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Cocrystal structure of camp-dependent protein kinase (PKA) in complex with a short-chained N-(2-AMINOETHYL)ISOQUINOLINE-5-sulfonamide) fasudil-derivative (ligand 03)

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
5M0B
Type
protein
Length
372 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
IQU
Pockets
5 · best druggability 0.72

Structure

x-ray diffraction · 2 distinct chains · 40% helix, 15% 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 alphaprotein1937% helix, 5% strandP61925

Ligands and binding sites

  • IQU · N-(2-aminoethyl)isoquinoline-5-sulfonamide · ligand · chains A, B
  • MOH · Methanol · additive · 2 copies · chains A, B
  • 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

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12130.720.8834IQU
21420.600.8422MPD
3960.460.8021empty
4940.350.7416empty
5610.280.7417MOH

Interfaces

1 interface between chains.

  • A–B · 890 Ų buried · 22 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 3 modified (phosphorylation).

Compared structures

  • 5M0B · 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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