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FAD/Oxygen-Peroxide Duplicate Reactions #639
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nice and thorough investigation, and a large chunk of the network would be affected by the proposed changes |
Please manually test all metabolic tasks can be filled before making the changes. |
I don't know what that means; which metabolic tasks are we talking about? |
The task list can be found here, and @haowang-bioinfo maybe you can guide how to test those tasks. I only find the RAVEN function taskStruct = parseTaskList('../data/metabolicTasks_Essential.txt'); |
When running checkTasks in this case, you can set the getEssential input to False, since you don’t need to get the essential reactions, just test if the tasks pass. So the second line could just be: checkTasks(bModel,[],true,false,false,taskStruct); This will greatly decrease run time, since the essentiality part takes a while. |
feel free to start a PR which can be made directly from a branch within Human-GEM, rather than from a forked repo (then we can check out the tasks). Is this clear? @Devlin-Moyer |
yea I can do that once #624 is merged; I've been holding off on opening any other PRs that add new reactions until #624 is merged since that adds new reactions, and having multiple PRs that add new reactions open at the same time seems like it'd set us up for some confusing/annoying/complicated merge conflicts and/or distinct reactions with the same IDs |
Addressed by #670 |
Problems
Similarly to #607, I found a number of pairs of reactions that are largely identical except one reduces FAD to FADH2 and the other reduces O2 to H2O2:
There's also this strange case:
MAR00059: 3alpha,7alpha-dihydroxy-5beta-cholest-24-enoyl-CoA [x] + FADH2 [x] + 0.5 O2 [x] ⇒ (24R,25R)3alpha,7alpha,24-trihydroxy-5beta-cholestanoyl-CoA [x] + FAD [x], GPR: ACOX2
Background/Rationale
ACOX2 irreversibly oxidizes its substrates (see Uniprot and this paper), so
MAR00059
definitely doesn't represent a reaction catalyzed by ACOX2 (see #634 for details and examples of reactions that ACOX2 should be associated with). However,MAR00059
is very similar toMAR01706
:MAR00059: 3alpha,7alpha-dihydroxy-5beta-cholest-24-enoyl-CoA [x] + FADH2 [x] + 0.5 O2 [x] ⇒ (24R,25R)3alpha,7alpha,24-trihydroxy-5beta-cholestanoyl-CoA [x] + FAD [x], GPR: ACOX2
MAR01706: 3alpha,7alpha-dihydroxy-5beta-cholest-24-enoyl-CoA [x] + H2O [x] ⇒ (24R,25R)3alpha,7alpha,24-trihydroxy-5beta-cholestanoyl-CoA [x], GPR: ACAA1 and EHHADH and HSD17B4
According to this paper about bile acid biosynthesis,
MAR01706
already accurately represents this step in the pathway and the catalytic activities of EHHADH and HSD17B4 (also see their Uniprot pages), soMAR00059
should just be removed for being a less-accurate version ofMAR01706
. Relatedly, ACAA1 is a 3-ketoacyl thiolase, andMAR01706
doesn't involve any thiolysis, so it should be removed from the GPR ofMAR01706
.Most similar reactions (i.e. the ~100 other reactions associated with ACOX1, ACOX2, or ACOX3 that involve peroxisomal metabolites) reduce O2 to H2O2 and not FAD to FADH2, so it would be easier/simpler to remove the FAD-dependent versions and keep the O2-dependent versions. However, that would be inconsistent with the changes and rationale in #607, where we kept the FAD-dependent versions of the reactions to explicitly account for its role in the transfer of electrons from various substrates to ubiquinone. Also, FAD cofactors are not covalently attached to most human enzymes (source), FAD cannot be biosynthesized in human peroxisomes (source), and SLC25A17 (
ENSG00000100372
) exchanges cytosolic FAD for peroxisomal FMN in humans (same source as before). Keeping the FAD-dependent members of each of these pairs, replacing O2 and H2O2 with FAD and FADH2 in all similar reactions, and adding a separate reaction for reduction of O2 to H2O2 by FADH2 would be a lot of work, but it would be more realistic (and consistent with #607).Proposed Changes
MAR00059
for being a less accurate version ofMAR01706
MAR01706
toENSG00000113790 or ENSG00000133835
and addPMID:19357427
to its referencesMAR01639
for being redundant withMAR01638
MAR03301
for being redundant withMAR02804
MAR03306
for being redundant withMAR02808
MAR03311
for being redundant withMAR02810
MAR04966
for being redundant withMAR02818
MAR03364
for being redundant withMAR03276
MAR03369
for being redundant withMAR03289
MAM02630x
(O2) withMAM01802x
(FAD) andMAM02041x
(H2O2) withMAM01803x
(FADH2) inMAR00442, MAR00759, MAR00777, MAR00800, MAR00833, MAR00872, MAR00952, MAR00968, MAR00974, MAR00975, MAR00977, MAR00978, MAR00982, MAR01001, MAR01005, MAR01018, MAR01162, MAR01205, MAR01254, MAR01271, MAR01291, MAR01296, MAR01303, MAR01600, MAR01704, MAR02408, MAR02510, MAR03053, MAR03054, MAR03055, MAR03056, MAR03057, MAR03062, MAR03066, MAR03070, MAR03074, MAR03078, MAR03082, MAR03086, MAR03090, MAR03094, MAR03098, MAR03102, MAR03326, MAR03330, MAR03334, MAR03338, MAR03342, MAR03346, MAR03350, MAR03356, MAR03360, MAR03459, MAR03466, MAR03470, MAR03498, MAR03506, MAR03512, MAR03849, MAR03984, MAR04001, MAR04650, MAR04789, MAR04981, MAR05025, MAR05026, MAR05028, MAR05097, MAR05100, MAR05108, MAR05119, MAR05175, MAR05178, MAR05180, MAR05182, MAR05184, MAR05189, MAR05196, MAR05300, MAR05327, MAR05331, MAR05350, MAR05366, MAR05372, MAR05374, MAR05377, MAR05382, MAR05421, MAR05428, MAR05431, MAR06284, MAR06285, MAR06322, MAR06344, MAR06345, MAR06933, MAR06936, MAR06943, MAR06946, MAR06949, MAR06952, MAR06959, MAR06962, MAR06964, MAR07641, MAR07647, MAR07704, MAR07706, MAR08017, MAR08021, MAR08415, MAR08689, MAR08690, MAR08755, MAR11529, MAR11534, MAR11539, MAR12372, MAR12808, and MAR20066
(every reaction that consumes O2 and produces H2O2 in the peroxisome except the ones that already have FAD-dependent versions)MAM02630x + MAM01803x -> MAM02041x + MAM01802x
, GPR:ENSG00000161533 or ENSG00000168306 or ENSG00000087008 or ENSG00000110887 or ENSG00000203797 or ENSG00000007171 or ENSG00000148832 or ENSG00000179761 or ENSG00000158125
(every enzyme mentioned here except ACOXL, which the paper says is not known to be catalytically active, UOX, which is a pseudogene in humans, and HAO1 and HAO2, which use FMN and not FAD according to this paper)The text was updated successfully, but these errors were encountered: