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The structure of T4 lysozyme I3C/C54T/R125C/E128C complex with zinc ions

Analyse The structure of T4 lysozyme I3C/C54T/R125C/E128C complex with zinc ions in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7DWS
Type
protein
Length
421 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Endolysin
EC
3.2.1.17
UniProt
D9IEF7
Ligands
ZN
Pockets
5 · best druggability 0.67

Structure

x-ray diffraction · 3 distinct chains · 63% helix, 2% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AEndolysin (EC 3.2.1.17)protein16459% helix, 6% strandD9IEF7
BEndolysin (EC 3.2.1.17)protein13365% helix, 0% strandD9IEF7
CEndolysin (EC 3.2.1.17)protein12468% helix, 0% strandD9IEF7

Ligands and binding sites

  • ZN · Zinc ion · metal · 4 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, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13370.670.8143empty
21880.600.8230empty
3500.500.8713empty
41170.470.7924empty
5720.280.7223empty

Interfaces

2 interfaces between chains.

  • A–C · 517 Ų buried · 6 hydrogen bonds · protein-protein
  • B–C · 217 Ų buried · 0 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 1 disulfide (disulfide).

Compared structures

  • 7DWS · The structure of T4 Lysozyme I3C/C54T/R125C/E128C complex with Zinc ions · the same entry in another collection · chain A against A, TM-score 1.00

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