Difference between revisions of "Talk:Protein coding sequences"

Revision as of 16:47, 3 March 2009

Protein naming

what do we actually want for proteins?

1. A link to information in the outside world about that protein
   • Based on this information, it would be nice to automatically identify some sort of family or classification that the protein belongs to.
2. A measure of what other proteins in the registry the protein is similar to.

The first problem can likely be solved simply by searching for the protein sequence in UNIParc (what about UNIRef?). If that doesn't return an exact match, we can turn to blast to see what the protein is most similar to. Can have this run ahead of time on every protein sequence.

The second problem can be solved by using something like BLink to return all related pid numbers and then comparing that list to the list of pid numbers in the registry. If that fails, turn to a precompiled Blast search on all registry proteins.

Alphabet soup

• [http://uniprot.org Uniprot] - this is the umbrella organization of Swissprot and TrEMBL
• [http://www.uniprot.org/help/uniprotkb UniprotKB] - this database is the superset of Swissprot (manually curated) and TrEMBL (autogenerated)
  • The protein sequences are derived from the translation of the coding sequences (CDS) which have been submitted to the public nucleic acid database, the EMBL/GenBank/DDBJ database. All these sequences, as well as the related data submitted by the authors, are automatically integrated into UniProtKB/TrEMBL.
• [http://www.uniprot.org/help/uniref Uniref] - The UniRef databases provide clustered sets of sequences from UniProt Knowledgebase (including splice variants and isoforms) and selected UniParc records, in order to obtain complete coverage of sequence space at several resolutions while hiding redundant sequences (but not their descriptions) from view.
• [http://www.genome.ad.jp/kegg/ KEGG] - they maintain their own database of proteins with KEGG numbers. Proteins are grouped the function, structure, etc.
• [http://www.cs.utk.edu/~rcollins/bioinf/tutorial/home.html Blink] - BLink (BLAST Link) is a tool that displays the pre-computed results of BLAST searches that have been completed for every protein sequence in the Entrez Proteins data domain. If you know the pid, you can access the Blink results from this url - http://www.ncbi.nlm.nih.gov/sutils/blink.cgi?pid=insert pid here&all=1.
  • Here is a php [http://www.cs.utk.edu/~rcollins/bioinf/tutorial/tutorial4.html script] that will return all related proteins based on a protein pid.
• [http://www.uniprot.org/help/uniparc UniParc] - a non-redundant archive of all protein sequences that are or have been listed in the major protein databases including the UniprotKB, RefSeq, PDB and others. Simply contains the protein sequences and any identifiers from the different databases that share that exact sequence.
• When doing a Blast search of the NCBI databases, the "nr" database is a non-redundant collection of protein sequences from translated genbank CDS, RefSeq proteins, items from the NCBI protein database and a few others. This is equivalent to UniParc but I'm not sure it lives as a standalone database.
• [http://www.ncbi.nlm.nih.gov/Structure/lexington/lexington.cgi?cmd=rps Cdart] might be a quick way to find proteins with domains similar to the query.
• [CDD] - the conserved domain database. Searching this database from NCBI returns matches to annotated domains and also protein superfamilies. The superfamily information is pretty useful. for example, searching for the amino acid sequence of C0062 returns this [http://www.ncbi.nlm.nih.gov/Structure/cdd/cddsrv.cgi?ascbin=8&maxaln=10&seltype=2&uid=127388&query=MKNINADDTYRIINKIKACRSNNDINQCLSDMTKMVHCEYYLLAIIYPHSMVKSDISILDNYPKKWRQYYDDANLIKYDPIVDYSNSNHSPINWNIFENNAVNKKSPNVIKEAKTSGLITGFSFPIHTANNGFGMLSFAHSEKDNYIDSLFLHACMNIPLIVPSLVDNYRKINIANNKSNNDLTKREKECLAWACEGKSSWDISKILGCSERTVTFHLTNAQMKLNTTNRCQSISKAILTGAIDCPYFKN&aln=1,182,0,57 LuxR] protein family, and this [http://www.ncbi.nlm.nih.gov/Structure/cdd/cddsrv.cgi?ascbin=8&maxaln=10&seltype=2&uid=112297&query=MKNINADDTYRIINKIKACRSNNDINQCLSDMTKMVHCEYYLLAIIYPHSMVKSDISILDNYPKKWRQYYDDANLIKYDPIVDYSNSNHSPINWNIFENNAVNKKSPNVIKEAKTSGLITGFSFPIHTANNGFGMLSFAHSEKDNYIDSLFLHACMNIPLIVPSLVDNYRKINIANNKSNNDLTKREKECLAWACEGKSSWDISKILGCSERTVTFHLTNAQMKLNTTNRCQSISKAILTGAIDCPYFKN&aln=1,20,0,124 autoinducer binding superfamily].

Papers

• [http://www.biomedcentral.com/1471-2105/8/401 Biomed] paper about a protein identifier cross-referencing tool, [http://www.ebi.ac.uk/Tools/picr/ PCIR]. Written by the folks at the EBI, the tool is now available from the Uniprot website.
• [http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pubmed&pubmedid=18697767 Bioinformatics] paper about [http://llama.med.harvard.edu/synergizer/translate/ the synergizer] which translates protein identifiers from one database to another.

Old material

• BBa_J31004 - change the vector of this part
• BBa_Y00029 - remove the prefix and suffix
• Rename chromatinremodeling to chromatin

Questions

• How do we want to indicate relationships between parts? - i.e. protein coding sequences and generators, transcriptional regulators and cognate promoters, similar versions of protein coding sequences,

Categories

Part level function

• //cds/reporter
  • //cds/reporter/fluorescentprotein
  • //cds/reporter/color
  • //cds/reporter/luciferase
• //cds/selectionmarker/antibioticresistance
• //cds/enzyme
  • //cds/enzyme/selectionmarker/antibioticresistance (//protein/enzyme/antibiotic_resistance)
  • //cds/enzyme/recombinase (//protein/enzyme/dna_excision_integration)
  • //cds/enzyme/biosynthesis/odorant (//protein/enzyme/smell)
  • //cds/enzyme/biosynthesis/AHL (//protein/enzyme/hsl_synthesis) --> synthases?
  • //cds/enzyme/protease
  • //cds/enzyme/degradation/AHL --> lyases?
  • //cds/enzyme/methylation --> should be split into methylases, demethylases
  • //cds/enzyme/phosphorylation --> should be split into phosphorylases, kinases, and phosphatases
• //cds/transcriptionalregulator (//protein/repact/uncategorized)
  • //cds/transcriptionalregulator/activator
  • //cds/transcriptionalregulator/repressor
• //cds/membrane
  • //cds/membrane/receptor
  • //cds/membrane/transporter
  • //cds/membrane/channel
  • //cds/membrane/pump
  • //cds/membrane/binding
  • //cds/membrane/surfacedisplay
• //cds/binding
  • //cds/binding/DNA
  • //cds/binging/lead
• //cds/chromatin

Device level function

• //function/motility
• //function/conjugation
• //function/sensor
  • //function/sensor/light
  • //function/sensor/lead
  • //function/sensor/odor
• //function/odor

Parameters

The following parameters can be auto-selected by the computer.

• Completeness <-- need a better name here
  • Full-length
    • begins with ATG/GTG and ends with TAA/TGA/TAG
    • begins with TTA/TCA/CTA and ends with CAT/CAC
  • N-terminus
    • begins with ATG/GTG or ends with TAA/TGA/TAG
  • C-terminus
    • begins with TTA/TCA/CTA or ends with CAT/CAC
  • Fusion
  • Domain
    • has neither an ATG/GTG nor a TAA/TGA/TAG
• Direction
  • Forward
    • begins with ATG/GTG or ends with TAA/TGA/TAG
  • Reverse
    • begins with TTA/TCA/CTA or ends with CAT/CAC
• Degradation tag
  • probably ought to be able to auto-detect and annotate the different degradation tags as well. I'll compile the different sequences and tag names. May want to somehow tie this with the Protein tags and modifiers parts.
• Signal sequences
  • do the same with N-terminal tags?

Columns

• all protein coding sequences
  • Protein
  • Description
  • Direction (auto-generated)
  • Completeness (auto-generated)
  • Tags (auto-generated based on sequence search)
  • SwissProt
  • KEGG
  • Length
• all enzymes
  • EC number
  • substrate
  • product

• fluorescent_reporter_protein_coding_sequences
  • excitation
  • emission
  • color
• luminescent_reporter_protein_coding_sequences
• color_reporter_protein_coding_sequences
  • color
• antibiotic_resistance_marker
  • antibiotic
• recombination_protein_coding_sequences
  • recombination site
• transcriptional_regulators
  • operator site sequence
  • ligand