Crystal structures of allosamidin derivatives in complex with human macrophage chitinase
about
Structure of human stabilin-1 interacting chitinase-like protein (SI-CLP) reveals a saccharide-binding cleft with lower sugar-binding selectivityStructure and ligand-induced conformational change of the 39-kDa glycoprotein from human articular chondrocytesCommon G102S polymorphism in chitotriosidase differentially affects activity towards 4-methylumbelliferyl substratesInteractions of a family 18 chitinase with the designed inhibitor HM508 and its degradation product, chitobiono-delta-lactoneTriad of polar residues implicated in pH specificity of acidic mammalian chitinaseCrystal Structures of Bacillus cereus NCTU2 Chitinase Complexes with Chitooligomers Reveal Novel Substrate Binding for Catalysis: A CHITINASE WITHOUT CHITIN BINDING AND INSERTION DOMAINSAcetazolamide-based fungal chitinase inhibitorsPotent Family-18 Chitinase InhibitorsFully Deacetylated Chitooligosaccharides Act as Efficient Glycoside Hydrolase Family 18 Chitinase InhibitorsScreening-based discovery ofAspergillus fumigatusplant-type chitinase inhibitorsCrystal structures and inhibitor binding properties of plant class V chitinases: the cycad enzyme exhibits unique structural and functional featuresSequence and structural analysis of the chitinase insertion domain reveals two conserved motifs involved in chitin-bindingBiomarkers in the diagnosis of lysosomal storage disorders: proteins, lipids, and inhibodies.Targeting AMCase reduces esophageal eosinophilic inflammation and remodeling in a mouse model of egg induced eosinophilic esophagitis.Novel methylxanthine derivative-mediated anti-inflammatory effects in inflammatory bowel disease.Gaucher disease: a model disorder for biomarker discovery.Novel biological activities of allosamidins.Interaction of di-N-acetylchitobiosyl moranoline with a family GH19 chitinase from moss, Bryum coronatum.A computational analysis of the binding mode of closantel as inhibitor of the Onchocerca volvulus chitinase: insights on macrofilaricidal drug design.A single histidine residue modulates enzymatic activity in acidic mammalian chitinase.Acidic Chitinase-Chitin Complex Is Dissociated in a Competitive Manner by Acetic Acid: Purification of Natural Enzyme for Supplementation Purposes.Screening-based discovery and structural dissection of a novel family 18 chitinase inhibitor.
P2860
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P2860
Crystal structures of allosamidin derivatives in complex with human macrophage chitinase
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2003 nî lūn-bûn
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2003 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի մայիսին հրատարակված գիտական հոդված
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2003年の論文
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2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
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name
Crystal structures of allosamidin derivatives in complex with human macrophage chitinase
@ast
Crystal structures of allosamidin derivatives in complex with human macrophage chitinase
@en
Crystal structures of allosamidin derivatives in complex with human macrophage chitinase
@nl
type
label
Crystal structures of allosamidin derivatives in complex with human macrophage chitinase
@ast
Crystal structures of allosamidin derivatives in complex with human macrophage chitinase
@en
Crystal structures of allosamidin derivatives in complex with human macrophage chitinase
@nl
prefLabel
Crystal structures of allosamidin derivatives in complex with human macrophage chitinase
@ast
Crystal structures of allosamidin derivatives in complex with human macrophage chitinase
@en
Crystal structures of allosamidin derivatives in complex with human macrophage chitinase
@nl
P2093
P2860
P50
P356
P1476
Crystal structures of allosamidin derivatives in complex with human macrophage chitinase
@en
P2093
Douglas R Houston
Francesco V Rao
Shohei Sakuda
P2860
P304
20110-20116
P356
10.1074/JBC.M300362200
P407
P577
2003-03-14T00:00:00Z