Question from NMRWiki Q&A forum Problems about VnmrJ 2.3A

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[Question from NMRWiki Q&A forum] Problems about VnmrJ 2.3A

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NMR processing:

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Rosetta-NMR (Robetta)

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GeNMR

I-TASSER

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Amber

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Torsion angles from chemical shifts:

Preditor

TALOS

Promega- Proline

Secondary structure from chemical shifts:

CSI (via RCI server)

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MICS caps, β-turns

d2D

PECAN

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RCI

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HADDOCK

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FANDAS

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V-NMR

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Methyl S2

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Shiftx2

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CH3shift- Methyl

ArShift- Aromatic

ShiftS

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

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DisMeta

Protein solubility:

Isotope labeling:

Solid-state NMR:

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02-25-2011, 11:33 AM

nmrlearner

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Problems about VnmrJ 2.3A

Problems about VnmrJ 2.3A

I have encountered some problems when getting started on the solid VNS system with VnmrJ 2.3A software.

when shimming with Fid scan, the fid/spectrum can't be displayed in real time.
when shimming with shimDriver, there may be an error message as 'usage - dfid or dfid#' and then the autoshim procedure quits.
How can I change the line style of the spectrum or fid? The line of spectrum seems too narrow.

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