Changes between Version 66 and Version 67 of Release1.4
- Timestamp:
- Dec 2, 2008, 11:45:00 AM (17 years ago)
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Release1.4
v66 v67 18 18 1. Need "effects" command for controlling all Effects via script. ECM 19 19 1. Reduce mmcif template file download 20 1. Framework for invoking chimeraservices.rbvi.ucsf.edu and other web services CH 21 * Security, transactions with IDs 22 1. connect to our own Web service (using the above framework) to BLAST on PDB, provide dialog for choosing which hit structures to open, whether to show pairwise sequence alignment from BLAST (in MAV), whether to superimpose hit and query structures (with Matchmaker). Input is sequence of molecule model already open in Chimera. ECM 23 * (search other databases such as NR? PSI-BLAST on NR?) 20 24 21 25 == Features Desired for 1.4 == … … 24 28 * Implement cron job to continuously update mmcif template file 25 29 30 26 31 === Documentation === 27 32 28 33 === Core 2 === 34 1. Electron tomography: Visualization of objects embedded in membranes e.g. nuclear pores in nuclear envelope, spikes in virus membranes. 35 1. be able to map volume gray levels onto curved membrane surfaces 36 1. move membrane surface along normals while viewing gray levels 37 1. place markers on surfaces 38 1. extract volume regions around surface markers for subtomogram averaging (average density for several nuclear pores, virus spikes to achieve higher resolution). Requires alignment capability and handling of tens to thousands of map subregions 29 39 30 40 === Core 4 === 41 1. allow specifying "sequence to add" by accession code (Uniprot?). Its feature annotations would automatically come along as regions. ECM 42 * would we want Fetch by ID for sequences? (would we want a sequence with no structure and not aligned with any other sequences?) 43 * perhaps allow specifying Uniprot accession or BLAST on Uniprot for existing sequences, retrieve and load feature annotations as sequence regions (would require global alignment to Uniprot sequence for correct mapping of features when the existing sequence is not identical) 44 * on my secondary MAV to-do list. EFP 45 1. When aligning in a structure sequence, consider secondary structure markups of non-structure sequences 46 1. If gaps are created while adding a sequence, make corresponding gaps in any markups 47 1. Aqua background -> gray, or put black border around sequence-name color swatches 48 31 49 32 50 == Features Postponed to 1.5 == 33 51 We will re-evaluate these features for the 1.5 release, but we think they are likely to be included. 34 52 1. Implement mmcif template web service to update templates dynamically from chimera 53 1. Allow sending template structure and template/target sequence alignment to comparative modeling program, either local or Web. ECM 54 * This will require discussion/clarification between Andre and Tom to align the research goals of the two groups 35 55 36 56 == Features Postponed to 1.5+ ==
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