scholarly article | Q13442814 |
P2093 | author name string | Bärbel S Blaum | |
Andrew J Benie | |||
Georg Sczakiel | |||
Hannelore Peters | |||
Thomas Peters | |||
Verena Gauss-Müller | |||
Winfried Wünsche | |||
Yuri Kusov | |||
P2860 | cites work | NMR study of parallel-stranded tetraplex formation by the hexadeoxynucleotide d(TG4T) | Q59060282 |
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Sequence and structural determinants of the interaction between the 5'-noncoding region of picornavirus RNA and rhinovirus protease 3C | Q72315781 | ||
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Specific binding of a hexanucleotide to HIV-1 reverse transcriptase: a novel class of bioactive molecules | Q38308590 | ||
Cell type-specific proteins which interact with the 5' nontranslated region of hepatitis A virus RNA. | Q38314556 | ||
Poliovirus RNA synthesis utilizes an RNP complex formed around the 5'-end of viral RNA. | Q38316546 | ||
Role of loop residues and cations on the formation and stability of dimeric DNA G-quadruplexes | Q38318880 | ||
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Specific recognition of proteins by array-bound hexanucleotides | Q38337802 | ||
Modeling the electrophoresis of rigid polyions: application to lysozyme | Q39661671 | ||
The 5' nontranslated region of hepatitis A virus RNA: secondary structure and elements required for translation in vitro | Q40113123 | ||
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Replication of a hepatitis A virus replicon detected by genetic recombination in vivo | Q40710005 | ||
Potassium-dependent folding: a key to intracellular delivery of G-quartet oligonucleotides as HIV inhibitors | Q40736451 | ||
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Inhibition of hepatitis C virus IRES-mediated translation by oligonucleotides | Q42990544 | ||
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Mutations at KFRDI and VGK domains of enterovirus 71 3C protease affect its RNA binding and proteolytic activities | Q44765873 | ||
A new model of dual interacting ligand binding sites on integrin alphaIIbbeta3. | Q45171116 | ||
Crystal structure of foot-and-mouth disease virus 3C protease. New insights into catalytic mechanism and cleavage specificity | Q45226865 | ||
Structure-assisted design of mechanism-based irreversible inhibitors of human rhinovirus 3C protease with potent antiviral activity against multiple rhinovirus serotypes | Q27619756 | ||
Crystal structure of an inhibitor complex of the 3C proteinase from hepatitis A virus (HAV) and implications for the polyprotein processing in HAV | Q27620759 | ||
The structure of the stemloop D subdomain of coxsackievirus B3 cloverleaf RNA and its interaction with the proteinase 3C | Q27643129 | ||
NMR solution structures of the apo and peptide-inhibited human rhinovirus 3C protease (Serotype 14): structural and dynamic comparison | Q27648817 | ||
Sequence variant (CTAGGG)n in the human telomere favors a G-quadruplex structure containing a G·C·G·C tetrad | Q27657084 | ||
Insights into cleavage specificity from the crystal structure of foot-and-mouth disease virus 3C protease complexed with a peptide substrate | Q27658042 | ||
The high-resolution crystal structure of a parallel-stranded guanine tetraplex | Q27730831 | ||
The refined crystal structure of the 3C gene product from hepatitis A virus: specific proteinase activity and RNA recognition | Q27734773 | ||
Refined X-ray crystallographic structure of the poliovirus 3C gene product | Q27747494 | ||
NMRPipe: a multidimensional spectral processing system based on UNIX pipes | Q27860859 | ||
Combinatorially selected guanosine-quartet structure is a potent inhibitor of human immunodeficiency virus envelope-mediated cell fusion | Q28368943 | ||
Utilization of site-directed spin labeling and high-resolution heteronuclear nuclear magnetic resonance for global fold determination of large proteins with limited nuclear overhauser effect data | Q29617299 | ||
Structure of human rhinovirus 3C protease reveals a trypsin-like polypeptide fold, RNA-binding site, and means for cleaving precursor polyprotein | Q30194279 | ||
Adaptive recognition by nucleic acid aptamers | Q30836242 | ||
DNA-XPA interactions: a (31)P NMR and molecular modeling study of dCCAATAACC association with the minimal DNA-binding domain (M98-F219) of the nucleotide excision repair protein XPA. | Q30993262 | ||
Identification of cellular proteins enhancing activities of internal ribosomal entry sites by competition with oligodeoxynucleotides | Q31049788 | ||
A DNA aptamer prevents influenza infection by blocking the receptor binding region of the viral hemagglutinin | Q31111010 | ||
In vitro evolution of nucleic acids | Q34089633 | ||
Dual modes of modification of hepatitis A virus 3C protease by a serine-derived beta-lactone: selective crystallization and formation of a functional catalytic triad in the active site | Q34467806 | ||
CheckShift: automatic correction of inconsistent chemical shift referencing | Q34694377 | ||
CheckShift improved: fast chemical shift reference correction with high accuracy | Q34990468 | ||
NMR studies of protein interactions. | Q36374377 | ||
Characterization of RNA aptamers that disrupt the RUNX1-CBFbeta/DNA complex | Q37421114 | ||
Design, synthesis, and amplification of DNA pools for in vitro selection | Q37611706 | ||
P275 | copyright license | Creative Commons Attribution-NonCommercial 3.0 Unported | Q18810331 |
P6216 | copyright status | copyrighted | Q50423863 |
P433 | issue | 7 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | hepatitis A | Q157661 |
Hepatitis A virus | Q4112120 | ||
P304 | page(s) | 3042-3055 | |
P577 | publication date | 2011-12-10 | |
P1433 | published in | Nucleic Acids Research | Q135122 |
P1476 | title | Functional binding of hexanucleotides to 3C protease of hepatitis A virus | |
P478 | volume | 40 |
Q26775640 | Direct-acting Antivirals and Host-targeting Agents against the Hepatitis A Virus |
Q40037886 | Functional RNA during Zika virus infection |
Q36870503 | G-quadruplex-interacting compounds alter latent DNA replication and episomal persistence of KSHV. |
Q34489819 | G-quadruplexes in viruses: function and potential therapeutic applications |
Q54239430 | Identification of G-quadruplex forming sequences in three manatee papillomaviruses. |
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