Deoxyuridine monophosphate

Deoxyuridine monophosphate
Names
	Other names dUMP
Identifiers
CAS Number	964-26-1 ;
3D model (JSmol)	Interactive image;
ChEMBL	ChEMBL211312 ;
ChemSpider	58574 ;
ECHA InfoCard	100.012.290
MeSH	uridine-4'-monophosphate
PubChem CID	688;
CompTox Dashboard (EPA)	DTXSID20242223 ;
	InChI InChI=1S/C9H13N2O8P/c12-5-3-8(11-2-1-7(13)10-9(11)14)19-6(5)4-18-20(15,16)17/h1-2,5-6,8,12H,3-4H2,(H,10,13,14)(H2,15,16,17)/t5-,6+,8+/m0/s1 Key: JSRLJPSBLDHEIO-SHYZEUOFSA-N ; InChI=1/C9H13N2O8P/c12-5-3-8(11-2-1-7(13)10-9(11)14)19-6(5)4-18-20(15,16)17/h1-2,5-6,8,12H,3-4H2,(H,10,13,14)(H2,15,16,17)/t5-,6+,8+/m0/s1 Key: JSRLJPSBLDHEIO-SHYZEUOFBW;
	SMILES O=P(O)(O)OC[C@H]2O[C@@H](N\1C(=O)NC(=O)/C=C/1)C[C@@H]2O;
Properties
Chemical formula	C9H13N2O8P
Molar mass	308.182
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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	Infobox references

Deoxyuridine monophosphate (dUMP), also known as deoxyuridylic acid or deoxyuridylate in its conjugate acid and conjugate base forms, respectively, is a deoxynucleotide.

It is an intermediate in the metabolism of deoxyribonucleotides.

Biosynthesis

Deoxyuridine monophosphate (dUMP) is the deoxygenated form of uridine monophosphate (UMP), and is the precursor to deoxythymine monophosphate (dTMP), a component of DNA nucleotide biosynthesis.[1] By replacing the hydroxyl group at the 2' carbon of ribose with a hydrogen, UMP becomes deoxygenated to dUMP.

The synthesis of deoxyuridine monophosphate (dUMP) is a multi-step process that begins with uridine monophosphate (UMP), the product of pyrimidine biosynthesis.[2] The enzyme nucleoside monophosphate kinase converts UMP and ATP to uridine diphosphate (UDP) and ADP.

In the presence of excess ATP, the enzyme ribonucleotide reductase initiates a chain reaction with UDP, which catalyzes the formation of deoxyuridine diphosphate (dUDP), which is then converted to deoxyuridine triphosphate (dUTP), then deoxyuridine monophosphate (dUMP) via the addition or removal of phosphate groups.[3]

Interactive pathway map

Click on genes, proteins and metabolites below to link to respective articles.[§ 1]

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|{{{bSize}}}px|alt=Fluorouracil (5-FU) Activity edit]]

Fluorouracil (5-FU) Activity edit

The interactive pathway map can be edited at WikiPathways: "FluoropyrimidineActivity_WP1601".

gollark: ++magic py bot.load_extension("duckduckgo")

gollark: Oh right.

gollark: Hmm. That probably should have done something.

gollark: ++search bee neuron data

gollark: It is actually down, though.

Notes

Berg, J. M.; Tymoczko, J. L.; Stryer, L. (2002). Biochemistry (5th ed.). New York: W H Freeman. ISBN 978-1-4641-2610-9.
Shambaugh, G. E. (June 1979). "Pyrimidine biosynthesis". The American Journal of Clinical Nutrition. 32 (6): 1290–1297. doi:10.1093/ajcn/32.6.1290. PMID 35970.
Garrett, Reginald H.; Grisham, Charles M. (2013). Biochemistry (6th ed.). Belmont, CA: Brooks/Cole, Cengage Learning. p. 949. ISBN 9781133106296.

This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.

[WikiPathways-4] The interactive pathway map can be edited at WikiPathways: "FluoropyrimidineActivity_WP1601".

[1] Berg, J. M.; Tymoczko, J. L.; Stryer, L. (2002). Biochemistry (5th ed.). New York: W H Freeman. ISBN 978-1-4641-2610-9.

[2] Shambaugh, G. E. (June 1979). "Pyrimidine biosynthesis". The American Journal of Clinical Nutrition. 32 (6): 1290–1297. doi:10.1093/ajcn/32.6.1290. PMID 35970.

[:2-3] Garrett, Reginald H.; Grisham, Charles M. (2013). Biochemistry (6th ed.). Belmont, CA: Brooks/Cole, Cengage Learning. p. 949. ISBN 9781133106296.

Deoxyuridine monophosphate

Biosynthesis

Interactive pathway map

See also

Notes