BMRB

Biological Magnetic Resonance Data Bank


A Repository for Data from NMR Spectroscopy on Proteins, Peptides, Nucleic Acids, and other Biomolecules
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BMRB Entry 17953

Title: NMR Structure of protoporphyrin-IX bound murine p22HBP

Deposition date: 2011-09-22 Original release date: 2012-09-24

Authors: Goodfellow, Brian; Dias, J.; Macedo, A.; Ferreira, G.; Peterson, F.; Volkman, B.; Duarte, I.

Citation: Goodfellow, Brian; Dias, J.; Macedo, A.; Ferreira, G.; Peterson, F.; Volkman, B.; Duarte, I.. "The NMR Structure of protoporphyrin-IX bound murine p22HBP"  to be published ., .-..

Assembly members:
HEME-BINDING_PROTEIN_1, polymer, 195 residues, 21737.3322 Da.

Natural source:   Common Name: Mouse   Taxonomy ID: 10090   Superkingdom: Eukaryota   Kingdom: Metazoa   Genus/species: Mus musculus

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

Entity Sequences (FASTA):
HEME-BINDING_PROTEIN_1: MKNSTHHHHHHNSLFGSVET WPWQVLSTGGKEDVSYEERA CEGGKFATVEVTDKPVDEAL REAMPKIMKYVGGTNDKGVG MGMTVPVSFAVFPNEDGSLQ KKLKVWFRIPNQFQGSPPAP SDESVKIEEREGITVYSTQF GGYAKEADYVAHATQLRTTL EGTPATYQGDVYYCAGYDPP MKPYGRRNEVWLVKA

Data sets:
Data typeCount
13C chemical shifts639
15N chemical shifts166
1H chemical shifts1031

Additional metadata:

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

Assembly:

Entity Assembly IDEntity NameEntity ID
1HEME-BINDING PROTEIN 11

Entities:

Entity 1, HEME-BINDING PROTEIN 1 195 residues - 21737.3322 Da.

1   METLYSASNSERTHRHISHISHISHISHIS
2   HISASNSERLEUPHEGLYSERVALGLUTHR
3   TRPPROTRPGLNVALLEUSERTHRGLYGLY
4   LYSGLUASPVALSERTYRGLUGLUARGALA
5   CYSGLUGLYGLYLYSPHEALATHRVALGLU
6   VALTHRASPLYSPROVALASPGLUALALEU
7   ARGGLUALAMETPROLYSILEMETLYSTYR
8   VALGLYGLYTHRASNASPLYSGLYVALGLY
9   METGLYMETTHRVALPROVALSERPHEALA
10   VALPHEPROASNGLUASPGLYSERLEUGLN
11   LYSLYSLEULYSVALTRPPHEARGILEPRO
12   ASNGLNPHEGLNGLYSERPROPROALAPRO
13   SERASPGLUSERVALLYSILEGLUGLUARG
14   GLUGLYILETHRVALTYRSERTHRGLNPHE
15   GLYGLYTYRALALYSGLUALAASPTYRVAL
16   ALAHISALATHRGLNLEUARGTHRTHRLEU
17   GLUGLYTHRPROALATHRTYRGLNGLYASP
18   VALTYRTYRCYSALAGLYTYRASPPROPRO
19   METLYSPROTYRGLYARGARGASNGLUVAL
20   TRPLEUVALLYSALA

Samples:

sample_1: HEME-BINDING_PROTEIN_1, [U-13C; U-15N], 1 mM

sample_conditions_1: ionic strength: 150.000 mM; pH: 8.000; pressure: 1.000 atm; temperature: 303.000 K

Experiments:

NameSampleSample stateSample conditions
2D/3D 15N NOESYsample_1solutionsample_conditions_1
2D/3D 13C NOESY (aliphatic and aromatic)sample_1solutionsample_conditions_1

Software:

AutoDep v4.3, AutoDep -

CYANA vany, Guntert, Mumenthaler and Wuthrich - chemical shift assignment, data analysis

NMR spectrometers:

  • Bruker DMX 600 MHz

Related Database Links:

UNP HEBP1_MOUSE
PDB
DBJ BAA33770
EMBL CAJ18470
GB AAD32096 AAH12654 AAI68221 EDL10544 EDM01631
REF NP_038574 XP_006237591 XP_011239526
SP Q9R257

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