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MolNFT v1 · #167558 · protein

Chloroplast ATP synthase (R3, CF1FO)

6VOJ · ATP synthase subunit alpha, chloroplastic: “Chloroplast ATP synthase (R3, CF1FO)”. Electron microscopy, 3 ligands (ATP, ADP, TTX), 20 pockets (best druggability 0.87). MolNFT v1 #167558 on GenesisL1: 3D structure, binding sites and…

PDB
6VOJ
Type
protein
Length
5,185 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, P00833, P05435, P06453, P31853, P06451, P69447
Ligands
ATP, ADP, TTX
Pockets
20 · best druggability 0.87

Structure

electron microscopy · 13 distinct chains · 46% helix, 15% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AATP synthase subunit alpha, chloroplastic (EC 7.1.2.2)protein49842% helix, 17% strandP06450
BATP synthase subunit alpha, chloroplastic (EC 7.1.2.2)protein50139% helix, 14% strandP06450
CATP synthase subunit alpha, chloroplastic (EC 7.1.2.2)protein50140% helix, 17% strandP06450
DATP synthase subunit beta, chloroplastic (EC 7.1.2.2)protein48036% helix, 19% strandP00825
EATP synthase subunit beta, chloroplastic (EC 7.1.2.2)protein47836% helix, 19% strandP00825
FATP synthase subunit beta, chloroplastic (EC 7.1.2.2)protein47935% helix, 18% strandP00825
dATP synthase delta chain, chloroplasticprotein17959% helix, 13% strandP11402
eATP synthase epsilon chain, chloroplasticprotein13130% helix, 33% strandP00833
gATP synthase gamma chain, chloroplasticprotein32254% helix, 7% strandP05435
IATP synthase subunit B, chloroplasticprotein15492% helix, 0% strandP06453
JATP synthase subunit B', chloroplasticprotein13496% helix, 0% strandP31853
aATP synthase subunit a, chloroplasticprotein22268% helix, 3% strandP06451
M, N, O, P, Q, R, S, T, U, V, W, X, Y, ZATP synthase subunit C, chloroplasticprotein7987% 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 B, D, F
  • TTX · Tentoxin · ligand · chains C, 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, 20 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110860.870.88112ATP
27840.860.89102empty
36940.840.8876ATP
411650.830.84108ATP
54820.830.9076ADP

Interfaces

63 interfaces between chains.

  • B–D · 2870 Ų buried · 34 hydrogen bonds · protein-protein
  • I–J · 2487 Ų buried · 10 hydrogen bonds · protein-protein
  • B–E · 2354 Ų buried · 20 hydrogen bonds · protein-protein
  • A–D · 2349 Ų buried · 26 hydrogen bonds · protein-protein
  • C–E · 2253 Ų buried · 18 hydrogen bonds · protein-protein

Compared structures

  • 6VOJ · Chloroplast ATP synthase (R3, CF1FO) · the same entry in another collection · chain g against g, TM-score 1.00

Analyse

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