ライフサイエンスコーパス: conjugase

1 O to target proteins is catalyzed by SUMO E2 conjugase.

2 to date possess a single indispensable SUMO conjugase.

3 desaturase-type enzymes that we have termed "conjugase."

4 ct in the endomembranes, where the ubiquitin conjugase activity of PHO2 is required for PHO1 degradat

5 n active-site cysteine crucial for ubiquitin conjugase activity.

6 gene shows that CrUBC9 is an authentic SUMO conjugase and, more importantly, that SUMOylation is ess

7 of NLA and phosphate2 (pho2; a ubiquitin E2 conjugase) and the synergistic effect of the accumulatio

8 -linked ubiquitination, and E1 activases, E2 conjugases, and E3 ligases involved in ubiquitination an

9 studies identified the Drosophila ubiquitin conjugase bendless (ben) to be important for central syn

10 Expression of tung tree FA conjugase/desaturase in Arabidopsis produced approximate

11 ber of the UbcH5 family of protein ubiquitin conjugase E2 enzymes, is a critical component of biologi

12 eristic of the catalytic domain of ubiquitin conjugase (E2) enzymes but lacking an active-site cystei

13 ression of 20S-proteasome alpha subunits, E2 conjugases, E3 ligases, and autophagy were measured with

14 MocD is a homolog of Mas2, the anabolic conjugase encoded by mas2'.

15 iously shown that acetylation of the SUMO E2 conjugase enzyme, Ubc9, at K65 downregulates its binding

16 CLNs are produced by conjugase enzymes that are homologs of the oleate desatu

17 protease, alpha-amylase and chicken pancreas conjugase) extraction treatment.

18 methyltransferases and histone H2B ubiquitin conjugase facilitate GAL10 antisense transcription, whil

19 the domain(s) within the Momordica charantia conjugase (FADX) responsible for CLN formation.

20 Like the Momordica conjugase, FADX G111V and FADX D115E produced predominan

21 in which the previously identified SUMO conjugase gene C. reinhardtii ubiquitin-conjugating enzy

22 GH3 amino acid conjugases have been identified in many plant and bacter

23 the presence of at least one additional SUMO conjugase in C. reinhardtii, a conjugase tentatively ide

24 at least two distinct and functional SUMO E2 conjugases in C. reinhardtii, with a clear division of l

25 including those for F-box factors, ubiquitin conjugases, Leucine-rich repeat proteins, and metabolic

26 d by previously characterized Z11-desaturase/conjugase MsexD2.

27 We found that the cyclin selective ubiquitin conjugase murine E2-C, was up regulated in NIH3T3 cells

28 onal activity was inhibited by Ubc9 (SUMO E2 conjugase) or PIAS1 (E3 ligase), but not in the ERK5-SUM

29 was inhibited by expression of Ubc9 (SUMO E2 conjugase) or PIAS1 (E3 ligase), suggesting the involvem

30 ost-translationally using individual sets of conjugase pathways that attach the polypeptides via an i

31 the first histidine box as a determinant of conjugase product partitioning into punicic acid (18:3 D

32 first histidine box, as key determinants of conjugase product partitioning.

33 t Rtf1 directly interacts with the ubiquitin conjugase Rad6 and stimulates H2Bub independently of tra

34 biquitin-activating enzyme E1, and ubiquitin conjugase Rad6, and eluted column fraction II (CFII) inc

35 out by Bre1p, an E3 ligase, along with an E2 conjugase, Rad6p.

36 ated knockdown of UBC9, an essential SUMO E2 conjugase, resulted in downregulation of FOXA2 protein l

37 , hydroxylase, epoxygenase, acetylenase, and conjugase) revealed several amino acid positions near th

38 mutant C93A, which is a defective E2-SUMO-1 conjugase, suggests that this activity may not be requir

39 ditional SUMO conjugase in C. reinhardtii, a conjugase tentatively identified as CrUBC3.

40 ucible ubiquitin ligase WSB-1, the ubiquitin conjugase UBC-7, and VDU-1, a D2-specific deubiquitinase

41 PHO2 encodes a putative E2 conjugase, UBC24.

42 eracting proteins and identified the SUMO E2 conjugase Ubc9 as one such partner.

43 The cellular E2 Sumo conjugase, Ubc9 interacts with HIV-1 Gag, and is importa

44 We show here that the ubiquitin conjugase, UbcH10, is significantly overexpressed in man

45 Together with its E2 conjugase Ube2J2, TMEM129 is responsible for the ubiquit

46 TRIM6 and the E2-ubiquitin conjugase UbE2K cooperated in the synthesis of unanchore

47 lelic germline mutations in the ubiquitin E2 conjugase UBE2T.

48 cid desaturases and hydroxylases rather than conjugases, which is consistent with its desaturase acti