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peptide antibiotic catabolic process
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GO_0030652 |
[The chemical reactions and pathways resulting in the breakdown of peptides with antibiotic activity.] |
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antibiotic catabolic process
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GO_0017001 |
[The chemical reactions and pathways resulting in the breakdown of antibiotic, a substance produced by or derived from certain fungi, bacteria, and other organisms, that can destroy or inhibit the growth of other microorganisms.] |
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heparan sulfate proteoglycan biosynthetic process
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GO_0015012 |
[The chemical reactions and pathways resulting in the formation of the heparan sulfate proteoglycan, a glycosaminoglycan with repeat unit consisting of alternating alpha-(1->4)-linked hexuronic acid and glucosamine residues; the former are a mixture of sulfated and nonsulfated D-glucuronic acid and L-iduronic acid; the L-iduronic acid is either sulfated or acetylated on its amino group as well as being sulfated on one of its hydroxyl groups; heparan sulfate chains are covalently linked to peptidyl-serine by a glycosidic attachment through the trisaccharide galactosyl-galactosyl-xylosyl to serine residues.] |
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obsolete heparan sulfate proteoglycan biosynthetic process, linkage to polypeptide
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GO_0015013 |
[OBSOLETE. The polymerization of one or more heparan sulfate chains via a xylose link onto serine residues in the core protein of a proteoglycan.] |
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obsolete centromere
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GO_0005698 |
[OBSOLETE. The region of a eukaryotic chromosome that is attached to the spindle during nuclear division. It is defined genetically as the region of the chromosome that always segregates at the first division of meiosis; the region of the chromosome in which no crossing over occurs. At the start of M phase, each chromosome consists of two sister chromatids with a constriction at a point which forms the centromere. During late prophase two kinetochores assemble on each centromere, one kinetochore on each sister chromatid.] |
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GO_0005699
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GO_0005699 |
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tetrahydrocorphin metabolic process
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GO_0015010 |
[The chemical reactions and pathways involving tetrahydrocorphins, tetrapyrroles that combine the structural elements of both porphyrins and corrins.] |
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nickel-tetrapyrrole coenzyme metabolic process
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GO_0015011 |
[The chemical reactions and pathways involving an enzyme cofactor consisting of a tetrapyrrole structure containing nickel, such as the F-430 cofactor found in methyl-coenzyme M reductase.] |
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obsolete regulation of coenzyme and prosthetic group metabolic process
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GO_0030657 |
[OBSOLETE. Any process that modulates the frequency, rate or extent of the chemical reactions and pathways involving coenzymes and prosthetic groups.] |
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vesicle membrane
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GO_0012506 |
[The lipid bilayer surrounding any membrane-bounded vesicle in the cell.] |
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obsolete internalization receptor activity
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GO_0015029 |
[OBSOLETE. (Was not defined before being made obsolete).] |
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GO_0015027
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GO_0015027 |
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GO_0015028
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GO_0015028 |
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obsolete GPI-anchored membrane-bound receptor
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GO_0015025 |
[OBSOLETE. (Was not defined before being made obsolete).] |
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coreceptor activity
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GO_0015026 |
[Combining with an extracellular or intracellular messenger, and in cooperation with a nearby primary receptor, initiating a change in cell activity.] |
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regulation of cellular pH
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GO_0030641 |
[Any process involved in the maintenance of an internal equilibrium of hydrogen ions (protons) within a cell or between a cell and its external environment.] |
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obsolete syndecan
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GO_0015023 |
[OBSOLETE. (Was not defined before being made obsolete).] |
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glucuronate-2-sulfatase activity
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GO_0015024 |
[Catalysis of the hydrolysis of the 2-sulfate groups of the 2-O-sulfo-D-glucuronate residues of chondroitin sulfate, heparin and heparitin sulfate.] |
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heparin-sulfate lyase activity
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GO_0015021 |
[Catalysis of the elimination of sulfate; appears to act on linkages between N-acetyl-D-glucosamine and uronate. Product is an unsaturated sugar.] |
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GO_0015022
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GO_0015022 |
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