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AKR1C4 AKR1C4 AKR1E2 AKR1E2 AKR1CL1 AKR1CL1 GCLM GCLM SUMF1 SUMF1 SUMF2 SUMF2 AKR1A1 AKR1A1 AKR1B10 AKR1B10 AKR1B1 AKR1B1 AGTRAP AGTRAP AKR1D1 AKR1D1 MCEE MCEE AKR1C3 AKR1C3 AKR1C2 AKR1C2 GCC1 GCC1 AKR1C1 AKR1C1 ALDH6A1 ALDH6A1 PCCB PCCB RPS21 RPS21 PCCA PCCA AKR1B15 AKR1B15 ECHDC1 ECHDC1 CMTM5 CMTM5 MMAA MMAA C4orf27 C4orf27 MUT MUT
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splice isoforms or post-translational modifications are collapsed, i.e. each node represents all the proteins produced by a single, protein-coding gene locus.
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small nodes:
protein of unknown 3D structure
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large nodes:
some 3D structure is known or predicted
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colored nodes:
query proteins and first shell of interactors
non-colored protein node
white nodes:
second shell of interactors
Edges:
Edges represent protein-protein associations
associations are meant to be specific and meaningful, i.e. proteins jointly contribute to a shared function; this does not necessarily mean they are physically binding each other.
Known Interactions
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from curated databases
experiment edge
experimentally determined
Predicted Interactions
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gene neighborhood
fusion edge
gene fusions
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gene co-occurrence
Others
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textmining
coexpression edge
co-expression
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AKR1D1aldo-keto reductase family 1, member D1 (delta 4-3-ketosteroid-5-beta-reductase); Efficiently catalyzes the reduction of progesterone, androstenedione, 17-alpha-hydroxyprogesterone and testosterone to 5-beta-reduced metabolites. The bile acid intermediates 7- alpha,12-alpha-dihydroxy-4-cholesten-3-one and 7-alpha-hydroxy-4- cholesten-3-one can also act as substrates (326 aa)
MCEEmethylmalonyl CoA epimerase (176 aa)
AKR1C4aldo-keto reductase family 1, member C4 (chlordecone reductase; 3-alpha hydroxysteroid dehydrogenase, type I; dihydrodiol dehydrogenase 4) (323 aa)
SUMF1sulfatase modifying factor 1 (374 aa)
MUTmethylmalonyl CoA mutase; Involved in the degradation of several amino acids, odd- chain fatty acids and cholesterol via propionyl-CoA to the tricarboxylic acid cycle. MCM has different functions in other species (750 aa)
MMAAmethylmalonic aciduria (cobalamin deficiency) cblA type; Probable GTPase. May function as chaperone. May be involved in the transport of cobalamin (Cbl) into mitochondria for the final steps of adenosylcobalamin (AdoCbl) synthesis (418 aa)
AKR1B1aldo-keto reductase family 1, member B1 (aldose reductase); Catalyzes the NADPH-dependent reduction of a wide variety of carbonyl-containing compounds to their corresponding alcohols with a broad range of catalytic efficiencies (316 aa)
AKR1E2aldo-keto reductase family 1, member E2; Catalyzes the NADPH-dependent reduction of 1,5-anhydro- D-fructose (AF) to 1,5-anhydro-D-glucitol. Can also catalyze the reduction of various aldehydes and quinones (By similarity). Has low NADPH-dependent reductase activity towards 9,10- phenanthrenequinone (in vitro) (320 aa)
AKR1A1aldo-keto reductase family 1, member A1 (aldehyde reductase); Catalyzes the NADPH-dependent reduction of a variety of aromatic and aliphatic aldehydes to their corresponding alcohols. Catalyzes the reduction of mevaldate to mevalonic acid and of glyceraldehyde to glycerol. Has broad substrate specificity. In vitro substrates include succinic semialdehyde, 4- nitrobenzaldehyde, 1,2-naphthoquinone, methylglyoxal, and D- glucuronic acid. Plays a role in the activation of procarcinogens, such as polycyclic aromatic hydrocarbon trans-dihydrodiols, and in the metabolism of various xenobiotic [...] (325 aa)
GCC1GRIP and coiled-coil domain containing 1; Probably involved in maintaining Golgi structure (775 aa)
AGTRAPangiotensin II receptor-associated protein; Appears to be a negative regulator of type-1 angiotensin II receptor-mediated signaling by regulating receptor internalisation as well as mechanism of receptor desensitization such as phosphorylation. Induces also a decrease in cell proliferation and angiotensin II-stimulated transcriptional activity (159 aa)
SUMF2sulfatase modifying factor 2 (358 aa)
RPS21ribosomal protein S21 (83 aa)
CMTM5CKLF-like MARVEL transmembrane domain containing 5 (156 aa)
AKR1B10aldo-keto reductase family 1, member B10 (aldose reductase); Acts as all-trans-retinaldehyde reductase. Can efficiently reduce aliphatic and aromatic aldehydes, and is less active on hexoses (in vitro). May be responsible for detoxification of reactive aldehydes in the digested food before the nutrients are passed on to other organs (316 aa)
GCLMglutamate-cysteine ligase, modifier subunit (274 aa)
PCCApropionyl CoA carboxylase, alpha polypeptide (728 aa)
AKR1C3aldo-keto reductase family 1, member C3 (3-alpha hydroxysteroid dehydrogenase, type II) (323 aa)
AKR1C2aldo-keto reductase family 1, member C2 (dihydrodiol dehydrogenase 2; bile acid binding protein; 3-alpha hydroxysteroid dehydrogenase, type III) (323 aa)
AKR1C1aldo-keto reductase family 1, member C1 (dihydrodiol dehydrogenase 1; 20-alpha (3-alpha)-hydroxysteroid dehydrogenase) (323 aa)
AKR1B15aldo-keto reductase family 1, member B15; Possesses weak oxidoreductase activity (344 aa)
C4orf27chromosome 4 open reading frame 27 (346 aa)
AKR1CL1aldo-keto reductase family 1, member C-like 1 (152 aa)
PCCBpropionyl CoA carboxylase, beta polypeptide (559 aa)
ECHDC1enoyl CoA hydratase domain containing 1 (307 aa)
ALDH6A1aldehyde dehydrogenase 6 family, member A1; Plays a role in valine and pyrimidine metabolism. Binds fatty acyl-CoA (535 aa)
Your Current Organism:
Homo sapiens
NCBI taxonomy Id: 9606
Other names: H. sapiens, Homo, Homo sapiens, human, man
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