Soo-Chen Cheng
Cheng, Soo-Chen, 1955-
VIAF ID: 63042755 (Personal)
Permalink: http://viaf.org/viaf/63042755
Preferred Forms
- 100 1 _ ‡a Cheng, Soo-Chen ‡d 1955-
- 100 1 _ ‡a Cheng, Soo-Chen, ‡d 1955-
- 100 0 _ ‡a Soo-Chen Cheng
4xx's: Alternate Name Forms (2)
Works
Title | Sources |
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Both catalytic steps of nuclear pre-mRNA splicing are reversible | |
A central role of Cwc25 in spliceosome dynamics during the catalytic phase of pre-mRNA splicing. | |
Cwc23 is a component of the NTR complex and functions to stabilize Ntr1 and facilitate disassembly of spliceosome intermediates. | |
Cwc25 is a novel splicing factor required after Prp2 and Yju2 to facilitate the first catalytic reaction | |
DEAH-box ATPase Prp16 has dual roles in remodeling of the spliceosome in catalytic steps | |
Dynamic interactions of Ntr1-Ntr2 with Prp43 and with U5 govern the recruitment of Prp43 to mediate spliceosome disassembly | |
Dynamic protein-RNA interactions in mediating splicing catalysis | |
Enzymatic and genetic ... 1983 | |
Evidence for complex dynamics during U2 snRNP selection of the intron branchpoint | |
Functional roles of protein splicing factors | |
The interaction of Prp2 with a defined region of the intron is required for the first splicing reaction | |
Link of NTR-mediated spliceosome disassembly with DEAH-box ATPases Prp2, Prp16, and Prp22. | |
A novel mechanism for Prp5 function in prespliceosome formation and proofreading the branch site sequence | |
The Prp19p-associated complex in spliceosome activation | |
RNA splicing for 30 years | |
Role of Cwc24 in the First Catalytic Step of Splicing and Fidelity of 5' Splice Site Selection | |
Sad1 counteracts Brr2-mediated dissociation of U4/U6.U5 in tri-snRNP homeostasis | |
The spliceosome catalyzes debranching in competition with reverse of the first chemical reaction | |
Spliceosome disassembly catalyzed by Prp43 and its associated components Ntr1 and Ntr2. | |
Structural requirement of Ntc77 for spliceosome activation and first catalytic step | |
A weak spliceosome-binding domain of Yju2 functions in the first step and bypasses Prp16 in the second step of splicing |