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Crystal structure of mouse P-cadherin extracellular domains EC1-EC2

Analyse Crystal structure of mouse P-cadherin extracellular domains EC1-EC2 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4NQQ
Type
protein
Length
847 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Cadherin-3
UniProt
P10287
Ligands
CA, CU
Pockets
4 · best druggability 0.78

Structure

x-ray diffraction · 3 distinct chains · 3% helix, 45% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BCadherin-3protein2133% helix, 45% strandP10287
CCadherin-3protein2103% helix, 47% strandP10287
DCadherin-3protein2113% helix, 45% strandP10287

Ligands and binding sites

  • CA · Calcium ion · metal · 14 copies · chains A, B, C, D
  • CU · Copper (II) ion · metal · 9 copies · chains A, C, B, D

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16170.780.8455empty
2680.700.9618empty
35000.660.7747empty
41800.460.7531empty

Interfaces

3 interfaces between chains.

  • A–B · 901 Ų buried · 18 hydrogen bonds · protein-protein
  • A–C · 506 Ų buried · 9 hydrogen bonds · protein-protein
  • C–D · 488 Ų buried · 7 hydrogen bonds · protein-protein

Compared structures

  • 4NQQ · Crystal structure of mouse P-cadherin extracellular domains EC1-EC2 · the same entry in another collection · chain D against D, TM-score 1.00
  • P10287 · AlphaFold monomer V2.0 prediction for cadherin-3 (P10287) · a predicted model of the same protein · chain C against A, TM-score 0.99

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