scholarly article | Q13442814 |
P356 | DOI | 10.1074/JBC.M408130200 |
P698 | PubMed publication ID | 15569683 |
P50 | author | Shigetsugu Hatakeyama | Q39908557 |
P2093 | author name string | Keiichi I Nakayama | |
Hisato Saitoh | |||
Hidehisa Takahashi | |||
P2860 | cites work | Identification of the enzyme required for activation of the small ubiquitin-like protein SUMO-1 | Q22009137 |
A RA-dependent, tumour-growth suppressive transcription complex is the target of the PML-RARalpha and T18 oncoproteins | Q22010974 | ||
Regulation and localization of the Bloom syndrome protein in response to DNA damage | Q24291133 | ||
Common properties of nuclear body protein SP100 and TIF1alpha chromatin factor: role of SUMO modification | Q24291154 | ||
U box proteins as a new family of ubiquitin-protein ligases | Q24291397 | ||
PML colocalizes with and stabilizes the DNA damage response protein TopBP1 | Q24303540 | ||
Human thymine DNA glycosylase binds to apurinic sites in DNA but is displaced by human apurinic endonuclease 1. | Q38330113 | ||
SUMO-1 modification of histone deacetylase 1 (HDAC1) modulates its biological activities | Q42816242 | ||
Generation of SUMO-1 modified proteins in E. coli: towards understanding the biochemistry/structural biology of the SUMO-1 pathway | Q44849258 | ||
Interaction of U-box-type ubiquitin-protein ligases (E3s) with molecular chaperones | Q44930825 | ||
Retinoic acid receptors interact physically and functionally with the T:G mismatch-specific thymine-DNA glycosylase | Q47724741 | ||
Separating substrate recognition from base hydrolysis in human thymine DNA glycosylase by mutational analysis | Q47838612 | ||
p300 Transcriptional Repression Is Mediated by SUMO Modification | Q60304936 | ||
A small ubiquitin-related polypeptide involved in targeting RanGAP1 to nuclear pore complex protein RanBP2 | Q24317523 | ||
Cloning and expression of human G/T mismatch-specific thymine-DNA glycosylase | Q24320042 | ||
An F-box protein, FWD1, mediates ubiquitin-dependent proteolysis of beta-catenin | Q24534109 | ||
Modification of the human thymine-DNA glycosylase by ubiquitin-like proteins facilitates enzymatic turnover | Q24534803 | ||
The SUMO E3 ligase RanBP2 promotes modification of the HDAC4 deacetylase | Q24534918 | ||
SUMO-1 conjugation to topoisomerase I: A possible repair response to topoisomerase-mediated DNA damage | Q24682811 | ||
Phosphorylation of serine 303 is a prerequisite for the stress-inducible SUMO modification of heat shock factor 1 | Q24685095 | ||
RAD6-dependent DNA repair is linked to modification of PCNA by ubiquitin and SUMO. | Q27937465 | ||
The nucleoporin RanBP2 has SUMO1 E3 ligase activity | Q28115025 | ||
The polycomb protein Pc2 is a SUMO E3 | Q28115324 | ||
Activation of p53 by conjugation to the ubiquitin-like protein SUMO-1. | Q28117154 | ||
The transcriptional role of PML and the nuclear body | Q28144176 | ||
Covalent modification of p73alpha by SUMO-1. Two-hybrid screening with p73 identifies novel SUMO-1-interacting proteins and a SUMO-1 interaction motif | Q28144708 | ||
Functional heterogeneity of small ubiquitin-related protein modifiers SUMO-1 versus SUMO-2/3 | Q28145507 | ||
An E3-like factor that promotes SUMO conjugation to the yeast septins | Q28188846 | ||
Involvement of PIAS1 in the sumoylation of tumor suppressor p53 | Q28189956 | ||
PML protein isoforms and the RBCC/TRIM motif | Q28204823 | ||
SUMO-1 modification of IkappaBalpha inhibits NF-kappaB activation | Q28282094 | ||
Identification of three major sentrinization sites in PML | Q28284098 | ||
Covalent modification of the Werner's syndrome gene product with the ubiquitin-related protein, SUMO-1 | Q28512334 | ||
The nuclear dot protein sp100, characterization of domains necessary for dimerization, subcellular localization, and modification by small ubiquitin-like modifiers | Q28616490 | ||
Regulation of Membrane Protein Transport by Ubiquitin and Ubiquitin-Binding Proteins | Q29619145 | ||
Nuclear and unclear functions of SUMO | Q29903594 | ||
Regulation of double-strand break-induced mammalian homologous recombination by UBL1, a RAD51-interacting protein | Q33615409 | ||
SUMO, ubiquitin's mysterious cousin | Q33939449 | ||
A ubiquitin-interacting motif conserved in components of the proteasomal and lysosomal protein degradation systems | Q33951379 | ||
SUMO: of branched proteins and nuclear bodies | Q34435551 | ||
Role and fate of PML nuclear bodies in response to interferon and viral infections | Q34435571 | ||
Ubc9p and the conjugation of SUMO-1 to RanGAP1 and RanBP2. | Q34452072 | ||
A new RING for SUMO: wrestling transcriptional responses into nuclear bodies with PIAS family E3 SUMO ligases | Q34455419 | ||
A superfamily of protein tags: ubiquitin, SUMO and related modifiers | Q35162583 | ||
RanBP2 associates with Ubc9p and a modified form of RanGAP1 | Q36105014 | ||
Preferential interaction of sentrin with a ubiquitin-conjugating enzyme, Ubc9. | Q36888922 | ||
P433 | issue | 7 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | leukemia | Q29496 |
thymine | Q171973 | ||
Thymine DNA glycosylase | Q21989641 | ||
P304 | page(s) | 5611-5621 | |
P577 | publication date | 2004-11-29 | |
P1433 | published in | Journal of Biological Chemistry | Q867727 |
P1476 | title | Noncovalent SUMO-1 binding activity of thymine DNA glycosylase (TDG) is required for its SUMO-1 modification and colocalization with the promyelocytic leukemia protein | |
P478 | volume | 280 |
Q24297984 | A functional SUMO-interacting motif in the transactivation domain of c-Myb regulates its myeloid transforming ability |
Q36119061 | A nuclear envelope protein linking nuclear pore basket assembly, SUMO protease regulation, and mRNA surveillance |
Q50567128 | Analysis of Small Ubiquitin-Like Modifier (SUMO) Targets Reflects the Essential Nature of Protein SUMOylation and Provides Insight to Elucidate the Role of SUMO in Plant Development. |
Q40119051 | Anchoring of the 26S proteasome to the organellar membrane by FKBP38. |
Q35646746 | Association of Dnmt3a and thymine DNA glycosylase links DNA methylation with base-excision repair. |
Q36853499 | Base excision repair, aging and health span. |
Q91522304 | Cell cycle-dependent localization of the proteasome to chromatin |
Q35227096 | Characterization of the SUMO-binding activity of the myeloproliferative and mental retardation (MYM)-type zinc fingers in ZNF261 and ZNF198 |
Q36884795 | Characterizing Requirements for Small Ubiquitin-like Modifier (SUMO) Modification and Binding on Base Excision Repair Activity of Thymine-DNA Glycosylase in Vivo |
Q39944664 | DNA methyltransferase 3B mutant in ICF syndrome interacts non-covalently with SUMO-1. |
Q55446744 | Defining the impact of sumoylation on substrate binding and catalysis by thymine DNA glycosylase. |
Q24650867 | Direct binding of CoREST1 to SUMO-2/3 contributes to gene-specific repression by the LSD1/CoREST1/HDAC complex |
Q40213321 | Doxorubicin down-regulates Kruppel-associated box domain-associated protein 1 sumoylation that relieves its transcription repression on p21WAF1/CIP1 in breast cancer MCF-7 cells |
Q36228483 | Dual roles of the SUMO-interacting motif in the regulation of Srs2 sumoylation |
Q34076047 | E2-mediated small ubiquitin-like modifier (SUMO) modification of thymine DNA glycosylase is efficient but not selective for the enzyme-product complex |
Q42729876 | Extent and significance of non-covalent SUMO interactions in plant development |
Q39135992 | Functions of SUMO in the Maintenance of Genome Stability |
Q34029103 | Gene expression in the third dimension: the ECM-nucleus connection |
Q47402178 | Generation of specific inhibitors of SUMO-1- and SUMO-2/3-mediated protein-protein interactions using Affimer (Adhiron) technology |
Q38932313 | Global Analysis of SUMO-Binding Proteins Identifies SUMOylation as a Key Regulator of the INO80 Chromatin Remodeling Complex |
Q34093782 | Identification of RING finger protein 4 (RNF4) as a modulator of DNA demethylation through a functional genomics screen |
Q33395720 | Identification of SUMO-interacting proteins by yeast two-hybrid analysis |
Q91657262 | Isoforms of Base Excision Repair Enzymes Produced by Alternative Splicing |
Q24319821 | Mechanism and consequences for paralog-specific sumoylation of ubiquitin-specific protease 25 |
Q40161850 | Modulation of Abeta generation by small ubiquitin-like modifiers does not require conjugation to target proteins |
Q42369960 | Multilevel Regulation of Abiotic Stress Responses in Plants |
Q26996127 | New perspectives on oxidized genome damage and repair inhibition by pro-oxidant metals in neurological diseases |
Q30495084 | One SUMO is sufficient to silence the dimeric potassium channel K2P1 |
Q37721763 | Oxidative stress-induced assembly of PML nuclear bodies controls sumoylation of partner proteins |
Q31060298 | PIAS1 is a GATA4 SUMO ligase that regulates GATA4-dependent intestinal promoters independent of SUMO ligase activity and GATA4 sumoylation |
Q38008909 | PML body meets telomere: the beginning of an ALTernate ending? |
Q22065791 | PML nuclear bodies |
Q42630066 | Phosphorylable tyrosine residue 162 in the double-stranded RNA-dependent kinase PKR modulates its interaction with SUMO |
Q24301465 | Poly-small ubiquitin-like modifier (PolySUMO)-binding proteins identified through a string search |
Q36516772 | Post-translational modifications of PML: consequences and implications |
Q37553976 | Protein SUMOylation in neuropathological conditions. |
Q24307773 | Protein interaction analysis of senataxin and the ALS4 L389S mutant yields insights into senataxin post-translational modification and uncovers mutant-specific binding with a brain cytoplasmic RNA-encoded peptide |
Q39466076 | Regulation of vaccinia virus E3 protein by small ubiquitin-like modifier proteins |
Q36499051 | Role of SUMO/Ubc9 in DNA damage repair and tumorigenesis |
Q28262535 | Role of base excision repair in maintaining the genetic and epigenetic integrity of CpG sites |
Q39613985 | Role of the SUMO-interacting motif in HIPK2 targeting to the PML nuclear bodies and regulation of p53. |
Q33649477 | SUMO Wrestles with Recombination |
Q41983297 | SUMO binding by the Epstein-Barr virus protein kinase BGLF4 is crucial for BGLF4 function. |
Q36839119 | SUMO junction-what's your function? New insights through SUMO-interacting motifs |
Q33809955 | SUMO-1 regulates the conformational dynamics of thymine-DNA Glycosylase regulatory domain and competes with its DNA binding activity |
Q40216483 | SUMO-1-dependent allosteric regulation of thymine DNA glycosylase alters subnuclear localization and CBP/p300 recruitment |
Q33870712 | SUMOylation and de-SUMOylation in response to DNA damage. |
Q64968755 | SUMOylation of periplakin is critical for efficient reorganization of keratin filament network. |
Q33985238 | Small ubiquitin-like modifier (SUMO) isoforms and conjugation-independent function in DNA double-strand break repair pathways |
Q46182845 | Small ubiquitin-like modifier (SUMO) recognition of a SUMO binding motif: a reversal of the bound orientation |
Q43252764 | Small ubiquitin-related modifier (SUMO) binding determines substrate recognition and paralog-selective SUMO modification |
Q27318485 | Sumoylated NHR-25/NR5A regulates cell fate during C. elegans vulval development |
Q45420080 | Sumoylation of Rta of Epstein-Barr virus is preferentially enhanced by PIASxbeta. |
Q36155106 | The SUMO pathway promotes basic helix-loop-helix proneural factor activity via a direct effect on the Zn finger protein senseless |
Q39010225 | The TRIM-FLMN protein TRIM45 directly interacts with RACK1 and negatively regulates PKC-mediated signaling pathway. |
Q38738431 | The novel heart-specific RING finger protein 207 is involved in energy metabolism in cardiomyocytes. |
Q35604640 | The role of small ubiquitin-like modifier-interacting motif in the assembly and regulation of metal-responsive transcription factor 1. |
Q29614358 | Ubiquitin-binding domains |
Q28540592 | Versatile recombinant SUMOylation system for the production of SUMO-modified protein |
Q36525452 | Viruses and sumoylation: recent highlights |
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