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Crystal structure of activated binary complex of hutp, an RNA binding anti-termination protein

Analyse Crystal structure of activated binary complex of hutp, an RNA binding… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1WPV
Type
protein
Length
441 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Hut operon positive regulatory protein
UniProt
P10943
Ligands
HIS, MG
Pockets
4 · best druggability 0.69

Structure

x-ray diffraction · 1 distinct chain · 37% helix, 30% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, CHut operon positive regulatory proteinprotein14737% helix, 30% strandP10943

Ligands and binding sites

  • HIS · Histidine · ligand · 3 copies · chains A, C, B
  • 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, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1750.690.9421HIS
2740.680.9421HIS
3730.640.9220HIS
41490.470.7728empty

Interfaces

3 interfaces between chains.

  • A–B · 568 Ų buried · 4 hydrogen bonds · protein-protein
  • B–C · 565 Ų buried · 4 hydrogen bonds · protein-protein
  • A–C · 558 Ų buried · 4 hydrogen bonds · protein-protein

Compared structures

  • 1WPV · Crystal Structure of Activated Binary complex of HutP, an RNA binding anti-termination… · the same entry in another collection · chain A against A, TM-score 1.00
  • P10943 · AlphaFold monomer V2.0 prediction for hut operon positive regulatory protein (P10943) · a predicted model of the same protein · chain A against A, TM-score 1.00

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