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Cocrystal structure of camp-dependent protein kinase (PKA) in complex with a S-methyl-piperazine substituted fasudil-derivative (ligand 01)

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

PDB
5LCU
Type
protein
Length
373 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
IQP
Pockets
6 · best druggability 0.80

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)protein35341% helix, 15% strandP25321
BCamp-dependent protein kinase inhibitor alphaprotein2035% helix, 0% strandP61925

Ligands and binding sites

  • IQP · 1-(5-isoquinolinesulfonyl)-2-methylpiperazine · ligand · chains A, B
  • MOH · Methanol · additive · 3 copies · chains A
  • MPD · (4S)-2-methyl-2,4-pentanediol · additive · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13930.800.8950IQP
21500.570.8223MOH, MPD
3820.330.7519empty
4670.330.7615empty
5950.330.7315empty

Interfaces

1 interface between chains.

  • A–B · 934 Ų buried · 18 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 3 modified (phosphorylation).

Compared structures

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

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