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NMR processing:
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NMR assignment:
Backbone:
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PINE
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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Fragment-based:
BMRB CS-Rosetta
Rosetta-NMR (Robetta)
Template-based:
GeNMR
I-TASSER
Refinement:
Amber
Structure from chemical shifts:
Fragment-based:
WeNMR CS-Rosetta
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Homology-based:
CS23D
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Torsion angles from chemical shifts:
Preditor
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Secondary structure from chemical shifts:
CSI (via RCI server)
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MICS caps, β-turns
d2D
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Flexibility from chemical shifts:
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Interactions from chemical shifts:
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Chemical shifts re-referencing:
Shiftcor
UNIO Shiftinspector
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CheckShift
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NMR model quality:
NOEs, other restraints:
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RPF scores
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Chemical shifts:
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Vasco
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RDCs:
DC
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Pseudocontact shifts:
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Protein geomtery:
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What-If
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PSVS
MolProbity
SAVES2 or SAVES4
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MetaMQAPII
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Ramachandran Plot
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Verify_3D
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NMR spectrum prediction:
FANDAS
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Flexibility from structure:
Backbone S2
Methyl S2
B-factor
Molecular dynamics:
Gromacs
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Chemical shifts prediction:
From structure:
Shiftx2
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CH3shift- Methyl
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Proshift
PPM
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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
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Zyggregator
Isotope labeling:
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Solid-state NMR:
sedNMR


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Old 07-10-2012, 06:01 PM
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Default processing cosy

processing cosy

Hi all, We have collected a magnitude cosy data using a bruker NMR (pulse sequence: cosygpqf) but having problems with nmrPIPE processing. We tried Real and QF

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