(Q27648368)

Cancer in xeroderma pigmentosum and related disorders of DNA repair

GOA release 2020-03-11

author name string

Jung-Hyun Min

series ordinal

1

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Nikola P Pavletich

series ordinal

2

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language of work or name

English

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publication date

4 October 2007

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published in

Nature

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volume

449

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page(s)

570-5

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issue

7162

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cites work

1 reference

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7 January 2021

Molecular mechanisms of mammalian global genome nucleotide excision repair.

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Expression cloning of a human DNA repair gene involved in xeroderma pigmentosum group C

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Purification and cloning of a nucleotide excision repair complex involving the xeroderma pigmentosum group C protein and a human homologue of yeast RAD23

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The comings and goings of nucleotide excision repair factors on damaged DNA

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Xeroderma pigmentosum group C protein complex is the initiator of global genome nucleotide excision repair

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Stable binding of human XPC complex to irradiated DNA confers strong discrimination for damaged sites

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Diversity of the damage recognition step in the global genomic nucleotide excision repair in vitro

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The XPC-HR23B complex displays high affinity and specificity for damaged DNA in a true-equilibrium fluorescence assay

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Sequential assembly of the nucleotide excision repair factors in vivo

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Mechanisms of DNA damage recognition and strand discrimination in human nucleotide excision repair

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In vivo recruitment of XPC to UV-induced cyclobutane pyrimidine dimers by the DDB2 gene product

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Rad23 and Rpn10: perennial wallflowers join the melee

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Identification and characterization of XPC-binding domain of hHR23B.

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A novel regulation mechanism of DNA repair by damage-induced and RAD23-dependent stabilization of xeroderma pigmentosum group C protein

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Rad23 stabilizes Rad4 from degradation by the Ub/proteasome pathway

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Solution conformation of the (-)-cis-anti-benzo[a]pyrenyl-dG adduct opposite dC in a DNA duplex: intercalation of the covalently attached BP ring into the helix with base displacement of the modified deoxyguanosine into the major groove

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Solution structure of the (+)-cis-anti-benzo[a]pyrene-dA ([BP]dA) adduct opposite dT in a DNA duplex

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Influence of benzo[a]pyrene diol epoxide chirality on solution conformations of DNA covalent adducts: the (-)-trans-anti-[BP]G.C adduct structure and comparison with the (+)-trans-anti-[BP]G.C enantiomer

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Thermodynamic and structural factors in the removal of bulky DNA adducts by the nucleotide excision repair machinery

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Structural characterization of an N-acetyl-2-aminofluorene (AAF) modified DNA oligomer by NMR, energy minimization, and molecular dynamics

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The solution structure of DNA duplex-decamer containing the (6-4) photoproduct of thymidylyl(3'-->5')thymidine by NMR and relaxation matrix refinement

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Solution-state structure of a DNA dodecamer duplex containing a Cis-syn thymine cyclobutane dimer, the major UV photoproduct of DNA

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Thermodynamic and base-pairing studies of matched and mismatched DNA dodecamer duplexes containing cis-syn, (6-4) and Dewar photoproducts of TT.

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Recognition of DNA adducts by human nucleotide excision repair. Evidence for a thermodynamic probing mechanism

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Structure and recognition of sheared tandem G x A base pairs associated with human centromere DNA sequence at atomic resolution

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Solution structure of a DNA double helix incorporating four consecutive non-Watson-Crick base-pairs

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7 January 2021

A multistep damage recognition mechanism for global genomic nucleotide excision repair

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DNA quality control by conformational readout on the undamaged strand of the double helix

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Peptide-N-glycanases and DNA repair proteins, Xp-C/Rad4, are, respectively, active and inactivated enzymes sharing a common transglutaminase fold

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Solution structure of the DNA- and RPA-binding domain of the human repair factor XPA

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Recognition of nonhybridizing base pairs during nucleotide excision repair of DNA

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Specific and efficient binding of xeroderma pigmentosum complementation group A to double-strand/single-strand DNA junctions with 3'- and/or 5'-ssDNA branches

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RPA stabilizes the XPA-damaged DNA complex through protein-protein interaction

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DNA-XPA interactions: a (31)P NMR and molecular modeling study of dCCAATAACC association with the minimal DNA-binding domain (M98-F219) of the nucleotide excision repair protein XPA.

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Recognition of helical kinks by xeroderma pigmentosum group A protein triggers DNA excision repair

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7 January 2021

A molecular mechanism for DNA damage recognition by the xeroderma pigmentosum group C protein complex

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7 January 2021

Solution conformation of the (+)-trans-anti-[BPh]dA adduct opposite dT in a DNA duplex: intercalation of the covalently attached benzo[c]phenanthrene to the 5'-side of the adduct site without disruption of the modified base pair

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Solution conformation of the (-)-trans-anti-benzo[c]phenanthrene-dA ([BPh]dA) adduct opposite dT in a DNA duplex: intercalation of the covalently attached benzo[c]phenanthrenyl ring to the 3'-side of the adduct site and comparison with the (+)-trans

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7 January 2021

DNA base damage recognition and removal: new twists and grooves

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7 January 2021

Finding a basis for flipping bases.

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7 January 2021

Flexibility and plasticity of human centrin 2 binding to the xeroderma pigmentosum group C protein (XPC) from nuclear excision repair.

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The structure of the human centrin 2-xeroderma pigmentosum group C protein complex.

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Processing of X-ray diffraction data collected in oscillation mode

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7 January 2021

[27] Maximum-likelihood heavy-atom parameter refinement for multiple isomorphous replacement and multiwavelength anomalous diffraction methods.

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Improved methods for building protein models in electron density maps and the location of errors in these models

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Crystallography & NMR System: A New Software Suite for Macromolecular Structure Determination

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Identifiers

DOI

10.1038/NATURE06155

1 reference

Consolidated OpenCitations Corpus – April 2017

Dimensions Publication ID

625511

1025933337

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625511

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

1 reference