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Yeast cytochrome BC1 complex with stigmatellin

Analyse Yeast cytochrome BC1 complex with stigmatellin in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2IBZ
Type
protein
Length
2,179 residues
Chains
11
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Ubiquinol-cytochrome-C reductase complex core protein 1; Ubiquinol-cytochrome-C reductase…
EC
1.10.2.2
UniProt
P07256, P07257, P00163, P07143, P08067, P00127, P00128, P08525, P22289
Ligands
HEC, UQ6, SMA, FES
Pockets
20 · best druggability 0.85

Structure

x-ray diffraction · 11 distinct chains · 44% helix, 16% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AUbiquinol-cytochrome-C reductase complex core protein 1 (EC 1.10.2.2)protein43144% helix, 18% strandP07256
BUbiquinol-cytochrome-C reductase complex core protein 2 (EC 1.10.2.2)protein35238% helix, 20% strandP07257
CCytochrome B (EC 1.10.2.2)protein38571% helix, 2% strandP00163
DCytochrome C1, heme protein, mitochondrial precursor (EC 1.10.2.2)protein24540% helix, 7% strandP07143
EUbiquinol-cytochrome C reductase iron-sulfur subunit, mitochondrial precursor (EC 1.10.2.2)protein18528% helix, 24% strandP08067
HUbiquinol-cytochrome C reductase complex 17 kda protein (EC 1.10.2.2)protein7468% helix, 0% strandP00127
FUbiquinol-cytochrome C reductase complex 14 kda protein (EC 1.10.2.2)protein12570% helix, 0% strandP00128
GUbiquinol-cytochrome C reductase complex ubiquinone-binding protein qp-C (EC 1.10.2.2)protein9341% helix, 11% strandP08525
IUbiquinol-cytochrome C reductase complex 7.3 kda protein (EC 1.10.2.2)protein5569% helix, 0% strandP22289
XVariable heavy chain of antibody fragmentprotein1272% helix, 52% strand—
YVariable light chain of antibody fragmentprotein1070% helix, 42% strand—

Ligands and binding sites

  • HEC · Heme C · ligand · 3 copies · chains C, D
  • UQ6 · 5-(3,7,11,15,19,23-hexamethyl-tetracosa-2,6,10,14,18, 22-hexaenyl)-2,3-dimethoxy-6-methyl-benzene-1,4-diol · ligand · chains C, E
  • SMA · Stigmatellin A · ligand · chains C
  • 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
16430.850.8965HEC
21720.820.9734empty
310210.800.8199empty
45020.790.8647HEC, UQ6
53460.770.8834empty

Interfaces

24 interfaces between chains.

  • C–F · 1809 Ų buried · 11 hydrogen bonds · protein-protein
  • C–D · 1723 Ų buried · 12 hydrogen bonds · protein-protein
  • A–B · 1651 Ų buried · 14 hydrogen bonds · protein-protein
  • C–G · 1477 Ų buried · 9 hydrogen bonds · protein-protein
  • D–H · 1227 Ų buried · 15 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 disulfide, 2 cofactor (disulfide, heme c attachment).

Compared structures

  • 2IBZ · Yeast Cytochrome BC1 Complex with Stigmatellin · the same entry in another collection · chain Y against Y, TM-score 1.00
  • P00163 · AlphaFold monomer V2.0 prediction for cytochrome B (P00163) · a predicted model of the same protein · chain C against A, TM-score 1.00

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