Details of Protein
General Information of Protein (ID: PRT00319) | |||||
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Name | Kynureninase (KYNU) | ||||
Synonyms |
Click to Show/Hide Synonyms of This Protein
L-kynurenine hydrolase; KYNU
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Gene Name | KYNU | Gene ID | |||
UniProt ID | |||||
Family | Hydrolases (EC 3) | ||||
EC Number | EC: 3.7.1.3 (Click to Show/Hide the Complete EC Tree) | ||||
Click to Show/Hide the Molecular/Functional Data (Sequence/Structure/Function) of This Protein | |||||
Sequence |
MEPSSLELPADTVQRIAAELKCHPTDERVALHLDEEDKLRHFRECFYIPKIQDLPPVDLS
LVNKDENAIYFLGNSLGLQPKMVKTYLEEELDKWAKIAAYGHEVGKRPWITGDESIVGLM KDIVGANEKEIALMNALTVNLHLLMLSFFKPTPKRYKILLEAKAFPSDHYAIESQLQLHG LNIEESMRMIKPREGEETLRIEDILEVIEKEGDSIAVILFSGVHFYTGQHFNIPAITKAG QAKGCYVGFDLAHAVGNVELYLHDWGVDFACWCSYKYLNAGAGGIAGAFIHEKHAHTIKP ALVGWFGHELSTRFKMDNKLQLIPGVCGFRISNPPILLVCSLHASLEIFKQATMKALRKK SVLLTGYLEYLIKHNYGKDKAATKKPVVNIITPSHVEERGCQLTITFSVPNKDVFQELEK RGVVCDKRNPNGIRVAPVPLYNSFHDVYKFTNLLTSILDSAETKN |
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Structure | |||||
Function | Catalyzes the cleavage of L-kynurenine (L-Kyn) and L-3-hydroxykynurenine (L-3OHKyn) into anthranilic acid (AA) and 3-hydroxyanthranilic acid (3-OHAA), respectively. Has a preference for the L-3-hydroxy form. Also has cysteine-conjugate-beta-lyase activity. | ||||
Regulatory Network | |||||
Full List of Metabolite(s) Regulated by This Protein | ||||||
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Nucleosides, nucleotides, and analogues | ||||||
NAD | Click to Show/Hide the Full List of Regulating Pair(s): 1 Pair(s) | |||||
Detailed Information |
Metabo Info
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Regulating Pair |
Experim Info
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[1] | ||||
Introduced Variation | Mutation (c.468T-A, c.1045_1051delTTTAAGC) of KYNU | |||||
Induced Change | NAD concentration: decrease | |||||
Summary | Introduced Variation
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Disease Status | Hereditary methemoglobinemia [ICD-11: 3A92] | |||||
Details | It is reported that mutation (c.468T-A, c.1045_1051delTTTAAGC) of KYNU leads to the decrease of NAD levels compared with control group. | |||||
Organic oxygen compounds | ||||||
L-3-Hydroxykynurenine | Click to Show/Hide the Full List of Regulating Pair(s): 1 Pair(s) | |||||
Detailed Information |
Metabo Info
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Regulating Pair |
Experim Info
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[1] | ||||
Introduced Variation | Mutation (c.468T-A, c.1045_1051delTTTAAGC) of KYNU | |||||
Induced Change | L-3-Hydroxykynurenine concentration: increase (FC = 160.7) | |||||
Summary | Introduced Variation
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Disease Status | Hereditary methemoglobinemia [ICD-11: 3A92] | |||||
Details | It is reported that mutation (c.468T-A, c.1045_1051delTTTAAGC) of KYNU leads to the increase of L-3-hydroxykynurenine levels compared with control group. | |||||
L-Kynurenine | Click to Show/Hide the Full List of Regulating Pair(s): 1 Pair(s) | |||||
Detailed Information |
Metabo Info
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Regulating Pair |
Experim Info
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[1] | ||||
Introduced Variation | Mutation (c.468T-A, c.1045_1051delTTTAAGC) of KYNU | |||||
Induced Change | L-Kynurenine concentration: increase (FC = 2.3) | |||||
Summary | Introduced Variation
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Disease Status | Hereditary methemoglobinemia [ICD-11: 3A92] | |||||
Details | It is reported that mutation (c.468T-A, c.1045_1051delTTTAAGC) of KYNU leads to the increase of L-kynurenine levels compared with control group. | |||||
Organoheterocyclic compounds | ||||||
Picolinic acid | Click to Show/Hide the Full List of Regulating Pair(s): 1 Pair(s) | |||||
Detailed Information |
Metabo Info
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Regulating Pair |
Experim Info
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[1] | ||||
Introduced Variation | Mutation (c.468T-A, c.1045_1051delTTTAAGC) of KYNU | |||||
Induced Change | Picolinic acid concentration: increase (FC = 1.4) | |||||
Summary | Introduced Variation
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Disease Status | Hereditary methemoglobinemia [ICD-11: 3A92] | |||||
Details | It is reported that mutation (c.468T-A, c.1045_1051delTTTAAGC) of KYNU leads to the increase of picolinic acid levels compared with control group. | |||||
Tryptophan | Click to Show/Hide the Full List of Regulating Pair(s): 1 Pair(s) | |||||
Detailed Information |
Metabo Info
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Regulating Pair |
Experim Info
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[1] | ||||
Introduced Variation | Mutation (c.468T-A, c.1045_1051delTTTAAGC) of KYNU | |||||
Induced Change | Tryptophan concentration: increase (FC = 1.2) | |||||
Summary | Introduced Variation
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Disease Status | Hereditary methemoglobinemia [ICD-11: 3A92] | |||||
Details | It is reported that mutation (c.468T-A, c.1045_1051delTTTAAGC) of KYNU leads to the increase of tryptophan levels compared with control group. | |||||
References | |||||
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1 | NAD Deficiency, Congenital Malformations, and Niacin Supplementation. N Engl J Med. 2017 Aug 10;377(6):544-552. |
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