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: 0 |
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: 0, no: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
GO:0016020 | membrane | 2 | 2 |
Related structures:
AlphaFold database: Q4QJC7
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 9 |
GO:0006396 | RNA processing | 6 | 9 |
GO:0006399 | tRNA metabolic process | 7 | 9 |
GO:0006400 | tRNA modification | 6 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 9 |
GO:0006807 | nitrogen compound metabolic process | 2 | 9 |
GO:0008033 | tRNA processing | 8 | 9 |
GO:0008152 | metabolic process | 1 | 9 |
GO:0009058 | biosynthetic process | 2 | 2 |
GO:0009451 | RNA modification | 5 | 2 |
GO:0009987 | cellular process | 1 | 9 |
GO:0016070 | RNA metabolic process | 5 | 9 |
GO:0031590 | wybutosine metabolic process | 4 | 2 |
GO:0031591 | wybutosine biosynthetic process | 5 | 2 |
GO:0034470 | ncRNA processing | 7 | 9 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 9 |
GO:0034660 | ncRNA metabolic process | 6 | 9 |
GO:0043170 | macromolecule metabolic process | 3 | 9 |
GO:0043412 | macromolecule modification | 4 | 2 |
GO:0044237 | cellular metabolic process | 2 | 9 |
GO:0044238 | primary metabolic process | 2 | 9 |
GO:0046483 | heterocycle metabolic process | 3 | 9 |
GO:0071704 | organic substance metabolic process | 2 | 9 |
GO:0090304 | nucleic acid metabolic process | 4 | 9 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 2 |
GO:1901137 | carbohydrate derivative biosynthetic process | 4 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 9 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 2 |
GO:1901576 | organic substance biosynthetic process | 3 | 2 |
GO:1901657 | glycosyl compound metabolic process | 4 | 2 |
GO:1901659 | glycosyl compound biosynthetic process | 5 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 9 |
GO:0003824 | catalytic activity | 1 | 9 |
GO:0005488 | binding | 1 | 9 |
GO:0010181 | FMN binding | 4 | 9 |
GO:0016829 | lyase activity | 2 | 9 |
GO:0032553 | ribonucleotide binding | 3 | 9 |
GO:0036094 | small molecule binding | 2 | 9 |
GO:0043167 | ion binding | 2 | 9 |
GO:0043168 | anion binding | 3 | 9 |
GO:0043169 | cation binding | 3 | 9 |
GO:0046872 | metal ion binding | 4 | 9 |
GO:0051536 | iron-sulfur cluster binding | 3 | 9 |
GO:0051539 | 4 iron, 4 sulfur cluster binding | 4 | 9 |
GO:0051540 | metal cluster binding | 2 | 9 |
GO:0097159 | organic cyclic compound binding | 2 | 9 |
GO:0097367 | carbohydrate derivative binding | 2 | 9 |
GO:1901265 | nucleoside phosphate binding | 3 | 9 |
GO:1901363 | heterocyclic compound binding | 2 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 175 | 179 | PF00656 | 0.311 |
CLV_C14_Caspase3-7 | 366 | 370 | PF00656 | 0.597 |
CLV_NRD_NRD_1 | 207 | 209 | PF00675 | 0.305 |
CLV_NRD_NRD_1 | 812 | 814 | PF00675 | 0.498 |
CLV_PCSK_KEX2_1 | 209 | 211 | PF00082 | 0.324 |
CLV_PCSK_KEX2_1 | 606 | 608 | PF00082 | 0.230 |
CLV_PCSK_PC1ET2_1 | 209 | 211 | PF00082 | 0.324 |
CLV_PCSK_PC1ET2_1 | 606 | 608 | PF00082 | 0.230 |
CLV_PCSK_SKI1_1 | 193 | 197 | PF00082 | 0.251 |
CLV_PCSK_SKI1_1 | 449 | 453 | PF00082 | 0.291 |
CLV_PCSK_SKI1_1 | 483 | 487 | PF00082 | 0.206 |
CLV_PCSK_SKI1_1 | 534 | 538 | PF00082 | 0.228 |
CLV_PCSK_SKI1_1 | 585 | 589 | PF00082 | 0.222 |
CLV_PCSK_SKI1_1 | 610 | 614 | PF00082 | 0.206 |
CLV_PCSK_SKI1_1 | 633 | 637 | PF00082 | 0.214 |
CLV_PCSK_SKI1_1 | 667 | 671 | PF00082 | 0.240 |
CLV_PCSK_SKI1_1 | 755 | 759 | PF00082 | 0.291 |
DEG_MDM2_SWIB_1 | 613 | 621 | PF02201 | 0.406 |
DEG_MDM2_SWIB_1 | 758 | 766 | PF02201 | 0.369 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.471 |
DOC_CKS1_1 | 710 | 715 | PF01111 | 0.449 |
DOC_CYCLIN_yCln2_LP_2 | 12 | 18 | PF00134 | 0.406 |
DOC_MAPK_DCC_7 | 500 | 510 | PF00069 | 0.473 |
DOC_MAPK_gen_1 | 286 | 293 | PF00069 | 0.416 |
DOC_MAPK_gen_1 | 629 | 640 | PF00069 | 0.408 |
DOC_MAPK_MEF2A_6 | 502 | 510 | PF00069 | 0.473 |
DOC_MAPK_MEF2A_6 | 585 | 593 | PF00069 | 0.412 |
DOC_MAPK_MEF2A_6 | 79 | 88 | PF00069 | 0.540 |
DOC_PIKK_1 | 389 | 397 | PF02985 | 0.536 |
DOC_PP2B_LxvP_1 | 12 | 15 | PF13499 | 0.413 |
DOC_PP2B_LxvP_1 | 240 | 243 | PF13499 | 0.334 |
DOC_PP4_FxxP_1 | 245 | 248 | PF00568 | 0.344 |
DOC_SPAK_OSR1_1 | 210 | 214 | PF12202 | 0.263 |
DOC_USP7_MATH_1 | 102 | 106 | PF00917 | 0.333 |
DOC_USP7_MATH_1 | 297 | 301 | PF00917 | 0.648 |
DOC_USP7_MATH_1 | 317 | 321 | PF00917 | 0.393 |
DOC_USP7_MATH_1 | 373 | 377 | PF00917 | 0.657 |
DOC_USP7_UBL2_3 | 625 | 629 | PF12436 | 0.406 |
DOC_WW_Pin1_4 | 292 | 297 | PF00397 | 0.596 |
DOC_WW_Pin1_4 | 472 | 477 | PF00397 | 0.286 |
DOC_WW_Pin1_4 | 528 | 533 | PF00397 | 0.406 |
DOC_WW_Pin1_4 | 585 | 590 | PF00397 | 0.432 |
DOC_WW_Pin1_4 | 598 | 603 | PF00397 | 0.394 |
DOC_WW_Pin1_4 | 709 | 714 | PF00397 | 0.460 |
DOC_WW_Pin1_4 | 71 | 76 | PF00397 | 0.616 |
DOC_WW_Pin1_4 | 788 | 793 | PF00397 | 0.308 |
DOC_WW_Pin1_4 | 80 | 85 | PF00397 | 0.534 |
DOC_WW_Pin1_4 | 88 | 93 | PF00397 | 0.370 |
LIG_14-3-3_CanoR_1 | 203 | 207 | PF00244 | 0.334 |
LIG_14-3-3_CanoR_1 | 262 | 272 | PF00244 | 0.352 |
LIG_14-3-3_CanoR_1 | 274 | 278 | PF00244 | 0.275 |
LIG_14-3-3_CanoR_1 | 446 | 452 | PF00244 | 0.394 |
LIG_14-3-3_CanoR_1 | 534 | 541 | PF00244 | 0.446 |
LIG_14-3-3_CanoR_1 | 569 | 574 | PF00244 | 0.489 |
LIG_14-3-3_CanoR_1 | 619 | 627 | PF00244 | 0.462 |
LIG_14-3-3_CanoR_1 | 637 | 641 | PF00244 | 0.341 |
LIG_14-3-3_CanoR_1 | 817 | 822 | PF00244 | 0.582 |
LIG_Actin_WH2_2 | 256 | 272 | PF00022 | 0.396 |
LIG_Actin_WH2_2 | 590 | 608 | PF00022 | 0.430 |
LIG_BRCT_BRCA1_1 | 184 | 188 | PF00533 | 0.240 |
LIG_BRCT_BRCA1_1 | 495 | 499 | PF00533 | 0.430 |
LIG_Clathr_ClatBox_1 | 750 | 754 | PF01394 | 0.348 |
LIG_deltaCOP1_diTrp_1 | 759 | 765 | PF00928 | 0.369 |
LIG_FHA_1 | 118 | 124 | PF00498 | 0.403 |
LIG_FHA_1 | 167 | 173 | PF00498 | 0.282 |
LIG_FHA_1 | 175 | 181 | PF00498 | 0.360 |
LIG_FHA_1 | 255 | 261 | PF00498 | 0.342 |
LIG_FHA_1 | 264 | 270 | PF00498 | 0.283 |
LIG_FHA_1 | 280 | 286 | PF00498 | 0.395 |
LIG_FHA_1 | 317 | 323 | PF00498 | 0.535 |
LIG_FHA_1 | 473 | 479 | PF00498 | 0.240 |
LIG_FHA_1 | 490 | 496 | PF00498 | 0.406 |
LIG_FHA_1 | 586 | 592 | PF00498 | 0.385 |
LIG_FHA_1 | 644 | 650 | PF00498 | 0.417 |
LIG_FHA_1 | 807 | 813 | PF00498 | 0.576 |
LIG_FHA_2 | 157 | 163 | PF00498 | 0.334 |
LIG_FHA_2 | 173 | 179 | PF00498 | 0.207 |
LIG_FHA_2 | 364 | 370 | PF00498 | 0.541 |
LIG_FHA_2 | 599 | 605 | PF00498 | 0.406 |
LIG_FHA_2 | 762 | 768 | PF00498 | 0.296 |
LIG_FHA_2 | 781 | 787 | PF00498 | 0.210 |
LIG_GBD_Chelix_1 | 17 | 25 | PF00786 | 0.482 |
LIG_LIR_Gen_1 | 185 | 196 | PF02991 | 0.240 |
LIG_LIR_Gen_1 | 223 | 233 | PF02991 | 0.264 |
LIG_LIR_Gen_1 | 662 | 671 | PF02991 | 0.259 |
LIG_LIR_Gen_1 | 767 | 775 | PF02991 | 0.299 |
LIG_LIR_Gen_1 | 780 | 790 | PF02991 | 0.309 |
LIG_LIR_Nem_3 | 185 | 191 | PF02991 | 0.200 |
LIG_LIR_Nem_3 | 223 | 229 | PF02991 | 0.309 |
LIG_LIR_Nem_3 | 259 | 264 | PF02991 | 0.318 |
LIG_LIR_Nem_3 | 418 | 424 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 462 | 466 | PF02991 | 0.306 |
LIG_LIR_Nem_3 | 662 | 666 | PF02991 | 0.259 |
LIG_LIR_Nem_3 | 764 | 768 | PF02991 | 0.288 |
LIG_LIR_Nem_3 | 769 | 775 | PF02991 | 0.311 |
LIG_LIR_Nem_3 | 780 | 785 | PF02991 | 0.325 |
LIG_LIR_Nem_3 | 786 | 790 | PF02991 | 0.305 |
LIG_LIR_Nem_3 | 791 | 797 | PF02991 | 0.259 |
LIG_LYPXL_S_1 | 420 | 424 | PF13949 | 0.360 |
LIG_LYPXL_S_1 | 554 | 558 | PF13949 | 0.206 |
LIG_LYPXL_yS_3 | 421 | 424 | PF13949 | 0.369 |
LIG_LYPXL_yS_3 | 555 | 558 | PF13949 | 0.406 |
LIG_Pex14_2 | 613 | 617 | PF04695 | 0.406 |
LIG_Pex14_2 | 758 | 762 | PF04695 | 0.384 |
LIG_PTB_Apo_2 | 574 | 581 | PF02174 | 0.406 |
LIG_SH2_CRK | 433 | 437 | PF00017 | 0.342 |
LIG_SH2_CRK | 518 | 522 | PF00017 | 0.473 |
LIG_SH2_CRK | 710 | 714 | PF00017 | 0.485 |
LIG_SH2_CRK | 787 | 791 | PF00017 | 0.297 |
LIG_SH2_NCK_1 | 772 | 776 | PF00017 | 0.352 |
LIG_SH2_NCK_1 | 787 | 791 | PF00017 | 0.257 |
LIG_SH2_STAP1 | 166 | 170 | PF00017 | 0.274 |
LIG_SH2_STAP1 | 22 | 26 | PF00017 | 0.467 |
LIG_SH2_STAP1 | 251 | 255 | PF00017 | 0.431 |
LIG_SH2_STAP1 | 652 | 656 | PF00017 | 0.406 |
LIG_SH2_STAP1 | 768 | 772 | PF00017 | 0.380 |
LIG_SH2_STAT3 | 101 | 104 | PF00017 | 0.303 |
LIG_SH2_STAT5 | 176 | 179 | PF00017 | 0.240 |
LIG_SH2_STAT5 | 594 | 597 | PF00017 | 0.406 |
LIG_SH2_STAT5 | 671 | 674 | PF00017 | 0.240 |
LIG_SH3_3 | 131 | 137 | PF00018 | 0.412 |
LIG_SH3_3 | 177 | 183 | PF00018 | 0.305 |
LIG_SH3_3 | 243 | 249 | PF00018 | 0.356 |
LIG_SH3_3 | 290 | 296 | PF00018 | 0.444 |
LIG_SH3_3 | 546 | 552 | PF00018 | 0.406 |
LIG_SH3_3 | 83 | 89 | PF00018 | 0.697 |
LIG_Sin3_3 | 188 | 195 | PF02671 | 0.174 |
LIG_SUMO_SIM_anti_2 | 724 | 729 | PF11976 | 0.502 |
LIG_SUMO_SIM_par_1 | 749 | 754 | PF11976 | 0.347 |
LIG_TRAF2_1 | 601 | 604 | PF00917 | 0.430 |
LIG_TRAF2_1 | 729 | 732 | PF00917 | 0.515 |
LIG_TRAF2_2 | 581 | 586 | PF00917 | 0.404 |
LIG_TYR_ITIM | 20 | 25 | PF00017 | 0.491 |
LIG_TYR_ITIM | 419 | 424 | PF00017 | 0.353 |
LIG_TYR_ITIM | 553 | 558 | PF00017 | 0.406 |
LIG_TYR_ITIM | 785 | 790 | PF00017 | 0.403 |
LIG_UBA3_1 | 750 | 755 | PF00899 | 0.356 |
LIG_WRC_WIRS_1 | 1 | 6 | PF05994 | 0.528 |
LIG_WRC_WIRS_1 | 570 | 575 | PF05994 | 0.406 |
LIG_WW_1 | 248 | 251 | PF00397 | 0.332 |
LIG_WW_3 | 181 | 185 | PF00397 | 0.334 |
MOD_CDK_SPxK_1 | 528 | 534 | PF00069 | 0.406 |
MOD_CK1_1 | 105 | 111 | PF00069 | 0.353 |
MOD_CK1_1 | 117 | 123 | PF00069 | 0.364 |
MOD_CK1_1 | 174 | 180 | PF00069 | 0.240 |
MOD_CK1_1 | 273 | 279 | PF00069 | 0.412 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.513 |
MOD_CK1_1 | 320 | 326 | PF00069 | 0.650 |
MOD_CK1_1 | 675 | 681 | PF00069 | 0.240 |
MOD_CK1_1 | 777 | 783 | PF00069 | 0.375 |
MOD_CK2_1 | 156 | 162 | PF00069 | 0.431 |
MOD_CK2_1 | 297 | 303 | PF00069 | 0.622 |
MOD_CK2_1 | 381 | 387 | PF00069 | 0.741 |
MOD_CK2_1 | 598 | 604 | PF00069 | 0.406 |
MOD_CMANNOS | 762 | 765 | PF00535 | 0.256 |
MOD_Cter_Amidation | 206 | 209 | PF01082 | 0.261 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.590 |
MOD_GlcNHglycan | 310 | 313 | PF01048 | 0.483 |
MOD_GlcNHglycan | 322 | 325 | PF01048 | 0.655 |
MOD_GlcNHglycan | 349 | 352 | PF01048 | 0.604 |
MOD_GlcNHglycan | 373 | 376 | PF01048 | 0.592 |
MOD_GlcNHglycan | 439 | 442 | PF01048 | 0.281 |
MOD_GlcNHglycan | 63 | 66 | PF01048 | 0.543 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.554 |
MOD_GlcNHglycan | 776 | 779 | PF01048 | 0.348 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.239 |
MOD_GSK3_1 | 250 | 257 | PF00069 | 0.364 |
MOD_GSK3_1 | 299 | 306 | PF00069 | 0.611 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.422 |
MOD_GSK3_1 | 489 | 496 | PF00069 | 0.430 |
MOD_GSK3_1 | 569 | 576 | PF00069 | 0.408 |
MOD_GSK3_1 | 61 | 68 | PF00069 | 0.581 |
MOD_GSK3_1 | 667 | 674 | PF00069 | 0.278 |
MOD_GSK3_1 | 777 | 784 | PF00069 | 0.427 |
MOD_GSK3_1 | 817 | 824 | PF00069 | 0.528 |
MOD_N-GLC_1 | 317 | 322 | PF02516 | 0.516 |
MOD_N-GLC_1 | 381 | 386 | PF02516 | 0.568 |
MOD_N-GLC_1 | 466 | 471 | PF02516 | 0.373 |
MOD_N-GLC_2 | 153 | 155 | PF02516 | 0.459 |
MOD_N-GLC_2 | 482 | 484 | PF02516 | 0.206 |
MOD_NEK2_1 | 171 | 176 | PF00069 | 0.268 |
MOD_NEK2_1 | 20 | 25 | PF00069 | 0.457 |
MOD_NEK2_1 | 291 | 296 | PF00069 | 0.556 |
MOD_NEK2_1 | 346 | 351 | PF00069 | 0.737 |
MOD_NEK2_1 | 435 | 440 | PF00069 | 0.287 |
MOD_NEK2_1 | 573 | 578 | PF00069 | 0.408 |
MOD_NEK2_1 | 636 | 641 | PF00069 | 0.406 |
MOD_NEK2_1 | 774 | 779 | PF00069 | 0.332 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.493 |
MOD_NEK2_2 | 166 | 171 | PF00069 | 0.258 |
MOD_NEK2_2 | 281 | 286 | PF00069 | 0.479 |
MOD_NEK2_2 | 459 | 464 | PF00069 | 0.271 |
MOD_OFUCOSY | 741 | 747 | PF10250 | 0.280 |
MOD_PIKK_1 | 100 | 106 | PF00454 | 0.316 |
MOD_PIKK_1 | 182 | 188 | PF00454 | 0.274 |
MOD_PIKK_1 | 254 | 260 | PF00454 | 0.410 |
MOD_PIKK_1 | 340 | 346 | PF00454 | 0.676 |
MOD_PIKK_1 | 466 | 472 | PF00454 | 0.371 |
MOD_PKA_1 | 286 | 292 | PF00069 | 0.512 |
MOD_PKA_2 | 202 | 208 | PF00069 | 0.334 |
MOD_PKA_2 | 273 | 279 | PF00069 | 0.420 |
MOD_PKA_2 | 445 | 451 | PF00069 | 0.306 |
MOD_PKA_2 | 568 | 574 | PF00069 | 0.436 |
MOD_PKA_2 | 636 | 642 | PF00069 | 0.406 |
MOD_PKA_2 | 816 | 822 | PF00069 | 0.519 |
MOD_Plk_1 | 317 | 323 | PF00069 | 0.597 |
MOD_Plk_1 | 780 | 786 | PF00069 | 0.417 |
MOD_Plk_2-3 | 781 | 787 | PF00069 | 0.401 |
MOD_Plk_4 | 156 | 162 | PF00069 | 0.391 |
MOD_Plk_4 | 166 | 172 | PF00069 | 0.246 |
MOD_Plk_4 | 256 | 262 | PF00069 | 0.350 |
MOD_Plk_4 | 317 | 323 | PF00069 | 0.646 |
MOD_Plk_4 | 447 | 453 | PF00069 | 0.332 |
MOD_Plk_4 | 459 | 465 | PF00069 | 0.229 |
MOD_Plk_4 | 544 | 550 | PF00069 | 0.406 |
MOD_Plk_4 | 569 | 575 | PF00069 | 0.433 |
MOD_Plk_4 | 636 | 642 | PF00069 | 0.416 |
MOD_Plk_4 | 761 | 767 | PF00069 | 0.268 |
MOD_ProDKin_1 | 292 | 298 | PF00069 | 0.597 |
MOD_ProDKin_1 | 472 | 478 | PF00069 | 0.257 |
MOD_ProDKin_1 | 528 | 534 | PF00069 | 0.406 |
MOD_ProDKin_1 | 585 | 591 | PF00069 | 0.432 |
MOD_ProDKin_1 | 598 | 604 | PF00069 | 0.394 |
MOD_ProDKin_1 | 709 | 715 | PF00069 | 0.453 |
MOD_ProDKin_1 | 71 | 77 | PF00069 | 0.617 |
MOD_ProDKin_1 | 788 | 794 | PF00069 | 0.307 |
MOD_ProDKin_1 | 80 | 86 | PF00069 | 0.534 |
MOD_ProDKin_1 | 88 | 94 | PF00069 | 0.359 |
MOD_SUMO_rev_2 | 598 | 608 | PF00179 | 0.431 |
MOD_SUMO_rev_2 | 662 | 669 | PF00179 | 0.240 |
TRG_DiLeu_BaEn_1 | 415 | 420 | PF01217 | 0.393 |
TRG_ENDOCYTIC_2 | 22 | 25 | PF00928 | 0.587 |
TRG_ENDOCYTIC_2 | 421 | 424 | PF00928 | 0.369 |
TRG_ENDOCYTIC_2 | 433 | 436 | PF00928 | 0.305 |
TRG_ENDOCYTIC_2 | 518 | 521 | PF00928 | 0.473 |
TRG_ENDOCYTIC_2 | 555 | 558 | PF00928 | 0.406 |
TRG_ENDOCYTIC_2 | 594 | 597 | PF00928 | 0.406 |
TRG_ENDOCYTIC_2 | 652 | 655 | PF00928 | 0.406 |
TRG_ENDOCYTIC_2 | 768 | 771 | PF00928 | 0.293 |
TRG_ENDOCYTIC_2 | 772 | 775 | PF00928 | 0.317 |
TRG_ENDOCYTIC_2 | 787 | 790 | PF00928 | 0.496 |
TRG_ER_diArg_1 | 208 | 211 | PF00400 | 0.283 |
TRG_ER_diArg_1 | 452 | 455 | PF00400 | 0.282 |
TRG_ER_diArg_1 | 733 | 736 | PF00400 | 0.377 |
TRG_NES_CRM1_1 | 586 | 598 | PF08389 | 0.404 |
TRG_Pf-PMV_PEXEL_1 | 231 | 235 | PF00026 | 0.334 |
TRG_Pf-PMV_PEXEL_1 | 610 | 614 | PF00026 | 0.206 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I710 | Leptomonas seymouri | 67% | 93% |
A0A3S5H5J8 | Leishmania donovani | 94% | 100% |
A0A3S5IRA8 | Trypanosoma rangeli | 54% | 100% |
A4H4B8 | Leishmania braziliensis | 80% | 98% |
A4HSJ7 | Leishmania infantum | 95% | 100% |
C9ZU99 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 54% | 99% |
E9AKI1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q8BJM7 | Mus musculus | 43% | 100% |