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MolNFT v1 · #51057 · protein

Structure of pkb-beta (AKT2) complexed with 4-(4-chloro- phenyl)-4-(4-(1H-pyrazol-4-yl)-phenyl)-piperidine

2UW9 · Rac-beta SERINE/THREONINE-protein kinase: “Structure of pkb-beta (AKT2) complexed with 4-(4-chloro- phenyl)-4-(4-(1H-pyrazol-4-yl)-phenyl)-piperidine”. X-ray diffraction, 1 ligand (GVP), 5 pockets (best druggability 0.82). MolNFT v1…

PDB
2UW9
Type
protein
Length
327 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Rac-beta SERINE/THREONINE-protein kinase; Glycogen synthase kinase-3 beta
EC
2.7.11.1, 2.7.11.26
UniProt
P31751, P49841
Ligands
GVP
Pockets
5 · best druggability 0.82

Structure

x-ray diffraction · 2 distinct chains · 35% helix, 18% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ARac-beta SERINE/THREONINE-protein kinase (EC 2.7.11.1)protein31736% helix, 18% strandP31751
CGlycogen synthase kinase-3 beta (EC 2.7.11.26)protein100% helix, 20% strandP49841

Ligands and binding sites

  • GVP · 4-(4-chlorophenyl)-4-[4-(1H-pyrazol-4-yl)phenyl]piperidine · ligand · chains A, C

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
14700.820.8951GVP
2620.400.8017empty
3820.370.7615empty
4980.350.7414empty
5730.340.7617empty

Interfaces

1 interface between chains.

  • A–C · 698 Ų buried · 18 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 1 modified (phosphorylation).

Compared structures

  • 2UW9 · STRUCTURE OF PKB-BETA (AKT2) COMPLEXED WITH 4-(4-chloro-phenyl)-4-(4-(1H-pyrazol-4-yl)-phe… · the same entry in another collection · chain A against A, TM-score 1.00
  • P31751 · AlphaFold monomer V2.0 prediction for rac-beta SERINE/THREONINE- protein kinase (P31751) · a predicted model of the same protein · chain A against A, TM-score 0.98

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