Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 2 |
Forrest at al. (procyclic) | no | yes: 2 |
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: 16 |
NetGPI | no | yes: 0, no: 16 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005874 | microtubule | 6 | 12 |
GO:0099080 | supramolecular complex | 2 | 12 |
GO:0099081 | supramolecular polymer | 3 | 12 |
GO:0099512 | supramolecular fiber | 4 | 12 |
GO:0099513 | polymeric cytoskeletal fiber | 5 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005871 | kinesin complex | 3 | 1 |
GO:0005875 | microtubule associated complex | 2 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
Related structures:
AlphaFold database: A4HZT3
Term | Name | Level | Count |
---|---|---|---|
GO:0007017 | microtubule-based process | 2 | 17 |
GO:0007018 | microtubule-based movement | 3 | 17 |
GO:0009987 | cellular process | 1 | 17 |
GO:0006810 | transport | 3 | 1 |
GO:0030705 | cytoskeleton-dependent intracellular transport | 4 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 17 |
GO:0003774 | cytoskeletal motor activity | 1 | 17 |
GO:0003777 | microtubule motor activity | 2 | 17 |
GO:0003824 | catalytic activity | 1 | 10 |
GO:0005488 | binding | 1 | 17 |
GO:0005515 | protein binding | 2 | 17 |
GO:0005524 | ATP binding | 5 | 17 |
GO:0008017 | microtubule binding | 5 | 17 |
GO:0008092 | cytoskeletal protein binding | 3 | 17 |
GO:0015631 | tubulin binding | 4 | 17 |
GO:0016787 | hydrolase activity | 2 | 10 |
GO:0017076 | purine nucleotide binding | 4 | 17 |
GO:0030554 | adenyl nucleotide binding | 5 | 17 |
GO:0032553 | ribonucleotide binding | 3 | 17 |
GO:0032555 | purine ribonucleotide binding | 4 | 17 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 17 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 17 |
GO:0036094 | small molecule binding | 2 | 17 |
GO:0043167 | ion binding | 2 | 17 |
GO:0043168 | anion binding | 3 | 17 |
GO:0097159 | organic cyclic compound binding | 2 | 17 |
GO:0097367 | carbohydrate derivative binding | 2 | 17 |
GO:0140657 | ATP-dependent activity | 1 | 17 |
GO:1901265 | nucleoside phosphate binding | 3 | 17 |
GO:1901363 | heterocyclic compound binding | 2 | 17 |
GO:0008574 | plus-end-directed microtubule motor activity | 3 | 1 |
GO:0016462 | pyrophosphatase activity | 5 | 1 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 1 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 1 |
GO:0016887 | ATP hydrolysis activity | 7 | 1 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 260 | 264 | PF00656 | 0.568 |
CLV_NRD_NRD_1 | 300 | 302 | PF00675 | 0.552 |
CLV_NRD_NRD_1 | 458 | 460 | PF00675 | 0.472 |
CLV_NRD_NRD_1 | 476 | 478 | PF00675 | 0.503 |
CLV_NRD_NRD_1 | 773 | 775 | PF00675 | 0.645 |
CLV_PCSK_FUR_1 | 428 | 432 | PF00082 | 0.372 |
CLV_PCSK_KEX2_1 | 300 | 302 | PF00082 | 0.607 |
CLV_PCSK_KEX2_1 | 430 | 432 | PF00082 | 0.401 |
CLV_PCSK_KEX2_1 | 773 | 775 | PF00082 | 0.673 |
CLV_PCSK_KEX2_1 | 815 | 817 | PF00082 | 0.367 |
CLV_PCSK_PC1ET2_1 | 430 | 432 | PF00082 | 0.395 |
CLV_PCSK_PC1ET2_1 | 815 | 817 | PF00082 | 0.371 |
CLV_PCSK_SKI1_1 | 147 | 151 | PF00082 | 0.275 |
CLV_PCSK_SKI1_1 | 313 | 317 | PF00082 | 0.355 |
CLV_PCSK_SKI1_1 | 335 | 339 | PF00082 | 0.268 |
CLV_PCSK_SKI1_1 | 354 | 358 | PF00082 | 0.439 |
CLV_PCSK_SKI1_1 | 430 | 434 | PF00082 | 0.268 |
CLV_PCSK_SKI1_1 | 459 | 463 | PF00082 | 0.453 |
CLV_PCSK_SKI1_1 | 472 | 476 | PF00082 | 0.409 |
CLV_PCSK_SKI1_1 | 532 | 536 | PF00082 | 0.511 |
DEG_SCF_FBW7_2 | 409 | 414 | PF00400 | 0.372 |
DOC_CYCLIN_RxL_1 | 456 | 466 | PF00134 | 0.426 |
DOC_MAPK_gen_1 | 428 | 438 | PF00069 | 0.344 |
DOC_MAPK_gen_1 | 813 | 822 | PF00069 | 0.365 |
DOC_MAPK_gen_1 | 823 | 831 | PF00069 | 0.359 |
DOC_MAPK_MEF2A_6 | 104 | 113 | PF00069 | 0.393 |
DOC_MAPK_MEF2A_6 | 240 | 249 | PF00069 | 0.246 |
DOC_MAPK_MEF2A_6 | 815 | 824 | PF00069 | 0.359 |
DOC_MIT_MIM_1 | 694 | 702 | PF04212 | 0.514 |
DOC_PP1_RVXF_1 | 789 | 795 | PF00149 | 0.346 |
DOC_USP7_MATH_1 | 173 | 177 | PF00917 | 0.388 |
DOC_USP7_MATH_1 | 412 | 416 | PF00917 | 0.313 |
DOC_USP7_MATH_1 | 498 | 502 | PF00917 | 0.676 |
DOC_USP7_MATH_1 | 760 | 764 | PF00917 | 0.468 |
DOC_USP7_UBL2_3 | 316 | 320 | PF12436 | 0.242 |
DOC_USP7_UBL2_3 | 854 | 858 | PF12436 | 0.401 |
DOC_WW_Pin1_4 | 102 | 107 | PF00397 | 0.351 |
DOC_WW_Pin1_4 | 174 | 179 | PF00397 | 0.369 |
DOC_WW_Pin1_4 | 184 | 189 | PF00397 | 0.308 |
DOC_WW_Pin1_4 | 407 | 412 | PF00397 | 0.311 |
DOC_WW_Pin1_4 | 494 | 499 | PF00397 | 0.646 |
LIG_14-3-3_CanoR_1 | 170 | 178 | PF00244 | 0.425 |
LIG_14-3-3_CanoR_1 | 227 | 234 | PF00244 | 0.256 |
LIG_14-3-3_CanoR_1 | 246 | 250 | PF00244 | 0.355 |
LIG_14-3-3_CanoR_1 | 284 | 292 | PF00244 | 0.689 |
LIG_14-3-3_CanoR_1 | 365 | 373 | PF00244 | 0.388 |
LIG_14-3-3_CanoR_1 | 420 | 424 | PF00244 | 0.238 |
LIG_14-3-3_CanoR_1 | 567 | 571 | PF00244 | 0.525 |
LIG_14-3-3_CanoR_1 | 617 | 626 | PF00244 | 0.491 |
LIG_14-3-3_CanoR_1 | 701 | 709 | PF00244 | 0.568 |
LIG_APCC_ABBA_1 | 139 | 144 | PF00400 | 0.292 |
LIG_APCC_ABBA_1 | 381 | 386 | PF00400 | 0.255 |
LIG_APCC_ABBAyCdc20_2 | 127 | 133 | PF00400 | 0.372 |
LIG_BIR_III_4 | 154 | 158 | PF00653 | 0.267 |
LIG_FHA_1 | 179 | 185 | PF00498 | 0.256 |
LIG_FHA_1 | 373 | 379 | PF00498 | 0.340 |
LIG_FHA_1 | 388 | 394 | PF00498 | 0.301 |
LIG_FHA_1 | 401 | 407 | PF00498 | 0.292 |
LIG_FHA_1 | 408 | 414 | PF00498 | 0.269 |
LIG_FHA_1 | 456 | 462 | PF00498 | 0.464 |
LIG_FHA_1 | 464 | 470 | PF00498 | 0.428 |
LIG_FHA_1 | 555 | 561 | PF00498 | 0.459 |
LIG_FHA_1 | 57 | 63 | PF00498 | 0.243 |
LIG_FHA_1 | 571 | 577 | PF00498 | 0.501 |
LIG_FHA_1 | 650 | 656 | PF00498 | 0.554 |
LIG_FHA_1 | 694 | 700 | PF00498 | 0.466 |
LIG_FHA_2 | 272 | 278 | PF00498 | 0.640 |
LIG_FHA_2 | 359 | 365 | PF00498 | 0.388 |
LIG_FHA_2 | 534 | 540 | PF00498 | 0.430 |
LIG_FHA_2 | 56 | 62 | PF00498 | 0.357 |
LIG_FHA_2 | 706 | 712 | PF00498 | 0.655 |
LIG_FHA_2 | 749 | 755 | PF00498 | 0.437 |
LIG_Integrin_RGD_1 | 659 | 661 | PF01839 | 0.458 |
LIG_LIR_Gen_1 | 115 | 122 | PF02991 | 0.285 |
LIG_LIR_Gen_1 | 132 | 142 | PF02991 | 0.277 |
LIG_LIR_Gen_1 | 401 | 409 | PF02991 | 0.243 |
LIG_LIR_Gen_1 | 48 | 57 | PF02991 | 0.285 |
LIG_LIR_Gen_1 | 680 | 688 | PF02991 | 0.434 |
LIG_LIR_Gen_1 | 94 | 102 | PF02991 | 0.303 |
LIG_LIR_Nem_3 | 115 | 120 | PF02991 | 0.280 |
LIG_LIR_Nem_3 | 132 | 138 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 195 | 201 | PF02991 | 0.334 |
LIG_LIR_Nem_3 | 380 | 384 | PF02991 | 0.261 |
LIG_LIR_Nem_3 | 401 | 405 | PF02991 | 0.243 |
LIG_LIR_Nem_3 | 48 | 52 | PF02991 | 0.285 |
LIG_LIR_Nem_3 | 680 | 684 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 725 | 731 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 94 | 98 | PF02991 | 0.283 |
LIG_NRBOX | 145 | 151 | PF00104 | 0.275 |
LIG_NRBOX | 388 | 394 | PF00104 | 0.283 |
LIG_NRBOX | 726 | 732 | PF00104 | 0.386 |
LIG_PCNA_yPIPBox_3 | 143 | 151 | PF02747 | 0.384 |
LIG_SH2_CRK | 681 | 685 | PF00017 | 0.548 |
LIG_SH2_NCK_1 | 221 | 225 | PF00017 | 0.372 |
LIG_SH2_NCK_1 | 53 | 57 | PF00017 | 0.228 |
LIG_SH2_SRC | 221 | 224 | PF00017 | 0.204 |
LIG_SH2_SRC | 53 | 56 | PF00017 | 0.390 |
LIG_SH2_STAP1 | 221 | 225 | PF00017 | 0.256 |
LIG_SH2_STAP1 | 479 | 483 | PF00017 | 0.575 |
LIG_SH2_STAP1 | 53 | 57 | PF00017 | 0.339 |
LIG_SH2_STAP1 | 63 | 67 | PF00017 | 0.288 |
LIG_SH2_STAT3 | 142 | 145 | PF00017 | 0.220 |
LIG_SH2_STAT3 | 479 | 482 | PF00017 | 0.533 |
LIG_SH2_STAT5 | 201 | 204 | PF00017 | 0.250 |
LIG_SH2_STAT5 | 254 | 257 | PF00017 | 0.609 |
LIG_SH2_STAT5 | 468 | 471 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 663 | 666 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 95 | 98 | PF00017 | 0.265 |
LIG_SH3_3 | 879 | 885 | PF00018 | 0.473 |
LIG_SUMO_SIM_anti_2 | 215 | 221 | PF11976 | 0.179 |
LIG_SUMO_SIM_par_1 | 189 | 195 | PF11976 | 0.275 |
LIG_SxIP_EBH_1 | 375 | 385 | PF03271 | 0.228 |
LIG_TRAF2_1 | 212 | 215 | PF00917 | 0.324 |
LIG_TRAF2_1 | 273 | 276 | PF00917 | 0.661 |
LIG_TRAF2_1 | 628 | 631 | PF00917 | 0.474 |
LIG_TRAF2_2 | 742 | 747 | PF00917 | 0.444 |
LIG_UBA3_1 | 844 | 851 | PF00899 | 0.462 |
LIG_WRC_WIRS_1 | 378 | 383 | PF05994 | 0.179 |
MOD_CK1_1 | 165 | 171 | PF00069 | 0.452 |
MOD_CK1_1 | 174 | 180 | PF00069 | 0.373 |
MOD_CK1_1 | 226 | 232 | PF00069 | 0.291 |
MOD_CK1_1 | 238 | 244 | PF00069 | 0.297 |
MOD_CK1_1 | 287 | 293 | PF00069 | 0.736 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.465 |
MOD_CK1_1 | 355 | 361 | PF00069 | 0.317 |
MOD_CK1_1 | 368 | 374 | PF00069 | 0.203 |
MOD_CK1_1 | 387 | 393 | PF00069 | 0.315 |
MOD_CK1_1 | 419 | 425 | PF00069 | 0.243 |
MOD_CK1_1 | 494 | 500 | PF00069 | 0.638 |
MOD_CK1_1 | 501 | 507 | PF00069 | 0.671 |
MOD_CK1_1 | 569 | 575 | PF00069 | 0.525 |
MOD_CK1_1 | 665 | 671 | PF00069 | 0.347 |
MOD_CK1_1 | 705 | 711 | PF00069 | 0.438 |
MOD_CK1_1 | 781 | 787 | PF00069 | 0.598 |
MOD_CK1_1 | 91 | 97 | PF00069 | 0.308 |
MOD_CK2_1 | 134 | 140 | PF00069 | 0.282 |
MOD_CK2_1 | 189 | 195 | PF00069 | 0.269 |
MOD_CK2_1 | 209 | 215 | PF00069 | 0.266 |
MOD_CK2_1 | 270 | 276 | PF00069 | 0.671 |
MOD_CK2_1 | 33 | 39 | PF00069 | 0.243 |
MOD_CK2_1 | 412 | 418 | PF00069 | 0.338 |
MOD_CK2_1 | 489 | 495 | PF00069 | 0.653 |
MOD_CK2_1 | 5 | 11 | PF00069 | 0.410 |
MOD_CK2_1 | 533 | 539 | PF00069 | 0.521 |
MOD_CK2_1 | 55 | 61 | PF00069 | 0.310 |
MOD_CK2_1 | 587 | 593 | PF00069 | 0.497 |
MOD_CK2_1 | 617 | 623 | PF00069 | 0.421 |
MOD_CK2_1 | 781 | 787 | PF00069 | 0.482 |
MOD_Cter_Amidation | 298 | 301 | PF01082 | 0.529 |
MOD_GlcNHglycan | 164 | 167 | PF01048 | 0.440 |
MOD_GlcNHglycan | 173 | 176 | PF01048 | 0.218 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.150 |
MOD_GlcNHglycan | 228 | 231 | PF01048 | 0.272 |
MOD_GlcNHglycan | 292 | 295 | PF01048 | 0.651 |
MOD_GlcNHglycan | 414 | 417 | PF01048 | 0.334 |
MOD_GlcNHglycan | 500 | 503 | PF01048 | 0.632 |
MOD_GlcNHglycan | 731 | 734 | PF01048 | 0.456 |
MOD_GlcNHglycan | 780 | 783 | PF01048 | 0.586 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.319 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.455 |
MOD_GSK3_1 | 245 | 252 | PF00069 | 0.358 |
MOD_GSK3_1 | 283 | 290 | PF00069 | 0.712 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.296 |
MOD_GSK3_1 | 368 | 375 | PF00069 | 0.334 |
MOD_GSK3_1 | 412 | 419 | PF00069 | 0.353 |
MOD_GSK3_1 | 494 | 501 | PF00069 | 0.638 |
MOD_GSK3_1 | 562 | 569 | PF00069 | 0.579 |
MOD_GSK3_1 | 693 | 700 | PF00069 | 0.367 |
MOD_GSK3_1 | 718 | 725 | PF00069 | 0.604 |
MOD_GSK3_1 | 748 | 755 | PF00069 | 0.559 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.306 |
MOD_N-GLC_1 | 102 | 107 | PF02516 | 0.321 |
MOD_N-GLC_1 | 352 | 357 | PF02516 | 0.292 |
MOD_N-GLC_1 | 489 | 494 | PF02516 | 0.462 |
MOD_N-GLC_1 | 705 | 710 | PF02516 | 0.446 |
MOD_N-GLC_1 | 79 | 84 | PF02516 | 0.282 |
MOD_NEK2_1 | 292 | 297 | PF00069 | 0.528 |
MOD_NEK2_1 | 392 | 397 | PF00069 | 0.265 |
MOD_NEK2_1 | 455 | 460 | PF00069 | 0.476 |
MOD_NEK2_1 | 570 | 575 | PF00069 | 0.516 |
MOD_NEK2_1 | 584 | 589 | PF00069 | 0.427 |
MOD_NEK2_1 | 642 | 647 | PF00069 | 0.433 |
MOD_NEK2_1 | 677 | 682 | PF00069 | 0.556 |
MOD_NEK2_1 | 702 | 707 | PF00069 | 0.438 |
MOD_NEK2_1 | 722 | 727 | PF00069 | 0.304 |
MOD_NEK2_1 | 98 | 103 | PF00069 | 0.278 |
MOD_NEK2_2 | 189 | 194 | PF00069 | 0.372 |
MOD_NEK2_2 | 748 | 753 | PF00069 | 0.443 |
MOD_NEK2_2 | 79 | 84 | PF00069 | 0.346 |
MOD_NEK2_2 | 862 | 867 | PF00069 | 0.398 |
MOD_PIKK_1 | 271 | 277 | PF00454 | 0.702 |
MOD_PIKK_1 | 285 | 291 | PF00454 | 0.715 |
MOD_PIKK_1 | 570 | 576 | PF00454 | 0.527 |
MOD_PIKK_1 | 584 | 590 | PF00454 | 0.548 |
MOD_PIKK_1 | 642 | 648 | PF00454 | 0.471 |
MOD_PIKK_1 | 679 | 685 | PF00454 | 0.382 |
MOD_PIKK_1 | 693 | 699 | PF00454 | 0.357 |
MOD_PIKK_1 | 735 | 741 | PF00454 | 0.535 |
MOD_PIKK_1 | 752 | 758 | PF00454 | 0.345 |
MOD_PIKK_1 | 852 | 858 | PF00454 | 0.561 |
MOD_PKA_1 | 773 | 779 | PF00069 | 0.513 |
MOD_PKA_2 | 226 | 232 | PF00069 | 0.273 |
MOD_PKA_2 | 23 | 29 | PF00069 | 0.597 |
MOD_PKA_2 | 245 | 251 | PF00069 | 0.223 |
MOD_PKA_2 | 283 | 289 | PF00069 | 0.719 |
MOD_PKA_2 | 384 | 390 | PF00069 | 0.292 |
MOD_PKA_2 | 419 | 425 | PF00069 | 0.261 |
MOD_PKA_2 | 455 | 461 | PF00069 | 0.501 |
MOD_PKA_2 | 566 | 572 | PF00069 | 0.528 |
MOD_PKA_2 | 697 | 703 | PF00069 | 0.591 |
MOD_PKA_2 | 718 | 724 | PF00069 | 0.633 |
MOD_PKA_2 | 752 | 758 | PF00069 | 0.473 |
MOD_PKA_2 | 773 | 779 | PF00069 | 0.513 |
MOD_Plk_1 | 249 | 255 | PF00069 | 0.314 |
MOD_Plk_1 | 32 | 38 | PF00069 | 0.418 |
MOD_Plk_1 | 352 | 358 | PF00069 | 0.279 |
MOD_Plk_1 | 489 | 495 | PF00069 | 0.509 |
MOD_Plk_1 | 665 | 671 | PF00069 | 0.418 |
MOD_Plk_1 | 705 | 711 | PF00069 | 0.417 |
MOD_Plk_2-3 | 257 | 263 | PF00069 | 0.576 |
MOD_Plk_2-3 | 33 | 39 | PF00069 | 0.372 |
MOD_Plk_4 | 134 | 140 | PF00069 | 0.290 |
MOD_Plk_4 | 358 | 364 | PF00069 | 0.260 |
MOD_Plk_4 | 377 | 383 | PF00069 | 0.253 |
MOD_Plk_4 | 463 | 469 | PF00069 | 0.406 |
MOD_Plk_4 | 501 | 507 | PF00069 | 0.648 |
MOD_Plk_4 | 511 | 517 | PF00069 | 0.569 |
MOD_Plk_4 | 718 | 724 | PF00069 | 0.450 |
MOD_Plk_4 | 79 | 85 | PF00069 | 0.298 |
MOD_Plk_4 | 93 | 99 | PF00069 | 0.255 |
MOD_ProDKin_1 | 102 | 108 | PF00069 | 0.351 |
MOD_ProDKin_1 | 174 | 180 | PF00069 | 0.369 |
MOD_ProDKin_1 | 184 | 190 | PF00069 | 0.308 |
MOD_ProDKin_1 | 407 | 413 | PF00069 | 0.311 |
MOD_ProDKin_1 | 494 | 500 | PF00069 | 0.619 |
MOD_SUMO_rev_2 | 529 | 536 | PF00179 | 0.538 |
MOD_SUMO_rev_2 | 600 | 607 | PF00179 | 0.585 |
MOD_SUMO_rev_2 | 807 | 814 | PF00179 | 0.376 |
TRG_DiLeu_BaEn_1 | 621 | 626 | PF01217 | 0.421 |
TRG_DiLeu_BaEn_4 | 529 | 535 | PF01217 | 0.550 |
TRG_DiLeu_BaEn_4 | 631 | 637 | PF01217 | 0.485 |
TRG_DiLeu_BaLyEn_6 | 650 | 655 | PF01217 | 0.440 |
TRG_DiLeu_BaLyEn_6 | 726 | 731 | PF01217 | 0.372 |
TRG_ENDOCYTIC_2 | 681 | 684 | PF00928 | 0.555 |
TRG_ENDOCYTIC_2 | 95 | 98 | PF00928 | 0.255 |
TRG_ER_diArg_1 | 14 | 17 | PF00400 | 0.371 |
TRG_ER_diArg_1 | 788 | 791 | PF00400 | 0.483 |
TRG_ER_diArg_1 | 875 | 878 | PF00400 | 0.560 |
TRG_NES_CRM1_1 | 662 | 675 | PF08389 | 0.389 |
TRG_NES_CRM1_1 | 818 | 833 | PF08389 | 0.365 |
TRG_NLS_Bipartite_1 | 300 | 322 | PF00514 | 0.473 |
TRG_NLS_MonoExtN_4 | 316 | 322 | PF00514 | 0.242 |
TRG_NLS_MonoExtN_4 | 428 | 434 | PF00514 | 0.372 |
TRG_Pf-PMV_PEXEL_1 | 793 | 797 | PF00026 | 0.416 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HVM1 | Leptomonas seymouri | 65% | 96% |
A0A0S4INA4 | Bodo saltans | 41% | 100% |
A0A1X0NUN6 | Trypanosomatidae | 41% | 95% |
A0A3Q8IG88 | Leishmania donovani | 30% | 100% |
A0A3R7NW09 | Trypanosoma rangeli | 30% | 85% |
A0A3S7WX05 | Leishmania donovani | 100% | 100% |
A0A422N2N4 | Trypanosoma rangeli | 42% | 100% |
A4H4I4 | Leishmania braziliensis | 25% | 100% |
A4H8S6 | Leishmania braziliensis | 25% | 86% |
A4HCA1 | Leishmania braziliensis | 78% | 100% |
A4IBA7 | Leishmania infantum | 30% | 100% |
E9AF32 | Leishmania major | 29% | 100% |
E9AVN8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
E9B0F9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9B687 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
Q0DV28 | Oryza sativa subsp. japonica | 25% | 94% |
Q4QBU1 | Leishmania major | 92% | 100% |
V5BLH7 | Trypanosoma cruzi | 42% | 100% |