About: New enzymes and methods for chemoenzymatic synthesis of bioactive glycosides

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An Entity of Type : http://linked.opendata.cz/ontology/domain/vavai/Projekt, within Data Space : linked.opendata.cz associated with source document(s)

Attributes	Values
rdf:type	http://linked.opendata.cz/ontology/domain/vavai/Projekt
rdfs:seeAlso	http://www.isvav.cz/projectDetail.do?rowId=GA203/01/1018
Description	Novel methods for enzymatic synthesis of bioactive glycosides based on aminosugars will be developed. New reaction conditions will be tested in enzymatic glycosylation to improve effectiveness of these reactions. New enzymes for synthesis of oligoglycosi (en) Budou vyvinuty nové postupy enzymové synthesy biologicky aktivních aminocukrů. Pro zlepšení účinnosti těchto reakcí budou vyzkoušeny nové reakční podmínky. Nové enzymy pro tyto synthesy budou systematicky vyhledávány a testovány, půjde především o dosud
Title	New enzymes and methods for chemoenzymatic synthesis of bioactive glycosides (en) Nové enzymy a metodiky pro chemoenzymatickou syntézu bioaktivních glykosidů
skos:notation	GA203/01/1018
http://linked.open...avai/cep/aktivita	Standard projects
http://linked.open...kovaStatniPodpora	http://linked.opendata.cz/resource/domain/vavai/projekt/GA203%2F01%2F1018/celkovaStatniPodpora
http://linked.open...ep/celkoveNaklady	http://linked.opendata.cz/resource/domain/vavai/projekt/GA203%2F01%2F1018/celkoveNaklady
http://linked.open...datumDodatniDoRIV	2008-05-30 (xsd:date)
http://linked.open...i/cep/druhSouteze	VS - Veřejná soutěž ve výzkumu a vývoji
http://linked.open...ep/duvernostUdaju	S - Úplné a pravdivé údaje nepodléhající ochraně podle zvláštních právních předpisů
http://linked.open.../cep/fazeProjektu	1222772
http://linked.open...ai/cep/hlavniObor	CE - Biochemie
http://linked.open...hodnoceniProjektu	V - Vynikající výsledky (s mezinárodním významem apod.). Zároveň byly splněny cíle a předpokládané výsledky uvedené ve smlouvě / rozhodnutí o poskytnutí podpory.
http://linked.open.../cep/klicovaSlova	Neuvedeno. (en)
http://linked.open...ep/partnetrHlavni	Mikrobiologický ústav AV ČR, v.v.i.
http://linked.open...inujicichPrijemcu	0 (xsd:int)
http://linked.open...cep/pocetPrijemcu	1 (xsd:int)
http://linked.open...ocetSpoluPrijemcu	2 (xsd:int)
http://linked.open.../pocetVysledkuRIV	33 (xsd:int)
http://linked.open...enychVysledkuVRIV	33 (xsd:int)
http://linked.open...iciPoslednihoRoku	2004
http://linked.open...atUdajeProjZameru	2004
http://linked.open.../vavai/cep/soutez	SGA02002GA-ST
http://linked.open...usZobrazovaneFaze	DUU
http://linked.open...ai/cep/typPojektu	P - Projekt výzkumu a vývoje financovaný ze státního rozpočtu
http://linked.open.../cep/vedlejsiObor	CC - Organická chemie EE - Mikrobiologie, virologie
http://linked.open...jektu+dodavatelem	Odborný přínos projektu vyplývá z doložené publikační aktivity řešitelů. Ve zprávě je uvedeno 12 publikovaných původních sdělení a 4 práce přijaté k publikaci. Výsledkem řešení projektu je popis některých enzymových reakcí. Získané poznatky byly využity (cs)
http://linked.open...tniCyklusProjektu	ZBKU
is http://linked.open...vavai/riv/projekt of	Hydrolytic and transglycosylation ractions of N-acyl modified substrates catalysed by Beta-N-acetylhexosaminidases. Enzymatic glycosylation of lincomycin. Exploitation of a Library of alfa-Galactosidases for the Sysnthesis of Building Blocks for Glycopolymers. The isoforms of rat natural killer cell receptor NKR-P1 display a distinct binding of complex saccharide ligands The isoforms of rat natural killer cell receptor NKR-P1 display a distinct binding of complex syccharide ligands Fungal beta-N-acetylhexosaminidases with high beta-N-acetylgalactosaminidase activity and their use for synthesis of beta-GalNAc-containing oligosaccharides. Enzymatic Discrimination of 2-Acetamido-2-deoxy-D-mannopyranose-Containing Disaccharides Using Beta-N-Acetylhexosaminedases. Enzymatic synthesis of N-acetylglucosaminobioses by reverse hydrolysis: Characterisation and application of the library of fungal -N-acetylhexosaminidases Fluorescent Labelled Thiourea-Bridged Glycodendrons Fluorescent Labelled Thiourea-Bridged Glycodendrons A concise synthesis of 4-nitrophenyl 2-azido-2-deoxy- and 2-acetamido-2-deoxy-D-mannopyranosides Toward an optimal oligosaccharide ligand for rat natural killer cell activation receptor NKR-P1 Toward on optimal oligasaccharide ligand for rat natural killer cell activation receptor NKR-P1. Activation carbohydrate receptors of natural killer lymphocytes: from genes and proteins to ligands and therapies Activation carbohydrate receptors of natural killer lymphocytes Determination of glycoclusters in the complex matrixes by HPAEC-PAD Design, functional evaluation and biomedical applications of carbohydrate dendrimers (glycodendrimers). Chemistry and mass spectrometry applied to protein microidentification Exploitation of a Library of alfa-Galactosidases for the Synthesis of Building Blocks for Glycopolymers. Interaction of CD69, the earliest activation antigen of lymphocytes, with calcium and saccharides in three dimensions p-Nitrofenyl-azidodeoxy-D-hexopyranosidy ß-N-Acetylhexosaminidase-catalysed synthesis of non-reducing oligosaccharides Molecular Xharacterization of Binding of Calcium and Carbohydrates by an Early Activation Antigen of Lymphocytes CD69. Synthesis of chitooligomer-based glycoconjugates and their binding to the rat natural killer cell activation receptor NKR-P1. Application of selectively acylated glycosides for the -D-galactosidase-catalysed synthesis of disaccharides Branched N-acetylglucosamine-terminated oligosaccharides are high-affinity ligands for CD69 antigen that may be important for the recognition of stressed cells. Application of Selectively Acylated Glycosides for the alfa-Galactosidase-Catalyzed Synthesis of Disaccharides. High affinity ligands for human lymphocyte receptor CD69. Protein chemistry and mass spectrometry in structural analysis of large proteins. Protein chimistry and massspectromtry in strictural analysis of large proteins. Synthesis of 4-nitrophenyl 2-acetamido-2-deoxy-beta-D-mannopyranoside and 4-nitrophenyl 2-acetamido-2-deoxy-alfa-D-mannopyranoside. Beta-N-Acetylhexosaminidase-catalysed synthesis of non-reducing oligosaccharides Regioselective enzymatic acylation ofN-acetylhexosamines
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