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Structure of a novel beta-mannanase BaMan113A with mannobiose, N236Y mutation.

Analyse Structure of a novel beta-mannanase BaMan113A with mannobiose, N236Y mutation. in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7DW8
Type
protein
Length
637 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
1.9
Source
Bacillus sp. N16-5
Molecule
Endo-beta-1,4-mannanase
UniProt
A0A140EH91
Ligands
BMA
Pockets
3 · best druggability 0.71

Structure

x-ray diffraction · resolution 1.9 · 2 distinct chains · 41% helix, 20% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AEndo-beta-1,4-mannanaseprotein32340% helix, 20% strandA0A140EH91
BEndo-beta-1,4-mannanaseprotein31441% helix, 20% strandA0A140EH91

Ligands and binding sites

  • BMA · beta-D-mannopyranose · sugar · 4 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16830.710.7881BMA
2580.380.8011empty
3630.370.7912empty

Interfaces

1 interface between chains.

  • A–B · 1015 Ų buried · 4 hydrogen bonds · protein-protein

Compared structures

  • 7DW8 · Structure of a novel beta-mannanase BAMAN113A with mannobiose, N236Y mutation. · the same entry in another collection · chain A against A, TM-score 1.00

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