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The structure of the catalytic domain of NCLPMO9C from the filamentous fungus neurospora crassa

Analyse The structure of the catalytic domain of NCLPMO9C from the filamentous fungus… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4D7U
Type
protein
Length
454 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Endoglucanase II
UniProt
Q7SHI8
Ligands
CU
Pockets
3 · best druggability 0.54

Structure

x-ray diffraction · 1 distinct chain · 7% helix, 35% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BEndoglucanase IIprotein2277% helix, 35% strandQ7SHI8

Ligands and binding sites

  • CU · Copper (II) ion · metal · 2 copies · chains A, B
  • GOL · Glycerol · additive · 5 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12640.540.7631empty
2600.330.7716GOL
3730.330.7516empty

Interfaces

1 interface between chains.

  • A–B · 288 Ų buried · 4 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 disulfide (disulfide).

Compared structures

  • 4D7U · The structure of the catalytic domain of NcLPMO9C from the filamentous fungus Neurospora… · the same entry in another collection · chain A against A, TM-score 1.00

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