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Ligands
Code Name Style Show Link
9HP 9-(4-hydroxyphenyl)-2,7-phenanthroline
CL Chloride ion
Non-standard Residues
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Glycosylation
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Modification
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Code : 1PMU   PDBj   RCSB PDB   PDBe
Header : TRANSFERASE
Title : The crystal structure of JNK3 in complex with a phenantroline 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 BL21(DE3)  (taxid:469008)
gene: MK10_HUMAN
expression_system_strain: BL21(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, selectivity, TRANSFERASE
Exp. method : X-RAY DIFFRACTION ( 2.7 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 -
-