Paper Published on NMR Restraint Validation

JY
Jasmine Young
Mon, Mar 25, 2024 2:57 PM

Dear PDB-l,

We are pleased to announce the publication of this manuscript,
addressing the challenge of validation of experimental biomolecular NMR
structures against restraint data.

The NMR exchange (NEF) and NMR-STAR formats provide a standardized
approach for representing commonly used NMR restraints. Using these
restraint formats, a standardized validation system for assessing
structural models of biopolymers against restraints has been developed
and implemented in the wwPDB OneDep data harvesting system.

The resulting wwPDB Restraint Violation Report provides a model vs data
assessment of biomolecule structures determined using distance and
dihedral restraints, with extensions to other restraint types currently
being implemented. These tools are useful for assessing NMR models, as
well as for assessing biomolecular structure predictions based on
distance restraints.

We present the rationale for model-vs-data restraint validation by the
wwPDB, together with summary of validation tools and reports for NMR
distance and dihedral restraints that have been developed, as
implemented in the wwPDB validation pipeline and recommended by the
wwPDB NMR-VTF committee.

*Restraint Validation of Biomolecular Structures Determined by NMR
in the Protein Data Bank*
Kumaran Baskaran, Eliza Ploskon, Roberto Tejero, Masashi Yokochi,
Deborah Harrus, Yuhe Liang, Ezra Peisach, Irina Persikova, Theresa A
Ramelot, Monica Sekharan, James Tolchard, John D Westbrook, Benjamin
Bardiaux, Charles Schwieters, Ardan Patwardhan, Sameer Velankar,
Stephen K Burley, Genji Kurisu, Jeffrey C Hoch, Gaetano T
Montelione, Geerten W Vuister, Jasmine Y Young
(2024) /Structure/ 32, 1–14: doi: 10.1016/j.str.2024.02.011
<https://doi.org/10.1016/j.str.2024.02.011> 

The wwPDB plans to further enhance validation report by providing
model-vs-data quality assessment for other kinds of restraints based on
community recommendation and improve data representation on structures
with multiple conformation states.

--
Regards,

Jasmine

---==========================
Jasmine Young, Ph.D.
Biocuration Team Lead
RCSB Protein Data Bank
Research Professor
Institute for Quantitative Biomedicine
Rutgers, The State University of New Jersey
174 Frelinghuysen Rd
Piscataway, NJ 08854-8087

Email:jasmine@rcsb.rutgers.edu
Phone: (848)445-0103 ext 4920
Fax: (732)445-4320

---==========================

Dear PDB-l, We are pleased to announce the publication of this manuscript, addressing the challenge of validation of experimental biomolecular NMR structures against restraint data. The NMR exchange (NEF) and NMR-STAR formats provide a standardized approach for representing commonly used NMR restraints. Using these restraint formats, a standardized validation system for assessing structural models of biopolymers against restraints has been developed and implemented in the wwPDB OneDep data harvesting system. The resulting wwPDB Restraint Violation Report provides a model vs data assessment of biomolecule structures determined using distance and dihedral restraints, with extensions to other restraint types currently being implemented. These tools are useful for assessing NMR models, as well as for assessing biomolecular structure predictions based on distance restraints. We present the rationale for model-vs-data restraint validation by the wwPDB, together with summary of validation tools and reports for NMR distance and dihedral restraints that have been developed, as implemented in the wwPDB validation pipeline and recommended by the wwPDB NMR-VTF committee. *Restraint Validation of Biomolecular Structures Determined by NMR in the Protein Data Bank* Kumaran Baskaran, Eliza Ploskon, Roberto Tejero, Masashi Yokochi, Deborah Harrus, Yuhe Liang, Ezra Peisach, Irina Persikova, Theresa A Ramelot, Monica Sekharan, James Tolchard, John D Westbrook, Benjamin Bardiaux, Charles Schwieters, Ardan Patwardhan, Sameer Velankar, Stephen K Burley, Genji Kurisu, Jeffrey C Hoch, Gaetano T Montelione, Geerten W Vuister, Jasmine Y Young (2024) /Structure/ 32, 1–14: doi: 10.1016/j.str.2024.02.011 <https://doi.org/10.1016/j.str.2024.02.011> The wwPDB plans to further enhance validation report by providing model-vs-data quality assessment for other kinds of restraints based on community recommendation and improve data representation on structures with multiple conformation states. -- Regards, Jasmine =========================================================== Jasmine Young, Ph.D. Biocuration Team Lead RCSB Protein Data Bank Research Professor Institute for Quantitative Biomedicine Rutgers, The State University of New Jersey 174 Frelinghuysen Rd Piscataway, NJ 08854-8087 Email:jasmine@rcsb.rutgers.edu Phone: (848)445-0103 ext 4920 Fax: (732)445-4320 ===========================================================