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3-Fosfoglicerinska kiselina
	(2R)-2-Hidroksi-3-fosfonooksipropanska kiselina
Identifikacija
CAS registarski broj	820-11-1
PubChem	439183
ChemSpider	388326
ChEBI	17794
ChEMBL	CHEMBL1160563
Jmol-3D slike	Slika 1
SMILES
	C([C@H](C(=O)O)O)OP(=O)(O)O
InChI
	InChI=1S/C3H7O7P/c4-2(3(5)6)1-10-11(7,8)9/h2,4H,1H2,(H,5,6)(H2,7,8,9)/t2-/m1/s1 ; Kod: OSJPPGNTCRNQQC-UWTATZPHSA-N
Svojstva
Molekulska formula	C3H7O7P
Molarna masa	186.06 g mol−1
	(šta je ovo?) (verifikuj) ; Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje (25 °C, 100 kPa) materijala
	Infobox references

3-Fosfoglicerinska kiselina (3PG, glicerat 3-fosfat, GP) je biohemijski značajan trougljenični molekul koji je metabolički intermedijer u glikolizi^[5] i Kalvinovom ciklusu.^[6] Ovo jedinjenje se često naziva PGA u kontekstu Kalvinovog ciklusa. 3-Fosfoglicerat je rezultant razlaganja šestougljeničnog intermedijera koji je veoma nestabilan. Dva molekula 3-fosfoglicerata se formiraju za svaki molekul CO₂.

Glikoliza

1,3-bisfosfo-D-glicerat	3-fosfoglicerat kinaza		3-fosfo-D-glicerat	Bisfosfogliceratna mutaza	2-fosfo-D-glicerat

	ADP	ATP

	ADP	ATP

	3-fosfoglicerat kinaza			Fosfogliceromutaza

Jedinjenje C00236 u KEGG bazi podataka metaboličkig puteva. Enzim 2.7.2.3 u KEGG bazi podataka metaboličkig puteva. Jedinjenje C00197 u KEGG bazi podataka metaboličkig puteva. Enzim 5.4.2.1 u KEGG bazi podataka metaboličkig puteva. Jedinjenje C00631 u KEGG bazi podataka metaboličkig puteva.

Reference

↑ Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today 15 (23-24): 1052-7. DOI:10.1016/j.drudis.2010.10.003. PMID 20970519. edit
↑ Evan E. Bolton, Yanli Wang, Paul A. Thiessen, Stephen H. Bryant (2008). „Chapter 12 PubChem: Integrated Platform of Small Molecules and Biological Activities”. Annual Reports in Computational Chemistry 4: 217-241. DOI:10.1016/S1574-1400(08)00012-1.
↑ Hettne KM, Williams AJ, van Mulligen EM, Kleinjans J, Tkachenko V, Kors JA. (2010). „Automatic vs. manual curation of a multi-source chemical dictionary: the impact on text mining”. J Cheminform 2 (1): 3. DOI:10.1186/1758-2946-2-3. PMID 20331846. edit
↑ Gaulton A, Bellis LJ, Bento AP, Chambers J, Davies M, Hersey A, Light Y, McGlinchey S, Michalovich D, Al-Lazikani B, Overington JP. (2012). „ChEMBL: a large-scale bioactivity database for drug discovery”. Nucleic Acids Res 40 (Database issue): D1100-7. DOI:10.1093/nar/gkr777. PMID 21948594. edit
↑ Bailey, Regina. „10 Steps of Glycolysis”.
↑ Campbell, Neil A.; Brad Williamson; Robin J. Heyden (2006). Biology: Exploring Life. Boston, Massachusetts: Pearson Prentice Hall. ISBN 0-13-250882-6.

Povezano

2-Fosfoglicerinska kiselina

[1] Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today 15 (23-24): 1052-7. DOI:10.1016/j.drudis.2010.10.003. PMID 20970519. edit

[2] Evan E. Bolton, Yanli Wang, Paul A. Thiessen, Stephen H. Bryant (2008). „Chapter 12 PubChem: Integrated Platform of Small Molecules and Biological Activities”. Annual Reports in Computational Chemistry 4: 217-241. DOI:10.1016/S1574-1400(08)00012-1.

[3] Hettne KM, Williams AJ, van Mulligen EM, Kleinjans J, Tkachenko V, Kors JA. (2010). „Automatic vs. manual curation of a multi-source chemical dictionary: the impact on text mining”. J Cheminform 2 (1): 3. DOI:10.1186/1758-2946-2-3. PMID 20331846. edit

[4] Gaulton A, Bellis LJ, Bento AP, Chambers J, Davies M, Hersey A, Light Y, McGlinchey S, Michalovich D, Al-Lazikani B, Overington JP. (2012). „ChEMBL: a large-scale bioactivity database for drug discovery”. Nucleic Acids Res 40 (Database issue): D1100-7. DOI:10.1093/nar/gkr777. PMID 21948594. edit

[5] Bailey, Regina. „10 Steps of Glycolysis”.

[6] Campbell, Neil A.; Brad Williamson; Robin J. Heyden (2006). Biology: Exploring Life. Boston, Massachusetts: Pearson Prentice Hall. ISBN 0-13-250882-6.

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