International
Tables for
Crystallography
Volume F
Crystallography of biological macromolecules
Edited by M. G. Rossmann and E. Arnold

International Tables for Crystallography (2006). Vol. F. ch. 24.2, pp. 659-662   | 1 | 2 |

Section 24.2.5.3. NDB searches

H. M. Berman,a* Z. Feng,a B. Schneider,a J. Westbrooka and C. Zardeckia

aThe Nucleic Acid Database Project, Department of Chemistry, Rutgers University, 610 Taylor Road, Piscataway, NJ 08854-8077, USA
Correspondence e-mail:  berman@rcsb.rutgers.edu

24.2.5.3. NDB searches

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A web interface was designed to make the query capabilities of the NDB as widely accessible as possible. To highlight the special features of NDB, the interface operates in two modes. In the quick search/quick report mode, several items, including structure ID, author, classification and special features, can be limited either by entering text in a box or by selecting an option from the pull-down menu. Any combination of these items may be used to constrain the structure selection. If none are used, the entire database will be selected. After selecting `Execute Selection', the user will be presented with a list of structure IDs and descriptors that match the desired conditions. Several viewing options for each structure in this list are possible. These include retrieving the coordinate files in either mmCIF or PDB format, retrieving the coordinates for the biological unit, viewing the structure with RasMol (Sayle & Milner-White, 1995[link]), or viewing an NDB Atlas page.

Preformatted quick reports can then be generated for the structures in this results list. The user selects a report from a list of 13 report options (Table 24.2.5.1)[link], and the report is created automatically. Multiple reports can be easily generated. These reports are particularly convenient for being able to produce reports quickly based on derived features, such as torsion angles and base morphology (Fig. 24.2.5.2)[link].

Table 24.2.5.1| top | pdf |
Quick reports available from the NDB

Report nameContents
NDB statusProcessing status information
Cell dimensionsCrystallographic cell constants
Primary citationPrimary bibliographic citations
Structure identifierIdentifiers, descriptor, coordinate availability
SequenceSequence
Nucleic acid sequenceNucleic acid sequence only
Protein sequenceProtein sequence only
Refinement information R factor, resolution and number of reflections used in refinement
Nucleic acid backbone torsions (NDB)Sugar–phosphate backbone torsion angles using NDB residue numbers
Nucleic acid backbone torsions (PDB)Sugar–phosphate backbone torsion angles using PDB residue numbers
Base-pair parameters (global)Global base-pair parameters calculated using Curves 5.1 (Lavery & Sklenar, 1989[link])
Base-pair step parameters (local)Local base-pair step parameters calculated using Curves 5.1
Groove dimensionsGroove dimensions using Stoffer & Lavery definitions from Curves 5.1
[Figure 24.2.5.2]

Figure 24.2.5.2| top | pdf |

Examples of quick reports. Clockwise from top left: base-pair parameters [global; calculated using Curves 5.1 (Lavery & Sklenar, 1989[link])] report for ribozyme structures; nucleic acid backbone torsions (NDB) report for ribozyme structures; structure identifier report for protein–DNA structures; citation report for protein–DNA structures.

In the full search/full report mode, it is possible to access most of the tables in the NDB to build more complex queries. Instead of limiting items that are listed on a single page, the user builds a search by selecting the tables and then the items that contain the desired features. These queries can use Boolean and logical operators to make complex queries.

After selecting structures using the full search, a variety of reports can be written. The report columns are selected from a variety of database tables, and then the full report is automatically generated. Multiple reports can be generated for the same group of selected structures; for example, reports on crystallization, base modification, or a combination of these reports can be generated for a particular group of structures.

References

First citation Sayle, R. & Milner-White, E. J. (1995). RasMol: biomolecular graphics for all. Trends Biochem. Sci. 20, 374.Google Scholar








































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