Denaturation by guanidinium chloride of dimeric MM-creatine kinase and its proteinase K-nicked form: evidence for a multiple-step process (Q73164730)

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1 November 2019

title

Denaturation by guanidinium chloride of dimeric MM-creatine kinase and its proteinase K-nicked form: evidence for a multiple-step process (English)

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1 November 2019

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E Clottes

1

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1 November 2019

C Leydier

2

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1 November 2019

F Couthon

3

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1 November 2019

O Marcillat

4

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1 November 2019

C Vial

5

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1 November 2019

language of work or name

English

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publication date

1 March 1997

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Biochimica et Biophysica Acta

1 November 2019

published in

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1 November 2019

volume

1338

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1 November 2019

issue

1

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1 November 2019

page(s)

37-46

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Structure of mitochondrial creatine kinase

1 November 2019

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Identification by protein microsequencing of a proteinase-V8-cleavage site in a folding intermediate of chick muscle creatine kinase

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Heterogeneity of rabbit muscle creatine kinase and limited proteolysis by proteinase K

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The effect of limited proteolysis on rabbit muscle creatine kinase

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Differential sensitivity of chicken MM-creatine kinase to trypsin and proteinase-K

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Monoclonal-antibody studies of creatine kinase. The proteinase K-cleavage site

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Specific proteolytic modification of creatine kinase isoenzymes. Implication of C-terminal involvement in enzymic activity but not in subunit-subunit recognition

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Study of the "molten globule" intermediate state in protein folding by a hydrophobic fluorescent probe

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Reversible dissociation and unfolding of dimeric creatine kinase isoenzyme MM in guanidine hydrochloride and urea

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Multiple-state equilibrium unfolding of guanidino kinases

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"Partly folded" state, a new equilibrium state of protein molecules: four-state guanidinium chloride-induced unfolding of beta-lactamase at low temperature.

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Further evidence on the equilibrium "pre-molten globule state": four-state guanidinium chloride-induced unfolding of carbonic anhydrase B at low temperature

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Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

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Assay of proteins in the presence of interfering materials

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Heart mitochondrial creatine kinase solubilization. Effect of mitochondrial swelling and SH group reagents

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Tricine-sodium dodecyl sulfate-polyacrylamide gel electrophoresis for the separation of proteins in the range from 1 to 100 kDa

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Size exclusion chromatography and universal calibration of gel columns

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Use of fast protein size-exclusion liquid chromatography to study the unfolding of proteins which denature through the molten globule

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Determination of tyrosine exposure in proteins by second-derivative spectroscopy

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Creatine kinase compactness and thiol accessibility during sodium dodecyl sulfate denaturation estimated by resonance energy transfer and 2-nitro-5-thiocyanobenzoic acid cleavage

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Fluorescence and the location of tryptophan residues in protein molecules

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Solute perturbation of protein fluorescence. Quenching of the tryptophyl fluorescence of model compounds and of lysozyme by iodide ion

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7 January 2021

Discrimination between the four tryptophan residues of MM-creatine kinase on the basis of the effect of N-bromosuccinimide on activity and spectral properties

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7 January 2021

ATP binding site of mitochondrial creatine kinase

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7 January 2021

Isolation and characterization of independently folding regions of the β chain of Escherichia coli tryptophan synthetase

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7 January 2021

Guanidine hydrochloride induced unfolding of the alpha subunit of tryptophan synthase and of the two alpha proteolytic fragments: evidence for stepwise unfolding of the two alpha domains

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Reversible unfolding of the beta 2 subunit of Escherichia coli tryptophan synthetase and its proteolytic fragments

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Reconstitution of active octameric mitochondrial creatine kinase from two genetically engineered fragments

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Identifiers

DOI

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1 November 2019

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