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Rabbit-muscle G-actin in complex with myxobacterial rhizopodin

Analyse Rabbit-muscle G-actin in complex with myxobacterial rhizopodin in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2VYP
Type
protein
Length
687 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Actin, alpha skeletal muscle
UniProt
P68135
Ligands
ATP, RH9, CA
Pockets
5 · best druggability 0.75

Structure

x-ray diffraction · 2 distinct chains · 45% helix, 20% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AActin, alpha skeletal muscleprotein35844% helix, 20% strandP68135
BActin, alpha skeletal muscleprotein32946% helix, 19% strandP68135

Ligands and binding sites

  • ATP · Adenosine-5'-triphosphate · ligand · 2 copies · chains A, B
  • RH9 · Rhizopodin · ligand · chains A, B
  • CA · Calcium ion · metal · 4 copies · chains A, B
  • HEZ · Hexane-1,6-diol · additive · 3 copies · chains A, B

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

Pockets

5 pockets found on a 1 Å grid, 4 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13530.750.8655ATP, CA
22720.710.8642ATP, CA
34670.570.7349HEZ
41580.530.7933empty
51560.470.7723empty

Interfaces

1 interface between chains.

  • A–B · 203 Ų buried · 2 hydrogen bonds · protein-protein

Compared structures

  • 2VYP · Rabbit-muscle G-actin in complex with myxobacterial rhizopodin · the same entry in another collection · chain A against A, TM-score 1.00
  • P68135 · AlphaFold monomer V2.0 prediction for actin, alpha skeletal muscle (P68135) · a predicted model of the same protein · chain A against A, TM-score 1.00

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