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PDBsum entry 3zrm

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protein ligands Protein-protein interface(s) links
Transferase/peptide PDB id
3zrm

 

 

 

 

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JSmol PyMol  
Contents
Protein chains
346 a.a.
23 a.a.
22 a.a.
Ligands
SO4 ×6
GOL ×2
ZRM ×2
Waters ×183
PDB id:
3zrm
Name: Transferase/peptide
Title: Identification of 2-(4-pyridyl)thienopyridinones as gsk-3beta inhibitors
Structure: Glycogen synthase kinase-3 beta. Chain: a, b. Fragment: residues 23-393. Synonym: gsk-3 beta. Engineered: yes. Proto-oncogene frat1. Chain: x, y. Fragment: residues 197-226. Synonym: frequently rearranged in advanced t-cell lymphomas 1, frat.
Source: Homo sapiens. Human. Organism_taxid: 9606. Expressed in: spodoptera frugiperda. Expression_system_taxid: 7108. Expression_system_cell_line: sf9.
Resolution:
2.49Å     R-factor:   0.190     R-free:   0.247
Authors: G.Gentile,G.Bernasconi,A.Pozzan,G.Merlo,P.Marzorati,P.Bamborough, B.Bax,A.Bridges,C.Brough,P.Carter,G.Cutler,M.Neu,M.Takada
Key ref: G.Gentile et al. (2011). Identification of 2-(4-pyridyl)thienopyridinones as GSK-3β inhibitors. Bioorg Med Chem Lett, 21, 4823-4827. PubMed id: 21764580
Date:
17-Jun-11     Release date:   29-Jun-11    
PROCHECK
Go to PROCHECK summary
 Headers
 References

Protein chains
Pfam   ArchSchema ?
P49841  (GSK3B_HUMAN) -  Glycogen synthase kinase-3 beta from Homo sapiens
Seq:
Struc:
420 a.a.
346 a.a.
Protein chain
Pfam   ArchSchema ?
Q92837  (FRAT1_HUMAN) -  Proto-oncogene FRAT1 from Homo sapiens
Seq:
Struc:
279 a.a.
23 a.a.
Protein chain
Pfam   ArchSchema ?
Q92837  (FRAT1_HUMAN) -  Proto-oncogene FRAT1 from Homo sapiens
Seq:
Struc:
279 a.a.
22 a.a.
Key:    PfamA domain  Secondary structure  CATH domain

 Enzyme reactions 
   Enzyme class 1: Chains A, B: E.C.2.7.11.1  - non-specific serine/threonine protein kinase.
[IntEnz]   [ExPASy]   [KEGG]   [BRENDA]
      Reaction:
1. L-seryl-[protein] + ATP = O-phospho-L-seryl-[protein] + ADP + H+
2. L-threonyl-[protein] + ATP = O-phospho-L-threonyl-[protein] + ADP + H+
L-seryl-[protein]
+ ATP
= O-phospho-L-seryl-[protein]
+ ADP
+ H(+)
L-threonyl-[protein]
+ ATP
= O-phospho-L-threonyl-[protein]
+ ADP
+ H(+)
   Enzyme class 2: Chains A, B: E.C.2.7.11.26  - [tau protein] kinase.
[IntEnz]   [ExPASy]   [KEGG]   [BRENDA]
      Reaction:
1. L-seryl-[tau protein] + ATP = O-phospho-L-seryl-[tau protein] + ADP + H+
2. L-threonyl-[tau protein] + ATP = O-phospho-L-threonyl-[tau protein] + ADP + H+
L-seryl-[tau protein]
+ ATP
= O-phospho-L-seryl-[tau protein]
+ ADP
+ H(+)
L-threonyl-[tau protein]
+ ATP
= O-phospho-L-threonyl-[tau protein]
+ ADP
+ H(+)
Note, where more than one E.C. class is given (as above), each may correspond to a different protein domain or, in the case of polyprotein precursors, to a different mature protein.
Molecule diagrams generated from .mol files obtained from the KEGG ftp site

 

 
    reference    
 
 
Bioorg Med Chem Lett 21:4823-4827 (2011)
PubMed id: 21764580  
 
 
Identification of 2-(4-pyridyl)thienopyridinones as GSK-3β inhibitors.
G.Gentile, G.Bernasconi, A.Pozzan, G.Merlo, P.Marzorati, P.Bamborough, B.Bax, A.Bridges, C.Brough, P.Carter, G.Cutler, M.Neu, M.Takada.
 
  ABSTRACT  
 
No abstract given.

 

 

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