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NMR processing:
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Side-chains:
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NOEs:
UNIO ATNOS-Candid
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Structure from NMR restraints:
Ab initio:
GeNMR
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ASDP
UNIO ATNOS-Candid
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Fragment-based:
BMRB CS-Rosetta
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Template-based:
GeNMR
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Refinement:
Amber
Structure from chemical shifts:
Fragment-based:
WeNMR CS-Rosetta
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CS23D
Simshift
Torsion angles from chemical shifts:
Preditor
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Secondary structure from chemical shifts:
CSI (via RCI server)
TALOS
MICS caps, β-turns
d2D
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Flexibility from chemical shifts:
RCI
Interactions from chemical shifts:
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Chemical shifts re-referencing:
Shiftcor
UNIO Shiftinspector
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NMR model quality:
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Pseudocontact shifts:
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NMR spectrum prediction:
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Flexibility from structure:
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Molecular dynamics:
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Chemical shifts prediction:
From structure:
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CH3shift- Methyl
ArShift- Aromatic
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Proshift
PPM
CheShift-2- Cα
From sequence:
Shifty
Camcoil
Poulsen_rc_CS
Disordered proteins:
MAXOCC
Format conversion & validation:
CCPN
From NMR-STAR 3.1
Validate NMR-STAR 3.1
NMR sample preparation:
Protein disorder:
DisMeta
Protein solubility:
camLILA
ccSOL
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camGroEL
Zyggregator
Isotope labeling:
UPLABEL
Solid-state NMR:
sedNMR


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Default log: Failed to find Z0 - low s/n

log: Failed to find Z0 - low s/n

Hi, everybody! I met a problem on Varian 400 MR: DMSO samples don't lock by "find Z0" button, but I can find lock signal manually in a quite unusual range of Z0 values (30000). After adjusting shims i still have pour s/n. Probe is tuned and matched. It happened after VT experiments, I ran. Samples in CDCl3 looks perfect! What am I doing wrong and why that's happened? Thanks.



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