Lineage for d2e1fa1 (2e1f A:1142-1235)

  1. Root: SCOP 1.75
  2. 758332Class a: All alpha proteins [46456] (284 folds)
  3. 770823Fold a.60: SAM domain-like [47768] (16 superfamilies)
    4-5 helices; bundle of two orthogonally packed alpha-hairpins; involved in the interactions with DNA and proteins
  4. 771280Superfamily a.60.8: HRDC-like [47819] (4 families) (S)
  5. 771281Family a.60.8.1: HRDC domain from helicases [47820] (2 proteins)
  6. 771289Protein Werner syndrome ATP-dependent helicase, WRN [140640] (1 species)
  7. 771290Species Human (Homo sapiens) [TaxId:9606] [140641] (3 PDB entries)
    Uniprot Q14191 1140-1239! Uniprot Q14191 1142-1235
  8. 771291Domain d2e1fa1: 2e1f A:1142-1235 [131964]
    automatically matched to 2E1E A:1142-1235
    complexed with cl

Details for d2e1fa1

PDB Entry: 2e1f (more details), 2 Å

PDB Description: Crystal structure of the HRDC Domain of Human Werner Syndrome Protein, WRN
PDB Compounds: (A:) Werner syndrome ATP-dependent helicase

SCOP Domain Sequences for d2e1fa1:

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

>d2e1fa1 a.60.8.1 (A:1142-1235) Werner syndrome ATP-dependent helicase, WRN {Human (Homo sapiens) [TaxId: 9606]}

SCOP Domain Coordinates for d2e1fa1:

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Timeline for d2e1fa1: