63
|
220
|
3kl7A |
Crystal structure of putative metal-dependent hydrolase (yp_001302908.1) from parabacteroides distasonis atcc 8503 at 2.30 a resolution |
70
|
214
|
3knsA |
Bacillus cereus metallo-beta-lactamase cys221asp mutant, 20 mm zn(ii) |
101
|
305
|
3jxpA |
Crystal structure of the coenzyme pqq synthesis protein (pqqb) from pseudomonas putida |
77
|
227
|
3iofA |
Crystal structure of cpha n220g mutant with inhibitor 10a |
81
|
227
|
3iogA |
Crystal structure of cpha n220g mutant with inhibitor 18 |
130
|
431
|
3ie2A |
Crystal structure of h400v mutant ttha0252 from thermus thermophilus hb8 |
138
|
431
|
3iekA |
Crystal structure of native ttha0252 from thermus thermophilus hb8 |
136
|
431
|
3ielA |
Crystal structure of ttha0252 from thermus thermophilus hb8 complexed with ump |
133
|
431
|
3ie0A |
Crystal structure of s378y mutant ttha0252 from thermus thermophilus hb8 |
137
|
431
|
3idzA |
Crystal structure of s378q mutant ttha0252 from thermus thermophilus hb8 |
68
|
221
|
3i13A |
Bacillus cereus zn-dependent metallo-beta-lactamase at ph 5.8 |
69
|
221
|
3i0vA |
Bacillus cereus metallo-beta-lactamase: apo form |
70
|
222
|
3i14A |
Cobalt-substituted metallo-beta-lactamase from bacillus cereus: residue cys168 partially oxidized |
69
|
222
|
3i11A |
Cobalt-substituted metallo-beta-lactamase from bacillus cereus |
81
|
256
|
3h3eA |
Crystal structure of tm1679, a metal-dependent hydrolase of the beta-lactamase superfamily |
70
|
249
|
3g1pA |
Crystals structure of phnp from e.coli k-12 |
69
|
222
|
3fczA |
Adaptive protein evolution grants organismal fitness by improving catalysis and flexibility |
79
|
227
|
3faiA |
The di zinc carbapenemase cpha n220g mutant |
76
|
226
|
3f9oA |
Crystal structure of the di-zinc carbapenemase cpha from aeromonas hydrophila |
72
|
277
|
3eshA |
Crystal structure of a probable metal-dependent hydrolase from staphylococcus aureus. northeast structural genomics target zr314 |
80
|
254
|
3dhaA |
An ultral high resolution structure of n-acyl homoserine lactone hydrolase with the product n-hexanoyl-l-homoserine bound at an alternative site |
100
|
299
|
3dh8A |
Structure of pseudomonas quinolone signal response protein pqse |
82
|
250
|
3dhcA |
1.3 angstrom structure of n-acyl homoserine lactone hydrolase with the product n-hexanoyl-l-homocysteine bound to the catalytic metal center |
81
|
250
|
3dhbA |
1.4 angstrom structure of n-acyl homoserine lactone hydrolase with the product n-hexanoyl-l-homoserine bound at the catalytic metal center |
168
|
549
|
3bk2A |
Crystal structure analysis of the rnase j/ump complex |
112
|
353
|
3bv6A |
Crystal structure of uncharacterized metallo protein from vibrio cholerae with beta-lactamase like fold |
167
|
551
|
3bk1A |
Crystal structure analysis of rnase j |
69
|
220
|
3bc2A |
Metallo beta-lactamase ii from bacillus cereus 569/h/9 at ph 6.0, monoclinic crystal form |
215
|
643
|
3af5A |
The crystal structure of an archaeal cpsf subunit, ph1404 from pyrococcus horikoshii |
86
|
273
|
3aj3A |
Crystal structure of selenomethionine substituted 4-pyridoxolactonase from mesorhizobium loti |
76
|
259
|
3adrA |
The first crystal structure of an archaeal metallo-beta-lactamase superfamily protein; st1585 from sulfolobus tokodaii |
140
|
431
|
3a4yA |
Crystal structure of h61a mutant ttha0252 from thermus thermophilus hb8 |
74
|
228
|
2znbA |
Metallo-beta-lactamase (cadmium-bound form) |
53
|
198
|
2zziA |
Crystal structure of ttha1623 in a di-iron-bound form |
56
|
200
|
2zwrA |
Crystal structure of ttha1623 from thermus thermophilus hb8 |
66
|
225
|
2yz3A |
Crystallographic investigation of inhibition mode of the vim-2 metallo-beta-lactamase from pseudomonas aeruginosa with mercaptocarboxylate inhibitor |
100
|
315
|
2zo4A |
Crystal structure of metallo-beta-lactamase family protein ttha1429 from thermus thermophilus hb8 |
233
|
639
|
2yheA |
Structure determination of the stereoselective inverting sec- alkylsulfatase pisa1 from pseudomonas sp. |
62
|
217
|
2ynuA |
Apo gim-1 with 2mol. crystal structures of pseudomonas aeruginosa gim-1: active site plasticity in metallo-beta-lactamases |
72
|
219
|
2yntB |
Gim-1-3mol native. crystal structures of pseudomonas aeruginosa gim- 1: active site plasticity in metallo-beta-lactamases |
66
|
217
|
2ynwA |
Gim-1-2mol native. crystal structures of pseudomonas aeruginosa gim- 1: active site plasticity in metallo-beta-lactamases |
202
|
634
|
2ycbA |
Structure of the archaeal beta-casp protein with n-terminal kh domains from methanothermobacter thermautotrophicus |
65
|
217
|
2ynvA |
Cys221 oxidized, mono zinc gim-1 - gim-1-ox. crystal structures of pseudomonas aeruginosa gim-1: active site plasticity in metallo-beta- lactamases |
66
|
221
|
2yntA |
Gim-1-3mol native. crystal structures of pseudomonas aeruginosa gim- 1: active site plasticity in metallo-beta-lactamases |
57
|
217
|
2ynvB |
Cys221 oxidized, mono zinc gim-1 - gim-1-ox. crystal structures of pseudomonas aeruginosa gim-1: active site plasticity in metallo-beta- lactamases |
200
|
635
|
2xr1A |
Dimeric archaeal cleavage and polyadenylation specificity factor with n-terminal kh domains (kh-cpsf) from methanosarcina mazei |
64
|
226
|
2y8aA |
Vim-7 with oxidised. structural and computational investigations of vim-7: insights into the substrate specificity of vim metallo-beta- lactamases |
66
|
227
|
2y87A |
Native vim-7. structural and computational investigations of vim-7: insights into the substrate specificity of vim metallo-beta- lactamases |
67
|
226
|
2y8bA |
Vim-7 with oxidised. structural and computational investigations of vim-7: insights into the substrate specificity of vim metallo-beta- lactamases |
65
|
210
|
2xf4A |
Crystal structure of salmonella enterica serovar typhimurium ycbl |