spacer
spacer

PDBsum entry 2z7l

Go to PDB code: 
protein ligands links
Transferase PDB id
2z7l
Jmol
Contents
Protein chain
329 a.a. *
Ligands
SO4
S91
BME ×3
Waters ×129
* Residue conservation analysis
PDB id:
2z7l
Name: Transferase
Title: Unphosphorylated mitogen activated protein kinase erk2 in complex with (4-{[5-carbamoyl-4-(3-methylanilino)pyrimidin 2-yl]amino}phenyl)acetic acid
Structure: Mitogen-activated protein kinase 1. Chain: a. Synonym: extracellular signal-regulated kinase 2, erk-2, mitogen-activated protein kinase 2, map kinase 2, mapk 2, p42-mapk, ert1. Engineered: yes
Source: Rattus norvegicus. Rat. Organism_taxid: 10116. Gene: mapk1, erk2, mapk, prkm1. Expressed in: escherichia coli. Expression_system_taxid: 562.
Resolution:
2.41Å     R-factor:   0.223     R-free:   0.276
Authors: N.Katayama,H.Kurihara
Key ref:
N.Katayama et al. (2008). Identification of a key element for hydrogen-bonding patterns between protein kinases and their inhibitors. Proteins, 73, 795-801. PubMed id: 18767165 DOI: 10.1002/prot.22207
Date:
27-Aug-07     Release date:   12-Aug-08    
PROCHECK
Go to PROCHECK summary
 Headers
 References

Protein chain
Pfam   ArchSchema ?
P63086  (MK01_RAT) -  Mitogen-activated protein kinase 1
Seq:
Struc:
358 a.a.
329 a.a.
Key:    PfamA domain  Secondary structure  CATH domain

 Enzyme reactions 
   Enzyme class: E.C.2.7.11.24  - Mitogen-activated protein kinase.
[IntEnz]   [ExPASy]   [KEGG]   [BRENDA]
      Reaction: ATP + a protein = ADP + a phosphoprotein
ATP
+ protein
= ADP
+ phosphoprotein
Molecule diagrams generated from .mol files obtained from the KEGG ftp site
 Gene Ontology (GO) functional annotation 
  GO annot!
  Cellular component     mitotic spindle   21 terms 
  Biological process     intracellular signal transduction   40 terms 
  Biochemical function     nucleotide binding     15 terms  

 

 
    reference    
 
 
DOI no: 10.1002/prot.22207 Proteins 73:795-801 (2008)
PubMed id: 18767165  
 
 
Identification of a key element for hydrogen-bonding patterns between protein kinases and their inhibitors.
N.Katayama, M.Orita, T.Yamaguchi, H.Hisamichi, S.Kuromitsu, H.Kurihara, H.Sakashita, Y.Matsumoto, S.Fujita, T.Niimi.
 
  ABSTRACT  
 
In this article, we report crystal structures for inhibitor-kinase complexes in which the inhibitor has different binding orientations and hydrogen-bonding patterns with extracellular-signal regulated kinase 2 and insulin receptor tyrosine kinase. Our crystallographic studies, and sequence and structural analyses of 532 coordinates of kinases held in the Protein Data Bank, suggest that the length of the "specificity linker" described here is a key structural element of the hydrogen-bonding patterns between protein kinases and their inhibitors. Proteins 2008. (c) 2008 Wiley-Liss, Inc.
 
  Selected figure(s)  
 
Figure 1.
Figure 1. Schematics showing the binding mode of ligands to protein kinases. (a) ATP. (b) Purvalanol B in CDK2 (PDB code 1CKP). (c) NU2058 in CDK2 (PDB code 1E1V). Hydrogen bonds are indicated by broken lines.
Figure 5.
Figure 5. Key elements for the hydrogen-bonding pattern of an ATP-mimetic compound. The orientation of R3-O of the group A kinase is more favorable for that of the group B kinase because of the difference in the length of the specificity linker.
 
  The above figures are reprinted by permission from John Wiley & Sons, Inc.: Proteins (2008, 73, 795-801) copyright 2008.  
  Figures were selected by an automated process.  

Literature references that cite this PDB file's key reference

  PubMed id Reference
20306284 A.Del Rio, M.Sgobba, M.D.Parenti, G.Degliesposti, R.Forestiero, C.Percivalle, P.F.Conte, M.Freccero, and G.Rastelli (2010).
A computational workflow for the design of irreversible inhibitors of protein kinases.
  J Comput Aided Mol Des, 24, 183-194.  
19689374 K.Burkhard, S.Smith, R.Deshmukh, A.D.MacKerell, and P.Shapiro (2009).
Development of extracellular signal-regulated kinase inhibitors.
  Curr Top Med Chem, 9, 678-689.  
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.