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P53 DNA binding domain in complex with NB139

Analyse P53 DNA binding domain in complex with NB139 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4QO1
Type
protein
Length
326 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
NB139 nanobody against the DNA-binding domain of P53; Cellular tumor antigen P53
UniProt
P04637
Ligands
ZN
Pockets
1 · best druggability 0.61

Structure

x-ray diffraction · 2 distinct chains · 10% helix, 40% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ANB139 nanobody against the DNA-binding domain of P53protein12711% helix, 48% strand—
BCellular tumor antigen P53protein1999% helix, 34% strandP04637

Ligands and binding sites

  • ZN · Zinc ion · metal · chains B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12450.610.8147empty

Interfaces

1 interface between chains.

  • A–B · 508 Ų buried · 7 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 1 disulfide (disulfide).

Compared structures

  • 4QO1 · p53 DNA binding domain in complex with Nb139 · the same entry in another collection · chain A against A, TM-score 1.00

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