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Structural and thermodynamic dissection of specific mannan recognition by a carbohydrate-binding module, TMCBM27

Analyse Structural and thermodynamic dissection of specific mannan recognition by a… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1OF3
Type
protein
Length
350 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Beta-mannosidase
UniProt
Q9RIK9
Ligands
CA
Pockets
3 · best druggability 0.48

Structure

x-ray diffraction · 2 distinct chains · 9% helix, 57% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ABeta-mannosidaseprotein1769% helix, 56% strandQ9RIK9
BBeta-mannosidaseprotein1749% helix, 57% strandQ9RIK9

Ligands and binding sites

  • CA · Calcium ion · metal · 2 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, 0 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11130.480.8018empty
21510.430.7521empty
3720.310.7413empty

Interfaces

1 interface between chains.

  • A–B · 607 Ų buried · 7 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 3 modified (engineered).

Compared structures

  • 1OF3 · Structural and thermodynamic dissection of specific mannan recognition by a… · the same entry in another collection · chain A against A, TM-score 1.00

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