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adenylyl sulfate-ammonia adenylyltransferase

forms adenosine 5'-phosphoramidate

Also Known As:

AS-AAT; adenylyl sulphate-ammonia adenylyltransferase

Networked: 9 relevant articles (0 outcomes, 0 trials/studies)

Bio-Agent Context: Research Results

Enzymes and Coenzymes: 1
- Enzymes: 152586
  - Transferases: 6589
    - Phosphotransferases: 42769
      - Nucleotidyltransferases: 29
        adenylyl sulfate-ammonia adenylyltransferase: 9

Experts

1.	Aytug, Nilüfer: 1 article (12/2017)
2.	Cerón, Jose Joaquin: 1 article (12/2017)
3.	Cihan, Hüseyin: 1 article (12/2017)
4.	Escribano, Damián: 1 article (12/2017)
5.	Kocaturk, Meric: 1 article (12/2017)
6.	Levent, Pinar: 1 article (12/2017)
7.	Martínez-Subiela, Silvia: 1 article (12/2017)
8.	Tvarijonaviciute, Asta: 1 article (12/2017)
9.	Yilmaz, Zeki: 1 article (12/2017)
10.	Jorgensen, Marda: 1 article (05/2011)

Related Diseases

1.	Liver Diseases (Liver Disease) 05/01/2011 - "AT-MSC-based gene therapy presents a novel approach for the treatment of liver diseases, such as AAT deficiency." 03/01/1989 - "As AAT is also synthesised in the liver, we investigated whether liver disease itself may result in low AAT levels. "
2.	Ehrlichiosis 12/01/2017 - "It can be concluded that there are significant changes in the serum proteome of dogs with ehrlichiosis with modifications in proteins related with the acute phase response such as Hp, albumin and AGP, with vitamin A transport such as RBP-4, with inhibitors of serine proteases and anti-inflammatory proteins such as AAT, and vitamin D metabolism and actin scavengers such as VDBP."
3.	Prostatic Neoplasms (Prostate Cancer) 06/01/1997 - "Finasteride and flutamide were safe and well tolerated as AAT for advanced prostate cancer. "
4.	Pneumonia (Pneumonitis) 12/01/2023 - "Our results indicate that inhibition of sCX3CL1 as well as AAT augmentation may be effective approaches to decrease excessive monocyte lung recruitment during acute and chronic inflammatory states.NEW & NOTEWORTHY Our novel findings that AAT and other inhibitors of TACE, the sheddase that controls full-length fractalkine (CX3CL1) endothelial expression, may provide fine-tuning of the CX3CL1-CX3CR1 axis specifically involved in endothelial-monocyte cross talk and leukocyte recruitment to the alveolar space, suggests that AAT and inhibitors of sCX3CL1 signaling may be harnessed to reduce lung inflammation."
5.	Neoplasms (Cancer) 09/01/2004 - "As AAT does not completely eliminate circulating androgens, sufficient concentrations of dihydrotestosterone may accumulate in tumor cells to maintain AR signaling, especially in the context of upregulated receptor levels or increased sensitivity of the AR for activation. "

Related Drugs and Biologics

1.	Proteins (Proteins, Gene)
2.	Serine Proteases (Serine Protease)
3.	Chemokine CX3CL1
4.	Proteome
5.	Finasteride (Propecia)
6.	Vitamin D
7.	Vitamin A (Retinol)
8.	Dihydrotestosterone (Androstanolone)
9.	Flutamide (Eulexin)
10.	Androgens