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Crystal structure of cortisol complexed with its nanobody at pH 10.5

Analyse Crystal structure of cortisol complexed with its nanobody at pH 10.5 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6ITQ
Type
protein
Length
489 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Anti-cortisol camelid antibody
Ligands
HCY, SO4
Pockets
6 · best druggability 0.81

Structure

x-ray diffraction · 3 distinct chains · 6% helix, 52% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, DAnti-cortisol camelid antibodyprotein1225% helix, 52% strand—
BAnti-cortisol camelid antibodyprotein1208% helix, 53% strand—
CAnti-cortisol camelid antibodyprotein1255% helix, 51% strand—

Ligands and binding sites

  • HCY · (11alpha,14beta)-11,17,21-trihydroxypregn-4-ene-3,20-dione · ligand · 4 copies · chains A, B, C, D
  • SO4 · Sulfate ion · ion · 2 copies · chains C, D

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110510.810.82112HCY
22080.590.8141empty
31890.570.8129HCY
41650.560.8123HCY
51400.420.7525empty

Interfaces

5 interfaces between chains.

  • A–C · 703 Ų buried · 12 hydrogen bonds · protein-protein
  • A–B · 432 Ų buried · 10 hydrogen bonds · protein-protein
  • C–D · 426 Ų buried · 8 hydrogen bonds · protein-protein
  • B–D · 246 Ų buried · 2 hydrogen bonds · protein-protein
  • B–C · 50 Ų buried · 0 hydrogen bonds · protein-protein

Compared structures

  • 6ITQ · Crystal structure of cortisol complexed with its nanobody at pH 10.5 · the same entry in another collection · chain A against A, TM-score 1.00

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