VLDB 2026 Research / reviewers in the wild / expert
Mark S. Johnson
dblp:30/3157
· DBLP profile ↗
2ranked-venue papers
0as first author
0since 2021 · last 2002
0000-0002-0496-358XORCID · corroborated
Domains — the database's venue-derived domains; a paper can count in several
Applied, interdisciplinary, general and emerging computing · 2
Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.
| Interdisciplinary, comprehensive, and emerging computing
2 papers |
Bioinformatics and computational biology · 100% |
Topics — the 4 heaviest of 4, each with the papers that count most for it
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Bioinformatics and computational biology › protein analysis
protein-ligand interaction |
0.0 | 1 | 2002 | A dissimilarity matrix between protein atom classes based on Gaussian mixtures · Bioinform. 2002 |
Bioinformatics and computational biology
protein structure analysis |
0.0 | 1 | 1998 | JOY: protein sequence-structure representation and analysis · Bioinform. 1998 |
Bioinformatics and computational biology › protein structure analysis
protein structure annotation |
0.0 | 1 | 1998 | JOY: protein sequence-structure representation and analysis · Bioinform. 1998 |
Bioinformatics and computational biology
structural bioinformatics |
0.0 | 1 | 2002 | A dissimilarity matrix between protein atom classes based on Gaussian mixtures · Bioinform. 2002 |
Methods — techniques the papers use, named apart from their topics
multidimensional scaling · 0.0jeffreys distance · 0.0hierarchical clustering · 0.0expectation-maximization · 0.0sequence-structure representation · 0.0
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2002 | A dissimilarity matrix between protein atom classes based on Gaussian mixturesabstractMOTIVATION: Previously, Rantanen et al. (2001; J. Mol. Biol., 313, 197-214) constructed a protein atom-ligand fragment interaction library embodying experimentally solved, high-resolution three-dimensional (3D) structural data from the Protein Data Bank (PDB). The spatial locations of protein atoms that surround ligand fragments were modeled with Gaussian mixture models, the parameters of which were estimated with the expectation-maximization (EM) algorithm. In the validation analysis of this library, there was strong indication that the protein atom classification, 24 classes, was too large and that a reduction in the classes would lead to improved predictions. RESULTS: Here, a dissimilarity (distance) matrix that is suitable for comparison and fusion of 24 pre-defined protein atom classes has been derived. Jeffreys' distances between Gaussian mixture models are used as a basis to estimate dissimilarities between protein atom classes. The dissimilarity data are analyzed both with a hierarchical clustering method and independently by using multidimensional scaling analysis. The results provide additional insight into the relationships between different protein atom classes, giving us guidance on, for example, how to readjust protein atom classification and, thus, they will help us to improve protein--ligand interaction predictions. CONTACT: [email protected] Ville-Veikko Rantanen, Mats Gyllenberg, Timo Koski, Mark S. Johnson |
Bioinform. | 4 |
| 1998 | JOY: protein sequence-structure representation and analysisabstractMOTIVATION: JOY is a program to annotate protein sequence alignments with three-dimensional (3D) structural features. It was developed to display 3D structural information in a sequence alignment and to help understand the conservation of amino acids in their specific local environments. RESULTS: : The JOY representation now constitutes an essential part of the two databases of protein structure alignments: HOMSTRAD (http://www-cryst.bioc.cam.ac.uk/homstrad ) and CAMPASS (http://www-cryst.bioc.cam.ac. uk/campass). It has also been successfully used for identifying distant evolutionary relationships. AVAILABILITY: The program can be obtained via anonymous ftp from torsa.bioc.cam.ac.uk from the directory /pub/joy/. The address for the JOY server is http://www-cryst.bioc.cam.ac.uk/cgi-bin/joy.cgi. CONTACT: [email protected] Kenji Mizuguchi, Charlotte M. Deane, Tom L. Blundell, Mark S. Johnson, John P. Overington |
Bioinform. | 4 |