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Proceedings of the National Academy of Sciences of the United States of America
|
October 5, 2017
De novo design of covalently constrained mesosize protein scaffolds with unique tertiary structures
Bobo Dang, Haifan Wu, Vikram Khipple Mulligan, et al.
Biorxiv : the Preprint Server for Biology
|
February 24, 2023
Designed Transmembrane Proteins Inhibit the Erythropoietin Receptor in a Custom Binding Topology
Marco Mravic, Li He, Huong Kratochvil, et al.
Plos One
|
June 14, 2012
NMR structure of lipoprotein YxeF from Bacillus subtilis reveals a calycin fold and distant homology with the lipocalin Blc from Escherichia coli
Yibing Wu, Marco Punta, Rong Xiao, et al.
Nature Chemistry
|
November 24, 2017
De novo design of a hyperstable non-natural protein-ligand complex with sub-Å accuracy
Nicholas F Polizzi, Yibing Wu, Thomas Lemmin, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
December 16, 2010
NMR analysis of the alphaIIb beta3 cytoplasmic interaction suggests a mechanism for integrin regulation
Douglas G Metcalf, David T Moore, Yibing Wu, et al.
Nature Chemical Biology
|
March 14, 2024
De novo-designed transmembrane proteins bind and regulate a cytokine receptor
Marco Mravic, Li He, Huong T Kratochvil, et al.
Biochemistry
|
May 15, 2007
Solution structures of a DNA dodecamer duplex with and without a cisplatin 1,2-d(GG) intrastrand cross-link: comparison with the same DNA duplex containing an oxaliplatin 1,2-d(GG) intrastrand cross-link
Yibing Wu, Debadeep Bhattacharyya, Candice L King, et al.
Journal of the American Chemical Society
|
December 4, 2014
Flipping in the pore: discovery of dual inhibitors that bind in different orientations to the wild-type versus the amantadine-resistant S31N mutant of the influenza A virus M2 proton channel
Yibing Wu, Belgin Canturk, Hyunil Jo, et al.
Journal of Medicinal Chemistry
|
November 19, 2013
3-Azatetracyclo[5.2.1.1(5,8).0(1,5)]undecane derivatives: from wild-type inhibitors of the M2 ion channel of influenza A virus to derivatives with potent activity against the V27A mutant
Matias Rey-Carrizo, Eva Torres, Chunlong Ma, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
June 2, 2017
Zinc-binding structure of a catalytic amyloid from solid-state NMR
Myungwoon Lee, Tuo Wang, Olga V Makhlynets, et al.
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Search research articles
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Showing results (71-80 of 95) with videos related to
Sort By:
Page
of 10
Proceedings of the National Academy of Sciences of the United States of America
|
October 5, 2017
De novo design of covalently constrained mesosize protein scaffolds with unique tertiary structures
Bobo Dang, Haifan Wu, Vikram Khipple Mulligan, et al.
Biorxiv : the Preprint Server for Biology
|
February 24, 2023
Designed Transmembrane Proteins Inhibit the Erythropoietin Receptor in a Custom Binding Topology
Marco Mravic, Li He, Huong Kratochvil, et al.
Plos One
|
June 14, 2012
NMR structure of lipoprotein YxeF from Bacillus subtilis reveals a calycin fold and distant homology with the lipocalin Blc from Escherichia coli
Yibing Wu, Marco Punta, Rong Xiao, et al.
Nature Chemistry
|
November 24, 2017
De novo design of a hyperstable non-natural protein-ligand complex with sub-Å accuracy
Nicholas F Polizzi, Yibing Wu, Thomas Lemmin, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
December 16, 2010
NMR analysis of the alphaIIb beta3 cytoplasmic interaction suggests a mechanism for integrin regulation
Douglas G Metcalf, David T Moore, Yibing Wu, et al.
Nature Chemical Biology
|
March 14, 2024
De novo-designed transmembrane proteins bind and regulate a cytokine receptor
Marco Mravic, Li He, Huong T Kratochvil, et al.
Biochemistry
|
May 15, 2007
Solution structures of a DNA dodecamer duplex with and without a cisplatin 1,2-d(GG) intrastrand cross-link: comparison with the same DNA duplex containing an oxaliplatin 1,2-d(GG) intrastrand cross-link
Yibing Wu, Debadeep Bhattacharyya, Candice L King, et al.
Journal of the American Chemical Society
|
December 4, 2014
Flipping in the pore: discovery of dual inhibitors that bind in different orientations to the wild-type versus the amantadine-resistant S31N mutant of the influenza A virus M2 proton channel
Yibing Wu, Belgin Canturk, Hyunil Jo, et al.
Journal of Medicinal Chemistry
|
November 19, 2013
3-Azatetracyclo[5.2.1.1(5,8).0(1,5)]undecane derivatives: from wild-type inhibitors of the M2 ion channel of influenza A virus to derivatives with potent activity against the V27A mutant
Matias Rey-Carrizo, Eva Torres, Chunlong Ma, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
June 2, 2017
Zinc-binding structure of a catalytic amyloid from solid-state NMR
Myungwoon Lee, Tuo Wang, Olga V Makhlynets, et al.
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