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Complex III2 from candida albicans, inhibitor free, rieske head domain in intermediate position

Analyse Complex III2 from candida albicans, inhibitor free, rieske head domain in… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7RJC
Type
protein
Length
1,907 residues
Chains
10
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Ubiquinol--cytochrome-C reductase subunit; Cytochrome B; Ubiquinol--cytochrome-C…
EC
7.1.1.8
UniProt
A0A1D8PP59, P0C8L0, A0A1D8PHA3, Q5ABS1, A0A1D8PHA2, A0A1D8PJT8, A0A1D8PLP3, P83782, A0A1D8PJX3
Ligands
HEM, U10, HEC, FES
Pockets
20 · best druggability 0.82

Structure

electron microscopy · 10 distinct chains · 52% helix, 10% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AUbiquinol--cytochrome-C reductase subunitprotein41647% helix, 16% strandA0A1D8PP59
KCytochrome Bprotein38372% helix, 2% strandP0C8L0
DUbiquinol--cytochrome-C reductase catalytic subunitprotein24441% helix, 8% strandA0A1D8PHA3
GCytochrome B-C1 complex subunit 7protein12268% helix, 1% strandQ5ABS1
FUbiquinol--cytochrome-C reductase subunit 8protein8555% helix, 7% strandA0A1D8PHA2
HUbiquinol--cytochrome-C reductase subunit 6protein7275% helix, 0% strandA0A1D8PJT8
IUbiquinol--cytochrome-C reductase subunit 9protein3982% helix, 0% strandA0A1D8PLP3
BCytochrome B-C1 complex subunit 2, mitochondrialprotein36441% helix, 19% strandP83782
MCytochrome B-C1 complex subunit rieske, mitochondrial (EC 7.1.1.8)protein5068% helix, 0% strandA0A1D8PJX3
ECytochrome B-C1 complex subunit rieske, mitochondrial (EC 7.1.1.8)protein13215% helix, 21% strandA0A1D8PJX3

Ligands and binding sites

  • HEM · Protoporphyrin IX containing Fe · ligand · 2 copies · chains K
  • U10 · Ubiquinone-10 · ligand · 2 copies · chains K
  • HEC · Heme C · ligand · chains D
  • FES · Fe2/s2 (inorganic) cluster · ligand · chains E

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

Pockets

20 pockets found on a 1 Å grid, 18 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15640.820.8765HEM
24590.770.8550HEM, U10
38900.770.8086HEC
47510.750.7974empty
510720.730.76113empty

Interfaces

19 interfaces between chains.

  • K–G · 1837 Ų buried · 10 hydrogen bonds · protein-protein
  • A–B · 1796 Ų buried · 13 hydrogen bonds · protein-protein
  • K–D · 1748 Ų buried · 16 hydrogen bonds · protein-protein
  • K–F · 1376 Ų buried · 5 hydrogen bonds · protein-protein
  • D–H · 1137 Ų buried · 6 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 3 cofactor, 1 covalent, 1 disulfide (heme c attachment, heme attachment, covalent ligand, disulfide).

Compared structures

  • 7RJC · Complex III2 from Candida albicans, inhibitor free, Rieske head domain in intermediate… · the same entry in another collection · chain E against E, TM-score 1.00
  • P0C8L0 · AlphaFold monomer V2.0 prediction for cytochrome B (P0C8L0) · a predicted model of the same protein · chain K against A, TM-score 0.99
  • P83782 · AlphaFold monomer V2.0 prediction for cytochrome B-C1 complex subunit 2, mitochondrial… · a predicted model of the same protein · chain B against A, TM-score 0.98

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