BMRB Entry 17857

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

Click here to enlarge.

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
MolProbity Validation Chart

NMR-STAR file interactive viewer.
NMR-STAR v3 text file.
XML gzip file.
RDF gzip file.
All files associated with the entry

Nicholas Rego and David Koes
3Dmol.js: molecular visualization with WebGL
Bioinformatics (2015) 31 (8): 1322-1324 doi:10.1093/bioinformatics/btu829

Select model:

I am color blind

Download raw data. Direct link to this display. Help

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:

Citation: Ruszczynska-Bartnik, Katarzyna; Zdanowski, Konrad; Zhukov, Igor; Bierzynski, Andrzej; Ejchart, Andrzej. "Chemical Shift Assignments and solution structure of human apo-S100A1 E32Q mutant" .

Assembly members:

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

Natural source:

Natural source: Common Name: Escherichia 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: pET30a+

Entity Sequences (FASTA):

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
Spectrometers
Hide all

Assembly:

Entity Assembly ID	Entity Name	Entity ID
1	S100A1E32Q_1	1
2	S100A1E32Q_2	1

Entities:

Entity 1, S100A1E32Q_1 93 residues - 10424.699 Da.

1

GLY

SER

GLU

LEU

GLU

THR

ALA

MET

GLU

THR

2

LEU

ILE

ASN

VAL

PHE

HIS

ALA

HIS

SER

GLY

3

LYS

GLU

GLY

ASP

LYS

TYR

LYS

LEU

SER

LYS

4

LYS

GLN

LEU

LYS

GLU

LEU

GLN

THR

GLU

5

LEU

SER

GLY

PHE

LEU

ASP

ALA

GLN

LYS

ASP

6

VAL

ASP

ALA

VAL

ASP

LYS

VAL

MET

LYS

GLU

7

LEU

ASP

GLU

ASN

GLY

ASP

GLY

GLU

VAL

ASP

8

PHE

GLN

GLU

TYR

VAL

LEU

VAL

ALA

9

LEU

THR

VAL

ALA

CYS

ASN

PHE

TRP

10

GLU

ASN

SER

Samples:

sample_1: S100A1E32Q, [U-98% 13C; U-98% 15N], 1 mM; TRIS-d11 50 mM; EDTA 1 mM; sodium chloride 50 mM; D2O 10%; H2O 90%

sample_conditions_1: ionic strength: 0.05 M; pH: 7.0; pressure: 1 atm; temperature: 310 K

Experiments:

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

Software:

Analysis-CCPN v2.1.5, CCPN - chemical shift assignment

CARA v1.8, Keller and Wuthrich - chemical shift assignment

SPARKY, Goddard - data analysis

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

X-PLOR NIH v2.26, Schwieters, Kuszewski, Tjandra and Clore - structure solution

NMR spectrometers:

Varian INOVA 400 MHz
Varian UnityPlus 500 MHz
Varian Varian NMR System 700 MHz
Varian Varian NMR System 800 MHz

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
AlphaFold	P02639 P23297 Q5RC36