All terms in GO

Label Id Description
mitotic nuclear bridge stalk GO_0140511
Either of the regions of a mitotic nuclear bridge proximal to the main portion of each daughter nucleus. The nuclear envelope in the stalk regions is depleted of nuclear pore complexes.
mitotic nuclear bridge GO_0140510
A narrow constricted region of the nucleus that forms around the anaphase spindle during closed mitosis, and connects the main portions of the newly forming daughter nuclei.
GO_0042089 GO_0042089
protein-RNA adaptor activity GO_0140517
The binding activity of a protein that brings together another protein and an RNA, permitting those molecules to function in a coordinated way.
T-helper 1 type immune response GO_0042088
An immune response which is associated with resistance to intracellular bacteria, fungi, and protozoa, and pathological conditions such as arthritis, and which is typically orchestrated by the production of particular cytokines by T-helper 1 cells, most notably interferon-gamma, IL-2, and lymphotoxin.
mitotic nuclear pore complex disassembly GO_0140516
The mitotic cell cycle process in which the controlled breakdown of the nuclear pores occurs during open or closed mitosis.
mitotic nuclear membrane disassembly GO_0007077
The mitotic cell cycle process in which the controlled partial or complete breakdown of the nuclear membranes during occurs during mitosis.
nuclear pore organization GO_0006999
A process that is carried out at the cellular level which results in the assembly, arrangement of constituent parts, or disassembly of the nuclear pore.
GO_0042087 GO_0042087
mitotic nuclear bridge organization GO_0140515
A mitotic cell cycle process which results in the assembly, arrangement, or disassembly of the mitotic nuclear bridge during closed mitosis.
5-methyltetrahydropteroyltri-L-glutamate-dependent methyltransferase activity GO_0042085
Catalysis of the transfer of a methyl group to an acceptor molecule; dependent on the presence of 5-methyltetrahydropteroyltri-L-glutamate.
epithelium-like organization GO_0140509
The organization of a polarized cell layer during morphogenesis in protozoa; an example is found during culmination in D. discoideum, involving alpha and beta catenins.
granzyme-mediated programmed cell death signaling pathway GO_0140507
The series of molecular signals induced by granzymes which triggers the cell death of a cell. The pathway starts with reception of a granzyme signal, and ends when the execution phase of cell death is triggered. Granzymes are serine proteases that are secreted by cytotoxic T cells and natural killer cells to induce cell death in target cells.
effector-mediated suppression of host salicylic acid-mediated innate immune signalling GO_0140502
A process mediated by a molecule secreted by a symbiont that results in the suppression of host salicylic acid-mediated innate immune signalling.
suppression by symbiont of defense-related host salicylic acid-mediated signal transduction pathway GO_0052003
Any process in which a symbiont stops, prevents, or reduces the frequency, rate or extent of host salicylic acid-mediated signal transduction pathways during the host defense response. The host is defined as the larger of the organisms involved in a symbiotic interaction.
positive regulation of reticulophagy GO_0140501
Any process that increases the frequency, rate or extent of reticulophagy.
regulation of reticulophagy GO_0140500
Any process that modulates the frequency, rate or extent of reticulophagy.
endoplasmic reticulum-autophagosome adaptor activity GO_0140506
The binding activity of a molecule that brings together an ER membrane and an autophagosome during reticulophagy.
regulation of microlipophagy GO_0140505
Any process that modulates the frequency, rate or extent of microlipophagy, the microautophagy-mediated direct internalization of lipid droplets into a lysosome-like vacuole during nutrient depletion.
microlipophagy GO_0140504
Microautophagy-mediated direct internalization of lipid droplets into a lysosome-like vacuole during nutrient depletion, such as during the transition to stationary phase or in response to nutrient limitation. Microlipophagy is mediated by the formation of sterol-enriched vacuolar microdomains at sites of engulfment. Initiation of microautophagy is defined as the point where liquid-ordered microdomains are formed at sites of engulfment, that requires S. cerevisiae Atg32p and Atg21p, as well as Niemann-Pick type C (NPC) sterol transporter proteins, Ncr1p and Npc2p. This is followed by redistribution of Atg14p from ER exit sites onto liquid-ordered vacuole membrane domains through interaction with stabilized AMP-activated protein kinase (AMPK), and together with Atg6p facilities docking and internalization of lipid droplets (LDs) at sites of invagination.