Sandbox 2ju1

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One of the [[CBI Molecules]] being studied in the [http://www.umass.edu/cbi/ University of Massachusetts Amherst Chemistry-Biology Interface Program] at UMass Amherst and on display at the [http://www.molecularplayground.org/ Molecular Playground].
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<applet load='2ju1'
<applet load='2ju1'
size='[450,338]'
size='[450,338]'
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align='right'
align='right'
caption='Acyl carrier protein DEBS'/>
caption='Acyl carrier protein DEBS'/>
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Polyketides are a medicinally important class of natural products. The architecture of modular polyketide synthases (PKSs), composed of multiple covalently linked domains grouped into modules, provides an attractive framework for engineering novel polyketide-producing assemblies. However, impaired domain-domain interactions can compromise the efficiency of engineered polyketide biosynthesis. To facilitate the study of these domain-domain interactions, we have used nuclear magnetic resonance (NMR) spectroscopy to determine the first solution structure of an acyl carrier protein (ACP) domain from a modular PKS, 6-deoxyerythronolide B synthase (DEBS). The tertiary fold of this 10-kD domain is a three-helical bundle; an additional short helix in the second loop also contributes to the core helical packing. Superposition of residues 14-94 of the ensemble on the mean structure yields an average atomic RMSD of 0.64 +/- 0.09 Angstrom for the backbone atoms (1.21 +/- 0.13 Angstrom for all non-hydrogen atoms). The three major helices superimpose with a backbone RMSD of 0.48 +/- 0.10 Angstrom (0.99 +/- 0.11 Angstrom for non-hydrogen atoms). Based on this solution structure, homology models were constructed for five other DEBS ACP domains. Comparison of their steric and electrostatic surfaces at the putative interaction interface (centered on helix II) suggests a model for protein-protein recognition of ACP domains, consistent with the previously observed specificity. Site-directed mutagenesis experiments indicate that two of the identified residues influence the specificity of ACP recognition. <ref name="DEBS "> Cafreyy P "Identification of DEBS 1, DEBS 2 and DEBS 3, the multienzyme polypeptides of the erythromycin-producing polyketide synthase from Saccharopolyspora erythraea" FEBS letters,15 June 1992, PMID:[http://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B6T36-44XN1WB-JW&_user=1516330&_coverDate=06/15/1992&_rdoc=1&_fmt=high&_orig=search&_origin=search&_sort=d&_docanchor=&view=c&_acct=C000053443&_version=1&_urlVersion=0&_userid=1516330&md5=31280cf1875244246efcef45bfb71fdf&searchtype=a 1618327]</ref>
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Polyketides are a medicinally important class of natural products. The architecture of modular polyketide synthases (PKSs), composed of multiple covalently linked domains grouped into modules, provides an attractive framework for engineering novel polyketide-producing assemblies. The tertiary fold of this 10-kD ACP domain is a three-helical bundle; an additional short helix in the second loop also contributes to the core helical packing. This is the <scene name='Sandbox_2ju1/Apo-acp/1'> ''apo''- form</scene> with the hydroxyl of serine that gets modified to ''holo''-form after post-translational modification which is the active form.
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<ref name="DEBS "> Cafreyy P "Identification of DEBS 1, DEBS 2 and DEBS 3, the multienzyme polypeptides of the erythromycin-producing polyketide synthase from Saccharopolyspora erythraea" FEBS letters,15 June 1992, PMID:[http://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B6T36-44XN1WB-JW&_user=1516330&_coverDate=06/15/1992&_rdoc=1&_fmt=high&_orig=search&_origin=search&_sort=d&_docanchor=&view=c&_acct=C000053443&_version=1&_urlVersion=0&_userid=1516330&md5=31280cf1875244246efcef45bfb71fdf&searchtype=a 1618327]</ref>
[http://en.wikipedia.org/wiki/Polyketide_synthase PKS]
[http://en.wikipedia.org/wiki/Polyketide_synthase PKS]
<ref name="DEBS "> Cafreyy P "Identification of DEBS 1, DEBS 2 and DEBS 3, the multienzyme polypeptides of the erythromycin-producing polyketide synthase from Saccharopolyspora erythraea" FEBS letters,15 June 1992, PMID:[http://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B6T36-44XN1WB-JW&_user=1516330&_coverDate=06/15/1992&_rdoc=1&_fmt=high&_orig=search&_origin=search&_sort=d&_docanchor=&view=c&_acct=C000053443&_version=1&_urlVersion=0&_userid=1516330&md5=31280cf1875244246efcef45bfb71fdf&searchtype=a 1618327]</ref>
<ref name="DEBS "> Cafreyy P "Identification of DEBS 1, DEBS 2 and DEBS 3, the multienzyme polypeptides of the erythromycin-producing polyketide synthase from Saccharopolyspora erythraea" FEBS letters,15 June 1992, PMID:[http://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B6T36-44XN1WB-JW&_user=1516330&_coverDate=06/15/1992&_rdoc=1&_fmt=high&_orig=search&_origin=search&_sort=d&_docanchor=&view=c&_acct=C000053443&_version=1&_urlVersion=0&_userid=1516330&md5=31280cf1875244246efcef45bfb71fdf&searchtype=a 1618327]</ref>
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<scene name='Sandbox_2ju1/Basic_residues/1'>basic residues in ACP</scene>
 

Current revision

One of the CBI Molecules being studied in the University of Massachusetts Amherst Chemistry-Biology Interface Program at UMass Amherst and on display at the Molecular Playground.

Acyl carrier protein DEBS

Drag the structure with the mouse to rotate

Polyketides are a medicinally important class of natural products. The architecture of modular polyketide synthases (PKSs), composed of multiple covalently linked domains grouped into modules, provides an attractive framework for engineering novel polyketide-producing assemblies. The tertiary fold of this 10-kD ACP domain is a three-helical bundle; an additional short helix in the second loop also contributes to the core helical packing. This is the with the hydroxyl of serine that gets modified to holo-form after post-translational modification which is the active form.

[1]

PKS [1]

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