Q9KU37
Gene name |
nagZ |
Protein name |
Beta-hexosaminidase |
Names |
Beta-N-acetylhexosaminidase, N-acetyl-beta-glucosaminidase |
Species |
Vibrio cholerae serotype O1 (strain ATCC 39315 / El Tor Inaba N16961) |
KEGG Pathway |
vch:VC_0692 |
EC number |
3.2.1.52: Glycosidases, ie enzymes hydrolyzing O- and S-glycosyl compounds |
Protein Class |
|
Descriptions
The autoinhibited protein was predicted that may have potential autoinhibitory elements via cis-regPred.
Autoinhibitory domains (AIDs)
Target domain |
|
Relief mechanism |
|
Assay |
cis-regPred |
Accessory elements
No accessory elements
No variants for Q9KU37
| Variant ID(s) | Position | Change | Description | Diseaes Association | Provenance |
|---|---|---|---|---|---|
| No variants for Q9KU37 | |||||
No associated diseases with Q9KU37
Functions
| Description | ||
|---|---|---|
| EC Number | 3.2.1.52 | Glycosidases, ie enzymes hydrolyzing O- and S-glycosyl compounds |
| Subcellular Localization |
|
|
| PANTHER Family | ||
| PANTHER Subfamily | ||
| PANTHER Protein Class | ||
| PANTHER Pathway Category | No pathway information available | |
1 GO annotations of cellular component
| Name | Definition |
|---|---|
| cytoplasm | The contents of a cell excluding the plasma membrane and nucleus, but including other subcellular structures. |
2 GO annotations of molecular function
| Name | Definition |
|---|---|
| beta-N-acetylhexosaminidase activity | Catalysis of the hydrolysis of terminal non-reducing N-acetyl-D-hexosamine residues in N-acetyl-beta-D-hexosaminides. |
| N-acetyl-beta-D-galactosaminidase activity | Catalysis of the reaction: H2O + an N-acetyl-beta-D-galactosalaminyl- |
8 GO annotations of biological process
| Name | Definition |
|---|---|
| carbohydrate metabolic process | The chemical reactions and pathways involving carbohydrates, any of a group of organic compounds based of the general formula Cx(H2O)y. |
| cell cycle | The progression of biochemical and morphological phases and events that occur in a cell during successive cell replication or nuclear replication events. Canonically, the cell cycle comprises the replication and segregation of genetic material followed by the division of the cell, but in endocycles or syncytial cells nuclear replication or nuclear division may not be followed by cell division. |
| cell division | The process resulting in division and partitioning of components of a cell to form more cells; may or may not be accompanied by the physical separation of a cell into distinct, individually membrane-bounded daughter cells. |
| cell wall organization | A process that results in the assembly, arrangement of constituent parts, or disassembly of the cell wall, the rigid or semi-rigid envelope lying outside the cell membrane of plant, fungal and most prokaryotic cells, maintaining their shape and protecting them from osmotic lysis. |
| peptidoglycan biosynthetic process | The chemical reactions and pathways resulting in the formation of peptidoglycans, any of a class of glycoconjugates found in bacterial cell walls. |
| peptidoglycan turnover | The continual breakdown and regeneration of peptidoglycan required to maintain the cell wall. |
| regulation of cell shape | Any process that modulates the surface configuration of a cell. |
| response to antibiotic | Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of an antibiotic stimulus. An antibiotic is a chemical substance produced by a microorganism which has the capacity to inhibit the growth of or to kill other microorganisms. |
No homologous proteins in AiPD
| UniProt AC | Gene Name | Protein Name | Species | Evidence Code |
|---|---|---|---|---|
| No homologous proteins | ||||
| 10 | 20 | 30 | 40 | 50 | 60 |
| MGPLWLDVAG | YELSAEDREI | LQHPTVGGVI | LFGRNYHDNQ | QLLALNKAIR | QAAKRPILIG |
| 70 | 80 | 90 | 100 | 110 | 120 |
| VDQEGGRVQR | FREGFSRIPP | AQYYARAENG | VELAEQGGWL | MAAELIAHDV | DLSFAPVLDM |
| 130 | 140 | 150 | 160 | 170 | 180 |
| GFACKAIGNR | AFGEDVQTVL | KHSSAFLRGM | KAVGMATTGK | HFPGHGAVIA | DSHLETPYDE |
| 190 | 200 | 210 | 220 | 230 | 240 |
| RETIAQDMAI | FRAQIEAGVL | DAMMPAHVVY | PHYDAQPASG | SSYWLKQVLR | EELGFKGIVF |
| 250 | 260 | 270 | 280 | 290 | 300 |
| SDDLSMEGAA | VMGGPVERSH | QALVAGCDMI | LICNKREAAV | EVLDNLPIME | VPQAEALLKK |
| 310 | 320 | ||||
| QQFSYSELKR | LERWQQASAN | MQRLIEQFSE |