| Type |
Details |
Score |
| GXD Expression |
| Probe: |
MGI:1927951 |
| Assay Type: |
RNA in situ |
| Annotation Date: |
2001-01-09 |
| Strength: |
Present |
| Sex: |
Not Specified |
| Emaps: |
EMAPS:1937619 |
| Pattern: |
Regionally restricted |
| Stage: |
TS19 |
| Assay Id: |
MGI:1928658 |
| Age: |
embryonic day 11.5 |
| Image: |
8. O., P. |
| Note: |
Expression is detected in the vertebrae from thoracic 11 up to the boundary between cervical vertebrae 1 and 2 for 2 of 4 specimens. The boundary is between C2/3 for two other specimens. Data posterior to C5 is summarized in Fig. 9. |
| Specimen Label: |
8. O., P. |
| Detected: |
true |
| Specimen Num: |
2 |
|
•
•
•
•
•
|
| GXD Expression |
| Probe: |
MGI:6175006 |
| Assay Type: |
RNA in situ |
| Annotation Date: |
2018-07-25 |
| Strength: |
Present |
| Sex: |
Not Specified |
| Emaps: |
EMAPS:1689419 |
| Pattern: |
Not Specified |
| Stage: |
TS19 |
| Assay Id: |
MGI:6190549 |
| Age: |
embryonic day 11.5 |
|
|
| Specimen Label: |
Table S2 - E11.5 - Hoxb5 |
| Detected: |
true |
| Specimen Num: |
1 |
|
•
•
•
•
•
|
| GXD Expression |
| Probe: |
MGI:6175006 |
| Assay Type: |
RNA in situ |
| Annotation Date: |
2018-07-25 |
| Strength: |
Present |
| Sex: |
Not Specified |
| Emaps: |
EMAPS:1689421 |
| Pattern: |
Not Specified |
| Stage: |
TS21 |
| Assay Id: |
MGI:6190549 |
| Age: |
embryonic day 13.5 |
|
|
| Specimen Label: |
Table S2 - E13.5 - Hoxb5 |
| Detected: |
true |
| Specimen Num: |
2 |
|
•
•
•
•
•
|
| GXD Expression |
| Probe: |
MGI:6175006 |
| Assay Type: |
RNA in situ |
| Annotation Date: |
2018-07-25 |
| Strength: |
Present |
| Sex: |
Male |
| Emaps: |
EMAPS:1689424 |
| Pattern: |
Not Specified |
| Stage: |
TS24 |
| Assay Id: |
MGI:6190549 |
| Age: |
embryonic day 15.5 |
|
|
| Specimen Label: |
Table S2 - E15.5 - Hoxb5 |
| Detected: |
true |
| Specimen Num: |
3 |
|
•
•
•
•
•
|
| GXD Expression |
| Probe: |
MGI:6175006 |
| Assay Type: |
RNA in situ |
| Annotation Date: |
2018-07-25 |
| Strength: |
Present |
| Sex: |
Male |
| Emaps: |
EMAPS:1689426 |
| Pattern: |
Not Specified |
| Stage: |
TS26 |
| Assay Id: |
MGI:6190549 |
| Age: |
embryonic day 18.5 |
|
|
| Specimen Label: |
Table S2 - E18.5 - Hoxb5 |
| Detected: |
true |
| Specimen Num: |
4 |
|
•
•
•
•
•
|
| GXD Expression |
| Probe: |
MGI:6175006 |
| Assay Type: |
RNA in situ |
| Annotation Date: |
2018-07-25 |
| Strength: |
Present |
| Sex: |
Male |
| Emaps: |
EMAPS:1689428 |
| Pattern: |
Not Specified |
| Stage: |
TS28 |
| Assay Id: |
MGI:6190549 |
| Age: |
postnatal day 4 |
|
|
| Specimen Label: |
Table S2 - P4 - Hoxb5 |
| Detected: |
true |
| Specimen Num: |
5 |
|
•
•
•
•
•
|
| GXD Expression |
| Probe: |
MGI:6175006 |
| Assay Type: |
RNA in situ |
| Annotation Date: |
2018-07-25 |
| Strength: |
Present |
| Sex: |
Male |
| Emaps: |
EMAPS:1689428 |
| Pattern: |
Not Specified |
| Stage: |
TS28 |
| Assay Id: |
MGI:6190549 |
| Age: |
postnatal day 14 |
|
|
| Specimen Label: |
Table S2 - P14 - Hoxb5 |
| Detected: |
true |
| Specimen Num: |
6 |
|
•
•
•
•
•
|
| GXD Expression |
| Probe: |
MGI:6175006 |
| Assay Type: |
RNA in situ |
| Annotation Date: |
2018-07-25 |
| Strength: |
Present |
| Sex: |
Male |
| Emaps: |
EMAPS:1689428 |
| Pattern: |
Not Specified |
| Stage: |
TS28 |
| Assay Id: |
MGI:6190549 |
| Age: |
postnatal day 28 |
|
|
| Specimen Label: |
Table S2 - P28 - Hoxb5 |
| Detected: |
true |
| Specimen Num: |
7 |
|
•
•
•
•
•
|
| GXD Expression |
| Probe: |
MGI:1927951 |
| Assay Type: |
RNA in situ |
| Annotation Date: |
2001-01-09 |
| Strength: |
Present |
| Sex: |
Not Specified |
| Emaps: |
EMAPS:1933719 |
| Pattern: |
Regionally restricted |
| Stage: |
TS19 |
| Assay Id: |
MGI:1928658 |
| Age: |
embryonic day 11.5 |
| Image: |
8. M., N. |
| Note: |
Expression is detected in the vertebrae from thoracic 11 up to the boundary between cervical vertebrae 1 and 2. Data posterior to C5 is summarized in Fig. 9. |
| Specimen Label: |
8. M., N. |
| Detected: |
true |
| Specimen Num: |
1 |
|
•
•
•
•
•
|
| GXD Expression |
| Probe: |
MGI:1927951 |
| Assay Type: |
RNA in situ |
| Annotation Date: |
2001-01-09 |
| Strength: |
Present |
| Sex: |
Not Specified |
| Emaps: |
EMAPS:1933719 |
| Pattern: |
Regionally restricted |
| Stage: |
TS19 |
| Assay Id: |
MGI:1928658 |
| Age: |
embryonic day 11.5 |
| Image: |
8. O., P. |
| Note: |
Expression is detected in the vertebrae from thoracic 11 up to the boundary between cervical vertebrae 1 and 2 for 2 of 4 specimens. The boundary is between C2/3 for two other specimens. Data posterior to C5 is summarized in Fig. 9. |
| Specimen Label: |
8. O., P. |
| Detected: |
true |
| Specimen Num: |
2 |
|
•
•
•
•
•
|
| GXD Expression |
| Probe: |
MGI:12545 |
| Assay Type: |
RNA in situ |
| Annotation Date: |
2020-08-07 |
| Strength: |
Strong |
| Sex: |
Not Specified |
| Emaps: |
EMAPS:2778224 |
| Pattern: |
Regionally restricted |
| Stage: |
TS24 |
| Assay Id: |
MGI:6448965 |
| Age: |
embryonic day 16.0 |
| Image: |
8C/D/E |
| Note: |
Expressed predominantly in the epithelial cells. |
| Specimen Label: |
8C/D/E |
| Detected: |
true |
| Specimen Num: |
14 |
|
•
•
•
•
•
|
| GXD Expression |
| Probe: |
MGI:12545 |
| Assay Type: |
RNA in situ |
| Annotation Date: |
2020-08-07 |
| Strength: |
Strong |
| Sex: |
Not Specified |
| Emaps: |
EMAPS:1881228 |
| Pattern: |
Regionally restricted |
| Stage: |
TS28 |
| Assay Id: |
MGI:6448965 |
| Age: |
postnatal adult |
| Image: |
9A/B |
| Note: |
Expressed in dispersed cells in the connective tissue. |
| Specimen Label: |
9A/B |
| Detected: |
true |
| Specimen Num: |
15 |
|
•
•
•
•
•
|
| GXD Expression |
| Probe: |
MGI:5484761 |
| Assay Type: |
RNA in situ |
| Annotation Date: |
2013-05-13 |
| Strength: |
Present |
| Sex: |
Not Specified |
| Emaps: |
EMAPS:1625515 |
| Pattern: |
Regionally restricted |
| Stage: |
TS15 |
| Assay Id: |
MGI:5484883 |
| Age: |
embryonic day 9.5 |
|
| Note: |
Expression is proximal and extends to where the liver will develop. |
| Specimen Label: |
1 |
| Detected: |
true |
| Specimen Num: |
1 |
|
•
•
•
•
•
|
| GXD Expression |
| Probe: |
MGI:6460027 |
| Assay Type: |
Immunohistochemistry |
| Annotation Date: |
2020-10-07 |
| Strength: |
Present |
| Sex: |
Not Specified |
| Emaps: |
EMAPS:3704926 |
| Pattern: |
Regionally restricted |
| Stage: |
TS26 |
| Assay Id: |
MGI:6460028 |
| Age: |
embryonic day 18.0 |
|
|
| Specimen Label: |
2A |
| Detected: |
true |
| Specimen Num: |
1 |
|
•
•
•
•
•
|
| GXD Expression |
| Probe: |
MGI:6460027 |
| Assay Type: |
Immunohistochemistry |
| Annotation Date: |
2020-10-07 |
| Strength: |
Present |
| Sex: |
Not Specified |
| Emaps: |
EMAPS:3705023 |
| Pattern: |
Regionally restricted |
| Stage: |
TS23 |
| Assay Id: |
MGI:6460028 |
| Age: |
embryonic day 15.0 |
|
| Note: |
Expression in ventral horns and area around central canal. |
| Specimen Label: |
2B |
| Detected: |
true |
| Specimen Num: |
2 |
|
•
•
•
•
•
|
| GXD Expression |
| Probe: |
MGI:6460027 |
| Assay Type: |
Immunohistochemistry |
| Annotation Date: |
2020-10-07 |
| Strength: |
Present |
| Sex: |
Not Specified |
| Emaps: |
EMAPS:3705026 |
| Pattern: |
Regionally restricted |
| Stage: |
TS26 |
| Assay Id: |
MGI:6460028 |
| Age: |
embryonic day 18.0 |
|
| Note: |
Authors report that intensity of expression changes from 15 to 18 days. Expression in ventral horns and area around central canal. |
| Specimen Label: |
2C |
| Detected: |
true |
| Specimen Num: |
3 |
|
•
•
•
•
•
|
| GXD Expression |
| Probe: |
MGI:6460027 |
| Assay Type: |
Immunohistochemistry |
| Annotation Date: |
2020-10-07 |
| Strength: |
Present |
| Sex: |
Not Specified |
| Emaps: |
EMAPS:3705026 |
| Pattern: |
Regionally restricted |
| Stage: |
TS26 |
| Assay Id: |
MGI:6460028 |
| Age: |
embryonic day 18.0 |
|
| Note: |
Expression in motor regions of spinal cord. Intensity of expression varied in nuclei from one cell type to another. |
| Specimen Label: |
2D |
| Detected: |
true |
| Specimen Num: |
4 |
|
•
•
•
•
•
|
| GXD Expression |
| Probe: |
MGI:12553 |
| Assay Type: |
RNA in situ |
| Annotation Date: |
2020-08-07 |
| Strength: |
Weak |
| Sex: |
Not Specified |
| Emaps: |
EMAPS:3705413 |
| Pattern: |
Not Specified |
| Stage: |
TS13 |
| Assay Id: |
MGI:6448968 |
| Age: |
embryonic day 8.5 |
| Image: |
1A/B |
|
| Specimen Label: |
1A/B |
| Detected: |
true |
| Specimen Num: |
1 |
|
•
•
•
•
•
|
| GXD Expression |
| Probe: |
MGI:12553 |
| Assay Type: |
RNA in situ |
| Annotation Date: |
2020-08-07 |
| Strength: |
Weak |
| Sex: |
Not Specified |
| Emaps: |
EMAPS:3705413 |
| Pattern: |
Not Specified |
| Stage: |
TS13 |
| Assay Id: |
MGI:6448968 |
| Age: |
embryonic day 8.5 |
| Image: |
1D/E |
|
| Specimen Label: |
1D/E |
| Detected: |
true |
| Specimen Num: |
2 |
|
•
•
•
•
•
|
| GXD Expression |
| Probe: |
MGI:256280 |
| Assay Type: |
RNA in situ |
| Annotation Date: |
2019-12-16 |
| Strength: |
Present |
| Sex: |
Not Specified |
| Emaps: |
EMAPS:3806722 |
| Pattern: |
Not Specified |
| Stage: |
TS22 |
| Assay Id: |
MGI:6381375 |
| Age: |
embryonic day 14.5 |
| Image: |
1C43 |
|
| Specimen Label: |
1C43 |
| Detected: |
true |
| Specimen Num: |
1 |
|
•
•
•
•
•
|
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Liu YH |
| Year: |
1991 |
| Journal: |
J Biol Chem |
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Characterization of estrogen-responsive mouse lactoferrin promoter. |
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266 |
| Issue: |
32 |
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•
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J Biol Chem |
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Organization, sequence, and expression of the murine S100 beta gene. Transcriptional regulation by cell type-specific cis-acting regulatory elements. |
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OASIS regulates chondroitin 6-O-sulfotransferase 1 gene transcription in the injured adult mouse cerebral cortex. |
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Elucidation of the role of fructose 2,6-bisphosphate in the regulation of glucose fluxes in mice using in vivo (13)C NMR measurements of hepatic carbohydrate metabolism. |
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Interaction of zonula occludens-1 (ZO-1) with alpha-actinin-4: application of functional proteomics for identification of PDZ domain-associated proteins. |
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J Immunol Methods |
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Biochem J |
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Eur J Pharmacol |
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Cancer Gene Ther |
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Different efficacy of in vivo herpes simplex virus thymidine kinase gene transduction and ganciclovir treatment on the inhibition of tumor growth of murine and human melanoma cells and rat glioblastoma cells. |
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•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
225
 |
| Fragment?: |
false |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
113
 |
| Fragment?: |
false |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
302
 |
| Fragment?: |
false |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
58
 |
| Fragment?: |
true |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
150
 |
| Fragment?: |
false |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
54
 |
| Fragment?: |
true |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
104
 |
| Fragment?: |
true |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
238
 |
| Fragment?: |
true |
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•
•
•
•
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Nakai H |
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2010 |
| Journal: |
FEBS J |
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Aspergillus nidulans alpha-galactosidase of glycoside hydrolase family 36 catalyses the formation of alpha-galacto-oligosaccharides by transglycosylation. |
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17 |
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3538-51 |
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•
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Rigden DJ |
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2002 |
| Journal: |
FEBS Lett |
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Iterative database searches demonstrate that glycoside hydrolase families 27, 31, 36 and 66 share a common evolutionary origin with family 13. |
| Volume: |
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1-3 |
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17-22 |
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•
•
•
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| Year: |
2011 |
| Journal: |
J Biol Chem |
| Title: |
α-Galactosidase/sucrose kinase (AgaSK), a novel bifunctional enzyme from the human microbiome coupling galactosidase and kinase activities. |
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47 |
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40814-23 |
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•
•
•
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Way M |
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1995 |
| Journal: |
J Cell Sci |
| Title: |
beta-Scruin, a homologue of the actin crosslinking protein scruin, is localized to the acrosomal vesicle of Limulus sperm. |
| Volume: |
108 ( Pt 10) |
|
| Pages: |
3155-62 |
|
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•
•
•
•
|
| Publication |
| First Author: |
Bork P |
| Year: |
1994 |
| Journal: |
J Mol Biol |
| Title: |
Drosophila kelch motif is derived from a common enzyme fold. |
| Volume: |
236 |
| Issue: |
5 |
| Pages: |
1277-82 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Oda S |
| Year: |
2009 |
| Journal: |
Structure |
| Title: |
Structural basis for targeting of human RNA helicase DDX3 by poxvirus protein K7. |
| Volume: |
17 |
| Issue: |
11 |
| Pages: |
1528-37 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Maluquer de Motes C |
| Year: |
2011 |
| Journal: |
PLoS Pathog |
| Title: |
Inhibition of apoptosis and NF-κB activation by vaccinia protein N1 occur via distinct binding surfaces and make different contributions to virulence. |
| Volume: |
7 |
| Issue: |
12 |
| Pages: |
e1002430 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Tang Q |
| Year: |
2018 |
| Journal: |
J Biol Chem |
| Title: |
Mechanism of vaccinia viral protein B14-mediated inhibition of IκB kinase β activation. |
| Volume: |
293 |
| Issue: |
26 |
| Pages: |
10344-10352 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Hadders MA |
| Year: |
2007 |
| Journal: |
Science |
| Title: |
Structure of C8alpha-MACPF reveals mechanism of membrane attack in complement immune defense. |
| Volume: |
317 |
| Issue: |
5844 |
| Pages: |
1552-4 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Noutoshi Y |
| Year: |
2006 |
| Journal: |
Plant Mol Biol |
| Title: |
Loss of Necrotic Spotted Lesions 1 associates with cell death and defense responses in Arabidopsis thaliana. |
| Volume: |
62 |
| Issue: |
1-2 |
| Pages: |
29-42 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Slade DJ |
| Year: |
2008 |
| Journal: |
J Mol Biol |
| Title: |
Crystal structure of the MACPF domain of human complement protein C8 alpha in complex with the C8 gamma subunit. |
| Volume: |
379 |
| Issue: |
2 |
| Pages: |
331-42 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Ishino T |
| Year: |
2005 |
| Journal: |
Cell Microbiol |
| Title: |
A Plasmodium sporozoite protein with a membrane attack complex domain is required for breaching the liver sinusoidal cell layer prior to hepatocyte infection. |
| Volume: |
7 |
| Issue: |
2 |
| Pages: |
199-208 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Satoh H |
| Year: |
2007 |
| Journal: |
Toxicon |
| Title: |
Characterization of PsTX-60B, a new membrane-attack complex/perforin (MACPF) family toxin, from the venomous sea anemone Phyllodiscus semoni. |
| Volume: |
49 |
| Issue: |
8 |
| Pages: |
1208-10 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Morita-Yamamuro C |
| Year: |
2005 |
| Journal: |
Plant Cell Physiol |
| Title: |
The Arabidopsis gene CAD1 controls programmed cell death in the plant immune system and encodes a protein containing a MACPF domain. |
| Volume: |
46 |
| Issue: |
6 |
| Pages: |
902-12 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Ponting CP |
| Year: |
1999 |
| Journal: |
Curr Biol |
| Title: |
Chlamydial homologues of the MACPF (MAC/perforin) domain. |
| Volume: |
9 |
| Issue: |
24 |
| Pages: |
R911-3 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Ruszczycky MW |
| Year: |
2012 |
| Journal: |
Biochim Biophys Acta |
| Title: |
Radical SAM enzymes in the biosynthesis of sugar-containing natural products. |
| Volume: |
1824 |
| Issue: |
11 |
| Pages: |
1231-44 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Sulzenbacher G |
| Year: |
2004 |
| Journal: |
J Mol Biol |
| Title: |
Crystal structure of E.coli alcohol dehydrogenase YqhD: evidence of a covalently modified NADP coenzyme. |
| Volume: |
342 |
| Issue: |
2 |
| Pages: |
489-502 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Jarboe LR |
| Year: |
2011 |
| Journal: |
Appl Microbiol Biotechnol |
| Title: |
YqhD: a broad-substrate range aldehyde reductase with various applications in production of biorenewable fuels and chemicals. |
| Volume: |
89 |
| Issue: |
2 |
| Pages: |
249-57 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Liu X |
| Year: |
2009 |
| Journal: |
Microbiology (Reading) |
| Title: |
Two novel metal-independent long-chain alkyl alcohol dehydrogenases from Geobacillus thermodenitrificans NG80-2. |
| Volume: |
155 |
| Issue: |
Pt 6 |
| Pages: |
2078-2085 |
|
•
•
•
•
•
|
| Protein Domain |
| Type: |
Repeat |
| Description: |
Kelch is a 50-residue motif, named after the Drosophila mutant in which it was first identified []. This sequence motif represents one β-sheet blade, and several of these repeats can associate to form a β-propeller. For instance, the motif appears 6 times in Drosophila egg-chamber regulatory protein (also known as ring canal kelch protein), creating a 6-bladed β-propeller. The motif is also found in mouse protein MIPP []and in a number of poxviruses. In addition, kelch repeats have been recognised in alpha- and beta-scruin [, ], and in galactose oxidase from the fungus Dactylium dendroides [, ]. The structure of galactose oxidase reveals that the repeated sequence corresponds to a 4-stranded antiparallel β-sheet motif that forms the repeat unit in a super-barrel structural fold [].The known functions of kelch-containing proteins are diverse: scruin is an actin cross-linking protein; galactose oxidase catalyses the oxidation of the hydroxyl group at the C6 position in D-galactose; and kelch may have a cytoskeletal function, as it is localised to the actin-rich ring canals that connect the 15 nurse cells to the developing oocyte in Drosophila []. Nevertheless, based on the location of the kelch pattern in the catalytic unit in galactose oxidase, functionally important residues have been predicted in glyoxal oxidase [].This entry represents a type of kelch sequence motif that comprises one β-sheet blade. |
|
•
•
•
•
•
|
| Protein Domain |
| Type: |
Family |
| Description: |
O-Glycosyl hydrolases () are a widespread group of enzymes that hydrolyse the glycosidic bond between two or more carbohydrates, or between a carbohydrate and a non-carbohydrate moiety. A classification system for glycosyl hydrolases, based on sequence similarity, has led to the definition of 85 different families [, ]. This classification is available on the CAZy (CArbohydrate-Active EnZymes) website.Glycoside hydrolase family 36 () occur in prokaryotes, eukaryotes, and archaea with a wide range of hydrolytic activities, including alpha-galactosidase, alpha-N-acetylgalactosaminidase, stachyose synthase, and raffinose synthase [, ]. All GH36 enzymes cleave a terminal carbohydrate moiety from a substrate that varies considerably in size, depending on the enzyme, and may be either a starch or a glycoprotein. GH36 members are retaining enzymes that cleave their substrates via an acid/base-catalyzed, double-displacement mechanism involving a covalent glycosyl-enzyme intermediate []. Two aspartic acid residues have been identified as the catalytic nucleophile and the acid/base, respectively.Proteins in this entry also include AgaSK, a bifunctional protein that contains two domains: one closely related to alpha-galactosidases from glycoside hydrolase family GH36 and the other containing a nucleotide-binding motif. It can hydrolyze melibiose and raffinose to galactose and either glucose or sucrose, respectively, and can specifically phosphorylate sucrose on the C6 position of glucose in the presence of ATP []. |
|
•
•
•
•
•
|
| Protein Domain |
| Type: |
Family |
| Description: |
Butanol dehydrogenase (BDH) is involved in the final step of the butanol formation pathway, in which it catalyses the conversion of butyraldehyde to butanol with the cofactor NAD(P)H being oxidised in the process. The NADH-BDH has higher activity with longer chained aldehydes and is inhibited by metabolites containing an adenine moiety. This protein family belongs to the so-called iron-containing alcohol dehydrogenase superfamily. Members in this family use divalent ions, preferentially iron or zinc []. This family also includes E. coli YqhD enzyme, an NADP-dependent dehydrogenase whose activity measurements with several alcohols demonstrate preference for alcohols longer than C3 [, ]. The active site of YqhD contains a zinc atom, and a modified NADPH cofactor bearing OH groups on the saturated C5 and C6 atoms, possibly due to oxygen stress on the enzyme, which would functionally work under anaerobic conditions.This entry also includes Long-chain-alcohol dehydrogenase 2 from Geobacillus thermodenitrificans which is able to oxidise a broad range of alkyl alcohols from methanol to 1-triacontanol (C1 to C30), whose best substrate is 1-octanol. In contrast to other members of the family, it apparently does not use iron or other metals as cofactor []. |
|
•
•
•
•
•
|
| Protein Domain |
| Type: |
Homologous_superfamily |
| Description: |
Kelch is a 50-residue motif, named after the Drosophila mutant in which it was first identified []. This sequence motif represents one β-sheet blade, and several of these repeats can associate to form a β-propeller. For instance, the motif appears 6 times in Drosophila egg-chamber regulatory protein (also known as ring canal kelch protein), creating a 6-bladed β-propeller. The motif is also found in mouse protein MIPP []and in a number of poxviruses. In addition, kelch repeats have been recognised in alpha- and beta-scruin [, ], and in galactose oxidase from the fungus Dactylium dendroides [, ]. The structure of galactose oxidase reveals that the repeated sequence corresponds to a 4-stranded antiparallel β-sheet motif that forms the repeat unit in a super-barrel structural fold [].The known functions of kelch-containing proteins are diverse: scruin is an actin cross-linking protein; galactose oxidase catalyses the oxidation of the hydroxyl group at the C6 position in D-galactose; and kelch may have a cytoskeletal function, as it is localised to the actin-rich ring canals that connect the 15 nurse cells to the developing oocyte in Drosophila []. Nevertheless, based on the location of the kelch pattern in the catalytic unit in galactose oxidase, functionally important residues have been predicted in glyoxal oxidase [].This entry represents the 6-bladed Kelch β-propeller, which consists of six 4-stranded β-sheet motifs (or six Kelch repeats). |
|
•
•
•
•
•
|
| Protein Domain |
| Type: |
Homologous_superfamily |
| Description: |
This entry represents a β-propeller domain found in galactose oxidase and in Kelch repeat-containing proteins.The known functions of kelch-containing proteins are diverse: scruin is an actin cross-linking protein; galactose oxidase catalyses the oxidation of the hydroxyl group at the C6 position in D-galactose; neuraminidase hydrolyses sialic acid residues from glycoproteins; and kelch may have a cytoskeletal function, as it is localised to the actin-rich ring canals that connect the 15 nurse cells to the developing oocyte in Drosophila []. Nevertheless, based on the location of the kelch pattern in the catalytic unit in galactose oxidase, functionally important residues have been predicted in glyoxal oxidase [].Galactose oxidase () is a monomeric enzyme that contains a single copper ion and catalyses the stereospecific oxidation of primary alcohols to their corresponding aldehyde []. The protein contains an unusual covalent thioether bond between a tyrosine and a cysteine that forms during its maturation []. Galactose oxidase is a three-domain protein: the N-terminal domain forms a jelly-roll sandwich, the central domain forms a seven 4-bladed β-propeller, and the C-terminal domain has an immunoglobulin-like fold. |
|
•
•
•
•
•
|
| Protein Domain |
| Type: |
Repeat |
| Description: |
Kelch is a 50-residue motif, named after the Drosophila mutant in which it was first identified []. This sequence motif represents one β-sheet blade, and several of these repeats can associate to form a β-propeller. For instance, the motif appears 6 times in Drosophila egg-chamber regulatory protein (also known as ring canal kelch protein), creating a 6-bladed β-propeller. The motif is also found in mouse protein MIPP []and in a number of poxviruses. In addition, kelch repeats have been recognised in alpha- and beta-scruin [, ], and in galactose oxidase from the fungus Dactylium dendroides [, ]. The structure of galactose oxidase reveals that the repeated sequence corresponds to a 4-stranded antiparallel β-sheet motif that forms the repeat unit in a super-barrel structural fold [].The known functions of kelch-containing proteins are diverse: scruin is an actin cross-linking protein; galactose oxidase catalyses the oxidation of the hydroxyl group at the C6 position in D-galactose; and kelch may have a cytoskeletal function, as it is localised to the actin-rich ring canals that connect the 15 nurse cells to the developing oocyte in Drosophila []. Nevertheless, based on the location of the kelch pattern in the catalytic unit in galactose oxidase, functionally important residues have been predicted in glyoxal oxidase [].This entry represents a type of kelch sequence motif that comprises one β-sheet blade. |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Dasen JS |
| Year: |
2008 |
| Journal: |
Cell |
| Title: |
Hox repertoires for motor neuron diversity and connectivity gated by a single accessory factor, FoxP1. |
| Volume: |
134 |
| Issue: |
2 |
| Pages: |
304-16 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Amin S |
| Year: |
2016 |
| Journal: |
Cell Rep |
| Title: |
Cdx and T Brachyury Co-activate Growth Signaling in the Embryonic Axial Progenitor Niche. |
| Volume: |
17 |
| Issue: |
12 |
| Pages: |
3165-3177 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Sawai A |
| Year: |
2022 |
| Journal: |
Elife |
| Title: |
PRC1 sustains the integrity of neural fate in the absence of PRC2 function. |
| Volume: |
11 |
|
|
|
•
•
•
•
•
|
| Publication |
| First Author: |
Jung H |
| Year: |
2010 |
| Journal: |
Neuron |
| Title: |
Global control of motor neuron topography mediated by the repressive actions of a single hox gene. |
| Volume: |
67 |
| Issue: |
5 |
| Pages: |
781-96 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Sabharwal P |
| Year: |
2011 |
| Journal: |
Neuron |
| Title: |
GDE2 regulates subtype-specific motor neuron generation through inhibition of Notch signaling. |
| Volume: |
71 |
| Issue: |
6 |
| Pages: |
1058-70 |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
783
 |
| Fragment?: |
false |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
760
 |
| Fragment?: |
false |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
713
 |
| Fragment?: |
false |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
341
 |
| Fragment?: |
false |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
702
 |
| Fragment?: |
false |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
216
 |
| Fragment?: |
true |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
284
 |
| Fragment?: |
false |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
250
 |
| Fragment?: |
true |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
187
 |
| Fragment?: |
false |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
720
 |
| Fragment?: |
false |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
752
 |
| Fragment?: |
false |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Guo B |
| Year: |
2011 |
| Journal: |
J Biol Chem |
| Title: |
Structure of the autocatalytic cysteine protease domain of potyvirus helper-component proteinase. |
| Volume: |
286 |
| Issue: |
24 |
| Pages: |
21937-43 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Alam J |
| Year: |
1994 |
| Journal: |
J Biol Chem |
| Title: |
Isolation and characterization of the mouse heme oxygenase-1 gene. Distal 5' sequences are required for induction by heme or heavy metals. |
| Volume: |
269 |
| Issue: |
2 |
| Pages: |
1001-9 |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
355
 |
| Fragment?: |
false |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
311
 |
| Fragment?: |
false |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
343
 |
| Fragment?: |
false |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Wisler GC |
| Year: |
1995 |
| Journal: |
J Gen Virol |
| Title: |
Characterization of the P1 protein and coding region of the zucchini yellow mosaic virus. |
| Volume: |
76 ( Pt 1) |
|
| Pages: |
37-45 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Verchot J |
| Year: |
1992 |
| Journal: |
Virology |
| Title: |
Mutational analysis of the tobacco etch potyviral 35-kDa proteinase: identification of essential residues and requirements for autoproteolysis. |
| Volume: |
190 |
| Issue: |
1 |
| Pages: |
298-306 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Pasin F |
| Year: |
2020 |
| Journal: |
Plant Commun |
| Title: |
Abscisic Acid Connects Phytohormone Signaling with RNA Metabolic Pathways and Promotes an Antiviral Response that Is Evaded by a Self-Controlled RNA Virus. |
| Volume: |
1 |
| Issue: |
5 |
|
|
•
•
•
•
•
|
| Publication |
| First Author: |
Firbank SJ |
| Year: |
2001 |
| Journal: |
Proc Natl Acad Sci U S A |
| Title: |
Crystal structure of the precursor of galactose oxidase: an unusual self-processing enzyme. |
| Volume: |
98 |
| Issue: |
23 |
| Pages: |
12932-7 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Whittaker JW |
| Year: |
2002 |
| Journal: |
Adv Protein Chem |
| Title: |
Galactose oxidase. |
| Volume: |
60 |
|
| Pages: |
1-49 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Rosado CJ |
| Year: |
2007 |
| Journal: |
Science |
| Title: |
A common fold mediates vertebrate defense and bacterial attack. |
| Volume: |
317 |
| Issue: |
5844 |
| Pages: |
1548-51 |
|
•
•
•
•
•
|