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Crystal structure of ATP binding domain of prrb from mycobacterium tuberculosis

Analyse Crystal structure of ATP binding domain of prrb from mycobacterium tuberculosis in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1YSR
Type
protein
Length
410 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Sensor-type histidine kinase prrb
EC
2.7.3.-
UniProt
P0A5Z8
Pockets
5 · best druggability 0.74

Structure

x-ray diffraction · 3 distinct chains · 36% helix, 32% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ASensor-type histidine kinase prrb (EC 2.7.3.-)protein13736% helix, 31% strandP0A5Z8
BSensor-type histidine kinase prrb (EC 2.7.3.-)protein13736% helix, 33% strandP0A5Z8
CSensor-type histidine kinase prrb (EC 2.7.3.-)protein13636% helix, 32% strandP0A5Z8

Ligands and binding sites

  • TRS · 2-amino-2-hydroxymethyl-propane-1,3-diol · additive · 3 copies · chains A, B, C
  • GOL · Glycerol · additive · 3 copies · chains A, B, C

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1900.740.9626TRS
2950.720.9526TRS
3530.570.9118empty
43780.550.7339empty
5650.320.7512empty

Interfaces

3 interfaces between chains.

  • A–B · 615 Ų buried · 6 hydrogen bonds · protein-protein
  • A–C · 603 Ų buried · 6 hydrogen bonds · protein-protein
  • B–C · 105 Ų buried · 2 hydrogen bonds · protein-protein

Compared structures

  • 1YSR · Crystal Structure of ATP binding domain of PrrB from Mycobacterium Tuberculosis · the same entry in another collection · chain A against A, TM-score 1.00

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