-
Accelrys stopped offering ViewerLite in 2003, but on 2006 started offering a new version, "Discovery Studio Visualizer", with more features.
A macromolecular visualization utility including ribbon, tube and schematic renderings of protein secondary structure. This is the free version of the commercial WebLab Viewer Pro. The free version lacks many of the features of the latter, such as crystal visualization, animations, script playback, some modeling capabilities, hardware stereo, and sketching of molecular structures. WebLab Viewer Lite gives the highest quality images for printing available in freeware. (Molecular Simulations Inc. was renamed Accelrys Inc. on June 1, 2001.)- Submitted by: Herraez, Angel. (Entry 8).
- A successor to WebLab Viewer Lite and Discovery Studio Viewer.
A visualization utility for small molecules and macromolecules, including ribbon, tube and schematic renderings of protein secondary structure. Mostly a viewer, but has limited editing capabilities. Runs on Windows 2000 and XP, and on Red Hat Enterprise Linux 3.0 and 4.0.
Features (copied from website):
- Import/export several file formats for 3D structures, amino acid sequence, and graphics.
- Insert SMILES string as a 3D molecule.
- Manipulate the view of 3D structures.
- Change charges, bonds, hybridization, oxidation state, and stereochemistry.
- Create groups, surfaces, isosurfaces, crystal cells, Catalyst or ISIS query features and labels.
- Monitor distances, angles, torsion, H-bonds, bumps and more.
- Calculate solvent accessibility and RMSD.
- Predict secondary structure.
- Optimize structures using a fast, Dreiding-like forcefield.
- Superimpose by tethers, sequence alignment, residues or matrices.
- Change the display of atoms, proteins, nucleotides, surfaces, sequences, and graphs.
- Perform 3D small molecule sketching, editing and animation.
- Control lighting, depth cueing, and graphical quality.
- Animate.
- Output high-quality graphics to present results to your colleagues.
- Submitted by: Herraez, Angel. (Entry 83).
- gabedit is a Graphical User Interface for Gamess-US, Gaussian, Molcas, Molpro, MPQC and Q-Chem computational chemistry packages.
Gabedit includes an advanced Molecule Builder.
Gabedit can graphically display a variety of Gamess-US, Gaussian, Molcas, Molpro, MPQC, Q-Chem and (partially) ADF calculation results, including the following :
- Molecular orbitals
- Surfaces from the electron density, electrostatic potential, NMR shielding density, and other properties. Surfaces may be displayed in solid, translucent and wire mesh modes. they are can be colorcoded by a separate property.
- Contours (colorcoded), Planes colorcoded, Dipole. XYZ axes and the principal axes of the molecule.
- Animation of the normal modes corresponding to vibrational frequencies.
- Animation of the rotation of geometry, surfaces, contours, planes colorcoded, xyz and the principal axes of the molecule.
- Animation of contours, Animation of planes colorcoded.
Gabedit can display IR and Raman computed spectra. It can generate a povray file for geometry (including hydrogen's bond), surfaces (including colorcoded surfaces), contours, planes colorcoded.
Gabedit can save picture in BMP, JPEG, PNG, PPM and PS format.
Gabedit can generate automatically a series of pictures for animation
(vibration, geometry convergence, rotation, contours, planes colorcoded).
- Submitted by: the author. (Entry 91).
- CMD bioscience specializes in the use of novel proprietary computational methods to model and engineer clinically important protein-protein and protein-peptide interactions. Our "Affinity" algorithm is designed to predict protein-protein / protein-peptide binding affinities; it is fast enough for use as a scoring function and will be made freely available to the academic community.
- Submitted by: the author. (Entry 94).
- RasMol is a program for molecular graphics visualisation originally developed by Roger Sayle. This site is provided for the convenience of users and software developers of open source versions of RasMol. In order to ensure continuing availability of source code and documentation most programs and documents on this site are subject to copyright. This does not prevent you from using the open-source versions of RasMol, from making copies and changes, but prevents the creation of "closed source" versions out of the open source versions. Appropriate copyrights and licenses appear with the relevant sources and documents. See
Copyright and NOTICE for applicable Copyright and other Notices.
- Co-authors: Sayle, Roger; Mueller, Arne; Grossman, Gary; Molinaro, Marco; Valadon, P.; and many others. Submitted by: the author. (Entry 10).
- ChemFileBrowser is a win32 free sotfware for chemistry designed to visualize and works with SDFile (MDL® format) to exchange and analyse information associated with chemical structure. It includes descriptors calculation like TPSA, molecular weight, HBd and HBa.
ChemFileBrowser since version 0.1.6 integrates Chemistry 2D viewer as a free reusable ActiveX control.
- Submitted by: the author. (Entry 69).
- Interprobe Chemical Services supplies molecular modelling software for use with two operating systems: SGI Irix (6.5.x) systems and Microsoft Windows systems (NT4, 95, 98, 2000, XP). The more extensive range of software is for the SGI systems and includes INTERCHEM (general structure modelling including biomolecules, PRESTO (protein sequence analysis), CHEMSPREAD (statistical package for analysing properties of structures), and a range of non-graphical programs; CONVERT (structure file format interconversion), PROTEINS (conversion of PDB files to INTERCHEM formate etc), COMPARISONS (programs for comparing and overlaying structures), ICMECH (molecular mechanics), STRAUSS (stand-alone programs for translating SMILES sttrings), AUTOBUILD (building of small molecule libraries), and structure database searching tools. At present the Windows inventory is limited to INTERCHEM-PC, PRESTO-PC, and PROTEINS-PC. Source code and executables are provided as standard. (N.B. The Windows programs require copies of the Salford Fortran-95 compiler and Clearwin+ graphics tools if the software is to be recompiled).
An ever expanding range of 3D structures derived from the 2D structure catalogues of the so-called "diversity suppliers" is being produced. A total of around 1.25 million "drug-like" structures is available now.
The programs are distributed under a cost-free license to academics and other not-for-profit organisations (i.e. charities). Industrial and government organisations are charged a (relatively) small fee (currently 2500 UK pounds) for a perpetual site license. The databases are distributed for no cost to all users.
- Submitted by: the author. (Entry 64).
PDB to MultiGIF 
Visualization of chemical 3D structures on the web comes with problems because the web browser cannot display chemical structures without the help of additional software. If you create a page with a 3D structure of a molecule and the visitor of your page does not use this special viewer software for displaying molecules it cannot get the whole information of the page which should be meditated. PDB2MultiGIF takes the 3D structure and generates an animated image which can be displayed using any browser. Thus every visitor of your page can get the whole information. It has many controls including size, number of frames, speed and axis of rotation, and if you wish, you can supply your own view as a RasMol script.
Bohne A.
PDB2MultiGIF: a web Tool to Create Animated Images of Molecules
J. Mol. Model. 4 (1998) 344-34- Submitted by: the author. (Entry 14).
AISMIG - An Interactive Server-side Molecule Image Generator 
AISMIG is a free web-service that enables molecule visualizion without any additional software
like Java or Plug-ins next to a web-browser. You can generate high quality and high resolution
images. It is nice alternative to the standart web-based visualizations techniques because
the user can see and interact with the structure in any case, independend of the software installed
locally. AISMIG is based on PyMol and PovRay.- Co-authors: Ranzinger, René. Submitted by: the author. (Entry 70).
- A new computer-based molecular visualization tool has been developed for teaching, and learning, molecular structure. This java-based ‘jmol Amalgamated Molecular Visualization Learning Environment’ (jAMVLE) is platform-independent, integrated, and interactive. It has an overall graphical user interface that is intuitive and easy to use. Students found that the jAMVLE application stimulated their interest, was a more active learning environment, provided better guidance, and made learning molecular structures fun. The application can be downloaded free from the internet at: wabri.org.au/jamvle.
- Co-authors: Chandler, David; Morgan, Eleanor; Helmerhorst, Erik. Submitted by: the author. (Entry 88).
- The free ChemDraw Net Plugin (Windows, Macintosh) will allow you to view and manipulate chemical structures, however, the save
and print functions are disabled.
Search Web databases by structure or substructure, such as the ChemFinder WebServer.
View ChemDraw documents that others have placed on the WWW.
- Submitted by: Martz, Eric. (Entry 7).
- FPV is a protein visualization software built using Java 3D API. FPV reads PDB files as input. It can load large molecules (e.g. 3000-4000 amino acids) and has a few display modes: spacefill, backbone, bonds, ribbon. It is available with source code.
- Co-authors: Wang, Yujun. Submitted by: the author. (Entry 43).
Marvin Applets and JavaBeans can be applied in web or stand-alone applications for sketching or viewing structures, queries and reactions. Marvin Applets are free for free web sites. MarvinSketch and MarvinView applications are free for academic/home users or for anyone if accessed at the ChemAxon web site. These Java tools are useful in the front end of chemical database systems.
A list of features:- maximum portability (Windows, Unix, Mac, several browsers, like IE, Netscape, Mozilla)
- several import/export formats (Molfile, SDfile, RDfile, Rgfile, Rxnfile, SMILES, SMARTS, XYZ, PDB, CML, etc.)
- image export (JPG, PNG, SVG, POV-Ray, etc.)
- chemical calculation plugin tools: pKa, logP, logD, polar surface area (PSA), charge distribution, polarizability prediction, H-bond aceptor/donor, major microspecies, reactivity, refractivity, elemental analysis, topology analysis, etc
- Advanced stereochemistry, E/Z double bonds, R/S chirality, ABS/OR/AND enhanced stereo, query stereo configuration
- query atoms and bonds
- R-groups and R-logic
- reactions, atom-mapping; several 3D models (wireframe, sticks, ball-and-stick, etc.), Various 2D and 3D cleaning options
- coordinate calculation; animation
- tables of structures with labels, buttons, check boxes, edit boxes,
- text and graphics input
- displaying and editing files containing molecule lists (SDfiles, SMILES)
- custom coloring
- copy and paste
- printing
Free for teaching and academic research through ChemAxon's Academic Package. Introduction, terms and application available from http://www.chemaxon.hu/forum/viewpost570.html#570- Submitted by: Allardyce, Alex. (Entry 38).
-
Calculator Plugins are modules of Marvin and JChem applications which perform calculations based on chemical structures.
Separate Calculator Plugins currently cover a range of calculations and physicochemical predictions. The plugin format is open to third party development, within ChemAxon we have ongoing plugin development, currently available plugins:- Elemental Analysis
- pKa
- logP
- logD
- Polar Surface Area
- Charge
- Huckel Analysis
- Hydrogen Bond Donor-Acceptor
- Major Microspecies
- Polarizability
- Refractivity
- Topology Analysis
Free unlimited structure based prediction implemetation here: http://www.chemaxon.com/demos/try_marvin.html
Free for teaching and academic research through ChemAxon's Academic Package. Introduction, terms and application available from http://www.chemaxon.hu/forum/viewpost570.html#570- Submitted by: Allardyce, Alex. (Entry 59).
-
JChem Base is a Java tool for the development of applications that allow for the search of mixed structural and non-structural data. JChem Base can integrate a variety of database systems (Oracle, SQL, Access, etc) with web interfaces and fully supports all ChemAxon technology.
Via the JChem Cartridge many JChem functions, such as structure searching or property predictions are directly available from within Oracle's SQL.
The system includes Marvin, a fast substructure, similarity, and exact search engine using 2D hashed fingerprints. Structures are stored in database tables. Structural and non-structural data can be combined. SDF, SMILES, etc. can be imported and exported. There is API with low and high level classes. Key features:- Graph based topology search algorithm
- Fingerprint-based database search accelerator technology
- Advanced query features;
- exact structure and substructure searching
- similarity searching using chemical and pharmacophore fingerprints
- generic query atoms
- SMARTS query property support
- R-group query expressions
- reaction queries
- stereo specific structure and reaction specifications
- supports Chemical Terms
To find out more please visit this implementation: http://www.jchem.com/index.html?content=examples.html or download and evaluate from our website
Free for teaching and academic research through ChemAxon's Academic Package. Introduction, terms and application available from http://www.chemaxon.hu/forum/viewpost570.html#570- Submitted by: Allardyce, Alex. (Entry 60).
- Pharmacophore Analysis;
- customizable pharmacophore definition framework (fragment- and calculation-based solutions)
- integration of physico-chemical prediction plugins; pKa, logP, logD, charge distribution, and polarizability predictions.
- supporting Chemical Terms
- Configurable Molecule Descriptor Generation;
- chemical topology fingerprints
- pharmacophore topology fingerprints
- BCUT
- plug-and-play custom and third party fingerprints
- hypothesis calculation
- fuzzy smoothing
- Virtual Screening;
- dissimilarity metrics (Euclidean, Tanimoto)
- variable metric modifiers (normalization, scaling, weighting, directing)
- enrichment enhancement by selectivity optimizer
- screening performance statistics
Free for teaching and academic research through ChemAxon's Academic Package. Introduction, terms and application available from http://www.chemaxon.hu/forum/viewpost570.html#570
To find out more or download JChem to evaluate the Screen tools, please visit the Screen page
- Submitted by: Allardyce, Alex. (Entry 61).
- Pharmacophore Analysis;
-
Fragmenter is the virtual building block creation component of ChemAxon’s Java based chemical software technology.
Fragmenter cleaves molecules to generate fragments which retain their associated cleavage route information.
Using the cleavage route information, the library of fragments generated can be used as building blocks to more easily create small molecule libraries during lead discovery and optimization.
- Customizable fragmentation rules
- Built in RECAP fragmentation module allows "more synthesisable" chemistry
- Rapid fragmentation
- Exhaustive fragmentation can be performed
- Fragmentation information is stored with fragments
Free for teaching and academic research through ChemAxon's Academic Package. Introduction, terms and application available from http://www.chemaxon.hu/forum/viewpost570.html#570
- Submitted by: Allardyce, Alex. (Entry 62).
-
Reactor is the virtual reaction engine of Chemaxon's JChem technology. It supports "smart" reactions (generic reaction equations combined with reaction rules) generating chemically feasible products even in batch mode. The professional version of the tool includes support for multi-step virtual synthesis and filtering of chemically feasible molecules which are not of interest.
Key features:
- chemoselectivity (advanced reaction site and functional group recognition)
- regioselectivity (directing rules, main product detection)
- stereoselectivity (inversion/retention)
- reverse reaction processing
- random synthesis for lead discovery
- exhaustive synthesis for metabolism applications
- intramolecular reactions
- sequential and combinatorial modes
- memory, file and database operation modes
- synthesis tree generation
- synthesis rules for each synthetic step (for on-the-fly filtering of intermediers)
- graphical user interface for browsing the synthesis database
- colored visualization of the original building blocks in the
generated library
- wide range of file formats supported (MOL, RXN, RDF, SMILES, SMARTS
- rapid execution
To find out more about Reactor please visit our public implementation or download JChem Base (containing Reactor) from our web site.
Free for teaching and academic research through ChemAxon's Academic Package. Introduction, terms and application available from http://www.chemaxon.hu/forum/viewpost570.html#570
- Submitted by: Allardyce, Alex. (Entry 63).
- NOC provides an intelligent and flexible environment for displaying, manipulating, and analyzing small molecules, proteins and their interactions. The program is suitable for most common crystallographic work. Furthermore there are many unique features in NOC.
- Submitted by: the author. (Entry 71).
-
Spock is a full-featured molecular graphics program developed by Jon A. Christopher while in the lab of Thomas O. Baldwin of the Department of Biochemistry and Biophysics at Texas A&M University. Spock has been designed from the ground up to be powerful, flexible and most of all, easy to use. Many of the features of spock are designed to bring molecular modeling programs into the age of the internet.
Spock has the features users have come to expect from molecular graphics software including several bond and atom rendering types, and a complete array of backbone "worm" representations. Further, spock can calculate and display molecular and accessible surfaces, and color code these surfaces by properties (such as electrostatic potential). Images can be publication quality, and renderings include cylinders for alpha helices. Unix/irix/linux only. Free for non-profit use; fee for commercial use.
- Submitted by: Herraez, Angel. (Entry 41).
- YAPView is a simple OpenGL-based visualization program for displaying protein structure and folding trajectories. It supports different styles (ribbon, ball and stick, space filling, etc.), individual configuration for each residue, transparency effects, high resolution and postscript output of the rendered 3D images, among other features.
YAPView has three aims:
1) To offer a basic, easy-to-use, multiplatform graphical tool for protein visualization. It doesn't try to match more complete and sophisticated visualization tools.
2) To focus in the display of dynamical information (e.g.: folding trajectories).
3) To provide an open and extensible interface allowing the addition of new features through the use of plugins.
- Submitted by: the author. (Entry 48).
- Once a macromolecular structure has been determined, the challenge is to communicate that information to a widely diverse audience of scientists, educators and students. Current options include the printed literature and dissemination over the Internet, either via online journals or directly on personal web pages. Printed literature has the advantage of wide acceptance and availability, but presents static images. Web pages can be powerful, but lack a uniform format. Furthermore, any dynamic images that are presented are subject to the whims of the providers of the browsers and plug-ins that are required to view them. At the University of California, San Diego and the Scripps Institute, we are developing the BioEditor as a tool to bridge the gap between the printed literature and current Internet presentation formats. It is a standalone Windows application that can be used to prepare and present structure annotations containing formatted text, graphics, sequence data, and interactive molecular views.
BioEditor includes a built-in browser based on Internet Explorer; molecular visualizations are done using the Chime plug-in. The executable includes a help file that has a quick-start tutorial to explain how to use all the components of the software. The web site (http://bioeditor.sdsc.edu) includes a download site and some sample documentaries that you can view to see the potential of BioEditor.
- Co-authors: Yang, Peng; Bourne, Phil; Goodsell, David. Submitted by: the author. (Entry 42).
- ProteinShop is an interactive tool for manipulating protein structures. It was designed to quickly create a set of protein configurations using human knowledge and intuition. These configurations can be subjected to local or global optimization.
- Co-authors: Kreylos, Oliver; Max, Nelson; Bethel, Wes; Lu, Ting-Cheng; Crawford, Clark. Submitted by: the author. (Entry 76).
- The program TRITON is a graphical tool for modelling protein mutants and assessment of their activities. Protein mutants are modelled based on the wild type structure by homology modelling using the external program MODELLER. Chemical reactions taking place in the mutants' active site are modelled using the semi-empirical quantum mechanic program MOPAC. Semi-quantitative predictions of the mutants' activities can be achieved by evaluating the changes in energies of the system and partial atomic charges of the active site residues during the reaction. The program TRITON offers graphical tools for the preparation of the input data files, for calculation and for the analysis of the generated output data. Implementation ensures the overall integrity of consecutive steps of the modelling of mutants and calculation of reaction coordinates, but the program can also be used simply for combinatorial generation of multiple mutants by homology modelling.
- Co-authors: Prokop, Martin; Bohac, Michal; Kuty, Michal; Koca, Jaroslav. Submitted by: the author. (Entry 20).
- Co-authors: Grosse-Kunstleve, Ralf W.. Submitted by: the author. (Entry 24).
- The software for this resource is open source and is availble for download. A web server outfitted with php and mysql is required to setup your own relational database. The software is OS independent.
This site provides access to a chemical and safety relational database developed in 2003 at Nebraska Wesleyan University. The site is designed specifically for local users but access to the database content is not restricted. This database has many features similar to chemfinder.com and the NIST webbook. The major difference is that the content of the database is determined by local interests and needs and is cross indexed to hazard information (specifically NFPA ratings). For example the database presently contains chemical and safety data for materials used in lab experiments in our first and second year chemistry courses.
The database can be searched by CAS numbers, molecular formula, chemical names, or by specific (NFPA) hazards. Included in the database are files of Chime-pdb files [Chime plugin required for viewing], MSDS's, NFPA ratings (graphic view), and 2D graphics of the molecules. In addition local users can cross-index an unlimited number of web-links to other material (such as IR, NMR, UV-vis and MS spectra, experimental data, potential maps, animations, etc) to each molecule in the database.
- Co-authors: Shoemaker, Austin. Submitted by: the author. (Entry 53).
- An OpenGL based viewer for windows (95, 98, NT, 00) supporting the following features:
- Display wire frame, stick figure, ball and stick, point, space-filling, ribbon, tube and spline molecular structures from a PDB file.
- Assign secondary structure via STRIDE
- Animate molecular trajectories stored in the DCD file format (both big- and little-endian).
- Kabsch rotate all structures in a trajectory against the initial structure.
- Interactively measure bond lengths, bond angles and torsion angles.
- Dynamically adjust user selected torsion angles.
- Display atom labels.
- Display coordinate axis.
- Dynamic modification of the color scheme (including color-by-element, color-by-atom-number, color-by-temperature and color-by-occupancy).
- Dynamic lighting.
- Adjust atomic radii (including radii-by-temperature and radii-by-occupancy).
- Print to any Windows supported printer and copy images to the Windows clip board.
- Generate AVI movies from a molecular trajectory.
- Directly query the PDB.
- Submitted by: the author. (Entry 19).
- STRAP is a work bench for multiple sequence alignments of proteins.
It is used to visualize three-dimensional structures, to align several
proteins using the amino-acid sequences or the xyz-coordinates of the
c-alpha atoms and to highlight residues in the sequence and the
3D-structure. Superimposed proteins are shown in Pymol. STRAP currently integrates the protein viewers
Jmol, Pymol, VMD and Rasmol. It is scriptable using java.
- Submitted by: the author. (Entry 65).
-
ConSurf identifies, in Chime (actually, in Protein Explorer) the most conserved residues, and the hypervariable residues, based on a multiple sequence alignment and phylogenetic tree. It work on any protein for which a 3D structure is available. ConSurf is completely automatic. All you have to provide is the PDB code for a 3D structure. Optionally, you can provide your own multiple sequence alignment. Image at left: enolase -- click on it to see the ConSurf Gallery.
- Co-authors: Ben-Tal, Nir; Pupko, Tal; Martz, Eric. Submitted by: Martz, Eric. (Entry 37).
XdomView (Version 2.1)
A Chime-based Graphical Tool for Protein Domain and Exon Position VisualizationXdomView is a chime-based visualization tool that maps the domain boundaries of the input PDB chain, obtained from protein structure classification databases (CATH, SCOP, NCBI, 3DEE and DALI) to its tertiary structure. It also runs BLAST2 for the input PDB chain sequence against all protein sequences in the ExInt* database and maps the intron positions and phases of aligned search results on the input protein's 3D structure. Xdom is a useful visualization tool for scientists working on gene and protein evolution and structural modeling and classification.
Contact Details :
Gopalan Vivek, Dr. Tan Tin Wee, Dr. Shoba Ranganathan
Bioinformatics Centre
Department of Biochemistry
National University of Singapore
*ExInt - Repository of intron positions, phase and protein sequences of all multi-exonic eukaryotic genes available in GenBank 122.- Co-authors: Shoba Ranganathan; Tan Tin Wee. Submitted by: the author. (Entry 36).
- For Deep View resources, go to the
Deep View / Swiss-PDBViewer section.
- Co-authors: Diemand, Alexandre; Schwede, Torsten; Peitsch, Manuel C.. Submitted by: Martz, Eric. (Entry 5).
- This review compares five chemical drawing programs, ISIS/Draw, ChemDraw, ChemWindow, ChemSketch and Chemistry 4-D Draw. ISIS/Draw and ChemSketch are free; the others are commercial software. This review is extensive and detailed, with helpful supplementary information (such as why to use gif rather than jpeg files for the web), and sample output from all 5 programs.
- Submitted by: Martz, Eric. (Entry 33).
Ghemical is a computational chemistry software package released under the GNU GPL. It means that full source code of the package is available, and users are free to study and modify the package. Ghemical is written in C++. It has a graphical user interface (which is based on GNOME), and it supports both quantum-mechanics (semi-empirical and ab initio) models and molecular mechanics models (there is an experimental Tripos 5.2-like force field for organic molecules). Also a tool for reduced protein models [1] is included. Geometry optimization, molecular dynamics and a large set of visualization tools are currently available.
Ghemical relies on external code to provide the quantum-mechanical calculations. Semi-empirical methods MNDO, MINDO/3, AM1 and PM3 come from the MOPAC7 package (Public Domain), and are included in the source distribution. The MPQC package (GNU GPL) is used to provide ab initio methods: the methods based on Hartree-Fock theory are currently supported with basis sets ranging from STO-3G to 6-31G**. The MPQC code is not included in the source distribution. In order to use the MPQC-based ab initio methods in Ghemical, you must first compile and install the MPQC program for your system, and then compile Ghemical using some specific settings that link the programs together. Ghemical also contains the OpenBabel package for import and export of many different file formats (as well as other tasks).
- Co-authors: Cruz, Mike; Heikkilä, Ville; Hutchison, Geoff; Huuskonen, Jarno; Rowley, Christopher. Submitted by: Bizzaro, J.W.. (Entry 73).
Viewmol is an open source graphical front end for computational chemistry programs. It is able to graphically aid in the generation of molecular structures for computations and to visualize their results. Viewmol has originally been developed by Jörg-Rüdiger Hill and Andreas Bleiber in the Quantum Chemistry Group of Humboldt University with contributions by Arne Dummer, Mariann Krossner, Andreas Bünger, and Andries de Man. Viewmol was named an outstanding product in the German/Austrian Academic Software Award 1993.
What can I do with Viewmol ?
- Building and editing of molecules
- Visualization of the geometry of a molecule as wire frame, stick, ball-and-stick, or CPK models
- Tracing of a geometry optimization or a MD trajectory
- Animation of normal vibrations or to show them as arrows
- Drawing of IR, Raman, and inelastic neutron scattering spectra
- Drawing of an MO energy level or density of states diagram
- Drawing of basis functions, molecular orbitals, and electron densities
- Drawing of properties defined on a grid
- Display of forces acting on each atom in a certain configuration
- Calculation of thermodynamic quantities for molecules and reactions between them
- Drawings generated by Viewmol can be saved as TIFF, PNG, HPGL, or PostScript files
- Animations of normal modes can be converted to a video file (MPEG), e. g. for inclusion into World Wide Web documents (requires additional programs available on the Internet)
- Interface to the ray tracing program Povray (input file generation and use of Povray from within Viewmol)
- Input and output in a variety of formats, new formats can be added easily by the user
- Embedded Python interpreter for automation
What files can Viewmol read ?
Viewmol is currently capable to work with- Gaussian outputs
- Discover files
- DMol3 outputs
- Gamess outputs
- Gaussian outputs
- Gulp outputs
- Mopac outputs
- PDB files
- PQS outputs
- Turbomole files
- Vamp outputs
- any molecular structure file supported by Open Babel
What files can Viewmol write ?
Viewmol can currently write- Turbomole files
- Accelrys car and arc files
- Gaussian input files
- MDL files
- any molecular structure file supported by Open Babel
- Co-authors: Bleiber, Andreas; Dummer, Arne; Krossner, Mariann; Bünger, Andreas; de Man, Andries. Submitted by: Parsons, Drew. (Entry 68).
The Ramachandran Plot Explorer is designed to make it easy to examine the conformation of a polypeptide - through the interactive
Ramachandran plot (phi-psi angles) and chi-angle tool. Simply click on a residue, then drag the marker on the Ramachandran plot.
To see how conformational changes might affect the energetics, I've included real-time calculation of H-bonds, weak H-bonds and steric clashes. This makes it easy to see why (i) certain regions of the Ramachandran plot are forbidden, and (ii) certain sidechain chi angles are favoured, (iii) the core is packed so tightly.
You can also edit (cut/paste/insert) protein sequences and mutate residues, with a simple click of the mouse.
I've worked hard to make an intuitive interface with lots of visual cues and feedback, and I've included what, I think, is a necessary set of navigating tools (sequence-bar, z-slab-bar, snake-measure tool).
There is a 3-point-clamp function, that (i) explores discrete solutions of a loop with fixed anchors and 3 hinge-residues, and (ii) allows the exploration of the phi/psi angles of residues inside the clamp without disturbing the rest of the protein.
This new version uses native widgets (standard file open/save dialogs!) and you can resize the window to your heart's content.
Limited to a single protein.
Now available for Linux, Windows and MacOSX.
- Submitted by: the author. (Entry 51).
- eMovie is a free tool that makes the creation of molecular movies both easy and intuitive via a breakthrough storyboard interface, similar in nature to what is used in the creation of traditional movies. eMovie is a plug-in for PyMOL, a powerful, open source, and multi-platform molecular graphics program. To download eMovie, please visit our download/install page.
Through eMovie, the user has the ability to construct an animation of any length out of building blocks like rotations, zooming, color changes, fading of selections, view changes, and even execution of specific PyMOL commands or scripts. Conformation changes and docking actions can be added as well (requires incentive version of PyMOL). Movies can be saved and loaded at a later time, and optionally exported as a ray-traced image sequences to be merged into a traditional movie file (e.g. .mov or .gif) using available external programs.
- Co-authors: Schreiber, Gideon; Rother, Kristian; Sussman, Joel L. Submitted by: the author. (Entry 96).
- Excel spreadsheet macros for reading PDB files, manipulating them, and exporting the modified data in PDB format. These "Renumbering Macros" take a number of PDB-Files in a directory (no more than 250, since the size of an EXCEL workbook is limited to 255 worksheets), read the ATOM and HETATM records of each file into an EXCEL worksheet, and extract the sequences, chain and residue labels into separate worksheets. The user can then process (gap) the sequence alignment manually or export it to gap it automatically with programs such as the GCG module PILEUP and reimport the sequence alignment into the EXCEL workbook. Further macros will then change the chain and residue labels of the PDB files according to a common numbering scheme indicated in the header row (for sequence alignments shorter than 250 amino acids) or in the header column (for sequence alignments longer than 250 amino acids) of the alignment and reexport the PDB coordinate files. At the page
Renumbering PDB Files don't miss the How To button, which opens a slide show explaining how to use the PDB macros.
- Submitted by: Martz, Eric. (Entry 66).
An interactive molecular modeling system developed by the the UCSF Resource for Biocomputing, Visualization, and Informatics. It is free for academic and non-profit use and is available for Windows, Mac OS X, Linux, and other platforms. UCSF Chimera development is funded by the NIH National Center for Research Resources (grant P41-RR01081). Features include:
- Atom-type and hydrogen-bond identification based on detailed geometric criteria
- Display of attributes such as B-factor and hydrophobicity with color, radii, and backbone worms; easy import of arbitrary user-defined attributes
- Display of three-dimensional data sets (electron densities, etc.) as isosurfaces or transparent solids, with interactive threshold adjustment
- Display of sequence alignments (many formats), automatic association of sequences with structures, sequence-structure crosstalk
- Playback of molecular dynamics trajectories (AMBER, CHARMM, GROMACS, GROMOS, MMTK, NAMD, PDB, X-PLOR formats)
- Interface to facilitate screening ligands from DOCK
- Multiscale visualization including low-resolution surfaces
- Generation of publication-quality images
- Movie recorder for saving image frames and assembling them into movie files
- Demo mechanism for scripting and replaying presentations
- Complete and searchable user documentation (HTML) included with download
- Extensibility as a design principle, allowing users to create custom modules without changing Chimera code
- Co-authors: Couch, Greg; Pettersen, Eric; Goddard, Tom; Greenblatt, Daniel; Meng, Elaine; Ferrin, Thomas. Submitted by: Meng, Elaine. (Entry 45).
- Friend is a bioinformatics application designed for simultaneous analysis and visualization of multiple structures and sequences of proteins and/or DNA/RNA. The application provides basic functionalities such as: structure visualization with different rendering and coloring, sequence alignment, and simple phylogeny analysis, along with a number of extended features to perform more complex analyses of sequence structure relationships, including: structural alignment of proteins, investigation of specific interaction motifs, studies of protein-protein and protein-DNA interactions, and protein super-families. It is also useful for functional annotation of proteins, protein modeling, and protein folding studies. Friend provides three levels of usage; 1) an extensive GUI for a scientist with no programming experience, 2) a command line interface for scripting for a scientist with some programming experience, and 3) the ability to extend Friend with user written libraries for an experienced programmer. The application is linked and communicates with local and remote sequence and structure databases.
- Co-authors: Abyzov, Alex. Submitted by: the author. (Entry 84).
- A unified description of protein structure is essential when structural similarity judgment, motif transitions or general folding are considered. In the applied approach, an assumption that all polypeptide chain conformations can be classified as helix-derived coerced invention of a new method of protein structure description based on geometrical parameters: radius of curvature R and dihedral angle between two consecutive peptide bond planes V. Developed basing on the model pentapeptides it helped to determine the general conformational subspace that turned out to be more useful than traditional φ/ψ mapping. The viewer allows to assign colors to the chain according to V/R parameters.
- Submitted by: the author. (Entry 89).
- The model oriented on localization of areas responsible for ligand binding or protein-protein complex creation is based on characteristics of spatial distribution of hydrophobicity in a protein molecule: It is assumed that hydrophobicity changes from protein interior (maximal) to exterior (close to zero) according to the three-dimensional Gauss distribution (fuzzy oil-drop model). It is generally accepted that the core region is not well described by a spheroid of buried residues surrounded by surfaces residues due to hydrophobic channels that permeate the molecule. Therefore the simple comparison of theoretical (idealized according to Gauss function) and empirical spatial distribution of hydrophobicity in protein gives the opportunity to identify the regions with high deviation versus the ideal model. The viewer 'reveals' regions recognized by high hydrophobicity density discrepancy to be possibly functionally important sites in proteins.
- Submitted by: the author. (Entry 90).
XCrySDen is a crystalline and molecular structure visualisation program, which aims at display of isosurfaces and contours, which can be superimposed on crystalline structures and interactively rotated and manipulated. It can run on most UNIX platforms, without any special hardware requirements.
XCrySDen has been also ported to MAC OSX (requires X11) and Windows (requires CYGWIN).
XCrySDen also provides a (partial) graphical user interface for CRYSTAL ab initio program, and a visualization system for PWscf and WIEN2k and initio programs.
Molecular (and general) visualising features: XCrySDen possesses more or less all the features that are expected from a modern molecular visualiser:
- representation of molecular-models in several display modes (wireframe, sticks, ball-and-sticks, spacefill, ...)
- display of forces acting on atoms
- real time operations such as rotation, translation and zooming of displayed structure
- animations
- measurement of distances, angles, and dihedrals
- contour-plane and isosurface representation of scalar fields
- "arrows" representation of the vector field
- setting various attributes, such as colours of atoms and bonds, radii of atoms, thicknesses of bonds and lines, sizes of points, balls and spacefills, just to name a few
- and more ...
Crystalline visualising features: In addition to the above described ``standard'' molecular visualising features, XCrySDen comes with an additional set of features that are necessary for visualising crystalline structures. Therefore XCrySDen is able to:
- switch between primitive and conventional cell settings
- change the number of the displayed unit cells, that is, display smaller or larger portions of a crystal
- display the crystal lattice
- visualise the Wigner-Seitz cell and Brillouin-zone
- k-path selection for band-structure calculations
- visualization of Fermi surfaces
- and more ...
- Submitted by: Voznyy, Oleksandr. (Entry 85).
-
MOLMOL is a molecular graphics program for display, analysis, and manipulation of three-dimensional structures of biological macromolecules, with special emphasis on nuclear magnetic resonance (NMR) solution structures of proteins and nucleic acids. MOLMOL has a graphical user interface with menus, dialog boxes and on-line help. The display possibilities include conventional presentations, as well as novel schematic drawings, with the option of displaying different presentations in one view. The covalent molecular structures can be modified by addition or removal of individual atoms and bonds; the three-dimensional structure can be manipulated by interactive rotation about individual dihedral angles. Special efforts were made to allow for appropriate display and analysis of sets of (typically 20-40) conformers that are conventionally used to represent the result of a NMR structure determination, using functions for superimposing sets of conformers, calculation of root mean square distance (RMSD) values, identification of hydrogen bonds, checking and displaying violations of NMR constraints, and identification and listing of short distances between pairs of hydrogen atoms. MOLMOL is publicly available at no charge, and runs on UNIX and Windows NT/95/98/2000.
MolMol has been cited by over 500 scientific journal articles (search for "molmol" at highwire.stanford.edu). It ranks among the most popular free visualization programs, including RasMol (>700) and KineMages (>450).
- Co-authors: Billeter, Martin; Wuethrich, Kurt; et al.. Submitted by: Martz, Eric. (Entry 46).
- Free license required for academic/not-for-profit use (fee for commercial use). Unix program for molecular visualization. MolScript has been used for probably the majority of published high-resolution macromolecular images. Learning its command language takes some time. It puts out a meta-language image description that must then be rendered with a separate engine, such as Raster3D or POV-Ray.
- Submitted by: Martz, Eric. (Entry 22).
is a
molecular graphics and modeling program for Linux and Windows with a
very intuitive user interface.
YASARA is powered by PVL (Portable Vector Language), a new development framework that provides performance way above traditional software. PVL allows you to visualize even the largest protein complexes at high frame rates.
Central features:
- OpenGL graphics engine, up to 35 times faster than usually. Publication quality ray-traced images including labels and arrows.
- Modeling and analysis tools, including structural superpositions.
- Yanaconda macro language for complicated tasks. Plugins can be programmed easily using the Python scripting language.
- Interactive tutorials, you can create your own molecular movies and animations to accompany your next talk.
- Quick upgrade to the higher stages YASARA Model, Dynamics & Structure (see commercial section). This adds support for affordable shutter glasses, data gloves, autostereoscopic displays, interactive real-time simulations using well known (AMBER) and newly developed (NOVA, YAMBER, YASARA) force fields, structure determination & prediction, docking etc. etc.
- A list of all features is available here.
Click here to download YASARA now for free...
- Submitted by: the author. (Entry 47).
- The most up-to-date Linux software for chemistry, biochemistry, genetics:
molecular modeling, visualization, graphics, computational chemistry calculations, molecular and quantum mechanics, dynamics, kinetics, calcultors, biochemistry and genetics related and evens some drug discovery software
- Submitted by: the author. (Entry 15).
- gOpenMol is the graphics interface to the OpenMol set of programs. gOpenMol
can also be used for the analysis and display of molecular dynamics
trajectories and the display of molecular orbitals, electron densities and
electrostatic potentials from programs like the GaussianXX, PC GAMESS and
Jaguar.
gOpenMol can import, display and analyse a wide range of different input atomic coordinate
file formats and binary trajectory file formats. The program has a graphical
user interface (GUI) based on the Motif set of widgets. The internal line
command interpreter is implemented using the Tool command language (Tcl).
gOpenMol can be used for a wide range of analysis and display tasks like the
display of isocontour surfaces. Available for linux, Windows, SGI Irix, and other platforms. See also the
gOpenMol Gallery.
- Submitted by: Martz, Eric. (Entry 28).
- For Chime and Chime resources, go to other sections of the
World Index of Molecular Visualization Resources.
- Co-authors: van Vliet, Bryan; Adler, Franklin; Holt, Jean. Submitted by: Martz, Eric. (Entry 3).
- Featuring RasMol 2.6, authored by Roger Sayle, this site was founded in 1995. Here is the most extensive collection of RasMol resources and reference documents of any in the world. This site is visited by over 5,000 people per week, and RasMol has been downloaded from this site over half a million times. The site includes:
- RasMol Quick Start! and RasMol Tutorials
- Origin of RasMol
- History of Molecular Visualization
- RasMol 2.6 Downloads for Windows, Macintosh, and other platforms
- RasMol 2.6 Reference Manual
- FAQ for RasMol and Chime including public domain status, literature citation, stereo viewing, printing in high resolution, showing double bonds, and control of covalent and noncovalent bond displays.
- Educational Molecular Visualization
- Guides to Select Commands, Coloring, and van der Waals radii and Covalent Bond Assignment Mechanisms.
- And more (see Contents)
See also RasMol Home Pages.- Co-authors: Sayle, Roger. Submitted by: the author. (Entry 1).
Protein Explorer
is free software for visualizing the three-dimensional structures of protein, DNA, and RNA macromolecules, and their interactions and binding of ligands, inhibitors, and drugs. It is arguably the easiest-to-use software of its kind. It is suitable for high school and college students (ages 16 years and older), yet it is also widely used by graduate students and researchers.
More
about what Protein Explorer does.
Protein Explorer makes the power of Chime accessible, offering extensive features both for novices and advanced features for protein structure specialists. Much easier to use, and much more powerful than RasMol. Extensive built-in context-sensitive help, QuickTour, Tutorials. For details, see
Snapshots of Protein Explorer in Action, and
Protein Explorer for Novices/Protein Explorer, Advanced.
- Submitted by: the author. (Entry 4).
- This site lists some molecular visualization freeware packages not yet indexed in the World Index, along with sample images from most of them. There are also links to sites with more extensive lists of molecular visualization freeware.
- Submitted by: the author. (Entry 6).
- There are two main RasMol websites:
- The
Home Page for RasMol and OpenRasMol is actively maintained by Herb Bernstein. It offers the latest version of RasMol (2.7 or later) with a number of enhancements documented in an updated reference manual. This site does not duplicate most of the extensive help for beginners and usage guides offered at the UMass RasMol site. RasMol 2.7's license requires that all derivatives be free with open source code.
- The RasMol Home Page at UMass, started in 1995 by Eric Martz, provides extensive help for beginners as well as reference materials and guides for advanced users. This site offers RasMol 2.6; its documents pertain to version 2.6 and largely stopped being updated in 1999, when Martz changed his focus to Protein Explorer and other Chime-based resources. This site does not document enhancements in RasMol 2.7, available from the OpenRasMol site. RasMol 2.6 and its source code are in the public domain due to the generosity of its author, Roger Sayle.
- Co-authors: Bernstein, Herb. Submitted by: the author. (Entry 49).
- The
Home Page for RasMol and OpenRasMol is actively maintained by Herb Bernstein. It offers the latest version of RasMol (2.7 or later) with a number of enhancements documented in an updated reference manual. This site does not duplicate most of the extensive help for beginners and usage guides offered at the UMass RasMol site. RasMol 2.7's license requires that all derivatives be free with open source code.
- FirstGlance in Jmol is a free, open source, browser-based application for viewing macromolecular structures online. It uses the free, open-source Jmol java applet (jmol.org).
FirstGlance is an HTML "wrapper" or "user interface" for Jmol. It enables you to see key features of the molecule by clicking on menus or buttons, without learning the (complicated) Jmol menu, or the Jmol command language.
- Submitted by: Foley, Brian. (Entry 82).
- Moilin is a molecular modelling program which can be operated in stand alone mode or as part of the Oscail package under PC-Windows. The download includes Mopac and Iconc. The program will also drive Tinker and PC-Gamess both of which are available free to academics. Thus calculations from molecular mechanics (including dynamics movies) to high level dft are possible. Moilin can generate plots of molecular orbitals from Mopac or Gamess.
Moilin uses opengl graphics with high resolution hard copy (up to 2400 x 1800).
Moilin interacts with the Oscail package which provides access to crystallographic software, file format conversion software, coordination polyhedra and Raster3D photorealism.
Downloads include "on-line tutorials" and "on-line" help.
Commercial users must obtain permission to use this software.
- Submitted by: the author. (Entry 54).
- Co-authors: Bacon, David; Murphy, Michael. Submitted by: the author. (Entry 32).
- Reported structures for several thousand inorganic crystals and small organic compounds. All data on this site have been placed in the public domain by the contributors (http://crystallography.net). Data are in Crystallographic Information File (CIF, not PDB) format. Visualizations of the crystal structures and molecules are in three dimensions using Jmol. CIFs can be downloaded.
- Submitted by: the author. (Entry 77).
BALLView is an extensible tool for visualizing and modeling bio-molecular structures. It provides a variety of different models for molecular visualization, e.g. ball-and-stick models, molecular surfaces, or ribbon models.
In contrast to most existing visualization tools, BALLView also offers rich functionality for molecular modeling and simulation, including molecular mechanics methods (AMBER and CHARMM force fields), continuum electrostatics methods employing a Finite-Difference Poisson Boltzmann solver, and secondary structure calculation. Results of these computations can be exported as publication quality images or as movies. Even unexperienced users have direct access to this functionality through an intuitive graphical user interface, which makes BALLView particularly useful for teaching.
For more advanced users, BALLView is extensible in different ways. Owing to its framework design, extension on the level of C++ code is very convenient. In addition, an interface to the scripting language Python allows the interactive rapid prototyping of new methods.
BALLView is portable and runs on all major platforms (Windows, MacOS X, Linux, most Unix flavors). It is open source software and available free of charge under the GNU Public License (GPL) from our website.- Co-authors: Hildebrandt, A.; Lenhof, H.P.; Kohlbacher O.. Submitted by: the author. (Entry 79).
The Molecular Interactive Collaborative Environment (MICE) is a Java/Java3D based molecular structure viewer. As a pure Java application, MICE will run without modification on any platform for which Java version 2 and Java3D are available. We have successfully run MICE on Windows 98/NT4.0, Solaris and Linux.
Using a simple form interface, users can users can create custom representations of any molecule in the Protein Databank (PDB), via a network-based scene generator (MSG) that uses MolScript to create VRML representations of the molecule of interest. Once loaded into MICE, the custom view can then be viewed interactively and queried using rudimentary scene interrogation tools.
As well as allowing a user to manipulate and examine a molecule locally, MICE can also share views of molecules across a network. In a collaborative session, multiple users at different geographical locations can view the same representation of the molecule of interest. Any user can take control of the session and alter the view of the molecule, with these changes being seen by all members of the collaboration.
- Co-authors: Tate, John; Gramada, Apostol; Bourne, Phil. Submitted by: the author. (Entry 12).
- Designed to predict how
small molecules, such as
substrates or drug
candidates, bind to a
receptor of known 3D
structure.
The
atomic affinity grids can be
visualised. This can help, for
example, to guide organic
synthetic chemists design
better binders.
Free to academics and educational institutions for non-commercial use.
For unix or linux; comes with C++ source code included.
- Co-authors: Goodsell, DS; Huey, R; Hart, WE; Halliday, S; Belew, R; Olson, AJ. Submitted by: Martz, Eric. (Entry 13).
- Cn3D is an open-source code visualization tool for biomolecular structures,
sequences, and sequence alignments. What sets Cn3D apart from
other software is its ability to correlate structure and sequence
information: for example, a scientist can quickly find the residues in
a crystal structure that correspond to known disease mutations, or
conserved active site residues from a family of sequence
homologs. Cn3D displays structure-structure alignments along with
their structure-based sequence alignments, to emphasize what
regions of a group of related proteins are most conserved in
structure and sequence. Also included are custom labeling
features, high-quality OpenGL graphics, and a variety of file
exports that together make Cn3D a powerful tool for literature
annotation. Cn3D is typically run from a WWW browser as a helper
application for NCBI's Entrez system, but it can also be used as a
standalone application.
Cn3D is available for Windows, Macintosh, and various UNIX
platforms.
- Submitted by: Martz, Eric. (Entry 23).
- GRASS is designed to facilitate the study of macromolecular function by mapping a number of structural, chemical, and biological properties onto various representations of molecular structure (molecular surfaces, wireframe, CPK spheres, or backbone tracing ribbons). The available properties currently include surface curvature, atomic charges, electrostatic potential, sequence variability, hydrophobicity, temperature factors, and distances from a ligand. The molecular properties and graphics are calculated on our server and sent to be viewed on the user's machine using any of three widely available visualization programs: a Virtual Reality Modeling Language (VRML) viewer, Chime, or Grasp.
- Co-authors: Hitz, Ben. Submitted by: the author. (Entry 55).
- STING is a PDB Viewer and Interactive WWW TOOL with
emphasis on bi-directional coupling of sequence and 3D
information. STING offers a simple and easy way to map single
amino acid letter code information in a sequence to its position
in 3D and vice versa!
Special attention in STING is given to MacroMolecular
INTERFACE analysis.
- Co-authors: Togawa,Roberto; Campos, Tharsis; Vilella, Wellington; Honig, Barry. Submitted by: the author. (Entry 17).
STING Millennium is a web based suite of programs that starts with visualizing molecular structure and then leads a user through a series of operations resulting in a comprehensive structure analysis:
amino acid sequence and structure
positions,with emphasis on bi-directional coupling of sequence and 3D
information
pattern search, neighbors identification,
H-bonds, angles and distances
between atoms are easy to obtain thanks to the intuitive graphic and menu interface.
In addition, a user can obtain:
sequence to structure relationships,
analysis of a quality of the
structure,
nature and volume of atomic
contacts of intra and inter chain type,
analysis of amino acid relative
conservation at specified position among homologous proteins, and
Accessible Surface Area
relationship of relative conservation
to the intra-chain contacts
functional parameters deciphered
etc..
Such powerful combination of tools is available from a single site, eliminating needs for time-consuming data parsing. As a real treat, STING Millennium offers to the users a compilation of all these data through Protein Dossier module.
STING Millennium can also be used as an application that provides a user friendly interface allowing to analyze several proteins at the same time. The proteins previously superimposed, can be displayed simultaneously and then analyzed. A user can compare active sites or any other relevant parts of structural alignment.
STING Millennium has been developed from original STING concept, however, we have completely rewritten all code and made a STING concept much more versatile. In terms of the system design the package is implemented using a variety of programming languages, each one better suited to a specific task:
Chime€ molecular visualization
plugin (MDL inc.) to provide the molecular rendering
Sequence window written in
Java€ that permits a complete control over the plugin and offers a series of
services
A JavaScript interface making
the bridge over the Java-plugin communication, which is specific for Netscape€
browsers
The PERL language is used as
a wrapper for processing web requests
The C++ classes are used for
more intensive programming tasks in structure parameter calculations
STING Millennium has several working modes permitting its use with:
A single
PDB structure (either from a database or single modeled structure in PDB format)
A structural alignment of several
structures (structures previously aligned with CE or PRISM software)
A PDB structure
along with a sequence alignment, containing the respective PDB sequence.
This offers a way to visualize sequence conservation/variation and correlate it with structural regions in the target protein. The structure can also have its residues colored by an index that indicates sequence conservation (sequence entropy) promoting a rapid identification of the sites subject to differential selective pressure
Several analytical programs developed by our group are listed under the modules entry in the main menu. They perform several tasks providing a powerful combination of tools to analyze the given PDB structure. These modules are:
HeSSper Graphical
Contacts Ramachandran
Plot IFR
Contacts PDB
file Text STINGPaint HORNET PDB
Cartoon SCORPION Protein
Dossier FORMIGA ConSSeq
The HeSSper data base is being re - generated now. For this reason, HESPER option on STING Millennium Modules menu is inactive. As son as the data base is re - generated, this option will become available.- Co-authors: Torres V.,Welolington; Campos F.,Tharsis; Lima F.,Leonardo; Luna M.,Fabio; Oliveira G.,Adilton; Miura T., Ronald; Inoue K,Marcus; Horita,Luiz Gustavo; Pappas,Georgios Jr.; Honig,Barry. Submitted by: the author. (Entry 18).