Literature DB >> 3910099

1H-15N heteronuclear NMR studies of Escherichia coli thioredoxin in samples isotopically labeled by residue type.

D M LeMaster, F M Richards.   

Abstract

Ten samples of Escherichia coli thioredoxin were individually isotopically enriched by residue type via growth of an appropriate auxotrophic strain on media supplemented with one 2H, 15N-enriched amino acid. 1H observe-heteronuclear decoupling experiments were conducted on these samples making use of the 95-Hz 1H-15N amide J1 coupling. Subtraction of near-resonance from off-resonance 15N decoupled spectra generated difference patterns corresponding only to protons directly bonded to 15N nuclei. For the ten different enriched residue types observed to date, every labeled position (60) has been observed as a resolved resonance. The spectral dispersion in both the 1H and the 15N dimensions was roughly 1500 Hz (at 500-MHz field strength) with rather little apparent dependence on residue type. With the exception of the glycine-enriched sample, the range of the J1 coupling constants was not much greater than the precision of the measurements (1.5-2.0 Hz). However, for the glycine residues the J1 amide coupling values varied over a range of 10 Hz.

Entities:  

Mesh:

Substances:

Year:  1985        PMID: 3910099     DOI: 10.1021/bi00346a036

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  69 in total

1.  Structure of the LpxC deacetylase with a bound substrate-analog inhibitor.

Authors:  Brian E Coggins; Xuechen Li; Amanda L McClerren; Ole Hindsgaul; Christian R H Raetz; Pei Zhou
Journal:  Nat Struct Biol       Date:  2003-08

2.  Mars -- robust automatic backbone assignment of proteins.

Authors:  Young-Sang Jung; Markus Zweckstetter
Journal:  J Biomol NMR       Date:  2004-09       Impact factor: 2.835

3.  Using codon optimization, chaperone co-expression, and rational mutagenesis for production and NMR assignments of human eIF2 alpha.

Authors:  Takuhiro Ito; Gerhard Wagner
Journal:  J Biomol NMR       Date:  2004-04       Impact factor: 2.835

4.  Crystallization and preliminary X-ray analysis of FlgA, a periplasmic protein essential for flagellar P-ring assembly.

Authors:  Hideyuki Matsunami; Fadel A Samatey; Shigehiro Nagashima; Katsumi Imada; Keiichi Namba
Journal:  Acta Crystallogr Sect F Struct Biol Cryst Commun       Date:  2012-02-23

5.  Transcriptional repression mediated by a TetR family protein, PfmR, from Thermus thermophilus HB8.

Authors:  Yoshihiro Agari; Keiko Sakamoto; Seiki Kuramitsu; Akeo Shinkai
Journal:  J Bacteriol       Date:  2012-06-29       Impact factor: 3.490

6.  Crystallization and preliminary X-ray analysis of a novel esterase Rv0045c from Mycobacterium tuberculosis.

Authors:  Lipeng Xu; Jiubiao Guo; Xiangdong Zheng; Tingyi Wen; Fei Sun; Siguo Liu; Hai Pang
Journal:  Acta Crystallogr Sect F Struct Biol Cryst Commun       Date:  2010-11-16

7.  Structure of RizA, an L-amino-acid ligase from Bacillus subtilis.

Authors:  Wataru Kagawa; Toshinobu Arai; Shun Ishikura; Kuniki Kino; Hitoshi Kurumizaka
Journal:  Acta Crystallogr F Struct Biol Commun       Date:  2015-08-25       Impact factor: 1.056

8.  CASA: an efficient automated assignment of protein mainchain NMR data using an ordered tree search algorithm.

Authors:  Jianyong Wang; Tianzhi Wang; Erik R P Zuiderweg; Gordon M Crippen
Journal:  J Biomol NMR       Date:  2005-12       Impact factor: 2.835

9.  Crystal structure of the histidine-containing phosphotransfer protein ZmHP2 from maize.

Authors:  Hajime Sugawara; Yoshiaki Kawano; Tomomitsu Hatakeyama; Tomoyuki Yamaya; Nobuo Kamiya; Hitoshi Sakakibara
Journal:  Protein Sci       Date:  2004-12-02       Impact factor: 6.725

10.  Crystallization and preliminary X-ray analysis of the ergothioneine-biosynthetic methyltransferase EgtD.

Authors:  Allegra Vit; Laëtitia Misson; Wulf Blankenfeldt; Florian Peter Seebeck
Journal:  Acta Crystallogr F Struct Biol Commun       Date:  2014-04-25       Impact factor: 1.056

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.