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A de novo designed heptameric coiled coil cc-hept

Analyse A de novo designed heptameric coiled coil cc-hept in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4PNA
Type
protein
Length
208 residues
Chains
7
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Cc-hept
Ligands
ACE
Pockets
1 · best druggability 0.88

Structure

x-ray diffraction · 2 distinct chains · 93% helix, 0% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, D, GCc-heptprotein3093% helix, 0% strand—
E, FCc-heptprotein2993% helix, 0% strand—

Ligands and binding sites

  • ACE · Acetyl group · ligand · 7 copies · chains A, C, B, G, D, E, F
  • GOL · Glycerol · additive · 4 copies · chains B, C, E, G, A, D, F

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
17810.880.8956GOL

Interfaces

7 interfaces between chains.

  • D–E · 821 Ų buried · 5 hydrogen bonds · protein-protein
  • B–E · 800 Ų buried · 4 hydrogen bonds · protein-protein
  • A–C · 798 Ų buried · 3 hydrogen bonds · protein-protein
  • F–G · 792 Ų buried · 9 hydrogen bonds · protein-protein
  • C–D · 788 Ų buried · 4 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 7 covalent (covalent ligand).

Compared structures

  • 4PNA · A de novo designed heptameric coiled coil CC-Hept · the same entry in another collection · chain A against A, TM-score 1.00

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