ライフサイエンスコーパス: complexes

1 uctural contexts of G-quadruplexes and their complexes.

2 5 can out-compete eIF2B to stabilize TC/eIF5 complexes.

3 A10 led to glomerular deposits of IgG1/IgG2a complexes.

4 cs simulations of ligands and protein-ligand complexes.

5 ein-protein interactions in membrane protein complexes.

6 teins used for assembling synaptic signaling complexes.

7 that recruit activating chromatin remodeling complexes.

8 reparation of milk protein-Vitamin A (Vit A) complexes.

9 ause it facilitates rapid formation of HA-HC complexes.

10 cular hydrogen bonds in carbohydrate-protein complexes.

11 series of multi-component synthetic protein complexes.

12 effector RhoGEFs can engage Galpha13.R7-RGS complexes.

13 ar how this complex differs from nonspecific complexes.

14 omplexes is much higher than hairpin-hairpin complexes.

15 n minimizing the formation of off-target DNA complexes.

16 to those of wildtype Synechocystis PSII core complexes.

17 irectly interacted with late endosomal SNARE complexes.

18 structure of vesicles formed by COPI protein complexes.

19 sure the equilibrium constant of noncovalent complexes.

20 s of KaiB-KaiC,KaiA-KaiB-KaiC, and CikA-KaiB complexes.

21 e expression, and function of the polycystin complexes.

22 ing heat stress and form high molecular mass complexes.

23 of these domains provides crosstalk between complexes.

24 st in plasma membrane (PM)-localised protein complexes.

25 ynamics of GreB interactions with elongation complexes.

26 ed different structures or were fuzzy in the complexes.

27 res Nup2, suggesting a role for nuclear pore complexes.

28 slow divergence and speciation in polyploid complexes.

29 or five illustrative cases of binary protein complexes.

30 assembled as diheteromeric or triheteromeric complexes.

31 oextraction as diethyldithiophosphate (DDTP) complexes.

32 ources of stability in Int*attL and Int*attR complexes.

33 oimmunoprecipitated with Apaf-1-procaspase-9 complexes.

34 e homology-modeled backbones to generate the complexes.

35 ding dose-sensitive subunits of multiprotein complexes.

36 her oxidoreductase enzymes and to biomimetic complexes.

37 mirrored in genomic loci bound by Sox2/Oct4 complexes.

38 brium with the respective [Co(I)(salophen)M] complexes.

39 as associated with the dissociation of these complexes.

40 he assembly of ATF1-containing transcription complexes.

41 ms biology to automatically identify protein complexes.

42 ate that is rarely seen for transition-metal complexes.

43 ool designed to help researchers study these complexes.

44 the formation of 1:1 stoichiometric sandwich complexes.

45 TA(+) making pi-contact with cyanostar-anion complexes.

46 ro-TGF-beta is secreted and stored in latent complexes.

47 ied a novel therapeutic target: DAT oligomer complexes.

48 ed with the salivary protein to form ternary complexes.

49 CT) excited states were observed in all four complexes.

50 nary and JACKDAW (JKD)/IDD10-SHR-SCR ternary complexes.

51 efficiency decreases for larger multiprotein complexes.

52 O80 protein interaction network by isolating complexes after protein complex components were deleted

53 The size of complexes also diminished significantly with the enzymat

54 Z[Cu(II)OH] complexes, although shown to be inactive, are identified

55 ous, but there was a correlation between NET complexes and both microbiota diversity (P = .009) and d

56 Crystal structures of the muPA:nanobody complexes and hydrogen-deuterium exchange mass spectrome

57 olecular organization of cytosolic transport complexes and identifies a novel regulator of slow trans

58 membrane protein Sun1 antagonizes Sun2 LINC complexes and inhibits RhoA activation and focal adhesio

59 locus-specific chromatin-regulating protein complexes and long-range DNA interactions.

60 pecific organic and inorganic bonds in metal complexes and minerals and therefore, has been employed

61 gnals recruitment of other noncanonical PRC1 complexes and of PRC2, the latter leading to deposition

62 n extraction of the SDS from the protein-SDS complexes and refolding of betaLG, BSA, and lysozyme, wh

63 metry of the mitochondrial respiratory chain complexes and skin inflammation and suggest that severe

64 nerated mono-, di- and tri-substituted sugar complexes and their hydrolysis products of mono-ribosyla

65 ncing, we identified locations of elongation complexes and transcription-repair coupling events in ge

66 raph, with nodes corresponding to junctional complexes and with edges corresponding to spectrin tetra

67 ylation, signaling recruitment of other PRC1 complexes, and PRC2.

68 the network, participation in supramolecular complexes, and regulatory interactions) using CellDesign

69 ocessing protein substrates in nucleoprotein complexes, and that Lon may help regulate DNA replicatio

70 in, we provide a geometric analysis of M2nLn complexes, and we discuss how size and geometry of the l

71 No known iron complexes are considered photoluminescent at room temper

72 cohols and tetrasubstituted alpha-borylamido complexes are discussed.

73 se findings show that 14-3-3 adaptor protein complexes are druggable targets and identify a new class

74 Spatially organized macromolecular complexes are essential for cell and tissue function, bu

75 These data support that SMN:HuD complexes are essential for normal motoneuron developmen

76 ct molecular mechanisms of their function in complexes are largely unknown.

77 arge igneous provinces characterized by sill complexes are more likely to trigger catastrophic global

78 ble to low-affinity interactions because the complexes are not observed directly, but rather leave a

79 eview how the expression and function of TCR complexes are orchestrated by several fine-tuned cellula

80 The X-ray crystal structures of two active complexes are reported, 1-I (R(1) =OEt, R(2) =H) and 2-I

81 mide-barbiturate hydrogen-bonding host-guest complexes are separately incorporated into heteroditopic

82 Main-group complexes are shown to be viable electrocatalysts for th

83 the transmembrane domains (TMDs) of t-SNARE complexes are shown to form aggregates leading to format

84 at the composition and stoichiometry of Hrd1 complexes are strongly influenced by Hrd1 expression lev

85 All complexes are well poised for dCTP insertion.

86 In Ni(II) salicylaldiminato complexes as an example case, these highly electron-with

87 The existence of the dihydrogen complexes, as well as isotope exchange reactions, provid

88 findings shed light on how mammalian dynein complexes associate with dynamic microtubules and help c

89 ds on the recognition of MHC class I-epitope complexes at the cell surface.

90 reading by transcript cleavage in elongation complexes backtracked by nucleotide misincorporation.

91 tic disorder initiated by antibodies against complexes between human platelet factor 4 (hPF4) and hep

92 umber of CCCTC-binding factor (CTCF)-cohesin complexes between the interacting DNA segments.

93 iffening of the polar regions of the stomata complexes, both in Arabidopsis and other plants, suggest

94 Iron complexes bound by redox-active pyridine dialdimine (PDA

95 phosphorylated by Mps1, recruits checkpoint complexes Bub1-Bub3 and BubR1-Bub3 to unattached kinetoc

96 verall solid-state packing of the Th-nitrato complexes but also influences the composition of the Th-

97 arget DNA gyrase by stabilizing DNA-cleavage complexes, but their clinical utility has been compromis

98 ake and presentation of in vivo-formed Ag-Ab complexes by i.v. injecting mice with Ag-specific Abs fo

99 a initiates the formation of death signaling complexes by mediating RIP1 dissociation from TNF recept

100 ting and stabilizing specific 14-3-3 protein complexes by small molecules, peptide mimetics, and natu

101 to prevent the formation of nonphysiological complexes by specializing protein-protein interactions.

102 ggests that pi-pi stacking in supramolecular complexes can be characterized by strong contributions t

103 ted serine protease-2 bound to LP-activation complexes captured on ligand-coated surfaces.

104 sis begins when a network of pigment-protein complexes captures solar energy and transports it to the

105 Signaling properties of G protein complexes carrying mutant Gbeta1 subunits were further a

106 electrogenerated low-valent transition metal complexes catalysts designed with considerable ingenuity

107 nd Fe) and their ligands and by mixing these complexes, coatings with a wide range of colors can be a

108 In both complexes CodY was tetrameric.

109 d that FDCs took up and retained self-immune complexes composed of ribonucleotide proteins, autoantib

110 ecules longer than 40 bp, and two CAF1-H3-H4 complexes concertedly associate with DNA molecules of th

111 of the Fpr4 FKBP with recombinant chromatin complexes condenses nucleosome arrays independently of i

112 er of nucleoskeleton and cytoskeleton (LINC) complexes connecting the nucleus to cytoskeletal element

113 Multicomponent efflux complexes constitute a primary mechanism for Gram-negati

114 Complexes containing a series of N-terminally and C-term

115 active reaction cycle by characterization of complexes containing AK and each of four different adeno

116 NACK is recruited to the ternary complexes containing Maml1 and Maml3, but not Maml2.

117 A series of heterobimetallic complexes containing three-center, two-electron Au-H-Cu

118 them, the ATP-dependent chromatin remodeling complexes control the chromatin architecture and have im

119 Also, as part of CP10-SE complexes, CP10 interacted with the salivary protein to

120 Bifunctional Mo complexes, [CpMo(CO)(kappa(3)-P2N2)](+) (P2N2 = 1,5-diaz

121 and, the (5)Hsigma pathways for these Cpd II complexes cross below the triplet states.

122 cargo reaches endosomes, where it encounters complexes dedicated to opposing functions: recycling and

123 Coimmunoprecipitation of CB1R protein complexes demonstrated that central or distal C-terminal

124 structural investigation of the cerium imido complexes demonstrated the impact of the alkali metal co

125 s that activity of heteromeric NLR signaling complexes depends on the sum of activation potentials of

126 this molecule resemble those of Meisenheimer complexes, derivatives of (CH)5CH2(-).

127 lear maturation of oocytes in cumulus-oocyte complexes derived from immature pig ovaries and provides

128 Although the complexes display considerable diversity in their compos

129 s in culture, the FLI-matured cumulus-oocyte complexes display distinctly different kinetics of MAPK

130 thods on two typical examples of noncovalent complexes drawn from a broad class of nucleic acids and

131 The persistence of these complexes during cultivation indicates that they may be

132 o distinct mSWI/SNF assemblies, BAF and PBAF complexes, enhancers and promoters, respectively, sugges

133 pectra of both D1-N87A and D1-N87D PSII core complexes exhibited characteristics similar to those of

134 homology models of the three antibody-gp120 complexes, extended the sampling times for large bulky r

135 A family of neodymium complexes featuring a redox-active ligand in three diffe

136 rom this work can be used to design improved complexes for applications that require efficient ligand

137 o efficiently target orphans of multiprotein complexes for degradation.

138 uilt structural models of TARP-AMPA receptor complexes for TARPs gamma2 and gamma8, combining recent

139 Our results suggest that protein-lipid complexes form via contacts between proteins and mixed l

140 ve localized spatially in the cell different complexes formed between RIG-I, TRIM25, and MAVS, in the

141 n, the nature and stability of the GSH-Cu(I) complexes formed under biologically relevant conditions

142 class of nucleic acids and transient protein complexes found in aqueous droplets.

143 ion to the phycobiliprotein light harvesting complexes from cryptophyte algae.

144 al residues for RNA interaction in PRC2 core complexes from Homo sapiens and Chaetomium thermophilum,

145 ociation pathways and near-crystal structure complexes from protein-protein association simulations.

146 membrane, and actively exports phospholipid complexes from the cytoplasmic to the exocytoplasmic lea

147 F2, indicating that the constitutive TMM-ERf complexes function as the receptors of EPF1 and EPF2.

148 Several metalloindene complexes have been isolated and crystallographically ch

149 ro carbonyl compounds catalyzed by palladium complexes have been reported, but palladium fluoroenolat

150 ide variety of synthetic metalloporphyrinoid complexes have been synthesized to generate and stabiliz

151 DFT calculations to determine the both complexes have free rotation around the CPh-B1 bond.

152 In particular, CB7 based host-guest complexes have received much attention for the controlle

153 Ruthenium(iii) complexes have successfully been used in clinical resear

154 ses in the mitochondrial phospholipidome and complexes I, IV, and V activities.

155 ed reverse-dative sigma-bond of metal-borane complexes (i.e., M-->BR3 ) remains limited.

156 and uptake of allergen-containing IgG immune complexes (Ig-ICs) by gut dendritic cells (DCs).

157 dent transfer of maternal IgG and OVA immune complexes (IgG-IC) via breast milk and induction of alle

158 is protection is sustained by heme-hemopexin complexes in biological fluids that resist oxidative dam

159 rences in free energy between the individual complexes in bulk water and at their most favorable posi

160 antrone-induced TOP2A and TOP2B-DNA covalent complexes in cells, which are converted to DNA double-st

161 r and the RSC, Arp2/Arp3, CPF, CF 1A and Lsm complexes in chromatin.

162 ces, pointing to a select role of BRD4S-BRG1 complexes in genomic silencing of invasive retroelements

163 icability of FRET-FLIM for visualizing SNARE complexes in live cells with subcellular spatial resolut

164 interaction interfaces in large biomolecular complexes in the solid state.

165 itial segments, and form channel-transporter complexes in vitro and in vivo KCNQ2/3 coexpression prot

166 that identification of PRC1-Br140 "bivalent complexes" in fly embryos supports and extends the bival

167 pressed in the Ni(II)- and Co(II)-bound RcnR complexes, in particular in the peptide corresponding to

168 ted with vascular endothelial cadherin-based complexes, including beta- and gamma-catenin and actin,

169 The activity of other Cul3-anchored complexes, including Cul3(KLHL9/KLHL13), was intact in S

170 res of ACKR3:CXCL12 and ACKR3:small-molecule complexes, including dynamic regions that proved unresol

171 tructures and dynamics of large biomolecular complexes, including ones that are not accessible to oth

172 caffold protein that assembles multi-protein complexes involved in DNA single-strand break repair.

173 cribes the synthesis of two transition metal complexes, [Ir{dF(CF3)2ppy}2(bpy)]PF6 (1a) and [Ru(bpy)3

174 tions in the formation of lysozyme/LM pectin complexes is discussed in relation to the overall struct

175 Ligand metathesis of Pd(II) complexes is mechanistically essential for cross-couplin

176 reveal that the stability of hairpin-monomer complexes is much higher than hairpin-hairpin complexes.

177 crystallography of supramolecular host-guest complexes is reviewed and discussed as a part of small m

178 late ablation of AnkG from established nodal complexes leads to slow but progressive nodal destabiliz

179 These complexes limit intracellular vesicular trafficking and

180 Several protein complexes localize to the gating zone and may regulate c

181 Bacterial cell envelope protein (CEP) complexes mediate a range of processes, including membra

182 The TORC1 and TORC2 complexes mediate the integration of nutritional cues to

183 ipotency and development.Polycomb repressive complexes modify histones but it is unclear how changes

184 For the cooked starch/lipid complexes, more profound effect was evident (22.2-67.7%)

185 t the compositional heterogeneity of protein complexes, mostly due to technical barriers of studying

186 TOR kinase acts in two functionally distinct complexes, mTOR complex 1 (mTORC1) and 2 (mTORC2), whose

187 target of rapamycin (mTOR), existing in two complexes, mTORC1 and mTORC2.

188 substrate, supporting a mechanism where CglI complexes must communicate along the one-dimensional DNA

189 f NMR shifts for a series of lanthanide(III) complexes, namely [LnL(1)] (Ln = Eu, Tb, Dy, Ho, Er, Tm,

190 hetic nontronites forms identical adsorption complexes, namely inner-sphere binuclear bidentate.

191 Neither the ferryl complexes nor their fleeting precursors have been crysta

192 Transport through nuclear pore complexes (NPCs) during interphase is facilitated by the

193 , and CK1delta were distributed into several complexes of approximately 0.9-1.1 MDa that appear to co

194 structures and properties of the adsorption complexes of arsenous acid (As(OH)3) on hydrated mackina

195 The re-dispersed soluble complexes of casein-iron-orthophosphate generated using

196 Copigmented complexes of chondroitin sulfate and anthocyanin were pr

197 ent proteins are assembled into multiprotein complexes of defined stoichiometry.

198 This suggests that complexes of Hg(II) with DOM thiols have similar bioavai

199 to negatively regulate Akt by downregulating complexes of mTORC2 and CDK2/cyclin A2 and upregulating

200 e ions are shown to interact with lanthanide complexes of phenacylDO3A derivatives in aqueous solutio

201 ent stabilities between the classical alkyne complexes of Pt(II) and their drastically more reactive

202 rt an association with dendritic trafficking complexes of Ptchd1.

203 dent on the multimerization of Dnmt3a/Dnmt3L complexes on the DNA.

204 GreB is selectively recruited to backtracked complexes or is ejected from RNAP by catalytic turnover.

205 It affords either the [Co(I)((R)salophen)K] complexes or the [Co(II)2(bis-salophen)M2] (M = Li, Na)

206 ult of inactivation of either of the protein complexes or variations in the external conditions are m

207 ated client proteins from membranes, protein complexes, or chromatin and has an essential role in aut

208 ing the central metal ion of the polypyridyl complexes (Os, Ru, and Fe) and their ligands and by mixi

209 thesized by polyketide synthase (PKS) enzyme complexes predominantly from acetate and propionate.

210 aling states, suggesting that core signaling complexes produce kinase activity over a range of recept

211 iated vesicles can form intervesicular SNARE complexes, providing mechanistic insight into compound f

212 We studied PSII core complexes purified from D1-N87A and D1-N87D variant stra

213 icular tachycardia and premature ventricular complexes (PVCs) most frequently occur in the context of

214 ructures in the cytoplasm called replication complexes (RCs).

215 Multiple protein complexes regulate the Rag GTPases in response to amino

216 rs in the slower phase (>10 s), when stalled complexes release their short RNA and make another witho

217 een described in some detail, the maturation complexes remain ill characterized.

218 Thus, vasohibin/SVBP complexes represent long-sought TCP enzymes.

219 These complexes restrict AMPAR dendritic mobility, leading to

220 Here we show purification of SCF(Fbxo4) complexes results in the identification of fragile X pro

221 sferase and 14-3-3:heat shock protein beta-6 complexes revealed similarities in the 3D structures of

222 f proteins in immunoprecipitates of mediator complexes revealed specific interactions between Mediato

223 phy study of the rabbit muscle GPb inhibitor complexes revealed structural features of the strong bin

224 fur derivative (thio-chrysin), and ruthenium-complexes (Ru-chrysin and Ru-thio-chrysin) were synthesi

225 at Tetrahymena telomerase holoenzyme and RPA complexes share subunits and that RPA subunits have dist

226 sive structural analyses of antigen-antibody complexes.Single-particle electron cryomicroscopy (cryoE

227 s independently acquired aerobic respiratory complexes, supporting the hypothesis that aerobic respir

228 substrates with H2O2 catalyzed by manganese complexes, supporting the hypothesis that both reactions

229 Injection of Cas9-guide RNA-lipid complexes targeting the Tmc1(Bth) allele into the cochle

230 2CH2P(t)Bu2)2) to generate octahedral ammine complexes that are kappa(2)-chelated by the conjugate ba

231 y markedly similar to those of other protein complexes that bind nucleic acid.

232 involved in the formation of protein-protein complexes that bridge the junctions between neighboring

233 romeres nucleate kinetochores, multi-subunit complexes that capture spindle microtubules to promote c

234 Here, we show that intercellular Celsr1 complexes that connect dividing cells with their neighbo

235 proteins associate with each other in large complexes that contain no other detectable protein subun

236 cription requires alteration of chromatin by complexes that increase the accessibility of nucleosomal

237 hment and regulation of cortical NuMA-dynein complexes that position the mitotic spindle.

238 fs known to be associated with the enzymatic complexes that regulate m(6)A dynamics, and expression e

239 inescence properties of square-planar Pt(II) complexes that result from the formation of supramolecul

240 n the formation of [(YbLD)2Tbx] (x = 1 to 3) complexes that, upon NIR excitation at 980 nm, showed an

241 For about one-quarter of these complexes, the absence of conformational entropy would r

242 es of themselves and assemble into homomeric complexes, the overwhelming majority of which (>96%) are

243 In all four complexes, the VHHs bind to a site on the top surface of

244 f two biochemically distinct DAXX-containing complexes: the ATRX-DAXX complex involved in gene repres

245 9 increases the capacity for Hsp90 and Hsc70 complexes to bind ATP and enhances their ATPase activiti

246 ng RNAs, guide Argonaute-containing effector complexes to complementary nascent RNAs to initiate hist

247 uous transactivator, and it blocks repressor complexes to enable viral gene transcription.

248 iation is important for active Ipl1/Aurora B complexes to preferentially destabilize misattached kine

249 tment of Cas9 and transcriptional activation complexes to target loci by modified single guide RNAs.

250 ents that recruit male-specific lethal (MSL) complexes to the X chromosome to upregulate expression o

251 Cadherin complexes transduce force fluctuations at junctions to a

252 In mitochondria, TOM and TIM complexes transport nuclear-encoded proteins, whereas th

253 rapid and highly processive, with individual complexes traveling an average distance of >/=10 kilobas

254 nsported to the Golgi apparatus, where those complexes trigger Galphai3-mediated ERK signaling.

255 rmation of the pre-fusion Env-CD4-coreceptor complexes triggers non-apoptotic cell surface exposure o

256 while mechanically stiffening the associated complexes under the applied membrane stretches.

257 structures of small or medium-sized protein complexes, up to approximately 30-40 kDa.

258 e dissociation rate constants of the ternary complexes varied dramatically with the guest structure a

259 Within Cav2.2-PKCbeta and Cav2.2-NOS1 complexes voltage-triggered Ca(2+) influx through the Ca

260 t the dose used, a single wave of elongation complexes was blocked within the first 25 kb of genes.

261 TCR occurred where the elongation complexes were blocked, and repair was associated with t

262 When SMC5/6 complexes were completely absent in oocytes during meiot

263 Nine crystal complexes were determined.

264 ts, electron transfer capable cytb 5 - cyt c complexes were formed in the presence of bicelles and na

265 The complexes were nontoxic to either bacterial or mammalian

266 ited when approximately 2700 IgE-FcepsilonRI complexes were occupied with specific IgE and challenged

267 Macrocyclic enyne and dienyne complexes were readily synthesized by palladium(II)-cata

268 The proton conductivities for the La and Pr complexes were roughly an order of magnitude higher than

269 romotes the formation of dinuclear palladium complexes, wherein only a single metal center is directl

270 he formation of virus-associated replication complexes, which are required for the amplification and

271 capture lipid antigens within CD1d-lipid-TCR complexes, while excluding CD1d bound to nonantigenic li

272 view of its ability to form triply H-bonded complexes with a suitably complementary 2,6-diacetylamin

273 r the assembly of essential enhancer-protein complexes with an impact on timely gene activation.

274 g actin protein expression and that GJA1-20k complexes with both actin and tubulin.

275 is, in which chiral organocatalysts or metal complexes with chiral ligands are used, has become the m

276 metry, affinity, and shape of macromolecular complexes with dissociation equilibrium constants from p

277 a unique methyltransferase for H3K79, forms complexes with distinct sets of co-factors.

278 s result, co-IP experiments showed that GpsB complexes with EzrA, StkP, PBP2a, PBP2b and MreC in pneu

279 termined the structures of the CL40 and CL59 complexes with gHgL using X-ray crystallography and EM t

280 l properties of soluble and insoluble starch complexes with linoleic acid when a beta-amylase treatme

281 ge to access Earth-abundant transition-metal complexes with long-lived charge-transfer excited states

282 hiols have similar bioavailability to Hg(II) complexes with low-molecular-weight thiols.

283 ng the door to design main-group metal-boron complexes with multiple bonding.

284 Enterobacterial MlaA proteins form stable complexes with OmpF/C (5,6) , but the porins do not appe

285 minent examples of unmodified CDs' inclusion complexes with organometallic guests and update the rese

286 ollective charge fluctuations-in contrast to complexes with other types of bonding.

287 d et al. show that in pneumococci GpsB forms complexes with PBP2a and PBP2b, and that deletion or dep

288 ation has been derived for only a few 14-3-3 complexes with phosphopeptide-containing proteins and a

289 o be measured within nucleic acids and their complexes with proteins.

290 in-10 exhibits differential participation in complexes with PSD-95 and gephyrin, which may underlie i

291 munoprecipitations indicated that TCTP forms complexes with Rad51 in vivo, and the stability maintena

292 ion, and promote collisions of transcription complexes with replisomes.

293 All proteins and their complexes with SDS were attempted to be refolded by the

294 peptide-containing proteins and a variety of complexes with short synthetic peptides.

295 y TGF-beta or by BMP receptors form trimeric complexes with Smad4 to target specific genes for cell f

296 Designing complexes with sufficiently long values of T2 requires a

297 ups forming five- and six-membered chelation complexes with the iodine atom.

298 The crystal structures of apo PllA and complexes with three different ligands revealed the mole

299 oduced 16 SCO-active [Fe(II)(bpp(X,Y))2](Z)2 complexes (Z = BF4 or in one case PF6) in (CD3)2CO solut

300 diphenylalanine (FF) and zinc phthalocyanine complexes (ZnPc) in water.