Structural Homology, Protein < Structure-Activity Relationship < Students

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List of bibliographic references

Number of relevant bibliographic references: 187.
[0-20] [0 - 20][0 - 50][20-40]

Ident.	Authors (with country if any)	Title
000007 (2000)	F. Zouhiri [France] ; J F Mouscadet ; K. Mekouar ; D. Desmaële ; D. Savouré ; H. Leh ; F. Subra ; M. Le Bret ; C. Auclair ; J. D'Angelo	Structure-activity relationships and binding mode of styrylquinolines as potent inhibitors of HIV-1 integrase and replication of HIV-1 in cell culture.
000010 (2001)	A. Johansson [Suède] ; I. Hubatsch ; E. Akerblom ; G. Lindeberg ; S. Winiwarter ; U H Danielson ; A. Hallberg	Inhibition of hepatitis C virus NS3 protease activity by product-based peptides is dependent on helicase domain.
000013 (2001)	D J Hwang [Corée du Sud] ; S N Kim ; J H Choi ; Y S Lee	Dicaffeoyl- or digalloyl pyrrolidine and furan derivatives as HIV integrase inhibitors.
000025 (2003)	Aurelio Bonavia [États-Unis] ; Bruce D. Zelus ; David E. Wentworth ; Pierre J. Talbot ; Kathryn V. Holmes	Identification of a receptor-binding domain of the spike glycoprotein of human coronavirus HCoV-229E.
000333 (2003)	Evelena Ontiveros [États-Unis] ; Taeg S. Kim ; Thomas M. Gallagher ; Stanley Perlman	Enhanced virulence mediated by the murine coronavirus, mouse hepatitis virus strain JHM, is associated with a glycine at residue 310 of the spike glycoprotein.
000339 (1992)	E L Oleszak ; S. Perlman ; J L Leibowitz	MHV S peplomer protein expressed by a recombinant vaccinia virus vector exhibits IgG Fc-receptor activity.
000360 (2003)	Christopher Mcguigan [Royaume-Uni] ; Alison Jukes ; Sally Blewett ; Hubert Barucki ; Jonathan T. Erichsen ; Graciella Andrei ; Robert Snoeck ; Erik De Clercq ; Jan Balzarini	Halophenyl furanopyrimidines as potent and selective anti-VZV agents.
000420 (2003)	Ekachai Jenwitheesuk [États-Unis] ; Ram Samudrala	Identifying inhibitors of the SARS coronavirus proteinase.
000502 (2004)	Hideka S. Miura [Japon] ; Keiko Nakagaki ; Fumihiro Taguchi	N-terminal domain of the murine coronavirus receptor CEACAM1 is responsible for fusogenic activation and conformational changes of the spike protein.
000546 (2004)	Ponraj Prabakaran [États-Unis] ; Xiaodong Xiao ; Dimiter S. Dimitrov	A model of the ACE2 structure and function as a SARS-CoV receptor.
000744 (2004)	Gregory J. Babcock [États-Unis] ; Diana J. Esshaki ; William D. Thomas ; Donna M. Ambrosino	Amino acids 270 to 510 of the severe acute respiratory syndrome coronavirus spike protein are required for interaction with receptor.
000769 (2004)	Usman Bacha [États-Unis] ; Jennifer Barrila ; Adrian Velazquez-Campoy ; Stephanie A. Leavitt ; Ernesto Freire	Identification of novel inhibitors of the SARS coronavirus main protease 3CLpro.
000798 (2004)	Mayuko Takeda-Shitaka [Japon] ; Hiroyuki Nojima ; Daisuke Takaya ; Kazuhiko Kanou ; Mitsuo Iwadate ; Hideaki Umeyama	Evaluation of homology modeling of the severe acute respiratory syndrome (SARS) coronavirus main protease for structure based drug design.
000A65 (2004)	Rajendram V. Rajnarayanan [États-Unis] ; Sivanesan Dakshanamurthy ; Nagarajan Pattabiraman	"Teaching old drugs to kill new bugs": structure-based discovery of anti-SARS drugs.
000A77 (2005)	Gaurav Sachdeva [Inde] ; Kaushal Kumar ; Preti Jain ; Srinivasan Ramachandran	SPAAN: a software program for prediction of adhesins and adhesin-like proteins using neural networks.
000B29 (2004)	Matthew J. Huentelman [États-Unis] ; Jasenka Zubcevic ; Jose A. Hernández Prada ; Xiaodong Xiao ; Dimiter S. Dimitrov ; Mohan K. Raizada ; David A. Ostrov	Structure-based discovery of a novel angiotensin-converting enzyme 2 inhibitor.
000D25 (2005)	Jaime Guillén [Espagne] ; Ana J. Pérez-Berná [Espagne] ; Miguel R. Moreno [Espagne] ; José Villalaín [Espagne]	Identification of the Membrane-Active Regions of the Severe Acute Respiratory Syndrome Coronavirus Spike Membrane Glycoprotein Using a 16/18-Mer Peptide Scan: Implications for the Viral Fusion Mechanism
000D46 (2005)	Naoyuki Masuda [Japon] ; Osamu Yamamoto ; Masahiro Fujii ; Tetsuro Ohgami ; Jiro Fujiyasu ; Toru Kontani ; Ayako Moritomo ; Masaya Orita ; Hiroyuki Kurihara ; Hironobu Koga ; Shunji Kageyama ; Mitsuaki Ohta ; Hiroshi Inoue ; Toshifumi Hatta ; Masafumi Shintani ; Hiroshi Suzuki ; Kenji Sudo ; Yasuaki Shimizu ; Eiichi Kodama ; Masao Matsuoka ; Masatoshi Fujiwara ; Tomoyuki Yokota ; Shiro Shigeta ; Masanori Baba	Studies of non-nucleoside HIV-1 reverse transcriptase inhibitors. Part 2: synthesis and structure-activity relationships of 2-cyano and 2-hydroxy thiazolidenebenzenesulfonamide derivatives.
000D91 (2005)	Gerold Hoever [Allemagne] ; Lidia Baltina ; Martin Michaelis ; Rimma Kondratenko ; Lia Baltina ; Genrich A. Tolstikov ; Hans W. Doerr ; Jindrich Cinatl	Antiviral activity of glycyrrhizic acid derivatives against SARS-coronavirus.
000F53 (2005)	Li-Rung Chen [République populaire de Chine] ; Yu-Chin Wang ; Yi Wen Lin ; Shan-Yen Chou ; Shyh-Fong Chen ; Lee Tai Liu ; Ying-Ta Wu ; Chih-Jung Kuo ; Tom Shieh-Shung Chen ; Shin-Hun Juang	Synthesis and evaluation of isatin derivatives as effective SARS coronavirus 3CL protease inhibitors.
001021 (2005)	Jiun-Jie Shie [Taïwan] ; Jim-Min Fang ; Chih-Jung Kuo ; Tun-Hsun Kuo ; Po-Huang Liang ; Hung-Jyun Huang ; Wen-Bin Yang ; Chun-Hung Lin ; Jiun-Ling Chen ; Yin-Ta Wu ; Chi-Huey Wong	Discovery of potent anilide inhibitors against the severe acute respiratory syndrome 3CL protease.

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