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This is just an ASCII text version of the manuscript describing
Clustal W, without the figures. It was published:
Nucleic Acids Research, 22(22):4673-4680.
CLUSTAL W: improving the sensitivity of progressive multiple
sequence alignment through sequence weighting, position specific
gap penalties and weight matrix choice.
Julie D. Thompson, Desmond G. Higgins1 and Toby J. Gibson*
European Molecular Biology Laboratory
Postfach 102209
Meyerhofstrasse 1
D-69012 Heidelberg
Germany
Phone: +49-6221-387398
Fax: +49-6221-387306
E-mail: Gibson@EMBL-Heidelberg.DE
Des.Higgins@EBI.AC.UK
Thompson@EMBL-Heidelberg.DE
Keywords: Multiple alignment, phylogenetic tree, weight matrix, gap
penalty, dynamic programming, sequence weighting.
1 Current address:
European Bioinformatics Institute
Hinxton Hall
Hinxton
Cambridge CB10 1RQ
UK.
* To whom correspondence should be addressed
ABSTRACT
The sensitivity of the commonly used progressive multiple sequence
alignment method has been greatly improved for the alignment of divergent
protein sequences. Firstly, individual weights are assigned to each sequence
in a partial alignment in order to downweight near-duplicate sequences and
upweight the most divergent ones. Secondly, amino acid substitution
matrices are varied at different alignment stages according to the divergence
of the sequences to be aligned. Thirdly, residue specific gap penalties and
locally reduced gap penalties in hydrophilic regions encourage new gaps in
potential loop regions rather than regular secondary structure. Fourthly,
positions in early alignments where gaps have been opened receive locally
reduced gap penalties to encourage the opening up of new gaps at these
positions. These modifications are incorporated into a new program,
CLUSTAL W which is freely available.
INTRODUCTION
The simultaneous alignment of many nucleotide or amino acid sequences is
now an essential tool in molecular biology. Multiple alignments are used to
find diagnostic patterns to characterise protein families; to detect or
demonstrate homology between new sequences and existing families of
sequences; to help predict the secondary and tertiary structures of new
sequences; to suggest oligonucleotide primers for PCR; as an essential prelude
to molecular evolutionary analysis. The rate of appearance of new sequence
data is steadily increasing and the development of efficient and accurate
automatic methods for multiple alignment is, therefore, of major
importance. The majority of automatic multiple alignments are now carried
out using the "progressive" approach of Feng and Doolittle (1). In this paper,
we describe a number of improvements to the progressive multiple
alignment method which greatly improve the sensitivity without sacrificing
any of the speed and efficiency which makes this approach so practical. The
new methods are made available in a program called CLUSTAL W which is
freely available and portable to a wide variety of computers and operating
systems.
In order to align just two sequences, it is standard practice to use dynamic
programming (2). This guarantees a mathematically optimal alignment,
given a table of scores for matches and mismatches between all amino acids
or nucleotides (e.g. the PAM250 matrix (3) or BLOSUM62 matrix (4)) and
penalties for insertions or deletions of different lengths. Attempts at
generalising dynamic programming to multiple alignments are limited to
small numbers of short sequences (5). For much more than eight or so
proteins of average length, the problem is uncomputable given current
computer power. Therefore, all of the methods capable of handling larger
problems in practical timescales, make use of heuristics. Currently, the most
widely used approach is to exploit the fact that homologous sequences are
evolutionarily related. One can build up a multiple alignment progressively
by a series of pairwise alignments, following the branching order in a
phylogenetic tree (1). One first aligns the most closely related sequences,
gradually adding in the more distant ones. This approach is sufficiently fast
to allow alignments of virtually any size. Further, in simple cases, the
quality of the alignments is excellent, as judged by the ability to correctly align
corresponding domains from sequences of known secondary or tertiary
structure (6). In more difficult cases, the alignments give good starting points
for further automatic or manual refinement.
This approach works well when the data set consists of sequences of different
degrees of divergence. Pairwise alignment of very closely related sequences
can be carried out very accurately. The correct answer may often be obtained
using a wide range of parameter values (gap penalties and weight matrix). By
the time the most distantly related sequences are aligned, one already has a
sample of aligned sequences which gives important information about the
variability at each position. The positions of the gaps that were introduced
during the early alignments of the closely related sequences are not changed
as new sequences are added. This is justified because the placement of gaps
in alignments between closely related sequences is much more accurate than
between distantly related ones. When all of the sequences are highly
divergent (e.g. less than approximately 25-30% identity between any pair of
sequences), this progressive approach becomes much less reliable.
There are two major problems with the progressive approach: the local
minimum problem and the choice of alignment parameters. The local
minimum problem stems from the "greedy" nature of the alignment strategy.
The algorithm greedily adds sequences together, following the initial tree.
There is no guarantee that the global optimal solution, as defined by some
overall measure of multiple alignment quality (7,8), or anything close to it,
will be found. More specifically, any mistakes (misaligned regions) made
early in the alignment process cannot be corrected later as new information
from other sequences is added. This problem is frequently thought of as
mainly resulting from an incorrect branching order in the initial tree. The
initial trees are derived from a matrix of distances between separately aligned
pairs of sequences and are much less reliable than trees from complete
multiple alignments. In our experience, however, the real problem is caused
simply by errors in the initial alignments. Even if the topology of the guide
tree is correct, each alignment step in the multiple alignment process may
have some percentage of the residues misaligned. This percentage will be
very low on average for very closely related sequences but will increase as
sequences diverge. It is these misalignments which carry through from the
early alignment steps that cause the local minimum problem. The only way
to correct this is to use an iterative or stochastic sampling procedure (e.g.
7,9,10). We do not directly address this problem in this paper.
The alignment parameter choice problem is, in our view, at least as serious as
the local minimum problem. Stochastic or iterative algorithms will be just
as badly affected as progressive ones if the parameters are inappropriate: they
will arrive at a false global minimum. Traditionally, one chooses one weight
matrix and two gap penalties (one for opening a new gap and one for
extending an existing gap) and hope that these will work well over all parts of
all the sequences in the data set. When the sequences are all closely related,
this works. The first reason is that virtually all residue weight matrices give
most weight to identities. When identities dominate an alignment, almost
any weight matrix will find approximately the correct solution. With very
divergent sequences, however, the scores given to non-identical residues will
become critically important; there will be more mismatches than identities.
Different weight matrices will be optimal at different evolutionary distances
or for different classes of proteins.
The second reason is that the range of gap penalty values that will find the
correct or best possible solution can be very broad for highly similar sequences
(11). As more and more divergent sequences are used, however, the exact
values of the gap penalties become important for success. In each case, there
may be a very narrow range of values which will deliver the best alignment.
Further, in protein alignments, gaps do not occur randomly (i.e. with equal
probability at all positions). They occur far more often between the major
secondary structural elements of alpha helices and beta strands than within
(12).
The major improvements described in this paper attempt to address the
alignment parameter choice problem. We dynamically vary the gap
penalties in a position and residue specific manner. The observed relative
frequencies of gaps adjacent to each of the 20 amino acids (12) are used to
locally adjust the gap opening penalty after each residue. Short stretches of
hydrophilic residues (e.g. 5 or more) usually indicate loop or random coil
regions and the gap opening penalties are locally reduced in these stretches.
In addition, the locations of the gaps found in the early alignments are also
given reduced gap opening penalties. It has been observed in alignments
between sequences of known structure that gaps tend not to be closer than
roughly eight residues on average (12). We increase the gap opening penalty
within eight residues of exising gaps. The two main series of amino acid
weight matrices that are used today are the PAM series (3) and the BLOSUM
series (4). In each case, there is a range of matrices to choose from. Some
matrices are appropriate for aligning very closely related sequences where
most weight by far is given to identities, with only the most frequent
conservative substitutions receiving high scores. Other matrices work better
at greater evolutionary distances where less importance is attached to
identities (13). We choose different weight matrices, as the alignment
proceeds, depending on the estimated divergence of the sequences to be
aligned at each stage.
Sequences are weighted to correct for unequal sampling across all
evolutionary distances in the data set (14). This downweights sequences that
are very similar to other sequences in the data set and upweights the most
divergent ones. The weights are calculated directly from the branch lengths
in the initial guide tree (15). Sequence weighting has already been shown to
be effective in improving the sensitivity of profile searches (15,16). In the
original CLUSTAL programs (17-19), the initial guide trees, used to guide the
multiple alignment, were calculated using the UPGMA method (20). We
now use the Neighbour-Joining method (21) which is more robust against the
effects of unequal evolutionary rates in different lineages and which gives
better estimates of individual branch lengths. This is useful because it is these
branch lengths which are used to derive the sequence weights. We also allow
users to choose between fast approximate alignments (22) or full dynamic
programming for the distance calculations used to make the guide tree.
The new improvements dramatically improve the sensitivity of the
progressive alignment method for difficult alignments involving highly
diverged sequences. We show one very demanding test case of over 60 SH3
domains (23) which includes sequence pairs with as little as 12% identity and
where there is only one exactly conserved residue across all of the sequences.
Using default parameters, we can achieve an alignment that is almost exactly
correct, according to available structural information (24). Using the program
in a wide variety of situations, we find that it will normally find the correct
alignment, in all but the most difficult and pathological of cases.
MATERIAL AND METHODS
The basic alignment method
The basic multiple alignment algorithm consists of three main stages: 1) all
pairs of sequences are aligned separately in order to calculate a distance matrix
giving the divergence of each pair of sequences; 2) a guide tree is calculated
from the distance matrix; 3) the sequences are progressively aligned according
to the branching order in the guide tree. An example using 7 globin
sequences of known tertiary structure (25) is given in figure 1.
1) The distance matrix/pairwise alignments
In the original CLUSTAL programs, the pairwise distances were calculated
using a fast approximate method (22). This allows very large numbers of
sequences to be aligned, even on a microcomputer. The scores are calculated
as the number of k-tuple matches (runs of identical residues, typically 1 or 2
long for proteins or 2 to 4 long for nucleotide sequences) in the best alignment
between two sequences minus a fixed penalty for every gap. We now offer a
choice between this method and the slower but more accurate scores from full
dynamic programming alignments using two gap penalties (for opening or
extending gaps) and a full amino acid weight matrix. These scores are
calculated as the number of identities in the best alignment divided by the
number of residues compared (gap positions are excluded). Both of these
scores are initially calculated as percent identity scores and are converted to
distances by dividing by 100 and subtracting from 1.0 to give number of
differences per site. We do not correct for multiple substitutions in these
initial distances. In figure 1 we give the 7x7 distance matrix between the 7
globin sequences calculated using the full dynamic programming method.
2) The guide tree
The trees used to guide the final multiple alignment process are calculated
from the distance matrix of step 1 using the Neighbour-Joining method (21).
This produces unrooted trees with branch lengths proportional to estimated
divergence along each branch. The root is placed by a "mid-point" method
(15) at a position where the means of the branch lengths on either side of the
root are equal. These trees are also used to derive a weight for each sequence
(15). The weights are dependent upon the distance from the root of the tree
but sequences which have a common branch with other sequences share the
weight derived from the shared branch. In the example in figure 1, the
leghaemoglobin (Lgb2_Luplu) gets a weight of 0.442 which is equal to the
length of the branch from the root to it. The Human beta globin
(Hbb_Human) gets a weight consisting of the length of the branch leading to
it that is not shared with any other sequences (0.081) plus half the length of
the branch shared with the horse beta globin (0.226/2) plus one quarter the
length of the branch shared by all four haemoglobins (0.061/4) plus one fifth
the branch shared between the haemoglobins and the myoglobin (0.015/5)
plus one sixth the branch leading to all the vertebrate globins (0.062). This
sums to a total of 0.221. By contrast, in the normal progressive alignment
algorithm, all sequences would be equally weighted. The rooted tree with
branch lengths and sequence weights for the 7 globins is given in figure 1.
3) Progressive alignment
The basic procedure at this stage is to use a series of pairwise alignments to
align larger and larger groups of sequences, following the branching order in
the guide tree. You proceed from the tips of the rooted tree towards the root.
In the globin example in figure 1 you align the sequences in the following
order: human vs. horse beta globin; human vs. horse alpha globin; the 2
alpha globins vs. the 2 beta globins; the myoglobin vs. the haemoglobins; the
cyanohaemoglobin vs the haemoglobins plus myoglobin; the leghaemoglobin
vs. all the rest. At each stage a full dynamic programming (26,27) algorithm is
used with a residue weight matrix and penalties for opening and extending
gaps. Each step consists of aligning two existing alignments or sequences.
Gaps that are present in older alignments remain fixed. In the basic
algorithm, new gaps that are introduced at each stage get full gap opening and
extension penalties, even if they are introduced inside old gap positions (see
the section on gap penalties below for modifications to this rule). In order to
calculate the score between a position from one sequence or alignment and
one from another, the average of all the pairwise weight matrix scores from
the amino acids in the two sets of sequences is used i.e. if you align 2
alignments with 2 and 4 sequences respectively, the score at each position is
the average of 8 (2x4) comparisons. This is illustrated in figure 2. If either set
of sequences contains one or more gaps in one of the positions being
considered, each gap versus a residue is scored as zero. The default amino
acid weight matrices we use are rescored to have only positive values.
Therefore, this treatment of gaps treats the score of a residue versus a gap as
having the worst possible score. When sequences are weighted (see
improvements to progressive alignment, below), each weight matrix value is
multiplied by the weights from the 2 sequences, as illustrated in figure 2.
Improvements to progressive alignment
All of the remaining modifications apply only to the final progressive
alignment stage. Sequence weighting is relatively straightforward and is
already widely used in profile searches (15,16). The treatment of gap penalties
is more complicated. Initial gap penalties are calculated depending on the
weight matrix, the similarity of the sequences, and the length of the
sequences. Then, an attempt is made to derive sensible local gap opening
penalties at every position in each pre-aligned group of sequences that will
vary as new sequences are added. The use of different weight matrices as the
alignment progresses is novel and largely by-passes the problem of initial
choice of weight matrix. The final modification allows us to delay the
addition of very divergent sequences until the end of the alignment process
when all of the more closely related sequences have already been aligned.
Sequence weighting
Sequence weights are calculated directly from the guide tree. The weights
are normalised such that the biggest one is set to 1.0 and the rest are all less
than one. Groups of closely related sequences receive lowered weights
because they contain much duplicated information. Highly divergent
sequences without any close relatives receive high weights. These weights
are used as simple multiplication factors for scoring positions from different
sequences or prealigned groups of sequences. The method is illustrated in
figure 2. In the globin example in figure 1, the two alpha globins get
downweighted because they are almost duplicate sequences (as do the two
beta globins); they receive a combined weight of only slightly more than if a
single alpha globin was used.
Initial gap penalties
Initially, two gap penalties are used: a gap opening penalty (GOP) which gives
the cost of opening a new gap of any length and a gap extension penalty (GEP)
which gives the cost of every item in a gap. Initial values can be set by the
user from a menu. The software then automatically attempts to choose
appropriate gap penalties for each sequence alignment, depending on the
following factors.
1) Dependence on the weight matrix
It has been shown (16,28) that varying the gap penalties used with different
weight matrices can improve the accuracy of sequence alignments. Here, we
use the average score for two mismatched residues (ie. off-diagonal values in
the matrix) as a scaling factor for the GOP.
2) Dependence on the similarity of the sequences
The percent identity of the two (groups of) sequences to be aligned is used to
increase the GOP for closely related sequences and decrease it for more
divergent sequences on a linear scale.
3) Dependence on the lengths of the sequences
The scores for both true and false sequence alignments grow with the length
of the sequences. We use the logarithm of the length of the shorter sequence
to increase the GOP with sequence length.
Using these three modifications, the initial GOP calculated by the program is:
GOP->(GOP+log(MIN(N,M))) * (average residue mismatch score) *
(percent identity scaling factor)
where N, M are the lengths of the two sequences.
4) Dependence on the difference in the lengths of the sequences
The GEP is modified depending on the difference between the lengths of the
two sequences to be aligned. If one sequence is much shorter than the other,
the GEP is increased to inhibit too many long gaps in the shorter sequence.
The initial GEP calculated by the program is:
GEP -> GEP*(1.0+|log(N/M)|)
where N, M are the lengths of the two sequences.
Position-specific gap penalties
In most dynamic programming applications, the initial gap opening and
extension penalties are applied equally at every position in the sequence,
regardless of the location of a gap, except for terminal gaps which are usually
allowed at no cost. In CLUSTAL W, before any pair of sequences or
prealigned groups of sequences are aligned, we generate a table of gap opening
penalties for every position in the two (sets of) sequences. An example is
shown in figure 3. We manipulate the initial gap opening penalty in a
position specific manner, in order to make gaps more or less likely at different
positions.
The local gap penalty modification rules are applied in a hierarchical manner.
The exact details of each rule are given below. Firstly, if there is a gap at a
position, the gap opening and gap extension penalties are lowered; the other
rules do not apply. This makes gaps more likely at positions where there are
already gaps. If there is no gap at a position, then the gap opening penalty is
increased if the position is within 8 residues of an existing gap. This
discourages gaps that are too close together. Finally, at any position within a
run of hydrophilic residues, the penalty is decreased. These runs usually
indicate loop regions in protein structures. If there is no run of hydrophilic
residues, the penalty is modified using a table of residue specific gap
propensities (12). These propensities were derived by counting the frequency
of each residue at either end of gaps in alignments of proteins of known
structure. An illustration of the application of these rules from one part of
the globin example, in figure 1, is given in figure 3.
1) Lowered gap penalties at existing gaps
If there are already gaps at a position, then the GOP is reduced in proportion
to the number of sequences with a gap at this position and the GEP is lowered
by a half. The new gap opening penalty is calculated as:
GOP -> GOP*0.3*(no. of sequences without a gap/no. of sequences).
2) Increased gap penalties near existing gaps
If a position does not have any gaps but is within 8 residues of an existing gap,
the GOP is increased by:
GOP -> GOP*(2+((8-distance from gap)*2)/8)
3) Reduced gap penalties in hydrophilic stretches
Any run of 5 hydrophilic residues is considered to be a hydrophilic stretch.
The residues that are to be considered hydrophilic may be set by the user but
are conservatively set to D, E, G, K, N, Q, P, R or S by default. If, at any
position, there are no gaps and any of the sequences has such a stretch, the
GOP is reduced by one third.
4) Residue specific penalties
If there is no hydrophilic stretch and the position does not contain any gaps,
then the GOP is multiplied by one of the 20 numbers in table 1, depending on
the residue. If there is a mixture of residues at a position, the multiplication
factor is the average of all the contributions from each sequence.
Weight matrices
Two main series of weight matrices are offered to the user: the Dayhoff PAM
series (3) and the BLOSUM series (4). The default is the BLOSUM series. In
each case, there is a choice of matrix ranging from strict ones, useful for
comparing very closely related sequences to very "soft" ones that are useful
for comparing very distantly related sequences. Depending on the distance
between the two sequences or groups of sequences to be compared, we switch
between 4 different matrices. The distances are measured directly from the
guide tree. The ranges of distances and tables used with the PAM series of
matrices is: 80-100%:PAM20, 60-80%:PAM60, 40-60%:PAM120, 0-40%:PAM350.
The range used with the BLOSUM series is:80-100%:BLOSUM80,
60-80%:BLOSUM62, 30-60%:BLOSUM45, 0-30%:BLOSUM30.
Divergent sequences
The most divergent sequences (most different, on average from all of the
other sequences) are usually the most difficult to align correctly. It is
sometimes better to delay the incorporation of these sequences until all of the
more easily aligned sequences are merged first. This may give a better chance
of correctly placing the gaps and matching weakly conserved positions against
the rest of the sequences. A choice is offered to set a cut off (default is 40%
identity or less with any other sequence) that will delay the alignment of the
divergent sequences until all of the rest have been aligned.
Software and Algorithms
Dynamic Programming
The most demanding part of the multiple alignment strategy, in terms of
computer processing and memory usage, is the alignment of two (groups of)
sequences at each step in the final progressive alignment. To make it
possible to align very long sequences (e.g. dynein heavy chains at ~ 5,000
residues) in a reasonable amount of memory, we use the memory efficient
dynamic programming algorithm of Myers and Miller (26). This sacrifices
some processing time but makes very large alignments practical in very little
memory. One disadvantage of this algorithm is that it does not allow
different gap opening and extension penalties at each position. We have
modified the algorithm so as to allow this and the details are described in a
separate paper (27).
Menus/file formats
Six different sequence input formats are detected automatically and read by
the program: EMBL/Swiss Prot, NBRF/PIR, Pearson/FASTA (29), GCG/MSF
(30), GDE (Steven Smith, Harvard University Genome Center) and CLUSTAL
format alignments. The last three formats allow users to read in complete
alignments (e.g. for calculating phylogenetic trees or for addition of new
sequences to an existing alignment). Alignment output may be requested in
standard CLUSTAL format (self-explanatory blocked alignments) or in
formats compatible with the GDE, PHYLIP (31) or GCG (30) packages. The
program offers the user the ability to calculate Neighbour-Joining
phylogenetic trees from existing alignments with options to correct for
multiple hits (32,33) and to estimate confidence levels using a bootstrap
resampling procedure (34). The trees may be output in the "New
Hampshire" format that is compatible with the PHYLIP package (31).
Alignment to an alignment
Profile alignment is used to align two existing alignments (either of which
may consist of just one sequence) or to add a series of new sequences to an
existing alignment. This is useful because one may wish to build up a
multiple alignment gradually, choosing different parameters manually, or
correcting intermediate errors as the alignment proceeds. Often, just a few
sequences cause misalignments in the progressive algorithm and these can be
removed from the process and then added at the end by profile alignment. A
second use is where one has a high quality reference alignment and wishes to
keep it fixed while adding new sequences automatically.
Portability/Availability
The full source code of the package is provided free to academic users. The
program will run on any machine with a full ANSI conforming C compiler.
It has been tested on the following hardware/software combinations:
Decstation/Ultrix, Vax or ALPHA/VMS, Silicon Graphics/IRIX. The source
code and documentation are available by E-mail from the EMBL file server
(send the words HELP and HELP SOFTWARE on two lines to the internet
address:
Netserv@EMBL-Heidelberg.DE) or by anonymous FTP from
FTP.EMBL-Heidelberg.DE. Queries may be addressed by E-mail to
Des.Higgins@EBI.AC.UK or Gibson@EMBL-Heidelberg.DE.
RESULTS AND DISCUSSION
Alignment of SH3 Domains
The ~60 residue SH3 domain was chosen to illustrate the performance of
CLUSTAL W, as there is a reference manual alignment (23) and the fold is
known (24). SH3 domains, with a minimum similarity below 12% identity,
are poorly aligned by progressive alignment programs such as CLUSTAL V
and PILEUP: neither program can generate the correct blocks corresponding to
the secondary structure elements.
Figure 4 shows an alignment generated by CLUSTAL W of the example set of
SH3 domains. The alignment was generated in two steps. After progressive
alignment, five blocks were produced, corresponding to structural elements,
with gaps inserted exclusively in the known loop regions. The beta strands in
blocks 1, 4 and 5 were all correctly superposed. However, four sequences in
block 2 and one sequence in block 3 were misaligned by 1-2 residues
(underlined in figure 4). A second progressive alignment of the aligned
sequences, including the gaps, improved this alignment: A single misaligned
sequence, H_P55, remains in block 2 (boxed in figure 4), while block 3 is now
completely aligned. This alignment corrects several errors (eg. P85A, P85B
and FUS1) in the manual alignment (23).
The SH3 alignment illustrates several features of CLUSTAL W usage. Firstly,
in a practical application involving divergent sequences, the initial
progressive alignment is likely to be a good but not perfect approximation to
the correct alignment. The alignment quality can be improved in a number of
ways. If the block structure of the alignment appears to be correct, realignment
of the alignment will usually improve most of the misaligned blocks: the
existing gaps allow the blocks to "float" cheaply to a locally optimal position
without disturbing the rest of the alignment. Remaining sequences which are
doubtfully aligned can then be individually tested by profile alignment to the
remainder: the misaligned H_P55 SH3 domain can be correctly aligned by
profile (with GOP <= 8). The indel regions in the final alignment can then be
manually cleaned up: Usually the exact alignment in the loop regions is not
determinable, and may have no meaning in structural terms. It is then
desirable to have a single gap per structural loop. CLUSTAL W achieved this
for two of the four SH3 loop regions (figure 4).
If the block structure of the alignment appears suspect, greater intervention by
the user may be required. The most divergent sequences, especially if they
have large insertions (which can be discerned with the aid of dot matrix
plots), should be left out of the progressive alignment. If there are sets of
closely related sequences that are deeply diverged from other sets, these can be
separately aligned and then merged by profile alignment. Incorrectly
determined sequences, containing frameshifts, can also confound regions of
an alignment: these can be hard to detect but sometimes they have been
grouped within the excluded divergent sequences: then they may be revealed
when they are individually compared to the alignment as having apparently
nonsense segments with respect to the other sequences.
Finding the best alignment
In cases where all of the sequences in a data set are very similar (e.g. no pair
less than 35% identical), CLUSTAL W will find an alignment which is
difficult to improve by eye. In this sense, the alignment is optimal with
regard to the alternative of manual alignment. Mathematically, this is vague
and can only be put on a more systematic footing by finding an objective
function (a measure of multiple alignment quality) that exactly mirrors the
information used by an "expert" to evaluate an alignment. Nonetheless, if an
alignment is impossible to improve by eye, then the program has achieved a
very useful result.
In more difficult cases, as more divergent sequences are included, it becomes
increasingly difficult to find good alignments and to evaluate them. What
we find with CLUSTAL W is that the basic block-like structure of the
alignment (corresponding to the major secondary structure elements) is
usually recovered, with some of the most divergent sequences misaligned in
small regions. This is a very useful starting point for manual refinement as it
helps define the major blocks of similarity. The problem sequences can be
removed from the analysis and realigned to the rest of the sequences
automatically or with different parameter settings. An examination of the
tree used to guide the alignment will usually show which sequences will be
most unreliably placed (those that branch off closest to the root and/or those
that align to other single sequences at a very low level of sequence identity
rather than align to a group of pre-aligned sequences). Finally, one can
simply iterate the multiple alignment process by feeding an output alignment
back into CLUSTAL W and repeating the multiple alignment process (using
the same or different parameters). The SH3 domain alignment in figure 4
was derived in this way by 2 passes using default parameters. In the second
pass, the local gap penalties are dominated by the placement of the initial
major gap positions. The alignment will either remain unchanged or will
converge rapidly (after 1 or 2 extra passes) on a better solution. If the
placement of the initial gaps is approximately correct but some of the
sequences are locally misaligned, this works well.
Comparison with other methods
Recently, several papers have addressed the problem of position specific
parameters for multiple alignment. In one case (35), local gap penalties are
increased in alpha helical and beta strand regions, when the 3-D structures of
one or more of the sequences are known. In a second case (36), a hidden
Markov model was used to estimate position specific gap penalties and
residue substitution weight matrices when large numbers of examples of a
protein domain were known. With CLUSTAL W, we attempt to derive the
same information purely from the set of sequences to be aligned. Therefore,
we can apply the method to any set of sequences. The success of this approach
will depend on the number of available sequences and their evolutionary
relationships. It will also depend on the decision making process during
multiple alignment (e.g. when to change weight matrix) and the accuracy and
appropriateness of our parameterisation. In the long term, this can only be
evaluated by exhaustive testing of sets of sequences where the correct
alignment (or parts of it) are known from structural information. What is
clear, however, is that the modifications described here significantly improve
the sensitivity of the progressive multiple alignment approach. This is
achieved with almost no sacrifice in speed and efficiency.
There are several areas where further improvements in sensitivity and
accuracy can be made. Firstly, the residue weight matrices and gap settings
can be made more accurate as more and more data accumulate, while
matrices for specific sequence types can be derived (e.g. for transmembrane
regions (37)). Secondly, stochastic or iterative optimisation methods can be
used to refine initial alignments (7,9,10). CLUSTAL W could be run with
several sets of starting parameters and in each case, the alignments refined
according to an objective function. The search for a good objective function,
that takes into account the sequence and position specific information used in
CLUSTAL W is a key area of research. Finally, the average number of
examples of each protein domain or family is growing steadily. It is not only
important that programs can cope with the large volumes of data that are
being generated, they should be able to exploit the new information to make
the alignments more and more accurate. Globally optimal alignments
(according to an objective function) may not always be possible but the
problem may be avoided if sufficiently large volumes of data become
available. CLUSTAL W is a step in this direction.
ACKNOWLEDGEMENTS
Numerous people have offered advice and suggestions for improvements to
earlier versions of the CLUSTAL programs. D.H. wishes to apologise to all of
the irate CLUSTAL V users who had to live with the bugs and lack of facilities
for getting trees in the New Hampshire format. We wish to specifically thank
Jeroen Coppieters who suggested using a series of weight matrices and Steven
Henikoff for advice on using the BLOSUM matrices. We are grateful to Rein
Aasland, Peer Bork, Ariel Blocker and Brtrand Seraphin for providing
challenging alignment problems. T.G. and J.T. thank Kevin Leonard for
support and encouragement. Finally, we thank all of the people who were
involved with various CLUSTAL programs over the years, namely: Paul
Sharp, Rainer Fuchs and Alan Bleasby.
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FIGURE LEGENDS
Figure 1. The basic progressive alignment procedure, illustrated using a set of
7 globins of known tertiary structure. The sequence names are from Swiss
Prot (38): Hba_Horse: horse alpha globin; Hba_Human: human alpha globin;
Hbb_Horse: horse beta globin; Hbb_Human: human beta globin; Myg_Phyca:
sperm whale myoglobin; Glb5_Petma: lamprey cyanohaemoglobin;
Lgb2_Luplu: lupin leghaemoglobin. In the distance matrix, the mean
number of differences per residue is given. The unrooted tree shows all
branch lengths drawn to scale. In the rooted tree, all branch lengths (mean
number of differences per residue along each branch) are given as well as
weights for each sequence. In the multiple alignment, the approximate
positions of the 7 alpha helices, common to all 7 proteins are shown. This
alignment was derived using CLUSTAL W with default parameters and the
PAM (3) series of weight matrices.
Figure 2. The scoring scheme for comparing two positions from two
alignments. Two sections of alignment with 4 and 2 sequences respectively
are shown. The score of the position with amino acids T,L,K,K versus the
position with amino acids V and I is given with and without sequence
weights. M(X,Y) is the weight matrix entry for amino acid X versus amino
acid Y. Wn is the weight for sequence n.
Figure 3. The variation in local gap opening penalty is plotted for a section of
alignment. The inital gap opening penalty is indicated by a dotted line. Two
hydrophilic stretches are underlined. The lowest penalties correspond to the
ends of the alignment, the hydrophilic stretches and the two positions with
gaps. The highest values are within 8 residues of the two gap positions. The
rest of the variation is caused by the residue specific gap penalties (12).
Figure 4. CLUSTAL W Alignment of a set of SH3 domains taken from (23).
Secondary structure assignments for the solved Spectrin (24) and Fyn (39)
domains are according to DSSP (40). The alignment was generated in two
steps using default parameters. After full multiple alignment, the aligned
sequences were realigned. Segments which were correctly aligned in the
second pass are underlined. The single misaligned segment in H_P55 and the
misaligned residue in H_NCK/2 are boxed.
The sequences are coloured to illustrate significant features. All G (orange)
and P (yellow) are coloured. Other residues matching a frequent occurrence of
a property in a column are coloured: hydrophobic = blue; hydrophobic
tendency = light blue; basic = red; acidic = purple; hydrophilic = green; White
= unconserved. The alignment figure was prepared with the GDE sequence
editor (S. Smith, Harvard University) and COLORMASK (J. Thompson,
EMBL).
Table 1. Pascarella and Argos residue specific gap modification factors.
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A 1.13 M 1.29
C 1.13 N 0.63
D 0.96 P 0.74
E 1.31 Q 1.07
F 1.20 R 0.72
G 0.61 S 0.76
H 1.00 T 0.89
I 1.32 V 1.25
K 0.96 Y 1.00
L 1.21 W 1.23
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The values are normalised around a mean value of 1.0 for H. The lower the
value, the greater the chance of having an adjacent gap. These are derived
from the original table of relative frequencies of gaps adjacent to each residue
(12) by subtraction from 2.0.
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