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3-D structure of myosin-V inhibited state

Analyse 3-D structure of myosin-V inhibited state in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2DFS
Type
protein
Length
3,668 residues
Chains
14
Method
electron crystallography
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Myosin-5A; Calmodulin
UniProt
Q02440, P62204
Pockets
20 · best druggability 0.74

Structure

electron crystallography · 3 distinct chains · 56% helix, 11% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, MMyosin-5Aprotein99458% helix, 12% strandQ02440
B, D, F, N, P, RCalmodulinprotein13948% helix, 9% strandP62204
C, E, G, O, Q, SCalmodulinprotein14153% helix, 9% strandP62204

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
17040.740.8060empty
27330.740.7966empty
34240.650.7854empty
41570.640.8636empty
55400.620.7547empty

Interfaces

26 interfaces between chains.

  • A–M · 2411 Ų buried · 23 hydrogen bonds · protein-protein
  • A–G · 1872 Ų buried · 32 hydrogen bonds · protein-protein
  • M–O · 1561 Ų buried · 27 hydrogen bonds · protein-protein
  • M–S · 1560 Ų buried · 34 hydrogen bonds · protein-protein
  • M–Q · 1548 Ų buried · 17 hydrogen bonds · protein-protein

Compared structures

  • 2DFS · 3-D structure of Myosin-V inhibited state · the same entry in another collection · chain S against S, TM-score 1.00

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