BMRB Entry 26004

Title:
HIGH RESOLUTION SOLUTION NMR STRUCTURE OF THE SPIDER VENOM PEPTIDE U5-SCYTOTOXIN-STH1A
Deposition date:
2016-03-18
Original release date:
2016-06-01
Authors:
Loening, Nikolaus
Citation:

Citation: Ariki, Nathanial; Munoz, Lisa; Armitage, Elizabeth; Goodstein, Francesca; George, Kathryn; Smith, Vanessa; Vetter, Irina; Herzig, Volker; King, Glenn; Loening, Nikolaus. "Characterization of Three Venom Peptides from the Spitting Spider Scytodes thoracica"  PLoS One 11, e0156291-e0156291 (2016).
PubMed: 27227898

Assembly members:

Assembly members:
U5-scytotoxin-Sth1a, polymer, 36 residues, 3912.2498 Da.

Natural source:

Natural source:   Common Name: spitting spider   Taxonomy ID: 1112478   Superkingdom: Eukaryota   Kingdom: Metazoa   Genus/species: Scytodes thoracica

Experimental source:

Experimental source:   Production method: recombinant technology   Host organism: Escherichia coli   Vector: PLIC-MBP

Entity Sequences (FASTA):

Entity Sequences (FASTA):
U5-scytotoxin-Sth1a: DETPDECVTRGNFCATPEVH GDWCCGSLKCVSNSCR

Data typeCount
13C chemical shifts146
15N chemical shifts75
1H chemical shifts430

Additional metadata:

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

Assembly:

Entity Assembly IDEntity NameEntity ID
1SYTXE1

Entities:

Entity 1, SYTXE 36 residues - 3912.2498 Da.

1   ASPGLUTHRPROASPGLUCYSVALTHRARG
2   GLYASNPHECYSALATHRPROGLUVALHIS
3   GLYASPTRPCYSCYSGLYSERLEULYSCYS
4   VALSERASNSERCYSARG

Samples:

sample_new_2: U5-scytotoxin-Sth1a, [U-13C; U-15N], 0.40 ± 0.10 mM

13C-15N: SYTXE, [U-98% 13C; U-98% 15N], 0.32 ± 0.0001 mM

15N: SYTXE, [U-98% 13C; U-98% 15N], 0.4 ± 0.0001 mM

sample_new_1: U5-scytotoxin-Sth1a, [U-13C; U-15N], 0.32 ± 0.10 mM

Standard: ionic strength: 0.030 M; pH: 6.500; pressure: 1.000 atm; temperature: 298.000 K

Experiments:

NameSampleSample stateSample conditions
3D HNCO13C-15NisotropicStandard
HNCACO (H[N[ca[CO]]])13C-15NisotropicStandard
HNCOCACB (H[N[co[{CA|ca[C]}]]])13C-15NisotropicStandard
3D HNCACB13C-15NisotropicStandard
2D 1H-13C HSQC/HMQC13C-15NisotropicStandard
2D 1H-13C HSQC/HMQC13C-15NisotropicStandard
2D 1H-13C HSQC/HMQC13C-15NisotropicStandard
2D 1H-13C HSQC/HMQC13C-15NisotropicStandard
2D 1H-15N HSQC/HMQC15NisotropicStandard
2D 1H-15N HSQC/HMQC15NisotropicStandard
2D 1H-1H TOCSY15NisotropicStandard
2D 1H-1H NOESY15NisotropicStandard
3D 1H-15N NOESY15NisotropicStandard
3D 1H-15N TOCSY15NisotropicStandard
2D 1H-15N HSQC/HMQC13C-15NisotropicStandard
3D HCCH-TOCSY13C-15NisotropicStandard
13C CT-HSQCsample_new_1solutionStandard
13C HSQCsample_new_1solutionStandard
13C AROMATIC HSQCsample_new_1solutionStandard
13C AROMATIC HSQC2sample_new_1solutionStandard
15N HMQC (13C/15N SAMPLE)sample_new_1solutionStandard
HCCH TOCSYsample_new_1solutionStandard
HNCACBsample_new_1solutionStandard
HNCACOsample_new_1solutionStandard
HNCOsample_new_1solutionStandard
HNCOCACBsample_new_1solutionStandard
15N HMQCsample_new_2solutionStandard
15N HMQC2sample_new_2solutionStandard
15N HSQC-NOESYsample_new_2solutionStandard
15N HSQC-TOCSYsample_new_2solutionStandard
1H NOESYsample_new_2solutionStandard
1H TOCSYsample_new_2solutionStandard

Software:

ARIA v2.3.2, Rieping W., Habeck M., Bardiaux B., Bernard A., Malliavin T.E., Nilges M. - NOE assignment, structure calculation

AutoDep v4.3, PDBe - chemical shift assignment

CNS v1.2, Brunger, Adams, Clore, Gros, Nilges and Read - chemical shift assignment

CcpNmr_Analysis v2.4, CCPN - chemical shift assignment, project management

Talos-N v4.12, Yang Shen and Ad Bax - protein backbone dihedral angle prediction

NMR spectrometers:

  • Bruker Avance III 600 MHz
  • Bruker AVANCE 600 MHz

Related Database Links:

ArachnoServer U5-scytotoxin-Sth1a

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