| EC Number | Cloned (Comment) | Organism |
|---|---|---|
| 1.13.11.31 | sequence comparisons and phylogenetic analysis | Homo sapiens |
| 1.13.11.31 | sequence comparisons and phylogenetic analysis | Macaca mulatta |
| 1.13.11.31 | sequence comparisons and phylogenetic analysis | Nomascus leucogenys |
| 1.13.11.31 | sequence comparisons and phylogenetic analysis | Oryctolagus cuniculus |
| 1.13.11.31 | sequence comparisons and phylogenetic analysis | Pan paniscus |
| 1.13.11.31 | sequence comparisons and phylogenetic analysis | Pan troglodytes |
| 1.13.11.31 | sequence comparisons and phylogenetic analysis | Papio anubis |
| 1.13.11.31 | sequence comparisons and phylogenetic analysis | Pongo abelii |
| 1.13.11.31 | sequence comparisons and phylogenetic analysis | Pongo pygmaeus |
| 1.13.11.33 | sequence comparisons and phylogenetic analysis | Homo sapiens |
| 1.13.11.33 | sequence comparisons and phylogenetic analysis | Macaca mulatta |
| 1.13.11.33 | sequence comparisons and phylogenetic analysis | Nomascus leucogenys |
| 1.13.11.33 | sequence comparisons and phylogenetic analysis | Oryctolagus cuniculus |
| 1.13.11.33 | sequence comparisons and phylogenetic analysis | Pan paniscus |
| 1.13.11.33 | sequence comparisons and phylogenetic analysis | Pan troglodytes |
| 1.13.11.33 | sequence comparisons and phylogenetic analysis | Papio anubis |
| 1.13.11.33 | sequence comparisons and phylogenetic analysis | Pongo abelii |
| 1.13.11.33 | sequence comparisons and phylogenetic analysis | Pongo pygmaeus |
| EC Number | Protein Variants | Comment | Organism |
|---|---|---|---|
| 1.13.11.31 | I417A | naturally occuring mutation, the mutant produces 94% 12-hydroperoxyicosatetraenoate and 6% 15-hydroperoxyicosatetraenoate, in contrast to the wild-type, that produces 15% 12-hydroperoxyicosatetraenoate and 85% 15-hydroperoxyicosatetraenoate | Homo sapiens |
| 1.13.11.31 | I417A | naturally occuring mutation, the mutant produces 82% 12-hydroperoxyicosatetraenoate and 18% 15-hydroperoxyicosatetraenoate, in contrast to the wild-type, that produces 14% 12-hydroperoxyicosatetraenoate and 86% 15-hydroperoxyicosatetraenoate | Pongo pygmaeus |
| 1.13.11.31 | I418A | naturally occuring mutation, the mutant produces exclusively 12-hydroperoxyicosatetraenoate and almost no 15-hydroperoxyicosatetraenoate, in contrast to the wild-type, that produces about equal amounts of both | Nomascus leucogenys |
| 1.13.11.31 | I418A | naturally occuring mutation, the mutant produces 92% 12-hydroperoxyicosatetraenoate and 8% 15-hydroperoxyicosatetraenoate, in contrast to the wild-type, that produces 3% 12-hydroperoxyicosatetraenoate and 97% 15-hydroperoxyicosatetraenoate | Oryctolagus cuniculus |
| 1.13.11.31 | I418F | naturally occuring mutation, the mutant produces more 15-hydroperoxyicosatetraenoate compared to 12-hydroperoxyicosatetraenoate, in contrast to the wild-type, that produces about equal amounts of both | Nomascus leucogenys |
| 1.13.11.31 | I419A | naturally occuring mutation, the mutant produces exclusively 12-hydroperoxyicosatetraenoate and almost no 15-hydroperoxyicosatetraenoate, in contrast to the wild-type, that produces about 80% 15-hydroperoxyicosatetraenoate | Pan troglodytes |
| 1.13.11.31 | M419T | naturally occuring mutation, the mutant produces more 12-hydroperoxyicosatetraenoate compared to 15-hydroperoxyicosatetraenoate, incontrast to the wild-type, inversed substrate specificity | Homo sapiens |
| 1.13.11.31 | T594V | naturally occuring mutation, the mutant produces more 12-hydroperoxyicosatetraenoate compared to 15-hydroperoxyicosatetraenoate, incontrast to the wild-type, inversed substrate specificity | Homo sapiens |
| 1.13.11.33 | I417A | naturally occuring mutation, the mutant produces 82% 12-hydroperoxyicosatetraenoate and 18% 15-hydroperoxyicosatetraenoate, in contrast to the wild-type, that produces 14% 12-hydroperoxyicosatetraenoate and 86% 15-hydroperoxyicosatetraenoate | Pongo pygmaeus |
| 1.13.11.33 | I417A | naturally occuring mutation, the mutant produces 94% 12-hydroperoxyicosatetraenoate and 6% 15-hydroperoxyicosatetraenoate, in contrast to the wild-type, that produces 15% 12-hydroperoxyicosatetraenoate and 85% 15-hydroperoxyicosatetraenoate | Homo sapiens |
| 1.13.11.33 | I418A | naturally occuring mutation, the mutant produces 92% 12-hydroperoxyicosatetraenoate and 8% 15-hydroperoxyicosatetraenoate, in contrast to the wild-type, that produces 3% 12-hydroperoxyicosatetraenoate and 97% 15-hydroperoxyicosatetraenoate | Oryctolagus cuniculus |
| 1.13.11.33 | I418A | naturally occuring mutation, the mutant produces exclusively 12-hydroperoxyicosatetraenoate and almost no 15-hydroperoxyicosatetraenoate, in contrast to the wild-type, that produces about equal amounts of both | Nomascus leucogenys |
| 1.13.11.33 | I418F | naturally occuring mutation, the mutant produces more 15-hydroperoxyicosatetraenoate compared to 12-hydroperoxyicosatetraenoate, in contrast to the wild-type, that produces about equal amounts of both | Nomascus leucogenys |
| 1.13.11.33 | I419A | naturally occuring mutation, the mutant produces exclusively 12-hydroperoxyicosatetraenoate and almost no 15-hydroperoxyicosatetraenoate, in contrast to the wild-type, that produces about 80% 15-hydroperoxyicosatetraenoate | Pan troglodytes |
| 1.13.11.33 | M419T | naturally occuring mutation, the mutant produces more 12-hydroperoxyicosatetraenoate compared to 15-hydroperoxyicosatetraenoate, incontrast to the wild-type, inversed substrate specificity | Homo sapiens |
| 1.13.11.33 | T594V | naturally occuring mutation, the mutant produces more 12-hydroperoxyicosatetraenoate compared to 15-hydroperoxyicosatetraenoate, incontrast to the wild-type, inversed substrate specificity | Homo sapiens |
| EC Number | Natural Substrates | Organism | Comment (Nat. Sub.) | Natural Products | Comment (Nat. Pro.) | Rev. | Reac. |
|---|---|---|---|---|---|---|---|
| 1.13.11.31 | arachidonate + O2 | Homo sapiens | - |
(5Z,8Z,10E,14Z)-(12S)-12-hydroperoxyicosa-5,8,10,14-tetraenoate | - |
? | |
| 1.13.11.31 | arachidonate + O2 | Nomascus leucogenys | - |
(5Z,8Z,10E,14Z)-(12S)-12-hydroperoxyicosa-5,8,10,14-tetraenoate | - |
? | |
| 1.13.11.31 | arachidonate + O2 | Pan troglodytes | - |
(5Z,8Z,10E,14Z)-(12S)-12-hydroperoxyicosa-5,8,10,14-tetraenoate | - |
? | |
| 1.13.11.31 | arachidonate + O2 | Pongo pygmaeus | - |
(5Z,8Z,10E,14Z)-(12S)-12-hydroperoxyicosa-5,8,10,14-tetraenoate | - |
? | |
| 1.13.11.31 | arachidonate + O2 | Oryctolagus cuniculus | - |
(5Z,8Z,10E,14Z)-(12S)-12-hydroperoxyicosa-5,8,10,14-tetraenoate | - |
? | |
| 1.13.11.31 | arachidonate + O2 | Papio anubis | - |
(5Z,8Z,10E,14Z)-(12S)-12-hydroperoxyicosa-5,8,10,14-tetraenoate | - |
? | |
| 1.13.11.31 | arachidonate + O2 | Homo sapiens neanderthalensis | - |
(5Z,8Z,10E,14Z)-(12S)-12-hydroperoxyicosa-5,8,10,14-tetraenoate | - |
? | |
| 1.13.11.31 | arachidonate + O2 | Homo sapiens subsp. 'Denisova' | - |
(5Z,8Z,10E,14Z)-(12S)-12-hydroperoxyicosa-5,8,10,14-tetraenoate | - |
? | |
| 1.13.11.31 | arachidonate + O2 | Macaca mulatta | - |
(5Z,8Z,10E,14Z)-(12S)-12-hydroperoxyicosa-5,8,10,14-tetraenoate | - |
? | |
| 1.13.11.31 | arachidonate + O2 | Pongo abelii | - |
(5Z,8Z,10E,14Z)-(12S)-12-hydroperoxyicosa-5,8,10,14-tetraenoate | - |
? | |
| 1.13.11.31 | arachidonate + O2 | Pan paniscus | - |
(5Z,8Z,10E,14Z)-(12S)-12-hydroperoxyicosa-5,8,10,14-tetraenoate | - |
? | |
| 1.13.11.31 | additional information | Homo sapiens | 15-lipoxygenating ALOX15 orthologs exhibit significantly higher lipoxin-synthesizing capacities than 12-lipoxygenating. Product pattern of primate ALOX15 orthologues, overview. The wild-type subject produces 21% 12-hydroperoxyicosatetraenoate and 79% 15-hydroperoxyicosatetraenoate | ? | - |
? | |
| 1.13.11.31 | additional information | Nomascus leucogenys | 15-lipoxygenating ALOX15 orthologs exhibit significantly higher lipoxin-synthesizing capacities than 12-lipoxygenating. Product pattern of primate ALOX15 orthologues, overview. The wild-type animal produces 54% 12-hydroperoxyicosatetraenoate and 46% 15-hydroperoxyicosatetraenoate with 76% overall activity compared to the human enzyme activity | ? | - |
? | |
| 1.13.11.31 | additional information | Pan troglodytes | 15-lipoxygenating ALOX15 orthologs exhibit significantly higher lipoxin-synthesizing capacities than 12-lipoxygenating. Product pattern of primate ALOX15 orthologues, overview. The wild-type animal produces 20% 12-hydroperoxyicosatetraenoate and 80% 15-hydroperoxyicosatetraenoate with 135% overall activity compared to the human enzyme activity | ? | - |
? | |
| 1.13.11.31 | additional information | Pongo pygmaeus | 15-lipoxygenating ALOX15 orthologs exhibit significantly higher lipoxin-synthesizing capacities than 12-lipoxygenating. Product pattern of primate ALOX15 orthologues, overview. The wild-type animal produces 14% 12-hydroperoxyicosatetraenoate and 86% 15-hydroperoxyicosatetraenoate | ? | - |
? | |
| 1.13.11.31 | additional information | Oryctolagus cuniculus | 15-lipoxygenating ALOX15 orthologs exhibit significantly higher lipoxin-synthesizing capacities than 12-lipoxygenating. Product pattern of primate ALOX15 orthologues, overview. The wild-type animal produces 3% 12-hydroperoxyicosatetraenoate and 97% 15-hydroperoxyicosatetraenoate | ? | - |
? | |
| 1.13.11.31 | additional information | Papio anubis | 15-lipoxygenating ALOX15 orthologs exhibit significantly higher lipoxin-synthesizing capacities than 12-lipoxygenating. Product pattern of primate ALOX15 orthologues, overview. The wild-type animal produces 78% 12-hydroperoxyicosatetraenoate and 22% 15-hydroperoxyicosatetraenoate with 37% overall activity compared to the human enzyme activity | ? | - |
? | |
| 1.13.11.31 | additional information | Homo sapiens neanderthalensis | 15-lipoxygenating ALOX15 orthologs exhibit significantly higher lipoxin-synthesizing capacities than 12-lipoxygenating. Product pattern of primate ALOX15 orthologues, overview | ? | - |
? | |
| 1.13.11.31 | additional information | Homo sapiens subsp. 'Denisova' | 15-lipoxygenating ALOX15 orthologs exhibit significantly higher lipoxin-synthesizing capacities than 12-lipoxygenating. Product pattern of primate ALOX15 orthologues, overview | ? | - |
? | |
| 1.13.11.31 | additional information | Macaca mulatta | 15-lipoxygenating ALOX15 orthologs exhibit significantly higher lipoxin-synthesizing capacities than 12-lipoxygenating. Product pattern of primate ALOX15 orthologues, overview | ? | - |
? | |
| 1.13.11.31 | additional information | Pongo abelii | 15-lipoxygenating ALOX15 orthologs exhibit significantly higher lipoxin-synthesizing capacities than 12-lipoxygenating. Product pattern of primate ALOX15 orthologues, overview | ? | - |
? | |
| 1.13.11.31 | additional information | Pan paniscus | 15-lipoxygenating ALOX15 orthologs exhibit significantly higher lipoxin-synthesizing capacities than 12-lipoxygenating. Product pattern of primate ALOX15 orthologues, overview | ? | - |
? | |
| 1.13.11.33 | arachidonate + O2 | Pongo pygmaeus | - |
(5Z,8Z,11Z,13E)-(15S)-15-hydroperoxyicosa-5,8,11,13-tetraenoate | - |
? | |
| 1.13.11.33 | arachidonate + O2 | Oryctolagus cuniculus | - |
(5Z,8Z,11Z,13E)-(15S)-15-hydroperoxyicosa-5,8,11,13-tetraenoate | - |
? | |
| 1.13.11.33 | arachidonate + O2 | Papio anubis | - |
(5Z,8Z,11Z,13E)-(15S)-15-hydroperoxyicosa-5,8,11,13-tetraenoate | - |
? | |
| 1.13.11.33 | arachidonate + O2 | Homo sapiens neanderthalensis | - |
(5Z,8Z,11Z,13E)-(15S)-15-hydroperoxyicosa-5,8,11,13-tetraenoate | - |
? | |
| 1.13.11.33 | arachidonate + O2 | Homo sapiens subsp. 'Denisova' | - |
(5Z,8Z,11Z,13E)-(15S)-15-hydroperoxyicosa-5,8,11,13-tetraenoate | - |
? | |
| 1.13.11.33 | arachidonate + O2 | Macaca mulatta | - |
(5Z,8Z,11Z,13E)-(15S)-15-hydroperoxyicosa-5,8,11,13-tetraenoate | - |
? | |
| 1.13.11.33 | arachidonate + O2 | Pongo abelii | - |
(5Z,8Z,11Z,13E)-(15S)-15-hydroperoxyicosa-5,8,11,13-tetraenoate | - |
? | |
| 1.13.11.33 | arachidonate + O2 | Pan paniscus | - |
(5Z,8Z,11Z,13E)-(15S)-15-hydroperoxyicosa-5,8,11,13-tetraenoate | - |
? | |
| 1.13.11.33 | arachidonate + O2 | Homo sapiens | - |
(5Z,8Z,11Z,13E)-(15S)-15-hydroperoxyicosa-5,8,11,13-tetraenoate | - |
? | |
| 1.13.11.33 | arachidonate + O2 | Nomascus leucogenys | - |
(5Z,8Z,11Z,13E)-(15S)-15-hydroperoxyicosa-5,8,11,13-tetraenoate | - |
? | |
| 1.13.11.33 | arachidonate + O2 | Pan troglodytes | - |
(5Z,8Z,11Z,13E)-(15S)-15-hydroperoxyicosa-5,8,11,13-tetraenoate | - |
? | |
| 1.13.11.33 | additional information | Pongo pygmaeus | 15-lipoxygenating ALOX15 orthologs exhibit significantly higher lipoxin-synthesizing capacities than 12-lipoxygenating. Product pattern of primate ALOX15 orthologues, overview. The wild-type animal produces 14% 12-hydroperoxyicosatetraenoate and 86% 15-hydroperoxyicosatetraenoate | ? | - |
? | |
| 1.13.11.33 | additional information | Oryctolagus cuniculus | 15-lipoxygenating ALOX15 orthologs exhibit significantly higher lipoxin-synthesizing capacities than 12-lipoxygenating. The wild-type animal produces 3% 12-hydroperoxyicosatetraenoate and 97% 15-hydroperoxyicosatetraenoate | ? | - |
? | |
| 1.13.11.33 | additional information | Papio anubis | 15-lipoxygenating ALOX15 orthologs exhibit significantly higher lipoxin-synthesizing capacities than 12-lipoxygenating. Product pattern of primate ALOX15 orthologues, overview. The wild-type animal produces 78% 12-hydroperoxyicosatetraenoate and 22% 15-hydroperoxyicosatetraenoate with 37% overall activity compared to the human enzyme activity | ? | - |
? | |
| 1.13.11.33 | additional information | Homo sapiens neanderthalensis | 15-lipoxygenating ALOX15 orthologs exhibit significantly higher lipoxin-synthesizing capacities than 12-lipoxygenating. Product pattern of primate ALOX15 orthologues, overview | ? | - |
? | |
| 1.13.11.33 | additional information | Homo sapiens subsp. 'Denisova' | 15-lipoxygenating ALOX15 orthologs exhibit significantly higher lipoxin-synthesizing capacities than 12-lipoxygenating. Product pattern of primate ALOX15 orthologues, overview | ? | - |
? | |
| 1.13.11.33 | additional information | Macaca mulatta | 15-lipoxygenating ALOX15 orthologs exhibit significantly higher lipoxin-synthesizing capacities than 12-lipoxygenating. Product pattern of primate ALOX15 orthologues, overview | ? | - |
? | |
| 1.13.11.33 | additional information | Pongo abelii | 15-lipoxygenating ALOX15 orthologs exhibit significantly higher lipoxin-synthesizing capacities than 12-lipoxygenating. Product pattern of primate ALOX15 orthologues, overview | ? | - |
? | |
| 1.13.11.33 | additional information | Pan paniscus | 15-lipoxygenating ALOX15 orthologs exhibit significantly higher lipoxin-synthesizing capacities than 12-lipoxygenating. Product pattern of primate ALOX15 orthologues, overview | ? | - |
? | |
| 1.13.11.33 | additional information | Homo sapiens | 15-lipoxygenating ALOX15 orthologs exhibit significantly higher lipoxin-synthesizing capacities than 12-lipoxygenating. Product pattern of primate ALOX15 orthologues, overview. The wild-type subject produces 21% 12-hydroperoxyicosatetraenoate and 79% 15-hydroperoxyicosatetraenoate | ? | - |
? | |
| 1.13.11.33 | additional information | Nomascus leucogenys | 15-lipoxygenating ALOX15 orthologs exhibit significantly higher lipoxin-synthesizing capacities than 12-lipoxygenating. Product pattern of primate ALOX15 orthologues, overview. The wild-type animal produces 54% 12-hydroperoxyicosatetraenoate and 46% 15-hydroperoxyicosatetraenoate with 76% overall activity compared to the human enzyme activity | ? | - |
? | |
| 1.13.11.33 | additional information | Pan troglodytes | 15-lipoxygenating ALOX15 orthologs exhibit significantly higher lipoxin-synthesizing capacities than 12-lipoxygenating. Product pattern of primate ALOX15 orthologues, overview. The wild-type animal produces 20% 12-hydroperoxyicosatetraenoate and 80% 15-hydroperoxyicosatetraenoate with 135% overall activity compared to the human enzyme activity | ? | - |
? |
| EC Number | Organism | UniProt | Comment | Textmining |
|---|---|---|---|---|
| 1.13.11.31 | Homo sapiens | P16050 | - |
- |
| 1.13.11.31 | Homo sapiens neanderthalensis | - |
- |
- |
| 1.13.11.31 | Homo sapiens subsp. 'Denisova' | - |
- |
- |
| 1.13.11.31 | Macaca mulatta | F7EPQ4 | - |
- |
| 1.13.11.31 | Nomascus leucogenys | G1S6D2 | - |
- |
| 1.13.11.31 | Oryctolagus cuniculus | P12530 | - |
- |
| 1.13.11.31 | Pan paniscus | - |
- |
- |
| 1.13.11.31 | Pan troglodytes | H2QBX9 | - |
- |
| 1.13.11.31 | Papio anubis | A0A096P2G1 | - |
- |
| 1.13.11.31 | Pongo abelii | Q5RBE8 | - |
- |
| 1.13.11.31 | Pongo pygmaeus | Q5RBE8 | - |
- |
| 1.13.11.33 | Homo sapiens | P16050 | - |
- |
| 1.13.11.33 | Homo sapiens neanderthalensis | - |
- |
- |
| 1.13.11.33 | Homo sapiens subsp. 'Denisova' | - |
- |
- |
| 1.13.11.33 | Macaca mulatta | F7EPQ4 | - |
- |
| 1.13.11.33 | Nomascus leucogenys | G1S6D2 | - |
- |
| 1.13.11.33 | Oryctolagus cuniculus | P12530 | - |
- |
| 1.13.11.33 | Pan paniscus | - |
- |
- |
| 1.13.11.33 | Pan troglodytes | H2QBX9 | - |
- |
| 1.13.11.33 | Papio anubis | A0A096P2G1 | - |
- |
| 1.13.11.33 | Pongo abelii | Q5RBE8 | - |
- |
| 1.13.11.33 | Pongo pygmaeus | Q5RBE8 | - |
- |
| EC Number | Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
|---|---|---|---|---|---|---|---|
| 1.13.11.31 | arachidonate + O2 | - |
Homo sapiens | (5Z,8Z,10E,14Z)-(12S)-12-hydroperoxyicosa-5,8,10,14-tetraenoate | - |
? | |
| 1.13.11.31 | arachidonate + O2 | - |
Nomascus leucogenys | (5Z,8Z,10E,14Z)-(12S)-12-hydroperoxyicosa-5,8,10,14-tetraenoate | - |
? | |
| 1.13.11.31 | arachidonate + O2 | - |
Pan troglodytes | (5Z,8Z,10E,14Z)-(12S)-12-hydroperoxyicosa-5,8,10,14-tetraenoate | - |
? | |
| 1.13.11.31 | arachidonate + O2 | - |
Pongo pygmaeus | (5Z,8Z,10E,14Z)-(12S)-12-hydroperoxyicosa-5,8,10,14-tetraenoate | - |
? | |
| 1.13.11.31 | arachidonate + O2 | - |
Oryctolagus cuniculus | (5Z,8Z,10E,14Z)-(12S)-12-hydroperoxyicosa-5,8,10,14-tetraenoate | - |
? | |
| 1.13.11.31 | arachidonate + O2 | - |
Papio anubis | (5Z,8Z,10E,14Z)-(12S)-12-hydroperoxyicosa-5,8,10,14-tetraenoate | - |
? | |
| 1.13.11.31 | arachidonate + O2 | - |
Homo sapiens neanderthalensis | (5Z,8Z,10E,14Z)-(12S)-12-hydroperoxyicosa-5,8,10,14-tetraenoate | - |
? | |
| 1.13.11.31 | arachidonate + O2 | - |
Homo sapiens subsp. 'Denisova' | (5Z,8Z,10E,14Z)-(12S)-12-hydroperoxyicosa-5,8,10,14-tetraenoate | - |
? | |
| 1.13.11.31 | arachidonate + O2 | - |
Macaca mulatta | (5Z,8Z,10E,14Z)-(12S)-12-hydroperoxyicosa-5,8,10,14-tetraenoate | - |
? | |
| 1.13.11.31 | arachidonate + O2 | - |
Pongo abelii | (5Z,8Z,10E,14Z)-(12S)-12-hydroperoxyicosa-5,8,10,14-tetraenoate | - |
? | |
| 1.13.11.31 | arachidonate + O2 | - |
Pan paniscus | (5Z,8Z,10E,14Z)-(12S)-12-hydroperoxyicosa-5,8,10,14-tetraenoate | - |
? | |
| 1.13.11.31 | additional information | 15-lipoxygenating ALOX15 orthologs exhibit significantly higher lipoxin-synthesizing capacities than 12-lipoxygenating. Product pattern of primate ALOX15 orthologues, overview. The wild-type subject produces 21% 12-hydroperoxyicosatetraenoate and 79% 15-hydroperoxyicosatetraenoate | Homo sapiens | ? | - |
? | |
| 1.13.11.31 | additional information | 15-lipoxygenating ALOX15 orthologs exhibit significantly higher lipoxin-synthesizing capacities than 12-lipoxygenating. Product pattern of primate ALOX15 orthologues, overview. The wild-type animal produces 54% 12-hydroperoxyicosatetraenoate and 46% 15-hydroperoxyicosatetraenoate with 76% overall activity compared to the human enzyme activity | Nomascus leucogenys | ? | - |
? | |
| 1.13.11.31 | additional information | 15-lipoxygenating ALOX15 orthologs exhibit significantly higher lipoxin-synthesizing capacities than 12-lipoxygenating. Product pattern of primate ALOX15 orthologues, overview. The wild-type animal produces 20% 12-hydroperoxyicosatetraenoate and 80% 15-hydroperoxyicosatetraenoate with 135% overall activity compared to the human enzyme activity | Pan troglodytes | ? | - |
? | |
| 1.13.11.31 | additional information | 15-lipoxygenating ALOX15 orthologs exhibit significantly higher lipoxin-synthesizing capacities than 12-lipoxygenating. Product pattern of primate ALOX15 orthologues, overview. The wild-type animal produces 14% 12-hydroperoxyicosatetraenoate and 86% 15-hydroperoxyicosatetraenoate | Pongo pygmaeus | ? | - |
? | |
| 1.13.11.31 | additional information | 15-lipoxygenating ALOX15 orthologs exhibit significantly higher lipoxin-synthesizing capacities than 12-lipoxygenating. Product pattern of primate ALOX15 orthologues, overview. The wild-type animal produces 3% 12-hydroperoxyicosatetraenoate and 97% 15-hydroperoxyicosatetraenoate | Oryctolagus cuniculus | ? | - |
? | |
| 1.13.11.31 | additional information | 15-lipoxygenating ALOX15 orthologs exhibit significantly higher lipoxin-synthesizing capacities than 12-lipoxygenating. Product pattern of primate ALOX15 orthologues, overview. The wild-type animal produces 78% 12-hydroperoxyicosatetraenoate and 22% 15-hydroperoxyicosatetraenoate with 37% overall activity compared to the human enzyme activity | Papio anubis | ? | - |
? | |
| 1.13.11.31 | additional information | 15-lipoxygenating ALOX15 orthologs exhibit significantly higher lipoxin-synthesizing capacities than 12-lipoxygenating. Product pattern of primate ALOX15 orthologues, overview | Homo sapiens neanderthalensis | ? | - |
? | |
| 1.13.11.31 | additional information | 15-lipoxygenating ALOX15 orthologs exhibit significantly higher lipoxin-synthesizing capacities than 12-lipoxygenating. Product pattern of primate ALOX15 orthologues, overview | Homo sapiens subsp. 'Denisova' | ? | - |
? | |
| 1.13.11.31 | additional information | 15-lipoxygenating ALOX15 orthologs exhibit significantly higher lipoxin-synthesizing capacities than 12-lipoxygenating. Product pattern of primate ALOX15 orthologues, overview | Macaca mulatta | ? | - |
? | |
| 1.13.11.31 | additional information | 15-lipoxygenating ALOX15 orthologs exhibit significantly higher lipoxin-synthesizing capacities than 12-lipoxygenating. Product pattern of primate ALOX15 orthologues, overview | Pongo abelii | ? | - |
? | |
| 1.13.11.31 | additional information | 15-lipoxygenating ALOX15 orthologs exhibit significantly higher lipoxin-synthesizing capacities than 12-lipoxygenating. Product pattern of primate ALOX15 orthologues, overview | Pan paniscus | ? | - |
? | |
| 1.13.11.31 | additional information | prediction of reaction specificity of mammalian ALOX15 orthologues, and reaction specificity of ALOX15 orthologues during late primate evolution | Homo sapiens | ? | - |
? | |
| 1.13.11.31 | additional information | prediction of reaction specificity of mammalian ALOX15 orthologues, and reaction specificity of ALOX15 orthologues during late primate evolution | Nomascus leucogenys | ? | - |
? | |
| 1.13.11.31 | additional information | prediction of reaction specificity of mammalian ALOX15 orthologues, and reaction specificity of ALOX15 orthologues during late primate evolution | Pan troglodytes | ? | - |
? | |
| 1.13.11.31 | additional information | prediction of reaction specificity of mammalian ALOX15 orthologues, and reaction specificity of ALOX15 orthologues during late primate evolution | Pongo pygmaeus | ? | - |
? | |
| 1.13.11.31 | additional information | prediction of reaction specificity of mammalian ALOX15 orthologues, and reaction specificity of ALOX15 orthologues during late primate evolution | Oryctolagus cuniculus | ? | - |
? | |
| 1.13.11.31 | additional information | prediction of reaction specificity of mammalian ALOX15 orthologues, and reaction specificity of ALOX15 orthologues during late primate evolution | Papio anubis | ? | - |
? | |
| 1.13.11.31 | additional information | prediction of reaction specificity of mammalian ALOX15 orthologues, and reaction specificity of ALOX15 orthologues during late primate evolution | Homo sapiens neanderthalensis | ? | - |
? | |
| 1.13.11.31 | additional information | prediction of reaction specificity of mammalian ALOX15 orthologues, and reaction specificity of ALOX15 orthologues during late primate evolution | Homo sapiens subsp. 'Denisova' | ? | - |
? | |
| 1.13.11.31 | additional information | prediction of reaction specificity of mammalian ALOX15 orthologues, and reaction specificity of ALOX15 orthologues during late primate evolution | Macaca mulatta | ? | - |
? | |
| 1.13.11.31 | additional information | prediction of reaction specificity of mammalian ALOX15 orthologues, and reaction specificity of ALOX15 orthologues during late primate evolution | Pongo abelii | ? | - |
? | |
| 1.13.11.31 | additional information | prediction of reaction specificity of mammalian ALOX15 orthologues, and reaction specificity of ALOX15 orthologues during late primate evolution | Pan paniscus | ? | - |
? | |
| 1.13.11.33 | arachidonate + O2 | - |
Pongo pygmaeus | (5Z,8Z,11Z,13E)-(15S)-15-hydroperoxyicosa-5,8,11,13-tetraenoate | - |
? | |
| 1.13.11.33 | arachidonate + O2 | - |
Oryctolagus cuniculus | (5Z,8Z,11Z,13E)-(15S)-15-hydroperoxyicosa-5,8,11,13-tetraenoate | - |
? | |
| 1.13.11.33 | arachidonate + O2 | - |
Papio anubis | (5Z,8Z,11Z,13E)-(15S)-15-hydroperoxyicosa-5,8,11,13-tetraenoate | - |
? | |
| 1.13.11.33 | arachidonate + O2 | - |
Homo sapiens neanderthalensis | (5Z,8Z,11Z,13E)-(15S)-15-hydroperoxyicosa-5,8,11,13-tetraenoate | - |
? | |
| 1.13.11.33 | arachidonate + O2 | - |
Homo sapiens subsp. 'Denisova' | (5Z,8Z,11Z,13E)-(15S)-15-hydroperoxyicosa-5,8,11,13-tetraenoate | - |
? | |
| 1.13.11.33 | arachidonate + O2 | - |
Macaca mulatta | (5Z,8Z,11Z,13E)-(15S)-15-hydroperoxyicosa-5,8,11,13-tetraenoate | - |
? | |
| 1.13.11.33 | arachidonate + O2 | - |
Pongo abelii | (5Z,8Z,11Z,13E)-(15S)-15-hydroperoxyicosa-5,8,11,13-tetraenoate | - |
? | |
| 1.13.11.33 | arachidonate + O2 | - |
Pan paniscus | (5Z,8Z,11Z,13E)-(15S)-15-hydroperoxyicosa-5,8,11,13-tetraenoate | - |
? | |
| 1.13.11.33 | arachidonate + O2 | - |
Homo sapiens | (5Z,8Z,11Z,13E)-(15S)-15-hydroperoxyicosa-5,8,11,13-tetraenoate | - |
? | |
| 1.13.11.33 | arachidonate + O2 | - |
Nomascus leucogenys | (5Z,8Z,11Z,13E)-(15S)-15-hydroperoxyicosa-5,8,11,13-tetraenoate | - |
? | |
| 1.13.11.33 | arachidonate + O2 | - |
Pan troglodytes | (5Z,8Z,11Z,13E)-(15S)-15-hydroperoxyicosa-5,8,11,13-tetraenoate | - |
? | |
| 1.13.11.33 | additional information | 15-lipoxygenating ALOX15 orthologs exhibit significantly higher lipoxin-synthesizing capacities than 12-lipoxygenating. Product pattern of primate ALOX15 orthologues, overview. The wild-type animal produces 14% 12-hydroperoxyicosatetraenoate and 86% 15-hydroperoxyicosatetraenoate | Pongo pygmaeus | ? | - |
? | |
| 1.13.11.33 | additional information | 15-lipoxygenating ALOX15 orthologs exhibit significantly higher lipoxin-synthesizing capacities than 12-lipoxygenating. The wild-type animal produces 3% 12-hydroperoxyicosatetraenoate and 97% 15-hydroperoxyicosatetraenoate | Oryctolagus cuniculus | ? | - |
? | |
| 1.13.11.33 | additional information | 15-lipoxygenating ALOX15 orthologs exhibit significantly higher lipoxin-synthesizing capacities than 12-lipoxygenating. Product pattern of primate ALOX15 orthologues, overview. The wild-type animal produces 78% 12-hydroperoxyicosatetraenoate and 22% 15-hydroperoxyicosatetraenoate with 37% overall activity compared to the human enzyme activity | Papio anubis | ? | - |
? | |
| 1.13.11.33 | additional information | 15-lipoxygenating ALOX15 orthologs exhibit significantly higher lipoxin-synthesizing capacities than 12-lipoxygenating. Product pattern of primate ALOX15 orthologues, overview | Homo sapiens neanderthalensis | ? | - |
? | |
| 1.13.11.33 | additional information | 15-lipoxygenating ALOX15 orthologs exhibit significantly higher lipoxin-synthesizing capacities than 12-lipoxygenating. Product pattern of primate ALOX15 orthologues, overview | Homo sapiens subsp. 'Denisova' | ? | - |
? | |
| 1.13.11.33 | additional information | 15-lipoxygenating ALOX15 orthologs exhibit significantly higher lipoxin-synthesizing capacities than 12-lipoxygenating. Product pattern of primate ALOX15 orthologues, overview | Macaca mulatta | ? | - |
? | |
| 1.13.11.33 | additional information | 15-lipoxygenating ALOX15 orthologs exhibit significantly higher lipoxin-synthesizing capacities than 12-lipoxygenating. Product pattern of primate ALOX15 orthologues, overview | Pongo abelii | ? | - |
? | |
| 1.13.11.33 | additional information | 15-lipoxygenating ALOX15 orthologs exhibit significantly higher lipoxin-synthesizing capacities than 12-lipoxygenating. Product pattern of primate ALOX15 orthologues, overview | Pan paniscus | ? | - |
? | |
| 1.13.11.33 | additional information | 15-lipoxygenating ALOX15 orthologs exhibit significantly higher lipoxin-synthesizing capacities than 12-lipoxygenating. Product pattern of primate ALOX15 orthologues, overview. The wild-type subject produces 21% 12-hydroperoxyicosatetraenoate and 79% 15-hydroperoxyicosatetraenoate | Homo sapiens | ? | - |
? | |
| 1.13.11.33 | additional information | 15-lipoxygenating ALOX15 orthologs exhibit significantly higher lipoxin-synthesizing capacities than 12-lipoxygenating. Product pattern of primate ALOX15 orthologues, overview. The wild-type animal produces 54% 12-hydroperoxyicosatetraenoate and 46% 15-hydroperoxyicosatetraenoate with 76% overall activity compared to the human enzyme activity | Nomascus leucogenys | ? | - |
? | |
| 1.13.11.33 | additional information | 15-lipoxygenating ALOX15 orthologs exhibit significantly higher lipoxin-synthesizing capacities than 12-lipoxygenating. Product pattern of primate ALOX15 orthologues, overview. The wild-type animal produces 20% 12-hydroperoxyicosatetraenoate and 80% 15-hydroperoxyicosatetraenoate with 135% overall activity compared to the human enzyme activity | Pan troglodytes | ? | - |
? | |
| 1.13.11.33 | additional information | prediction of reaction specificity of mammalian ALOX15 orthologues, and reaction specificity of ALOX15 orthologues during late primate evolution | Pongo pygmaeus | ? | - |
? | |
| 1.13.11.33 | additional information | prediction of reaction specificity of mammalian ALOX15 orthologues, and reaction specificity of ALOX15 orthologues during late primate evolution | Oryctolagus cuniculus | ? | - |
? | |
| 1.13.11.33 | additional information | prediction of reaction specificity of mammalian ALOX15 orthologues, and reaction specificity of ALOX15 orthologues during late primate evolution | Papio anubis | ? | - |
? | |
| 1.13.11.33 | additional information | prediction of reaction specificity of mammalian ALOX15 orthologues, and reaction specificity of ALOX15 orthologues during late primate evolution | Homo sapiens neanderthalensis | ? | - |
? | |
| 1.13.11.33 | additional information | prediction of reaction specificity of mammalian ALOX15 orthologues, and reaction specificity of ALOX15 orthologues during late primate evolution | Homo sapiens subsp. 'Denisova' | ? | - |
? | |
| 1.13.11.33 | additional information | prediction of reaction specificity of mammalian ALOX15 orthologues, and reaction specificity of ALOX15 orthologues during late primate evolution | Macaca mulatta | ? | - |
? | |
| 1.13.11.33 | additional information | prediction of reaction specificity of mammalian ALOX15 orthologues, and reaction specificity of ALOX15 orthologues during late primate evolution | Pongo abelii | ? | - |
? | |
| 1.13.11.33 | additional information | prediction of reaction specificity of mammalian ALOX15 orthologues, and reaction specificity of ALOX15 orthologues during late primate evolution | Pan paniscus | ? | - |
? | |
| 1.13.11.33 | additional information | prediction of reaction specificity of mammalian ALOX15 orthologues, and reaction specificity of ALOX15 orthologues during late primate evolution | Homo sapiens | ? | - |
? | |
| 1.13.11.33 | additional information | prediction of reaction specificity of mammalian ALOX15 orthologues, and reaction specificity of ALOX15 orthologues during late primate evolution | Nomascus leucogenys | ? | - |
? | |
| 1.13.11.33 | additional information | prediction of reaction specificity of mammalian ALOX15 orthologues, and reaction specificity of ALOX15 orthologues during late primate evolution | Pan troglodytes | ? | - |
? |
| EC Number | Synonyms | Comment | Organism |
|---|---|---|---|
| 1.13.11.31 | 12/15-lipoxygenase | - |
Homo sapiens |
| 1.13.11.31 | 12/15-lipoxygenase | - |
Nomascus leucogenys |
| 1.13.11.31 | 12/15-lipoxygenase | - |
Pan troglodytes |
| 1.13.11.31 | 12/15-lipoxygenase | - |
Pongo pygmaeus |
| 1.13.11.31 | 12/15-lipoxygenase | - |
Oryctolagus cuniculus |
| 1.13.11.31 | 12/15-lipoxygenase | - |
Papio anubis |
| 1.13.11.31 | 12/15-lipoxygenase | - |
Homo sapiens neanderthalensis |
| 1.13.11.31 | 12/15-lipoxygenase | - |
Homo sapiens subsp. 'Denisova' |
| 1.13.11.31 | 12/15-lipoxygenase | - |
Macaca mulatta |
| 1.13.11.31 | 12/15-lipoxygenase | - |
Pongo abelii |
| 1.13.11.31 | 12/15-lipoxygenase | - |
Pan paniscus |
| 1.13.11.31 | Alox15 | - |
Homo sapiens |
| 1.13.11.31 | Alox15 | - |
Nomascus leucogenys |
| 1.13.11.31 | Alox15 | - |
Pan troglodytes |
| 1.13.11.31 | Alox15 | - |
Pongo pygmaeus |
| 1.13.11.31 | Alox15 | - |
Oryctolagus cuniculus |
| 1.13.11.31 | Alox15 | - |
Papio anubis |
| 1.13.11.31 | Alox15 | - |
Homo sapiens neanderthalensis |
| 1.13.11.31 | Alox15 | - |
Homo sapiens subsp. 'Denisova' |
| 1.13.11.31 | Alox15 | - |
Macaca mulatta |
| 1.13.11.31 | Alox15 | - |
Pongo abelii |
| 1.13.11.31 | Alox15 | - |
Pan paniscus |
| 1.13.11.33 | 12/15-lipoxygenase | - |
Pongo pygmaeus |
| 1.13.11.33 | 12/15-lipoxygenase | - |
Oryctolagus cuniculus |
| 1.13.11.33 | 12/15-lipoxygenase | - |
Papio anubis |
| 1.13.11.33 | 12/15-lipoxygenase | - |
Homo sapiens neanderthalensis |
| 1.13.11.33 | 12/15-lipoxygenase | - |
Homo sapiens subsp. 'Denisova' |
| 1.13.11.33 | 12/15-lipoxygenase | - |
Macaca mulatta |
| 1.13.11.33 | 12/15-lipoxygenase | - |
Pongo abelii |
| 1.13.11.33 | 12/15-lipoxygenase | - |
Pan paniscus |
| 1.13.11.33 | 12/15-lipoxygenase | - |
Homo sapiens |
| 1.13.11.33 | 12/15-lipoxygenase | - |
Nomascus leucogenys |
| 1.13.11.33 | 12/15-lipoxygenase | - |
Pan troglodytes |
| 1.13.11.33 | Alox15 | - |
Pongo pygmaeus |
| 1.13.11.33 | Alox15 | - |
Oryctolagus cuniculus |
| 1.13.11.33 | Alox15 | - |
Papio anubis |
| 1.13.11.33 | Alox15 | - |
Homo sapiens neanderthalensis |
| 1.13.11.33 | Alox15 | - |
Homo sapiens subsp. 'Denisova' |
| 1.13.11.33 | Alox15 | - |
Macaca mulatta |
| 1.13.11.33 | Alox15 | - |
Pongo abelii |
| 1.13.11.33 | Alox15 | - |
Pan paniscus |
| 1.13.11.33 | Alox15 | - |
Homo sapiens |
| 1.13.11.33 | Alox15 | - |
Nomascus leucogenys |
| 1.13.11.33 | Alox15 | - |
Pan troglodytes |
| EC Number | General Information | Comment | Organism |
|---|---|---|---|
| 1.13.11.31 | evolution | mammals (mice, rats, pigs) express 12-lipoxygenating ALOX15 orthologues. 15-lipoxygenating isoforms are found in primates (orangutans, humans), suggesting an evolution of ALOX15 specificity. Other primates (baboons, rhesus monkeys) express 12-lipoxygenating enzymes. Gibbons, which are flanked in evolution by rhesus monkeys (12-lipoxygenating ALOX15) and orangutans (15-lipoxygenating ALOX15), express an ALOX15 ortholog with pronounced dual specificity, an evolution of ALOX15 specificity, which is aimed at optimizing the biosynthetic capacity for antiinflammatory and proresolving lipoxins. Phylogenetic analysis | Homo sapiens |
| 1.13.11.31 | evolution | mammals (mice, rats, pigs) express 12-lipoxygenating ALOX15 orthologues. 15-lipoxygenating isoforms are found in primates (orangutans, humans), suggesting an evolution of ALOX15 specificity. Other primates (baboons, rhesus monkeys) express 12-lipoxygenating enzymes. Gibbons, which are flanked in evolution by rhesus monkeys (12-lipoxygenating ALOX15) and orangutans (15-lipoxygenating ALOX15), express an ALOX15 ortholog with pronounced dual specificity, an evolution of ALOX15 specificity, which is aimed at optimizing the biosynthetic capacity for antiinflammatory and proresolving lipoxins. Phylogenetic analysis | Nomascus leucogenys |
| 1.13.11.31 | evolution | mammals (mice, rats, pigs) express 12-lipoxygenating ALOX15 orthologues. 15-lipoxygenating isoforms are found in primates (orangutans, humans), suggesting an evolution of ALOX15 specificity. Other primates (baboons, rhesus monkeys) express 12-lipoxygenating enzymes. Gibbons, which are flanked in evolution by rhesus monkeys (12-lipoxygenating ALOX15) and orangutans (15-lipoxygenating ALOX15), express an ALOX15 ortholog with pronounced dual specificity, an evolution of ALOX15 specificity, which is aimed at optimizing the biosynthetic capacity for antiinflammatory and proresolving lipoxins. Phylogenetic analysis | Pan troglodytes |
| 1.13.11.31 | evolution | mammals (mice, rats, pigs) express 12-lipoxygenating ALOX15 orthologues. 15-lipoxygenating isoforms are found in primates (orangutans, humans), suggesting an evolution of ALOX15 specificity. Other primates (baboons, rhesus monkeys) express 12-lipoxygenating enzymes. Gibbons, which are flanked in evolution by rhesus monkeys (12-lipoxygenating ALOX15) and orangutans (15-lipoxygenating ALOX15), express an ALOX15 ortholog with pronounced dual specificity, an evolution of ALOX15 specificity, which is aimed at optimizing the biosynthetic capacity for antiinflammatory and proresolving lipoxins. Phylogenetic analysis | Pongo pygmaeus |
| 1.13.11.31 | evolution | mammals (mice, rats, pigs) express 12-lipoxygenating ALOX15 orthologues. 15-lipoxygenating isoforms are found in primates (orangutans, humans), suggesting an evolution of ALOX15 specificity. Other primates (baboons, rhesus monkeys) express 12-lipoxygenating enzymes. Gibbons, which are flanked in evolution by rhesus monkeys (12-lipoxygenating ALOX15) and orangutans (15-lipoxygenating ALOX15), express an ALOX15 ortholog with pronounced dual specificity, an evolution of ALOX15 specificity, which is aimed at optimizing the biosynthetic capacity for antiinflammatory and proresolving lipoxins. Phylogenetic analysis | Oryctolagus cuniculus |
| 1.13.11.31 | evolution | mammals (mice, rats, pigs) express 12-lipoxygenating ALOX15 orthologues. 15-lipoxygenating isoforms are found in primates (orangutans, humans), suggesting an evolution of ALOX15 specificity. Other primates (baboons, rhesus monkeys) express 12-lipoxygenating enzymes. Gibbons, which are flanked in evolution by rhesus monkeys (12-lipoxygenating ALOX15) and orangutans (15-lipoxygenating ALOX15), express an ALOX15 ortholog with pronounced dual specificity, an evolution of ALOX15 specificity, which is aimed at optimizing the biosynthetic capacity for antiinflammatory and proresolving lipoxins. Phylogenetic analysis | Papio anubis |
| 1.13.11.31 | evolution | mammals (mice, rats, pigs) express 12-lipoxygenating ALOX15 orthologues. 15-lipoxygenating isoforms are found in primates (orangutans, humans), suggesting an evolution of ALOX15 specificity. Other primates (baboons, rhesus monkeys) express 12-lipoxygenating enzymes. Gibbons, which are flanked in evolution by rhesus monkeys (12-lipoxygenating ALOX15) and orangutans (15-lipoxygenating ALOX15), express an ALOX15 ortholog with pronounced dual specificity, an evolution of ALOX15 specificity, which is aimed at optimizing the biosynthetic capacity for antiinflammatory and proresolving lipoxins. Phylogenetic analysis | Homo sapiens neanderthalensis |
| 1.13.11.31 | evolution | mammals (mice, rats, pigs) express 12-lipoxygenating ALOX15 orthologues. 15-lipoxygenating isoforms are found in primates (orangutans, humans), suggesting an evolution of ALOX15 specificity. Other primates (baboons, rhesus monkeys) express 12-lipoxygenating enzymes. Gibbons, which are flanked in evolution by rhesus monkeys (12-lipoxygenating ALOX15) and orangutans (15-lipoxygenating ALOX15), express an ALOX15 ortholog with pronounced dual specificity, an evolution of ALOX15 specificity, which is aimed at optimizing the biosynthetic capacity for antiinflammatory and proresolving lipoxins. Phylogenetic analysis | Homo sapiens subsp. 'Denisova' |
| 1.13.11.31 | evolution | mammals (mice, rats, pigs) express 12-lipoxygenating ALOX15 orthologues. 15-lipoxygenating isoforms are found in primates (orangutans, humans), suggesting an evolution of ALOX15 specificity. Other primates (baboons, rhesus monkeys) express 12-lipoxygenating enzymes. Gibbons, which are flanked in evolution by rhesus monkeys (12-lipoxygenating ALOX15) and orangutans (15-lipoxygenating ALOX15), express an ALOX15 ortholog with pronounced dual specificity, an evolution of ALOX15 specificity, which is aimed at optimizing the biosynthetic capacity for antiinflammatory and proresolving lipoxins. Phylogenetic analysis | Macaca mulatta |
| 1.13.11.31 | evolution | mammals (mice, rats, pigs) express 12-lipoxygenating ALOX15 orthologues. 15-lipoxygenating isoforms are found in primates (orangutans, humans), suggesting an evolution of ALOX15 specificity. Other primates (baboons, rhesus monkeys) express 12-lipoxygenating enzymes. Gibbons, which are flanked in evolution by rhesus monkeys (12-lipoxygenating ALOX15) and orangutans (15-lipoxygenating ALOX15), express an ALOX15 ortholog with pronounced dual specificity, an evolution of ALOX15 specificity, which is aimed at optimizing the biosynthetic capacity for antiinflammatory and proresolving lipoxins. Phylogenetic analysis | Pongo abelii |
| 1.13.11.31 | evolution | mammals (mice, rats, pigs) express 12-lipoxygenating ALOX15 orthologues. 15-lipoxygenating isoforms are found in primates (orangutans, humans), suggesting an evolution of ALOX15 specificity. Other primates (baboons, rhesus monkeys) express 12-lipoxygenating enzymes. Gibbons, which are flanked in evolution by rhesus monkeys (12-lipoxygenating ALOX15) and orangutans (15-lipoxygenating ALOX15), express an ALOX15 ortholog with pronounced dual specificity, an evolution of ALOX15 specificity, which is aimed at optimizing the biosynthetic capacity for antiinflammatory and proresolving lipoxins. Phylogenetic analysis | Pan paniscus |
| 1.13.11.31 | additional information | molecular dynamics simulations and quantum mechanics/molecular mechanics calculations | Homo sapiens |
| 1.13.11.31 | additional information | molecular dynamics simulations and quantum mechanics/molecular mechanics calculations | Nomascus leucogenys |
| 1.13.11.31 | additional information | molecular dynamics simulations and quantum mechanics/molecular mechanics calculations | Pan troglodytes |
| 1.13.11.31 | additional information | molecular dynamics simulations and quantum mechanics/molecular mechanics calculations | Pongo pygmaeus |
| 1.13.11.31 | additional information | molecular dynamics simulations and quantum mechanics/molecular mechanics calculations | Oryctolagus cuniculus |
| 1.13.11.31 | additional information | molecular dynamics simulations and quantum mechanics/molecular mechanics calculations | Papio anubis |
| 1.13.11.31 | additional information | molecular dynamics simulations and quantum mechanics/molecular mechanics calculations | Homo sapiens neanderthalensis |
| 1.13.11.31 | additional information | molecular dynamics simulations and quantum mechanics/molecular mechanics calculations | Homo sapiens subsp. 'Denisova' |
| 1.13.11.31 | additional information | molecular dynamics simulations and quantum mechanics/molecular mechanics calculations | Macaca mulatta |
| 1.13.11.31 | additional information | molecular dynamics simulations and quantum mechanics/molecular mechanics calculations | Pongo abelii |
| 1.13.11.31 | additional information | molecular dynamics simulations and quantum mechanics/molecular mechanics calculations | Pan paniscus |
| 1.13.11.31 | physiological function | ALOX15-encoded 12/15-lipoxygenase orthologs are implicated in maturational degradation of intracellular organelles and in the biosynthesis of antiinflammatory and proresolving eicosanoids | Homo sapiens |
| 1.13.11.31 | physiological function | ALOX15-encoded 12/15-lipoxygenase orthologs are implicated in maturational degradation of intracellular organelles and in the biosynthesis of antiinflammatory and proresolving eicosanoids | Nomascus leucogenys |
| 1.13.11.31 | physiological function | ALOX15-encoded 12/15-lipoxygenase orthologs are implicated in maturational degradation of intracellular organelles and in the biosynthesis of antiinflammatory and proresolving eicosanoids | Pan troglodytes |
| 1.13.11.31 | physiological function | ALOX15-encoded 12/15-lipoxygenase orthologs are implicated in maturational degradation of intracellular organelles and in the biosynthesis of antiinflammatory and proresolving eicosanoids | Pongo pygmaeus |
| 1.13.11.31 | physiological function | ALOX15-encoded 12/15-lipoxygenase orthologs are implicated in maturational degradation of intracellular organelles and in the biosynthesis of antiinflammatory and proresolving eicosanoids | Oryctolagus cuniculus |
| 1.13.11.31 | physiological function | ALOX15-encoded 12/15-lipoxygenase orthologs are implicated in maturational degradation of intracellular organelles and in the biosynthesis of antiinflammatory and proresolving eicosanoids | Papio anubis |
| 1.13.11.31 | physiological function | ALOX15-encoded 12/15-lipoxygenase orthologs are implicated in maturational degradation of intracellular organelles and in the biosynthesis of antiinflammatory and proresolving eicosanoids | Homo sapiens neanderthalensis |
| 1.13.11.31 | physiological function | ALOX15-encoded 12/15-lipoxygenase orthologs are implicated in maturational degradation of intracellular organelles and in the biosynthesis of antiinflammatory and proresolving eicosanoids | Homo sapiens subsp. 'Denisova' |
| 1.13.11.31 | physiological function | ALOX15-encoded 12/15-lipoxygenase orthologs are implicated in maturational degradation of intracellular organelles and in the biosynthesis of antiinflammatory and proresolving eicosanoids | Macaca mulatta |
| 1.13.11.31 | physiological function | ALOX15-encoded 12/15-lipoxygenase orthologs are implicated in maturational degradation of intracellular organelles and in the biosynthesis of antiinflammatory and proresolving eicosanoids | Pongo abelii |
| 1.13.11.31 | physiological function | ALOX15-encoded 12/15-lipoxygenase orthologs are implicated in maturational degradation of intracellular organelles and in the biosynthesis of antiinflammatory and proresolving eicosanoids | Pan paniscus |
| 1.13.11.33 | evolution | mammals (mice, rats, pigs) express 12-lipoxygenating ALOX15 orthologues. 15-lipoxygenating isoforms are found in primates (orangutans, humans), suggesting an evolution of ALOX15 specificity. Other primates (baboons, rhesus monkeys) express 12-lipoxygenating enzymes. Gibbons, which are flanked in evolution by rhesus monkeys (12-lipoxygenating ALOX15) and orangutans (15-lipoxygenating ALOX15), express an ALOX15 ortholog with pronounced dual specificity, an evolution of ALOX15 specificity, which is aimed at optimizing the biosynthetic capacity for antiinflammatory and proresolving lipoxins. Phylogenetic analysis | Pongo pygmaeus |
| 1.13.11.33 | evolution | mammals (mice, rats, pigs) express 12-lipoxygenating ALOX15 orthologues. 15-lipoxygenating isoforms are found in primates (orangutans, humans), suggesting an evolution of ALOX15 specificity. Other primates (baboons, rhesus monkeys) express 12-lipoxygenating enzymes. Gibbons, which are flanked in evolution by rhesus monkeys (12-lipoxygenating ALOX15) and orangutans (15-lipoxygenating ALOX15), express an ALOX15 ortholog with pronounced dual specificity, an evolution of ALOX15 specificity, which is aimed at optimizing the biosynthetic capacity for antiinflammatory and proresolving lipoxins. Phylogenetic analysis | Oryctolagus cuniculus |
| 1.13.11.33 | evolution | mammals (mice, rats, pigs) express 12-lipoxygenating ALOX15 orthologues. 15-lipoxygenating isoforms are found in primates (orangutans, humans), suggesting an evolution of ALOX15 specificity. Other primates (baboons, rhesus monkeys) express 12-lipoxygenating enzymes. Gibbons, which are flanked in evolution by rhesus monkeys (12-lipoxygenating ALOX15) and orangutans (15-lipoxygenating ALOX15), express an ALOX15 ortholog with pronounced dual specificity, an evolution of ALOX15 specificity, which is aimed at optimizing the biosynthetic capacity for antiinflammatory and proresolving lipoxins. Phylogenetic analysis | Papio anubis |
| 1.13.11.33 | evolution | mammals (mice, rats, pigs) express 12-lipoxygenating ALOX15 orthologues. 15-lipoxygenating isoforms are found in primates (orangutans, humans), suggesting an evolution of ALOX15 specificity. Other primates (baboons, rhesus monkeys) express 12-lipoxygenating enzymes. Gibbons, which are flanked in evolution by rhesus monkeys (12-lipoxygenating ALOX15) and orangutans (15-lipoxygenating ALOX15), express an ALOX15 ortholog with pronounced dual specificity, an evolution of ALOX15 specificity, which is aimed at optimizing the biosynthetic capacity for antiinflammatory and proresolving lipoxins. Phylogenetic analysis | Homo sapiens neanderthalensis |
| 1.13.11.33 | evolution | mammals (mice, rats, pigs) express 12-lipoxygenating ALOX15 orthologues. 15-lipoxygenating isoforms are found in primates (orangutans, humans), suggesting an evolution of ALOX15 specificity. Other primates (baboons, rhesus monkeys) express 12-lipoxygenating enzymes. Gibbons, which are flanked in evolution by rhesus monkeys (12-lipoxygenating ALOX15) and orangutans (15-lipoxygenating ALOX15), express an ALOX15 ortholog with pronounced dual specificity, an evolution of ALOX15 specificity, which is aimed at optimizing the biosynthetic capacity for antiinflammatory and proresolving lipoxins. Phylogenetic analysis | Homo sapiens subsp. 'Denisova' |
| 1.13.11.33 | evolution | mammals (mice, rats, pigs) express 12-lipoxygenating ALOX15 orthologues. 15-lipoxygenating isoforms are found in primates (orangutans, humans), suggesting an evolution of ALOX15 specificity. Other primates (baboons, rhesus monkeys) express 12-lipoxygenating enzymes. Gibbons, which are flanked in evolution by rhesus monkeys (12-lipoxygenating ALOX15) and orangutans (15-lipoxygenating ALOX15), express an ALOX15 ortholog with pronounced dual specificity, an evolution of ALOX15 specificity, which is aimed at optimizing the biosynthetic capacity for antiinflammatory and proresolving lipoxins. Phylogenetic analysis | Macaca mulatta |
| 1.13.11.33 | evolution | mammals (mice, rats, pigs) express 12-lipoxygenating ALOX15 orthologues. 15-lipoxygenating isoforms are found in primates (orangutans, humans), suggesting an evolution of ALOX15 specificity. Other primates (baboons, rhesus monkeys) express 12-lipoxygenating enzymes. Gibbons, which are flanked in evolution by rhesus monkeys (12-lipoxygenating ALOX15) and orangutans (15-lipoxygenating ALOX15), express an ALOX15 ortholog with pronounced dual specificity, an evolution of ALOX15 specificity, which is aimed at optimizing the biosynthetic capacity for antiinflammatory and proresolving lipoxins. Phylogenetic analysis | Pongo abelii |
| 1.13.11.33 | evolution | mammals (mice, rats, pigs) express 12-lipoxygenating ALOX15 orthologues. 15-lipoxygenating isoforms are found in primates (orangutans, humans), suggesting an evolution of ALOX15 specificity. Other primates (baboons, rhesus monkeys) express 12-lipoxygenating enzymes. Gibbons, which are flanked in evolution by rhesus monkeys (12-lipoxygenating ALOX15) and orangutans (15-lipoxygenating ALOX15), express an ALOX15 ortholog with pronounced dual specificity, an evolution of ALOX15 specificity, which is aimed at optimizing the biosynthetic capacity for antiinflammatory and proresolving lipoxins. Phylogenetic analysis | Pan paniscus |
| 1.13.11.33 | evolution | mammals (mice, rats, pigs) express 12-lipoxygenating ALOX15 orthologues. 15-lipoxygenating isoforms are found in primates (orangutans, humans), suggesting an evolution of ALOX15 specificity. Other primates (baboons, rhesus monkeys) express 12-lipoxygenating enzymes. Gibbons, which are flanked in evolution by rhesus monkeys (12-lipoxygenating ALOX15) and orangutans (15-lipoxygenating ALOX15), express an ALOX15 ortholog with pronounced dual specificity, an evolution of ALOX15 specificity, which is aimed at optimizing the biosynthetic capacity for antiinflammatory and proresolving lipoxins. Phylogenetic analysis | Homo sapiens |
| 1.13.11.33 | evolution | mammals (mice, rats, pigs) express 12-lipoxygenating ALOX15 orthologues. 15-lipoxygenating isoforms are found in primates (orangutans, humans), suggesting an evolution of ALOX15 specificity. Other primates (baboons, rhesus monkeys) express 12-lipoxygenating enzymes. Gibbons, which are flanked in evolution by rhesus monkeys (12-lipoxygenating ALOX15) and orangutans (15-lipoxygenating ALOX15), express an ALOX15 ortholog with pronounced dual specificity, an evolution of ALOX15 specificity, which is aimed at optimizing the biosynthetic capacity for antiinflammatory and proresolving lipoxins. Phylogenetic analysis | Nomascus leucogenys |
| 1.13.11.33 | evolution | mammals (mice, rats, pigs) express 12-lipoxygenating ALOX15 orthologues. 15-lipoxygenating isoforms are found in primates (orangutans, humans), suggesting an evolution of ALOX15 specificity. Other primates (baboons, rhesus monkeys) express 12-lipoxygenating enzymes. Gibbons, which are flanked in evolution by rhesus monkeys (12-lipoxygenating ALOX15) and orangutans (15-lipoxygenating ALOX15), express an ALOX15 ortholog with pronounced dual specificity, an evolution of ALOX15 specificity, which is aimed at optimizing the biosynthetic capacity for antiinflammatory and proresolving lipoxins. Phylogenetic analysis | Pan troglodytes |
| 1.13.11.33 | additional information | molecular dynamics simulations and quantum mechanics/molecular mechanics calculations | Pongo pygmaeus |
| 1.13.11.33 | additional information | molecular dynamics simulations and quantum mechanics/molecular mechanics calculations | Oryctolagus cuniculus |
| 1.13.11.33 | additional information | molecular dynamics simulations and quantum mechanics/molecular mechanics calculations | Papio anubis |
| 1.13.11.33 | additional information | molecular dynamics simulations and quantum mechanics/molecular mechanics calculations | Homo sapiens neanderthalensis |
| 1.13.11.33 | additional information | molecular dynamics simulations and quantum mechanics/molecular mechanics calculations | Homo sapiens subsp. 'Denisova' |
| 1.13.11.33 | additional information | molecular dynamics simulations and quantum mechanics/molecular mechanics calculations | Macaca mulatta |
| 1.13.11.33 | additional information | molecular dynamics simulations and quantum mechanics/molecular mechanics calculations | Pongo abelii |
| 1.13.11.33 | additional information | molecular dynamics simulations and quantum mechanics/molecular mechanics calculations | Pan paniscus |
| 1.13.11.33 | additional information | molecular dynamics simulations and quantum mechanics/molecular mechanics calculations | Homo sapiens |
| 1.13.11.33 | additional information | molecular dynamics simulations and quantum mechanics/molecular mechanics calculations | Nomascus leucogenys |
| 1.13.11.33 | additional information | molecular dynamics simulations and quantum mechanics/molecular mechanics calculations | Pan troglodytes |
| 1.13.11.33 | physiological function | ALOX15-encoded 12/15-lipoxygenase orthologs are implicated in maturational degradation of intracellular organelles and in the biosynthesis of antiinflammatory and proresolving eicosanoids | Pongo pygmaeus |
| 1.13.11.33 | physiological function | ALOX15-encoded 12/15-lipoxygenase orthologs are implicated in maturational degradation of intracellular organelles and in the biosynthesis of antiinflammatory and proresolving eicosanoids | Oryctolagus cuniculus |
| 1.13.11.33 | physiological function | ALOX15-encoded 12/15-lipoxygenase orthologs are implicated in maturational degradation of intracellular organelles and in the biosynthesis of antiinflammatory and proresolving eicosanoids | Papio anubis |
| 1.13.11.33 | physiological function | ALOX15-encoded 12/15-lipoxygenase orthologs are implicated in maturational degradation of intracellular organelles and in the biosynthesis of antiinflammatory and proresolving eicosanoids | Homo sapiens neanderthalensis |
| 1.13.11.33 | physiological function | ALOX15-encoded 12/15-lipoxygenase orthologs are implicated in maturational degradation of intracellular organelles and in the biosynthesis of antiinflammatory and proresolving eicosanoids | Homo sapiens subsp. 'Denisova' |
| 1.13.11.33 | physiological function | ALOX15-encoded 12/15-lipoxygenase orthologs are implicated in maturational degradation of intracellular organelles and in the biosynthesis of antiinflammatory and proresolving eicosanoids | Macaca mulatta |
| 1.13.11.33 | physiological function | ALOX15-encoded 12/15-lipoxygenase orthologs are implicated in maturational degradation of intracellular organelles and in the biosynthesis of antiinflammatory and proresolving eicosanoids | Pongo abelii |
| 1.13.11.33 | physiological function | ALOX15-encoded 12/15-lipoxygenase orthologs are implicated in maturational degradation of intracellular organelles and in the biosynthesis of antiinflammatory and proresolving eicosanoids | Pan paniscus |
| 1.13.11.33 | physiological function | ALOX15-encoded 12/15-lipoxygenase orthologs are implicated in maturational degradation of intracellular organelles and in the biosynthesis of antiinflammatory and proresolving eicosanoids | Homo sapiens |
| 1.13.11.33 | physiological function | ALOX15-encoded 12/15-lipoxygenase orthologs are implicated in maturational degradation of intracellular organelles and in the biosynthesis of antiinflammatory and proresolving eicosanoids | Nomascus leucogenys |
| 1.13.11.33 | physiological function | ALOX15-encoded 12/15-lipoxygenase orthologs are implicated in maturational degradation of intracellular organelles and in the biosynthesis of antiinflammatory and proresolving eicosanoids | Pan troglodytes |