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Camp-dependent protein kinase a from cricetulus griseus in complex with fragment like molecule 3-amino-5-(trifluoromethyl)-1H-pyridin-2- one

Analyse Camp-dependent protein kinase a from cricetulus griseus in complex with… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5N33
Type
protein
Length
364 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, A0A061IH64
Ligands
8JW
Pockets
3 · best druggability 0.82

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)protein35139% helix, 15% strandP25321
BCamp-dependent protein kinase inhibitor alpha-like proteinprotein130% helix, 8% strandA0A061IH64

Ligands and binding sites

  • 8JW · 3-azanyl-5-(trifluoromethyl)-1~{H}-pyridin-2-one · ligand · chains A
  • MPD · (4S)-2-methyl-2,4-pentanediol · 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

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14020.820.91408JW
22590.590.7936MPD
3540.280.7414empty

Interfaces

1 interface between chains.

  • A–B · 950 Ų buried · 24 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 modified (phosphorylation).

Compared structures

  • 5N33 · cAMP-dependent Protein Kinase A from Cricetulus griseus in complex with fragment like… · the same entry in another collection · chain A against A, TM-score 1.00

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