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Structural mechanism for the fine-tuning of ccpa function by the small molecule effectors glucose-6-phosphate and fructose-1,6-bisphosphate

Analyse Structural mechanism for the fine-tuning of ccpa function by the small molecule… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2OEN
Type
protein
Length
362 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Catabolite control protein; Phosphocarrier protein hpr
UniProt
P46828, O69250
Pockets
4 · best druggability 0.72

Structure

x-ray diffraction · 2 distinct chains · 37% helix, 16% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
GCatabolite control proteinprotein27538% helix, 15% strandP46828
LPhosphocarrier protein hprprotein8733% helix, 17% strandO69250

Pockets

4 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1530.720.9816empty
21480.680.8828empty
31470.520.8022empty
4690.370.7815empty

Interfaces

1 interface between chains.

  • G–L · 702 Ų buried · 6 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 1 modified (phosphorylation).

Compared structures

  • 2OEN · Structural mechanism for the fine-tuning of CcpA function by the small molecule effectors… · the same entry in another collection · chain G against G, TM-score 1.00
  • P46828 · AlphaFold monomer V2.0 prediction for catabolite control protein a (P46828) · a predicted model of the same protein · chain G against A, TM-score 0.99
  • O69250 · AlphaFold monomer V2.0 prediction for phosphocarrier protein hpr (O69250) · a predicted model of the same protein · chain L against A, TM-score 0.96

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