D-Index & Metrics Best Publications

D-Index & Metrics

Discipline name D-index D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines. Citations Publications World Ranking National Ranking
Biology and Biochemistry D-index 47 Citations 14,897 108 World Ranking 11958 National Ranking 5145

Overview

What is he best known for?

The fields of study he is best known for:

  • Enzyme
  • Amino acid
  • Biochemistry

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.

His most cited work include:

  • Mechanism Of Cell Surface Activation Of 72-kDa Type IV Collagenase ISOLATION OF THE ACTIVATED FORM OF THE MEMBRANE METALLOPROTEASE (1475 citations)
  • SV40-transformed human lung fibroblasts secrete a 92-kDa type IV collagenase which is identical to that secreted by normal human macrophages. (1000 citations)
  • H-ras oncogene-transformed human bronchial epithelial cells (TBE-1) secrete a single metalloprotease capable of degrading basement membrane collagen. (935 citations)

What are the main themes of his work throughout his whole career to date?

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.

He most often published in these fields:

  • Biochemistry (67.44%)
  • Stereochemistry (24.03%)
  • Enzyme (23.26%)

What were the highlights of his more recent work (between 2009-2019)?

  • Biochemistry (67.44%)
  • Enzyme (23.26%)
  • Dehydratase (5.43%)

In recent papers he was focusing on the following fields of study:

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.

Between 2009 and 2019, his most popular works were:

  • Contrasting catalytic and allosteric mechanisms for phosphoglycerate dehydrogenases. (42 citations)
  • D-3-Phosphoglycerate Dehydrogenase. (20 citations)
  • Regulation of Mycobacterium tuberculosis D-3-phosphoglycerate dehydrogenase by phosphate-modulated quaternary structure dynamics and a potential role for polyphosphate in enzyme regulation. (14 citations)

In his most recent research, the most cited papers focused on:

  • Enzyme
  • Amino acid
  • Biochemistry

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.

Best Publications

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)

1929 Citations

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)

1573 Citations

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)

1509 Citations

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)

905 Citations

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)

863 Citations

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)

851 Citations

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)

811 Citations

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)

441 Citations

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)

432 Citations

Synthetic Peptides: A User's Guide

Gregory A. Grant.
(2002)

390 Citations

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