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- PDB-2i8l: Solution Structure of an endopeptidase HycI from Escherichia coli -

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Basic information

Entry
Database: PDB / ID: 2i8l
TitleSolution Structure of an endopeptidase HycI from Escherichia coli
ComponentsHydrogenase 3 maturation protease
KeywordsHYDROLASE / ALPHA-BETA SANDWICH
Function / homology
Function and homology information


HycI peptidase / enzyme activator activity / protein processing / endopeptidase activity / aspartic-type endopeptidase activity / metal ion binding
Similarity search - Function
Peptidase A31, hydrogenase maturation protease HycI / Hydrogenase maturation protease / HybD-like / Peptidase A31 family / Peptidase HybD-like domain superfamily / Rossmann fold / 3-Layer(aba) Sandwich / Alpha Beta
Similarity search - Domain/homology
Hydrogenase 3 maturation protease
Similarity search - Component
Biological speciesEscherichia coli (E. coli)
MethodSOLUTION NMR / molecular dynamics simulated annealing
AuthorsYang, F. / Hu, W. / Jin, C.
CitationJournal: J.Biol.Chem. / Year: 2007
Title: Solution structure and backbone dynamics of an endopeptidase HycI from Escherichia coli: implications for mechanism of the [NiFe] hydrogenase maturation
Authors: Yang, F. / Hu, W. / Xu, H. / Li, C. / Xia, B. / Jin, C.
History
DepositionSep 2, 2006Deposition site: RCSB / Processing site: PDBJ
Revision 1.0Dec 5, 2006Provider: repository / Type: Initial release
Revision 1.1May 1, 2008Group: Version format compliance
Revision 1.2Jul 13, 2011Group: Version format compliance
Revision 1.3May 1, 2024Group: Data collection / Database references
Category: chem_comp_atom / chem_comp_bond ...chem_comp_atom / chem_comp_bond / database_2 / pdbx_nmr_software / pdbx_nmr_spectrometer
Item: _database_2.pdbx_DOI / _database_2.pdbx_database_accession ..._database_2.pdbx_DOI / _database_2.pdbx_database_accession / _pdbx_nmr_software.name / _pdbx_nmr_spectrometer.model

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Structure visualization

Structure viewerMolecule:
MolmilJmol/JSmol

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Assembly

Deposited unit
A: Hydrogenase 3 maturation protease


Theoretical massNumber of molelcules
Total (without water)17,0661
Polymers17,0661
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 / 100structures with the lowest energy
RepresentativeModel #1lowest energy

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Components

#1: Protein Hydrogenase 3 maturation protease / endopeptidase HycI


Mass: 17066.432 Da / Num. of mol.: 1
Source method: isolated from a genetically manipulated source
Source: (gene. exp.) Escherichia coli (E. coli) / Plasmid: pET21a(+) / Production host: Escherichia coli (E. coli)
References: UniProt: P0AEV9, Hydrolases; Acting on peptide bonds (peptidases)

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Experimental details

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Experiment

ExperimentMethod: SOLUTION NMR
NMR experiment
Conditions-IDExperiment-IDSolution-IDType
1113D 15N-separated NOESY
1223D 13C-separated NOESY

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Sample preparation

Details
Solution-IDContentsSolvent system
11mM HycI U-15N; 50mM phosphate buffer; 50mM NaCl; 1mM EDTA, 90% H2O, 10% D2O90% H2O/10% D2O
21mM HycI U-15N, 13C; 50mM phosphate buffer; 50mM NaCl; 1mM EDTA, 90% H2O, 10% D2O90% H2O/10% D2O
Sample conditionsIonic strength: 50mM NaCl, 50mM sodium phosphate / pH: 7 / Pressure: ambient / Temperature: 298 K

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NMR measurement

NMR spectrometer
TypeManufacturerModelField strength (MHz)Spectrometer-ID
Bruker AVANCEBrukerAVANCE6001
Bruker AVANCEBrukerAVANCE8002

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Processing

NMR software
NameVersionDeveloperClassification
XwinNMR3.5Brukercollection
NMRPipe2.1F. Delaglioprocessing
NMRView5B. Johnsondata analysis
CYANA2P. Guntertstructure solution
Amber7D. Caserefinement
RefinementMethod: molecular dynamics simulated annealing / Software ordinal: 1
NMR representativeSelection criteria: lowest energy
NMR ensembleConformer selection criteria: structures with the lowest energy
Conformers calculated total number: 100 / Conformers submitted total number: 20

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