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Structure and allostery of the PKA riib tetrameric holoenzyme

Analyse Structure and allostery of the PKA riib tetrameric holoenzyme in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3TNP
Type
protein
Length
1,214 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Camp-dependent protein kinase catalytic subunit alpha; Camp-dependent protein kinase type…
EC
2.7.11.11
UniProt
P05132, P31324
Pockets
20 · best druggability 0.78

Structure

x-ray diffraction · 2 distinct chains · 33% helix, 23% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
C, FCamp-dependent protein kinase catalytic subunit alpha (EC 2.7.11.11)protein33736% helix, 16% strandP05132
B, ECamp-dependent protein kinase type II-beta regulatory subunitprotein27029% helix, 32% strandP31324

Pockets

20 pockets found on a 1 Å grid, 9 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14080.780.8753empty
22560.770.9037empty
33400.630.7941empty
42770.580.7825empty
52850.570.7736empty

Interfaces

5 interfaces between chains.

  • C–B · 2026 Ų buried · 41 hydrogen bonds · protein-protein
  • F–E · 2025 Ų buried · 41 hydrogen bonds · protein-protein
  • B–E · 358 Ų buried · 2 hydrogen bonds · protein-protein
  • B–F · 352 Ų buried · 3 hydrogen bonds · protein-protein
  • C–E · 348 Ų buried · 3 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 6 modified (phosphorylation).

Compared structures

  • 3TNP · Structure and Allostery of the PKA RIIb Tetrameric Holoenzyme · the same entry in another collection · chain C against C, TM-score 1.00
  • P31324 · AlphaFold monomer V2.0 prediction for camp-dependent protein kinase type II-beta… · a predicted model of the same protein · chain B against A, TM-score 0.87

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