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Calculating conservation and predicting hENT1 structure using the amino acid sequence

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dc.date.accessioned 2012-10-30T12:28:28Z und
dc.date.accessioned 2017-10-24T12:21:46Z
dc.date.available 2012-10-30T12:28:28Z und
dc.date.available 2017-10-24T12:21:46Z
dc.date.issued 2012-10-30T12:28:28Z
dc.identifier.uri http://radr.hulib.helsinki.fi/handle/10138.1/2084 und
dc.identifier.uri http://hdl.handle.net/10138.1/2084
dc.title Calculating conservation and predicting hENT1 structure using the amino acid sequence en
ethesis.department.URI http://data.hulib.helsinki.fi/id/61364eb4-647a-40e2-8539-11c5c0af8dc2
ethesis.department Institutionen för matematik och statistik sv
ethesis.department Department of Mathematics and Statistics en
ethesis.department Matematiikan ja tilastotieteen laitos fi
ethesis.faculty Matematisk-naturvetenskapliga fakulteten sv
ethesis.faculty Matemaattis-luonnontieteellinen tiedekunta fi
ethesis.faculty Faculty of Science en
ethesis.faculty.URI http://data.hulib.helsinki.fi/id/8d59209f-6614-4edd-9744-1ebdaf1d13ca
ethesis.university.URI http://data.hulib.helsinki.fi/id/50ae46d8-7ba9-4821-877c-c994c78b0d97
ethesis.university Helsingfors universitet sv
ethesis.university University of Helsinki en
ethesis.university Helsingin yliopisto fi
dct.creator Ng, Kim
dct.issued 2012
dct.language.ISO639-2 eng
dct.abstract In analysis of structural information for transmembrane (TM) proteins it is ideal to work with a three-dimensional (3D) structure. This is not always possible as determining an accurate 3D structure can be challenging and expensive as pursuing one can take large amounts of time. Sequence analysis is often used as a surrogate to determine a subset of information regarding secondary and tertiary protein structure given the primary structure (an amino acid sequence). Using Equilibrative Nucleoside Transporter member 1 (ENT1) as a model, the objective of predicting secondary and tertiary structure given primary structure is attempted through computational (in silico) methods. The in silico methods include the use of a pipeline of programs spanning both custom made and ready built software. A set of 2034 homologous protein sequences are first obtained from the initial human ENT1 (hENT1) sequence through a BLASTp. This sequence information is then processed to acquire information on variation, conservation, and hydrophobicity through topology prediction, hydropathic moment plots and variation moment plots. Comparing these results with data acquired from Glycerol-3-Phosphate Transporter (GlpT), a protein with a known 3D structure of 3.3 Angstrom resolution is done to assess evidence of evolutionary origin. This in turn allows estimation on the reliability of predictions to be made on aspects of the secondary and tertiary structure for hENT1. The results show that within predicted TM alpha helical regions that there is some level of correlation between the variation of the amino acids within the alpha helical TM region and its orientation towards the membrane. This can be further refined by gathering statistics on other known proteins with a 3D structure for their relationships in TM regions to hydrophobicity and variability. This will aid in secondary and tertiary structure predictions of other TM proteins given further refinement and additional data. In addition, the sequence conservation information obtained should prove to be robust and allow for a large number of sequences to be analyzed to determine conservation of amino acids given a reference protein. Ideally this information will provide aid in determining interesting amino acids for experiments to be done on hENT1. en
dct.language en
ethesis.language.URI http://data.hulib.helsinki.fi/id/languages/eng
ethesis.language English en
ethesis.language englanti fi
ethesis.language engelska sv
ethesis.thesistype pro gradu-avhandlingar sv
ethesis.thesistype pro gradu -tutkielmat fi
ethesis.thesistype master's thesis en
ethesis.thesistype.URI http://data.hulib.helsinki.fi/id/thesistypes/mastersthesis
ethesis.degreeprogram Bioinformatics en
dct.identifier.urn URN:NBN:fi-fe2017112251646
dc.type.dcmitype Text

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