2bdg | pdb_00002bdg

Human Kallikrein 4 complex with nickel and p-aminobenzamidine

spinqualitylabelsall models 2bdg, resolution 1.95Å Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image   Print3D Structural highlights 2bdg is a 2 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA. For a guided tour on the structure components use FirstGlance. Method: X-ray diffraction, Resolution 1.95Å Ligands: CL, NA, NI, PBZ Resources: FirstGlance, OCA, PDBe, RCSB, PDBsum, ProSAT Disease KLK4_HUMAN Defects in KLK4 are the cause of amelogenesis imperfecta hypomaturation type 2A1 (AI2A1) [MIM:204700. AI2A1 is an autosomal recessive defect of enamel formation. The disorder involves both primary and secondary dentitions. The teeth have a shiny agar jelly appearance and the enamel is softer than normal. Brown pigment is present in middle layers of enamel. Function KLK4_HUMAN Involved in enamel formation. Evolutionary Conservation Check, as determined by ConSurfDB. You may read the explanation of the method and the full data available from ConSurf. See Also Kallikrein 3D structures

Proteopedia Page Contributors and Editors (what is this?)

OCA