SCOPe Funding Alert: SCOPe support from the NIH ended in April 2016. John-Marc Chandonia is the primary maintainer and has continued to develop SCOPe using vacation time. Three proposals to the NIH for continued funding have been unsuccessful. If our current NIH proposal is not funded, SCOPe will shut down permanently in Summer 2017 as Dr. Chandonia will need to seek a new position.

Lineage for Class i: Low resolution protein structures

  1. Root: SCOP 1.55
  2. Class i: Low resolution protein structures [58117] (12 folds)

Folds:

  1. i.1: Ribosome and ribosomal fragments [58118] (1 superfamily)
  2. i.2: Helicase [58135] (1 superfamily)
  3. i.3: ATP synthase [58140] (1 superfamily)
  4. i.4: Electron transport chains [58146] (1 superfamily)
  5. i.5: Photosystems [58155] (1 superfamily)
  6. i.6: Virus and virus-receptor complexes [58162] (1 superfamily)
  7. i.7: Reovirus core [58175] (1 superfamily)
  8. i.8: RNA polymerase [58180] (1 superfamily)
  9. i.9: Blood clotting [58187] (1 superfamily)
  10. i.10: Tubulin:stathmin-like domain complex [58193] (1 superfamily)
  11. i.11: Computational models partly based on NMR data [58198] (1 superfamily)
  12. i.12: Proteins of incorrect, partial and unknown sequence [58207] (1 superfamily)

More info for Class i: Low resolution protein structures

Timeline for Class i: Low resolution protein structures: