|
86
|
266
|
2fm6A |
Zinc-beta-lactamase l1 from stenotrophomonas maltophilia (native form) |
|
86
|
266
|
2fu8A |
Zinc-beta-lactamase l1 from stenotrophomonas maltophilia (d-captopril complex) |
|
125
|
358
|
2ffyA |
Ampc beta-lactamase n289a mutant in complex with a boronic acid deacylation transition state analog compound sm3 |
|
88
|
266
|
2fu7A |
Zinc-beta-lactamase l1 from stenotrophomonas maltophilia (cu-substituted form) |
|
73
|
245
|
2fhxB |
Pseudomonas aeruginosa spm-1 metallo-beta-lactamase |
|
85
|
266
|
2fu6A |
Zinc-beta-lactamase l1 from stenotrophomonas maltophilia (apo form) |
|
75
|
245
|
2fhxA |
Pseudomonas aeruginosa spm-1 metallo-beta-lactamase |
|
65
|
216
|
2dooA |
The structure of imp-1 complexed with the detecting reagent (dansylc4sh) by a fluorescent probe |
|
90
|
262
|
2cc1A |
Crystal structure of the class a beta-lactamase from mycobacterium fortuitum |
|
69
|
221
|
2bgaA |
Bacillus cereus metallo-beta-lactamase (bcii) arg (121) cys mutant. solved at ph7 using 20 micromolar znso4 in the buffer. 1mm dtt was used as a reducing agent. cys221 is oxidized. |
|
92
|
263
|
2b5rA |
1b lactamase / b lactamase inhibitor |
|
73
|
228
|
2bmiA |
Metallo-beta-lactamase |
|
71
|
221
|
2bg2A |
Bacillus cereus metallo-beta-lactamase (bcii) arg (121) cys mutant. solved at ph4.5 using 20mm znso4 in the buffer. 1mm dtt and 1mm tcep- hcl were used as reducing agents. cys221 is reduced. |
|
71
|
221
|
2bc2A |
Metallo beta-lactamase ii from bacillus cereus 569/h/9 at ph 6.0, trigonal crystal form |
|
67
|
221
|
2bfzA |
Bacillus cereus metallo-beta-lactamase (bcii) arg (121) cys mutant. solved at ph4.5 using 20mm znso4 in buffer. 1mm dtt was used as a reducing agent. cys221 is oxidized. |
|
70
|
221
|
2bg7A |
Bacillus cereus metallo-beta-lactamase (bcii) arg (121) cys mutant. solved at ph4.5 using 20 micromolar znso4 in the buffer. 1mm dtt was used as a reducing agent. cys221 is oxidized. |
|
73
|
222
|
2bfzB |
Bacillus cereus metallo-beta-lactamase (bcii) arg (121) cys mutant. solved at ph4.5 using 20mm znso4 in buffer. 1mm dtt was used as a reducing agent. cys221 is oxidized. |
|
73
|
221
|
2bflA |
Bacillus cereus metallo-beta-lactamase (bcii) arg (121) cys mutant. solved at ph5 using 20mm znso4 in buffer. 1mm dtt was used as a reducing agent. |
|
69
|
221
|
2bg6A |
Bacillus cereus metallo-beta-lactamase (bcii) arg (121) cys mutant. solved at ph5 using 20 micromolar znso4 in the buffer. 1mm dtt was used as a reducing agent. cys221 is oxidized. |
|
76
|
222
|
2bg8B |
Bacillus cereus metallo-beta-lactamase (bcii) arg (121) cys mutant. solved at ph4.5 using 20 micromolar znso4 in the buffer. 1mm dtt and 1mm tcep-hcl were used as reducing agents. |
|
68
|
221
|
2bg8A |
Bacillus cereus metallo-beta-lactamase (bcii) arg (121) cys mutant. solved at ph4.5 using 20 micromolar znso4 in the buffer. 1mm dtt and 1mm tcep-hcl were used as reducing agents. |
|
114
|
357
|
2blsA |
Ampc beta-lactamase from escherichia coli |
|
73
|
221
|
2bfkA |
Bacillus cereus metallo-beta-lactamase (bcii) arg (121) cys mutant. solved at ph7 using 20mm znso4 in buffer. 1mm dtt was used as a reducing agent |
|
85
|
266
|
2aioA |
Metallo beta lactamase l1 from stenotrophomonas maltophilia complexed with hydrolyzed moxalactam |
|
111
|
353
|
1zkjA |
Structural basis for the extended substrate spectrum of cmy-10, a plasmid-encoded class c beta-lactamase |
|
96
|
265
|
2a3uA |
Crystal structure of sulbactam bound to e166a variant of shv-1 beta-lactamase |
|
111
|
358
|
1zc2A |
Crystal structure of plasmid-encoded class c beta-lactamase cmy-2 complexed with citrate molecule |
|
93
|
263
|
1zg4A |
Tem1 beta lactamase |
|
97
|
263
|
1zg6A |
Tem1 beta lactamase mutant s70g |
|
72
|
230
|
1znbA |
Metallo-beta-lactamase |
|
97
|
265
|
2a49A |
Crystal structure of clavulanic acid bound to e166a variant of shv-1 beta-lactamase |
|
112
|
354
|
1z6fA |
Crystal structure of penicillin-binding protein 5 from e. coli in complex with a boronic acid inhibitor |
|
99
|
263
|
1ylpA |
Atomic resolution structure of ctx-m-27 beta-lactamase |
|
97
|
263
|
1ym1A |
X-ray crystallographic structure of ctx-m-9 beta-lactamase complexed with a boronic acid inhibitor (sm2) |
|
95
|
263
|
1ylwA |
X-ray structure of ctx-m-16 beta-lactamase |
|
111
|
359
|
1xx2A |
Refinement of p99 beta-lactamase from enterobacter cloacae |
|
93
|
262
|
1ymxA |
X-ray crystallographic structure of ctx-m-9 beta-lactamase covalently linked to cefoxitin |
|
101
|
263
|
1yljA |
Atomic resolution structure of ctx-m-9 beta-lactamase |
|
97
|
263
|
1yt4A |
Crystal structure of tem-76 beta-lactamase at 1.4 angstrom resolution |
|
97
|
263
|
1ymsA |
X-ray crystallographic structure of ctx-m-9 beta-lactamase complexed with nafcinin-like boronic acid inhibitor |
|
109
|
359
|
1y54A |
Crystal structure of the native class c beta-lactamase from enterobacter cloacae 908r complexed with brl42715 |
|
97
|
263
|
1yltA |
Atomic resolution structure of ctx-m-14 beta-lactamase |
|
96
|
263
|
1ylyA |
X-ray crystallographic structure of ctx-m-9 beta-lactamase complexed with ceftazidime-like boronic acid |
|
98
|
263
|
1ylzA |
X-ray crystallographic structure of ctx-m-14 beta-lactamase complexed with ceftazidime-like boronic acid |
|
90
|
263
|
1xxmA |
The modular architecture of protein-protein binding site |
|
112
|
358
|
1xgiA |
Ampc beta-lactamase in complex with 3-(3-nitro-phenylsulfamoyl)-thiophene-2-carboxylic acid |
|
95
|
263
|
1xpbA |
Structure of beta-lactamase tem1 |
|
112
|
358
|
1xgjA |
Ampc beta-lactamase in complex with 3-(4-carboxy-2-hydroxy-phenylsulfamoyl)-thiophene-2-carboxylic acid |
|
61
|
219
|
1wuoA |
Crystal structure of metallo-beta-lactamase imp-1 mutant (d81a) |
|
82
|
224
|
1x8gA |
Crystal structure of the mono-zinc carbapenemase cpha from aeromonas hydrophyla |
