BMRB Entry 15848

Title:
Solution NMR Structure of Putative N-Acetyl Transferase YhhK from E. coli Bound to Coenzyme A: Northeast Structural Genomics Consortium Target ET106
Deposition date:
2008-06-30
Original release date:
2008-09-19
Authors:
Cort, John; Yee, Adelinda; Arrowsmith, Cheryl; Kennedy, Michael
Citation:

Citation: Cort, John; Yee, Adelinda; Arrowsmith, Cheryl; Kennedy, Michael. "Solution NMR Structure of Putative N-Acetyl Transferase YhhK from E. coli Bound to Coenzyme A"  .

Assembly members:

Assembly members:
YhhK, polymer, 128 residues, Formula weight is not available
COENZYME A, non-polymer, 767.534 Da.

Natural source:

Natural source:   Common Name: E. coli   Taxonomy ID: 562   Superkingdom: Bacteria   Kingdom: not available   Genus/species: Escherichia coli

Experimental source:

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

Data sets:
Data typeCount
13C chemical shifts388
15N chemical shifts130
1H chemical shifts795

Additional metadata:

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

Assembly:

Entity Assembly IDEntity NameEntity ID
1YhhK1
2CoA2

Entities:

Entity 1, YhhK 128 residues - Formula weight is not available

1   METLYSLEUTHRILEILEARGLEUGLULYS
2   PHESERASPGLNASPARGILEASPLEUGLN
3   LYSILETRPPROGLUTYRSERPROSERSER
4   LEUGLNVALASPASPASNHISARGILETYR
5   ALAALAARGPHEASNGLUARGLEULEUALA
6   ALAVALARGVALTHRLEUSERGLYTHRGLU
7   GLYALALEUASPSERLEUARGVALARGGLU
8   VALTHRARGARGARGGLYVALGLYGLNTYR
9   LEULEUGLUGLUVALLEUARGASNASNPRO
10   GLYVALSERCYSTRPTRPMETALAASPALA
11   GLYVALGLUASPARGGLYVALMETTHRALA
12   PHEMETGLNALALEUGLYPHETHRTHRGLN
13   GLNGLYGLYTRPGLULYSCYSGLY

Entity 2, CoA - C21 H36 N7 O16 P3 S - 767.534 Da.

1   COA

Samples:

sample_1: YhhK, [U-100% 13C; U-100% 15N], 0.6 ± 0.2 mM; Coenzyme A 5 ± 1 mM; D2O 7%; sodium chloride 300 ± 5 mM; TRIS 25 ± 1 mM; DTT 5 ± .1 mM

sample_2: YhhK, [U-100% 13C; U-100% 15N], 0.6 ± 0.2 mM; Coenzyme A 5 ± 1 mM; D2O 100%; sodium chloride 300 ± 5 mM; TRIS 25 ± 1 mM; DTT 5 ± .1 mM

sample_conditions_1: ionic strength: 300 mM; pH: 7; pressure: 1 atm; temperature: 293 K

Experiments:

NameSampleSample stateSample conditions
2D 1H-15N HSQCsample_1isotropicsample_conditions_1
2D 1H-13C HSQCsample_1isotropicsample_conditions_1
3D CBCA(CO)NHsample_1isotropicsample_conditions_1
3D HNCACBsample_1isotropicsample_conditions_1
3D HNCOsample_1isotropicsample_conditions_1
3D HCCH-TOCSYsample_1isotropicsample_conditions_1
3D HCCH-COSYsample_1isotropicsample_conditions_1
3D HBHA(CO)NHsample_1isotropicsample_conditions_1
3D 1H-15N NOESYsample_1isotropicsample_conditions_1
3D 1H-13C NOESYsample_1isotropicsample_conditions_1
4D 13C HMQC-NOESY-HMQCsample_2isotropicsample_conditions_1

Software:

FELIX, Accelrys Software Inc. - chemical shift assignment, data analysis, processing

SPARKY, Goddard - chemical shift assignment, data analysis, processing

AutoStruct, Huang, Tejero, Powers and Montelione - refinement, structure solution

CNS, Brunger, Adams, Clore, Gros, Nilges and Read - refinement, structure solution

X-PLOR NIH, Schwieters, Kuszewski, Tjandra and Clore - refinement, structure solution

NMR spectrometers:

  • Varian INOVA 750 MHz
  • Varian INOVA 600 MHz

Related Database Links:

GB NP417916 AAB18434 AAC76484 AAG58566 AAN44936 AAP19246
SWS P37613
PDB
DBJ BAB37729 BAE77834 BAG79250 BAI27716 BAI32887
EMBL CAQ33778 CAR00402 CAR05068 CAV00264 CBJ03206
REF NP_312333 NP_417916 NP_709229 WP_000176384 WP_000778768
SP P37613
AlphaFold P37613

Download HSQC peak lists in one of the following formats:
CSV: Backbone or all simulated peaks
SPARKY: Backbone or all simulated peaks