About: Synthesis and study of normal, enantio, retro, and retroenantio isomers of cecropin A-melittin hybrids, their end group effects and selective enzyme inactivation

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About: Synthesis and study of normal, enantio, retro, and retroenantio isomers of cecropin A-melittin hybrids, their end group effects and selective enzyme inactivation Goto Sponge NotDistinct Permalink

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scientific article published on 01 January 1998

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в січні 1998 (uk) articolo scientifico (pubblicato il 1998) (it) im Januar 1998 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu en xineru de 1998 (ast) scientific article published on 01 January 1998 (en) artikull shkencor i botuar më 01 janar 1998 (sq)
publication date	wds:Q74293368-FF20CB86-1F0B-41EE-9DE8-197B46F26357
publication date	1998-01-01 00:00:00Z (xsd:dateTime)
author name string	wds:Q74293368-03E65FE6-BFE9-4C84-B5AC-5EFE2243E88C wds:Q74293368-0E8DD82E-BAB1-420C-9BDF-E67C5529EB25 wds:Q74293368-D40C5528-C3F1-4880-A7DE-E7C03C21E65E wds:Q74293368-E1DF7B85-38EC-4AAF-9749-66CB0FF0A9E0
author name string	R B Merrifield S Vunnam P Juvvadi K S Rotondi
rdfs:label	Synthesis and study of normal, enantio, retro, and retroenantio isomers of cecropin A-melittin hybrids, their end group effects and selective enzyme inactivation (en) Synthesis and study of normal, enantio, retro, and retroenantio isomers of cecropin A-melittin hybrids, their end group effects and selective enzyme inactivation (nl) Synthesis and study of normal, enantio, retro, and retroenantio isomers of cecropin A-melittin hybrids, their end group effects and selective enzyme inactivation (sq)
skos:prefLabel	Synthesis and study of normal, enantio, retro, and retroenantio isomers of cecropin A-melittin hybrids, their end group effects and selective enzyme inactivation (en) Synthesis and study of normal, enantio, retro, and retroenantio isomers of cecropin A-melittin hybrids, their end group effects and selective enzyme inactivation (nl) Synthesis and study of normal, enantio, retro, and retroenantio isomers of cecropin A-melittin hybrids, their end group effects and selective enzyme inactivation (sq)
name	Synthesis and study of normal, enantio, retro, and retroenantio isomers of cecropin A-melittin hybrids, their end group effects and selective enzyme inactivation (en) Synthesis and study of normal, enantio, retro, and retroenantio isomers of cecropin A-melittin hybrids, their end group effects and selective enzyme inactivation (nl) Synthesis and study of normal, enantio, retro, and retroenantio isomers of cecropin A-melittin hybrids, their end group effects and selective enzyme inactivation (sq)
title	wds:Q74293368-1C78B998-47DA-4742-9A4C-24063E472945
title	Synthesis and study of normal, enantio, retro, and retroenantio isomers of cecropin A-melittin hybrids, their end group effects and selective enzyme inactivation (en)
page(s)	wds:Q74293368-ADA0046D-93CA-4AF8-AB1D-1F11A2516476
page(s)	38-44
instance of	wds:Q74293368-DA47A809-62B9-4BA1-85AB-0F05AC86990B
instance of	scholarly article
PubMed ID	wds:Q74293368-4EC39C03-AEDC-4EAE-909F-CA4B13170A00
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/9495589
PubMed ID	9495589
published in	wds:Q74293368-13FDA42E-22FA-4159-8E74-3D7CB49449D1
published in	Chemical Biology and Drug Design
issue	wds:Q74293368-CBF1FD1F-1470-4C54-A96C-9E5A1F634849
volume	wds:Q74293368-C792FB8D-4EBC-424D-8C4B-929E96FD0CF7
issue	1
volume	51
DOI	wds:Q74293368-49AC4257-B70F-4C74-AD20-F20686A94903
DOI	http://dx.doi.org/10.1111/J.1399-3011.1998.TB00414.X
DOI	10.1111/J.1399-3011.1998.TB00414.X
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q74293368
is cites work of	Alpha-helical cationic antimicrobial peptides: relationships of structure and function The interactions of histidine-containing amphipathic helical peptide antibiotics with lipid bilayers. The effects of charges and pH Structure-function studies on the cyclic peptide MT-II, lactam derivative of alpha-melanotropin Conformational Fine-Tuning of Pore-Forming Peptide Potency and Selectivity. Effect of α,α-Dialkyl Amino Acids on the Protease Resistance of Peptides Plasticity in structure and interactions is critical for the action of indolicidin, an antibacterial peptide of innate immune origin
is cites work of	wds:Q73041195-BB4CB788-D13E-4B88-8D23-C06A59451B4A wds:Q36639362-2E50B6AE-C0FC-498D-A91F-6336A7B9A638 wds:Q37825833-EBC2CFDA-0F87-481A-9702-7CFE25BB1933 wds:Q78125324-04F66485-92AB-475B-A83C-6C2B2B6C8A33 wds:Q35859779-EA637EDA-1FA8-462C-BEAC-5167FA46CE63 wds:Q44637113-31421BD8-3C65-4C8B-B696-C1FC16EC4789

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