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Cryo-EM structure of euglena gracilis mitochondrial ATP synthase, membrane region

Analyse Cryo-EM structure of euglena gracilis mitochondrial ATP synthase, membrane… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6TDV
Type
protein
Length
5,464 residues
Chains
38
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
ATPTB1; ATPTB3; ATPTB6; ATPTB12; Subunit a; Subunit B; Subunit D; Subunit F; Subunit I/J…
Ligands
CDL, TRT, LPP
Pockets
20 · best druggability 0.86

Structure

electron microscopy · 19 distinct chains · 59% helix, 5% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, aATPTB1protein48656% helix, 7% strand—
B, bATPTB3protein3187% helix, 0% strand—
D, dATPTB6protein18673% helix, 1% strand—
E, eATPTB12protein9668% helix, 5% strand—
F, fSubunit aprotein27468% helix, 2% strand—
G, gSubunit Bprotein11149% helix, 14% strand—
H, hSubunit Dprotein38851% helix, 11% strand—
I, iSubunit Fprotein9768% helix, 1% strand—
J, jSubunit I/Jprotein10364% helix, 1% strand—
K, kSubunit Kprotein10365% helix, 1% strand—
L, lSubunit 8protein5751% helix, 0% strand—
M, mATPEG1protein16685% helix, 0% strand—
N, nATPEG2protein13140% helix, 1% strand—
O, oATPEG3protein10058% helix, 11% strand—
P, pATPEG4protein11444% helix, 1% strand—
Q, qATPEG5protein8970% helix, 0% strand—
R, rATPEG6protein6938% helix, 6% strand—
S, sATPEG7protein6546% helix, 8% strand—
T, tATPEG8protein6629% helix, 8% strand—

Ligands and binding sites

  • CDL · Cardiolipin · ligand · 25 copies · chains A, D, O, F, K, J, E, Q, M, f, m, n, p, N, P, R, a, d, o, k, j, e, q, G, I, g, i, r
  • TRT · Fragment of triton X-100 · ligand · 16 copies · chains F, G, I, P, n, M, N, g, i, K, R, f, p, m, k, r
  • LPP · 2-(hexadecanoyloxy)-1-[(phosphonooxy)methyl]ethyl hexadecanoate · ligand · 12 copies · chains F, K, Q, G, I, P, S, N, i, p, L, O, J, n, R, f, k, q, g, s, l, o, j, r
  • LMT · Dodecyl-beta-D-maltoside · additive · 8 copies · chains D, F, J, L, O, G, I, N, f, Q, R, d, j, l, o, g, i, n, q, r

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
17420.860.8987LMT
28230.850.88104LMT
35990.840.8976empty
48650.830.8593empty
57350.820.8571empty

Interfaces

202 interfaces between chains.

  • G–H · 3832 Ų buried · 37 hydrogen bonds · protein-protein
  • g–h · 3821 Ų buried · 37 hydrogen bonds · protein-protein
  • A–H · 3231 Ų buried · 30 hydrogen bonds · protein-protein
  • a–h · 3230 Ų buried · 30 hydrogen bonds · protein-protein
  • a–f · 2239 Ų buried · 26 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 disulfide (disulfide).

Compared structures

  • 6TDV · Cryo-EM structure of Euglena gracilis mitochondrial ATP synthase, membrane region · the same entry in another collection · chain B against B, TM-score 1.00

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