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MolNFT v1 · #147733 · protein

Crystal structure of the protein-kinase a catalytic subunit from criteculus griseus in complex with compounds RKP032 and ADP

6EM6 · Camp-dependent protein kinase catalytic subunit alpha: “Crystal structure of the protein-kinase a catalytic subunit from criteculus griseus in complex with compounds…”. X-ray diffraction, 3 ligands (ADP, RIP, MG), 4 pockets (best…

PDB
6EM6
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; UPF0418 protein FAM164A
EC
2.7.11.11
UniProt
P25321, G3HK48
Ligands
ADP, RIP, MG
Pockets
4 · best druggability 0.71

Structure

x-ray diffraction · 2 distinct chains · 39% helix, 14% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ACamp-dependent protein kinase catalytic subunit alpha (EC 2.7.11.11)protein34039% helix, 15% strandP25321
CUPF0418 protein FAM164Aprotein1844% helix, 0% strandG3HK48

Ligands and binding sites

  • ADP · Adenosine-5'-diphosphate · ligand · chains A
  • RIP · beta-D-ribopyranose · ligand · chains C
  • MG · Magnesium ion · metal · 2 copies · chains A

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
14930.710.8149ADP, MG
21040.500.8113empty
3790.360.7620empty
4520.250.7311empty

Interfaces

1 interface between chains.

  • A–C · 707 Ų buried · 13 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 3 modified, 1 covalent (phosphorylation, covalent ligand).

Compared structures

  • 6EM6 · Crystal structure of the Protein-Kinase A catalytic subunit from Criteculus Griseus in… · the same entry in another collection · chain A against A, TM-score 1.00

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