scholarly article | Q13442814 |
P2093 | author name string | S Acharya | |
R Fishel | |||
S Gradia | |||
P2860 | cites work | Ras-GTPase activating protein (GAP): a putative effector for Ras | Q24314651 |
Mutations of two PMS homologues in hereditary nonpolyposis colon cancer | Q24318484 | ||
Mutation of MSH3 in endometrial cancer and evidence for its functional role in heteroduplex repair | Q24318892 | ||
hMSH2 forms specific mispair-binding complexes with hMSH3 and hMSH6 | Q24323176 | ||
Distantly related sequences in the alpha- and beta-subunits of ATP synthase, myosin, kinases and other ATP-requiring enzymes and a common nucleotide binding fold | Q24556499 | ||
Ras-catalyzed hydrolysis of GTP: a new perspective from model studies | Q24630231 | ||
Genetic and biochemical analysis of Msh2p-Msh6p: role of ATP hydrolysis and Msh2p-Msh6p subunit interactions in mismatch base pair recognition. | Q27932001 | ||
Binding of mismatched microsatellite DNA sequences by the human MSH2 protein | Q28241673 | ||
The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer | Q28256988 | ||
Escherichia coli mutS-encoded protein binds to mismatched DNA base pairs | Q28287503 | ||
Identification of mismatch repair genes and their role in the development of cancer | Q28288647 | ||
Isolation of an hMSH2-p160 Heterodimer That Restores DNA Mismatch Repair to Tumor Cells | Q28292781 | ||
MutS homologs in mammalian cells | Q28303186 | ||
Guanine nucleotide exchange factors: activators of the Ras superfamily of proteins | Q28303508 | ||
hMutSbeta, a heterodimer of hMSH2 and hMSH3, binds to insertion/deletion loops in DNA | Q28610839 | ||
Redundancy of Saccharomyces cerevisiae MSH3 and MSH6 in MSH2-dependent mismatch repair | Q29615027 | ||
Mismatch repair in replication fidelity, genetic recombination, and cancer biology | Q29616483 | ||
Strand-specific mismatch correction in nuclear extracts of human and Drosophila melanogaster cell lines | Q33720790 | ||
MutS mediates heteroduplex loop formation by a translocation mechanism | Q33887145 | ||
Restoration of mismatch repair to nuclear extracts of H6 colorectal tumor cells by a heterodimer of human MutL homologs | Q34554581 | ||
Dominant negative mutator mutations in the mutS gene of Escherichia coli | Q34726651 | ||
Fate of mismatched base-pair regions in polyoma heteroduplex DNA during infection of mouse cells | Q35022697 | ||
DNA mismatch repair detected in human cell extracts | Q36833208 | ||
Mechanisms and biological effects of mismatch repair | Q37041860 | ||
Identification of homologous pairing and strand-exchange activity from a human tumor cell line based on Z-DNA affinity chromatography | Q37479375 | ||
Signal transduction by guanine nucleotide binding proteins | Q38172744 | ||
Signal transduction pathways involving Ras. Mini review | Q40626683 | ||
Emerging concepts in the Ras superfamily of GTP-binding proteins. | Q40824986 | ||
Replacement of gly815 in helicase motif V alters the single-stranded DNA-dependent ATPase activity of the herpes simplex virus type 1 helicase-primase | Q41192630 | ||
Messenger RNA translation in prokaryotes: GTPase centers associated with translational factors | Q41257104 | ||
RGS proteins and signaling by heterotrimeric G proteins | Q41378270 | ||
Strand-specific mismatch repair in mammalian cells | Q41602506 | ||
MLH1, PMS1, and MSH2 interactions during the initiation of DNA mismatch repair in yeast | Q42427955 | ||
Mutation in the DNA mismatch repair gene homologue hMLH1 is associated with hereditary non-polyposis colon cancer | Q48084125 | ||
Interaction of MutS protein with the major and minor grooves of a heteroduplex DNA. | Q54565774 | ||
Direct visualization of dynamics and co-operative conformational changes within RecA filaments that appear to be associated with the hydrolysis of adenosine 5'-O-(3-thiotriphosphate). | Q54679045 | ||
The mismatch-repair protein hMSH2 binds selectively to DNA adducts of the anticancer drug cisplatin | Q71533749 | ||
Influence of the kinesin neck domain on dimerization and ATPase kinetics | Q73144368 | ||
P433 | issue | 7 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 995-1005 | |
P577 | publication date | 1997-12-26 | |
P1433 | published in | Cell | Q655814 |
P1476 | title | The human mismatch recognition complex hMSH2-hMSH6 functions as a novel molecular switch | |
P478 | volume | 91 |
Q27934451 | A mutation in the MSH6 subunit of the Saccharomyces cerevisiae MSH2-MSH6 complex disrupts mismatch recognition |
Q35447437 | A quantitative model of nucleosome dynamics. |
Q37683114 | ATP alters the diffusion mechanics of MutS on mismatched DNA. |
Q40762229 | ATP binding and hydrolysis by Saccharomyces cerevisiae Msh2-Msh3 are differentially modulated by mismatch and double-strand break repair DNA substrates |
Q27939412 | ATP-dependent assembly of a ternary complex consisting of a DNA mismatch and the yeast MSH2-MSH6 and MLH1-PMS1 protein complexes |
Q38316177 | ATP-hydrolysis-dependent conformational switch modulates the stability of MutS-mismatch complexes |
Q24292069 | Activation of human MutS homologs by 8-oxo-guanine DNA damage |
Q28212223 | Adenosine nucleotide modulates the physical interaction between hMSH2 and BRCA1 |
Q28359649 | Affinity of mismatch-binding protein MutS for heteroduplexes containing different mismatches |
Q33889534 | An ATP-ADP switch in MuB controls progression of the Mu transposition pathway |
Q39448525 | An ATP/ADP-dependent molecular switch regulates the stability of p53-DNA complexes. |
Q27938988 | Analysis of the functional domains of the mismatch repair homologue Msh1p and its role in mitochondrial genome maintenance. |
Q24300627 | Analysis of the human MutLalpha.MutSalpha complex |
Q38328409 | Analysis of the interaction between the Saccharomyces cerevisiae MSH2-MSH6 and MLH1-PMS1 complexes with DNA using a reversible DNA end-blocking system. |
Q38332082 | Application of stopped-flow kinetics methods to investigate the mechanism of action of a DNA repair protein |
Q73893732 | Arabidopsis MutS homologs-AtMSH2, AtMSH3, AtMSH6, and a novel AtMSH7-form three distinct protein heterodimers with different specificities for mismatched DNA |
Q92339722 | Array comparative genomic hybridization based identification of key genetic alterations at 2p21-p16.3 (MSH2, MSH6, EPCAM), 3p23-p14.2 (MLH1), 7p22.1 (PMS2) and 1p34.1-p33 (MUTYH) regions in hereditary non polyposis colorectal cancer (Lynch syndrome) |
Q40720210 | Association of p53 and MSH2 with recombinative repair complexes during S phase |
Q39656345 | Asymmetric ATP binding and hydrolysis activity of the Thermus aquaticus MutS dimer is key to modulation of its interactions with mismatched DNA. |
Q34130576 | BRCA1 and cell signaling |
Q34270970 | Biochemical basis for dominant mutations in the Saccharomyces cerevisiae MSH6 gene |
Q43882487 | Biochemical characterization of the human RAD51 protein. I. ATP hydrolysis |
Q43882490 | Biochemical characterization of the human RAD51 protein. II. Adenosine nucleotide binding and competition |
Q38320783 | Biochemical characterization of the interaction between the Saccharomyces cerevisiae MSH2-MSH6 complex and mispaired bases in DNA. |
Q24798955 | Cadmium inhibits mismatch repair by blocking the ATPase activity of the MSH2-MSH6 complex |
Q51324871 | Cascading MutS and MutL sliding clamps control DNA diffusion to activate mismatch repair. |
Q34713695 | Change is good: variations in common biological mechanisms in the epsilonproteobacterial genera Campylobacter and Helicobacter |
Q27629464 | Composite active site of an ABC ATPase: MutS uses ATP to verify mismatch recognition and authorize DNA repair |
Q33559854 | Construction and characterization of mismatch-containing circular DNA molecules competent for assessment of nick-directed human mismatch repair in vitro |
Q34133630 | Cooperation and competition in mismatch repair: very short-patch repair and methyl-directed mismatch repair in Escherichia coli |
Q57060631 | Coordinated protein and DNA conformational changes govern mismatch repair initiation by MutS |
Q57784307 | Coordinating Multi-Protein Mismatch Repair by Managing Diffusion Mechanics on the DNA |
Q27640487 | Crystal structure and biochemical analysis of the MutS.ADP.beryllium fluoride complex suggests a conserved mechanism for ATP interactions in mismatch repair |
Q27627633 | Crystal structures of mismatch repair protein MutS and its complex with a substrate DNA |
Q34385782 | DNA bending and unbending by MutS govern mismatch recognition and specificity |
Q73054412 | DNA binding and protein-protein interaction sites in MutS, a mismatched DNA recognition protein from Thermus thermophilus HB8 |
Q43664681 | DNA chain length dependence of formation and dynamics of hMutSalpha.hMutLalpha.heteroduplex complexes |
Q37602208 | DNA mismatch repair (MMR)-dependent 5-fluorouracil cytotoxicity and the potential for new therapeutic targets. |
Q36527421 | DNA mismatch repair and Lynch syndrome |
Q28211143 | DNA mismatch repair and mutation avoidance pathways |
Q34141513 | DNA mismatch repair: MutS structures bound to mismatches. |
Q35132526 | DNA mismatch repair: from structure to mechanism. |
Q34144865 | DNA mismatch repair: the hands of a genome guardian. |
Q64387816 | DNA template requirements for human mismatch repair in vitro |
Q38331192 | DNA-dependent activation of the hMutSalpha ATPase |
Q33356760 | Decoding the histone code: Role of H3K36me3 in mismatch repair and implications for cancer susceptibility and therapy |
Q74456713 | Deletion mutation analysis of the mutS gene in Escherichia coli |
Q44353892 | Differential and simultaneous adenosine di- and triphosphate binding by MutS. |
Q24337694 | Differential specificities and simultaneous occupancy of human MutSalpha nucleotide binding sites |
Q27690717 | Discovery of a new motion mechanism of biomotors similar to the earth revolving around the sun without rotation |
Q38349552 | Dissimilar mispair-recognition spectra of Arabidopsis DNA-mismatch-repair proteins MSH2{middle dot}MSH6 (MutS ) and MSH2{middle dot}MSH7 (MutS ) |
Q78037753 | Dissociation of mismatch recognition and ATPase activity by hMSH2-hMSH3 |
Q43675423 | Distinct MutS DNA-binding modes that are differentially modulated by ATP binding and hydrolysis |
Q42081270 | Distinct nucleotide binding/hydrolysis properties and molar ratio of MutSalpha and MutSbeta determine their differential mismatch binding activities |
Q40823475 | Distinct requirements within the Msh3 nucleotide binding pocket for mismatch and double-strand break repair |
Q38289639 | Dominant Saccharomyces cerevisiae msh6 mutations cause increased mispair binding and decreased dissociation from mispairs by Msh2-Msh6 in the presence of ATP. |
Q37210972 | Dual daughter strand incision is processive and increases the efficiency of DNA mismatch repair |
Q38316881 | Dual role of MutS glutamate 38 in DNA mismatch discrimination and in the authorization of repair. |
Q36764079 | Endonuclease activities of MutLα and its homologs in DNA mismatch repair |
Q36436073 | Engineered disulfide-forming amino acid substitutions interfere with a conformational change in the mismatch recognition complex Msh2-Msh6 required for mismatch repair |
Q27939116 | Eukaryotic DNA mismatch repair |
Q77753605 | Eukaryotic mismatch repair: an update |
Q37446019 | Evidence that nucleosomes inhibit mismatch repair in eukaryotic cells |
Q30841579 | Evolutionary Covariance Combined with Molecular Dynamics Predicts a Framework for Allostery in the MutS DNA Mismatch Repair Protein |
Q36421123 | Exonuclease 1 (Exo1) is required for activating response to S(N)1 DNA methylating agents |
Q36862037 | Functional analysis helps to clarify the clinical importance of unclassified variants in DNA mismatch repair genes |
Q34425450 | Functional interactions and signaling properties of mammalian DNA mismatch repair proteins |
Q34322248 | G-quadruplex recognition activities of E. Coli MutS. |
Q33836026 | Genomic and epigenetic instability in colorectal cancer pathogenesis |
Q44068446 | HNPCC mutations in hMSH2 result in reduced hMSH2-hMSH6 molecular switch functions |
Q36968380 | Hereditary cancer-associated missense mutations in hMSH6 uncouple ATP hydrolysis from DNA mismatch binding |
Q42975008 | Heteroduplex DNA and ATP induced conformational changes of a MutS mismatch repair protein from Thermus aquaticus |
Q36389371 | How DNA-repair proteins find their targets |
Q24812717 | Human AP endonuclease suppresses DNA mismatch repair activity leading to microsatellite instability. |
Q33536382 | Human DNA repair systems: an overview |
Q35562811 | Human MSH2 (hMSH2) protein controls ATP processing by hMSH2-hMSH6 |
Q31119964 | Human MutL homolog (MLH1) function in DNA mismatch repair: a prospective screen for missense mutations in the ATPase domain |
Q43514135 | Human mismatch repair and G*T mismatch binding by hMutSalpha in vitro is inhibited by adriamycin, actinomycin D, and nogalamycin |
Q28140727 | Identification of mismatch repair protein complexes in HeLa nuclear extracts and their interaction with heteroduplex DNA |
Q37371661 | In vitro and in vivo modulations of benzo[c]phenanthrene-DNA adducts by DNA mismatch repair system |
Q42700921 | Inhibition of colorectal cancer genomic copy number alterations and chromosomal fragile site tumor suppressor FHIT and WWOX deletions by DNA mismatch repair |
Q39991083 | Inhibition of the 5' to 3' exonuclease activity of hEXO1 by 8-oxoguanine |
Q24629057 | Interaction between the Msh2 and Msh6 nucleotide-binding sites in the Saccharomyces cerevisiae Msh2-Msh6 complex |
Q73923892 | Interaction of Escherichia coli MutS and MutL at a DNA mismatch |
Q33555210 | Interaction of MutS and Vsr: some dominant-negative mutS mutations that disable methyladenine-directed mismatch repair are active in very-short-patch repair |
Q24298420 | Interactions between p53, hMSH2-hMSH6 and HMG I(Y) on Holliday junctions and bulged bases |
Q22003969 | Interactions of human hMSH2 with hMSH3 and hMSH2 with hMSH6: examination of mutations found in hereditary nonpolyposis colorectal cancer |
Q35750965 | Interplay between mismatch repair and chromatin assembly |
Q35227178 | Is thymidine glycol containing DNA a substrate of E. coli DNA mismatch repair system? |
Q28264548 | Large conformational changes in MutS during DNA scanning, mismatch recognition and repair signalling |
Q73075608 | MSH2 and MSH6 are required for removal of adenine misincorporated opposite 8-oxo-guanine in S. cerevisiae |
Q34394298 | MSH2-MSH6 stimulates DNA polymerase eta, suggesting a role for A:T mutations in antibody genes |
Q50287452 | MSH2:MSH6 exchanges ADP for ATP |
Q27659930 | Magnesium Coordination Controls the Molecular Switch Function of DNA Mismatch Repair Protein MutS |
Q37713815 | Maintaining a sense of direction during long-range communication on DNA. |
Q28262719 | Mechanisms and functions of DNA mismatch repair |
Q28608973 | Mechanisms of human DNA repair: an update |
Q43919200 | Mechanisms of pathogenicity in human MSH2 missense mutants. |
Q38684481 | Meiotic Chromosome Association 1 Interacts with TOP3α and Regulates Meiotic Recombination in Rice. |
Q35910256 | Meiotic recombination intermediates and mismatch repair proteins |
Q43864989 | Milestones of Lynch syndrome: 1895-2015. |
Q38254881 | Mismatch binding, ADP-ATP exchange and intramolecular signaling during mismatch repair |
Q50335571 | Mismatch recognition and DNA-dependent stimulation of the ATPase activity of hMutSalpha is abolished by a single mutation in the hMSH6 subunit |
Q39656168 | Mismatch recognition-coupled stabilization of Msh2-Msh6 in an ATP-bound state at the initiation of DNA repair |
Q36283640 | Mismatch repair |
Q35164333 | Mismatch repair during homologous and homeologous recombination |
Q34194518 | Mismatch repair in correction of replication errors and processing of DNA damage |
Q43990123 | Mismatch repair in human nuclear extracts. Time courses and ATP requirements for kinetically distinguishable steps leading to tightly controlled 5' to 3' and aphidicolin-sensitive 3' to 5' mispair-provoked excision |
Q44447213 | Mismatch repair in human nuclear extracts: effects of internal DNA-hairpin structures between mismatches and excision-initiation nicks on mismatch correction and mismatch-provoked excision |
Q33960642 | Mismatch repair processing of carcinogen-DNA adducts triggers apoptosis |
Q30569509 | Mismatch repair protein hMSH2-hMSH6 recognizes mismatches and forms sliding clamps within a D-loop recombination intermediate |
Q34723491 | Mismatch-repair protein MSH6 is associated with Ku70 and regulates DNA double-strand break repair |
Q37691675 | Mispair-specific recruitment of the Mlh1-Pms1 complex identifies repair substrates of the Saccharomyces cerevisiae Msh2-Msh3 complex |
Q77734679 | Mobile DNA elements: controlling transposition with ATP-dependent molecular switches |
Q38168515 | Modern aspects of the structural and functional organization of the DNA mismatch repair system |
Q34293069 | Molecular mechanisms of DNA mismatch repair |
Q59356833 | Molecular switch-like regulation enables global subunit coordination in a viral ring ATPase |
Q44522189 | Msh2 separation of function mutations confer defects in the initiation steps of mismatch repair |
Q38271431 | Multiple factors insulate Msh2-Msh6 mismatch repair activity from defects in Msh2 domain I. |
Q91404367 | MutL sliding clamps coordinate exonuclease-independent Escherichia coli mismatch repair |
Q90721497 | MutS homolog sliding clamps shield the DNA from binding proteins |
Q43797701 | MutS preferentially recognizes cisplatin- over oxaliplatin-modified DNA. |
Q78239852 | MutS recognition of exocyclic DNA adducts that are endogenous products of lipid oxidation |
Q34698570 | MutS switches between two fundamentally distinct clamps during mismatch repair |
Q42409924 | MutS/MutL crystal structure reveals that the MutS sliding clamp loads MutL onto DNA. |
Q35914165 | Mutations in the nucleotide binding and hydrolysis domains of Helicobacter pylori MutS2 lead to altered biochemical activities and inactivation of its in vivo function |
Q35063954 | Mutator phenotypes of yeast strains heterozygous for mutations in the MSH2 gene. |
Q24679608 | N-terminus of hMLH1 confers interaction of hMutLalpha and hMutLbeta with hMutSalpha |
Q35259130 | Native mass spectrometry provides direct evidence for DNA mismatch-induced regulation of asymmetric nucleotide binding in mismatch repair protein MutS. |
Q27011117 | New insights and challenges in mismatch repair: getting over the chromatin hurdle |
Q33643516 | Nuclear reorganization of DNA mismatch repair proteins in response to DNA damage |
Q41479268 | Nucleosome remodeling by hMSH2-hMSH6. |
Q28610864 | Nucleotide-promoted release of hMutSalpha from heteroduplex DNA is consistent with an ATP-dependent translocation mechanism |
Q28366275 | Nucleotides and heteroduplex DNA preserve the active conformation of Pseudomonas aeruginosa MutS by preventing protein oligomerization |
Q30751633 | Oligomerization of a MutS mismatch repair protein from Thermus aquaticus |
Q41838980 | P1 ParA interacts with the P1 partition complex at parS and an ATP-ADP switch controls ParA activities |
Q34272353 | PCR candidate region mismatch scanning: adaptation to quantitative, high-throughput genotyping |
Q39600696 | Phosphorylation of mismatch repair proteins MSH2 and MSH6 affecting MutSalpha mismatch-binding activity |
Q28256131 | Prokaryotic DNA mismatch repair |
Q28142999 | Proliferating cell nuclear antigen and Msh2p-Msh6p interact to form an active mispair recognition complex |
Q42139576 | Rad50 ATPase activity is regulated by DNA ends and requires coordination of both active sites. |
Q41886077 | Recognition of DNA alterations by the mismatch repair system |
Q38005951 | Recognition of damaged DNA: structure and dynamic markers |
Q37319600 | Reconstitution of long and short patch mismatch repair reactions using Saccharomyces cerevisiae proteins |
Q36540486 | Regulation of mismatch repair by histone code and posttranslational modifications in eukaryotic cells |
Q42660015 | Replication errors: cha(lle)nging the genome |
Q34612512 | Requirement for Msh6, but not for Swi4 (Msh3), in Msh2-dependent repair of base-base mismatches and mononucleotide loops in Schizosaccharomyces pombe |
Q38018051 | Research on plants for the understanding of diseases of nuclear and mitochondrial origin |
Q34057743 | Roles for mismatch repair factors in regulating genetic recombination |
Q36540776 | Roles for mismatch repair family proteins in promoting meiotic crossing over |
Q33640393 | Saccharomyces cerevisiae Msh2-Msh6 DNA binding kinetics reveal a mechanism of targeting sites for DNA mismatch repair |
Q27932017 | Saccharomyces cerevisiae Msh2p and Msh6p ATPase activities are both required during mismatch repair |
Q37132714 | Sequence context effect for hMSH2-hMSH6 mismatch-dependent activation |
Q40921833 | Signaling from DNA mispairs to mismatch-repair excision sites despite intervening blockades |
Q73143600 | Signaling mismatch repair in cancer |
Q35132521 | Signaling mismatch repair: the mechanics of an adenosine-nucleotide molecular switch |
Q35027619 | Single molecule studies of DNA mismatch repair |
Q30528236 | Single-molecule imaging reveals target-search mechanisms during DNA mismatch repair |
Q41884304 | Single-molecule multiparameter fluorescence spectroscopy reveals directional MutS binding to mismatched bases in DNA |
Q26999680 | Single-molecule views of MutS on mismatched DNA. |
Q42929083 | Slow conformational changes in MutS and DNA direct ordered transitions between mismatch search, recognition and signaling of DNA repair |
Q38324036 | Specific binding of human MSH2.MSH6 mismatch-repair protein heterodimers to DNA incorporating thymine- or uracil-containing UV light photoproducts opposite mismatched bases. |
Q33896699 | Steady-state regulation of the human DNA mismatch repair system. |
Q57784305 | Stochastic Processes and Component Plasticity Governing DNA Mismatch Repair |
Q28484788 | Structural and functional divergence of MutS2 from bacterial MutS1 and eukaryotic MSH4-MSH5 homologs |
Q27625340 | Structural biology of Rad50 ATPase: ATP-driven conformational control in DNA double-strand break repair and the ABC-ATPase superfamily |
Q28285134 | Structural, molecular and cellular functions of MSH2 and MSH6 during DNA mismatch repair, damage signaling and other noncanonical activities |
Q36579583 | Structure and function of ABC transporters: the ATP switch provides flexible control |
Q36521428 | Structure and function of the components of the human DNA mismatch repair system |
Q27667527 | Structures of Human Exonuclease 1 DNA Complexes Suggest a Unified Mechanism for Nuclease Family |
Q34353789 | The ATP switch model for ABC transporters |
Q36627936 | The Kub5-Hera/RPRD1B interactome: a novel role in preserving genetic stability by regulating DNA mismatch repair |
Q38295775 | The Phe-X-Glu DNA binding motif of MutS. The role of hydrogen bonding in mismatch recognition |
Q28306188 | The Saccharomyces cerevisiae Mlh1-Mlh3 heterodimer is an endonuclease that preferentially binds to Holliday junctions |
Q27935147 | The Saccharomyces cerevisiae Msh2 mismatch repair protein localizes to recombination intermediates in vivo. |
Q27640375 | The alternating ATPase domains of MutS control DNA mismatch repair |
Q44530427 | The coordinated functions of the E. coli MutS and MutL proteins in mismatch repair |
Q27627644 | The crystal structure of DNA mismatch repair protein MutS binding to a G x T mismatch |
Q44584724 | The effect of curcumin on mismatch repair (MMR) proteins hMSH2 and hMLH1 after ultraviolet (UV) irradiation on HL-60 cells |
Q41860625 | The effects of nucleotides on MutS-DNA binding kinetics clarify the role of MutS ATPase activity in mismatch repair |
Q34989790 | The genetic pathogenesis of colorectal cancer |
Q36447028 | The hMSH2(M688R) Lynch syndrome mutation may function as a dominant negative |
Q24339204 | The histone mark H3K36me3 regulates human DNA mismatch repair through its interaction with MutSα |
Q24291370 | The interaction of DNA mismatch repair proteins with human exonuclease I |
Q34533276 | The mechanism of mismatch repair and the functional analysis of mismatch repair defects in Lynch syndrome |
Q36448284 | The multifaceted mismatch-repair system |
Q35563361 | The predicted truncation from a cancer-associated variant of the MSH2 initiation codon alters activity of the MSH2-MSH6 mismatch repair complex |
Q91595501 | The properties of Msh2-Msh6 ATP binding mutants suggest a signal amplification mechanism in DNA mismatch repair |
Q28610649 | The role of mismatched nucleotides in activating the hMSH2-hMSH6 molecular switch |
Q36162012 | The unstructured linker arms of Mlh1-Pms1 are important for interactions with DNA during mismatch repair |
Q90622154 | The unstructured linker arms of MutL enable GATC site incision beyond roadblocks during initiation of DNA mismatch repair |
Q44219222 | Transfer of the MSH2.MSH6 complex from proliferating cell nuclear antigen to mispaired bases in DNA. |
Q46602231 | Uncertain pathogenicity of MSH2 variants N127S and G322D challenges their classification. |
Q38361436 | Vanadate inhibits the ATPase activity and DNA binding capability of bacterial MutS. A structural model for the vanadate-MutS interaction at the Walker A motif |
Q38336441 | hMSH2 and hMSH6 play distinct roles in mismatch binding and contribute differently to the ATPase activity of hMutSalpha |
Q28138775 | hMSH2-hMSH6 forms a hydrolysis-independent sliding clamp on mismatched DNA |
Q24622206 | hMSH4-hMSH5 adenosine nucleotide processing and interactions with homologous recombination machinery |
Q24292227 | hMutSalpha forms an ATP-dependent complex with hMutLalpha and hMutLbeta on DNA. |
Q34276816 | hMutSbeta is required for the recognition and uncoupling of psoralen interstrand cross-links in vitro |
Q44881166 | hXRCC2 enhances ADP/ATP processing and strand exchange by hRAD51. |
Q40749074 | p53 binds telomeric single strand overhangs and t-loop junctions in vitro |
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