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Crystal structure analysis of klebsiella pneumoniae pullulanase complexed with maltotetraose

Analyse Crystal structure analysis of klebsiella pneumoniae pullulanase complexed with… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2FHF
Type
protein
Length
1,052 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Alpha-dextrin endo-1,6-alpha-glucosidase
EC
3.2.1.41
UniProt
W9BQ28
Ligands
GLC, CA
Pockets
7 · best druggability 0.63

Structure

x-ray diffraction · 1 distinct chain · 27% helix, 24% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AAlpha-dextrin endo-1,6-alpha-glucosidase (EC 3.2.1.41)protein105227% helix, 24% strandW9BQ28

Ligands and binding sites

  • GLC · alpha-D-glucopyranose · sugar · 10 copies · chains A
  • CA · Calcium ion · metal · 5 copies · chains A

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

Pockets

7 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12620.630.8141empty
23290.570.7637GLC
31490.480.7826empty
41340.420.7520empty
5980.390.7618empty

Modifications

Observed in the structure: 3 disulfide (disulfide).

Compared structures

  • 2FHF · Crystal Structure Analysis of Klebsiella pneumoniae pullulanase complexed with… · the same entry in another collection · chain A against A, TM-score 1.00

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