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NMR structure of Neuromedin C in aqueous solution.
Authors
Adrover, M., Sanchis, P., Vilanova, B., Pauwels, K., Martorell, G., Perez, J.
Assembly
Neuromedin C in water
Entity
1. Neuromedin C in water (polymer, Thiol state: not present), 11 monomers, 1119.278 Da Detail

GNHWAVGHLM X


Formula weight
1119.278 Da
Source organism
Homo sapiens
Exptl. method
solution NMR
Refine. method
distance geometry
Data set
assigned_chemical_shifts, heteronucl_NOEs, heteronucl_T1_relaxation, heteronucl_T2_relaxation
Chem. Shift Complete
Sequence coverage: 90.9 %, Completeness: 89.3 %, Completeness (bb): 80.0 % Detail

Polymer type: polypeptide(L)

Total1H13C15N
All89.3 % (100 of 112)98.2 % (55 of 56)77.3 % (34 of 44)91.7 % (11 of 12)
Backbone80.0 % (48 of 60)95.5 % (21 of 22)64.3 % (18 of 28)90.0 % (9 of 10)
Sidechain100.0 % (60 of 60)100.0 % (34 of 34)100.0 % (24 of 24)100.0 % (2 of 2)
Aromatic100.0 % (20 of 20)100.0 % (10 of 10)100.0 % (9 of 9)100.0 % (1 of 1)
Methyl100.0 % (10 of 10)100.0 % (5 of 5)100.0 % (5 of 5)

1. Neuromedin C

GNHWAVGHLM X

Sample

Solvent system 90% H2O/10% D2O, Pressure 1 atm, Temperature 273 K, pH 4.0, Details The sample was prepared in 10mM acetate buffer at pH 4.0


#NameIsotope labelingTypeConcentration
1Neuromedin Cnatural abundance5.0 (±0.1) mM
2sodium acetatenatural abundance10 (±0.1) mM
3DSSnatural abundance1.6 (±0.1) mM
4H2Onatural abundance90 %
5D2Onatural abundance10 %

Protein Blocks Logo
Calculated from 18 models in PDB: 2N0B, Strand ID: A Detail


Heteronucl. T1
10 T1 values in 1 lists
Coherence Iz, Field strength (1H) 600 MHz, Pressure 1 atm, Temperature 273 K, pH 4.0 Detail
Heteronucl. T2
10 T2 values in 1 lists
Coherence I(+,-), Field strength (1H) 600 MHz, Pressure 1 atm, Temperature 273 K, pH 4.0 Detail
Heteronucl. NOE
10 NOE values in 1 lists
Value type peak height, Field strength (1H) 600 MHz, Pressure 1 atm, Temperature 273 K, pH 4.0 Detail
Heteronucl. T1/T2
10 T1/T2 values in 1 lists
Field strength (1H) 600 MHz, Pressure 1 atm, Temperature 273 K, pH 4.0 Detail
Release date
2015-10-11
Citation
Conformational ensembles of neuromedin C reveal a progressive coil-helix transition within a binding-induced folding mechanism
Adrover, M., Sanchis, P., Vilanova, B., Pauwels, K., Martorell, G., Perez, J.
RSC ADV (2015), 5, 83074-83088, PubMed , DOI:
Related entities 1. Neuromedin C in water, : 10 : 9 entities Detail
Experiments performed 8 experiments Detail
NMR combined restraints 3 contents Detail
Keywords Feeding regulation, Growth and differentiation of human tumors, Neuropeptide