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Crystal structure of the V. cholerae histidine kinase dctb sensor domain

Analyse Crystal structure of the V. cholerae histidine kinase dctb sensor domain in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3BY9
Type
protein
Length
517 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Sensor protein
EC
2.7.13.3
UniProt
Q9KQS3
Ligands
CA
Pockets
2 · best druggability 0.31

Structure

x-ray diffraction · 2 distinct chains · 31% helix, 28% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ASensor protein (EC 2.7.13.3)protein25933% helix, 28% strandQ9KQS3
BSensor protein (EC 2.7.13.3)protein25830% helix, 28% strandQ9KQS3

Ligands and binding sites

  • CA · Calcium ion · metal · 2 copies · chains A
  • SIN · Succinic acid · additive · 2 copies · chains A, B

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

Pockets

2 pockets found on a 1 Å grid, 0 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1720.310.7415empty
2550.290.7516empty

Interfaces

1 interface between chains.

  • A–B · 70 Ų buried · 0 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 5 modified (engineered).

Compared structures

  • 3BY9 · Crystal structure of the V. cholerae Histidine Kinase DctB Sensor Domain · the same entry in another collection · chain A against A, TM-score 1.00

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