{"database":"Pride","file_versions":[{"headers":{"Content-Type":["application/json"]},"body":{"files":{"Raw":["ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2019/02/PXD012560/10132017_Jonikas_XL_192_MS3_frac3-2.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2019/02/PXD012560/10132017_Jonikas_XL_192_MS3_frac2-2.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2019/02/PXD012560/10132017_Jonikas_XL_192_MS3_frac2-1.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2019/02/PXD012560/10132017_Jonikas_XL_192_MS3_frac3-3.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2019/02/PXD012560/10132017_Jonikas_XL_192_MS3_frac4-3.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2019/02/PXD012560/10132017_Jonikas_XL_192_MS3_frac1.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2019/02/PXD012560/10132017_Jonikas_XL_192_MS3_frac2-3.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2019/02/PXD012560/10132017_Jonikas_XL_192_MS3_frac4-1.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2019/02/PXD012560/10132017_Jonikas_XL_192_MS3_frac3-1.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2019/02/PXD012560/10132017_Jonikas_XL_192_MS3_frac4-2.raw"],"Mzid":["ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2019/02/PXD012560/Mudpit_10132017_Jonikas_XL_192_MS3_frac_ITMSwindow_10132017_Jonikas_XL_192_MS3_frac1.mzid_Mudpit_10132017_Jonikas_XL_192_MS3_frac_ITMSwindow__10132017_Jonikas_XL_192_MS3_frac1.MGF","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2019/02/PXD012560/Mudpit_10132017_Jonikas_XL_192_MS3_frac_ITMSwindow_10132017_Jonikas_XL_192_MS3_frac1.mzid"]},"type":"primary"},"statusCodeValue":200,"statusCode":"OK"}],"scores":null,"additional":{"labhead_mail":["mjonikas@princeton.edu"],"submitter":["Xiaobo Li"],"technology_type":["Mass Spectrometry","Shotgun proteomics"],"software":[""],"submitter_keywords":["Lc-ms","Tmt labeling","Algae","Photosynthesis","Chlamydomonas"],"full_dataset_link":["https://www.ebi.ac.uk/pride/archive/projects/PXD012560"],"tissue":["Plant Cell"],"sample_protocol":["TAP-dark-grown cells were collected by centrifugation and flash-frozen. Proteins were extracted from the frozen pellets by resuspension in lysis buffer (6M guandium Hydrochloride, 10mM tris(2-carboxyethyl)phosphine, 40mM chloroacetamide, 100mM Tris pH8.5, 1x MS-Safe protease inhibitor, 1x Phosphatase inhibitor cocktail II), grinding with liquid nitrogen, followed by sonication. Protein lysates were then digested with trypsin (Promega) into peptides. Three biological replicates were processed for each strain. The samples were labeled with tandem mass tags (TMTs), multiplexed and then fractionated before tandem mass spectrometry analyses. Briefly, each sample was labeled with the TMT labeling reagent (Thermo Fisher) according to the manufacturer’s instructions. The samples were then mixed in equimolar amounts and desalted using C18-stage tips. The dried peptide mix was then separated using strong cation exchange (SCX) stage-tips into four fractions. Each of the four fractions were then diluted with 1% trifluoroacetic acid (TFA) and separated into three fractions using SDB-RPS stage tips. This procedure initially resulted in a total of 12 fractions. Fractions 1-3 (the children of the first SCX fraction) were pooled together yielding 10 final fractions. Each final fraction was diluted and injected per run using an Easy-nLC 1200 UPLC system (Thermo Fisher). Samples were loaded onto a nano capillary column packed with 1.9 µm C18-AQ (Dr. Maisch) mated to metal emitter in-line with a Fusion Lumos (Thermo Fisher). Samples were eluted using a split gradient of 10-20% solution B (80% ACN with 0.1% FA) in 32 min and 20-40% solution B in 92 min followed column wash at 100% solution B for 10 min. The mass spectrometer was operated in a data-dependent mode with the 60,000 resolution MS1 scan (380-1500 m/z), AGC target of 4e5 and max injection time of 50ms. Peptides above threshold 5e3 and charges 2-7 were selected for fragmentation with dynamic exclusion after 1 time for 60 s and 10 ppm tolerance. MS1 isolation windows of 1.6m/z, MS2 isolation windows 2 and HCD NCE of 55% were selected. MS3 fragments were detected in the Orbitrap at 50,000 resolution in the mass range of 120-500 with AGC 5e4 and max injection time of 86 ms. The total duty cycle was set to 3.0 sec."],"repository":["Pride"],"quantification_method":[""],"modification":[""],"data_protocol":["Raw files were searched with MaxQuant, using default settings for MS3 reporter TMT 10-plex data. Files were searched against sequences of nuclear, mitochondrial, and chloroplast-encoded Chlamydomonas proteins supplemented with common contaminants. Raw files were also analyzed within the Proteome Discoverer (Thermo Fisher) using the Byonic70 search node (Protein Metrics). Data from Maxquant and Proteome Discoverer were combined in Scaffold Q+ (Proteome Software Inc.), which was used to validate MS/MS based peptide and protein identifications. Peptide identifications were accepted if they could be established at greater than 80.0% probability by the Scaffold Local FDR algorithm. Protein identifications were accepted if they could be established at greater than 96.0% probability and contained at least 2 identified peptides. Scaffold Q+ un-normalized data were exported in the format of the log2 value of the reporter ion intensities, which reflect the relative abundances of the same protein among different samples multiplexed. Each sample was then normalized to a median of 0 (by subtracting the original median from the raw values, since the values are log2). For each gene, for each pair of samples, the normalized log2 intensity values from the three replicates of one sample were compared against those for the other sample using a standard t-test. The resulting P values were adjusted for multiple testing, yielding a false discovery rate (FDR) for each gene in each pair of samples. We note that our calculation of FDR does not take into account the spectral count of each protein, which is related to the absolute abundance of the protein and impacts the accuracy of proteomic measurements. Specifically, proteins with a low spectral count are likely of low abundance in cells and often exhibit a large variation in the intensity value between the biological replicates."],"omics_type":["Proteomics"],"labhead":["Martin Jonikas"],"instrument_platform":[""],"labhead_affiliation":["Princeton University"],"submission_type":["PARTIAL"],"species":["Chlamydomonas Reinhardtii"],"submitter_mail":["lixiaobo@westlake.edu.cn"],"publication":["30886426 Li X, Patena W, Fauser F, Jinkerson RE, Saroussi S, Meyer MT, Ivanova N, Robertson JM, Yue R, Zhang R, Vilarrasa-Blasi J, Wittkopp TM, Ramundo S, Blum SR, Goh A, Laudon M, Srikumar T, Lefebvre PA, Grossman AR, Jonikas MC. A genome-wide algal mutant library and functional screen identifies genes required for eukaryotic photosynthesis. Nat Genet. 2019 10.1038/s41588-019-0370-6"],"curator_keywords":["Biological"],"submitter_affiliation":["Westlake University"],"submitter_country":["China"],"pubmed_abstract":["Photosynthetic organisms provide food and energy for nearly all life on Earth, yet half of their protein-coding genes remain uncharacterized<sup>1,2</sup>. Characterization of these genes could be greatly accelerated by new genetic resources for unicellular organisms. Here we generated a genome-wide, indexed library of mapped insertion mutants for the unicellular alga Chlamydomonas reinhardtii. The 62,389 mutants in the library, covering 83% of nuclear protein-coding genes, are available to the community. Each mutant contains unique DNA barcodes, allowing the collection to be screened as a pool. We performed a genome-wide survey of genes required for photosynthesis, which identified 303 candidate genes. Characterization of one of these genes, the conserved predicted phosphatase-encoding gene CPL3, showed that it is important for accumulation of multiple photosynthetic protein complexes. Notably, 21 of the 43 higher-confidence genes are novel, opening new opportunities for advances in understanding of this biogeochemically fundamental process. This library will accelerate the characterization of thousands of genes in algae, plants, and animals."],"pubmed_title":["A genome-wide algal mutant library and functional screen identifies genes required for eukaryotic photosynthesis."],"pubmed_authors":["Li Xiaobo X, Patena Weronika W, Fauser Friedrich F, Jinkerson Robert E RE, Saroussi Shai S, Meyer Moritz T MT, Ivanova Nina N, Robertson Jacob M JM, Yue Rebecca R, Zhang Ru R, Vilarrasa-Blasi Josep J, Wittkopp Tyler M TM, Ramundo Silvia S, Blum Sean R SR, Goh Audrey A, Laudon Matthew M, Srikumar Tharan T, Lefebvre Paul A PA, Grossman Arthur R AR, Jonikas Martin C MC"],"description_synonyms":["MGC130048, gamma sarcoglycan, increased, SGCG_HUMAN, DMDA1, 35 kDa dystrophin-associated glycoprotein, increased number, Proteins, SG-gamma, A4, Gene, decreased number, gamma (35kDa dystrophin-associated glycoprotein), supernumerary, TYPE, SGCG, Protein Gene Products, DAGA4, Gene Proteins, present in greater numbers in organism, decreased, DMDA, reduced, subnumerary, 35kD dystrophin-associated glycoprotein, Protein, SCARMD2, 35DAG, Gene Products, gamma-sarcoglycan, sarcoglycan, LGMD2C., MAM, gamma-SG, present in fewer numbers in organism, SCG3, accessory"],"pubmed_title_synonyms":["Materials, wide/broad, Genetic, Genomes, Photosynthetic, Photosynthesis Dark Reaction, Gene, Calvin Benson Bassham Cycle, Reductive Pentose Phosphate Cycle, whole genome, Calvin Benson Cycle, broad, Calvin-Benson-Bassham, Cistrons, Photosynthetic Carbon Fixation., wide, Material, Calvin Cycle, Photosynthesis Dark Reactions, Cycle, Genetic Materials, Calvin-Benson-Bassham Cycle, Cistron, Calvin, Calvin-Benson Cycle, Dark Reactions of Photosynthesis, Calvin-Benson, Carbon Fixation, Library, Genetic Material"],"data_synonyms":["Bru, Materials, Raw, ion, False, acetylglucosaminyltransferase-like protein, Mbp1, Gene, protein, Computer, protein-containing complex, LARGE1, froggy, peptide, Polypeptides, peptido, Gyltl1a., dorsal marginal zone, Gene Products, Del(8)44H, Software Engineering, Low, protein aggregate, myd, Computer Program, Application, Svc, Open Source Softwares, me75, F, Genetic, peptides, like-acetylglucosaminyltransferase, MS3, nodus primitivus, Software Application, iones, MDDGB6, Open, Open Source Software, Computer Programs and Programming, Mbp-1, LARGE, ions, D17Mit170, T1, Chloroplast, Etioplast, Probabilities, Computer Software Application, BPFD#36, Tools, stem node, sample, peptidos, thiol methyltransferase activity, Applications Software, Open Source, Computer Software, cou, gyltl1b-b, protein complex, Proteins, total expressed protein, Etioplasts, Tl3, Cistrons, Tl2, Source Softwares, Peptide, Cell, Software Tools, Tool, Programs, polypeptide, Program, Computer Applications, TPSG1, S-adenosyl-L-methionine:thiol S-methyltransferase activity, Software Tool, Lr, native protein, count, Ionen, MDDGA6, Algorithm, mKIAA0609, Protein, Computer Applications Software, Chlamydomona, Computer Applications Softwares, Henson's node, Genetic Materials, median, Softwares, KIAA0609, Software, Genetic Material, acetylglucosaminyltransferase-like 1A, fg, Software Applications, Col4a-1, Exhibit, gyltl1b, nodal stem, Source Software, Engineering, mdc1d, common, INSDC_feature:gene, LARGE_HUMAN, sample population, Protein Gene Products, Computer Programs, Gene Proteins, MDC1D, Applications, Applications Softwares, like-glycosyltransferase, enr, Ion, Material, PRSS31, DMZ, Bra, Peptid, Cistron, Polypeptide, TMT, Proteomes, glycosyltransferase-like protein LARGE1, Computer Software Applications"],"name_synonyms":["Chlamydomona, Peptidomics."],"pubmed_abstract_synonyms":["lifespan, Materials, DNS, (Deoxyribonucleotide)n, Phosphatase, FON1, Chlamydomonas, Diatomophyceae, metazoans, Chromophyta, Gene, Diatomeae, SUPERMAN, reinhardtii, Reductive Pentose Phosphate Cycle, protein, broad, FLORAL ORGAN NUMBER 1, Monoester Hydrolase, protein-containing complex, animals, cryptophytes, Deoxyribonucleic acids, Photosynthetic Carbon Fixation, protrusion, Phosphatases, Hydrolase, Readability, Chlorophyta sensu Bremer 1985, Deoxyribonucleic Acid, Photosynthesis Dark Reactions, Cycle, SUP, Gene Products, glaucocystophytes, Animal, protein aggregate, Carbon Fixation, Animalia, reinhardius, thymus nucleic acid, ostium, Genetic, algae, Genomes, entire lifespan, entire life cycle, Bdr, Double Stranded, Deoxyribonucleic acid, plants, Super protein, Calvin-Benson-Bassham, Phosphomonoesterases, sp, SNAP-25, Phosphoric Monoester Hydrolase, genetic, Dinoflagellata, Mif1, Chlamydomonas reihhardtii, Chlamydomonas reinhardii, Calvin-Benson-Bassham Cycle, Calvin, Dinophyta, Double-Stranded DNA, diatoms, (Deoxyribonucleotide)m, deoxyribonucleic acids, DNAn, dinoflagellates, cryptomonads, constitutitional genetic, Dark Reactions of Photosynthesis, phosphatase, ostia, Chlamydomonas smithii, Pyrrhophyta, foramen, anatomical protrusion, wide/broad, protein complex, Photosynthetic, DNAn+1, land plants, Proteins, familial, Photosynthesis Dark Reaction, Metazoa., Synaptosomal-associated 25 kDa protein, Calvin Benson Cycle, Double-Stranded, foramina, Chlamydomonas reinhardtius, Cistrons, predicted, (Deoxyribonucleotide)n+m, Phosphomonoesterase, Glaucophyta, native protein, Protein, Genetic Materials, GENA70, Calvin-Benson Cycle, Cryptomonadida, ds-DNA, desoxyribose nucleic acid, Foods, Library, Genetic Material, Phosphoric Monoester, green algae, Dinophycidae, Diatomea, life, INS, Plant, Calvin Benson Bassham Cycle, phosphoric monoester hydrolase activity, Pyrrophyta, FLO10, INSDC_feature:gene, whole genome, Understanding, Chlamydomonas reinhardius, HERP, Chlorophycota, Phosphohydrolases, Protein Gene Products, Glaucophyceae, multicellular animals, Gene Proteins, wide, Phosphohydrolase, higher plants, Material, Calvin Cycle, spine, SNAP, Phosphoric, opening, ds DNA, Cryptophyta, Desoxyribonukleinsaeure, Cistron, inherited genetic, DNA, earth, Calvin-Benson, Hydrolases, hereditary, Chlamydomonas smithii R.W.Howshaw & H.Ettl, Chlamydomonas reinhardtii P.A.Dangeard, FLORAL DEFECTIVE 10"],"sample_synonyms":["Kation, FLN-B, SCT, dmMOF, Bhlha41, Scx, SCX, Tandem, Phosphatase, hypersomnia with periodic respiration, fond, Abcb2, bHLHa48, CycEI, Apaf-1, heavy chain disease, Long Term, Ham1, DmelCG9648, 5730420M11Rik, Trifluoroacetate, Polypeptides, hydrogen chloride, Drug Tolerance, Ly6, scx, Method, Protease Inhibitor, FLASH, dMOF, B1, SEC, mixed central and obstructive sleep apnea, WMS, strong, SET, Divorced, C79325, hac-1, DmelCG13176, N, sleep, sec, hypopnea, ORF19, Divorces, T6G21.3, RIP25, Phosphomonoesterases, ecotype, SURGICAL AND MEDICAL PROCEDURES, AI047805, DmelCG4299, isolation and purification, set, Wasserstoffchlorid, Peptidohydrolase Inhibitor, column, bHLHa41, ACN, sample, D1, Acn, n, stage, autolysin activity, phosphatase, drug tolerance, SGS, Stars, Ly-6A.2, bHLHc9, immune system tolerance, anon-53Fa, Longterm Effect, l(2)SH0173, mixed central and obstructive, mixed sleep apnea, Procedure, Cyc E, ACMICD, bHLHd7, RING4, bHLHd6, bHLHd9, bHLHd8, TPSG1, bHLHd5, bHLHd4, BG:DS07108.3, Stickstoff, Dm1, Tap-1, Hydrolase Inhibitor, Chlorwasserstoff, 1110049F14Rik, l(2)05206, CG6829, dark/hac-1/dapaf-1, Acid, DmelCG7659, HLA-DR-associated protein II, Antagonists, DI-2, FLN3, I-2Dm, pooled, reagent, Methodological, beta Trypsin, Children, MEX67, apnea syndromes, I-2PP1, Phosphohydrolase, breathing, nitrogen, Self Tolerance, TAF-IBETA, antagonists and inhibitors, Mex67, Phosphoric, Charges and Fees, PRSS31, Indicator, bacteriolytic toxin activity, TAF-Ibeta, Endopeptidase, Peptide Peptidohydrolase Inhibitor, chlorane, STARS, TMT, l(3)01658, T-cell-activating protein, dipeptide chemoreceptor protein, sleep-disordered, cycline, Effects, chlorure d'hydrogene, Endopeptidase Inhibitors, Protein USO1 homolog, DmcyclinE, developmental stage, Antp P1, Stem cell antigen 1, Antp P2, protein-containing complex, thomson, SCXB, 17alpha)-isomer, sleep apnea, CG7826, SCXA, mass-to-charge ratio, cdi7, sleep hypopneas, DmelCG3025, cyclinE, TAP1, isolation, Mex67h, tough, Hu, Gene Products, CG7835, Cdi7, CDI7, CG42273, Peptide Hydrolase, 3.4, Technique, Cesium Trifluoroacetate, T6K12_14, MAX, ABP-280-like protein, anatomical systems, FAM39E, Acinus, Hydrogen chloride, interventionDescription, Longterm, beta-Trypsin, 2pp2a, Long-Term, DmcycE, MCP-IV, Antagonist, 2-7, CG1028, CG10574, T6K12.14., Solution, CD156, Phosphoric Monoester Hydrolase, acinusL, Study, Injectable, max, 2PP2A, Protease Antagonists, acinusS, dSET, dSet, Peptide Peptidohydrolase Inhibitors, peptidos, Ly-6A.2|Ly-6E.1, Squalene transfer protein, Ly6a, PTHB1, C22orf6, inhibitors, dark/dapaf-1/hac-1, Spf, SPF, dApaf-1, Proteins, Kationen, CG3025, Ly-6E.1, Sca-1, chloridohydrogen, DmAntp, buffer, Cell, mKIAA0670, polypeptide, APAF1, Wash2, Wash1, l(2)k02514, native protein, Immune Tolerance, DmCycE, Hac-1, I-2PP2A, C18, Long Term Effects, Dm I-2, Strain, MFS1, 5alpha, MIXL, Intervention, AU020952, Ant, holin, l(2)k02602, Alpha-tocopherol-associated protein, mixed, ensemble, PSF1, Separations, Striated muscle activator of Rho-dependent signaling, Dark/Dapaf-1/HAC1, azote, Mass Spectrometry-Mass Spectrometry, Peptidohydrolase Inhibitors, CD156a, AOI, Supernatant protein factor, Longterm Effects, ME-IV, Gene Proteins, D-CycE, Peptidase, bps, SCA-1, Ns, DmelCG1028, Antiprotease, MTP1, Fees, DRO15DC96Z, Peptide Hydrolase Inhibitors, Vesicle-docking protein, hydrochloric acid, Immunological Tolerance, Hac-1/Dark, IPP2A2, Endopeptidase Inhibitor, ANT-C, DmelCG6829, cation, Antp1, classic hairy cell leukaemia, Peptide Hydrolase Inhibitor, Ly-6A|E, Hydrogenchlorid, protein, Mass Spectrometry Mass Spectrometry, peptide, Phosphatases, Hydrolase, Techniques, peptido, Ccne, BANF, hTAP, AntP1, sleep apneas, Inhibitors, Min, Apaf1, Hydrolase Inhibitors, protein aggregate, ARK, Injectables, Effect, MIX, DmelCG42273, 3-hydroxy-5-estrane-17-carbonitrile, Sca1, peptides, TAF-I, dMax, 2610036I19Rik, 2610510L13Rik, E430039A18Rik, arc, min, mAPC, Mass Spectrometry, purification, ABC17, ark, SCAN, xscleraxis, T1, BG:DS07700.1, IGAAD, fSAP152, LRS1, Methodological Studies, mKIAA1315, DmelCG10574, 380, ppm, trifluoro-, CG7659, ANT-P, stem cell antigen 1, dApaf1, necrosis, Strains, hypopneas, Reagents, GPHYSD2, 115kDa, Long-Term Effects, reagents, phapii, D-Apaf-1, Peptidase Inhibitor, Dmel_CG7826, CG9648, StF-IT-1, Th, CED-4, classic hairy cell leukemia, Peptide Peptidohydrolase, br37, Aus, S-adenosyl-L-methionine:thiol S-methyltransferase activity, AA387232, HCD, BB114693, dmax, Immunologic Tolerance, bacteriocin activity, cultivar, sleep hypopnea, WASH, reactif, Acetic acid, Dmel_CG7835, Mnb, MNB, MILD1, CHARGES, MS/MS, AI256582, Sonications, HCl, Trifluoroacetic, APT1, hac1, MASS, CG4299, AW124434, Methodological Study, chloracetamide, dapaf-1S, apaf-1, MOF, Mof, dapaf-1L, lysin activity, Peptidase Inhibitors, l35Dd, Charge, Tolerance, Cesium, Antiproteases, Polypeptide, mixed sleep Apneas, 7N, Hydrolases, Y3, Inhibitor, Strains and Sprains, i2pp2a, apnea syndrome, Dapaf-1/HAC-1, Procedures, Ly-6A.2/Ly-6E.1, Reagent, FBN, DMANTPE1, D4Ertd659e, Gene, Protease, cycE, ACINUS, Monoester Hydrolase, 1300013M05Rik, l(2)br37, PHAPII, CYCLE, Buffer, Intervention or Procedure, Dark/Hac-1/dApaf1, Hac1, Dark/Hac-1/dApaf-1, resilient, Ms1, ECTOL1, Injection, p63, p65, Studies, AW536553, Protease Antagonist, Sprains, Separated, cloruro de hidrogeno, Reagents and Indicators, apneas, Ham-1, Pro-Mega, ANTC, antp, Ly-6A/E, CYCE, reactivo, MS1, MS3, MS2, DmelCG3938, CyclE, Selb, ipp2a2, dapaf-1, inhibiteur, 3938, Interventional, dapaf, labeling, dark, Charges, TABP, Indicators, OCTD, l(2)k05007, cations, Vdp, VDP, dm-cycE, inhibidor, Fee, 10^[-6], DARK, taf-ibeta, male sterility 1, apnea, Cation, liquid, Long-Term Effect, AntP, ANTP, dArk, Dapaf-1, FLN1L, TCEP, thiol methyltransferase activity, TAP, Tap, Intervention Strategies, ABP-278, DYRK1, 5E4, protein complex, Sprain, igaad, inhibitor, apaf1, Peptide, cationes, group, strain, AI875693, tap, [HCl], Phosphomonoesterase, secret agent, FH1, Protein, I2PP2A, Hydrochloride, Dyrk1, Dark, l(3)84Ba, CyeE, (3alpha, Dark/Apaf-I, Mvb1, tandem MS, ABP-280, WMS2, CG13176, antagonists, Phosphoric Monoester, Separation, 10^[-9], PRSS, MALE STERILITY 1 PROTEIN, CC1, l(2)35Dd, Tripcellim, phosphoric monoester hydrolase activity, dApaf-1/DARK/HAC-1, sample population, nitrogeno, P115, Protein Gene Products, Phosphohydrolases, Trypure, dSET/TAF-Ibeta, 2610030F17Rik, Transcytosis-associated protein, SSKS, AA960152, Peptid, SCH, AA407739, CG3938, dAPAF-1, Scl, RCB1376, 3-OHECN"],"additional_accession":[]},"is_claimable":false,"name":"Chlamydomonas cpl3 mutant proteomics","description":"This project aims to identify proteins with increased or decreased abundance in the photosynthetically-deficient cpl3 mutant compared to the wild 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