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5ZGM
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CRYSTAL STRUCTURE OF PARVALBUMIN SPVI, THE MAJOR ALLERGENS IN MUSTELUS GRISEUS
Descriptor:Parvalbumin SPVI, CALCIUM ION, SULFATE ION
Authors:Yang, R.Q., Chen, Y.L., Jin, T.C., Cao, M.J.
Deposit date:2018-03-09
Release date:2018-08-01
Last modified:2018-08-08
Method:X-RAY DIFFRACTION (1.399 Å)
Cite:Purification, Characterization, and Crystal Structure of Parvalbumins, the Major Allergens in Mustelus griseus.
J. Agric. Food Chem., 66, 2018
5ZH6
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CRYSTAL STRUCTURE OF PARVALBUMIN SPV-II OF MUSTELUS GRISEUS
Descriptor:Parvalbumin SPV-II, CALCIUM ION, SULFATE ION
Authors:Yang, R.Q., Chen, Y.L., Jin, T.C., Cao, M.J.
Deposit date:2018-03-11
Release date:2018-08-01
Last modified:2019-08-28
Method:X-RAY DIFFRACTION (1.54 Å)
Cite:Purification, Characterization, and Crystal Structure of Parvalbumins, the Major Allergens in Mustelus griseus.
J. Agric. Food Chem., 66, 2018
2J7U
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DENGUE VIRUS NS5 RNA DEPENDENT RNA POLYMERASE DOMAIN
Descriptor:RNA DEPENDENT RNA POLYMERASE, ZINC ION, MAGNESIUM ION, ...
Authors:Yap, T.L., Xu, T., Chen, Y.L., Malet, H., Egloff, M.P., Canard, B., Vasudevan, S.G., Lescar, J.
Deposit date:2006-10-17
Release date:2007-03-13
Last modified:2011-07-13
Method:X-RAY DIFFRACTION (1.85 Å)
Cite:Crystal Structure of the Dengue Virus RNA- Dependent RNA Polymerase Catalytic Domain at 1.85 Angstrom Resolution.
J.Virol., 81, 2007
2J7W
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DENGUE VIRUS NS5 RNA DEPENDENT RNA POLYMERASE DOMAIN COMPLEXED WITH 3' DGTP
Descriptor:POLYPROTEIN, ZINC ION, GUANOSINE-5'-TRIPHOSPHATE, ...
Authors:Yap, T.L., Xu, T., Chen, Y.L., Malet, H., Egloff, M.P., Canard, B., Vasudevan, S.G., Lescar, J.
Deposit date:2006-10-17
Release date:2007-03-13
Last modified:2011-07-13
Method:X-RAY DIFFRACTION (2.6 Å)
Cite:Crystal Structure of the Dengue Virus RNA- Dependent RNA Polymerase Catalytic Domain at 1.85 Angstrom Resolution.
J.Virol., 81, 2007
3PB4
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CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF HUMAN GOLGI-RESIDENT GLUTAMINYL CYCLASE AT PH 6.0
Descriptor:Glutaminyl-peptide cyclotransferase-like protein, ZINC ION
Authors:Huang, K.F., Liaw, S.S., Huang, W.L., Chia, C.Y., Lo, Y.C., Chen, Y.L., Wang, A.H.J.
Deposit date:2010-10-20
Release date:2011-02-02
Last modified:2011-08-03
Method:X-RAY DIFFRACTION (1.13 Å)
Cite:Structures of human Golgi-resident glutaminyl cyclase and its complexes with inhibitors reveal a large loop movement upon inhibitor binding
J.Biol.Chem., 286, 2011
3PB6
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CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF HUMAN GOLGI-RESIDENT GLUTAMINYL CYCLASE AT PH 6.5
Descriptor:Glutaminyl-peptide cyclotransferase-like protein, CACODYLATE ION, ZINC ION
Authors:Huang, K.F., Liaw, S.S., Huang, W.L., Chia, C.Y., Lo, Y.C., Chen, Y.L., Wang, A.H.J.
Deposit date:2010-10-20
Release date:2011-02-02
Last modified:2011-08-03
Method:X-RAY DIFFRACTION (1.05 Å)
Cite:Structures of human Golgi-resident glutaminyl cyclase and its complexes with inhibitors reveal a large loop movement upon inhibitor binding
J.Biol.Chem., 286, 2011
3PB7
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CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF HUMAN GOLGI-RESIDENT GLUTAMINYL CYCLASE IN COMPLEX WITH PBD150
Descriptor:Glutaminyl-peptide cyclotransferase-like protein, 1-(3,4-dimethoxyphenyl)-3-[3-(1H-imidazol-1-yl)propyl]thiourea, ZINC ION
Authors:Huang, K.F., Liaw, S.S., Huang, W.L., Chia, C.Y., Lo, Y.C., Chen, Y.L., Wang, A.H.J.
Deposit date:2010-10-20
Release date:2011-02-02
Last modified:2011-08-03
Method:X-RAY DIFFRACTION (1.4 Å)
Cite:Structures of human Golgi-resident glutaminyl cyclase and its complexes with inhibitors reveal a large loop movement upon inhibitor binding
J.Biol.Chem., 286, 2011
3PB8
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CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF HUMAN GOLGI-RESIDENT GLUTAMINYL CYCLASE IN COMPLEX WITH N-ACETYLHISTAMINE
Descriptor:Glutaminyl-peptide cyclotransferase-like protein, N-[2-(1H-IMIDAZOL-4-YL)ETHYL]ACETAMIDE, ZINC ION
Authors:Huang, K.F., Liaw, S.S., Huang, W.L., Chia, C.Y., Lo, Y.C., Chen, Y.L., Wang, A.H.J.
Deposit date:2010-10-20
Release date:2011-02-02
Last modified:2011-08-03
Method:X-RAY DIFFRACTION (1.13 Å)
Cite:Structures of human Golgi-resident glutaminyl cyclase and its complexes with inhibitors reveal a large loop movement upon inhibitor binding
J.Biol.Chem., 286, 2011
3PB9
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CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF HUMAN GOLGI-RESIDENT GLUTAMINYL CYCLASE IN COMPLEX WITH 1-BENZYLIMIDAZOLE
Descriptor:Glutaminyl-peptide cyclotransferase-like protein, 1-BENZYL-1H-IMIDAZOLE, ZINC ION
Authors:Huang, K.F., Liaw, S.S., Huang, W.L., Chia, C.Y., Lo, Y.C., Chen, Y.L., Wang, A.H.J.
Deposit date:2010-10-20
Release date:2011-02-02
Last modified:2011-08-03
Method:X-RAY DIFFRACTION (1.12 Å)
Cite:Structures of human Golgi-resident glutaminyl cyclase and its complexes with inhibitors reveal a large loop movement upon inhibitor binding
J.Biol.Chem., 286, 2011
3PBB
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CRYSTAL STRUCTURE OF HUMAN SECRETORY GLUTAMINYL CYCLASE IN COMPLEX WITH PBD150
Descriptor:Glutaminyl-peptide cyclotransferase, 1-(3,4-dimethoxyphenyl)-3-[3-(1H-imidazol-1-yl)propyl]thiourea, ZINC ION
Authors:Huang, K.F., Liaw, S.S., Huang, W.L., Chia, C.Y., Lo, Y.C., Chen, Y.L., Wang, A.H.J.
Deposit date:2010-10-20
Release date:2011-02-02
Last modified:2011-08-03
Method:X-RAY DIFFRACTION (1.95 Å)
Cite:Structures of human Golgi-resident glutaminyl cyclase and its complexes with inhibitors reveal a large loop movement upon inhibitor binding
J.Biol.Chem., 286, 2011
3PBE
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CRYSTAL STRUCTURE OF THE MUTANT W207F OF HUMAN SECRETORY GLUTAMINYL CYCLASE
Descriptor:Glutaminyl-peptide cyclotransferase, ZINC ION, SULFATE ION
Authors:Huang, K.F., Liaw, S.S., Huang, W.L., Chia, C.Y., Lo, Y.C., Chen, Y.L., Wang, A.H.J.
Deposit date:2010-10-20
Release date:2011-02-02
Last modified:2011-08-03
Method:X-RAY DIFFRACTION (1.95 Å)
Cite:Structures of human Golgi-resident glutaminyl cyclase and its complexes with inhibitors reveal a large loop movement upon inhibitor binding
J.Biol.Chem., 286, 2011
4QR3
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BRD4 BROMODOMAIN 1 COMPLEX WITH ITS NOVEL INHIBITORS
Descriptor:Bromodomain-containing protein 4, N-cyclopentyl-3-(2-oxo-2,3-dihydro-1,3-thiazol-4-yl)benzenesulfonamide
Authors:Xiong, B., Cao, D.Y., Chen, T.T., Xu, Y.C.
Deposit date:2014-06-30
Release date:2015-07-01
Method:X-RAY DIFFRACTION (1.374 Å)
Cite:Fragment-based drug discovery of 2-thiazolidinones as BRD4 inhibitors: 2. Structure-based optimization
J.Med.Chem., 58, 2015
4QR4
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BRD4 BROMODOMAIN 1 COMPLEX WITH ITS NOVEL INHIBITORS
Descriptor:Bromodomain-containing protein 4, 2-chloro-N-cyclopentyl-5-(2-oxo-2,3-dihydro-1,3-thiazol-4-yl)benzenesulfonamide
Authors:Xiong, B., Cao, D.Y., Chen, T.T., Xu, Y.C.
Deposit date:2014-06-30
Release date:2015-07-01
Method:X-RAY DIFFRACTION (1.28 Å)
Cite:Fragment-based drug discovery of 2-thiazolidinones as BRD4 inhibitors: 2. Structure-based optimization
J.Med.Chem., 58, 2015
4QR5
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BRD4 BROMODOMAIN 1 COMPLEX WITH ITS NOVEL INHIBITORS
Descriptor:Bromodomain-containing protein 4, N-[3-(cyclopentylsulfamoyl)-5-(2-oxo-2,3-dihydro-1,3-thiazol-4-yl)phenyl]cyclopropanecarboxamide
Authors:Xiong, B., Cao, D.Y., Chen, T.T., Xu, Y.C.
Deposit date:2014-06-30
Release date:2015-07-01
Method:X-RAY DIFFRACTION (1.41 Å)
Cite:Fragment-based drug discovery of 2-thiazolidinones as BRD4 inhibitors: 2. Structure-based optimization
J.Med.Chem., 58, 2015
4OEA
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CRYSTAL STRUCTURE OF AR-LBD
Descriptor:Androgen receptor, 5-ALPHA-DIHYDROTESTOSTERONE
Authors:Liu, J.S., Hsu, C.L., Wu, W.G.
Deposit date:2014-01-12
Release date:2014-08-20
Last modified:2014-12-24
Method:X-RAY DIFFRACTION (2.12 Å)
Cite:Identification of a new androgen receptor (AR) co-regulator BUD31 and related peptides to suppress wild-type and mutated AR-mediated prostate cancer growth via peptide screening and X-ray structure analysis.
Mol Oncol, 8, 2014
4OED
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CRYSTAL STRUCTURE OF AR-LBD BOUND WITH CO-REGULATOR PEPTIDE
Descriptor:Androgen receptor, Protein BUD31 homolog, SULFATE ION, ...
Authors:Liu, J.S., Hsu, C.L., Wu, W.G.
Deposit date:2014-01-13
Release date:2014-08-20
Last modified:2014-12-24
Method:X-RAY DIFFRACTION (2.79 Å)
Cite:Identification of a new androgen receptor (AR) co-regulator BUD31 and related peptides to suppress wild-type and mutated AR-mediated prostate cancer growth via peptide screening and X-ray structure analysis.
Mol Oncol, 8, 2014
4OEY
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CRYSTAL STRUCTURE OF AR-LBD BOUND WITH CO-REGULATOR PEPTIDE
Descriptor:Androgen receptor, co-regulator peptide, SULFATE ION, ...
Authors:Liu, J.S., Hsu, C.L., Wu, W.G.
Deposit date:2014-01-14
Release date:2014-08-20
Last modified:2014-12-24
Method:X-RAY DIFFRACTION (1.83 Å)
Cite:Identification of a new androgen receptor (AR) co-regulator BUD31 and related peptides to suppress wild-type and mutated AR-mediated prostate cancer growth via peptide screening and X-ray structure analysis.
Mol Oncol, 8, 2014
4OEZ
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CRYSTAL STRUCTURE OF AR-LBD BOUND WITH CO-REGULATOR PEPTIDE
Descriptor:Androgen receptor, co-regulator peptide, SULFATE ION, ...
Authors:Liu, J.S., Hsu, C.L., Wu, W.G.
Deposit date:2014-01-14
Release date:2014-08-20
Last modified:2014-12-24
Method:X-RAY DIFFRACTION (1.8 Å)
Cite:Identification of a new androgen receptor (AR) co-regulator BUD31 and related peptides to suppress wild-type and mutated AR-mediated prostate cancer growth via peptide screening and X-ray structure analysis.
Mol Oncol, 8, 2014
4OFR
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CRYSTAL STRUCTURE OF AR-LBD BOUND WITH CO-REGULATOR PEPTIDE
Descriptor:Androgen receptor, co-regulator peptide, 5-ALPHA-DIHYDROTESTOSTERONE
Authors:Liu, J.S., Hsu, C.L., Wu, W.G.
Deposit date:2014-01-15
Release date:2014-08-20
Last modified:2014-12-24
Method:X-RAY DIFFRACTION (2.26 Å)
Cite:Identification of a new androgen receptor (AR) co-regulator BUD31 and related peptides to suppress wild-type and mutated AR-mediated prostate cancer growth via peptide screening and X-ray structure analysis.
Mol Oncol, 8, 2014
4OFU
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CRYSTAL STRUCTURE OF AR-LBD BOUND WITH CO-REGULATOR PEPTIDE
Descriptor:Androgen receptor, co-regulator peptide, 5-ALPHA-DIHYDROTESTOSTERONE
Authors:Liu, J.S., Hsu, C.L., Wu, W.G.
Deposit date:2014-01-15
Release date:2014-08-20
Last modified:2014-12-24
Method:X-RAY DIFFRACTION (2.12 Å)
Cite:Identification of a new androgen receptor (AR) co-regulator BUD31 and related peptides to suppress wild-type and mutated AR-mediated prostate cancer growth via peptide screening and X-ray structure analysis.
Mol Oncol, 8, 2014
4OGH
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CRYSTAL STRUCTURE OF T877A-AR-LBD
Descriptor:Androgen receptor, HYDROXYFLUTAMIDE, SULFATE ION
Authors:Liu, J.S., Hsu, C.L., Wu, W.G.
Deposit date:2014-01-16
Release date:2014-08-20
Last modified:2014-12-24
Method:X-RAY DIFFRACTION (2.98 Å)
Cite:Identification of a new androgen receptor (AR) co-regulator BUD31 and related peptides to suppress wild-type and mutated AR-mediated prostate cancer growth via peptide screening and X-ray structure analysis.
Mol Oncol, 8, 2014
4OH5
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CRYSTAL STRUCTURE OF T877A-AR-LBD BOUND WITH CO-REGULATOR PEPTIDE
Descriptor:Androgen receptor, co-regulator peptide, HYDROXYFLUTAMIDE, ...
Authors:Liu, J.S., Hsu, C.L., Wu, W.G.
Deposit date:2014-01-17
Release date:2014-08-20
Last modified:2014-12-24
Method:X-RAY DIFFRACTION (2 Å)
Cite:Identification of a new androgen receptor (AR) co-regulator BUD31 and related peptides to suppress wild-type and mutated AR-mediated prostate cancer growth via peptide screening and X-ray structure analysis.
Mol Oncol, 8, 2014
4OH6
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CRYSTAL STRUCTURE OF T877A-AR-LBD BOUND WITH CO-REGULATOR PEPTIDE
Descriptor:Androgen receptor, Protein BUD31 homolog, HYDROXYFLUTAMIDE, ...
Authors:Liu, J.S., Hsu, C.L., Wu, W.G.
Deposit date:2014-01-17
Release date:2014-08-20
Last modified:2014-12-24
Method:X-RAY DIFFRACTION (3.56 Å)
Cite:Identification of a new androgen receptor (AR) co-regulator BUD31 and related peptides to suppress wild-type and mutated AR-mediated prostate cancer growth via peptide screening and X-ray structure analysis.
Mol Oncol, 8, 2014
4OHA
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CRYSTAL STRUCTURE OF T877A-AR-LBD BOUND WITH CO-REGULATOR PEPTIDE
Descriptor:Androgen receptor, co-regulator peptide, HYDROXYFLUTAMIDE, ...
Authors:Liu, J.S., Hsu, C.L., Wu, W.G.
Deposit date:2014-01-17
Release date:2014-08-20
Last modified:2014-12-24
Method:X-RAY DIFFRACTION (1.42 Å)
Cite:Identification of a new androgen receptor (AR) co-regulator BUD31 and related peptides to suppress wild-type and mutated AR-mediated prostate cancer growth via peptide screening and X-ray structure analysis.
Mol Oncol, 8, 2014
4OIL
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CRYSTAL STRUCTURE OF T877A-AR-LBD BOUND WITH CO-REGULATOR PEPTIDE
Descriptor:Androgen receptor, co-regulator peptide, HYDROXYFLUTAMIDE
Authors:Liu, J.S., Hsu, C.L., Wu, W.G.
Deposit date:2014-01-19
Release date:2014-08-20
Last modified:2014-12-24
Method:X-RAY DIFFRACTION (2.51 Å)
Cite:Identification of a new androgen receptor (AR) co-regulator BUD31 and related peptides to suppress wild-type and mutated AR-mediated prostate cancer growth via peptide screening and X-ray structure analysis.
Mol Oncol, 8, 2014
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