about
CyBase: a database of cyclic protein sequence and structureCombined X-ray and NMR Analysis of the Stability of the Cyclotide Cystine Knot Fold That Underpins Its Insecticidal Activity and Potential Use as a Drug ScaffoldIsolation and characterization of peptides from Momordica cochinchinensis seedsDespite a Conserved Cystine Knot Motif, Different Cyclotides Have Different Membrane Binding ModesThe role of conserved Glu residue on cyclotide stability and activity: a structural and functional study of kalata B12, a naturally occurring Glu to Asp mutantPromiscuity of carbonic anhydrase II. Unexpected ester hydrolysis of carbohydrate-based sulfamate inhibitorsInsights into the Membrane Interactions of the Saposin-Like Proteins Na-SLP-1 and Ac-SLP-1 from Human and Dog HookwormHookworm SCP/TAPS protein structure--A key to understanding host-parasite interactions and developing new interventionsAlpha-1 giardin is an annexin with highly unusual calcium-regulated mechanismsThe cyclic cystine ladder of theta-defensins as a stable, bifunctional scaffold: A proof-of-concept study using the integrin-binding RGD motifAnticancer and toxic properties of cyclotides are dependent on phosphatidylethanolamine phospholipid targetingRacemic and quasi-racemic X-ray structures of cyclic disulfide-rich peptide drug scaffoldsMirror Images of Antimicrobial Peptides Provide Reflections on Their Functions and Amyloidogenic PropertiesEfficient enzymatic cyclization of an inhibitory cystine knot-containing peptideExtensions of PDZ domains as important structural and functional elementsComparison of VILIP-1 and VILIP-3 binding to phospholipid monolayers.NMRDyn: a program for NMR relaxation studies of protein association.Divalent cations and redox conditions regulate the molecular structure and function of visinin-like protein-1SBAL: a practical tool to generate and edit structure-based amino acid sequence alignments.Cyclotide isolation and characterization.Rational design and synthesis of an orally bioavailable peptide guided by NMR amide temperature coefficients.Alanine scanning mutagenesis of the prototypic cyclotide reveals a cluster of residues essential for bioactivity.Phosphorylation of CRN2 by CK2 regulates F-actin and Arp2/3 interaction and inhibits cell migration.Improving the Selectivity of Engineered Protease Inhibitors: Optimizing the P2 Prime Residue Using a Versatile Cyclic Peptide Library.Design of substrate-based BCR-ABL kinase inhibitors using the cyclotide scaffold.Design of Potent and Selective Cathepsin G Inhibitors Based on the Sunflower Trypsin Inhibitor-1 Scaffold.Cyclotides insert into lipid bilayers to form membrane pores and destabilize the membrane through hydrophobic and phosphoethanolamine-specific interactionsCyclotides as natural anti-HIV agents.Atypical (RIO) protein kinases from Haemonchus contortus--promise as new targets for nematocidal drugs.Disulfide-rich macrocyclic peptides as templates in drug design.Chlorotoxin: Structure, activity, and potential uses in cancer therapy.Using the MCoTI-II Cyclotide Scaffold To Design a Stable Cyclic Peptide Antagonist of SET, a Protein Overexpressed in Human Cancer.Cyclic peptide oral bioavailability: Lessons from the past.The role of disulfide bonds in structure and activity of chlorotoxin.Inhibition of tau aggregation using a naturally-occurring cyclic peptide scaffold.Isolation and characterization of cytotoxic cyclotides from Viola tricolor.The anthelmintic activity of the cyclotides: natural variants with enhanced activity.Anti-HIV cyclotides from the Chinese medicinal herb Viola yedoensis.Translational diffusion of cyclic peptides measured using pulsed-field gradient NMR.Cycloviolacin H4, a hydrophobic cyclotide from Viola hederaceae.
P50
Q25257489-271B7044-13FB-4B70-A668-F787E4E7D052Q27653739-9B8B827A-ADB7-4E2F-8DC1-D3993EBF3B0BQ27657200-02CFD3BC-0A53-4D4D-9B5D-096A38D9CE05Q27657245-3878E218-EB9C-4E7F-99CA-03BE34BBF99CQ27667166-6BBCE651-47A5-4B60-9339-43E787C9BFF8Q27674593-F659F240-3B21-4731-8FB0-082B9B1952D6Q27674983-E6FE39DC-31A3-41AB-BE00-46C43408F4A8Q27675830-B00CBD39-F633-4C7F-A882-CF134F02B2F4Q27681755-28EEFDA8-BF07-433B-B5ED-997F9BC06386Q27688055-F4BFD00F-EBD8-4D9F-B2B7-6C0FB92DC8D4Q27694726-9B88121B-4399-45FC-96AF-616AFBD6912CQ27694819-1C8D0121-9AD4-44AD-8D77-EF71CF90A989Q27704538-6DC4762A-9198-4A7C-8358-A56F0FDEE41AQ27704653-2D78E51F-D76F-4FEA-B699-0AC5DAC6F226Q30398142-1412D9F6-2CA6-4294-AFFF-E51A8247EC7BQ31156372-73F0B667-DDC3-4058-B8C0-CCE96845816BQ33388229-380E285D-0B7B-45DD-928D-83751C88742BQ34071615-B3AEA721-441C-424A-91E0-3F70FFDACBB9Q34158310-C9E5193D-3A07-4DD3-B812-D72453118F6BQ34433160-59E50770-08DC-4DEA-99E8-DD9D51AD7AE5Q34709012-255FFCE3-F66A-4A45-9DC9-042CED396E31Q34747442-53A3004A-B572-49E6-9A0F-F1AC1BF189A7Q35712790-71FAD5E3-B7CE-4637-B311-CFFDFF0450C7Q35783014-3DDFA0B8-BEA0-4B4C-9B18-0138985C7B36Q35942258-B76EC97F-ABF7-442E-82A9-FAE121E5C0B7Q36237689-EB9513D9-B15C-4B60-AA59-93B048ACB6BDQ36481904-1701E889-D93B-4AFC-A616-D38859C8BF4AQ37002917-91876841-F7C7-4D09-AC74-0C8854A7ADB1Q37832015-8F23DCFC-375D-431B-8431-E6AD06401095Q38197792-D771235B-4628-4AA6-B21A-8CAC81932636Q38595154-60A1E1BE-9E51-44C8-A6D4-B8123D4942EEQ38810458-C7C3F8A3-5884-476B-BDEF-175DF3EC3644Q38834152-DF2EE3CD-0B2B-494F-8A20-35D31D71258FQ39096712-98E52120-8172-4E3E-A557-9478C8B48F92Q40065016-5145444E-20F2-486D-B4CD-8DE545895108Q43004571-E029FB58-9E35-4EC4-A483-E2EEEB02553EQ45741061-BDAAE5BB-CE5A-4BBA-8A44-08D3D8BAB6DCQ46849544-576794FB-B152-4F3B-BDFE-3115528B7860Q46909798-E4A09B28-9D9F-4B97-B69B-8B1E4F50E1D6Q46914746-9A74C603-AC34-451A-95A0-383CEBC85090
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Conan K Wang
@ast
Conan K Wang
@en
Conan K Wang
@es
Conan K Wang
@nl
Conan K Wang
@sl
type
label
Conan K Wang
@ast
Conan K Wang
@en
Conan K Wang
@es
Conan K Wang
@nl
Conan K Wang
@sl
altLabel
Conan Wang
@en
prefLabel
Conan K Wang
@ast
Conan K Wang
@en
Conan K Wang
@es
Conan K Wang
@nl
Conan K Wang
@sl
P1053
D-1481-2010
P106
P21
P31
P3829
P496
0000-0002-7973-7632
P569
2000-01-01T00:00:00Z