Molecular basis for covalent inhibition of glyceraldehyde-3-phosphate dehydrogenase by a 2-phenoxy-1,4-naphthoquinone small molecule.

about

Identification of common immunodominant antigens of Eimeria tenella, Eimeria acervulina and Eimeria maxima by immunoproteomic analysis.Protective Efficacy of Coccidial Common Antigen Glyceraldehyde 3-Phosphate Dehydrogenase (GAPDH) against Challenge with Three Eimeria Species.

P2860

Q33798659-99094D05-744E-449C-8866-8A93D57A2AE1 Q40109106-13162460-0D6A-4DCE-9BAC-DD04A8362633

P2860

Molecular basis for covalent inhibition of glyceraldehyde-3-phosphate dehydrogenase by a 2-phenoxy-1,4-naphthoquinone small molecule.

Item

http://www.wikidata.org/entity/Q38924209

description

2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年学术文章

@wuu

2017年学术文章

@zh-cn

2017年学术文章

@zh-hans

2017年学术文章

@zh-my

2017年学术文章

@zh-sg

2017年學術文章

@yue

2017年學術文章

@zh

2017年學術文章

@zh-hant

name

Molecular basis for covalent i ...... naphthoquinone small molecule.

@en

type

Item

label

Molecular basis for covalent i ...... naphthoquinone small molecule.

@en

prefLabel

Molecular basis for covalent i ...... naphthoquinone small molecule.

@en

P1476

Molecular basis for covalent i ...... -naphthoquinone small molecule

@en

P2093

Andrea Cavalli

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

Christian Bergamini

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

Elisa Uliassi

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

Federica Prati

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

Gianluca Paredi

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

Maria Paola Costi

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

Marilena Margiotta

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

Paola Conti

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

Riccardo Amorati

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

Romana Fato

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

P2860

A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding

Evidence for the two phosphate binding sites of an analogue of the thioacyl intermediate for the Trypanosoma cruzi glyceraldehyde-3-phosphate dehydrogenase-catalyzed reaction, from its crystal structure

Trapping of the thioacylglyceraldehyde-3-phosphate dehydrogenase intermediate from Bacillus stearothermophilus. Direct evidence for a flip-flop mechanism

GAPDH, a novel regulator of the pro-apoptotic mitochondrial membrane permeabilization

Vesicular glycolysis provides on-board energy for fast axonal transport

Naphthoquinone derivatives exert their antitrypanosomal activity via a multi-target mechanism

Acrylonitrile irreversibly inactivates glyceraldehyde-3-phosphate dehydrogenase by alkylating the catalytically active cysteine 149.

Site-specific binding of quinones to proteins through thiol addition and addition-elimination reactions.

Structure-activity relationships of novel inhibitors of glyceraldehyde-3-phosphate dehydrogenase.

2-(Quinazolin-4-ylamino)-[1,4]benzoquinones as covalent-binding, irreversible inhibitors of the kinase domain of vascular endothelial growth factor receptor-2.

P304

225-235

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

P31

scholarly article

P356

10.1111/CBDD.12941

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

P433

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

P478

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

P50

Stefano Bruno

Marcel Kaiser

Maria Laura Bolognesi

Mirko Zaffagnini

P577

2017-03-06T00:00:00Z

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

P698

28079302

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

Molecular basis for covalent inhibition of glyceraldehyde-3-phosphate dehydrogenase by a 2-phenoxy-1,4-naphthoquinone small molecule.

about

P2860

P2860

Molecular basis for covalent inhibition of glyceraldehyde-3-phosphate dehydrogenase by a 2-phenoxy-1,4-naphthoquinone small molecule.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698