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- PDB-2e3f: NMR structure of DEF-BAT, a mutant of anopheles defensin DEF-AAA -

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Basic information

Entry
Database: PDB / ID: 2e3f
TitleNMR structure of DEF-BAT, a mutant of anopheles defensin DEF-AAA
Componentsdefensin, mutant DEF-BAT
KeywordsANTIMICROBIAL PROTEIN / insect defensin / CSab motif / antibacterial
Function / homology
Function and homology information


humoral immune response / defense response to Gram-positive bacterium / defense response to bacterium / innate immune response / extracellular space
Similarity search - Function
Arthropod defensin / Invertebrate defensins family profile. / Defensin, invertebrate/fungal / Knottin, scorpion toxin-like / Knottin, scorpion toxin-like superfamily / Defensin A-like / 2-Layer Sandwich / Alpha Beta
Similarity search - Domain/homology
Biological speciesAnopheles gambiae (African malaria mosquito)
MethodSOLUTION NMR / Simulated annealing with torsion angle space (ARIA, CNS)
AuthorsLandon, C. / Barbault, F. / Vovelle, F.
CitationJournal: Proteins / Year: 2008
Title: Rational design of peptides active against the gram positive bacteria Staphylococcus aureus
Authors: Landon, C. / Barbault, F. / Legrain, M. / Guenneugues, M. / Vovelle, F.
History
DepositionNov 22, 2006Deposition site: PDBJ / Processing site: RCSB
Revision 1.0Nov 13, 2007Provider: repository / Type: Initial release
Revision 1.1Jul 13, 2011Group: Version format compliance
Revision 1.2Oct 20, 2021Group: Database references / Derived calculations
Category: database_2 / pdbx_struct_assembly ...database_2 / pdbx_struct_assembly / pdbx_struct_oper_list / struct_ref_seq_dif
Item: _database_2.pdbx_DOI / _database_2.pdbx_database_accession / _struct_ref_seq_dif.details
Revision 1.3Oct 30, 2024Group: Data collection / Structure summary
Category: chem_comp_atom / chem_comp_bond ...chem_comp_atom / chem_comp_bond / pdbx_entry_details / pdbx_modification_feature

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Structure visualization

Structure viewerMolecule:
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Assembly

Deposited unit
A: defensin, mutant DEF-BAT


Theoretical massNumber of molelcules
Total (without water)4,7471
Polymers4,7471
Non-polymers00
Water00
1


  • Idetical with deposited unit
  • defined by author
TypeNameSymmetry operationNumber
identity operation1_5551
NMR ensembles
DataCriteria
Number of conformers (submitted / calculated)10 / 100structures with the lowest energy and the least restraint violations
RepresentativeModel #1lowest restraint energy

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Components

#1: Protein/peptide defensin, mutant DEF-BAT


Mass: 4747.454 Da / Num. of mol.: 1 / Fragment: residues 63-102
Source method: isolated from a genetically manipulated source
Source: (gene. exp.) Anopheles gambiae (African malaria mosquito)
Gene: DEF1 / Production host: Saccharomyces cerevisiae (brewer's yeast) / References: UniProt: Q17027
Has protein modificationY

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Experimental details

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Experiment

ExperimentMethod: SOLUTION NMR
NMR experiment
Conditions-IDExperiment-IDSolution-IDType
111DQF-COSY
1212D TOCSY
1312D NOESY
241DQF-COSY
2512D TOCSY
2612D NOESY
NMR detailsText: This structure was determined using standard 2D homonuclear techniques.

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Sample preparation

DetailsContents: 2mM DEF-BAT, 40mM sodium acetate buffer / Solvent system: 90% H2O/10% D2O
Sample conditions
Conditions-IDIonic strengthpHPressure (kPa)Temperature (K)
140mM sodium acetate buffer 4.9ambient 293 K
240mM sodium acetate buffer 4.9ambient 303 K

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NMR measurement

NMR spectrometerType: Varian INOVA / Manufacturer: Varian / Model: INOVA / Field strength: 600 MHz

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Processing

NMR software
NameVersionDeveloperClassification
NMRPipe2.2Delaglioprocessing
NMRView5Johnsondata analysis
ARIA1.1Linge & Nilgesstructure solution
CNS1.1Brungerstructure solution
CNS1.1Brungerrefinement
RefinementMethod: Simulated annealing with torsion angle space (ARIA, CNS)
Software ordinal: 1
Details: The structures are based on a total of 625 NOE-derived distance constraints.
NMR representativeSelection criteria: lowest restraint energy
NMR ensembleConformer selection criteria: structures with the lowest energy and the least restraint violations
Conformers calculated total number: 100 / Conformers submitted total number: 10

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