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Crystal structure of a 6-helix coiled coil cc-hex-L24C

Analyse Crystal structure of a 6-helix coiled coil cc-hex-L24C in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4KVT
Type
protein
Length
181 residues
Chains
6
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
6-helix coiled coil cc-hex-L24C peptide
Ligands
ACE
Pockets
1 · best druggability 0.85

Structure

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

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, E, F6-helix coiled coil cc-hex-L24C peptideprotein3093% helix, 0% strand—
D6-helix coiled coil cc-hex-L24C peptideprotein3194% helix, 0% strand—

Ligands and binding sites

  • ACE · Acetyl group · ligand · 6 copies · chains A, C, B, F, D, E

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
14280.850.9152empty

Interfaces

6 interfaces between chains.

  • B–D · 733 Ų buried · 1 hydrogen bond · protein-protein
  • A–C · 710 Ų buried · 1 hydrogen bond · protein-protein
  • A–B · 708 Ų buried · 2 hydrogen bonds · protein-protein
  • D–E · 685 Ų buried · 1 hydrogen bond · protein-protein
  • C–F · 682 Ų buried · 0 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 6 covalent (covalent ligand).

Compared structures

  • 4KVT · Crystal structure of a 6-helix coiled coil CC-Hex-L24C · the same entry in another collection · chain A against A, TM-score 1.00

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