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Cytochrome C peroxidase bccp of shewanella oneidensis

Analyse Cytochrome C peroxidase bccp of shewanella oneidensis in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3O5C
Type
protein
Length
1,226 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Cytochrome C551 peroxidase
UniProt
Q8EF24
Ligands
HEM, CA
Pockets
19 · best druggability 0.86

Structure

x-ray diffraction · 3 distinct chains · 41% helix, 5% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ACytochrome C551 peroxidaseprotein30840% helix, 5% strandQ8EF24
B, DCytochrome C551 peroxidaseprotein30741% helix, 5% strandQ8EF24
CCytochrome C551 peroxidaseprotein30441% helix, 5% strandQ8EF24

Ligands and binding sites

  • HEM · Protoporphyrin IX containing Fe · ligand · 8 copies · chains A, B, C, D
  • CA · Calcium ion · metal · 4 copies · chains A, B, C, D
  • BU3 · (R,R)-2,3-butanediol · additive · chains C, D

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

Pockets

19 pockets found on a 1 Å grid, 8 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15530.860.9177HEM, CA
25870.860.9078HEM
35340.850.9174HEM, CA
42640.830.9442HEM
51700.820.9744empty

Interfaces

4 interfaces between chains.

  • A–B · 1977 Ų buried · 14 hydrogen bonds · protein-protein
  • C–D · 1962 Ų buried · 14 hydrogen bonds · protein-protein
  • A–C · 354 Ų buried · 7 hydrogen bonds · protein-protein
  • A–D · 180 Ų buried · 2 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 9 cofactor (heme attachment).

Compared structures

  • 3O5C · Cytochrome c Peroxidase BccP of Shewanella oneidensis · the same entry in another collection · chain A against A, TM-score 1.00

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