Found 335 chains in Genus chains table. Displaying 251 - 300. Applied filters: Proteins

Search results query: Neutral Protease; domain 2

Total Genus Sequence Length pdb Title
222 610 3choA Crystal structure of leukotriene a4 hydrolase in complex with 2-amino-n-[4-(phenylmethoxy)phenyl]-acetamide
215 608 3chpA Crystal structure of leukotriene a4 hydrolase in complex with (3s)-3-amino-4-oxo-4-[(4-phenylmethoxyphenyl)amino]butanoic acid
212 610 3chsA Crystal structure of leukotriene a4 hydrolase in complex with (2s)-2-amino-5-[[4-[(2s)-2-hydroxy-2-phenyl-ethoxy]phenyl]amino]-5-oxo-pentanoic acid
207 610 3chrA Crystal structure of leukotriene a4 hydrolase in complex with 4-amino-n-[4-(phenylmethoxy)phenyl]-butanamide
213 607 3chqA Crystal structure of leukotriene a4 hydrolase in complex with n5-[4-(phenylmethoxy)phenyl]-l-glutamine
177 592 3ciaA Crystal structure of cold-aminopeptidase from colwellia psychrerythraea
323 866 3b34A Crystal structure of e. coli aminopeptidase n in complex with phenylalanine
316 866 3b2pA Crystal structure of e. coli aminopeptidase n in complex with arginine
320 866 3b3bA Crystal structure of e. coli aminopeptidase n in complex with tryptophan
322 866 3b37A Crystal structure of e. coli aminopeptidase n in complex with tyrosine
320 866 3b2xA Crystal structure of e. coli aminopeptidase n in complex with lysine
216 610 3b7rL Leukotriene a4 hydrolase complexed with inhibitor rb3040
215 610 3b7tA [e296q]lta4h in complex with arg-ala-arg substrate
222 610 3b7sA [e296q]lta4h in complex with rsr substrate
215 610 3b7uX Leukotriene a4 hydrolase complexed with kelatorphan
320 866 2zxgA Aminopeptidase n complexed with the aminophosphinic inhibitor of pl250, a transition state analogue
326 895 2yd0A Crystal structure of the soluble domain of human endoplasmic reticulum aminopeptidase 1 erap1
205 632 2xpzA Structure of native yeast lta4 hydrolase
216 632 2xpyA Structure of native leukotriene a4 hydrolase from saccharomyces cerevisiae
221 632 2xq0A Structure of yeast lta4 hydrolase in complex with bestatin
122 316 2wi0A Dipeptide inhibitors of thermolysin
119 316 2whzA Dipeptide inhibitors of thermolysin
118 336 2vqxA Precursor of protealysin, metalloproteinase from serratia proteamaculans.
221 610 2vj8A Complex of human leukotriene a4 hydrolase with a hydroxamic acid inhibitor
120 316 2tlxA Thermolysin (native)
114 316 2tmnE Crystallographic structural analysis of phosphoramidates as inhibitors and transition-state analogs of thermolysin
121 316 2tliA Thermolysin (5% isopropanol soaked crystals)
212 610 2r59A Leukotriene a4 hydrolase complexed with inhibitor rb3041
321 866 2hpoA Structure of aminopeptidase n from e. coli suggests a compartmentalized, gated active site
304 864 2gtqA Crystal structure of aminopeptidase n from human pathogen neisseria meningitidis
118 316 2g4zA Anomalous substructure of thermolysin
309 867 2dqmA Crystal structure of aminopeptidase n complexed with bestatin
307 865 2dq6A Crystal structure of aminopeptidase n from escherichia coli
280 780 1z5hA Crystal structures of the tricorn interacting factor f3 from thermoplasma acidophilum
115 316 1zdpE Crystal structure analysis of thermolysin complexed with the inhibitor (s)-thiorphan
255 780 1z1wA Crystal structures of the tricorn interacting facor f3 from thermoplasma acidophilum, a zinc aminopeptidase in three different conformations
116 316 2a7gE On the routine use of soft x-rays in macromolecular crystallography, part iii- the optimal data collection wavelength
114 316 1z9gE Crystal structure analysis of thermolysin complexed with the inhibitor (r)-retro-thiorphan
116 316 1y3gE Crystal structure of a silanediol protease inhibitor bound to thermolysin
110 298 1u4gA Elastase of pseudomonas aeruginosa with an inhibitor
24 62 1trlA Nmr solution structure of the c-terminal fragment 255-316 of thermolysin: a dimer formed by subunits having the native structure
117 316 1thlA Thermolysin complexed with a novel glutaramide derivative, n-(1-(2(r,s)-carboxy-4-phenylbutyl) cyclopentylcarbonyl)-(s)-tryptophan
115 316 1tmnE Binding of n-carboxymethyl dipeptide inhibitors to thermolysin determined by x-ray crystallography. a novel class of transition-state analogues for zinc peptidases
117 316 1tlpE Crystallographic structural analysis of phosphoramidates as inhibitors and transition-state analogs of thermolysin
121 316 1tlxA Thermolysin (native)
121 316 1tliA Thermolysin (2% isopropanol soaked crystals)
222 610 1sqmA Structure of [r563a] leukotriene a4 hydrolase
116 316 1qf2A Thermolysin (e.c.3.4.24.27) complexed with (2-sulphanyl-3-phenylpropanoyl)-gly-(5-phenylproline). parameters for zn-monodentation of mercaptoacyldipeptides in metalloendopeptidase
116 316 1qf0A Thermolysin (e.c.3.4.24.27) complexed with (2-sulphanyl-3-phenylpropanoyl)-phe-tyr. parameters for zn-bidentation of mercaptoacyldipeptides in metalloendopeptidase
117 316 1qf1A Thermolysin (e.c.3.4.24.27) complexed with (2-sulphanylheptanoyl)-phe-ala. parameters for zn-bidentation of mercaptoacyldipeptides in metalloendopeptidase