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Camp-dependent protein kinase a from cricetulus griseus in complex with fragment like molecule 2-amino-1-(4-FLUOROPHENYL)ETHANOL

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
5N1K
Type
protein
Length
357 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
489
Pockets
4 · best druggability 0.79

Structure

x-ray diffraction · 2 distinct chains · 36% helix, 15% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ACamp-dependent protein kinase catalytic subunit alpha (EC 2.7.11.11)protein34437% helix, 16% strandP25321
BCamp-dependent protein kinase inhibitor alpha-like proteinprotein130% helix, 8% strandA0A061IH64

Ligands and binding sites

  • 489 · (1S)-2-amino-1-(4-fluorophenyl)ethanol · ligand · 3 copies · chains A, B
  • DMS · Dimethyl sulfoxide · additive · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13530.790.8942489, DMS
21460.550.8120489
3530.280.7515empty
4600.270.7315empty

Interfaces

1 interface between chains.

  • A–B · 939 Ų buried · 24 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 3 modified (phosphorylation).

Compared structures

  • 5N1K · 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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