Search Results - "Coll, Joyce T"

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  1. 1

    Crystal Structure of the Ectodomain Complex of the CGRP Receptor, a Class-B GPCR, Reveals the Site of Drug Antagonism by ter Haar, Ernst, Koth, Christopher M., Abdul-Manan, Norzehan, Swenson, Lora, Coll, Joyce T., Lippke, Judith A., Lepre, Christopher A., Garcia-Guzman, Miguel, Moore, Jonathan M.

    Published in Structure (London) (01-09-2010)
    “…Dysregulation of the calcitonin gene-related peptide (CGRP), a potent vasodilator, is directly implicated in the pathogenesis of migraine. CGRP binds to and…”
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  2. 2
  3. 3

    Crystal Structure of Aurora-2, an Oncogenic Serine/Threonine Kinase by Cheetham, Graham M T, Knegtel, Ronald M A, Coll, Joyce T, Renwick, Suzanne B, Swenson, Lora, Weber, Peter, Lippke, Judith A, Austen, Douglas A

    Published in The Journal of biological chemistry (08-11-2002)
    “…Aurora-2 is a key member of a closely related subgroup of serine/threonine kinases that plays important roles in the completion of essential mitotic events…”
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  4. 4

    Crystal structure of JNK3: a kinase implicated in neuronal apoptosis by Xie, Xiaoling, Gu, Yong, Fox, Ted, Coll, Joyce T, Fleming, Mark A, Markland, William, Caron, Paul R, Wilson, Keith P, Su, Michael S-S

    Published in Structure (London) (15-08-1998)
    “…Background: The c-Jun N-terminal kinases (JNKs) are members of the mitogen-activated protein (MAP) kinase family, and regulate signal transduction in response…”
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  5. 5

    Nonstructural protein 5A (NS5A) and human replication protein A increase the processivity of hepatitis C virus NS5B polymerase activity in vitro by Mani, Nagraj, Yuzhakov, Alexander, Yuzhakov, Olga, Coll, Joyce T, Black, Jim, Saxena, Kumkum, Fulghum, John R, Lippke, Judith A, Rao, B Govinda, Rijnbrand, Rene, Kwong, Ann D

    Published in Journal of virology (01-01-2015)
    “…The precise role(s) and topological organization of different factors in the hepatitis C virus (HCV) RNA replication complex are not well understood. In order…”
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  6. 6

    The structures of caspases-1, -3, -7 and -8 reveal the basis for substrate and inhibitor selectivity by Wei, Yunyi, Fox, Ted, Chambers, Steve P, Sintchak, JoAnne, Coll, Joyce T, Golec, Julian MC, Swenson, Lora, Wilson, Keith P, Charifson, Paul S

    Published in Chemistry & biology (01-06-2000)
    “…Background: Peptide inhibitors of caspases have helped define the role of these cysteine proteases in biology. Structural and biochemical characterization of…”
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  7. 7

    Development of a protease production platform for structure-based drug design by Fox, Ted, Brennan, Debra, Austen, Douglas A, Swalley, Susanne E, Coll, Joyce T, Raybuck, Scott A, Chambers, Stephen P

    Published in Current protein & peptide science (01-10-2007)
    “…Structure-based drug design (SBDD) has played an integral role in the development of highly specific, potent protease inhibitors resulting in a number of drugs…”
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  8. 8

    Structure of GSK3β reveals a primed phosphorylation mechanism by ter Haar, Ernst, Coll, Joyce T, Austen, Douglas A, Hsiao, Hsun-Mei, Swenson, Lora, Jain, Jugnu

    Published in Nature structural biology (01-07-2001)
    “…GSK3β was identified as the kinase that phosphorylates glycogen synthase but is now known to be involved in multiple signaling pathways. GSK3β prefers prior…”
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  9. 9

    A single amino acid substitution makes ERK2 susceptible to pyridinyl imidazole inhibitors of p38 MAP kinase by Fox, Ted, Coll, Joyce T., Xie, Xiaoling, Ford, Pamella J., Germann, Ursula A., Porter, Margaret D., Pazhanisamy, S., Fleming, Mark A., Galullo, Vincent, Su, Michael S. S., Wilson, Keith P.

    Published in Protein science (01-11-1998)
    “…Mitogen‐activated protein (MAP) kinases are serine/threonine kinases that mediate intracellular signal transduction pathways.Pyridinyl imidazole compounds…”
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