About: Covalent chromatography by thiol-disulfide interchange

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scientific article published on 01 January 1974

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в січні 1974 (uk) articolo scientifico (pubblicato il 1974) (it) article scientifique publié en 1974 (fr) im Januar 1974 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu en xineru de 1974 (ast) artikull shkencor i botuar më 01 janar 1974 (sq) scientific article published on 01 January 1974 (en)
publication date	wds:Q68872808-249CD481-2C82-4654-AB1B-2B32AE04C3DE
publication date	1974-01-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q68872808-69A4078D-54DC-4DA0-AB4A-C65078127EBE
language of work or name	English
cites work	wds:Q68872808-1011F5E5-E051-4764-A2B1-0F32ABB490F6 wds:Q68872808-34909373-FD9D-4A94-A00D-FD042FE9ED93 wds:Q68872808-35A25A5D-B082-4203-9CC1-859DB61E3434 wds:Q68872808-58844716-C104-4E1E-A492-BFCFBCB7BAA7 wds:Q68872808-891B08A8-6AEF-496D-B313-FDCE3429EF89 wds:Q68872808-C420862E-8055-4A13-BB84-31DAAA641937 wds:Q68872808-CF369CDC-7160-4C01-830F-CE6B0F4C0C3B wds:Q68872808-DC58FB92-51FE-43F6-875B-2137CDE29CBA wds:Q68872808-DCF17027-A126-4784-B371-C2FABAF444B1 wds:Q68872808-EFB75C73-E405-4851-A5F7-551E84B3ED03 wds:Q68872808-FB34F436-DF69-4AB8-944F-042D4363B348
cites work	Reactions of papain and of low-molecular-weight thiols with some aromatic disulphides. 2,2'-Dipyridyl disulphide as a convenient active-site titrant for papain even in the presence of other thiols Reactivities of the various protonic states in the reactions of papain and of L-cysteine with 2,2'- and with 4,4'- dipyridyl disulphide: evidence for nucleophilic reactivity in the un-ionized thiol group of the cysteine-25 residue of papain occasion A novel reactivity of papain and a convenient active site titration in the presence of other thiols Covalent chromatography. Preparation of fully active papain from dried papaya latex Chemical Coupling of Peptides and Proteins to Polysaccharides by Means of Cyanogen Halides The Purification of Papain by Affinity Chromatography Chemical Coupling of Proteins to Agarose Chemical Fixation of Enzymes to Cyanogen Halide Activated Polysaccharide Carriers Propapain and its Conversion to Papain: A New Type of Zymogen Activation Mechanism involving Intramolecular Thiol-Disulphide Interchange 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 A covalent affinity column for the purification of acetylcholinesterase
author name string	wds:Q68872808-471F8AFA-9669-4C16-AD79-AA227C8F8CC7 wds:Q68872808-9428F9F3-621F-4B83-B211-21A06053106F wds:Q68872808-F1D571CA-C934-42AB-BBCF-76565C5D8D3D wds:Q68872808-F5CF7B81-D1FF-4F73-BCA3-EDC1204DB387
author name string	K Brocklehurst J Carlsson E M Crook M P Kierstan
rdfs:label	Covalent chromatography by thiol-disulfide interchange (en) Covalent chromatography by thiol-disulfide interchange (nl) Covalent chromatography by thiol-disulfide interchange (sq)
skos:prefLabel	Covalent chromatography by thiol-disulfide interchange (en) Covalent chromatography by thiol-disulfide interchange (nl) Covalent chromatography by thiol-disulfide interchange (sq)
name	Covalent chromatography by thiol-disulfide interchange (en) Covalent chromatography by thiol-disulfide interchange (nl) Covalent chromatography by thiol-disulfide interchange (sq)
title	wds:Q68872808-8324B5D2-23DF-4C3D-805A-481C01EC56A8
title	Covalent chromatography by thiol-disulfide interchange (en)
page(s)	wds:Q68872808-235FFE41-D298-4076-9861-F59BBFA8D49B
page(s)	531-544
instance of	wds:Q68872808-F952EC43-9D10-4CCF-991C-B4CA90A72C8C
instance of	scholarly article
PubMed ID	wds:Q68872808-E6AFD5BA-A413-487C-B47F-54989E36A74E
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/4449470
PubMed ID	4449470
published in	wds:Q68872808-43CDD9CD-7905-49FC-8B97-8774C4A4BA98
published in	Methods in Enzymology
volume	wds:Q68872808-D28FFAD2-158C-4493-9537-554091DAC595
volume	34
DOI	wds:Q68872808-83662194-8FA5-4041-AC74-A6877DC7F121
DOI	http://dx.doi.org/10.1016/S0076-6879(74)34069-4
DOI	10.1016/S0076-6879(74)34069-4
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q68872808
is cites work of	Structure of chymopapain M the late-eluted chymopapain deduced by comparative modelling techniques and active-centre characteristics determined by pH-dependent kinetics of catalysis and reactions with time-dependent inhibitors: the Cys-25/His-159 io A reporter group delivery system with both absolute and selective specificity for thiol groups and an improved fluorescent probe containing the 7-nitrobenzo-2-oxa-1,3-diazole moiety Preparation of fully active ficin from Ficus glabrata by covalent chromatography and characterization of its active centre by using 2,2'-depyridyl disulphide as a reactivity probe A necessary modification to the preparation of papain from any high-quality latex of Carica papaya and evidence for the structural integrity of the enzyme produced by traditional methods Differences in the interaction of the catalytic groups of the active centres of actinidin and papain. Rapid purification of fully active actinidin by covalent chromatography and characterization of its active centre by use of two-protonic-state reac A spectrophotometric method for the detection of contaminant chymopapains in preparations of papain. Selective modification of one type of thiol group in the chymopapains by a two-protonic-state reagent Characterization of the papain active centre by using two-protonic-state electrophiles as reactivity probes. Evidence for nucleophilic reactivity in the un-interrupted cysteine-25-histidine-159 interactive system Quantitative proteomics strategy involving the selection of peptides containing both cysteine and histidine from tryptic digests of cell lysates Interaction Between Isolated Cytochrome c1 and Cytochrome c Affinity chromatography purification of cytochrome c binding enzymes Immobilization of enzymes to agar, agarose, and Sephadex supports Immobilization of enzymes on heterofunctional epoxy supports. Purification and characterization of Clostridium perfringens delta-toxin Specific covalent modification of thiols: Applications in the study of enzymes and other biomolecules Evaluation of benzofuroxan as a chromophoric oxidizing agent for thiol groups by using its reactions with papain, ficin, bromelain and low-molecular-weight thiols Proteomics based on selecting and quantifying cysteine containing peptides by covalent chromatography A convenient method of preparation of high-activity urease from Canavalia ensiformis by covalent chromatography and an investigation of its thiol groups with 2,2'-dipyridyl disulphide as a thiol titrant and reactivity probe The structural origins of the unusual specificities observed in the isolation of chymopapain M and actinidin by covalent chromatography and the lack of inhibition of chymopapain M by cystatin Chymopapain A. Purification and investigation by covalent chromatography and characterization by two-protonic-state reactivity-probe kinetics, steady-state kinetics and resonance Raman spectroscopy of some dithioacyl derivatives Resolution of protein disulphide-isomerase and glutathione-insulin transhydrogenase activities by covalent chromatography Purification and characterization of a Bacillus megaterium disulfide reductase specific for disulfides containing pantethine 4',4"-diphosphate. Evidence that binding to the s2-subsite of papain may be coupled with catalytically relevant structural change involving the cysteine-25-histidine-159 diad. Kinetics of the reaction of papain with a two-protonic-state reactivity probe containing a h Comparison of low- and high-pressure affinity chromatography for the purification of serine and sulfhydryl esterases Immobilized bovine lactose synthase A method of topographical analysis of the active site Resolution of thiol-containing proteins by sequential-elution covalent chromatography Purification of papain by affinity chromatography Immobilization of proteins as a tool for studying primary structure around their cysteinyl residues. Resolution of sulphydryl oxidase from γ-glutamyltransferase in bovine milk by covalent chromatography on cysteinylsuccinamidopropyl-glass A high-yield method to extract peptides from rat brain tissue
is cites work of	wds:Q36291031-DF0AB119-B1FD-4E40-B190-291C64028341 wds:Q39125159-E3494885-BB15-43A0-BEA7-367CC15108F3

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