2-Fosfoglicerinska kiselina

2-Fosfoglicerinska kiselina
	3-hidroksi-2-fosfonoksipropanska kiselina
Drugi nazivi	2PG
Identifikacija
CAS registarski broj	2553-59-5
PubChem	59
ChemSpider	58
Jmol-3D slike	Slika 1; Slika 2
SMILES
	C(C(C(=O)O)OP(=O)(O)O)O O=P(O)(O)OC(C(=O)O)CO
InChI
	InChI=1S/C3H7O7P/c4-1-2(3(5)6)10-11(7,8)9/h2,4H,1H2,(H,5,6)(H2,7,8,9) ; Kod: GXIURPTVHJPJLF-UHFFFAOYSA-N InChI=1/C3H7O7P/c4-1-2(3(5)6)10-11(7,8)9/h2,4H,1H2,(H,5,6)(H2,7,8,9); Kod: GXIURPTVHJPJLF-UHFFFAOYAQ
Svojstva
Molekulska formula	C3H7O7P
Molarna masa	186,06 g/mol
	(šta je ovo?) (verifikuj) ; Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje (25 °C, 100 kPa) materijala
	Infobox references

2-Fosfoglicerinska kiselina (2PG, 2-fosfoglicerat) je glicerinska kiselina koja služi kao supstrat u glikolizi.^[4]^[5] Ona se posredstvom enolaze pretvara u fosfoenolpiruvat (PEP), što je predzadnji korak konverzije glukoze u piruvat.

U glikolizi

3-fosfo-D-glicerat	Fosfogliceromutaza	2-fosfo-D-glicerat	Enolaza		fosfoenolpiruvat

				H₂O

				H₂O

	Fosfogliceromutaza		Enolaza

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. Enzim 4.2.1.11 u KEGG bazi podataka metaboličkig puteva. Jedinjenje C00074 u KEGG bazi podataka metaboličkig puteva.

Povezano

3-Fosfoglicerinska kiselina

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
↑ 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.

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

[5] 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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