Glucocerebrosidase sequence based prediction
Contents
Secondary structure prediction
General
The secondary structure of a protein is the three-dimensional form. In contrast to the tertiary structure it describes the local segments. Because of weak chemical forces like hydrogen bonds and the values of the φ and ψ angles they form different structures. The main types are α-helices and parallel and anti-parallel β-sheets. Some rare structures are π-helices and 3,10-helices. Another possibility are coils, which are irregular formed elements.
A protein consists of several secondary structure elements which build together the tertiary structure. <ref>http://en.wikipedia.org/wiki/Biomolecular_structure#Secondary_structure</ref>
PSIPRED
PSIPRED is a method by David T. Jones, published 1999 in JMB with "Protein Secondary Structure Prediction Based on Position-specific Scoring Matrices". PSIPRED works with a two-stage neural network to predict secondary structure. These are based on the position specific scoring matrices generated by PSI-BLAST, which is run before.<ref>David T. Jones, Protein Secondary Structure Prediction Based on Position-specific Scoring Matrices, JMB, 1999</ref>
We run the online and the local version of PSIPRED and got different results. In the following it is compared to the secondary structure given in Uniprot<ref>http://www.uniprot.org/uniprot/P04062</ref>.
Conf: | 988898954488887622315999999999998641038968865325999649995388
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online: | CCCCCCCCCCCCCCCCCHHHHHHHHHHHHHHHHHHHHCCCCCCCCCCCCCCCEEEEECCC
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Conf: | 987898955489988742200466888998986410038977877777863169974474
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local: | CCCCCCCCCCCCCCCCCEEEEHHHHHHHHHHHHHHHCCCCCCCCCCCCCCCEEEEEECCC
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uniprot: | ------------------------------------------------EEEE-EEEEEE-
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AA: | MEFSSPSREECPKPLSRVSIMAGSLTGLLLLQAVSWASGARPCIPKSFGYSSVVCVCNAT
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Conf: | 558889998889992599996377885421237645688875108995378301079247
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online: | CCCCCCCCCCCCCCCEEEEEECCCCCCCCCCCCCCCCCCCCCCCEEEECCCCCEEEEEEE
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Conf: | 148899998788875431100345640022100111177897107840966454557422
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local: | CCCCCCCCCCCCCCCCCCCCCCCCCCCEEEEEEEEECCCCCCCCEEEECCCCCCCEEEEE
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uniprot: | -------------EEEEEEEE-----EEEEEEE-EEE----EEEEEEEEEEEEEE--EEE
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AA: | YCDSFDPPTFPALGTFSRYESTRSGRRMELSMGPIQANHTGTGLLLTLQPEQKFQKVKGF
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Conf: | 300233899997249999999999860597882105999750588999986666899999
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online: | EECCCHHHHHHHHCCCHHHHHHHHHHCCCCCCCEEEEEEEEECCCCCCCCCCCCCCCCCC
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Conf: | 011335889987508927898998851396893001358621344677653324799999
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local: | CCCCCHHHHHHHHHCCHHHHHHHHHHHCCCCCCEEEEEEEECCCCCCCCCCCCCCCCCCC
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uniprot: | EE--HHHHHHH----HHHHHHHHHHHH-CCCC---EEEEEEE--EEEEE------EEE--
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AA: | GGAMTDAAALNILALSPPAQNLLLKSYFSEEGIGYNIIRVPMASCDFSIRTYTYADTPDD
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Conf: | 689999994100245289999999971999389971377785612147247999889999
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online: | CCCCCCCCCHHCCCCCHHHHHHHHHHCCCCCEEEECCCCCCCCCEECCCCCCCCCCCCCC
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Conf: | 721111368543220024799998733999689957899974220056347854325899
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local: | CCCCCCCCCCCCCCCHHHHHHHHHHHCCCCCEEEECCCCCCCCCCCCCCCCCCCCCCCCC
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uniprot: | --------HHHH--HHHHHHHHHHH-----EEEEEEE---HHH----EEEEE-EEEE---
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AA: | FQLHNFSLPEEDTKLKIPLIHRALQLAQRPVSLLASPWTSPTWLKTNGAVNGKGSLKGQP
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Conf: | 922699999999999999975490786872012579899999999986349999999999
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online: | CCHHHHHHHHHHHHHHHHHHHCCEEEEEEECCCCCCCCCCCCCCCCCCCCCHHHHHHHHH
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Conf: | 971468799999999967663395143898112789787678873222114422121122
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local: | CCHHHHHHHHHHHHHHHHHHHCCCCEEEEEEECCCCCCCCCCCCCCCCCCCCCCCCHHHH
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uniprot: | -HHHHHHHHHHHHHHHHHHH-----EEEEE-----HHH------------HHHHHHHHHH
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AA: | GDIYHQTWARYFVKFLDAYAEHKLQFWAVTAENEPSAGLLSGYPFQCLGFTPEHQRDFIA
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Conf: | 955799851689972999944888873334664149955640224689831699998033
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online: | HHHHHHHHCCCCCCEEEEEECCCCCCHHHHHHHHCCCHHHHCCCCEEEEEECCCCCCHHH
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Conf: | 111332310577410134212544556520222238976651151878702212236320
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local: | HHHHHHHHCCCCCCCEEEEECCCCCCCCCCHHHHCCCHHHHHCCEEEEEECCCCCCCCCC
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uniprot: | -HHHHHH--CCCCEEEEEEEEEHHH--HHHHHHH--HHHH----EEEEEEE------HHH
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AA: | RDLGPTLANSTHHNVRLLMLDDQRLLLPHWAKVVLTDPEAAKYVHGIAVHWYLDFLAPAK
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Conf: | 412688750999509994343699998866567831444255999999996402335772
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online: | HHHHHHHHCCCCCEEEEECCCCCCCCCCCCCCCCCHHHHHHHHHHHHHHHHHCCEEEEEE
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Conf: | 011111126898001101210389653344579861210143212566552001100000
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local: | CCCCCCCCCCCCCCEEHHHHCCCCCCCCCCCCCCCHHHHCCCCHHHHHHHHHHHHHHEEE
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uniprot: | HHHHHHHH---EEEEEEEEE--------------HHHHHHHHHHHHHHHH--EEEEEEEE
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AA: | ATLGETHRLFPNTMLFASEACVGSKFWEQSVRLGSWDRGMQYSHSIITNLLYHVVGWTDW
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Conf: | 000169999986689878535895679769986202333102244469939999542389
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online: | EECCCCCCCCCCCCCCCCCCEEEECCCCEEEECCHHHHHHHHCCCCCCCCEEEEEEECCC
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Conf: | 023699999860001325228998208703226821232123444679927984435078
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local: | CCCCCCCCCCCCEECCCCCCEEEEECCCCEEECCCEEEECCCCCCCCCCCEEEEEEEECC
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uniprot: | E-----------------EEEEEHHH-EEEE-HHHHHHHHHH-------EEEEEEEEE--
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AA: | NLALNPEGGPNWVRNFVDSPIIVDITKDTFYKQPMFYHLGHFSKFIPEGSQRVGLVASQK
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Conf: | 99028999928998999999099993779999099304998518951899999309
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online: | CCCEEEEEECCCCCEEEEEECCCCCCEEEEEEECCCCEEEEECCCCEEEEEEEEEC
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Conf: | 99538995649997799999146898214741998642000389842568774139
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local: | CCCCEEEEECCCCCEEEEEEECCCCCEEEEECCCCCCCCCCCCCCCEEEEEEEECC
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uniprot: | EEEEEEEE-----EEEEEEE-EEE-EEEEEEECCCEEEEEEE---EEEEEEE----
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AA: | NDLDAVALMHPDGSAVVVVLNRSSKDVPLTIKDPAVGFLETISPGYSIHTYLWRRQ
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The results differ a lot. The online version of PSIPRED seems to have different parameters than the local version. So we got different results. Compared to the given secondary structure in Uniprot there are many regions that are predicted wrong.
Jpred3
Comparison with DSSP
Prediction of disordered regions
General
DISOPRED
POODLE
IUPRED
Prediction of transmembrane alpha-helices and signal peptides
General
Why is the prediction of transmembrane helices and signal peptides grouped together here?
signal peptides
TMHMM
Phobius and PolyPhobius
Phobius
PolyPhobius
OCTOPUS and SPOCTOPUS
OCTOPUS
SOCTOPUS
SignalIP
TargetP
Prediction of GO terms
General
GOPET
Pfam
ProtFun 2.2
References
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