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Metal ion dependency of the antiterminator protein, hutp, for binding to the terminator region of hut mRNA- a structural basis

Analyse Metal ion dependency of the antiterminator protein, hutp, for binding to the… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1WRO
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, BA
Pockets
6 · best druggability 0.66

Structure

x-ray diffraction · 1 distinct chain · 39% helix, 30% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, CHut operon positive regulatory proteinprotein14739% helix, 30% strandP10943

Ligands and binding sites

  • HIS · Histidine · ligand · 3 copies · chains A, C, B
  • BA · Barium ion · metal · 6 copies · chains A, B, C

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1870.660.9122BA, HIS
2840.630.9020HIS
3760.620.9022HIS
41660.490.7728empty
5560.340.7812empty

Interfaces

3 interfaces between chains.

  • B–C · 556 Ų buried · 3 hydrogen bonds · protein-protein
  • A–B · 554 Ų buried · 3 hydrogen bonds · protein-protein
  • A–C · 543 Ų buried · 3 hydrogen bonds · protein-protein

Compared structures

  • 1WRO · Metal Ion dependency of the antiterminator protein, HutP, for binding to the terminator… · 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 C against A, TM-score 0.99

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