All terms in MI

Label Id Description
n-acetyl-proline MI_0137 [Residue modification. OBSOLETE remap to MOD:00059.]
n-acetyl-serine MI_0138 [Residue modification. OBSOLETE remap to MOD:00060.]
attached carbohydrate disrupting interaction rate MI_2315 [Carbohydrate species chemically attached to proteins, or other organic molecules involved in an interaction that disrupts interaction rate (in the case of interactions inferred from enzymatic reaction) when compared with the non-glycosylated molecule.]
formylated residue MI_0146 [Residue modification. OBSOLETE remap to MOD:00493.]
nanoluc luciferase protein tag MI_2325 [NanoLuc luciferase (Nluc) is a small (19 kDa), highly stable, ATP independent, bioluminescent protein derived from the luciferase complex of the deep-sea shrimp O. gracilirostris.]
luciferase tag MI_1205 [Luciferase is a generic term for the class of oxidative enzymes used in bioluminescence and is distinct from a photoprotein. Luciferase catalyzes a bioluminescent reaction which requires the substrate luciferin as well as Mg2+ and ATP, produces green light with a wavelength of 562 nm.]
dbsnp MI_2324 [dbSNP contains human single nucleotide variations, microsatellites, and small-scale insertions and deletions along with publication, population frequency, molecular consequence, and genomic and RefSeq mapping information for both common variations and clinical mutations.]
feature database MI_0447 [A database describing a feature on a molecule.]
n-formyl-methionine MI_0147 [Residue modification. OBSOLETE remap to MOD:00030.]
kiss MI_2323 [KISS (KInase Substrate Sensor) is a protein complementation technology that allows in situ analysis of protein-protein interactions in intact mammalian cells. In this method, which is derived from MAPPIT (mammalian protein-protein interaction trap), the bait protein is coupled to the kinase domain of TYK2, while the prey protein is fused to a fragment of the gp130 cytokine receptor chain. Bait and prey interaction leads to phosphorylation of the gp130 anchor by TYK2, followed by recruitment and activation of STAT3, resulting in transcription of a STAT3-dependent reporter system. This approach enables the identification of interactions between proteins, including transmembrane and cytosolic proteins, and their modulation in response to physiological or pharmacological challenges.]
protein complementation assay MI_0090 [In the protein-fragment complementation assay, the proteins of interest ("Bait" and "Prey") are covalently linked at the genetic level to incomplete fragments of a third protein (known as the "reporter") and are expressed in vivo, Interaction between the "bait" and the "prey" proteins brings the fragments of the "reporter" protein in close enough proximity to allow them to reform and become the functional reporter protein. Typically enzymes which confer resistance to antibiotics, such as Dihydrofolate reductase or Beta-lactamase, or proteins that give colorimetric or fluorescent signals are used. The Bait protein is generally the protein under study and the methods are readily adaptable to highthroughput mode.]
arginine amide MI_0145 [Residue modification. OBSOLETE remap to MOD:00091.]
Illumina dye sequencing MI_2322 [This method generates several billion bases of accurate nucleotide sequence per experiment at low cost. Single molecules of DNA are attached to a flat surface, amplified in situ and used as templates for synthetic sequencing with fluorescent reversible terminator deoxyribonucleotides. Images of the surface are analysed to generate high-quality sequence.]
high-throughput sequencing MI_2321 [High-throughput (a.k.a. "next-generation") sequencing applies to methods that allow for sequencing of genome-scale number of bases.]
nucleotide sequence identification MI_0078 [Identification of a nucleotide sequence. Depending on the experimental design, nucleotide sequence can be determined before the interaction detection while building a collection of clones or after the selection of randomly generated clones.]
n-acetyl-valine MI_0142 [Residue modification. OBSOLETE remap to MOD:00063.]
amidated residue MI_0143 [Residue modification. OBSOLETE remap to MOD:00674.]
aruk-ucl MI_2320 [The Alzheimer's Research UK Gene Ontology Project represents a collaboration between University College London, the European Bioinformatics Institute (EBI) and the University of Manchester, funded by Alzheimer's Research UK. This annotation group is a member of the IMEx Consortium. www.ucl.ac.uk/functional-gene-annotation/neurological]
interaction database MI_0461 [Databases that contain experimental or predictive molecular interaction data.]
n-acetyl-tryptophan MI_0140 [Residue modification. OBSOLETE remap to MOD:00785.]