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5-fluorotryptophan incorporated SCFV10 complexed to hen egg lysozyme

Analyse 5-fluorotryptophan incorporated SCFV10 complexed to hen egg lysozyme in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2ZNX
Type
protein
Length
700 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Scfv; Lysozyme C
EC
3.2.1.17
UniProt
P00698
Ligands
1PG
Pockets
11 · best druggability 0.75

Structure

x-ray diffraction · 2 distinct chains · 19% helix, 35% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BScfvprotein2215% helix, 50% strand—
Y, ZLysozyme C (EC 3.2.1.17)protein12941% helix, 11% strandP00698

Ligands and binding sites

  • 1PG · 2-(2-{2-[2-(2-methoxy-ethoxy)-ethoxy]-ethoxy}-ethoxy)-ethanol · ligand · 2 copies · chains A, Y, B, Z

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

Pockets

11 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14240.750.8567empty
21680.660.86281PG
31970.650.84331PG
4960.380.7519empty
5840.370.7617empty

Interfaces

5 interfaces between chains.

  • B–Z · 970 Ų buried · 24 hydrogen bonds · protein-protein
  • A–Y · 949 Ų buried · 27 hydrogen bonds · protein-protein
  • Y–B · 499 Ų buried · 7 hydrogen bonds · protein-protein
  • A–Z · 496 Ų buried · 7 hydrogen bonds · protein-protein
  • A–B · 261 Ų buried · 0 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 12 disulfide, 12 modified (disulfide, nonstandard).

Compared structures

  • 2ZNX · 5-Fluorotryptophan Incorporated ScFv10 Complexed to Hen Egg Lysozyme · the same entry in another collection · chain A against A, TM-score 1.00

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