Urate oxidase: Difference between revisions
m (Protected "Urate oxidase": Bot: Protecting all pages from category Drug ([Edit=Allow only administrators] (indefinite) [Move=Allow only administrators] (indefinite))) |
imported>Boghog (→Significance of absence in humans: consistent citation formatting) |
||
(One intermediate revision by one other user not shown) | |||
Line 1: | Line 1: | ||
{{Infobox_gene}} | |||
{{ | |||
:[[Uric acid]] + O<sub>2</sub> + H<sub>2</sub>O → [[5-hydroxyisourate]] + [[hydrogen peroxide|H<sub>2</sub>O<sub>2</sub>]] → [[allantoin]] + CO<sub>2</sub> | The enzyme '''urate oxidase''' ('''UO'''), or '''uricase''' or '''factor-independent urate hydroxylase''', absent in humans, catalyzes the [[oxidation]] of [[uric acid]] to [[5-hydroxyisourate]]:<ref name="PUB00002471">{{cite journal | vauthors = Motojima K, Kanaya S, Goto S | title = Cloning and sequence analysis of cDNA for rat liver uricase | journal = The Journal of Biological Chemistry | volume = 263 | issue = 32 | pages = 16677–81 | date = November 1988 | pmid = 3182808 }}</ref> | ||
:[[Uric acid]] + O<sub>2</sub> + H<sub>2</sub>O → [[5-hydroxyisourate]] + [[hydrogen peroxide|H<sub>2</sub>O<sub>2</sub>]] | |||
:[[5-hydroxyisourate]] + H<sub>2</sub>O → [[allantoin]] + CO<sub>2</sub> | |||
{| | {| | ||
|- valign="top" | |- valign="top" | ||
| [[Image:Uric acid.png|thumb|150px|[[Uric acid]]]] | | [[Image:Uric acid.png|thumb|150px|[[Uric acid]]]] | ||
| [[Image:5-Hydroxyisourate. | | [[Image:5-Hydroxyisourate.svg|left|thumb|150px|[[5-hydroxyisourate]]]] | ||
| [[Image:Allantoin. | | [[Image:Allantoin.svg|left|thumb|150px|[[Allantoin]]]] | ||
|} | |} | ||
==Structure== | == Structure == | ||
Urate oxidase is a [[tetrameric protein|homotetrameric]] enzyme containing four identical active sites situated at the interfaces between its four subunits. UO from ''[[Aspergillus flavus|A. flavus]]'' is made up of 301 residues and has a molecular weight of 33438 [[dalton (unit)| | Urate oxidase is mainly localised in the liver, where it forms a large electron-dense paracrystalline core in many [[peroxisome]]s.<ref name="PUB00001587">{{cite journal | vauthors = Motojima K, Goto S | title = Organization of rat uricase chromosomal gene differs greatly from that of the corresponding plant gene | journal = FEBS Letters | volume = 264 | issue = 1 | pages = 156–8 | date = May 1990 | pmid = 2338140 | doi = 10.1016/0014-5793(90)80789-L }}</ref> The enzyme exists as a tetramer of identical subunits, each containing a possible type 2 copper-binding site.<ref name="PUB00004693">{{cite journal|vauthors=Wu XW, Lee CC, Muzny DM, Caskey CT|date=December 1989|title=Urate oxidase: primary structure and evolutionary implications|journal=Proceedings of the National Academy of Sciences of the United States of America|volume=86|issue=23|pages=9412–6|doi=10.1073/pnas.86.23.9412|pmc=298506|pmid=2594778}}</ref> | ||
Urate oxidase is a [[tetrameric protein|homotetrameric]] enzyme containing four identical active sites situated at the interfaces between its four subunits. UO from ''[[Aspergillus flavus|A. flavus]]'' is made up of 301 residues and has a molecular weight of 33438 [[dalton (unit)|daltons]]. It is unique among the [[oxidase]]s in that it does not require a metal atom or an organic co-factor for [[catalysis]]. Sequence analysis of several organisms has determined that there are 24 amino acids which are conserved, and of these, 15 are involved with the active site. | |||
{| | {| | ||
|- valign="top" | |- valign="top" | ||
| {{enzyme | |||
| Name = factor-independent urate hydroxylase | |||
| EC_number = 1.7.3.3 | |||
| CAS_number = 9002-12-4 | |||
| IUBMB_EC_number = 1/7/3/3 | |||
| GO_code = 0004846 | |||
| image = | |||
| width = | |||
| caption = | |||
}} | |||
| {{Pfam_box | | {{Pfam_box | ||
| Symbol = Uricase | | Symbol = Uricase | ||
Line 38: | Line 48: | ||
}} | }} | ||
|} | |} | ||
== Reaction mechanism == | |||
Urate oxidase is the first in a pathway of three enzymes to convert uric acid to S-(+)-allantoin. After uric acid is converted to 5-hydroxyisourate by urate oxidase, 5-hydroxyisourate (HIU) is converted to 2-oxo-4-hydroxy-4-carboxy-5-ureidoimidazoline (OHCU) by HIU [[hydrolase]], and then to S-(+)-allantoin by [[2-oxo-4-hydroxy-4-carboxy-5-ureidoimidazoline decarboxylase]] (OHCU decarboxylase). Without HIU hydrolase and OHCU decarboxylase, HIU will spontaneously decompose into [[Racemic mixture|racemic]] allantoin.<ref>{{cite journal | vauthors = Ramazzina I, Folli C, Secchi A, Berni R, Percudani R | title = Completing the uric acid degradation pathway through phylogenetic comparison of whole genomes | language = En | journal = Nature Chemical Biology | volume = 2 | issue = 3 | pages = 144–8 | date = March 2006 | pmid = 16462750 | doi = 10.1038/nchembio768 | url = http://www.nature.com/doifinder/10.1038/nchembio768 }}</ref> | |||
Within the active site of urate oxidase, there is a catalytic site that holds uric acid and its analogues in the same orientation and a common catalytic site where oxygen, water, and hydrogen peroxide are sequentially driven. This mechanism is similar to that of [[catalase]], which reverses hydrogen peroxide back to oxygen and also sequentially drives hydrogen peroxide and water through the common catalytic site.<ref>{{cite journal | vauthors = Gabison L, Prangé T, Colloc'h N, El Hajji M, Castro B, Chiadmi M | title = Structural analysis of urate oxidase in complex with its natural substrate inhibited by cyanide: mechanistic implications | journal = BMC Structural Biology | volume = 8 | pages = 32 | date = July 2008 | pmid = 18638417 | doi = 10.1186/1472-6807-8-32 }}</ref> [[X-ray crystallography]] has shown that uric acid first binds to the active site as a monoanion, and is then deprotonated to a dianion. The dianion is stabilized by [[Arginine|Arg]] 176 and [[Glutamine|Gln]] 228 of the enzyme.<ref>{{cite journal | vauthors = Colloc'h N, el Hajji M, Bachet B, L'Hermite G, Schiltz M, Prangé T, Castro B, Mornon JP | title = Crystal structure of the protein drug urate oxidase-inhibitor complex at 2.05 A resolution | language = En | journal = Nature Structural Biology | volume = 4 | issue = 11 | pages = 947–52 | date = November 1997 | pmid = 9360612 | doi = 10.1038/nsb1197-947 }}</ref> Oxygen will subsequently accept an electron pair from the uric acid dianion and be converted to hydrogen peroxide, which is replaced by water that performs a nucleophilic attack on the intermediate to produce 5-hydroxyisourate.<ref>{{cite journal | vauthors = Oksanen E, Blakeley MP, El-Hajji M, Ryde U, Budayova-Spano M | title = The neutron structure of urate oxidase resolves a long-standing mechanistic conundrum and reveals unexpected changes in protonation | journal = PLOS One | volume = 9 | issue = 1 | pages = e86651 | date = 2014-01-23 | pmid = 24466188 | doi = 10.1371/journal.pone.0086651 }}</ref> | |||
Urate oxidase is known to be inhibited by both [[cyanide]] and [[chloride]] ions. This occurs because of anion-π interactions between the inhibitor and the uric acid substrate.<ref>{{cite journal | vauthors = Estarellas C, Frontera A, Quiñonero D, Deyà PM | title = Relevant anion-π interactions in biological systems: the case of urate oxidase | journal = Angewandte Chemie | volume = 50 | issue = 2 | pages = 415–8 | date = January 2011 | pmid = 21132687 | doi = 10.1002/anie.201005635 }}</ref> | |||
==Significance of absence in humans== | ==Significance of absence in humans== | ||
Urate oxidase is found in nearly all organisms, from [[bacteria]] to [[mammals]], but is [[Pseudogene|inactive]] in humans and several other great apes, having been lost in early [[primate]] [[evolution]]<ref name="PUB00004693" />. This means that instead of producing [[allantoin]] as the end product of [[purine]] oxidation, the pathway ends with uric acid. This leads to humans having much higher and more highly variable levels of urate in the blood than most other mammals.<ref>{{cite journal | vauthors = So A, Thorens B | title = Uric acid transport and disease | journal = The Journal of Clinical Investigation | volume = 120 | issue = 6 | pages = 1791–9 | date = June 2010 | pmid = 20516647 | pmc = 2877959 | doi = 10.1172/JCI42344 }}</ref> | |||
Genetically, the loss of urate oxidase function in humans was caused by two nonsense mutations at codons 33 and 187 and an aberrant splice site.<ref>{{cite journal | vauthors = Wu XW, Muzny DM, Lee CC, Caskey CT | title = Two independent mutational events in the loss of urate oxidase during hominoid evolution | journal = Journal of Molecular Evolution | volume = 34 | issue = 1 | pages = 78–84 | date = January 1992 | pmid = 1556746 }}</ref> | |||
It has been proposed that the loss of urate oxidase [[ | It has been proposed that the loss of urate oxidase [[gene expression]] has been advantageous to [[hominid]]s, since uric acid is a powerful [[antioxidant]] and scavenger of singlet oxygen and [[Radical (chemistry)|radical]]s.<ref name="pmid6947260">{{cite journal | vauthors = Ames BN, Cathcart R, Schwiers E, Hochstein P | title = Uric acid provides an antioxidant defense in humans against oxidant- and radical-caused aging and cancer: a hypothesis | journal = Proceedings of the National Academy of Sciences of the United States of America | volume = 78 | issue = 11 | pages = 6858–62 | date = November 1981 | pmid = 6947260 | pmc = 349151 | doi = 10.1073/pnas.78.11.6858 }}</ref> Its presence provides the body with protection from [[oxidative]] damage, thus prolonging life and decreasing age-specific cancer rates. | ||
Urate oxidase is formulated as a protein drug ([[rasburicase]]) for the treatment of acute [[hyperuricemia]] in patients receiving [[chemotherapy]]. A [[PEGylation|PEGylated]] form of urate oxidase | However, uric acid plays a complex physiological role in several processes, including [[inflammation]] and danger signalling<ref>{{cite journal | vauthors = Ghaemi-Oskouie F, Shi Y | title = The role of uric acid as an endogenous danger signal in immunity and inflammation | journal = Current Rheumatology Reports | volume = 13 | issue = 2 | pages = 160–6 | date = April 2011 | pmid = 21234729 | pmc = 3093438 | doi = 10.1007/s11926-011-0162-1 }}</ref>, and modern purine-rich diets can lead to [[Hyperuricemia|hyperuricaemia]], which is linked to many diseases including an increased risk of developing [[gout]].<ref>{{cite journal | vauthors = So A, Thorens B | title = Uric acid transport and disease | journal = The Journal of Clinical Investigation | volume = 120 | issue = 6 | pages = 1791–9 | date = June 2010 | pmid = 20516647 | pmc = 2877959 | doi = 10.1172/JCI42344 }}</ref> | ||
== Disease relevance == | |||
{{Medical citations needed|section|date=March 2018}} | |||
Urate oxidase is formulated as a protein drug ([[rasburicase]]) for the treatment of acute [[hyperuricemia]] in patients receiving [[chemotherapy]]. A [[PEGylation|PEGylated]] form of urate oxidase, [[pegloticase]], was FDA approved in 2010 for the treatment of chronic gout in adult patients refractory to "conventional therapy".<ref>{{cite web|title=Pegloticase Drug Approval Package|url=https://www.accessdata.fda.gov/drugsatfda_docs/nda/2010/125293s0000TOC.cfm|publisher=US FDA|access-date=15 May 2017}}</ref> | |||
Children with [[Non-Hodgkin lymphoma|non-Hodgkin's lymphoma]] (NHL), specifically with [[Burkitt's lymphoma]] and B-cell [[acute lymphoblastic leukemia]] (B-ALL), often experience [[tumor lysis syndrome]] (TLS), which occurs when breakdown of tumor cells by chemotherapy releases uric acid and cause the formation of uric acid crystals in the [[Nephron|renal tubules]] and [[Collecting duct system|collecting ducts]]. This can lead to [[kidney failure]] and even death. Studies suggest that patients at a high risk of developing TLS may benefit from the administration of urate oxidase.<ref>{{cite journal | vauthors = Wössmann W, Schrappe M, Meyer U, Zimmermann M, Reiter A | title = Incidence of tumor lysis syndrome in children with advanced stage Burkitt's lymphoma/leukemia before and after introduction of prophylactic use of urate oxidase | journal = Annals of Hematology | volume = 82 | issue = 3 | pages = 1605 | date = March 2003 | pmid = 12634948 | doi = 10.1007/s00277-003-0608-2 }}</ref> However, humans lack the subsequent enzyme HIU hydroxylase in the pathway to degrade uric acid to allantoin, so long-term urate oxidase therapy could potentially have harmful effects because of toxic effects of HIU.<ref>{{cite journal | vauthors = Stevenson WS, Hyland CD, Zhang JG, Morgan PO, Willson TA, Gill A, Hilton AA, Viney EM, Bahlo M, Masters SL, Hennebry S, Richardson SJ, Nicola NA, Metcalf D, Hilton DJ, Roberts AW, Alexander WS | title = Deficiency of 5-hydroxyisourate hydrolase causes hepatomegaly and hepatocellular carcinoma in mice | journal = Proceedings of the National Academy of Sciences of the United States of America | volume = 107 | issue = 38 | pages = 16625–30 | date = September 2010 | pmid = 20823251 | doi = 10.1073/pnas.1010390107 | url = http://www.pnas.org/cgi/doi/10.1073/pnas.1010390107 | pmc = 2944704 }}</ref> | |||
Higher uric acid levels have also been associated with [[epilepsy]]. However, it was found in mouse models that disrupting urate oxidase actually decreases brain excitability and susceptibility to seizures.<ref>{{cite journal | vauthors = Thyrion L, Portelli J, Raedt R, Glorieux G, Larsen LE, Sprengers M, Van Lysebettens W, Carrette E, Delbeke J, Vonck K, Boon P | title = Disruption, but not overexpression of urate oxidase alters susceptibility to pentylenetetrazole- and pilocarpine-induced seizures in mice | journal = Epilepsia | volume = 57 | issue = 7 | pages = e146-50 | date = July 2016 | pmid = 27158916 | doi = 10.1111/epi.13410 }}</ref> | |||
[[Graft-versus-host disease]] (GVHD) is often a side effect of allogeneic [[hematopoietic stem cell transplantation]] (HSCT), driven by donor [[T cell]]s destroying host tissue. Uric acid has been shown to increase T cell response, so clinical trials have shown that urate oxidase can be administered to decrease uric acid levels in the patient and subsequently decrease the likelihood of GVHD.<ref>{{cite journal | vauthors = Yeh AC, Brunner AM, Spitzer TR, Chen YB, Coughlin E, McAfee S, Ballen K, Attar E, Caron M, Preffer FI, Yeap BY, Dey BR | title = Phase I study of urate oxidase in the reduction of acute graft-versus-host disease after myeloablative allogeneic stem cell transplantation | journal = Biology of Blood and Marrow Transplantation | volume = 20 | issue = 5 | pages = 730–4 | date = May 2014 | pmid = 24530972 | doi = 10.1016/j.bbmt.2014.02.003 }}</ref> | |||
==In legumes== | ==In legumes== | ||
UO is also an essential enzyme in the ureide pathway, where [[nitrogen fixation]] occurs in the root nodules of [[legume]]s. The fixed nitrogen is converted to [[metabolite]]s that are transported from the roots throughout the plant to provide the needed nitrogen for [[amino acid]] biosynthesis. | UO is also an essential enzyme in the ureide pathway, where [[nitrogen fixation]] occurs in the root nodules of [[legume]]s. The fixed nitrogen is converted to [[metabolite]]s that are transported from the roots throughout the plant to provide the needed nitrogen for [[amino acid]] biosynthesis. | ||
In legumes, 2 forms of uricase are found: in the roots, the tetrameric form; and, in the uninfected cells of root nodules, a monomeric form, which plays an important role in nitrogen-fixation.<ref name="PUB00004611">{{cite journal | | In legumes, 2 forms of uricase are found: in the roots, the tetrameric form; and, in the uninfected cells of root nodules, a monomeric form, which plays an important role in nitrogen-fixation.<ref name="PUB00004611">{{cite journal | vauthors = Nguyen T, Zelechowska M, Foster V, Bergmann H, Verma DP | title = Primary structure of the soybean nodulin-35 gene encoding uricase II localized in the peroxisomes of uninfected cells of nodules | journal = Proceedings of the National Academy of Sciences of the United States of America | volume = 82 | issue = 15 | pages = 5040–4 | date = August 1985 | pmid = 16593585 | pmc = 390494 | doi = 10.1073/pnas.82.15.5040 }}</ref> | ||
== See also == | |||
*[[2-oxo-4-hydroxy-4-carboxy-5-ureidoimidazoline decarboxylase]] | |||
== References == | == References == | ||
{{Reflist| | {{Reflist}} | ||
{{Nucleotide metabolism}} | |||
{{Nitrogenous donor oxidoreductases}} | |||
{{Enzymes}} | |||
{{Portal bar|Molecular and Cellular Biology|border=no}} | |||
{{InterPro content|IPR002042}} | {{InterPro content|IPR002042}} | ||
[[Category:EC 1.7.3]] | |||
[[Category: |
Latest revision as of 15:01, 13 December 2018
VALUE_ERROR (nil) | |||||||
---|---|---|---|---|---|---|---|
Identifiers | |||||||
Aliases | |||||||
External IDs | GeneCards: [1] | ||||||
Orthologs | |||||||
Species | Human | Mouse | |||||
Entrez |
|
| |||||
Ensembl |
|
| |||||
UniProt |
|
| |||||
RefSeq (mRNA) |
|
| |||||
RefSeq (protein) |
|
| |||||
Location (UCSC) | n/a | n/a | |||||
PubMed search | n/a | n/a | |||||
Wikidata | |||||||
|
The enzyme urate oxidase (UO), or uricase or factor-independent urate hydroxylase, absent in humans, catalyzes the oxidation of uric acid to 5-hydroxyisourate:[1]
- Uric acid + O2 + H2O → 5-hydroxyisourate + H2O2
- 5-hydroxyisourate + H2O → allantoin + CO2
![]() |
Structure
Urate oxidase is mainly localised in the liver, where it forms a large electron-dense paracrystalline core in many peroxisomes.[2] The enzyme exists as a tetramer of identical subunits, each containing a possible type 2 copper-binding site.[3]
Urate oxidase is a homotetrameric enzyme containing four identical active sites situated at the interfaces between its four subunits. UO from A. flavus is made up of 301 residues and has a molecular weight of 33438 daltons. It is unique among the oxidases in that it does not require a metal atom or an organic co-factor for catalysis. Sequence analysis of several organisms has determined that there are 24 amino acids which are conserved, and of these, 15 are involved with the active site.
|
|
Reaction mechanism
Urate oxidase is the first in a pathway of three enzymes to convert uric acid to S-(+)-allantoin. After uric acid is converted to 5-hydroxyisourate by urate oxidase, 5-hydroxyisourate (HIU) is converted to 2-oxo-4-hydroxy-4-carboxy-5-ureidoimidazoline (OHCU) by HIU hydrolase, and then to S-(+)-allantoin by 2-oxo-4-hydroxy-4-carboxy-5-ureidoimidazoline decarboxylase (OHCU decarboxylase). Without HIU hydrolase and OHCU decarboxylase, HIU will spontaneously decompose into racemic allantoin.[4]
Within the active site of urate oxidase, there is a catalytic site that holds uric acid and its analogues in the same orientation and a common catalytic site where oxygen, water, and hydrogen peroxide are sequentially driven. This mechanism is similar to that of catalase, which reverses hydrogen peroxide back to oxygen and also sequentially drives hydrogen peroxide and water through the common catalytic site.[5] X-ray crystallography has shown that uric acid first binds to the active site as a monoanion, and is then deprotonated to a dianion. The dianion is stabilized by Arg 176 and Gln 228 of the enzyme.[6] Oxygen will subsequently accept an electron pair from the uric acid dianion and be converted to hydrogen peroxide, which is replaced by water that performs a nucleophilic attack on the intermediate to produce 5-hydroxyisourate.[7]
Urate oxidase is known to be inhibited by both cyanide and chloride ions. This occurs because of anion-π interactions between the inhibitor and the uric acid substrate.[8]
Significance of absence in humans
Urate oxidase is found in nearly all organisms, from bacteria to mammals, but is inactive in humans and several other great apes, having been lost in early primate evolution[3]. This means that instead of producing allantoin as the end product of purine oxidation, the pathway ends with uric acid. This leads to humans having much higher and more highly variable levels of urate in the blood than most other mammals.[9]
Genetically, the loss of urate oxidase function in humans was caused by two nonsense mutations at codons 33 and 187 and an aberrant splice site.[10]
It has been proposed that the loss of urate oxidase gene expression has been advantageous to hominids, since uric acid is a powerful antioxidant and scavenger of singlet oxygen and radicals.[11] Its presence provides the body with protection from oxidative damage, thus prolonging life and decreasing age-specific cancer rates.
However, uric acid plays a complex physiological role in several processes, including inflammation and danger signalling[12], and modern purine-rich diets can lead to hyperuricaemia, which is linked to many diseases including an increased risk of developing gout.[13]
Disease relevance
This section with questionable factual accuracy needs more medical references for verification or relies too heavily on primary sources. (March 2018) |
Urate oxidase is formulated as a protein drug (rasburicase) for the treatment of acute hyperuricemia in patients receiving chemotherapy. A PEGylated form of urate oxidase, pegloticase, was FDA approved in 2010 for the treatment of chronic gout in adult patients refractory to "conventional therapy".[14]
Children with non-Hodgkin's lymphoma (NHL), specifically with Burkitt's lymphoma and B-cell acute lymphoblastic leukemia (B-ALL), often experience tumor lysis syndrome (TLS), which occurs when breakdown of tumor cells by chemotherapy releases uric acid and cause the formation of uric acid crystals in the renal tubules and collecting ducts. This can lead to kidney failure and even death. Studies suggest that patients at a high risk of developing TLS may benefit from the administration of urate oxidase.[15] However, humans lack the subsequent enzyme HIU hydroxylase in the pathway to degrade uric acid to allantoin, so long-term urate oxidase therapy could potentially have harmful effects because of toxic effects of HIU.[16]
Higher uric acid levels have also been associated with epilepsy. However, it was found in mouse models that disrupting urate oxidase actually decreases brain excitability and susceptibility to seizures.[17]
Graft-versus-host disease (GVHD) is often a side effect of allogeneic hematopoietic stem cell transplantation (HSCT), driven by donor T cells destroying host tissue. Uric acid has been shown to increase T cell response, so clinical trials have shown that urate oxidase can be administered to decrease uric acid levels in the patient and subsequently decrease the likelihood of GVHD.[18]
In legumes
UO is also an essential enzyme in the ureide pathway, where nitrogen fixation occurs in the root nodules of legumes. The fixed nitrogen is converted to metabolites that are transported from the roots throughout the plant to provide the needed nitrogen for amino acid biosynthesis.
In legumes, 2 forms of uricase are found: in the roots, the tetrameric form; and, in the uninfected cells of root nodules, a monomeric form, which plays an important role in nitrogen-fixation.[19]
See also
References
- ↑ Motojima K, Kanaya S, Goto S (November 1988). "Cloning and sequence analysis of cDNA for rat liver uricase". The Journal of Biological Chemistry. 263 (32): 16677–81. PMID 3182808.
- ↑ Motojima K, Goto S (May 1990). "Organization of rat uricase chromosomal gene differs greatly from that of the corresponding plant gene". FEBS Letters. 264 (1): 156–8. doi:10.1016/0014-5793(90)80789-L. PMID 2338140.
- ↑ 3.0 3.1 Wu XW, Lee CC, Muzny DM, Caskey CT (December 1989). "Urate oxidase: primary structure and evolutionary implications". Proceedings of the National Academy of Sciences of the United States of America. 86 (23): 9412–6. doi:10.1073/pnas.86.23.9412. PMC 298506. PMID 2594778.
- ↑ Ramazzina I, Folli C, Secchi A, Berni R, Percudani R (March 2006). "Completing the uric acid degradation pathway through phylogenetic comparison of whole genomes". Nature Chemical Biology. 2 (3): 144–8. doi:10.1038/nchembio768. PMID 16462750.
- ↑ Gabison L, Prangé T, Colloc'h N, El Hajji M, Castro B, Chiadmi M (July 2008). "Structural analysis of urate oxidase in complex with its natural substrate inhibited by cyanide: mechanistic implications". BMC Structural Biology. 8: 32. doi:10.1186/1472-6807-8-32. PMID 18638417.
- ↑ Colloc'h N, el Hajji M, Bachet B, L'Hermite G, Schiltz M, Prangé T, Castro B, Mornon JP (November 1997). "Crystal structure of the protein drug urate oxidase-inhibitor complex at 2.05 A resolution". Nature Structural Biology. 4 (11): 947–52. doi:10.1038/nsb1197-947. PMID 9360612.
- ↑ Oksanen E, Blakeley MP, El-Hajji M, Ryde U, Budayova-Spano M (2014-01-23). "The neutron structure of urate oxidase resolves a long-standing mechanistic conundrum and reveals unexpected changes in protonation". PLOS One. 9 (1): e86651. doi:10.1371/journal.pone.0086651. PMID 24466188.
- ↑ Estarellas C, Frontera A, Quiñonero D, Deyà PM (January 2011). "Relevant anion-π interactions in biological systems: the case of urate oxidase". Angewandte Chemie. 50 (2): 415–8. doi:10.1002/anie.201005635. PMID 21132687.
- ↑ So A, Thorens B (June 2010). "Uric acid transport and disease". The Journal of Clinical Investigation. 120 (6): 1791–9. doi:10.1172/JCI42344. PMC 2877959. PMID 20516647.
- ↑ Wu XW, Muzny DM, Lee CC, Caskey CT (January 1992). "Two independent mutational events in the loss of urate oxidase during hominoid evolution". Journal of Molecular Evolution. 34 (1): 78–84. PMID 1556746.
- ↑ Ames BN, Cathcart R, Schwiers E, Hochstein P (November 1981). "Uric acid provides an antioxidant defense in humans against oxidant- and radical-caused aging and cancer: a hypothesis". Proceedings of the National Academy of Sciences of the United States of America. 78 (11): 6858–62. doi:10.1073/pnas.78.11.6858. PMC 349151. PMID 6947260.
- ↑ Ghaemi-Oskouie F, Shi Y (April 2011). "The role of uric acid as an endogenous danger signal in immunity and inflammation". Current Rheumatology Reports. 13 (2): 160–6. doi:10.1007/s11926-011-0162-1. PMC 3093438. PMID 21234729.
- ↑ So A, Thorens B (June 2010). "Uric acid transport and disease". The Journal of Clinical Investigation. 120 (6): 1791–9. doi:10.1172/JCI42344. PMC 2877959. PMID 20516647.
- ↑ "Pegloticase Drug Approval Package". US FDA. Retrieved 15 May 2017.
- ↑ Wössmann W, Schrappe M, Meyer U, Zimmermann M, Reiter A (March 2003). "Incidence of tumor lysis syndrome in children with advanced stage Burkitt's lymphoma/leukemia before and after introduction of prophylactic use of urate oxidase". Annals of Hematology. 82 (3): 1605. doi:10.1007/s00277-003-0608-2. PMID 12634948.
- ↑ Stevenson WS, Hyland CD, Zhang JG, Morgan PO, Willson TA, Gill A, Hilton AA, Viney EM, Bahlo M, Masters SL, Hennebry S, Richardson SJ, Nicola NA, Metcalf D, Hilton DJ, Roberts AW, Alexander WS (September 2010). "Deficiency of 5-hydroxyisourate hydrolase causes hepatomegaly and hepatocellular carcinoma in mice". Proceedings of the National Academy of Sciences of the United States of America. 107 (38): 16625–30. doi:10.1073/pnas.1010390107. PMC 2944704. PMID 20823251.
- ↑ Thyrion L, Portelli J, Raedt R, Glorieux G, Larsen LE, Sprengers M, Van Lysebettens W, Carrette E, Delbeke J, Vonck K, Boon P (July 2016). "Disruption, but not overexpression of urate oxidase alters susceptibility to pentylenetetrazole- and pilocarpine-induced seizures in mice". Epilepsia. 57 (7): e146–50. doi:10.1111/epi.13410. PMID 27158916.
- ↑ Yeh AC, Brunner AM, Spitzer TR, Chen YB, Coughlin E, McAfee S, Ballen K, Attar E, Caron M, Preffer FI, Yeap BY, Dey BR (May 2014). "Phase I study of urate oxidase in the reduction of acute graft-versus-host disease after myeloablative allogeneic stem cell transplantation". Biology of Blood and Marrow Transplantation. 20 (5): 730–4. doi:10.1016/j.bbmt.2014.02.003. PMID 24530972.
- ↑ Nguyen T, Zelechowska M, Foster V, Bergmann H, Verma DP (August 1985). "Primary structure of the soybean nodulin-35 gene encoding uricase II localized in the peroxisomes of uninfected cells of nodules". Proceedings of the National Academy of Sciences of the United States of America. 82 (15): 5040–4. doi:10.1073/pnas.82.15.5040. PMC 390494. PMID 16593585.
- Genes on human chromosome
- Pages with broken file links
- Protein pages needing a picture
- Articles needing additional medical references from March 2018
- Articles with invalid date parameter in template
- All articles needing additional references
- Articles requiring reliable medical sources
- Portal templates with all redlinked portals
- EC 1.7.3