BMRB Entry 51398

Title:
PARP14 macro domain 2 free form
Deposition date:
2022-04-14
Original release date:
2022-09-19
Authors:
Charalampous, Periklis; Fourkiotis, Nikolaos; Tsika, Aikaterini; Gallo, Angelo; Spyroulias, Georgios
Citation:

Citation: Fourkiotis, Nikolaos; Charalampous, Periklis; Tsika, Aikaterini; Kravvariti, Konstantina; Sideras-Bisdekis, Christos; Gallo, Angelo; Spyroulias, Georgios. "NMR study of human macroPARPs domains: 1 H, 15 N and 13 C resonance assignment of hPARP14 macro domain 2 in the free and the ADPr bound state"  Biomol. NMR Assign. 16, 399-406 (2022).
PubMed: 36107366

Assembly members:

Assembly members:
entity_1, polymer, 197 residues, Formula weight is not available

Natural source:

Natural source:   Common Name: Human   Taxonomy ID: 9606   Superkingdom: Eukaryota   Kingdom: Metazoa   Genus/species: Homo sapiens

Experimental source:

Experimental source:   Production method: recombinant technology   Host organism: Escherichia coli   Vector: pETm41

Data sets:
Data typeCount
13C chemical shifts703
15N chemical shifts171
1H chemical shifts1211

Additional metadata:

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

Assembly:

Entity Assembly IDEntity NameEntity ID
1P14MD21

Entities:

Entity 1, P14MD2 197 residues - Formula weight is not available

The str file includes a cloning tag (GAMG) so the native sequence starts at G5. The number correspond in the gene is G999 (native sequence start).

1   GLYALAMETGLYGLYLYSTHRSERTRPGLU
2   LYSGLYSERLEUVALSERPROGLYGLYLEU
3   GLNMETLEULEUVALLYSGLUGLYVALGLN
4   ASNALALYSTHRASPVALVALVALASNSER
5   VALPROLEUASPLEUVALLEUSERARGGLY
6   PROLEUSERLYSSERLEULEUGLULYSALA
7   GLYPROGLULEUGLNGLUGLULEUASPTHR
8   VALGLYGLNGLYVALALAVALSERMETGLY
9   THRVALLEULYSTHRSERSERTRPASNLEU
10   ASPCYSARGTYRVALLEUHISVALVALALA
11   PROGLUTRPARGASNGLYSERTHRSERSER
12   LEULYSILEMETGLUASPILEILEARGGLU
13   CYSMETGLUILETHRGLUSERLEUSERLEU
14   LYSSERILEALAPHEPROALAILEGLYTHR
15   GLYASNLEUGLYPHEPROLYSASNILEPHE
16   ALAGLULEUILEILESERGLUVALPHELYS
17   PHESERSERLYSASNGLNLEULYSTHRLEU
18   GLNGLUVALHISPHELEULEUHISPROSER
19   ASPHISGLUASNILEGLNALAPHESERASP
20   GLUPHEALAARGARGALAASN

Samples:

sample_1: PARP14 macro domain 2, [U-100% 13C; U-100% 15N], 0.6 mM; D2O, [U-100% 2H], 10%; H2O 90%; DTT 2 mM; HEPES 50 mM; EDTA 0.4 mM; sodium chloride 100 mM; proteases inhibitors 0.1%; DSS 1%

sample_conditions_1: ionic strength: 150 mM; pH: 7; pressure: 1 atm; temperature: 298 K

Experiments:

NameSampleSample stateSample conditions
2D 1H-15N HSQCsample_1isotropicsample_conditions_1
2D 1H-13C HSQCsample_1isotropicsample_conditions_1
3D HNCOsample_1isotropicsample_conditions_1
3D HN(CA)COsample_1isotropicsample_conditions_1
3D HNCAsample_1isotropicsample_conditions_1
3D HN(CO)CAsample_1isotropicsample_conditions_1
3D CBCA(CO)NHsample_1isotropicsample_conditions_1
3D CBCANHsample_1isotropicsample_conditions_1
3D (H)CCH-TOCSYsample_1isotropicsample_conditions_1

Software:

TOPSPIN v4.1.1 - collection, processing

CARA v1.9.1.7 - chemical shift assignment, peak picking

NMR spectrometers:

  • Bruker AVANCE III 700 MHz

Related Database Links:

UNP Q460N5
AlphaFold Q9ULF2

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