| Basic Information | |
|---|---|
| Species | Mimulus guttatus |
| Cazyme ID | mgv1a006381m |
| Family | GT47 |
| Protein Properties | Length: 447 Molecular Weight: 51013.6 Isoelectric Point: 9.7738 |
| Chromosome | Chromosome/Scaffold: 196 Start: 490668 End: 494517 |
| Description | FRA8 homolog |
| View CDS | |
| External Links |
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| CAZyDB |
| Signature Domain Download full data set without filtering | |||
|---|---|---|---|
| Family | Start | End | Evalue |
| GT47 | 91 | 389 | 0 |
| SGMKVYVYDLPAEYNSDWLSNERCGSHLFASEVAVHRALMKSPARTFDPWEADFFFVPVYVSCNFSKVNGFPAIGHARALMASAVVHVSSHLPFWNRSGG ADHVFVASHDFGSCFHTMEDAAVAEGVPEFMRNSIVLQTFGVEGNHPCQDVENVVIPPYVSPESVRTTLEKSPVTGRRDIFAFFRGKMEVHPKNISGRFY SKRVRTVILRKYGSDRRFYLRRHRFAGYQSEIVRSTFCLCPLGWAPWSPRLVESVALGCVPVIIADGIRLPFPSAVPWPEISLTVAESDVDNLGKILAH | |||
| Full Sequence |
|---|
| Protein Sequence Length: 447 Download |
| MINMAETTKR PLRNRGFYLK MKFLHNNTRH RYFKWILWFS ISFYFFSYFL ITQNKPIITS 60 LSRTTFSRTQ ASRAVVEESP LSYLQRFEEN SGMKVYVYDL PAEYNSDWLS NERCGSHLFA 120 SEVAVHRALM KSPARTFDPW EADFFFVPVY VSCNFSKVNG FPAIGHARAL MASAVVHVSS 180 HLPFWNRSGG ADHVFVASHD FGSCFHTMED AAVAEGVPEF MRNSIVLQTF GVEGNHPCQD 240 VENVVIPPYV SPESVRTTLE KSPVTGRRDI FAFFRGKMEV HPKNISGRFY SKRVRTVILR 300 KYGSDRRFYL RRHRFAGYQS EIVRSTFCLC PLGWAPWSPR LVESVALGCV PVIIADGIRL 360 PFPSAVPWPE ISLTVAESDV DNLGKILAHV AATNLTAIQK NLWDPEVRKA LLYHDPIIEG 420 DATWQILVSL KEKLGRSHRR SRVSIQ* |
| Functional Domains Download unfiltered results here | ||||||
|---|---|---|---|---|---|---|
| Cdd ID | Domain | E-Value | Start | End | Length | Domain Description |
| pfam03016 | Exostosin | 5.0e-72 | 90 | 388 | 306 | + Exostosin family. The EXT family is a family of tumour suppressor genes. Mutations of EXT1 on 8q24.1, EXT2 on 11p11-13, and EXT3 on 19p have been associated with the autosomal dominant disorder known as hereditary multiple exostoses (HME). This is the most common known skeletal dysplasia. The chromosomal locations of other EXT genes suggest association with other forms of neoplasia. EXT1 and EXT2 have both been shown to encode a heparan sulphate polymerase with both D-glucuronyl (GlcA) and N-acetyl-D-glucosaminoglycan (GlcNAC) transferase activities. The nature of the defect in heparan sulphate biosynthesis in HME is unclear. |
| Gene Ontology | |
|---|---|
| GO Term | Description |
| GO:0016020 | membrane |
| Annotations - NR Download unfiltered results here | |||||||
|---|---|---|---|---|---|---|---|
| Source | Hit ID | E-Value | Query Start | Query End | Hit Start | Hit End | Description |
| GenBank | AAX33322.1 | 0 | 12 | 444 | 3 | 440 | secondary cell wall-related glycosyltransferase family 47 [Populus tremula x Populus tremuloides] |
| GenBank | ABI64067.1 | 0 | 12 | 446 | 3 | 442 | glycosyltransferase GT47C [Populus tremula x Populus alba] |
| RefSeq | XP_002275679.1 | 0 | 10 | 434 | 6 | 440 | PREDICTED: hypothetical protein [Vitis vinifera] |
| RefSeq | XP_002314302.1 | 0 | 4 | 446 | 1 | 462 | predicted protein [Populus trichocarpa] |
| RefSeq | XP_002523710.1 | 0 | 4 | 446 | 1 | 461 | transferase, putative [Ricinus communis] |
