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Crystal structure of a domain of the sensory box sensor histidine KINASE/RESPONSE regulator from geobacter sulfurreducens

Analyse Crystal structure of a domain of the sensory box sensor histidine… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2R78
Type
protein
Length
460 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Sensor protein
EC
2.7.13.3
UniProt
Q74DN1
Pockets
3 · best druggability 0.69

Structure

x-ray diffraction · 3 distinct chains · 30% helix, 31% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ASensor protein (EC 2.7.13.3)protein11431% helix, 31% strandQ74DN1
B, DSensor protein (EC 2.7.13.3)protein11530% helix, 31% strandQ74DN1
CSensor protein (EC 2.7.13.3)protein11630% helix, 31% strandQ74DN1

Ligands and binding sites

  • ACT · Acetate ion · additive · 10 copies · chains A, B, C, D

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11140.690.9025ACT
2950.670.9024ACT
3650.540.8723ACT

Interfaces

4 interfaces between chains.

  • A–B · 1523 Ų buried · 7 hydrogen bonds · protein-protein
  • C–D · 1433 Ų buried · 6 hydrogen bonds · protein-protein
  • A–C · 385 Ų buried · 11 hydrogen bonds · protein-protein
  • B–C · 188 Ų buried · 0 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 modified (engineered).

Compared structures

  • 2R78 · Crystal structure of a domain of the sensory box sensor histidine kinase/response… · the same entry in another collection · chain A against A, TM-score 1.00

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