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DNA-templated DNA replication maintenance of fidelity
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GO_0045005 |
[A DNA metabolic process that prevents or corrects errors to ensure that DNA is replicated accurately. Errors can be corrected either by intrinsic DNA polymerase proofreading activity or via mismatch repair.] |
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pre-replicative complex assembly involved in cell cycle DNA replication
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GO_1902299 |
[Any pre-replicative complex assembly that is involved in cell cycle DNA replication.] |
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pre-replicative complex assembly
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GO_0036388 |
[The aggregation, arrangement and bonding together of a set of components to form the pre-replicative complex, a protein-DNA complex that forms at the origin of replication during the initial step of DNA replication and allows the origin to become competent, or 'licensed', for replication.] |
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archaeal-type flagellum-dependent cell motility
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GO_0097590 |
[Cell motility due to the motion of one or more archaeal-type flagella. An archaeal-type flagellum (also called archaellum) is a non-membrane-bounded organelle superficially similar to a bacterial-type flagellum, but having a different molecular structure and lacking a central channel.] |
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ventral disc lateral crest
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GO_0097591 |
[Fibrillar repetitive structure surrounding the ventral disc edge in Giardia species (trophozoite stage). The composition of the lateral crest is not fully known yet.] |
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ventral disc overlap zone
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GO_0097592 |
[A region of the ventral disc of Giardia species (trophozoite stage) where two portions of the same array of microtubules overlap (the microtubule array makes a complete circle and overlaps on itself).] |
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ventral disc microtubule array
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GO_0097593 |
[A part of the ventral disc of Giardia species (trophozoite stage) consisting of a spiral array of microtubules linked to the ventral membrane. These microtubules form the base of the ventral disc dorsal microribbons that extend nearly perpendicular from the membrane.] |
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ventral disc dorsal microribbon
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GO_0097594 |
[Trilaminar structure extending perpendicularly into the cytoplasm along the length of ventral disc microtubules in Giardia species (trophozoite stage). Constituents of dorsal microribbons (also called dorsal ribbons or microribbons) include alpha-coiled-helix proteins approximately 29 to 38 kDa in size. These proteins line the edges of the microribbons but are not found in microtubules. Tubulins are not found in microribbons.] |
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ventral disc crossbridge
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GO_0097595 |
[Structure horizontally linking adjacent microribbons of the ventral disc in Giardia species (trophozoite stage). The composition of crossbridges is not fully known yet.] |
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ventral disc supernumerary microtubule array
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GO_0097596 |
[A partial left-handed spiral array of microtubules that lies generally dorsal to the main ventral disc microtubule array in Giardia species (trophozoite stage).] |
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ventral disc
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GO_0097597 |
[Specialized organelle found in Giardia species (trophozoite stage) and characterized by a spiral array of microtubules and microtubule-associated structures including dorsal microribbons and crossbridges. The edge of the ventral disc narrows into a lateral crest. The ventral disk mediates mechanical attachment of the trophozoite to the host's intestinal wall, and contains the contractile proteins actinin, alpha-actinin, myosin, and tropomyosin working towards contraction of the disk involved in adherence.] |
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sperm cytoplasmic droplet
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GO_0097598 |
[A small amount of cytoplasm surrounded by a cell membrane that is generally retained in spermatozoa after spermiogenesis, when the majority of the cytoplasm is phagocytosed by Sertoli cells to produce what are called residual bodies. Initially, the droplet is located at the neck just behind the head of an elongated spermatid. During epididymal transit, the cytoplasmic droplet migrates caudally to the annulus at the end of the midpiece; the exact position and time varies by species. The cytoplasmic droplet consists of lipids, lipoproteins, RNAs, a variety of hydrolytic enzymes, receptors, ion channels, and Golgi-derived vesicles. The droplet may be involved in regulatory volume loss (RVD) at ejaculation, and in most species, though not in humans, the cytoplasmic droplet is lost at ejaculation. Note that the cytoplasmic droplet is distinct from 'excessive residual cytoplasm' that sometimes remains in epididymal spermatozoa, particularly when spermiogenesis has been disrupted.] |
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2-polyprenyl-6-hydroxyphenol O-methyltransferase activity
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GO_1990888 |
[Catalysis of the reaction: 2-polyprenyl-6-hydroxyphenol + S-adenosyl-L-methionine = 2-polyprenyl-6-methoxyphenol + S-adenosyl-L-homocysteine + H+.] |
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H4K20me3 modified histone binding
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GO_1990889 |
[Binding to a histone H4 in which the lysine residue at position 20 has been modified by trimethylation.] |
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methylated histone binding
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GO_0035064 |
[Binding to a histone in which a residue has been modified by methylation.] |
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GO_1990886
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GO_1990886 |
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obsolete 2-polyprenyl-3-methyl-5-hydroxy-6-methoxy-1,4-benzoquinol O-methyltransferase activity
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GO_1990887 |
[OBSOLETE. Catalysis of the reaction: 2-polyprenyl-3-methyl-5-hydroxy-6-methoxy-1,4-benzoquinol + S-adenosyl-L-methionine = ubiquinol-n + S-adenosyl-L-homocysteine + H+.] |
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RNA acetylation
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GO_1990884 |
[The posttranscriptional addition of one or more acetyl groups to specific residues in an RNA molecule.] |
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obsolete protein serine/threonine kinase binding
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GO_1990885 |
[OBSOLETE. Binding to a protein serine/threonine kinase.] |
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rRNA acetylation
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GO_1990882 |
[The modification of rRNA structure by addition of an acetyl group to rRNA. An acetyl group is CH3CO-, derived from acetic [ethanoic] acid.] |