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Cytochrome domain of myriococcum thermophilum cellobiose dehydrogenase, mtcyt

Analyse Cytochrome domain of myriococcum thermophilum cellobiose dehydrogenase, mtcyt in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4QI3
Type
protein
Length
416 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Cellobiose dehydrogenase
UniProt
A9XK88
Ligands
HEM, MAN, NAG, MG
Pockets
6 · best druggability 0.68

Structure

x-ray diffraction · 1 distinct chain · 7% helix, 46% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BCellobiose dehydrogenaseprotein2087% helix, 46% strandA9XK88

Ligands and binding sites

  • HEM · Protoporphyrin IX containing Fe · ligand · 2 copies · chains A, B
  • MAN · alpha-D-mannopyranose · sugar · 8 copies · chains A, B
  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 2 copies · chains A, B
  • MG · Magnesium ion · metal · 3 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12020.680.8630HEM, MG
21940.670.8630HEM
33920.600.7638empty
41710.450.7529empty
51170.440.7717empty

Interfaces

1 interface between chains.

  • A–B · 466 Ų buried · 6 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 10 glycan, 4 disulfide, 2 modified (O-glycosylation, disulfide, N-glycosylation, cyclization).

Compared structures

  • 4QI3 · Cytochrome domain of Myriococcum thermophilum cellobiose dehydrogenase, MtCYT · the same entry in another collection · chain A against A, TM-score 1.00

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