Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/6579
Title: <smarttagtype namespaceuri="urn:schemas-microsoft-com:office:smarttags" name="State"><smarttagtype namespaceuri="urn:schemas-microsoft-com:office:smarttags" name="place"> Synthesis of a modified peptide fragment analog Val-Tyr (<i>P</i>)-Val-Ala-Ala-OH of cAMP protein kinase regulatory sub unit type II employing Fmoc chemistry </smarttagtype></smarttagtype>
Authors: Devaraju, Kuramkote Shivanna
Patil, Basanagoud S
Tantry, Subramanyam J
Babu, S V Suresh
Shetty K, Taranath
Babu, Vommina V Suresh
Keywords: Phosphorylation
cAMP protein kinase
phosphatases
Fmoc-chemistry
bis-TMS method
Issue Date: Jul-2006
Publisher: CSIR
Series/Report no.: <b>Int.Cl.<sup>8 </sup>C07D</b>
Abstract: The synthesis of new peptide fragment analog (Val-Tyr(<i>P</i>)-Val-Ala-Ala-OH) incorporating Tyr into the phosphorylation site of the cAMP protein kinase regulatory sub unit type II in place of Ser (Val-Ser(<i>P</i>)-Val-Ala-Ala-OH) has been described. The phosphopentapeptide fragment is prepared by Fmoc chemistry employing the global phosphorylation method. The yield (68%) as well as purity of the final peptide is satisfactory. The peptide is fully characterized by HPLC, NMR and mass spectral data.
Description: 1747-1752
URI: http://hdl.handle.net/123456789/6579
ISSN: 0975-0983(Online); 0376-4699(Print)
Appears in Collections:IJC-B Vol.45B(07) [July 2006]

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