Inter- and intramolecular aldol reactions promiscuously catalyzed by a proline-based tautomerase.

about

Engineering a Promiscuous Tautomerase into a More Efficient Aldolase for Self-Condensations of Linear Aliphatic Aldehydes.Amide rotation trajectories probed by symmetry.

P2860

Q36351769-3D33EB5C-73DC-4D1A-A0A8-40B0DAA3793E Q48001048-A7519A28-8404-4E9F-97EC-3FB296338E60

P2860

Inter- and intramolecular aldol reactions promiscuously catalyzed by a proline-based tautomerase.

Item

http://www.wikidata.org/entity/Q48145667

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

Inter- and intramolecular aldo ...... y a proline-based tautomerase.

@en

Inter- and intramolecular aldo ...... y a proline-based tautomerase.

@nl

type

Item

label

Inter- and intramolecular aldo ...... y a proline-based tautomerase.

@en

Inter- and intramolecular aldo ...... y a proline-based tautomerase.

@nl

prefLabel

Inter- and intramolecular aldo ...... y a proline-based tautomerase.

@en

Inter- and intramolecular aldo ...... y a proline-based tautomerase.

@nl

P1476

Inter- and intramolecular aldo ...... y a proline-based tautomerase.

@en

P2093

Edzard M Geertsema

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

Ellen Zandvoort

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

Jan-Ytzen van der Meer

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

Mehran Rahimi

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

Thea van den Bosch

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

Yufeng Miao

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

P2860

Observation of covalent intermediates in an enzyme mechanism at atomic resolution

Sequential Aldol Condensation Catalyzed by Hyperthermophilic 2-Deoxy-D-Ribose-5-Phosphate Aldolase

Evidence for the formation of an enamine species during aldol and Michael-type addition reactions promiscuously catalyzed by 4-oxalocrotonate tautomerase

The 4-oxalocrotonate tautomerase family of enzymes: how nature makes new enzymes using a beta-alpha-beta structural motif

Physically associated enzymes produce and metabolize 2-hydroxy-2,4-dienoate, a chemically unstable intermediate formed in catechol metabolism via meta cleavage in Pseudomonas putida

The chemical versatility of the beta-alpha-beta fold: catalytic promiscuity and divergent evolution in the tautomerase superfamily.

Microbial aldolases as C-C bonding enzymes--unknown treasures and new developments.

Evolution of enzymatic activity in the tautomerase superfamily: mechanistic and structural consequences of the L8R mutation in 4-oxalocrotonate tautomerase

Directed evolution of aldolases for exploitation in synthetic organic chemistry

Catalytic asymmetric aldol reactions in aqueous media.

P304

2809-2816

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

P31

scholarly article

P356

10.1039/C7OB00302A

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

P433

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

P478

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

P50

Gerrit J Poelarends

Pim de Haan

P577

2017-03-09T00:00:00Z

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

P698

28277572

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

Inter- and intramolecular aldol reactions promiscuously catalyzed by a proline-based tautomerase.

about

P2860

P2860

Inter- and intramolecular aldol reactions promiscuously catalyzed by a proline-based tautomerase.

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