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Crystal structure of mitochondrial cytochrome BC1 in complex with antimycin A1

Analyse Crystal structure of mitochondrial cytochrome BC1 in complex with antimycin A1 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1NTK
Type
protein
Length
2,114 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, AY1, FES
Pockets
20 · best druggability 0.83

Structure

x-ray diffraction · 11 distinct chains · 51% helix, 12% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AUbiquinol-cytochrome C reductase complex core protein I, mitochondrial (EC 1.10.2.2)protein44646% helix, 19% strandP31800
BUbiquinol-cytochrome C reductase complex core protein 2, mitochondrial (EC 1.10.2.2)protein42346% helix, 20% strandP23004
CCytochrome Bprotein37870% helix, 2% strandP00157
DCytochrome C1protein24142% helix, 6% strandP00125
EUbiquinol-cytochrome C reductase iron-sulfur subunit, mitochondrial (EC 1.10.2.2)protein19630% helix, 22% strandP13272
FUbiquinol-cytochrome C reductase complex 14 kda protein (EC 1.10.2.2)protein10569% helix, 0% strandP00129
GUbiquinol-cytochrome C reductase complex ubiquinone-binding protein qp-C (EC 1.10.2.2)protein7952% helix, 9% strandP13271
HUbiquinol-cytochrome C reductase complex 11 kda protein (EC 1.10.2.2)protein7676% helix, 0% strandP00126
IUbiquinol-cytochrome C reductase 8 kda protein (EC 1.10.2.2)protein5712% helix, 11% strandP13272
JUbiquinol-cytochrome C reductase complex 7.2 kda protein (EC 1.10.2.2)protein6072% helix, 0% strandP00130
KUbiquinol-cytochrome C reductase complex 6.4 kda protein (EC 1.10.2.2)protein5360% helix, 0% strandP07552

Ligands and binding sites

  • HEM · Protoporphyrin IX containing Fe · ligand · 3 copies · chains C, D
  • AY1 · [(2R,3S,6S,7R,8R)-3-[(3-formamido-2-oxidanyl-phenyl)carbonylamino]-8-hexyl-2,6-dimethyl-4,9-bis(oxidanylidene)-1,5-dioxonan-7-yl] 2-methylpropanoate · 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, 17 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
17930.830.8688HEM
29690.830.85102empty
38720.830.8596empty
46130.800.8553empty
54940.800.8652HEM, AY1

Interfaces

24 interfaces between chains.

  • A–B · 2198 Ų buried · 38 hydrogen bonds · protein-protein
  • B–I · 1955 Ų buried · 25 hydrogen bonds · protein-protein
  • C–D · 1681 Ų buried · 14 hydrogen bonds · protein-protein
  • A–I · 1523 Ų buried · 31 hydrogen bonds · protein-protein
  • C–F · 1266 Ų buried · 9 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 disulfide (disulfide).

Compared structures

  • 1NTK · Crystal Structure of Mitochondrial Cytochrome bc1 in Complex with Antimycin A1 · 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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