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Calcium-free campari V0.2

Analyse Calcium-free campari V0.2 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4OY4
Type
protein
Length
334 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Chimera protein of calmodulin, gpf-like protein eosfp, and myosin light chain kinase
UniProt
P62161, Q5S6Z9, Q6LDG3
Ligands
CR8, SO4
Pockets
4 · best druggability 0.73

Structure

x-ray diffraction · 1 distinct chain · 22% helix, 39% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AChimera protein of calmodulin, gpf-like protein eosfp, and myosin light chain kinaseprotein33422% helix, 39% strandP62161, Q5S6Z9, Q6LDG3

Ligands and binding sites

  • CR8 · 2-[1-amino-2-(1H-imidazol-5-yl)ethyl]-1-(carboxymethyl)-4-[(4-oxocyclohexa-2,5-dien-1-ylidene)methyl]-1H-imidazol-5-olate · ligand · chains A
  • SO4 · Sulfate ion · ion · 2 copies · chains A
  • GOL · Glycerol · additive · 2 copies · chains A

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

Pockets

4 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1700.730.9820CR8
24590.680.7956empty
3820.380.7717empty
4700.300.7422empty

Modifications

Observed in the structure: 2 covalent (covalent ligand).

Compared structures

  • 4OY4 · calcium-free CaMPARI v0.2 · the same entry in another collection · chain A against A, TM-score 1.00

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