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PDBsum entry 5ftp
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PDB id:
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Cell cycle
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Title:
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Sulfur sad phasing of cdc23nterm: data collection with a tailored x- ray beam size at 2.69 a wavelength (4.6 kev)
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Structure:
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Anaphase-promoting complex subunit 8. Chain: a, b. Fragment: n-term, unp residues 19-301. Synonym: 20s cyclosome/apc complex protein apc8,cell untimely torn protein 23,20s cyclosome/apc complex protein apc8, cell untimely torn protein 23. Engineered: yes
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Source:
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Schizosaccharomyces pombe. Organism_taxid: 4896. Expressed in: escherichia coli. Expression_system_taxid: 562. Other_details: source details are the same as 3zn3
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Resolution:
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3.10Å
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R-factor:
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0.190
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R-free:
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0.260
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Authors:
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M.Cianci,M.R.Groves,D.Barford,T.R.Schneider
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Key ref:
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M.Cianci
et al.
(2016).
Data collection with a tailored X-ray beam size at 2.69 Å wavelength (4.6 keV): sulfur SAD phasing of Cdc23(Nterm).
Acta Crystallogr D Struct Biol,
72,
403-412.
PubMed id:
DOI:
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Date:
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14-Jan-16
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Release date:
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16-Mar-16
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PROCHECK
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Headers
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References
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DOI no:
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Acta Crystallogr D Struct Biol
72:403-412
(2016)
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PubMed id:
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Data collection with a tailored X-ray beam size at 2.69 Å wavelength (4.6 keV): sulfur SAD phasing of Cdc23(Nterm).
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M.Cianci,
M.R.Groves,
D.Barford,
T.R.Schneider.
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ABSTRACT
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The capability to reach wavelengths of up to 3.1 Å at the newly established
EMBL P13 beamline at PETRA III, the new third-generation synchrotron at DESY in
Hamburg, provides the opportunity to explore very long wavelengths to harness
the sulfur anomalous signal for phase determination. Data collection at λ =
2.69 Å (4.6 keV) allowed the crystal structure determination by sulfur SAD
phasing of Cdc23(Nterm), a subunit of the multimeric anaphase-promoting complex
(APC/C). At this energy, Cdc23(Nterm) has an expected Bijvoet ratio
〈|Fanom|〉/〈F〉 of 2.2%, with 282 residues, including six cysteines and
five methionine residues, and two molecules in the asymmetric unit (65.4 kDa;
12 Cys and ten Met residues). Selectively illuminating two separate portions of
the same crystal with an X-ray beam of 50 µm in diameter allowed crystal
twinning to be overcome. The crystals diffracted to 3.1 Å resolution, with
unit-cell parameters a = b = 61.2, c = 151.5 Å, and belonged to space group
P43. The refined structure to 3.1 Å resolution has an R factor of 18.7% and
an Rfree of 25.9%. This paper reports the structure solution, related methods
and a discussion of the instrumentation.
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');
}
}
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