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- PDB-1orx: Solution Structure of the acyclic permutant des-(24-28)-kalata B1. -

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Basic information

Entry
Database: PDB / ID: 1orx
TitleSolution Structure of the acyclic permutant des-(24-28)-kalata B1.
Componentskalata B1
KeywordsANTIBIOTIC / acyclic permutation / cyclotides / kalata B1
Function / homologyCyclotide, moebius, conserved site / Cyclotides Moebius subfamily signature. / Cyclotides profile. / Cyclotide / Cyclotide superfamily / Cyclotide family / killing of cells of another organism / defense response to bacterium / Kalata-B1
Function and homology information
MethodSOLUTION NMR / torsion angle dynamics
AuthorsBarry, D.G. / Daly, N.L. / Clark, R.J. / Sando, L. / Craik, D.J.
CitationJournal: Biochemistry / Year: 2003
Title: Linearization of a naturally occurring circular protein maintains structure but eliminates hemolytic activity
Authors: Barry, D.G. / Daly, N.L. / Clark, R.J. / Sando, L. / Craik, D.J.
History
DepositionMar 17, 2003Deposition site: RCSB / Processing site: PDBJ
Revision 1.0Jun 24, 2003Provider: repository / Type: Initial release
Revision 1.1Apr 29, 2008Group: Version format compliance
Revision 1.2Jul 13, 2011Group: Version format compliance
Revision 1.3Feb 23, 2022Group: Data collection / Database references / Derived calculations
Category: database_2 / pdbx_nmr_software ...database_2 / pdbx_nmr_software / pdbx_struct_assembly / pdbx_struct_oper_list
Item: _database_2.pdbx_DOI / _database_2.pdbx_database_accession / _pdbx_nmr_software.name
Revision 1.4Oct 9, 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:
MolmilJmol/JSmol

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Assembly

Deposited unit
A: kalata B1


Theoretical massNumber of molelcules
Total (without water)2,3791
Polymers2,3791
Non-polymers00
Water00
1


  • Idetical with deposited unit
  • defined by author
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
NMR ensembles
DataCriteria
Number of conformers (submitted / calculated)20 / 50structures with the lowest energy
Representative

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Components

#1: Protein/peptide kalata B1


Mass: 2378.724 Da / Num. of mol.: 1 / Fragment: RESIUDES 1-24 / Source method: obtained synthetically
Details: This sequence is a synthetic acyclic permutant of the cyclic plant protein kalata B1.
References: UniProt: P56254
Has protein modificationY

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Experimental details

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Experiment

ExperimentMethod: SOLUTION NMR
NMR experiment
Conditions-IDExperiment-IDSolution-IDType
1112D TOCSY
1212D NOESY
131DQF-COSY
142E-COSY
152H-D exchange experiment
NMR detailsText: This structure was determined using standard 2D homonuclear techniques.

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Sample preparation

Details
Solution-IDContentsSolvent system
1Unlabelled90% H2O/10% D2O
2Unlabelled99.99% D2O
Sample conditionspH: 4 / Pressure: ambient / Temperature: 295 K
Crystal grow
*PLUS
Method: other / Details: NMR

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NMR measurement

RadiationProtocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M
Radiation wavelengthRelative weight: 1
NMR spectrometer
TypeManufacturerModelField strength (MHz)Spectrometer-ID
Bruker DMXBrukerDMX7501
Bruker ARXBrukerARX5002

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Processing

NMR software
NameClassification
XwinNMRcollection
XEASYdata analysis
DYANAstructure solution
CNSrefinement
RefinementMethod: torsion angle dynamics / Software ordinal: 1
NMR ensembleConformer selection criteria: structures with the lowest energy
Conformers calculated total number: 50 / Conformers submitted total number: 20

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