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English	No label defined	scientific article

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scholarly article

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Kinetics of the hydrolysis of N-benzoyl-L-serine methyl ester catalysed by bromelain and by papain. Analysis of modifier mechanisms by lattice nomography, computational methods of parameter evaluation for substrate-activated catalyses and consequences of postulated non-productive binding in bromelain- and papain-catalysed hydrolyses (English)

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author name string

C W Wharton

1

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A Cornish-Bowden

2

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K Brocklehurst

3

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E M Crook

4

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language of work or name

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publication date

August 1974

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Biochemical Journal

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141

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2

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365-381

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Application of a Theory of Enzyme Specificity to Protein Synthesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1168089

20 March 2017

Tissue sulfhydryl groups

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1168089

20 March 2017

A COMPARISON OF ESTIMATES OF MICHAELIS-MENTEN KINETIC CONSTANTS FROM VARIOUS LINEAR TRANSFORMATIONS

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1168089

29 September 2017

Mapping the active site of papain with the aid of peptide substrates and inhibitors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1168089

29 September 2017

PAPAIN-CATALYSED HYDROLYSIS OF SOME HIPPURIC ESTERS. A NEW MECHANISM FOR PAPAIN-CATALYSED HYDROLYSIS.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1168089

2 June 2018

Demonstration of a change in the rate-determining step in papain- and ficin-catalyzed acyl-transfer reactions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1168089

2 June 2018

Ficin- and papain-catalyzed reactions. Changes in reactivity of the essential sulfhydryl group in the presence of substrates and competitive inhibitors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1168089

2 June 2018

Multiple molecular forms of stem bromelain. Isolation and characterization of two closely related components, SB1 and SB2.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1168089

2 June 2018

A general method for the quantitative determination of saturation curves for multisubunit proteins.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1168089

2 June 2018

Negatively co-operative ligand binding

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1168089

27 November 2018

The mutability of stem bromelain: evidence for perturbation by structural transitions of the parameters that characterize the reaction of the essential thiol group of bromelain with 2,2'-dipyridyl disulphide

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1168089

27 November 2018

The Nature of the Perturbation of the Michaelis Constant of the Bromelain-Catalysed Hydrolysis of alpha-N-Benzoyl-l-Arginine Ethyl Ester Consequent upon Attachment of Bromelain to O-(Carboxymethyl)-Cellulose

1 reference

https://pubmed.ncbi.nlm.nih.gov/4455211

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

KINETICS OF PAPAIN-CATALYZED HYDROLYSIS OF ALPHA-N-BENZOYL-L-ARGININE ETHYL ESTER AND ALPHA-N-BENZOYL-L-ARGININAMIDE

1 reference

https://pubmed.ncbi.nlm.nih.gov/4455211

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sequence of amino acids in the vicinity of the reactive thiol group of stem bromelain

1 reference

https://pubmed.ncbi.nlm.nih.gov/4455211

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

PREPARATION AND CHEMICAL PROPERTIES OF PURIFIED STEM AND FRUIT BROMELAINS

1 reference

https://pubmed.ncbi.nlm.nih.gov/4455211

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Preparation and Some Properties of Bromelain Covalently Attached to O-(Carboxymethyl)-Cellulose

1 reference

https://pubmed.ncbi.nlm.nih.gov/4455211

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

STUDIES ON THE ACTIVE CENTER OF TRYPSIN. THE BINDING OF AMIDINES AND GUANIDINES AS MODELS OF THE SUBSTRATE SIDE CHAIN

1 reference

https://pubmed.ncbi.nlm.nih.gov/4455211

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The alpha-chymotrypsin catalyzed hydrolysis of a series of acylated glycine methyl esters

1 reference

https://pubmed.ncbi.nlm.nih.gov/4455211

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

FRACTIONATION AND PARTIAL CHARACTERIZATION OF THE PROTEOLYTIC ENZYMES OF STEM BROMELAIN

1 reference

https://pubmed.ncbi.nlm.nih.gov/4455211

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

PURIFICATION AND PHYSICAL CHARACTERIZATION OF STEM BROMELAIN

1 reference

https://pubmed.ncbi.nlm.nih.gov/4455211

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

KINETIC STUDIES OF BROMELAIN CATALYSIS

1 reference

https://pubmed.ncbi.nlm.nih.gov/4455211

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

THE MECHANISM OF THE SPECIFICITY OF TRYPSIN CATALYSIS. 3. ACTIVATION OF THE CATALYTIC SITE OF TRYPSIN BY ALKYLAMMONIUM IONS IN THE HYDROLYSIS OF ACETYLGLYCINE ETHYL ESTER

1 reference

https://pubmed.ncbi.nlm.nih.gov/4455211

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Substrate activation of trypsin and acetyltrypsin caused by -N-benzoyl-L-arginine p-nitroanilide

1 reference

https://pubmed.ncbi.nlm.nih.gov/4455211

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phenolic hydroxyl ionization in papain

1 reference

https://pubmed.ncbi.nlm.nih.gov/4455211

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The kinetic analysis of hydrolytic enzyme catalyses: Consequences of non-productive binding

1 reference

https://pubmed.ncbi.nlm.nih.gov/4455211

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Kinetics of Papain-Catalyzed Hydrolyses of Neutral Substrates*

1 reference

https://pubmed.ncbi.nlm.nih.gov/4455211

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

SUBSTRATE ACTIVATION OF TRYPSIN

1 reference

https://pubmed.ncbi.nlm.nih.gov/4455211

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

ON THE MOLECULAR WEIGHTS OF THE PROTEOLYTIC ENZYMES OF STEM BROMELAIN

1 reference

https://pubmed.ncbi.nlm.nih.gov/4455211

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The rate-limiting reaction in papain action as derived from the reaction of the enzyme with chloroacetic acid

1 reference

https://pubmed.ncbi.nlm.nih.gov/4455211

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A Kinetic Analysis of the Papain-Catalyzed Hydrolysis of α-N-Benzoyl-L-citrulline Methyl Ester*

1 reference

https://pubmed.ncbi.nlm.nih.gov/4455211

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1042/BJ1410365

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