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Vladislav V. Flemming M. The latter interaction either with the NCAM or FGFR is probably unspecific, and is very unlikely to have any physiological relevance, but it turned out to be quite useful in showing the presence of the second site. The first cluster is located in close proximity to the binding sites for FGF, heparin, and Ig2 itself Fig. If you are not the author of this article and you wish to reproduce material from it in a third party non-RSC publication you must formally request permission using Copyright Clearance Center. Association between the first two immunoglobulin-like domains of the neural cell adhesion molecule N-CAM. Fortunately, one of the identified sites is located in the vicinity of the Ig2 module's site for heparin, and the presence of this site was confirmed by inhibition of the Ig2—NCAM binding by a heparin analog, SOS. However, interactions between the individual modules were minimally detected by SPR, indicating that both NCAM modules as well as both FGFR modules are involved in binding or are necessary for maximal binding. Figure 6.

  • Structural basis for the activation of FGFR by NCAM

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    Structural basis for the activation of FGFR by NCAM

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    This indicates that the C-terminal part of the F3 1 module of the NCAM, together with the N-terminal part of the F3 2 module, might form a single binding site for FGFR, and this site may be destroyed when the modules are separated.

    You do not have JavaScript enabled. This may take some time to load. Insights into the molecular basis for fibroblast growth factor receptor autoinhibition and ligand-binding promiscuity.

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    This article has been cited by other articles in PMC. Current Journals.

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    Protein Sci. Using surface plasmon resonance and nuclear magnetic resonance analyses, the present study demonstrates that the second Ig module of FGFR also is involved in binding to the NCAM.

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    The experiment was repeated nine times. However, the fact that the competition isotherm clearly demonstrates the presence of two binding sites in the FGFR Ig2 module makes it quite plausible that the two clusters of perturbed residues identified by NMR correspond to real binding events. However, this model cannot be excluded based on our data alone.

    The K d value for this binding was estimated to be

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    Actions. T/98 ECLI:EU:T, Unión de Pequeños Agricultores, [25]. Figure 1.

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    This indicates that the exchange between the bound and unbound form of the Ig2 module is intermediate on the NMR timescale. Support Center Support Center.

    Origin software version 6. Whether or not the model is true requires further investigation.

    Elucidation of the mechanism of the regulatory function of the Ig1 module of the fibroblast growth factor receptor 1. Current Journals. Structure and interactions of NCAM modules 1 and 2, basic elements in neural cell adhesion.

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    FEBS Lett.

    From the journal: Chemical Communications. Download Citation: Chem. Issue 24, The experimental setup was the same as described in Figure 1.

    4 comments

    1. Arashirisar:

      The Ig1 and Ig2 modules of the NCAM were demonstrated to bind to each other, which indicates that these modules are involved in a symmetrical double-reciprocal interaction Kiselyov et al. Education in Chemistry.

    2. Mujind:

      This article has been cited by other articles in PMC. Addition of F3 1—2 modules of the NCAM led to either line-broadening, chemical shift changes or, for certain residues, disappearance of the NMR signals.

    3. Kigazuru:

      Open in a separate window. Authors contributing to RSC publications journal articles, books or book chapters do not need to formally request permission to reproduce material contained in this article provided that the correct acknowledgement is given with the reproduced material.

    4. Mezisida:

      Another way of demonstrating the presence of two binding sites is to estimate the K d values for the two sites from the concentration dependence of the chemical shifts changes. Patrick a.