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Cul4A-RING E3 ubiquitin ligase complex
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GO_0031464 |
[A ubiquitin ligase complex in which a cullin from the Cul4A subfamily and a RING domain protein form the catalytic core; substrate specificity is conferred by an adaptor protein.] |
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Cul4-RING E3 ubiquitin ligase complex
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GO_0080008 |
[A ubiquitin ligase complex in which a cullin from the Cul4 family and a RING domain protein form the catalytic core; substrate specificity is conferred by an adaptor protein.] |
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Cul4B-RING E3 ubiquitin ligase complex
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GO_0031465 |
[A ubiquitin ligase complex in which a cullin from the Cul4B subfamily and a RING domain protein form the catalytic core; substrate specificity is conferred by unknown subunits.] |
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Cul5-RING ubiquitin ligase complex
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GO_0031466 |
[A ubiquitin ligase complex in which a cullin from the Cul5 subfamily and a RING domain protein form the catalytic core; substrate specificity is conferred by an elongin-BC adaptor and a SOCS/BC box protein.] |
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Cul7-RING ubiquitin ligase complex
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GO_0031467 |
[A ubiquitin ligase complex in which a cullin from the Cul7 subfamily and a RING domain protein form the catalytic core; substrate specificity is conferred by a Skp1 linker and an F-box protein.] |
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nuclear membrane reassembly
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GO_0031468 |
[The reformation of the nuclear membranes following their breakdown in the context of a normal process.] |
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bacterial microcompartment
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GO_0031469 |
[An organelle found in bacteria consisting of a proteinaceous coat containing metabolic enzymes whose purpose is the sequestration or concentration of metabolites and which has the appearance of a polygonal granule by electron microscopy.] |
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negative regulation of slow-twitch skeletal muscle fiber contraction
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GO_0031450 |
[Any process that stops, prevents, or reduces the frequency, rate or extent of slow-twitch skeletal muscle contraction.] |
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positive regulation of slow-twitch skeletal muscle fiber contraction
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GO_0031451 |
[Any process that activates or increases the frequency, rate or extent of slow-twitch skeletal muscle contraction.] |
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negative regulation of heterochromatin formation
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GO_0031452 |
[Any process that stops, prevents, or reduces the frequency, rate or extent of heterochromatin formation.] |
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negative regulation of heterochromatin organization
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GO_0120262 |
[Any process that stops, prevents, or reduces the frequency, rate or extent of heterochromatin organization.] |
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positive regulation of heterochromatin organization
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GO_0120263 |
[Any process that activates or increases the frequency, rate or extent of heterochromatin organization.] |
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GO_0031454
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GO_0031454 |
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obsolete glycine betaine metabolic process
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GO_0031455 |
[OBSOLETE. The chemical reactions and pathways involving glycine betaine, N-trimethylglycine.] |
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glycine betaine catabolic process
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GO_0031457 |
[The chemical reactions and pathways resulting in the breakdown of glycine betaine, N-trimethylglycine.] |
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ABC-type betaine transporter activity
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GO_0031458 |
[Catalysis of the reaction: ATP + H2O + a betaine(out) = ADP + phosphate + a betaine(in).] |
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ABC-type glycine betaine transporter activity
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GO_0031459 |
[Catalysis of the reaction: ATP + H2O + glycine betaine(out) = ADP + phosphate + glycine betaine(in).] |
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amino-acid betaine transmembrane transporter activity
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GO_0015199 |
[Enables the transfer of betaine from one side of a membrane to the other. Betaine is the N-trimethyl derivative of an amino acid.] |
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ABC-type quaternary ammonium compound transporting activity
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GO_0015418 |
[Catalysis of the reaction: ATP + H2O + quaternary ammonium(out) = ADP + H+ + phosphate + quaternary ammonium(in).] |
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myosin XI complex
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GO_0031481 |
[A myosin complex containing a dimer of class XI myosin heavy chains and associated light chains. Myosin XI heavy chain sizes are similar in molecular structure to the class V myosins with 5 to 6 IQ motifs and tail regions with predicted coiled coil domains (forming dimeric molecules) and large C-terminal regions.] |