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Resolution: standard / high Figure 2.
Conformational rearrangements in E1 enzymes. Cartoon representations
of distinct states in the catalytic cycle of canonical E1 enzymes.
(a) The adenylation state based on the crystal structure of
NAE1-UBA3 in complex with NEDD8 and ATP/Mg2+ [PDB: 1R4N] [32]. The carboxy-terminal tail of the Ubl is in the adenylation site
of the active Rossmann-type subunit of the E1, ready to nucleophilically
attack the α-phosphate of the ATP to form the Ubl-AMP intermediate. The
catalytic cysteine residue in the E1 cysteine domain is part of an
α-helix and is removed from the adenylation site, giving rise to an
open conformation of the cysteine domain. (b) The thioesterification
state as seen in a crystal structure of SAE1-UBA2 and SUMO covalently
coupled to an AMP analogue that mimics the tetrahedral intermediate
generated during thioesterification [PDB: 3KYD] [8]. Mediated by large conformational changes in the crossover and
re-entry loops, the cysteine domain is rotated with respect to the
Rossmann-type subunits. The helix containing the active site cysteine seen
in (a) has melted. In this closed conformation of the cysteine domain, the
catalytic cysteine nucleophile is in position to attack the adenylated
carboxyl terminus of the Ubl. The positive dipole of helix H2 in the active
Rossmann-type subunit (colored purple) is thought to favor this reaction [8]. (c) The trans-thioesterification state as represented by
a crystal structure of NAE1-UBA3 thioester-linked to NEDD8 and in complex
with an additional NEDD8 molecule, an E2 enzyme (Ubc12) and
ATP/Mg2+[35]. The cysteine domain of the E1 adopts an open orientation similar
to the adenylation state (a), but now holds the carboxyl terminus of the
thioester-linked Ubl close to the E2 active site (a Cys-to-Ala mutant of the
E2 was used in this study (see text)). The ubiquitin-fold domain has swung
away from its position in the previous states (a,b) to accommodate the E2
and contributes to E2 binding. In (a,c) domains found in NAE1-UBA3 but not
in SAE1-UBA2 were omitted for clarity. To see a rendition of a dynamic
transition between the structures shown in the lower panels of (a-c), see
Additional file 1. As noted in the movie legend,
the details of the trajectory linking individual structures is not realistic
and is simply meant to illustrate the nature of the conformational changes
rather than identify the nature of the transition pathway.
Lorenz et al. BMC Biology 2013 11:65 doi:10.1186/1741-7007-11-65 |