BMRB

Biological Magnetic Resonance Data Bank


A Repository for Data from NMR Spectroscopy on Proteins, Peptides, Nucleic Acids, and other Biomolecules
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BMRB Entry 17613

Title: Solution NMR Structure of DE NOVO DESIGNED PROTEIN, P-LOOP NTPASE FOLD, Northeast Structural Genomics Consortium Target OR36

Deposition date: 2011-04-29 Original release date: 2011-06-01

Authors: Liu, Gaohua; Koga, Nobuyasu; Koga, Rie; Xiao, Rong; Janjua, Haleema; Ciccosanti, colleen; Lee, Hsiau-Wei; Acton, Thomas; Everett, John; Baker, David; Montelione, Gaetano; Northeast Structural Genomics Consortium, NESG

Citation: Liu, Gaohua; Koga, Nobuyasu; Koga, Rie; Xiao, Rong; Lee, Hsiau-Wei; Janjua, Haleema; Ciccosanti, colleen; Acton, Thomas; Everett, John; Baker, David; Montelione, Gaetano. "Northeast Structural Genomics Consortium Target OR36"  To be published ., .-..

Assembly members:
OR36, polymer, 134 residues, 16031.576 Da.

Natural source:   Common Name: Denove Design   Taxonomy ID: not available   Superkingdom: not available   Kingdom: not available   Genus/species: not available not available

Experimental source:   Production method: recombinant technology   Host organism: Escherichia coli

Entity Sequences (FASTA):
OR36: MKILILINTNNDELIKKIKK EVENQGYQVRDVNDSDELKK EMKKLAEEKNFEKILIISND KQLLKEMLELISKLGYKVFL LLQDQDENELEEFKRKIESQ GYEVRKVTDDEEALKIVREF MQKAGSLEHHHHHH

Data sets:
Data typeCount
13C chemical shifts598
15N chemical shifts139
1H chemical shifts1003

Time Domain Data

Additional metadata:

  • Assembly
  • Samples and Experiments
  • Software
  • Spectrometers
  • Hide all

Assembly:

Entity Assembly IDEntity NameEntity ID
1OR361

Entities:

Entity 1, OR36 134 residues - 16031.576 Da.

1   METLYSILELEUILELEUILEASNTHRASN
2   ASNASPGLULEUILELYSLYSILELYSLYS
3   GLUVALGLUASNGLNGLYTYRGLNVALARG
4   ASPVALASNASPSERASPGLULEULYSLYS
5   GLUMETLYSLYSLEUALAGLUGLULYSASN
6   PHEGLULYSILELEUILEILESERASNASP
7   LYSGLNLEULEULYSGLUMETLEUGLULEU
8   ILESERLYSLEUGLYTYRLYSVALPHELEU
9   LEULEUGLNASPGLNASPGLUASNGLULEU
10   GLUGLUPHELYSARGLYSILEGLUSERGLN
11   GLYTYRGLUVALARGLYSVALTHRASPASP
12   GLUGLUALALEULYSILEVALARGGLUPHE
13   METGLNLYSALAGLYSERLEUGLUHISHIS
14   HISHISHISHIS

Samples:

sample_NC: OR36, [U-100% 13C; U-100% 15N], 0.71 mM; H2O 90%; D2O 10%; NaN3 0.02%; DTT 10 mM; CaCL2 5 mM; NaCL 100 mM; MES 20 mM; DSS 50 uM; Proteinase Inhibitors 1 x

sample_NC5: OR36, [U-10% 13C; U-100% 15N], 0.95 mM; H2O 90%; D2O 10%; NaN3 0.02%; DTT 10 mM; CaCL2 5 mM; NaCL 100 mM; MES 20 mM; DSS 50 uM; Proteinase Inhibitors 1 x

sample_NC5_RDC: OR36, [U-10% 13C; U-100% 15N], 0.95 mM; H2O 90%; D2O 10%; NaN3 0.02%; DTT 10 mM; CaCL2 5 mM; NaCL 100 mM; MES 20 mM; DSS 50 uM; Proteinase Inhibitors 1 x

sample_conditions_1: pH: 6.5; pressure: 1 atm; temperature: 298 K

Experiments:

NameSampleSample stateSample conditions
2D 1H-15N HSQCsample_NCisotropicsample_conditions_1
2D 1H-13C HSQCsample_NC5isotropicsample_conditions_1
3D HNCOsample_NCisotropicsample_conditions_1
3D CBCA(CO)NHsample_NCisotropicsample_conditions_1
3D HNCACBsample_NCisotropicsample_conditions_1
3D 1H-13C arom NOESYsample_NCisotropicsample_conditions_1
3D simutaneous 13C-aromatic,13C-aliphatic,15N edited 1H-1H NOESYsample_NCisotropicsample_conditions_1
2D 1H-15N HSQCsample_NC5_RDCisotropicsample_conditions_1
2D HetNOEsample_NC5isotropicsample_conditions_1

Software:

CNS, Brunger, Adams, Clore, Gros, Nilges and Read - refinemen,structure solution,geometry optimization

CYANA v3.0, Guntert, Mumenthaler and Wuthrich - refinement,geometry optimization,structure solution

AutoStruct v2.1, Huang, Tejero, Powers and Montelione - data analysis,refinement

AutoAssign v2.1, Zimmerman, Moseley, Kulikowski and Montelione - data analysis,chemical shift assignment

NMRPipe, Delaglio, Grzesiek, Vuister, Zhu, Pfeifer and Bax - processing

XEASY, Bartels et al. - data analysis,peak picking,chemical shift assignment

TOPSPIN, Bruker Biospin - collection

VNMRJ, Varian - collection

SPARKY, Goddard - data analysis

TALOS+, Shen, Cornilescu, Delaglio and Bax - geometry optimization

NMR spectrometers:

  • Bruker Avance 800 MHz
  • Varian INOVA 600 MHz
  • Varian INOVA 600 MHz

Related Database Links:

BMRB 18337 18372
PDB

Download simulated HSQC data in one of the following formats:
CSV: Backbone or all simulated shifts
SPARKY: Backbone or all simulated shifts