8YS7 | pdb_00008ys7

Crystal structure of actinomycin D and Echinomycin-d(ACGGGCT/AGCCCCGT) complex


Experimental Data Snapshot

  • Method: X-RAY DIFFRACTION
  • Resolution: 3.24 Å
  • R-Value Free: 
    0.292 (Depositor), 0.292 (DCC) 
  • R-Value Work: 
    0.277 (Depositor), 0.278 (DCC) 
  • R-Value Observed: 
    0.279 (Depositor) 

Starting Model: experimental
View more details

wwPDB Validation   3D Report Full Report


Ligand Structure Quality Assessment 


This is version 1.0 of the entry. See complete history


Literature

Crystal structure of actinomycin D and Echinomycin-d(ACGGGCT/AGCCCCGT) complex

Lee, Y.Y.Hou, M.H.

To be published.

Macromolecules

Find similar proteins by:  Sequence   |   3D Structure  

Entity ID: 3
MoleculeChains Sequence LengthOrganismDetailsImage
EchinomycinE,
H [auth A]
8StreptomycesMutation(s): 0 
Sequence Annotations
Expand
  • Reference Sequence

Find similar proteins by:  Sequence   |   3D Structure  

Entity ID: 4
MoleculeChains Sequence LengthOrganismDetailsImage
actinomycin DF [auth I],
G [auth D]
11StreptomycesMutation(s): 0 
Entity Groups  
Sequence Clusters30% Identity50% Identity70% Identity90% Identity95% Identity100% Identity
Sequence Annotations
Expand
  • Reference Sequence

Find similar nucleic acids by:  Sequence   |   3D Structure  

Entity ID: 1
MoleculeChains LengthOrganismImage
DNA (5'-D(P*AP*GP*CP*CP*CP*CP*GP*T)-3')A [auth B],
C [auth K]
8synthetic construct
Sequence Annotations
Expand
  • Reference Sequence

Find similar nucleic acids by:  Sequence   |   3D Structure  

Entity ID: 2
MoleculeChains LengthOrganismImage
DNA (5'-D(P*AP*CP*GP*GP*GP*CP*T)-3')B [auth C],
D [auth L]
7synthetic construct
Sequence Annotations
Expand
  • Reference Sequence
Experimental Data & Validation

Experimental Data

  • Method: X-RAY DIFFRACTION
  • Resolution: 3.24 Å
  • R-Value Free:  0.292 (Depositor), 0.292 (DCC) 
  • R-Value Work:  0.277 (Depositor), 0.278 (DCC) 
  • R-Value Observed: 0.279 (Depositor) 
Space Group: H 3 2
Unit Cell:
Length ( Å )Angle ( ˚ )
a = 132.661α = 90
b = 132.661β = 90
c = 50.052γ = 120
Software Package:
Software NamePurpose
PHENIXrefinement
HKL-2000data scaling
HKL-2000data reduction
PHENIXphasing

Structure Validation

View Full Validation Report



Ligand Structure Quality Assessment 


Entry History & Funding Information

Deposition Data


Funding OrganizationLocationGrant Number
Ministry of Science and Technology (MoST, Taiwan)Taiwan--

Revision History  (Full details and data files)

  • Version 1.0: 2025-04-09
    Type: Initial release