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NMR processing:
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Structure from NMR restraints:
Ab initio:
GeNMR
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Fragment-based:
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Template-based:
GeNMR
I-TASSER
Refinement:
Amber
Structure from chemical shifts:
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WeNMR CS-Rosetta
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CS23D
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Torsion angles from chemical shifts:
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Secondary structure from chemical shifts:
CSI (via RCI server)
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Flexibility 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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RDCs:
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Pseudocontact shifts:
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Protein geomtery:
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What-If
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PSVS
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NMR spectrum prediction:
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Flexibility from structure:
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B-factor
Molecular dynamics:
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Chemical shifts prediction:
From structure:
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From sequence:
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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:
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Protein solubility:
camLILA
ccSOL
Camfold
camGroEL
Zyggregator
Isotope labeling:
UPLABEL
Solid-state NMR:
sedNMR


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Default [ASAP] Nanobody GPS by PCS: An Efficient New NMR Analysis Method for G Protein Coupled Receptors and Other Large Proteins

[ASAP] Nanobody GPS by PCS: An Efficient New NMR Analysis Method for G Protein Coupled Receptors and Other Large Proteins

Feng-Jie Wu, Pascal S. Rieder, Layara Akemi Abiko, Philip Ro?฿ler, Alvar D. Gossert, Daniel Ha?ussinger, and Stephan Grzesiek



Journal of the American Chemical Society
DOI: 10.1021/jacs.2c09692



Source: Journal of the American Chemical Society
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