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PDBsum entry 3dy7

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protein ligands metals links
Transferase PDB id
3dy7

 

 

 

 

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JSmol PyMol  
Contents
Protein chain
260 a.a. *
Ligands
ATP
1CX
Metals
_MG
* Residue conservation analysis
PDB id:
3dy7
Name: Transferase
Title: X-ray structure of the human mitogen-activated protein kinase kinase 1 (mek1) in a complex with ligand and mgatp
Structure: Dual specificity mitogen-activated protein kinase kinase 1. Chain: a. Fragment: protein kinase domain, unp residues 62-393. Synonym: map kinase kinase 1, mapkk 1, erk activator kinase 1, mapk/erk kinase 1, mek1. Engineered: yes
Source: Homo sapiens. Human. Organism_taxid: 9606. Gene: map2k1, mek1, prkmk1. Expressed in: escherichia coli. Expression_system_taxid: 562.
Resolution:
2.70Å     R-factor:   0.248     R-free:   0.269
Authors: J.F.Ohren,A.Pavlovsky,E.Zhang
Key ref: H.Tecle et al. (2009). Beyond the MEK-pocket: can current MEK kinase inhibitors be utilized to synthesize novel type III NCKIs? Does the MEK-pocket exist in kinases other than MEK? Bioorg Med Chem Lett, 19, 226-229. PubMed id: 19019675
Date:
25-Jul-08     Release date:   16-Jun-09    
PROCHECK
Go to PROCHECK summary
 Headers
 References

Protein chain
Pfam   ArchSchema ?
Q02750  (MP2K1_HUMAN) -  Dual specificity mitogen-activated protein kinase kinase 1 from Homo sapiens
Seq:
Struc:
393 a.a.
260 a.a.
Key:    PfamA domain  Secondary structure  CATH domain

 Enzyme reactions 
   Enzyme class: E.C.2.7.12.2  - mitogen-activated protein kinase 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+
3. L-tyrosyl-[protein] + ATP = O-phospho-L-tyrosyl-[protein] + ADP + H+
L-seryl-[protein]
Bound ligand (Het Group name = ATP)
corresponds exactly
+ ATP
= O-phospho-L-seryl-[protein]
+ ADP
+ H(+)
L-threonyl-[protein]
Bound ligand (Het Group name = ATP)
corresponds exactly
+ ATP
= O-phospho-L-threonyl-[protein]
+ ADP
+ H(+)
L-tyrosyl-[protein]
Bound ligand (Het Group name = ATP)
corresponds exactly
+ ATP
= O-phospho-L-tyrosyl-[protein]
+ ADP
+ H(+)
Molecule diagrams generated from .mol files obtained from the KEGG ftp site

 

 
    reference    
 
 
Bioorg Med Chem Lett 19:226-229 (2009)
PubMed id: 19019675  
 
 
Beyond the MEK-pocket: can current MEK kinase inhibitors be utilized to synthesize novel type III NCKIs? Does the MEK-pocket exist in kinases other than MEK?
H.Tecle, J.Shao, Y.Li, M.Kothe, S.Kazmirski, J.Penzotti, Y.H.Ding, J.Ohren, D.Moshinsky, R.Coli, N.Jhawar, E.Bora, S.Jacques-O'Hagan, J.Wu.
 
  ABSTRACT  
 
An approach and preliminary results for utilizing legacy MEK inhibitors as templates for a reiterative structural based design and synthesis of novel, type III NCKIs (non-classical kinase inhibitors) is described. Evidence is provided that the MEK-pocket or pockets closely related to it may exist in kinases other than MEK.
 

Literature references that cite this PDB file's key reference

  PubMed id Reference
20154661 O.Fedorov, S.Müller, and S.Knapp (2010).
The (un)targeted cancer kinome.
  Nat Chem Biol, 6, 166-169.  
19568781 L.A.Smyth, and I.Collins (2009).
Measuring and interpreting the selectivity of protein kinase inhibitors.
  J Chem Biol, 2, 131-151.  
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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