BMRB Entry 17857

Name: Chemical Shift Assignments and solution structure of human apo-S100A1 E32Q mutant
Published: 2012-08-01

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PDB ID: 2m3w
Entry in NMR Restraints Grid
Validation report in NRG-CING
Chem Shift validation: AVS_anomalous, AVS_full, LACS, SPARTA
BMRB Entry DOI: doi:10.13018/BMR17857
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Bioinformatics (2015) 31 (8): 1322-1324 doi:10.1093/bioinformatics/btu829

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Title: Chemical Shift Assignments and solution structure of human apo-S100A1 E32Q mutant

Deposition date: 2011-08-12 Original release date: 2012-08-01

Authors: Ruszczynska-Bartnik, Katarzyna; Zdanowski, Konrad; Zhukov, Igor; Bierzynski, Andrzej; Ejchart, Andrzej

Citation: Ruszczynska-Bartnik, Katarzyna; Zdanowski, Konrad; Zhukov, Igor; Bierzynski, Andrzej; Ejchart, Andrzej. "Chemical Shift Assignments and solution structure of human apo-S100A1 E32Q mutant" Not known ., .-..

Assembly members:
S100A1E32Q_calcium_binding_protein, polymer, 93 residues, 10424.699 Da.

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

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

Entity Sequences (FASTA):
S100A1E32Q_calcium_binding_protein: GSELETAMETLINVFHAHSG KEGDKYKLSKKQLKELLQTE LSGFLDAQKDVDAVDKVMKE LDENGDGEVDFQEYVVLVAA LTVACNNFFWENS

Data sets:

assigned_chemical_shifts
- assigned_chem_shift_list_1
heteronucl_NOEs
heteronucl_T1_relaxation
heteronucl_T2_relaxation

Data type	Count
13C chemical shifts	415
15N chemical shifts	101
1H chemical shifts	663
heteronuclear NOE values	230
T1 relaxation values	231
T2 relaxation values	231

Additional metadata:

Assembly
Samples and Experiments
Software
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Entity Assembly ID	Entity Name	Entity ID
1	S100A1E32Q_1	1
2	S100A1E32Q_2	1

Name	Sample	Sample state	Sample conditions
2D 1H-15N HSQC	sample_1	isotropic	sample_conditions_1
2D 1H-13C HSQC	sample_1	isotropic	sample_conditions_1
3D 1H-13C NOESY aliphatic	sample_1	isotropic	sample_conditions_1
3D 1H-13C NOESY aromatic	sample_1	isotropic	sample_conditions_1
3D C(CO)NH	sample_1	isotropic	sample_conditions_1
3D HBHA(CO)NH	sample_1	isotropic	sample_conditions_1
3D CBCA(CO)NH	sample_1	isotropic	sample_conditions_1
3D HN(CO)CA	sample_1	isotropic	sample_conditions_1
3D HNCACB	sample_1	isotropic	sample_conditions_1
3D 1H-15N NOESY	sample_1	isotropic	sample_conditions_1
3D HNCO	sample_1	isotropic	sample_conditions_1
3D HNCA	sample_1	isotropic	sample_conditions_1
3D HCCH-TOCSY	sample_1	isotropic	sample_conditions_1
2D 1H-15N T2 relaxation	sample_1	isotropic	sample_conditions_1
2D 1H-15N T1 relaxation	sample_1	isotropic	sample_conditions_1
2D 1H-15N heteronuclear NOE	sample_1	isotropic	sample_conditions_1

BMRB	16360 18087 18088 18089 18101 18230 18231 18545
PDB	2L0P 2LHL 2LLS 2LLT 2LLU 2LP2 2LP3 2LUX 2M3W
DBJ	BAE90380 BAG35086 BAG70130 BAG70260
EMBL	CAA41107 CAH90674
GB	AAH14392 AAI41992 AAI48020 AAP35584 AAP36328
PRF	2003367A
REF	NP_001092512 NP_001127319 NP_001270255 NP_006262 XP_001111015
SP	P02639 P23297 Q5RC36
TPG	DAA31796

Biological Magnetic Resonance Data Bank

BMRB Entry 17857

Title: Chemical Shift Assignments and solution structure of human apo-S100A1 E32Q mutant

Additional metadata:

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