 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
111160.790.8090NAG, NGO
211060.770.7988NGO, NAG
32150.530.7837empty
41260.450.7827empty

Interfaces

1 interface between chains.

  • A–B · 1383 Ų buried · 22 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 disulfide (disulfide).

Compared structures

  • 1E6Z · Chitinase B from serratia marcescens wildtype in complex with catalytic intermediate · the same entry in another collection · chain A against A, TM-score 1.00

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