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Crystal structure of the receiver domain of cpxr from E. COLI (phosphorylated)

Analyse Crystal structure of the receiver domain of cpxr from E. COLI (phosphorylated) in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4UHK
Type
protein
Length
386 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Transcriptional regulatory protein cpxr
UniProt
P0AE88
Ligands
MG
Pockets
4 · best druggability 0.56

Structure

x-ray diffraction · 2 distinct chains · 49% helix, 18% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ATranscriptional regulatory protein cpxrprotein13048% helix, 18% strandP0AE88
B, CTranscriptional regulatory protein cpxrprotein12849% helix, 18% strandP0AE88

Ligands and binding sites

  • MG · Magnesium ion · metal · 3 copies · chains A, B, C

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
12560.560.7729empty
21650.550.8021empty
31160.480.8019empty
41050.390.7717empty

Interfaces

2 interfaces between chains.

  • B–C · 1468 Ų buried · 29 hydrogen bonds · protein-protein
  • A–B · 231 Ų buried · 6 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 3 modified (phosphorylation).

Compared structures

  • 4UHK · Crystal structure of the receiver domain of CpxR from E. coli (phosphorylated) · the same entry in another collection · chain A against A, TM-score 1.00
  • P0AE88 · AlphaFold monomer V2.0 prediction for transcriptional regulatory protein cpxr (P0AE88) · a predicted model of the same protein · chain C against A, TM-score 0.93

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