190 related articles for article (PubMed ID: 31056463)
1. Allosteric Regulation of Oligomerization by a B
Ruetz M; Campanello GC; McDevitt L; Yokom AL; Yadav PK; Watkins D; Rosenblatt DS; Ohi MD; Southworth DR; Banerjee R
Cell Chem Biol; 2019 Jul; 26(7):960-969.e4. PubMed ID: 31056463
[TBL] [Abstract][Full Text] [Related]
2. Protein destabilization and loss of protein-protein interaction are fundamental mechanisms in cblA-type methylmalonic aciduria.
Plessl T; Bürer C; Lutz S; Yue WW; Baumgartner MR; Froese DS
Hum Mutat; 2017 Aug; 38(8):988-1001. PubMed ID: 28497574
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Structures of the human GTPase MMAA and vitamin B12-dependent methylmalonyl-CoA mutase and insight into their complex formation.
Froese DS; Kochan G; Muniz JR; Wu X; Gileadi C; Ugochukwu E; Krysztofinska E; Gravel RA; Oppermann U; Yue WW
J Biol Chem; 2010 Dec; 285(49):38204-13. PubMed ID: 20876572
[TBL] [Abstract][Full Text] [Related]
5. Energetics of interaction between the G-protein chaperone, MeaB, and B12-dependent methylmalonyl-CoA mutase.
Padovani D; Labunska T; Banerjee R
J Biol Chem; 2006 Jun; 281(26):17838-44. PubMed ID: 16641088
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. A switch III motif relays signaling between a B12 enzyme and its G-protein chaperone.
Lofgren M; Padovani D; Koutmos M; Banerjee R
Nat Chem Biol; 2013 Sep; 9(9):535-9. PubMed ID: 23873214
[TBL] [Abstract][Full Text] [Related]
8. Delineating the clinical spectrum of isolated methylmalonic acidurias: cblA and mut.
Hörster F; Tuncel AT; Gleich F; Plessl T; Froese SD; Garbade SF; Kölker S; Baumgartner MR;
J Inherit Metab Dis; 2021 Jan; 44(1):193-214. PubMed ID: 32754920
[TBL] [Abstract][Full Text] [Related]
9. Role of vitamin B12 on methylmalonyl-CoA mutase activity.
Takahashi-Iñiguez T; García-Hernandez E; Arreguín-Espinosa R; Flores ME
J Zhejiang Univ Sci B; 2012 Jun; 13(6):423-37. PubMed ID: 22661206
[TBL] [Abstract][Full Text] [Related]
10. Autoinhibition and signaling by the switch II motif in the G-protein chaperone of a radical B12 enzyme.
Lofgren M; Koutmos M; Banerjee R
J Biol Chem; 2013 Oct; 288(43):30980-9. PubMed ID: 23996001
[TBL] [Abstract][Full Text] [Related]
11. Structure of metallochaperone in complex with the cobalamin-binding domain of its target mutase provides insight into cofactor delivery.
Vaccaro FA; Born DA; Drennan CL
Proc Natl Acad Sci U S A; 2023 Feb; 120(8):e2214085120. PubMed ID: 36787360
[TBL] [Abstract][Full Text] [Related]
12. Switch I-dependent allosteric signaling in a G-protein chaperone-B
Campanello GC; Lofgren M; Yokom AL; Southworth DR; Banerjee R
J Biol Chem; 2017 Oct; 292(43):17617-17625. PubMed ID: 28882898
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. Crystal structure and mutagenesis of the metallochaperone MeaB: insight into the causes of methylmalonic aciduria.
Hubbard PA; Padovani D; Labunska T; Mahlstedt SA; Banerjee R; Drennan CL
J Biol Chem; 2007 Oct; 282(43):31308-16. PubMed ID: 17728257
[TBL] [Abstract][Full Text] [Related]
16. Long-term outcome in methylmalonic acidurias is influenced by the underlying defect (mut0, mut-, cblA, cblB).
Hörster F; Baumgartner MR; Viardot C; Suormala T; Burgard P; Fowler B; Hoffmann GF; Garbade SF; Kölker S; Baumgartner ER
Pediatr Res; 2007 Aug; 62(2):225-30. PubMed ID: 17597648
[TBL] [Abstract][Full Text] [Related]
17. Clustering of mutations in methylmalonyl CoA mutase associated with mut- methylmalonic acidemia.
Crane AM; Ledley FD
Am J Hum Genet; 1994 Jul; 55(1):42-50. PubMed ID: 7912889
[TBL] [Abstract][Full Text] [Related]
18. Redox-Linked Coordination Chemistry Directs Vitamin B
Banerjee R; Gouda H; Pillay S
Acc Chem Res; 2021 Apr; 54(8):2003-2013. PubMed ID: 33797888
[TBL] [Abstract][Full Text] [Related]
19. Complementation studies in the cblA class of inborn error of cobalamin metabolism: evidence for interallelic complementation and for a new complementation class (cblH).
Watkins D; Matiaszuk N; Rosenblatt DS
J Med Genet; 2000 Jul; 37(7):510-3. PubMed ID: 10882753
[TBL] [Abstract][Full Text] [Related]
20. Inherited defects of cobalamin metabolism.
Watkins D; Rosenblatt DS
Vitam Horm; 2022; 119():355-376. PubMed ID: 35337626
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]