戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 dy, we report that PSY is a substrate of the Clp protease.
2 cted the degradation activity of the stromal Clp protease.
3 errogate the in vivo essentiality of the Mtb Clp protease.
4  of GluTR1, thus making it accessible to the Clp protease.
5  symmetry mismatch is a universal feature of Clp proteases.
6 ure; a result in contrast to other bacterial Clp proteases.
7 nce to the family of heat-shock proteins and Clp proteases.
8 usceptible to ATP-dependent degradation by a Clp protease, a finding that supports a proposed mechani
9 ot all stromal ClpC functions as part of the Clp protease; a proposal supported by the near abolition
10            Inactivation of components of the Clp protease alters abundance of several Isd proteins, i
11                                          The Clp protease and Isd complex are widely conserved in bac
12                                              Clp proteases and chaperones are ubiquitous among prokar
13 x with ClpC (the HSP100 chaperone partner of Clp proteases) and phycobiliproteins in vitro.
14 ured by expression of heat shock protein 60, Clp protease, and Lon peptidase 1.
15 the regulatory partner for the ATP-dependent Clp protease, and yet this and many other important char
16                                              Clp proteases are found in prokaryotes, mitochondria, an
17 lpC appears to function primarily within the Clp protease, as the principle stromal protease responsi
18             Phenylalanine partially restores Clp protease assembly and activity, providing a rational
19 s isolated from diabetic lesions encoded the Clp proteases, associated with the misfolded protein res
20                                          The Clp protease ATPase subunit and chaperone ClpX is dispen
21 ized PAA2 transporter for degradation by the Clp protease, but not several other chloroplast protease
22 oteome phenotypes were driven by the loss of CLP protease capacity, with little impact from the PREP
23 s in ClpPR core subunits, indicating reduced Clp protease capacity.
24 he proteolytic component of the caseinolytic Clp protease (ClpP) from E. coli at 2.3 A resolution usi
25 ic activity of S. aureus Strains lacking the Clp proteases ClpX, ClpC, and ClpP were significantly at
26    Collectively, these results show that the Clp protease complex and chaperones control several proc
27                                          The Clp protease complex in Mycobacterium tuberculosis is un
28         We have applied this strategy to the Clp protease complex of tobacco (Nicotiana tabacum) and
29  the proteolytic subunits of the chloroplast Clp protease complex, was identified and validated as th
30                                          The Clp protease complexes provide a means for quality contr
31 nd binds to Mycobacterium tuberculosis (Mtb) Clp protease complexes.
32          Unlike in Escherichia coli, the Mtb Clp protease consists of two distinct proteolytic subuni
33                                    Likewise, Clp protease constitutes a central part of the plastid p
34                               Tetradecameric Clp protease core complexes in non-photosynthetic plasti
35              Plastids contain tetradecameric Clp protease core complexes, with five ClpP Ser-type pro
36  in one subunit of the chloroplast-localized Clp protease core, ClpR1.
37 is proposed that the proteolytic activity of Clp protease counteracts GBP binding to assure the appro
38 ion result in loss of intracellular Rsh in a Clp protease-dependent manner.
39 eme, induced by feeding with ALA, stimulates Clp-protease-dependent degradation of Arabidopsis GluTR1
40 s lactis clpE gene, encoding a member of the Clp protease family; and the third product showed no sig
41                                          The Clp protease gene regulator, Rv2745c (clgR), is induced
42                            The ATP-dependent Clp protease has been well-characterized in Escherichia
43   Although the structure and function of the Clp protease have been studied in great detail in both b
44 R4 null allele demonstrate a central role of Clp protease in chloroplast biogenesis and protein homeo
45 ein turnover, further supporting the role of Clp protease in degrading PSY protein.
46                                          The Clp protease in the chloroplasts of plant cells is a lar
47 oteolytic subunit, ClpP4, of the chloroplast Clp protease in vivo, and ubiquitylates ClpP4 in vitro.
48 tion of protein degradation by mycobacterial Clp proteases in vitro and describe novel features of th
49      Upon hypoxic and reaeration conditions, Clp protease induction occurred within wild-type Mtb, in
50 ivation of clgR, which subsequently leads to Clp protease induction, is crucial for degradation of mi
51 ms should facilitate identification of novel Clp protease inhibitors and activators.
52                       Protein degradation by Clp proteases is regulated primarily by substrate recogn
53 , the proteolytic component of ATP-dependent Clp proteases, is a hollow-cored particle composed of tw
54 s study sought to identify the effect of the Clp protease on the iron-regulated surface determinant (
55 ClpP protein (a component of the cytoplasmic Clp protease) participates in biofilm formation in this
56 tants, we demonstrate that the P. falciparum Clp protease (PfClpP) has robust enzymatic activity that
57 g these are regulatory components of Lon and Clp proteases, proteins involved in DNA replication, rec
58        The role of such an envelope membrane Clp protease remains unclear although it appears uninvol
59 ion by sub-stoichiometric binding at the Mtb Clp protease sites.
60 nt progress and breakthroughs in identifying Clp protease structures, substrates, substrate adaptors
61 nes of the single gene for the mitochondrial CLP protease subunit, CLPP2, in Arabidopsis (Arabidopsis
62 ncovered to physically interact with various Clp protease subunits (i.e., ClpS1, ClpC1, and ClpD).
63 sed coexpression networks showed that all 12 CLP protease subunits tightly coexpressed as a single cl
64 as well as most of the chloroplast-localized Clp protease subunits, is inhibited in clpR1-1.
65 istic interactions were observed between the CLP protease system (clpr1-2, clpr2-1, clpc1-1, clpt1, c
66                                    Thus, the Clp protease system and GBP contribute to GluTR accumula
67                                          The Clp protease system destabilizes a zinc-bound form of Mp
68                                          The Clp protease system is a promising, noncanonical drug ta
69 wed strong genetic interactions with stromal CLP protease system mutants, resulting in reduced growth
70 d one of these virulence determinants is the Clp protease system.
71 ry of substrate selection by the chloroplast CLP protease system.
72                   The caseinolytic protease (Clp) protease system has been expanded in plant plastids
73 ely acts as an adaptor protein that guides a Clp protease to the phycobiliproteins, thereby initiatin
74      These results indicate that the Lon and Clp proteases use the same mechanism of substrate discri
75                                          The Clp proteases were found to be partially glucose regulat
76                                We found that Clp proteases, widely reported to form biologically rele