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Cocrystal structure of camp-dependent protein kinase (PKA) in complex with the fasudil-fragment isoquinoline-5-sulfonamide

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

PDB
5M0C
Type
protein
Length
357 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
7CB
Pockets
4 · best druggability 0.80

Structure

x-ray diffraction · 2 distinct chains · 37% helix, 15% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ACamp-dependent protein kinase catalytic subunit alpha (EC 2.7.11.11)protein33837% helix, 15% strandP25321
BCamp-dependent protein kinase inhibitor alphaprotein1932% helix, 5% strandP61925

Ligands and binding sites

  • 7CB · isoquinoline-5-sulfonamide · ligand · chains A, B
  • MRD · (4R)-2-methylpentane-2,4-diol · additive · chains A
  • DMS · Dimethyl sulfoxide · 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, 1 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13050.800.91437CB
2640.440.8112empty
3620.320.7615empty
4510.260.7316empty

Interfaces

1 interface between chains.

  • A–B · 980 Ų buried · 22 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 modified (phosphorylation).

Compared structures

  • 5M0C · Cocrystal structure of cAMP-dependent Protein Kinase (PKA) in complex with the… · the same entry in another collection · chain A against A, TM-score 1.00

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