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Camp-dependent protein kinase a from cricetulus griseus in complex with fragment like molecule 4-methyl-5-(1-methylimidazol-2-yl)-1,3- thiazol-2-amine

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
5N3A
Type
protein
Length
366 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
46P
Pockets
3 · 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)protein35338% helix, 15% strandP25321
BCamp dependent protein kinase inhibitor alpha-like proteinprotein130% helix, 8% strand—

Ligands and binding sites

  • 46P · 4-methyl-5-(1-methyl-1H-imidazol-2-yl)-1,3-thiazol-2-amine · ligand · chains A
  • DMS · Dimethyl sulfoxide · additive · 2 copies · chains A
  • 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

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13340.800.904346P
22520.590.7938MPD
3650.330.7618empty

Interfaces

1 interface between chains.

  • A–B · 914 Ų buried · 23 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 modified (phosphorylation).

Compared structures

  • 5N3A · 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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