132
|
389
|
4wucA |
N-terminal 43 kda fragment of the e. coli dna gyrase b subunit grown from 100 mm nacl condition |
131
|
389
|
4wubA |
N-terminal 43 kda fragment of the e. coli dna gyrase b subunit grown from 100 mm kcl condition |
115
|
345
|
4utgA |
Burkholderia pseudomallei heptokinase wcbl,amppnp (atp analogue) complex. |
92
|
267
|
4u3bA |
Lpxc from a.aaeolicus in complex with the mmp inhibitor 4-[[4-(4-chlorophenoxy)phenyl]sulfanylmethyl]tetrahydropyran-4-carbohydroxamic acid - compound 2 |
92
|
267
|
4u3dA |
Lpxc from a.aaeolicus in complex with 4-[[4-[2-[4-(morpholinomethyl)phenyl]ethynyl]phenoxy]methyl]tetrahydropyran-4-carbohydroxamic acid (compound 9) |
61
|
184
|
4qnjA |
The structure of wt a. thaliana igpd2 in complex with mn2+ and formate at 1.3a resolution |
92
|
310
|
4rpfA |
Crystal structure of homoserine kinase from yersinia pestis nepal516, nysgrc target 032715 |
58
|
185
|
4qnkA |
The structure of wt a. thaliana igpd2 in complex with mn2+ and phosphate |
113
|
394
|
4r1fA |
Re-refined human dna topoisomerase iia (atpase and transducer domains) in complex with adp and so4 |
123
|
385
|
4pu9A |
E. coli gyrb 43-kda n-terminal fragment in complex with adp-bef3 |
95
|
266
|
4ozeA |
A.aolicus lpxc in complex with native product |
124
|
382
|
4prvA |
E. coli gyrb 43-kda n-terminal fragment in complex with adp |
89
|
315
|
4p52A |
Crystal structure of homoserine kinase from cytophaga hutchinsonii atcc 33406, nysgrc target 032717. |
108
|
374
|
4prxA |
E. coli gyrb 43-kda n-terminal fragment in complex with adp+pi |
88
|
334
|
4p7aA |
Crystal structure of human mlh1 |
167
|
683
|
4myuA |
Crystal structure of elongation factor g mutant(efg) |
88
|
299
|
4okgA |
Lpxc from p.aeruginosa with the inhibitor 6-(benzimidazol-1-yl)-5-[4-[2-[6-[(4-methylpiperazin-1-yl)methyl]-3-pyridyl]ethynyl]phenyl]pyridine-3-carbohydroxamic acid |
156
|
683
|
4mytA |
Crystal structure of elongation factor g (efg) |
98
|
342
|
4n3oA |
2.4 angstrom resolution crystal structure of putative sugar kinase from campylobacter jejuni. |
174
|
693
|
4nbqA |
Structure of the polynucleotide phosphorylase (cbu_0852) from coxiella burnetii |
63
|
199
|
4mu4A |
The form b structure of an e21q catalytic mutant of a. thaliana igpd2 in complex with mn2+ and its substrate, 2r3s-igp, to 1.41 a resolution |
54
|
185
|
4mu1A |
The structure of wt a. thaliana igpd2 in complex with mn2+, imidazole, and sulfate at 1.5 a resolution |
58
|
186
|
4mu3A |
The form a structure of an e21q catalytic mutant of a. thaliana igpd2 in complex with mn2+ and a mixture of its substrate, 2r3s-igp, and an inhibitor, 2s3s-igp, to 1.12 a resolution |
87
|
302
|
4mqyA |
Crystal structure of the escherichia coli lpxc/lpc-138 complex |
57
|
191
|
4lomA |
Crystal structure of mycobacterium tuberculosis hisb in complex with its substrate |
182
|
683
|
4m1kA |
Crystal structure of elongation factor g (efg) |
58
|
185
|
4mu0A |
The structure of wt a. thaliana igpd2 in complex with mn2+ and 1,2,4-triazole at 1.3 a resolution |
60
|
190
|
4lpfA |
Crystal structure of mycobacterium tuberculosis imidazole glycerol phosphate dehydratase in complex with an inhibitor |
91
|
300
|
4mdtA |
Structure of lpxc bound to the reaction product udp-(3-o-(r-3-hydroxymyristoyl))-glucosamine |
93
|
296
|
4lcgA |
Crystal structure of the pseudomonas aeruginosa lpxc/lpc-050 complex |
108
|
374
|
4kqvA |
Topoisomerase iv atp binding domain of francisella tularensis in complex with a small molecule inhibitor |
94
|
296
|
4lchA |
Crystal structure of the pseudomonas aeruginosa lpxc/lpc-051 complex |
95
|
298
|
4lcfA |
Crystal structure of the pseudomonas aeruginosa lpxc/lpc-014 complex |
83
|
300
|
4is9A |
Crystal structure of the escherichia coli lpxc/l-161,240 complex |
84
|
297
|
4j3dA |
Pseudomonas aeruginosa lpxc in complex with a hydroxamate inhibitor |
107
|
376
|
4hxzA |
Pyrrolopyrimidine inhibitors of dna gyrase b and topoisomerase iv, part i: structure guided discovery and optimization of dual targeting agents with potent, broad-spectrum enzymatic activity. |
52
|
202
|
4izjB |
Crystal structure of yellowtail ascites virus vp4 protease with a wild-type active site reveals acyl-enzyme complexes and product complexes. |
109
|
371
|
4hy1A |
Pyrrolopyrimidine inhibitors of dna gyrase b and topoisomerase iv, part i: structure guided discovery and optimization of dual targeting agents with potent, broad-spectrum enzymatic activity. |
90
|
300
|
4isaA |
Crystal structure of the escherichia coli lpxc/bb-78485 complex |
37
|
114
|
4jg4A |
Ligand concentration regulates the pathways of coupled protein folding and binding |
53
|
203
|
4izjD |
Crystal structure of yellowtail ascites virus vp4 protease with a wild-type active site reveals acyl-enzyme complexes and product complexes. |
51
|
203
|
4izkB |
Crystal structure of yellowtail ascites virus vp4 protease active site mutant (k674a) reveals both an acyl-enzyme complex and an empty active site |
50
|
203
|
4izjA |
Crystal structure of yellowtail ascites virus vp4 protease with a wild-type active site reveals acyl-enzyme complexes and product complexes. |
53
|
202
|
4izkA |
Crystal structure of yellowtail ascites virus vp4 protease active site mutant (k674a) reveals both an acyl-enzyme complex and an empty active site |
110
|
371
|
4hymA |
Pyrrolopyrimidine inhibitors of dna gyrase b and topoisomerase iv, part i: structure guided discovery and optimization of dual targeting agents with potent, broad-spectrum enzymatic activity. |
89
|
312
|
4hacA |
Crystal structure of the mevalonate kinase from an archaeon methanosarcina mazei |
89
|
308
|
4hacB |
Crystal structure of the mevalonate kinase from an archaeon methanosarcina mazei |
62
|
191
|
4gquA |
Crystal structure of hisb from mycobacterium tuberculosis |
184
|
712
|
4fwhA |
Crystal structure of the lon-like protease mtalonc in complex with mg262 |
88
|
302
|
4fw3A |
Crystal structure of the lpxc in complex with n-[(2s)-3-amino-1-(hydroxyamino)-1-oxopropan-2-yl]-4-(4-phenylbuta-1,3-diyn-1-yl)benzamide inhibitor |