Gene Ontology annotation through association of InterPro records with GO terms
TreeGrafter-generated GO annotations
Combined Automated Annotation using Multiple IEA Methods
UniProtKB A0A5M3MRX5 flat file (Coniophora puteana)
PAINT IBD nodes for PTHR11540
PANTHER PTHR11540 reviewed member entries with subfamily assignments
Targeting-signal analysis for Coniophora puteana MDH A0A5M3MRX5
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The target has a presequence-like N-terminal extension (5 Arg/Lys, 0 Asp/Glu) and no PTS1, while its paralog A0A5M3MC96 lacks the extension and ends in SKL.
"The target has no PTS1 (ends in FVA). Its paralog A0A5M3MC96 ends in SKL, a canonical PTS1, and lacks the presequence, matching yeast peroxisomal MDH3."
Gene sequence and primary structure of mitochondrial malate dehydrogenase from Saccharomyces cerevisiae.
Isolation and expression of the gene encoding yeast mitochondrial malate dehydrogenase.
A physiological role for oxalic acid biosynthesis in the wood-rotting basidiomycete Fomitopsis palustris.
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MDH activity is very high in oxalate-producing F. palustris extracts.
"the greatest activity was found for MDH: 5,840 nmol"
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Malate, not oxaloacetate, is proposed to leave mitochondria and be oxidized to oxaloacetate for oxalate synthesis.
"oxaloacetate cannot be shuttled through the membrane system of mitochondria and glyoxysomes, and not oxaloacetate but malate may flow out from Cycle A or B to be oxidized to form oxaloacetate"
Evidence for a cytoplasmic pathway of oxalate biosynthesis in Aspergillus niger.
The Paleozoic origin of enzymatic lignin decomposition reconstructed from 31 fungal genomes.