Insights into Ubiquitination from the Unique Clamp-like Binding of the RING E3 AO7 to the E2 UbcH5B*

Background: The RING E3 AO7/RNF25 binds its E2 with unusually high affinity. Results: AO7 has a secondary E2 binding site adjacent to the RING. Conclusion: This site prevents the stimulatory effect of non-covalent backside binding of ubiquitin, has unique agonist properties, and allows for structural analysis of RING mutants. Significance: Knowledge of how RING E3s mediate ubiquitination is critical to understanding cellular protein regulation. RING proteins constitute the largest class of E3 ubiquitin ligases. Unlike most RINGs, AO7 (RNF25) binds the E2 ubiquitin-conjugating enzyme, UbcH5B (UBE2D2), with strikingly high affinity. We have defined, by co-crystallization, the distinctive means by which AO7 binds UbcH5B. AO7 contains a structurally unique UbcH5B binding region (U5BR) that is connected by an 11-amino acid linker to its RING domain, forming a clamp surrounding the E2. The U5BR interacts extensively with a region of UbcH5B that is distinct from both the active site and the RING-interacting region, referred to as the backside of the E2. An apparent paradox is that the high-affinity binding of the AO7 clamp to UbcH5B, which is dependent on the U5BR, decreases the rate of ubiquitination. We establish that this is a consequence of blocking the stimulatory, non-covalent, binding of ubiquitin to the backside of UbcH5B. Interestingly, when non-covalent backside ubiquitin binding cannot occur, the AO7 clamp now enhances the rate of ubiquitination. The high-affinity binding of the AO7 clamp to UbcH5B has also allowed for the co-crystallization of previously described and functionally important RING mutants at the RING-E2 interface. We show that mutations having marked effects on function only minimally affect the intermolecular interactions between the AO7 RING and UbcH5B, establishing a high degree of complexity in activation through the RING-E2 interface.

Specificity in ubiquitination is conferred in large part by E3 ubiquitin ligases. Each E3 functions with a subset of the ϳ40 different (in mammals) E2 ubiquitin-conjugating enzymes. E3s mediate the direct or indirect transfer of ubiquitin from the active site Cys of an activated E2 (E2ϳUb) 6 to, most frequently, primary amines (Lys or the N termini of proteins). RING-type E3s (consisting primarily of RING finger and U-box proteins), which constitute the large majority of E3s, mediate the direct transfer of ubiquitin from E2 (for review, see Refs. 1 and 2). The isopeptide or peptide bonds formed with ubiquitin can be on heterologous substrates or on the E3 itself; the latter is usually referred to as autoubiquitination (Ref. 3; for review, see Ref. 4). Proteins can be modified with a single ubiquitin on one or more residues (monoubiquitination), or substrate-conjugated ubiquitin can itself be ubiquitinated on any of its seven Lys residues or its N terminus (5), forming multi-or polyubiquitin chains. Some polyubiquitin linkages represent particularly potent proteasome-targeting signals, whereas others specify different functions.
RING-type E3s bind both E2ϳUb and substrates and allosterically activate E2ϳUb (for review, see Ref. 1). Structural studies have revealed that RING-type domains bind E2s in a canonical manner using the RING's two Zn 2ϩ -coordinating loops and the intervening central ␣-helix. This RING-E2 binding is generally of low affinity (for review, see Ref. 1). For this reason, differentiating the activating function of specific residues at the RING-E2 interface from their effects on overall RING-E2 affinity can be problematic.
Key residues required for the allosteric activation of E2s have been identified (6). More recently, it has become clear that activation of E2ϳUb is dependent, in part, on the RING domain stabilizing a "closed" conformation of E2ϳUb that is primed for ubiquitin transfer. This conformation, where the orientation of the E2ϳUb thioester bond is optimal for nucleophilic attack, is a consequence of critical interactions of ubiquitin with both E2 and RING-type domains (Refs. 7-16; for review, see Ref. 1). Understanding precisely how this orientation and these stabilizing interactions enhance catalysis remains an area of intense investigation.
Other than at the E2 active site, ubiquitin also binds to a specific region on the "backside" of a subset of E2s (Ub B binding), which enhances RING:E2 affinity and stimulates ubiquitination (17)(18)(19)(20). Several E3s also bind their cognate E2s on secondary sites away from the RING-E2 interface. For the most part these overlap the backside Ub B binding site. E2 backside binding by E3s has also been shown to have substantial effects on ubiquitination (16,18,19,(21)(22)(23)(24)(25). Backside binding to ubiquitin E2s is shared with plant proteins that target E2s to the plasma membrane (26,27), and remarkable parallels exist in the SUMO conjugating system (Refs. 28 -34; for review, see Ref. 1). Determining the varied structures, functions, and dynamics of secondary E2 binding sites, including ones that await discovery, is critical to understanding the in vivo regulation of modification by ubiquitin and ubiquitin-like proteins. AO7 (RNF25) was first identified because of its unusually high-affinity binding to the E2 UbcH5B (UBE2D2) (3,35). This binding, which is dependent on both an intact AO7 RING and a C-terminal extension, helped lead to the determination that RING proteins are generally ubiquitin ligases (3). Although its cellular role remains obscure, the high-affinity AO7-UbcH5B binding led us to revisit AO7 as a model for RING:E2 interactions.
We establish herein that the structurally atypical RING domain of AO7 is part of a unique "clamp"-like structure that is comprised of the RING and the C-terminal extension. This clamp surrounds UbcH5B and includes a secondary UbcH5B binding site that overlaps the Ub B binding site on UbcH5B. The effects of disrupting this clamp provide insights into the functional consequences of both the AO7 clamp and Ub B binding (17). In addition, the unique nature of the AO7 clamp has facilitated the co-crystallization of UbcH5B together with AO7 RING mutants, which are analogous to mutations in other RINGs that have been shown to result in either compromised function or E2 binding (36 -39). This provides a means to begin to systematically dissociate overall RING:E2 affinity from functions of specific amino acids at the RING-E2 interface.

Experimental Procedures
Antibodies and Plasmids-Rat monoclonal HA antibody was from Roche Applied Science (catalog #11867423001). Rabbit polyclonal UbcH5 antiserum was from US Biological (catalog #U1000-86-M). Rabbit polyclonal GFP antiserum was from Santa Cruz (SC-8334). Rabbit polyclonal ubiquitin antibody has been described (40). pET15b-UbcH5B has been described (35) and was used as the template for point mutations. Plasmids encoding UbcM2/UbcH9/Ube2e3 were gifts from Scott Plafker and from Wade Harper (Addgene plasmid #15789) and have been described (41,42). All AO7-encoding constructs were generated by PCR from human AO7 EST (Thermo Scientific Clone ID: 4811222). AO7R (Fig. 1A) and AO7 217-258 were cloned into pGEX-6P-1 (GE Healthcare) from BamHI to XhoI. Sequence-encoding AO7RE (Fig. 1A) was cloned into the first multiple cloning site of a modified pETDUET-1 (Novagen) vector containing an N-terminal GST fusion protein in place of His 6 (pETDUET-GST), from BamHI to HindIII. A PreScission Protease (GE Healthcare) sequence (LEVLFQGP) was included in all N-terminal primers for AO7 constructs, enabling removal of GST. All GST fusions cleaved by PreScission Protease have residual Gly-Pro remaining at their N termini. To generate plasmids encoding both AO7RE and UbcH5B, cDNA encoding the E2 was amplified from pET15b-UbcH5B and cloned into the second multiple cloning site of pETDUET-GST from NdeI to XhoI. To generate UbcH5B for FlAsH labeling (UbcH5B-Green), an HHHHHHGSGCCPGCCGGSGGS tag was inserted directly upstream of UbcH5B, and the entire sequence cloned into pGEX-6P-1 from BamHI to XhoI. N-terminal HA-tagged human AO7 (RNF25) encoding amino acids 2-439 was generated by PCR and subcloned into pcDNA3.1 (ϩ) (Invitrogen) from EcoRI to XhoI. Human ubiquitin was amplified by PCR from pGL-ubiquitin (a gift from R. Andrew Byrd) as template and cloned into pETDUET-GST from BamHI to HindIII with a PreScission Protease recognition sequence at the N terminus. I44A ubiquitin (Ub I44A ) was generated by site-specific mutagenesis of this plasmid. Point mutations and deletions were generated using QuikChange (Stratagene) and verified by sequencing. pEGFP-C1 plasmid encoding GFP was purchased from Clontech.
Protein Expression and Purification-Except where noted, Escherichia coli BL21 (DE3) (Invitrogen) transformed with expression plasmids were grown at 37°C until A 600 0.8 -1.0. Protein expression was induced with isopropyl ␤-D-1-thiogalactopyranoside (0.15 mM) at 23°C for 20 h. When the RING finger of AO7 was expressed, 50 -500 M ZnSO 4 was included. For GST fusion proteins and protein complexes with UbcH5B, cell lysis was performed using an APV-2000 homogenizer in binding buffer (50 mM Tris, pH 7.5, 150 mM NaCl) with 1 mM PMSF. For UbcH5B-Green, 1 mM DTT was included in the binding buffer. After centrifugation at 27,000 ϫ g for 30 min, supernatants were collected and incubated with glutathione-Sepharose (GS) 4B (GE Healthcare) for 2 h at 4°C, after which beads were collected by centrifugation and thoroughly washed with binding buffer. GST fusion proteins were either eluted using elution buffer (50 mM Tris-HCl, 10 mM reduced glutathione, pH 8.0) and thoroughly dialyzed against binding buffer, or the GST tag was removed by on-column cleavage by incubating the GST fusion protein bound to GS 4B with PreScission Protease (GE Healthcare) overnight at 4°C. After concentrating to about 5 ml using Vivaspin 20 (10-kDa cut off) (GE Healthcare) or Ultra-15 Centrifugal Filter Units (3-kDa cut off) (Millipore), target proteins were further purified by gel filtration chromatography (HiPrep 16/60 Sephacryl S-300 HR, GE Healthcare) on an Akta FPLC system using binding buffer as necessary. To generate UbcM2 for ubiquitination reactions from GST-UbcM2, bacterial lysate was passed over GS 4B followed by cleavage using 5 units of thrombin (Amersham Biosciences) for 4 h. Thrombin was removed using benzamidine-Sepharose 6B (GE Healthcare) followed by passage through a Pierce Spin Cup (Thermo Scientific) to remove residual beads.
For purification of UbcH5B, cell lysis was performed as described above in 50 mM acetic acid-sodium acetate, pH 5.4. Purification from supernatant was performed by cation exchange chromatography (HiTrap SP HP 5 ml, GE Healthcare) using a gradient of 0 -1.0 M NaCl. The peak was subjected to further separation by gel filtration (HiPrep 16/60 Sephacryl S-300 HR, GE Healthcare) using Akta FPLC with binding buffer.
UbcH5B for NMR was transformed, expressed, and lysed as described (22) except that 50 mM acetic acid-sodium acetate, pH 5.4, 4 mM DTT was used for lysis. The supernatant was separated as described (22) by sequential cation exchange and gel filtration chromatography carried out on an S200 column (GE Healthcare) in 50 mM Tris-HCl, pH 7.5, 2 mM tris(2-carboxyethyl)phosphine as described (22). The extent of 15 N incorporation was determined by mass spectroscopy to be Ͼ98%.
Freshly purified samples of WT AO7RE (Fig. 1A) and its mutants, in complex with UbcH5B, were used for crystallization. Samples were otherwise immediately frozen and stored at Ϫ80°C for further functional assays.
Crystallization, Data Collection, and Structure Determination-Crystals of AO7RE⅐UbcH5B were obtained using the hanging drop vapor diffusion method at 19 Ϯ 1°C by mixing 1 l of protein solution and 2 l of reservoir solution (Table 2), and the premixed 3-l droplets were equilibrated against 200 l of reservoir solution. The diamond-shaped crystals grew to full size (ϳ0.1 mm ϫ 0.1 mm ϫ 0.1 mm) in 3 days. Crystals were flash-cooled in cold nitrogen stream after a brief soak in 100% paraffin oil as the cryo-protectant. X-ray diffraction data were collected from a single crystal on a MAR345 image plate detector mounted on a RIGAKU MicroMax TM -007 HF microfocus x-ray generator and processed using the HKL-3000 program suite (43). Crystals of the AO7RE Y165A ⅐UbcH5B and AO7RE P199A ⅐UbcH5B complexes were obtained using a similar protocol, and the data were collected on the same diffractometer system. Crystallization conditions and data collection statistics of the three samples are summarized in Table 2.
The AO7RE⅐UbcH5B structure was determined by molecular replacement using phenix.automr of the PHENIX program suite (44). The crystal structure of WT UbcH5B (PDB entry 2ESK) (6) was used as the search model. The AO7RE structure including zinc ions coordinated by the AO7 RING domain were built into the electron density map, first using phenix.autobuild and then by manual interpretation. The structure was refined with phenix.refine of PHENIX, and the model building and adjustment was done with COOT (45). About 1000 reflections were randomly selected for cross-validation. Ethylene glycol, di(hydroxyethyl) ether, and oxalate molecules from the crystallization solutions and water molecules were included at the last stage of the refinement on the basis of difference electron density (F o Ϫ F c , above 3) and verified with omit maps. The refined structure was validated using the PROCHECK (46) and WHATIF (47) programs. The AO7RE Y165A ⅐UbcH5B and AO7RE P199A ⅐UbcH5B structures were determined with the difference Fourier method using the AO7RE⅐UbcH5B structure as the start model, and the structures were refined with the same strategy as the AO7RE⅐UbcH5B structure. The figures were generated with PyMol (DeLano Scientific LLC). Refinement statistics of the three structures are listed in Table 2. 35 S-Labeled E2 Binding Assay-Binding was carried out using equimolar amounts (ϳ50 picomoles) of each GST fusion protein. In vitro translated [ 35 S]methionine-labeled E2s were generated using the E. coli T7-S30 Extract System (Promega) from pET15b-UbcH5B or pDEST17-Ube2E3. Binding assays using in vitro translated UbcH5B were carried out by incubating purified GST fusion proteins prebound to GS 4B with ϳ10 5 cpm (ϳ180 fmol) of [ 35 S]methionine-labeled E2 in 25 mM Tris-HCl, pH 7.4, 50 mM NaCl, 5 mM DTT, 0.5% Nonidet P-40 overnight at 4°C in 250 l. Beads were washed with the same buffer and resolved by SDS-PAGE under reducing conditions.
In Vitro Ubiquitination-Autoubiquitination assays employed equimolar amounts (ϳ1 M) of purified GST fusion proteins that were prebound to GS 4B in 50 l of ubiquitination assay buffer (50 mM Tris-HCl, pH 7.4, 0.2 mM ATP, 0.5 mM MgCl 2 , 0.1 mM DTT). Approximately 2 M UbcH5B and 50 -100 nM His-tagged purified mouse ubiquitin-activating enzyme (E1) were used in all reactions. Baculovirus encoding His 6 -tagged mouse E1 was a gift from Kazuhiro Iwai. For experiments involving Ub I44A , purified recombinant WT ubiquitin was used in parallel. Purified bovine WT ubiquitin from Sigma (catalog #U6253) was employed in all other experiments. WT ubiquitin was used at 4.0 M in all reactions. Samples were incubated at 37°C for 2 h (unless otherwise indicated) with continuous shaking. Beads were washed and processed as described (22). Autoubiquitination assays using ϳ190 fmol of [ 35 S]methionine-labeled in vitro transcribed and translated forms of AO7 were carried out in solution using UbcH5B and E1 in 25 l of ubiquitination assay buffer. Reactions were quenched with SDS sample buffer and resolved by SDS-PAGE under reducing conditions and assessed by Storm phosphorimaging (GE Healthcare) and quantified using ImageQuant (GE Healthcare).
Single-round Ubiquitin Turnover-Loading of 35 S-labeled UbcH5B in the presence of excess ubiquitin (5 M) using Histagged purified mouse E1 ubiquitin-activating enzyme was carried out as described (22). To assess discharge of ubiquitin from UbcH5B, E1 activity was quenched with apyrase (Sigma) (23). Then [ 35 S]methionine-labeled ubiquitin-loaded UbcH5B (ϳ2 nM) was combined with ubiquitin (80 M) and purified GST fusion proteins (ϳ1 M) in 50 l of 50 mM Tris-HCl, pH 7.4. E2ϳUb was allowed to bind to GST fusions at 4°C for 10 min before raising the temperature to 25°C and beginning turnover reactions. Samples were resolved by SDS-PAGE without reducing agent and processed for visualization and quantification as above. Discharge was monitored by measuring the fraction of UbcH5BϳUb remaining at each time point. Data analysis was carried out with Prism (GraphPad Software). Data shown are the average of three independent experiments; error bars represent S.D.
Cell Experiments-HEK-293 cells were cultured in DMEM containing 10% (v/v) fetal bovine serum, 2 mM glutamine, 100 units/ml penicillin, and 100 g/ml streptomycin in a humidified incubator at 37°C. Cells were transfected as described (48) with a 4:1 ratio of plasmids encoding forms of HA-AO7 and GFP. After 36 -48 h, cells were treated with 80 g/ml cycloheximide, 10 M lactacystin, or 50 M MG132 (all from Sigma) and lysed and processed as described (49).
Microscale Thermophoresis (MST)-UbcH5B-Green was expressed in E. coli BL21 (DE3) and purified with GS 4B. The immobilized protein was incubated on beads with FlAsH-EDT2 for 20 min at room temperature, thoroughly washed in buffer consisting of 50 mM Tris-HCl, pH 7.5, and 100 mM NaCl, and released from beads by cleavage with PreScission Protease. Microscale Thermophoresis was performed with titration of AO7 RING constructs with labeled UbcH5B in Monolith NT.115 (NanoTemper Technologies GmbH). Measurements were repeated at least twice in triplicates. Data were fitted with the equation for mass action by nonlinear least squares to estimate K d . For UbcH5B-Green binding to ubiquitin, the apparent K d was reported, as saturation was not achieved even at the highest concentration of ubiquitin (1 mM).
NMR Spectroscopy-NMR samples were prepared in 50 mM Tris-HCl, pH 7.5, 2 mM tris(2-carboxyethyl)phosphine; exper-iments were performed at 25°C. For titration experiments, 15 N-labeled UbcH5B samples were concentrated up to 0.3 mM, whereas the concentration of AO7 217-258 ranged from 0.15 to 1.5 mM. NMR spectra were acquired on 600-MHz Bruker spectrometers equipped with cryoprobes. Titration experiments were monitored by recording two-dimensional 1 H, 15 N correlated spectra at various ratios of UbcH5B to AO7 217-258. All NMR data were processed using NMRPipe. The assignments and analysis were derived using software SPARKY (50). Titration curves were fitted to 1:1 model by software written in MATLAB (kindly provided by David Fushman) (51).

A Region Beyond the AO7 RING Finger Is Required for E2
Binding-Analogous to mouse AO7 (3), a RING-containing fragment of human AO7 that extends 15 amino acids beyond the last predicted Zn 2ϩ -coordinating Cys (AO7R) (see Fig. 1A for a schematic) was insufficient to bind UbcH5B, as assessed using GST fusion proteins and GS pulldown (Fig. 1B). However, an extension of 57 amino acids beyond the last RING Cys (AO7R extended; AO7RE), terminating at residue 258, was adequate for stable E2 binding. This difference was validated by MST where AO7RE showed an ϳ80-fold greater affinity for UbcH5B relative to AO7R (180 nM versus 14 M; Fig. 1C and Table 1).
AO7 Forms a Clamp-like Structure around UbcH5B-Attempts were first undertaken to crystallize AO7RE alone. The large scale purification of AO7RE or variants, including FIGURE 1. A region beyond the AO7 RING finger is required for high-affinity UbcH5B binding. A, schematic of human AO7 (above). Components of the AO7 clamp are indicated in white (L, Linker). Sequence of AO7RE (below) with Zn 2ϩ -coordinating residues and structural features noted in "Results"; disordered regions are indicated with dashed lines. B, binding of in vitro transcribed and translated 35 S-labeled UbcH5B to N-terminal GST fusions of AO7 prebound to GS. GST fusions were provided in excess relative to UbcH5B, and each was present in equimolar amounts as determined by Coomassie Blue. C, UbcH5B-Green modified with FlAsH was added to increasing amounts of AO7 from which GST had been cleaved. Binding was assessed by MST.

The AO7 Clamp and Insights into Ubiquitination
AO7R, necessary for crystallography or NMR, resulted in nonrefoldable precipitated protein. To circumvent this difficulty, AO7RE and UbcH5B were co-expressed (see "Experimental Procedures"). This AO7RE⅐UbcH5B complex was crystallized and diffracted to 1.8 Å (Table 2). There is one AO7RE⅐UbcH5B complex in the asymmetric unit, which includes two Zn 2ϩ ions ( Fig. 2A).
In comparison to other published structures, UbcH5B in the AO7RE⅐UbcH5B complex features a typical E2 fold (for review, see Ref. 52) and does not change significantly upon binding AO7RE. The root mean square deviations between UbcH5B in the AO7RE⅐UbcH5B complex and several free UbcH5B structures (PDB entries 2ESK, 2ESO, 2ESP, and 2ESQ) are ϳ0.5 Å. The number and property of residues involved in RING binding as well as those surrounding the active site Cys, including the highly conserved Asn-77 (53,54), are similar among all structures.
In the complex, AO7RE is clamp-shaped and surrounds UbcH5B ( Fig. 2A; for linear representation see Fig. 1A). The buried surface between UbcH5B and AO7RE is ϳ2950 Å 2 . The AO7RE fragment contains three structural motifs: a highly atypical N-terminal RING domain (residues 129 -216), a secondary UbcH5B-binding region (residues 228 -255, U5BR), and an extended linker region connecting the RING to the U5BR domain (residues 217-227, Linker) ( Fig. 2A). The RING contains a ␤-hairpin, a central ␣-helix (␣1), and two loops that contribute, as predicted, four of the eight coordinating residues of the C3H2C3 RING to Zn 2ϩ 1 and Zn 2ϩ 2 (3). This core of the RING is followed by a region that is unique to AO7, which contains a second ␣-helix (␣2) that stacks "underneath" the core and interacts extensively through hydrophobic interactions with the structural elements of the core of this RING ( Fig.  2A). This region connects directly to the Linker. The AO7 RING is also unique among canonical RING fingers in that the ␣1 helix has two additional turns at its C-terminal end and a 17-residue disordered Gln-Glu-rich region in loop 2 (residues 178 -194; Fig. 2B, for sequence see Fig. 1A).
Residues equivalent to AO7 Arg-202, which immediately follows the last Zn 2ϩ -coordinating Cys, have been implicated in binding to thioester-linked ubiquitin in RING-type E3⅐E2-Ub structures 7 (8,9,11,15,16) and potentially serve as "allosteric linchpins" in the activation of E2ϳUb by RING-type domains (9). Interestingly, unlike most RING-type E3s in complex with E2s, Arg-202 exhibited static disorder with two conformations in a 0.56/0.44 ratio (Fig. 2C, see also Fig. 6C). The major conformation allows for the conserved hydrogen bonding with UbcH5B Gln-92 or the equivalent in other E2s (e.g. Refs. 39, 56, and 57; for review, see Ref. 1), whereas the minor conformation, which is not generally observed, led to a hydrogen bond with the AO7 Gln-197 side chain and a van der Waal interaction with UbcH5B Ser-94. The AO7RE⅐UbcH5B structure was, of necessity, determined in the absence of thioester-linked ubiquitin because of the need for co-expression.
The AO7RE Linker covers the outer surface of the UbcH5B ␣1 helix (Fig. 2D). On one side of the Linker, Met-222, Leu-224, and Tyr-225 of AO7 contact Leu-3, His-7, and Leu-10 of UbcH5B, respectively, and on the other side, salt bridges and hydrogen bonds are formed between the proteins. . UbcH5B is shown in cyan. AO7RE is shown in yellow except for the Linker, in red. Helices, strands, and loops are illustrated as spirals, arrows, and tubes, respectively. The N and C termini and secondary structure elements are labeled in black and red for UbcH5B and AO7, respectively. The disordered peptide (residues 178 -194 after the ␣1 helix) of AO7RE is represented with a dashed curve. Two zinc ions in AO7 RING are illustrated. B, superposition of AO7 RING with other RING and U-box structures (PDB entries 3FL2, 1Z6U, 1FBV, 3HCT, 1LDJ, 2CKL, 2C2V, 3EB6, and 3LRQ). The AO7 RING is shown in yellow, the central ␣-helix of AO7 RING is labeled, and the disordered peptide in loop 2 of the AO7 RING is indicated with a dashed curve. C-E, the interactions of UbcH5B with AO7 RING (C), Linker (D), and U5BR (E, viewed from two directions). UbcH5B is shown in cyan, RING and U5BR are in yellow, and Linker is in red. The residues involved in electrostatic (cutoff distance ϭ 3.5 Å) and van der Waals (cutoff distance ϭ 4.0 Å) interactions at the interface are shown as sticks. Dashed lines in black indicate salt bridges and hydrogen bonds. The residues involved in the interactions are labeled in black and red for UbcH5B and AO7, respectively.
The U5BR of AO7RE contains a long ␣-helix (␣3) and a short C-terminal loop that interacts extensively with the backside of UbcH5B (Fig. 2E). From the middle of the ␣3 helix to the C terminus of AO7RE, several hydrophobic side chains (Leu-241, Tyr-242, Ile-251, Ile-252, and Leu-254) interact with UbcH5B. AO7 Tyr-242 forms an edge-to-face interaction with UbcH5B Phe-51, whereas the AO7 Ile-252 side chain penetrates deeply into a hydrophobic pocket formed by side chains from the UbcH5B ␣4␣2 loop (Fig. 2E). A number of hydrogen bonds and salt bridges surround the hydrophobic interface. The guanidinium groups of AO7 Arg-244 and Arg-248 each form a salt bridge with the C-terminal (Met-147) carboxyl group of UbcH5B. In addition, the AO7 Arg-238 and Gln-245 side chains form hydrogen bonds with side chains from the UbcH5B ␤-sheet, whereas the main chain groups of AO7 Gly-249, Gly-250, and Ile-252 are hydrogen-bonded to several UbcH5B side chains (Fig. 2E). The U5BR is hook-shaped in general, anchoring on the backside of UbcH5B on the opposite side of the E2 from the site of covalent binding of UbcH5B to Ub and from the closed conformation of UbcH5BϳUb (for review, see Ref. 1). By NMR, the U5BR together with the Linker exhibited a dissociation constant (K d ) of 173 Ϯ 40 M for UbcH5B (Fig. 3D). Assessment of binding of this region by NMR using 15 N-labeled UbcH5B demonstrated that, in solution, as in the crystal structure, most contacts with UbcH5B distal to the RING finger are in the U5BR (Fig. 3E). Notably, the site of U5BR binding to UbcH5B overlaps the site of non-covalent Ub B binding to the UbcH5 family of E2s (K d Ͼ 200 M; Table 1) (17,20).
Requirements for AO7-UbcH5B Binding and Ubiquitination-To begin to assess the significance of the U5BR, we carried out a structure-based mutational analysis. Mutation of two U5BR residues that contact the ␤-sheet core of UbcH5B (Fig. 2E), Y242A and Q245A (AO7RE YQ-AA ), significantly diminished binding (Fig. 4A). Deletions within the U5BR of either amino acids 238 -245, referred to hereafter as AO7RE⌬, or amino acids 246 -252 resulted in loss of high-affinity UbcH5B binding, as did deletion of amino acids 217-222 of the Linker (Fig. 4A). . The secondary structure assignments of the residues are illustrated. Residues in red were mutated to Ala, and co-crystallization was undertaken or attempted as described in the "Results" section. D, trajectories of two 15 N-labeled UbcH5B residues that shift upon titration with AO7 fragment 217-258 (Linker and U5BR) used to calculate K d . E, chemical shift perturbations in the UbcH5B upon interaction with the AO7 fragment (residues 217-258). Unlabeled AO7 was titrated onto 15 N-labeled UbcH5B. Upon titration of 15 N-labeled UbcH5B, residues on the UbcH5B backside ␤-sheet are perturbed significantly in areas corresponding to U5BR binding. In contrast, the Linker does not perturb the UbcH5B significantly. The perturbation (⌬␦) is defined as the difference in peak frequencies of the free and AO7-saturated states. ⌬␦ is calculated by the formula ⌬␦ ϭ [(␦N f Ϫ ␦N s ) 2 /5 ϩ (␦H f Ϫ ␦H s ) 2 ] 1/2 , where ␦H f, ␦H s and ␦N f, ␦N s are the proton and nitrogen frequencies in free and saturated state, respectively. UbcH5B residues contacting AO7 in the crystal structure are shown as circles on the data. Black circles represent UbcH5B contacts with the AO7 U5BR in the crystal structure, whereas gray-filled circles represent UbcH5B contacts with the AO7 Linker. DECEMBER 18, 2015 • VOLUME 290 • NUMBER 51

JOURNAL OF BIOLOGICAL CHEMISTRY 30231
A GST fusion of AO7RE was next compared with AO7R and AO7RE⌬, both of which lack an intact U5BR, in autoubiquitination assays with UbcH5B (Fig. 4B). In these assays, except for free ubiquitin, essentially all of the ubiquitin immunoreactivity is found on the AO7 fusion proteins (data not shown). Compared with AO7RE, both AO7R and AO7RE⌬ exhibited a substantial increase in ubiquitination, including a marked increase in higher molecular weight forms (Fig. 4B). This suggests increased activity with loss of the U5BR. As results with AO7RE⌬ and AO7R were indistinguishable, most experiments that follow were carried out comparing AO7RE to AO7RE⌬.
Immunoblotting for ubiquitin was corroborated by directly assessing ubiquitination of 35 S-labeled AO7 (Fig. 4, C and D). A higher proportion of AO7RE⌬ molecules was modified at each time accompanied by a greater upward shift in migration compared with AO7RE, even after extended incubation. Singleround discharge experiments where UbcH5BϳUb was first preincubated with an ϳ500-fold excess of AO7RE or AO7RE⌬ confirmed that AO7RE⌬, which lacks an intact U5BR, had greater activity than AO7RE (Fig. 4, E and F). These demonstrate that the differences observed in autoubiquitination assays are due to activity and are not accounted for by differences in the rate of exchange of UbcH5B for UbcH5BϳUb (58,59). Thus, loss of the U5BR enhances AO7 activity despite its decreased affinity for UbcH5B.
AO7RE⌬ Reveals a Role for Ubiquitin Backside Binding-One explanation for the unexpected increase in reactivity with disruption of the U5BR could lie in the increased accessibility of Ub B to UbcH5B when the U5BR is not intact. To address this we employed an UbcH5B mutant that cannot bind Ub B (UbcH5B S22R ) (17). This mutant does not significantly alter UbcH5B binding to AO7RE (Fig. 5A) and has relatively minor effects on AO7RE autoubiquitination (Fig. 5B, compare lanes 1,  7, and 13 to lanes 2, 8, and 14). In sharp contrast, when either AO7RE⌬ or AO7R was evaluated with UbcH5B S22R , there was a dramatic decrease in ubiquitination, with low molecular weight ubiquitin-modified forms of the E3 only detectable at later time points (Fig. 5B).
To understand the mechanistic basis for this difference, we once again carried out single round turnover experiments (Fig.  5C). In the presence of AO7RE, the rate of ubiquitin transfer from UbcH5B S22R was comparable with WT UbcH5B. In contrast, using AO7RE⌬, ubiquitin transfer from UbcH5B S22R was dramatically diminished relative to the rate from WT UbcH5B. This strongly supports the idea that Ub B binding plays a critical role in ubiquitination mediated by AO7RE⌬ but not by AO7RE, where this binding is blocked by the high-affinity interaction with the U5BR.
To complement our findings with S22R, we wished to assess the impact of mutating Ile-44 of ubiquitin (Ub I44A ). Ile-44 is central to, and essential for, the interaction of Ub B with the backside of UbcH5B (17). Unfortunately, mutating Ile-44 disrupts E2 function, as exemplified in studies using the E2, Cdc34, for which Ub B binding is not implicated in function (12). This disruption is due, at least in part, to loss of a critical interaction of the E2 with ubiquitin covalently bound to its active site (E2ϳUb) (8,9,11). However, in Cdc34, a complementary muta-tion restores function (12). Similarly, for AO7RE, where Ub B binding to UbcH5B was blocked by the U5BR, Ub I44A resulted in a loss of function, but a mutation of UbcH5B analogous to that made in Cdc34 (UbcH5B S108L ) resulted in a significant restoration of activity (Fig. 5D, lanes 1-4). The restoration of function with UbcH5B S108L allowed us to assess the role of disrupting Ub B binding using Ub I44A and AO7RE⌬. Unlike the significant restoration of activity seen with AO7RE, this combination failed to restore function with AO7RE⌬ (Fig. 5D, lanes  5-8). Together with the results obtained with UbcH5B S22R , these findings demonstrated the stimulatory role of Ub B bind-  Fig. 4B. C, loss of E2ϳUb was assessed as in Fig. 4E. Data are from three independent experiments. D, ubiquitination was carried out as in Fig. 4B. E, binding assay was carried out as in Fig. 1B. IB, immunoblot. F, ubiquitination assay was carried out as in Fig. 4B for 90 min using UbcM2 as the E2. G, purified, bacterially expressed WT or S22R UbcH5B was loaded with equimolar amounts of ubiquitin lacking Lys (UbK0), and the release of UbK0 was assessed during incubation in the presence or absence of added UbK0 (160 M) and with AO7RE⌬ from which GST had been cleaved. UbcH5B was detected by immunoblotting. Note the ratio of E2ϳUb to E2 over the time course. Efficiency of loading is less than in experiments using 35 S-labeled E2 and WT ubiquitin (e.g. Fig. 4F), as the amount of UbK0 used was kept low during loading to maximize the effect of UbK0 added during the discharge phase. DECEMBER 18, 2015 • VOLUME 290 • NUMBER 51 ing to UbcH5B when the U5BR is disrupted. An additional important finding that arises from these experiments is that, when Ub B binding is precluded, an intact U5BR is required for significant ubiquitination (Fig. 5, B-D).

The AO7 Clamp and Insights into Ubiquitination
To further evaluate the positive role of the U5BR when Ub B binding is lost or diminished, we turned to another E2, UbcM2/ Ube2e3/UbcH9, which tightly binds AO7 (3,60). This binding is also U5BR-dependent (Fig. 5E). In contrast to UbcH5, UbcM2 shows very little Ub B binding and exhibits markedly decreased activity with AO7 relative to UbcH5B (60). When ubiquitination was assessed, activity was seen with AO7RE ( Fig.  5F). However, ubiquitination was essentially undetectable with UbcM2 when the U5BR was interrupted (AO7RE⌬, AO7R), reinforcing the importance of the U5BR in facilitating ubiquitination in the absence of significant Ub B binding.
The stimulatory effect of Ub B binding was originally postulated to be due to this ubiquitin itself being linked to an E2 (E2ϳUb B ), resulting in concatemerization of E2ϳUb molecules through backside binding. This would then facilitate chain formation, with backside-bound ubiquitin serving as the acceptor ubiquitin (17,18). To evaluate whether this is indeed a requirement, a purified protein system was used to assess ubiquitin transfer from E2, with AO7RE⌬ as the E3. UbcH5B was loaded in the presence of an equimolar amount of UbK0, which does not function as an ubiquitin acceptor, and then allowed to discharge in the presence of excess free Lys 8 (400 M) (61, 62). When UbK0 was added during the discharge assay at a significantly higher concentration than at the loading step (160 versus 5 M), the rate of discharge increased with WT UbcH5B (Fig.  5G, top two panels, compare the relative amounts of E2 and E2ϳUbK0 as a function of time). In contrast, excess UbK0 had no effect on discharge when ubiquitin backside binding was disrupted by the S22R mutation (Fig. 5G, bottom two panels). This suggests that, although Ub B binding is critical for ubiquitin transfer by UbcH5B, Ub B does not necessarily serve as an acceptor. This is consistent with recent results using the RING E3 RNF38 (20).
Ubiquitin Backside Binding Can Be Functionally Important in Cells-In cells some E3s undergo autoubiquitination, often resulting in ubiquitin chains that target them for proteasomal degradation (for review, see Ref. 4). If this is true for AO7 and Ub B binding is important in cells, which has not been previously assessed, then disruption of the U5BR should destabilize AO7 by enhancing autoubiquitination. Indeed, HA-AO7 (amino acids 2-439) lacking U5BR amino acids 238 -245 (HA-AO7⌬), is short-lived relative to a version containing an intact U5BR (HA-AO7; Fig. 6A) and is stabilized by inhibitors of the proteasome (Fig. 6, B and C). Importantly, degradation of HA-AO7⌬ is markedly diminished when its own ligase activity is compromised by mutation of a conserved residue in the RING-E2 interface (Y165〈; Fig. 6D, see also below), demonstrating that the accelerated loss of HA-AO7⌬ is not due to misfolding. These findings are highly suggestive of the cellular relevance of noncovalent Ub B binding.

Structures of AO7 RING Finger Mutations in Complex with
UbcH5B-For other RING-type E3s, specific E3s residues at the canonical interface with E2 have been shown to affect the ability of RINGs to bind to E2 or activate E2ϳUb (Refs. 8, 9, 16, 36 -39, 63, and 64; for review, see Ref. 1). However, parsing the effects of these mutations on low-affinity RING-E2 binding versus ligase function is difficult. Included among conserved interface residues shown to be important are bulky hydrophobic residues in loop 1 between the first two Zn 2ϩ -coordinating cysteines (usually an Ile) (36) and at the beginning of the central ␣-helix (37,38) as well as a highly-conserved Pro in loop 2 (39), also between the Zn 2ϩ -coordinating residues (for review, see Ref. 1). Importantly, the effects of these mutations on the RING-E2 interface have not been assessed at a detailed structural level. We took advantage of the AO7 clamp and its high affinity for UbcH5B to evaluate mutations in each of these positions by 8 The excess Lys added as an acceptor did not substantively accelerate the rate of discharge in the presence of AO7RE⌬. co-crystallization (Zn 2ϩ 1 loop, I137A; central ␣-helix, Y165A; Zn 2ϩ 2 loop, P199A). AO7RE Y165A ⅐UbcH5B and AO7RE P199A ⅐ UbcH5B were successfully crystallized, but crystals for AO7RE I137A ⅐UbcH5B were not obtained. Neither the Y165A nor the P199A mutation caused significant overall conformational changes in the proteins (Fig. 7A). The root mean square deviation values for the three structures are ϳ0.5 Å. All three mutated AO7 RING residues are located at the hydrophobic interface between AO7 and UbcH5B ( Fig. 2A). The Ile-137 side chain faces the hydrophobic pocket surrounded by Pro-61, Phe-62, and Pro-95 of UbcH5B, contributing most to the hydrophobic interactions between AO7 RING and UbcH5B, providing a possible explanation for the inability to obtain a crystal structure of this mutant with E2. Although the Y165A and P199A mutations of AO7 do not bring significant changes to the overall structure of the AO7RE-UbcH5B complex, they each cause localized changes to the hydrophobic environment at the RING-UbcH5B interface. In AO7RE Y165A ⅐UbcH5B, the mutation induced the rearrangement of three side chains on the E2 binding surface of the RING central ␣-helix and invasion of several water molecules (Fig.  7B). Consequently, the landscape of the E2 binding surface of the RING is reshaped in the localized area of the mutation, and the hydrophobicity in the center of the RING-UbcH5B interface is changed. This leads to an alteration of several interactions, including the formation of two new RING interactions with Lys-63 of UbcH5B (Fig. 3B, compare with Fig. 3A). In AO7RE P199A ⅐UbcH5B, there is no notable conformational change in other interface residues, but the mutation brings a water molecule (W1) into the hydrophobic core of AO7RE ( Fig.  7C and Fig. 3C compare with Fig. 3A). We observed no significant alterations in E2 residues in the ␣2 helix and the 3 10 (1) helix with the Y165A and P199A mutations. These are regions that recent RING-type E3⅐UbcH5-Ub structures have implicated as being involved in RING-dependent ubiquitin binding and in formation of the activated closed conformation of E2ϳUb (for review, see Ref. 1). Additionally, AO7 Arg-202 remained disordered (Fig. 7C). The critical Asp-87 of UbcH5B was similarly disordered as it is in the WT complex. Asn-77 (53, 54) also did not change with mutations in the RING-E2 interface.
Consequence of RING Finger Mutations-The crystallographic analyses demonstrate that structural changes seen with AO7RE Y165A and AO7RE P199A , as compared with WT AO7RE, are largely limited to local changes in the AO7RE-UbcH5B binding landscape, without substantial decreases in interactions at the RING-E2 interface. This is surprising considering their consequences for other RINGs. Consistent with limited alteration of interactions, binding of UbcH5B as assessed by GS pulldown showed no difference between AO7RE WT, Y165A, and P199A after extensive washing, whereas I137A demonstrated diminished binding (Fig. 8A). The affinity of Tyr-165 and Pro-199 mutants of AO7RE for UbcH5B were found to be greater than (Y165A) or similar to (P199A) that of AO7RE, whereas the affinity of I137A was marginally less than AO7RE (Ͻ1.5-fold) ( Table 1 and Fig. 8B).
In contrast, autoubiquitination with the Y165A and P199A mutants was markedly reduced compared with AO7RE (Fig.  8C). The I137A mutation (36) dramatically decreased ubiquitination. Similarly, mutation of Arg-202, whose equivalent in other RING type E3s has been shown, using E2-Ub, to be essential to maintain the closed conformation necessary for ubiquitin transfer (8,9,11,15,16), severely inhibits ubiquitination. The functional effects of the I137A, Y165A, and P199A RING mutations were confirmed in single turnover experiments (Fig.  8D). All of these mutations reduce the rate of ubiquitin transfer. In the context of the AO7 clamp, this cannot be explained by a FIGURE 7. Structures of UbcH5B in complex with AO7RE mutants. A, superimposition of the AO7RE⅐UbcH5B (in cyan), AO7RE Y165A ⅐UbcH5B (in magenta), and AO7RE P199A ⅐UbcH5B (in orange) complexes. B, the Y165A mutation resulted in a change in the AO7 Met-169 side-chain orientation inasmuch as the Met-169 side chain partially occupies the space created by the Y165A mutation, causing the AO7 Glu-172 side chain to bend toward the Met-169 side chain such that Glu-172 forms a new salt bridge with Lys-63 in the ␤3␤4 loop of UbcH5B. The His-168 side chain, which is disordered in the WT, is stabilized in the mutant. Such conformational changes reshape the local E2-binding surface of the RING. Furthermore, several water molecules (W1, W2, and W3) invade into the cavity created by the Y165A mutation. The mutant and WT structures are shown in magenta and cyan, respectively. Residues at the RING-E2 interface are shown as sticks. The water molecules are shown as spheres. C, the P199A mutation brings a water molecule (W1) into the hydrophobic core of AO7 RING, which is hydrogen-bonded to the main chain amide of the Ala-199 residue. This does not disturb the conformation of nearby side chains. The residues on the interface or surrounding the hydrophobic core and the water molecule are illustrated. The mutant and WT structures are shown in orange and cyan, respectively. DECEMBER 18, 2015 • VOLUME 290 • NUMBER 51 simple effect on affinity for E2. This is particularly the case for Y165A and P199A, where the RING-E2 interface is largely unaltered and there are no substantial changes in E2 residues identified as being important for binding ubiquitin (8,9,11,15,16,20). Accordingly, both Tyr-165 and Pro-199 play substantial roles in AO7 function without having significant effects on the E2-RING interface.

Discussion
Backside Binding to E2s-A central issue in RING-type E3 function is to understand how ubiquitination efficiently occurs despite generally low-affinity interactions between these E3s and E2s. As this study and others clearly demonstrate, noncovalent binding of ubiquitin to the backside of a subset of E2s (Ub B ) is one means by which ubiquitination is stimulated. This binding occurs between the Ile-44 "hydrophobic patch" on ubiquitin and a specific region on the backside of these E2s (17)(18)(19)(20). The U5BR, which is a primarily helical, secondary E2 binding domain that forms the upper part of the AO7 clamp, traverses the Ub B binding site on UbcH5B and precludes Ub B binding (Fig. 9A).
Several other RING-type E3s also contain secondary E2 binding domains, most of which are characterized by a prominent ␣-helix that crosses the Ub B binding site, although some contain additional N-or C-terminal features that enhance interactions with E2. For the mammalian endoplasmic reticulum-associated degradation (ERAD) E3 gp78 and the yeast CUE1 protein, which functions with the ERAD E3s HRD1 and DOA10, these E2 binding helices cross the Ub B binding site at a markedly different orientation then that of the U5BR when aligned based on the conserved E2 fold (Fig. 9B) (16,(21)(22)(23). Unlike the U5BR, these regions all allosterically stimulate ubiquitination with ERAD E2s (16,22,23). Single helices that cross the Ub B binding site are also found in the RING-type E3s Rad18 and Bre1, which function with the E2 Rad6. These exhibit yet a different orientation (Fig. 9B) and limit ubiquitination by blocking Ub B binding, favoring monoubiquitination (18,19). More complex E2 backside binding is provided by the binding of the "winged-helix B" domain of the cullin-like subunit of the anaphase promoting complex/cyclosome to UbcH10. In this case the first of two involved helices exhibits an orientation that resembles a severely truncated U5BR (24).
In all cases, these secondary E2 binding domains are either separated from the RING by Ͼ100 amino acids or are on distinct polypeptides (16,18,19,(21)(22)(23)(24). The AO7 U5BR represents the first known example of an E2 backside binding region that is contiguous with a RING-type domain, the two being separated only by the short Linker necessary to traverse the N-terminal ␣-helix of UbcH5B. These contiguous domains result in a clamp-like structure that binds to UbcH5B with high affinity. Despite the tight binding conferred by the AO7 clamp, the rate of transfer of ubiquitin from E2ϳUb is slower when the clamp is intact. This is due to blocking of Ub B binding by the U5BR region of AO7. However, in the absence of the potential for Ub B binding (e.g. when an E2 with limited Ub B binding is used or potentially when the local concentration of ubiquitin is limited), the high-affinity binding of the intact clamp increases activity relative to a disrupted clamp. Thus, the AO7 clamp uniquely has context-dependent effects that either decrease or increase catalysis of E2ϳUb.
The question arises as to why there is a more substantial stimulation of catalysis by Ub B binding and a disrupted AO7 clamp (AO7R or AO7RE⌬) compared with the high-affinity intact clamp, where Ub B binding is blocked (see Figs. 4E and 5C). A definitive answer cannot be discerned from the structures presented herein. There are hints that arise from recent elegant work of Buetow et al. (20), where the authors provide evidence that Ub B increases the affinity of UbcH5B-Ub for the RNF38 RING. This is marginally greater (ϳ2-fold) than the affinity between AO7RE and UbcH5B. Importantly, they also find alterations in the structure of the ␣1 helix and the ␣1␤1 loop of UbcH5B in the context of RING⅐UbcH5B-Ub and, with Ub B binding, changes in dynamics of this region are noted. This promotes conformations of UbcH5BϳUb that facilitate catalysis (20). A possibility, therefore, is that combinatorial differences in these factors (affinity, structure, and dynamics) account for the differential effect of Ub B relative to the U5BR.  Fig. 1B. B, data were from MST as in Fig. 1C, including the same data set for WT AO7RE. See Table 1 for calculated the K d values. C, equal amounts of the indicated AO7RE mutations were purified in complex with UbcH5B by washing co-expressed complexes only once, and ubiquitination was assessed after the addition of an equal amount of purified UbcH5B. Twice as much E2 was added in the GST control reaction. A Coomassie stain of the purified complexes is shown below. D, single round turnover experiments were carried out as in Fig. 4E. Data are graphed as the fraction of E2ϳUb remaining at each time point and are the average of three independent experiments.
Interestingly, the three AO7RE⅐UbcH5B structures in this study also exhibit conformational changes in UbcH5B in the ␣1 helix and the ␣1␤1 loop (compared with free UbcH5B, PDB entries 2ESK, 2ESP, 2ESO, and 2ESQ). However, these changes are not identical with, or directly comparable with those observed by Buetow et al. (20); regardless, they are all within the conformational space of this region. Definitively assessing the effects of the AO7 clamp versus Ub B on E2ϳUb structure and dynamics will require additional extensive structural and biochemical studies.
It now becomes important to understand whether Ub B binding is relevant in vivo. The fact that binding of UbcH5B-Ub to RING increases the affinity of Ub B from 200 to 14 M in the case of RNF38 (20) makes cellular levels of ubiquitin (20 -80 M; Refs. 65 and 66) sufficient to have an effect. Our cellular data showing proteasomal degradation of AO7 when the clamp is disrupted and the site of Ub B binding is accessible provide in vivo data consistent with its importance. Whether this apparent in vivo Ub B binding effect is due to the free ubiquitin pool, polyubiquitin chains, ubiquitin already attached to substrates, E2ϳUb, or a combination thereof, and whether ubiquitin-like domains also contribute are interesting questions that remain to be addressed.
Complexity of the E2-RING Interface-The significance of specific conserved RING residues at the E2 interface is gener-ally poorly understood. Taking advantage of the AO7 clamp we have, for the first time, explored the importance of mutations of critical residues in the central ␣1 helix and the second Zn 2ϩcoordinating loop (Y165A and P199A, respectively) at a structural level. Interestingly, we find that, for both mutants, there is (i) no significant decrease in RING affinity for UbcH5B, (ii) only minimal changes in the RING-E2 interface, and (iii) compared with AO7RE, no difference in the positions of residues implicated in the allosteric RING-mediated activation of E2ϳUb (Refs. 6, 8, 9, 11, 14 -16, and 20; for review, see Ref. 1). Despite this, mutation of either Tyr-165 or Pro-199 resulted in a marked decrease in activity with UbcH5B. How this occurs is not clear, but there are at least two possibilities. First, although neither of these residues is predicted to have direct interactions with ubiquitin covalently linked to E2 (E2ϳUb), it is possible that through local changes they indirectly affect its positioning. However, there is no evidence to support this based on other structural studies in which the positioning of ubiquitin in E2-Ub was examined (Refs. 8, 9, 11, 14 -16, and 20; for review, see Ref. 1). A second, attractive, possibility is that one or both of these residues are involved in transmitting allosteric changes from the RING to the active site of UbcH5B and thereby affect ubiquitin transfer. Understanding this will require analysis of the effect of these mutations on structure and dynamics using E2-Ub with either AO7 or other RING E3s. Regardless, our data