| Basic Information | |
|---|---|
| Species | Glycine max |
| Cazyme ID | Glyma19g29730.1 |
| Family | GT47 |
| Protein Properties | Length: 521 Molecular Weight: 59589.8 Isoelectric Point: 8.8435 |
| Chromosome | Chromosome/Scaffold: 19 Start: 37457990 End: 37461737 |
| Description | exostosin family protein |
| View CDS | |
| External Links |
|---|
| NCBI Taxonomy |
| Plaza |
| CAZyDB |
| Signature Domain Download full data set without filtering | |||
|---|---|---|---|
 | |||
| Family | Start | End | Evalue |
| GT47 | 123 | 444 | 0 |
| AVLRVFMYDLPPEFHFGLLDWKPEENVNNVWPDIKTKAPHYPGGLNLQHSIEYWLTLDLLASELPESEAPSNARSVIRVRNSSEADVIFVPFFSSLCYNR LSKTGPHEKRSRNKLLQEKLVKYVTAQEEWKRSGGKDHVILAHHPNSMLDARMKLWPGTFILSDFGRYPTNIANVEKDVIAPYKHVVGSYDNDQSSFDSR TTLLYFQGAIYRKDGGHVRHELYYLLKNEKDVHFSFGSVQKGGVRKATEGMRSSKFCLNIAGDTPSSNRLFDAIASHCVPVIISDDIELPYEDVLDYSQF CIFVRTRDALKKRYLINFIRSI | |||
| Full Sequence |
|---|
| Protein Sequence Length: 521 Download |
| MVERTVSGSA IKVVSKKSLC GFFTMTTLLF MLSWLFVLRS TRSEASPNSN LFSSYSNSDF 60 DHSVQQQKNV EEEVEPSFGN RAILVDNIEA AAAATTTTTT TTHDDKQQVL EEQGVKCKAH 120 DKAVLRVFMY DLPPEFHFGL LDWKPEENVN NVWPDIKTKA PHYPGGLNLQ HSIEYWLTLD 180 LLASELPESE APSNARSVIR VRNSSEADVI FVPFFSSLCY NRLSKTGPHE KRSRNKLLQE 240 KLVKYVTAQE EWKRSGGKDH VILAHHPNSM LDARMKLWPG TFILSDFGRY PTNIANVEKD 300 VIAPYKHVVG SYDNDQSSFD SRTTLLYFQG AIYRKDGGHV RHELYYLLKN EKDVHFSFGS 360 VQKGGVRKAT EGMRSSKFCL NIAGDTPSSN RLFDAIASHC VPVIISDDIE LPYEDVLDYS 420 QFCIFVRTRD ALKKRYLINF IRSIGKEEWT RMWNRLKEVE SFFEFQFPSK EGDAVQMIWK 480 AIARKVPFMK LKTNRSRRFL RSLYGNDMGN KSITTPANFW * |
| Functional Domains Download unfiltered results here | ||||||||
|---|---|---|---|---|---|---|---|---|
 | ||||||||
| Cdd ID | Domain | E-Value | Start | End | Length | Domain Description | ||
| pfam03016 | Exostosin | 3.0e-55 | 125 | 444 | 330 | + 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 | AAX33321.1 | 0 | 7 | 520 | 6 | 509 | secondary cell wall-related glycosyltransferase family 47 [Populus tremula x Populus tremuloides] |
| RefSeq | XP_002268382.1 | 0 | 76 | 520 | 42 | 488 | PREDICTED: hypothetical protein [Vitis vinifera] |
| RefSeq | XP_002319201.1 | 0 | 7 | 499 | 8 | 449 | predicted protein [Populus trichocarpa] |
| RefSeq | XP_002325457.1 | 0 | 122 | 520 | 70 | 463 | predicted protein [Populus trichocarpa] |
| RefSeq | XP_002530948.1 | 0 | 76 | 517 | 65 | 497 | catalytic, putative [Ricinus communis] |
