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Crystal structure of short hoefavidin-hoef-PEPTIDE(L9F) complex

Analyse Crystal structure of short hoefavidin-hoef-PEPTIDE(L9F) complex in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4Z2P
Type
protein
Length
274 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Avidin family; Hoef-peptide (L9F)
UniProt
A9D857
Pockets
3 · best druggability 0.49

Structure

x-ray diffraction · 4 distinct chains · 4% helix, 58% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AAvidin familyprotein1276% helix, 62% strandA9D857
PHoef-peptide (L9F)protein100% helix, 20% strand—
BAvidin familyprotein1263% helix, 60% strandA9D857
CHoef-peptide (L9F)protein110% helix, 18% strand—

Pockets

3 pockets found on a 1 Å grid, 0 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1630.490.8517empty
21200.470.7933empty
3520.460.8518empty

Interfaces

3 interfaces between chains.

  • A–B · 1642 Ų buried · 15 hydrogen bonds · protein-protein
  • A–P · 597 Ų buried · 8 hydrogen bonds · protein-protein
  • B–C · 571 Ų buried · 10 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 disulfide (disulfide).

Compared structures

  • 4Z2P · Crystal structure of short hoefavidin-hoef-peptide(L9F) complex · the same entry in another collection · chain B against B, TM-score 1.00
  • A9D857 · AlphaFold monomer V2.0 prediction for hoefavidin (A9D857) · a predicted model of the same protein · chain A against A, TM-score 0.99

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