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3-d Structure Configuration & Conformation

Date post: 08-Apr-2018
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    Subho Brato Mukherjee

    MSc Applied Genetics

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    CONTENTS-y BRIEF INTRODUCTION OF BIOMOLECULES

    y 3-D STRUCTURES

    y CONFIGURATION

    y CONFORMATION

    y BIBLIOGRAPHY

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    BIOMOLECULES

    y

    The chemistry of living organisms isorganized around CARBON.

    CARBON CANFORM SINGLE

    BOND

    WITHHYDROGEN

    WITHANOTHERCARBONATOM

    CARBON CANFORM DOUBLE

    BOND

    WITH

    OXYGEN

    WITHANOTHERCARBONATOM

    CARBON CANFORM TRIPLE

    BOND

    WITH

    NITROGEN

    WITHANOTHERCARBONATOM

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    Functional Groups determine

    chemical propertiesMost biomolecules can be regarded as derivatives

    of hydrocarbons, compounds with a covalentlylinked Carbon backbone to which only Hydrogen

    atoms are bonded.

    The Hydrogen atoms may be replaced by a varietyof functional groups to yield different families oforganic compounds.

    The chemical personality of a compound can bedetermined by the chemistry of its functionalgroups and their disposition in 3 dimensional space.

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    EXAMPLES OF FUNCTIONAL

    GROUPS

    CARBOXYGROUP

    CARBONYLGROUP

    AMINOGROUPS

    HYDROXYLGROUP

    ALCOHOLS AMINES

    CARBOXYLIC

    ACIDS

    ALDEHYDES

    &

    KETONES

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    3 d structure- configuration &

    conformationCompounds of Carbon commonly exist as

    STEREOISOMERS, different molecules in which

    the order of bonding is the same, but thespatial relationship among the atoms isdifferent.

    Molecular interactions between biomoleculesare invariably STEREOSPECIFIC; that is, theyrequire specific stereochemistry in theinteracting molecules.

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    CONFIGURATION-Molecule is changed only by

    breaking a bond

    It refers to the fixed spatial arrangement ofatoms-Double bonds & Chiral centres

    It refers to interconversion by temporarybreaking of one or more covalent bonds.

    H H HOOC HC=C C=C

    HOOC COOH H COOH

    Maleic Acid (cis) Fumaric Acid (trans)

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    Stereoisomers

    CHIRALCARBON

    DIASTEREOMER

    S

    ENANTI-OMER

    RACEMIC

    MIXTURE

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    Biological interactions

    RSSYSTEM

    R(Rectus)-

    Clockwise

    S (Sinister)-

    Anticlockwise

    DLSYSTEM

    DextroRotatory

    LaevoRotatory

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    CONFORMATION

    o It refers to the Spatial Arrangement ofsubstituent groups , without breaking anybonds.

    o The 2 main types are-

    o Freely interconvertible-not possible to isolate.

    More stable (predominates)Staggered

    Less stable (less predominan e)E lipsed

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    BIBLIOGRAPHY

    Google.co.in----thebiggest search engine.

    Satyanarayan panikar

    Leninger Principles of

    Biochemistry byNelson & Cox.

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    THANK YOU !!

    For paying attention..

    - SUBHO


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