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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 UBs) counter the signal induced by ubiquitin conjugases and ligases by removing ubiquitin from these
8  of NLA and phosphate2 (pho2; a ubiquitin E2 conjugase) and the synergistic effect of the accumulatio
9 -linked ubiquitination, and E1 activases, E2 conjugases, and E3 ligases involved in ubiquitination an
10 12)-ATG5-ATG16L1 in complex with the E2-like conjugase ATG3 docks LC3 onto the membrane in three step
11  studies identified the Drosophila ubiquitin conjugase bendless (ben) to be important for central syn
12                                The ubiquitin conjugase BRUCE (BIR Repeat containing Ubiquitin-Conjuga
13                   Expression of tung tree FA conjugase/desaturase in Arabidopsis produced approximate
14 ber of the UbcH5 family of protein ubiquitin conjugase E2 enzymes, is a critical component of biologi
15 eristic of the catalytic domain of ubiquitin conjugase (E2) enzymes but lacking an active-site cystei
16 ression of 20S-proteasome alpha subunits, E2 conjugases, E3 ligases, and autophagy were measured with
17      MocD is a homolog of Mas2, the anabolic conjugase encoded by mas2'.
18 iously shown that acetylation of the SUMO E2 conjugase enzyme, Ubc9, at K65 downregulates its binding
19                         CLNs are produced by conjugase enzymes that are homologs of the oleate desatu
20 protease, alpha-amylase and chicken pancreas conjugase) extraction treatment.
21 methyltransferases and histone H2B ubiquitin conjugase facilitate GAL10 antisense transcription, whil
22 the domain(s) within the Momordica charantia conjugase (FADX) responsible for CLN formation.
23                           Like the Momordica conjugase, FADX G111V and FADX D115E produced predominan
24      in which the previously identified SUMO conjugase gene C. reinhardtii ubiquitin-conjugating enzy
25 nscription elongation factor and a ubiquitin conjugase guides substrate selection toward a highly con
26                               GH3 amino acid conjugases have been identified in many plant and bacter
27 the presence of at least one additional SUMO conjugase in C. reinhardtii, a conjugase tentatively ide
28 at least two distinct and functional SUMO E2 conjugases in C. reinhardtii, with a clear division of l
29  The primary function of the UBE2T ubiquitin conjugase is in the monoubiquitination of the FANCI-FANC
30 ctors allowed us to identify the UBE2D2/3 E2 conjugase LET-70 working with UBR-5 to exit stem fate.
31 including those for F-box factors, ubiquitin conjugases, Leucine-rich repeat proteins, and metabolic
32 6 and other TLR-related ubiquitin ligase and conjugase levels.
33 d by previously characterized Z11-desaturase/conjugase MsexD2.
34 We found that the cyclin selective ubiquitin conjugase murine E2-C, was up regulated in NIH3T3 cells
35 onal activity was inhibited by Ubc9 (SUMO E2 conjugase) or PIAS1 (E3 ligase), but not in the ERK5-SUM
36 was inhibited by expression of Ubc9 (SUMO E2 conjugase) or PIAS1 (E3 ligase), suggesting the involvem
37 ost-translationally using individual sets of conjugase pathways that attach the polypeptides via an i
38  the first histidine box as a determinant of conjugase product partitioning into punicic acid (18:3 D
39  first histidine box, as key determinants of conjugase product partitioning.
40 t Rtf1 directly interacts with the ubiquitin conjugase Rad6 and stimulates H2Bub independently of tra
41 biquitin-activating enzyme E1, and ubiquitin conjugase Rad6, and eluted column fraction II (CFII) inc
42  Paf1C directly interacts with the ubiquitin conjugase Rad6, leading to the stimulation of H2BK123ub
43 out by Bre1p, an E3 ligase, along with an E2 conjugase, Rad6p.
44 ated knockdown of UBC9, an essential SUMO E2 conjugase, resulted in downregulation of FOXA2 protein l
45 , hydroxylase, epoxygenase, acetylenase, and conjugase) revealed several amino acid positions near th
46  mutant C93A, which is a defective E2-SUMO-1 conjugase, suggests that this activity may not be requir
47 ditional SUMO conjugase in C. reinhardtii, a conjugase tentatively identified as CrUBC3.
48 ucible ubiquitin ligase WSB-1, the ubiquitin conjugase UBC-7, and VDU-1, a D2-specific deubiquitinase
49                   PHO2 encodes a putative E2 conjugase, UBC24.
50 eracting proteins and identified the SUMO E2 conjugase Ubc9 as one such partner.
51              Msh4 is directly targeted by E2 conjugase Ubc9, initially becoming mono-SUMOylated in re
52                         The cellular E2 Sumo conjugase, Ubc9 interacts with HIV-1 Gag, and is importa
53              We show here that the ubiquitin conjugase, UbcH10, is significantly overexpressed in man
54                         Together with its E2 conjugase Ube2J2, TMEM129 is responsible for the ubiquit
55                   TRIM6 and the E2-ubiquitin conjugase UbE2K cooperated in the synthesis of unanchore
56 lelic germline mutations in the ubiquitin E2 conjugase UBE2T.
57 cid desaturases and hydroxylases rather than conjugases, which is consistent with its desaturase acti