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Membrane Guanylate Cyclase catalytic Subdomain: Structure and Linkage with Calcium Sensors and Bicarbonate.

  1. Author:
    Ravichandran, Ravi
    Duda, Teresa
    Pertzev, Alexandre
    Sharma, Rameshwar K
  2. Author Address

    Advanced Biomedical Computing Center, Frederick National Laboratory for Cancer Research, Leidos Biomedical Research Inc., FredrickMD, United States., The Unit of Regulatory and Molecular Biology, Research Divisions of Biochemistry and Molecular Biology, Salus University, Elkins ParkPA, United States.,
    1. Year: 2017
    2. Date: Jun 7
  1. Journal: Frontiers in molecular neuroscience
    1. 10
    2. Pages: 173
  2. Type of Article: Article
  3. Article Number: 173
  4. ISSN: 1662-5099
  1. Abstract:

    Membrane guanylate cyclase (MGC) is a ubiquitous multi-switching cyclic GMP generating signaling machine linked with countless physiological processes. In mammals it is encoded by seven distinct homologous genes. It is a single transmembrane spanning multi-modular protein; composed of integrated blocks and existing in homo-dimeric form. Its core catalytic domain (CCD) module is a common transduction center where all incoming signals are translated into the production of cyclic GMP, a cellular signal second messenger. Crystal structure of the MGC 39;s CCD does not exist and its precise identity is ill-defined. Here, we define it at a sub-molecular level for the phototransduction-linked MGC, the rod outer segment guanylate cyclase type 1, ROS-GC1. (1) The CCD is a conserved 145-residue structural unit, represented by the segment V(820)-P(964). (2) It exists as a homo-dimer and contains seven conserved catalytic elements (CEs) wedged into seven conserved motifs. (3) It also contains a conserved 21-residue neurocalcin d-modulated structural domain, V(836)-L(857). (4) Site-directed mutagenesis documents that each of the seven CEs governs the cyclase 39;s catalytic activity. (5) In contrast to the soluble and the bacterium MGC which use Mn(2+)-GTP substrate for catalysis, MGC CCD uses the natural Mg(2+)-GTP substrate. (6) Strikingly, the MGC CCD requires anchoring by the Transmembrane Domain (TMD) to exhibit its major (~92%) catalytic activity; in isolated form the activity is only marginal. This feature is not linked with any unique sequence of the TMD; there is minimal conservation in TMD. Finally, (7) the seven CEs control each of four phototransduction pathways- -two Ca(2+)-sensor GCAPs-, one Ca(2+)-sensor, S100B-, and one bicarbonate-modulated. The findings disclose that the CCD of ROS-GC1 has built-in regulatory elements that control its signal translational activity. Due to conservation of these regulatory elements, it is proposed that these elements also control the physiological activity of other members of MGC family.

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External Sources

  1. DOI: 10.3389/fnmol.2017.00173
  2. PMID: 28638321
  3. PMCID: PMC5461267
  4. WOS: 000402940000001

Library Notes

  1. Fiscal Year: FY2016-2017
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