Polyprotein cleavage mechanism of SARS CoV Mpro and chemical modification of the octapeptide

scientific article published in November 2004

Polyprotein cleavage mechanism of SARS CoV Mpro and chemical modification of the octapeptide is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1016/J.PEPTIDES.2004.06.018
P932PMC publication ID7115412
P698PubMed publication ID15501516
P5875ResearchGate publication ID257052268

P50authorKuo-Chen ChouQ30069869
Dong-Qing WeiQ78691557
P2093author name stringHong Guo
Yu Zhu
Qi-Shi Du
Shu-Qing Wang
Suzanne Sirois
P2860cites workSolution structure of BID, an intracellular amplifier of apoptotic signalingQ27617719
Coronavirus main proteinase (3CLpro) structure: basis for design of anti-SARS drugsQ27641252
The crystal structures of severe acute respiratory syndrome virus main protease and its complex with an inhibitorQ27642450
Solution structure of the RAIDD CARD and model for CARD/CARD interaction in caspase-2 and caspase-9 recruitmentQ27764927
Identification of a novel coronavirus in patients with severe acute respiratory syndromeQ29615907
A novel coronavirus associated with severe acute respiratory syndromeQ29617553
A model of the complex between cyclin-dependent kinase 5 and the activation domain of neuronal Cdk5 activatorQ33333805
Subcellular location prediction of apoptosis proteinsQ34163319
Kinetics of processive nucleic acid polymerases and nucleasesQ34293063
Prediction of Protein Structural ClassesQ34297604
Steady-state kinetic studies with the non-nucleoside HIV-1 reverse transcriptase inhibitor U-87201E.Q34305893
Kinetic studies with the non-nucleoside HIV-1 reverse transcriptase inhibitor U-88204E.Q34306379
A vectorized sequence-coupling model for predicting HIV protease cleavage sites in proteins.Q34352547
Predicting cleavability of peptide sequences by HIV protease via correlation-angle approachQ34357106
Predicting human immunodeficiency virus protease cleavage sites in proteins by a discriminant function methodQ34379398
Prediction of human immunodeficiency virus protease cleavage sites in proteinsQ34395418
N-terminal domain of the murine coronavirus receptor CEACAM1 is responsible for fusogenic activation and conformational changes of the spike proteinQ34554080
Severe acute respiratory syndrome and influenza: virus incursions from southern ChinaQ35605213
Steady-state kinetic studies with the polysulfonate U-9843, an HIV reverse transcriptase inhibitorQ38312049
Kinetic studies with the non-nucleoside human immunodeficiency virus type-1 reverse transcriptase inhibitor U-90152E.Q42275206
The quinoline U-78036 is a potent inhibitor of HIV-1 reverse transcriptase.Q42278148
The benzylthio-pyrimidine U-31,355, a potent inhibitor of HIV-1 reverse transcriptaseQ42556920
Prediction of the tertiary structure of the beta-secretase zymogenQ43939436
Identification of the N-terminal functional domains of Cdk5 by molecular truncation and computer modelingQ44060634
Virtual screening for SARS-CoV protease based on KZ7088 pharmacophore pointsQ44904083
A formulation for correlating properties of peptides and its application to predicting human immunodeficiency virus protease-cleavable sites in proteinsQ45774564
Binding mechanism of coronavirus main proteinase with ligands and its implication to drug design against SARS.Q51661127
An alternate-subsite-coupled model for predicting HIV protease cleavage sites in proteins.Q52384852
Prediction of the tertiary structure of a caspase-9/inhibitor complexQ73616626
Prediction of the tertiary structure and substrate binding site of caspase-8Q74028194
P433issue11
P921main subjectSARSr-CoVQ278567
SARS-CoV-1Q85438966
P1104number of pages8
P304page(s)1857-1864
P577publication date2004-11-01
P1433published inPeptidesQ7166533
P1476titlePolyprotein cleavage mechanism of SARS CoV Mpro and chemical modification of the octapeptide
P478volume25

Reverse relations

cites work (P2860)
Q44727152A novel fingerprint map for detecting SARS-CoV.
Q38028553Advances in visual representation of molecular potentials
Q53501563Cleavage mechanism of the H5N1 hemagglutinin by trypsin and furin.
Q45764150Computational studies of the binding modes of A 2A adenosine receptor antagonists
Q51907535Estimating residue evolutionary conservation by introducing von Neumann entropy and a novel gap-treating approach.
Q45421991From genome to drug lead: identification of a small-molecule inhibitor of the SARS virus
Q46580414Inhibition of the severe acute respiratory syndrome 3CL protease by peptidomimetic alpha,beta-unsaturated esters
Q100514026Molecular mechanisms of the novel coronavirus SARS-CoV-2 and potential anti-COVID19 pharmacological targets since the outbreak of the pandemic
Q34390896Molecular modeling and chemical modification for finding peptide inhibitor against severe acute respiratory syndrome coronavirus main proteinase
Q43486256Peptide reagent design based on physical and chemical properties of amino acid residues
Q34461791Synthesis and activity of an octapeptide inhibitor designed for SARS coronavirus main proteinase
Q42858751Synthesis and evaluation of pyrazolone compounds as SARS-coronavirus 3C-like protease inhibitors

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