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Crystal structure of a pl 26 exo-rhamnogalacturonan lyase from penicillium chrysogenum complexed with tetrameric substrate

Analyse Crystal structure of a pl 26 exo-rhamnogalacturonan lyase from penicillium… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5XQO
Type
protein
Length
1,780 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Pcrglx protein
UniProt
A0A0C6EFY4
Ligands
GAD, RAM, ADA, CA
Pockets
19 · best druggability 0.91

Structure

x-ray diffraction · 2 distinct chains · 30% helix, 26% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
APcrglx proteinprotein89930% helix, 26% strandA0A0C6EFY4
BPcrglx proteinprotein88130% helix, 26% strandA0A0C6EFY4

Ligands and binding sites

  • GAD · 2,6-anhydro-3-deoxy-L-threo-hex-2-enonic acid · ligand · 2 copies · chains A, B
  • RAM · alpha-L-rhamnopyranose · sugar · 4 copies · chains A, B
  • ADA · alpha-D-galactopyranuronic acid · sugar · 2 copies · chains A, B
  • 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

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110320.910.93130empty
21350.800.9731empty
31240.780.9725empty
4680.740.9818empty
5540.710.9817empty

Interfaces

1 interface between chains.

  • A–B · 5153 Ų buried · 102 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 6 modified, 2 disulfide, 2 glycan (engineered, disulfide, glycosylation).

Compared structures

  • 5XQO · Crystal structure of a PL 26 exo-rhamnogalacturonan lyase from Penicillium chrysogenum… · the same entry in another collection · chain A against A, TM-score 1.00

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