186 related articles for article (PubMed ID: 23996001)
21. Structural basis of the stereospecificity of bacterial B12-dependent 2-hydroxyisobutyryl-CoA mutase.
Kurteva-Yaneva N; Zahn M; Weichler MT; Starke R; Harms H; Müller RH; Sträter N; Rohwerder T
J Biol Chem; 2015 Apr; 290(15):9727-37. PubMed ID: 25720495
[TBL] [Abstract][Full Text] [Related]
22. Homology modeling of human methylmalonyl-CoA mutase: a structural basis for point mutations causing methylmalonic aciduria.
Thomä NH; Leadlay PF
Protein Sci; 1996 Sep; 5(9):1922-7. PubMed ID: 8880917
[TBL] [Abstract][Full Text] [Related]
23. High resolution melting analysis of the MMAB gene in cblB patients and in those with undiagnosed methylmalonic aciduria.
Illson ML; Dempsey-Nunez L; Kent J; Huang Q; Brebner A; Raff ML; Watkins D; Gilfix BM; Wittwer CT; Rosenblatt DS
Mol Genet Metab; 2013; 110(1-2):86-9. PubMed ID: 23707710
[TBL] [Abstract][Full Text] [Related]
24. The coenzyme b12 analog 5'-deoxyadenosylcobinamide-gdp supports catalysis by methylmalonyl-coa mutase in the absence of trans-ligand coordination.
Chowdhury S; Thomas MG; Escalante-Semerena JC; Banerjee R
J Biol Chem; 2001 Jan; 276(2):1015-9. PubMed ID: 11031263
[TBL] [Abstract][Full Text] [Related]
25. Adenosyltransferase tailors and delivers coenzyme B12.
Padovani D; Labunska T; Palfey BA; Ballou DP; Banerjee R
Nat Chem Biol; 2008 Mar; 4(3):194-6. PubMed ID: 18264093
[TBL] [Abstract][Full Text] [Related]
26. A G-protein editor gates coenzyme B12 loading and is corrupted in methylmalonic aciduria.
Padovani D; Banerjee R
Proc Natl Acad Sci U S A; 2009 Dec; 106(51):21567-72. PubMed ID: 19955418
[TBL] [Abstract][Full Text] [Related]
27. Patient mutations in human ATP:cob(I)alamin adenosyltransferase differentially affect its catalytic versus chaperone functions.
Gouda H; Mascarenhas R; Pillay S; Ruetz M; Koutmos M; Banerjee R
J Biol Chem; 2021 Dec; 297(6):101373. PubMed ID: 34757128
[TBL] [Abstract][Full Text] [Related]
28. Naturally occurring cobalamin (B
Sokolovskaya OM; Plessl T; Bailey H; Mackinnon S; Baumgartner MR; Yue WW; Froese DS; Taga ME
Biochimie; 2021 Apr; 183():35-43. PubMed ID: 32659443
[TBL] [Abstract][Full Text] [Related]
29. G-protein signaling: A switch saves B12 radical status.
Toraya T
Nat Chem Biol; 2013 Sep; 9(9):530-1. PubMed ID: 23873213
[No Abstract] [Full Text] [Related]
30. Adenosyltransferase: an enzyme and an escort for coenzyme B12?
Yamanishi M; Vlasie M; Banerjee R
Trends Biochem Sci; 2005 Jun; 30(6):304-8. PubMed ID: 15950874
[TBL] [Abstract][Full Text] [Related]
31. Itaconyl-CoA forms a stable biradical in methylmalonyl-CoA mutase and derails its activity and repair.
Ruetz M; Campanello GC; Purchal M; Shen H; McDevitt L; Gouda H; Wakabayashi S; Zhu J; Rubin EJ; Warncke K; Mootha VK; Koutmos M; Banerjee R
Science; 2019 Nov; 366(6465):589-593. PubMed ID: 31672889
[TBL] [Abstract][Full Text] [Related]
32. Architecture of the human G-protein-methylmalonyl-CoA mutase nanoassembly for B
Mascarenhas R; Ruetz M; Gouda H; Heitman N; Yaw M; Banerjee R
Nat Commun; 2023 Jul; 14(1):4332. PubMed ID: 37468522
[TBL] [Abstract][Full Text] [Related]
33. Isolation and Expression of a cDNA Encoding Methylmalonic Aciduria Type A Protein from Euglena gracilis Z.
Yabuta Y; Takamatsu R; Kasagaki S; Watanabe F
Metabolites; 2013 Feb; 3(1):144-54. PubMed ID: 24957894
[TBL] [Abstract][Full Text] [Related]
34. Characterization of a succinyl-CoA radical-cob(II)alamin spin triplet intermediate in the reaction catalyzed by adenosylcobalamin-dependent methylmalonyl-CoA mutase.
Mansoorabadi SO; Padmakumar R; Fazliddinova N; Vlasie M; Banerjee R; Reed GH
Biochemistry; 2005 Mar; 44(9):3153-8. PubMed ID: 15736925
[TBL] [Abstract][Full Text] [Related]
35. Mutation and biochemical analysis of patients belonging to the cblB complementation class of vitamin B12-dependent methylmalonic aciduria.
Lerner-Ellis JP; Gradinger AB; Watkins D; Tirone JC; Villeneuve A; Dobson CM; Montpetit A; Lepage P; Gravel RA; Rosenblatt DS
Mol Genet Metab; 2006 Mar; 87(3):219-25. PubMed ID: 16410054
[TBL] [Abstract][Full Text] [Related]
36. Renal involvement in a patient with cobalamin A type (cblA) methylmalonic aciduria: a 42-year follow-up.
Haarmann A; Mayr M; Kölker S; Baumgartner ER; Schnierda J; Hopfer H; Devuyst O; Baumgartner MR
Mol Genet Metab; 2013 Dec; 110(4):472-6. PubMed ID: 24095221
[TBL] [Abstract][Full Text] [Related]
37. Impact of cblB mutations on the function of ATP:cob(I)alamin adenosyltransferase in disorders of vitamin B12 metabolism.
Zhang J; Dobson CM; Wu X; Lerner-Ellis J; Rosenblatt DS; Gravel RA
Mol Genet Metab; 2006 Apr; 87(4):315-22. PubMed ID: 16439175
[TBL] [Abstract][Full Text] [Related]
38. Ligand-binding by catalytically inactive mutants of the cblB complementation group defective in human ATP:cob(I)alamin adenosyltransferase.
Zhang J; Wu X; Padovani D; Schubert HL; Gravel RA
Mol Genet Metab; 2009 Nov; 98(3):278-84. PubMed ID: 19625202
[TBL] [Abstract][Full Text] [Related]
39. The crystal structure of the small GTPase Rab11b reveals critical differences relative to the Rab11a isoform.
Scapin SM; Carneiro FR; Alves AC; Medrano FJ; Guimarães BG; Zanchin NI
J Struct Biol; 2006 Jun; 154(3):260-8. PubMed ID: 16545962
[TBL] [Abstract][Full Text] [Related]
40. Importance of the histidine ligand to coenzyme B12 in the reaction catalyzed by methylmalonyl-CoA mutase.
Vlasie M; Chowdhury S; Banerjee R
J Biol Chem; 2002 May; 277(21):18523-7. PubMed ID: 11893736
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
