Difference between revisions of "Fabry:Sequence alignments (sequence searches and multiple alignments):Results"
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TODO: Add pictures of MSA and find a way to present them, since they are _very_ wide --[[User:Rackersederj|Rackersederj]] 07:06, 5 May 2012 (UTC)<br> |
TODO: Add pictures of MSA and find a way to present them, since they are _very_ wide --[[User:Rackersederj|Rackersederj]] 07:06, 5 May 2012 (UTC)<br> |
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− | Maybe only interesting parts or the active site...? --[[User:Rackersederj|Rackersederj]] 13:07, 5 May 2012 (UTC) |
+ | Maybe only interesting parts or the active site...? --[[User:Rackersederj|Rackersederj]] 13:07, 5 May 2012 (UTC) ... Active site (D179 and D231) and partly the surrounding parts are highly conserved! Functional sites... maybe also Glycosylation site (139,192,215,408) and Disulfide bonds (52 ↔ 94, 56 ↔ 63, 142 ↔ 172, 202 ↔ 223, 378 ↔ 382) |
Revision as of 16:16, 5 May 2012
Please see Task 2 for our scripts and line of action on this topic.
Contents
Reference sequence
The reference sequence of α-Galactosidase A that will be used in this task was obtained from Swissprot P06280.
>gi|4504009|ref|NP_000160.1| alpha-galactosidase A precursor [Homo sapiens] MQLRNPELHLGCALALRFLALVSWDIPGARALDNGLARTPTMGWLHWERFMCNLDCQEEPDSCISEKLFM EMAELMVSEGWKDAGYEYLCIDDCWMAPQRDSEGRLQADPQRFPHGIRQLANYVHSKGLKLGIYADVGNK TCAGFPGSFGYYDIDAQTFADWGVDLLKFDGCYCDSLENLADGYKHMSLALNRTGRSIVYSCEWPLYMWP FQKPNYTEIRQYCNHWRNFADIDDSWKSIKSILDWTSFNQERIVDVAGPGGWNDPDMLVIGNFGLSWNQQ VTQMALWAIMAAPLFMSNDLRHISPQAKALLQDKDVIAINQDPLGKQGYQLRQGDNFEVWERPLSGLAWA VAMINRQEIGGPRSYTIAVASLGKGVACNPACFITQLLPVKRKLGFYEWTSRLRSHINPTGTVLLQLENT MQMSLKDLL
Sequence searches
Blast
<figtable id="blastidev">
</figtable>
First we performed a BLAST search with the default parameter. Since all hits were significant we raised the number of shown one line descriptions (-v) as well as the number of database sequences to show alignments for (-b). This led to 663 hits with an E-value smaller or equal to 0.003, which we declared as significant in our search. For these proteins we extracted the E-value and the number of positive and also of identical amino acids of the pairwise alignments, as well as the length of each hit. You can see a histogram of each of these features on the left.
For the comparison of the GO terms, we obtained the set of terms for each hit and analyzed the number of those in common with the GO terms of the search protein α-Galactosidase A . We devided the number of common terms by the number of GO terms of P06280 (49). Since these proportions are very small, we thought it would also make sense to explore the fraction of the hits GO terms shared with the reference terms. Thus we devided the number if common terms by the number of terms of the hit. The histogram of the second rate show that in average over 80% of the GO terms of each hit are common with those of AGAL. The small amount of average accordance of the Galactosidase terms to the hit terms may be due to the fact that humans are a lot more complex than the species the homologous hits belong to. So the protein has to fullfill more needs in a more complex organism and thus has more GO terms assigned.
The average length fits the length of the α-Galactosidase A protein very well. This can be seen in the left picture Histogram of the length of the BLAST hits for P06280. On average over 51% of the residues are positive and almost 36% are identical hits. Thus on average 87% of the residues in each alignment are similar to the protein sequence of AGAL.
Psi-Blast
HHblits
We searched the "big80" database with HHblits using the default settings and also with the maximum number of possible iterations (8).
2 iterations - default
<figtable id="blastidev">
</figtable>
Number of hits with Evalue < 0.003: 326
8 iterations
<figtable id="blastidev">
</figtable>
Number of hits with Evalue < 0.003: 729
The first HHblits run took about 2.5 minutes, the second one about 16 minutes (see section Time).
Comparison sequence searches
Comparing the hits
Venn diagrams created with Oliveros, J.C. (2007) VENNY. An interactive tool for comparing lists with Venn Diagrams.
In the Venn diagrams one realises, that only a small portion of the found hits is shared by all three methods. Each method seems to have a very unique set of findings. The biggest overlap is between the BLAST and Psi-BLAST hits, which is according to our expectations, since these two use similar approaches, while HHBlits searches by using iterative HMM-HMM comparison. These facts become most obvious in the last picture, where only the 100 best hits of all three methods are compared. Only eleven hits are common among all methods. The remaining 89 are shared by BLAST and Psi-BLAST and are unique in the HHBlits search. The comparison of all hits with E-value smaller or equal to 0.03 in all methods looks similar. It is noteworthy that here even a small number of hits is even shared only by HHBlits and BLAST (52), as well as Psi-BLAST and HHBlits (2). The overlap of the two different HHBlits searched with 2 and 8 iterations shows also a great amount of overlap.
Comparing the Evalues
![Fabry animation.gif](/wiki/images/0/08/Fabry_animation.gif)
Above you can see an animated histogram of the distribution of the E-values, for the search performed with different methods. The R Script is based on Andrea's R Script psiBlast.evalueHist.Rscript
As one can clearly see, the number of significant hits in the Psi-Blast search exceeds the number of hits in any of the other two searches by far. Also this histogram looks more like a normal distribution with mean -80, while the histograms of the BLAST and the HHBlits search do not, but rather tend towards the zero point. The least hits are generated by the "ordinary" BLAST search (663), the Psi-BLAST search finds the ten-fold number (6868). Thus in respect to the E-values I would prefer using Psi-Blast.
Time
We evaluated the time the programs ran with the command "time"
Method | Parameter | Time |
---|---|---|
Blast v = 700 | b = 700, v = 700 | 1m53.944s |
HHBlits | default | 2m19.519s |
HHBlits | n = 8 | 16m7.754s |
Multiple sequence alignments
Dataset
We used the following 21 proteins to create multiple sequence alignments with the different methods. Since we only had three sequences for the first group, we added an additional sequence to each of the other ones to have a sufficiently large number of proteins in our datasets.
#99 - 90% sequence identity >tr|B4DLT5|B4DLT5_HUMAN cDNA FLJ56739, highly similar to Alpha-galactosidase A (EC 3.2.1.22) OS=Homo sapiens | Identities = 183/183 (100%) >tr|G3SI81|G3SI81_GORGO Uncharacterized protein OS=Gorilla gorilla|Identities = 390/432 (90%) >UP20|LOZLIBUBA|1|64 Alpha-galactosidase A (Fragment). [Ateles belzebuth chamek]|O97898|Identities=97% #89 - 60% sequence identity >tr|G1P280|G1P280_MYOLU Uncharacterized protein OS=Myotis lucifugus|Identities = 341/410 (83%) >tr|G1T044|G1T044_RABIT Uncharacterized protein OS=Oryctolagus|Identities = 348/420 (82%) >tr|E1B725|E1B725_BOVIN Uncharacterized protein OS=Bos taurus GN=GLA|Identities = 334/413 (80%) >tr|D3ZJF9|D3ZJF9_RAT Galactosidase, alpha (Mapped), isoform CRA_a|Identities = 331/418 (79%) >tr|H2L5H7|H2L5H7_ORYLA Uncharacterized protein (Fragment)|Identities = 255/402 (63%) >tr|E1BT44|E1BT44_CHICK Uncharacterized protein OS=Gallus gallus|Identities = 276/385 (71%) #59 - 40% sequence identity >tr|E2B637|E2B637_HARSA Alpha-N-acetylgalactosaminidase|Identities = 204/411 (49%) >tr|F4WJD6|F4WJD6_ACREC Alpha-N-acetylgalactosaminidase|Identities = 195/394 (49%) >tr|D2T1A8|D2T1A8_CHOPA Putative alpha-N-acetylgalactosaminidase|Identities = 202/413 (48%) >tr|G5BPR2|G5BPR2_HETGA Alpha-N-acetylgalactosaminidase|Identities = 168/292 (57%) >tr|F5BFS9|F5BFS9_TOBAC Alpha-galactosidase OS=Nicotiana tabacum|Identities = 145/329 (44%) >tr|Q3UZX5|Q3UZX5_MOUSE Putative uncharacterized protein OS=Mus|Identities = 140/239 (58%) #39 - 20% sequence identity >tr|F1T8Q0|F1T8Q0_9CLOT Alpha-galactosidase (Precursor)|Identities = 164/416 (39%) >tr|G6DHZ5|G6DHZ5_DANPL Alpha-N-acetylgalactosaminidase OS=Danaus|Identities = 110/294 (37%) >tr|C7G8V8|C7G8V8_9FIRM Alpha-galactosidase OS=Roseburia|Identities = 134/347 (38%) >tr|F8EMB8|F8EMB8_RUNSL Alpha-galactosidase (Precursor) OS=Runella|Identities = 106/366 (28%) >tr|G0FV12|G0FV12_AMYMD Melibiase OS=Amycolatopsis mediterranei S699|Identities = 104/411 (25%) >tr|B9TQP6|B9TQP6_RICCO Alpha-galactosidase/alpha-n-acetylgalactosaminidase|Identities = 31/93 (33%)
TODO: Add pictures of MSA and find a way to present them, since they are _very_ wide --Rackersederj 07:06, 5 May 2012 (UTC)
Maybe only interesting parts or the active site...? --Rackersederj 13:07, 5 May 2012 (UTC) ... Active site (D179 and D231) and partly the surrounding parts are highly conserved! Functional sites... maybe also Glycosylation site (139,192,215,408) and Disulfide bonds (52 ↔ 94, 56 ↔ 63, 142 ↔ 172, 202 ↔ 223, 378 ↔ 382)