Invanz Sandbox

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== Function ==
== Function ==
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Invanz is used to treat a range of bacterial infections caused by Gram positive and Gram negative bacteria as well as a range of both aerobic and anaerobic bacteria. Invanz works by inhibiting cell wall synthesis via binding to penicillin binding proteins (PBPs). Invanz is stable against hydrolysis from many beta-lactamases including penicillinases and cephalosporinases, but is unstable against metallo-beta-lactamases <ref name="merck" />. Beta-lactamases are secreted by bacteria to provide resistance to antibiotics; however, Invanz is relatively unaffected by these beta-lactamases and thus is an effective treatment for various bacterial infections <ref>PMID: 25561890</ref>. Beta-lactamases work by attacking and cleaving the beta-lactam ring of antibiotics before the antibiotic reaches its target such as the penicilling binding proteins <ref>PMID: 25485972</ref>. The unique structural features of Invanz equip this drug with some of the widest spectrum and most potent antimicrobial activity of carbapenem antibiotics today <ref>PMID: 12951340</ref>.
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Invanz is used to treat a range of bacterial infections caused by Gram positive and Gram negative bacteria as well as a range of both aerobic and anaerobic bacteria. Invanz works by inhibiting cell wall synthesis via binding to penicillin binding proteins (PBPs). Invanz is stable against hydrolysis from many beta-lactamases including penicillinases and cephalosporinases, but is unstable against metallo-beta-lactamases <ref name="merck" />. Beta-lactamases are secreted by bacteria to provide resistance to antibiotics; however, Invanz is relatively unaffected by these beta-lactamases and thus is an effective treatment for various bacterial infections <ref>PMID: 25561890</ref>. The unique structural features of Invanz equip this drug with some of the widest spectrum and most potent antimicrobial activity of carbapenem antibiotics today <ref>PMID: 12951340</ref>.
== Structural highlights ==
== Structural highlights ==
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Invanz is a carbapenem which is a beta-lactam antibiotic (contains a beta lactam ring) that has antimicrobial action via inhibition of cell wall synthesis. This class of antibiotics is known for its broad spectrum of activity, and its structure allows it to bind penicillin binding proteins (PBPs) to inhibit bacterial cell wall synthesis in a variety of bacterial types <ref>PMID: 17488146</ref><ref name="Invanz1">...</ref>. Some Invanz inhibiting proteins include <scene name='74/746003/4qu3/1'>4QU3</scene>, <scene name='74/746003/3zgp/1'>3ZGP</scene>, <scene name='74/746003/3m6b/1'>3M6B</scene> , and <scene name='74/746003/3m6h/1'>3M6H</scene>. REF Antibiotic resistance to carbapenems largely results from ability of the bacterial species to secrete beta-lactamase enzymes that can degrade the antimicrobial. Invanz has resistance to many beta-lactamases since it has a trans-1-hydroxyethyl group that confers resistance of the antibiotic to degradation by most beta-lactamases <ref>PMID: 15150178 </ref> <ref name="hammond">...</ref>. The beta lactam ring is a four-membered, nitrogen-containing ring that binds to PBPs, thus making them unable to continue bacterial cell wall synthesis. PBPs are enzymes found in the cell membrane that aid in cross-linking of peptidoglycan during cell wall synthesis <ref>PMID: 18266856</ref>. By inactivating PBPs and inhibiting cell wall synthesis, bacterial cell death will occur as the cells lyse due to osmotic pressure <ref>Page, M.L. The mechanisms of reactions of beta lactam antibiotics. Accounts of Chemical Research, 1984, 17(4), 144-151 DOI: 10.1021/ar00100a005</ref>.
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Invanz is a carbapenem which is a beta-lactam antibiotic (contains a beta lactam ring) that has antimicrobial action via inhibition of cell wall synthesis. This class of antibiotics is known for its broad spectrum of activity, and its structure allows it to bind penicillin binding proteins (PBPs) to inhibit bacterial cell wall synthesis in a variety of bacterial types <ref>PMID: 17488146</ref><ref name="Invanz1">...</ref>. Antibiotic resistance to carbapenems largely results from ability of the bacterial species to secrete beta-lactamase enzymes that prevent the antimicrobial from accomplishing its job. Beta-lactamases work by attacking and cleaving the beta-lactam ring of antibiotics before the antibiotic reaches its target such as the penicilling binding proteins <ref>PMID: 25485972</ref>. Invanz has resistance to many beta-lactamases since it has a trans-1-hydroxyethyl group that confers resistance of the antibiotic to degradation by most beta-lactamases <ref>PMID: 15150178 </ref> <ref name="hammond">...</ref>. The beta lactam ring is a four-membered, nitrogen-containing ring that binds to PBPs, thus making them unable to continue bacterial cell wall synthesis. PBPs are enzymes found in the cell membrane that aid in cross-linking of peptidoglycan during cell wall synthesis <ref>PMID: 18266856</ref>. By inactivating PBPs and inhibiting cell wall synthesis, bacterial cell death will occur as the cells lyse due to osmotic pressure <ref>Page, M.L. The mechanisms of reactions of beta lactam antibiotics. Accounts of Chemical Research, 1984, 17(4), 144-151 DOI: 10.1021/ar00100a005</ref>. Some Invanz inhibiting proteins include <scene name='74/746003/4qu3/1'>4QU3</scene>, <scene name='74/746003/3zgp/1'>3ZGP</scene>, <scene name='74/746003/3m6b/1'>3M6B</scene> , and <scene name='74/746003/3m6h/1'>3M6H</scene>.

Revision as of 23:44, 4 December 2016

Invanz (Ertapenem) is a 1-beta-methyl carbapenem antibiotic that is designed to treat multi drug resistant bacterial infections such as intra-abdominal infections, skin and skin suture infections, community-acquired pneumonia, complicated urinary tract infections including pyelonephritis, acute pelvic infections, and can be used as a prophylactic measure prior to colorectal surgery. Invanz is an injectable antibiotic that can be administered intramuscularly [1][2].

Beta-lactamase Ges-2 Acyl Enzyme Complex(PDB code 4QU3)

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Proteopedia Page Contributors and Editors (what is this?)

Courtney Stout, Madeline Henwood, Swokiya Bhandari.

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