Fingerprint Fingerprint is based on mining the text of the person's scientific documents to create an index of weighted terms, which defines the key subjects of each individual researcher.

  • 10 Similar Profiles
Peptidyl-Dipeptidase A Medicine & Life Sciences
Clostridium difficile Medicine & Life Sciences
Catalytic Domain Medicine & Life Sciences
Neurotoxins Medicine & Life Sciences
Proteins Medicine & Life Sciences
Angiotensin-Converting Enzyme Inhibitors Medicine & Life Sciences
Pancreatic Ribonuclease Medicine & Life Sciences
Glycosyltransferases Medicine & Life Sciences

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Projects 2002 2020

Research Output 2001 2018

A comparative bioinformatic analysis of C9orf72

Iyer, S., Acharya, K. R. & Subramanian, V. 19 Feb 2018 In : PeerJ. 6, p. e4391

Research output: Contribution to journalArticle

Open Access
Saimiriine herpesvirus 2
Supravalvular Aortic Stenosis
Cyclic AMP Receptor Protein
Frontotemporal Dementia
Submandibular Gland

Crystal structures of sampatrilat and sampatrilat-Asp in complex with human ACE: a molecular basis for domain-selectivity

Cozier, G. E., Schwager, S. L., Sharma, R. K., Chibale, K., Sturrock, E. D. & Acharya, K. R. 24 Feb 2018 In : FEBS Journal.

Research output: Contribution to journalArticle

Open Access
Peptidyl-Dipeptidase A
Hydrophobic and Hydrophilic Interactions
Angiotensin-Converting Enzyme Inhibitors
Catalytic Domain

High resolution crystal structures of the receptor-binding domain of neurotoxin serotypes A and FA

Davies, J. R., Hackett, G. S., Liu, S. M. & Acharya, K. R. 21 Mar 2018 In : PeerJ. 6, e4552

Research output: Contribution to journalArticle

Open Access
Cytochrome c Group
botulinum toxin
1 Citations

Investigation into the Mechanism of Homo- and Heterodimerization of Angiotensin-Converting Enzyme

Abrie, J. A., Moolman, W. J. A., Cozier, G. E., Schwager, S. L. U., Acharya, K. R. & Sturrock, E. D. 1 Apr 2018 In : Molecular Pharmacology. 93, 4, p. 344-354

Research output: Contribution to journalArticle

Open Access
Peptidyl-Dipeptidase A
Renin-Angiotensin System
Amyotrophic Lateral Sclerosis
Motor Neuron Disease
Missense Mutation