2wd2 | pdb_00002wd2

A CHIMERIC MICROTUBULE DISRUPTOR WITH EFFICACY ON A TAXANE RESISTANT CELL LINE

spinqualitylabelsall models 2wd2, resolution 1.49Å Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image   Print3D Structural highlights 2wd2 is a 1 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA. For a guided tour on the structure components use FirstGlance. Ligands: FMT, MS5, ZN Related: 1okl, 1i9q, 1zfq, 1if7, 1cam, 1t9n, 1cnw, 1okn, 1f2w, 1g52, 2h4n, 1bnm, 1bnq, 1cnh, 1ugc, 1xev, 1ugg, 1if9, 1g53, 1fqm, 1ca2, 1cal, 1fql, 1i9n, 1g4o, 2cba, 1ydc, 1ccs, 1lzv, 1bnv, 1fqr, 1rzb, 1a42, 1th9, 1zsb, 1cnb, 1hed, 1i8z, 1g48, 1lg5, 1g0f, 1bv3, 1tg3, 1cvc, 1ugd, 1i90, 1yo0, 1fsn, 1hva, 1rze, 1ugb, 1z9y, 2fmz, 1cnk, 1bn1, 1teq, 1rza, 2vvb, 1ccu, 1i9l, 2cbc, 1g46, 1cvb, 1cao, 1fsq, 6ca2, 5ca2, 1caj, 1g1d, 1cvf, 2fou, 1lgd, 1if6, 1bn4, 1teu, 1cra, 1ze8, 1if4, 1hea, 1hca, 1cah, 1g4j, 1kwq, 1raz, 1cim, 1cvh, 1if8, 1cin, 1i9m, 1zfk, 1fqn, 1zsa, 1lg6, 1cnc, 1bnn, 1uga, 2foq, 1tb0, 1cai, 1dcb, 2ax2, 1cnx, 5cac, 2hd6, 4cac, 1ttm, 1cak, 1i9o, 1cni, 1can, 2eu3, 1yda, 1eou, 1yo2, 1mua, 2ca2, 1cct, 1oq5, 2abe, 1ugf, 1rzc, 2cbe, 1thk, 1kwr, 1zgf, 1cay, 1cng, 1moo, 1hec, 2ez7, 9ca2, 1fr7, 8ca2, 1zh9, 1ydd, 1bic, 1lug, 1caz, 7ca2, 1cvd, 1fr4, 4ca2, 1cil, 2geh, 1g45, 1ydb, 1dca, 1fsr, 2cbb, 1i9p, 12ca, 1avn, 1bcd, 1am6, 1i91, 1cve, 1g3z, 1heb, 2cbd, 1zsc, 3ca2, 1bnu, 1zge, 1bnw, 2fov, 1te3, 1bnt, 1if5, 1yo1, 1g54, 1rzd, 1uge, 1ray, 2fmg, 1g0e, 1cva, 1ca3, 2eu2, 1tg9, 1tbt, 1xeg, 1bn3, 1okm, 1cny, 1cnj, 1h9n, 2vva, 2aw1, 1h4n, 2fos, 1h9q, 2wd3 Activity: Carbonate dehydratase, with EC number 4.2.1.1 Resources: FirstGlance, OCA, RCSB, PDBsum Disease [CAH2_HUMAN] Defects in CA2 are the cause of osteopetrosis autosomal recessive type 3 (OPTB3) [MIM:259730]; also known as osteopetrosis with renal tubular acidosis, carbonic anhydrase II deficiency syndrome, Guibaud-Vainsel syndrome or marble brain disease. Osteopetrosis is a rare genetic disease characterized by abnormally dense bone, due to defective resorption of immature bone. The disorder occurs in two forms: a severe autosomal recessive form occurring in utero, infancy, or childhood, and a benign autosomal dominant form occurring in adolescence or adulthood. Autosomal recessive osteopetrosis is usually associated with normal or elevated amount of non-functional osteoclasts. OPTB3 is associated with renal tubular acidosis, cerebral calcification (marble brain disease) and in some cases with mental retardation. Function [CAH2_HUMAN] Essential for bone resorption and osteoclast differentiation (By similarity). Reversible hydration of carbon dioxide. Can hydrate cyanamide to urea. Involved in the regulation of fluid secretion into the anterior chamber of the eye. Evolutionary Conservation Check, as determined by ConSurfDB. You may read the explanation of the method and the full data available from ConSurf. Publication Abstract from PubMed A chimeric approach is used to discover microtubule disruptors with excellent in vitro activity and oral bioavailability; a ligand-protein interaction with carbonic anhydrase that enhances bioavailability is characterised by protein X-ray crystallography. Dosing of a representative chimera in a tumour xenograft model confirms the excellent therapeutic potential of the class. Chimeric microtubule disruptors.,Leese MP, Jourdan F, Kimberley MR, Cozier GE, Thiyagarajan N, Stengel C, Regis-Lydi S, Foster PA, Newman SP, Acharya KR, Ferrandis E, Purohit A, Reed MJ, Potter BV Chem Commun (Camb). 2010 May 7;46(17):2907-9. Epub 2010 Mar 20. PMID:20386818 From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine. See Also Carbonic anhydrase

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