Brand  (β version)

  The number of atoms exceeds 100,000.
  So, it can not be displayed here.

Select unit:

Select hetatm:   

close
information
centroid:
interaction residue:

Select chain:   Sequence  

Data format:   

Color scheme of protein:

Ligands
Code Name Style Show Link
FRZ 5-(2-phenylpyrazolo[1,5-a]pyridin-3-yl)-1h-pyrazolo[3,4-C]pyridazin-3-amine
Non-standard Residues
Code Name Show
Glycosylation
Code Name Emphasize
Modification
Code Name Show
Code : 1TVO   PDBj   RCSB PDB   PDBe
Header : TRANSFERASE
Title : The structure of ERK2 in complex with a small molecule inhibitor
Release Data : 2005-09-13
Compound :
mol_id molecule chains synonym
1 Mitogen-activated protein kinase 1 A ERK2, Extracellular signal-regulated kinase 2, ERK-2, Mitogen-activated protein kinase 2, MAP kinase 2, MAPK 2, p42-MAPK, ERT1
ec: 2.7.1.37
Source :
mol_id organism_scientific organism_common expression_system
1 Homo sapiens  (taxid:9606) Human Escherichia coli  (taxid:562)
expression_system_cell: DH5alfa
expression_system_vector_type: plasmid
expression_system_plasmid: pGEX-6p-1
Authors : Kinoshita, T.
Keywords : KINASE, PROTEIN-INHIBITOR COMPLEX, TRANSFERASE
Exp. method : X-RAY DIFFRACTION ( 2.50 Å )
Citation :

Identification of a selective ERK inhibitor and structural determination of the inhibitor-ERK2 complex

Ohori, M.,Kinoshita, T.,Okubo, M.  et al.
(2005)  Biochem.Biophys.Res.Commun.  336 : 357 - 363

PubMed: 16139248
DOI: 10.1016/j.bbrc.2005.08.082

Chain : A
UniProt : P28482 (MK01_HUMAN)
Reaction: EC: Evidence:
Physiological Direction:
ATP + L-seryl-[protein] = ADP + H(+) + O-phospho-L-seryl- [protein] 2.7.11.24 -
-
ATP + L-threonyl-[protein] = ADP + H(+) + O-phospho-L- threonyl-[protein] 2.7.11.24 -
-