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1 and its gene does not encode a recognizable signal peptide sequence.
2 a potential endoplasmic reticulum-targeting signal peptide sequence.
3 putative CPA3 protein contains a 16-residue signal peptide sequence, a 95-residue NH2-terminal activ
4 in organization to that of CNA, with typical signal peptide sequences, a non-repetitive A region foll
5 This is the first study to establish that a signal peptide sequence alone, administered as a gene va
6 sists of a probable 25-amino-acid N-terminal signal peptide sequence, an extracellular region of 4398
8 cluding a potential 17-amino acid N-terminal signal peptide sequence and a putative C-terminal membra
9 ignated otoraplin, has a predicted secretion signal peptide sequence and shows a high degree of cross
11 novel 266-amino acid protein that contains a signal peptide sequence and two cysteine-rich domains wi
12 the reactive antigens contained a predicted signal peptide sequence and were classified as outer mem
13 fficult to identify as they lack discernable signal peptide sequences and can make use of diverse sec
15 rotein isoforms have a conserved N-terminus (signal peptide sequence) and are dissimilar in amino aci
16 second is an uncharacterized protein with a signal peptide sequence, and the third is an ortholog of
17 les a subset of cytosolic proteins devoid of signal peptide sequences, and thus unable to access the
18 as to why so many large proteins, without a signal peptide sequence, are present in the prostatic fl
20 HB1, residues 12-31) is part of a tripartite signal peptide sequence, comprising n, h, and c regions.
21 s are substituted for specific COOH-terminal signal peptide sequences contained in nascent polypeptid
22 rs of Bacteroides secretion, we characterize signal peptide sequence features, post-secretion extrace
23 stem (HptARS), the N-terminal SecB-dependent signal peptide sequence for recombinant protein secretio
24 lier by using a B(1)-hordein promoter with a signal peptide sequence for targeting to the protein bod
25 1)-hordein promoter either with or without a signal peptide sequence for targeting to the protein bod
26 l region of the 1,001-residue form resembles signal peptide sequences for mitochondrial import, and f
27 eze protein genes, both with and without the signal peptide sequence (for protein secretion), were ex
28 ing het-c constructs deleted for a predicted signal peptide sequence formed HET-C heterocomplexes in
30 a secretory protein that contains a distinct signal peptide sequence in its first 19 amino acids.
31 iation of this pathway normally requires two signals: peptide sequences in unassembled outer-membrane
32 (TM) region of SrtC2, predicted to contain a signal peptide sequence, is cleaved off the mature prote
33 ALDH2 cDNA with or without the mitochondrial signal peptide sequence led to selective expression of t
35 previously characterized the release of the signal peptide sequence-less fibroblast growth factor (F
36 amine the effect of a cleavable leucine-rich signal peptide sequence (Lucy tag) on OR surface express
43 formed with the B(1)-hordein promoter with a signal peptide sequence produced a higher level of wheat
44 e pathway combined with reengineering of the signal peptide sequence results in display levels 24-fol
45 mino acids in length featuring a hydrophobic signal peptide sequence separated from the more hydrophi
46 Surprisingly, the +2 leucine in the DmsA signal peptide (sequence SRRGLV) appears to play an equa
47 tension encompassing a 42-residue N-terminal signal peptide sequence, sufficient for targeting protei
49 l canine MDA-7 has a potential 28 amino acid signal peptide sequence that can target it for active se
50 lational start site for secM, defining a new signal peptide sequence with an extended amino-terminal
51 studies showed that replacing the hGLA cDNA signal peptide sequence with that of human iduronate 2-s
52 s showed that TfsA and TfsB possess putative signal peptide sequences with cleavage sites at alanine