#METABOLOMICS WORKBENCH Tom_Metz_20140707_9470461_mwtab.txt DATATRACK_ID:135 STUDY_ID:ST000084 ANALYSIS_ID:AN000136 PROJECT_ID:PR000075
VERSION             	1
CREATED_ON          	2016-09-17
#PROJECT
PR:PROJECT_TITLE                 	Systems Biology for EnteroPathogens
PR:PROJECT_TYPE                  	MS analysis
PR:PROJECT_SUMMARY               	sysbep.org
PR:INSTITUTE                     	Pacific Northwest National Laboratory
PR:DEPARTMENT                    	Biological Separation and Mass Spectrometry
PR:LAST_NAME                     	Joshua
PR:FIRST_NAME                    	Adkins
PR:ADDRESS                       	-
PR:EMAIL                         	Joshua.Adkins@pnnl.gov
PR:PHONE                         	-
#STUDY
ST:STUDY_TITLE                   	Model-driven multi-omic data analysis elucidates metabolic immunomodulators of
ST:STUDY_TITLE                   	activation
ST:STUDY_TYPE                    	growth condition, timecourse
ST:STUDY_SUMMARY                 	Macrophages are central players in immune response, manifesting divergent
ST:STUDY_SUMMARY                 	to control inflammation and innate immunity through release of cytokines and
ST:STUDY_SUMMARY                 	signaling factors. Recently, the focus on metabolism has been reemphasized as
ST:STUDY_SUMMARY                 	signaling and regulatory pathways of human pathophysiology, ranging from cancer
ST:STUDY_SUMMARY                 	aging, often converge on metabolic responses. Here, we used genome-scale
ST:STUDY_SUMMARY                 	and multi-omics (transcriptomics, proteomics, and metabolomics) analysis to
ST:STUDY_SUMMARY                 	metabolic features that are critical for macrophage activation. A genome-scale
ST:STUDY_SUMMARY                 	network for the RAW 264.7 cell line was constructed to determine metabolic
ST:STUDY_SUMMARY                 	of activation. Metabolites well-known to be associated with immunoactivation
ST:STUDY_SUMMARY                 	and arginine) and immunosuppression (tryptophan and vitamin D3) were among the
ST:STUDY_SUMMARY                 	critical effectors. Intracellular metabolic mechanisms were assessed,
ST:STUDY_SUMMARY                 	a suppressive role for de-novo nucleotide synthesis. Finally, underlying
ST:STUDY_SUMMARY                 	mechanisms of macrophage activation were identified by analyzing multi-omic
ST:STUDY_SUMMARY                 	obtained from LPS-stimulated RAW cells in the context of our flux-based
ST:STUDY_SUMMARY                 	This study demonstrates that the role of metabolism in regulating activation
ST:STUDY_SUMMARY                 	be greater than previously anticipated and elucidates underlying connections
ST:STUDY_SUMMARY                 	activation and metabolic effectors. This submission corresponds to the
ST:STUDY_SUMMARY                 	data from this study.
ST:INSTITUTE                     	Pacific Northwest National Laboratory
ST:DEPARTMENT                    	Biological Separation and Mass Spectrometry
ST:LAST_NAME                     	Metz
ST:FIRST_NAME                    	Thomas
ST:ADDRESS                       	-
ST:EMAIL                         	thomas.metz@pnnl.gov
ST:PHONE                         	-
ST:NUM_GROUPS                    	2
ST:TOTAL_SUBJECTS                	12
#SUBJECT
SU:SUBJECT_TYPE                  	Cells
SU:SUBJECT_SPECIES               	Mus musculus
SU:TAXONOMY_ID                   	10090
SU:GENOTYPE_STRAIN               	RAW 264.7
SU:CELL_STRAIN_DETAILS           	RAW 264.7
SU:CELL_PRIMARY_IMMORTALIZED     	immortalized
SU:SPECIES_GROUP                 	Mammal
#SUBJECT_SAMPLE_FACTORS:         	SUBJECT(optional)[tab]SAMPLE[tab]FACTORS(NAME:VALUE pairs separated by |)[tab]Additional sample data
SUBJECT_SAMPLE_FACTORS           	-	SBEP_Metab_LPSactivated1	Lipopolysaccharide Treatment:100 ng/ml	
SUBJECT_SAMPLE_FACTORS           	-	SBEP_Metab_LPSactivated2	Lipopolysaccharide Treatment:100 ng/ml	
SUBJECT_SAMPLE_FACTORS           	-	SBEP_Metab_LPSactivated3	Lipopolysaccharide Treatment:100 ng/ml	
SUBJECT_SAMPLE_FACTORS           	-	SBEP_Metab_Control1	Lipopolysaccharide Treatment:None	
SUBJECT_SAMPLE_FACTORS           	-	SBEP_Metab_Control2	Lipopolysaccharide Treatment:None	
SUBJECT_SAMPLE_FACTORS           	-	SBEP_Metab_Control3	Lipopolysaccharide Treatment:None	
#COLLECTION
CO:COLLECTION_SUMMARY            	After stimulation, cells were washed twice with Dulbecco?s PBS, scraped out and
CO:COLLECTION_SUMMARY            	into 15-mL centrifuge tubes.
CO:SAMPLE_TYPE                   	Cell
CO:COLLECTION_METHOD             	After stimulation, cells were washed twice with Dulbecco?s PBS, scraped out and
CO:COLLECTION_METHOD             	into 15-mL centrifuge tubes.
CO:COLLECTION_TIME               	24 hours
CO:COLLECTION_VIALS              	15-mL centrifuge tubes
CO:TISSUE_CELL_QUANTITY_TAKEN    	All
#TREATMENT
TR:TREATMENT_SUMMARY             	Macrophages (RAW 264.7 cells) grown for two day with suplimentation of 100ng |
TR:TREATMENT_SUMMARY             	lipopolysaccharide | Macrophages (RAW 264.7 cells) grown for two days without
TR:TREATMENT_PROTOCOL_COMMENTS   	Macrophages (RAW 264.7 cells) were seeded at a density of 3.0E6 cells in 150 mm
TR:TREATMENT_PROTOCOL_COMMENTS   	using Dulbecco's Modified Eagle's Medium supplemented with 10% fetal calf
TR:TREATMENT_PROTOCOL_COMMENTS   	then grown for 2 days and stimulated for 24 hours with 100 ng/mL of
TR:TREATMENT_PROTOCOL_COMMENTS   	diluted in fresh medium. A control culture was run in parallel by incubating
TR:TREATMENT_PROTOCOL_COMMENTS   	the same period of time with fresh medium only. Three biological replicates
TR:TREATMENT_PROTOCOL_COMMENTS   	performed per condition, and two dishes were used for each replicate. /
TR:TREATMENT_PROTOCOL_COMMENTS   	(RAW 264.7 cells) were seeded at a density of 3.0E6 cells in 150 mm dishes
TR:TREATMENT_PROTOCOL_COMMENTS   	Dulbecco's Modified Eagle's Medium supplemented with 10% fetal calf serum, then
TR:TREATMENT_PROTOCOL_COMMENTS   	for 2 days and stimulated for 24 hours with 100 ng/mL of lipopolysaccharide
TR:TREATMENT_PROTOCOL_COMMENTS   	in fresh medium. A control culture was run in parallel by incubating for the
TR:TREATMENT_PROTOCOL_COMMENTS   	period of time with fresh medium only. Three biological replicates were
TR:TREATMENT_PROTOCOL_COMMENTS   	per condition, and two dishes were used for each replicate.
TR:TREATMENT                     	Abiotic
TR:TREATMENT_COMPOUND            	lipopolysaccharide / fresh medium
TR:TREATMENT_DOSE                	100 ng/mL /--
TR:TREATMENT_VEHICLE             	fresh medium
TR:CELL_GROWTH_CONTAINER         	150 mm dishes
TR:CELL_INOC_PROC                	Macrophages (RAW 264.7 cells) were seeded at a density of 3.0E6 cells in 150 mm
TR:CELL_MEDIA                    	Dulbecco's Modified Eagle's Medium supplemented with 10% fetal calf serum
TR:CELL_HARVESTING               	After stimulation, cells were washed twice with Dulbecco?s PBS, scraped out and
TR:CELL_HARVESTING               	into 15-mL centrifuge tubes.
#SAMPLEPREP
SP:SAMPLEPREP_SUMMARY            	Suspentions softly centrifuged, buffer removed, amonium bicarbonate added,
SP:SAMPLEPREP_SUMMARY            	extraxted with chloroform/methanol (2:1, v/v), vortexed, centrifuged, aqueous
SP:SAMPLEPREP_SUMMARY            	dried in vacuum concentrator, derivatization with methoxyamine in pyridine,
SP:SAMPLEPREP_SUMMARY            	(MSTFA), and 1% trimethylchlorosilane (TMCS)
SP:SAMPLEPREP_PROTOCOL_COMMENTS  	Cell suspensions were softly centrifuged (230 × g for 5 min) and as much
SP:SAMPLEPREP_PROTOCOL_COMMENTS  	as possible was removed. Then, 170 µL of 150 mM ammonium bicarbonate was added
SP:SAMPLEPREP_PROTOCOL_COMMENTS  	the cell pellet and the cell suspensions were transferred to 2 mL
SP:SAMPLEPREP_PROTOCOL_COMMENTS  	tubes for extraction. Subsequently, the water soluble metabolites were
SP:SAMPLEPREP_PROTOCOL_COMMENTS  	with four volumes of chilled (-20°C) chloroform/methanol (2:1, v/v). After
SP:SAMPLEPREP_PROTOCOL_COMMENTS  	the samples were centrifuged (12,000 × g for 5 min) and the upper (aqueous)
SP:SAMPLEPREP_PROTOCOL_COMMENTS  	containing water-soluble metabolites were transferred into glass vials,
SP:SAMPLEPREP_PROTOCOL_COMMENTS  	by drying in a vacuum concentrator. For the derivatization, 20 µL of
SP:SAMPLEPREP_PROTOCOL_COMMENTS  	in pyridine (30 mg/mL) were added to each sample, followed by incubation at
SP:SAMPLEPREP_PROTOCOL_COMMENTS  	with shaking for 90 min to protect carbonyl groups. Next, 80 µL of
SP:SAMPLEPREP_PROTOCOL_COMMENTS  	(MSTFA) with 1% trimethylchlorosilane (TMCS) were added to each vial, followed
SP:SAMPLEPREP_PROTOCOL_COMMENTS  	incubation at 37°C with shaking for 30 min to derivatize hydroxyl and amine
SP:SAMPLEPREP_PROTOCOL_COMMENTS  	The samples were then allowed to cool to room temperature.
SP:PROCESSING_METHOD             	Homogenization
SP:EXTRACTION_METHOD             	The water soluble metabolites were extracted with four volumes of chilled
SP:EXTRACTION_METHOD             	chloroform/methanol (2:1, v/v). After vortexing, the samples were centrifuged
SP:EXTRACTION_METHOD             	× g for 5 min) and the upper (aqueous) layers containing water-soluble
SP:EXTRACTION_METHOD             	were transferred into glass vials, followed by drying in a vacuum concentrator.
SP:EXTRACT_ENRICHMENT            	Vacuum Concentrator
SP:SAMPLE_RESUSPENSION           	20 µL of methoxyamine in pyridine (30 mg/mL)
SP:SAMPLE_DERIVATIZATION         	20 µL of methoxyamine in pyridine (30 mg/mL), 80 µL of
SP:SAMPLE_DERIVATIZATION         	(MSTFA) with 1% trimethylchlorosilane (TMCS),
SP:CELL_TYPE                     	Macrophage
#CHROMATOGRAPHY
CH:CHROMATOGRAPHY_SUMMARY        	Agilent 7890A gas chromatograph with a HP-5MS gas chromatography column using
CH:CHROMATOGRAPHY_TYPE           	GC
CH:INSTRUMENT_NAME               	Agilent 7890A
CH:COLUMN_NAME                   	Agilent HP5-MS (30m × 0.25mm, 0.25 um)
CH:CHROMATOGRAPHY_COMMENTS       	Chromatography was carried out on an Agilent 7890A gas chromatograph using the
CH:CHROMATOGRAPHY_COMMENTS       	software (Chemstation) and a HP-5MS gas chromatography column (Agilent
CH:CHROMATOGRAPHY_COMMENTS       	Santa Clara, CA; 30 m x 0.25 mm x 0.25 m film thickness). The sample injection
CH:CHROMATOGRAPHY_COMMENTS       	was splitless, and 1 L of each sample was injected. The injection port
CH:CHROMATOGRAPHY_COMMENTS       	was held at 250 C throughout the analysis. The GC oven was held at 60 C for 1
CH:CHROMATOGRAPHY_COMMENTS       	after injection, and the temperature was then increased to 325 C by 10 C/min,
CH:CHROMATOGRAPHY_COMMENTS       	by a 5 min hold at 325 C. The helium gas flow rates for each Experiment were
CH:CHROMATOGRAPHY_COMMENTS       	by the Agilent Retention Time Locking function based on analysis of deuterated
CH:CHROMATOGRAPHY_COMMENTS       	acid and were in the range of 0.450.5 mL/min.
CH:FLOW_RATE                     	0.45-0.5mL/min
CH:INJECTION_TEMPERATURE         	250 C
CH:SAMPLE_INJECTION              	1 L, Splitless
CH:ANALYTICAL_TIME               	37.5 min
CH:OVEN_TEMPERATURE              	60 C for 1 min, then increased to 325 C by 10 C/min, followed by a 5 min hold
CH:OVEN_TEMPERATURE              	325 C
CH:SAMPLE_SYRINGE_SIZE           	10 L
#ANALYSIS
AN:ANALYSIS_TYPE                 	MS
AN:LABORATORY_NAME               	Biological Separations & Mass Spectrometry group, Pacific Northwest National
AN:LABORATORY_NAME               	(www.omics.pnl.gov)
AN:ACQUISITION_DATE              	2012
AN:SOFTWARE_VERSION              	Metabolite Detector vs. 2.0.6 beta
AN:DATA_FORMAT                   	Raw .D.Zip; Processed .CDF
#MS
MS:INSTRUMENT_NAME               	Agilent 5975C
MS:INSTRUMENT_TYPE               	Single quadrupole
MS:MS_TYPE                       	EI
MS:ION_MODE                      	POSITIVE
MS:MS_COMMENTS                   	An Agilent GC 7890A coupled with a single quadrupole MSD 5975C (Agilent
MS:MS_COMMENTS                   	Inc.; Santa Clara, CA, USA) was used, and the samples were blocked and analyzed
MS:MS_COMMENTS                   	random order for each experiment. Data were collected over the mass range
MS:MS_COMMENTS                   	m/z. A mixture of FAMEs (C8-C28) was analyzed once per day together with the
MS:MS_COMMENTS                   	for retention index alignment purposes during subsequent data analysis.
MS:SCAN_RANGE_MOVERZ             	50-550 m/z
MS:MS_COMMENTS                   	After converting raw data to netCDF format, the data were processed by the
MS:MS_COMMENTS                   	software for peak deconvolution and chromatographic alignment. Retention
MS:MS_COMMENTS                   	(RI) were calculated based on the analysis of a mixture of fatty acid methyl
MS:MS_COMMENTS                   	(C8 - C30) (Agilent Technologies) as external retention time standards, then
MS:MS_COMMENTS                   	retention index information was subsequently applied to all experimental
MS:MS_COMMENTS                   	for retention time alignment. MetaboliteDetector parameters for peak detection
MS:MS_COMMENTS                   	deconvolution are as follows: Peak threshold, 7; minimum peak height, 7;
MS:MS_COMMENTS                   	width, 8. Deconvoluted features were identified by matching to the Agilent
MS:MS_COMMENTS                   	Metabolomics Retention Time Locked Library, which contains mass spectral and
MS:MS_COMMENTS                   	indix information for approximately 700 metabolites. Each initial match to the
MS:MS_COMMENTS                   	was manually inspected to confirm a confident identification. The data were
MS:MS_COMMENTS                   	matched against the NIST 08 library to identify additional peaks not included
MS:MS_COMMENTS                   	the Fiehn library. MetaboliteDetector software was used for database matching
MS:MS_COMMENTS                   	batch identification/quantification parameters are as follows: required score,
MS:MS_COMMENTS                   	?RI, 25; minimum S/N, 20; maximum peak discrepancy index, 100. Ions 73 and 143
MS:MS_COMMENTS                   	excluded from use as metabolite quantification ions, since these are due to
MS:MS_COMMENTS                   	of the trimethylsilyl groups. Otherwise, three unique fragment ions were
MS:MS_COMMENTS                   	to each metabolite for quantification and used for each individual GC-MS
MS:MS_COMMENTS                   	when processing the data in batch mode. The summed areas of the three
MS:MS_COMMENTS                   	ions were exported from MetaboliteDetector and used in further statistical
MS:MS_COMMENTS                   	All identifications were manually validated by inspection of retention index
MS:MS_COMMENTS                   	spectrum matches.
#MS_METABOLITE_DATA
MS_METABOLITE_DATA:UNITS         	Peak area
MS_METABOLITE_DATA_START
Samples	SBEP_Metab_LPSactivated1	SBEP_Metab_LPSactivated2	SBEP_Metab_LPSactivated3	SBEP_Metab_Control1	SBEP_Metab_Control2	SBEP_Metab_Control3
Factors	Lipopolysaccharide Treatment:100 ng/ml	Lipopolysaccharide Treatment:100 ng/ml	Lipopolysaccharide Treatment:100 ng/ml	Lipopolysaccharide Treatment:None	Lipopolysaccharide Treatment:None	Lipopolysaccharide Treatment:None
1-methyl nicotinamide	1128844.9000	990557.0975	1142586.6960	1117011.1816	1315764.9690	1609434.2165
2-aminoethanethiol	941833.5000	868973.5000	953831.6860	1600093.6015	1964054.9380	2213228.8040
3-hydroxybenzaldehyde	501242.7073	431011.4386	477214.9231			
3-phosphoglyceric acid	1303610.3515	1504818.0300	1740486.5540	877204.8435	1211525.0710	1272797.0990
4-guanidinobutyric acid	1859373.2670	1685591.6650	1858273.8870	2645271.9460	2600277.8205	3854828.0225
4-hydroxyquinoline-2-carboxylic acid	177836.4865	168974.9107	193569.5687	2110118.1290	2221603.0990	2535250.0470
5^-deoxy-5^-(methylthio)adenosine	2882511.8800	2957775.4975	2724568.3550	464864.2507	589460.9126	780203.1709
adenosine	1537097.8750	1214250.8015	1316169.5090	4053242.8525	4148655.7665	4784051.0780
adenosine-5-monophosphate	9454142.7335	8121689.6410	8463618.3950	27543792.1050	34940220.5400	42146640.0400
alpha ketoglutaric acid				2092664.4335	2059916.6520	2437121.8085
arabitol	390153.2435	387118.4070	454665.9208			
beta- alanine	12036820.1650	10851261.8450	13599141.0650	23432641.8050	24002849.8650	30832474.5100
citraconic acid	6589380.9000	6127515.1420	7514006.2660			
citric acid	682651.2431	498260.2384	538841.7364	1070709.0001	948590.2074	1063573.1426
creatinine	10452669.1560	10339577.5660	11304334.0600	14319437.0950	12841146.2800	16519702.7700
Cysteinylglycine				747331.7561	634460.2773	848180.1665
D-galactose				523849.8309	545109.2323	811281.7084
D-glucosaminic acid	26639733.4550	28680203.6300	29834683.9500	1869625.0015	2704562.6160	3391397.5005
D-glucose-6-phosphate	1721774.7810	1643900.4280	1763549.7790			
DL-3-aminoisobutyric acid	172434.6981	92082.6045	141553.3294	1511728.4585	1461268.2315	2514955.0150
DL-threo-beta-Hydroxyaspartic acid	95146.8605	103992.0491	120882.9009	170726.0954	335916.9590	425773.9757
D-malic acid	1147617.8690	1135687.1810	1415029.3205	4107528.9195	3486786.6035	4118208.6520
D-mannitol	2946232.9380	2897797.4370	3412819.1040	1900178.9300	1597070.3660	1223019.2760
D-Ribose 5-phosphate	2229996.4555	2427192.3445	2573543.4410	3592947.2585	5229012.1725	8143540.4925
D-sorbitol	589958.5707	435463.2498	518026.4727	249105.8004	207333.6954	190275.6371
D-threitol	1081927.9775	1084599.8660	1233440.0695	1162887.3080	1628252.2225	1772900.8970
fructose	2037004.2305	2114549.7710	2326119.2610	481045.2352	709047.3964	789425.1007
fumaric acid				3276814.9275	3400546.9545	4137408.8530
glucoheptonic acid	2634651.2925	2829935.9925	2869015.6730	1288067.9260	1342649.3530	1229431.2395
gluconic acid	494827.0838	699589.9422	617827.3551			
glycerol 1-phosphate	10264178.5300	10798000.4200	9612604.6905			
glycine	37465350.1100	33155757.6900	40856466.0700	53534675.3200	55540492.2750	69796232.4650
guanosine				975057.3367	1245361.9060	1440699.5980
guanosine-5^-monophosphate	32649491.4100	29851123.1350	33411172.9700	66815175.9950	72595108.8700	81348058.1400
hypotaurine	3802828.5805	3079498.0710	4089572.1595	5823187.2135	6589528.6090	9111528.9630
hypoxanthine	46279.6424	46244.4621	47779.0448	54423.4678	77548.7990	113037.4879
inosine	3807795.3400	3671602.6305	4020506.4480	5453101.7045	6577889.8230	7621978.0705
L-alanine	2966422.2705	2527379.4385	2874097.5210	9763688.5645	10716948.6250	14565213.9750
L-aspartic acid	1611386.4610	854706.8746	1149295.5377	17758208.6450	11004554.3600	13441915.2450
L-cysteine	6594124.7115	6239553.3880	6916586.0315	4363129.8585	4647791.9710	5261679.3860
L-glutamic acid	19048241.4500	17688103.9950	22072682.5300	32429901.4500	31172798.7500	37958720.7050
L-leucine	921691.1742	927836.8475	1013165.8040	1733967.8160	1628935.4350	2075679.0600
L-lysine	3397988.6500	3137480.4855	4116308.9395	4663940.2620	5255705.5005	6985776.7045
L-methionine	778737.0805	823831.7756	869545.9695	449913.1699		
L-ornithine	895489.0345	1786521.5760	338658.3193	2462425.0610	2398847.8915	3367301.2360
L-serine	1567014.7625	1635960.1275	1790927.5215	2503343.5225	2284952.7000	3016039.1185
L-sorbose	1445182.5500	926870.9442	1067504.9490	2227343.3225	2465901.1845	3205120.3090
L-threonine	4206167.4105	3813468.4815	4105387.5070	6327888.6420	7315329.1770	10419036.5800
L-tyrosine				2494203.6000	3139766.7630	4027543.5960
L-valine	2032012.8800	1984586.5770	2182315.5285	1921864.9465	1993920.9160	2503465.9570
maltitol	1017471.4548	923455.5432	982604.0935	1232980.4005	1316691.3385	1617773.4420
mucic acid	218055.6989	207827.6139	195215.3010			
oxalic acid	22672.0000	27759.5000	26053.0000	31231.8201	37874.1906	35845.2230
palmitic acid	321087.4780	251727.9914	290664.8260	1144873.4435	1430828.4635	1885948.7900
pantothenic acid	1494386.4495	1474212.0750	1509237.7320	2246904.2570	2593580.9985	2915574.7765
porphine	487431.0139	489637.8323	510780.0168	425471.3115	889348.9603	1129465.8540
putrescine	24086631.4450	23407531.2800	26341519.8150	6759718.3870	7405081.2425	9908081.7660
pyruvic acid	728753.8819	862734.1556	926361.1350	1394193.6825	1288652.5820	1390265.1600
ribonic acid gamma-lactone				586224.1754	764691.0749	863848.2198
spermidine	7597352.8600	4974057.2150	8640064.2905	11585311.2750	14707324.2150	17969750.7550
spermine	1297630.8355	554069.7708	1612147.8085	5256107.3915	7576976.7175	11210265.5350
stearic acid	1102517.7490	1011344.8775	1270094.6065	1759707.1405	1897270.9630	2297010.1180
tagatose	1463995.6225	1649932.2850	1673612.2225			
thymine				722755.5389	1000376.5401	2537650.6245
tyramine	5108178.3740	5342080.0920	4457680.0675	1121906.5485	758655.2526	766216.4064
uridine 5^-monophosphate	1193945.2940	1132687.3275	1274190.3945	3593946.2695	3647580.9585	4667846.3210
xanthine	1545967.6430	1433454.6040	1812530.9525	3681925.3400	5000439.1170	5864402.9620
xylitol	654501.6410	657450.6469	678320.9415	298665.5000	440508.5775	618706.6942
5-deoxy-5-(methylthio)adenosine	2731021	2843049	2631001	397555	576958	585647
guanosine-5-monophosphate	31644175	29383169	32762698	63475745	69081290	77607095
uridine 5-monophosphate	1228226	1179639	1279919	3472964	3654297	4544097
Unidentified_01	667852	503774	691478	847455	1012036	1294021
Unidentified_02	3871892	2507673	2860159	16526784	21532416	29651772
Unidentified_03	1898544	1469469	1691181	2300752	2357821	2473606
Unidentified_04	10059442	8389064	7407525	2864880	4723176	7005910
Unidentified_05	534036	611976	659420	6285391	6906213	8899782
Unidentified_06	9427201	9919212	8469552	30604478	37724103	44658661
Unidentified_07	4118621	2335308	2673643	5588379	7580617	9610814
Unidentified_08	569459	529109	548205	492286	426787	504992
Unidentified_09	1175370	1127782	1262448	1953747	1686602	1886616
Unidentified_10	872574	865073	871272	403826	435012	464220
Unidentified_11	438110	319398	400521	1346161	1653397	2208702
Unidentified_12	155837	536296	487104	1181248	1128942	1477804
Unidentified_13	3618923	3406644	3513440	3126937	2882708	2950750
Unidentified_14	10612748	10141421	11406521	47435112	49258838	50256978
Unidentified_15	642425	759665	962899	131519	166594	301300
Unidentified_16	3742451	3812143	4161443	1582753	1704383	2040883
Unidentified_17	680163	601501	667084	711982	673185	890280
Unidentified_18	3510703	3494722	4093260	3788163	4946855	6167557
Unidentified_19	409948	315735	630997	652759	1031449	1822350
Unidentified_20	640052	392679	759300	1034596	1556482	2608259
Unidentified_21	3149606	3614620	3387828	3510301	3895706	4760973
Unidentified_22	3907777	3521515	3758783	992634	907774	1286177
Unidentified_23	1535597	1590410	1536950	3315486	3990111	4478393
Unidentified_24	581187	515310	726577	649528	833006	887258
ribonic acid ?-lactone	N	N	N	609096	744730	729124
pyrophosphate	10011647	5910492	8783192	N	N	N
MS_METABOLITE_DATA_END
#METABOLITES
METABOLITES_START
metabolite_name	moverz_quant	ri	ri_type	pubchem_id	inchi_key	kegg_id	other_id	other_id_type
1-methyl nicotinamide				10129985			CHEBI:16797	PNNL_ID
2-aminoethanethiol				6058			CHEBI:17141	PNNL_ID
3-hydroxybenzaldehyde				101			CHEBI:16207	PNNL_ID
3-phosphoglyceric acid				724			CHEBI:17794	PNNL_ID
4-guanidinobutyric acid				500			CHEBI:15728	PNNL_ID
4-hydroxyquinoline-2-carboxylic acid				3845			CHEBI:18344	PNNL_ID
5'-deoxy-5'-(methylthio)adenosine				149			CHEBI:17509	PNNL_ID
adenosine							CHEBI:16335	PNNL_ID
adenosine-5-monophosphate							CHEBI:16027	PNNL_ID
alpha ketoglutaric acid							CHEBI:30915	PNNL_ID
arabitol				94154			CHEBI:18333	PNNL_ID
beta- alanine							CHEBI:16958	PNNL_ID
citraconic acid							CHEBI:17626	PNNL_ID
citric acid							CHEBI:30769	PNNL_ID
creatinine							CHEBI:16737	PNNL_ID
Cysteinylglycine				65270			CID65270	PNNL_ID
D-galactose				439353			CHEBI:4139	PNNL_ID
D-glucosaminic acid				235915			CHEBI:17784	PNNL_ID
D-glucose-6-phosphate				439427			CID44134741	PNNL_ID
DL-3-aminoisobutyric acid				64956			CHEBI:27389	PNNL_ID
DL-threo-beta-Hydroxyaspartic acid				443239			CHEBI:10696	PNNL_ID
D-malic acid				92824			CHEBI:30796	PNNL_ID
D-mannitol							CHEBI:16899	PNNL_ID
D-Ribose 5-phosphate				77982			CHEBI:52742	PNNL_ID
D-sorbitol				453			CHEBI:17924	PNNL_ID
D-threitol				169019			CHEBI:48300	PNNL_ID
fructose				5984			CHEBI:48095	PNNL_ID
fumaric acid				444972			CHEBI:18012	PNNL_ID
glucoheptonic acid							CID25588	PNNL_ID
gluconic acid				10690			CHEBI:33198	PNNL_ID
glycerol 1-phosphate				754			CHEBI:14336	PNNL_ID
glycine				750			CHEBI:15428	PNNL_ID
guanosine				6802			CHEBI:16750	PNNL_ID
guanosine-5'-monophosphate				6804			CHEBI:17345	PNNL_ID
hypotaurine				107812			CHEBI:16668	PNNL_ID
hypoxanthine							CHEBI:17368	PNNL_ID
inosine							CHEBI:17596	PNNL_ID
L-alanine				5950			CHEBI:16977	PNNL_ID
L-aspartic acid				5960			CHEBI:17053	PNNL_ID
L-cysteine				5862			CHEBI:17561	PNNL_ID
L-glutamic acid				33032			CHEBI:16015	PNNL_ID
L-leucine				6106			CHEBI:15603	PNNL_ID
L-lysine				5962			CHEBI:18019	PNNL_ID
L-methionine				6137			CHEBI:16643	PNNL_ID
L-ornithine							CHEBI:15729	PNNL_ID
L-serine				5951			CHEBI:17115	PNNL_ID
L-sorbose				6904			CHEBI:13172	PNNL_ID
L-threonine				6288			CHEBI:16857	PNNL_ID
L-tyrosine				6057			CHEBI:17895	PNNL_ID
L-valine				6287			CHEBI:16414	PNNL_ID
maltitol				493591			HMDB02928	PNNL_ID
mucic acid				607			CHEBI:30852	PNNL_ID
oxalic acid				18676629			CHEBI:16995	PNNL_ID
palmitic acid				5326436			CHEBI:15756	PNNL_ID
pantothenic acid				11777341			CHEBI:46905	PNNL_ID
porphine				5481287			CHEBI:8337	PNNL_ID
putrescine				1045			CHEBI:17148	PNNL_ID
pyruvic acid							CHEBI:32816	PNNL_ID
ribonic acid gamma-lactone							HMDB01900	PNNL_ID
spermidine							CHEBI:16610	PNNL_ID
spermine				1103			CHEBI:15746	PNNL_ID
stearic acid							CHEBI:28842	PNNL_ID
tagatose				92092			CHEBI:47693	PNNL_ID
thymine				1135			CHEBI:17821	PNNL_ID
tyramine				5610			CHEBI:15760	PNNL_ID
uridine 5'-monophosphate				45109815			CHEBI:16695	PNNL_ID
xanthine							CHEBI:17712	PNNL_ID
xylitol							CHEBI:17151	PNNL_ID
5-deoxy-5-(methylthio)adenosine							
guanosine-5-monophosphate							
uridine 5-monophosphate							
Unidentified_01							
Unidentified_02							
Unidentified_03							
Unidentified_04							
Unidentified_05							
Unidentified_06							
Unidentified_07							
Unidentified_08							
Unidentified_09							
Unidentified_10							
Unidentified_11							
Unidentified_12							
Unidentified_13							
Unidentified_14							
Unidentified_15							
Unidentified_16							
Unidentified_17							
Unidentified_18							
Unidentified_19							
Unidentified_20							
Unidentified_21							
Unidentified_22							
Unidentified_23							
Unidentified_24							
ribonic acid ?-lactone							
pyrophosphate							
METABOLITES_END
#END