| Basic Information | |
|---|---|
| Species | Brachypodium distachyon |
| Cazyme ID | Bradi3g28012.1 |
| Family | GT47 |
| Protein Properties | Length: 522 Molecular Weight: 57704.4 Isoelectric Point: 7.2263 |
| Chromosome | Chromosome/Scaffold: 3 Start: 29347833 End: 29349738 |
| Description | Exostosin family protein |
| View CDS | |
| External Links |
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| NCBI Taxonomy |
| Plaza |
| CAZyDB |
| Signature Domain Download full data set without filtering | |||
|---|---|---|---|
| Family | Start | End | Evalue |
| GT47 | 111 | 452 | 0 |
| CDGRYIYMYDMPPRFNDDLVRHCGKGELHPWLDMCPYVANDGMGEPLGDEGGVFPGHGWYATDQFTLDLIFHSRMKRSYECLTNDTTLAAAVFVPFYAGL DAGRFLYNHSTSIRDKLQLEFIDWLVNRPEWRAMGGRDHFLVAGRTTWDFRREADVDALWGTKLLTHPAVKNMTAFVLEKSPSSRNNFAIPYPTYFHPEA AADVVAWQQKVREIPRRWLFSFAGAPRPGSNKTVRAELIRQCGASSLCNLFHCGGKDGDGAADCNSPGGVMRVFEGSDFCLQPRGDTATRRSTFDALLAG CVPVFFHRDSAYTQYALHFPRDHARYSVLIPHAGVAAGRVSI | |||
| Full Sequence |
|---|
| Protein Sequence Length: 522 Download |
| MKMTATFATK IHEDPDPVDA ANKPDGSGAV LRPFRVCHLT VLATAFCALV FYAHYAIRGN 60 MASALFKPPV TISSSSLPLL SSTSTIDPSL QPEKPATNRS AAAPASESDH CDGRYIYMYD 120 MPPRFNDDLV RHCGKGELHP WLDMCPYVAN DGMGEPLGDE GGVFPGHGWY ATDQFTLDLI 180 FHSRMKRSYE CLTNDTTLAA AVFVPFYAGL DAGRFLYNHS TSIRDKLQLE FIDWLVNRPE 240 WRAMGGRDHF LVAGRTTWDF RREADVDALW GTKLLTHPAV KNMTAFVLEK SPSSRNNFAI 300 PYPTYFHPEA AADVVAWQQK VREIPRRWLF SFAGAPRPGS NKTVRAELIR QCGASSLCNL 360 FHCGGKDGDG AADCNSPGGV MRVFEGSDFC LQPRGDTATR RSTFDALLAG CVPVFFHRDS 420 AYTQYALHFP RDHARYSVLI PHAGVAAGRV SIEERLGRIP AEEVRRMREA VIRLIPRVVY 480 ADPRAGRAGF NDAFDVAVEA IIDRVAKRRC GEDEVTAGTT E* 540 |
| Functional Domains Download unfiltered results here | ||||||||
|---|---|---|---|---|---|---|---|---|
| Cdd ID | Domain | E-Value | Start | End | Length | Domain Description | ||
| pfam03016 | Exostosin | 2.0e-60 | 110 | 459 | 363 | + 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 | EEC74507.1 | 0 | 35 | 509 | 28 | 535 | hypothetical protein OsI_09988 [Oryza sativa Indica Group] |
| RefSeq | NP_001048945.1 | 0 | 35 | 509 | 28 | 535 | Os03g0144800 [Oryza sativa (japonica cultivar-group)] |
| RefSeq | NP_001150032.1 | 0 | 108 | 511 | 55 | 456 | xyloglucan galactosyltransferase KATAMARI 1 [Zea mays] |
| Swiss-Prot | Q8H038 | 0 | 35 | 509 | 12 | 519 | KATAM_ORYSJ RecName: Full=Xyloglucan galactosyltransferase KATAMARI1 homolog |
| RefSeq | XP_002464524.1 | 0 | 19 | 512 | 14 | 485 | hypothetical protein SORBIDRAFT_01g020080 [Sorghum bicolor] |
