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Camp-dependent protein kinase a from cricetulus griseus in complex with fragment like molecule N-methyl-1-(5-pyridin-3-yloxyfuran-2-yl) methanamine

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
5N1D
Type
protein
Length
369 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
8FZ
Pockets
4 · best druggability 0.76

Structure

x-ray diffraction · 2 distinct chains · 40% helix, 14% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ACamp-dependent protein kinase catalytic subunit alpha (EC 2.7.11.11)protein35140% helix, 15% strandP25321
BCamp-dependent protein kinase inhibitor alpha-like proteinprotein1839% helix, 0% strandA0A061IH64

Ligands and binding sites

  • 8FZ · (5-pyridin-3-yloxyfuran-2-yl)methanamine · ligand · chains A
  • MPD · (4S)-2-methyl-2,4-pentanediol · additive · 2 copies · 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
14450.760.85428FZ
21310.590.8421MPD
31140.380.7415empty
4720.310.7422empty

Interfaces

1 interface between chains.

  • A–B · 857 Ų buried · 18 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 3 modified (phosphorylation).

Compared structures

  • 5N1D · 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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