Mechanism of NanR gene repression and allosteric induction of bacterial sialic acid metabolism
Horne C,
Venugopal H,
Panjikar S,
Henrickson A,
Brookes E,
North R,
Murphy J,
Friemann R,
Griffin M,
Ramm G,
Demeler B,
Dobson R
(2020 Apr 24)
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Sample: |
HTH-type transcriptional repressor NanR dimer, 59 kDa Escherichia coli protein
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Buffer: |
20 mM Tris, 150 mM NaCl, 0.1 % (w/v) sodium azide, pH: 8 |
Experiment: |
SAXS
data collected at SAXS/WAXS, Australian Synchrotron on 2019 Apr 20
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RgGuinier |
3.2 |
nm |
Dmax |
10.5 |
nm |
VolumePorod |
110 |
nm3 |
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Sample: |
HTH-type transcriptional repressor NanR dimer, 59 kDa Escherichia coli protein
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Buffer: |
20 mM Tris, 150 mM NaCl, 20 mM Neu5Ac and 0.1 % (w/v) sodium azide, pH: 8 |
Experiment: |
SAXS
data collected at SAXS/WAXS, Australian Synchrotron on 2019 Apr 20
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RgGuinier |
3.1 |
nm |
Dmax |
10.1 |
nm |
VolumePorod |
105 |
nm3 |
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Sample: |
HTH-type transcriptional repressor NanR dimer, 59 kDa Escherichia coli protein
(GGTATA)2 repeat DNA monomer, 11 kDa DNA
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Buffer: |
20 mM Tris, 150 mM NaCl, 0.1 % (w/v) sodium azide, pH: 8 |
Experiment: |
SAXS
data collected at SAXS/WAXS, Australian Synchrotron on 2019 Apr 20
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RgGuinier |
3.3 |
nm |
Dmax |
9.8 |
nm |
VolumePorod |
108 |
nm3 |
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