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Cryo-EM structure of F-actin in complex with ADP

Analyse Cryo-EM structure of F-actin in complex with ADP in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5ONV
Type
protein
Length
1,855 residues
Chains
5
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Actin, alpha skeletal muscle
UniProt
P68135
Ligands
ADP, MG
Pockets
17 · best druggability 0.83

Structure

electron microscopy · 1 distinct chain · 44% helix, 20% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, D, EActin, alpha skeletal muscleprotein37144% helix, 20% strandP68135

Ligands and binding sites

  • ADP · Adenosine-5'-diphosphate · ligand · 5 copies · chains A, B, C, D, E
  • MG · Magnesium ion · metal · 5 copies · chains A, B, C, D, E

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

Pockets

17 pockets found on a 1 Å grid, 11 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
111160.830.84100empty
23140.810.9158ADP, MG
35270.800.8665empty
42730.800.9248ADP, MG
52880.790.9047ADP, MG

Interfaces

7 interfaces between chains.

  • B–D · 1198 Ų buried · 13 hydrogen bonds · protein-protein
  • A–C · 1197 Ų buried · 13 hydrogen bonds · protein-protein
  • C–E · 1193 Ų buried · 13 hydrogen bonds · protein-protein
  • C–D · 485 Ų buried · 6 hydrogen bonds · protein-protein
  • B–C · 484 Ų buried · 6 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 5 modified (methylation).

Compared structures

  • 5ONV · Cryo-EM structure of F-actin in complex with ADP · the same entry in another collection · chain E against E, TM-score 1.00
  • P68135 · AlphaFold monomer V2.0 prediction for actin, alpha skeletal muscle (P68135) · a predicted model of the same protein · chain E against A, TM-score 0.96

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