Use B-factor related features for accurate classification between protein binding interfaces and crystal packing contacts

Abstract

Background

Distinction between true protein interactions and crystal packing contacts is important for structural bioinformatics studies to respond to the need of accurate classification of the rapidly increasing protein structures. There are many unannotated crystal contacts and there also exist false annotations in this rapidly expanding volume of data. Previous tools have been proposed to address this problem. However, challenging issues still remain, such as low performance when the training and test data contain mixed interfaces having diverse sizes of contact areas.

Methods and results

B factor is a measure to quantify the vibrational motion of an atom, a more relevant feature than interface size to characterize protein binding. We propose to use three features related to B factor for the classification between biological interfaces and crystal packing contacts. The first feature is the sum of the normalized B factors of the interfacial atoms in the contact area, the second is the average of the interfacial B factor per residue in the chain, and the third is the average number of interfacial atoms with a negative normalized B factor per residue in the chain. We investigate the distribution properties of these basic features and a compound feature on four datasets of biological binding and crystal packing, and on a protein binding-only dataset with known binding affinity. We also compare the cross-dataset classification performance of these features with existing methods and with a widely-used and the most effective feature interface area. The results demonstrate that our features outperform the interface area approach and the existing prediction methods remarkably for many tests on all of these datasets.

Conclusions

The proposed B factor related features are more effective than interface area to distinguish crystal packing from biological binding interfaces. Our computational methods have a potential for large-scale and accurate identification of biological interactions from the experimentally determined structural data stored at PDB which may have diverse interface sizes.

Background

With the breakthrough of protein structure determination technologies, in particular X-ray crystallography, rapidly increasing 3D structures of proteins become available. For example, PDB (protein data bank) has stored 90,358 entries which are solved by X-ray crystallography as of July 2014. These quaternary structures can be used to uncover the binding mechanisms of proteins and to annotate protein functions. However, crystal packing contacts, which are a kind of false protein binding, also exist in PDB to blur the analysis of quaternary structures. In fact, crystal packing is due to the artifact of the crystallographic packing environments and it is randomly formed during the crystallization process. It does not occur in solution or in physiological states [1]. The immediate question is how to accurately determine whether a crystal contact produced from a PDB entry is a true biological interaction. This problem is difficult especially when a protein complex consists of a large number of protein chains, a common situation in PDB and also in real biological systems.

This research problem has attracted intensive interests. Methods have been proposed to understand the difference of interfacial properties between biological binding and crystal packing. For example, biological interfaces were found to be much larger [2–8], or more conserved than crystal packing [2, 3], or more abundant in aromatic residues [3]. Biological interactions were also found to have different residue composition from the rest of protein surfaces [4, 9, 10], while crystal packing interfaces possess similar composition to the rest of protein surfaces as a whole [8].

Complicated computational methods have also been proposed to classify true biological binding and false binding. An idea is to break an interface down to contacting atomic or residue pairs, and then uses the enrichment or frequency of these pairs as features for the classification. Based on the atomic pair representation idea, Weng's group [11] and Klebe's group [12] have both utilized machine-learning algorithms to construct effective classifiers for distinguishing different types of protein binding, such as crystal packing, permanent and transient interactions [11, 12]. Liu et al. have used a new definition of atomic contacts named β contacts in atomic pair representation for interfaces, and demonstrated that it is a novel idea to outperform the existing methods in distinguishing crystal packing from homodimers [13]. Using residue pairs to describe interfaces, Bernauer et al. have constructed an SVM classifier DiMoVo for identifying biological protein interactions [14]. Liu and Li have designed the propensity vector of residue contacts within the O-ring to develop OringPV for the distinction between crystal packing and biological interactions [15]. Many other features have also been used. For example, the PITA method scores crystal packing using the properties of contact size and chemical complementarity [16]. Zhu et al. [3] have extracted six properties from interfaces, such as interface size, amino acid composition and gap volume, and then used them as an SVM input to train their NOXclass classifier to discriminate between crystal packing, obligate and non-obligate interactions [3]. Recently, Capitani's group [17] have proposed to use core size and evolutionary metrics of interfacial residues to classify small biological interfaces from large crystal contacts. Their method EPPIC can outperform a widely-used method PISA [18].

Despite the intensive research on the characterization of crystal packing and biological binding, it still remains an important issue to design a good method which can be always effective across multiple datasets containing interfaces of diverse sizes, and especially on those datasets where crystal packing and biological binding have similar interface sizes [14, 17]. It is even more challenging to detect one single discriminative feature which can clearly characterize crystal packing interfaces having different sizes across multiple datasets.

In this work, we propose to use B factor to distinguish biological interfaces from crystal packing contacts. B factor is a measure to capture the atomic vibrational motion. We propose to use three features derived from B factor for this classification problem. One is denoted as ΣB; it is the sum of the normalized B factors of the interfacial atoms at a binding interface. The second is the ratio of ΣB over the logarithm of min _r + 1 (the smaller one of the average numbers of residues per chain in the two units of an interaction). This feature is denoted by avgΣB. The third feature is denoted by avgNo.B which represents the ratio of the number of interfacial atoms with a negative normalized B factor over the logarithm of min _r + 1. The fourth new feature is a compound feature by integrating avgΣB and avgNo.B through multiplication to amplify these two features' collective synergy.

To show the effectiveness and the interpretability of the four features, we visualize their distribution properties from four datasets of biological binding and crystal packing, and from a biological protein-protein and protein-peptide binding dataset newly constructed from PDBbind [19]. For the protein interactions in this new dataset, their binding affinity is known and the complexes have diverse interface sizes.

Because interface area is considered as one of the most effective features by the existing research, we especially compare our features with interface area. To show the overall classification performance of these features, we also compare the cross-dataset classification performance of each of the four features with the performances achieved by the interface area approach and those by existing methods. The results have demonstrated that each of our four features, in particular avgΣB, avgNo.B and their multiplication, consistently outperforms the feature interface area and existing prediction methods across almost all of the datasets. These features based on B factor thus have a strong capability to distinguish true and false biological interfaces of diverse sizes for real-world applications.

Data sets

Four datasets in the literature and a new dataset are used to investigate the four features derived from B factor.

The first dataset (Bahadur) contains 187 crystal packing interfaces and 122 biological homodimers [4, 5]. DiMoVo was trained on this dataset [14].

The second dataset (Ponstingl) has 92 crystal packing interfaces and 76 homodimers [20]. This dataset was used by several existing works [11, 12], including PITA [16] and PISA [18].

The third dataset (BNCPCS) comprises 75 obligate interactions and 106 crystal packing interfaces [3]. NOXclass was trained on this dataset.

The fourth dataset (DC) is composed of 82 crystal packing interfaces and 82 biological interfaces [17]. The uniqueness of this dataset is that crystal packing interfaces are larger and biological interfaces are smaller than those in the first three datasets. EPPIC was trained and optimized on this dataset [17].

A new dataset is constructed from the protein-protein binding and protein-peptide binding data stored at PDBbind [19]. All the complexes are annotated with a binding affinity extracted from PDBbind. The binding biological units in PDB structures are obtained using an automatic process according to the information provided in PDBbind. An interface is included in this dataset, if the PDB structure satisfies the following requirements. (i) The PDB structure is determined by X-ray crystallography rather than other techniques, and (ii) the resolution is better than 2.5 Å. (iii) In the PDB entry, the number of atoms should be 3+ times than the number of residues in order to remove those PDB entries with a possible error. (iv) In the complex, both of the binding partners have more than 5 residues. (v) In the interface, the number of atomic contacts from non-standard residues is less than 20% of all atomic contacts. This newly constructed dataset is composed of 799 protein-protein or protein-peptide complexes with binding affinity information. This dataset is denoted as PDBbind. It is a bench-marking dataset for testing algorithms on classifying biological binding interfaces of diverse area sizes.

Methods

In this section, we describe what is B factor and how it is normalized. Then, we describe how to derive B factor related features to represent an interface. We also show how to detect the optimal distinguishability of each feature on training datasets and then test it on other datasets.

B factor and its normalization

B factor is also known as temperature factor or Debye-Waller factor. It measures and quantities the uncertainty/mobility of an atom in dynamic protein 3D structures, namely, the displacement of the atomic positions from its mean position. B factor is an indicator of the relative vibrational motion or the disorder of an atom in protein crystal. It is calculated using $B^i=8{\pi }^2{U}_i^2$, where $U_i^2$ is the mean square displacement of atom i. B factor increases as $U_i^2$ increases. A low B factor implies that the atom is in the well-ordered parts of the structure, while a large B factor generally suggests a very high flexibility of this atom.

Protein flexibility is closely related to protein functions such as catalysis and allostery [21]. Deeply buried atoms in the core of the protein are usually rigid with a low B factor [22], and interfacial residues in protein binding complexes also have lower B-factors in comparison to the rest of the tertiary structural surface [23]. For different PDB structures, the distribution of B factors varies greatly. Thus, a normalized B factor is used in this work and calculated by Equation 1.

$$\begin{array}{c}{B}_{norm}^i=\frac{B^i-\bar{\overline{B}}}{{\delta }_B}\times \frac{1}{1.645}\\ {\ddot{B}}_{norm}^i=min\left[max\left(B_{norm}^i,-1\right),1\right]\end{array}$$

(1)

where Bⁱ is the B factor of atom i, $\overline{B}$ and δ _B are the mean and the standard deviation of the B factor of all atoms within a binding unit of the PDB biological complexes, and $B_{norm}^i$ is the normalized B factor of atom i. The number 1.645 is a typical threshold under a standard normal distribution, indicating the 0.05 probability of a value outside [−1.645, 1.645] for each of the two tails. min means the minimum of two values, while max returns the maximum. The first equation in Equation 1 is used to normalize and scale the 90% confidence interval of the B factor to [-1, 1]. The second equation in Equation 1 is used to set any value outside the 90% confidence interval to either -1 or 1, whichever is closer. The normalization is performed individually on each contact partner in a complex, no matter the contact is false or true.

Using B factor related features to characterize an interface

Interfacial atoms

An atom from a biological unit is defined as an interfacial atom if it has at least one β contacts with the partner biological unit. We note that a biological unit may contain more than one chain. β contact is a new definition of atomic contact [13]. It requires that there is no other atom interrupting the contact. Formally, given a quaternary structure of a protein complex p, a β contact between two atoms i and j in p requires that (i) the spatial distance between i and j is less than a threshold Td plus the sum of their van der Waals radii defined by [24], (ii) i and j share a Voronoi facet in p's Voronoi diagram, and (iii) the contact cannot break p's β-skeleton. The β-skeleton [25] of a discrete set p is an undirected graph in computational geometry. In this graph, two points i and j have an edge if angle ikj is sharper than a threshold determined by β, ∀k ∈ p, k ≠ i, j. This angle threshold is denoted as ∠β, which actually defines a forbidden region fr of the contact between i and j. The forbidden region fr of a β contact usually does not cover any other atoms. Otherwise, if there is an atom k in fr, the contact between i and j is not a β contact. A β contact suggests that its two atoms should have enough direct contact area to form an important interaction. The number of atomic β contacts in protein binding interfaces is only a small fraction number of distance-based contacts or less than half the number of contacts in the Voronoi diagrams [13]. Interestingly, it has been demonstrated that the use of β contacts can achieve better prediction performance for distinguishing false binding of crystal packing from homodimers [13], for predicting binding hot spots and the change of binding free energy after mutations [26], and for estimating protein-ligand binding affinity [27].

In this work, an interfacial atom is used for further analysis if and only when the number of its local contacts across the interface is more than 2. The local contacts of an atom include the contacts of the atom itself and the contacts of its covalently-bonded nearby atoms. The covalently-bonded nearby atoms of a given atom i are those atoms within two covalent-bond steps from i. For example, given a chain of covalent bonds i − j − k − l − m, where − indicates a covalent bond. From i, the covalently-bonded step is 0 to i, is 1 to j, is 2 to k, is 3 to l, and is 4 to m. Thus, i, j and k are the covalently-bonded nearby atoms of atom i, while l and m are not. The requirement of the number of local contacts is used to detect non-isolated atomic contacts.

Four interfacial features related to B factor

B factor score (denoted by ΣB) The first feature to describe an interface is the sum of the normalized B factors of all of the interfacial atoms. That is, $\Sigma B={\sum }_{j=1}^N{\ddot{B}}_{norm}^{i_j}$, where N is the number of interfacial atoms and ij is an interfacial atom, 1 ≤ j ≤ N.

Average ΣB (denoted by avg ΣB) A recent published work has suggested that the area size of protein interfaces is related to the size of proteins [28]. Thus, we calculate the ratio of ΣB over the logarithm of min _r + 1, and name this ratio average ΣB, denoted by avgΣB. Formally, avgΣB = ΣB/log(min _r + 1). Here, min _r is the smaller number of the average numbers of residues per chain for the two biological units in a complex. The logarithm is used to decrease the effect of min _r on avgΣB when min _r is extremely large.

The number of interfacial atoms with a negative normalized B factor (denoted by No.B) We also calculate the number of interfacial atoms having a normalized B factor less than 0. It is denoted by No.B. Similarly, we produce the ratio of No.B over log(min _r + 1) based on the same reason for avgΣB. This ratio feature is denoted by avgNo.B.

A combined feature--avg ΣB*avgNo.B We also multiply avgNo.B and avgΣB/100 as a feature to describe an interface. This feature is denoted by avgΣB*avgNo.B. The intuition behind this new feature is to amplify the collective synergy of avgΣB and avgNo.B through multiplication.

Interface area (ΔASA)

An effective feature widely used by the existing works to distinguish biological binding and crystal packing is interface area (ΔASA). Interface area measures half of the change of a surface area upon protein complex formation. The classification performance of this feature is considered as a baseline performance here. ΔASA of a protein complex is calculated through Equation 2.

$$\Delta ASA=\left(AS{A}_1+AS{A}_2-AS{A}_C\right)/2$$

(2)

where ASA₁ and ASA₂ are the surface areas of the two biological units of the protein complex and ASA _C is the surface area of the protein complex.

Similarly, the ratio of ΔASA over the logarithm of min _r + 1 is denoted by avgΔASA. Both ΔASA and avgΔASA are compared with the B factor based features for identifying biological binding interfaces from PDB structure data.

Optimization of the scoring threshold for each feature

For each of the features introduced above, we use the following process to find the best threshold point on a learning dataset for the classification of test data. We explore all possible split points for a feature, and assess the MCC performance with regard to every split point. Then, we collect all those split points which produce the top 10% performance, and take the average of these split points as the optimal split threshold for the feature in the learning process. This threshold is used to predict interaction types (biological binding or crystal packing) for the structure data from the other datasets. Using the average of the top 10% best split points instead of the best split point is for the purpose of increasing performance stability and generalizability of the feature. When the PDBbind dataset is used for learning, the value at the first 25% quantile, which is close to 0, is used as the threshold and tested on the other datasets. This is because PDBbind is constructed using an automatic process without manual checking, and it is possible that some true complexes are wrongly collected. The threshold value 25% is not optimal. There is no gold standard to select an optimal threshold on PDBbind, because only positive samples are given.

Assessment measures

Prediction performance is measured by precision(pre.), recall(rec.), specificity(spec.) accuracy(acc.) and MCC whose definitions are given in Equation 3.

$$\begin{array}{ccc}precision\left(pre.\right)\hfill & =\hfill & \frac{TP}{TP+FP}\hfill \\ recall\left(rec.\right)\hfill & =\hfill & \frac{TP}{TP+FN}\hfill \\ specificity\left(spec.\right)\hfill & =\hfill & \frac{TN}{TN+FP}\hfill \\ accuracy\left(acc.\right)\hfill & =\hfill & \frac{TP+TN}{TP+TN+FP+FN}\hfill \\ MCC\hfill & =\hfill & \frac{TP*TN-FP*FN}{\sqrt{\left(TP+FP\right)\left(TP+FN\right)\left(TN+FP\right)\left(TN+FN\right)}}\hfill \end{array}$$

(3)

where binding complexes are considered as the true cases, while crystal packing as the false cases; TP, FP, TN and FN are the number of true positives, false positives, true negatives and false negatives, respectively. Hence, precision is the number of correct binding complex predictions divided by the number of positive predictions, recall is the fraction of correct binding complex predictions over all true binding complexes, while accuracy is the number of correct predictions divided by the number of all true or false complexes.

Results

We report cross-dataset classification performances achieved by each of the B-factor based features in comparison with the performance by the feature interface size (ΔASA). It is observed that avgΣB, avgNo.B and avgΣB*avgNo.B have much better performance than ΔASA. We then present a detailed distribution analysis for these features' scores of the protein structures from the five datasets. We also compare avgΣB with two published methods EPPIC [17] and PISA [18] to highlight our better classification performance.

Cross-dataset classification performance by single features

Comparison between ΣB and ΔASA: ΔASA is a geometrical feature widely used by existing methods, and it is considered as an effective approach to the classification between crystal packing and true biological binding. It has been suggested to use 856 Ų [20] as a threshold to distinguish crystal packing contacts from homodimers, achieving an accuracy of 85% on the Ponstingl data set. In [3], it is shown that a cutoff of ΔASA at 650Ų has approximately 7% error rates on the BNCPCS dataset including 62 non-obligate interactions. However, these methods have limits to achieve good performance when the biological binding interfaces and crystal packing contact areas have diverse interface sizes.

Table 1 shows the classification performance for ΣB and ΔASA on the five datasets. It can be seen that ΣB has much better classification performances than ΔASA under almost all of these tests. In particular, when tested on DC, ΔASA has three negative MCC performance and another two low MCC values less than 0.3. But, ΣB always has positive MCC values larger than 0.3. This performance difference is mainly attributed to the hard case that similar sizes of the interface areas exist between the crystal packing contacts and the real biological binding interfaces in DC. Under this situation, the classification capability of ΔASA is lost.

Table 1 Cross-dataset classification performances.

When tested on the Bahadur and Ponstingl datasets, ΣB outperforms ΔASA for all cases, achieving at least 0.1 MCC improvement in 5 of the 8 cross-dataset comparisons, and achieving 0.05 - 0.1 MCC improvement in another 2 comparisons. When tested on BNCPCS, ΣB has also achieved higher MCC performance than ΔASA when both ΣB and ΔASA are optimized on DC and Bahadur. ΔASA has only achieved a higher MCC performance than ΣB on BNCPCS, when optimized on the Ponstingl dataset. We note that crystal packing contacts from BNCPCS are easy to be distinguished--both ΣB and ΔASA have achieved an accuracy higher than 0.94. When PDBbind is used in learning process and the other datasets are used for testing, ΣB always outperforms ΔASA remarkably.

Comparison between avgΣB and avgΔASA: When the two average-smoothed features, i.e., avgΣB and avgΔASA, are used in the classification, their performance is better than the non-smoothed features ΣB and ΔASA, respectively. This affirms that taking average is a good way to deal with the issue of relative size of an interface compared to its chains. This idea is especially meaningful when protein-peptide binding interfaces are considered for classification where peptides are usually of small sizes and the corresponding binding interfaces are always much smaller than protein-protein binding interfaces. Table 1 also shows the superior performance of avgΣB in comparison with avgΔASA for almost all of the cross-dataset tests.

The performance of avgNo.B and of avgΣB*avgNo.B: The feature avgNo.B is also useful to classify crystal packing from biological binding. But its performance is a bit unstable in comparison with ΣB or avgΣB. Nevertheless, it still has a stabler than ΔASA. The cross-dataset classification performance by avgΣB*avgNo.B (the multiplication of avgΣB and avgNo.B) is presented in the middle row of Table 1 for each of the datasets. This performance is competitive to the best performance achieved by avgΣB or avgNo.B. This feature also outperforms ΔASA and avgΔASA for almost all of the across-dataset tests.

The value distributions of our B factor based features and the value distribution of the feature interface size

The value distributions of the features on the five datasets are drawn in Figures 1, 2 and 3. The p-values of these distributions for the two types of interfaces are reported in Table 2. It is clear from Figure 1(a) and Figure 2(a) that B factor related features such as ΣB are more powerful than interface size to distinguish between biological binding interfaces and crystal packing interfaces.

Figure 1

The score distributions of ΣB and ΔASA in boxplot for the five datasets. The p-values are shown in Table 2. The horizontal lines represent the best split points for each of the four datasets and the 25% quantile point for PDBbind.

Figure 2

The score distributions of AvgΣB and avgΔASA in boxplot for the five datasets. The p-values are shown in Table 2. The horizontal lines represent the best split points for each of the four datasets and the 25% quantile point on PDBbind.

Figure 3

The score distributions of Average No.B (avgNo.B) and avgΣB*avgNo.B in boxplot for the five datasets. The p-values are shown in Table 2. The horizontal lines represent the best split points for each of the four datasets and the 25% quantile point on PDBbind. avgΣB*avgNo.B is divided by 100 for better visualization but without changing its value distribution between the two types of interfaces.

Table 2 p-values of different features for the two types of interfaces in the four datasets.

In particular on the DC dataset, crystal packing contacts have very similar area sizes with those of the biological binding interfaces. Features ΣB and avgΣB can classify these two types of interfaces very well. This classification is quantified as in Table 2 where B factor related features always have much smaller and more significant p-values than those of ΔASA. However, ΔASA even has insignificant p-value 0.184 on the DC dataset. Features avgNo.B and avgΣB*avgNo.B (Figure 3) can also separate the two types of interfaces with a clearer boundary than ΔASA does (Figure 1(b) and Figure 2(b)).

The scatter plots of avgΣB and ΔASA on the five datasets are presented in Figure 4. Figure 4(a) indicates that ΔASA wrongly classifies many of those protein binding interfaces of PDBbind below the horizontal line as crystal packing contacts, while avgΣB misclassifies much less number of protein binding interfaces on the right-hand side of the vertical line (142 vs 322). Further, Figure 4(b) suggests that a cross-dataset ΔASA threshold is useless on DC. Figure 4(c) on the Bahadur dataset and Figure 4(d) on the Ponstingl dataset both demonstrate that many of the crystal packing contacts with a large interfaces can have a small avgΣB values and thus they can be correctly classified by avgΣB. In Figure 4(e) on BNCPCS, both ΔASA and avgΣB are powerful to distinguish between crystal packing and biological binding.

Figure 4

The relationship of ΔASA and avgΣB. Sign + represents a true binding interface, while ○ represents a crystal packing interface. Those complexes with ΔASA larger than 2200 Å or avgΣB smaller than -16 are all true binding and thus are not drawn. The horizontal lines have ΔASA = 800 Å, while the vertical lines have avgΣB = -5. Both the values are not optimized but used only for a better visualization of the different distribution across datasets.

In conclusion, avgΣB and avgΣB*avgNo.B have a consistent classification performance across the datasets with diverse interface sizes, including those large interfaces of crystal packing and small interfaces of biological binding.

Classification performance comparison with PISA and EPPIC

The performances by avgΣB and avgΣB*avgNo.B are compared with a widely-used method PISA and a newly published method EPPIC (Table 3). Although much less number of features are used by our approach, our single feature avgΣB can outperform both EPPIC and PISA. On both the Ponstingl and the Bahadur datasets, the MCC scores of EPPIC are quite close to those of avgΣB, and also much higher than those of PISA.

Table 3 Comparison with existing methods PISA and EPPIC.

Our method also has much higher specificity and higher precision, indicating that the predicted biological binding interfaces are more likely to be true binding. It is thus quite useful to automatically compile protein-binding datasets from PDB for large-scale structural analysis where crystal packing contacts should be correctly labeled and then excluded to enhance the analysis results.

Feature avg ΣB can be used to correct errors in biological binding annotation: an example

The B factor feature avgΣB is able to correct annotation errors. We demonstrate such corrections in Figure 5 by examining two derived protein complexes from PDB entry 1UBY.

Figure 5

Two interfaces derived from the PDB entry 1UBY. (a) The used dimer structure in the Bahadur dataset which is derived by a computational tool with regard to the biomolecule 2 of REMARK 350 in 1UBY; (b) the dimer structure determined by the authors of 1UBY. The original B factors in 1UBY are ranged between 13.22 and 83.45 according to Equation 1. The colors from blue to white and to red indicate B factors from small to large. The structures are shown in the surface view. The regions without any surface view are the binding sites on chain A. The binding sites on chain B are not shown due to the symmetry of the interfaces.

Figure 5(a) shows a one-side binding site of the interface for a derived complex with regard to the biomolecule 2 of the REMARK 350 of 1UBY. This interface has a ΔASA = 1766.75 Ų and it is predicted to be dimeric by a computational tool [29]. However, there are no biological evidences so far to claim it as a true dimer. Figure 5(b) displays a one-side binding site of another derived dimeric interface (according to the biomolecule 1 of the REMARK 350 in 1UBY). This binding interface is actually recommended by the authors of 1UBY[30].

The interface in Figure 5(a) is manually mistaken as a biological binding interface in the Bahadur dataset. But, it is the interface in Figure 5(b), instead of that in Figure 5(a), that should be in this dataset. Feature avgΣB can correct this mistake with two reasonable evidences as follows. Firstly, the interface in Figure 5(a) has an avgΣB value of 14.96, which is in the top-right region of Figure 4(c) with '+'. This avgΣB value is extremely different from the avgΣB values of other biological binding interfaces as shown in Figure 4. Secondly, the interface in Figure 5(a) has atoms with larger B factor in red, while the interface in Figure 5(b) has atoms with much smaller B factor in blue. Thus, avgΣB can make a reasonable prediction that the interface in Figure 5(b) is dimeric and the interface in Figure 5(a) should not be. This is also consistent with the biological evidence in the REMARK 350 of 1UBY[30]. Thus, the interface in Figure 5(a) needs more biological evidences to be claimed as a true dimer. This example illustrates that the B factor feature avgΣB can be used to correct wrong annotations of biological binding interfaces.

Conclusion

In this work, we have proposed to use B factor as a new characteristic to distinguish between crystal packing contacts and biological binding interfaces. Assessed on five datasets, all of the B factor related features have exhibited their excellent capability for classifying various biological binding interfaces with diverse interface sizes. Our B factor features have also achieved better classification performances than the widely-used feature interface size and two published methods PISA and EPPIC. In particular, the average sum of normalized B factor of interfacial atoms is a clear indictor for biological binding. As a future work, the B factor related features and our method will be employed for a large scale annotation of potential biological binding interfaces for PDB.