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High-Resolution Solution Structure of a Sweet Protein Single-Chain Monellin (SCM) determined by Nuclear Magnetic Resonance Spectroscopy and Dynamical Simulated Annealing Calculations
Authors
Lee, S., Lee, J., Chang, H., Cho, J., Jung, J., Lee, W.
Assembly
monellin
Entity
1. monellin (polymer, Thiol state: not reported), 94 monomers, 11067.49 Da Detail

GEWEIIDIGP FTQNLGKFAV DEENKIGQYG RLTFNKVIRP CMKKTIYENE REIKGYEYQL YVYASDKLFR ADISEDYKTR GRKLLRFNGP VPPP


Formula weight
11067.49 Da
Source organism
Dioscoreophyllum cumminsii
Exptl. method
NMR
Refine. method
HYBRID GEOMETRY/DYNAMICAL SIMULATED ANNEALING CALCULATIONS
Data set
assigned_chemical_shifts
Chem. Shift Complete
Sequence coverage: 95.7 %, Completeness: 77.1 %, Completeness (bb): 96.0 % Detail

Polymer type: polypeptide(L)

Total1H15N
All77.1 % (553 of 717)75.2 % (466 of 620)89.7 % (87 of 97)
Backbone96.0 % (267 of 278)95.8 % (182 of 190)96.6 % (85 of 88)
Sidechain65.1 % (286 of 439)66.0 % (284 of 430)22.2 % (2 of 9)
Aromatic60.0 % (36 of 60)61.0 % (36 of 59) 0.0 % (0 of 1)
Methyl55.8 % (24 of 43)55.8 % (24 of 43)

1. monellin

GEWEIIDIGP FTQNLGKFAV DEENKIGQYG RLTFNKVIRP CMKKTIYENE REIKGYEYQL YVYASDKLFR ADISEDYKTR GRKLLRFNGP VPPP

Sample

Temperature 298 K, pH 7.0


#NameIsotope labelingTypeConcentration
1monellin0.0 ~ 0.0 mM

Protein Blocks Logo
Calculated from 21 models in PDB: 1MNL, Strand ID: A Detail


Release date
2000-04-30
Citation
Solution structure of a sweet protein single-chain monellin determined by nuclear magnetic resonance and dynamical simulated annealing calculations
Lee, S., Lee, J., Chang, H., Cho, J., Jung, J., Lee, W.
Biochemistry (1999), 38, 2340-2346, PubMed 10029527 , DOI 10.1021/bi9822731 ,
Related entities 1. monellin, : 1 : 1 : 2 : 42 entities Detail
Experiments performed 7 experiments Detail
nullKeywords alpha/beta motif, sweet protein, sweet receptor binding