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Crystal structure of computationally designed armadillo repeat proteins for modular peptide recognition.

Analyse Crystal structure of computationally designed armadillo repeat proteins for… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4D49
Type
protein
Length
988 residues
Chains
8
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Armadillo repeat protein ARM00027; Poly arg decapeptide
Ligands
ARG
Pockets
3 · best druggability 0.76

Structure

x-ray diffraction · 2 distinct chains · 76% helix, 0% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, E, FArmadillo repeat protein ARM00027protein23879% helix, 0% strand—
C, D, G, HPoly arg decapeptideprotein90% helix, 0% strand—

Ligands and binding sites

  • ARG · Arginine · ligand · 2 copies · chains D, E

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
111740.760.78117empty
29440.750.7888empty
33740.730.8452empty

Interfaces

13 interfaces between chains.

  • B–D · 964 Ų buried · 31 hydrogen bonds · protein-protein
  • F–H · 961 Ų buried · 32 hydrogen bonds · protein-protein
  • E–G · 935 Ų buried · 33 hydrogen bonds · protein-protein
  • A–C · 934 Ų buried · 23 hydrogen bonds · protein-protein
  • E–F · 504 Ų buried · 10 hydrogen bonds · protein-protein

Compared structures

  • 4D49 · Crystal structure of computationally designed armadillo repeat proteins for modular… · the same entry in another collection · chain E against E, TM-score 1.00

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