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14-3-3 sigma with RELA/P65 binding site PS45 and covalently bound TCF521-173

Analyse 14-3-3 sigma with RELA/P65 binding site PS45 and covalently bound TCF521-173 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7O5X
Type
protein
Length
236 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
14-3-3 protein sigma; Transcription factor P65
UniProt
P31947, Q04206
Ligands
V3W, CA, CL
Pockets
2 · best druggability 0.55

Structure

x-ray diffraction · 2 distinct chains · 79% helix, 0% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A14-3-3 protein sigmaprotein22782% helix, 0% strandP31947
PTranscription factor P65protein90% helix, 0% strandQ04206

Ligands and binding sites

  • V3W · 4-(4-methoxypiperidin-1-yl)carbonylbenzaldehyde · ligand · chains A, P
  • CA · Calcium ion · metal · chains A
  • CL · Chloride ion · ion · 2 copies · chains A
  • PEG · Di(hydroxyethyl)ether · additive · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11930.550.7927V3W
2560.350.7917empty

Interfaces

1 interface between chains.

  • A–P · 574 Ų buried · 12 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 modified, 1 covalent (covalent ligand, oxidation, phosphorylation).

Compared structures

  • 7O5X · 14-3-3 sigma with RelA/p65 binding site pS45 and covalently bound TCF521-173 · the same entry in another collection · chain A against A, TM-score 1.00
  • P31947 · AlphaFold monomer V2.0 prediction for 14-3-3 protein sigma (P31947) · a predicted model of the same protein · chain A against A, TM-score 0.97

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