202 related articles for article (PubMed ID: 36840719)
41. Key role of phosphorylation sites in ATPase domain and Linker region of MLH1 for DNA binding and functionality of MutLα.
Firnau MB; Plotz G; Zeuzem S; Brieger A
Sci Rep; 2023 Aug; 13(1):12503. PubMed ID: 37532794
[TBL] [Abstract][Full Text] [Related]
42. Human MutLalpha: the jack of all trades in MMR is also an endonuclease.
Yang W
DNA Repair (Amst); 2007 Jan; 6(1):135-9. PubMed ID: 17142111
[TBL] [Abstract][Full Text] [Related]
43. Insights into DNA cleavage by MutL homologs from analysis of conserved motifs in eukaryotic Mlh1.
Putnam CD; Kolodner RD
Bioessays; 2023 Sep; 45(9):e2300031. PubMed ID: 37424007
[TBL] [Abstract][Full Text] [Related]
44. Dual daughter strand incision is processive and increases the efficiency of DNA mismatch repair.
Hermans N; Laffeber C; Cristovão M; Artola-Borán M; Mardenborough Y; Ikpa P; Jaddoe A; Winterwerp HH; Wyman C; Jiricny J; Kanaar R; Friedhoff P; Lebbink JH
Nucleic Acids Res; 2016 Aug; 44(14):6770-86. PubMed ID: 27174933
[TBL] [Abstract][Full Text] [Related]
45. Endonuclease Activity of MutL Protein of the Rhodobacter sphaeroides Mismatch Repair System.
Monakhova MV; Penkina AI; Pavlova AV; Lyaschuk AM; Kucherenko VV; Alexeevski AV; Lunin VG; Friedhoff P; Klug G; Oretskaya TS; Kubareva EA
Biochemistry (Mosc); 2018 Mar; 83(3):281-293. PubMed ID: 29625547
[TBL] [Abstract][Full Text] [Related]
46. Recurrent mismatch binding by MutS mobile clamps on DNA localizes repair complexes nearby.
Hao P; LeBlanc SJ; Case BC; Elston TC; Hingorani MM; Erie DA; Weninger KR
Proc Natl Acad Sci U S A; 2020 Jul; 117(30):17775-17784. PubMed ID: 32669440
[TBL] [Abstract][Full Text] [Related]
47. PCNA and Msh2-Msh6 activate an Mlh1-Pms1 endonuclease pathway required for Exo1-independent mismatch repair.
Goellner EM; Smith CE; Campbell CS; Hombauer H; Desai A; Putnam CD; Kolodner RD
Mol Cell; 2014 Jul; 55(2):291-304. PubMed ID: 24981171
[TBL] [Abstract][Full Text] [Related]
48. Activity of Vsr endonucleases encoded by Neisseria gonorrhoeae FA1090 is influenced by MutL and MutS proteins.
Adamczyk-Popławska M; Bandyra K; Kwiatek A
BMC Microbiol; 2018 Aug; 18(1):95. PubMed ID: 30165819
[TBL] [Abstract][Full Text] [Related]
49. SMARCAD1-mediated recruitment of the DNA mismatch repair protein MutLα to MutSα on damaged chromatin induces apoptosis in human cells.
Takeishi Y; Fujikane R; Rikitake M; Obayashi Y; Sekiguchi M; Hidaka M
J Biol Chem; 2020 Jan; 295(4):1056-1065. PubMed ID: 31843968
[TBL] [Abstract][Full Text] [Related]
50. Modulation of microRNA processing by mismatch repair protein MutLα.
Mao G; Lee S; Ortega J; Gu L; Li GM
Cell Res; 2012 Jun; 22(6):973-85. PubMed ID: 22290424
[TBL] [Abstract][Full Text] [Related]
51. The PMS2 subunit of human MutLalpha contains a metal ion binding domain of the iron-dependent repressor protein family.
Kosinski J; Plotz G; Guarné A; Bujnicki JM; Friedhoff P
J Mol Biol; 2008 Oct; 382(3):610-27. PubMed ID: 18619468
[TBL] [Abstract][Full Text] [Related]
52. The functions of MutL in mismatch repair: the power of multitasking.
Guarné A
Prog Mol Biol Transl Sci; 2012; 110():41-70. PubMed ID: 22749142
[TBL] [Abstract][Full Text] [Related]
53. Interactions of Exo1p with components of MutLalpha in Saccharomyces cerevisiae.
Tran PT; Simon JA; Liskay RM
Proc Natl Acad Sci U S A; 2001 Aug; 98(17):9760-5. PubMed ID: 11481425
[TBL] [Abstract][Full Text] [Related]
54. The Mlh1-Pms1 endonuclease uses ATP to preserve DNA discontinuities as strand discrimination signals to facilitate mismatch repair.
Piscitelli JM; Witte SJ; Sakinejad YS; Manhart CM
bioRxiv; 2024 Jun; ():. PubMed ID: 38915520
[TBL] [Abstract][Full Text] [Related]
55. Stoichiometry of MutS and MutL at unrepaired mismatches in vivo suggests a mechanism of repair.
Elez M; Radman M; Matic I
Nucleic Acids Res; 2012 May; 40(9):3929-38. PubMed ID: 22241777
[TBL] [Abstract][Full Text] [Related]
56. A possible mechanism for exonuclease 1-independent eukaryotic mismatch repair.
Kadyrov FA; Genschel J; Fang Y; Penland E; Edelmann W; Modrich P
Proc Natl Acad Sci U S A; 2009 May; 106(21):8495-500. PubMed ID: 19420220
[TBL] [Abstract][Full Text] [Related]
57. Mutations affecting a putative MutLalpha endonuclease motif impact multiple mismatch repair functions.
Erdeniz N; Nguyen M; Deschênes SM; Liskay RM
DNA Repair (Amst); 2007 Oct; 6(10):1463-70. PubMed ID: 17567544
[TBL] [Abstract][Full Text] [Related]
58. Involvement of DNA mismatch repair in the maintenance of heterochromatic DNA stability in Saccharomyces cerevisiae.
Dahal BK; Kadyrova LY; Delfino KR; Rogozin IB; Gujar V; Lobachev KS; Kadyrov FA
PLoS Genet; 2017 Oct; 13(10):e1007074. PubMed ID: 29069084
[TBL] [Abstract][Full Text] [Related]
59. MutLα heterodimers modify the molecular phenotype of Friedreich ataxia.
Ezzatizadeh V; Sandi C; Sandi M; Anjomani-Virmouni S; Al-Mahdawi S; Pook MA
PLoS One; 2014; 9(6):e100523. PubMed ID: 24971578
[TBL] [Abstract][Full Text] [Related]
60. Spatial coupling between DNA replication and mismatch repair in Caulobacter crescentus.
Chai T; Terrettaz C; Collier J
Nucleic Acids Res; 2021 Apr; 49(6):3308-3321. PubMed ID: 33677508
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
