Carries an ATP pyrophosphate-lyase domain on its cytoplasmic segment. Likely acts as a receptor for some unknown extracellular stimulus. Extremely expanded kinetoplastid protein family.. Expressed in the insect stage (promastigote) but not in the mammalian host stage of the parasite life cycle.. Localization: Cell surface (by feature)
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 20 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 31, no: 23 |
NetGPI | no | yes: 0, no: 54 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 51 |
GO:0110165 | cellular anatomical entity | 1 | 52 |
Related structures:
AlphaFold database: E8NHJ6
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 47 |
GO:0006163 | purine nucleotide metabolic process | 5 | 47 |
GO:0006164 | purine nucleotide biosynthetic process | 6 | 47 |
GO:0006171 | cAMP biosynthetic process | 8 | 47 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 47 |
GO:0006753 | nucleoside phosphate metabolic process | 4 | 47 |
GO:0006793 | phosphorus metabolic process | 3 | 47 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 47 |
GO:0006807 | nitrogen compound metabolic process | 2 | 47 |
GO:0007165 | signal transduction | 2 | 47 |
GO:0008152 | metabolic process | 1 | 47 |
GO:0009058 | biosynthetic process | 2 | 47 |
GO:0009117 | nucleotide metabolic process | 5 | 47 |
GO:0009150 | purine ribonucleotide metabolic process | 6 | 47 |
GO:0009152 | purine ribonucleotide biosynthetic process | 7 | 47 |
GO:0009165 | nucleotide biosynthetic process | 6 | 47 |
GO:0009187 | cyclic nucleotide metabolic process | 6 | 47 |
GO:0009190 | cyclic nucleotide biosynthetic process | 7 | 47 |
GO:0009259 | ribonucleotide metabolic process | 5 | 47 |
GO:0009260 | ribonucleotide biosynthetic process | 6 | 47 |
GO:0009987 | cellular process | 1 | 47 |
GO:0018130 | heterocycle biosynthetic process | 4 | 47 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 47 |
GO:0019637 | organophosphate metabolic process | 3 | 47 |
GO:0019693 | ribose phosphate metabolic process | 4 | 47 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 47 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 47 |
GO:0035556 | intracellular signal transduction | 3 | 47 |
GO:0044237 | cellular metabolic process | 2 | 47 |
GO:0044238 | primary metabolic process | 2 | 47 |
GO:0044249 | cellular biosynthetic process | 3 | 47 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 47 |
GO:0044281 | small molecule metabolic process | 2 | 47 |
GO:0046058 | cAMP metabolic process | 7 | 47 |
GO:0046390 | ribose phosphate biosynthetic process | 5 | 47 |
GO:0046483 | heterocycle metabolic process | 3 | 47 |
GO:0050789 | regulation of biological process | 2 | 47 |
GO:0050794 | regulation of cellular process | 3 | 47 |
GO:0052652 | cyclic purine nucleotide metabolic process | 6 | 47 |
GO:0055086 | nucleobase-containing small molecule metabolic process | 3 | 47 |
GO:0065007 | biological regulation | 1 | 47 |
GO:0071704 | organic substance metabolic process | 2 | 47 |
GO:0072521 | purine-containing compound metabolic process | 4 | 47 |
GO:0072522 | purine-containing compound biosynthetic process | 5 | 47 |
GO:0090407 | organophosphate biosynthetic process | 4 | 47 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 47 |
GO:1901137 | carbohydrate derivative biosynthetic process | 4 | 47 |
GO:1901293 | nucleoside phosphate biosynthetic process | 5 | 47 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 47 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 47 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 47 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 47 |
GO:1901576 | organic substance biosynthetic process | 3 | 47 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 41 |
GO:0016829 | lyase activity | 2 | 41 |
GO:0004016 | adenylate cyclase activity | 3 | 3 |
GO:0009975 | cyclase activity | 2 | 3 |
GO:0016849 | phosphorus-oxygen lyase activity | 3 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 395 | 399 | PF00656 | 0.438 |
CLV_C14_Caspase3-7 | 769 | 773 | PF00656 | 0.392 |
CLV_C14_Caspase3-7 | 91 | 95 | PF00656 | 0.327 |
CLV_NRD_NRD_1 | 217 | 219 | PF00675 | 0.556 |
CLV_NRD_NRD_1 | 26 | 28 | PF00675 | 0.471 |
CLV_NRD_NRD_1 | 41 | 43 | PF00675 | 0.408 |
CLV_NRD_NRD_1 | 437 | 439 | PF00675 | 0.439 |
CLV_NRD_NRD_1 | 535 | 537 | PF00675 | 0.481 |
CLV_NRD_NRD_1 | 670 | 672 | PF00675 | 0.522 |
CLV_PCSK_FUR_1 | 215 | 219 | PF00082 | 0.552 |
CLV_PCSK_FUR_1 | 27 | 31 | PF00082 | 0.298 |
CLV_PCSK_KEX2_1 | 217 | 219 | PF00082 | 0.557 |
CLV_PCSK_KEX2_1 | 26 | 28 | PF00082 | 0.474 |
CLV_PCSK_KEX2_1 | 29 | 31 | PF00082 | 0.426 |
CLV_PCSK_KEX2_1 | 41 | 43 | PF00082 | 0.411 |
CLV_PCSK_PC1ET2_1 | 29 | 31 | PF00082 | 0.496 |
CLV_PCSK_SKI1_1 | 117 | 121 | PF00082 | 0.613 |
CLV_PCSK_SKI1_1 | 218 | 222 | PF00082 | 0.538 |
CLV_PCSK_SKI1_1 | 265 | 269 | PF00082 | 0.472 |
CLV_PCSK_SKI1_1 | 29 | 33 | PF00082 | 0.397 |
CLV_PCSK_SKI1_1 | 315 | 319 | PF00082 | 0.432 |
CLV_PCSK_SKI1_1 | 515 | 519 | PF00082 | 0.540 |
CLV_PCSK_SKI1_1 | 664 | 668 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 799 | 803 | PF00082 | 0.468 |
CLV_PCSK_SKI1_1 | 93 | 97 | PF00082 | 0.583 |
DEG_APCC_DBOX_1 | 40 | 48 | PF00400 | 0.649 |
DEG_APCC_DBOX_1 | 721 | 729 | PF00400 | 0.291 |
DEG_APCC_DBOX_1 | 798 | 806 | PF00400 | 0.215 |
DEG_APCC_KENBOX_2 | 616 | 620 | PF00400 | 0.184 |
DEG_MDM2_SWIB_1 | 492 | 499 | PF02201 | 0.163 |
DEG_ODPH_VHL_1 | 697 | 708 | PF01847 | 0.153 |
DEG_SPOP_SBC_1 | 300 | 304 | PF00917 | 0.392 |
DOC_CDC14_PxL_1 | 529 | 537 | PF14671 | 0.229 |
DOC_CDC14_PxL_1 | 774 | 782 | PF14671 | 0.177 |
DOC_CYCLIN_yCln2_LP_2 | 246 | 252 | PF00134 | 0.350 |
DOC_CYCLIN_yCln2_LP_2 | 518 | 524 | PF00134 | 0.370 |
DOC_MAPK_FxFP_2 | 504 | 507 | PF00069 | 0.362 |
DOC_MAPK_gen_1 | 169 | 176 | PF00069 | 0.203 |
DOC_MAPK_gen_1 | 215 | 224 | PF00069 | 0.243 |
DOC_MAPK_gen_1 | 26 | 37 | PF00069 | 0.492 |
DOC_MAPK_gen_1 | 41 | 51 | PF00069 | 0.519 |
DOC_MAPK_gen_1 | 616 | 623 | PF00069 | 0.175 |
DOC_MAPK_gen_1 | 93 | 102 | PF00069 | 0.380 |
DOC_MAPK_MEF2A_6 | 42 | 51 | PF00069 | 0.426 |
DOC_MAPK_MEF2A_6 | 520 | 529 | PF00069 | 0.367 |
DOC_MAPK_MEF2A_6 | 722 | 729 | PF00069 | 0.272 |
DOC_MAPK_MEF2A_6 | 799 | 806 | PF00069 | 0.226 |
DOC_MAPK_MEF2A_6 | 93 | 102 | PF00069 | 0.384 |
DOC_MAPK_RevD_3 | 203 | 218 | PF00069 | 0.182 |
DOC_MAPK_RevD_3 | 601 | 617 | PF00069 | 0.159 |
DOC_PP1_RVXF_1 | 169 | 176 | PF00149 | 0.278 |
DOC_PP1_RVXF_1 | 313 | 319 | PF00149 | 0.361 |
DOC_PP1_RVXF_1 | 552 | 558 | PF00149 | 0.322 |
DOC_PP2B_LxvP_1 | 246 | 249 | PF13499 | 0.357 |
DOC_PP2B_PxIxI_1 | 610 | 616 | PF00149 | 0.165 |
DOC_PP4_FxxP_1 | 175 | 178 | PF00568 | 0.372 |
DOC_PP4_FxxP_1 | 504 | 507 | PF00568 | 0.362 |
DOC_PP4_FxxP_1 | 608 | 611 | PF00568 | 0.188 |
DOC_PP4_FxxP_1 | 622 | 625 | PF00568 | 0.263 |
DOC_PP4_FxxP_1 | 677 | 680 | PF00568 | 0.370 |
DOC_PP4_FxxP_1 | 787 | 790 | PF00568 | 0.373 |
DOC_PP4_FxxP_1 | 817 | 820 | PF00568 | 0.276 |
DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.314 |
DOC_USP7_MATH_1 | 240 | 244 | PF00917 | 0.277 |
DOC_USP7_MATH_1 | 300 | 304 | PF00917 | 0.388 |
DOC_USP7_MATH_1 | 394 | 398 | PF00917 | 0.343 |
DOC_USP7_MATH_1 | 643 | 647 | PF00917 | 0.393 |
DOC_USP7_MATH_1 | 686 | 690 | PF00917 | 0.393 |
DOC_USP7_UBL2_3 | 380 | 384 | PF12436 | 0.399 |
DOC_WW_Pin1_4 | 328 | 333 | PF00397 | 0.375 |
DOC_WW_Pin1_4 | 602 | 607 | PF00397 | 0.283 |
DOC_WW_Pin1_4 | 767 | 772 | PF00397 | 0.393 |
DOC_WW_Pin1_4 | 791 | 796 | PF00397 | 0.279 |
LIG_14-3-3_CanoR_1 | 215 | 224 | PF00244 | 0.308 |
LIG_14-3-3_CanoR_1 | 301 | 308 | PF00244 | 0.337 |
LIG_14-3-3_CanoR_1 | 36 | 44 | PF00244 | 0.514 |
LIG_14-3-3_CanoR_1 | 438 | 442 | PF00244 | 0.225 |
LIG_14-3-3_CanoR_1 | 484 | 488 | PF00244 | 0.350 |
LIG_14-3-3_CanoR_1 | 671 | 679 | PF00244 | 0.337 |
LIG_14-3-3_CanoR_1 | 694 | 698 | PF00244 | 0.335 |
LIG_14-3-3_CanoR_1 | 756 | 761 | PF00244 | 0.390 |
LIG_14-3-3_CanoR_1 | 842 | 846 | PF00244 | 0.384 |
LIG_Actin_WH2_2 | 199 | 214 | PF00022 | 0.202 |
LIG_Actin_WH2_2 | 221 | 237 | PF00022 | 0.205 |
LIG_Actin_WH2_2 | 520 | 538 | PF00022 | 0.253 |
LIG_Actin_WH2_2 | 578 | 596 | PF00022 | 0.181 |
LIG_AP2alpha_2 | 198 | 200 | PF02296 | 0.159 |
LIG_APCC_ABBA_1 | 151 | 156 | PF00400 | 0.372 |
LIG_APCC_ABBA_1 | 318 | 323 | PF00400 | 0.368 |
LIG_APCC_ABBA_1 | 354 | 359 | PF00400 | 0.177 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.732 |
LIG_BRCT_BRCA1_1 | 164 | 168 | PF00533 | 0.363 |
LIG_BRCT_BRCA1_1 | 604 | 608 | PF00533 | 0.167 |
LIG_BRCT_BRCA1_1 | 746 | 750 | PF00533 | 0.189 |
LIG_BRCT_BRCA1_1 | 802 | 806 | PF00533 | 0.321 |
LIG_DLG_GKlike_1 | 756 | 763 | PF00625 | 0.172 |
LIG_EH1_1 | 310 | 318 | PF00400 | 0.139 |
LIG_eIF4E_1 | 223 | 229 | PF01652 | 0.167 |
LIG_eIF4E_1 | 777 | 783 | PF01652 | 0.183 |
LIG_FHA_1 | 206 | 212 | PF00498 | 0.234 |
LIG_FHA_1 | 223 | 229 | PF00498 | 0.160 |
LIG_FHA_1 | 349 | 355 | PF00498 | 0.283 |
LIG_FHA_1 | 409 | 415 | PF00498 | 0.257 |
LIG_FHA_1 | 587 | 593 | PF00498 | 0.274 |
LIG_FHA_1 | 674 | 680 | PF00498 | 0.297 |
LIG_FHA_1 | 73 | 79 | PF00498 | 0.223 |
LIG_FHA_1 | 792 | 798 | PF00498 | 0.285 |
LIG_FHA_1 | 8 | 14 | PF00498 | 0.692 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.176 |
LIG_FHA_1 | 849 | 855 | PF00498 | 0.404 |
LIG_FHA_2 | 193 | 199 | PF00498 | 0.352 |
LIG_FHA_2 | 329 | 335 | PF00498 | 0.380 |
LIG_FHA_2 | 347 | 353 | PF00498 | 0.320 |
LIG_FHA_2 | 569 | 575 | PF00498 | 0.245 |
LIG_FHA_2 | 657 | 663 | PF00498 | 0.323 |
LIG_FHA_2 | 707 | 713 | PF00498 | 0.316 |
LIG_FHA_2 | 767 | 773 | PF00498 | 0.208 |
LIG_FHA_2 | 850 | 856 | PF00498 | 0.439 |
LIG_FHA_2 | 89 | 95 | PF00498 | 0.331 |
LIG_GBD_Chelix_1 | 289 | 297 | PF00786 | 0.496 |
LIG_GBD_Chelix_1 | 416 | 424 | PF00786 | 0.499 |
LIG_GBD_Chelix_1 | 425 | 433 | PF00786 | 0.448 |
LIG_Integrin_isoDGR_2 | 115 | 117 | PF01839 | 0.434 |
LIG_Integrin_RGD_1 | 196 | 198 | PF01839 | 0.363 |
LIG_IRF3_LxIS_1 | 598 | 605 | PF10401 | 0.187 |
LIG_LIR_Apic_2 | 172 | 178 | PF02991 | 0.354 |
LIG_LIR_Apic_2 | 461 | 465 | PF02991 | 0.382 |
LIG_LIR_Apic_2 | 605 | 611 | PF02991 | 0.262 |
LIG_LIR_Apic_2 | 676 | 680 | PF02991 | 0.401 |
LIG_LIR_Apic_2 | 814 | 820 | PF02991 | 0.357 |
LIG_LIR_Gen_1 | 198 | 207 | PF02991 | 0.284 |
LIG_LIR_Gen_1 | 219 | 229 | PF02991 | 0.369 |
LIG_LIR_Gen_1 | 526 | 535 | PF02991 | 0.241 |
LIG_LIR_Gen_1 | 556 | 565 | PF02991 | 0.306 |
LIG_LIR_Gen_1 | 577 | 585 | PF02991 | 0.259 |
LIG_LIR_Gen_1 | 618 | 627 | PF02991 | 0.375 |
LIG_LIR_Gen_1 | 731 | 739 | PF02991 | 0.172 |
LIG_LIR_Gen_1 | 747 | 758 | PF02991 | 0.282 |
LIG_LIR_Gen_1 | 759 | 765 | PF02991 | 0.339 |
LIG_LIR_Nem_3 | 198 | 203 | PF02991 | 0.269 |
LIG_LIR_Nem_3 | 219 | 224 | PF02991 | 0.351 |
LIG_LIR_Nem_3 | 273 | 278 | PF02991 | 0.218 |
LIG_LIR_Nem_3 | 526 | 532 | PF02991 | 0.285 |
LIG_LIR_Nem_3 | 556 | 560 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 577 | 583 | PF02991 | 0.207 |
LIG_LIR_Nem_3 | 618 | 623 | PF02991 | 0.327 |
LIG_LIR_Nem_3 | 630 | 635 | PF02991 | 0.215 |
LIG_LIR_Nem_3 | 731 | 735 | PF02991 | 0.168 |
LIG_LIR_Nem_3 | 736 | 742 | PF02991 | 0.170 |
LIG_LIR_Nem_3 | 747 | 753 | PF02991 | 0.292 |
LIG_LIR_Nem_3 | 759 | 763 | PF02991 | 0.336 |
LIG_LIR_Nem_3 | 775 | 780 | PF02991 | 0.254 |
LIG_LIR_Nem_3 | 855 | 861 | PF02991 | 0.436 |
LIG_LYPXL_yS_3 | 275 | 278 | PF13949 | 0.197 |
LIG_LYPXL_yS_3 | 777 | 780 | PF13949 | 0.163 |
LIG_MYND_3 | 624 | 628 | PF01753 | 0.347 |
LIG_NRBOX | 597 | 603 | PF00104 | 0.192 |
LIG_NRBOX | 797 | 803 | PF00104 | 0.142 |
LIG_PCNA_TLS_4 | 358 | 366 | PF02747 | 0.356 |
LIG_PCNA_yPIPBox_3 | 406 | 420 | PF02747 | 0.355 |
LIG_PDZ_Class_2 | 858 | 863 | PF00595 | 0.198 |
LIG_Pex14_2 | 175 | 179 | PF04695 | 0.368 |
LIG_Pex14_2 | 492 | 496 | PF04695 | 0.359 |
LIG_Pex14_2 | 746 | 750 | PF04695 | 0.213 |
LIG_Pex14_2 | 783 | 787 | PF04695 | 0.161 |
LIG_PTB_Apo_2 | 399 | 406 | PF02174 | 0.422 |
LIG_PTB_Apo_2 | 73 | 80 | PF02174 | 0.366 |
LIG_PTB_Apo_2 | 781 | 788 | PF02174 | 0.171 |
LIG_PTB_Phospho_1 | 399 | 405 | PF10480 | 0.382 |
LIG_PTB_Phospho_1 | 73 | 79 | PF10480 | 0.379 |
LIG_SH2_CRK | 252 | 256 | PF00017 | 0.405 |
LIG_SH2_CRK | 462 | 466 | PF00017 | 0.359 |
LIG_SH2_GRB2like | 400 | 403 | PF00017 | 0.437 |
LIG_SH2_GRB2like | 580 | 583 | PF00017 | 0.182 |
LIG_SH2_NCK_1 | 252 | 256 | PF00017 | 0.404 |
LIG_SH2_NCK_1 | 658 | 662 | PF00017 | 0.407 |
LIG_SH2_SRC | 451 | 454 | PF00017 | 0.351 |
LIG_SH2_STAP1 | 322 | 326 | PF00017 | 0.375 |
LIG_SH2_STAP1 | 583 | 587 | PF00017 | 0.318 |
LIG_SH2_STAP1 | 836 | 840 | PF00017 | 0.297 |
LIG_SH2_STAT3 | 478 | 481 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 107 | 110 | PF00017 | 0.377 |
LIG_SH2_STAT5 | 111 | 114 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 193 | 196 | PF00017 | 0.256 |
LIG_SH2_STAT5 | 223 | 226 | PF00017 | 0.270 |
LIG_SH2_STAT5 | 306 | 309 | PF00017 | 0.252 |
LIG_SH2_STAT5 | 364 | 367 | PF00017 | 0.171 |
LIG_SH2_STAT5 | 400 | 403 | PF00017 | 0.394 |
LIG_SH2_STAT5 | 451 | 454 | PF00017 | 0.261 |
LIG_SH2_STAT5 | 478 | 481 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 512 | 515 | PF00017 | 0.307 |
LIG_SH2_STAT5 | 580 | 583 | PF00017 | 0.395 |
LIG_SH2_STAT5 | 620 | 623 | PF00017 | 0.222 |
LIG_SH2_STAT5 | 632 | 635 | PF00017 | 0.228 |
LIG_SH2_STAT5 | 658 | 661 | PF00017 | 0.337 |
LIG_SH2_STAT5 | 79 | 82 | PF00017 | 0.349 |
LIG_SH3_3 | 147 | 153 | PF00018 | 0.265 |
LIG_SH3_3 | 494 | 500 | PF00018 | 0.323 |
LIG_SH3_3 | 585 | 591 | PF00018 | 0.300 |
LIG_SH3_3 | 600 | 606 | PF00018 | 0.321 |
LIG_SH3_3 | 676 | 682 | PF00018 | 0.336 |
LIG_SUMO_SIM_anti_2 | 131 | 138 | PF11976 | 0.381 |
LIG_SUMO_SIM_anti_2 | 201 | 208 | PF11976 | 0.176 |
LIG_SUMO_SIM_anti_2 | 584 | 589 | PF11976 | 0.174 |
LIG_SUMO_SIM_anti_2 | 599 | 605 | PF11976 | 0.240 |
LIG_SUMO_SIM_anti_2 | 709 | 718 | PF11976 | 0.292 |
LIG_SUMO_SIM_anti_2 | 800 | 806 | PF11976 | 0.189 |
LIG_SUMO_SIM_par_1 | 546 | 551 | PF11976 | 0.309 |
LIG_SUMO_SIM_par_1 | 599 | 605 | PF11976 | 0.210 |
LIG_SUMO_SIM_par_1 | 726 | 731 | PF11976 | 0.335 |
LIG_TRFH_1 | 244 | 248 | PF08558 | 0.214 |
LIG_TRFH_1 | 85 | 89 | PF08558 | 0.208 |
LIG_TYR_ITIM | 633 | 638 | PF00017 | 0.340 |
LIG_UBA3_1 | 206 | 213 | PF00899 | 0.319 |
LIG_WRC_WIRS_1 | 241 | 246 | PF05994 | 0.273 |
LIG_WRC_WIRS_1 | 716 | 721 | PF05994 | 0.294 |
LIG_WRC_WIRS_1 | 729 | 734 | PF05994 | 0.166 |
LIG_WRC_WIRS_1 | 757 | 762 | PF05994 | 0.403 |
MOD_CK1_1 | 239 | 245 | PF00069 | 0.331 |
MOD_CK1_1 | 339 | 345 | PF00069 | 0.390 |
MOD_CK1_1 | 432 | 438 | PF00069 | 0.296 |
MOD_CK1_1 | 688 | 694 | PF00069 | 0.325 |
MOD_CK1_1 | 718 | 724 | PF00069 | 0.332 |
MOD_CK1_1 | 767 | 773 | PF00069 | 0.374 |
MOD_CK2_1 | 346 | 352 | PF00069 | 0.316 |
MOD_CK2_1 | 483 | 489 | PF00069 | 0.351 |
MOD_CK2_1 | 643 | 649 | PF00069 | 0.288 |
MOD_CK2_1 | 819 | 825 | PF00069 | 0.348 |
MOD_CK2_1 | 849 | 855 | PF00069 | 0.330 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.515 |
MOD_GlcNHglycan | 238 | 241 | PF01048 | 0.524 |
MOD_GlcNHglycan | 303 | 306 | PF01048 | 0.553 |
MOD_GlcNHglycan | 339 | 342 | PF01048 | 0.588 |
MOD_GlcNHglycan | 37 | 40 | PF01048 | 0.359 |
MOD_GlcNHglycan | 420 | 423 | PF01048 | 0.532 |
MOD_GlcNHglycan | 508 | 511 | PF01048 | 0.528 |
MOD_GlcNHglycan | 556 | 560 | PF01048 | 0.531 |
MOD_GlcNHglycan | 597 | 601 | PF01048 | 0.499 |
MOD_GlcNHglycan | 659 | 662 | PF01048 | 0.537 |
MOD_GlcNHglycan | 688 | 691 | PF01048 | 0.503 |
MOD_GlcNHglycan | 825 | 828 | PF01048 | 0.587 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.279 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.247 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.621 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.676 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.350 |
MOD_GSK3_1 | 236 | 243 | PF00069 | 0.293 |
MOD_GSK3_1 | 250 | 257 | PF00069 | 0.317 |
MOD_GSK3_1 | 295 | 302 | PF00069 | 0.322 |
MOD_GSK3_1 | 336 | 343 | PF00069 | 0.370 |
MOD_GSK3_1 | 425 | 432 | PF00069 | 0.190 |
MOD_GSK3_1 | 523 | 530 | PF00069 | 0.281 |
MOD_GSK3_1 | 592 | 599 | PF00069 | 0.280 |
MOD_GSK3_1 | 643 | 650 | PF00069 | 0.335 |
MOD_GSK3_1 | 685 | 692 | PF00069 | 0.348 |
MOD_GSK3_1 | 740 | 747 | PF00069 | 0.372 |
MOD_GSK3_1 | 766 | 773 | PF00069 | 0.277 |
MOD_GSK3_1 | 819 | 826 | PF00069 | 0.370 |
MOD_GSK3_1 | 83 | 90 | PF00069 | 0.201 |
MOD_GSK3_1 | 841 | 848 | PF00069 | 0.346 |
MOD_N-GLC_1 | 109 | 114 | PF02516 | 0.410 |
MOD_N-GLC_1 | 527 | 532 | PF02516 | 0.524 |
MOD_N-GLC_1 | 565 | 570 | PF02516 | 0.524 |
MOD_N-GLC_1 | 581 | 586 | PF02516 | 0.537 |
MOD_N-GLC_1 | 791 | 796 | PF02516 | 0.502 |
MOD_N-GLC_1 | 81 | 86 | PF02516 | 0.458 |
MOD_N-GLC_1 | 845 | 850 | PF02516 | 0.552 |
MOD_NEK2_1 | 106 | 111 | PF00069 | 0.214 |
MOD_NEK2_1 | 157 | 162 | PF00069 | 0.304 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.318 |
MOD_NEK2_1 | 222 | 227 | PF00069 | 0.285 |
MOD_NEK2_1 | 236 | 241 | PF00069 | 0.328 |
MOD_NEK2_1 | 271 | 276 | PF00069 | 0.262 |
MOD_NEK2_1 | 35 | 40 | PF00069 | 0.620 |
MOD_NEK2_1 | 420 | 425 | PF00069 | 0.215 |
MOD_NEK2_1 | 429 | 434 | PF00069 | 0.198 |
MOD_NEK2_1 | 446 | 451 | PF00069 | 0.172 |
MOD_NEK2_1 | 548 | 553 | PF00069 | 0.347 |
MOD_NEK2_1 | 555 | 560 | PF00069 | 0.308 |
MOD_NEK2_1 | 758 | 763 | PF00069 | 0.184 |
MOD_NEK2_1 | 81 | 86 | PF00069 | 0.192 |
MOD_NEK2_1 | 823 | 828 | PF00069 | 0.286 |
MOD_NEK2_2 | 306 | 311 | PF00069 | 0.198 |
MOD_NEK2_2 | 7 | 12 | PF00069 | 0.528 |
MOD_PKA_2 | 11 | 17 | PF00069 | 0.694 |
MOD_PKA_2 | 216 | 222 | PF00069 | 0.371 |
MOD_PKA_2 | 300 | 306 | PF00069 | 0.352 |
MOD_PKA_2 | 35 | 41 | PF00069 | 0.641 |
MOD_PKA_2 | 437 | 443 | PF00069 | 0.201 |
MOD_PKA_2 | 483 | 489 | PF00069 | 0.343 |
MOD_PKA_2 | 568 | 574 | PF00069 | 0.352 |
MOD_PKA_2 | 670 | 676 | PF00069 | 0.335 |
MOD_PKA_2 | 693 | 699 | PF00069 | 0.284 |
MOD_PKA_2 | 740 | 746 | PF00069 | 0.173 |
MOD_PKA_2 | 841 | 847 | PF00069 | 0.374 |
MOD_Plk_1 | 201 | 207 | PF00069 | 0.170 |
MOD_Plk_1 | 370 | 376 | PF00069 | 0.401 |
MOD_Plk_1 | 446 | 452 | PF00069 | 0.281 |
MOD_Plk_1 | 555 | 561 | PF00069 | 0.344 |
MOD_Plk_1 | 581 | 587 | PF00069 | 0.321 |
MOD_Plk_1 | 643 | 649 | PF00069 | 0.361 |
MOD_Plk_1 | 664 | 670 | PF00069 | 0.328 |
MOD_Plk_1 | 81 | 87 | PF00069 | 0.280 |
MOD_Plk_2-3 | 88 | 94 | PF00069 | 0.185 |
MOD_Plk_4 | 143 | 149 | PF00069 | 0.357 |
MOD_Plk_4 | 158 | 164 | PF00069 | 0.256 |
MOD_Plk_4 | 201 | 207 | PF00069 | 0.232 |
MOD_Plk_4 | 370 | 376 | PF00069 | 0.361 |
MOD_Plk_4 | 420 | 426 | PF00069 | 0.350 |
MOD_Plk_4 | 429 | 435 | PF00069 | 0.287 |
MOD_Plk_4 | 483 | 489 | PF00069 | 0.217 |
MOD_Plk_4 | 715 | 721 | PF00069 | 0.315 |
MOD_Plk_4 | 800 | 806 | PF00069 | 0.186 |
MOD_ProDKin_1 | 328 | 334 | PF00069 | 0.376 |
MOD_ProDKin_1 | 602 | 608 | PF00069 | 0.283 |
MOD_ProDKin_1 | 767 | 773 | PF00069 | 0.387 |
MOD_ProDKin_1 | 791 | 797 | PF00069 | 0.277 |
MOD_SUMO_for_1 | 615 | 618 | PF00179 | 0.190 |
MOD_SUMO_rev_2 | 231 | 237 | PF00179 | 0.306 |
MOD_SUMO_rev_2 | 373 | 382 | PF00179 | 0.393 |
MOD_SUMO_rev_2 | 432 | 440 | PF00179 | 0.292 |
MOD_SUMO_rev_2 | 88 | 98 | PF00179 | 0.395 |
TRG_DiLeu_BaEn_2 | 617 | 623 | PF01217 | 0.308 |
TRG_DiLeu_BaEn_2 | 648 | 654 | PF01217 | 0.163 |
TRG_DiLeu_BaLyEn_6 | 588 | 593 | PF01217 | 0.362 |
TRG_DiLeu_LyEn_5 | 775 | 780 | PF01217 | 0.177 |
TRG_ENDOCYTIC_2 | 275 | 278 | PF00928 | 0.197 |
TRG_ENDOCYTIC_2 | 321 | 324 | PF00928 | 0.352 |
TRG_ENDOCYTIC_2 | 620 | 623 | PF00928 | 0.366 |
TRG_ENDOCYTIC_2 | 635 | 638 | PF00928 | 0.348 |
TRG_ENDOCYTIC_2 | 739 | 742 | PF00928 | 0.272 |
TRG_ENDOCYTIC_2 | 777 | 780 | PF00928 | 0.354 |
TRG_ER_diArg_1 | 214 | 217 | PF00400 | 0.345 |
TRG_ER_diArg_1 | 40 | 42 | PF00400 | 0.598 |
TRG_Pf-PMV_PEXEL_1 | 315 | 319 | PF00026 | 0.536 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A1X0NPQ6 | Trypanosomatidae | 28% | 95% |
A0A1X0P171 | Trypanosomatidae | 25% | 67% |
A0A3R7KBB6 | Trypanosoma rangeli | 26% | 97% |
A0A3R7R8G4 | Trypanosoma rangeli | 27% | 84% |
A4H8V6 | Leishmania braziliensis | 62% | 97% |
A4H8V7 | Leishmania braziliensis | 49% | 75% |
A4HX88 | Leishmania infantum | 50% | 95% |
C9ZM79 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 69% |
C9ZM80 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 69% |
C9ZM81 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 69% |
C9ZM82 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 69% |
C9ZM83 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 67% |
C9ZM86 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 70% |
C9ZN26 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 68% |
C9ZN41 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 70% |
C9ZN43 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 72% |
C9ZN44 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 70% |
C9ZN45 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 70% |
C9ZN46 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 70% |
C9ZN86 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 100% |
C9ZNA5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 70% |
C9ZNA6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 71% |
C9ZNH3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 67% |
C9ZNT1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 69% |
C9ZPZ6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 69% |
C9ZQ51 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 69% |
C9ZQ89 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 68% |
C9ZQ91 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 23% | 93% |
C9ZQ92 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 23% | 71% |
C9ZTS4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 68% |
C9ZTS5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 68% |
C9ZTS6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 72% |
C9ZUE6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 72% |
C9ZWQ5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 68% |
C9ZWU2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 71% |
C9ZWU3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 78% |
C9ZWY7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 70% |
C9ZZQ4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 69% |
D0A0U3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 70% |
D0A0W7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 69% |
D0A0X5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 68% |
D0A1S1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 69% |
D0A5D2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 71% |
D0A5D5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 70% |
D0A5U0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 70% |
D0A5U1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 70% |
D0A7A0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 69% |
D0A9R3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 71% |
D0AAV3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 69% |
Q26721 | Trypanosoma brucei brucei | 29% | 70% |
Q4QEI1 | Leishmania major | 49% | 68% |
Q99279 | Trypanosoma brucei brucei | 22% | 69% |
Q99280 | Trypanosoma brucei brucei | 24% | 70% |
V5AW53 | Trypanosoma cruzi | 28% | 100% |
V5AYH7 | Trypanosoma cruzi | 27% | 67% |
V5BBK5 | Trypanosoma cruzi | 28% | 72% |