Biosynthetic Pathways

"Biosynthetic Pathways" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

Sets of enzymatic reactions occurring in organisms and that form biochemicals by making new covalent bonds.

Descriptor ID	D053898
MeSH Number(s)	G02.111.098 G03.493.100
Concept/Terms	Biosynthetic Pathways Biosynthetic Pathways Biosynthetic Pathway Pathway, Biosynthetic Pathways, Biosynthetic

Below are MeSH descriptors whose meaning is more general than "Biosynthetic Pathways".

Biological Sciences [G]
Chemical Phenomena [G02]
Biochemical Phenomena [G02.111]
Biosynthetic Pathways [G02.111.098]
Metabolism [G03]
Metabolic Networks and Pathways [G03.493]
Biosynthetic Pathways [G03.493.100]

Below are MeSH descriptors whose meaning is related to "Biosynthetic Pathways".

Below are MeSH descriptors whose meaning is more specific than "Biosynthetic Pathways".

publications

Timeline | Most Recent

This graph shows the total number of publications written about "Biosynthetic Pathways" by people in this website by year, and whether "Biosynthetic Pathways" was a major or minor topic of these publications.

Bar chart showing 10 publications over 7 distinct years, with a maximum of 2 publications in 2013 and 2014 and 2021

To see the data from this visualization as text, click here.

Year	Major Topic	Minor Topic	Total
2010	0	1	1
2011	0	1	1
2013	1	1	2
2014	0	2	2
2015	0	1	1
2018	0	1	1
2021	1	1	2

Below are the most recent publications written about "Biosynthetic Pathways" by people in Profiles.

Davis EW, Okrent RA, Manning VA, Trippe KM. Unexpected distribution of the 4-formylaminooxyvinylglycine (FVG) biosynthetic pathway in Pseudomonas and beyond. PLoS One. 2021; 16(4):e0247348.

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Seale LA, Ogawa-Wong AN, Watanabe LM, Khadka VS, Menor M, Torres DJ, Carlson BA, Hatfield DL, Berry MJ. Adaptive Thermogenesis in a Mouse Model Lacking Selenoprotein Biosynthesis in Brown Adipocytes. Int J Mol Sci. 2021 Jan 09; 22(2).

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Zhou W, Debnath A, Jennings G, Hahn HJ, Vanderloop BH, Chaudhuri M, Nes WD, Podust LM. Enzymatic chokepoints and synergistic drug targets in the sterol biosynthesis pathway of Naegleria fowleri. PLoS Pathog. 2018 09; 14(9):e1007245.

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Lin CJ, Smibert P, Zhao X, Hu JF, Ramroop J, Kellner SM, Benton MA, Govind S, Dedon PC, Sternglanz R, Lai EC. An extensive allelic series of Drosophila kae1 mutants reveals diverse and tissue-specific requirements for t6A biogenesis. RNA. 2015 Dec; 21(12):2103-18.

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Fox DT, Schmidt EN, Tian H, Dhungana S, Valentine MC, Warrington NV, Phillips PD, Finney KB, Cope EK, Leid JG, Testa CA, Koppisch AT. Sub-inhibitory fosmidomycin exposures elicits oxidative stress in Salmonella enterica serovar Typhimurium LT2. PLoS One. 2014; 9(4):e95271.

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Christie AE, Fontanilla TM, Roncalli V, Cieslak MC, Lenz PH. Diffusible gas transmitter signaling in the copepod crustacean Calanus finmarchicus: identification of the biosynthetic enzymes of nitric oxide (NO), carbon monoxide (CO) and hydrogen sulfide (H2S) using a de novo assembled transcriptome. Gen Comp Endocrinol. 2014 Jun 01; 202:76-86.

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Quintana AM, Picchione F, Klein Geltink RI, Taylor MR, Grosveld GC. Zebrafish ETV7 regulates red blood cell development through the cholesterol synthesis pathway. Dis Model Mech. 2014 Feb; 7(2):265-70.

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Christie AE, Fontanilla TM, Roncalli V, Cieslak MC, Lenz PH. Identification and developmental expression of the enzymes responsible for dopamine, histamine, octopamine and serotonin biosynthesis in the copepod crustacean Calanus finmarchicus. Gen Comp Endocrinol. 2014 Jan 01; 195:28-39.

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Ouellet H, Johnston JB, de Montellano PR. Cholesterol catabolism as a therapeutic target in Mycobacterium tuberculosis. Trends Microbiol. 2011 Nov; 19(11):530-9.

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Liang D, Meyer L, Chang DW, Lin J, Pu X, Ye Y, Gu J, Wu X, Lu K. Genetic variants in MicroRNA biosynthesis pathways and binding sites modify ovarian cancer risk, survival, and treatment response. Cancer Res. 2010 Dec 01; 70(23):9765-76.

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