(Q30713425)

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Are phylogenetic trees suitable for chemogenomics analyses of bioactivity data sets: the importance of shared active compounds and choosing a suitable data embedding method, as exemplified on Kinases

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

Are phylogenetic trees suitable for chemogenomics analyses of bioactivity data sets: the importance of shared active compounds and choosing a suitable data embedding method, as exemplified on Kinases (English)

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

0 references

5

object named as

Andreas Bender

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

author name string

Shardul Paricharak

1

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

Tom Klenka

2

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

Martin Augustin

3

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

Umesh A Patel

4

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

publication date

13 December 2013

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

Journal of Cheminformatics

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

5

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

1

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

49

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

copyright license

Creative Commons Attribution 2.0 Generic

1 December 2013

1 reference

April 2022 Public Data File from Crossref

copyright status

1 reference

April 2022 Public Data File from Crossref

A broad activity screen in support of a chemogenomic map for kinase signalling research and drug discovery.

1 reference

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T-REX: a web server for inferring, validating and visualizing phylogenetic trees and networks

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14 July 2018

Structural approaches to obtain kinase selectivity

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Kinase-kernel models: accurate in silico screening of 4 million compounds across the entire human kinome

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Comprehensive analysis of kinase inhibitor selectivity

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Comprehensive assay of kinase catalytic activity reveals features of kinase inhibitor selectivity

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14 July 2018

Chemogenomic profiling provides insights into the limited activity of irreversible EGFR Inhibitors in tumor cells expressing the T790M EGFR resistance mutation

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Targeting the cancer kinome through polypharmacology

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14 July 2018

Through the "gatekeeper door": exploiting the active kinase conformation

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14 July 2018

Which aspects of HTS are empirically correlated with downstream success?

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14 July 2018

''R"--project for statistical computing

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A quantitative analysis of kinase inhibitor selectivity

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14 July 2018

Chemogenomic data analysis: prediction of small-molecule targets and the advent of biological fingerprint

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Molecular recognition of protein kinase binding pockets for design of potent and selective kinase inhibitors

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3900467

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The protein kinase complement of the human genome

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[Current therapy of chronic myeloid leukemia].

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based on heuristic

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The eukaryotic protein kinase superfamily: kinase (catalytic) domain structure and classification 1

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2 January 2022

Identifiers

10.1186/1758-2946-5-49

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

DBLP publication ID

journals/jcheminf/ParicharakKAPB13a

1 reference

DBLP Dataset 2021-01-02

28 January 2021

Dimensions Publication ID

0 references

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

ResearchGate publication ID

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