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Crystal structure of the alpha-kinase domain of myosin heavy chain kinase a complex with ADP

Analyse Crystal structure of the alpha-kinase domain of myosin heavy chain kinase a… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3LMH
Type
protein
Length
488 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Myosin heavy chain kinase a
EC
2.7.11.7
UniProt
P42527
Ligands
ADP, ZN, PO4
Pockets
5 · best druggability 0.77

Structure

x-ray diffraction · 2 distinct chains · 24% helix, 29% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AMyosin heavy chain kinase a (EC 2.7.11.7)protein24823% helix, 29% strandP42527
BMyosin heavy chain kinase a (EC 2.7.11.7)protein24024% helix, 30% strandP42527

Ligands and binding sites

  • ADP · Adenosine-5'-diphosphate · ligand · 2 copies · chains A, B
  • ZN · Zinc ion · metal · 2 copies · chains A, B
  • PO4 · Phosphate ion · ion · 2 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, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
111500.770.79106empty
22750.600.7938ADP
32180.550.7835ADP
4920.340.7417empty
5590.310.7512empty

Interfaces

1 interface between chains.

  • A–B · 1076 Ų buried · 15 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 modified (phosphorylation).

Compared structures

  • 3LMH · Crystal Structure of the Alpha-kinase Domain of Myosin Heavy Chain Kinase A Complex with… · the same entry in another collection · chain A against A, TM-score 1.00
  • P42527 · AlphaFold monomer V2.0 prediction for myosin heavy chain kinase a (P42527) · a predicted model of the same protein · chain A against A, TM-score 0.80

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