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Structure of phis Fab (SC44-8) in complex with phis mimetic peptide

Analyse Structure of phis Fab (SC44-8) in complex with phis mimetic peptide in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6X1V
Type
protein
Length
438 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
SC44-8 light chain; SC44-8 heavy chain; Aclyana-3-ptza peptide
Pockets
4 · best druggability 0.64

Structure

x-ray diffraction · 3 distinct chains · 7% helix, 52% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
LSC44-8 light chainprotein2158% helix, 57% strand—
HSC44-8 heavy chainprotein2166% helix, 48% strand—
DAclyana-3-ptza peptideprotein70% helix, 0% strand—

Ligands and binding sites

  • EDO · 1,2-ethanediol · additive · 2 copies · chains L, H

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15960.640.7557EDO
2890.370.7622empty
3730.310.7421empty
4560.290.7514empty

Interfaces

3 interfaces between chains.

  • L–H · 1877 Ų buried · 21 hydrogen bonds · protein-protein
  • L–D · 319 Ų buried · 7 hydrogen bonds · protein-protein
  • H–D · 284 Ų buried · 9 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 7 disulfide, 1 modified (disulfide, nonstandard).

Compared structures

  • 6X1V · Structure of pHis Fab (SC44-8) in complex with pHis mimetic peptide · the same entry in another collection · chain L against L, TM-score 1.00

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