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Structure of phage TP901-1 rbp (ORF49) in complex with nanobody 11.

Analyse Structure of phage TP901-1 rbp (ORF49) in complex with nanobody 11. in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4IOS
Type
protein
Length
861 residues
Chains
8
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Bpp; Llama nanobody 11
UniProt
Q9G096
Pockets
9 · best druggability 0.74

Structure

x-ray diffraction · 6 distinct chains · 3% helix, 50% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, HBppprotein1003% helix, 49% strandQ9G096
B, CBppprotein993% helix, 49% strandQ9G096
DLlama nanobody 11protein1133% helix, 50% strand—
ELlama nanobody 11protein1183% helix, 50% strand—
FLlama nanobody 11protein1153% helix, 50% strand—
GLlama nanobody 11protein1173% helix, 49% strand—

Ligands and binding sites

  • GOL · Glycerol · additive · chains B

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

Pockets

9 pockets found on a 1 Å grid, 5 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1720.740.9819empty
22900.660.8237empty
32480.620.8138empty
42230.610.8230empty
53640.540.7349empty

Interfaces

12 interfaces between chains.

  • B–C · 819 Ų buried · 10 hydrogen bonds · protein-protein
  • A–C · 782 Ų buried · 11 hydrogen bonds · protein-protein
  • A–B · 758 Ų buried · 9 hydrogen bonds · protein-protein
  • C–F · 532 Ų buried · 12 hydrogen bonds · protein-protein
  • D–H · 529 Ų buried · 15 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 disulfide (disulfide).

Compared structures

  • 4IOS · Structure of phage TP901-1 RBP (ORF49) in complex with nanobody 11. · the same entry in another collection · chain A against A, TM-score 1.00

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