(Q41697600)

7 October 2017

title

Modulating pyridoxamine-mediated transamination through a betabeta alpha motif peptide scaffold (English)

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7 October 2017

Shogren-Knaak MA

1

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7 October 2017

Imperiali B

series ordinal

2

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7 October 2017

language of work or name

English

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publication date

1 September 1999

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Bioorganic & Medicinal Chemistry

7 October 2017

published in

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7 October 2017

volume

7

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7 October 2017

issue

9

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7 October 2017

page(s)

1993-2002

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Pyridoxal enzymes: mechanistic diversity and uniformity

7 October 2017

cites work

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https://api.crossref.org/works/10.1016%2FS0968-0896%2899%2900112-1

7 January 2021

Pyridoxamine-amino acid chimeras in semisynthetic aminotransferase mimics

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2899%2900112-1

7 January 2021

Design of a monomeric 23-residue polypeptide with defined tertiary structure

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2899%2900112-1

7 January 2021

Design and NMR analyses of compact, independently folded BBA motifs

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2899%2900112-1

7 January 2021

2.8-A-resolution crystal structure of an active-site mutant of aspartate aminotransferase from Escherichia coli

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2899%2900112-1

7 January 2021

Site-directed mutagenesis of aspartate aminotransferase from E. coli.

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2899%2900112-1

7 January 2021

Direct Brønsted analysis of the restoration of activity to a mutant enzyme by exogenous amines

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2899%2900112-1

7 January 2021

Stereochemistry of enzymic transamination

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2899%2900112-1

7 January 2021

Stereochemistry of transamination catalyzed by pyridoxamine--pyruvate transaminase

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2899%2900112-1

7 January 2021

o-Phthalaldehyde—N-acetyl-L-cysteine as a chiral derivatization reagent for liquid chromatographic optical resolution of amino acid ernantiomers and its application to conventional amino acid analysis

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2899%2900112-1

7 January 2021

High-performance liquid chromatographic determination of enantiomeric amino acids and amino alcohols after derivatization with o-phthaldialdehyde and various chiral mercaptans. Application to peptide hydrolysates

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2899%2900112-1

7 January 2021

10.1016/S0968-0896(99)00112-1

Identifiers

DOI

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7 October 2017

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