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PDBsum entry 4dpe

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protein ligands metals Protein-protein interface(s) links
Hydrolase/hydrolase inhibitor PDB id
4dpe

 

 

 

 

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Contents
Protein chain
168 a.a.
Ligands
NGH
Metals
_PT ×6
_ZN ×4
_CA ×6
_CL ×2
Waters ×161
PDB id:
4dpe
Name: Hydrolase/hydrolase inhibitor
Title: Structure of mmp3 complexed with a platinum-based inhibitor.
Structure: Stromelysin-1. Chain: a, b. Fragment: unp residues 100-272. Synonym: sl-1, matrix metalloproteinase-3, mmp-3, transin-1. Engineered: yes
Source: Homo sapiens. Human. Organism_taxid: 9606. Gene: mmp3, stmy1. Expressed in: escherichia coli. Expression_system_taxid: 562
Resolution:
1.96Å     R-factor:   0.184     R-free:   0.231
Authors: B.D.Belviso,F.Arnesano,V.Calderone,R.Caliandro,G.Natile,D.Siliqi
Key ref: B.D.Belviso et al. (2013). Structure of matrix metalloproteinase-3 with a platinum-based inhibitor. Chem Commun (camb), 49, 5492-5494. PubMed id: 23660647 DOI: 10.1039/c3cc41278d
Date:
13-Feb-12     Release date:   20-Feb-13    
PROCHECK
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 Headers
 References

Protein chains
Pfam   ArchSchema ?
P08254  (MMP3_HUMAN) -  Stromelysin-1 from Homo sapiens
Seq:
Struc:
477 a.a.
168 a.a.
Key:    PfamA domain  Secondary structure  CATH domain

 Enzyme reactions 
   Enzyme class: E.C.3.4.24.17  - stromelysin 1.
[IntEnz]   [ExPASy]   [KEGG]   [BRENDA]
      Reaction: Preferential cleavage where P1', P2' and P3' are hydrophobic residues.
      Cofactor: Ca(2+); Zn(2+)

 

 
DOI no: 10.1039/c3cc41278d Chem Commun (camb) 49:5492-5494 (2013)
PubMed id: 23660647  
 
 
Structure of matrix metalloproteinase-3 with a platinum-based inhibitor.
B.D.Belviso, R.Caliandro, D.Siliqi, V.Calderone, F.Arnesano, G.Natile.
 
  ABSTRACT  
 
An X-ray investigation has been performed with the aim of characterizing the binding sites of a platinum-based inhibitor (K[PtCl3(DMSO)]) of matrix metalloproteinase-3 (stromelysin-1). The platinum complex targets His224 in the S1' specificity loop, representing the first step in the selective inhibition process (PDB ID code ).
 

 

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