218 related articles for article (PubMed ID: 27251438)
1. Role of the tryptophan residues in proton-coupled folate transporter (PCFT-SLC46A1) function.
Najmi M; Zhao R; Fiser A; Goldman ID
Am J Physiol Cell Physiol; 2016 Jul; 311(1):C150-7. PubMed ID: 27251438
[TBL] [Abstract][Full Text] [Related]
2. Substituted-cysteine accessibility and cross-linking identify an exofacial cleft in the 7th and 8th helices of the proton-coupled folate transporter (SLC46A1).
Aluri S; Zhao R; Fiser A; Goldman ID
Am J Physiol Cell Physiol; 2018 Mar; 314(3):C289-C296. PubMed ID: 29167151
[TBL] [Abstract][Full Text] [Related]
3. Identification of Tyr residues that enhance folate substrate binding and constrain oscillation of the proton-coupled folate transporter (PCFT-SLC46A1).
Visentin M; Unal ES; Najmi M; Fiser A; Zhao R; Goldman ID
Am J Physiol Cell Physiol; 2015 Apr; 308(8):C631-41. PubMed ID: 25608532
[TBL] [Abstract][Full Text] [Related]
4. Substituted cysteine accessibility reveals a novel transmembrane 2-3 reentrant loop and functional role for transmembrane domain 2 in the human proton-coupled folate transporter.
Wilson MR; Hou Z; Matherly LH
J Biol Chem; 2014 Sep; 289(36):25287-95. PubMed ID: 25053408
[TBL] [Abstract][Full Text] [Related]
5. Residues in the eighth transmembrane domain of the proton-coupled folate transporter (SLC46A1) play an important role in defining the aqueous translocation pathway and in folate substrate binding.
Aluri S; Zhao R; Fiser A; Goldman ID
Biochim Biophys Acta Biomembr; 2017 Nov; 1859(11):2193-2202. PubMed ID: 28802835
[TBL] [Abstract][Full Text] [Related]
6. A proton-coupled folate transporter mutation causing hereditary folate malabsorption locks the protein in an inward-open conformation.
Zhan HQ; Najmi M; Lin K; Aluri S; Fiser A; Goldman ID; Zhao R
J Biol Chem; 2020 Nov; 295(46):15650-15661. PubMed ID: 32893190
[TBL] [Abstract][Full Text] [Related]
7. A P425R mutation of the proton-coupled folate transporter causing hereditary folate malabsorption produces a highly selective alteration in folate binding.
Shin DS; Zhao R; Yap EH; Fiser A; Goldman ID
Am J Physiol Cell Physiol; 2012 May; 302(9):C1405-12. PubMed ID: 22345511
[TBL] [Abstract][Full Text] [Related]
8. Properties of the Arg376 residue of the proton-coupled folate transporter (PCFT-SLC46A1) and a glutamine mutant causing hereditary folate malabsorption.
Mahadeo K; Diop-Bove N; Shin D; Unal ES; Teo J; Zhao R; Chang MH; Fulterer A; Romero MF; Goldman ID
Am J Physiol Cell Physiol; 2010 Nov; 299(5):C1153-61. PubMed ID: 20686069
[TBL] [Abstract][Full Text] [Related]
9. Functional roles of the A335 and G338 residues of the proton-coupled folate transporter (PCFT-SLC46A1) mutated in hereditary folate malabsorption.
Shin DS; Zhao R; Fiser A; Goldman DI
Am J Physiol Cell Physiol; 2012 Oct; 303(8):C834-42. PubMed ID: 22843796
[TBL] [Abstract][Full Text] [Related]
10. Substitutions that lock and unlock the proton-coupled folate transporter (PCFT-SLC46A1) in an inward-open conformation.
Aluri S; Zhao R; Lin K; Shin DS; Fiser A; Goldman ID
J Biol Chem; 2019 May; 294(18):7245-7258. PubMed ID: 30858177
[TBL] [Abstract][Full Text] [Related]
11. Role of the fourth transmembrane domain in proton-coupled folate transporter function as assessed by the substituted cysteine accessibility method.
Shin DS; Zhao R; Fiser A; Goldman ID
Am J Physiol Cell Physiol; 2013 Jun; 304(12):C1159-67. PubMed ID: 23552283
[TBL] [Abstract][Full Text] [Related]
12. Role of the glutamate 185 residue in proton translocation mediated by the proton-coupled folate transporter SLC46A1.
Unal ES; Zhao R; Goldman ID
Am J Physiol Cell Physiol; 2009 Jul; 297(1):C66-74. PubMed ID: 19403800
[TBL] [Abstract][Full Text] [Related]
13. Identification of an Extracellular Gate for the Proton-coupled Folate Transporter (PCFT-SLC46A1) by Cysteine Cross-linking.
Zhao R; Najmi M; Fiser A; Goldman ID
J Biol Chem; 2016 Apr; 291(15):8162-72. PubMed ID: 26884338
[TBL] [Abstract][Full Text] [Related]
14. The proton-coupled folate transporter (PCFT-SLC46A1) and the syndrome of systemic and cerebral folate deficiency of infancy: Hereditary folate malabsorption.
Zhao R; Aluri S; Goldman ID
Mol Aspects Med; 2017 Feb; 53():57-72. PubMed ID: 27664775
[TBL] [Abstract][Full Text] [Related]
15. Vulnerability of the cysteine-less proton-coupled folate transporter (PCFT-SLC46A1) to mutational stress associated with the substituted cysteine accessibility method.
Zhao R; Shin DS; Goldman ID
Biochim Biophys Acta; 2011 Apr; 1808(4):1140-5. PubMed ID: 21256110
[TBL] [Abstract][Full Text] [Related]
16. Hereditary folate malabsorption due to a mutation in the external gate of the proton-coupled folate transporter SLC46A1.
Aluri S; Zhao R; Lubout C; Goorden SMI; Fiser A; Goldman ID
Blood Adv; 2018 Jan; 2(1):61-68. PubMed ID: 29344585
[TBL] [Abstract][Full Text] [Related]
17. Functional and mechanistic roles of the human proton-coupled folate transporter transmembrane domain 6-7 linker.
Wilson MR; Hou Z; Wilson LJ; Ye J; Matherly LH
Biochem J; 2016 Oct; 473(20):3545-3562. PubMed ID: 27514717
[TBL] [Abstract][Full Text] [Related]
18. The functional roles of the His247 and His281 residues in folate and proton translocation mediated by the human proton-coupled folate transporter SLC46A1.
Unal ES; Zhao R; Chang MH; Fiser A; Romero MF; Goldman ID
J Biol Chem; 2009 Jun; 284(26):17846-57. PubMed ID: 19389703
[TBL] [Abstract][Full Text] [Related]
19. Functional roles of aspartate residues of the proton-coupled folate transporter (PCFT-SLC46A1); a D156Y mutation causing hereditary folate malabsorption.
Shin DS; Min SH; Russell L; Zhao R; Fiser A; Goldman ID
Blood; 2010 Dec; 116(24):5162-9. PubMed ID: 20805364
[TBL] [Abstract][Full Text] [Related]
20. Identification of a functionally critical GXXG motif and its relationship to the folate binding site of the proton-coupled folate transporter (PCFT-SLC46A1).
Zhao R; Shin DS; Fiser A; Goldman ID
Am J Physiol Cell Physiol; 2012 Sep; 303(6):C673-81. PubMed ID: 22785121
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
