Glycosylator: a Python framework for the rapid modeling of glycans
Background Carbohydrates are a class of large and diverse biomolecules, ranging from a simple monosaccharide to large multi-branching glycan structures. The covalent linkage of a carbohydrate to the nitrogen atom of an asparagine, a process referred to as N- linked glycosylation, plays an important...
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          | Published in | BMC bioinformatics Vol. 20; no. 1; pp. 513 - 7 | 
|---|---|
| Main Authors | , | 
| Format | Journal Article | 
| Language | English | 
| Published | 
        London
          BioMed Central
    
        22.10.2019
     BioMed Central Ltd BMC  | 
| Subjects | |
| Online Access | Get full text | 
| ISSN | 1471-2105 1471-2105  | 
| DOI | 10.1186/s12859-019-3097-6 | 
Cover
| Abstract | Background
Carbohydrates are a class of large and diverse biomolecules, ranging from a simple monosaccharide to large multi-branching glycan structures. The covalent linkage of a carbohydrate to the nitrogen atom of an asparagine, a process referred to as
N-
linked glycosylation, plays an important role in the physiology of many living organisms. Most software for glycan modeling on a personal desktop computer requires knowledge of molecular dynamics to interface with specialized programs such as CHARMM or AMBER. There are a number of popular web-based tools that are available for modeling glycans (e.g., GLYCAM-WEB (http://
https://dev.glycam.org/gp/
) or Glycosciences.db (
http://www.glycosciences.de/
)). However, these web-based tools are generally limited to a few canonical glycan conformations and do not allow the user to incorporate glycan modeling into their protein structure modeling workflow.
Results
Here, we present Glycosylator, a Python framework for the identification, modeling and modification of glycans in protein structure that can be used directly in a Python script through its application programming interface (API) or through its graphical user interface (GUI). The GUI provides a straightforward two-dimensional (2D) rendering of a glycoprotein that allows for a quick visual inspection of the glycosylation state of all the sequons on a protein structure. Modeled glycans can be further refined by a genetic algorithm for removing clashes and sampling alternative conformations. Glycosylator can also identify specific three-dimensional (3D) glycans on a protein structure using a library of predefined templates.
Conclusions
Glycosylator was used to generate models of glycosylated protein without steric clashes. Since the molecular topology is based on the CHARMM force field, new complex sugar moieties can be generated without modifying the internals of the code. Glycosylator provides more functionality for analyzing and modeling glycans than any other available software or webserver at present. Glycosylator will be a valuable tool for the glycoinformatics and biomolecular modeling communities. | 
    
|---|---|
| AbstractList | Carbohydrates are a class of large and diverse biomolecules, ranging from a simple monosaccharide to large multi-branching glycan structures. The covalent linkage of a carbohydrate to the nitrogen atom of an asparagine, a process referred to as N-linked glycosylation, plays an important role in the physiology of many living organisms. Most software for glycan modeling on a personal desktop computer requires knowledge of molecular dynamics to interface with specialized programs such as CHARMM or AMBER. There are a number of popular web-based tools that are available for modeling glycans (e.g., GLYCAM-WEB (http://https://dev.glycam.org/gp/) or Glycosciences.db (http://www.glycosciences.de/)). However, these web-based tools are generally limited to a few canonical glycan conformations and do not allow the user to incorporate glycan modeling into their protein structure modeling workflow. Here, we present Glycosylator, a Python framework for the identification, modeling and modification of glycans in protein structure that can be used directly in a Python script through its application programming interface (API) or through its graphical user interface (GUI). The GUI provides a straightforward two-dimensional (2D) rendering of a glycoprotein that allows for a quick visual inspection of the glycosylation state of all the sequons on a protein structure. Modeled glycans can be further refined by a genetic algorithm for removing clashes and sampling alternative conformations. Glycosylator can also identify specific three-dimensional (3D) glycans on a protein structure using a library of predefined templates. Glycosylator was used to generate models of glycosylated protein without steric clashes. Since the molecular topology is based on the CHARMM force field, new complex sugar moieties can be generated without modifying the internals of the code. Glycosylator provides more functionality for analyzing and modeling glycans than any other available software or webserver at present. Glycosylator will be a valuable tool for the glycoinformatics and biomolecular modeling communities. Abstract Background Carbohydrates are a class of large and diverse biomolecules, ranging from a simple monosaccharide to large multi-branching glycan structures. The covalent linkage of a carbohydrate to the nitrogen atom of an asparagine, a process referred to as N-linked glycosylation, plays an important role in the physiology of many living organisms. Most software for glycan modeling on a personal desktop computer requires knowledge of molecular dynamics to interface with specialized programs such as CHARMM or AMBER. There are a number of popular web-based tools that are available for modeling glycans (e.g., GLYCAM-WEB (http://https://dev.glycam.org/gp/) or Glycosciences.db (http://www.glycosciences.de/)). However, these web-based tools are generally limited to a few canonical glycan conformations and do not allow the user to incorporate glycan modeling into their protein structure modeling workflow. Results Here, we present Glycosylator, a Python framework for the identification, modeling and modification of glycans in protein structure that can be used directly in a Python script through its application programming interface (API) or through its graphical user interface (GUI). The GUI provides a straightforward two-dimensional (2D) rendering of a glycoprotein that allows for a quick visual inspection of the glycosylation state of all the sequons on a protein structure. Modeled glycans can be further refined by a genetic algorithm for removing clashes and sampling alternative conformations. Glycosylator can also identify specific three-dimensional (3D) glycans on a protein structure using a library of predefined templates. Conclusions Glycosylator was used to generate models of glycosylated protein without steric clashes. Since the molecular topology is based on the CHARMM force field, new complex sugar moieties can be generated without modifying the internals of the code. Glycosylator provides more functionality for analyzing and modeling glycans than any other available software or webserver at present. Glycosylator will be a valuable tool for the glycoinformatics and biomolecular modeling communities. Background Carbohydrates are a class of large and diverse biomolecules, ranging from a simple monosaccharide to large multi-branching glycan structures. The covalent linkage of a carbohydrate to the nitrogen atom of an asparagine, a process referred to as N-linked glycosylation, plays an important role in the physiology of many living organisms. Most software for glycan modeling on a personal desktop computer requires knowledge of molecular dynamics to interface with specialized programs such as CHARMM or AMBER. There are a number of popular web-based tools that are available for modeling glycans (e.g., GLYCAM-WEB ( Results Here, we present Glycosylator, a Python framework for the identification, modeling and modification of glycans in protein structure that can be used directly in a Python script through its application programming interface (API) or through its graphical user interface (GUI). The GUI provides a straightforward two-dimensional (2D) rendering of a glycoprotein that allows for a quick visual inspection of the glycosylation state of all the sequons on a protein structure. Modeled glycans can be further refined by a genetic algorithm for removing clashes and sampling alternative conformations. Glycosylator can also identify specific three-dimensional (3D) glycans on a protein structure using a library of predefined templates. Conclusions Glycosylator was used to generate models of glycosylated protein without steric clashes. Since the molecular topology is based on the CHARMM force field, new complex sugar moieties can be generated without modifying the internals of the code. Glycosylator provides more functionality for analyzing and modeling glycans than any other available software or webserver at present. Glycosylator will be a valuable tool for the glycoinformatics and biomolecular modeling communities. Keywords: N-linked glycosylation, Glycan modeling, Glycoprotein, Biomolecular modeling Background Carbohydrates are a class of large and diverse biomolecules, ranging from a simple monosaccharide to large multi-branching glycan structures. The covalent linkage of a carbohydrate to the nitrogen atom of an asparagine, a process referred to as N- linked glycosylation, plays an important role in the physiology of many living organisms. Most software for glycan modeling on a personal desktop computer requires knowledge of molecular dynamics to interface with specialized programs such as CHARMM or AMBER. There are a number of popular web-based tools that are available for modeling glycans (e.g., GLYCAM-WEB (http:// https://dev.glycam.org/gp/ ) or Glycosciences.db ( http://www.glycosciences.de/ )). However, these web-based tools are generally limited to a few canonical glycan conformations and do not allow the user to incorporate glycan modeling into their protein structure modeling workflow. Results Here, we present Glycosylator, a Python framework for the identification, modeling and modification of glycans in protein structure that can be used directly in a Python script through its application programming interface (API) or through its graphical user interface (GUI). The GUI provides a straightforward two-dimensional (2D) rendering of a glycoprotein that allows for a quick visual inspection of the glycosylation state of all the sequons on a protein structure. Modeled glycans can be further refined by a genetic algorithm for removing clashes and sampling alternative conformations. Glycosylator can also identify specific three-dimensional (3D) glycans on a protein structure using a library of predefined templates. Conclusions Glycosylator was used to generate models of glycosylated protein without steric clashes. Since the molecular topology is based on the CHARMM force field, new complex sugar moieties can be generated without modifying the internals of the code. Glycosylator provides more functionality for analyzing and modeling glycans than any other available software or webserver at present. Glycosylator will be a valuable tool for the glycoinformatics and biomolecular modeling communities. Carbohydrates are a class of large and diverse biomolecules, ranging from a simple monosaccharide to large multi-branching glycan structures. The covalent linkage of a carbohydrate to the nitrogen atom of an asparagine, a process referred to as N-linked glycosylation, plays an important role in the physiology of many living organisms. Most software for glycan modeling on a personal desktop computer requires knowledge of molecular dynamics to interface with specialized programs such as CHARMM or AMBER. There are a number of popular web-based tools that are available for modeling glycans (e.g., GLYCAM-WEB (http:// https://dev.glycam.org/gp/ ) or Glycosciences.db ( http://www.glycosciences.de/ )). However, these web-based tools are generally limited to a few canonical glycan conformations and do not allow the user to incorporate glycan modeling into their protein structure modeling workflow.BACKGROUNDCarbohydrates are a class of large and diverse biomolecules, ranging from a simple monosaccharide to large multi-branching glycan structures. The covalent linkage of a carbohydrate to the nitrogen atom of an asparagine, a process referred to as N-linked glycosylation, plays an important role in the physiology of many living organisms. Most software for glycan modeling on a personal desktop computer requires knowledge of molecular dynamics to interface with specialized programs such as CHARMM or AMBER. There are a number of popular web-based tools that are available for modeling glycans (e.g., GLYCAM-WEB (http:// https://dev.glycam.org/gp/ ) or Glycosciences.db ( http://www.glycosciences.de/ )). However, these web-based tools are generally limited to a few canonical glycan conformations and do not allow the user to incorporate glycan modeling into their protein structure modeling workflow.Here, we present Glycosylator, a Python framework for the identification, modeling and modification of glycans in protein structure that can be used directly in a Python script through its application programming interface (API) or through its graphical user interface (GUI). The GUI provides a straightforward two-dimensional (2D) rendering of a glycoprotein that allows for a quick visual inspection of the glycosylation state of all the sequons on a protein structure. Modeled glycans can be further refined by a genetic algorithm for removing clashes and sampling alternative conformations. Glycosylator can also identify specific three-dimensional (3D) glycans on a protein structure using a library of predefined templates.RESULTSHere, we present Glycosylator, a Python framework for the identification, modeling and modification of glycans in protein structure that can be used directly in a Python script through its application programming interface (API) or through its graphical user interface (GUI). The GUI provides a straightforward two-dimensional (2D) rendering of a glycoprotein that allows for a quick visual inspection of the glycosylation state of all the sequons on a protein structure. Modeled glycans can be further refined by a genetic algorithm for removing clashes and sampling alternative conformations. Glycosylator can also identify specific three-dimensional (3D) glycans on a protein structure using a library of predefined templates.Glycosylator was used to generate models of glycosylated protein without steric clashes. Since the molecular topology is based on the CHARMM force field, new complex sugar moieties can be generated without modifying the internals of the code. Glycosylator provides more functionality for analyzing and modeling glycans than any other available software or webserver at present. Glycosylator will be a valuable tool for the glycoinformatics and biomolecular modeling communities.CONCLUSIONSGlycosylator was used to generate models of glycosylated protein without steric clashes. Since the molecular topology is based on the CHARMM force field, new complex sugar moieties can be generated without modifying the internals of the code. Glycosylator provides more functionality for analyzing and modeling glycans than any other available software or webserver at present. Glycosylator will be a valuable tool for the glycoinformatics and biomolecular modeling communities.  | 
    
| ArticleNumber | 513 | 
    
| Audience | Academic | 
    
| Author | Soto, Cinque Lemmin, Thomas  | 
    
| Author_xml | – sequence: 1 givenname: Thomas orcidid: 0000-0001-5705-4964 surname: Lemmin fullname: Lemmin, Thomas email: thomas.lemmin@inf.ethz.ch organization: DS3Lab, System Group, Department of Computer Sciences, ETH Zurich, Institute of Medical Virology, University of Zurich (UZH) – sequence: 2 givenname: Cinque surname: Soto fullname: Soto, Cinque email: cinque.soto@vumc.org organization: Vanderbilt Vaccine Center, Vanderbilt University Medical Center, Department of Pediatrics, Vanderbilt University Medical Center  | 
    
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| Cites_doi | 10.1016/j.carres.2017.04.015 10.1016/S0304-4165(99)00165-8 10.1007/s11427-015-4980-7 10.1093/nar/gky994 10.1021/ct200328p 10.1002/(SICI)1097-0282(199609)39:3<417::AID-BIP13>3.0.CO;2-8 10.1016/0263-7855(96)00018-5 10.1186/1471-2105-5-69 10.1002/jcc.21886 10.1093/bioinformatics/btr168 10.1155/2010/148178 10.1002/jcc.20820 10.1002/jcc.20289 10.1109/MCSE.2007.55 10.1021/acs.jcim.7b00237 10.1093/glycob/cwz003 10.1016/j.cell.2016.04.010 10.1074/jbc.R400036200 10.1021/acs.jctc.8b01066 10.1093/protein/3.5.433 10.1002/cbic.201600665 10.3390/v11040374 10.1093/bioinformatics/btx358 10.3390/v6031294 10.1093/bioinformatics/15.9.767 10.1016/j.bbagen.2010.03.013 10.1016/j.str.2017.07.018 10.1002/star.200890000 10.1002/jcc.20945 10.3390/ijms19020580 10.1093/glycob/12.4.43R 10.1016/j.tim.2007.03.003 10.1038/nrm4073  | 
    
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| References | Y Gavel (3097_CR4) 1990; 3 IG Ferreira (3097_CR6) 2018; 19 S Shahzad-Ul-Hussan (3097_CR34) 2017; 18 R Danne (3097_CR14) 2017; 57 JC Phillips (3097_CR31) 2005; 26 M Böhm (3097_CR20) 2019; 47 3097_CR16 JD Hunter (3097_CR27) 2007; 9 DJ Vigerust (3097_CR11) 2007; 15 W Humphrey (3097_CR30) 1996; 14 A Yan (3097_CR2) 2005; 280 S Jo (3097_CR23) 2008; 29 J Lee (3097_CR24) 2019; 15 RG Spiro (3097_CR3) 2002; 12 F Zhu (3097_CR9) 2016; 59 T Lemmin (3097_CR35) 2017; 25 ME Janik (3097_CR7) 2010; 1800 O Guvench (3097_CR22) 2011; 7 S Tsuchiya (3097_CR12) 2017; 445 A Bakan (3097_CR25) 2011; 27 Anne Dell (3097_CR8) 2010; 2010 3097_CR26 S Jo (3097_CR17) 2011; 32 GBE Stewart-Jones (3097_CR33) 2016; 165 P Le Mercier (3097_CR28) 2019; 11 R Apweiler (3097_CR1) 1999; 1473 S-J Park (3097_CR18) 2017; 33 MD Tate (3097_CR10) 2014; 6 T Lütteke (3097_CR32) 2004; 5 C Xu (3097_CR5) 2015; 16 S-J Park (3097_CR19) 2019; 29 KN Kirschner (3097_CR21) 2008; 29 F Schierbaum (3097_CR29) 2008; 60 A Bohne (3097_CR15) 1999; 15 SB Engelsen (3097_CR13) 1996; 39  | 
    
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Carbohydrates are a class of large and diverse biomolecules, ranging from a simple monosaccharide to large multi-branching glycan structures. The... Carbohydrates are a class of large and diverse biomolecules, ranging from a simple monosaccharide to large multi-branching glycan structures. The covalent... Background Carbohydrates are a class of large and diverse biomolecules, ranging from a simple monosaccharide to large multi-branching glycan structures. The... Abstract Background Carbohydrates are a class of large and diverse biomolecules, ranging from a simple monosaccharide to large multi-branching glycan...  | 
    
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| SubjectTerms | Algorithms Applications programming Asparagine Biochemistry Bioinformatics Biomedical and Life Sciences Biomolecular modeling Biotechnology Computational biology Computational Biology/Bioinformatics Computer Appl. in Life Sciences Fructose Glycan modeling Glycoprotein Graphical user interfaces Life Sciences Methods Microarrays Molecular dynamics N-linked glycosylation Nitrogen (Chemical element) Polysaccharides Software Structural analysis Sugar Web site management software Workflow software  | 
    
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| Title | Glycosylator: a Python framework for the rapid modeling of glycans | 
    
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