Potent inhibitors of beta-tryptase and human leukocyte elastase based on the MCoTI-II scaffold.
about
Cyclic Peptides Arising by Evolutionary Parallelism via Asparaginyl-Endopeptidase-Mediated BiosynthesisIn Vivo Activation of the p53 Tumor Suppressor Pathway by an Engineered CyclotideStructural Insights into the Role of the Cyclic Backbone in a Squash Trypsin InhibitorOxytocic plant cyclotides as templates for peptide G protein-coupled receptor ligand designSemienzymatic Cyclization of Disulfide-rich Peptides Using Sortase ATransforming conotoxins into cyclotides: Backbone cyclization of P-superfamily conotoxinsComputational Design of Hypothetical New Peptides Based on a Cyclotide Scaffold as HIV gp120 InhibitorJuggling jobs: roles and mechanisms of multifunctional protease inhibitors in plants.Reversible and noncompetitive inhibition of beta-tryptase by protein surface binding of tetravalent peptide ligands identified from a combinatorial split-mix library.Cytotoxic potency of small macrocyclic knot proteins: structure-activity and mechanistic studies of native and chemically modified cyclotides.Identification and characterization of a new family of cell-penetrating peptides: cyclic cell-penetrating peptides.Polycyclic peptide therapeutics.Dynamic scenario of membrane binding process of kalata b1Neutrophil elastase inhibitors.The evolution of Momordica cyclic peptides.Inhibition of Human Prolyl Oligopeptidase Activity by the Cyclotide Psysol 2 Isolated from Psychotria solitudinum.Review seed biopharmaceutical cyclic peptides: From discovery to applications.Host-defense activities of cyclotides.Biological activities of natural and engineered cyclotides, a novel molecular scaffold for peptide-based therapeutics.Cyclotides, a novel ultrastable polypeptide scaffold for drug discoveryUterotonic plants and their bioactive constituentsCyclic thrombospondin-1 mimetics: grafting of a thrombospondin sequence into circular disulfide-rich frameworks to inhibit endothelial cell migration.Design of a novel cyclotide-based CXCR4 antagonist with anti-human immunodeficiency virus (HIV)-1 activity.Cyclotides insert into lipid bilayers to form membrane pores and destabilize the membrane through hydrophobic and phosphoethanolamine-specific interactionsChemical and biological production of cyclotides.Molecular grafting onto a stable framework yields novel cyclic peptides for the treatment of multiple sclerosis.Plant antimicrobial peptides.Protein scaffold-based molecular probes for cancer molecular imaging.Engineered cystine-knot miniproteins for diagnostic applications.Cyclotides as a basis for drug design.Joseph Rudinger memorial lecture: discovery and applications of cyclotides.Cyclotides as grafting frameworks for protein engineering and drug design applications.Cystine-knot peptides: emerging tools for cancer imaging and therapy.Cyclotides: a natural combinatorial peptide library or a bioactive sequence player?Neutrophil elastase inhibitors: a patent review and potential applications for inflammatory lung diseases (2010 - 2014).Structural and functional characterization of chimeric cyclotides from the Möbius and trypsin inhibitor subfamilies.Discovery, structure, function, and applications of cyclotides: circular proteins from plants.Formyl peptide receptor modulators: a patent review and potential applications for inflammatory diseases (2012-2015).Cyclotides: Overview and Biotechnological Applications.Making Ends Meet: Microwave-Accelerated Synthesis of Cyclic and Disulfide Rich Proteins Via In Situ Thioesterification and Native Chemical Ligation.
P2860
Q27670873-E05A9289-D21D-4208-B86E-364778F7A81CQ27679062-45850FEA-516F-4C05-B06F-79BB4A257A59Q27680481-C0623E64-8ED4-4B04-BC86-64F06735B62FQ27680631-0EE0F9CF-19F5-40DB-BE6F-78A0A726638AQ27681346-6E7E8774-2725-4EA5-BBAD-4D9D2962CA63Q27701553-69EA65BF-C9B9-4B61-ADB1-9AC995FA94ACQ28550563-131C72EA-8EF0-4523-BD66-5483F49FF8BAQ30383793-BF0691F9-325F-4BF6-B190-357F9882F461Q33568820-1337CD03-9CAF-4464-938B-F53EB8A8B8C1Q33872337-D0E4EEE4-093E-4119-8ECF-7699305A07F4Q34004482-B1BA4311-5ABC-4199-946A-5672DDE1DFAAQ34324717-B6577619-7732-4F15-A439-F5F623E43C14Q34634734-775646D3-6B32-484D-A51C-1BD6FF8E0B2AQ34814104-65A0ED8E-972E-4CD4-8CC0-D909AF69E82EQ35400491-8B66B0A7-22BA-4665-90ED-C8F15C8E5AC5Q35610164-DEC9BB62-89DD-4F53-8506-BBF973FE7AC9Q35780886-1A3BF067-25D3-40BD-BC91-E2C7671C3BB7Q35864573-ADCDF3C4-0189-4146-B21A-D63557B1AEE9Q35893500-F20630D3-F76F-46EE-9E76-D8E944286EACQ35900582-1C37C3A3-8D6A-484E-B40B-2D680F32923BQ36126255-FCE6D9F5-EBB5-462E-B2B3-988B61AF30DAQ36321375-3E07A3A4-635B-4CDD-AFF3-1ABC37EB9E53Q36465556-1189F9BF-180F-417C-ADE3-EB5ECB81C280Q36481904-627AE128-F4C8-48A8-87E7-7BDBCE3469C9Q36771109-1AA4FCC7-EF44-4DE7-A4EC-C90E1623EA17Q37503343-CB379201-C105-4226-B8E8-831075EEB3FBQ37677077-3B0C3547-39B6-4D99-9B5F-524FE9E2F5B8Q37696357-5AF076EB-C027-4459-802E-DA9048774FD5Q37724879-0600BFB0-0BC0-4BA2-BFC2-DB58D6668507Q37999102-255D5CD9-DE36-4D90-A7DF-7CE223FCB2BDQ38112084-A01D3143-BC31-4E33-847B-6B2701A00B93Q38124801-CF507081-ABA7-4010-A870-53816EB96324Q38243927-85CE5AB4-855C-40A2-8D3C-75F0054C16C5Q38253141-C4B7F589-538B-4EA5-9DAF-EBD42DD2CADAQ38539470-73255D69-95DE-4C63-9EED-9A546A23C7B1Q38834923-0DC71502-A6C1-434C-8DF9-BF73B02430FAQ38843873-AD87ABD1-E6E7-4B32-80C9-D071B4E71CFDQ38907435-9B56F897-42E1-4525-BF48-A919E9BD7B82Q39330201-8710C51C-918A-458E-BF7A-CB1095B73215Q41138668-7A020428-6541-4D7D-882E-F349935D5AFA
P2860
Potent inhibitors of beta-tryptase and human leukocyte elastase based on the MCoTI-II scaffold.
description
2009 nî lūn-bûn
@nan
2009年の論文
@ja
2009年学术文章
@wuu
2009年学术文章
@zh
2009年学术文章
@zh-cn
2009年学术文章
@zh-hans
2009年学术文章
@zh-my
2009年学术文章
@zh-sg
2009年學術文章
@yue
2009年學術文章
@zh-hant
name
Potent inhibitors of beta-tryp ...... ased on the MCoTI-II scaffold.
@en
Potent inhibitors of beta-tryp ...... ased on the MCoTI-II scaffold.
@nl
type
label
Potent inhibitors of beta-tryp ...... ased on the MCoTI-II scaffold.
@en
Potent inhibitors of beta-tryp ...... ased on the MCoTI-II scaffold.
@nl
prefLabel
Potent inhibitors of beta-tryp ...... ased on the MCoTI-II scaffold.
@en
Potent inhibitors of beta-tryp ...... ased on the MCoTI-II scaffold.
@nl
P50
P356
P1476
Potent inhibitors of beta-tryp ...... ased on the MCoTI-II scaffold.
@en
P2093
Camille Bonomelli
P304
P356
10.1021/JM901233U
P407
P577
2009-10-01T00:00:00Z