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MolNFT v1 · #19074 · protein

The catalytic subunit of camp-dependent protein kinase (PKA) in complex with rho-kinase inhibitor Y-27632

1Q8T · Camp-dependent protein kinase, alpha-catalytic subunit: “The catalytic subunit of camp-dependent protein kinase (PKA) in complex with rho-kinase inhibitor Y-27632”. X-ray diffraction, 1 ligand (Y27), 6 pockets (best druggability…

PDB
1Q8T
Type
protein
Length
361 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Camp-dependent protein kinase, alpha-catalytic subunit; Camp-dependent protein kinase…
EC
2.7.1.37
UniProt
P00517, P04541
Ligands
Y27
Pockets
6 · best druggability 0.82

Structure

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

ChainMoleculeTypeResiduesSecondary structureUniProt
ACamp-dependent protein kinase, alpha-catalytic subunit (EC 2.7.1.37)protein34138% helix, 16% strandP00517
BCamp-dependent protein kinase inhibitor, alpha formprotein2030% helix, 5% strandP04541

Ligands and binding sites

  • Y27 · (R)-trans-4-(1-aminoethyl)-N-(4-pyridyl) cyclohexanecarboxamide · ligand · 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
13540.820.9142Y27
21170.530.8116empty
31140.450.7818empty
4870.310.7319empty
5580.290.7417empty

Interfaces

1 interface between chains.

  • A–B · 1050 Ų buried · 21 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 3 modified (phosphorylation).

Compared structures

  • 1Q8T · The Catalytic Subunit of cAMP-dependent Protein Kinase (PKA) in Complex with Rho-kinase… · the same entry in another collection · chain A against A, TM-score 1.00

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