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Complex structure of virulence factor sgha mutant with its substrate sag

Analyse Complex structure of virulence factor sgha mutant with its substrate sag in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6RK2
Type
protein
Length
905 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Beta-glucosidase
EC
3.2.1.21
UniProt
A0A2I4PGZ0
Ligands
6GR
Pockets
7 · best druggability 0.76

Structure

x-ray diffraction · 2 distinct chains · 44% helix, 16% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ABeta-glucosidase (EC 3.2.1.21)protein45445% helix, 16% strandA0A2I4PGZ0
BBeta-glucosidase (EC 3.2.1.21)protein45144% helix, 16% strandA0A2I4PGZ0

Ligands and binding sites

  • 6GR · 2-(alpha-L-altropyranosyloxy)benzoic acid · ligand · 2 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12410.760.9033empty
25220.710.80516GR
34850.700.80496GR
4830.400.7816empty
5720.360.7816empty

Interfaces

1 interface between chains.

  • A–B · 1033 Ų buried · 13 hydrogen bonds · protein-protein

Compared structures

  • 6RK2 · Complex structure of virulence factor SghA mutant with its substrate SAG · the same entry in another collection · chain A against A, TM-score 1.00

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