All terms in GO
| Label | Id | Description |
|---|---|---|
| heparan sulfate proteoglycan biosynthetic process | 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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| heparan sulfate proteoglycan biosynthetic process, linkage to polypeptide | GO_0015013 |
The polymerization of one or more heparan sulfate chains via a xylose link onto serine residues in the core protein of a proteoglycan.
|
| protein O-linked glycosylation via serine | GO_0018242 |
The glycosylation of protein via the O3 atom of peptidyl-serine, forming O3-glycosyl-L-serine; the most common forms are N-acetylgalactosaminyl, mannosyl, galactosyl, and xylosyl serine.
|
| obsolete centromere | 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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| tetrahydrocorphin metabolic process | 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 | 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.
|
| GO_0005699 | GO_0005699 | |
| cellular lactam biosynthetic process | GO_0072339 |
The chemical reactions and pathways resulting in the formation of lactams, any cyclic amides of amino carboxylic acids, having a 1-azacycloalkan-2-one structure, or analogues having unsaturation or heteroatoms replacing one or more carbon atoms of the ring.
|
| obsolete regulation of coenzyme and prosthetic group metabolic process | 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 | GO_0012506 |
The lipid bilayer surrounding any membrane-bounded vesicle in the cell.
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| obsolete internalization receptor activity | GO_0015029 |
OBSOLETE. (Was not defined before being made obsolete).
|
| GO_0015027 | GO_0015027 | |
| GO_0015028 | GO_0015028 | |
| obsolete GPI-anchored membrane-bound receptor | GO_0015025 |
OBSOLETE. (Was not defined before being made obsolete).
|
| regulation of cellular pH | 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 | GO_0015023 |
OBSOLETE. (Was not defined before being made obsolete).
|
| glucuronate-2-sulfatase activity | 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 | 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 | GO_0015022 | |
| cellular sulfate ion homeostasis | GO_0030642 |
Any process involved in the maintenance of an internal steady state of sulfate ions at the level of a cell.
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