Lineage for d2n79c_ (2n79 C:)

  1. Root: SCOPe 2.06
  2. 1976409Class a: All alpha proteins [46456] (289 folds)
  3. 1994319Fold a.39: EF Hand-like [47472] (4 superfamilies)
    core: 4 helices; array of 2 hairpins, opened
  4. 1994320Superfamily a.39.1: EF-hand [47473] (12 families) (S)
    Duplication: consists of two EF-hand units: each is made of two helices connected with calcium-binding loop
  5. 1994753Family a.39.1.5: Calmodulin-like [47502] (24 protein domains)
    Duplication: made with two pairs of EF-hands
  6. 1995301Protein automated matches [190064] (20 species)
    not a true protein
  7. 1995342Species Human (Homo sapiens) [TaxId:9606] [186813] (23 PDB entries)
  8. 1995364Domain d2n79c_: 2n79 C: [278710]
    automated match to d2kfxt_
    complexed with ca; mutant

Details for d2n79c_

PDB Entry: 2n79 (more details)

PDB Description: the structural and functional effects of the familial hypertrophic cardiomyopathy-linked cardiac troponin c mutation, l29q
PDB Compounds: (C:) troponin c, slow skeletal and cardiac muscles

SCOPe Domain Sequences for d2n79c_:

Sequence; same for both SEQRES and ATOM records: (download)

>d2n79c_ a.39.1.5 (C:) automated matches {Human (Homo sapiens) [TaxId: 9606]}

SCOPe Domain Coordinates for d2n79c_:

Click to download the PDB-style file with coordinates for d2n79c_.
(The format of our PDB-style files is described here.)

Timeline for d2n79c_: