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MolNFT v1 · #162609 · protein

Cryo-EM structure of polytomella F-ATP synthase, rotary substate 2C, monomer-masked refinement

6RE6 · Asa-10: polytomella F-ATP synthase associated subunit 10: “Cryo-EM structure of polytomella F-ATP synthase, rotary substate 2C, monomer-masked refinement”. Electron microscopy, 4 ligands (ATP, ADP, MG), 20 pockets (best druggability…

PDB
6RE6
Type
protein
Length
7,099 residues
Chains
31
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Asa-10: polytomella F-ATP synthase associated subunit 10; ATP synthase associated protein…
EC
7.1.2.2
UniProt
Q85JD5, K0J903, D7NIZ2, A0A024FSR7, D7P897, D8V7I2, D8V7I7, D7P7X5, H8PGG3, D8V7I1, D7P7X6, Q4LDE7, A0ZW40, A0ZW41
Ligands
ATP, ADP, MG, ZN
Pockets
20 · best druggability 0.89

Structure

electron microscopy · 21 distinct chains · 48% helix, 11% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
0Asa-10: polytomella F-ATP synthase associated subunit 10protein8132% helix, 2% strand—
1ATP synthase associated protein ASA1protein59561% helix, 1% strandQ85JD5
2Asa-2: polytomella F-ATP synthase associated subunit 2protein44162% helix, 5% strand—
3Mitochondrial F1F0 ATP synthase associated 32 kda proteinprotein24569% helix, 2% strandK0J903
4Mitochondrial ATP synthase associated protein ASA4protein29070% helix, 1% strandD7NIZ2
5Mitochondrial F1F0 ATP synthase associated 14 kda proteinprotein12368% helix, 0% strandA0A024FSR7
6Mitochondrial ATP synthase subunit ASA6protein12455% helix, 0% strandD7P897
7Mitochondrial ATP synthase associated protein ASA7protein17647% helix, 13% strandD8V7I2
8Mitochondrial ATP synthase subunit ASA8protein8857% helix, 0% strandD8V7I7
9Asa-9: polytomella F-ATP synthase associated subunit 9protein9748% helix, 0% strand—
A, B, C, D, E, F, G, H, I, JMitochondrial ATP synthase subunit Cprotein7491% helix, 0% strandD7P7X5
MMitochondrial ATP synthase subunit 6protein21768% helix, 2% strandH8PGG3
PMitochondrial ATP synthase subunit oscpprotein19353% helix, 12% strandD8V7I1
QEpsilon: polytomella F-ATP synthase epsilon subunitprotein7232% helix, 17% strand—
RMitochondrial ATP synthase subunit deltaprotein17725% helix, 28% strandD7P7X6
SATP synthase gamma chain, mitochondrialprotein27757% helix, 14% strandQ4LDE7
T, UATP synthase subunit alphaprotein52337% helix, 18% strandA0ZW40
VATP synthase subunit alphaprotein52038% helix, 18% strandA0ZW40
XATP synthase subunit beta (EC 7.1.2.2)protein53835% helix, 19% strandA0ZW41
YATP synthase subunit beta (EC 7.1.2.2)protein52035% helix, 18% strandA0ZW41
ZATP synthase subunit beta (EC 7.1.2.2)protein53933% helix, 18% strandA0ZW41

Ligands and binding sites

  • ATP · Adenosine-5'-triphosphate · ligand · 3 copies · chains T, X, U, Z, V, Y
  • ADP · Adenosine-5'-diphosphate · ligand · 2 copies · chains T, Y, V, Z
  • MG · Magnesium ion · metal · 5 copies · chains T, U, V, Y, Z
  • ZN · Zinc ion · metal · chains 6, M

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
111390.890.9091empty
27810.880.91115ATP, MG
37390.840.8865ATP, MG
46010.840.8981ATP, MG
59470.820.8389empty

Interfaces

101 interfaces between chains.

  • V–Z · 4214 Ų buried · 40 hydrogen bonds · protein-protein
  • 1–5 · 3917 Ų buried · 33 hydrogen bonds · protein-protein
  • U–X · 3662 Ų buried · 31 hydrogen bonds · protein-protein
  • T–Y · 3354 Ų buried · 35 hydrogen bonds · protein-protein
  • 4–7 · 3088 Ų buried · 33 hydrogen bonds · protein-protein

Compared structures

  • 6RE6 · Cryo-EM structure of Polytomella F-ATP synthase, Rotary substate 2C, monomer-masked… · the same entry in another collection · chain 1 against 1, TM-score 1.00

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