(Q27730708)

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High-resolution structure of Ascaris trypsin inhibitor in solution: direct evidence for a pH-induced conformational transition in the reactive site

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28 October 2019

High-resolution structure of Ascaris trypsin inhibitor in solution: direct evidence for a pH-induced conformational transition in the reactive site (English)

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28 October 2019

G. Marius Clore

2

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28 October 2019

Angela Gronenborn

3

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28 October 2019

author name string

B L Grasberger

1

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28 October 2019

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1 July 1994

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28 October 2019

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28 October 2019

2

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28 October 2019

669-678

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28 October 2019

7

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28 October 2019

Protein inhibitors of proteinases

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Crystallographic refinement of the structure of bovine pancreatic trypsin inhibitor at l.5 Å resolution

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Crystal structure of a bacterial protein proteinase inhibitor (Streptomyces subtilisin inhibitor) at 2·6 Å resolution

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Structure of bovine pancreatic trypsin inhibitor. Results of joint neutron and X-ray refinement of crystal form II

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Structure of form III crystals of bovine pancreatic trypsin inhibitor

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Solution conformation of proteinase inhibitor IIA from bull seminal plasma by 1H nuclear magnetic resonance and distance geometry

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Protein structures in solution by nuclear magnetic resonance and distance geometry. The polypeptide fold of the basic pancreatic trypsin inhibitor determined using two different algorithms, DISGEO and DISMAN.

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Three-dimensional structure of potato carboxypeptidase inhibitor in solution. A study using nuclear magnetic resonance, distance geometry, and restrained molecular dynamics

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Solution structure of recombinant hirudin and the Lys-47 .fwdarw. Glu mutants: a nuclear magnetic resonance and hybrid distance geometry-dynamical simulated annealing study

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Determination of the complete three-dimensional structure of the trypsin inhibitor from squash seeds in aqueous solution by nuclear magnetic resonance and a combination of distance geometry and dynamical simulated annealing

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Crystal structures of Streptomyces subtilisin inhibitor and its complex with subtilisin BPN'

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The isoinhibitors of chymotrypsin/elastase from Ascaris lumbricoides: isolation by affinity chromatography and association with the enzymes.

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The isoinhibitors of chymotrypsin/elastase from Ascaris lumbricoides: the reactive site

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The isoinhibitors of chymotrypsin/elastase from Ascaris lumbricoides: the primary structure

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Sequential resonance assignment and secondary structure determination of the Ascaris trypsin inhibitor, a member of a novel class of proteinase inhibitors

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Inhibition of human blood clotting by extracts of Ascaris suum

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Structures of larger proteins in solution: three- and four-dimensional heteronuclear NMR spectroscopy

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Determination of the three-dimensional solution structure of the C-terminal domain of cellobiohydrolase I from Trichoderma reesei. A study using nuclear magnetic resonance and hybrid distance geometry-dynamical simulated annealing

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High-resolution three-dimensional structure of reduced recombinant human thioredoxin in solution

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High-resolution three-dimensional structure of interleukin 1 beta in solution by three- and four-dimensional nuclear magnetic resonance spectroscopy

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The three-dimensional structure of alpha1-purothionin in solution: combined use of nuclear magnetic resonance, distance geometry and restrained molecular dynamics

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Determination of three-dimensional structures of proteins from interproton distance data by dynamical simulated annealing from a random array of atoms. Circumventing problems associated with folding

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The anatomy and taxonomy of protein structure

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Isolation of the trypsin inhibitors in Ascaris lumbricoides var. suum using affinity chromatography

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Application of phase sensitive two-dimensional correlated spectroscopy (COSY) for measurements of 1H-1H spin-spin coupling constants in proteins

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Determination of three-dimensional structures of proteins in solution by nuclear magnetic resonance spectroscopy

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On the size of the active site in proteases. I. Papain

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Identifiers

10.1016/S0969-2126(00)00067-8

1 reference

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28 October 2019

1 reference

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28 October 2019

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