2,5-diaminopentanoic acid

2,5-diaminopentanoic acid is a lipid of Fatty Acyls (FA) class. The involved functions are known as Vasodilation, Intestinal Absorption and Pinocytosis. 2,5-diaminopentanoic acid often locates in Mitochondria, Microfilaments, NADH dehydrogenase complex and respiratory chain complex III location sensu Eukarya. The associated genes with 2,5-diaminopentanoic acid are GAPDH gene and iberiotoxin.

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Introduction

To understand associated biological information of 2,5-diaminopentanoic acid, we collected biological information of abnormalities, associated pathways, cellular/molecular locations, biological functions, related genes/proteins, lipids and common seen animal/experimental models with organized paragraphs from literatures.

What diseases are associated with 2,5-diaminopentanoic acid?

There are no associated biomedical information in the current reference collection.

Possible diseases from mapped MeSH terms on references

We collected disease MeSH terms mapped to the references associated with 2,5-diaminopentanoic acid

MeSH term MeSH ID Detail
Retinal Dysplasia D015792 1 associated lipids
Lip Diseases D008047 1 associated lipids
Argininosuccinic Aciduria D056807 1 associated lipids
Hernia D006547 1 associated lipids
Hyperopia D006956 1 associated lipids
Choroideremia D015794 1 associated lipids
Acute Chest Syndrome D056586 1 associated lipids
Heart Failure, Diastolic D054144 1 associated lipids
Paraparesis, Spastic D020336 1 associated lipids
Opsoclonus-Myoclonus Syndrome D053578 1 associated lipids
Lens Diseases D007905 1 associated lipids
Chorioretinitis D002825 1 associated lipids
Hyperargininemia D020162 1 associated lipids
Myotonia Congenita D009224 1 associated lipids
Laurence-Moon Syndrome D007849 1 associated lipids
Central Nervous System Bacterial Infections D020806 1 associated lipids
Ornithine Carbamoyltransferase Deficiency Disease D020163 2 associated lipids
Amyloid Neuropathies, Familial D028227 2 associated lipids
Gyrate Atrophy D015799 2 associated lipids
Myopia D009216 2 associated lipids
Urea Cycle Disorders, Inborn D056806 2 associated lipids
Spastic Paraplegia, Hereditary D015419 2 associated lipids
Scotoma D012607 2 associated lipids
Papilledema D010211 2 associated lipids
Uveal Diseases D014603 2 associated lipids
Pressure Ulcer D003668 2 associated lipids
alpha-Thalassemia D017085 2 associated lipids
Cystinuria D003555 2 associated lipids
Proteus Infections D011512 2 associated lipids
Aortic Aneurysm, Thoracic D017545 2 associated lipids
Coma D003128 2 associated lipids
Malaria, Vivax D016780 2 associated lipids
Craniopharyngioma D003397 2 associated lipids
Colonic Polyps D003111 3 associated lipids
Cockayne Syndrome D003057 3 associated lipids
Macular Edema D008269 3 associated lipids
HIV Wasting Syndrome D019247 3 associated lipids
Spinocerebellar Degenerations D013132 3 associated lipids
Colitis, Ischemic D017091 3 associated lipids
Melioidosis D008554 4 associated lipids
Retinal Diseases D012164 4 associated lipids
Acinetobacter Infections D000151 4 associated lipids
Yersinia Infections D015009 4 associated lipids
Intracranial Hypertension D019586 4 associated lipids
Histiocytosis, Non-Langerhans-Cell D015616 4 associated lipids
Urogenital Neoplasms D014565 4 associated lipids
Foot Ulcer D016523 4 associated lipids
Language Development Disorders D007805 4 associated lipids
Hyperammonemia D022124 5 associated lipids
Fatigue Syndrome, Chronic D015673 5 associated lipids
Protein Deficiency D011488 5 associated lipids
Purine-Pyrimidine Metabolism, Inborn Errors D011686 5 associated lipids
Trypanosomiasis D014352 5 associated lipids
Growth Disorders D006130 5 associated lipids
Myotonic Dystrophy D009223 5 associated lipids
Leishmaniasis, Cutaneous D016773 6 associated lipids
Infection D007239 6 associated lipids
Leukemia, Myelomonocytic, Acute D015479 6 associated lipids
Acromegaly D000172 6 associated lipids
Dysentery, Bacillary D004405 6 associated lipids
Malnutrition D044342 6 associated lipids
Atrophy D001284 7 associated lipids
Adenoma, Islet Cell D007516 7 associated lipids
Rhabdomyosarcoma D012208 7 associated lipids
Trichostrongyloidiasis D014252 7 associated lipids
Femoral Fractures D005264 7 associated lipids
Hypopituitarism D007018 7 associated lipids
Arthralgia D018771 8 associated lipids
Irritable Bowel Syndrome D043183 8 associated lipids
Poisoning D011041 9 associated lipids
Hepatic Encephalopathy D006501 9 associated lipids
Retinal Degeneration D012162 9 associated lipids
Fetal Growth Retardation D005317 9 associated lipids
Brain Diseases, Metabolic, Inborn D020739 10 associated lipids
Hearing Disorders D006311 10 associated lipids
Vision Disorders D014786 10 associated lipids
Infertility, Male D007248 11 associated lipids
Uveitis, Anterior D014606 11 associated lipids
Liver Failure, Acute D017114 11 associated lipids
Learning Disorders D007859 11 associated lipids
Radiation Injuries, Experimental D011833 11 associated lipids
Carcinoma, Renal Cell D002292 12 associated lipids
Eye Diseases D005128 12 associated lipids
Acute-Phase Reaction D000210 12 associated lipids
Metabolic Diseases D008659 12 associated lipids
Critical Illness D016638 13 associated lipids
Reye Syndrome D012202 14 associated lipids
Brain Neoplasms D001932 15 associated lipids
Tremor D014202 15 associated lipids
Synovitis D013585 15 associated lipids
Amino Acid Metabolism, Inborn Errors D000592 16 associated lipids
Malabsorption Syndromes D008286 16 associated lipids
Ulcer D014456 16 associated lipids
Swine Diseases D013553 16 associated lipids
Choline Deficiency D002796 16 associated lipids
Brain Infarction D020520 17 associated lipids
Cough D003371 19 associated lipids
Heart Defects, Congenital D006330 20 associated lipids
Wounds and Injuries D014947 20 associated lipids
Prostatic Hyperplasia D011470 20 associated lipids
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PubChem Associated disorders and diseases

What pathways are associated with 2,5-diaminopentanoic acid

There are no associated biomedical information in the current reference collection.

PubChem Biomolecular Interactions and Pathways

Link to PubChem Biomolecular Interactions and Pathways

What cellular locations are associated with 2,5-diaminopentanoic acid?

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What functions are associated with 2,5-diaminopentanoic acid?


Related references are published most in these journals:

Function Cross reference Weighted score Related literatures

What lipids are associated with 2,5-diaminopentanoic acid?

There are no associated biomedical information in the current reference collection.

What genes are associated with 2,5-diaminopentanoic acid?

Related references are published most in these journals:


Gene Cross reference Weighted score Related literatures

What common seen animal models are associated with 2,5-diaminopentanoic acid?

There are no associated biomedical information in the current reference collection.

NCBI Entrez Crosslinks

All references with 2,5-diaminopentanoic acid

Download all related citations
Per page 10 20 50 100 | Total 4676
Authors Title Published Journal PubMed Link
Macedo JP et al. Ornithine uptake and the modulation of drug sensitivity in Trypanosoma brucei. 2017 FASEB J. pmid:28679527
Aguilera S et al. Temperature-mediated biosynthesis of the phytotoxin phaseolotoxin by Pseudomonas syringae pv. phaseolicola depends on the autoregulated expression of the phtABC genes. 2017 PLoS ONE pmid:28570637
Ye Q et al. The value of grip test, lysophosphatidlycholines, glycerophosphocholine, ornithine, glucuronic acid decrement in assessment of nutritional and metabolic characteristics in hepatitis B cirrhosis. 2017 PLoS ONE pmid:28384211
Noens EE and Lolkema JS Convergent evolution of the arginine deiminase pathway: the ArcD and ArcE arginine/ornithine exchangers. 2017 Microbiologyopen pmid:27804281
Biron BM et al. Cl-Amidine Prevents Histone 3 Citrullination and Neutrophil Extracellular Trap Formation, and Improves Survival in a Murine Sepsis Model. 2017 J Innate Immun pmid:27622642
Falone S et al. Regular and Moderate Exercise Counteracts the Decline of Antioxidant Protection but Not Methylglyoxal-Dependent Glycative Burden in the Ovary of Reproductively Aging Mice. 2016 Oxid Med Cell Longev pmid:28116035
Qadri SK et al. Milder Form of Urea Cycle Defect Revisited: Report and Review of Hyperornithinaemia-Hyperammonaemia-Homocitrullinuria (HHH) Syndrome Diagnosed in a Teenage Girl Presenting with Recurrent Encephalopathy. 2016 Ann. Acad. Med. Singap. pmid:28062886
Papadaki G et al. Neutrophil extracellular traps exacerbate Th1-mediated autoimmune responses in rheumatoid arthritis by promoting DC maturation. 2016 Eur. J. Immunol. pmid:27585946
Koseki J et al. A Trans-omics Mathematical Analysis Reveals Novel Functions of the Ornithine Metabolic Pathway in Cancer Stem Cells. 2016 Sci Rep pmid:26864636
Kobylarz MJ et al. Deciphering the Substrate Specificity of SbnA, the Enzyme Catalyzing the First Step in Staphyloferrin B Biosynthesis. 2016 Biochemistry pmid:26794841