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Crystal structure analysis of bovine BC1 with uhdbt

Analyse Crystal structure analysis of bovine BC1 with uhdbt in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1SQV
Type
protein
Length
2,100 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
HEC, UHD, UQ2, FES
Pockets
20 · best druggability 0.86

Structure

x-ray diffraction · 11 distinct chains · 50% helix, 12% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AUbiquinol-cytochrome C reductase complex core protein I, mitochondrial (EC 1.10.2.2)protein44645% helix, 19% strandP31800
BUbiquinol-cytochrome C reductase complex core protein 2, mitochondrial (EC 1.10.2.2)protein42345% helix, 20% strandP23004
CCytochrome B (EC 1.10.2.2)protein37874% helix, 2% strandP00157
DCytochrome C1, heme protein, mitochondrial (EC 1.10.2.2)protein24138% helix, 5% strandP00125
EUbiquinol-cytochrome C reductase iron-sulfur subunit (EC 1.10.2.2)protein19627% helix, 19% strandP13272
FUbiquinol-cytochrome C reductase complex 14 kda protein (EC 1.10.2.2)protein10564% helix, 1% strandP00129
GUbiquinol-cytochrome C reductase complex ubiquinone-binding protein qp-C (EC 1.10.2.2)protein7548% helix, 12% strandP13271
HUbiquinol-cytochrome C reductase complex 11 kda protein (EC 1.10.2.2)protein6772% helix, 0% strandP00126
IUbiquinol-cytochrome C reductase complex 8 kda protein (EC 1.10.2.2)protein577% helix, 11% strandP13272
JUbiquinol-cytochrome C reductase complex 7.2 kda protein (EC 1.10.2.2)protein6170% helix, 0% strandP00130
KUbiquinol-cytochrome C reductase complex 6.4 kda protein (EC 1.10.2.2)protein5163% helix, 0% strandP07552

Ligands and binding sites

  • HEC · Heme C · ligand · 3 copies · chains C, D
  • UHD · 6-hydroxy-5-undecyl-1,3-benzothiazole-4,7-dione · ligand · chains C
  • UQ2 · Ubiquinone-2 · 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
14390.860.9357HEC
28340.820.84100empty
35110.800.8650HEC, UQ2
46490.790.8454empty
56660.790.8459empty

Interfaces

24 interfaces between chains.

  • A–B · 2315 Ų buried · 38 hydrogen bonds · protein-protein
  • B–I · 2058 Ų buried · 21 hydrogen bonds · protein-protein
  • C–D · 1734 Ų buried · 14 hydrogen bonds · protein-protein
  • A–I · 1484 Ų buried · 19 hydrogen bonds · protein-protein
  • C–F · 1248 Ų buried · 8 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 3 disulfide (disulfide).

Compared structures

  • 1SQV · Crystal Structure Analysis of Bovine Bc1 with UHDBT · 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 0.99

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