You can find more information about
protein kinase 7
using the following links:
PFID
PFID Old
Formal Annotation
PlasmoDB
TDR Targets
Subcellular Localization
Affecting Drugs
Drug Name
PubMed Articles (year of publication)
PF3D7_0213400
PFB0605w
protein kinase 7
PlasmoDB
TDR
Picture 1
1nm-pp1
Structures of P. falciparum protein kinase 7 identify an activation motif and leads for inhibitor design
3-(1,2,3-triazol-4-yl)pyrazolo[3,4-d]pyrimidin
Synthesis of 3-(1,2,3-triazol-1-yl)- and 3-(1,2,3-triazol-4-yl)-substituted pyrazolo[3,4-d]pyrimidin-4-amines via click chemistry: potential inhibitors of the Plasmodium falciparum PfPK7 protein kinase
Hymenialdisine
PfPK7, an atypical MEK-related protein kinase, reflects the absence of classical three-component MAPK pathways in the human malaria parasite Plasmodium falciparum
Hymenialdisine 01
PfPK7, an atypical MEK-related protein kinase, reflects the absence of classical three-component MAPK pathways in the human malaria parasite Plasmodium falciparum
Imidazopyridazine
Synthesis and in vitro evaluation of imidazopyridazines as novel inhibitors of the malarial kinase PfPK7
Structural insight for imidazopyridazines as malarial kinase PfPK7 inhibitors using QSAR techniques
Luzindole
Ubiquitin proteasome system and the atypical kinase PfPK7 are involved in melatonin signaling in Plasmodium falciparum
Melatonin
Ubiquitin proteasome system and the atypical kinase PfPK7 are involved in melatonin signaling in Plasmodium falciparum
Pp2
Structures of P. falciparum protein kinase 7 identify an activation motif and leads for inhibitor design
pyrazolo[3,4-d]pyrimidin-4-amine
Synthesis of 3-(1,2,3-triazol-1-yl)- and 3-(1,2,3-triazol-4-yl)-substituted pyrazolo[3,4-d]pyrimidin-4-amines via click chemistry: potential inhibitors of the Plasmodium falciparum PfPK7 protein kinase
Staurosporine
PfPK7, an atypical MEK-related protein kinase, reflects the absence of classical three-component MAPK pathways in the human malaria parasite Plasmodium falciparum
TCMDC-136692
Biochemical Screening of Five Protein Kinases from Plasmodium falciparum against 14,000 Cell-Active Compounds
TCMDC-136693
Biochemical Screening of Five Protein Kinases from Plasmodium falciparum against 14,000 Cell-Active Compounds
Expasy - NiceZime View
Brenda - The Comprehensive Enzyme Information System