His scientific interests lie mostly in Biochemistry, Collagenase, Molecular biology, Peptide and Enzyme. His work in Biochemistry covers topics such as Signal peptide which are related to areas like HT1080. Gregory A. Grant interconnects Type I collagen, Enzyme inhibitor, Trypsin and MMP1 in the investigation of issues within Collagenase.
His study in Molecular biology is interdisciplinary in nature, drawing from both Cell culture, Interstitial collagenase and Metalloproteinase. His work carried out in the field of Peptide brings together such families of science as Protein structure, Binding domain and Thrombospondin. His Enzyme research is multidisciplinary, incorporating perspectives in Protein primary structure and Primary.
Biochemistry, Stereochemistry, Enzyme, Serine and Allosteric regulation are his primary areas of study. His research links Molecular biology with Biochemistry. His Molecular biology research incorporates themes from Secretion, Cell culture, Monoclonal antibody and Metalloproteinase.
His work in Stereochemistry addresses subjects such as Active site, which are connected to disciplines such as Dehydratase. The concepts of his Serine study are interwoven with issues in Protein structure, Conformational change, Cooperativity and Binding site. His Allosteric enzyme study in the realm of Allosteric regulation connects with subjects such as Legionella pneumophila.
Gregory A. Grant focuses on Biochemistry, Enzyme, Dehydratase, Allosteric regulation and ACT domain. Gregory A. Grant integrates many fields, such as Biochemistry and Legionella pneumophila, in his works. His Dehydratase research incorporates elements of L serine, Cysteine, Stereochemistry and Active site.
In his study, Substrate concentration and Kinetic inhibition is inextricably linked to Enzyme activator, which falls within the broad field of Stereochemistry. His study looks at the intersection of Active site and topics like Protein structure with Peptide, Crystallography and Protein quaternary structure. His Allosteric regulation research includes themes of Plasma protein binding and Neuroscience.
His primary areas of study are Biochemistry, Allosteric regulation, ACT domain, Enzyme and Legionella pneumophila. He combines topics linked to Stereochemistry with his work on Biochemistry. His studies in Stereochemistry integrate themes in fields like Activator, Cofactor and Phosphate.
His Protein structure research integrates issues from Cooperativity, Serine, Active site, Protein quaternary structure and Tetramer. Gregory A. Grant has included themes like Phosphoserine and Biosynthesis in his D-3-Phosphoglycerate Dehydrogenase study. His biological study spans a wide range of topics, including Allosteric enzyme, Structural motif, Function and Effector.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Mechanism Of Cell Surface Activation Of 72-kDa Type IV Collagenase ISOLATION OF THE ACTIVATED FORM OF THE MEMBRANE METALLOPROTEASE
Alex Y. Strongin;Ivan Collier;Gregory Bannikov;Barry L. Marmer.
Journal of Biological Chemistry (1995)
SV40-transformed human lung fibroblasts secrete a 92-kDa type IV collagenase which is identical to that secreted by normal human macrophages.
S M Wilhelm;I E Collier;B L Marmer;A Z Eisen.
Journal of Biological Chemistry (1989)
H-ras oncogene-transformed human bronchial epithelial cells (TBE-1) secrete a single metalloprotease capable of degrading basement membrane collagen.
I E Collier;S M Wilhelm;A Z Eisen;B L Marmer.
Journal of Biological Chemistry (1988)
Human fibroblast collagenase. Complete primary structure and homology to an oncogene transformation-induced rat protein.
G I Goldberg;S M Wilhelm;A Kronberger;E A Bauer.
Journal of Biological Chemistry (1986)
Human 72-kilodalton type IV collagenase forms a complex with a tissue inhibitor of metalloproteases designated TIMP-2
Gregory I. Goldberg;Barry L. Marmer;Gregory A. Grant;Arthur Z. Eisen.
Proceedings of the National Academy of Sciences of the United States of America (1989)
Tissue cooperation in a proteolytic cascade activating human interstitial collagenase.
Chengshi He;Scott M. Wilhelm;Alice P. Pentland;Barry L. Marmer.
Proceedings of the National Academy of Sciences of the United States of America (1989)
Modification of the NADH of the Isoniazid Target (InhA) from Mycobacterium tuberculosis
Denise A. Rozwarski;Gregory A. Grant;Derek H. R. Barton;William R. Jacobs.
Science (1998)
Human skin fibroblast stromelysin: structure, glycosylation, substrate specificity, and differential expression in normal and tumorigenic cells
Scott M. Wilhelm;Ivan E. Collier;Annemarie Kronberger;Arthur Z. Eisen.
Proceedings of the National Academy of Sciences of the United States of America (1987)
Plasma membrane-dependent activation of the 72-kDa type IV collagenase is prevented by complex formation with TIMP-2.
A Y Strongin;B L Marmer;G A Grant;G I Goldberg.
Journal of Biological Chemistry (1993)
Synthetic Peptides: A User's Guide
Gregory A. Grant.
(2002)
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