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1H, 13C, and 15N Chemical Shift Assignments of the dimeric mutant of GB1
Authors
Byeon, I.L., Louis, J.M., Gronenborn, A.M.
Assembly
The B1 Domain of Streptococcal Protein G
Entity
1. The B1 Domain of Streptococcal Protein G (polymer, Thiol state: not present), 56 monomers, 6220.783 × 2 Da Detail

MQYKVILNGK TLKGETTTEA VDAATAEKVV KQFFNDNGVD GEWTYDDATK TFTVTE


Total weight
12441.566 Da
Max. entity weight
6220.783 Da
Source organism
Streptococcus sp.
Exptl. method
NMR
Data set
assigned_chemical_shifts
Chem. Shift Complete
Sequence coverage: 100.0 %, Completeness: 84.9 %, Completeness (bb): 84.8 % Detail

Polymer type: polypeptide(L)

Total1H13C15N
All84.9 % (538 of 634)91.6 % (295 of 322)72.8 % (182 of 250)98.4 % (61 of 62)
Backbone84.8 % (285 of 336)99.1 % (115 of 116)70.1 % (115 of 164)98.2 % (55 of 56)
Sidechain87.1 % (305 of 350)87.4 % (180 of 206)86.2 % (119 of 138)100.0 % (6 of 6)
Aromatic48.3 % (28 of 58)62.1 % (18 of 29)32.1 % (9 of 28)100.0 % (1 of 1)
Methyl100.0 % (66 of 66)100.0 % (33 of 33)100.0 % (33 of 33)

1. Immunoglobulin Binding domain 1 of Protein G

MQYKVILNGK TLKGETTTEA VDAATAEKVV KQFFNDNGVD GEWTYDDATK TFTVTE

Sample

Temperature 298 (±1) K, pH 6.0 (±0.2)


#NameIsotope labelingTypeConcentration
1Immunoglobulin Binding domain 1 of Protein G[U-95% 13C; U-95% 15N]1.7 mM

LACS Plot; CA
Referencing offset: -0.15 ppm, Outliers: 1 Detail
LACS Plot; CB
Referencing offset: -0.15 ppm, Outliers: 1 Detail
LACS Plot; HA
Referencing offset: -0.15 ppm, Outliers: 2 Detail
Release date
2003-12-04
Citation
A protein contortionist: core mutations of GB1 that induce dimerization and domain swapping
Byeon, I.L., Louis, J.M., Gronenborn, A.M.
J. Mol. Biol. (2003), 333, 141-152, PubMed 14516749 ,
Related entities 1. The B1 Domain of Streptococcal Protein G, : 1 : 2 : 104 entities Detail
Interaction partners 1. The B1 Domain of Streptococcal Protein G, : 1 interactors Detail
Experiments performed 18 experiments Detail
nullKeywords core mutants, domain-swapping, GB1, NMR structure, oligomerization