Found 587 chains in Genus chains table. Displaying 301 - 350. Applied filters: Proteins

Search results query: Ribosomal Protein S5; domain 2

Total Genus Sequence Length pdb Title
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