BMRB Entry 50381

Title:
The Structural Basis of PTEN Regulation by Multi-Site Phosphorylation
Deposition date:
2020-07-08
Original release date:
2021-10-10
Authors:
Dempsey, Daniel; Viennet, Thibault; Arthanari, Haribabu; Cole, Philipp
Citation:

Citation: Dempsey, Daniel; Viennet, Thibault; Iwase, Reina; Park, Eunyoung; Henriquez, Stephanie; Chen, Zan; Jeliazkov, Jeliazko; Palanski, Brad; Phan, Kim; Coote, Paul; Gray, Jeffrey; Eck, Michael; Gabelli, Sandra; Arthanari, Haribabu; Cole, Philip. "The Structural Basis of PTEN Regulation by Multi-Site Phosphorylation"  Nat. Struct. Mol. Biol. 28, 858-868 (2021).
PubMed: 34625746

Assembly members:

Assembly members:
entity_1, polymer, 336 residues, Formula weight is not available
entity_2, polymer, 18 residues, Formula weight is not available

Natural source:

Natural source:   Common Name: vase tunicate   Taxonomy ID: 7719   Superkingdom: Eukaryota   Kingdom: Metazoa   Genus/species: Ciona intestinalis

Experimental source:

Experimental source:   Production method: recombinant technology   Host organism: Escherichia coli   Vector: pET28a

Data sets:
Data typeCount
13C chemical shifts165
15N chemical shifts91
1H chemical shifts91
molecule interaction chemical shift values180

Additional metadata:

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

Assembly:

Entity Assembly IDEntity NameEntity ID
1VSP1
24P PTEN C-tail2

Entities:

Entity 1, VSP 336 residues - Formula weight is not available

VSP soluble domain, aa 241-576

1   LYSALASERSERARGARGTHRILESERGLN
2   ASNLYSARGARGTYRARGLYSASPGLYPHE
3   ASPLEUASPLEUTHRTYRVALTHRASPHIS
4   VALILEALAMETSERPHEPROSERSERGLY
5   ARGGLNSERLEUPHEARGASNPROILEGLY
6   GLUVALSERARGPHEPHELYSTHRLYSHIS
7   PROASPLYSPHEARGILETYRASNLEUCYS
8   SERGLUARGGLYTYRASPGLUTHRLYSPHE
9   ASPASNHISVALTYRARGVALMETILEASP
10   ASPHISASNVALPROTHRLEUVALASPLEU
11   LEULYSPHEILEASPASPALALYSVALTRP
12   METTHRSERASPPROASPHISVALILEALA
13   ILEHISSERLYSGLYGLYLYSGLYARGTHR
14   GLYTHRLEUVALSERSERTRPLEULEUGLU
15   ASPGLYLYSPHEASPTHRALALYSGLUALA
16   LEUGLUTYRPHEGLYSERARGARGTHRASP
17   PHEGLUVALGLYASPVALPHEGLNGLYVAL
18   GLUTHRALASERGLNILEARGTYRVALGLY
19   TYRPHEGLULYSILELYSLYSASNTYRGLY
20   GLYGLNLEUPROPROMETLYSLYSLEULYS
21   VALTHRGLYVALTHRILETHRALAILEGLN
22   GLYVALGLYARGGLYASNGLYSERASPLEU
23   SERMETGLNILEVALSERGLUARGGLNGLU
24   VALLEULEUCYSLYSPHEALAGLUGLYTYR
25   ASNCYSALALEUGLNTYRASPALATHRASP
26   ASPCYSVALTHRCYSGLUVALLYSASNCYS
27   PROVALLEUALAGLYASPILELYSVALARG
28   PHEMETSERTHRSERLYSSERLEUPROARG
29   GLYTYRASPASNCYSPROPHETYRPHETRP
30   PHEASNTHRSERLEUVALGLUGLYASPHIS
31   VALTHRLEULYSARGGLUGLUILEASPASN
32   PROHISLYSLYSLYSTHRTRPLYSILETYR
33   ARGASPASNPHETHRVALLYSLEUTHRPHE
34   SERASPALAGLUASPILE

Entity 2, 4P PTEN C-tail 18 residues - Formula weight is not available

1   CYSTYRSEPASPTPOTPOASPSEPASPPRO
2   GLUASNGLUPROPHEASPGLUASP

Samples:

sample_1: Voltage Sensing Phosphatase, [U-13C; U-15N; U-2H], 175 uM; Tetra-phosphorylated PTEN C-tail 800 uM

sample_conditions_1: ionic strength: 0.05 M; pH: 7.5; pressure: 1 atm; temperature: 298 K

Experiments:

NameSampleSample stateSample conditions
2D 1H-15N HSQCsample_1isotropicsample_conditions_1
3D HNCAsample_1isotropicsample_conditions_1
3D HN(CO)CAsample_1isotropicsample_conditions_1
3D HN(CA)COsample_1isotropicsample_conditions_1
3D HNCOsample_1isotropicsample_conditions_1
2D 1H-15N HSQCsample_1isotropicsample_conditions_1
2D 1H-15N HSQCsample_1isotropicsample_conditions_1

Software:

TOPSPIN v3 - collection

NMRPipe - processing

CcpNMR v2.4 - chemical shift assignment

NMR spectrometers:

  • Bruker AVANCE III 800 MHz
  • Bruker AVANCE NEO 900 MHz
  • Bruker AVANCE III 800 MHz

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