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Crystal structure of apocalmodulin

Analyse Crystal structure of apocalmodulin in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1QX5
Type
protein
Length
1,159 residues
Chains
8
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Calmodulin
UniProt
P62161
Pockets
20 · best druggability 0.72

Structure

x-ray diffraction · 4 distinct chains · 56% helix, 8% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
D, I, B, T, YCalmodulinprotein14558% helix, 9% strandP62161
JCalmodulinprotein14458% helix, 7% strandP62161
KCalmodulinprotein14352% helix, 8% strandP62161
RCalmodulinprotein14755% helix, 8% strandP62161

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19500.720.76111empty
26710.710.7885empty
33640.640.7945empty
43090.640.8035empty
53000.640.8145empty

Interfaces

20 interfaces between chains.

  • J–T · 2710 Ų buried · 36 hydrogen bonds · protein-protein
  • I–R · 2709 Ų buried · 38 hydrogen bonds · protein-protein
  • B–K · 2694 Ų buried · 32 hydrogen bonds · protein-protein
  • D–Y · 2680 Ų buried · 34 hydrogen bonds · protein-protein
  • I–K · 368 Ų buried · 2 hydrogen bonds · protein-protein

Compared structures

  • 1QX5 · Crystal structure of apoCalmodulin · the same entry in another collection · chain D against D, TM-score 1.00

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