General Information of DME (ID: DME1471) |
DME Name |
L-malate:NADP(+) oxidoreductase (maeB), Hungateiclostridium thermocellum
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Synonyms |
L-malate:NADP oxidoreductase; NADP-dependent malic enzyme; Bacterial NADP-ME
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Gene Name |
maeB
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UniProt ID |
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Gene ID |
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EC Number |
EC: 1.1.1.40 (Click to Show/Hide the Complete EC Tree)
Oxidoreductase
CH-OH donor oxidoreductase
NAD/NADP oxidoreductase
EC: 1.1.1.40
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Lineage |
Species: Hungateiclostridium thermocellum (Click to Show/Hide the Complete Species Lineage)
Kingdom: Bacteria
Phylum: Firmicutes
Class: Clostridia
Order: Clostridiales
Family: Hungateiclostridiaceae
Genus: Hungateiclostridium
Species: Hungateiclostridium thermocellum
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Interactome(loading-time for this interactome depdends on the speed of web connection)
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Interactions between Host Protein and DME (HOSPPI)
Jump to Detailed Interactome Data
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Click to Show/Hide the Molecular/Functional Data (Sequence/Structure/Pathway/Function) of This DME
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Tissue Distribution |
Primarily distributed in human gut.
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Sequence |
MDDQLKQSALDFHEFPVPGKIQVSPTKPLATQRDLALAYSPGVAAPCLEIEKDPLKAYKY TARGNLVAVISNGTAVLGLGNIGALAGKPVMEGKGVLFKKFAGIDVFDIEVDELDPDKFI EVVAALEPTFGGINLEDIKAPECFYIEQKLRERMNIPVFHDDQHGTAIISTAAILNGLRV VEKNISDVRMVVSGAGAAAIACMNLLVALGLQKHNIVVCDSKGVIYQGREPNMAETKAAY AVVDDGKRTLDDVIEGADIFLGCSGPKVLTQEMVKKMARAPMILALANPEPEILPPLAKE VRPDAIICTGRSDYPNQVNNVLCFPFIFRGALDVGATAINEEMKLAAVRAIAELAHAEQS EVVASAYGDQDLSFGPEYIIPKPFDPRLIVKIAPAVAKAAMESGVATRPIADFDVYIDKL TEFVYKTNLFMKPIFSQARKAPKRVVLPEGEEARVLHATQELVTLGLAKPILIGRPNVIE MRIQKLGLQIKAGVDFEIVNNESDPRFKEYWTEYFQIMKRRGVTQEQAQRALISNPTVIG AIMVQRGEADAMICGTVGDYHEHFSVVKNVFGYRDGVHTAGAMNALLLPSGNTFIADTYV NDEPDAEELAEITLMAAETVRRFGIEPRVALLSHSNFGSSDCPSSSKMRQALELVRERAP ELMIDGEMHGDAALVEAIRNDRMPDSSLKGSANILVMPNMEAARISYNLLRVSSSEGVTV GPVLMGVAKPVHVLTPIASVRRIVNMVALAVVEAQTQPL
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Pathway |
Carbon metabolism (ecj01200 ) |
Metabolic pathways (ecj01100 ) |
Microbial metabolism in diverse environments (ecj01120 ) |
Pyruvate metabolism (ecj00620 ) |
Function |
This enzyme catalyzes the oxidative decarboxylation of (S)-malate in the presence of NADP+ and divalent metal ions, and the decarboxylation of oxaloacetate.
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