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PDBsum entry 4zt1

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protein metals Protein-protein interface(s) links
Cell adhesion PDB id
4zt1

 

 

 

 

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JSmol PyMol  
Contents
Protein chains
209 a.a.
Metals
_CA ×6
Waters ×382
PDB id:
4zt1
Name: Cell adhesion
Title: Crystal structure of human e-cadherin (residues 3-213) in x-dimer conformation
Structure: Cadherin-1. Chain: a, b. Fragment: unp residues 157-367. Synonym: cam 120/80,epithelial cadherin,e-cadherin,uvomorulin. Engineered: yes
Source: Homo sapiens. Human. Organism_taxid: 9606. Gene: cdh1, cdhe, uvo. Expressed in: escherichia coli bl21(de3). Expression_system_taxid: 469008. Expression_system_variant: plyss.
Resolution:
1.92Å     R-factor:   0.194     R-free:   0.219
Authors: V.Nardone,A.P.Lucarelli,A.Dalle Vedove,E.Parisini
Key ref: V.Nardone et al. (2016). Crystal Structure of Human E-Cadherin-EC1EC2 in Complex with a Peptidomimetic Competitive Inhibitor of Cadherin Homophilic Interaction. J Med Chem, 59, 5089-5094. PubMed id: 27120112 DOI: 10.1021/acs.jmedchem.5b01487
Date:
14-May-15     Release date:   01-Jun-16    
PROCHECK
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 Headers
 References

Protein chains
Pfam   ArchSchema ?
P12830  (CADH1_HUMAN) -  Cadherin-1 from Homo sapiens
Seq:
Struc:
 
Seq:
Struc:
882 a.a.
209 a.a.
Key:    PfamA domain  Secondary structure  CATH domain

 

 
DOI no: 10.1021/acs.jmedchem.5b01487 J Med Chem 59:5089-5094 (2016)
PubMed id: 27120112  
 
 
Crystal Structure of Human E-Cadherin-EC1EC2 in Complex with a Peptidomimetic Competitive Inhibitor of Cadherin Homophilic Interaction.
V.Nardone, A.P.Lucarelli, A.Dalle Vedove, R.Fanelli, A.Tomassetti, L.Belvisi, M.Civera, E.Parisini.
 
  ABSTRACT  
 
Cadherins are transmembrane cell adhesion proteins whose aberrant expression often correlates with cancer development and proliferation. We report the crystal structure of an E-cadherin extracellular fragment in complex with a peptidomimetic compound that was previously shown to partially inhibit cadherin homophilic adhesion. The structure reveals an unexpected binding mode and allows the identification of a druggable cadherin interface, thus paving the way to a future structure-guided design of cell adhesion inhibitors against cadherin-expressing solid tumors.
 

 

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