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
ANP Phosphoaminophosphonic acid-adenylate ester
MG Magnesium ion
CHU N-(3-fluoro-4-{[4-methyl-2-oxo-7-(pyrimidin-2-yloxy)-2h-chromen-3-yl]methyl}pyridin-2-yl)-N'-methylsulfuric diamide
PG4 Tetraethylene glycol
CL Chloride ion
Non-standard Residues
Code Name Show
Glycosylation
Code Name Emphasize
Modification
Code Name Show
Code : 3WIG   PDBj   RCSB PDB   PDBe
Header : TRANSFERASE/TRANSFERASE INHIBITOR
Title : Human MEK1 kinase in complex with CH5126766 and MgAMP-PNP
Release Data : 2014-06-04
Compound :
mol_id molecule chains synonym
1 Dual specificity mitogen-activated protein kinase kinase 1 A MAP kinase kinase 1, MAPKK 1, MKK1, ERK activator kinase 1, MAPK/ERK kinase 1, MEK 1
ec: 2.7.12.2
other_details: UNP RESIDUES 62-270, 303-393
Source :
mol_id organism_scientific organism_common expression_system
1 Homo sapiens  (taxid:9606) Human Escherichia coli  (taxid:562)
gene: MAP2K1, MEK1, PRKMK1
expression_system_vector_type: plasmid
Authors : Lukacs, C.M., Janson, C., Schuck, V.
Keywords : kinase, kinase inhibitor, allosteric, TRANSFERASE-TRANSFERASE INHIBITOR complex
Exp. method : X-RAY DIFFRACTION ( 2.7000 Å )
Citation :

Disruption of CRAF-Mediated MEK Activation Is Required for Effective MEK Inhibition in KRAS Mutant Tumors

Lito, P.,Saborowski, A.,Yue, J.  et al.
(2014)  Cancer Cell  25 : 697 - 710

PubMed: 24746704
DOI: 10.1016/j.ccr.2014.03.011

Chain : A
UniProt : Q02750 (MP2K1_HUMAN)
Reaction: EC: Evidence:
Physiological Direction:
ATP + L-seryl-[protein] = ADP + H(+) + O-phospho-L-seryl- [protein] 2.7.12.2 -
-
ATP + L-threonyl-[protein] = ADP + H(+) + O-phospho-L- threonyl-[protein] 2.7.12.2 -
-
ATP + L-tyrosyl-[protein] = ADP + H(+) + O-phospho-L-tyrosyl- [protein] 2.7.12.2 -
-