GL1X · GenesisL1 explorer

MolNFT v1 · #94901 · protein

Room temperature X-ray structure of camp dependent protein kinase a in complex with high MG2+ concentration, ADP and phosphorylated peptide PSP20

4IAF · Camp-dependent protein kinase catalytic subunit alpha: “Room temperature X-ray structure of camp dependent protein kinase a in complex with high MG2+ concentration…”. X-ray diffraction, 2 ligands (ADP, MG), 5 pockets (best…

PDB
4IAF
Type
protein
Length
356 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Camp-dependent protein kinase catalytic subunit alpha; Phosphorylated pseudo-substrate…
EC
2.7.11.11
UniProt
P05132
Ligands
ADP, MG
Pockets
5 · best druggability 0.80

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)protein33636% helix, 15% strandP05132
SPhosphorylated pseudo-substrate peptide PSP20protein2030% helix, 5% strand—

Ligands and binding sites

  • ADP · Adenosine-5'-diphosphate · ligand · chains A, S
  • MG · Magnesium ion · metal · 2 copies · chains A, S

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12050.800.9435MG, ADP
2800.420.7916empty
3520.390.8011empty
4650.290.7420empty
5650.280.7315empty

Interfaces

1 interface between chains.

  • A–S · 1103 Ų buried · 29 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 modified (phosphorylation).

Compared structures

  • 4IAF · Room temperature X-ray Structure OF cAMP dependent protein kinase A in complex with high… · the same entry in another collection · chain A against A, TM-score 1.00

Analyse

GL1X is a live explorer of the GenesisL1 blockchain. Turn on JavaScript for search, charts and interactive views.