A Decision Graph Explanation of Protein Secondary Structure Prediction
26th Hawaii International Conference on Systems Sciences (HICSS26), Vol 1, pp.669-678, January 1993
David L. Dowe,
function to be learned: class #1 = (@1 & @2) or (@3 & @4) class #2 = ~ #1 binary attributes @1, @2, @3 and @4.
Figure 1: Example Decision Tree.
A decision graph (figure 2) can contain join nodes in addition to decision nodes and leaves. A join node represents the disjunction of the paths leading to it: p or q or r or ... . For example, the sets of things matching <T,F,?,?> and <F,?,?,?> lead to the same join node. This does not add to the class of decision functions that can be described but it does make it much more efficient to describe a wide class of functions.
function to be learned: class #1 = (@1 & @2) or (@3 & @4) class #2 = ~ #1
Figure 2: Example Decision Graph.
The most obvious attributes in secondary structure prediction are the amino acids in a window but 20 is a very high arity or fan-out for an attribute. A decision node divides the training data into 20 subsets. 2 levels of decision nodes divide it into 400 subsets. This rapidly halts progress in the inference of a decision tree. On the other hand, decision graphs can delay this problem by joining paths with related outcomes, by adding the data flowing along these paths, and learning a richer theory. (We actually use a 21st pseudo amino acid to indicate "end of chain".) Note, it is also possible to add redundant attributes, possibly with lower arity such as classes that amino acids belong to, but that is not considered here.
There are a great many possible decision graphs for secondary structure prediction. Minimum message length (MML) encoding is used to evaluate graphs and to guide the search for a "good" one. The search can be difficult and lookahead and heuristics are necessary. A greedy algorithm is used with a specified amount of lookahead. Global optimality cannot generally be guaranteed in feasible time. However, any two graphs can be compared with confidence.
Minimum message length (MML) encoding is a general information-theoretic principle. Given data D we wish to infer an hypothesis H. In general there are many possible hypotheses and we can only speak of better or worse hypotheses. Imagine a transmitter who must send a message containing the data to a receiver who is a considerable distance away. If the transmitter can infer a good hypothesis it can be used to compress the data. However any details of the hypothesis that the receiver does not already know, ie. that are not common knowledge, must be included in the message or it will not be comprehensible. The message paradigm keeps us honest - nothing can be passed under the table. We therefore consider two-part messages, which transmit first an hypothesis H and then transmit D using a code which would be optimal if the hypothesis were true. From information-theory, the message length (ML) in an optimal code of an event E of probability P(E) is -log2(P(E)) bits. Therefore the best hypothesis is the one giving the shortest total message.
ML(E) = -log2(P(E)), where event E has probability P(E). Bayes' theorem: P(H&D)= P(D).P(H|D) = P(H).P(D|H) ML(H&D)=ML(D)+ML(H|D)=ML(H)+ML(D|H) posterior log odds-ratio: -log2(P(H|D)/P(H'|D)) = ML(H|D)-ML(H'|D) = (ML(H)+ML(D|H)) - (ML(H')+ML(D|H')) for hypotheses H and H', data D.
P(D|H) is the likelihood of the hypothesis - actually a function of the data given the hypothesis. P(H) is the prior probability of hypothesis H. Oliver and Wallace discuss a prior probablity distribution for decision graphs. P(H|D) is the posterior probability of hypothesis H. The posterior odds-ratio of two hypotheses H and H' can be calculated from the difference in total message lengths: the better one gives the shortest message. The raw data itself constitutes a null-theory and gives an hypothesis test: any hypothesis that gives an overall message length longer than that of the null-theory is not acceptable.
The MML principle has been successfully applied to clustering or classification[31, 32], decision trees[22, 33], decision graphs[19, 20], string alignment and other problems.
Our present decision graphs are hypotheses of secondary structure formation. A graph makes probabilistic predictions of structure. If they are good predictions then the states (E,H,O) can be transmitted very cheaply. Balancing this saving is the cost of transmitting the graph itself. Thus, simple and complex graphs are compared fairly. This prevents the fitting of noise in training data. Some learning techniques tend to generate more complex models given more data. This is not necessarily the case with MML encoding. Certainly small data-sets only justify simple models but large data-sets do not necessarily justify complex models unless there is genuine structure in the data.
The main database used in our experiments consists of 75 sequences from non-homologous proteins as used in a recent version of the GOR method[7, 8]. The list is given in table 2.
Test-Sets 1 carbanhy cpase flavodox g3pdh lysot4 ovomucod plipase rubredox tim (Size 1687) 2 adkinase app catalase cona dhfr glucagon neurotxb pti staphnuc (Size 1426) 3 bencejig bencejpr cobratox crambin elastase lysohen papainhy plastocy prealb subtilhy superoxd (Size 1569) 4 actinhyd arabbind cytb5 cytb562 cytc cytc550 cytc551 fecytc2 pglycmut rhodnese (Size 1676) 5 alph azurin ferredpa ferredsp hbchiron hbhorse1 hbhorse2 hbhuman1 hbhuman2 hblampry hipip myoglob (Size 1583) 6 adh asptc1 asptc2 chymoch2 chymocow ldh melittin protasea (Size 1617) 7 betatryp cabindpv glutred leghb malatedh rnasech2 rnasecow thermoly (Size 1717) 8 aprot2ap aprothyd aprotpen fab1 fab2 insulin1 insulin2 subinhib (Size 1557) Training set is the complement of the test-set in each case.Table 2: Proteins Used.
A window of size 7 was used in the main experiments. This gives reasonable predictions and infers a rich graph - and one that can be presented on a page. Windows of size 5 and 9 gave marginally worse results. Windows of size 1 and 3 gave worse results and large windows could not be justified in MML terms. The window was slid along each protein, the amino acids in the window becoming the attributes, and the state of the central position becoming the class, of a "thing". A 21st pseudo amino acid, denoted by `_', is used to indicate "end of chain".
Decision graphs were derived for the entire database. The parameters controlling the search process were varied to find the best graph, giving the shortest total message length. Additionally, in order to test the predictive power of graphs, the data was divided into various groups. Each group served as a test-set for a graph inferred from a training set which was the union of the other groups. This is perhaps the severest and least biased kind of test of a predictive method - testing on arbitrary proteins when trained on non-homologous proteins.
Figure 3 shows the decision graph inferred from all 75 sequences using a window size of 7. Attributes or positions are numbered 1 to 7 by the program (rather than -3 to +3), the central, predicted amino acid being at position 4, and this numbering is used in the discussion. Rectangular boxes represent collections of leaf nodes. The observed frequencies of the states, E/H/O, are given in the leaves and at other nodes in the graph. Those at node 1 are for the entire database. The frequencies yield estimates of the probabilities of states.
The message length for the graph's structure is 191 bits and for the data given the graph is 17.4 Kbits. The null-hypothesis requires 18.9 Kbits so the graph is statistically significant by a wide margin although we cannot be certain that it is the best possible graph because of the nature of the search process.
Study of the graph reveals various groups of amino acids at join nodes. These groups were formed automatically by the program and were not provided as background knowledge. A further possibility to be investigated is to provide these or other groupings or classes in the data to the program as background knowledge so that it could split on attributes of lower arity.
The graphs inferred for different data-sets vary slightly. It is a close thing whether it is better for the top-level test to be on the central amino acid (4), as in figure 3, or on the following one (5). This may be due to proline (P) which is a strong indicator of turns. When a smaller database was used, a top-level test on
ML(graph) = 191 bits, ML(states|graph) = 17.4 Kbits; Total = 17.6 Kbits ML(null-hypothesis) = 18.9 KbitsFigure 3: Decision Graph, PG, with Window Size 7.
proline at position 5 led directly to a leaf that was strongly `other', `O', in 270/310 cases. In the current graph, a top-level test on proline at position 4 leads to a leaf that is other in 416/538 cases. A second-level test on proline at position 5 leads to a leaf that is other in 314/367 cases. We also note more tests in the graph that refer to proline and lead to leaves that are strongly other. The earlier graph was based on approximately 8.5K things not directly comparable with the present database. The current graph has fewer decision nodes (7 versus 8) and more join nodes.
The leaves most biased to the extended state in the current graph (figure 3) lie towards the lower right of the graph as children of node 5. There are several paths to these nodes, most of which can be summarised by:
if @4 in [ACFHIKLMQRST VWY] & @3 in [ CF I L TQRVWY] & @5 in [ CF I L V Y] then probably extended
We see, for example, that runs of members of [CFILVY] tend to form extended strands. Robson and Suzuki[24, p336] found that these are the 6 strongest indicators of the extended state. They also performed a cluster analysis of amino acids based on secondary structure preferences and reported, "The best defined group is composed of non-polar residues. ... [FILMV]".
The leaves most biased to the helical state lie at the bottom of the graph as children of node 7. Many of the paths here are summarised by:
if @4 in [AC FHIKLM QR TVWY] & @3 in [A DE H K MNQRS ] & @5 in [A DE H K NQRS W ] & @2 in [AC EFHIKLMNQRSTVWY] & @6 in [AC EFHIKLM QR VWY] then probably helix
In addition @4=E tends to imply a helix. We conclude that runs of [AEHKQR] tend to form helices. A and E are known to be strong indicators of helices. [EKQH] are close to each other on the codon ring defined by Swanson[28, p155 fig1] where proximity indicates similarity of codons in the genetic code and similarity of physico-chemical properties.
There is an interesting sub-graph of nodes testing positions 3 and 5 in the centre of the graph. With simplification, the paths from node 2 to node 6, the latter of which is biased towards helix, can be approximated by:
@5 in [EK] or @3 in [AEHM] & @5 in [DGNST] or @5 in [ACFHILMQR VWY] & @3 in [AD KNQRS ] or @3 in [ CF IL QRTVWY] & @5 in [ADHKNQRSW]
[AEM] suggest helix and [DNS] are often at the start of turns, so the second line probably models the transition from a helix to a turn. Note the partial symmetry in lines 3 and 4 between positions 3 and 5 which would be on opposite sides of a helix. The groups on opposite sides in both cases are [CFILQRVWY] and [ADKNQRS]. Taking the differences of these sets gives [CFILVWY] and [ADKNS]. [CFILVY] are non-polar and [ADKNS] are polar which models the tendency of helices to have a hydrophobic side and a hydrophilic side.
The group [DGNST] is formed twice in quite separate parts of the graph although it does not seem to be very strongly biased to one structure. [DGNST] are all `small' and [DNST] are `polar' in Taylor's terms. [DNST] form a leaf-class in a classification of amino acids that Jimenez-Montano derived[11, p653 fig3] from Lim's work. [NST] are members of Robson and Suzuki's ambivalent group.
The above decision graph for secondary structure prediction does not model the serial correlation in secondary structure directly. It may be possible to extend the theory of decision trees and graphs to model series directly, and some alternatives are being investigated, but currently the initial predictions are smoothed by a further decision graph which models just the serial correlation in secondary structure. Two variations of smoothing were tried and others are possible. The first variation is somewhat ad hoc and does not have a simple MML interpretation but it improves the prediction rate by 3.3%. The second variation improves the prediction rate by 2.5% and does have a simple MML interpretation.
Figure 4 shows a smoothing graph, SG1, derived from all 75 sequences. The best graph happens to be a tree in this case. Note that the smoothing graph used on a test-set was inferred only from the appropriate training data. The states of the 6 flanking amino acids, positions 1 to 3 and 5 to 7, are the "attributes" of a "thing" and the state of the central amino acid (4) is the "class". This graph models the influence of the flanking states on the central state. When the smoothing graph is created, the actual states of the flanking positions are used as inputs. Each leaf in the graph has pattern(s) associated with it that correspond to the path(s) to the leaf.
The question arises of how to reconcile the possibly conflicting results of the prediction graph `PG' and the smoothing graph `SG1'. The following procedure was
Figure 4: Decision Graph, SG1, Demonstrating Serial Correlation in Conformations.
used to make a smoothed sequence of predictions for a test protein. Any given sequence of hypothetical states for the protein can be given a probability under PG. To do this the probabilities of the states can be found - from the counts at the leaves of the graph - and multiplied together. Equivalently, the -log probabilities are taken and added, which gives an empirical energy function for the sequence of states under the graph PG. This indicates how consistent the states are with the graph PG.
A similar process is followed for SG1 except that the counts observed in a leaf are used relative to those of the entire training data rather than relative to the total counts within the leaf - this gives more weight to frequent patterns such as ..OOO.. .
The energy is calculated for both PG and SG1 and the results added with a parameter to control the relative weight given to each graph. This ratio was optimised on the training set, being in the range 50:1 to 7:1 and showing that the unsmoothed predictions were fairly sound. A trinomial distribution is derived from the proportions of states (EHO) in the training data. A final term is included in the energy function for the -log probability of the proportion of (predicted) states occuring under the distribution. The search for a sequence of predicted states which minimises the energy function for a given protein was carried out by simulated annealing, starting from either the unsmoothed predictions or random predictions.
The second method of smoothing used a different decision graph, SG2. SG2 used the 7 predicted states from the prediction graph, PG, as attributes to predict the central state of a window. It can be thought of as a correction graph for PG. Again SG2 was inferred from the appropriate training data. Notionally SG2 was applied simultaneously, in parallel, to all the windows of the entire protein sequence to avoid the question of second-order corrections.
A typical instance of SG2 is quite large and not very interesting. It contains tests that look for isolated predictions of helix, say, which can be over-ridden by their neighbours.
A message length can be calculated for the combined use of PG and SG2. The message would include
unsmoothed +SG1 +SG2 tree graph PG graph graph set Train Test Train Test Train Test Train Test --- ---------- ---------- ---------- ---------- 1 55.3 50.8 56.0 54.2 58.8 59.7 58.7 56.5 2 53.4 50.7 54.0 53.3 56.7 56.7 57.0 57.2 3 53.1 53.0 54.0 51.7 57.6 58.1 57.2 55.8 4 54.8 54.3 54.8 56.4 58.4 58.7 58.2 60.3 5 55.3 42.3 57.9 46.8 61.5 49.5 61.1 48.6 6 55.0 51.0 55.5 49.0 60.0 49.9 58.6 50.9 7 54.7 50.1 56.0 52.8 58.2 55.3 57.2 54.7 8 53.9 53.8 55.3 54.6 57.4 57.0 57.6 54.0 ---- ---- ---- ---- ---- ---- ---- ---- avg 54.4 50.7 55.4 52.3 58.6 55.6 58.2 54.8 all 55.0 N/A 56.5 N/A 59.7 N/A 58.0 N/ATable 3: Prediction Success Rates for 3 States.
the structure of PG (191 bits),
SG2 saves about 500 bits on cost of the data alone (part (iv)), over the use of just PG, and the overall saving of about 300 bits is plainly significant.
Table 3 gives the success rates for 3 states (E/H/O) on the training data and on the test data for the 8 test-sets, for the prediction graph alone and for the smoothed results. Results are also given for the complete database. (Figures are also given for a decision tree without smoothing.)
The prediction graph alone achieves 56.5% on the full database and an average of 52.3% on the 8 test-sets. The first smoothing method returns 59.7% and 55.6% respectively, and the second smoothing method returns 58.0% and 54.8%. These results are about 2% better than those on the earlier, smaller database.
Test-set 5 causes the worst performance on a test set and the best on its training set. This contains several of the globins, and their absence from the training set probably causes the drop in the test-set results relative to the training set results. However the GOR method also performs less well than usual on some of these sequences[8, p449] so perhaps there is something difficult about them.
A decision graph is a theory or explanation of secondary structure prediction. The explanation can only be in terms of the information given - here the amino acid sequences. Decision trees are quite familiar in expert systems (a familiar example is in the diagnosis of car faults) and they are generally considered to be comprehensible. A decision graph can be more compact but also more involved, which can be good or bad for purposes of clarity. Logical rules can be extracted from the graph but are likely to be long and numerous if this is done automatically. Muggleton et al noted the difficulty of understanding a large set of logical rules generated by a computer program. To capture the "essence" of a graph in few rules may require simplification and approximation, as in section 4.2, and is not yet an automatic process.
As a prediction method, the performance of the current decision graph is fair. The success rate is in the 49% to 60% range, averaging 55.6% on the test-sets, for a database of 75 sequences and a window of 7. Future work includes giving the decision graph program some background knowledge in terms of amino acid classes, trying both larger databases and restricted classes of proteins, using different window sizes, using a larger number of secondary structure states and investigating different ways of modelling series.
Barry Robson very kindly provided the database from the Protean-II package.
Allison L., C. S. Wallace & C. N. Yee (1992).
Finite-state models in the alignment of macro-molecules.
Also see [TR90/148(HTML)].
Brooks B. R., R. E. Bruccoleri, B. D. Olafson, D. J. States, S. Swaminathan & M. Karplus (1983). CHARMM: a program for macromolecular energy minimization and dynamics calculations. J. Comput. Chem. 4(2) 187-217.
Chaitin G. J. (1966). On the length of programs for computing finite sequences. Jrnl. ACM. 13 547-549.
Chou P. Y. & G. D. Fasman (1974). Prediction of protein conformation. Biochemistry 13 222-245.
Dowe D. L., J. Oliver, L. Allison, T. I. Dix & C. S. Wallace (1992). Learning rules for protein secondary structure prediction. Dept. Res. Conf. 1-12, Dept. Comp. Sci., University of Western Australia; [TR92/163.ps].
Garnier J. & J. M. Levin (1991). The protein structure code: what is its present status. Comp. Appl. BioSci. 7(2) 133-142.
Garnier J., D. J. Osguthorpe & B. Robson (1978). Analysis of the accuracy and implications of simple methods for predicting the secondary structure of globular proteins. J. Mol. Biol. 120 97-120.
Garnier J. & B. Robson (1989). The GOR method of predicting secondary structures in proteins. Prediction of Protein Structure and the Principles of Protein Conformation, G. D. Fasman (ed), Plenum 417-465.
Gibrat J.-F., J. Garnier & B. Robson (1987). Further developments of protein secondary structure prediction using information theory. J. Mol. Biol. 198 425-443.
Holley L. H. & M. Karplus (1989). Protein secondary structure prediction with a neural network. Proc. Natl. Acad. Sci. USA. 86 152-156.
Jiminez-Montano M. A. (1984). On the syntactic structure of protein sequences and the concept of grammar complexity. Bull. Math. Biol. 46(4) 641-659.
Kabsch W. & C. Sander (1983). How good are predictions of protein secondary structure? FEBS Letters 155(2) 179-182.
King R. D. & M. J. E. Sternberg (1990). Machine learning approach for the prediction of protein secondary structure. J. Mol. Biol., 216 441-457.
Kirkpatrick S., C. D. Gelatt jnr. & M. P. Vecchi (1983). Optimization by simulated annealing. Science 220 671-679.
Lathrop R. H., T. A. Webster & T. F. Smith (1987). Ariadne: pattern-directed inference and hierarchical abstraction in protein structure recognition. Commun. ACM. 30(11) 909-921.
Lim V. I. (1974). Algorithms for prediction of alpha-helices and beta-structural regions on globular proteins. J. Mol. Biol. 88 873-894.
Muggleton S., R. D. King & M. J. E. Sternberg (1992). Using logic for protein structure prediction. 25th Hawaii Int. Conf. Sys. Sci. 685-696.
Muggleton S., R. D. King & M. J. E. Sternberg (1992). Protein secondary structure prediction using logic based machine learning. Protein Engineering, to appear.
Oliver J. & C. S. Wallace (1991). Inferring decision graphs. 12th Int. Joint Conf. on Artificial Intelligence (IJCAI), workshop 8, Sydney, Australia.
Oliver J, D. L. Dowe & C. S. Wallace (1992). Inferring decision graphs using the minimum message length principle. Australian Joint Conf. on Artificial Intelligence, Hobart, to appear.
Protean II User Guide. Proteus Molecular Design Limited, Marple, Cheshire, UK (1990).
Quinlan J. R. & R. L. Rivest (1989). Inferring decision trees using the minimum description length principle. Information & Computation 80 227-248.
Reeke jr. G. N. (1988). Protein folding: computational approaches to an exponential-time problem. Ann. Rev. Comput. Sci. 3 59-84.
Robson B. & E. Suzuki (1976). Conformational properties of amino acid residues in globular proteins. J. Mol. Biol. 107 327-356.
Robson B. (1986). The prediction of peptide and protein structure. Practical Protein Chemistry - a Handbook A. Darbre (ed), Wiley 567-607.
Schulz G. E. (1988). A critical evaluation of methods for prediction of protein secondary structures. Ann. Rev. Biophys. Biophys. Chem. 17 1-21.
Sternberg M. J. E. (1983). The analysis and prediction of protein structure. Computing in Biological Science Geisow & Barrett (eds), Elsevier 143-177.
Swanson R. (1984). A unifying concept for the amino acid code. Bull. Math. Biol. 46(2) 187-203.
Taylor W. R. (1986). The classification of amino acid conservation. J. Theor. Biol. 119 205-218.
Taylor W. R. (1987). Protein structure prediction. Nucleic Acid and Protein Sequence Analysis, a Practical Approach M. J. Bishop & C. J. Rawling (eds), IRL Press, 285-322.
Wallace C. S. & D. M. Boulton (1968).
An information measure for classification.
Comp. J. 11(2) 185-194.
Wallace C. S. (1990). Classification by minimum message length inference. Proc. Int. Conf. on Computing and Information (ICCI), Niagara, Lect. Notes in Comp. Sci 468, Springer-Verlag, 72-81.
Wallace C. S. & J. D. Patrick (1992). Coding Decision trees. Machine Learning, to appear.
↑ © L. Allison, www.allisons.org/ll/ (or as otherwise indicated).
Created with "vi (Linux)", charset=iso-8859-1, fetched Wednesday, 19-Sep-2018 09:45:53 EDT.
Free: Linux, Ubuntu operating-sys, OpenOffice office-suite, The GIMP ~photoshop, Firefox web-browser, FlashBlock flash on/off.