Glucocerebrosidase sequence alignments

Sequence searches

Several different tools were used in order to look for sequences that are related to glucocerebrosidase in the non-redundant sequence database.

• FASTA

As Fasta was not initially installed, it was downloaded from the EBI FTP Download Site <ref>ftp://ftp.ebi.ac.uk/pub/software/unix/fasta/fasta36/</ref>.

Command:

../bin/fasta36 gbaseq.fasta /data/blast/nr/nr > fasta_gba_search.out

• BLAST

Command:

blastall -p blastp -d /data/blast/nr/nr -i gbaseq.fasta -o blast.out

• PSI-BLAST

This tool was used 4 times with all different combinations of 3 or 5 iterations (x) and an E-value cut-off (y) of 0.005 or 10e-6.

Command:

blastpgp -d /data/blast/nr/nr -i gbaseq.fasta -o psi_blast_x_y.out -j x -h y

Furthermore the online version of HHSearch <ref>http://toolkit.lmb.uni-muenchen.de/hhpred</ref> was used to search against the pdb70 database of May 14th.

Results

The sequence search with FASTA returned 520 sequences. BLAST, as well as the different PSI-BLAST runs returned 500 sequences. The search with HHSearch against the pdb database only resulted in 100 sequences.

Overlap

Overlap of the results of the different sequence searches. (At most 5 different lists could be captured in one diagram).

The overlaps between the results of the different tools (FASTA, BLAST, 4 PSI-BLAST runs) have been investigated and are visualized using Venn-Diagrams (created with <ref>http://bioinformatics.psb.ugent.be/webtools/Venn/</ref>). The results of HHSearch are not included as a different database (pdb70) was used and therefore the results can not be compared.
In total, the 6 different sequence searches returned 626 unique sequences whereof 405 sequences were returned by each of the searches and 41 were only found by a single one. There were no sequences which have only been found by PSI-BLAST runs with 3 iterations whereas FASTA returned 25 sequences that have not been found by any other tool. These numbers indicate that the different sequence searches return very similar sequences and that each of the tools could be used to retrieve the related sequences of glucocerebrosidase.

Sequence Identity

As BLAST only shows details for the 250 "best" alignments, the sequence identitiy could only be analyzed for the 250 first sequences of the BLAST and PSI-BLAST results. The table below shows the number of sequences that fall into a certain interval. These numbers are also visualized in the diagram on the right. Most of the sequences which BLAST, PSI-BLAST and FASTA found lie within the range of 20 to 39 percent whereas HHSearch has its peak in the area of 0 to 19 percent. As HHSearch was applied to the pdb database, only sequences with a known 3D-structure could be found. The fact that no sequence was found with a sequence identity in the interval of 30 to 99 percent indicates, that there are no known structures of closely related proteins of glucocerebrosidase. The search returned one sequence with a 100% identity: 2NT0 <ref>http://www.pdb.org/pdb/explore/explore.do?structureId=2NT0</ref>, the structure of glucocerebrosidase with a pharmacological chaperone.

Identity distribution of the different sequence searches.

Identity	BLAST	PSI-BLAST 3 iterations e-value cutoff 0.005	PSI-BLAST 3 iterations e-value cutoff 10e-6	PSI-BLAST 5 iterations e-value cutoff 0.005	PSI-BLAST 5 iterations e-value cutoff 10e-6	FASTA	HHSearch
0-9 %	0	0	0	0	0	0	8
10-19%	0	0	0	0	0	0	89
20-29%	43	85	85	96	94	240	2
30-39 %	127	98	98	90	91	160	0
40-49 %	28	26	26	24	25	44	0
50-59 %	6	4	4	3	3	6	0
60-69 %	3	0	0	0	0	3	0
70-79 %	1	1	1	1	1	6	0
80-89 %	15	9	9	9	9	27	0
90-100 %	27	27	27	27	27	34	1
Total	250	250	250	250	250	520	100

Multiple sequence alignments

Sequences used for multiple sequence alignments

For the multiple sequence alignments we used our reference sequence and twenty sequences we had found with sequence searches. We tried to avoid hypothetical sequences and tried to take sequences, that have similiar identities in all sequence searches. For the multiple sequence alignments we have a variety of organisms with human, orang-utan, mouse and also bacteria and worms.
The following tables show the chosen sequences with their identities in the different searches. We only found one pdb structure.

our reference sequence: P04062, GLCM_HUMAN Glucosylceramidase

99 - 90% sequence identity
NP_001127488.1	glucosylceramidase precursor	Pongo abelii	95.0, 98.0, 98.0, 98.0, 98.0, 98.1
3KE0	A Chain A, Crystal Structure Of N370s Glucocerebrosidase At Acidic Ph.		97.0, 99.0, 99.0, 99.0, 99.0, 99.8
EAW53100.1	glucosidase, beta; acid (includes glucosylceramidase), isoform CRA_a	Homo sapiens	97.0, 99.0, 99.0, 99.0, 99.0, 99.6
NP_001165283.1	glucosylceramidase isoform 3 precursor	Homo sapiens	88.0, 90.0, 90.0, 90.0, 90.0, 90.9
NP_001128784.1	DKFZP469B0323 protein	Pongo abelii	95.0, 97.0, 97.0, 97.0, 97.0, 97.4
89 - 60% sequence identity
NP_032120.1	glucosylceramidase isoform 1	Mus musculus	84.0, 86.0, 86.0, 86.0, 86.0, 86.4
EDL15229.1	glucosidase, beta, acid, isoform CRA_a	Mus musculus	84.0, 86.0, 86.0, 86.0, 86.0, 86.3
NP_001121111.1	glucosidase, beta, acid	Rattus norvegicus	85.0, 87.0, 87.0, 87.0, 87.0, 87.6
NP_001039886.1	glucosylceramidase precursor	Bos taurus	86.0, 89.0, 89.0, 89.0, 89.0, 89.2
NP_001005730.1	glucosylceramidase precursor	Sus scrofa	87.0, 89.0, 89.0, 89.0, 89.0, 89.6
59 - 40% sequence identity
EFN73638.1	Glucosylceramidase	Camponotus floridanus	41.0, 40.0, 40.0, 41.0, 40.0, 42.2
CAG11843.1	unnamed protein product	Tetraodon nigroviridis	52.0, 53.0, 53.0, 53.0, 53.0, 54.2
NP_500785.1	hypothetical protein Y4C6B.6	Caenorhabditis elegans	41.0, 40.0, 39.0, 40.0, 39.0, 41.9
EFA07058.1	hypothetical protein TcasGA2_TC010035	Tribolium castaneum	41.0, 42.0, 41.0, 42.0, 41.0, 43.2
EFO26573.1	O-glycosyl hydrolase family 30 protein	Loa loa	40.0, 40.0, 40.0, 40.0, 40.0, 41.7
39 - 20% sequence identity
ZP_07040024.1	glucosylceramidase	Bacteroides sp. 3_1_23	26.0, 24.0, 24.0, 24.0, 24.0, 25.5
YP_244236.1	glycosyl hydrolase	Xanthomonas campestris pv. campestris str. 8004	33.0, 31.0, 30.0, 31.0, 31.0, 33.4
ZP_01885435.1	glycosyl hydrolase	Pedobacter sp. BAL39	36.0, 33.0, 32.0, 33.0, 33.0, 37.2
ZP_07388379.1	Glucan endo-1,6-beta-glucosidase	Paenibacillus curdlanolyticus YK9	28.0, 24.0, 23.0, 24.0, 24.0, 30.1
NP_623885.1	O-glycosyl hydrolase family protein	Thermoanaerobacter tengcongensis MB4	37.0, 34.0, 33.0, 34.0, 32.0, 37.5

Tools used

• Cobalt

Cobalt was not yet installed, so we downloaded it from the NCBI Server<ref>ftp://ftp.ncbi.nlm.nih.gov/pub/cobalt/executables/2.0.1/</ref>.

command
time /home/student/Desktop/ncbi-cobalt-2.0.1/cobalt -i multiple_alignment.fasta -norps T > cobalt_multiple_alignment.aln

	time
real	0m3.488s
user	0m2.320s
sys	0m0.180s

• ClustalW

command
time clustalw

	time
real	0m40.625s
user	0m5.320s
sys	0m0.070s

• Muscle

command
time muscle -in multiple_alignment.fasta -out muscle_multiple_alignment.aln

	time
real	0m3.018s
user	0m1.710s
sys	0m0.100s

• T-Coffee

command
time t_coffee multiple_alignment.fasta

	time
real	0m41.360s
user	0m34.000s
sys	0m0.920s

• 3D-Coffee/Expresso

command
time t_coffee -seq multiple_alignment.fasta -mode expresso -pdb_type dn

	time
real	12m19.825s
user	5m17.140s
sys	0m46.970s

The following pictures show cut-outs of the different alignments with Jalview.

Multiple Alignment by Cobalt in Jalview

Multiple Alignment by ClustalW in Jalview

Multiple Alignment by Muscle with Jalview

Multiple Alignment by T-Coffee with Jalview

Multiple Alignment by 3D-Coffee/Expresso in Jalview

Results

Conserved Columns

	Cobalt	ClustalW	Muscle	T-Coffee	3D-Coffee/Expresso
>50%	133	133	131	125	123
>60%	98	98	96	104	90
>70%	64	64	62	67	58
>80%	53	54	54	50	57
>90%	52	51	51	52	49
100%	25	23	26	26	25

If you look at the alignments in Jalview you can see, that after about 100-120 residues of glucoceribrosidase the conservation gets very high. The first part does not seem to be very important for the function of the protein and therefore mutated gradually in the different organisms. The conserved regions which follow may be necessary for the catalytic function of the protein. If there are mutations, there are amino acids with the same properties, for example arginine and lysine, so the function is maintained.

Functionally important residues

Glutamine residues 235 and 340 play key roles in the active site<ref>http://www.ncbi.nlm.nih.gov/books/NBK1269/</ref>. The alignments show almost the same conservation:

T-Coffee	15/21, 17/21
3D-Coffee	15/21, 16/21
Muscle	15/21, 17/21
Cobalt	15/21, 17/21
ClustalW	15/21, 17/21

In the other sequences asparagine and threonine are aligned to the glutamines, which also are polar amino acids.

Gaps in the reference structure

	Cobalt	ClustalW	Muscle	T-Coffee	3D-Coffee/Expresso
# Gaps	413	404	442	441	546

The reason for most of the gaps are sequences with inserts. The largest example is ZP_07388379.1 which has additionally 300 amino acids at the end. Another one is CAG11843.1 with two times 30 amino acids. The remaining gaps are from the alignment itself.
The 3D-Coffee alignment has the most gaps. It tried to align the structure, therefore there are more gaps because amino acids are only aligned, when also the structure fits. In the Jalview alignment there are a lot of very "gappy" parts, as you can see in the picture.

Example of a very "gappy" part of the 3D-coffee alignment

Gaps in secondary structure elements

sec. structure	position	Cobalt	ClustalW	Muscle	T-Coffee	3D-Coffee/Expresso
Beta strand	49-52	0	0	0	0	2
Beta strand	54-60	0	0	0	0	0
Beta strand	75-82	5	0	0	0	0
Beta strand	88-94	0	0	0	1	9
Beta strand	96-98	0	0	0	4	18
Beta strand	103-116	4	0	23	0	6
Beta strand	119-123	0	0	0	0	0
Helix	126-132	0	0	0	0	0
Helix	137-148	0	0	0	0	19
Turn	150-153	28	28	28	28	1
Beta strand	157-163	0	0	0	0	0
Beta strand	166-170	0	0	0	0	0
Beta strand	177-179	0	0	0	0	0
Helix	190-193	0	0	0	0	0
Helix	196-206	0	0	0	0	0
Beta strand	212-218	0	0	0	0	2
Helix	222-224	0	0	0	0	0
Beta strand	229-233	7	0	0	7	7
Beta strand	235-238	0	0	0	0	0
Helix	243-261	0	0	0	0	1
Beta strand	267-271	0	0	0	0	0
Helix	277-279	0	0	0	0	0
Helix	292-301	0	0	0	0	0
Helix	202-208	0	0	0	0	0
Turn	311-314	0	0	1	1	2
Beta strand	315-323	0	0	0	0	0
Helix	324-326	0	0	0	0	0
Helix	329-335	0	0	0	0	0
Helix	338-341	0	0	0	0	0
Beta strand	346-352	0	0	0	0	0
Helix	359-369	0	0	0	2	2
Beta strand	373-381	13	13	13	13	0
Helix	396-411	0	0	8	6	13
Beta strand	414-422	8	0	0	0	0
Beta strand	440-444	0	0	0	0	1
Helix	445-447	0	0	1	0	1
Beta strand	449-452	0	0	3	0	0
Helix	454-463	0	0	0	0	1
Beta strand	471-479	1	0	2	2	5
Beta strand	482-489	0	1	0	0	0
Beta strand	495-501	0	0	0	0	0
Beta strand	503-505	0	29	0	0	0
Beta strand	507-513	0	0	10	30	1
Turn	514-516	0	0	0	0	40
Beta strand	517-523	0	0	0	1	12
Beta strand	527-533	4	0	0	0	160

The secondary structure information is from Uniprot<ref>http://www.uniprot.org/uniprot/P04062</ref>.

References

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