Probable conserved Mce associated membrane protein (Mam1Adelta106) from M.tuberculosis (SANS)
Data type: SASBDB experimental dataStatus: PublishedCurve type: Single concentrationLast updated: 2026-05-05T11:41:40.417306+02:00
SANS data were collected on the Zoom time-of-flight SANS instrument (ISIS Neutron and Muon Source, Harwell, UK) using wavelength range 1.75-16.5Å. The source to sample and sample to detector distance was 4 m and the beam size was 12 mm. Mam1Adelta106 was solubilized with C12E9 in the lysis buffer where the deuteration of the C12E9 was 0.2 % v/v. Excess C12E9 was washed away throughout the purification, and replaced with D-C12E9 in the STFC SANS facilities using SEC Superdex200 column. From the highest point of the peak, 3 fractions were selected. Each of these fractions was loaded to Starna Scientific quartz round cuvette (match code 6,path length 1, type 32/Q/1), and SANS data were collected from each fraction with an exposure time of 1 h in 5 cycles (5 h total exposure time for each fraction). The neutron momentum transfer (q) standard deviation and truncated scattering data are provided as an additional file.
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1. Samples, Components and Experimental Conditions Sample & Experiment
Sample 1 · Probable conserved Mce associated membrane protein (Mam1Adelta106) from M.tuberculosis (SANS)
Mam1A/Rv0175 delta 106 is N-terminally truncated construct which lacks the alpha1-helix. Protein, despite the removal of TM-helix, is not soluble and required C12E9 detergent to be solubilized. Tetrameric form was calculated with SEC-MALS.
experiment.sample.buffer.name
50 mM Tris, 500 mM NaCl, D-C12E9
experiment.sample.buffer.concentration_unit
null
experiment.sample.buffer.comment
50mM Tris at pH8.5 with 500mM NaCl, supplemented with 0.003% Deuterated C12E9
experiment.sample.buffer.additive
null
experiment.sample.buffer.concentration
null
experiment.sample.buffer.pka
null
experiment.sample.buffer.ph
8.5
experiment.sample.buffer.deuteration
null
experiment.sample.purity_method
null
experiment.sample.name
Probable conserved Mce associated membrane protein (Mam1Adelta106) from M.tuberculosis (SANS)
SANS data were collected on the Zoom time-of-flight SANS instrument (ISIS Neutron and Muon Source, Harwell, UK) using wavelength range 1.75-16.5Å. The source to sample and sample to detector distance was 4 m and the beam size was 12 mm. Mam1Adelta106 was solubilized with C12E9 in the lysis buffer where the deuteration of the C12E9 was 0.2 % v/v. Excess C12E9 was washed away throughout the purification, and replaced with D-C12E9 in the STFC SANS facilities using SEC Superdex200 column. From the highest point of the peak, 3 fractions were selected. Each of these fractions was loaded to Starna Scientific quartz round cuvette (match code 6,path length 1, type 32/Q/1), and SANS data were collected from each fraction with an exposure time of 1 h in 5 cycles (5 h total exposure time for each fraction). The neutron momentum transfer (q) standard deviation and truncated scattering data are provided as an additional file.