Ampicillin

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<StructureSection load='' size='340' side='right' caption='Caption for this structure' scene=''>
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<StructureSection load='' size='340' side='right' caption='Ampicillin' scene='10/1040157/Cv/1'>
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Ampicillin is an antibiotic belonging to the aminopenicillin class of the penicillin family. The drug is used to prevent and treat a number of bacterial infections, such as respiratory tract infections, urinary tract infections, meningitis, salmonellosis, and endocarditis. It may also be used to prevent group B streptococcal infection in newborns.<ref name="a7">[https://www.drugs.com/monograph/ampicillin.html "Ampicillin".] The American Society of Health-System Pharmacists. Archived from the original on 12 July 2015. Retrieved 1 August 2015.</ref>
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'''Ampicillin''' is an antibiotic belonging to the aminopenicillin class of the penicillin family. The drug is used to prevent and treat a number of bacterial infections, such as respiratory tract infections, urinary tract infections, meningitis, salmonellosis, and endocarditis. It may also be used to prevent group B streptococcal infection in newborns.<ref name="a7">[https://www.drugs.com/monograph/ampicillin.html "Ampicillin".] The American Society of Health-System Pharmacists. Archived from the original on 12 July 2015. Retrieved 1 August 2015.</ref> See also [https://en.wikipedia.org/wiki/Ampicillin Ampicillin].
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Ampicillin is in the penicillin group of beta-lactam antibiotics and is part of the aminopenicillin family. It is roughly equivalent to amoxicillin in terms of activity.<ref name="a7">[https://www.drugs.com/monograph/ampicillin.html "Ampicillin".] The American Society of Health-System Pharmacists. Archived from the original on 12 July 2015. Retrieved 1 August 2015.</ref> Ampicillin is able to penetrate gram-positive and some gram-negative bacteria. It differs from penicillin G, or benzylpenicillin, only by the presence of an amino group. This amino group, present on both ampicillin and amoxicillin, helps these antibiotics pass through the pores of the outer membrane of gram-negative bacteria, such as E. coli, Proteus mirabilis, Salmonella enterica, and Shigella.<ref name="a19">Hauser AR (2012). Antibiotic Basics for Clinicians: The ABCs of Choosing the Right Antibacterial Agent. Lippincott Williams & Wilkins. pp. 25–28. ISBN 978-1-4511-1221-4.</ref>
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''E. coli'' PBP structure shows a distinct <scene name='47/478544/Cv/5'>3 domain structures</scene> ([[2ex6]]). The <scene name='47/478544/Cv/6'>active site</scene> contains the <scene name='47/478544/Cv/7'>covalently bond between Ser62 and antibiotic ampicillin</scene><ref>PMID:16411754</ref>. Water molecules are shown as red spheres.
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== References ==
== References ==
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Current revision

Ampicillin

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References

  1. 1.0 1.1 "Ampicillin". The American Society of Health-System Pharmacists. Archived from the original on 12 July 2015. Retrieved 1 August 2015.
  2. Hauser AR (2012). Antibiotic Basics for Clinicians: The ABCs of Choosing the Right Antibacterial Agent. Lippincott Williams & Wilkins. pp. 25–28. ISBN 978-1-4511-1221-4.
  3. Kishida H, Unzai S, Roper DI, Lloyd A, Park SY, Tame JR. Crystal structure of penicillin binding protein 4 (dacB) from Escherichia coli, both in the native form and covalently linked to various antibiotics. Biochemistry. 2006 Jan 24;45(3):783-92. PMID:16411754 doi:10.1021/bi051533t

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