Author results

2LRM
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ASSIGNMENT AND STRUCTURE OF E COLI PERIPLASMIC PROTEIN YMGD
Descriptor:Uncharacterized protein ymgD
Authors:Wu, K., Inouye, M., Baum, J., Hsu, S., Masuda, H.
Deposit date:2012-04-07
Release date:2013-04-10
Method:SOLUTION NMR
Cite:Solution structure of homodimeric periplasmic protein YmgD in E. coli
To be Published
2LRV
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ASSIGNMENT OF E COLI PERIPLASMIC PROTEIN YMGD
Descriptor:Uncharacterized protein ymgD
Authors:Wu, K., Inouye, M., Baum, J., Hsu, S., Masuda, H.
Deposit date:2012-04-13
Release date:2013-04-17
Method:SOLUTION NMR
Cite:Solution structure of homodimeric periplasmic protein YmgD in E. coli
To be Published
3KBH
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CRYSTAL STRUCTURE OF NL63 RESPIRATORY CORONAVIRUS RECEPTOR-BINDING DOMAIN COMPLEXED WITH ITS HUMAN RECEPTOR
Descriptor:Angiotensin-converting enzyme 2, Spike glycoprotein, N-ACETYL-D-GLUCOSAMINE
Authors:Wu, K., Li, W., Peng, G., Li, F.
Deposit date:2009-10-20
Release date:2009-12-15
Last modified:2018-04-18
Method:X-RAY DIFFRACTION (3.31 Å)
Cite:Crystal structure of NL63 respiratory coronavirus receptor-binding domain complexed with its human receptor.
Proc.Natl.Acad.Sci.USA, 106, 2009
3SCI
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CRYSTAL STRUCTURE OF SPIKE PROTEIN RECEPTOR-BINDING DOMAIN FROM A PREDICTED SARS CORONAVIRUS HUMAN STRAIN COMPLEXED WITH HUMAN RECEPTOR ACE2
Descriptor:Angiotensin-converting enzyme 2, Spike glycoprotein, ZINC ION, ...
Authors:Wu, K., Peng, G., Wilken, M., Geraghty, R., Li, F.
Deposit date:2011-06-07
Release date:2012-02-08
Last modified:2019-07-17
Method:X-RAY DIFFRACTION (2.9 Å)
Cite:SARS coronavirus: mechanism of host receptor adaptation and rational prediction of future evolution
To be Published
3SCJ
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CRYSTAL STRUCTURE OF SPIKE PROTEIN RECEPTOR-BINDING DOMAIN FROM A PREDICTED SARS CORONAVIRUS CIVET STRAIN COMPLEXED WITH HUMAN RECEPTOR ACE2
Descriptor:Angiotensin-converting enzyme 2, Spike glycoprotein, ZINC ION, ...
Authors:Wu, K., Peng, G., Wilken, M., Geraghty, R., Li, F.
Deposit date:2011-06-07
Release date:2012-02-08
Last modified:2019-07-17
Method:X-RAY DIFFRACTION (3 Å)
Cite:SARS coronavirus: mechanism of host receptor adaptation and rational prediction of future evolution
To be Published
3SCK
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CRYSTAL STRUCTURE OF SPIKE PROTEIN RECEPTOR-BINDING DOMAIN FROM A PREDICTED SARS CORONAVIRUS CIVET STRAIN COMPLEXED WITH HUMAN-CIVET CHIMERIC RECEPTOR ACE2
Descriptor:Angiotensin-converting enzyme 2 chimera, Spike glycoprotein, ZINC ION, ...
Authors:Wu, K., Peng, G., Wilken, M., Geraghty, R., Li, F.
Deposit date:2011-06-07
Release date:2012-02-08
Last modified:2019-07-17
Method:X-RAY DIFFRACTION (3 Å)
Cite:SARS coronavirus: mechanism of host receptor adaptation and rational prediction of future evolution
To be Published
3SCL
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CRYSTAL STRUCTURE OF SPIKE PROTEIN RECEPTOR-BINDING DOMAIN FROM SARS CORONAVIRUS EPIDEMIC STRAIN COMPLEXED WITH HUMAN-CIVET CHIMERIC RECEPTOR ACE2
Descriptor:Angiotensin-converting enzyme 2 chimera, Spike glycoprotein, ZINC ION, ...
Authors:Wu, K., Peng, G., Wilken, M., Geraghty, R., Li, F.
Deposit date:2011-06-07
Release date:2012-02-08
Last modified:2019-07-17
Method:X-RAY DIFFRACTION (3 Å)
Cite:SARS coronavirus: mechanism of host receptor adaptation and rational prediction of future evolution
To be Published
2L26
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RV0899 FROM MYCOBACTERIUM TUBERCULOSIS CONTAINS TWO SEPARATED DOMAINS
Descriptor:Uncharacterized protein Rv0899/MT0922
Authors:Shi, C., Li, J., Gao, Y., Wu, K., Huang, H., Tian, C.
Deposit date:2010-08-12
Release date:2011-08-17
Last modified:2011-12-07
Method:SOLUTION NMR
Cite:Structural Studies of Mycobacterium tuberculosis Rv0899 Reveal a Monomeric Membrane-Anchoring Protein with Two Separate Domains
J.Mol.Biol., 2011
1WD2
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SOLUTION STRUCTURE OF THE C-TERMINAL RING FROM A RING-IBR-RING (TRIAD) MOTIF
Descriptor:Ariadne-1 protein homolog, ZINC ION
Authors:Capili, A.D., Edghill, E.L., Wu, K., Borden, K.L.B.
Deposit date:2004-05-11
Release date:2004-07-20
Last modified:2011-07-13
Method:SOLUTION NMR
Cite:Structure of the C-terminal RING Finger from a RING-IBR-RING/TRIAD Motif Reveals a Novel Zinc-binding Domain Distinct from a RING
J.Mol.Biol., 340, 2004
1XT9
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CRYSTAL STRUCTURE OF DEN1 IN COMPLEX WITH NEDD8
Descriptor:Sentrin-specific protease 8, Neddylin
Authors:Reverter, D., Wu, K., Erdene, T.G., Pan, Z.Q., Wilkinson, K.D., Lima, C.D.
Deposit date:2004-10-21
Release date:2004-12-21
Last modified:2011-07-13
Method:X-RAY DIFFRACTION (2.2 Å)
Cite:Structure of a Complex between Nedd8 and the Ulp/Senp Protease Family Member Den1.
J.Mol.Biol., 345, 2005
5Z10
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STRUCTURE OF THE MECHANOSENSITIVE PIEZO1 CHANNEL
Descriptor:Piezo-type mechanosensitive ion channel component 1
Authors:Zhao, Q., Zhou, H., Chi, S., Wang, Y., Wang, J., Geng, J., Wu, K., Liu, W., Zhang, T., Dong, M.-Q., Wang, J., Li, X., Xiao, B.
Deposit date:2017-12-22
Release date:2018-01-31
Last modified:2018-03-07
Method:ELECTRON MICROSCOPY (3.97 Å)
Cite:Structure and mechanogating mechanism of the Piezo1 channel.
Nature, 554, 2018
6AGF
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STRUCTURE OF THE HUMAN VOLTAGE-GATED SODIUM CHANNEL NAV1.4 IN COMPLEX WITH BETA1
Descriptor:Sodium channel protein type 4 subunit alpha, Sodium channel subunit beta-1, N-ACETYL-D-GLUCOSAMINE, ...
Authors:Pan, X.J., li, Z.Q., Zhou, Q., Shen, H.Z., Wu, K., Huang, X.S., Chen, J.F., Zhang, J.R., Zhu, X.C., Lei, J.L., Xiong, W., Gong, H.P., Xiao, B.L., Yan, N.
Deposit date:2018-08-11
Release date:2018-10-10
Last modified:2018-12-26
Method:ELECTRON MICROSCOPY (3.2 Å)
Cite:Structure of the human voltage-gated sodium channel Nav1.4 in complex with beta 1.
Science, 362, 2018
4GG5
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CRYSTAL STRUCTURE OF CMET IN COMPLEX WITH NOVEL INHIBITOR
Descriptor:Hepatocyte growth factor receptor, 3-(4-methylpiperazin-1-yl)-N-(3-nitrobenzyl)-7-(trifluoromethyl)quinolin-5-amine
Authors:Liu, Q.F., Chen, T.T., Xu, Y.C.
Deposit date:2012-08-05
Release date:2012-10-03
Last modified:2012-10-17
Method:X-RAY DIFFRACTION (2.423 Å)
Cite:Multisubstituted quinoxalines and pyrido[2,3-d]pyrimidines: Synthesis and SAR study as tyrosine kinase c-Met inhibitors.
Bioorg.Med.Chem.Lett., 22, 2012
4GG7
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CRYSTAL STRUCTURE OF CMET IN COMPLEX WITH NOVEL INHIBITOR
Descriptor:Hepatocyte growth factor receptor, N-(3-nitrobenzyl)-6-[1-(piperidin-4-yl)-1H-pyrazol-4-yl]-2-(trifluoromethyl)pyrido[2,3-d]pyrimidin-4-amine
Authors:Liu, Q.F., Chen, T.T., Xu, Y.C.
Deposit date:2012-08-06
Release date:2012-10-03
Last modified:2012-10-17
Method:X-RAY DIFFRACTION (2.27 Å)
Cite:Multisubstituted quinoxalines and pyrido[2,3-d]pyrimidines: Synthesis and SAR study as tyrosine kinase c-Met inhibitors.
Bioorg.Med.Chem.Lett., 22, 2012
4G6G
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CRYSTAL STRUCTURE OF NDH WITH TRT
Descriptor:Rotenone-insensitive NADH-ubiquinone oxidoreductase, mitochondrial, FRAGMENT OF TRITON X-100, ...
Authors:Li, W., Feng, Y., Ge, J., Yang, M.
Deposit date:2012-07-19
Release date:2012-10-24
Last modified:2012-12-05
Method:X-RAY DIFFRACTION (2.39 Å)
Cite:Structural insight into the type-II mitochondrial NADH dehydrogenases.
Nature, 491, 2012
4G6H
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CRYSTAL STRUCTURE OF NDH WITH NADH
Descriptor:Rotenone-insensitive NADH-ubiquinone oxidoreductase, mitochondrial, FLAVIN-ADENINE DINUCLEOTIDE, ...
Authors:Li, W., Feng, Y., Ge, J., Yang, M.
Deposit date:2012-07-19
Release date:2012-10-24
Last modified:2013-11-06
Method:X-RAY DIFFRACTION (2.262 Å)
Cite:Structural insight into the type-II mitochondrial NADH dehydrogenases.
Nature, 491, 2012
4G73
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CRYSTAL STRUCTURE OF NDH WITH NADH AND QUINONE
Descriptor:Rotenone-insensitive NADH-ubiquinone oxidoreductase, mitochondrial, 2,3-DIMETHOXY-5-METHYL-6-(3,11,15,19-TETRAMETHYL-EICOSA-2,6,10,14,18-PENTAENYL)-[1,4]BENZOQUINONE, ...
Authors:Li, W., Feng, Y., Ge, J., Yang, M.
Deposit date:2012-07-19
Release date:2012-10-24
Last modified:2013-11-06
Method:X-RAY DIFFRACTION (2.522 Å)
Cite:Structural insight into the type-II mitochondrial NADH dehydrogenases.
Nature, 491, 2012
4G74
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CRYSTAL STRUCTURE OF NDH WITH QUINONE
Descriptor:Rotenone-insensitive NADH-ubiquinone oxidoreductase, mitochondrial, 2,3-DIMETHOXY-5-METHYL-6-(3,11,15,19-TETRAMETHYL-EICOSA-2,6,10,14,18-PENTAENYL)-[1,4]BENZOQUINONE, ...
Authors:Li, W., Feng, Y., Ge, J., Yang, M.
Deposit date:2012-07-19
Release date:2012-10-24
Last modified:2012-12-05
Method:X-RAY DIFFRACTION (2.48 Å)
Cite:Structural insight into the type-II mitochondrial NADH dehydrogenases.
Nature, 491, 2012
5C5S
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CRYSTAL STRUCTURE OF HUMAN MYOSIN 9B RHOGAP DOMAIN AT 2.2 ANGSTROM
Descriptor:Unconventional myosin-IXb
Authors:Yi, F.S., Ren, J.Q., Feng, W.
Deposit date:2015-06-22
Release date:2015-11-25
Last modified:2016-02-17
Method:X-RAY DIFFRACTION (2.2 Å)
Cite:Myo9b is a key player in SLIT/ROBO-mediated lung tumor suppression
J.Clin.Invest., 125, 2015
2LGV
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RBX1
Descriptor:E3 ubiquitin-protein ligase RBX1, ZINC ION
Authors:Spratt, D.E., Shaw, G.S.
Deposit date:2011-08-02
Release date:2012-03-28
Last modified:2012-06-06
Method:SOLUTION NMR
Cite:Selective recruitment of an e2~ubiquitin complex by an e3 ubiquitin ligase.
J.Biol.Chem., 287, 2012
3H6F
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CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS PROTEASOME MODIFIED BY INHIBITOR HT1171
Descriptor:Proteasome (Alpha subunit) PrcA, Proteasome (Beta subunit) PrcB, DIMETHYLFORMAMIDE
Authors:Li, D., Li, H., Lin, G.
Deposit date:2009-04-23
Release date:2009-09-15
Last modified:2011-07-13
Method:X-RAY DIFFRACTION (2.51 Å)
Cite:Inhibitors selective for mycobacterial versus human proteasomes.
Nature, 461, 2009
3H6I
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CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS PROTEASOME MODIFIED BY INHIBITOR GL1
Descriptor:Proteasome (Alpha subunit) PrcA, Proteasome (Beta subunit) PrcB, DIMETHYLFORMAMIDE
Authors:Li, D., Li, H., Lin, G.
Deposit date:2009-04-23
Release date:2009-09-15
Last modified:2011-07-13
Method:X-RAY DIFFRACTION (2.43 Å)
Cite:Inhibitors selective for mycobacterial versus human proteasomes.
Nature, 461, 2009
3HF9
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CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS PROTEASOME OPEN-GATE MUTANT MODIFIED BY INHIBITOR GL1
Descriptor:Proteasome (Alpha subunit) PrcA, Proteasome (Beta subunit) PrcB
Authors:Li, D., Li, H.
Deposit date:2009-05-11
Release date:2009-09-15
Last modified:2019-07-24
Method:X-RAY DIFFRACTION (2.878 Å)
Cite:Inhibitors selective for mycobacterial versus human proteasomes.
Nature, 461, 2009
3HFA
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CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS PROTEASOME OPEN-GATE MUTANT
Descriptor:Proteasome (Beta subunit) PrcB, Proteasome (Alpha subunit) PrcA, DIMETHYLFORMAMIDE
Authors:Li, D., Li, H.
Deposit date:2009-05-11
Release date:2009-09-15
Last modified:2019-07-24
Method:X-RAY DIFFRACTION (2.504 Å)
Cite:Inhibitors selective for mycobacterial versus human proteasomes.
Nature, 461, 2009
5UR5
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PYR1 BOUND TO THE RATIONALLY DESIGNED AGONIST 4M
Descriptor:Abscisic acid receptor PYR1, SULFATE ION, N-(4-cyano-3-ethyl-5-methylphenyl)-1-(4-methylphenyl)methanesulfonamide, ...
Authors:Peterson, F.C., Vaidya, A., Jensen, D.R., Volkman, B.F., Cutler, S.R.
Deposit date:2017-02-09
Release date:2017-11-29
Method:X-RAY DIFFRACTION (1.93 Å)
Cite:A Rationally Designed Agonist Defines Subfamily IIIA Abscisic Acid Receptors As Critical Targets for Manipulating Transpiration.
ACS Chem. Biol., 12, 2017
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