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MolNFT v1 · #21943 · protein

Crystal structure analysis of bovine BC1 with azoxystrobin

1SQB · Ubiquinol-cytochrome C reductase complex core protein I…: “Crystal structure analysis of bovine BC1 with azoxystrobin”. X-ray diffraction, 3 ligands (HEM, AZO, FES), 20 pockets (best druggability 0.82). MolNFT v1 #21943 on…

PDB
1SQB
Type
protein
Length
2,103 residues
Chains
11
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Ubiquinol-cytochrome C reductase complex core protein I, mitochondrial…
EC
1.10.2.2
UniProt
P31800, P23004, P00157, P00125, P13272, P00129, P13271, P00126, P00130, P07552
Ligands
HEM, AZO, FES
Pockets
20 · best druggability 0.82

Structure

x-ray diffraction · 11 distinct chains · 50% helix, 11% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AUbiquinol-cytochrome C reductase complex core protein I, mitochondrial (EC 1.10.2.2)protein44647% helix, 19% strandP31800
BUbiquinol-cytochrome C reductase complex core protein 2, mitochondrial (EC 1.10.2.2)protein42546% helix, 20% strandP23004
CCytochrome B (EC 1.10.2.2)protein37873% helix, 2% strandP00157
DCytochrome C1, heme protein, mitochondrial (EC 1.10.2.2)protein24136% helix, 10% strandP00125
EUbiquinol-cytochrome C reductase iron-sulfur subunit (EC 1.10.2.2)protein19625% helix, 13% strandP13272
FUbiquinol-cytochrome C reductase complex 14 kda protein (EC 1.10.2.2)protein10569% helix, 1% strandP00129
GUbiquinol-cytochrome C reductase complex ubiquinone-binding protein qp-C (EC 1.10.2.2)protein7544% helix, 12% strandP13271
HUbiquinol-cytochrome C reductase complex 11 kda protein (EC 1.10.2.2)protein6769% helix, 0% strandP00126
IUbiquinol-cytochrome C reductase 8 kda protein (EC 1.10.2.2)protein577% helix, 7% strandP13272
JUbiquinol-cytochrome C reductase complex 7.2 kda protein (EC 1.10.2.2)protein6177% helix, 0% strandP00130
KUbiquinol-cytochrome C reductase complex 6.4 kda protein (EC 1.10.2.2)protein5269% helix, 0% strandP07552

Ligands and binding sites

  • HEM · Protoporphyrin IX containing Fe · ligand · 3 copies · chains C, D
  • AZO · Methyl (2Z)-2-(2-{[6-(2-cyanophenoxy)pyrimidin-4-yl]oxy}phenyl)-3-methoxyacrylate · 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, 19 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15950.820.8766HEM
23960.800.8949empty
35140.800.8651HEM
45910.790.8554empty
56750.790.8485empty

Interfaces

25 interfaces between chains.

  • A–B · 2412 Ų buried · 44 hydrogen bonds · protein-protein
  • B–I · 2157 Ų buried · 23 hydrogen bonds · protein-protein
  • C–D · 1757 Ų buried · 15 hydrogen bonds · protein-protein
  • A–I · 1481 Ų buried · 20 hydrogen bonds · protein-protein
  • C–F · 1252 Ų buried · 8 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 3 disulfide (disulfide).

Compared structures

  • 1SQB · Crystal Structure Analysis of Bovine Bc1 with Azoxystrobin · the same entry in another collection · chain K against K, TM-score 1.00
  • P00157 · AlphaFold monomer V2.0 prediction for cytochrome B (P00157) · a predicted model of the same protein · chain C against A, TM-score 1.00

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