W5PND2
Gene name |
DDR1 |
Protein name |
receptor protein-tyrosine kinase |
Names |
|
Species |
Ovis aries (Sheep) |
KEGG Pathway |
mmu:12305 |
EC number |
|
Protein Class |
|

Descriptions
Autoinhibitory domains (AIDs)
Target domain |
614-908 (Protein kinase domain) |
Relief mechanism |
PTM |
Assay |
|
Accessory elements
No accessory elements
References
- Sammon D et al. (2020) "Two-step release of kinase autoinhibition in discoidin domain receptor 1", Proceedings of the National Academy of Sciences of the United States of America, 117, 22051-22060
- Fu HL et al. (2014) "Glycosylation at Asn211 regulates the activation state of the discoidin domain receptor 1 (DDR1)", The Journal of biological chemistry, 289, 9275-87
Autoinhibited structure

Activated structure

1 structures for W5PND2
Entry ID | Method | Resolution | Chain | Position | Source |
---|---|---|---|---|---|
AF-W5PND2-F1 | Predicted | AlphaFoldDB |
21 variants for W5PND2
Variant ID(s) | Position | Change | Description | Diseaes Association | Provenance |
---|---|---|---|---|---|
rs1092729259 | 20 | A>T | No | Ensembl | |
rs408471111 | 22 | M>V | No | Ensembl | |
rs1092224965 | 34 | A>E | No | Ensembl | |
rs415808807 | 99 | P>L | No | Ensembl | |
rs1094746247 | 100 | G>V | No | Ensembl | |
rs1093869742 | 101 | R>H | No | Ensembl | |
rs1092835531 | 103 | R>G | No | Ensembl | |
rs1091071610 | 145 | P>L | No | Ensembl | |
rs592363873 | 218 | T>M | No | Ensembl | |
rs605506291 | 263 | S>C | No | Ensembl | |
rs597224269 | 277 | R>Q | No | Ensembl | |
rs591003488 | 342 | R>H | No | Ensembl | |
rs603731954 | 345 | R>H | No | Ensembl | |
rs604052155 | 370 | V>L | No | Ensembl | |
rs590557710 | 379 | G>S | No | Ensembl | |
rs1089392286 | 399 | L>S | No | Ensembl | |
rs1090468552 | 494 | R>H | No | Ensembl | |
rs1092674640 | 634 | E>D | No | Ensembl | |
rs593566445 | 727 | T>M | No | Ensembl | |
rs1086313802 | 758 | R>C | No | Ensembl | |
rs1094840887 | 796 | A>T | No | Ensembl |
No associated diseases with W5PND2
4 regional properties for W5PND2
Type | Name | Position | InterPro Accession |
---|---|---|---|
domain | Cation-transporting P-type ATPase, N-terminal | 116 - 187 | IPR004014 |
domain | Cation-transporting P-type ATPase, C-terminal | 844 - 1013 | IPR006068 |
ptm | P-type ATPase, phosphorylation site | 460 - 466 | IPR018303 |
domain | P-type ATPase, haloacid dehalogenase domain | 439 - 812 | IPR044492 |
1 GO annotations of cellular component
Name | Definition |
---|---|
membrane | A lipid bilayer along with all the proteins and protein complexes embedded in it an attached to it. |
2 GO annotations of molecular function
Name | Definition |
---|---|
ATP binding | Binding to ATP, adenosine 5'-triphosphate, a universally important coenzyme and enzyme regulator. |
transmembrane receptor protein tyrosine kinase activity | Combining with a signal and transmitting the signal from one side of the membrane to the other to initiate a change in cell activity by catalysis of the reaction: ATP + a protein-L-tyrosine = ADP + a protein-L-tyrosine phosphate. |
1 GO annotations of biological process
Name | Definition |
---|---|
collagen-activated tyrosine kinase receptor signaling pathway | The series of molecular signals initiated by collagen binding to its receptor on the surface of a target cell where the receptor possesses tyrosine kinase activity, and ending with the regulation of a downstream cellular process, e.g. transcription. |
No homologous proteins in AiPD
UniProt AC | Gene Name | Protein Name | Species | Evidence Code |
---|---|---|---|---|
No homologous proteins |
10 | 20 | 30 | 40 | 50 | 60 |
MAPGALSFLL | LLLLVATGDA | DMKGHFDPAK | CRYALGMQDR | TIPDGDISAS | SSWSDSTAAR |
70 | 80 | 90 | 100 | 110 | 120 |
HSRLESSDGD | GAWCPAGPVF | PKEEEYLQVD | LRRLHLVAPG | RPRHAGGLGK | EFSPSYRLRY |
130 | 140 | 150 | 160 | 170 | 180 |
SRDGHRWMDW | RDRWGQEVIL | GNEDPGGVVL | KDLGPPMVAR | LVRFYPRADR | VMSVCLRVEL |
190 | 200 | 210 | 220 | 230 | 240 |
YGCLWKDGLL | SYTAPVGQTM | YLSEAVHLND | STYDGYTTHT | VGGLQYGGLG | QLADGVVGLD |
250 | 260 | 270 | 280 | 290 | 300 |
DFRKSQELRV | WPGYDYVGWS | NHSFPSGYVE | MEFEFDRLRA | FQAMQVHCNN | MHTLGARLPG |
310 | 320 | 330 | 340 | 350 | 360 |
GVECRFKRGP | AMAWEGEPVR | HALGGSLGDP | RARTVSVPLG | GRMGRFLQCR | FLFAGPWLLF |
370 | 380 | 390 | 400 | 410 | 420 |
SEISFISDVV | NDSSLALGGT | FPPAPWWPPG | PPPTNFSSLE | LEPRGQQPVA | KAEGSPTAIL |
430 | 440 | 450 | 460 | 470 | 480 |
IGCLVAIILL | LLLIIALMLW | RRLHWRRLLS | KDKAERRVLE | EELTVHLSVP | GDTILINNRP |
490 | 500 | 510 | 520 | 530 | 540 |
GPREPPPYQE | PRPRGNPPHS | APGVPNSSAL | LLSNPAYRLL | LATYARPPRG | PGPPTPAWAK |
550 | 560 | 570 | 580 | 590 | 600 |
PTNTQACSGD | YMEPEKPGAP | LLPPPPQNSV | PHYAEADIVT | LQGVTGGNTY | AVPALPPGAA |
610 | 620 | 630 | 640 | 650 | 660 |
GDGPPRVDFP | RSRLRFKEKL | GEGQFGEVHL | CEVESPQDLV | SLDFPLNVRK | GHPLLVAVKI |
670 | 680 | 690 | 700 | 710 | 720 |
LRPDATKNAR | NDFLKEVKIM | SRLKDPNIIR | LLGVCVQDDP | LCMITDYMEN | GDLNQFLSAH |
730 | 740 | 750 | 760 | 770 | 780 |
QLEDKATEGA | GDGEAAQGPT | ISYPMLLHVA | AQIASGMRYL | ATLNFVHRDL | ATRNCLVGEN |
790 | 800 | 810 | 820 | 830 | 840 |
FTIKIADFGM | SRNLYAGDYY | RVQGRAVLPI | RWMAWECILM | GKFTTASDVW | AFGVTLWEVL |
850 | 860 | 870 | 880 | 890 | 900 |
MLCRAQPFGQ | LTDEQVIENA | GEFFRDQGRQ | VYLSRPPACP | LSLYDLMLRC | WSREPEQRPP |
910 | |||||
FSQLHRFLAE | DAVNTV |