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Blosum62%s%s: cannot read 1st input file name %s: cannot read matrix (option -x) %d%s: cannot read P : type of analysis %f%s: cannot read gap open penalty (-G option) %s: cannot read gap extention penalty (-g option) %s: cannot read threshold (-W option) option -w: threshold is <= 0.0, setting it to %f %s: cannot read recovering ratio (-r option) option -r: recovering ratio is not in [0,1], setting it to %f %s: cannot read proba (-N option) option -N: proba is <= 0.0, setting it to %f %s: cannot read minimum score (-m option) %s: cannot read minimum rms (-M option) option -m: minimum rms is <= 0.0, setting it to %f %s: cannot read number of wanted best subalignments %s: subalignment number cannot be less than 1, setting it to %d %s: cannot read minimal length %s: minimal length cannot be less than 0, setting it to %d %s: cannot read number of shuffle %s: cannot read extend wCannot open out file (-i option) Cannot open error file (-j option) %s: cannot read maximum rrmsd a:b:D:e:Fg:G:hi:j:lL:m:M:n:N:pP:qr:s:u:UvVw:Wx:zABCDEFGHIJKLMNOPQRSTUVWXYZ%s: cannot read matrix in file %s %s: cannot read matrix in file Blosum62 ACGT%s: option inexistante %s%s.set.pml%s:: error: No input 1st file ! exiting... rb%s:: error: cannot open %s rt%s:: error: cannot open temporary file %s:: Problem uncompressing 1st file %s, exiting.... -> 1st file uncompressed (%s) Cannot open gz file %s, exiting.... %s:: Problem uncompressing 1st gz file %s, exiting.... %s:: Problem uncompressing 2nd file %s, exiting.... -> 2nd file uncompressed (%s) Problem uncompressing gz file %s, exiting.... Problem in reading protein structure in %s %d eme proteine , exiting...End of first database file, %d proteins have been read Problem in recoding protein %s angles exiting... **********Problem in reading sequence in %s %d th reading ... plus de %d residus, on passe a la suivante ... %s %d **************** reading %s temps %f num prot %d Problem in reading the %dth protein (ignored) End of second database file, %d proteins have been read Problem in recoding protein %s angles (ignored) ========Problem in reading sequence in %s %d th reading ...p0 : pb format binaire ...================ reading %s num prot %d probleme shuffle %s %s nmatch %d score : %f nb match %d threshold score=%f (ERR_SHUFFLE=%d) wtCan't open set file %s Print results for Gok in %s Can't open pymol file %s Print results for pymol in %s ************************no match Pb in reading %d sequences/structures Pb in recoding %d sequences/structures No protein read in one of the database file : file1 : %d file2 : %d ********** fin du fichier ************* ACDEFGHIKLMNPQRSTVWYsimalign:: not enough memory for swres! DNA:3D-STRUCTURE:PROTEIN:%s: match %d mismatch %d gap-open %d gap-ext %d SIM:: not enough memory for RMS computations (pp0,pp1) pb malloc avec %s (%d %s) (size=%d) CCsim.cDDRRSSEEFFHHWWIIJJXXYYSsROWSIM: not enough memory for salign sROW[i]LISTLIST[i]--> K = %d Kwanted = %d There are no %d alignments between two sequences--> match count = %d score = %d probleme proba waterman_vingron break: limit score, probability or length given is reached added match (%4d,%4d) (%4d,%4d) (score=%.2f len=%d) alignment discarded too much overlap (%.3f), restarting... (%4d,%4d) (%4d,%4d) (score=%f len=%d) sim: break cause length (%d) < minlength (%d) sim: break cause score (%f) < minscore (%f) sim: break cause proba (%f) < proba limit (%f) sim: break cause number of matches reached sim: break cause no more matches sim: break unknown cause !!! swalign:: not enough memory for crossed rms swalign:: not enough memory for group z %5d . : . %5d %s %s %5d %s swresswalign.cswres->posd0swres->posd1swres->posf0swres->posf1swres->scoreswres->score_freqswres->score_par_freqswres->score_GLswres->tm_scoreswres->score_blosangleswres->recoverswres->rmsswres->rev_rmsswres->saliswres->tProbaMTD_p0swres->tProbaMTD_p1swres->tProbaIndepswres->tProbaBiswres->alphaswres->betaswres->gammaswres->new_rmsswres->matrix4xpb realloc avec %s (%d %s) swres->sali[swres->nmatch]MYFREE null %s%-6c: %6d %6d %7.1f - ##3 %4d - ---- p0= %s%c p1= %s%c RESULTS ---- ********************************************************* Number %4d local alignment Begins at (%d,%d) [PDB=(%4d%c,%4d%c)] Ends at (%d,%d) Length protein1 %4d protein2 %4d Score %10.2f Score/Alignement Length %8.3f RMS or Probability %7.2f Overlap %4.2f Alignment length %4d MTD Probability protein1 %4.3f protein2 %4.3f Zscore %.3f Blosum score: %5d GL score : %5.2f Group : %1d Score_freq : %20.2f Blosum_angle : %5.3f TM score %5.3f RRMSD: %.2f Sequence alignment corresponding to structure match: Sequence alignment: Angle alignment: NUM GROUP %7d %5d [%3d] %7.2f Sum Log MTD Probability protein1 %6.5f protein2 %6.5f @p0 p1 #repeat start0 start1 lg_prot score rms/proba overlap lg_match match1 match2 blosum GLscore compat start0 start1 end0 end1 RRMSD%10s%c %10s%c %6d %6d %6d %7d %8.2f %11.2f %11.2f %8d #1 #2 #3 %6d %7.2f %6d %4d %4d %4d %4d %6.2f ##1 %s%c %s%c %4d ##2 ==1 ==2 %6.1f %cNucleic*pp0*pp1swalign:: not enough memory for RMS computations (pp0,pp1) swalign:: not enough memory for swres! swalign::not enough memory for NewMatrix alignsw:: cc <%c> %f is not s,i or d, this should not append! alignsw:: lastmove <%c> is not s,i or d, this should not append! aliswalign2.c*plensub*ppp0*ppp1swalign2: not enough memory for RMS computations gap_extsIisJjgap_ext[j]sIi[j]sJj[j]best_scoresbest_scores[i]salign%s %s too much overlap (%.3f), restarting... (%4d,%4d) (%4d,%4d) (score=%.2f len=%d) pas de match score %f score=%15.2f (minscore=%15.2f) normalized score = %15.2f stop on match: step %d (nmatch=%d): score %.2f (min=%.2f) proba %.4f (lim=%.4f) len %d (minlen=%d) stop on score: step %d (nmatch=%d): score %.2f (min=%.2f) proba %.4f (lim=%.4f) len %d (minlen=%d) stop on proba: step %d (nmatch=%d): score %.2f (min=%.2f) proba %.4f (lim=%.4f) len %d (minlen=%d) stop on length: step %d (nmatch=%d): score %.2f (min=%.2f) proba %.4f (lim=%.4f) len %d (minlen=%d) LitPdbProtAlpha:: Error: %s Pb in reading PDB file : residu null Problem in residue number reading in header End of file encountered while searching to read next header End of file encountered while reading header LitProtAlpha:: No residue to read in %s LitProtAlpha:: End of file encountered while reading LitProtAlpha:: Empty file Problem in allocation for pProt in LitProtAlpha pdb.entIncorrect number of residues: %d read residues over %d Problem with ReadPhipsiLine in LitProtAlpha Maximum number of chains/fragments (%d) exceeded for %s End of file reached nombre de residus incorrect: %d residus lus sur %d pb avec ReadPhipsiLine ds LitProtAlpha angle %f du residu %d de la proteine %s non valide , ignore End of data file Cannot read binary file (is file really in binary format?) BinaryReadProtAlpha: cannot allocate for pProt nb max de chaines/fragments (%d) depasse pour %s angle %f du residu %d de la proteine %s non valide, ignore BinaryReadProtAlpha:: debut frag 0 (frag %d) NewProt pb de mallocNO HEADERHEADERLitEnTete: pas de HEADER sur ligne [%s] LitEnTete: Fichier vide PATHLitEnTete: pas de PATH sur ligne [%s] NBRESLitEnTete: Cannot read number of residues LitEnTete: pas de NBRES sur ligne [%s] angle non valide: %f (%d) RecodeAngles:: pb de recodage, angle (%f) recode (%d) est > au maximum (%d) pb dans aa3to1: %s, pos: %s, cases %d indice %d not enought memory for temposeq (fasta) .. IO error 1 with sequence #%s IO error 2 with sequence #%s (flag ok 0) sequence non multiple de 3 !!! : %d Too much undefined characters in #%s not enought memory for pProt (fasta) .. Fin de ficher IO error 2 with sequence #%s (flag not ok) init_minimier:: Error: Not enough memory for result treePas de minimier a desallouer %s%s%s%s!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!! Minimier tree was sorted before all proteins were ranked Results impredictable !!!!!!!!!!!!!!! I think the score hasn't been computed: %f Unitaryr%d%d%s PAM %s Proximity %s Distance Matrix used : %s %s Vocabulary : %s %s Threshold : %d %s Values : %s %s %c %3d %s Classes : %s %c %s %c %d %d %s %3d%4.2f Matrix file is not symetric Matrix values < minval or > maxval Bad matrix (similarity should be distance) bad type matrix simple_convert: no proper conversion indicated MAT%c %c %f --> Sum %c %f (proba simple %f) Set_TableFreq:: can't open %s for statistics ReadTable1Dim:: premature end of frequencies file bad format for number of groups in ReadTable1Dim <%s> *t1stats.cReadTableFreq:: premature end of frequencies file %d %lfReadTableFreq:: bad format <%s> ReadTableFreq:: Cannot read line before 2-uple in frequency file *t2%d %d %lfReadTableFreq:: bad format (2) <%s> pb au recodage des angles dans CalculProbaBiAli, angleGroupe: %d, nbGroupes: %d lgMot: %d j: %d indxproblem in angle recoding in CalculProbaMtd avec %s indx[%d]= %d, max %d, angle %d (%d), : %f mot %d: %d a %d @ probabilites simples @ %20d%20d%3d %6d %10.2f %8.2f %10.2f %10.2f HEADER ZZZ %d %f %f %f Ecriture du fichier pour pymol impossibles (un des parametres est null) load %s.pdb , struct1 hide everything, struct1 show ribbon, struct1 color blue, struct1 load %s.pdb , struct2 hide everything, struct2 show ribbon, struct2 color red, struct2 select sel11, struct1 and resi %d-%d color forest, sel11 select sel12, struct1 and resi %d-%d color yellow, sel12 select sel21, struct2 and resi %d-%d color purple, sel21 select sel22, struct2 and resi %d-%d color orange, sel22 run fitting.py fitting struct1, i. %d-%d , struct2, i. %d-%d impossible d'afficher la proteine %d a parameter of EcritEnTeteSet is NULL name %s%d visible 1 color %d path %s adress %d end un des parametres de EcritEnTeteSet est NULL name match%d pdbref 0 %d %c-%d %c %d-%d %d-%d pdbref 1 %d %c-%d %c %d-%d %d-%d symbol alpha a parameter of EcritToutDansSet is NULL Cannot create "set" file *-PROTEIN-SET---ASCII-FILE--* * suite2 * END_PDB_REC Impossible de creer le fichier set END_WORD cant open file %s to readr+*Error* [%d] %s BUG: %s k-uple too big with this alphabetnot enough memory for hash table(i >= siz) in DistribRandom(i,j >= siz) in HashRandomswalign:: not enough memory for tempo file stat_sequences.c swalign:: not enough memory for temposeq Error in Shuffling: exit... (%d) wv1: score %f (%4d,%4d) (%4d,%4d) water_vingstats_sequence.cscorebisscoresscores[i]nbscorebis[i]scores[j]Invalid arguments in routine GAMMQa too large, ITMAX too small in routine GCFx less than 0 in routine GSERa too large, ITMAX too small in routine GSER> Numerical Recipes run-time error... > %s allocation failure in vector()allocation failure in ivector()allocation failure in dvector()allocation failure 1 in matrix()allocation failure 2 in matrix()allocation failure 1 in dmatrix()allocation failure 2 in dmatrix()allocation failure 1 in imatrix()allocation failure 2 in imatrix()allocation failure in submatrix()allocation failure in convert_matrix() @@@@@@@@@@@@@@@@@@@@@@@@@@@@@@@@@@@@@@@@@@@@ @@@@@@@@@@ Parameters used : @@@@@@@@@@ @@@@@@@@@@@@@@@@@@@@@@@@@@@@@@@@@@@@@@@@@@@@ @@ Type of file : 3D amino acid sequences DNA sequences @@ File : %s format PDB fasta binary alpha @@ Number of alignments to show : %3d @@ Minimum score %5.2f @@ Gap penalty : opening : %3.2f + k * extension : %3.2f (k total gap length) @@ Overlap allowed : %2.3f @@ Algorithm : Huang-Miller @@ Algorithm : Smith-Waterman @@ maximum RRMSD %3.2f @@ Threshold for the score %5.2f @@ Minimum length for repeats : %d @@ P-value %5.2f @@ Declumping method : %d @@ Substitution matrix %s @@ Number of random sequences : %5d @@@@@@@@@@@@@@@@@@@@@@@@@@@@@@@@@@@@@@@@@@@@ %s: Usage: -s input_file -P [0|1|2] options ******************** FILES ********************************** -s file : file is in PDB format or fasta format for sequences (PDB file can be compressed in .Z or .gz format) ******************** STRUCTURE / SEQUCENCE ********************************** -P<0/1/2> 0 : structure analysis -P<0/1/2> 1 : proteique sequence analysis -P<0/1/2> 2 : nucleique sequence analysis ******************** OPTIONS ********************************** -l output on one line per match (several lines output by default) -n number of best subalignments to show (even if they are not statistically significant for sequences) - default for structure: %d - default for sequence: -1, i.e. the algorithm rely on statistical criteria for stopping output) -L minimal length for the repeat %d -m : minimum score for output subalignment -z : use default minimum score for output subalignment(def structure %.0f protein %.0f nucleic %.0f) -N : probability for dna and protein (def:%f) gaps : -G -1 : default value for gap open and extension penalty : %5.2f structure, %5.2f protein, %5.2f nucleic) default gap extention penalty : %5.2f structure, %5.2f protein, %5.2f nucleic) gap cost = gap_open + k * gap_ext (k being total gap length) -G : other value for gap open penalty -g : other value for gap extension penalty -r : ratio of tolerated recovering [0,1] (def:%4.2f) -q : output matches are sorted by scores (default: sort is done on RMS) -i : standard output -j : error output -W : Smith/Waterman algorithm is to be used (default: Huang/Miller algorithm) -F : No sequence/structure size limit, (default:%d when SW is used) ******************** OPTIONS FOR SEQUENCES ONLY ********************************** -x matrix (if amino acid or DNA sequence) -D : number of shuffled sequences used to calculate the statistical significance of the scores, default : %d -p second method of Waterman and Vingron for statistical significance : declumping estimation ******************** OPTIONS FOR STRUCTURES ONLY ********************************** -M : minimum rms for output subalignment(def:%f) -u : normalize minimum rms for output subalignment (Betancourt, Skolnick, 2001) (def:%f) -U use RMSD instead of Relative RMSD -w : value of threshold for angle score (def:%10.2f) note: score is detailed in paper -e : to extend alignment for amino acid distant than less than x Angstrom PrintArbreScan:: No protein returned from the minimier Error in getrusage -------------------------------------- %s: CPU User Time : %8d sec %4d usec %s: mem size in Ko : ru_minflt:%d ru_majflt:%d %s: mem size in Ko : ru_maxrss:%d ru_ixrss:%d ru_idrss:%d ru_isrss:%d ru_minflt:%d ru_majflt:%d ru_inblock %d ru_oublock %d ru_nswap:%d no_nameprobleme ecriture binaire not enought memory for seq (fasta) .. fin du fichier !!! 1 IO error 1 with sequence #%s seq->seqlibfasta.c2 IO error 1 with sequence #%s %d /UNK/ALA/CYS/ASP/GLU/PHE/GLY/HIS/ILE/LYS/LEU/MET/ASN/PRO/GLN/ARG/SER/THR/VAL/TRP/TYR/MSE/CSE/ASX/GLX/CEA/HYP/ACD/HSE/HYL/ALB/ARO/PCA/BAS/SAR/BET/TAU//GLY/ALA//CYS/SER/THR/VAL//ILE/LEU/ASP/ASN/%d chain Chain %d %c first res %d%c nbRes %d new_residu:: not enough memoryput_atom_in_res:: not enough memoryset_residue_neighbours:: trop de voisinsCAget_CA_xyz:%3s %4d has no CA atom get_CA_TFactor:%3s %4d has no CA atom precedingfollowingget_distca_1_2:: residue does not existerreur distance : trou get_phi_psi get_chi get_alpha_tau get_distca_1_2get_distca_1_3has no CA atomhas no CB atomhas no N atomhas no CO atomhas no CG(1), OG(1) or SG atomhas no CD(1), OD(1), SD or ND(1) atomhas no CE, CE(1), OE(1), NE or NE(1) atomat start of chainat end of chain%s :: residue %s %4d %s residue %s %4d %s%s :: residue %s %4d %sget_phi_psi:: residue does not existCNget_chi:: residue does not existCBCGCG1OGOG1SGCDCD1OD1SDND1CECE1OE1NENE1get_alpha_tau:: residue does not exist%hdget_atom: bad atom format%creadPdbResidues: protein %s Cannot read key in line <%s> DESCCOMPNDSOURCEREMARK2 RESOLUTION.ATOMHETATMENDMDLENDTERpb malloc avec %s (%d %s) *tChainlibphipsi.creadPdbResiduesChain: protein %s Cannot read key in line <%s> EXPDTANMRTHEORETICALReadPhipsiLine: no line %3s %hd%c %f %f %f %f %f %fReading input file with x y z %3s %hd%c %f %f %fReading input file without x y z ReadPhipsiLine:: Bad file format in <%s> readBinary: Cannot read header readBinary: Cannot read path readBinary: Cannot read number of residues readBinary: Not enough memory for binres array ! readBinary: Cannot read residues, %d residues expected, %d residus read! Read errorunZ function: no fileFile is not in compressed format Not enough memory to process %d bitsWrite error failed fwritefailed gzclose1.2.3%c%c%c%c%c%c%c%c%c%c: deflate 1.2.3 Copyright 1995-2005 Jean-loup Gailly incorrect header checkunknown compression methodinvalid window sizeunknown header flags setheader crc mismatchinvalid block typeinvalid stored block lengthstoo many length or distance symbolsinvalid code lengths setinvalid bit length repeatinvalid literal/lengths setinvalid distances setinvalid literal/length codeinvalid distance codeinvalid distance too far backincorrect data checkincorrect length checkneed dictionarystream endfile errorstream errordata errorinsufficient memorybuffer errorincompatible versionuninitialized zip processingnot enough memorybad magic headerreserved field or compression methodEOF while processing headerInvalid compressed dataMore data to process at closeuncompressed size differs from recordedbad CRCwrite errorgeneric/internal error inflate 1.2.3 Copyright 1995-2005 Mark Adler ModelCopy: destination model is NULL NewModel: not enough memory for MTDModel %4d %6.4f Cannot read first line in input Cannot read order and nstates in line: <%s> readModel::Cannot allocate for model Cannot read line %d in input Cannot read state %d in input line <%s> %gNewModelSet:: Cannot allocate for set readModelSet::Cannot read %d-th value readModelSet::Cannot read line in input NewMTDJacobi: not enough memory for MTDJacobi NewMTDLJacobi: not enough memory for MTDLJacobi Error: %s fprintfsprintfsscanfprintf%s[%d,%d]=%f %s[%d]=%lf vlibqbestfit.cypMmatmat[i]fscanfvfprintfvsnprintf$LDBL128libSystem.C1%@kFp4q>-;@aKr @>04@ WTyK<0@d2,Bwcv^ @PH*~x& JԢ$聸4pXe,p:@M@\?Ϣ?W?ԣM+Yd@|@ h@ !nzjZ '}DhibW]egl6qnkv+zZgJoC`֣ѓ~8ORѻgWg?H6K +گ L6JAz``ègU1nFiyaf%oҠRh6 w G"U&/ź; (+Z\j1,ٞ[ޮd°c&ujm 6?rgWJz{+ 8Ҏվ | !Bhݳڃn&[owGwZjpf; \ebiaklE x NT9§g&a`IiGM>nwۮjJZ@ f7;𩼮S޻G0齽ʺŠS0$6TW)#gfz.aJ]h*o+ 7 Z-1A26b+-Sdl}wEVZOAي»IˬO ~M-JQS#xpaA.U7Y-۩6˚w]]llA?Z$㧲F waރ$Ųe]]DFok(vpi91k *Z  ,8mF6]pTqke0*1¶u4%y<8syjHA}X*ݹ1SbSW§ٖծ1k**kypH]oF*.f6TTcMe"¤0g)&Ůޟ:{kZ >8,$5*F21wsHpQkzF6c]wN̵ׄJ# pȄA#]F8l1?(gOB~TUyLbˁ8#^TO1ZbbySIOP~V{-b-4R^~Ge­lHnuS/:6# $Tj?e+y䏼Hf*'˼Ѝb# &??~p$iBF;[wzek~ZS 7H8v ?3$rj7nFY |OQ; U dؓS - \G=&pGw`)/ ai5&sL <:R=Pe6^X7}o5641W0ճ2k3$k%'1&-[#bML"'{ "!$*x(+)`F(> q-q,v.Ț/7pqXsYr3w%vQO+tru՛E~xKO} |b!ytxBz{l.m~Do8nkljw[h1Ri85bcm?a+f`Qeddf"giH IKSNJuyOcN LZMݥFĚGE@ND$A2D@XsBI*CThPU3gWu>V SR:P|Q~Z9[ SYfX]4\)^oEZ_/m5qs<\kg2z &J8 좞V`a/6i\lU,zB\uHƒ=&FW A+Ox]`غ7W>9q߳!7Kk ֩fض-bѠ3pj$]^Ĝ'*~@IWVÕ<ӂMʏş{ Dt͆mC-@mw+B.(>dT"ş~Ϝ8yo$w1J}50K_ ^ϋiBۉI#dXфTQc:r Р fΫnx|)Ko%3/uUv?A)ġ:C|sд@͉ ;IbeU"hH_S1ފZ^ھ4ge ȋbW72%k_ܝ8Ŵ(}OodJֿjw3XcVPW0Bq{gǧurCo&p-?О'sB zGɠ2>[ ;g/P8i_ Y=嗇e:ϏOZw3(?RXw@ Qh+HZ"0*WOIo@}m5N#+'*GA |􏒨HX=#?X1vjʨ`^pYL'!$UxAׯ3\Y;U^GP~b;!lڇF 2p(ԐQV_:X1: 3n :m@I)/NJ2"v+x xKH.jAf^O*9y]#Mk~`bю_޶ Rz7hFм!10cV"ajحn6 SrN){t*8Fv#fu`zrϮsɛW"G9E^vMcD&dA/yQA4S&ֿ EbLil!>aDƋΪ~7A8n&]|vYoᡱ Kyi׫w¡\~9$66 Qnf>q,o,ӹI 散 I{.C>HnY-Qg̰t zfa0w,aQ mjp5c飕d2yҗ+L |~-d jHqA}mQDžӃVlkdzbeO\lcc=  n;^iLA`rqgjm Zjz  ' }Dңhi]Wbgeq6lknv+ӉZzJgo߹ﾎCՎ`~ѡ8ROggW?K6H+ L J6`zA`Ugn1yiFafo%6hRw G "/&U;( Z+j\1е,[d&c윣ju m ?6grWJz+{8 Ғ |! ӆBhn[&wowGZpj;f\ eibkaElx TN³9a&g`MGiIwn>JjѮZf @;7SŞϲG0򽽊º0S$6к)WTg#.zfJah]+o*7 Z-A1b62S-+ldEw}ZVǖAOIъ OM~-QJ#SpxAaU׮.7׵Y-6]]wll?AԞZ͢$ Faw$eڪ]]FD(koipvk19Z* ,  m86F߲]qTp0ek*1u4yީ%8S1bSWĔՖk1**ykʬHpo].*F6fcTT"eM©g0&):{ϼkZ> 8$,52F*sw1pHkQ6Fzw]cN̵J #pAF]#l8?1(BOgT~yUbL8^#ܖTZ1ObbSyOIV~P-{b-R4٠~^eGnHl/Su6: #jT$+e?yHf'*b#ٽЧ ?&~?$pi;FBzw[keZ~7 Sv8H 3?r$7jnԄYFܨ |OQ;օ U d S - =G\ p&Gw)` /a߫i5&LsZ<#0zMzFM8,9; :R:(q-v,.7/pXqYs3r%w+OQvrtEux܉~OK }!b|tyBxʠz{.lD~m8onlk[wjR1h58ib?mcf+aQ`צedd"fig HINSKyuJcO NZLݘMFGN@E$DD2AsX@*IBCPhTg3U>uW ַVS:R|P~Q9ZS [fYX4])\ZEo^m/_5qϱ٥s\ۼqދ!K7 kfֶԁ-b3Πjp]$^'~*I@VW<âM˟ŏ{ tDCm-@wm.B+(铜>Td"ŀǼϭ~8y$owJ1}05_K^ iϏ은BI#ƈdX܁T̓cQ: rՆ⩗ fn|xK)o%ƭ/3vUuA?)C:|sĵ@͂ Ͳ;bIUeh"׻_HS1޼^Z4eg Wb27_k%8ם(ŊO}do׸Jj3wVcXWP0qB{߭gCru&op-?'Bs ưGz>2[Ȏg; i8P/ _Y=чe:ZO?(3wwXR @hQ+ğH*0"ZOWoI}@mNП5+#*'G| AH=XX?#1jvʬ`p^Y<L~i/{kHwâ hs)aLoD~Pf7VM'(@ﰤ ہg9x+n&;f?/X)T`D1 ߨMߒ.FgTp'Hq/L0UEc?kǃh6ry7]P\@TN%s7@'>$!AxUʰ\3;Y^U~PGl!;b F2ȂpԞ(Q_V:1X: n3 m:@/)IJNv"2x+ٗ Kx.HҥfAj^y9*O]#kM`~b_R 7zFh!1߈Vc0a"j6nS Nr)Υ{t*F8#vufz`rs"WG9^EMvc΍&DAdQy/4Aڱ&S֚E biLQ<6'5P..T&q]w4.6IE? v\[YI>U!lDa>Ԫ΋ϩ7~8A]&nv|oY yKiw\¹9~$ 66nQfq>,o,IӔ 渱{I .H>C-Yn馑gQz tafA@!  @a`10  @`Psp0  ` @ X ;x8 h( H T+t4  d$ D \ S|< l,  L R#r2  b" B Z Cz: j*  J V@3v6 f& F  ^ c~> n. 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