Title: Advanced Editing of Pathway/Genome Databases
1Advanced Editing of Pathway/Genome Databases
Ron Caspi
2General Curation
3User Preferences
4Create and Use Author and Organization Frames
5Using the Text Editor
- Formatting
- ltigtitaliclt/igt, ltbgtboldlt/igt
- know your alpha, beta
- Text wrapper need two newlines to force a new
paragraph - Text wrapper Never leave empty spaces at the end
of a line - An internal link to a reaction frame will print
the reaction equation - To print an enzymatic activity name use an
internal link to the enzymatic activity frame ID,
not the enzyme frame ID (important when an enzyme
is multifunctional e.g. CPLX-6934). - When providing multiple citations, use
CITSPMID1PMID2 (rather than CITSPMID1,
CITSPMID2. - Special characters
- Ã…ngstrom Aring (Ã…)
- Degree deg (?)
6Use Internal Hyperlinks
7Use Variant Classes
example Putrescin Biosynthesis
8Hypothetical Reactions, Excluded Enzymes
Specified in the Pathway Info Editor
- Enzymes Not Used useful when an enzyme is
associated with a reaction, but does not
participate in a specific pathway. For example, a
catabolic enzyme in a biosynthetic pathway (e.g.
EC 2.1.3.3, ornithine carbamoyltransferase) - Hypothetical reactions useful when a pathway
step is proposed, but has not been proven
9Super Pathways
- Need to keep pathways within well-defined end
points - Link pathways to upstream or downstream pathways
with pathway links. - Keep pathways simple
- Create more complex metabolic networks using
superpathways - Example superpathway of aromatic compound
degradation (aerobic) - is composed of
- catechol degradation II
- mandelate degradation I
- benzoate degradation (aerobic)
- b-ketoadipate degradation
- protocatechuate degradation II
- shikimate degradation
- quinate degradation
- 4-hydroxymandelate degradation
- tryptophan degradation I
10Advanced Curation
11Using the Frame Editor
- The frame editor is powerful, but dangerous Use
it when there are no alternatives. - Examples
- Renaming frames
- Modified proteins
- Modifying dates of author credits
- Replacing an enzyme or reaction in an
enzymatic-reaction frame - Removing mistakes from pathway frames, such as
predecessor pairs that the software ignores. - Removing duplicated values from slots that should
only have a single value (OFFIClAL-EC?) - Investigated orphan enzymatic reaction frames
reported by the consistency Checker
12Protein complexes
- Adenosylmethionine decarboxylase is first
synthesized as a proenzyme, and then self-cleaves
into two smaller polypeptides. Each cleavage
product forms a homotetramer, and the two
complexes form a heterooctamer. - A combination of editors enables creation of such
multi-level complexes.
Tutorial Creating Protein Complexes
13Classes and Instances
- Instance frames describe specific objects (e.g. a
specific gene) - Class frames describe general types of biological
objects (e.g. the class of all genes) - Proteins that are substrates of MetaCyc reactions
are classes - Every compound with an R in its structure
should be a class
14Converting an existing compound instance to a
class
Modifications of MetaCyc classes is considered a
schema change, and will be overwritten during the
next update! Only use this procedure to correct
curation errors that were introduced in your
PGDB!
- Open the compound editor
- Click Convert to Class and exit
- Rename the frame to follow class name convention
(if necessary) - Modify the common name to start with a
15The Ontology Editor
16The Ontology Editor
- Changing parent classes
- Adding parent classes
- Creating new classes to improve ontology
- Tutorial the Ontology Editor
17The Consistency Checker
Consistency Checking should be performed
routinely (every few months), and detected
problems should be addressed
18Consistency Checker Automatic Tasks
Bad Links MetaCyc pathways are extensively linked
to other pathways. When new PGDBs are created by
Pathologic, these links are still there, even if
they point to pathways that are not present in
the new PGDB. These links are only removed by the
Consistency Checker.
19Consistency Checker Manual Tasks
Example create an empty FRAME construct,
then run the task Check Frame References
20Exporting Pathways Between PGDBs
- To export a pathway to a file
- (optional inclusion of enzymes and genes)
- Edit gt Add Pathway to File Export List
- File gt Export gt Selected Pathways to
Lisp-format File - To import a pathway from file
- File gt Import gt Pathways from File
- To export a pathway directly to another PGDB
(both PGDBs must be installed on the same
system) - Edit -gt Export Pathway to DB
21Moving Objects Between PGDBs
- The following commands will import a frame from
MetaCyc to EcoCyc - Both databases must be open before this will
work. - (import-compounds '(CPD-ID) (kb-of-organism
'meta) (kb-of-organism 'ecoli)) - (import-reactions '(ID-RXN) (kb-of-organism
'meta) (kb-of-organism 'ecoli)) - (import-proteins '(ID-MONOMER) (kb-of-organism
'meta) (kb-of-organism 'ecoli))
22Exporting Graphics
- You can save any screen as a vector-based
postscript file by using File -gt Print - The PS files are easily converted to PDF by Adobe
Distiller (pat of the Acrobat Pro package) - Graphics programs like Corel Draw or Illustrator
can open the PDF files and let you manipulate the
graphics - The software also generates two posters the
cellular overview, and the genome poster. Those
are also generated in postscript format.
23Creating Links to External Databases
- To define a new external database link
- File ? Create ? External Database Description
- Enter frame name
- Fill fields as shown in next slide
- To edit an existing link
- Right-click on a link (from a Navigator page),
and select Edit External Database Info - Creating links to a PGDB
- see http//biocyc.org/linking.shtml
24External Database Editor
25Polymerization
example folate polyglutamylation I
26The Pathway Registry
27The Registry Schema Upgrades
28The Registry Uploading Your PGDB
- The process of uploading a PGDB to the Registry
is largely automated. See Publishing PGDBs in
the Registry in the User Guide for details