SASDWN5

N-acetylmuramoyl-L-alanine amidase (without His-Tag)

Data type: SASBDB experimental data Status: Published Curve type: Single concentration Last updated: 2025-11-10T15:23:43.804079+01:00

SAXS experiments were performed at the beamline B21 of the Diamond Light Source (Harwell Campus, UK) (Cowieson et al, 2020). Samples of 45 µl of 6His-tagged and untagged DS6AGH19-Ami2B protein at 5.6 and 5.9 mg/ml were loaded into a Sodex KW-403 column and a SRT-C SEC-300 (Sepax) column, respectively, equilibrated in buffer (20 mM Tris pH 8.0, 150 mM NaCl and 1 mM DTT) and connected to an Agilent 1200 HPLC system at 18 °C. Continuously eluting samples were exposed for 3 s in 10 s acquisition blocks using an X-ray wavelength of 1 Å, and a sample to detector (Eiger 4M) distance of 3.7 m. The data covered a momentum transfer range of 0.0032 < q < 0.34 Å−1. The frames recorded immediately before elution of the sample were subtracted from the protein scattering profiles. The Scåtter software package (www.bioisis.net) was used to analyse data, buffer-subtraction, scaling, merging and checking possible radiation damage of the samples. The Rg value was calculated with the Guinier approximation assuming that at very small angles q < 1.3/Rg. The particle distance distribution, Dmax, was calculated from the scattering pattern with GNOM, and shape estimation was carried out with DAMMIF/DAMMIN, all these programs included in the ATSAS package. The proteins molecular mass was estimated with GNOM. Interactively generated PDB-based homology models were made using the program COOT by manually adjusting the X-ray structures obtained in this work, into the envelope given by SAXS until a good correlation between the real-space scattering profile calculated for the homology model matched the experimental scattering data. This was computed with the program FoXS.

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1. Samples, Components and Experimental Conditions Sample & Experiment

Sample 1 · N-acetylmuramoyl-L-alanine amidase (without His-Tag)

Concentration— – 5.9 Buffer / pH20 mM Tris, 150 mM NaCl and 1 mM DTT / 8.0
Experimental temperature18.0 Facility / beamlineDiamond Light Source / B21
Wavelength1.0 nmExposure3.0 s × 600

Molecular Components

ComponentType / organismUniProt and ConstructOligomeric StateMolecular weight
N-acetylmuramoyl-L-alanine amidase
View sequence
>DS6AGPMMLTVESFAAAMGNSLSVDRYRQLFPAAVESMVACGCTTVNRAAMWLAQVGHESGGLRWMEELASGAAYEWRSDLGNTQAGDGVRFKGRGPIQITGRYNYRKVSEWAHAQGIVPTPTYFVDNPTQLASDQYGFIGVSWYWQHGGPRPGQINGFADAGDILSGSRCVNGWVTTPNGMPDRTERWNRCRAMGDQILPAGAGTDNGGDGMAWTGDPVWLEDVLRPVLGDRLRVLPSWQMYGHGDFKDIRGVMVHHTGNARETAESIRKGRPDLRGPLSNIHIAPDGTVTLVAAGVCWHAGAGSYPWLPTNNANWHMIGIECAWPTIRPNGTYDEREPWPDAQIIAMRDTCAALTKRLGWDASRVIGHKEYAGASQGKWDPGNLDMGWFRGEVAKAMRG
proteinMycobacterium phage DS6AG8I4E01–395monomerMolecule count 143.458 kDa

Experimental Curves

CurvePoints / columnsq rangeUncertainty qualityNegative-intensity pointsSource file
12572[3]0.0045–0.33986956 1/AHas uncertainty columnMissing 0115sasbdb/entries/n5/sasdwn5/source/SASDWN5.dat
▼

2. Measurements Reported by SASBDB Reported Results

MetricMethodValueUncertaintyUnit
dmaxP(r)9.5—Å
i0Guinier0.0390946—arbitrary
i0P(r)0.03921—arbitrary
mwExperimental39.21—kDa
mwGuinier I(0)37.75—kDa
mwPorod39.8—kDa
porod_volumePorod50.0—ų
rgGuinier2.7890.052Å
rgP(r)2.850.04Å

These values are reported by SASBDB; SAXSdb did not recalculate them from the experimental curve.

▼

3. Source Fits and Models Source Fits & Models

▶

4. Source File Index Source Files

▶

5. Experiment Description and Publication Experiment & Publication

▼

6. Complete Source Record Complete Source Record

The following content comes directly from the SASBDB entry. Missing values are shown as “—”; SAXSdb does not infer undeclared units.

Open the original SASBDB entry

Buffer and Sample Properties

Buffer name20 mM Tris, 150 mM NaCl and 1 mM DTTBuffer concentration—
pH8.0Additives—
Buffer description—
Purity measurement method—Extinction coefficient—
Absorbance—Scattering contrast—
Specific volume / dry volume— / —Mixture / deuteration— / —

Acquisition Conditions and Instrument

Measurement date2024-09-30Storage / measurement temperature4.0 / 18.0
Exposure time3.0Frames600
Wavelength1.0Sample-to-detector distance3.7
SourceX-ray synchrotronDetectorEiger 4M
Facility / beamlineDiamond Light Source / B21 · Didcot, UK
q range0.045 – 3.399Sample volume / flow rate— / —

Original SASBDB Plots

Experimental I(q)
Experimental I(q)
Experimental I(q), log-log
Experimental I(q), log-log
Guinier plot
Guinier plot
Kratky plot
Kratky plot
P(r) plot
P(r) plot

Downloadable Files

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All source fields (unfiltered)

Every source field is expanded here, including empty values, list members and fields already shown above.

summary.json:179 field values
Field pathRaw value
codeSASDWN5
statusPublished
type_of_curveSingle concentration
angular_unit1/A
project.titleDissecting the molecular basis underlying mycobacterial cell-wall hydrolysis by the catalytic domains of D29LysA and DS6ALysA phage endolysins.
project.publication.titleDissecting the molecular basis underlying mycobacterial cell-wall hydrolysis by the catalytic domains of D29LysA and DS6ALysA phage endolysins.
project.publication.author_listCeballos-Zúñiga F, Galvez-Larrosa L, Muñoz IG, Infantes L, Fernández-Carrillo J, Pérez-Dorado I
project.publication.journalInt J Biol Macromol
project.publication.doi10.1016/j.ijbiomac.2025.148896
project.publication.pmid41207583
project.publication.published_date2025 Nov 7
project.statusreleased
project.submitted_date2025-01-21
project.released_date2025-11-10
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experiment.instrument.detector.typenull
experiment.instrument.detector.nameEiger 4M
experiment.instrument.detector.resolution75.0
experiment.instrument.nameDiamond Light Source
experiment.instrument.cityDidcot
experiment.instrument.countryUK
experiment.instrument.beamline_nameB21
experiment.instrument.beam_geometrynull
experiment.instrument.type_of_sourceX-ray synchrotron
experiment.instrument.point_sourcenull
experiment.instrument.line_collimationnull
experiment.instrument.sample_path_lengthnull
experiment.instrument.line_collimation_slitlengthnull
experiment.instrument.line_collimation_integrationwidthnull
experiment.instrument.xray_energynull
experiment.instrument.beam_profile_ahnull
experiment.instrument.beam_profile_alnull
experiment.sample.molecule[0].long_nameN-acetylmuramoyl-L-alanine amidase
experiment.sample.molecule[0].short_nameDS6A
experiment.sample.molecule[0].sequence>DS6A GPMMLTVESFAAAMGNSLSVDRYRQLFPAAVESMVACGCTTVNRAAMWLAQVGHESGGLRWM EELASGAAYEWRSDLGNTQAGDGVRFKGRGPIQITGRYNYRKVSEWAHAQGIVPTPTYFV DNPTQLASDQYGFIGVSWYWQHGGPRPGQINGFADAGDILSGSRCVNGWVTTPNGMPDRT ERWNRCRAMGDQILPAGAGTDNGGDGMAWTGDPVWLEDVLRPVLGDRLRVLPSWQMYGHG DFKDIRGVMVHHTGNARETAESIRKGRPDLRGPLSNIHIAPDGTVTLVAAGVCWHAGAGS YPWLPTNNANWHMIGIECAWPTIRPNGTYDEREPWPDAQIIAMRDTCAALTKRLGWDASR VIGHKEYAGASQGKWDPGNLDMGWFRGEVAKAMRG
experiment.sample.molecule[0].organismMycobacterium phage DS6A
experiment.sample.molecule[0].uniprot_codeG8I4E0
experiment.sample.molecule[0].uniprot_range_first1
experiment.sample.molecule[0].uniprot_range_last395
experiment.sample.molecule[0].oligomerizationmonomer
experiment.sample.molecule[0].molecular_typeprotein
experiment.sample.molecule[0].uniprot_sequenceMMLTVESFAAAMGNSLSVDRYRQLFPAAVESMVACGCTTVNRAAMWLAQVGHESGGLRWM EELASGAAYEWRSDLGNTQAGDGVRFKGRGPIQITGRYNYRKVSEWAHAQGIVPTPTYFV DNPTQLASDQYGFIGVSWYWQHGGPRPGQINGFADAGDILSGSRCVNGWVTTPNGMPDRT ERWNRCRAMGDQILPAGAGTDNGGDGMAWTGDPVWLEDVLRPVLGDRLRVLPSWQMYGHG DFKDIRGVMVHHTGNARETAESIRKGRPDLRGPLSNIHIAPDGTVTLVAAGVCWHAGAGS YPWLPTNNANWHMIGIECAWPTIRPNGTYDEREPWPDAQIIAMRDTCAALTKRLGWDASR VIGHKEYAGASQGKWDPGNLDMGWFRGEVAKAMRGEFDPKAPAPAPNPPADNDNGGFLMA LNDKQQHDLYNAVMTIAAVAADIQTQLRGPGLRGWPQLGRNANGEALTLVDAVGVIKAIA DREAGR
experiment.sample.molecule[0].mw43.458
experiment.sample.molecule[0].total_mw43.458
experiment.sample.molecule[0].number_molecules1
experiment.sample.molecule[0].complex_stateFalse
experiment.sample.molecule[0].deuterationnull
experiment.sample.molecule[0].molecule_sourcebiological
experiment.sample.molecule[0].molecule_descriptionThe molecule beahves as a monomer in solution
experiment.sample.buffer.name20 mM Tris, 150 mM NaCl and 1 mM DTT
experiment.sample.buffer.concentration_unitnull
experiment.sample.buffer.commentnull
experiment.sample.buffer.additivenull
experiment.sample.buffer.concentrationnull
experiment.sample.buffer.pkanull
experiment.sample.buffer.ph8.0
experiment.sample.buffer.deuterationnull
experiment.sample.purity_methodnull
experiment.sample.nameN-acetylmuramoyl-L-alanine amidase (without His-Tag)
experiment.sample.ext_coefficientnull
experiment.sample.contrastnull
experiment.sample.specific_volnull
experiment.sample.dry_volnull
experiment.sample.absorbptionnull
experiment.sample.deuterationnull
experiment.sample.mixturenull
experiment.contributor[0].affiliation[0].short_namenull
experiment.contributor[0].affiliation[0].addressnull
experiment.contributor[0].affiliation[0].full_nameSpanish National Cancer Research Centre (CNIO)
experiment.contributor[0].affiliation[0].webpagenull
experiment.contributor[0].contributor_nameINÉS
experiment.contributor[0].contributor_surnameMUÑOZ
experiment.contributor[0].orcidhttps://orcid.org/0000-0001-6732-4059
experiment.concentration_methodnull
experiment.concentration_unitnull
experiment.date2024-09-30
experiment.storage_temperature4.0
experiment.cell_temperature18.0
experiment.exposure_time3.0
experiment.number_of_frames600
experiment.wavelength1.0
experiment.sample_detector_distance3.7
experiment.concentration_minnull
experiment.concentration_max5.9
experiment.sample_volumenull
experiment.flow_ratenull
experiment.s_min0.045
experiment.s_max3.399
experiment.total_exposure_timenull
experiment.seccolumnnull
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fits[0].softwareFoXS
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fits[0].p_value0.0
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fits[1].softwareDAMMIN
fits[1].chi_square_value0.85
fits[1].p_value0.0594
fits[1].fit_residual_plotSASDWN5_fit2_fitresiduals_img.png
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fits[1].fit_lognull
fits[1].software_versionnull
fits[1].description
estimated_volume_methodnull
pddf_softwareATSAS GNOM
pddf_software_version5.0
i0_calibration_standardnull
descriptionSAXS experiments were performed at the beamline B21 of the Diamond Light Source (Harwell Campus, UK) (Cowieson et al, 2020). Samples of 45 µl of 6His-tagged and untagged DS6AGH19-Ami2B protein at 5.6 and 5.9 mg/ml were loaded into a Sodex KW-403 column and a SRT-C SEC-300 (Sepax) column, respectively, equilibrated in buffer (20 mM Tris pH 8.0, 150 mM NaCl and 1 mM DTT) and connected to an Agilent 1200 HPLC system at 18 °C. Continuously eluting samples were exposed for 3 s in 10 s acquisition blocks using an X-ray wavelength of 1 Å, and a sample to detector (Eiger 4M) distance of 3.7 m. The data covered a momentum transfer range of 0.0032 < q < 0.34 Å−1. The frames recorded immediately before elution of the sample were subtracted from the protein scattering profiles. The Scåtter software package (www.bioisis.net) was used to analyse data, buffer-subtraction, scaling, merging and checking possible radiation damage of the samples. The Rg value was calculated with the Guinier approximation assuming that at very small angles q < 1.3/Rg. The particle distance distribution, Dmax, was calculated from the scattering pattern with GNOM, and shape estimation was carried out with DAMMIF/DAMMIN, all these programs included in the ATSAS package. The proteins molecular mass was estimated with GNOM. Interactively generated PDB-based homology models were made using the program COOT by manually adjusting the X-ray structures obtained in this work, into the envelope given by SAXS until a good correlation between the real-space scattering profile calculated for the homology model matched the experimental scattering data. This was computed with the program FoXS.
experiment_descriptionnull
tags[]
intensity_unitarbitrary
experimental_mw39.21
experimental_mw_errornull
guinier_i0_mw37.75
guinier_i0_mw_errornull
porod_mw39.8
porod_mw_errornull
pddf_i00.03921
pddf_i0_errornull
guinier_i00.0390946
guinier_i0_errornull
pddf_rg2.85
pddf_rg_error0.04
guinier_rg2.789
guinier_rg_error0.052
pddf_dmax9.5
pddf_dmax_errornull
porod_volume50.0
porod_volume_errornull
estimated_volumenull
estimated_volume_errornull
guinier_point_first80
guinier_point_last323
pddf_point_firstnull
pddf_point_lastnull
i0_calibration_standard_datanull
intensities_log_log_plotSASDWN5_datloglog_img.png
symmetrynull
last_modified2025-11-10T15:23:43.804079+01:00
bragg_peak[]
manifest.json:34 field values
Field pathRaw value
codeSASDWN5
statussuccess
started_at2026-08-11T14:52:12.573277+00:00
finished_at2026-08-11T14:52:22.815674+00:00
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View the complete summary.json source
{
  "code": "SASDWN5",
  "status": "Published",
  "type_of_curve": "Single concentration",
  "angular_unit": "1/A",
  "project": {
    "title": "Dissecting the molecular basis underlying mycobacterial cell-wall hydrolysis by the catalytic domains of D29LysA and DS6ALysA phage endolysins.",
    "publication": {
      "title": "Dissecting the molecular basis underlying mycobacterial cell-wall hydrolysis by the catalytic domains of D29LysA and DS6ALysA phage endolysins.",
      "author_list": "Ceballos-Zúñiga F, Galvez-Larrosa L, Muñoz IG, Infantes L, Fernández-Carrillo J, Pérez-Dorado I",
      "journal": "Int J Biol Macromol",
      "doi": "10.1016/j.ijbiomac.2025.148896",
      "pmid": "41207583",
      "published_date": "2025 Nov 7"
    },
    "status": "released",
    "submitted_date": "2025-01-21",
    "released_date": "2025-11-10"
  },
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View the complete manifest.json source
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