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Chloroplast ATP synthase (R2, CF1FO)

Analyse Chloroplast ATP synthase (R2, CF1FO) in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6VOL
Type
protein
Length
5,165 residues
Chains
26
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
ATP synthase subunit alpha, chloroplastic; ATP synthase subunit beta, chloroplastic; ATP…
EC
7.1.2.2
UniProt
P06450, P00825, P11402, P05435, P00833, P06453, P31853, P06451, P69447
Ligands
ATP, ADP, TTX
Pockets
20 · best druggability 0.87

Structure

electron microscopy · 13 distinct chains · 48% helix, 15% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AATP synthase subunit alpha, chloroplastic (EC 7.1.2.2)protein49741% helix, 16% strandP06450
BATP synthase subunit alpha, chloroplastic (EC 7.1.2.2)protein50142% helix, 17% strandP06450
CATP synthase subunit alpha, chloroplastic (EC 7.1.2.2)protein50044% helix, 18% strandP06450
DATP synthase subunit beta, chloroplastic (EC 7.1.2.2)protein47937% helix, 19% strandP00825
EATP synthase subunit beta, chloroplastic (EC 7.1.2.2)protein48038% helix, 20% strandP00825
FATP synthase subunit beta, chloroplastic (EC 7.1.2.2)protein47836% helix, 18% strandP00825
dATP synthase delta chain, chloroplasticprotein17963% helix, 12% strandP11402
gATP synthase gamma chain, chloroplasticprotein32156% helix, 12% strandP05435
eATP synthase epsilon chain, chloroplasticprotein13131% helix, 31% strandP00833
IATP synthase subunit B, chloroplasticprotein15097% helix, 0% strandP06453
JATP synthase subunit B', chloroplasticprotein13392% helix, 0% strandP31853
aATP synthase subunit a, chloroplasticprotein21075% helix, 0% strandP06451
M, N, O, P, Q, R, S, T, U, V, W, X, Y, ZATP synthase subunit C, chloroplasticprotein7985% helix, 0% strandP69447

Ligands and binding sites

  • ATP · Adenosine-5'-triphosphate · ligand · 4 copies · chains A, D, B, E, C, F
  • ADP · Adenosine-5'-diphosphate · ligand · 2 copies · chains D, C, E
  • TTX · Tentoxin · ligand · chains A, 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
17710.870.90107ATP
27960.870.9093ATP
36550.860.9075ATP
410610.840.85103TTX
58070.830.86100empty

Interfaces

60 interfaces between chains.

  • C–E · 3089 Ų buried · 41 hydrogen bonds · protein-protein
  • B–E · 2364 Ų buried · 31 hydrogen bonds · protein-protein
  • A–F · 2340 Ų buried · 32 hydrogen bonds · protein-protein
  • C–F · 2288 Ų buried · 24 hydrogen bonds · protein-protein
  • I–J · 2192 Ų buried · 7 hydrogen bonds · protein-protein

Compared structures

  • 6VOL · Chloroplast ATP synthase (R2, CF1FO) · the same entry in another collection · chain I against I, TM-score 1.00

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