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The Open Protein Structure Annotation Network
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2och

    Table of contents
    1. 1. Protein Summary
    2. 2. Ligand Summary

    Title X-ray crystal structure of J-domain of dnj-12 from Caenorhabditis elegans. To be Published
    Site MCSG
    PDB Id 2och Target Id
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    Molecular Characteristics
    Source
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    Alias Ids
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    TPS5961,O45502, 6239
    Molecular Weight
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    Da.
    Residues
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    Isoelectric Point
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    Sequence
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      BLAST   FFAS

    Structure Determination
    Method XRAY
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    Chains 1
    Resolution (Å)
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    Rfree
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    Matthews' coefficent 2.50 Rfactor 0.2191
    Waters
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    Solvent Content 50.83

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    Ligand Information
    Ligands
    Metals

    Jmol

     
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    Google Scholar output for 2och
    1. Synthesis and biological evaluation of chromium bioorganometallics based on the antibiotic platensimycin lead structure
    M Patra, G Gasser, A Pinto, K Merz, I Ott - , 2009 - Wiley Online Library
     
    2. Synthesis and biological evaluation of pyrazole derivatives containing thiourea skeleton as anticancer agents
    PC Lv, HQ Li, J Sun, Y Zhou, HL Zhu - Bioorganic & medicinal chemistry, 2010 - Elsevier
     
    3. Synthesis, molecular modeling studies, and selective inhibitory activity against monoamine oxidase of N, N_-bis [2-oxo-2 H-benzopyran]-3-
    F Chimenti, D Secci, A Bolasco, P Chimenti - Bioorganic & medicinal , 2006 - Elsevier
     
    4. Synthesis and biological evaluation of N-substituted-3, 5-diphenyl-2-pyrazoline derivatives as cyclooxygenase (COX-2) inhibitors
    R Fioravanti, A Bolasco, F Manna, F Rossi - European journal of , 2010 - Elsevier
     
    5. Virtual screening and synthesis of quinazolines as novel JAK2 inhibitors
    SH Yang, DB Khadka, SH Cho, HK Ju, KY Lee - Bioorganic & Medicinal , 2011 - Elsevier
     
    6. Peroxidase-like activity of Thermobifida fusca hemoglobin: The oxidation of dibenzylbutanolide
    R Torge, A Comandini, B Catacchio - Journal of Molecular , 2009 - Elsevier
     
    7. Homoisoflavonoids: natural scaffolds with potent and selective monoamine oxidase-B inhibition properties
    N Desideri, A Bolasco, R Fioravanti - Journal of Medicinal , 2011 - ACS Publications
     
    8. A convenient synthesis and molecular modeling study of novel purine and pyrimidine derivatives as CDK2/cyclin A3 inhibitors
    ASS Hamad Elgazwy, NSM Ismail - Bioorganic & medicinal , 2010 - Elsevier
     
    9. Synthesis of chromeno [3, 4- b] indoles as Lamellarin D analogues: A novel DYRK1A inhibitor class
    C Neagoie, E Vedrenne, F Buron, JY Mrour - European Journal of , 2012 - Elsevier
     
    10. Chiral 1, 5-disubstituted 1, 3, 5-hexahydrotriazine-2- N-nitroimine analogues as novel potent neonicotinoids: Synthesis, insecticidal evaluation and molecular
    C Sun, J Zhu, H Wang, J Jin, J Xing, D Yang - European journal of , 2011 - Elsevier
     
    11. Potent Clicked MMP2 Inhibitors: Synthesis, Molecular Modeling and Biological Exploration
    JM Zapico, P Serra, J Garca-Sanmartn, K Filipiak - Org. Biomol. , 2011 - xlink.rsc.org
     
    12. Mutants of glycoside hydrolases and uses thereof for synthesizing complex oligosaccharides and disaccharide intermediates
    L Mulard, I Andre, E Champion, C Moulis - EP Patent , 2009 - freepatentsonline.com
     

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    Protein Summary


    Ligand Summary

    Reviews

    References

     

    No references found.

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