Author results

4H5S
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COMPLEX STRUCTURE OF NECL-2 AND CRTAM
分子名称:Cytotoxic and regulatory T-cell molecule, Cell adhesion molecule 1
著者Zhang, S., Lu, G., Qi, J., Li, Y., Zhang, Z., Zhang, B., Yan, J., Gao, G.F.
登録日2012-09-18
公開日2013-08-07
最終更新日2014-05-07
実験手法X-RAY DIFFRACTION (1.7 Å)
主引用文献Competition of Cell Adhesion and Immune Recognition: Insights into the Interaction between CRTAM and Nectin-like 2
Structure, 21, 2013
5G04
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STRUCTURE OF THE HUMAN APC-CDC20-HSL1 COMPLEX
分子名称:ANAPHASE-PROMOTING COMPLEX SUBUNIT 1, ANAPHASE-PROMOTING COMPLEX SUBUNIT 11, CELL DIVISION CYCLE PROTEIN 23 HOMOLOG, ...
著者Zhang, S., Chang, L., Alfieri, C., Zhang, Z., Yang, J., Maslen, S., Skehel, M., Barford, D.
登録日2016-03-16
公開日2016-05-25
実験手法ELECTRON MICROSCOPY (4 Å)
主引用文献Molecular Mechanism of Apc/C Activation by Mitotic Phosphorylation.
Nature, 533, 2016
5G05
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CRYO-EM STRUCTURE OF COMBINED APO PHOSPHORYLATED APC
分子名称:ANAPHASE-PROMOTING COMPLEX SUBUNIT 1, ANAPHASE-PROMOTING COMPLEX SUBUNIT 11, CELL DIVISION CYCLE PROTEIN 23 HOMOLOG, ...
著者Zhang, S., Chang, L., Alfieri, C., Zhang, Z., Yang, J., Maslen, S., Skehel, M., Barford, D.
登録日2016-03-16
公開日2016-05-25
最終更新日2016-06-08
実験手法ELECTRON MICROSCOPY (3.5 Å)
主引用文献Molecular Mechanism of Apc/C Activation by Mitotic Phosphorylation.
Nature, 533, 2016
5IHW
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THE CRYSTAL STRUCTURE OF SDRE FROM STAPHYLOCOCCUS AUREUS
分子名称:Serine-aspartate repeat-containing protein E
著者Zhang, S., Wei, J., Wu, S., Zhang, X., Luo, M., Wang, D.
登録日2016-02-29
公開日2017-03-22
実験手法X-RAY DIFFRACTION (1.25 Å)
主引用文献The crystal structure of SdrE from staphylococcus aureus
To Be Published
5YY5
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STRUCTURAL DEFINITION OF A UNIQUE NEUTRALIZATION EPITOPE ON THE RECEPTOR-BINDING DOMAIN OF MERS-COV SPIKE GLYCOPROTEIN
分子名称:MERS-CoV RBD, Heavy chain, Light chain, ...
著者Zhang, S., Wang, P., Zhou, P., Wang, X., Zhang, L.
登録日2017-12-08
公開日2018-08-01
最終更新日2019-02-20
実験手法X-RAY DIFFRACTION (2.8 Å)
主引用文献Structural Definition of a Unique Neutralization Epitope on the Receptor-Binding Domain of MERS-CoV Spike Glycoprotein
Cell Rep, 24, 2018
4QTJ
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COMPLEX OF WOPR DOMAIN OF WOR1 IN CANDIDA ALBICANS WITH THE 13BP DSDNA
分子名称:White-opaque regulator 1, DNA (5'-D(*AP*AP*AP*AP*GP*TP*TP*TP*AP*AP*CP*TP*T)-3'), DNA (5'-D(*AP*AP*GP*TP*TP*AP*AP*AP*CP*TP*TP*TP*T)-3')
著者Zhang, S., Zhang, T., Ding, J.
登録日2014-07-08
公開日2014-08-13
最終更新日2017-11-22
実験手法X-RAY DIFFRACTION (2.1 Å)
主引用文献Crystal structure of the WOPR-DNA complex and implications for Wor1 function in white-opaque switching of Candida albicans.
Cell Res., 2014
4QTK
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COMPLEX OF WOPR DOMAIN OF WOR1 IN CANDIDA ALBICANS WITH THE 17BP DSDNA
分子名称:White-opaque regulator 1, DNA (5'-D(*TP*CP*AP*AP*AP*AP*AP*AP*GP*TP*TP*TP*AP*AP*CP*TP*T)-3'), DNA (5'-D(*AP*AP*GP*TP*TP*AP*AP*AP*CP*TP*TP*TP*TP*TP*TP*GP*A)-3')
著者Zhang, S., Zhang, T., Ding, J.
登録日2014-07-08
公開日2014-08-13
最終更新日2017-11-22
実験手法X-RAY DIFFRACTION (2.99 Å)
主引用文献Crystal structure of the WOPR-DNA complex and implications for Wor1 function in white-opaque switching of Candida albicans.
Cell Res., 2014
5XYN
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THE CRYSTAL STRUCTURE OF CSM2-PSY3-SHU1-SHU2 COMPLEX FROM BUDDING YEAST
分子名称:Platinum sensitivity protein 3, Chromosome segregation in meiosis protein 2, Suppressor of HU sensitivity involved in recombination protein 1, ...
著者Zhang, S., Zhang, T., Ding, J.
登録日2017-07-09
公開日2017-11-08
最終更新日2017-12-27
実験手法X-RAY DIFFRACTION (3.3 Å)
主引用文献Structural basis for the functional role of the Shu complex in homologous recombination.
Nucleic Acids Res., 45, 2017
5ZXV
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STRUCTURAL DEFINITION OF A UNIQUE NEUTRALIZATION EPITOPE ON THE RECEPTOR-BINDING DOMAIN OF MERS-COV SPIKE GLYCOPROTEIN
分子名称:MERS-CoV RBD, heavy chain, light chain
著者Zhang, S., Wang, X.
登録日2018-05-21
公開日2018-07-25
実験手法X-RAY DIFFRACTION (4.482 Å)
主引用文献Structural Definition of a Unique Neutralization Epitope on the Receptor-Binding Domain of MERS-CoV Spike Glycoprotein
Cell Rep, 24, 2018
5GN8
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STRUCTURE OF A 48-MER PROTEIN NANOCAGE FABRICATED FROM ITS 24-MER ANALOGUE BY SUBUNIT INTERFACE REDESIGN
分子名称:Ferritin heavy chain, CALCIUM ION
著者Zhang, S., Zang, J., Zhao, G., Mikami, B.
登録日2016-07-19
公開日2016-12-14
最終更新日2017-01-25
実験手法X-RAY DIFFRACTION (2.805 Å)
主引用文献"Silent" Amino Acid Residues at Key Subunit Interfaces Regulate the Geometry of Protein Nanocages
ACS Nano, 10, 2016
5GOU
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STRUCTURE OF A 16-MER PROTEIN NANOCAGE FABRICATED FROM ITS 24-MER ANALOGUE BY SUBUNIT INTERFACE REDESIGN
分子名称:Ferritin heavy chain
著者Zhang, S., Zang, J., Wang, W., Wang, H., Zhao, G.
登録日2016-07-29
公開日2017-02-22
実験手法X-RAY DIFFRACTION (2.91 Å)
主引用文献Conversion of the Native 24-mer Ferritin Nanocage into Its Non-Native 16-mer Analogue by Insertion of Extra Amino Acid Residues.
Angew. Chem. Int. Ed. Engl., 55, 2016
1HZ3
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ALZHEIMER'S DISEASE AMYLOID-BETA PEPTIDE (RESIDUES 10-35)
分子名称:A-BETA AMYLOID
著者Zhang, S., Iwata, K., Lachenmann, M.J., Peng, J.W., Li, S., Stimson, E.R., Lu, Y., Felix, A.M., Maggio, J.E., Lee, J.P.
登録日2001-01-23
公開日2001-01-31
最終更新日2011-07-13
実験手法SOLUTION NMR
主引用文献The Alzheimer's peptide a beta adopts a collapsed coil structure in water.
J.Struct.Biol., 130, 2000
3RL1
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HIV RT DERIVED PEPTIDE COMPLEXED TO HLA-A*0301
分子名称:HLA class I histocompatibility antigen, A-3 alpha chain, Beta-2-microglobulin, ...
著者Zhang, S., Liu, J., Cheng, H., Tan, S., Qi, J., Yan, J., Gao, G.F.
登録日2011-04-19
公開日2012-02-29
実験手法X-RAY DIFFRACTION (2 Å)
主引用文献Structural basis of cross-allele presentation by HLA-A*0301 and HLA-A*1101 revealed by two HIV-derived peptide complexes
Mol.Immunol., 49, 2011
3RL2
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HIV NEF DERIVED PEPTIDE NEF73 COMPLEXED TO HLA-A*0301
分子名称:HLA class I histocompatibility antigen, A-3 alpha chain, Beta-2-microglobulin, ...
著者Zhang, S., Liu, J., Cheng, H., Tan, S., Qi, J., Yan, J., Gao, G.F.
登録日2011-04-19
公開日2012-02-29
実験手法X-RAY DIFFRACTION (2.386 Å)
主引用文献Structural basis of cross-allele presentation by HLA-A*0301 and HLA-A*1101 revealed by two HIV-derived peptide complexes
Mol.Immunol., 49, 2011
5H30
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CRYO-EM STRUCTURE OF ZIKA VIRUS COMPLEXED WITH FAB C10 AT PH 6.5
分子名称:structural protein E, strutural protein M, IgG C10 heavy chain, ...
著者Zhang, S., Kostyuchenko, V., Ng, T.-S., Lok, S.-M.
登録日2016-10-19
公開日2016-11-30
最終更新日2017-01-25
実験手法ELECTRON MICROSCOPY (4.4 Å)
主引用文献Neutralization mechanism of a highly potent antibody against Zika virus
Nat Commun, 7, 2016
5H32
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CRYO-EM STRUCTURE OF ZIKA VIRUS COMPLEXED WITH FAB C10 AT PH 5.0
分子名称:structural protein E, C10 IgG heavy chain variable region, C10 IgG light chain variable region
著者Zhang, S., Kostyuchenko, V., Ng, T.-S., Lok, S.-M.
登録日2016-10-20
公開日2016-11-30
最終更新日2017-01-25
実験手法ELECTRON MICROSCOPY (12 Å)
主引用文献Neutralization mechanism of a highly potent antibody against Zika virus
Nat Commun, 7, 2016
5H37
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CRYO-EM STRUCTURE OF ZIKA VIRUS COMPLEXED WITH FAB C10 AT PH 8.0
分子名称:structural protein E, strutural protein M, C10 IgG heavy chain variable region, ...
著者Zhang, S., Kostyuchenko, V., Ng, T.-S., Lim, X.-N., Ooi, J.S.G., Lambert, S., Tan, T.Y., Widman, D., Shi, J., Baric, R.S., Lok, S.-M.
登録日2016-10-20
公開日2016-11-30
最終更新日2017-01-25
実験手法ELECTRON MICROSCOPY (4 Å)
主引用文献Neutralization mechanism of a highly potent antibody against Zika virus
Nat Commun, 7, 2016
2MDA
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THE SOLUTION STRUCTURE OF THE REGULATORY DOMAIN OF TYROSINE HYDROXYLASE
分子名称:Tyrosine 3-monooxygenase
著者Zhang, S., Huang, T., Hinck, A., Fitzpatrick, P.
登録日2013-09-08
公開日2014-01-01
最終更新日2014-03-26
実験手法SOLUTION NMR
主引用文献The solution structure of the regulatory domain of tyrosine hydroxylase.
J.Mol.Biol., 426, 2014
5CDI
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CHLOROPLAST CHAPERONIN 60B1 OF CHLAMYDOMONAS
分子名称:Chaperonin 60B1
著者Zhang, S., Zhou, H., Yu, F., Gao, F., He, J., Liu, C.
登録日2015-07-04
公開日2016-05-11
最終更新日2019-02-20
実験手法X-RAY DIFFRACTION (3.807 Å)
主引用文献Structural insight into the cooperation of chloroplast chaperonin subunits
Bmc Biol., 14, 2016
5CDJ
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APICAL DOMAIN OF CHLOROPLAST CHAPERONIN 60A
分子名称:RuBisCO large subunit-binding protein subunit alpha, chloroplastic
著者Zhang, S., Yu, F., Liu, C., Gao, F.
登録日2015-07-04
公開日2016-07-13
最終更新日2017-05-17
実験手法X-RAY DIFFRACTION (1.75 Å)
主引用文献Functional Partition of Cpn60 alpha and Cpn60 beta Subunits in Substrate Recognition and Cooperation with Co-chaperonins
Mol Plant, 9, 2016
5CDK
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APICAL DOMAIN OF CHLOROPLAST CHAPERONIN 60B1
分子名称:Chaperonin 60B1
著者Zhang, S., Yu, F., Liu, C., Gao, F.
登録日2015-07-04
公開日2016-07-13
最終更新日2017-10-04
実験手法X-RAY DIFFRACTION (1.5 Å)
主引用文献Functional Partition of Cpn60 alpha and Cpn60 beta Subunits in Substrate Recognition and Cooperation with Co-chaperonins
Mol Plant, 9, 2016
5H4D
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CRYSTAL STRUCTURE OF HSIRT3 IN COMPLEX WITH A SPECIFIC AGONIST AMIODARONE HYDROCHLORIDE
分子名称:NAD-dependent protein deacetylase sirtuin-3, mitochondrial, ARG-HIS-LYS, ...
著者Zhang, S., Fu, L., Liu, J., Liu, B.
登録日2016-10-31
公開日2017-11-08
最終更新日2017-11-22
実験手法X-RAY DIFFRACTION (3.21 Å)
主引用文献Crystal structure of hSIRT3 in complex with a specific agonist Amiodarone hydrochloride
To Be Published
4GE2
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CRYSTAL STRUCTURE OF HUMAN PROTEIN TYROSINE PHOSPHATASE PTPN9 (MEG2) COMPLEX WITH COMPOUND 3
分子名称:Tyrosine-protein phosphatase non-receptor type 9, N-acetyl-4-[difluoro(phosphono)methyl]-L-phenylalanyl-N~5~-(3-iodobenzoyl)-L-ornithinamide
著者Zhang, Z.-Y., Liu, S., Zhang, S.
登録日2012-08-01
公開日2012-10-31
最終更新日2012-11-14
実験手法X-RAY DIFFRACTION (1.8 Å)
主引用文献A Highly Selective and Potent PTP-MEG2 Inhibitor with Therapeutic Potential for Type 2 Diabetes.
J.Am.Chem.Soc., 134, 2012
4GE5
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CRYSTAL STRUCTURE OF HUMAN PROTEIN TYROSINE PHOSPHATASE PTPN9 (MEG2) COMPLEX WITH COMPOUND 5
分子名称:Tyrosine-protein phosphatase non-receptor type 9, N-(4-bromo-3-methylbenzoyl)-4-[difluoro(phosphono)methyl]-L-phenylalanyl-N~5~-(3-iodobenzoyl)-L-ornithinamide
著者Zhang, Z.-Y., Liu, S., Zhang, S.
登録日2012-08-01
公開日2012-10-31
最終更新日2012-11-14
実験手法X-RAY DIFFRACTION (2 Å)
主引用文献A Highly Selective and Potent PTP-MEG2 Inhibitor with Therapeutic Potential for Type 2 Diabetes.
J.Am.Chem.Soc., 134, 2012
4GE6
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CRYSTAL STRUCTURE OF HUMAN PROTEIN TYROSINE PHOSPHATASE PTPN9 (MEG2) COMPLEX WITH COMPOUND 7
分子名称:Tyrosine-protein phosphatase non-receptor type 9, N-(4-bromo-3-methylbenzoyl)-4-[difluoro(phosphono)methyl]-L-phenylalanyl-N~5~-(3-iodobenzoyl)-L-ornithyl-3-{[(4-hydroxy-3-methoxyphenyl)acetyl]amino}-D-alaninamide
著者Zhang, Z.-Y., Liu, S., Zhang, S.
登録日2012-08-01
公開日2012-10-31
最終更新日2012-11-14
実験手法X-RAY DIFFRACTION (1.4 Å)
主引用文献A Highly Selective and Potent PTP-MEG2 Inhibitor with Therapeutic Potential for Type 2 Diabetes.
J.Am.Chem.Soc., 134, 2012