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MolNFT v1 · #147738 · protein

Crystal structure of the protein-kinase a catalytic subunit from criteculus griseus in complex with compounds RKP153 and fasudil

6EMB · Camp-dependent protein kinase catalytic subunit alpha: “Crystal structure of the protein-kinase a catalytic subunit from criteculus griseus in complex with compounds…”. X-ray diffraction, 2 ligands (M77, RIP), 2 pockets (best…

PDB
6EMB
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
Ligands
M77, RIP
Pockets
2 · best druggability 0.74

Structure

x-ray diffraction · 2 distinct chains · 39% helix, 14% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ACamp-dependent protein kinase catalytic subunit alpha (EC 2.7.11.11)protein35339% helix, 15% strandP25321
DCamp-dependent protein kinase inhibitorprotein1844% helix, 0% strand—

Ligands and binding sites

  • M77 · 5-(1,4-diazepan-1-sulfonyl)isoquinoline · ligand · chains A, D
  • RIP · beta-D-ribopyranose · ligand · chains D

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15000.740.8351M77
22900.590.7838empty

Interfaces

1 interface between chains.

  • A–D · 819 Ų buried · 16 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 modified, 1 covalent (phosphorylation, covalent ligand).

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