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The crystal structure of an engineered phage lysin containing the binding domain of pesticin and the killing domain of T4-lysozyme

Analyse The crystal structure of an engineered phage lysin containing the binding… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4EXM
Type
protein
Length
1,244 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Pesticin, lysozyme chimera
EC
3.2.1.17
UniProt
Q57159, P00720
Pockets
16 · best druggability 0.73

Structure

x-ray diffraction · 3 distinct chains · 40% helix, 21% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
APesticin, lysozyme chimera (EC 3.2.1.17)protein29140% helix, 22% strandQ57159, P00720
BPesticin, lysozyme chimera (EC 3.2.1.17)protein29140% helix, 21% strandQ57159, P00720
C, DPesticin, lysozyme chimera (EC 3.2.1.17)protein33140% helix, 21% strandQ57159, P00720

Pockets

16 pockets found on a 1 Å grid, 6 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1600.730.9819empty
25350.700.7974empty
33670.670.8049empty
45040.650.7750empty
52990.610.7929empty

Interfaces

6 interfaces between chains.

  • B–C · 1469 Ų buried · 9 hydrogen bonds · protein-protein
  • A–D · 1462 Ų buried · 9 hydrogen bonds · protein-protein
  • A–B · 663 Ų buried · 11 hydrogen bonds · protein-protein
  • C–D · 413 Ų buried · 11 hydrogen bonds · protein-protein
  • A–C · 181 Ų buried · 2 hydrogen bonds · protein-protein

Compared structures

  • 4EXM · The crystal structure of an engineered phage lysin containing the binding domain of… · the same entry in another collection · chain A against A, TM-score 1.00

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