Identification of Highly Potent Protein Kinase C-Related Kinase 1 Inhibitors by Virtual Screening, Binding Free Energy Rescoring, and in vitro Testing.

about

Identification of Highly Potent Protein Kinase C-Related Kinase 1 Inhibitors by Virtual Screening, Binding Free Energy Rescoring, and in vitro Testing.

Item

http://www.wikidata.org/entity/Q36089876

description

2016 nî lūn-bûn

@nan

2016年の論文

@ja

2016年論文

@yue

2016年論文

@zh-hant

2016年論文

@zh-hk

2016年論文

@zh-mo

2016年論文

@zh-tw

2016年论文

@wuu

2016年论文

@zh

2016年论文

@zh-cn

name

Identification of Highly Poten ...... scoring, and in vitro Testing.

@ast

Identification of Highly Poten ...... scoring, and in vitro Testing.

@en

type

Item

label

Identification of Highly Poten ...... scoring, and in vitro Testing.

@ast

Identification of Highly Poten ...... scoring, and in vitro Testing.

@en

prefLabel

Identification of Highly Poten ...... scoring, and in vitro Testing.

@ast

Identification of Highly Poten ...... scoring, and in vitro Testing.

@en

P1476

Identification of Highly Poten ...... scoring, and in vitro Testing.

@en

P2093

Abdulkarim Najar

http://www.w3.org/2001/XMLSchema#string

Eric Metzger

http://www.w3.org/2001/XMLSchema#string

Inna Slynko

http://www.w3.org/2001/XMLSchema#string

Karin Schmidtkunz

http://www.w3.org/2001/XMLSchema#string

Roland Schüle

http://www.w3.org/2001/XMLSchema#string

Tobias Rumpf

http://www.w3.org/2001/XMLSchema#string

P2860

The structural basis of Rho effector recognition revealed by the crystal structure of human RhoA complexed with the effector domain of PKN/PRK1

Cooperative demethylation by JMJD2C and LSD1 promotes androgen receptor-dependent gene expression

Protein kinase C-related kinase targets nuclear localization signals in a subset of class IIa histone deacetylases

Phosphorylation of histone H3 at threonine 11 establishes a novel chromatin mark for transcriptional regulation

Phosphorylation of histone H3T6 by PKCbeta(I) controls demethylation at histone H3K4

A novel protein kinase with leucine zipper-like sequences: its catalytic domain is highly homologous to that of protein kinase C

Regulatory domain selectivity in the cell-type specific PKN-dependence of cell migration

A novel inducible transactivation domain in the androgen receptor: implications for PRK in prostate cancer

Translocation of PKN from the cytosol to the nucleus induced by stresses

Identification of 4-(2-(4-amino-1,2,5-oxadiazol-3-yl)-1-ethyl-7-{[(3S)-3-piperidinylmethyl]oxy}-1H-imidazo[4,5-c]pyridin-4-yl)-2-methyl-3-butyn-2-ol (GSK690693), a novel inhibitor of AKT kinase

P304

2084-2094

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1002/CMDC.201600284

http://www.w3.org/2001/XMLSchema#string

P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P50

P577

2016-07-29T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

27472906

http://www.w3.org/2001/XMLSchema#string