Lineage for d6ghdg1 (6ghd G:2-45)

  1. Root: SCOPe 2.07
  2. 2299346Class a: All alpha proteins [46456] (289 folds)
  3. 2347594Fold a.140: LEM/SAP HeH motif [63450] (6 superfamilies)
    helix-extended loop-helix; parallel helices
  4. 2347595Superfamily a.140.1: LEM domain [63451] (1 family) (S)
  5. 2347596Family a.140.1.1: LEM domain [63452] (3 proteins)
  6. 2347597Protein Inner nuclear membrane protein emerin [63455] (1 species)
  7. 2347598Species Human (Homo sapiens) [TaxId:9606] [63456] (5 PDB entries)
  8. 2347600Domain d6ghdg1: 6ghd G:2-45 [355884]
    Other proteins in same PDB: d6ghda_, d6ghdb_, d6ghdc_, d6ghdd_, d6ghde_, d6ghdf_, d6ghdg2
    automated match to d1jeia_
    complexed with edo, so4

Details for d6ghdg1

PDB Entry: 6ghd (more details), 2.1 Å

PDB Description: structural analysis of the ternary complex between lamin a/c, baf and emerin identifies an interface disrupted in autosomal recessive progeroid diseases
PDB Compounds: (G:) emerin

SCOPe Domain Sequences for d6ghdg1:

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

>d6ghdg1 a.140.1.1 (G:2-45) Inner nuclear membrane protein emerin {Human (Homo sapiens) [TaxId: 9606]}

SCOPe Domain Coordinates for d6ghdg1:

Click to download the PDB-style file with coordinates for d6ghdg1.
(The format of our PDB-style files is described here.)

Timeline for d6ghdg1: