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
984 Cyclopropyl-{4-[5-(3,4-dichlorophenyl)-2-[(1-methyl)-piperidin]-4-yl-3-propyl-3h-imidazol-4-yl]-pyrimidin-2-yl}amine
Non-standard Residues
Code Name Show
Glycosylation
Code Name Emphasize
Modification
Code Name Show
Code : 1PMN   PDBj   RCSB PDB   PDBe
Header : TRANSFERASE
Title : Crystal structure of JNK3 in complex with an imidazole-pyrimidine inhibitor
Release Data : 2003-09-09
Compound :
mol_id molecule chains synonym
1 Mitogen-activated protein kinase 10 A Stress-activated protein kinase JNK3, c-Jun N-terminal kinase 3, MAP kinase p49 3F12
ec: 2.7.1.-
Source :
mol_id organism_scientific organism_common expression_system
1 Homo sapiens  (taxid:9606) Human Escherichia coli  (taxid:562)
gene: MK10_HUMAN
expression_system_strain: BLD21(DE3)
expression_system_vector_type: Plasmid
expression_system_plasmid: pET15B
Authors : Scapin, G., Patel, S.B., Lisnock, J., Becker, J.W., LoGrasso, P.V.
Keywords : MAP kinase, apoptosis, inhibition, transferase
Exp. method : X-RAY DIFFRACTION ( 2.2 Å )
Citation :

The structure of JNK3 in complex with small molecule inhibitors: structural basis for potency and selectivity

Scapin, G.,Patel, S.B.,Lisnock, J.  et al.
(2003)  Chem.Biol.  10 : 705 - 712

PubMed: 12954329
DOI: 10.1016/S1074-5521(03)00159-5

Chain : A
UniProt : P53779 (MK10_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 -
-