INTRODUCTION

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Ubiquitin-conjugating enzymes (E2s) comprise a class of eukaryotic enzymes that function at an intermediate step in the reaction pathway leading to protein ubiquitination. Initially, E2s accept ubiquitin from the active-site cysteine of a ubiquitin-activating enzyme (E1) to their own active-site cysteine via a transthiolation reaction. Subsequently, thiol ester-linked ubiquitin is donated by E2s in one of two possible ways. E2s may transfer ubiquitin directly to a lysine side chain found either on a protein substrate or on a ubiquitin moiety in a growing multiubiquitin chain through the formation of an isopeptide bond. Alternatively, E2s transfer ubiquitin to a cysteine of a ubiquitin protein ligase (E3) through a second transthiolation reaction. In the former case, an E3 functions to assist the E2 in the recognition of a protein substrate, while in the latter case, it is believed that the E3 directly links ubiquitin to either the protein substrate or a growing multiubiquitin chain. Assembly of a multiubiquitin chain on a protein substrate by either an E2 or an E3 targets the protein for degradation by the 26S proteosome (35, 39, 43).

E2s have been shown to consist of a conserved catalytic domain that contains the active-site cysteine. This conservation is observed in both sequence and structural comparisons of E2s. For example, the 11 E2s and two ubiquitin-like conjugating enzymes (UBC9 and UBC12) from the yeast Saccharomyces cerevisiae exhibit between 20 and 92% identity. Superimposition of the six solved E2 crystal structures also makes it apparent that the three-dimensional folding of different E2s shows little variation (3-5, 16, 54, 58). It is thought that the requirement of E2s to interact with E1 and ubiquitin (or their cognates) during E2-ubiquitin thiol ester formation placed considerable evolutionary constraints on the E2 structure, resulting in the observed conservation (4, 50).

Although E2s have a function in common in ubiquitin thiol ester formation, they have also been shown to function within a wide range of cellular pathways resulting in the ubiquitination of protein substrates particular to those pathways. This requires that downstream of E2-ubiquitin thiol ester formation, an E2 must interact with proteins that are specific to that pathway, such as an E3 or a target, through unique points of contact other than those employed with ubiquitin and E1.

To acquire these individual functional characteristics, E2s have exploited tolerable levels of structural variation. One source of structural variety comes in the form of carboxy- and amino-terminal extensions to the conserved catalytic domain, the type II, III, and IV E2s (15). In addition, loop structures can result from amino acid insertions within the conserved catalytic domain. These additions to the catalytic domain have been reported to contribute to the unique functional characteristics of several E2s. For example, CDC34 (UBC3) from S. cerevisiae is required for the G₁ to S phase transition of the cell cycle (10) and is responsible for the degradation of several cell cycle-related proteins (7). CDC34 possesses both a carboxy-terminal extension and an insertion near its active-site cysteine, both of which play a role in its cell cycle function (26, 31, 50). Furthermore, the carboxy-terminal extension has been shown to help mediate the interaction between CDC34 and its E3, namely, the SCF complex (32).

The type I E2s (15), however, are capable of performing their unique cellular functions without the requirement of extensions or insertions. In these cases, protein interactions unique to an E2 must be determined solely by the distribution of specific amino acid side chains on the conserved catalytic domain surface. In the present work, we demonstrate that a single amino acid replacement within an E2 catalytic domain results in the acquisition of two other E2 functions in addition to its own. These results shed light on the nature of E2-E3 interactions and suggest that E2s may have evolved from a pluripotent progenitor.

	MATERIALS AND METHODS

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Plasmids and yeast strains. The S. cerevisiae high-copy-number, TRP1-based E2 expression plasmids used in growth and UV sensitivity studies are identical to YEP96 (8), except that the rad6C, ubc1C, and UBC4 coding sequences replace the ubiquitin coding sequence. The specific codon changes and the corresponding residue changes for each of these E2 sequences are listed in Table 1. Group A (plasmids 1 to 3) are the parental E2 constructs that were used as positive controls throughout this study. rad6C encodes a truncated version of RAD6 that contains the functionally active catalytic domain (residues 1 to 153) but lacks the C-terminal acidic tail (residues 154 to 172). Additional codon changes within rad6C reflect the creation of new restriction sites within the coding sequence to facilitate subsequent gene manipulation. Changes at codon positions 2 and 3, 51 and 52, 98 and 99, and 153 create the restriction sites SacI, KasI, SmaI, and EcoRV, respectively. Changes at codons 2, 51, 98, and 99 have no effect on the polypeptide sequence, whereas changes at codons 3, 52, and 153 result in conservative amino acid replacements (Table 1). The rad6C plasmid fully complements the UV sensitivity of a rad6-null strain in either the low-copy-number or the high-copy-number form.

View this table: [in this window] [in a new window]   TABLE 2.   Phenotypes of rad6C, ubc1C, and UBC4a

Phenotype analysis. For growth studies, strains MHY508 and KMY20 containing TRP1 vectors were grown in fully supplemented SD liquid medium lacking tryptophan (48) to exponential growth phase. Cells (10⁵) from each culture were then plated onto fully supplemented SD plates (lacking tryptophan) and grown at 30°C. Growth was scored on the basis of colony size. Colonies were given designations of + to ++++++ based on their sizes relative to colonies produced by cells expressing either rad6C (+) or UBC4 (++++++). For stress sensitivity experiments, MHY508 strains were grown at 30°C on plates in the presence or absence of canavanine sulfate (1.5 µg/ml) or at the temperatures indicated. Colonies were counted after 7 days. For UV sensitivity experiments, plates containing KMY20 strains were irradiated with 72 J of short-wavelength UV light (254 nm) per m². Plasmid rescue of the cdc34-null defect associated with YES71 was assessed by determining the persistence of cell viability upon loss of the URA3-CDC34 maintenance plasmid in the presence of FOA. Cells were grown to early exponential phase in fully supplemented SD liquid medium lacking uracil and tryptophan. Cells (10⁶) were then spread onto fully supplemented SD plates containing FOA (1 mg/ml) and then incubated at 25°C for 5 days. Colony formation indicated loss of the URA3-CDC34 maintenance plasmid and complementation of the cdc34-null defect by the E2 gene of the TRP1-based plasmid.

Protein expression and purification. Expression of protein from pET3a plasmids, cell harvesting, and lysis were performed as previously described for CDC34 (15). For the purification of rad6C and its derivatives, clarified supernatants were passed over a MonoQ HR 5/10 ion-exchange column (Pharmacia) equilibrated with 50 mM Tris-HCl (pH 7.5)-1 mM EDTA-1 mM dithiothreitol (DTT) and the proteins were eluted with an NaCl gradient of 0 to 1 M. rad6C eluted at approximately 240 mM NaCl. The Mono Q fractions were concentrated by Centricon (Amicon) filtration and then loaded onto a Superdex 75 HR 10/30 size exclusion column (Pharmacia) equilibrated with 50 mM HEPES (pH 7.5)-150 mM NaCl-1 mM EDTA-1 mM DTT. Peak fractions were collected, pooled, and concentrated to 500 µl. Glycerol was added to a final concentration of 5%, and the protein samples were stored at 80°C. Expression of ³⁵S-radiolabeled ubiquitin and subsequent cell lysis were carried out as previously described for ³⁵S-radiolabeled CDC34 (38). For the purification of ubc1C, its derivatives, and ³⁵S-radiolabeled ubiquitin, clarified supernatants were passed over a MonoQ HR5/10 ion-exchange column equilibrated with 50 mM Tris-HCl (pH 7.5)-1 mM EDTA-1 mM DTT. The flowthrough was concentrated to 2 ml by Centricon filtration and then run over a MonoS HR5/10 ion-exchange column (Pharmacia) equilibrated with 50 mM HEPES (pH 7.5)-1 mM EDTA-1 mM DTT. The flowthrough was again collected and concentrated to 500 µl and then passed over a Superdex 75 HR10/30 size exclusion column equilibrated with 50 mM HEPES (pH 7.5)-150 mM NaCl-1 mM EDTA-1 mM DTT. Peak fractions were collected, pooled, and concentrated to 500 µl. Glycerol was added to a final concentration of 5%, and the protein samples were stored at 80°C. Each of these protocols resulted in essentially pure protein with typical yields of 0.25 to 0.5 mg/100 ml of culture. Purified poly-His-tagged E1 from S. cerevisiae (Uba1-6His) was a gift from S. Sadis and D. Finley (Harvard Medical School).

E2-ubiquitin thiol ester formation. Thiol ester reactions were performed in 0.5 ml of buffer A (10 mM HEPES, 40 mM NaCl, 5 mM MgCl₂, 5 mM ATP, 50 µg of bovine serum albumin per ml [final pH 7.5]) supplemented with the protease inhibitors antipain, aprotinin, chymostatin, leupeptin, and pepstatin A (each at 20 µg/ml), phenylmethylsulfonyl fluoride (180 µg/ml), and an ATP regeneration system (5 µg of creatine kinase per ml, 0.6 U of inorganic pyrophosphatase per ml, 3.3 mg of phosphocreatine per ml). Also present in each reaction mixture were E2 (100 nM) and [³⁵S]ubiquitin (100 nM with a specific activity of 1.5 × 10⁵ cpm/µg). The reaction was initiated by the addition of ubiquitin-activating enzyme (Uba1-6His at 25 nM), followed by a 5-min incubation at 30°C prior to subsequent analysis. With these reaction conditions, E2-ubiquitin thiol ester yields varied linearly with respect to the E2 concentrations of the positive controls rad6C and ubc1C.

E2 structural alignment. Three-dimensional structures of S. cerevisiae UBC1 (unpublished data), RAD6 (UBC2; 58), UBC4, and UBC7 (4, 5) and Homo sapiens UBC9 (54) were aligned by using the Superimpose function contained within the Viewer module of Insight II, version 95.0 (Molecular Simulations Inc.). Alignments were performed by using nine structurally conserved amino acid positions distributed throughout the length of the polypeptide (positions 17, 34, 49, 66, 77, 86, 96, 110, and 135 according to the numbering of S. cerevisiae UBC4). The root mean square deviation for these four superimposed structures at the nine positions indicated equaled 0.83 Å. The resulting alignment served as the guide for the computer-aided alignment of the remaining E2 catalytic domains shown in Fig. 3 (1, 10, 11, 14, 20, 21, 30, 45-47, 52, 57). The evolutionary analysis shown in Fig. 2 was generated by the Clustal method (contained in MegAlign-DNA Star) using the multiple-protein sequence alignment described above.

Amino acid substitutions used for E2 surface maps (see Fig. 4). For rad6C, UBC4, and ubc1C, amino acid substitutions with and without phenotypic effects were taken from Table 2. Characterized substitutions from other sources were as follows (square brackets denote multiple substitutions) for RAD6: no effect on RAD6 DNA repair function, [K17A, E18A, D19A], [E58A, D60A, E61A, E62A], [K132A, D132A, K134A], and [K139A, R140A, K142A, E143A]; negative effect on RAD6 DNA repair function, [R6A, R7A, R8A], [K71A, E75A], and [E86A, D90A] (33). Those for CDC34 were as follows: no effect on CDC34 function, [R4A, K5A], [R14A, R17A, E18A], [D21A, K23A, K24A], [E32A, E34A, D35A, D36A], [E51A, D52A], [K61A, R65A], [E68A, D69A], R78A, E122A, [E133A, D134A], [D144A, D148A], [R150A, K151A, E154A], [K157A, R159A, K161A], [E163A, E165A, R166A], [K168A, D170A], [R14A, R17A, E18A, D21A, K23A, K24], and [D144A, D148A, R150A, K151A, E154A]; negative effect on CDC34 function, [R90A, D91A, R93A], [E109A, D111A, E113A] (36), [S97A or D], [S139A or D], and [G103 to T114 deleted] (31).

	RESULTS

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We approached the problem of E2 specificity with the simple assumption that the unique determinants of specificity for each E2 catalytic domain could be identified by searching for amino acids whose transposition from one E2 to another resulted in a corresponding transposition of function. Such an approach has previously been used to make a single amino acid substitution in NEDD8, making it a substrate for the ubiquitin pathway (56). The ubiquitin-conjugating enzymes UBC4 and RAD6 (UBC2) from S. cerevisiae were employed, as each carries out a distinct, nonoverlapping function and their respective biological properties can be easily measured by determining cell viability in simple plating experiments.

Initially, comparisons of the sequence similarities and differences both within and among the six members of the RAD6 and UBC4 families from S. cerevisiae, Schizosaccharomyces pombe, Drosophila melanogaster, Caenorhabditis elegans, Arabidopsis thaliana, and H. sapiens were carried out (6, 9, 24, 25, 28, 40, 41, 42, 45, 53, 55, 59). From these comparisons, we identified 21 positions that displayed strong conservation within each family but differed between families. These positions were distributed more or less uniformly throughout the E2 polypeptide, and notably, only one of these positions was not found on the protein surface (UBC4 A147, RAD6 W149).

Using this information, we attempted to convert the DNA repair function of S. cerevisiae RAD6 (14) to the growth and stress resistance functions of S. cerevisiae UBC4 (45) by replacing the amino acids at these 21 positions in RAD6, either singly or in combination, with their UBC4 counterparts (Table 1, plasmids 4 to 16). For these experiments, a derivative of RAD6 lacking its C-terminal polyaspartate tail (rad6C) was used because of both the absence of the tail in other members of the RAD6 family and the fact that the tail is not essential for its DNA repair function in S. cerevisiae (34).

Contrary to our initial expectation, substitutions at 18 of these 21 positions displayed no transposition of the UBC4 growth or stress resistance functions to rad6C. Furthermore, these 18 substitutions had no adverse effect on the DNA repair function of rad6C, even when present together in the various combinations listed in Table 1 (plasmids 4, 7, 10, 11, and 14 to 16). Thus, none of these 18 positions plays a significant role in determining the unique characteristics of RAD6 or UBC4.

On the other hand, two substitutions in rad6C resulted in the elimination of (S120D) or a strong reduction in (N123V) the DNA repair activity of RAD6 without affecting the efficiency of E2-ubiquitin thiol ester formation (Table 2, rows 8, 9, and 13). Neither of these substitutions imparted any UBC4 character to rad6C. Conversely, the transposition of their RAD6 counterparts into UBC4 had little, if any, effect on UBC4 function and failed to produce any degree of RAD6 function (Table 2, row 17). Thus, positions 120 and 123 are necessary, if not sufficient, determinants of RAD6 function whereas their UBC4 counterparts (positions 118 and 121) are not essential to the UBC4 functions tested.

The DNA repair function of RAD6 has also been previously shown to be dependent upon at least one of three arginines (residues R6, R7, and R8) at its amino terminus (33). It was expected that by replacing the amino-terminal residues of RAD6 with those of UBC4 (plasmid 19), the DNA repair function of RAD6 would be lost, as UBC4 has only one arginine residue (R6) in this region, corresponding to position R8 in RAD6. Contrary to this expectation, minimal loss of DNA repair function was observed (Table 2, row 19), indicating that of the three amino-terminal arginine residues in RAD6, R8 plays the pivotal role in its DNA repair function. We confirmed this by replacing R8 in RAD6 with Q (the residue found at the analogous position in UBC9), which resulted in complete loss of the DNA repair function (Table 2, row 17).

The most striking observation that emerged from this mutational analysis was that the single transposition of F63 from UBC4 to the N65 position of rad6C resulted in a functionally hybrid E2 that had acquired the growth and stress properties of UBC4 with minimal loss of its original DNA repair properties (Table 2, row 5). The N65F derivative of rad6C also acquired UBC4's ability to degrade a noncleaved ubiquitin--galactosidase fusion (data not shown), as originally reported by Johnson et al. (17, 18). A similar but weaker effect was observed when N80 of UBC4 was transposed to the Y82 position of rad6C, which also augmented the UBC4 character of rad6C when combined with the N65F transposition with minimal loss of its DNA repair function (Table 2, rows 6 and 12). Notably, the reciprocal F63N and N80Y transpositions into UBC4 had little, if any, effect on UBC4 function (Table 2, row 17) and these transpositions did not impart any RAD6 characteristics to UBC4.

Two conclusions can be drawn from this analysis. (i) The functional determinants of RAD6 and UBC4 are not spatially equivalent but map to different regions on the E2 surface. This accounts for the ability of one E2 to acquire the properties of the other while retaining its own characteristics. (ii) RAD6 has more functionally relevant surface properties in common with UBC4 than would be predicted on the basis of function or sequence comparisons.

A pluripotent E2. Previous studies have shown that appending the CDC34 tail to the catalytic domain of RAD6 (but not UBC4) creates an E2 chimera capable of fully substituting for the cell cycle function of CDC34 without loss of RAD6 DNA repair activity (26, 50). Given the observations cited above, it seemed reasonable to expect that by appending the CDC34 tail to the bifunctional rad6C F65 derivative, a pluripotent E2 could be created that incorporates the UBC4, RAD6, and CDC34 activities in a single polypeptide. Contrary to our expectation, we observed that a chimeric E2 consisting of rad6C F65 and the CDC34 tail could rescue the cdc34-null strain and the UV sensitivity of the rad6-null strain (Fig. 1) but severely exacerbated the growth phenotype of the ubc4 ubc5-null strain (data not shown). Thus, the CDC34 tail appears to interfere with an essential function, likely that of the remaining UBC4 family member, UBC1. This observation raises the possibility that one role of an E2s carboxy-terminal extension is to isolate a particular function to that E2.

View larger version (27K): [in this window] [in a new window]   FIG. 1.   A pluripotent E2. (A) Complementation of defects associated with the ubc4 ubc5 (35°C), rad6 (UV), or cdc34 (FOA) mutant strains by various rad6C derivatives. The positions of point substitutions introduced into the rad6C catalytic domain (gray) are indicated, as is the addition of the CDC34 tail domain (white) to the carboxy terminus of rad6C. The ability (+) or inability () of each derivative to allow colony formation by each strain under the conditions given was determined. (B) The ability of a plasmid expressing rad6C F65 to complement each disruption strain is compared to that of a negative control plasmid containing no E2 gene (null) or the appropriate positive control plasmid expressing either UBC4, CDC34, or rad6C (see Materials and Methods).

Evolutionary relationships. The ability of the RAD6 catalytic domain to accommodate the functions of UBC4 and CDC34 in addition to its own suggested the possibility that these three E2s diverged from a common RAD6-like E2 progenitor that embodied the functions related to stress response, cell cycle, and DNA repair. In light of the fundamental importance of these processes to cell viability, such a divergence may have been among the first in E2 evolution.

View larger version (11K): [in this window] [in a new window]   FIG. 2.   Evolutionary relationships among E2s from S. cerevisiae (see Materials and Methods). Also indicated are the lengths of major sequence landmarks for each E2. The letters a and b refer to the insertion positions highlighted in Fig. 3.

View larger version (55K): [in this window] [in a new window]   FIG. 3.   Structure-based sequence alignment of the E2 catalytic domains from S. cerevisiae (see Materials and Methods). The two positions that accommodate insertions are labeled a and b.

Mapping of the determinants of specificity. A picture of the structural relationships among RAD6, UBC4, and CDC34 emerges when the mutational analyses derived from this work and elsewhere (see Materials and Methods) are combined with protein sequence comparisons and viewed in three dimensions. In Fig. 4, a structurally based schematic of the RAD6 catalytic domain is used as a common template to highlight three different surface attributes of the three E2s. Gray areas highlight surface features that are common to all previously identified E2s and include the solvent-exposed backbone and residue side chains that are identical from protein to protein. These regions are expected to include sites of interactions for ubiquitin and E1 that are required for the universally shared process of E2-ubiquitin thiol ester formation. Ubc9 and Ubc12 were naturally excluded from this analysis because of their involvement in non-ubiquitin conjugation processes involving the ubiquitin homologues Smt3 (Sumo-1) and Rub1, respectively (19, 27). Open symbols correspond to the positions of individual side chains that are presumed to be functionally inessential based on their lack of conservation within a given E2 family (circles) or directly demonstrated to be inessential by site-specific mutagenesis (squares). Closed symbols denote side chains that have been shown to play a role in functional properties that are unique to a given E2 without affecting E2-ubiquitin thiol ester formation (squares) or side chains that are candidates for unique functional determinants based on their conservation within a given E2 family, coupled with their lack of conservation between E2 families, and which could not be excluded on the basis of existing mutational data (circles).

View larger version (49K): [in this window] [in a new window]   FIG. 4.   Surface map of three E2 catalytic domains based on function. For each E2, the catalytic domain of S. cerevisiae RAD6 has been used as the map template rotated through increments of 90°. Gray areas represent regions that are structurally conserved. The active-site cysteine is marked by the letter C. Amino acid substitutions with no effect on function are indicated with open boxes. Substitutions that affect functions that are specific to each E2 are indicated with filled boxes. Open circles denote residues that are unconserved within each E2 family indicated, while closed circles denote residues that exhibit conservation within an E2 family but variation between families.

View larger version (136K): [in this window] [in a new window]   FIG. 5.   Three-dimensional map of functionally important surfaces. The three-dimensional surface of S. cerevisiae RAD6 is used as the map template rotated to the left or right by 60°. The amino terminus is found at the top of the structures. The active-site cysteine is yellow. Conserved solvent-accessible regions are gray. Residues of clear specific functional importance for each E2 based on mutation studies are highlighted in dark green (UBC4), dark magenta (CDC34), or blue (RAD6). Residues of potential importance to E2 specificity according to the criteria described in Results are highlighted in light green (UBC4) or pink (CDC34).

	DISCUSSION

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Two opposing evolutionary forces appear to have shaped the forms of contemporary E2s. On the one hand, the evolutionary inertia that preserved the key catalytic elements common to all E2s resisted changes to their structures. On the other hand, the tendency toward structural variation provided a source for the diversity of functions observed among E2s today.

The generation of E2 diversity appears to have occurred in two possible ways: (i) changes in the distribution of amino acids on a common E2 frame through amino acid substitutions and (ii) the introduction of novel peptide elements through insertions and extensions.

We propose that E2s evolved from an ancestral E2 capable of carrying out multiple E2 functions. Phylogenetic evidence and the pluripotent nature of rad6C F65 suggest that RAD6 most closely resembles this ancestral E2 and that it consisted solely of the conserved E2 catalytic domain. Subsequent gene duplication, coupled with changes in the distribution of amino acids within the conserved catalytic domain, may have led to E2 diversity and functional specialization. In some instances, such changes appear to have been coupled with insertions and extensions, such as in the case of CDC34. Curiously, these additional peptide elements are not required for the cell cycle function of CDC34 based on the pluripotent nature of rad6C F65. Similarly, other work has shown that deletion of CDC34's catalytic domain insertion, in combination with proper amino acid substitutions, generates a fully functional derivative of CDC34 (31). Furthermore, these changes convert these positions to the residues found in RAD6, possibly accounting for the ability of rad6C F65 to carry out this cell cycle function in the absence of the catalytic domain insertion.

These examples highlight the fact that, even though insertions and extensions may have been acquired to define functional specificity, these functions remain an inherent part of the catalytic domain. These insertions and extensions appear to be dispensable with respect to E2 function and were likely acquired at some point after E2 functions had been established within the catalytic domain.

This interpretation is supported by sequence comparisons and phylogenetic analysis. With respect to insertions, this analysis suggests that the short and variable lengths of E2 insertions did not appear abruptly, carrying with them new functional attributes, but rather developed incrementally with time. Interestingly, the phylogenetic analysis presented in Fig. 2 indicates that most of the loops in present-day E2s arose fairly infrequently and independently from one another after the divergence of UBC4 and CDC34 from RAD6. The notable exceptions to this conclusion are the loops of UBC7 and CDC34, which were clearly acquired from a common ancestor. The observation that these loops are not absolutely required for the in vivo activity of these E2s is consistent with this phylogenetic interpretation (31). The infrequent and independent appearance of loops at only two positions within the catalytic domain attests to the tight evolutionary constraint placed on its modification.

Phylogenetic evidence also suggests that while extensions play a role in E2 specificity, they too were acquired relatively late in the chronology of E2, after many of their functions had been established (Fig. 2). The tails of CDC34, RAD6, and UBC1, for example, were all acquired following the divergences that led to their final forms. This conclusion is also supported by E2 comparisons across species. The tail of CDC34 shares only 9% identity with the tail of its human counterpart, tx61 (37), and the two are therefore unlikely to have the same evolutionary origin. The fact that tx61 can substitute for CDC34 in vivo argues against the notion that the tail plays a central role in substrate specificity. Similarly, the polyaspartate tail of RAD6 is not found on any of the other RAD6 homologues identified from other organisms and is not required for the DNA repair function of RAD6 (34). Finally, the tail of UBC1 exhibits only 13% identity with its bovine homologue, E2-25K, indicating that these tails are likely of independent origin. As in the case of RAD6, the tail of UBC1 is not required for its stress response activity (Table 2, row 2). The phylogenetic evidence therefore suggests that several essential E2 functions were fixed in a primordial E2 prior to the acquisition of inserts and extensions.

E2 structure and function. From the standpoint of structure, the most striking feature of the E2 surface is the distribution of residues that are conserved among all E2s, relative to residues that probably contributed to the functional divergence of UBC4, RAD6, and CDC34 (Fig. 5). Both classes of residues are found as a largely contiguous patchwork that surrounds the active-site cysteine. When combined, the determinants of UBC4, RAD6, and CDC34 form two clusters that are separated from one another by a conserved partition (Fig. 6). Residues that are important to the functions of each of these E2s can be found in both clusters (Fig. 5).

View larger version (124K): [in this window] [in a new window]   FIG. 6.   Surface determinants of E2 function are concentrated in two patches. Mapped onto the S. cerevisiae RAD6 crystal structure are all of the residues which play a role in the functional specificity of either UBC4, CDC34, or RAD6. The two views of RAD6 vary by a rotation of 30°, and the amino terminus is found at the top of the structures. Shown on the surface are (i) residues from UBCH7 which form contacts with the HECT domain of E6-AP (blue), (ii) residues identified as determinants of UBC4, CDC34, or RAD6 function (Fig. 5) that coincide with UBCH7/E6-AP HECT contact points (magenta), and (iii) residues identified as determinants of UBC4, CDC34, or RAD6 function (Fig. 5) that do not coincide with UBCH7/E6-AP HECT contact points (pink). The active-site cysteine is shown (yellow), as are conserved E2 residues (gray). Numbers indicate amino acid positions within rad6C that either play a role in the DNA repair function of RAD6 or allow it to acquire the UBC4 and CDC34 functions.