BMRB Entry 18087

Name: solution structure of human apo-S100A1 C85M
Published: 2013-01-08

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PDB ID: 2lls
Entry in NMR Restraints Grid
Validation report in NRG-CING
Chem Shift validation: AVS_full, LACS, SPARTA
BMRB Entry DOI: doi:10.13018/BMR18087
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Nicholas Rego and David Koes
3Dmol.js: molecular visualization with WebGL
Bioinformatics (2015) 31 (8): 1322-1324 doi:10.1093/bioinformatics/btu829

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Title:

solution structure of human apo-S100A1 C85M

Deposition date:

2011-11-17

Original release date:

2013-01-08

Authors:

Budzinska, Monika; Jaremko, Lukasz; Jaremko, Mariusz; Zdanowski, Konrad; Zhukov, Igor; Bierzynski, Andrzej; Ejchart, Andrzej

Citation:

Citation: Budzinska, Monika; Jaremko, Lukasz; Jaremko, Mariusz; Zdanowski, Konrad; Zhukov, Igor; Bierzynski, Andrzej; Ejchart, Andrzej. "Chemical Shift Assignments and solution structure of human apo-S100A1 C85M mutant" .

Assembly members:

Assembly members:
S100A1C85M, polymer, 93 residues, 10453.736 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-30a+

Entity Sequences (FASTA):

Entity Sequences (FASTA):
S100A1C85M: GSELETAMETLINVFHAHSG KEGDKYKLSKKELKELLQTE LSGFLDAQKDVDAVDKVMKE LDENGDGEVDFQEYVVLVAA LTVAMNNFFWENS

Data sets:

assigned_chemical_shifts
- assigned_chem_shift_list_1
heteronucl_NOEs
heteronucl_T1_relaxation
heteronucl_T2_relaxation

Data type	Count
13C chemical shifts	396
15N chemical shifts	95
1H chemical shifts	658
heteronuclear NOE values	194
T1 relaxation values	188
T2 relaxation values	190

Additional metadata:

Assembly
Samples and Experiments
Software
Spectrometers
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Assembly:

Entity Assembly ID	Entity Name	Entity ID
1	S100A1C85M, chain 1	1
2	S100A1C85M, chain 2	1

Entities:

Entity 1, S100A1C85M, chain 1 93 residues - 10453.736 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

GLU

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

MET

ASN

PHE

TRP

10

GLU

ASN

SER

Samples:

sample_1: TRIS-d11 50 mM; D2O 10%; sodium chloride 50 mM; S100A1C85M, [U-99% 13C; U-99% 15N], 1 mM; H2O 90%

sample_2: TRIS-d11 50 mM; sodium chloride 50 mM; S100A1C85M, [U-99% 13C; U-99% 15N], 1 mM; D2O 100%

sample_3: TRIS-d11 50 mM; D2O 10%; sodium chloride 50 mM; S100A1C85M, [U-99% 15N], 1 mM; H2O 90%

sample_conditions_1: ionic strength: 50 mM; pH: 6.8; pressure: 1 atm; temperature: 310 K

sample_conditions_2: ionic strength: 50 mM; pH: 7.2; pressure: 1 atm; temperature: 310 K

sample_conditions_3: ionic strength: 50 mM; pH: 6.8; 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-15N HSQC NH2 only	sample_1	isotropic	sample_conditions_1
2D 1H-13C HSQC aliphatic	sample_2	isotropic	sample_conditions_2
2D 1H-13C HSQC aromatic	sample_2	isotropic	sample_conditions_2
3D CBCA(CO)NH	sample_1	isotropic	sample_conditions_1
3D HNCO	sample_1	isotropic	sample_conditions_1
3D HNCA	sample_1	isotropic	sample_conditions_1
3D HNCACB	sample_1	isotropic	sample_conditions_1
3D HN(CO)CA	sample_1	isotropic	sample_conditions_1
3D HBHA(CO)NH	sample_1	isotropic	sample_conditions_1
3D HCCH-TOCSY	sample_2	isotropic	sample_conditions_2
3D 1H-15N NOESY	sample_1	isotropic	sample_conditions_1
3D 1H-13C NOESY aliphatic	sample_2	isotropic	sample_conditions_2
3D 1H-13C NOESY aromatic	sample_2	isotropic	sample_conditions_2
2D 1H-15N heteronuclear NOE	sample_3	isotropic	sample_conditions_3
2D 1H-15N heteronuclear NOE	sample_3	isotropic	sample_conditions_3
2D 1H-15N heteronuclear NOE	sample_3	isotropic	sample_conditions_3
2D 1H-15N T1 relaxation	sample_3	isotropic	sample_conditions_3
2D 1H-15N T1 relaxation	sample_3	isotropic	sample_conditions_3
2D 1H-15N T1 relaxation	sample_3	isotropic	sample_conditions_3
2D 1H-15N T2 relaxation	sample_3	isotropic	sample_conditions_3
2D 1H-15N T2 relaxation	sample_3	isotropic	sample_conditions_3
2D 1H-15N T2 relaxation	sample_3	isotropic	sample_conditions_3

Software:

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

CYANA, Guntert, Mumenthaler and Wuthrich - constraints assignments, data analysis, structure solution

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

SPARKY, Goddard - chemical shift assignment, data analysis

CARA, Keller and Wuthrich - chemical shift assignment

MARS, Jung, Zweckstetter - automated chemical shift assignments

NMR spectrometers:

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

BMRB	16360 17857 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