Human-GEM
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Duplicate Beta-Oxidation Pathways for Linoleoyl- and gamma-Linolenoyl-CoA
Current behavior:
There are two separate pathways for the β-oxidation of linoleoyl and γ-linolenoyl-CoA to 4-decenoyl-CoA:
| Overall Reaction | “Low-Resolution” Version | “High-Resolution” Version |
|---|---|---|
| γ-linolenoyl-CoA -> 4,7,10-hexadecatrienoyl-CoA | MAR05358 |
MAR03452 + MAR03453 + MAR03454 + MAR03455 |
| 4,7,10-hexadecatrienoyl-CoA -> 2,4,7,10-hexadecatetraenoyl-CoA | MAR05195 |
MAR03456 |
| 2,4,7,10-hexadecatetraenoyl-CoA -> 3,7,10-hexadecatrienoyl-CoA | MAR05302 |
MAR03457 |
| 3,7,10-hexadecatrienoyl-CoA -> 2,7,10-hexadecatrienoyl-CoA | MAR05229 |
MAR03458 |
| 2,7,10-hexadecatrienoyl-CoA -> 5,8-tetradecadienoyl-CoA | MAR05208 |
MAR03281 + MAR03282 + MAR03283 |
| linoleoyl-CoA -> 7,10-hexadecadienoyl-CoA | MAR05356 |
MAR03275 + MAR03277 + MAR03278 + MAR03279 |
| 7,10-hexadecadienoyl-CoA -> 5,8-tetradecadienoyl-CoA | MAR05191 |
MAR03280 + MAR03281 + MAR03282 + MAR03283 |
| 5,8-tetradecadienoyl-CoA -> 3,6-dodecadienoyl-CoA | MAR05123 |
MAR03284 + MAR03285 + MAR03286 + MAR03287 |
| 3,6-dodecadienoyl-CoA -> 2,6-dodecadienoyl-CoA | MAR05075 |
MAR03288 |
| 2,6-dodecadienoyl-CoA -> 4-decenoyl-CoA | MAR05072 |
MAR03290 + MAR03292 + MAR03293 |
| Metabolite | ID in “Low-Resolution” Pathway | ID in “High-Resolution” Pathway |
|---|---|---|
| 4,7,10-hexadecatrienoyl-CoA | MAM03274m |
MAM00091m |
| 2,4,7,10-hexadecatetraenoyl-CoA | MAM03653m |
MAM00072m |
| 3,7,10-hexadecatrienoyl-CoA | MAM03221m |
MAM00089m |
| 2,7,10-hexadecatrienoyl-CoA | MAM03182m |
MAM03009m |
| 5,8-tetradecadienoyl-CoA | MAM03978m |
MAM01576m |
| 3,6-dodecadienoyl-CoA | MAM03203m |
MAM01575m |
| 2,6-dodecadienoyl-CoA | MAM02698m |
MAM03021m |
| 7,10-hexadecadienoyl-CoA | MAM03650m |
MAM01577m |
Expected behavior:
Both of these pathways should not exist; I propose removing the “lower-resolution” one and keeping the “higher-resolution” one. The pathway for β-oxidation of (4Z,7Z,10Z,13Z,16Z)-docosapentaenoyl-CoA (mentioned in #746) joins with the “lower-resolution” pathway at 4,7,10-hexadecatrienoyl-CoA; replacing MAM03274m with MAM00091m in MAR05360 will be sufficient to keep that pathway intact after removing the “lower-resolution” pathway.
Proposed changes:
- [x] Remove
MAR05358for being a duplicate ofMAR03452+MAR03453+MAR03454+MAR03455 - [x] Remove
MAR05195for being a duplicate ofMAR03456 - [x] Remove
MAR05302for being a duplicate ofMAR03457 - [x] Remove
MAR05229for being a duplicate ofMAR03458 - [x] Remove
MAR05208for being a duplicate ofMAR03281+MAR03282+MAR03283 - [x] Remove
MAR05356for being a duplicate ofMAR03275+MAR03277+MAR03278+MAR03279 - [x] Remove
MAR05191for being a duplicate ofMAR03280+MAR03281+MAR03282+MAR03283 - [x] Remove
MAR05123for being a duplicate ofMAR03284+MAR03285+MAR03286+MAR03287 - [x] Remove
MAR05075for being a duplicate ofMAR03288 - [x] Remove
MAR05072for being a duplicate ofMAR03290+MAR03292+MAR03293 - [x] Replace
MAM03274mwithMAM00091minMAR05360 - [x] Remove
MAM03274mfor being a duplicate ofMAM00091m - [x] Remove
MAM03653mfor being a duplicate ofMAM00072m - [x] Remove
MAM03221mfor being a duplicate ofMAM00089m - [x] Remove
MAM03182mfor being a duplicate ofMAM03009m - [x] Remove
MAM03978mfor being a duplicate ofMAM01576m - [x] Remove
MAM03203mfor being a duplicate ofMAM01575m - [x] Remove
MAM02698mfor being a duplicate ofMAM03021m - [x] Remove
MAM03650mfor being a duplicate ofMAM01577m
this issue presents the duplicate pathways of beta-oxidation for linoleoyl- and gamma-Linolenoyl-CoA, which were from the rough merging from two sources, one from HMR2 while another from Recon3D.
the proposed removal of "low-resolution” version appears to be a reasonable solution, here are some ideas for implementation:
- better ignore potential inaccuracy of GPRs, and focus on reaction manipulation
- the
subsystemname of kept reactions probably should be renamed - the
H2O2[m]in MAR03456 may be replaced withFADH2[m]from MAR05195
Re: changing the subsystems of the reactions not being removed: it looks like MAR03452, MAR03453, MAR03454, MAR03455, MAR03456, MAR03457, and MAR03458 (the reactions between gamma-linolenoyl-CoA and the point where its beta-oxidation pathway merges with linoleoyl-CoA's beta-oxidation pathway) are all in the Omega-6 fatty acid metabolism subsystem, while the rest are in the Beta oxidation of di-unsaturated fatty acids (n-6) (mitochondrial) subsystem. The reactions being removed are all in the Fatty acid oxidation subsystem.
There are only 19 reactions in the Beta oxidation of di-unsaturated fatty acids (n-6) (mitochondrial) subsystem, and nearly all of them are mentioned above. It seems redundant to have separate subsystems for Beta oxidation of di-unsaturated fatty acids (n-6) (mitochondrial) and Omega-6 fatty acid metabolism, since the former is a subset of the latter, and they're both pretty specific. I feel like it'd make sense to either
- Reassign all reactions currently in the
Beta oxidation of di-unsaturated fatty acids (n-6) (mitochondrial)subsystem to theOmega-6 fatty acid metabolismsubsystem, or - Move
MAR03452,MAR03453,MAR03454,MAR03455,MAR03456,MAR03457, andMAR03458from theOmega-6 fatty acid metabolismsubsystem to theBeta oxidation of di-unsaturated fatty acids (n-6) (mitochondrial)subsystem, and look through the other reactions in theOmega-6 fatty acid metabolismsubsystem to see if they can also be reassigned to more specific subsystems, or - Add all reactions currently in the
Beta oxidation of di-unsaturated fatty acids (n-6) (mitochondrial)subsystem to theOmega-6 fatty acid metabolismandFatty acid oxidationsubsystems, and add all reactions currently in theOmega-6 fatty acid metabolismsubsystem to theFatty acid oxidationsubsystem without removing them from their current subsystems (i.e. have each reaction be in multiple subsystems simultaneously)
Depending on what the philosophy behind assigning reactions to subsystems is.
During check, I also identified the duplicate mets in Peroxisome compartment, should we also fix this?
| Metabolite | ID in “Low-Resolution” Pathway | ID in “High-Resolution” Pathway |
|---|---|---|
| 4,7,10-hexadecatrienoyl-CoA | MAM03274x | MAM00091x |
| 2,4,7,10-hexadecatetraenoyl-CoA | MAM03653x | MAM00072x |
| 3,7,10-hexadecatrienoyl-CoA | MAM03221x | MAM00089x |
| 2,7,10-hexadecatrienoyl-CoA | MAM03182x | MAM03009x |
| 5,8-tetradecadienoyl-CoA | MAM03978x | MAM01576x |
| 3,6-dodecadienoyl-CoA | MAM03203x | MAM01575x |
| 2,6-dodecadienoyl-CoA | MAM02698x | MAM03021x |
| 7,10-hexadecadienoyl-CoA | MAM03650x | MAM01577x |
yea I also noticed that when putting together #793 and wasn't sure if it would be better to address that here or to do separate issues for duplicate peroxisomal pathways. I'd sorta tentatively decided to hold off on bringing up peroxisomal equivalents to the various mitochondrial duplicate pathways/reactions I recently identified until more of this current batch of issues had been resolved.
Ok, I would say let's make it a separate issue later