Peter D'Eustachio

 ORCID
https://orcid.org/0000-0002-5494-626X
Project
Reactome
Affiliation
NYU School of Medicine, Department of Biochemistry
Authored Pathways (15/156)
Date Identifier Pathway Reference
2021-12-13 R-HSA-9759774 Diseases of mitochondrial beta oxidation BibTex
2021-07-09 R-HSA-9735804 Diseases of nucleotide metabolism BibTex
2021-07-02 R-HSA-9735786 Nucleotide catabolism defects BibTex
2021-07-02 R-HSA-9735763 Defective PNP disrupts phosphorolysis of (deoxy)guanosine and (deoxy)inosine BibTex
2021-07-02 R-HSA-9734207 Nucleotide salvage defects BibTex
2021-07-02 R-HSA-9734281 Defective HPRT1 disrupts guanine and hypoxanthine salvage BibTex
2021-07-02 R-HSA-9734735 Defective ADA disrupts (deoxy)adenosine deamination BibTex
2021-07-02 R-HSA-9734195 Defective APRT disrupts adenine salvage BibTex
2020-07-22 R-HSA-9694516 SARS-CoV-2 Infection BibTex
2020-01-06 R-HSA-9673163 Oleoyl-phe metabolism BibTex
2018-11-24 R-HSA-9629569 Protein hydroxylation BibTex
2017-01-13 R-HSA-8955332 Carboxyterminal post-translational modifications of tubulin BibTex
2016-12-30 R-HSA-8953897 Cellular responses to stimuli BibTex
2016-12-29 R-HSA-8953854 Metabolism of RNA BibTex
2015-12-10 R-HSA-8848584 Wax and plasmalogen biosynthesis BibTex
Show all authored pathways...
Authored Reactions (15/923)
Date Identifier Reaction Reference
2024-07-11 R-MMU-9915559 Slc27a1 transports arachidonate across the ER membrane BibTex
2024-06-20 R-HSA-9914143 SLC27A2-mediated ligation of peroxisomal fatty acid and CoASH BibTex
2024-06-10 R-HSA-9912889 SLC35D2 exchanges UDP-GlcA for UMP BibTex
2024-05-29 R-HSA-9911362 CPT1B transfers PALM to CAR BibTex
2024-04-29 R-HSA-9909159 HK1 phosphorylates Mannose to Man6P BibTex
2023-12-20 R-HSA-9856548 MLXIPL:MLX binds ACACB gene promoter BibTex
2023-12-20 R-HSA-9856605 Transcriptional activation of ACACB by ChREBP:MLX BibTex
2023-12-20 R-HSA-9856546 MLXIPL:MLX binds FASN gene promoter BibTex
2023-12-20 R-HSA-9856550 MLXIPL:MLX binds ACACA gene promoter BibTex
2023-12-20 R-HSA-9856549 MLXIPL:MLX binds ACLY gene promoter BibTex
2023-12-20 R-HSA-9856539 MLXIPL:MLX binds PKLR gene promoter BibTex
2023-12-20 R-HSA-9856604 MLXIPL:MLX binds AGPAT1 gene promoter BibTex
2023-06-13 R-HSA-9837419 PANK4 hydrolyzes PPANT to pantetheine BibTex
2023-06-13 R-MMU-9837342 Nudt8 hydrolyzes CoA-SH to PPANT BibTex
2023-06-13 R-HSA-9837354 NUDT8 hydrolyzes CoA-SH to PPANT BibTex
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Reviewed Pathways (15/354)
Date Identifier Pathway Reference
2024-08-21 R-HSA-9757110 Prednisone ADME BibTex
2024-08-21 R-HSA-427975 Proton/oligopeptide cotransporters BibTex
2024-08-18 R-HSA-5668914 Diseases of metabolism BibTex
2024-08-18 R-HSA-9865118 Diseases of branched-chain amino acid catabolism BibTex
2024-08-18 R-HSA-9915355 Beta-ketothiolase deficiency BibTex
2024-08-18 R-HSA-9865114 Maple Syrup Urine Disease BibTex
2024-08-18 R-HSA-9865113 Loss-of-function mutations in DBT cause MSUD2 BibTex
2024-08-18 R-HSA-9912529 H139Hfs13* PPM1K causes a mild variant of MSUD BibTex
2024-08-18 R-HSA-9907570 Loss-of-function mutations in DLD cause MSUD3/DLDD BibTex
2024-08-18 R-HSA-9865125 Loss-of-function mutations in BCKDHA or BCKDHB cause MSUD BibTex
2024-08-18 R-HSA-9909438 3-Methylcrotonyl-CoA carboxylase deficiency BibTex
2024-08-18 R-HSA-9916720 Mitochondrial short-chain enoyl-CoA hydratase deficiency 1 BibTex
2024-08-18 R-HSA-9912481 Branched-chain ketoacid dehydrogenase kinase deficiency BibTex
2024-08-18 R-HSA-9916722 3-hydroxyisobutyryl-CoA hydrolase deficiency BibTex
2024-08-18 R-HSA-9914274 3-methylglutaconic aciduria BibTex
Show all reviewed pathways...
Reviewed Reactions (15/2,028)
Date Identifier Reaction Reference
2024-08-21 R-HSA-508308 beta-methylglutaconyl-CoA + ADP + orthophosphate <=> beta-methylcrotonyl-CoA + ATP + CO2 (MCCA) BibTex
2024-08-21 R-HSA-70745 isovaleryl-CoA + FAD => beta-methylcrotonyl-CoA + FADH2 BibTex
2024-08-19 R-HSA-8863761 UXS1 tetramer decarboxylates UDP-glucuronate to UDP-xylose BibTex
2024-08-18 R-HSA-9915356 ACAT1 mutants don't synthesize propionyl-CoA or acetyl-CoA BibTex
2024-08-18 R-HSA-9865115 DBT loss-of-function mutants don't synthesize BCAA-CoA BibTex
2024-08-18 R-HSA-9912527 H139Hfs13* PPM1K does not dephosphorylate BCKDH BibTex
2024-08-18 R-HSA-9907572 Loss-of-function DLD mutants don't dehydrogenate dihydrolipoyl DBT BibTex
2024-08-18 R-HSA-9865121 BCKDHA or BCKDHB loss-of-function mutants don't synthesize BCAA-CoA BibTex
2024-08-18 R-HSA-9909466 MCCC mutants don't synthesize beta-methylglutaconyl-CoA BibTex
2024-08-18 R-HSA-9916717 ECHS1 mutants don't synthesize beta-hydroxyisobutyryl-CoA BibTex
2024-08-18 R-HSA-9912480 BCKDK loss-of-function mutations do not phosphorylate BCKDH BibTex
2024-08-18 R-HSA-9916727 HIBCH mutants don't synthesize beta-hydroxyisobutyrate BibTex
2024-08-18 R-HSA-9914271 AUH mutants don't synthesize 3-hydroxy-methylglutaryl-CoA BibTex
2024-08-18 R-HSA-9914837 IVD mutants don't synthesize beta-methylcrotonyl-CoA BibTex
2024-05-28 R-HSA-2534087 NMT1/2 transfer MYS to GNAT1 BibTex
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