Remarkably Stereospecific Utilization of ATP α,β-Halomethylene Analogues by Protein Kinases.

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Chemo-enzymatic synthesis of the exocyclic olefin isomer of thymidine monophosphate.Bisphosphonate-Generated ATP-Analogs Inhibit Cell Signaling Pathways.

P2860

Q52615043-60E5022A-F43C-469C-B770-A46F13CBAE52 Q54978574-41C66D86-AFBA-40E9-AE5F-34058F0812FB

P2860

Remarkably Stereospecific Utilization of ATP α,β-Halomethylene Analogues by Protein Kinases.

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http://www.wikidata.org/entity/Q40189472

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2017 nî lūn-bûn

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2017年の論文

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2017年論文

@yue

2017年論文

@zh-hant

2017年論文

@zh-hk

2017年論文

@zh-mo

2017年論文

@zh-tw

2017年论文

@wuu

2017年论文

@zh

2017年论文

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name

Remarkably Stereospecific Util ...... Analogues by Protein Kinases.

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type

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label

Remarkably Stereospecific Util ...... Analogues by Protein Kinases.

@en

prefLabel

Remarkably Stereospecific Util ...... Analogues by Protein Kinases.

@en

P1476

Remarkably Stereospecific Util ...... e Analogues by Protein Kinases

@en

P2093

Alvin Kung

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

Carolina D Amador

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

Charles E McKenna

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

Feng Ni

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

Lin Chen

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

Ming Guo

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

Vivek Shah

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

Xuegong Fan

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

Yankun Duan

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

Yongheng Chen

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

P2860

Halogen bonds in biological molecules

Mechanism of nitrogen fixation by nitrogenase: the next stage

Crystal structures of c-Src reveal features of its autoinhibitory mechanism

( R )-β,γ-Fluoromethylene-dGTP-DNA Ternary Complex with DNA Polymerase β

α,β-Difluoromethylene Deoxynucleoside 5′-Triphosphates: A Convenient Synthesis of Useful Probes for DNA Polymerase β Structure and Function

Halogenated β,γ-Methylene- and Ethylidene-dGTP-DNA Ternary Complexes with DNA Polymerase β: Structural Evidence for Stereospecific Binding of the Fluoromethylene Analogues

Stereospecific Formation of a Ternary Complex of (S)-α,β-Fluoromethylene-dATP with DNA Pol β

β,γ-CHF- and β,γ-CHCl-dGTP Diastereomers: Synthesis, Discrete 31 P NMR Signatures, and Absolute Configurations of New Stereochemical Probes for DNA Polymerases

Comprehensive characterization of the Published Kinase Inhibitor Set

Structural investigation of the antibiotic and ATP-binding sites in kanamycin nucleotidyltransferase

P304

7701-7704

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P31

scholarly article

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10.1021/JACS.7B03266

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P407

English

P433

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

P478

139

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

P50

Chao Zhang

P577

2017-06-02T00:00:00Z

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

P698

28535041

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

P932

5541949

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Remarkably Stereospecific Utilization of ATP α,β-Halomethylene Analogues by Protein Kinases.

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P2860

P2860

Remarkably Stereospecific Utilization of ATP α,β-Halomethylene Analogues by Protein Kinases.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P932