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Structural and biochemical evidence for a boat-like transition state in beta-mannosidases

Analyse Structural and biochemical evidence for a boat-like transition state in… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2VQT
Type
protein
Length
1,675 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Beta-mannosidase
EC
3.2.1.25
UniProt
Q8AAK6
Ligands
15A, CL, BR
Pockets
13 · best druggability 0.77

Structure

x-ray diffraction · 2 distinct chains · 24% helix, 36% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ABeta-mannosidase (EC 3.2.1.25)protein83623% helix, 37% strandQ8AAK6
BBeta-mannosidase (EC 3.2.1.25)protein83924% helix, 36% strandQ8AAK6

Ligands and binding sites

  • 15A · (2Z,3R,4S,5R,6R)-2-[(2-aminoethyl)imino]-6-(hydroxymethyl)piperidine-3,4,5-triol · ligand · 2 copies · chains A, B
  • CL · Chloride ion · ion · 13 copies · chains A, B
  • BR · Bromide ion · ion · 10 copies · chains A, B
  • EDO · 1,2-ethanediol · additive · 45 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16610.770.8255EDO, CL
25860.760.8357EDO, BR, CL
35520.720.8171EDO, CL
43200.670.812615A, CL
53190.660.8235EDO, CL

Interfaces

1 interface between chains.

  • A–B · 789 Ų buried · 8 hydrogen bonds · protein-protein

Compared structures

  • 2VQT · Structural and biochemical evidence for a boat-like transition state in beta-mannosidases · the same entry in another collection · chain A against A, TM-score 1.00

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