BMRB Entry 17226

Title:
1H, 15N, and 13C chemical shift assignments, and 15N dynamics for trHbN-cyanomet from M. tuberculosis
Deposition date:
2010-09-30
Original release date:
2011-10-28
Authors:
Savard, Pierre-Yves; Morin, Sebastien; Sebilo, Anne; Meindre, Fanny; Guertin, Michel; Gagne, Stephane
Citation:

Citation: Savard, Pierre-Yves; Daigle, Richard; Morin, Sebastien; Sebilo, Anne; Meindre, Fanny; Lague, Patrick; Guertin, Michel; Gagne, Stephane. "Structure and dynamics of Mycobacterium tuberculosis truncated hemoglobin N: insights from NMR spectroscopy and molecular dynamics simulations."  Biochemistry 50, 11121-11130 (2011).
PubMed: 21999759

Assembly members:

Assembly members:
trHbN, polymer, 136 residues, 14317.3 Da.
FE, non-polymer, 55.845 Da.
CYN, non-polymer, 26.017 Da.

Natural source:

Natural source:   Common Name: Mycobacterium tuberculosis   Taxonomy ID: 1773   Superkingdom: Bacteria   Kingdom: not available   Genus/species: Mycobacterium tuberculosis

Experimental source:

Experimental source:   Production method: recombinant technology   Host organism: Escherichia coli   Vector: pET3a

Data typeCount
13C chemical shifts446
15N chemical shifts123
1H chemical shifts555
heteronuclear NOE values303
order parameters101
T1 relaxation values303
T2 relaxation values201

Additional metadata:

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

Assembly:

Entity Assembly IDEntity NameEntity ID
1trHbN1
2iron ion2
3cyanide ion3

Entities:

Entity 1, trHbN 136 residues - 14317.3 Da.

1   METGLYLEULEUSERARGLEUARGLYSARG
2   GLUPROILESERILETYRASPLYSILEGLY
3   GLYHISGLUALAILEGLUVALVALVALGLU
4   ASPPHETYRVALARGVALLEUALAASPASP
5   GLNLEUSERALAPHEPHESERGLYTHRASN
6   METSERARGLEULYSGLYLYSGLNVALGLU
7   PHEPHEALAALAALALEUGLYGLYPROGLU
8   PROTYRTHRGLYALAPROMETLYSGLNVAL
9   HISGLNGLYARGGLYILETHRMETHISHIS
10   PHESERLEUVALALAGLYHISLEUALAASP
11   ALALEUTHRALAALAGLYVALPROSERGLU
12   THRILETHRGLUILELEUGLYVALILEALA
13   PROLEUALAVALASPVALTHRSERGLYGLU
14   SERTHRTHRALAPROVAL

Entity 2, iron ion - Fe - 55.845 Da.

1   FE

Entity 3, cyanide ion - C N - 26.017 Da.

1   CYN

Samples:

sample_1: trHbN, [U-99% 15N], 0.8 mM; D2O, [U-99% 2H], 10%; DSS 0.1 mM; potassium phosphate 20 mM; potassium cyanide 2.4 mM; EDTA 50 uM; H2O 90%

sample_2: trHbN, [U-99% 13C; U-99% 15N], 0.8 mM; D2O, [U-99% 2H], 10%; DSS 0.1 mM; potassium phosphate 20 mM; potassium cyanide 2.4 mM; EDTA 50 uM; H2O 90%

sample_conditions_1: pH: 7.5; pressure: 1 atm; temperature: 273 K

Experiments:

NameSampleSample stateSample conditions
2D 1H-15N HSQCsample_1isotropicsample_conditions_1
2D 1H-15N HSQCsample_1isotropicsample_conditions_1
2D 1H-15N HSQCsample_1isotropicsample_conditions_1
2D 1H-15N HSQCsample_2isotropicsample_conditions_1
3D CBCA(CO)NHsample_2isotropicsample_conditions_1
3D C(CO)NHsample_2isotropicsample_conditions_1
3D HNCOsample_2isotropicsample_conditions_1
3D HNCACBsample_2isotropicsample_conditions_1
3D HCCH-TOCSYsample_2isotropicsample_conditions_1
3D H(CCO)NHsample_2isotropicsample_conditions_1
3D HNHBsample_1isotropicsample_conditions_1
3D 1H-13C NOESYsample_2isotropicsample_conditions_1

Software:

VNMRJ v2.1b, Varian - collection

NMRPipe v5.0, Delaglio, Grzesiek, Vuister, Zhu, Pfeifer and Bax - processing

NMRDraw v5.0, Delaglio, Grzesiek, Vuister, Zhu, Pfeifer and Bax - processing

NMRView v5.2.2_01, Johnson, One Moon Scientific - chemical shift assignment

Relax v1.3, Edward D'Auvergne - curvefitting

ModelFree v4.20, Palmer - data analysis

NMR spectrometers:

  • Varian INOVA 500 MHz
  • Varian INOVA 600 MHz
  • Varian INOVA 800 MHz

Related Database Links:

PDB
DBJ BAH25857 BAL65514 BAQ05541 GAA45289
EMBL CAB56291 CAL71581 CCC26641 CCC43897 CCC64155
GB AAD28758 AAK45860 ABQ73299 ABR05918 ACT25509
REF NP_216058 NP_855221 WP_003407730 WP_003911564 WP_015289952
SP P0A593 P0A594 P9WN24 P9WN25
AlphaFold P0A593 P0A594 P9WN24 P9WN25

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