5ZR1

Saccharomyces Cerevisiae Origin Recognition Complex Bound to a 72-bp Origin DNA containing ACS and B1 element


Experimental Data Snapshot

  • Method: ELECTRON MICROSCOPY
  • Resolution: 3.00 Å
  • Aggregation State: PARTICLE 
  • Reconstruction Method: SINGLE PARTICLE 

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This is version 1.2 of the entry. See complete history


Literature

Structure of the origin recognition complex bound to DNA replication origin.

Li, N.Lam, W.H.Zhai, Y.Cheng, J.Cheng, E.Zhao, Y.Gao, N.Tye, B.K.

(2018) Nature 559: 217-222

  • DOI: https://doi.org/10.1038/s41586-018-0293-x
  • Primary Citation of Related Structures:  
    5ZR1

  • PubMed Abstract: 

    The six-subunit origin recognition complex (ORC) binds to DNA to mark the site for the initiation of replication in eukaryotes. Here we report a 3 Å cryo-electron microscopy structure of the Saccharomyces cerevisiae ORC bound to a 72-base-pair origin DNA sequence that contains the ARS consensus sequence (ACS) and the B1 element. The ORC encircles DNA through extensive interactions with both phosphate backbone and bases, and bends DNA at the ACS and B1 sites. Specific recognition of thymine residues in the ACS is carried out by a conserved basic amino acid motif of Orc1 in the minor groove, and by a species-specific helical insertion motif of Orc4 in the major groove. Moreover, similar insertions into major and minor grooves are also embedded in the B1 site by basic patch motifs from Orc2 and Orc5, respectively, to contact bases and to bend DNA. This work pinpoints a conserved role of ORC in modulating DNA structure to facilitate origin selection and helicase loading in eukaryotes.


  • Organizational Affiliation

    State Key Laboratory of Membrane Biology, Peking-Tsinghua Center for Life Sciences, School of Life Sciences, Peking University, Beijing, China.


Macromolecules

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Entity ID: 1
MoleculeChains Sequence LengthOrganismDetailsImage
Origin recognition complex subunit 1914Saccharomyces cerevisiae S288CMutation(s): 0 
Gene Names: ORC1YML065W
UniProt
Find proteins for P54784 (Saccharomyces cerevisiae (strain ATCC 204508 / S288c))
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Go to UniProtKB:  P54784
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UniProt GroupP54784
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Entity ID: 2
MoleculeChains Sequence LengthOrganismDetailsImage
Origin recognition complex subunit 2620Saccharomyces cerevisiae S288CMutation(s): 0 
Gene Names: ORC2RRR1SIR5YBR060CYBR0523
UniProt
Find proteins for P32833 (Saccharomyces cerevisiae (strain ATCC 204508 / S288c))
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UniProt GroupP32833
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Entity ID: 3
MoleculeChains Sequence LengthOrganismDetailsImage
Origin recognition complex subunit 3616Saccharomyces cerevisiae S288CMutation(s): 0 
Gene Names: ORC3OAF1OIF1YLL004WL1365
UniProt
Find proteins for P54790 (Saccharomyces cerevisiae (strain ATCC 204508 / S288c))
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UniProt GroupP54790
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Entity ID: 4
MoleculeChains Sequence LengthOrganismDetailsImage
Origin recognition complex subunit 4529Saccharomyces cerevisiae S288CMutation(s): 0 
Gene Names: ORC4YPR162CP9325.5
UniProt
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UniProt GroupP54791
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Entity ID: 5
MoleculeChains Sequence LengthOrganismDetailsImage
Origin recognition complex subunit 5479Saccharomyces cerevisiae S288CMutation(s): 0 
Gene Names: ORC5YNL261WN0834
UniProt
Find proteins for P50874 (Saccharomyces cerevisiae (strain ATCC 204508 / S288c))
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UniProt GroupP50874
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Entity ID: 6
MoleculeChains Sequence LengthOrganismDetailsImage
Origin recognition complex subunit 6435Saccharomyces cerevisiae S288CMutation(s): 0 
Gene Names: ORC6AAP1YHR118C
UniProt
Find proteins for P38826 (Saccharomyces cerevisiae (strain ATCC 204508 / S288c))
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UniProt GroupP38826
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Entity ID: 7
MoleculeChains LengthOrganismImage
72bp-oring DNA, ACS305, T-rich72Saccharomyces cerevisiae
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Entity ID: 8
MoleculeChains LengthOrganismImage
72bp-oring DNA, ACS305, A-rich72Saccharomyces cerevisiae
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Experimental Data & Validation

Experimental Data

  • Method: ELECTRON MICROSCOPY
  • Resolution: 3.00 Å
  • Aggregation State: PARTICLE 
  • Reconstruction Method: SINGLE PARTICLE 

Structure Validation

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Entry History 

Deposition Data

Revision History  (Full details and data files)

  • Version 1.0: 2018-07-11
    Type: Initial release
  • Version 1.1: 2018-07-25
    Changes: Data collection, Database references
  • Version 1.2: 2024-03-27
    Changes: Data collection, Database references, Derived calculations