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PDBsum entry 3v61
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Protein binding/DNA binding protein
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PDB id
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3v61
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Nature
483:59-63
(2012)
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PubMed id:
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Recognition of SUMO-modified PCNA requires tandem receptor motifs in Srs2.
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A.A.Armstrong,
F.Mohideen,
C.D.Lima.
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ABSTRACT
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Ubiquitin (Ub) and ubiquitin-like (Ubl) modifiers such as SUMO (also known as
Smt3 in Saccharomyces cerevisiae) mediate signal transduction through
post-translational modification of substrate proteins in pathways that control
differentiation, apoptosis and the cell cycle, and responses to stress such as
the DNA damage response. In yeast, the proliferating cell nuclear antigen PCNA
(also known as Pol30) is modified by ubiquitin in response to DNA damage and by
SUMO during S phase. Whereas Ub-PCNA can signal for recruitment of translesion
DNA polymerases, SUMO-PCNA signals for recruitment of the anti-recombinogenic
DNA helicase Srs2. It remains unclear how receptors such as Srs2 specifically
recognize substrates after conjugation to Ub and Ubls. Here we show, through
structural, biochemical and functional studies, that the Srs2 carboxy-terminal
domain harbours tandem receptor motifs that interact independently with PCNA and
SUMO and that both motifs are required to recognize SUMO-PCNA specifically. The
mechanism presented is pertinent to understanding how other receptors
specifically recognize Ub- and Ubl-modified substrates to facilitate signal
transduction.
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Literature references that cite this PDB file's key reference
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PubMed id
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Reference
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C.Otomo,
Z.Metlagel,
G.Takaesu,
and
T.Otomo
(2013).
Structure of the human ATG12~ATG5 conjugate required for LC3 lipidation in autophagy.
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Nat Struct Mol Biol,
20,
59-66.
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PDB codes:
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The most recent references are shown first.
Citation data come partly from CiteXplore and partly
from an automated harvesting procedure. Note that this is likely to be
only a partial list as not all journals are covered by
either method. However, we are continually building up the citation data
so more and more references will be included with time.
Where a reference describes a PDB structure, the PDB
codes are
shown on the right.
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