Sandbox PgpWWC

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==P-glycoprotein==
==P-glycoprotein==
<StructureSection load='4m1m' size='340' side='right' caption='P-glycoprotein: Both domains at 3.5 Å resolution ' scene=''>
<StructureSection load='4m1m' size='340' side='right' caption='P-glycoprotein: Both domains at 3.5 Å resolution ' scene=''>
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'''P-glycoprotein (P-gp, ABCB1)''' is an ATP casette transporter that hydrolyses ATP for conformational changes after a variety of substrates are transported. It is one of the membrane proteins responsible for the multi drug resistance (MDR) in cancer treatment, as well as various other drug therapies (Aller et. al 2009; He and Liu 2002). P-gp can be found in tumor cells, as well as in the liver, kidney, adrenal gland, intestine, blood-brain barrier (BBB), placenta, blood-testis barrier, and blood-ovarian barriers. An effective MDR transport protein, the high amount of active Pgp substrates stems from the polyspecificity for hydrophobic and aromatic compounds (Marchetti, Mazzanti, Beijnen, & Schellens 2007).
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P-glycoprotein (P-gp, ABCB1) is one of the membrane proteins responsible for the MDR in cancer treatment, as well as various other drug therapies beyond cancer (Aller et. al 2009; He and Liu 2002). P-gp can be found in tumor cells, as well as in the liver, kidney, adrenal gland, intestine, blood-brain barrier (BBB), placenta, blood-testis barrier, and blood-ovarian barriers. P-gp is an effective MDR transport protein because of the high amount of active substrates stemming from the polyspecificity for hydrophobic and aromatic compounds (Marchetti, Mazzanti, Beijnen, & Schellens 2007).
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== Function ==
== Function ==

Revision as of 15:14, 9 April 2015

P-glycoprotein

P-glycoprotein: Both domains at 3.5 Å resolution

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References

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