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Bovine mitochondrial F1-ATPase complexed with the inhibitor protein IF1

Analyse Bovine mitochondrial F1-ATPase complexed with the inhibitor protein IF1 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1OHH
Type
protein
Length
2,986 residues
Chains
8
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
ATP synthase alpha chain heart isoform, mitochondrial; ATP synthase beta chain…
EC
3.6.1.34
UniProt
P19483, P00829, P05631, P01096
Ligands
ANP, MG
Pockets
20 · best druggability 0.87

Structure

x-ray diffraction · 7 distinct chains · 43% helix, 19% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AATP synthase alpha chain heart isoform, mitochondrial (EC 3.6.1.34)protein48743% helix, 20% strandP19483
BATP synthase alpha chain heart isoform, mitochondrial (EC 3.6.1.34)protein47942% helix, 20% strandP19483
CATP synthase alpha chain heart isoform, mitochondrial (EC 3.6.1.34)protein48842% helix, 21% strandP19483
DATP synthase beta chain, mitochondrial (EC 3.6.1.34)protein46939% helix, 20% strandP00829
E, FATP synthase beta chain, mitochondrial (EC 3.6.1.34)protein46637% helix, 22% strandP00829
GATP synthase gamma chain, mitochondrial (EC 3.6.1.34)protein9487% helix, 0% strandP05631
HATPase inhibitor, mitochondrialprotein3781% helix, 0% strandP01096

Ligands and binding sites

  • ANP · Phosphoaminophosphonic acid-adenylate ester · ligand · 5 copies · chains A, D, B, E, C, F
  • MG · Magnesium ion · metal · 5 copies · chains A, B, C, D, F

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16980.870.9182ANP, MG
23040.850.9566empty
34760.840.9168empty
48340.840.8679ANP, MG
55780.830.8866empty

Interfaces

18 interfaces between chains.

  • A–D · 2651 Ų buried · 31 hydrogen bonds · protein-protein
  • C–F · 2393 Ų buried · 24 hydrogen bonds · protein-protein
  • B–F · 2227 Ų buried · 32 hydrogen bonds · protein-protein
  • C–D · 2157 Ų buried · 34 hydrogen bonds · protein-protein
  • B–E · 1977 Ų buried · 20 hydrogen bonds · protein-protein

Compared structures

  • 1OHH · BOVINE MITOCHONDRIAL F1-ATPASE complexed with the inhibitor protein IF1 · the same entry in another collection · chain H against H, TM-score 1.00
  • P19483 · AlphaFold monomer V2.0 prediction for ATP synthase subunit alpha, mitochondrial (P19483) · a predicted model of the same protein · chain A against A, TM-score 0.99
  • P00829 · AlphaFold monomer V2.0 prediction for ATP synthase subunit beta, mitochondrial (P00829) · a predicted model of the same protein · chain E against A, TM-score 0.98

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