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The crystal structure of sporulation kinase D mutant sensor domain, R131A, from bacillus subtilis subsp at 2.4A resolution

Analyse The crystal structure of sporulation kinase D mutant sensor domain, R131A, from… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4JGR
Type
protein
Length
408 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Sporulation kinase D
EC
2.7.13.3
UniProt
O31671
Pockets
4 · best druggability 0.51

Structure

x-ray diffraction · 2 distinct chains · 36% helix, 28% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ASporulation kinase D (EC 2.7.13.3)protein20236% helix, 28% strandO31671
BSporulation kinase D (EC 2.7.13.3)protein20637% helix, 28% strandO31671

Ligands and binding sites

  • GOL · Glycerol · additive · 3 copies · chains B, A
  • ACY · Acetic acid · additive · 2 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12230.510.7628GOL
22090.480.7536empty
3960.340.7415empty
4610.260.7218empty

Interfaces

1 interface between chains.

  • A–B · 974 Ų buried · 7 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 10 modified (engineered).

Compared structures

  • 4JGR · The crystal structure of sporulation kinase D mutant sensor domain, R131A, from Bacillus… · the same entry in another collection · chain A against A, TM-score 1.00
  • O31671 · AlphaFold monomer V2.0 prediction for sporulation kinase D (O31671) · a predicted model of the same protein · chain B against A, TM-score 0.98

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