Found 28394 chains in Genus chains table. Displaying 4001 - 4050. Applied filters: Proteins

Search results query: Orthogonal Bundle

Total Genus Sequence Length pdb Title
76 185 154lA The refined structures of goose lysozyme and its complex with a bound trisaccharide show that the "goose-type lysozymes lack a catalytic aspartate
57 162 177lA Protein flexibility and adaptability seen in 25 crystal forms of t4 lysozyme
59 162 198lA Thermodynamic and structural compensation in "size-switch" core-repacking variants of t4 lysozyme
59 162 197lA Thermodynamic and structural compensation in "size-switch" core-repacking variants of t4 lysozyme
75 185 153lA The refined structures of goose lysozyme and its complex with a bound trisaccharide show that the "goose-type lysozymes lack a catalytic aspartate
255 713 5sx2A Crystal structure of the d141e mutant of b. pseudomallei katg at ph 8.0.
257 713 5sykA Crystal structure of b. pseudomallei katg treated with hydrogen peroxide
262 713 5sx6A Crystal structure of the catalase-peroxidase katg of b. pseudomallei at ph 6.5
257 713 5syvA Crystal structure of burkholderia pseudomallei katg n240d variant
57 142 5sw7A Structure of the human hemoglobin mutant hb providence (a-gly-c:v1m; b,d:v1m,k82d; ferrous, carbonmonoxy bound)
102 332 5prcC Photosynthetic reaction center from rhodopseudomonas viridis (atrazine complex)
325 905 5lhdA Structure of glycosylated human aminopeptidase n
265 725 5mgbA Crystal structure of rat peroxisomal multifunctional enzyme type-1 (rpmfe1) complexed with acetoacetyl-coa and nad
335 903 5ldsA Structure of the porcine aminopeptidase n ectodomain
113 332 5m4uA Orthorhombic complex structure of human protein kinase ck2 catalytic subunit (isoform ck2alpha') with the inhibitor 4'-carboxy-6,8-chloro- flavonol (flc21)
116 331 5m56A Monoclinic complex structure of human protein kinase ck2 catalytic subunit (isoform ck2alpha') with the inhibitor 4'-carboxy-6,8-chloro-flavonol (flc21)
93 225 5m96A Synthesis and biological evaluation of new triazolo and imidazolopyridine rorgt inverse agonists
65 153 5mbnA Refinement of myoglobin and cytochrome c
115 329 5m4cA Complex structure of human protein kinase ck2 catalytic subunit with a thieno[2,3-d]pyrimidin inhibitor crystallized under low-salt conditions
57 146 5mbaA Binding mode of azide to ferric aplysia limacina myoglobin. crystallographic analysis at 1.9 angstroms resolution
80 277 5m57A Nek2 bound to arylaminopurine 6
297 905 5lg6A Structure of the deglycosylated porcine aminopeptidase n ectodomain
39 129 5lytA Comparison of radiation-induced decay and structure refinement from x-ray data collected from lysozyme crystals at low and ambient temperatures
43 129 5lxwA Atomic resolution x-ray crystal structure of cisplatin bound to hen egg white lysozyme stored for 5 years on the shelf
43 151 5llqA Crystal structure of sulfolobus solfataricus o6-methylguanine methyltransferase c119f variant
88 244 5lwpA Discovery of phenoxyindazoles and phenylthioindazoles as rorg inverse agonists
48 129 5lvjA Hen egg white lysozyme soaked with [h2ind][trans-rucl4(dmso)(hind)]
165 426 5lovB Dz-2384 tubulin complex
85 264 5l8lA Aurora-a kinase domain in complex with vnar-d01 (crystal form 1)
174 428 5lxtB Tubulin-discodermolide complex
89 271 5lmbA Human spleen tyrosine kinase kinase domain in complex with azanaphthyridine inhibitor
231 666 5lhhA Structure of the kdm1a/corest complex with the inhibitor 4-ethyl-n-[3-(methoxymethyl)-2-[[4-[[(3r)-pyrrolidin-3-yl]methoxy]phenoxy]methyl]phenyl]thieno[3,2-b]pyrrole-5-carboxamide
218 666 5l3cA Human lsd1/corest: lsd1 e379k mutation
188 512 5lfaA Crystal structure of iron-sulfur cluster containing bacterial (6-4) photolyase phrb - y424f mutant with impaired dna repair activity
96 290 5lwmA Crystal structure of jak3 in complex with compound 4 (fm381)
95 290 5lwnA Crystal structure of jak3 in complex with compound 5 (fm409)
140 409 5li8A Crystal structure of mycobacterium tuberculosis cyp126a1 in complex with ketoconazole
90 272 5m53A Nek2 bound to arylaminopurine inhibitor 11
201 666 5lhiA Structure of the kdm1a/corest complex with the inhibitor n-[3-(ethoxymethyl)-2-[[4-[[(3r)-pyrrolidin-3-yl]methoxy]phenoxy]methyl]phenyl]-4-methylthieno[3,2-b]pyrrole-5-carboxamide
101 329 5m44A Complex structure of human protein kinase ck2 catalytic subunit with a thieno[2,3-d]pyrimidin inhibitor crystallized under high-salt conditions
49 129 5la5A Room temperature x-ray diffraction of tetragonal hewl. second data set (0.62 mgy)
98 387 5lnk4 Entire ovine respiratory complex i
117 316 5lwdE Thermolysin in complex with inhibitor (jc96)
136 398 5livA Crystal structure of myxobacterial cyp260a1
49 129 5linA Lysozyme, collected at rotation 1 degree per second
82 292 5lqfA Cdk1/cyclinb1/cks2 in complex with nu6102
32 92 5m33A Structural tuning of cd81lel (space group p21)
87 247 5l86A Engineered ascorbate peroxidise
130 406 5li7A Crystal structure of mycobacterium tuberculosis cyp126a1 in complex with 1-(3-(1h-imidazol-1-yl)propyl)-3-((3s,5s,7s)-adamantan-1-yl)urea
191 639 5lpcA Crystal structure of vanadium-dependent haloperoxidase from a. marina