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PDBsum entry 2rg3

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protein ligands links
Hydrolase PDB id
2rg3

 

 

 

 

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Contents
Protein chain
218 a.a. *
Ligands
NAG-NAG-FUC
EPE
Waters ×121
* Residue conservation analysis
PDB id:
2rg3
Name: Hydrolase
Title: Covalent complex structure of elastase
Structure: Leukocyte elastase. Chain: a. Synonym: elastase-2, neutrophil elastase, pmn elastase, bone marrow serine protease, medullasin, human leukocyte elastase, hle. Engineered: yes
Source: Homo sapiens. Human. Gene: ela2. Expressed in: escherichia coli
Resolution:
1.80Å     R-factor:   0.200    
Authors: W.Huang,Y.Yamamoto
Key ref: W.Huang et al. (2008). X-ray snapshot of the mechanism of inactivation of human neutrophil elastase by 1,2,5-thiadiazolidin-3-one 1,1-dioxide derivatives. J Med Chem, 51, 2003-2008. PubMed id: 18318470
Date:
02-Oct-07     Release date:   01-Jul-08    
PROCHECK
Go to PROCHECK summary
 Headers
 References

Protein chain
Pfam   ArchSchema ?
P08246  (ELNE_HUMAN) -  Neutrophil elastase from Homo sapiens
Seq:
Struc:
267 a.a.
218 a.a.*
Key:    PfamA domain  Secondary structure  CATH domain
* PDB and UniProt seqs differ at 1 residue position (black cross)

 Enzyme reactions 
   Enzyme class: E.C.3.4.21.37  - leukocyte elastase.
[IntEnz]   [ExPASy]   [KEGG]   [BRENDA]
      Reaction: Hydrolysis of proteins, including elastin. Preferential cleavage: Val-|-Xaa > Ala-|-Xaa.

 

 
J Med Chem 51:2003-2008 (2008)
PubMed id: 18318470  
 
 
X-ray snapshot of the mechanism of inactivation of human neutrophil elastase by 1,2,5-thiadiazolidin-3-one 1,1-dioxide derivatives.
W.Huang, Y.Yamamoto, Y.Li, D.Dou, K.R.Alliston, R.P.Hanzlik, T.D.Williams, W.C.Groutas.
 
  ABSTRACT  
 
The mechanism of action of a general class of mechanism-based inhibitors of serine proteases, including human neutrophil elastase (HNE), has been elucidated by determining the X-ray crystal structure of an enzyme-inhibitor complex. The captured intermediate indicates that processing of inhibitor by the enzyme generates an N-sulfonyl imine functionality that is tethered to Ser195, in accordance with the postulated mechanism of action of this class of inhibitors. The identity of the HNE-N-sulfonyl imine species was further corroborated using electrospray ionization mass spectrometry.
 

Literature references that cite this PDB file's key reference

  PubMed id Reference
21511470 D.Dou, G.He, K.R.Alliston, and W.C.Groutas (2011).
Dual function inhibitors of relevance to chronic obstructive pulmonary disease.
  Bioorg Med Chem Lett, 21, 3177-3180.  
20423453 E.Hajjar, T.Broemstrup, C.Kantari, V.Witko-Sarsat, and N.Reuter (2010).
Structures of human proteinase 3 and neutrophil elastase--so similar yet so different.
  FEBS J, 277, 2238-2254.  
19394830 Y.Li, D.Dou, G.He, G.H.Lushington, and W.C.Groutas (2009).
Mechanism-based inhibitors of serine proteases with high selectivity through optimization of S' subsite binding.
  Bioorg Med Chem, 17, 3536-3542.  
The most recent references are shown first. Citation data come partly from CiteXplore and partly from an automated harvesting procedure. Note that this is likely to be only a partial list as not all journals are covered by either method. However, we are continually building up the citation data so more and more references will be included with time.

 

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