Author results

1YVL
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STRUCTURE OF UNPHOSPHORYLATED STAT1
分子名称:Signal transducer and activator of transcription 1-alpha/beta, 5-residue peptide, GOLD ION
著者Mao, X., Ren, Z., Parker, G.N., Sondermann, H., Pastorello, M.A., Wang, W., McMurray, J.S., Demeler, B., Darnell Jr., J.E., Chen, X.
登録日2005-02-16
公開日2005-03-22
最終更新日2011-07-13
実験手法X-RAY DIFFRACTION (3 Å)
主引用文献Structural bases of unphosphorylated STAT1 association and receptor binding.
Mol.Cell, 17, 2005
1RDE
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NMR STRUCTURE OF THE THROMBIN-BINDING DNA APTAMER STABILIZED BY SR2+
分子名称:Thrombin-binding DNA aptamer
著者Mao, X., Marky, L.A., Gmeiner, W.H.
登録日2003-11-05
公開日2003-11-11
最終更新日2011-07-13
実験手法SOLUTION NMR
主引用文献NMR structure of the thrombin-binding DNA aptamer stabilized by Sr2+.
J.Biomol.Struct.Dyn., 22, 2004
5Z6P
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THE CRYSTAL STRUCTURE OF AN AGARASE, AGWH50C
分子名称:B-agarase
著者Mao, X., Zhou, J., Zhang, P., Zhang, L., Zhang, J., Li, Y.
登録日2018-01-24
公開日2019-01-02
最終更新日2019-03-06
実験手法X-RAY DIFFRACTION (2.061 Å)
主引用文献Structure-based design of agarase AgWH50C from Agarivorans gilvus WH0801 to enhance thermostability.
Appl. Microbiol. Biotechnol., 103, 2019
1FLI
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DNA-BINDING DOMAIN OF FLI-1
分子名称:FLI-1
著者Liang, H., Mao, X., Olejniczak, E.T., Nettesheim, D.G., Yu, L., Meadows, R.P., Thompson, C.B., Fesik, S.W.
登録日1994-09-15
公開日1995-09-15
最終更新日2011-07-13
実験手法SOLUTION NMR
主引用文献Solution structure of the ets domain of Fli-1 when bound to DNA.
Nat.Struct.Biol., 1, 1994
1GHD
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CRYSTAL STRUCTURE OF THE GLUTARYL-7-AMINOCEPHALOSPORANIC ACID ACYLASE BY MAD PHASING
分子名称:GLUTARYL-7-AMINOCEPHALOSPORANIC ACID ACYLASE
著者Ding, Y., Jiang, W., Mao, X., He, H., Zhang, S., Tang, H., Bartlam, M., Ye, S., Jiang, F., Liu, Y., Zhao, G., Rao, Z.
登録日2000-12-07
公開日2003-07-08
最終更新日2017-10-04
実験手法X-RAY DIFFRACTION (2.4 Å)
主引用文献Affinity alkylation of the Trp-B4 residue of the beta -subunit of the glutaryl 7-aminocephalosporanic acid acylase of Pseudomonas sp. 130.
J.Biol.Chem., 277, 2002
3CWG
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UNPHOSPHORYLATED MOUSE STAT3 CORE FRAGMENT
分子名称:Signal transducer and activator of transcription 3
著者Ren, Z., Mao, X., Mertens, C., Krishnaraj, R., Qin, J., Mandal, P.K., Romanowshi, M.J., McMurray, J.S.
登録日2008-04-21
公開日2008-07-01
最終更新日2011-07-13
実験手法X-RAY DIFFRACTION (3.05 Å)
主引用文献Crystal structure of unphosphorylated STAT3 core fragment.
Biochem.Biophys.Res.Commun., 374, 2008
2ELA
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CRYSTAL STRUCTURE OF THE PTB DOMAIN OF HUMAN APPL1
分子名称:Adapter protein containing PH domain, PTB domain and leucine zipper motif 1
著者Li, J., Mao, X., Dong, L.Q., Liu, F., Tong, L.
登録日2007-03-27
公開日2007-05-29
最終更新日2011-07-13
実験手法X-RAY DIFFRACTION (2 Å)
主引用文献Crystal Structures of the BAR-PH and PTB Domains of Human APPL1
Structure, 15, 2007
2ELB
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CRYSTAL STRUCTURE OF THE BAR-PH DOMAIN OF HUMAN APPL1
分子名称:Adapter protein containing PH domain, PTB domain and leucine zipper motif 1
著者Li, J., Mao, X., Dong, L.Q., Liu, F., Tong, L.
登録日2007-03-27
公開日2007-05-29
最終更新日2011-07-13
実験手法X-RAY DIFFRACTION (2.6 Å)
主引用文献Crystal Structures of the BAR-PH and PTB Domains of Human APPL1
Structure, 15, 2007
4XCH
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S-RIBOSYLHOMOCYSTEINASE FROM STREPTOCOCCUS SUIS
分子名称:S-ribosylhomocysteine lyase, ZINC ION
著者Wang, Y., Mao, X., Lu, C.
登録日2014-12-18
公開日2015-06-24
最終更新日2017-10-04
実験手法X-RAY DIFFRACTION (2.2 Å)
主引用文献Crystal Structure of LuxS from Streptococcus suis
To Be Published
5GVU
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CRYSTAL STRUCTURE OF BVDV NS3 HELICASE DOMAIN
分子名称:NS3 helicase
著者Li, S., Mao, X.
登録日2016-09-06
公開日2017-09-13
実験手法X-RAY DIFFRACTION (2.82 Å)
主引用文献crystal structure of BVDV NS3 helicase
To Be Published
5WSO
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CRYSTAL STRUCTURE OF BVDV NS3 HELICASE
分子名称:NS3 helicase
著者Li, P., Shi, J., Wang, S., Li, S., Mao, X.
登録日2016-12-08
公開日2017-12-13
実験手法X-RAY DIFFRACTION (2.82 Å)
主引用文献Crystal structure of BVDV NS3 helicase
To Be Published
2HOG
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CRYSTAL STRUCTURE OF CHEK1 IN COMPLEX WITH INHIBITOR 20
分子名称:Serine/threonine-protein kinase Chk1, (5-{3-[5-(PIPERIDIN-1-YLMETHYL)-1H-INDOL-2-YL]-1H-INDAZOL-6-YL}-2H-1,2,3-TRIAZOL-4-YL)METHANOL
著者Yan, Y., Ikuta, M.
登録日2006-07-14
公開日2007-04-24
最終更新日2011-07-13
実験手法X-RAY DIFFRACTION (1.9 Å)
主引用文献3-(Indol-2-yl)indazoles as Chek1 kinase inhibitors: Optimization of potency and selectivity via substitution at C6.
Bioorg.Med.Chem.Lett., 16, 2006
2HXL
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CRYSTAL STRUCTURE OF CHEK1 IN COMPLEX WITH INHIBITOR 1
分子名称:Serine/threonine-protein kinase Chk1, 3-(5-{[4-(AMINOMETHYL)PIPERIDIN-1-YL]METHYL}-1H-INDOL-2-YL)-1H-INDAZOLE-6-CARBONITRILE
著者Yan, Y.
登録日2006-08-03
公開日2007-06-19
最終更新日2011-07-13
実験手法X-RAY DIFFRACTION (1.8 Å)
主引用文献Development of 6-substituted indolylquinolinones as potent Chek1 kinase inhibitors.
Bioorg.Med.Chem.Lett., 16, 2006
2HXQ
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CRYSTAL STRUCTURE OF CHEK1 IN COMPLEX WITH INHIBITOR 2
分子名称:Serine/threonine-protein kinase Chk1, 3-(5-{[4-(AMINOMETHYL)PIPERIDIN-1-YL]METHYL}-1H-INDOL-2-YL)QUINOLIN-2(1H)-ONE
著者Yan, Y.
登録日2006-08-03
公開日2007-06-19
最終更新日2011-07-13
実験手法X-RAY DIFFRACTION (2 Å)
主引用文献Development of 6-substituted indolylquinolinones as potent Chek1 kinase inhibitors.
Bioorg.Med.Chem.Lett., 16, 2006
2HY0
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CRYSTAL STRUCTURE OF CHEK1 IN COMPLEX WITH INHIBITOR 22
分子名称:Serine/threonine-protein kinase Chk1, 3-[5-(PIPERIDIN-1-YLMETHYL)-1H-INDOL-2-YL]-6-(1H-PYRAZOL-4-YL)QUINOLIN-2(1H)-ONE
著者Yan, Y.
登録日2006-08-04
公開日2007-06-19
最終更新日2011-07-13
実験手法X-RAY DIFFRACTION (1.7 Å)
主引用文献Development of 6-substituted indolylquinolinones as potent Chek1 kinase inhibitors.
Bioorg.Med.Chem.Lett., 16, 2006
2LKO
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STRUCTURAL BASIS OF PHOSPHOINOSITIDE BINDING TO KINDLIN-2 PLECKSTRIN HOMOLOGY DOMAIN IN REGULATING INTEGRIN ACTIVATION
分子名称:Fermitin family homolog 2, INOSITOL-(1,3,4,5)-TETRAKISPHOSPHATE
著者Liu, J., Fukuda, K., Xu, Z.
登録日2011-10-17
公開日2011-10-26
最終更新日2011-12-28
実験手法SOLUTION NMR
主引用文献Structural basis of phosphoinositide binding to kindlin-2 protein pleckstrin homology domain in regulating integrin activation.
J.Biol.Chem., 286, 2011
2QHM
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CRYSTAL STRUCTURE OF CHEK1 IN COMPLEX WITH INHIBITOR 2A
分子名称:Serine/threonine-protein kinase Chk1, (3-ENDO)-8-METHYL-8-AZABICYCLO[3.2.1]OCT-3-YL 1H-PYRROLO[2,3-B]PYRIDINE-3-CARBOXYLATE
著者Yan, Y., Munshi, S.
登録日2007-07-02
公開日2008-03-18
最終更新日2011-07-13
実験手法X-RAY DIFFRACTION (2 Å)
主引用文献Optimization of a pyrazoloquinolinone class of Chk1 kinase inhibitors.
Bioorg.Med.Chem.Lett., 17, 2007
2QHN
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CRYSTAL STRUCTURE OF CHEK1 IN COMPLEX WITH INHIBITOR 1A
分子名称:Serine/threonine-protein kinase Chk1, 5-ETHYL-3-METHYL-1,5-DIHYDRO-4H-PYRAZOLO[4,3-C]QUINOLIN-4-ONE
著者Yan, Y., Munshi, S.
登録日2007-07-02
公開日2008-03-18
最終更新日2011-07-13
実験手法X-RAY DIFFRACTION (1.7 Å)
主引用文献Optimization of a pyrazoloquinolinone class of Chk1 kinase inhibitors.
Bioorg.Med.Chem.Lett., 17, 2007
2R0U
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CRYSTAL STRUCTURE OF CHEK1 IN COMPLEX WITH INHIBITOR 54
分子名称:Serine/threonine-protein kinase Chk1, 6-(3-aminopropyl)-4-(3-hydroxyphenyl)-9-(1H-pyrazol-4-yl)benzo[h]isoquinolin-1(2H)-one
著者Yan, Y., Ikuta, M.
登録日2007-08-21
公開日2007-10-30
最終更新日2011-07-13
実験手法X-RAY DIFFRACTION (1.9 Å)
主引用文献Synthesis and evaluation of substituted benzoisoquinolinones as potent inhibitors of Chk1 kinase.
Bioorg.Med.Chem.Lett., 17, 2007
3F9N
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CRYSTAL STRUCTURE OF CHK1 KINASE IN COMPLEX WITH INHIBITOR 38
分子名称:Serine/threonine-protein kinase Chk1, 3-(3-chlorophenyl)-2-({(1S)-1-[(6S)-2,8-diazaspiro[5.5]undec-2-ylcarbonyl]pentyl}sulfanyl)quinazolin-4(3H)-one, SULFATE ION
著者Yan, Y., Munshi, S., Ikuta, M.
登録日2008-11-14
公開日2009-01-20
最終更新日2011-07-13
実験手法X-RAY DIFFRACTION (1.9 Å)
主引用文献Development of thioquinazolinones, allosteric Chk1 kinase inhibitors.
Bioorg.Med.Chem.Lett., 19, 2009
3NCW
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CRYSTAL STRUCTURE OF EHEC O157:H7 INTIMIN
分子名称:Intimin adherence protein
著者Yi, Y., Gao, F., Gao, G.F., Zou, Q.M.
登録日2010-06-06
公開日2011-01-05
最終更新日2011-07-13
実験手法X-RAY DIFFRACTION (2.8 Å)
主引用文献Crystal Structure of EHEC Intimin: Insights into the Complementarity between EPEC and EHEC
Plos One, 5, 2010
3NCX
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CRYSTAL STRUCTURE OF EHEC O157:H7 INTIMIN MUTANT
分子名称:Intimin adherence protein
著者Yi, Y., Gao, F., Gao, G.F., Zou, Q.M.
登録日2010-06-06
公開日2011-01-05
最終更新日2011-07-13
実験手法X-RAY DIFFRACTION (2.6 Å)
主引用文献Crystal Structure of EHEC Intimin: Insights into the Complementarity between EPEC and EHEC
Plos One, 5, 2010
3SWJ
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CRYSTAL STRUCTURE OF CAMPYLOBACTER JEJUNI CHUZ
分子名称:Putative uncharacterized protein, PROTOPORPHYRIN IX CONTAINING FE, AZIDE ION
著者Hu, Y.
登録日2011-07-14
公開日2011-11-09
最終更新日2013-07-10
実験手法X-RAY DIFFRACTION (2.409 Å)
主引用文献Crystal structure of Campylobacter jejuni ChuZ: a split-barrel family heme oxygenase with a novel heme-binding mode.
Biochem.Biophys.Res.Commun., 415, 2011
4DBF
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CRYSTAL STRUCTURES OF CG1458
分子名称:2-HYDROXYHEPTA-2,4-DIENE-1,7-DIOATE ISOMERASE, MAGNESIUM ION
著者Ran, T.T., Xu, D.Q., Wang, W.W., Gao, Y.Y., Wang, M.T.
登録日2012-01-15
公開日2012-11-28
実験手法X-RAY DIFFRACTION (1.9 Å)
主引用文献Crystal structures of Cg1458 reveal a catalytic lid domain and a common catalytic mechanism for FAH family.
Biochem.J., 449, 2013
4DBH
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CRYSTAL STRUCTURE OF CG1458 WITH INHIBITOR
分子名称:2-HYDROXYHEPTA-2,4-DIENE-1,7-DIOATE ISOMERASE, MAGNESIUM ION, OXALATE ION
著者Ran, T.T., Wang, W.W., Xu, D.Q., Gao, Y.Y.
登録日2012-01-15
公開日2012-11-28
実験手法X-RAY DIFFRACTION (1.94 Å)
主引用文献Crystal structures of Cg1458 reveal a catalytic lid domain and a common catalytic mechanism for FAH family.
Biochem.J., 449, 2013
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