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PDBsum entry 3pup

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protein ligands Protein-protein interface(s) links
Transferase PDB id
3pup

 

 

 

 

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JSmol PyMol  
Contents
Protein chains
346 a.a. *
Ligands
OS1 ×2
* Residue conservation analysis
PDB id:
3pup
Name: Transferase
Title: Structure of glycogen synthase kinase 3 beta (gsk3b) in complex with a ruthenium octasporine ligand (os1)
Structure: Glycogen synthase kinase-3 beta. Chain: a, b. Synonym: gsk-3 beta. Engineered: yes
Source: Homo sapiens. Human. Organism_taxid: 9606. Gene: gsk3b. Expressed in: escherichia coli. Expression_system_taxid: 562.
Resolution:
2.99Å     R-factor:   0.206     R-free:   0.249
Authors: P.Filippakopoulos,K.Kraling,L.O.Essen,E.Meggers,S.Knapp
Key ref: L.Feng et al. (2011). Structurally sophisticated octahedral metal complexes as highly selective protein kinase inhibitors. J Am Chem Soc, 133, 5976-5986. PubMed id: 21446733
Date:
06-Dec-10     Release date:   22-Dec-10    
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.
Key:    PfamA domain  Secondary structure  CATH domain

 Enzyme reactions 
   Enzyme class: 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(+)
Molecule diagrams generated from .mol files obtained from the KEGG ftp site

 

 
    reference    
 
 
J Am Chem Soc 133:5976-5986 (2011)
PubMed id: 21446733  
 
 
Structurally sophisticated octahedral metal complexes as highly selective protein kinase inhibitors.
L.Feng, Y.Geisselbrecht, S.Blanck, A.Wilbuer, G.E.Atilla-Gokcumen, P.Filippakopoulos, K.Kräling, M.A.Celik, K.Harms, J.Maksimoska, R.Marmorstein, G.Frenking, S.Knapp, L.O.Essen, E.Meggers.
 
  ABSTRACT  
 
No abstract given.

 

 

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