Sandbox Reserved 425

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(Introduction)
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==Introduction==
==Introduction==
<Structure load='4OTI' applet size='[450,338]' frame='true' align='right' caption='pdbcode, short caption for Molecular Playground here' scene='Insert optional scene name here' />
<Structure load='4OTI' applet size='[450,338]' frame='true' align='right' caption='pdbcode, short caption for Molecular Playground here' scene='Insert optional scene name here' />
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Protein kinase C, an enzyme that is activated by the receptor-mediated hydrolysis of inositol phospholipids, relays information in the form of a variety of extracellular signals across the membrane to regulate many Ca2+-dependent processes. At an early phase of cellular responses, the enzyme appears to have a dual effect, providing positive forward as well as negative feedback controls over various steps of its own and other signaling pathways, such as the receptors that are coupled to inositol phospholipid hydrolysis and those of some growth factors. In biological systems, a positive signal is frequently followed by immediate negative feedback regulation. Such a novel role of this <scene name='48/483882/4oti/1'>protein kinase</scene> system seems to give a logical basis for clarifying the biochemical mechanism of signal transduction, and to add a new dimension essential to our understanding of cell-to-cell communication.</scene> of the protein.
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Protein kinase C, an enzyme that is activated by the receptor-mediated hydrolysis of inositol phospholipids, relays information in the form of a variety of extracellular signals across the membrane to regulate many Ca2+-dependent processes. At an early phase of cellular responses, the enzyme appears to have a dual effect, providing positive forward as well as negative feedback controls over various steps of its own and other signaling pathways, such as the receptors that are coupled to inositol phospholipid hydrolysis and those of some growth factors. In biological systems, a positive signal is frequently followed by immediate negative feedback regulation. Such a novel role of this <scene name='48/483882/4oti/1'>protein kinase</scene> system seems to give a logical basis for clarifying the biochemical mechanism of signal transduction, and to add a new dimension essential to our understanding of cell-to-cell communication of the protein.
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==Overall Structure==
==Overall Structure==

Revision as of 18:05, 6 March 2015


This Sandbox is Reserved from January 19, 2016, through August 31, 2016 for use for Proteopedia Team Projects by the class Chemistry 423 Biochemistry for Chemists taught by Lynmarie K Thompson at University of Massachusetts Amherst, USA. This reservation includes Sandbox Reserved 425 through Sandbox Reserved 439.


'Protein kinase C related kinase/Tofacitinib (prostrate and ovarian cancer)-4OTI'

Contents

Introduction

pdbcode, short caption for Molecular Playground here

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Protein kinase C, an enzyme that is activated by the receptor-mediated hydrolysis of inositol phospholipids, relays information in the form of a variety of extracellular signals across the membrane to regulate many Ca2+-dependent processes. At an early phase of cellular responses, the enzyme appears to have a dual effect, providing positive forward as well as negative feedback controls over various steps of its own and other signaling pathways, such as the receptors that are coupled to inositol phospholipid hydrolysis and those of some growth factors. In biological systems, a positive signal is frequently followed by immediate negative feedback regulation. Such a novel role of this system seems to give a logical basis for clarifying the biochemical mechanism of signal transduction, and to add a new dimension essential to our understanding of cell-to-cell communication of the protein.



















Overall Structure

pdbcode, insert caption here

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Binding Interactions

pdbcode, Insert caption here

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Additional Features

pdbcode, Insert caption here

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Quiz Question 1

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Quiz Question 2

pdbcode, Insert caption here

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See Also

Credits

Introduction - name of team member

Overall Structure - name of team member

Drug Binding Site - name of team member

Additional Features - name of team member

Quiz Question 1 - name of team member

Quiz Question 2 - name of team member

References

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