| Structural highlights
2wd2 is a 1 chain structure with sequence from Human. Full crystallographic information is available from OCA. For a guided tour on the structure components use FirstGlance.
| | Ligands: | , , |
| 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, PDBe, RCSB, PDBsum, ProSAT |
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.[1] [2] [3] [4] [5]
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.[6] [7]
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[8]
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.
See Also
References
- ↑ Venta PJ, Welty RJ, Johnson TM, Sly WS, Tashian RE. Carbonic anhydrase II deficiency syndrome in a Belgian family is caused by a point mutation at an invariant histidine residue (107 His----Tyr): complete structure of the normal human CA II gene. Am J Hum Genet. 1991 Nov;49(5):1082-90. PMID:1928091
- ↑ Roth DE, Venta PJ, Tashian RE, Sly WS. Molecular basis of human carbonic anhydrase II deficiency. Proc Natl Acad Sci U S A. 1992 Mar 1;89(5):1804-8. PMID:1542674
- ↑ Soda H, Yukizane S, Yoshida I, Koga Y, Aramaki S, Kato H. A point mutation in exon 3 (His 107-->Tyr) in two unrelated Japanese patients with carbonic anhydrase II deficiency with central nervous system involvement. Hum Genet. 1996 Apr;97(4):435-7. PMID:8834238
- ↑ Hu PY, Lim EJ, Ciccolella J, Strisciuglio P, Sly WS. Seven novel mutations in carbonic anhydrase II deficiency syndrome identified by SSCP and direct sequencing analysis. Hum Mutat. 1997;9(5):383-7. PMID:9143915 doi:<383::AID-HUMU1>3.0.CO;2-5 10.1002/(SICI)1098-1004(1997)9:5<383::AID-HUMU1>3.0.CO;2-5
- ↑ Shah GN, Bonapace G, Hu PY, Strisciuglio P, Sly WS. Carbonic anhydrase II deficiency syndrome (osteopetrosis with renal tubular acidosis and brain calcification): novel mutations in CA2 identified by direct sequencing expand the opportunity for genotype-phenotype correlation. Hum Mutat. 2004 Sep;24(3):272. PMID:15300855 doi:10.1002/humu.9266
- ↑ Briganti F, Mangani S, Scozzafava A, Vernaglione G, Supuran CT. Carbonic anhydrase catalyzes cyanamide hydration to urea: is it mimicking the physiological reaction? J Biol Inorg Chem. 1999 Oct;4(5):528-36. PMID:10550681
- ↑ Kim CY, Whittington DA, Chang JS, Liao J, May JA, Christianson DW. Structural aspects of isozyme selectivity in the binding of inhibitors to carbonic anhydrases II and IV. J Med Chem. 2002 Feb 14;45(4):888-93. PMID:11831900
- ↑ 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. Chimeric microtubule disruptors. Chem Commun (Camb). 2010 May 7;46(17):2907-9. Epub 2010 Mar 20. PMID:20386818 doi:10.1039/c002558e
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