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Threonine synthase from bacillus subtilis atcc 6633 with plp and appa

Analyse Threonine synthase from bacillus subtilis atcc 6633 with plp and appa in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6NMX
Type
protein
Length
1,396 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Threonine synthase
EC
4.2.3.1
UniProt
A8HUA2
Ligands
LJS
Pockets
12 · best druggability 0.79

Structure

x-ray diffraction · 3 distinct chains · 49% helix, 17% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AThreonine synthase (EC 4.2.3.1)protein35049% helix, 17% strandA8HUA2
B, CThreonine synthase (EC 4.2.3.1)protein34948% helix, 17% strandA8HUA2
DThreonine synthase (EC 4.2.3.1)protein34848% helix, 17% strandA8HUA2

Ligands and binding sites

  • LJS · (2E,3Z)-2-{[(Z)-{3-hydroxy-2-methyl-5-[(phosphonooxy) methyl]pyridin-4(1H)-ylidene}methyl]imino}-5-phosphonopent-3-enoic acid · ligand · 4 copies · chains A, B, C, D

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

Pockets

12 pockets found on a 1 Å grid, 8 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11130.790.9831LJS
21100.790.9830LJS
33630.790.8875empty
41060.790.9829LJS
51040.780.9830LJS

Interfaces

4 interfaces between chains.

  • A–C · 3288 Ų buried · 26 hydrogen bonds · protein-protein
  • B–D · 3265 Ų buried · 28 hydrogen bonds · protein-protein
  • B–C · 370 Ų buried · 3 hydrogen bonds · protein-protein
  • A–B · 49 Ų buried · 0 hydrogen bonds · protein-protein

Compared structures

  • 6NMX · Threonine synthase from Bacillus subtilis ATCC 6633 with PLP and APPA · the same entry in another collection · chain A against A, TM-score 1.00

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