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2.55-ångström cryo-EM structure of cytochrome BO3 from escherichia COLI in native membrane

Analyse 2.55-ångström cryo-EM structure of cytochrome BO3 from escherichia COLI in… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7CUB
Type
protein
Length
1,199 residues
Chains
4
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Cytochrome BO(3) ubiquinol oxidase subunit 1; Cytochrome BO(3) ubiquinol oxidase subunit…
EC
7.1.1.3
UniProt
P0ABI8, P0ABJ1, P0ABJ3, P0ABJ6
Ligands
3PE, HEM, HEO, UQ8, CU
Pockets
19 · best druggability 0.90

Structure

electron microscopy · 4 distinct chains · 63% helix, 6% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ACytochrome BO(3) ubiquinol oxidase subunit 1 (EC 7.1.1.3)protein65967% helix, 2% strandP0ABI8
BCytochrome BO(3) ubiquinol oxidase subunit 2protein25934% helix, 24% strandP0ABJ1
CCytochrome BO(3) ubiquinol oxidase subunit 3protein18482% helix, 0% strandP0ABJ3
DCytochrome BO(3) ubiquinol oxidase subunit 4protein9775% helix, 2% strandP0ABJ6

Ligands and binding sites

  • 3PE · 1,2-diacyl-sn-glycero-3-phosphoethanolamine · ligand · 5 copies · chains A, C
  • HEM · Protoporphyrin IX containing Fe · ligand · chains A
  • HEO · Heme O · ligand · chains A, B
  • UQ8 · Ubiquinone-8 · ligand · chains A
  • CU · Copper (II) ion · metal · chains A

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
19300.900.92100HEM, HEO
211560.840.84743PE
32590.670.8329empty
43510.650.7933empty
52000.640.8428UQ8

Interfaces

5 interfaces between chains.

  • A–B · 3748 Ų buried · 29 hydrogen bonds · protein-protein
  • C–D · 1709 Ų buried · 3 hydrogen bonds · protein-protein
  • A–C · 1317 Ų buried · 8 hydrogen bonds · protein-protein
  • A–D · 933 Ų buried · 6 hydrogen bonds · protein-protein
  • B–D · 306 Ų buried · 2 hydrogen bonds · protein-protein

Compared structures

  • 7CUB · 2.55-Angstrom Cryo-EM structure of Cytochrome bo3 from Escherichia coli in Native Membrane · the same entry in another collection · chain D against D, TM-score 1.00
  • P0ABI8 · AlphaFold monomer V2.0 prediction for cytochrome BO(3) ubiquinol oxidase subunit 1… · a predicted model of the same protein · chain A against A, TM-score 1.00
  • P0ABJ1 · AlphaFold monomer V2.0 prediction for cytochrome BO(3) ubiquinol oxidase subunit 2… · a predicted model of the same protein · chain B against A, TM-score 0.98
  • P0ABJ3 · AlphaFold monomer V2.0 prediction for cytochrome BO(3) ubiquinol oxidase subunit 3… · a predicted model of the same protein · chain C against A, TM-score 0.89
  • P0ABJ6 · AlphaFold monomer V2.0 prediction for cytochrome BO(3) ubiquinol oxidase subunit 4… · a predicted model of the same protein · chain D against A, TM-score 0.66

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