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Structure of gh 38 jack bean alpha-mannosidase

Analyse Structure of gh 38 jack bean alpha-mannosidase in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6B9O
Type
protein
Length
1,872 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Alpha-mannosidase from canavalia ensiformis (jack bean)
EC
3.2.1.24
Ligands
MAN, NAG, BMA, ZN
Pockets
20 · best druggability 0.85

Structure

x-ray diffraction · 2 distinct chains · 26% helix, 29% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AAlpha-mannosidase from canavalia ensiformis (jack bean) (EC 3.2.1.24)protein93526% helix, 30% strand—
BAlpha-mannosidase from canavalia ensiformis (jack bean) (EC 3.2.1.24)protein93726% helix, 29% strand—

Ligands and binding sites

  • MAN · alpha-D-mannopyranose · sugar · 18 copies · chains A, B
  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 8 copies · chains A, B
  • BMA · beta-D-mannopyranose · sugar · 2 copies · chains A, B
  • ZN · Zinc ion · metal · 2 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
111840.850.8696NAG, BMA
26860.850.8949empty
35980.750.8258empty
44760.690.7940NAG, BMA
51120.650.8918empty

Interfaces

1 interface between chains.

  • A–B · 2371 Ų buried · 28 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 6 disulfide, 4 glycan (disulfide, N-glycosylation).

Compared structures

  • 6B9O · Structure of GH 38 Jack Bean alpha-mannosidase · the same entry in another collection · chain A against A, TM-score 1.00

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