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1 xtensions (NDGD1 and NDGD2) targeting to the outer envelope.
2 tein transport tube across the mycobacterial outer envelope.
3 losion of a massive star, passes through its outer envelope.
4 pid phosphatidylcholine is found only in the outer envelope.
5 mbrane lipid transfer protein present in the outer envelope.
6  proper delivery of cargo to the chloroplast outer envelope.
7 ave carotenoids localized in the chromoplast outer envelope.
8  is specifically incorporated into the viral outer envelope.
9 rvations of molecular lines that probe their outer envelopes.
10 culates called spermatophores composed of an outer envelope, an inner matrix, and a bolus of sperm.
11 e spontaneous insertion of proteins into the outer envelope and thylakoid, the role of cubic lipid st
12  These are the ER/plasmodesmata, chloroplast outer envelopes and membrane contact sites between them.
13 Here, we provide evidence that the plastidic outer envelope B-barrel proteins OEP21, OEP24, and OEP37
14 in-binding protein that was localized to the outer envelope based on susceptibility to proteinase K.
15          Tic22 physically interacts with the outer envelope biogenesis factor Omp85 in vitro and in v
16 last-targeting sequence, was targeted to the outer envelope by an ATP-independent and protease-insens
17 eton within the yolk cell and defects in the outer enveloping cell layer, which are both known mediat
18 rmatophore regions, the inner matrix and the outer envelope, differ in their protein composition and
19 enables a temporal release of two drugs: the outer envelope first releases an anti-angiogenesis agent
20 h the matrix and core from one clade and the outer envelope from another.
21                                 Two integral outer envelope GTPases, Toc34 and Toc86, are proposed to
22 the absence of energy, two components of the outer envelope import machinery, IAP86 and IAP75, cross-
23 ed that DGD1 was targeted to the chloroplast outer envelope in an ATP-independent manner.
24 res of cocoons at all three cocoon sections (outer envelope, inner envelope, and the intermediate sec
25 fish, the embryonic epidermis consists of an outer enveloping layer (EVL) and an inner basal layer th
26  a novel type I cytokeratin expressed in the outer enveloping layer.
27 ion limbo, unable to acquire the tegument or outer (envelope) layers.
28 ency towards overproduction of the bacterial outer envelope, leading to the formation and release dur
29  found that VAP27 proteins interact with the outer envelope membrane (OEM) of chloroplasts, where the
30 to identify factors required for chloroplast outer envelope membrane (OEM) protein degradation.
31 f three distinct membrane systems, i.e., the outer envelope membrane (OEM), inner envelope membrane (
32 ificantly (10-fold) upregulated but those of outer envelope membrane (Toc159), stromal (hsp93, cpn60)
33 esidue did not block PDV1 insertion into the outer envelope membrane but did abolish its localization
34 ermediate which has completely traversed the outer envelope membrane but has not yet reached the stro
35                                  OEP75 is an outer envelope membrane component of the chloroplastic p
36 the translocation of pea proteins across the outer envelope membrane is present within the six N-term
37                 Targeting of atToc159 to the outer envelope membrane is strictly dependent only on gu
38 dependent formation of the translocon at the outer envelope membrane of chloroplasts (TOC) and TIC su
39             The multimeric translocon at the outer envelope membrane of chloroplasts (Toc) initiates
40                        The translocon at the outer envelope membrane of chloroplasts (TOC) mediates c
41  interaction with several translocons at the outer envelope membrane of chloroplasts (TOC) proteins o
42 om the cytosol through the translocon at the outer envelope membrane of chloroplasts (TOC).
43 t of the import machinery [translocon at the outer envelope membrane of chloroplasts (Toc33), a 33-ki
44                       The translocons at the outer envelope membrane of chloroplasts (TOCs) initiate
45 75 is a protein translocation channel in the outer envelope membrane of chloroplasts and its presence
46                            Translocon at the outer envelope membrane of chloroplasts, 34 kDa (Toc34)
47 dicate that OEP40 is a "glucose-gate" in the outer envelope membrane of chloroplasts, facilitating se
48 ted that the TGD4 protein was present in the outer envelope membrane of chloroplasts, where it appear
49 , the protein-translocating channel from the outer envelope membrane of pea chloroplasts, in the geno
50 t of the protein import apparatus within the outer envelope membrane of plastids.
51                                  Toc75 is an outer envelope membrane protein of chloroplasts.
52 tified PLASTID DIVISION1 (PDV1), an integral outer envelope membrane protein, and its homolog PDV2 as
53                                        Three outer envelope membrane proteins (OEP86, OEP75, and OEP3
54  AKRA2, a targeting receptor for chloroplast outer envelope membrane proteins, binds chloroplast-spec
55      Reconstruction of DGDG synthesis in the outer envelope membrane was observed only with diglycosy
56 SFR2 protein is localized to the chloroplast outer envelope membrane, as revealed by the analysis of
57 iring steps: binding of the precursor to the outer envelope membrane, outer membrane transport, and i
58 of DAGK presence in the outer leaflet of the outer envelope membrane, phosphatidic acid accumulation
59     During energy-independent binding at the outer envelope membrane, preproteins interact with three
60 ing upon insertion of preproteins across the outer envelope membrane, supporting the proposal that bo
61 hatidic acid accumulation in the chloroplast outer envelope membrane, the location of MGDG synthase i
62 protein translocation channel at the plastid outer envelope membrane, Toc75, is essential for the via
63 protein translocation across the chloroplast outer envelope membrane.
64 rane or in the transfer of PtdOH through the outer envelope membrane.
65 ke ARC5 ring on the cytosolic surface of the outer envelope membrane.
66 DV2, an ARC5 recruitment factor spanning the outer envelope membrane.
67 ide, they provide the basis for an essential outer envelope membrane.
68 ner chloroplast envelope membrane facing the outer envelope membrane.
69 n translocation channel in the chloroplastic outer envelope membrane.
70 he functional Toc complex at the chloroplast outer envelope membrane.
71 transit peptides that target them across the outer envelope membrane.
72 110, associate with import components of the outer envelope membrane.
73  the targeting and insertion of IAP34 at the outer envelope membrane.
74 d coordinated fashion across their inner and outer envelope membranes.
75 coded proteins through the translocon at the outer envelope of chloroplasts (TOC) complexes.
76 nnel of the protein import translocon at the outer envelope of chloroplasts (TOC).
77                       The Toc complex at the outer envelope of chloroplasts initiates the import of n
78 mport is initiated by TOC (translocon at the outer envelope of chloroplasts) complexes in the plastid
79 ly specific, regulated solute channel in the outer envelope of chloroplasts, named OEP40.
80 with a density of about 107 atoms/cm3 and an outer envelope of density 10,000 atoms/cm3.
81 lipopolysaccharide (LPS), a component of the outer envelope of Gram-negative bacteria.
82 ynthesis of LPS, a critical component of the outer envelope of Gram-negative bacteria.
83 d molecule, termed S881, is localized to the outer envelope of M. tuberculosis and negatively regulat
84    Because of its unique localization at the outer envelope of plastids, LACS9 was regarded as a cand
85 embrane of Gram-negative bacteria and of the outer envelope of the endosymbiotically derived organell
86                                          The outer envelope of the extracellular form of vaccinia vir
87                                          The outer envelope of the extracellular form of vaccinia vir
88 id (FFA) released is then transferred to the outer envelope of the plastid where it is reactivated to
89                      These pixels are on the outer envelope of the principal component scores of the
90                    However, the indigestible outer envelope of the spermatophore delays female remati
91 a glycoprotein specifically localized to the outer envelope of vaccinia virus was shown to be encoded
92 n shown to be involved in the integration of outer envelope protein 14 (OEP14), whose outer membrane
93             We show that a paralog of Toc75, outer envelope protein 80 kD (OEP80), also uses a transi
94 tioning 1 (CHUP1) that encodes a chloroplast outer envelope protein constitutively induces stromules
95 (SAM) complex, and in chloroplasts it is the outer envelope protein Oep80.
96 A also binds specifically to the chloroplast OUTER ENVELOPE PROTEIN7 (OEP7) and is required for the b
97 specifies the mid-plastid positioning of the outer envelope proteins PDV1 and PDV2, which have parall
98 The Chlamydia family of human pathogens uses outer envelope proteins that are highly cross-linked by
99                                 In contrast, outer envelope proteins were initially oxidized without
100 s that were labeled with antibodies to other outer-envelope proteins and with protein A-colloidal gol
101 ptor (34-kD subunit of the translocon of the outer envelope) recognition in vitro, preprotein binding
102  segmentation; the presence or absence of an outer envelope; recombination frequency; duration of inf
103 rmation for targeting and insertion into the outer envelope resides in the N-terminal half of DGD1, b
104  components positioned on both the inner and outer envelope surfaces.
105                          Finally, we use the outer envelope-targeted DAGK line as a tool to probe the
106  Spike (S) protein, the protein on the viral outer envelope that binds to the human angiotensin-conve
107 e positioned on the cytosolic surface of the outer envelope, the stromal surface of the inner envelop
108                   Antibodies specific to the outer envelope translocation components OEP75 and OEP34,
109 ntain the 75-kD component of the chloroplast outer envelope translocon (Toc75) and are capable of imp
110 rates them), and found that variation in the outer envelope underlies the differences in architecture
111 ogenitor star must have retained much of its outer envelope until after helium fusion in the core was
112                          EBs posses a unique outer envelope where rigidity is achieved by disulfide b
113       Imported LeHPL was integrated into the outer envelope with most of the protein exposed to the i

 
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