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Side-chains:
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NOEs:
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UNIO Candid
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Structure from NMR restraints:
Ab initio:
GeNMR
Cyana
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ASDP
UNIO ATNOS-Candid
UNIO Candid
Fragment-based:
BMRB CS-Rosetta
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Template-based:
GeNMR
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Refinement:
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Structure from chemical shifts:
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WeNMR CS-Rosetta
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Torsion angles from chemical shifts:
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Secondary structure from chemical shifts:
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Flexibility from chemical shifts:
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Chemical shifts re-referencing:
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UNIO Shiftinspector
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NMR model quality:
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RPF scores
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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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From sequence:
Shifty
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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
Camfold
camGroEL
Zyggregator
Isotope labeling:
UPLABEL
Solid-state NMR:
sedNMR


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Default Bruker GRPDLY Parameter

Bruker GRPDLY Parameter

I am new to working with Bruker-style NMR data and am experiencing confusion with regard to Bruker's digital filtering. Some experiments on our Bruker spectrometers result in valid decim/dspfvs/grpdly values in the acqus output file, but other spectrometers give a value of -1 for grpdly. Does anyone know what this value means? More importantly, how can I calculate how many points to left-shift the Bruker fid for offline processing when grpdly does not contain the value?

Thank you.



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