Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/4675
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dc.contributor.advisorDAS, ALOKEen_US
dc.contributor.authorR.S., KAARTHIKen_US
dc.date.accessioned2020-06-11T10:02:27Z
dc.date.available2020-06-11T10:02:27Z
dc.date.issued2020-05en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/4675-
dc.description.abstractStructure-function relationship found in protein helps us to understand the function that a protein is capable of by knowing its structure. Following the secondary structure of a small peptide will give more information on the structure of the protein, which can be used to understand the functions of the protein in detail. Apart from covalent bonds, these secondary structures are shaped by non-covalent interactions like hydrogen bonds, hydrophobic interactions, and n→π* interactions. Though these non-covalent interactions are individually weak, many such interactions cumulatively contribute to stabilising the conformation of a peptide. Gas-phase studies on small peptides are carried out to study such non-covalent interactions that are supporting the peptides when there is no effect from the solvent medium or any other nearby molecules.en_US
dc.language.isoenen_US
dc.subjectPeptidesen_US
dc.subjectDouble resonance spectroscopyen_US
dc.subjectAmino acidsen_US
dc.subjectQuantum chemistryen_US
dc.subjectUltraviolet lasersen_US
dc.subject2020en_US
dc.titleConformational study of small peptides using spectroscopy and quantum chemistry calculationsen_US
dc.typeThesisen_US
dc.type.degreeBS-MSen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.contributor.registration20151014en_US
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