Activator convergence audit
Generated by audit_activator_convergence.py; do not edit by hand. Part of EXECUTABLE_MODELS. Full detail, including each connection's description, is in activator_convergence_audit.yaml.
Every step with two or more activating regulators, which the Boolean translation would OR together by default. ALTERNATIVE_VARIANTS steps are settled by the module's own structure (the activators are alternative variants); DECLARED steps carry activation_logic; UNDECIDED steps need a curator to read the module.
274 steps in 150 modules: ALTERNATIVE_VARIANTS 40, DECLARED 8, UNDECIDED 226.
| module | step | classification | default rule | declared rule |
|---|---|---|---|---|
adrenal_steroidogenesis |
17alpha-hydroxylation and 17,20-lyase (to 17OH-steroids and DHEA/androstenedione) | UNDECIDED | (cyp11a1_step | hsd3b2_step) |
|
adrenal_steroidogenesis |
21-hydroxylation (progesterone to DOC; 17OH-progesterone to 11-deoxycortisol) | UNDECIDED | (cyp17a1_step | hsd3b2_step) |
|
alginate_polymerization_export |
AlgK secretion scaffold | UNDECIDED | (alg8_alg44_synthase | algG_maturation) |
|
aliphatic_glucosinolate_myrosinase_defense |
Methylthioalkylmalate synthase (MAM) | UNDECIDED | (ipmdh_decarboxylation | met_deamination) |
|
aliphatic_glucosinolate_myrosinase_defense |
Myrosinase (thioglucosidase) hydrolysis | UNDECIDED | (alkenylation | sulfation) |
|
arginine_biosynthesis |
N-acetyl-L-glutamate to N-acetyl-L-glutamyl 5-phosphate | UNDECIDED | (argJ_transacetylation_variant | glutamate_acetylation_step) |
|
arginine_biosynthesis |
L-ornithine to L-citrulline | UNDECIDED | (argE_deacetylation_variant | argJ_transacetylation_variant | carbamoyl_phosphate_synthetase_a_step) |
|
auxin_polar_transport |
PIN-mediated polar auxin efflux | UNDECIDED | (abcb_auxin_export | auxin_influx | pin_kinase_regulation) |
|
bacterial_c_di_amp_signaling |
Phosphodiesterase hydrolysis of c-di-AMP to pApA | UNDECIDED | (c_di_amp_synthesis | papa_clearance) |
|
bacterial_chemotaxis_signal_transduction |
Flagellum-dependent motility output | UNDECIDED | (c_ring_motor_switch | flagellar_stator_conductance) |
|
bacterial_chromosomal_dna_replication |
DNA polymerase III alpha-epsilon core | UNDECIDED | (beta_clamp_processivity | dnag_priming) |
|
bacterial_cytochrome_c_maturation_system_i |
CcmE heme chaperone | UNDECIDED | (ccmc_heme_handling_subunit | ccmd_accessory_subunit) |
|
bacterial_cytochrome_c_maturation_system_i |
CcmF/CcmH heme-ligation machinery | UNDECIDED | (ccmab_energy_coupling | ccmh_redox_component) |
|
bacterial_flagellar_assembly_export |
Hook-filament junction, flagellin filament, and cap | UNDECIDED | (flagellar_late_transcription | rod_hook_assembly) |
|
bacterial_rna_degradation |
Processive 3'-to-5' RNA degradation | UNDECIDED | (degradosome_helicase_assistance | rne_endonucleolytic_cleavage) |
|
bacterial_rna_polymerase_core |
RpoB/RpoC catalytic cleft | UNDECIDED | (rpoa_alpha_dimer_platform | rpoz_omega_assembly_subunit) |
|
bacterial_ruvabc_holliday_junction_processing |
RuvC cleavage and resolution of the Holliday junction | UNDECIDED | (recg_branch_migration | ruvb_branch_migration) |
|
bacterial_twin_arginine_translocation |
Active Tat translocon assembly | UNDECIDED | (tatb_receptor_organization | tatc_substrate_recognition) |
|
bacterial_type_ii_secretion |
Type II secretion pseudopilus | UNDECIDED | (inner_membrane_platform | secretion_atpase) |
|
bile_acid_biosynthesis |
3-beta-hydroxy-Delta5-C27-steroid dehydrogenase (HSD3B7) | UNDECIDED | (cholesterol_7a_hydroxylation | oxysterol_7a_hydroxylation) |
|
bile_acid_synthesis_ring_modification |
7-alpha-hydroxycholesterol to 7-alpha-hydroxy-4-cholesten-3-one | UNDECIDED | (cyp7a1_step | cyp7b1_step) |
|
bile_acid_synthesis_sidechain_conjugation |
choloyl-CoA + glycine/taurine to glyco-/tauro-cholate | UNDECIDED | (acox2_step | slc27a5_step) |
|
branched_chain_amino_acid_biosynthesis |
Branched-chain 2-oxoacids to L-valine, L-leucine, and L-isoleucine | UNDECIDED | (ilvD_step | leuB_step) |
|
branched_chain_amino_acid_biosynthesis |
2-Isopropylmalate to 3-isopropylmalate | UNDECIDED | (ipm_export_step | leuA_step) |
|
c_elegans_cgmp_sensory_transduction |
TAX-4/TAX-2 heteromeric cyclic nucleotide-gated channel | UNDECIDED | (afd_thermosensory_rgc | daf11_gc | o2_sensing_sgc | odr1_gc) |
|
c_elegans_lysosomal_lipid_signaling |
LBP-8 lipid chaperone shuttle | UNDECIDED | (lipl4_lysosomal_lipolysis | nhr_reception) |
|
c_elegans_mutator_22g_rna_amplification |
RDE-3/MUT-2 poly(UG) tailing of target RNA | UNDECIDED | (mut14_helicase | mutator_scaffold | rde8_endonuclease) |
|
c_elegans_mutator_22g_rna_amplification |
RRF-1 RNA-dependent RNA polymerase synthesis of 22G-RNAs | UNDECIDED | (mutator_scaffold | pug_tailing) |
|
c_elegans_mutator_22g_rna_amplification |
Mutator-dependent WAGO silencing branch | UNDECIDED | (ego1_rdrp | rdrp_synthesis) |
|
c_elegans_p_granule_assembly_segregation |
PGL self-associating RNA-binding scaffold core | UNDECIDED | (glh_perinuclear_layer | meg_embryonic_shell) & !mex_gradient |
|
camalexin_biosynthesis |
Indole cyanohydrin / dehydro-IAN formation | UNDECIDED | (iaox_formation | wrky33_activity) |
|
camalexin_biosynthesis |
CYP71B15/PAD3: dihydrocamalexate synthase (no GO term yet) | UNDECIDED | (ggp_step | wrky33_activity) |
|
cardiac_specification_network |
Cardiogenic GATA factor | UNDECIDED | (nk2_factor | tbox_factor) |
|
cardiac_specification_network |
Hand bHLH factor | UNDECIDED | (gata_factor | nk2_factor) |
|
cardiac_specification_network |
MEF2 myocardial differentiation factor | UNDECIDED | (gata_factor | nk2_factor) |
|
carnitine_shuttle |
acylcarnitine (cytosolic side) / carnitine (matrix) antiport | UNDECIDED | (cpt1_step | cpt2_step) |
|
cdp_dag_phospholipid_synthesis |
CDP-DAG-dependent cardiolipin synthase (CRD1) | UNDECIDED | (cdp_dag_synthesis | pgp_dephosphorylation) |
|
cellulose_biosynthesis |
(1->4)-beta-D-glucan polymerization by the CSC | UNDECIDED | (accessory_factors | microtubule_guidance | udp_glucose_supply) |
|
cerebellum_development |
Purkinje-cell DNER contribution to Bergmann-glial maturation | UNDECIDED | (early_purkinje_plate_formation | gcp_smoothened_transducer | purkinje_shh_signal) |
|
cerebellum_development |
SMO transducer in granule-cell precursors | UNDECIDED | (early_purkinje_plate_formation | germinal_zone_lineage_specification | purkinje_shh_signal) |
|
cerebellum_development |
Granule-cell inward migration | UNDECIDED | (early_purkinje_plate_formation | gcp_smoothened_transducer | purkinje_shh_signal) |
|
cerebellum_development |
PTPN11-ERK Bergmann-glial specification program | UNDECIDED | (early_purkinje_plate_formation | gcp_smoothened_transducer | purkinje_shh_signal) |
|
cerebellum_development |
Regional cerebellar foliation | UNDECIDED | (dner_purkinje_signal | gcp_smoothened_transducer | granule_cell_migration | ptpn11_erk_bg_specification) |
|
cholesterol_synthesis_post_lanosterol |
Delta24-sterol to 24,25-dihydro sterol (desmosterol to cholesterol; zymosterol to zymostenol) | UNDECIDED | (dhcr7_step | hsd17b7_step) |
|
cholesterol_synthesis_post_lanosterol |
Delta(8)-sterol to Delta(7)-sterol | UNDECIDED | (dhcr24_step | hsd17b7_step) |
|
ciliary_transition_zone |
MKS module | UNDECIDED | (cep290_module | mks5_assembly_hub) |
|
coenzyme_a_biosynthesis |
Pantoate to 4-phosphopantoate | UNDECIDED | (aminopropanal_dehydrogenase_step | aspartate_decarboxylation_route | ketopantoate_reductase_step) |
|
coenzyme_a_biosynthesis |
(R)-pantoate and beta-alanine to pantothenate | UNDECIDED | (aminopropanal_dehydrogenase_step | aspartate_decarboxylation_route | ketopantoate_reductase_step) |
|
coenzyme_q10_biosynthesis |
C1 decarboxylation (COQ4) and C1 hydroxylation (COQ6) | UNDECIDED | (c5_hydroxylation | synthome_regulation) |
|
coenzyme_q10_biosynthesis |
3-demethoxyubiquinone hydroxylase (COQ7) | UNDECIDED | (c2_methylation | substrate_presentation) |
|
complex_i_assembly_factors |
Q-module intermediate assembly (NDUFAF3-NDUFAF4, NDUFAF6) | UNDECIDED | (ci_membrane_arm_assembly | ci_subunit_maturation) |
|
complex_iv_assembly_factors |
incorporation of the early COX7/COX8 nuclear subunits | UNDECIDED | (cua_metallation | cub_metallation) |
|
conidiation_regulatory_cascade |
BrlA master-switch induction | UNDECIDED | (flbB | flbC | flbD | flbE | fluG) |
|
conidiation_regulatory_cascade |
FL fluffy master regulator | UNDECIDED | (neu_acon2 | neu_frq | neu_wc1 | neu_wc2) |
|
creatine_phosphocreatine_system |
Phosphocreatine shuttle / creatine kinase system (see MODULE:phosphocreatine_shuttle) | UNDECIDED | (biosynthesis_part | transport_part) |
|
cuproptosis |
FDX1-mediated Cu(II) reduction (master trigger) | UNDECIDED | (atox1_copper_chaperone | copper_exporting_atpase | ctr1_copper_import) |
|
cuproptosis |
Lipoylated pyruvate dehydrogenase complex (copper targets) | UNDECIDED | (fdx1_trigger | lipoylation_machinery) |
|
dolichol_phosphate_sugar_donor_supply |
presentation/utilisation of Dol-P-Man and Dol-P-Glc | UNDECIDED | (alg5_step | dpm_complex_step) |
|
emp_glycolysis |
Ferredoxin-dependent oxidation (archaeal GAPOR) | UNDECIDED | (aldolase_step | tpi_step) |
|
emp_glycolysis |
G3P + phosphate + NAD(P)+ to 1,3-bisphospho-D-glycerate | UNDECIDED | (aldolase_step | tpi_step) |
|
emp_glycolysis |
Non-phosphorylating NADP+ oxidation (GAPN bypass) | UNDECIDED | (aldolase_step | tpi_step) |
|
er_unfolded_protein_response |
BiP ER HSP70 chaperones | UNDECIDED | (atf6_arm | hac1_transcription_factor | xbp1_transcription_factor) |
|
ergosterol_biosynthesis |
lanosterol to 4,4-dimethylcholesta-8,14,24-trienol + formate | UNDECIDED | (erg7_step | ncp1_activity) |
|
ergosterol_biosynthesis |
squalene + O2 + reduced P450 reductase to (S)-2,3-epoxysqualene | UNDECIDED | (erg9_step | ncp1_activity) |
|
ergosterol_biosynthesis |
4-methyl sterol to 4-carboxy sterol (three successive oxidations; twice per sterol) | UNDECIDED | (cyb5_activity | erg24_step) |
|
ergosterol_biosynthesis |
episterol to ergosta-5,7,24(28)-trienol | UNDECIDED | (cyb5_activity | erg2_step) |
|
ergosterol_biosynthesis |
ergosta-5,7,24(28)-trienol to ergosta-5,7,22,24(28)-tetraenol | UNDECIDED | (erg3_step | ncp1_activity) |
|
ergosterol_biosynthesis |
(S)-2,3-epoxysqualene to lanosterol | UNDECIDED | (erg1_step | erg27_activity) |
|
erythromycin_biosynthesis |
EryBV attaches L-mycarose to erythronolide B | UNDECIDED | (eryF_step | mycarose_pathway) |
|
erythromycin_biosynthesis |
EryCIII (activated by EryCII) attaches D-desosamine, forming erythromycin D | UNDECIDED | (desosamine_pathway | eryBV_step) |
|
ether_lipid_plasmalogen_biosynthesis |
Alkyldihydroxyacetone-phosphate synthase (AGPS) | UNDECIDED | (dhap_acylation | fatty_alcohol_synthesis) |
|
eukaryotic_thiamine_biosynthesis |
HMP-P to HMP-PP | UNDECIDED | (hmp_kinase_step | thi5_hmpp_synthase_step) |
|
eukaryotic_thiamine_biosynthesis |
Thiazole phosphate + HMP-PP to thiamine monophosphate (THI6) | UNDECIDED | (adt_processing_step | het_kinase_step | hmpp_kinase_step) |
|
ferroptosis |
Ferroptosis execution | UNDECIDED | (labile_iron_supply | pufa_phospholipid_supply) & !(dhodh_coq_defense | fsp1_coq_defense | gch1_bh4_defense | gpx4_gsh_defense) |
|
ferroptosis |
GPX4-glutathione defense | UNDECIDED | (atf4_isr_inducer | nrf2_master_antioxidant) & !tp53_context_regulator |
|
floral_meristem_identity |
AP1/CAL/FUL establish floral fate | UNDECIDED | (integrator_input | lfy_program) & !tfl1_inflorescence_maintenance |
|
floral_meristem_identity |
LEAFY floral meristem identity program | UNDECIDED | (ap1_floral_fate | integrator_input) & !tfl1_inflorescence_maintenance |
|
floral_organ_identity_abce |
Whorl-specific floral quartet complexes | UNDECIDED | (b_function | e_function) |
|
folate_one_carbon_interconversion |
5,10-methenyl-THF to 10-formyl-THF hydrolysis | UNDECIDED | (formyl_folate_salvage | methylene_methenyl_redox) |
|
g1_s_transition |
Activator E2F transcription factor | UNDECIDED | (g1_cdk_priming | g1s_cdk_activation) & !rb_corepressor |
|
g1_s_transition |
Fission-yeast MBF (Cdc10-Res1-Res2) | UNDECIDED | (g1_cdk_priming | g1s_cdk_activation) |
|
g1_s_transition |
G1/S cyclin-CDK activation | UNDECIDED | (e2f_activator | fission_yeast_mbf | sbf_mbf | scf_ligase) |
|
g1_s_transition |
SBF/MBF transcription factor | UNDECIDED | (g1_cdk_priming | g1s_cdk_activation) & !whi5_corepressor |
|
g2_m_transition |
Cdc25 dephosphorylation of CDK1 Tyr15/Thr14 | UNDECIDED | (cdk1_cyclinb_assembly | polo_reinforcement | wee1_inhibition) & !checkpoint_restraint |
|
g2_m_transition |
Cyclin B-CDK1 assembly and CAK phosphorylation | UNDECIDED | (cdc25_activation | endosulfine | pp2a_b55) |
|
g2_m_transition |
Inhibitory Tyr15/Thr14 phosphorylation by Wee1/Myt1 | UNDECIDED | (cdk1_cyclinb_assembly | checkpoint_restraint) & !(cdk1_cyclinb_assembly | polo_reinforcement) |
|
galactose_leloir_pathway |
alpha-D-galactose 1-phosphate + UDP-glucose to glucose-1-phosphate + UDP-galactose | UNDECIDED | (gale_step | galk1_step) |
|
gibberellin_della_signaling |
PIF-driven growth transcription | UNDECIDED | (della_degradation | della_recognition) |
|
glutathione_synthesis_gamma_glutamyl_cycle |
Cys-Gly dipeptidase (DUG1/CNDP2 M20A family) | UNDECIDED | (dug2_dug3_gsh_cleavage | extracellular_gsh_breakdown | intracellular_gsh_degradation) |
|
glutathione_synthesis_gamma_glutamyl_cycle |
gamma-glutamyl transpeptidase (GGT) | UNDECIDED | (glutathione_recycling | glutathione_synthesis) |
|
glutathione_synthesis_gamma_glutamyl_cycle |
5-oxoprolinase (OPLAH) | UNDECIDED | (gamma_glutamyl_cyclization | intracellular_gsh_degradation) |
|
glutathione_thioredoxin_redox_systems |
Thioredoxin-dependent thiol peroxidases | UNDECIDED | (sod_step | trx_step) |
|
glycogen_biosynthesis |
glycogen(n) + UDP-glucose to glycogen(n+1) + UDP | UNDECIDED | (gbe1_step | gyg1_step | ugp2_step) |
|
glycogen_synthesis_and_mobilization |
GlgP-dependent glycogen phosphorolysis | UNDECIDED | (glgb_branch_formation | glgx_branch_removal) |
|
glycolate_glyoxylate_assimilation |
Tartronate semialdehyde to glycerate | UNDECIDED | (glyoxylate_carboligase | hydroxypyruvate_isomerization) |
|
glycosphingolipid_biosynthesis |
GM2/GD2 synthase (B4GALNT1) | UNDECIDED | (ganglio_gd3 | ganglio_gm3) |
|
glycosphingolipid_lysosomal_degradation |
ceramide to sphingosine + fatty acid | UNDECIDED | (galc_step | gba_step | smpd1_step) |
|
heat_shock_response |
Cytosolic Hsp70 folding cycle with J-domain, HSP110 and BAG cofactors | UNDECIDED | (hsf_activation | shsp_holdase) |
|
hedgehog_signaling |
Slimb/beta-TrCP SCF substrate adaptor | UNDECIDED | (ck1_processive_kinase | gsk3_processive_kinase) |
|
hedgehog_signaling |
SUFU release and Fused-family phosphorylation of Ci/GLI | UNDECIDED | (smo_pka_inhibition | smo_transducer) |
|
hedgehog_signaling |
Smoothened pseudosubstrate inhibition of protein kinase A | UNDECIDED | (hh_coreceptor | hspg_ligand_distribution | patched_receptor | vertebrate_secreted_accessories) |
|
hedgehog_signaling |
Smoothened transducer | UNDECIDED | (hh_coreceptor | hspg_ligand_distribution | patched_receptor | vertebrate_secreted_accessories) & !patched_receptor |
|
hexosamine_biosynthesis |
Phosphoacetylglucosamine mutase (PGM3) | UNDECIDED | (glcn6p_acetylation | glcnac_salvage) |
|
homocysteine_metabolism |
L-homocysteine + 5-methyl-THF to L-methionine + THF | UNDECIDED | (cobalamin_support | mthfr_step) |
|
intraflagellar_transport |
Accessory homodimeric kinesin-2 transport | UNDECIDED | (dyf5_regulation | kinesin_ii_import) |
|
intraflagellar_transport |
Heterotrimeric kinesin-II transport of IFT trains | UNDECIDED | (ift_a_complex | ift_b_complex) & !dyf5_regulation |
|
jak_stat_signaling |
STAT recruitment and phosphorylation | UNDECIDED | (alt_stat_inputs | receptor_phosphorylation) |
|
lignin_monolignol_biosynthesis |
Monolignol transport across the plasma membrane | UNDECIDED | (c3h_step | cad_step | ccoaomt_step | comt_step | hct_step) |
|
lipid_a_raetz_biosynthesis |
Lipid A disaccharide synthesis | UNDECIDED | (lpxD_step | lpxH_step) |
|
malate_aspartate_shuttle |
Inner-membrane carriers (SLC25A11 OGC, SLC25A12 AGC1) | UNDECIDED | (mas_cytosolic_arm | mas_matrix_arm) |
|
metaphase_anaphase_transition_and_mitotic_exit |
Cdh1/Hct1/Ste9 coactivator | UNDECIDED | (apc_c | cdc14_scer | clp1_spom | cohesin_kleisin | metazoan_pp2a_b55_reactivation) |
|
metazoan_autophagosome_biogenesis |
LC3-subfamily Atg8 in phagophore elongation | UNDECIDED | (atg8_conjugation | cargo_recruitment) |
|
metazoan_autophagosome_biogenesis |
GABARAP-type LGG-1 in autophagosome formation | UNDECIDED | (atg8_conjugation | cargo_recruitment) |
|
methionine_cycle |
S-adenosyl-L-homocysteine -> L-homocysteine | UNDECIDED | (gnmt_activity | meth_activity) |
|
methionine_cycle |
Cystathionine beta-synthase activity | UNDECIDED | (ahc_step | amet_pool) |
|
methionine_cycle |
Glycine N-methyltransferase activity | UNDECIDED | (amet_pool | mat1_activity | mat3_activity) & !(ahcys_pool | mlthf_pool) |
|
methionine_cycle |
MAT-III methionine adenosyltransferase activity | UNDECIDED | (amet_pool | bhmt_route | met_pool | mete_route | ms_route) |
|
methionine_cycle |
Folate-dependent remethylation, cobalamin-independent (MetE-type methionine synthase) | UNDECIDED | (ahc_step | mthfr_activity) |
|
methionine_cycle |
Folate-dependent remethylation, cobalamin-dependent (MetH/MTR-type methionine synthase) | UNDECIDED | (ahc_step | mthfr_activity) |
|
mitochondrial_complex_v |
F1 sector (alpha3-beta3 catalytic head + central stalk) | UNDECIDED | (complex_v_assembly | complex_v_fo) |
|
mitochondrial_upr |
HSP60 and mtHSP70 matrix chaperone output | UNDECIDED | (dve1_activator | jmjd31_demethylase | lin65_cofactor | ubl5_coactivator | uprmt_transcription_factor) |
|
mitochondrial_upr |
ATFS-1/ATF5 nuclear transcriptional activation | UNDECIDED | (atf4_isr_activation | atfs1_import_checkpoint | dve1_activator | hri_eif2a_phosphorylation | jmjd31_demethylase | lin65_cofactor | ubl5_coactivator) & !atfs1_import_checkpoint |
|
muth_independent_mismatch_repair |
DNA polymerase-dependent gap filling | UNDECIDED | (excision_nuclease_choice | ssb_excision_scaffold) |
|
neural_crest_gene_regulatory_network |
FoxD3 crest specifier | UNDECIDED | (id3_competence | myc_competence | pax3_border | pax7_border | pou5f3_competence | tfap2c_border | zic1_border) |
|
neural_crest_gene_regulatory_network |
Neural crest delamination and migration | UNDECIDED | (foxd3_spec | snai2_spec | sox10_variant | sox8_spec | sox9_variant | tfap2a_spec | tfap2b_spec) |
|
neural_crest_gene_regulatory_network |
Pax3 border specifier | UNDECIDED | (gbx2_border | msx1_border | pou5f3_competence | tfap2a_border) |
|
neural_crest_gene_regulatory_network |
Snail1 early crest specifier | UNDECIDED | (id3_competence | myc_competence | pax3_border | pax7_border | pou5f3_competence | tfap2c_border | zic1_border) |
|
neural_crest_gene_regulatory_network |
Snai2 crest specifier | UNDECIDED | (pax3_border | snai1_spec) & !twist1_snai2_inhibition |
|
neural_crest_gene_regulatory_network |
Sox10 | UNDECIDED | (id3_competence | myc_competence | pax3_border | pax7_border | pou5f3_competence | tfap2c_border | zic1_border) |
|
neural_crest_gene_regulatory_network |
Sox8 crest specifier | UNDECIDED | (id3_competence | myc_competence | pax3_border | pax7_border | pou5f3_competence | tfap2c_border | zic1_border) |
|
neural_crest_gene_regulatory_network |
Sox9 | UNDECIDED | (id3_competence | myc_competence | pax3_border | pax7_border | pou5f3_competence | tfap2c_border | zic1_border) |
|
neural_crest_gene_regulatory_network |
AP-2alpha crest specifier | UNDECIDED | (id3_competence | myc_competence | pax3_border | pax7_border | pou5f3_competence | tfap2c_border | zic1_border) |
|
neural_crest_gene_regulatory_network |
AP-2beta (TFAP2A–TFAP2B) crest specifier | UNDECIDED | (id3_competence | myc_competence | pax3_border | pax7_border | pou5f3_competence | tfap2c_border | zic1_border) |
|
neural_crest_gene_regulatory_network |
Twist1 ectomesenchyme driver | UNDECIDED | (neural_crest_emigration | pax3_border) |
|
nicotine_biosynthesis |
nicotinic acid N-glucoside reduction (A622 / NaGR) | UNDECIDED | (mpo_step | ugt_step) |
|
nitrogen_assimilation_glutamate_glutamine |
L-glutamate + ammonium + ATP to L-glutamine | UNDECIDED | (glutamate_deamination_step | gs_gogat_route | nadp_gdh_route) |
|
nitrogen_cycle |
Ammonia assimilation (GS/GOGAT cycle) | UNDECIDED | (assim_nitrite_reduction | nitrogen_fixation) |
|
notch_signaling |
Notch receptor binds ligand in trans | UNDECIDED | (notch_fringe_elongation | notch_ligand_presentation) & !notch_cis_inhibition |
|
notch_signaling |
Notch target gene output | UNDECIDED | (csl_dna_binding | mastermind_coactivation) |
|
nucleokinesis |
Dynein-dynactin-LIS1-NDEL1 nuclear motor | UNDECIDED | (nuclear_envelope_motor_coupling | perinuclear_microtubule_track) |
|
oxphos |
F1 catalytic head | UNDECIDED | (complex_IV | respiratory_chain_variants) |
|
oxphos |
Fo proton-translocating sector | UNDECIDED | (complex_IV | respiratory_chain_variants) |
|
oxphos |
Proton-motive-force-driven ATP synthesis (rotational) | UNDECIDED | (complex_IV | respiratory_chain_variants) & !if1_inhibitor |
|
oxphos |
Quinone pool (ubiquinone/menaquinone) | UNDECIDED | (auxiliary_quinone_dehydrogenases | complex_I | complex_II) |
|
pentose_phosphate_nonoxidative_branch |
D-xylulose-5-P + D-ribose-5-P to sedoheptulose-7-P + D-glyceraldehyde-3-P | UNDECIDED | (rpe_step | rpia_step) |
|
pentose_phosphate_pathway |
Transketolase: xylulose 5-phosphate plus ribose 5-phosphate | UNDECIDED | (ribose_5_phosphate_isomerase_step | ribulose_phosphate_epimerase_step) |
|
pentose_phosphate_pathway |
Transketolase: xylulose 5-phosphate plus erythrose 4-phosphate | UNDECIDED | (ribulose_phosphate_epimerase_step | transaldolase_step) |
|
peptidoglycan_precursor_biosynthesis |
MurF pentapeptide ligation | UNDECIDED | (ddl_dipeptide_synthesis | murE_third_residue_ligation) |
|
peptidoglycan_recycling |
AnmK formation of MurNAc-6-phosphate | UNDECIDED | (ampD_peptide_release_step | nagZ_glycan_processing_step) |
|
peptidoglycan_recycling |
Mpl ligation of the recovered tripeptide to UDP-MurNAc | UNDECIDED | (ampD_peptide_release_step | murU_step) |
|
peroxisomal_beta_oxidation |
Acyl-CoA oxidases | UNDECIDED | (intraperoxisomal_activation | thiolytic_cleavage) |
|
peroxisomal_beta_oxidation |
Multifunctional proteins (D-specific MFE-2; L-specific bifunctional protein) | UNDECIDED | (acyl_coa_oxidation | enoyl_coa_isomerisation) |
|
phagophore_assembly_site |
Atg1-dependent Atg13 phosphorylation and Atg1 complex dissociation | UNDECIDED | (pas_atg2_atg18 | pas_atg8_conjugation | pas_membrane_component | pas_pi3k_complex_i) |
|
phagophore_organelle_contact_site |
ATG2-family ER-phagophore membrane tether | UNDECIDED | (atg9_rim_scramblase | wipi4_atg18_clamp) |
|
phagophore_organelle_contact_site |
Lipid flux through the contact site | UNDECIDED | (atg2_clr_rim_anchor | atg2_tether | donor_membrane_face) & !escrt_iii_rim_sealing |
|
phenylalanine_tyrosine_biosynthesis |
phenylpyruvate / 4-hydroxyphenylpyruvate to L-phenylalanine / L-tyrosine | UNDECIDED | (pdh_step | pdt_step) |
|
photosynthesis |
NADP-dependent glyceraldehyde-3-phosphate dehydrogenase | UNDECIDED | (atp_synthase | light_harvesting) & !cp12_scaffold |
|
photosynthesis |
Phosphoribulokinase | UNDECIDED | (atp_synthase | light_harvesting) & !cp12_scaffold |
|
photosynthesis |
Bisphosphatase regeneration steps (FBPase, SBPase) | UNDECIDED | (atp_synthase | light_harvesting) |
|
photosynthesis |
Rubisco activase and inhibitor removal | UNDECIDED | (atp_synthase | light_harvesting) |
|
photosynthesis |
Rubisco carboxylation of RuBP | UNDECIDED | (atp_synthase | carbon_concentrating_mechanism | light_harvesting) |
|
polyamine_metabolism |
FAD-dependent polyamine oxidation | UNDECIDED | (polyamine_acetylation | spermidine_to_spermine) |
|
polyamine_metabolism |
Spermidine synthase | UNDECIDED | (ornithine_to_putrescine | sam_decarboxylation) |
|
polyamine_metabolism |
Spermine synthase | UNDECIDED | (putrescine_to_spermidine | sam_decarboxylation) |
|
pqq_biosynthesis |
PqqC terminal PQQ formation | UNDECIDED | (pqqa_proteolysis | pqqb_oxygenation) |
|
primary_cilium_life_cycle |
ARL13B activates ARL3 | UNDECIDED | (ift81_ift74_tubulin | ift_a_complex | ift_b_scaffold) |
|
primary_cilium_life_cycle |
ARL3 releases lipidated cargo | UNDECIDED | (arl13b_arl3_gef | pde6d_prenyl_carrier | unc119b_myristoyl_carrier) & !rp2_arl3_gap |
|
primary_cilium_life_cycle |
Aurora A drives disassembly | UNDECIDED | (nedd9_aurka_activation | pitchfork_aurka_activation) |
|
primary_cilium_life_cycle |
Dynein-2 | UNDECIDED | (cep290_tz_scaffold | mks_module | nphp_module) & !cilium_length_control |
|
primary_cilium_life_cycle |
IFT81-IFT74 tubulin module | UNDECIDED | (cep290_tz_scaffold | mks_module | nphp_module) & !cilium_length_control |
|
primary_cilium_life_cycle |
INPP5E sets ciliary phosphoinositides | UNDECIDED | (ift81_ift74_tubulin | ift_a_complex | ift_b_scaffold) |
|
primary_cilium_life_cycle |
Heterotrimeric kinesin-2 | UNDECIDED | (cep290_tz_scaffold | mks_module | nphp_module) & !cilium_length_control |
|
primary_cilium_life_cycle |
Myosin-Va preciliary vesicle delivery | UNDECIDED | (cp110_cep97_cap | ttbk2_cap_removal) |
|
primary_cilium_life_cycle |
NEDD9 activates Aurora A | UNDECIDED | (arl3_cargo_release | inpp5e_pip2_hydrolysis | tulp3_gpcr_import) |
|
primary_cilium_life_cycle |
PDE6D carries farnesylated cargo | UNDECIDED | (ift81_ift74_tubulin | ift_a_complex | ift_b_scaffold) |
|
primary_cilium_life_cycle |
Pitchfork activates Aurora A | UNDECIDED | (arl3_cargo_release | inpp5e_pip2_hydrolysis | tulp3_gpcr_import) |
|
primary_cilium_life_cycle |
PLK1 activates KIF2A | UNDECIDED | (arl3_cargo_release | inpp5e_pip2_hydrolysis | tulp3_gpcr_import) |
|
primary_cilium_life_cycle |
Phosphorylated Tctex-1 promotes resorption | UNDECIDED | (arl3_cargo_release | inpp5e_pip2_hydrolysis | tulp3_gpcr_import) |
|
primary_cilium_life_cycle |
TULP3 links IFT-A to membrane cargo | UNDECIDED | (ift81_ift74_tubulin | ift_a_complex | ift_b_scaffold) |
|
primary_cilium_life_cycle |
UNC119B carries myristoylated cargo | UNDECIDED | (ift81_ift74_tubulin | ift_a_complex | ift_b_scaffold) |
|
proline_metabolism |
P5C dehydrogenase completion of proline catabolism | UNDECIDED | (oat_p5c_supply | prodh_p5c_formation) |
|
proline_metabolism |
P5C reductase-dependent L-proline formation | UNDECIDED | (aldh18a1_semialdehyde_formation | oat_p5c_supply | split_semialdehyde_formation) |
|
propionyl_coa_catabolism |
(R)-methylmalonyl-CoA to succinyl-CoA | UNDECIDED | (adocbl_supply | mcee_step) |
|
protein_prenylation_caax_processing |
CAAX endoprotease (RCE1) | UNDECIDED | (farnesylation | geranylgeranylation_I) |
|
purine_nucleotide_catabolism |
Adenosine deaminase (ADA) | UNDECIDED | (cyto_amp_5nt | ecto_amp_5nt) |
|
purine_nucleotide_catabolism |
Purine-nucleoside phosphorylase (PNP) | UNDECIDED | (adenosine_deamination | imp_gmp_5nt) |
|
purine_nucleotide_catabolism |
Xanthine dehydrogenase/oxidase (XDH) | UNDECIDED | (guanine_deamination | nucleoside_phosphorolysis) |
|
purine_nucleotide_interconversion |
IMP + L-aspartate + GTP to adenylosuccinate + GDP + Pi | UNDECIDED | (ampd_step | ndp_kinase_step) |
|
purine_salvage_and_catabolism |
hypoxanthine/guanine + PRPP to IMP/GMP + PPi | UNDECIDED | (adenine_moiety_deamination | pnp_step) |
|
purine_salvage_and_catabolism |
hypoxanthine to xanthine to urate | UNDECIDED | (guanine_deamination_step | pnp_step) |
|
pyrenoid_ccm |
Lumenal bicarbonate dehydration (CAH3) | UNDECIDED | (pyrenoid_tubule_biogenesis | thylakoid_bicarbonate_entry) |
|
pyrenoid_ccm |
Rubisco carboxylation in the pyrenoid matrix | UNDECIDED | (lumenal_co2_release | starch_sheath_barrier) |
|
pyrenoid_ccm |
Thylakoid bicarbonate entry (bestrophin-like channels) | UNDECIDED | (ccm_induction | ci_uptake | stromal_co2_recapture) |
|
pyrimidine_nucleotide_catabolism |
Dihydropyrimidine dehydrogenase (DPYD) | UNDECIDED | (thymidine_phosphorolysis | uridine_phosphorolysis) |
|
pyrimidine_nucleotide_catabolism |
Uridine phosphorylase (UPP1 / UPP2) | UNDECIDED | (cytidine_deamination | pyrimidine_5nt) |
|
pyrimidine_salvage |
uracil + PRPP to UMP + PPi | UNDECIDED | (cytosine_deamination_step | nucleoside_cleavage) |
|
retinal_determination_network |
Eyes absent transcriptional coactivator-phosphatase | UNDECIDED | (dach_cofactor | pax6_selector) |
|
retinal_determination_network |
Six-family homeodomain transcription factor | UNDECIDED | (eya_cofactor | pax6_selector) |
|
retinoid_visual_cycle |
11-cis retinol dehydrogenase (RDH5) | UNDECIDED | (cralbp_carrier | isomerohydrolysis | photoisomerase) |
|
riboflavin_biosynthesis |
6,7-dimethyl-8-ribityllumazine formation | UNDECIDED | (dhbp_branch | phosphoribitylaminouracil_phosphatase_step) |
|
root_radial_patterning_shr_scr |
Nuclear capture of SHR by SCR and BIRD/IDD proteins | UNDECIDED | (shr_mobile_signal | shr_scr_bird_activation) |
|
root_radial_patterning_shr_scr |
SHR-SCR-BIRD activation of SCR, MGP and CYCD6;1 | UNDECIDED | (cycd6_formative_division | shr_nuclear_capture) |
|
scer_hog1_cascade |
Ssk2/Ssk22 MAP kinase kinase kinase activation | UNDECIDED | (ssk1_rr | ste50_ste11_activation) |
|
selenocysteine_biosynthesis_incorporation |
SelA-dependent Sec-tRNA(Sec) synthesis | UNDECIDED | (selenophosphate_synthesis | ser_trna_sec_synthesis) |
|
selenocysteine_biosynthesis_incorporation |
EEFSEC-dependent Sec-tRNA(Sec) delivery | UNDECIDED | (secisbp2_recognition | sepsecs_sec_trna_formation) |
|
selenocysteine_biosynthesis_incorporation |
PSTK-dependent phosphoseryl-tRNA(Sec) formation | UNDECIDED | (selenophosphate_synthesis | ser_trna_sec_synthesis) |
|
selenocysteine_biosynthesis_incorporation |
SECISBP2-dependent SECIS recognition | UNDECIDED | (selenophosphate_synthesis | ser_trna_sec_synthesis) |
|
sialic_acid_metabolism |
CMP-N-acetylneuraminate synthetase (CMAS) | UNDECIDED | (lysosomal_sialic_acid_export | neu5ac9p_to_neu5ac) |
|
spytag_spycatcher |
FbaB fibronectin binding and host-cell adhesion/invasion | UNDECIDED | (fbab_cell_wall_anchoring | fbab_cnab2_isopeptide | fbab_thioester_host_capture) |
|
synaptic_vesicle_exocytosis |
NSF / alpha-SNAP disassembly of the cis-SNARE complex | UNDECIDED | (presynaptic_calcium_influx | vesicle_priming) |
|
taurine_biosynthesis_and_transport |
Taurine transporter TauT (SLC6A6) | UNDECIDED | (cysteamine_dioxygenation | cysteinesulfinate_decarboxylation) |
|
tetrahydrobiopterin_metabolism |
aromatic amino acid hydroxylation consumes BH4, producing pterin-4a-carbinolamine | UNDECIDED | (qdpr_step | spr_step) |
|
tetrahydrofolate_biosynthesis |
7,8-dihydroneopterin to 7,8-dihydropteroate | UNDECIDED | (adc_lyase_step | dihydroneopterin_dephosphorylation_step) |
|
thiamine_diphosphate_biosynthesis |
HMP diphosphate plus thiazole phosphate to thiamine phosphate | UNDECIDED | (thiD_step | thiG_step) |
|
thiamine_diphosphate_biosynthesis |
Thiazole phosphate synthesis | UNDECIDED | (dehydroglycine_supply | dxs_step | thiS_sulfur_carrier_role) |
|
thiamine_diphosphate_biosynthesis |
ThiI: sulfur transfer to ThiS | UNDECIDED | (cysteine_desulfurase_activity | thiF_this_adenylylation_activity) |
|
thiamine_uptake_and_activation |
Mitochondrial thiamine pyrophosphate carrier (SLC25A19) | UNDECIDED | (thiamine_activation | thtp_homeostasis) |
|
type_ii_fatty_acid_synthesis |
FabD malonyl-ACP loading | UNDECIDED | (acetyl_coa_carboxylation | acp_carrier_role) |
|
ubiquinone_biosynthesis |
4-Hydroxy-3-polyprenylbenzoate to 3,4-dihydroxy-5-polyprenylbenzoate | UNDECIDED | (hydroxybenzoate_prenylation | ubiquinone_biosynthesis_accessory_system) |
|
ubiquinone_biosynthesis |
UbiX: flavin prenyltransferase | UNDECIDED | (hydroxybenzoate_prenylation | ubiquinone_biosynthesis_accessory_system) |
|
ubiquinone_biosynthesis |
Polyprenylation of 4-hydroxybenzoate | UNDECIDED | (chorismate_lyase_route | hydroxybenzaldehyde_oxidation_step | polyprenyl_diphosphate_tail_synthesis) |
|
urea_cycle |
L-citrulline + L-aspartate + ATP to argininosuccinate + AMP + PPi | UNDECIDED | (citrin_aspartate_supply | ornithine_citrulline_transport) |
|
urea_cycle |
citrulline export / ornithine import across the inner membrane (SLC25A15) | UNDECIDED | (arg1_step | otc_step) |
|
ureide_urea_catabolism |
urea + HCO3- + ATP to allophanate + ADP + Pi | UNDECIDED | (allantoicase_route | ureidoglycine_aminohydrolase_step | ureidoglycolate_breakdown_step) |
|
ureide_urea_catabolism |
Nickel urease (one step; most fungi, plants, many bacteria) | UNDECIDED | (allantoicase_route | ureidoglycine_aminohydrolase_step | ureidoglycolate_breakdown_step) |
|
wnt_signaling |
Wnt-Frizzled-co-receptor engagement | UNDECIDED | (rspo_lgr_potentiation | wnt_ligand_biogenesis) & !(rnf43_znrf3_receptor_turnover | secreted_antagonists) |
|
aps_dependent_assimilatory_sulfate_reduction |
Assimilatory reduction of sulfite to sulfide | ALTERNATIVE_VARIANTS | (direct_aps_reduction_route | paps_reductase_activity) |
|
bacterial_alkanesulfonate_uptake_desulfonation |
SsuD alkanesulfonate monooxygenation | DECLARED | (ssuabc_import | ssue_fmn_reduction) |
ssuabc_import & ssue_fmn_reduction |
bacterial_isc_iron_sulfur_cluster_assembly |
IscU scaffold assembly | DECLARED | (fdx_electron_delivery | isc_sulfur_mobilization) |
isc_sulfur_mobilization & fdx_electron_delivery |
bacterial_methionine_cycle |
Folate-dependent methionine regeneration | ALTERNATIVE_VARIANTS | (ahcy_route | luxs_step) |
|
bacterial_nonhomologous_end_joining |
LigD-mediated DNA-end sealing | DECLARED | (ku_end_recognition | ligd_end_processing) |
ku_end_recognition |
bacterial_pst_phosphate_uptake |
PstSACB phosphate translocation | DECLARED | (pstb_energy_coupling | psts_phosphate_capture) |
psts_phosphate_capture & pstb_energy_coupling |
bacterial_purine_base_oxidation_to_urate |
XdhAB-dependent xanthine oxidation to urate | ALTERNATIVE_VARIANTS | (guanine_deamination_route | hypoxanthine_oxidation_route) |
|
bacterial_sec_posttranslational_protein_export |
SecYEG protein-conducting channel | DECLARED | (seca_atpase_motor | secdf_yajc_accessory_complex) |
seca_atpase_motor |
bacterial_shikimate_chorismate_biosynthesis |
EPSP to chorismate | ALTERNATIVE_VARIANTS | (arom_epsps_step | discrete_epsps_step) |
|
bacterial_type_iv_secretion_apparatus |
Type IV secretion pilus | DECLARED | (envelope_core_complex | mating_pair_stabilization | virb4_family_atpase) |
envelope_core_complex & virb4_family_atpase |
biotin_biosynthesis |
Pimelate thioester to 8-amino-7-oxononanoate (KAPA) | ALTERNATIVE_VARIANTS | (bioH_step | fungal_peroxisomal_beta_oxidation_variant | saccharomyces_bio1_variant) |
|
c_elegans_dbl1_body_size_signaling |
SMA-6/DAF-4 receptor activation | DECLARED | (dbl1_ligand | sma10_lrig) |
dbl1_ligand |
carotene_backbone_biosynthesis |
Epsilon cyclization (lycopene -> delta-carotene) | ALTERNATIVE_VARIANTS | (crti_type_desaturation | crtiso_step) |
|
chitin_perception |
BIK1 phosphorylation of RBOHD | ALTERNATIVE_VARIANTS | (atcerk1_kinase | oscerk1_kinase) |
|
chitin_perception |
PBL27/OsRLCK185 RLCK phosphorylation of the MAP3K | ALTERNATIVE_VARIANTS | (atcerk1_kinase | oscerk1_kinase) |
|
coenzyme_a_biosynthesis |
4'-phosphopantothenate to phosphopantothenoylcysteine | ALTERNATIVE_VARIANTS | (pantothenate_kinase_step | phosphopantothenate_synthetase_step) |
|
de_novo_purine_synthesis |
SAICAR synthetase | ALTERNATIVE_VARIANTS | (ade2_purE_domain_substep | direct_air_carboxylase_route | purE_substep) |
|
emp_glycolysis |
D-glucose 6-phosphate to D-fructose 6-phosphate | ALTERNATIVE_VARIANTS | (adp_kinase_entry_variant | atp_kinase_entry_variant | glucan_entry_variant | pts_entry_variant) |
|
emp_glycolysis |
3-phospho-D-glycerate to 2-phospho-D-glycerate | ALTERNATIVE_VARIANTS | (ferredoxin_oxidation_variant | nonphosphorylating_nadp_variant | pgk_step) |
|
glucarate_galactarate_catabolism |
5-dehydro-4-deoxyglucarate to 2,5-dioxopentanoate | ALTERNATIVE_VARIANTS | (galactarate_entry | glucarate_entry) |
|
glycogen_synthesis_and_mobilization |
GlgB-dependent glycogen branching | ALTERNATIVE_VARIANTS | (glga_adp_chain_extension | glga_udp_chain_extension) |
|
heme_biosynthesis |
ALA condensation | ALTERNATIVE_VARIANTS | (c4_alas_step | c5_heml_activity) |
|
jak_stat_signaling |
STAT-dependent transcription | DECLARED | (mapk_branch_interface | stat_dimerization_import) & !(pias_restraint | ptp_dephosphorylation) |
stat_dimerization_import & !(ptp_dephosphorylation | pias_restraint) |
metazoan_autophagosome_biogenesis |
EPG5-dependent autophagosome-lysosome fusion | ALTERNATIVE_VARIANTS | (gabarap_fusion | lgg2_late) |
|
methionine_biosynthesis |
Direct sulfhydrylation of O-acetylhomoserine (metY) | ALTERNATIVE_VARIANTS | (o_acetyl_activation | o_succinyl_activation) |
|
methionine_biosynthesis |
Direct sulfhydrylation of O-succinylhomoserine (metZ) | ALTERNATIVE_VARIANTS | (o_acetyl_activation | o_succinyl_activation) |
|
methionine_biosynthesis |
Cystathionine gamma-synthase | ALTERNATIVE_VARIANTS | (o_acetyl_activation | o_succinyl_activation) |
|
methionine_biosynthesis |
Homocysteine methylation to methionine | ALTERNATIVE_VARIANTS | (direct_sulfhydrylation | direct_sulfhydrylation_metZ | metC_node) |
|
methionine_cycle |
MAT-I methionine adenosyltransferase activity | ALTERNATIVE_VARIANTS | (bhmt_route | mete_route | ms_route) & !amet_pool |
|
methionine_cycle |
Methionine adenosyltransferase (MAT2A/MetK/SAM1-type) | ALTERNATIVE_VARIANTS | (bhmt_route | mete_route | ms_route) |
|
methionine_cycle |
SAM-dependent methyltransferase activity (general) | ALTERNATIVE_VARIANTS | (mat1_activity | mat3_activity | mat_single_chain_activity) & !ahcys_pool |
|
methionine_salvage_mta_cycle |
acireductone + O2 to 4-methylthio-2-oxobutanoate + formate | ALTERNATIVE_VARIANTS | (bifunctional_e1_variant | hkmtp_phosphatase_step) |
|
methionine_salvage_mta_cycle |
MTR-1-P to S-methyl-5-thio-D-ribulose 1-phosphate | ALTERNATIVE_VARIANTS | (mta_phosphorylase_route | mtr_kinase_step) |
|
methylcitrate_cycle |
2-methyl-cis-aconitate hydration | ALTERNATIVE_VARIANTS | (prpD_direct_route | prpF_isomerization) |
|
mitophagy |
Atg8-family docking of mitophagy receptors on the phagophore | ALTERNATIVE_VARIANTS | (allo1_receptor | bnip3_nix_receptor | fundc1_receptor | ubiquitin_binding_receptors) |
|
nad_biosynthesis_salvage |
NaMN adenylylation alternatives | ALTERNATIVE_VARIANTS | (nadc_step | nicotinate_preiss_handler_route | nmn_deamidating_route | pncb_after_pnca_step) |
|
nad_de_novo_and_salvage_fungal |
NaMN to nicotinate adenine dinucleotide (NaAD) | ALTERNATIVE_VARIANTS | (nicotinate_phosphoribosyltransferase_step | nrk1_nicotinate_riboside_kinase_activity | quinolinate_phosphoribosyltransferase_step) |
|
peroxisome-lifecycle |
Matrix protein cargo targeting | ALTERNATIVE_VARIANTS | (pex16_supported_pmp_route | pex3_family_membrane_docking | rrbp1_supported_er_biogenesis_route) |
|
pirna_mediated_germline_silencing |
HRDE-1 nuclear 22G-RNA Argonaute | ALTERNATIVE_VARIANTS | (piwil2_slicer | wago1_cytoplasmic_effector) |
|
pirna_mediated_germline_silencing |
Piwi-directed H3K9me3 heterochromatin (Drosophila) | ALTERNATIVE_VARIANTS | (piwil2_slicer | wago1_cytoplasmic_effector) |
|
pirna_mediated_germline_silencing |
PIWIL4/MIWI2 nuclear piRNA effector | ALTERNATIVE_VARIANTS | (piwil2_slicer | wago1_cytoplasmic_effector) |
|
pirna_mediated_germline_silencing |
WAGO-4 Z granule 22G-RNA Argonaute | ALTERNATIVE_VARIANTS | (piwil2_slicer | wago1_cytoplasmic_effector) |
|
primordial_germ_cell_specification |
piRNA-guided transposon silencing in the germline | ALTERNATIVE_VARIANTS | (pgc_tripartite_network | preformation) |
|
riboflavin_biosynthesis |
Pyrimidine-intermediate dephosphorylation | ALTERNATIVE_VARIANTS | (rib2_deaminase_step | ribd_reductase_step) |
|
triacylglycerol_biosynthesis |
1-Acylglycerol-3-phosphate O-acyltransferases (AGPAT/SLC1, MBOAT ALE1, LOA1) | ALTERNATIVE_VARIANTS | (acyl_dhap_reduction | g3p_route) |
|
type_ii_fatty_acid_synthesis |
Four-reaction FAS-II elongation cycle | ALTERNATIVE_VARIANTS | (kasIII_route | mad_route_first_condensation) |
|
ureide_urea_catabolism |
(S)-ureidoglycolate to glyoxylate | ALTERNATIVE_VARIANTS | (allantoicase_route | ureidoglycine_aminohydrolase_step) |
|
vitamin_b6_plp_metabolism |
PLP homeostasis (PDXP) | ALTERNATIVE_VARIANTS | (pdxs_pdxt_de_novo_variant | pnpo_step) |