Search Count: 42
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Crystal Structure Of Lumazine Synthase From Bacillus Anthracis
Organism: Bacillus anthracis
Method: X-RAY DIFFRACTION Resolution:3.50 Å Release Date: 2014-07-09 Classification: TRANSFERASE Ligands: PO4 |
Organism: Bacillus anthracis
Method: X-RAY DIFFRACTION
Release Date: 2014-07-09
Ligands: PO4
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Crystal Structure Of A Human Valpha7.2/Vbeta13.3 Mait Tcr In Complex With Bovine Mr1
Organism: Homo sapiens, Bos taurus
Method: X-RAY DIFFRACTION Resolution:2.90 Å Release Date: 2013-10-16 Classification: IMMUNE SYSTEM Ligands: SO4 |
Organism: Homo sapiens, Bos taurus
Method: X-RAY DIFFRACTION
Release Date: 2013-10-16
Ligands: SO4
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Crystal Structure Of A Human Valpha7.2/Vbeta13.2 Mait Tcr In Complex With Bovine Mr1
Organism: Bos taurus, Homo sapiens
Method: X-RAY DIFFRACTION Resolution:3.40 Å Release Date: 2013-10-16 Classification: IMMUNE SYSTEM Ligands: SO4 |
Organism: Bos taurus, Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-10-16
Ligands: SO4
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Crystal Structure Of A Human Mait Tcr In Complex With A Bacterial Antigen Bound To Humanized Bovine Mr1
Organism: Bos taurus, Homo sapiens
Method: X-RAY DIFFRACTION Resolution:3.26 Å Release Date: 2013-10-16 Classification: IMMUNE SYSTEM Ligands: 1XL, SO4 |
Organism: Bos taurus, Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-10-16
Ligands: 1XL, SO4
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Design, Synthesis And Biological Evaluation Of Potent Quinoline And Pyrroloquinoline Ammosamide Analogues As Inhibitors For Quinone Reductase 2
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.50 Å Release Date: 2012-01-18 Classification: OXIDOREDUCTASE/INHIBITOR Ligands: ZN, FAD, 465, GOL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2012-01-18
Ligands: ZN, FAD, 465, GOL
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Design, Synthesis And Biological Evaluation Of Potetent Quinoline And Pyrroloquinoline Ammosamide Analogues As Inhibitors Of Quinone Reductase 2
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.53 Å Release Date: 2012-01-18 Classification: OXIDOREDUCTASE/INHIBITOR Ligands: ZN, FAD, UXH |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2012-01-18
Ligands: ZN, FAD, UXH
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Casimiroin Analog Inhibitor Of Quinone Reductase 2
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.57 Å Release Date: 2012-01-11 Classification: OXIDOREDUCTASE/OXIDOREDUCTASE INHIBITOR Ligands: ZN, EWQ, FAD |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2012-01-11
Ligands: ZN, EWQ, FAD
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Crystal Structure Of Hiv-1 Reverse Transcriptase (Rt) In Complex With The Non-Nucleoside Rt Inhibitor (E)-S-Methyl 5-(1-(3,7-Dimethyl-2-Oxo-2,3-Dihydrobenzo[D]Oxazol-5-Yl)-5-(5-Methyl-1,3,4-Oxadiazol-2-Yl)Pent-1-Enyl)-2-Methoxy-3-Methylbenzothioate.
Organism: Human immunodeficiency virus type 1 bh10
Method: X-RAY DIFFRACTION Resolution:2.80 Å Release Date: 2010-04-07 Classification: transferase/hydrolase Ligands: UDR |
Organism: Human immunodeficiency virus type 1 bh10
Method: X-RAY DIFFRACTION
Release Date: 2010-04-07
Ligands: UDR
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Crystal Structure Of The Hiv-1 Reverse Transcriptase (Rt) In Complex With The Alkenyldiarylmethane (Adam) Non-Nucleoside Rt Inhibitor Dimethyl 3,3'-(6-Methoxy-6-Oxohex-1-Ene-1,1-Diyl)Bis(5-Cyano-6-Methoxybenzoate).
Organism: Human immunodeficiency virus type 1 bh10
Method: X-RAY DIFFRACTION Resolution:2.55 Å Release Date: 2010-04-07 Classification: transferase/hydrolase Ligands: AC7 |
Organism: Human immunodeficiency virus type 1 bh10
Method: X-RAY DIFFRACTION
Release Date: 2010-04-07
Ligands: AC7
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Synthesis Of Casimiroin And Optimization Of Its Quinone Reductase 2 And Aromatase Inhibitory Activity
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.84 Å Release Date: 2009-03-24 Classification: OXIDOREDUCTASE Ligands: ZN, XM5, FAD |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2009-03-24
Ligands: ZN, XM5, FAD
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Synthesis Of Casimiroin And Optimization Of Its Quinone Reductase 2 And Aromatase Inhibitory Activity
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.98 Å Release Date: 2009-03-24 Classification: OXIDOREDUCTASE Ligands: MXX, FAD, ZN |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2009-03-24
Ligands: MXX, FAD, ZN
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Lumazine Synthase From Mycobacterium Tuberculosis Bound To N-6-(Ribitylamino)Pyrimidine-2,4(1H,3H)-Dione-5-Yl-Propionamide
Organism: Mycobacterium tuberculosis
Method: X-RAY DIFFRACTION Resolution:2.30 Å Release Date: 2008-04-08 Classification: TRANSFERASE Ligands: Y19, K, PO4 |
Organism: Mycobacterium tuberculosis
Method: X-RAY DIFFRACTION
Release Date: 2008-04-08
Ligands: Y19, K, PO4
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3D Structure Of Lumazine Synthase From Candida Albicans
Organism: Candida albicans
Method: X-RAY DIFFRACTION Resolution:2.50 Å Release Date: 2007-05-01 Classification: TRANSFERASE Ligands: PO4, MPD |
Organism: Candida albicans
Method: X-RAY DIFFRACTION
Release Date: 2007-05-01
Ligands: PO4, MPD
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Lumazine Synthase From Mycobacterium Tuberculosis Bound To 3-(1,3,7- Trihydro-9-D-Ribityl-2,6,8-Purinetrione-7-Yl) Pentane 1 Phosphate
Organism: Mycobacterium tuberculosis
Method: X-RAY DIFFRACTION Resolution:1.60 Å Release Date: 2006-12-13 Classification: TRANSFERASE Ligands: TP6, K, DTU, MPD |
Organism: Mycobacterium tuberculosis
Method: X-RAY DIFFRACTION
Release Date: 2006-12-13
Ligands: TP6, K, DTU, MPD
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Lumazine Synthase From Mycobacterium Tuberculosis Bound To 3-(1,3,7- Trihydro-9-D-Ribityl-2,6,8-Purinetrione-7-Yl) 1,1 Difluoropentane-1- Phosphate
Organism: Mycobacterium tuberculosis
Method: X-RAY DIFFRACTION Resolution:1.90 Å Release Date: 2006-12-13 Classification: TRANSFERASE Ligands: TSF, K |
Organism: Mycobacterium tuberculosis
Method: X-RAY DIFFRACTION
Release Date: 2006-12-13
Ligands: TSF, K
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Lumazine Synthase From Mycobacterium Tuberculosis Bound To 4-(6- Chloro-2,4-Dioxo-1,2,3,4-Tetrahydropyrimidin-5-Yl)Butyl Phosphate
Organism: Mycobacterium tuberculosis
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2006-12-13 Classification: TRANSFERASE Ligands: JCL, K, ACT, MPD, DTD |
Organism: Mycobacterium tuberculosis
Method: X-RAY DIFFRACTION
Release Date: 2006-12-13
Ligands: JCL, K, ACT, MPD, DTD
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Lumazine Synthase From Mycobacterium Tuberculosus Bound To 3-(1,3,7- Trihydro-9-D-Ribityl-2,6,8-Purinetrione-7-Yl)
Organism: Mycobacterium tuberculosis
Method: X-RAY DIFFRACTION Resolution:2.75 Å Release Date: 2006-12-13 Classification: TRANSFERASE Ligands: PUG, K, PO4, MPD |
Organism: Mycobacterium tuberculosis
Method: X-RAY DIFFRACTION
Release Date: 2006-12-13
Ligands: PUG, K, PO4, MPD
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Lumazine Synthase From Mycobacterium Tuberculosis Bound To 3-(1,3,7- Trihydro-9-D-Ribityl-2,6,8-Purinetrione-7-Yl)Hexane 1-Phosphate
Organism: Mycobacterium tuberculosis
Method: X-RAY DIFFRACTION Resolution:2.80 Å Release Date: 2006-12-13 Classification: TRANSFERASE Ligands: PHR, K, MPD |
Organism: Mycobacterium tuberculosis
Method: X-RAY DIFFRACTION
Release Date: 2006-12-13
Ligands: PHR, K, MPD
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Crystal Structure Of An Archaeal Pentameric Riboflavin Synthase
Organism: Methanocaldococcus jannaschii
Method: X-RAY DIFFRACTION Resolution:2.30 Å Release Date: 2005-11-08 Classification: TRANSFERASE |
Organism: Methanocaldococcus jannaschii
Method: X-RAY DIFFRACTION
Release Date: 2005-11-08
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Crystal Structure Of An Archaeal Pentameric Riboflavin Synthase Complex With A Substrate Analog Inhibitor
Organism: Methanocaldococcus jannaschii
Method: X-RAY DIFFRACTION Resolution:2.22 Å Release Date: 2005-11-08 Classification: TRANSFERASE Ligands: RDL |
Organism: Methanocaldococcus jannaschii
Method: X-RAY DIFFRACTION
Release Date: 2005-11-08
Ligands: RDL