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PDBsum entry 4abj

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protein ligands metals links
Hydrolase/inhibitor PDB id
4abj

 

 

 

 

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Contents
Protein chain
223 a.a.
Ligands
ARG-CYS-THR-LYS-
SER-PLW-PRO-ILE-
CYS-PHE
DMF
GOL ×4
SO4
Metals
_CA
Waters ×283
PDB id:
4abj
Name: Hydrolase/inhibitor
Title: Co-complex structure of bovine trypsin with a modified bowman-birk inhibitor (ica)sfti-1(1,14), that was 1,5-disubstituted with 1,2,3- trizol to mimic a cis amide bond
Structure: Cationic trypsin. Chain: a. Synonym: beta-trypsin, alpha-trypsin chain 1, alpha-trypsin chain 2. Trypsin inhibitor 1. Chain: b. Synonym: ica-sfti inhibitor, sfti-1. Engineered: yes. Other_details: chemically synthesized
Source: Bos taurus. Cattle. Organism_taxid: 9913. Other_details: sigma-aldrich trypsin from bovine pancreas t1426. Synthetic: yes. Helianthus annuus. Common sunflower. Organism_taxid: 4232. Other_details: chemically synthesized
Resolution:
1.45Å     R-factor:   0.191     R-free:   0.204
Authors: S.Schmelz,M.Empting,M.Tischler,D.Nasu,D.Heinz,H.Kolmar
Key ref: M.Tischler et al. (2012). Braces for the peptide backbone: insights into structure-activity relationships of protease inhibitor mimics with locked amide conformations. Angew Chem Int Ed Engl, 51, 3708-3712. PubMed id: 22374650
Date:
08-Dec-11     Release date:   07-Mar-12    
PROCHECK
Go to PROCHECK summary
 Headers
 References

Protein chain
Pfam   ArchSchema ?
P00760  (TRY1_BOVIN) -  Serine protease 1 from Bos taurus
Seq:
Struc:
246 a.a.
223 a.a.
Key:    PfamA domain  Secondary structure  CATH domain

 Enzyme reactions 
   Enzyme class: E.C.3.4.21.4  - trypsin.
[IntEnz]   [ExPASy]   [KEGG]   [BRENDA]
      Reaction: Preferential cleavage: Arg-|-Xaa, Lys-|-Xaa.

 

 
Angew Chem Int Ed Engl 51:3708-3712 (2012)
PubMed id: 22374650  
 
 
Braces for the peptide backbone: insights into structure-activity relationships of protease inhibitor mimics with locked amide conformations.
M.Tischler, D.Nasu, M.Empting, S.Schmelz, D.W.Heinz, P.Rottmann, H.Kolmar, G.Buntkowsky, D.Tietze, O.Avrutina.
 
  ABSTRACT  
 
No abstract given.

 

 

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