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Crystal structure of an exo-alpha-1,6-mannosidase (BACOVA_03347) from bacteroides ovatus at 1.60 a resolution

Analyse Crystal structure of an exo-alpha-1,6-mannosidase (BACOVA_03347) from… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3P2C
Type
protein
Length
890 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Putative glycosyl hydrolase
UniProt
A7LZS1
Pockets
9 · best druggability 0.83

Structure

x-ray diffraction · 1 distinct chain · 46% helix, 13% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BPutative glycosyl hydrolaseprotein44546% helix, 13% strandA7LZS1

Ligands and binding sites

  • EDO · 1,2-ethanediol · additive · 13 copies · chains A, B
  • PGE · Triethylene glycol · additive · chains B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12110.830.9646empty
21720.540.7928EDO
31290.510.8024EDO
41320.490.7919EDO
51210.440.7720EDO

Interfaces

1 interface between chains.

  • A–B · 1566 Ų buried · 22 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 28 modified (engineered).

Compared structures

  • 3P2C · Crystal structure of an exo-alpha-1,6-mannosidase (bacova_03347) from bacteroides ovatus… · the same entry in another collection · chain A against A, TM-score 1.00

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