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1 ishing the releasable pool of this essential decapeptide.
2 esion mechanism that can be modulated by the decapeptide.
3 nd 4, but not exon 2, which encodes the GnRH decapeptide.
4 myxin B (PxB), a cationic amphipathic cyclic decapeptide.
5 ched amino acids present within this complex decapeptide.
6 and become almost the same for the octa- and decapeptide.
7 hown for the solid-phase assembly of the ACP decapeptide.
8  extracellular medium as a cleaved, modified decapeptide.
9 eability for a variety of thioether-cyclized decapeptides.
10 d EdTx, and binding to solid-phase LF and EF decapeptides.
11 utation in the eighth amino acid of the GnRH decapeptide, 1 nonsense mutation that causes premature t
12                                            A decapeptide 18-4a (NH(2)-WxEAAYQkFL-CONH(2)) [corrected]
13 for k(cat) for H-D-Phe-L-Pip-Arg-pNA and the decapeptide (2a) are most consistent with two identical
14 atory actions in vivo and that the ubiquitin-decapeptide 50-59 has immunosuppressive effects similar
15 ith the full-size Abeta protein (Abeta42), a decapeptide Abeta(14-23) and alpha-synuclein; all three
16        Applications to assembly of the model decapeptide ACP showed that HDATU was far more effective
17 mical labeling of the tripeptide LWL and the decapeptide ACTH 1-10 with amine-containing reagents.
18 mbinant C5a and to a conformationally biased decapeptide agonist of C5a (YSFKPMPLaR) by releasing IL-
19                    A conformationally biased decapeptide agonist of human C5a anaphylatoxin (YSFKPMPL
20                    A conformationally biased decapeptide agonist of human C5a anaphylatoxin (YSFKPMPL
21  (AII) is proteolytically processed from the decapeptide AI by angiotensin-converting enzyme (ACE), a
22  using MALDI TOF mass spectrometry, oxidized decapeptides all showed evidence of multimer formation a
23 1/9/11/9/11/16/9/12/10" H-bonding, while the decapeptide ("alpha-beta-alpha-beta-alpha-beta-delta-alp
24                                          The decapeptide ("alpha-beta-alpha-beta-alpha-beta-gamma-alp
25 -Ser-Tyr-Hyp-Hyp-Thr-DOPA-Lys (mPEG-MAPD), a decapeptide analogue of a protein found in Mytilus eduli
26                      The highly conserved NK decapeptide and homeodomain regions were identical betwe
27 ptide linkage between the MccE492 C-terminal decapeptide and monoglycosylated enterobactin (MGE) requ
28 llenging sequences such as the Jung-Redemann decapeptide and the 42-residue amyloid beta polypeptide
29 upt the 3 C-terminal amino acids of the GnRH decapeptide and to produce a premature stop codon was id
30 sor; Ps4, a prepro-TRH-derived TRH-enhancing decapeptide, and EEP (pGlu-Glu-Pro-NH(2)).
31 tely 92 kDa) and number of tandemly repeated decapeptides, and contained the same post-translational
32     Here an analysis of back-exchange in the decapeptide, angiotensin I, and a hexapeptide derived by
33 rtion of this prototypical second generation decapeptide antagonist can be replaced with a more compa
34 , the first amino acid incorporated into the decapeptide antibiotic gramicidin S.
35                     Starting from the cyclic decapeptide antibiotic tyrocidine A, this chemoenzymatic
36 f a decapeptide thioester to form the cyclic decapeptide antibiotic tyrocidine A.
37                                   The cyclic decapeptide antibiotic tyrocidine has D-Phe residues at
38  We wanted to test the effect of a synthetic decapeptide antimicrobial, KSL, on the development of or
39  only two residues (one near each end of the decapeptide) are critical for cyclization.
40                                  A synthetic decapeptide based on this sequence but with the N- and C
41         Here we show that adjacent phases of decapeptide-based multiphase model membraneless organell
42      A fluorescently labeled wild-type BACH1 decapeptide (BDP1) containing the critical phosphoserine
43                           MccE492 C-terminal decapeptides bearing fluorescein and biotin moieties on
44 presence of liquid plasma yielded two cyclic decapeptides, CGLIIQKNEC (CLT1) and CNAGESSKNC (CLT2).
45                             Here we screen a decapeptide combinatorial library arranged in a position
46 ons of decapeptides with all the millions of decapeptides contained in a protein database to rank and
47          The two proteins are connected by a decapeptide containing a protease recognition site speci
48 tion, we examine the folding of a homologous decapeptide containing an amino acid substitution linked
49 determined, each in complex with a hepta- or decapeptide corresponding to a natural or nonnatural PTS
50                                           In decapeptides corresponding to the basic domain, a R57S s
51 turnover modulation properties of SA1-III, a decapeptide derived from a serine protease inhibitor (se
52  polycations such as spermine and a cationic decapeptide derived from SV40 T-antigen were only modera
53                     Kisspeptin-10 (Kp-10), a decapeptide derived from the primary translation product
54 s studies allowed the identification of 4N1K decapeptide derived from the TSP-1/CD47 binding epitope.
55                                              Decapeptides derived from human HLA class I sequences ha
56 increases the rate of isomerization of three decapeptides derived from the N terminus of yeast histon
57 ead compound in a series of immunomodulating decapeptides discovered through activity-based screening
58             This behavior prompted design of decapeptide DP1 (DEHGTAVMLK) as a Mn(2+) ligand, and dev
59 library, we demonstrated previously that the decapeptide DWEYSVWLSN is specifically bound by the path
60  approximately 36 tandemly repeated His-rich decapeptides (e.g., HVHTHRVLHK) in the N-terminal half a
61 munochemistry of these proteins, overlapping decapeptides encompassing the whole protein were synthes
62                                       Lysine decapeptides enhance RPR function by promoting holoenzym
63                    GnRH is a multifunctional decapeptide essential for the development of secondary s
64 nworm, Manduca sexta, including the amidated decapeptide F10.
65 ; (iii) in water with a reduced density, the decapeptide forms a helix, indicating the sensitivity of
66 des a homeobox, an NK-2 box and a N-terminal decapeptide found in other Nk family members.
67 nd CHCA, is developed to directly sequence a decapeptide from a single cerebral ganglion B cell.
68 embrane using a dual-acylated amino-terminal decapeptide from Fyn is sufficient to restore the growth
69 a chimeric protein containing the N-terminal decapeptide from human group IIA PLA(2) joined with a (1
70 he glutamic acid of position 1 in the cyclic decapeptide G1TE, which is a potent inhibitor of tyrosin
71 ecognized the FITC-labeled LRAHAVDVNG-NH2, a decapeptide generated from the EC-1 domain of N-cadherin
72 mmortalized GT1-1 neurons, which secrete the decapeptide GnRH in a pulsatile manner conceptually iden
73 Insights into the active conformation of the decapeptide gonadotropin releasing hormone (GnRH) have b
74                                          The decapeptide gonadotropin-releasing hormone (GnRH) plays
75                                          The decapeptide gonadotropin-releasing hormone (GnRH), which
76                             The hypothalamic decapeptide gonadotropin-releasing hormone stimulates mo
77                             The hypothalamic decapeptide, gonadotropin-releasing hormone (GnRH), util
78 PSs which biosynthesize the symmetric cyclic decapeptide gramicidin S and the cyclic lipoheptapeptide
79 rences to scale the membrane affinity of the decapeptide Gramicidin S cyclo(d-Phe-Pro-Val-Orn-Leu-)2
80 e presented for the two charge states of the decapeptide Gramicidin S.
81 ha-thrombin bound to the factor XIII-(28-37) decapeptide has been determined.
82 Tandem mass spectrometry of isolated tryptic decapeptides has detected both C(2)-hexosylated tryptoph
83                                    Hexa- and decapeptides have been identified with sequence homologi
84  source of the immunodominant and protective decapeptide HF10 presented by the H-2L(d) major histocom
85 termine the self-assembled structures of the decapeptide hIAPP(20-29), which is considered to be the
86 co mosaic virus (TMV) virion with a mosquito decapeptide hormone, trypsin-modulating oostatic factor
87 in the Val-24-Lys-28 region of the wild-type decapeptide; (ii) in the presence of salt ions, salt bri
88 ce of either anti-E-cadherin antibody or the decapeptide in the assay medium.
89             We investigated a cyclic carrier decapeptide incorporating a B cell GAS peptide epitope,
90 eproduction in mammals by secreting the GnRH decapeptide into the portal blood vessels of the pituita
91                      The conformation of the decapeptide is an Omega-loop.
92                   We find that: (i) when the decapeptide is in water, hydrophobic interactions and tr
93    We find that the incorporated amphiphilic decapeptide is indeed helical.
94 uman group IB PLA(2) in which the N-terminal decapeptide is joined with the (13)C-labeled fragment, a
95               This MC1R hAGRP(109-118) based decapeptide is novel in that AGRP(83-132) itself does no
96 ation of cell-cell adhesion in BBMECs by the decapeptide is thought-provoking for creating channels f
97                                         This decapeptide (KKERKLARTA) is a fragment of the cardiac di
98 However, we found that true peptide bonds in decapeptide libraries were cleaved by the T1S mutant 10-
99  subsequently bioparmed against the original decapeptide library, the sole clone demonstrating inhibi
100 n the conserved cytochrome P450 heme-binding decapeptide loop resulted in the amplification of four c
101 ter Lys379 rather than Lys380, releasing the decapeptide Lys-bradykinin (kallidin).
102 ns of mouse dorsal root ganglia, Cat-S and a decapeptide mimicking the Cat-S-revealed tethered ligand
103 ted, and the minimal epitope was mapped to a decapeptide NS3-1J (10.4).
104 ing human secretory component to overlapping decapeptides of Calpha3, we confirm these residues and a
105                                              Decapeptides of prohevein were synthesized on derivatize
106              Probing an array of overlapping decapeptides of Rattus norvegicus (Rat) Krp1 with recomb
107 s I molecules of H-2d,u,p,q presented the V3 decapeptide P18-I10 (RGPGRAFVTI) to CTL.
108 an anti-GXM antibodies, we screened a random decapeptide phage display library with the human anti-GX
109  but both trophinin and GLH-1 contain unique decapeptide phenylalanine-glycine (FG)-repeat domains.
110 riants revealed a highly conserved consensus decapeptide PKISYPPTYK that is repeated 64 times and dif
111                        Screening of L- and D-decapeptide positional scanning combinatorial peptide li
112        The hydroxylation of tyrosines in the decapeptide proceeds sequentially.
113 s observed during tyrosinase incubation of a decapeptide related to the mussel adhesive protein mefp1
114 tryptophan-rich domain of Pvfp-1 contains 42 decapeptide repeats with the consensus sequences ATPKPW(
115 r its ability to liberate the amino-terminal decapeptide required for formation of a functional SakST
116 udied Abeta monomer folding and identified a decapeptide segment of Abeta, (21)Ala-(22)Glu-(23)Asp-(2
117  we probe the initial stages of folding of a decapeptide segment of Abeta, Abeta(21-30), shown experi
118                           Additionally, this decapeptide sequence attenuated complement-dependent VCA
119 conserved, vertebrate-specific non-enzymatic decapeptide sequence in the luminal stem domain plays a
120                               The N-terminal decapeptide sequence of protease IV is not homologous wi
121 sterase (anti-AChE10S) and (b) the identical decapeptide sequence phosphorylated at the active site s
122 yclonal antibodies were generated from (a) a decapeptide sequence that includes the active site serin
123 , PC5/6, PC7, and PACE4 in cleaving over 100 decapeptide sequences representing the R-X-(R/K/X)-R dow
124 hbor and near-neighbor amino acid pairs into decapeptide sequences that are flanked by unique dipepti
125     Furthermore, the 4-Cpa-containing cyclic decapeptide shows remarkable selectivity in the inhibiti
126 ct is interpreted using a model of the 5A/5B decapeptide substrate bound to the active site of the NS
127 lex also accepts and modifies the C-terminal decapeptide substrate fragments of the structurally rela
128                                  Using a Bid decapeptide substrate, we observed that phosphorylation
129 on has been characterized in crystals of the decapeptide t-butoxycarbonyl-Leu-Val-beta Phe-Val-(D)Pro
130 e specific enrichment of two phage-displayed decapeptides, TAASGVRSMH and LTLRWVGLMS.
131 em that replaces the gene III protein with a decapeptide tag for immunologic quantitation.
132                                              Decapeptides targeted at the alpha-/beta-synuclein inter
133  sequence analysis, BZAP45 contains a unique decapeptide that is part of a putative leucine-zipper pr
134 c gonadotropin-releasing hormone (GnRH) is a decapeptide that stimulates pituitary synthesis and secr
135                              Nine additional decapeptides that contained the same capping groups on t
136     These were encapsulated into amphiphilic decapeptides that form soluble filamentous structures wi
137 cture-permeability relationship of 24 cyclic decapeptides that share the same backbone N-methylation
138 lized further through the use of overlapping decapeptides that spanned this 26-mer.
139                  We identified more than 100 decapeptides that stimulate these T cells at nanomolar c
140 ynthesis of enkephalin-like model penta- and decapeptides, then octreotate amide and finally octreota
141 NRPS catalyzes head-to-tail cyclization of a decapeptide thioester to form gramicidin S, and the TE d
142 wn to catalyze head-to-tail cyclization of a decapeptide thioester to form the cyclic decapeptide ant
143                By systematically varying the decapeptide-thioester substrate and comparing cyclizatio
144 etase efficiently catalyses cyclization of a decapeptide-thioester to form the antibiotic tyrocidine
145            We report on the preparation of a decapeptide through the parallel operation of two rotaxa
146                We have been employing cyclic decapeptides to identify the determinants for substrate
147 ed for prostate and breast cancer treatments-decapeptide triptorelin.
148 cture-function studies of the hAGRP(109-118) decapeptide, Tyr-c[Cys-Arg-Phe-Phe-Asn-Ala-Phe-Cys]-Tyr-
149 urn of the cyclic beta-hairpin antimicrobial decapeptide tyrocidine A, (Tyrc A) was substituted with
150 responsible for the production of the cyclic decapeptide tyrocidine A, TycC TE, retains autonomous ab
151         Using a thioesterase domain from the decapeptide tyrocidine synthetase, 13 head-to-tail cycli
152  third DNA binding motif using the "AT hook" decapeptide unit (Lys(1)-Arg(2)-Prol(3)-Arg(4)-Gly(5)-Ar
153                                 Large cyclic decapeptides (up to 50-atom ring) were synthesized effic
154 tiomer) was successfully incorporated into a decapeptide using standard solid-phase peptide synthesis
155    A concentration-dependent binding of this decapeptide was also observed in the flow cytometry assa
156                   A library of Ac-XXXXXPAPRM decapeptides was prepared on a TentaGel solid support us
157    A bacteriophage library displaying random decapeptides was used to characterize the binding prefer
158 terestingly, three copies of a tyrosine-rich decapeptide were found interspersed in the RGG box regio
159    Six natural or synthetic variants of this decapeptide were subjected to oxidation by tyrosinase or
160                          The closely related decapeptides were labeled with the NIR dye, separated us
161   Gonadotropin-releasing hormone (GnRH) is a decapeptide widely known for its role in regulating repr
162 of a synthetic peptide based on the His-rich decapeptide with Fe3+, Co2+, Ni2+, Zn2+, and Cu2+ indica
163 des at the C-terminus provided access to the decapeptides with "hybrid HTH" motifs.
164 rom these libraries composed of trillions of decapeptides with all the millions of decapeptides conta
165                                              Decapeptides with Pro(3) modified to trans-4-hydroxyprol
166         We generated two libraries of cyclic decapeptides with stable cross-beta conformations, and f
167 the library (17(5) approximately 1.4 x 10(6) decapeptides) with a Lyme monoclonal antibody (H9724) an
168 ide (GAP), which lies C-terminal to the GnRH decapeptide within the GnRH precursor, and 2 sequence va
169 usly reported linear breast cancer targeting decapeptide WxEAAYQkFL, here we report the synthesis of
170 e minimal fission yeast CTD coding unit is a decapeptide Y(1)S(2)P(3)T(4)S(5)P(6)S(7)Y(1)S(2)P(3) and

 
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