Recent changes
From WikiPathways
Track the most recent changes to the wiki on this page.
21 December 2024
- Homo sapiens:Electron transport chain: OXPHOS system in mitochondria; 19:33 . . (+27) . . Egonw (Talk | contribs) (Correct Complex Portal data sources)
- Homo sapiens:Electron transport chain: OXPHOS system in mitochondria; 19:31 . . (+427) . . Egonw (Talk | contribs) (Added three complex nodes with Complex Portal IDs.)
- Homo sapiens:Mitochondrial carrier deficiency associated with shuttle disturbances; 15:50 . . (-46) . . Egonw (Talk | contribs) (Removed template comments)
- Homo sapiens:Disorders of galactose metabolism ; 14:28 . . (+24) . . Egonw (Talk | contribs) (galactose translocation)
- Homo sapiens:Amino acid metabolism; 14:20 . . (-5) . . Egonw (Talk | contribs) (Changed to the ChEBI identifier)
- Homo sapiens:Amino acid metabolism; 12:28 . . (+558) . . Egonw (Talk | contribs) (Converted labels into data nodes)
- Homo sapiens:Amino acid metabolism; 10:59 . . (+1,604) . . Egonw (Talk | contribs) (Converted a metabolite Label to DataNode with identifier)
- Mus musculus:Amino acid metabolism; 10:44 . . (-5) . . Egonw (Talk | contribs) (Use the ChEBI identifier )
- Homo sapiens:Amino acid metabolism; 10:43 . . (-5) . . Egonw (Talk | contribs) (The linked ChEBI entry seems to have the correct stereochemistry)
- Homo sapiens:Glycosaminoglycan degradation; 07:59 . . (+887) . . Egonw (Talk | contribs) (Added a literature reference, about drug targeting)
- Homo sapiens:Cytoplasmic ribosomal proteins; 07:55 . . (0) . . Egonw (Talk | contribs) (Oops, wrong species)
- Homo sapiens:Cytoplasmic ribosomal proteins; 07:37 . . (+15) . . Egonw (Talk | contribs) (Manually set the data source to Complex Portal)
- Homo sapiens:Cytoplasmic ribosomal proteins; 07:36 . . (+2,539) . . Egonw (Talk | contribs) (Added a literature reference and Complex Portal identifiers (with wrong datasource))
20 December 2024
- Homo sapiens:Disorders of NAD metabolism; 16:49 . . (+2,481) . . Mareknoga (Talk | contribs) (Fixing some of the missing annotations)
- Homo sapiens:Glycosaminoglycan degradation; 15:50 . . (+18) . . Egonw (Talk | contribs) (Completed the reference)
- Homo sapiens:Glycosaminoglycan degradation; 15:48 . . (+2,115) . . Egonw (Talk | contribs) (URL of the KEGG pathway)
- Homo sapiens:Proteoglycan biosynthesis; 15:35 . . (+36) . . Egonw (Talk | contribs) (mim-translocations)
- Homo sapiens:Pathways of nucleic acid metabolism and innate immune sensing; 14:41 . . (-315) . . Egonw (Talk | contribs) (Modified description)
- Homo sapiens:Disorders of Mitochondrial Homeostatis, Dynamics, Protein Import, and Quality Control; 14:30 . . (+36) . . Egonw (Talk | contribs) (mim-translocation and RoundedRectangle)
- Homo sapiens:Metabolic reprogramming in colon cancer; 14:27 . . (0) . . Egonw (Talk | contribs) (Not the polymer residue, but the compound. Fixed the ID)
- Homo sapiens:Disorders of NAD metabolism; 14:21 . . (+409) . . Mareknoga (Talk | contribs) (pushing unsaved changes)
- Homo sapiens:SCFA and skeletal muscle substrate metabolism; 12:33 . . (-168) . . Eweitz (Talk | contribs) (Ontology Term : 'cell of skeletal muscle' added !)
- Homo sapiens:SCFA and skeletal muscle substrate metabolism; 12:32 . . (-13) . . Eweitz (Talk | contribs) (Fix truncated text)
- Homo sapiens:SCFA and skeletal muscle substrate metabolism; 12:31 . . (+2) . . Eweitz (Talk | contribs) (Standardize case)
- Homo sapiens:SCFA and skeletal muscle substrate metabolism; 12:30 . . (-73) . . Eweitz (Talk | contribs) (Economize layout)
- Homo sapiens:Fatty acid beta-oxidation; 08:24 . . (+1,733) . . Egonw (Talk | contribs) (Added a literature reference)
- Homo sapiens:Pyrimidine metabolism; 08:16 . . (+2,295) . . Egonw (Talk | contribs) (Added a reference)
- Homo sapiens:Photodynamic therapy-induced AP-1 survival signaling; 02:20 . . (+900) . . Eweitz (Talk | contribs) (Clear cache for board dimensions)
- Homo sapiens:Somatic sex determination; 00:06 . . (+68) . . Khanspers (Talk | contribs) (Ontology Term : 'Leydig cell' added !)
19 December 2024
- Homo sapiens:Somatic sex determination; 18:06 . . (+29) . . Khanspers (Talk | contribs) (added xref for CTNNB1)
- Homo sapiens:SCFA and skeletal muscle substrate metabolism; 18:03 . . (+50) . . Khanspers (Talk | contribs) (added Wikidata for lipid storage)
- Homo sapiens:Somatic sex determination; 18:01 . . (+4,467) . . Khanspers (Talk | contribs) (overhaul for clarity, added Wikidata nodes, add NR5A1 interaction and reference)
- Homo sapiens:Disorders of NAD metabolism; 16:40 . . (+4,485) . . Mareknoga (Talk | contribs) (started working on the NAD consumption and salvage)
- Homo sapiens:Mitochondrial carrier deficiency associated with shuttle disturbances; 16:37 . . (+202) . . Daanvanbeek (Talk | contribs) (Rhea's added, check GLUD1, can go both directoins and NAD or NADP)
- Homo sapiens:Disorders of Mitochondrial Homeostatis, Dynamics, Protein Import, and Quality Control; 16:34 . . (-29) . . DeSl (Talk | contribs) (Changed two lines to graphical ones)
- Homo sapiens:Disorders of Mitochondrial Homeostatis, Dynamics, Protein Import, and Quality Control; 16:31 . . (+3,741) . . DeSl (Talk | contribs) (Added last molecular interactions for VCP)
- Homo sapiens:Mitochondrial carrier deficiency associated with shuttle disturbances; 16:25 . . (+535) . . Daanvanbeek (Talk | contribs) (Added Rhea identifiers)
- Homo sapiens:Disorders of Mitochondrial Homeostatis, Dynamics, Protein Import, and Quality Control; 16:22 . . (+12,183) . . DeSl (Talk | contribs) (Added molecular interactions for TMEM126A and VCP)
- Homo sapiens:Sandbox pathway test; 15:50 . . (+259) . . Mkutmon (Talk | contribs) (add data node test)
- Homo sapiens:Sandbox pathway test; 15:50 . . (+200) . . Mkutmon (Talk | contribs) (Ontology Term : 'Disease' added !)
- Homo sapiens:Sandbox pathway test; 15:50 . . (-95) . . Mkutmon (Talk | contribs) (Ontology Term : 'DOID:4' removed !)
- Homo sapiens:Mitochondrial carrier deficiency associated with shuttle disturbances; 15:47 . . (+5) . . Daanvanbeek (Talk | contribs) (layout change)
- Homo sapiens:Mitochondrial carrier deficiency associated with shuttle disturbances; 15:47 . . (+283) . . Daanvanbeek (Talk | contribs) (Layout change)
- Homo sapiens:Mitochondrial carrier deficiency associated with shuttle disturbances; 15:46 . . (+743) . . Daanvanbeek (Talk | contribs) (Added GOT2 disease)
- Homo sapiens:Mitochondrial carrier deficiency associated with shuttle disturbances; 15:43 . . (+3,670) . . Daanvanbeek (Talk | contribs) (Added diseases)
- Homo sapiens:Disorders of Mitochondrial Homeostatis, Dynamics, Protein Import, and Quality Control; 15:42 . . (-115) . . DeSl (Talk | contribs) (Added IDs for datanodes missing)
- Homo sapiens:Disorders of Mitochondrial Homeostatis, Dynamics, Protein Import, and Quality Control; 15:40 . . (+51) . . DeSl (Talk | contribs) (Added LOHN1 ID)
- Homo sapiens:Disorders of Mitochondrial Homeostatis, Dynamics, Protein Import, and Quality Control; 15:37 . . (+68) . . DeSl (Talk | contribs) (Updated the description)
- Homo sapiens:Disorders of Mitochondrial Homeostatis, Dynamics, Protein Import, and Quality Control; 15:35 . . (+13,826) . . DeSl (Talk | contribs) (Added all OMIM IDs for this chapter!!)
- (diff) . . N Homo sapiens:Mitochondrial carrier deficiency associated with shuttle disturbances; 15:08 . . (+24,159) . . Daanvanbeek (Talk | contribs) (New pathway)