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Crystal structure of Bacillus subtilis LytE in complex with IseA

Analyse Crystal structure of Bacillus subtilis LytE in complex with IseA in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
8I2E
Type
protein
Length
542 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
3.2
Source
Bacillus subtilis subsp. subtilis str. 168
Molecule
Uncharacterized protein YoeB; Probable peptidoglycan endopeptidase LytE
EC
3.4.-.-
UniProt
O34841, P54421
Pockets
5 · best druggability 0.64

Structure

x-ray diffraction · resolution 3.2 · 2 distinct chains · 26% helix, 32% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, CUncharacterized protein YoeBprotein15327% helix, 33% strandO34841
B, DProbable peptidoglycan endopeptidase LytE (EC 3.4.-.-)protein11825% helix, 31% strandP54421

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16250.640.7560empty
2800.430.8016empty
31120.390.7523empty
4830.350.7619empty
5700.310.7419empty

Interfaces

3 interfaces between chains.

  • A–B · 1154 Ų buried · 22 hydrogen bonds · protein-protein
  • C–D · 1131 Ų buried · 21 hydrogen bonds · protein-protein
  • A–C · 557 Ų buried · 6 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 disulfide (disulfide).

Compared structures

  • P54421 · AlphaFold monomer V2.0 prediction for probable peptidoglycan endopeptidase lyte (P54421) · a predicted model of the same protein · chain B against A, TM-score 0.98
  • O34841 · AlphaFold monomer V2.0 prediction for uncharacterized protein yoeb (O34841) · a predicted model of the same protein · chain A against A, TM-score 0.96

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