scholarly journals Symposium 20 - PABMB: Teaching biochemistry in a connected world: KEEPING 3D RESOURCES IN THE WEB TO LEARN ON PROTEIN STRUCTURE

2015 ◽  
Vol 13 ◽  
pp. 41
Author(s):  
Raul Herrera ◽  
M. A. Moya-León
Keyword(s):  
Protein Structure ◽  
Undergraduate Students ◽  
Dynamic Models ◽  
Protein Structures ◽  
Practical Experience ◽  
Dimensional Structure ◽  
New Paradigm ◽  
Ligand Interaction ◽  
Motivation For Learning ◽  
The Web

Symposium 20 - PABMB: Teaching biochemistry in a connected world Chair: Miguel Castanho, Universidade de Lisboa, PortugalAbstract:The new paradigm of higher education requires new teaching strategies to meet the learning objectives of biochemistry courses. Teaching biochemistry in the current state of science and society requires a special motivation for learning, especially for students of degrees other than Biochemistry. The traditional way of teaching, based on the teacher-student relationship, mostly unidirectional, does not fulfil the needs imposed in this era. Considering the current situation universities students require new abilities in their training and the use of computers can constitute a place for discovery and research, enabling the experience of new and diverse situations. The design of teaching material for undergraduate students who take biochemistry courses as complementary subject on their careers should be seen as an opportunity to complement theoretical aspects on the current courses. Three different approaches could be used: (I) a description of the basic concepts, like in a book but using dynamics figures. (II) Modelling proteins highlighting key motifs at the three-dimensional structure and residues where inhibitors can be attached. And (III) elaborating active quizzes where students can be driven on their learning. Building knowledge based on practical experience can improve student competences on basic science and the learning process can be complemented in the use of dynamics models. On the other hand, exploring protein structures from the web could give students a better comprehension of residues interaction and non-covalent forces involved in protein-protein or protein-ligand interaction. The use of dynamic models improves the comprehension of protein structure and their special link to amino acids residues or ligands. This work was supported by Anillo ACT1110 project. Key Words: protein structure, 3D source, learning activities.

Prediction of Structural and Functional Aspects of Protein

2014 ◽  
pp. 317-333
Author(s):  
Arun G. Ingale
Keyword(s):  
Protein Structure ◽  
Protein Structure Prediction ◽  
Structure Prediction ◽  
Tertiary Structure ◽  
Protein Structures ◽  
Three Dimensional ◽  
Dimensional Structure ◽  
Sequence Information ◽  
Predict Protein Structure ◽  
Basic Ideas

To predict the structure of protein from a primary amino acid sequence is computationally difficult. An investigation of the methods and algorithms used to predict protein structure and a thorough knowledge of the function and structure of proteins are critical for the advancement of biology and the life sciences as well as the development of better drugs, higher-yield crops, and even synthetic bio-fuels. To that end, this chapter sheds light on the methods used for protein structure prediction. This chapter covers the applications of modeled protein structures and unravels the relationship between pure sequence information and three-dimensional structure, which continues to be one of the greatest challenges in molecular biology. With this resource, it presents an all-encompassing examination of the problems, methods, tools, servers, databases, and applications of protein structure prediction, giving unique insight into the future applications of the modeled protein structures. In this chapter, current protein structure prediction methods are reviewed for a milieu on structure prediction, the prediction of structural fundamentals, tertiary structure prediction, and functional imminent. The basic ideas and advances of these directions are discussed in detail.

TOP: a new method for protein structure comparisons and similarity searches

2000 ◽  
Vol 33 (1) ◽  
pp. 176-183 ◽  
Author(s):  
Guoguang Lu
Keyword(s):  
User Interface ◽  
Protein Structure ◽  
Protein Structures ◽  
Three Dimensional ◽  
Data Bank ◽  
Structure Alignment ◽  
Dimensional Structure ◽  
Protein Structure Alignment ◽  
Protein Structure Analysis ◽  
Structure Comparison

In order to facilitate the three-dimensional structure comparison of proteins, software for making comparisons and searching for similarities to protein structures in databases has been developed. The program identifies the residues that share similar positions of both main-chain and side-chain atoms between two proteins. The unique functions of the software also include database processingviaInternet- and Web-based servers for different types of users. The developed method and its friendly user interface copes with many of the problems that frequently occur in protein structure comparisons, such as detecting structurally equivalent residues, misalignment caused by coincident match of Cαatoms, circular sequence permutations, tedious repetition of access, maintenance of the most recent database, and inconvenience of user interface. The program is also designed to cooperate with other tools in structural bioinformatics, such as the 3DB Browser software [Prilusky (1998).Protein Data Bank Q. Newslett.84, 3–4] and the SCOP database [Murzin, Brenner, Hubbard & Chothia (1995).J. Mol. Biol.247, 536–540], for convenient molecular modelling and protein structure analysis. A similarity ranking score of `structure diversity' is proposed in order to estimate the evolutionary distance between proteins based on the comparisons of their three-dimensional structures. The function of the program has been utilized as a part of an automated program for multiple protein structure alignment. In this paper, the algorithm of the program and results of systematic tests are presented and discussed.

scholarly journals A Probabilistic Programming Approach to Protein Structure Superposition

2019 ◽  
Author(s):  
Lys Sanz Moreta ◽  
Ahmad Salim Al-Sibahi ◽  
Douglas Theobald ◽  
William Bullock ◽  
Basile Nicolas Rommes ◽  
...  
Keyword(s):  
Protein Structure ◽  
Structure Prediction ◽  
Probabilistic Models ◽  
Protein Structures ◽  
Likelihood Estimation ◽  
Programming Approach ◽  
New Paradigm ◽  
Biomolecular Structure ◽  
Probabilistic Programming ◽  
Mean Structure

AbstractOptimal superposition of protein structures is crucial for understanding their structure, function, dynamics and evolution. We investigate the use of probabilistic programming to superimpose protein structures guided by a Bayesian model. Our model THESEUS-PP is based on the THESEUS model, a probabilistic model of protein superposition based on rotation, translation and perturbation of an underlying, latent mean structure. The model was implemented in the deep probabilistic programming language Pyro. Unlike conventional methods that minimize the sum of the squared distances, THESEUS takes into account correlated atom positions and heteroscedasticity (i.e., atom positions can feature different variances). THESEUS performs maximum likelihood estimation using iterative expectation-maximization. In contrast, THESEUS-PP allows automated maximum a-posteriori (MAP) estimation using suitable priors over rotation, translation, variances and latent mean structure. The results indicate that probabilistic programming is a powerful new paradigm for the formulation of Bayesian probabilistic models concerning biomolecular structure. Specifically, we envision the use of the THESEUS-PP model as a suitable error model or likelihood in Bayesian protein structure prediction using deep probabilistic programming.

scholarly journals Protein Structure Prediction Based on Improved Genetic Algorithm

2020 ◽  
Vol 11 (9) ◽  
pp. 450-454
Author(s):  
Jiaxi Liu ◽  
Keyword(s):  
Genetic Algorithm ◽  
Protein Structure ◽  
Amino Acid ◽  
Protein Structure Prediction ◽  
Structure Prediction ◽  
Protein Structures ◽  
Three Dimensional ◽  
Dimensional Structure ◽  
Improved Genetic Algorithm ◽  
Research Areas

The prediction of protein three-dimensional structure from amino acid sequence has been a challenge problem in bioinformatics, owing to the many potential applications for robust protein structure prediction methods. Protein structure prediction is essential to bioscience, and its research results are important for other research areas. Methods for the prediction an才d design of protein structures have advanced dramatically. The prediction of protein structure based on average hydrophobic values is discussed and an improved genetic algorithm is proposed to solve the optimization problem of hydrophobic protein structure prediction. An adjustment operator is designed with the average hydrophobic value to prevent the overlapping of amino acid positions. Finally, some numerical experiments are conducted to verify the feasibility and effectiveness of the proposed algorithm by comparing with the traditional HNN algorithm.

scholarly journals On the use of direct-coupling analysis with a reduced alphabet of amino acids combined with super-secondary structure motifs for protein fold prediction

2021 ◽  
Vol 3 (2) ◽  
Author(s):  
Bernat Anton ◽  
Mireia Besalú ◽  
Oriol Fornes ◽  
Jaume Bonet ◽  
Alexis Molina ◽  
...  
Keyword(s):  
Amino Acids ◽  
Protein Structure ◽  
Secondary Structure ◽  
Protein Structures ◽  
Three Dimensional ◽  
Direct Coupling ◽  
Dimensional Structure ◽  
Coupling Analysis ◽  
Multiple Sequence ◽  
Direct Coupling Analysis

Abstract Direct-coupling analysis (DCA) for studying the coevolution of residues in proteins has been widely used to predict the three-dimensional structure of a protein from its sequence. We present RADI/raDIMod, a variation of the original DCA algorithm that groups chemically equivalent residues combined with super-secondary structure motifs to model protein structures. Interestingly, the simplification produced by grouping amino acids into only two groups (polar and non-polar) is still representative of the physicochemical nature that characterizes the protein structure and it is in line with the role of hydrophobic forces in protein-folding funneling. As a result of a compressed alphabet, the number of sequences required for the multiple sequence alignment is reduced. The number of long-range contacts predicted is limited; therefore, our approach requires the use of neighboring sequence-positions. We use the prediction of secondary structure and motifs of super-secondary structures to predict local contacts. We use RADI and raDIMod, a fragment-based protein structure modelling, achieving near native conformations when the number of super-secondary motifs covers >30–50% of the sequence. Interestingly, although different contacts are predicted with different alphabets, they produce similar structures.

TOWARDS SCALEable PROTEIN STRUCTURE COMPARISON AND DATABASE SEARCH

2005 ◽  
Vol 14 (05) ◽  
pp. 827-848 ◽  
Author(s):  
CHERN-HOOI CHIONH ◽  
ZHIYONG HUANG ◽  
KIAN-LEE TAN ◽  
ZHEN YAO
Keyword(s):  
Protein Structure ◽  
Structural Properties ◽  
Protein Structures ◽  
Query Protein ◽  
Similarity Score ◽  
Three Dimensions ◽  
Dimensional Structure ◽  
Performance Study ◽  
Structure Comparison ◽  
Protein Structure Comparison

Comparing protein structures in three dimensions is a computationally expensive process that makes a full scan of a protein against a library of known protein structures impractical. To reduce the cost, we can use an approximation of the three dimensional structure that allows protein comparison to be performed quickly to filter away dissimilar proteins. In this paper, we present a new algorithm, called SCALE, for protein structure comparison. In SCALE, a protein is represented as a sequence of secondary structure elements (SSEs) augmented with 3D structural properties such as the distances and angles between the SSEs. As such, the comparison between two proteins is reduced to a sequence alignment problem between their corresponding sequences of SSEs. The 3-D structural properties of the proteins contribute to the similarity score between the two sequences. We have implemented SCALE, and compared its performance against existing schemes. Our performance study shows that SCALE outperforms existing methods in terms of both efficiency and effectiveness (measured in terms of precision and recall). To avoid exhaustive search, an index based on the structural properties is also proposed. The index prunes away a considerable amount of dissimilar proteins given a query protein.

scholarly journals Prediction of Structural and Functional Aspects of Protein

2017 ◽  
pp. 551-568
Author(s):  
Arun G. Ingale
Keyword(s):  
Protein Structure ◽  
Protein Structure Prediction ◽  
Structure Prediction ◽  
Tertiary Structure ◽  
Protein Structures ◽  
Three Dimensional ◽  
Dimensional Structure ◽  
Sequence Information ◽  
Predict Protein Structure ◽  
Basic Ideas

To predict the structure of protein from a primary amino acid sequence is computationally difficult. An investigation of the methods and algorithms used to predict protein structure and a thorough knowledge of the function and structure of proteins are critical for the advancement of biology and the life sciences as well as the development of better drugs, higher-yield crops, and even synthetic bio-fuels. To that end, this chapter sheds light on the methods used for protein structure prediction. This chapter covers the applications of modeled protein structures and unravels the relationship between pure sequence information and three-dimensional structure, which continues to be one of the greatest challenges in molecular biology. With this resource, it presents an all-encompassing examination of the problems, methods, tools, servers, databases, and applications of protein structure prediction, giving unique insight into the future applications of the modeled protein structures. In this chapter, current protein structure prediction methods are reviewed for a milieu on structure prediction, the prediction of structural fundamentals, tertiary structure prediction, and functional imminent. The basic ideas and advances of these directions are discussed in detail.

scholarly journals A COMPARATIVE STUDY OF PROTEIN TERTIARY STRUCTURE PREDICTION METHODS

2014 ◽  
pp. 15-18
Author(s):  
CHANDRAYANI N. ROKDE ◽  
DR.MANALI KSHIRSAGAR
Keyword(s):  
Protein Structure ◽  
Structure Prediction ◽  
Tertiary Structure ◽  
Sequence Data ◽  
Protein Structures ◽  
Three Dimensional ◽  
Data Bank ◽  
Dimensional Structure ◽  
X Ray Crystallography ◽  
Protein Tertiary Structure Prediction

Protein structure prediction (PSP) from amino acid sequence is one of the high focus problems in bioinformatics today. This is due to the fact that the biological function of the protein is determined by its three dimensional structure. The understanding of protein structures is vital to determine the function of a protein and its interaction with DNA, RNA and enzyme. Thus, protein structure is a fundamental area of computational biology. Its importance is intensed by large amounts of sequence data coming from PDB (Protein Data Bank) and the fact that experimentally methods such as X-ray crystallography or Nuclear Magnetic Resonance (NMR)which are used to determining protein structures remains very expensive and time consuming. In this paper, different types of protein structures and methods for its prediction are described.

scholarly journals Predicting the performance of automated crystallographic model-building pipelines

2021 ◽  
Vol 77 (12) ◽  
Author(s):  
Emad Alharbi ◽  
Paul Bond ◽  
Radu Calinescu ◽  
Kevin Cowtan
Keyword(s):  
Protein Structure ◽  
Model Building ◽  
Protein Structures ◽  
Software Tool ◽  
Crystallographic Data ◽  
Dimensional Structure ◽  
Data Sets ◽  
Data Set ◽  
Experimental Phasing ◽  
Computational Work

Proteins are macromolecules that perform essential biological functions which depend on their three-dimensional structure. Determining this structure involves complex laboratory and computational work. For the computational work, multiple software pipelines have been developed to build models of the protein structure from crystallographic data. Each of these pipelines performs differently depending on the characteristics of the electron-density map received as input. Identifying the best pipeline to use for a protein structure is difficult, as the pipeline performance differs significantly from one protein structure to another. As such, researchers often select pipelines that do not produce the best possible protein models from the available data. Here, a software tool is introduced which predicts key quality measures of the protein structures that a range of pipelines would generate if supplied with a given crystallographic data set. These measures are crystallographic quality-of-fit indicators based on included and withheld observations, and structure completeness. Extensive experiments carried out using over 2500 data sets show that the tool yields accurate predictions for both experimental phasing data sets (at resolutions between 1.2 and 4.0 Å) and molecular-replacement data sets (at resolutions between 1.0 and 3.5 Å). The tool can therefore provide a recommendation to the user concerning the pipelines that should be run in order to proceed most efficiently to a depositable model.

Sequence Specific Dihedral Angle Distribution: Application in Protein Structure Prediction and Evaluation

1970 ◽  
Vol 19 (2) ◽  
pp. 217-226
Author(s):  
S. M. Minhaz Ud-Dean ◽  
Mahdi Muhammad Moosa
Keyword(s):  
Protein Structure ◽  
Dihedral Angle ◽  
Protein Structure Prediction ◽  
Structure Prediction ◽  
Protein Structures ◽  
Angle Distribution ◽  
Ramachandran Plot ◽  
Specific Data ◽  
Specific Distribution ◽  
Structure Evaluation

Protein structure prediction and evaluation is one of the major fields of computational biology. Estimation of dihedral angle can provide information about the acceptability of both theoretically predicted and experimentally determined structures. Here we report on the sequence specific dihedral angle distribution of high resolution protein structures available in PDB and have developed Sasichandran, a tool for sequence specific dihedral angle prediction and structure evaluation. This tool will allow evaluation of a protein structure in pdb format from the sequence specific distribution of Ramachandran angles. Additionally, it will allow retrieval of the most probable Ramachandran angles for a given sequence along with the sequence specific data. Key words: Torsion angle, φ-ψ distribution, sequence specific ramachandran plot, Ramasekharan, protein structure appraisal D.O.I. 10.3329/ptcb.v19i2.5439 Plant Tissue Cult. & Biotech. 19(2): 217-226, 2009 (December)

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