BMRB

Biological Magnetic Resonance Data Bank


A Repository for Data from NMR Spectroscopy on Proteins, Peptides, Nucleic Acids, and other Biomolecules
Member of WWPDB

BMRB Entry 16837

Title: HAV 3C C24S   PubMed: 22156376

Deposition date: 2010-04-06 Original release date: 2011-12-15

Authors: Blaum, Baerbel; Winfried, Wuensche; Andrew, Benie

Citation: Blaum, Barbel; Wunsche, Winfried; Benie, Andrew; Kusov, Yuri; Peters, Hannelore; Gauss-Muller, Verena; Peters, Thomas; Sczakiel, Georg. "Functional binding of hexanucleotides to 3C protease of hepatitis A virus."  Nucleic Acids Res. 40, 3042-3055 (2012).

Assembly members:
HAV_3C_protease_C24S, polymer, 217 residues, Formula weight is not available

Natural source:   Common Name: Hepatitis A virus   Taxonomy ID: 12092   Superkingdom: Virus   Kingdom: not available   Genus/species: Hepatovirus not available

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

Entity Sequences (FASTA):
HAV_3C_protease_C24S: STLEIAGLVRKNLVQFGVGE KNGSVRWVMNALGVKDDWLL VPSHAYKFEKDYEMMEFYFN RGGTYYSISAGNVVIQSLDV GFQDVVLMKVPTIPKFRDIT QHFIKKGDVPRALNRLATLV TTVNGTPMLISEGPLKMEEK ATYVHKKNDGTTVDLTVDQA WRGKGEGLPGMCGGALVSSN QSIQNAILGIHVAGGNSILV AKLVTQEMFQNIDKKIE

Data sets:
Data typeCount
13C chemical shifts494
15N chemical shifts157
1H chemical shifts157

Additional metadata:

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

Assembly:

Entity Assembly IDEntity NameEntity ID
1HAV 3C C24S1

Entities:

Entity 1, HAV 3C C24S 217 residues - Formula weight is not available

1   SERTHRLEUGLUILEALAGLYLEUVALARG
2   LYSASNLEUVALGLNPHEGLYVALGLYGLU
3   LYSASNGLYSERVALARGTRPVALMETASN
4   ALALEUGLYVALLYSASPASPTRPLEULEU
5   VALPROSERHISALATYRLYSPHEGLULYS
6   ASPTYRGLUMETMETGLUPHETYRPHEASN
7   ARGGLYGLYTHRTYRTYRSERILESERALA
8   GLYASNVALVALILEGLNSERLEUASPVAL
9   GLYPHEGLNASPVALVALLEUMETLYSVAL
10   PROTHRILEPROLYSPHEARGASPILETHR
11   GLNHISPHEILELYSLYSGLYASPVALPRO
12   ARGALALEUASNARGLEUALATHRLEUVAL
13   THRTHRVALASNGLYTHRPROMETLEUILE
14   SERGLUGLYPROLEULYSMETGLUGLULYS
15   ALATHRTYRVALHISLYSLYSASNASPGLY
16   THRTHRVALASPLEUTHRVALASPGLNALA
17   TRPARGGLYLYSGLYGLUGLYLEUPROGLY
18   METCYSGLYGLYALALEUVALSERSERASN
19   GLNSERILEGLNASNALAILELEUGLYILE
20   HISVALALAGLYGLYASNSERILELEUVAL
21   ALALYSLEUVALTHRGLNGLUMETPHEGLN
22   ASNILEASPLYSLYSILEGLU

Samples:

sample_1: HAV 3C protease C24S, [U-100% 13C; U-100% 15N; U-75% 2H], 0.2 mM; H2O 90%; D2O 10%

sample_conditions_1: ionic strength: 200 mM; pH: 7.4; pressure: 1 atm; temperature: 303 K

Experiments:

NameSampleSample stateSample conditions
3D HNCOsample_1isotropicsample_conditions_1
3D HN(CA)COsample_1isotropicsample_conditions_1
3D HNCACBsample_1isotropicsample_conditions_1
3D HN(CO)CACBsample_1isotropicsample_conditions_1

Software:

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

SPARKY, Goddard - chemical shift assignment

NMR spectrometers:

  • Bruker Avance 700 MHz

Related Database Links:

PDB
DBJ BAA35102 BAA35103 BAA35104 BAA35105 BAA35106
EMBL CAA33491 CAA50195 CAA53024 CAA53025 CAA53026
GB AAA45465 AAA45466 AAA45467 AAA45468 AAA45469
PIR GNNYHB
REF NP_041007 NP_041008 NP_740558
SP A3FMB2 A5LGW7 P06441 P08617 P13901

Download simulated HSQC data in one of the following formats:
CSV: Backbone or all simulated shifts
SPARKY: Backbone or all simulated shifts