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1  of the TPR subunits Cdc16, Cdc23 and Cdc27 (Apc3).
2 sm that is reset after inactivation of bimA1(APC3).
3 bunit (Cks) to a hyperphosphorylated loop of Apc3.
4  to coimmunoprecipitate with Cdc20 and Cdc27/APC3.
5  bias for transition mutations to occur at 5'ApC3'/3'TpG5' sites (where bases 5'A and 3'T are mutated
6 de movements, whereas APC2 (aa 1034-2130) or APC3 (aa 2130-2844) reduced both anterograde and retrogr
7 renamed bimA10) and two other ts lethal bimA(APC3) alleles, bimA1 and bimA9.
8                                        Human APC3 also binds APC16 and APC7 and contains a >200-resid
9 ough highly temperature-sensitive, the bimA1(APC3) anaphase-promoting complex/cyclosome (APC/C) mutat
10  through coordinated phosphorylation between Apc3 and Apc1.
11 tratricopeptide repeat (TPR) proteins (APC7, APC3, APC6, and APC8) that homodimerize and stack with q
12             Here, we map the basis for human APC3 assembly with APC16 and APC7, report crystal struct
13 tein subunits, including BimE (APC1), CDC27 (APC3), CDC16 (APC6), and CDC23 (APC8).
14 repeat (TPR) proteins that form homo-dimers (Apc3/Cdc27, Apc6/Cdc16, Apc7 and Apc8/Cdc23).
15  APC16 binds asymmetrically to the symmetric APC3 dimer and, together with biochemistry and prior dat
16 require active NIMA, because a nimA5 + bimA1(APC3) double mutant arrests in a mitotic state with very
17                                  These bimA1(APC3)-induced cell cycle oscillations require active NIM
18 lated during mitosis, although the basis for APC3 interactions and whether loop phosphorylation is re
19         Instead, rapid inactivation of bimA1(APC3) is shown to promote repeating oscillations of chro
20 rylation of APC/C subunits, notably Apc1 and Apc3, is required for Cdc20 to activate the APC/C, where
21 r results demonstrate that mutations in bimA(APC3) lead to errors in DNA metabolism that indirectly b
22                                    The bimA1(APC3) mutation may also make the APC/C resistant to acti
23                                    The bimA1(APC3) mutation therefore first inactivates the APC/C but
24 in how APC16 recruits APC7 to APC3, show how APC3's C-terminal domain is rearranged in the full APC/C
25 -terminal domain of APC16, and test roles of APC3's loop and IR tail binding surfaces in APC/C-cataly
26                                              APC3's TPR motifs recruit substrate-binding coactivators
27                    Within the APC/C complex, APC3 serves as center for regulation.
28 ior data, explain how APC16 recruits APC7 to APC3, show how APC3's C-terminal domain is rearranged in
29  checkpoint inhibits septation in these bimA(APC3) strains.
30  C/EBPdelta induces expression of the Cdc27 (APC3) subunit of the anaphase promoting complex/cyclosom
31 1 mutation represents a novel allele of bimA(APC3), which encodes a conserved component of the anapha

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