Structural elucidation of the DFG-Asp in and DFG-Asp out states of TAM kinases and insight into the selectivity of their inhibitors.

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Highly Sensitive, Engineered Magnetic Nanosensors to Investigate the Ambiguous Activity of Zika Virus and Binding Receptors.

P2860

Q38156921-6F654BED-1634-4924-B729-912068D28807

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Structural elucidation of the DFG-Asp in and DFG-Asp out states of TAM kinases and insight into the selectivity of their inhibitors.

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2014 nî lūn-bûn

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2014年の論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

@zh-tw

2014年论文

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2014年论文

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2014年论文

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name

Structural elucidation of the ...... lectivity of their inhibitors.

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Structural elucidation of the ...... lectivity of their inhibitors.

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type

Item

label

Structural elucidation of the ...... lectivity of their inhibitors.

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Structural elucidation of the ...... lectivity of their inhibitors.

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Structural elucidation of the ...... lectivity of their inhibitors.

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Structural elucidation of the ...... lectivity of their inhibitors.

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P1476

Structural elucidation of the ...... electivity of their inhibitors

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P2093

Abdellah Messoussi

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

Clémence Feneyrolles

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

Lucile Peyronnet

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P2860

axl, a transforming gene isolated from primary human myeloid leukemia cells, encodes a novel receptor tyrosine kinase

Axl receptor tyrosine kinase stimulated by the vitamin K-dependent protein encoded by growth-arrest-specific gene 6

The protein kinase complement of the human genome

The Protein Data Bank

Dominant-negative inhibition of the Axl receptor tyrosine kinase suppresses brain tumor cell growth and invasion and prolongs survival

PROCHECK: a program to check the stereochemical quality of protein structures

Structural insights into the inhibited states of the Mer receptor tyrosine kinase

Discovery of N-(4-(2-amino-3-chloropyridin-4-yloxy)-3-fluorophenyl)-4-ethoxy-1-(4-fluorophenyl)-2-oxo-1,2-dihydropyridine-3-carboxamide (BMS-777607), a selective and orally efficacious inhibitor of the Met kinase superfamily

Discovery of 4-azaindoles as novel inhibitors of c-Met kinase

LY2801653 is an orally bioavailable multi-kinase inhibitor with potent activity against MET, MST1R, and other oncoproteins, and displays anti-tumor activities in mouse xenograft models

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16223-16239

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scholarly article

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10.3390/MOLECULES191016223

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English

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P478

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Gweneal Chevé

Abdelaziz Yasri

Khalid Bougrin

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2014-10-10T00:00:00Z

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267756084

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25310149

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6271404

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Structural elucidation of the DFG-Asp in and DFG-Asp out states of TAM kinases and insight into the selectivity of their inhibitors.

about

P2860

P2860

Structural elucidation of the DFG-Asp in and DFG-Asp out states of TAM kinases and insight into the selectivity of their inhibitors.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P5875

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P5875

P698

P932