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Cocrystal structure of camp-dependent protein kinase (PKA) in complex with long-chain fasudil-derivative (ligand 05)

Analyse Cocrystal structure of camp-dependent protein kinase (PKA) in complex with… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5LCQ
Type
protein
Length
371 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Camp-dependent protein kinase catalytic subunit alpha; Camp-dependent protein kinase…
EC
2.7.11.11
UniProt
P25321, P61925
Ligands
6TV
Pockets
4 · best druggability 0.72

Structure

x-ray diffraction · 2 distinct chains · 40% helix, 14% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ACamp-dependent protein kinase catalytic subunit alpha (EC 2.7.11.11)protein35340% helix, 15% strandP25321
BCamp-dependent protein kinase inhibitor alphaprotein1839% helix, 0% strandP61925

Ligands and binding sites

  • 6TV · ~{N}-[2-(propylamino)ethyl]isoquinoline-5-sulfonamide · ligand · chains A, B
  • MOH · Methanol · additive · 2 copies · chains A, B
  • MRD · (4R)-2-methylpentane-2,4-diol · additive · chains A

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

Pockets

4 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11840.720.89326TV
21260.600.8519MRD
3840.320.7316empty
4550.280.7414empty

Interfaces

1 interface between chains.

  • A–B · 820 Ų buried · 22 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 3 modified (phosphorylation).

Compared structures

  • 5LCQ · Cocrystal structure of cAMP-dependent Protein Kinase (PKA) in complex with long-chain… · the same entry in another collection · chain A against A, TM-score 1.00

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