Biosynthetically directed ²H labelling for stereospecific resonance assignments of glycine methylene groups.

about

Advances in NMR structures of integral membrane proteins.Selective (15)N-labeling of the side-chain amide groups of asparagine and glutamine for applications in paramagnetic NMR spectroscopy.

P2860

Q30431265-E0B56F7D-206B-4E74-81D6-3BD99F87F0FC Q53507939-69F2B27F-F36E-4ABC-92FB-8413D1A7773F

P2860

Biosynthetically directed ²H labelling for stereospecific resonance assignments of glycine methylene groups.

Item

http://www.wikidata.org/entity/Q54322329

description

2012 nî lūn-bûn

@nan

2012年の論文

@ja

2012年学术文章

@wuu

2012年学术文章

@zh

2012年学术文章

@zh-cn

2012年学术文章

@zh-hans

2012年学术文章

@zh-my

2012年学术文章

@zh-sg

2012年學術文章

@yue

2012年學術文章

@zh-hant

name

Biosynthetically directed ²H l ...... s of glycine methylene groups.

@en

Biosynthetically directed ²H l ...... s of glycine methylene groups.

@nl

type

Item

label

Biosynthetically directed ²H l ...... s of glycine methylene groups.

@en

Biosynthetically directed ²H l ...... s of glycine methylene groups.

@nl

prefLabel

Biosynthetically directed ²H l ...... s of glycine methylene groups.

@en

Biosynthetically directed ²H l ...... s of glycine methylene groups.

@nl

P1476

Biosynthetically directed ²H l ...... s of glycine methylene groups.

@en

P2093

Karin V Loscha

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

P2860

Stereospecific nuclear magnetic resonance assignments of the methyl groups of valine and leucine in the DNA-binding domain of the 434 repressor by biosynthetically directed fractional 13C labeling

Optimal isotope labelling for NMR protein structure determinations.

A practical method for cell-free protein synthesis to avoid stable isotope scrambling and dilution.

Floating stereospecific assignment revisited: application to an 18 kDa protein and comparison with J-coupling data.

Recommendations for the presentation of NMR structures of proteins and nucleic acids. IUPAC-IUBMB-IUPAB Inter-Union Task Group on the Standardization of Data Bases of Protein and Nucleic Acid Structures Determined by NMR Spectroscopy.

Suppression of isotope scrambling in cell-free protein synthesis by broadband inhibition of PLP enymes for selective 15N-labelling and production of perdeuterated proteins in H2O.

Hydrogen exchange during cell-free incorporation of deuterated amino acids and an approach to its inhibition

Serine hydroxymethyltransferase revisited.

SAIL--stereo-array isotope labeling.

Biosynthetic incorporation of 15N and 13C for assignment and interpretation of nuclear magnetic resonance spectra of proteins.

P2888

s10858-012-9690-x

P304

97-104

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

P31

scholarly article

P356

10.1007/S10858-012-9690-X

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

P433

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

P478

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

P50

Gottfried Otting

P577

2012-11-29T00:00:00Z

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

P698

23192292

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

Biosynthetically directed ²H labelling for stereospecific resonance assignments of glycine methylene groups.

about

P2860

P2860

Biosynthetically directed ²H labelling for stereospecific resonance assignments of glycine methylene groups.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P50

P577

P698

P356

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P50

P577

P698