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obsolete regulation of DNA ligation
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GO_0051105 |
[OBSOLETE. Any process that modulates the frequency, rate or extent of DNA ligation, the re-formation of a broken phosphodiester bond in the DNA backbone, carried out by DNA ligase.] |
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obsolete DNA-dependent DNA replication DNA ligation
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GO_0051104 |
[OBSOLETE. The re-formation of a broken phosphodiester bond in the DNA backbone, carried out by DNA ligase, that contributes to DNA-dependent DNA replication.] |
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acrosomal membrane
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GO_0002080 |
[The membrane that surrounds the acrosomal lumen. The acrosome is a special type of lysosome in the head of a spermatozoon that contains acid hydrolases and is concerned with the breakdown of the outer membrane of the ovum during fertilization.] |
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mitochondrial mRNA 3'-end processing
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GO_0090616 |
[Any process involved in forming the mature 3' end of an mRNA molecule that derives from the mitochondrial genome.] |
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mitochondrial mRNA processing
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GO_0090615 |
[Steps involved in processing precursor RNAs arising from transcription of operons in the mitochondrial genome into mature mRNAs.] |
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obsolete DNA clamp unloading
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GO_0090618 |
[OBSOLETE. The process of removing the PCNA complex from DNA when Okazaki fragments are completed or the replication fork terminates.] |
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mitochondrial mRNA 5'-end processing
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GO_0090617 |
[Any process involved in forming the mature 5' end of an mRNA molecule that derives from the mitochondrial genome.] |
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cAMP deaminase activity
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GO_0090612 |
[Catalysis of the reaction: cyclic adenosine monophosphate + H2O = cyclic inosine monophosphate + NH3.] |
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ubiquitin-independent protein catabolic process via the multivesicular body sorting pathway
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GO_0090611 |
[The chemical reactions and pathways resulting in the breakdown of a protein or peptide, via the multivesicular body (MVB) sorting pathway; proteins are sorted into MVBs, and delivered to a lysosome/vacuole for degradation. This process is independent of ubiquitination.] |
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5'-methylthioadenosine deaminase activity
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GO_0090614 |
[Catalysis of the reaction: 5'methyl thioadenosine + H2O = 5'methyl thioinosine + NH3.] |
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5'-deoxyadenosine deaminase activity
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GO_0090613 |
[Catalysis of the reaction: 5'deoxyadenosine + H2O = 5'deoxyinosine + NH3.] |
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microtubule minus-end binding
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GO_0051011 |
[Binding to the minus end of a microtubule.] |
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microtubule plus-end binding
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GO_0051010 |
[Binding to the plus end of a microtubule.] |
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microtubule severing
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GO_0051013 |
[The process in which a microtubule is broken down into smaller segments. Severing enzymes remove dimers from the middle of the filament to create new ends, unlike depolymerizing kinesins that use ATP to uncap microtubules at their ends.] |
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bundle sheath cell fate specification
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GO_0090610 |
[The process in which a cell becomes capable of differentiating autonomously into a bundle sheath cell in an environment that is neutral with respect to the developmental pathway; upon specification, the cell fate can be reversed.] |
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actin filament binding
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GO_0051015 |
[Binding to an actin filament, also known as F-actin, a helical filamentous polymer of globular G-actin subunits.] |
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actin binding
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GO_0003779 |
[Binding to monomeric or multimeric forms of actin, including actin filaments.] |
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inner acrosomal membrane
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GO_0002079 |
[The acrosomal membrane region that underlies the acrosomal vesicle and is located toward the sperm nucleus. This region is responsible for molecular interactions allowing the sperm to penetrate the zona pellucida and fuses with the egg plasma membrane.] |
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membrane fusion involved in acrosome reaction
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GO_0002078 |
[The fusion of the plasma membrane of the sperm with the outer acrosomal membrane.] |
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barbed-end actin filament capping
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GO_0051016 |
[The binding of a protein or protein complex to the barbed (or plus) end of an actin filament, thus preventing the addition, exchange or removal of further actin subunits.] |