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MolNFT v1 · #94923 · protein

Structure of camp dependent protein kinase a in complex with high K+ concentration, ADP and phosphorylated peptide PSP20

4IB1 · Camp-dependent protein kinase catalytic subunit alpha: “Structure of camp dependent protein kinase a in complex with high K+ concentration, ADP and phosphorylated…”. X-ray diffraction, 2 ligands (ADP, K), 5 pockets (best…

PDB
4IB1
Type
protein
Length
358 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, K
Pockets
5 · best druggability 0.81

Structure

x-ray diffraction · 2 distinct chains · 36% helix, 16% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ACamp-dependent protein kinase catalytic subunit alpha (EC 2.7.11.11)protein33837% helix, 16% strandP05132
SPhosphorylated pseudo-substrate peptide PSP20protein2030% helix, 10% strand—

Ligands and binding sites

  • ADP · Adenosine-5'-diphosphate · ligand · chains A, S
  • K · Potassium 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
12030.810.9541K, ADP
2960.480.8014empty
3820.420.8019empty
4510.290.7513empty
5680.280.7314empty

Interfaces

1 interface between chains.

  • A–S · 1133 Ų buried · 29 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 modified (phosphorylation).

Compared structures

  • 4IB1 · Structure of cAMP dependent protein kinase A in complex with high K+ concentration, ADP… · the same entry in another collection · chain A against A, TM-score 1.00

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