Alamethicin
WikiDoc Resources for Alamethicin |
Articles |
---|
Most recent articles on Alamethicin Most cited articles on Alamethicin |
Media |
Powerpoint slides on Alamethicin |
Evidence Based Medicine |
Clinical Trials |
Ongoing Trials on Alamethicin at Clinical Trials.gov Clinical Trials on Alamethicin at Google
|
Guidelines / Policies / Govt |
US National Guidelines Clearinghouse on Alamethicin
|
Books |
News |
Commentary |
Definitions |
Patient Resources / Community |
Patient resources on Alamethicin Discussion groups on Alamethicin Patient Handouts on Alamethicin Directions to Hospitals Treating Alamethicin Risk calculators and risk factors for Alamethicin
|
Healthcare Provider Resources |
Causes & Risk Factors for Alamethicin |
Continuing Medical Education (CME) |
International |
|
Business |
Experimental / Informatics |
Please Take Over This Page and Apply to be Editor-In-Chief for this topic: There can be one or more than one Editor-In-Chief. You may also apply to be an Associate Editor-In-Chief of one of the subtopics below. Please mail us [1] to indicate your interest in serving either as an Editor-In-Chief of the entire topic or as an Associate Editor-In-Chief for a subtopic. Please be sure to attach your CV and or biographical sketch.
Alamethicin is a peptide antibiotic, produced by the fungus Trichoderma viride. It contains the non-proteinogenic amino acid 2-aminoisobutyric acid (Aib), which strongly induces helical peptide structures. The peptide sequence is:
Ac-Aib-Pro-Aib-Ala-Aib-Ala-Gln-Aib-Val-Aib-Gly-Leu-Aib-Pro-Val-Aib-Aib-Glu-Gln-Phl
(Ac = acetyl, Phl = phenylalaninol)
- Molecular Formula: C92H150N22O25
- CAS number: 27061-78-5
- Appearance: Off white solid
- UV spectrum maxima: 265, 257
- Melting point: 255°C-270°C
- Solubility information: DMSO, Methanol, Ethanol. Not soluble in water
In cell membranes, it forms voltage-dependent ion channels by aggregation of four to six molecules.
data copied from Fermentek Alamethicin product page