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Backbone 1H, 13C, and 15N chemical shift assignments for the nucleotide-binding domain of E.coli DnaK in the ADP.Pi-bound state
Authors
Zhuravleva, A., Gierasch, L.M.
Assembly
NBD(1-388)
Entity
1. the nucleotide-binding domain of DnaK (polymer, Thiol state: all free), 388 monomers, 42009.22 Da Detail

MGKIIGIDLG TTNSCVAIMD GTTPRVLENA EGDRTTPSII AYTQDGETLV GQPAKRQAVT NPQNTLFAIK RLIGRRFQDE EVQRDVSIMP FKIIAADNGD AWVEVKGQKM APPQISAEVL KKMKKTAEDY LGEPVTEAVI TVPAYFNDAQ RQATKDAGRI AGLEVKRIIN EPTAAALAYG LDKGTGNRTI AVYDLGGGAF DISIIEIDEV DGEKTFEVLA TNGDTHLGGE DFDSRLINYL VEEFKKDQGI DLRNDPLAMQ RLKEAAEKAK IELSSAQQTD VNLPYITADA TGPKHMNIKV TRAKLESLVE DLVNRSIELL KVALQDAGLS VSDIDDVILV GGQTRMPMVQ KKVAEFFGKE PRKDVNPDEA VAIGAAVQGG VLTGDVKD


2. ADP (non-polymer), 427.201 Da
3. MG (non-polymer), 24.305 Da
4. PO4 (non-polymer), 94.971 Da
Total weight
42555.695 Da
Max. entity weight
42009.22 Da
Source organism
Escherichia coli
Exptl. method
solution NMR
Data set
assigned_chemical_shifts
Chem. Shift Complete
Sequence coverage: 95.4 %, Completeness: 45.7 %, Completeness (bb): 77.4 % Detail

Polymer type: polypeptide(L)

Total1H13C15N
All45.7 % (1998 of 4374)24.4 % (553 of 2267)64.9 % (1104 of 1701)84.0 % (341 of 406)
Backbone77.4 % (1777 of 2296)50.4 % (400 of 793)91.7 % (1037 of 1131)91.4 % (340 of 372)
Sidechain21.9 % (533 of 2433)10.4 % (153 of 1474)41.0 % (379 of 925) 2.9 % (1 of 34)
Aromatic10.8 % (19 of 176)14.8 % (13 of 88) 6.9 % (6 of 87) 0.0 % (0 of 1)
Methyl21.8 % (108 of 496)15.7 % (39 of 248)27.8 % (69 of 248)

1. the nucleotide-binding domain of DnaK

MGKIIGIDLG TTNSCVAIMD GTTPRVLENA EGDRTTPSII AYTQDGETLV GQPAKRQAVT NPQNTLFAIK RLIGRRFQDE EVQRDVSIMP FKIIAADNGD AWVEVKGQKM APPQISAEVL KKMKKTAEDY LGEPVTEAVI TVPAYFNDAQ RQATKDAGRI AGLEVKRIIN EPTAAALAYG LDKGTGNRTI AVYDLGGGAF DISIIEIDEV DGEKTFEVLA TNGDTHLGGE DFDSRLINYL VEEFKKDQGI DLRNDPLAMQ RLKEAAEKAK IELSSAQQTD VNLPYITADA TGPKHMNIKV TRAKLESLVE DLVNRSIELL KVALQDAGLS VSDIDDVILV GGQTRMPMVQ KKVAEFFGKE PRKDVNPDEA VAIGAAVQGG VLTGDVKD

Sample

Solvent system 95% H2O/5% D2O, Pressure 1 atm, Temperature 299 (±0.2) K, pH 7.0 (±0.1)


#NameIsotope labelingTypeConcentration
1potassium phosphatenatural abundance10 mM
2magnesium chloridenatural abundance10 mM
3AEBSF protease inhibitornatural abundance1 uM
4DTTnatural abundance5 mM
5DSSnatural abundance0.5 mM
6ADPnatural abundance10 mM
7potassium chloridenatural abundance10 mM
8the nucleotide-binding domain of DnaK[U-97% 2H; U-95% 13C; U-95% 15N]0.5 mM
9H2Onatural abundance95 %
10D2Onatural abundance5 %

LACS Plot; CA
Referencing offset: -0.04 ppm, Outliers: 3 Detail
LACS Plot; CB
Referencing offset: -0.04 ppm, Outliers: 3 Detail
LACS Plot; CO
Referencing offset: 0.11 ppm, Outliers: 2 Detail
Release date
2011-05-04
Citation 1
NMRPipe: a multidimensional spectral processing system based on UNIX pipes
Delaglio, F., Grzesiek, S., Vuister, G., Zhu, G., Pfeifer, J., Bax, A.
J. Biomol. NMR (1995), 6, 277-293, PubMed 8520220 ,
Citation 2
Allosteric signal transmission in the nucleotide-binding domain of 70-kDa heat shock protein (Hsp70) molecular chaperones
Zhuravleva, A., Gierasch, L.M.
Proc. Natl. Acad. Sci. U. S. A. (2011), 108, 6987-6992, PubMed 21482798 , DOI 10.1073/pnas.1014448108 ,
Citation 3
Automated analysis of protein NMR assignments using methods from artificial intelligence
Feng, W., Zimmerman, D., Kulikowski, C., Huang, Y., Tashiro, M., Shimotakahara, S., Chien, C., Powers, R., Montelione, G.
J. Mol. Biol. (1997), 269, 592-610, PubMed 9217263 , DOI 10.1006/jmbi.1997.1052 ,
Citation 4
Optimizing the process of nuclear magnetic resonance spectrum analysis and computer aided resonance assignment
Keller, R.
Related entities 1. the nucleotide-binding domain of DnaK, : 1 : 18 : 283 entities Detail
Interaction partners 1. the nucleotide-binding domain of DnaK, : 322 interactors Detail
Experiments performed 6 experiments Detail
Chemical shift validation 6 contents Detail
Keywords allostery, conformational ensemble, DnaK, Hsp70 molecular chaperone, interdomain linker, nucleotide-binding domain, subdomain motions