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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005819 | spindle | 5 | 1 |
GO:0005930 | axoneme | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0072686 | mitotic spindle | 6 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HFK9
Term | Name | Level | Count |
---|---|---|---|
GO:0000226 | microtubule cytoskeleton organization | 3 | 1 |
GO:0000281 | mitotic cytokinesis | 4 | 1 |
GO:0000910 | cytokinesis | 3 | 1 |
GO:0001539 | cilium or flagellum-dependent cell motility | 3 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007010 | cytoskeleton organization | 5 | 1 |
GO:0007017 | microtubule-based process | 2 | 1 |
GO:0007051 | spindle organization | 3 | 1 |
GO:0007052 | mitotic spindle organization | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022402 | cell cycle process | 2 | 1 |
GO:0048870 | cell motility | 2 | 1 |
GO:0060285 | cilium-dependent cell motility | 4 | 1 |
GO:0061640 | cytoskeleton-dependent cytokinesis | 4 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:1902850 | microtubule cytoskeleton organization involved in mitosis | 4 | 1 |
GO:1903047 | mitotic cell cycle process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 7 |
GO:0005509 | calcium ion binding | 5 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043169 | cation binding | 3 | 7 |
GO:0046872 | metal ion binding | 4 | 7 |
GO:0005515 | protein binding | 2 | 1 |
GO:0008092 | cytoskeletal protein binding | 3 | 1 |
GO:0015631 | tubulin binding | 4 | 1 |
GO:0043014 | alpha-tubulin binding | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 69 | 73 | PF00656 | 0.588 |
CLV_MEL_PAP_1 | 724 | 730 | PF00089 | 0.505 |
CLV_NRD_NRD_1 | 116 | 118 | PF00675 | 0.255 |
CLV_NRD_NRD_1 | 252 | 254 | PF00675 | 0.334 |
CLV_NRD_NRD_1 | 29 | 31 | PF00675 | 0.543 |
CLV_NRD_NRD_1 | 34 | 36 | PF00675 | 0.550 |
CLV_NRD_NRD_1 | 397 | 399 | PF00675 | 0.575 |
CLV_NRD_NRD_1 | 417 | 419 | PF00675 | 0.268 |
CLV_NRD_NRD_1 | 442 | 444 | PF00675 | 0.255 |
CLV_NRD_NRD_1 | 479 | 481 | PF00675 | 0.307 |
CLV_NRD_NRD_1 | 533 | 535 | PF00675 | 0.392 |
CLV_NRD_NRD_1 | 647 | 649 | PF00675 | 0.617 |
CLV_NRD_NRD_1 | 670 | 672 | PF00675 | 0.412 |
CLV_NRD_NRD_1 | 700 | 702 | PF00675 | 0.423 |
CLV_PCSK_FUR_1 | 648 | 652 | PF00082 | 0.383 |
CLV_PCSK_KEX2_1 | 149 | 151 | PF00082 | 0.255 |
CLV_PCSK_KEX2_1 | 29 | 31 | PF00082 | 0.543 |
CLV_PCSK_KEX2_1 | 34 | 36 | PF00082 | 0.550 |
CLV_PCSK_KEX2_1 | 397 | 399 | PF00082 | 0.575 |
CLV_PCSK_KEX2_1 | 417 | 419 | PF00082 | 0.268 |
CLV_PCSK_KEX2_1 | 442 | 444 | PF00082 | 0.255 |
CLV_PCSK_KEX2_1 | 479 | 481 | PF00082 | 0.255 |
CLV_PCSK_KEX2_1 | 650 | 652 | PF00082 | 0.386 |
CLV_PCSK_KEX2_1 | 670 | 672 | PF00082 | 0.412 |
CLV_PCSK_KEX2_1 | 700 | 702 | PF00082 | 0.500 |
CLV_PCSK_PC1ET2_1 | 149 | 151 | PF00082 | 0.255 |
CLV_PCSK_PC1ET2_1 | 650 | 652 | PF00082 | 0.404 |
CLV_PCSK_PC7_1 | 30 | 36 | PF00082 | 0.653 |
CLV_PCSK_PC7_1 | 475 | 481 | PF00082 | 0.255 |
CLV_PCSK_SKI1_1 | 189 | 193 | PF00082 | 0.431 |
CLV_PCSK_SKI1_1 | 246 | 250 | PF00082 | 0.336 |
CLV_PCSK_SKI1_1 | 253 | 257 | PF00082 | 0.294 |
CLV_PCSK_SKI1_1 | 272 | 276 | PF00082 | 0.285 |
CLV_PCSK_SKI1_1 | 355 | 359 | PF00082 | 0.255 |
CLV_PCSK_SKI1_1 | 443 | 447 | PF00082 | 0.255 |
CLV_PCSK_SKI1_1 | 572 | 576 | PF00082 | 0.494 |
CLV_PCSK_SKI1_1 | 671 | 675 | PF00082 | 0.423 |
CLV_PCSK_SKI1_1 | 718 | 722 | PF00082 | 0.494 |
CLV_Separin_Metazoa | 26 | 30 | PF03568 | 0.546 |
DEG_APCC_KENBOX_2 | 330 | 334 | PF00400 | 0.509 |
DEG_SIAH_1 | 199 | 207 | PF03145 | 0.585 |
DOC_ANK_TNKS_1 | 605 | 612 | PF00023 | 0.494 |
DOC_CDC14_PxL_1 | 15 | 23 | PF14671 | 0.660 |
DOC_CYCLIN_RxL_1 | 186 | 194 | PF00134 | 0.632 |
DOC_CYCLIN_RxL_1 | 569 | 580 | PF00134 | 0.465 |
DOC_CYCLIN_RxL_1 | 668 | 677 | PF00134 | 0.408 |
DOC_CYCLIN_RxL_1 | 696 | 707 | PF00134 | 0.511 |
DOC_MAPK_gen_1 | 115 | 123 | PF00069 | 0.457 |
DOC_MAPK_gen_1 | 243 | 251 | PF00069 | 0.452 |
DOC_MAPK_gen_1 | 440 | 448 | PF00069 | 0.461 |
DOC_MAPK_MEF2A_6 | 115 | 123 | PF00069 | 0.507 |
DOC_MAPK_MEF2A_6 | 559 | 568 | PF00069 | 0.333 |
DOC_PP4_FxxP_1 | 13 | 16 | PF00568 | 0.532 |
DOC_PP4_FxxP_1 | 390 | 393 | PF00568 | 0.640 |
DOC_SPAK_OSR1_1 | 373 | 377 | PF12202 | 0.333 |
DOC_USP7_MATH_1 | 209 | 213 | PF00917 | 0.346 |
DOC_USP7_MATH_1 | 632 | 636 | PF00917 | 0.674 |
DOC_USP7_MATH_1 | 685 | 689 | PF00917 | 0.533 |
DOC_USP7_MATH_1 | 726 | 730 | PF00917 | 0.526 |
DOC_USP7_MATH_1 | 749 | 753 | PF00917 | 0.543 |
DOC_USP7_UBL2_3 | 436 | 440 | PF12436 | 0.558 |
DOC_USP7_UBL2_3 | 531 | 535 | PF12436 | 0.540 |
DOC_WW_Pin1_4 | 156 | 161 | PF00397 | 0.443 |
DOC_WW_Pin1_4 | 228 | 233 | PF00397 | 0.561 |
DOC_WW_Pin1_4 | 383 | 388 | PF00397 | 0.596 |
LIG_14-3-3_CanoR_1 | 312 | 320 | PF00244 | 0.377 |
LIG_14-3-3_CanoR_1 | 373 | 383 | PF00244 | 0.343 |
LIG_14-3-3_CanoR_1 | 420 | 426 | PF00244 | 0.415 |
LIG_14-3-3_CanoR_1 | 67 | 71 | PF00244 | 0.605 |
LIG_14-3-3_CanoR_1 | 727 | 734 | PF00244 | 0.426 |
LIG_14-3-3_CanoR_1 | 735 | 743 | PF00244 | 0.417 |
LIG_AP2alpha_2 | 185 | 187 | PF02296 | 0.558 |
LIG_AP2alpha_2 | 299 | 301 | PF02296 | 0.455 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.564 |
LIG_BIR_III_2 | 183 | 187 | PF00653 | 0.567 |
LIG_BRCT_BRCA1_1 | 316 | 320 | PF00533 | 0.534 |
LIG_BRCT_BRCA1_1 | 326 | 330 | PF00533 | 0.468 |
LIG_BRCT_BRCA1_1 | 500 | 504 | PF00533 | 0.534 |
LIG_eIF4E_1 | 684 | 690 | PF01652 | 0.528 |
LIG_FHA_1 | 127 | 133 | PF00498 | 0.408 |
LIG_FHA_1 | 143 | 149 | PF00498 | 0.455 |
LIG_FHA_1 | 176 | 182 | PF00498 | 0.450 |
LIG_FHA_1 | 186 | 192 | PF00498 | 0.520 |
LIG_FHA_1 | 263 | 269 | PF00498 | 0.468 |
LIG_FHA_1 | 452 | 458 | PF00498 | 0.380 |
LIG_FHA_1 | 542 | 548 | PF00498 | 0.482 |
LIG_FHA_1 | 632 | 638 | PF00498 | 0.424 |
LIG_FHA_1 | 90 | 96 | PF00498 | 0.356 |
LIG_FHA_2 | 259 | 265 | PF00498 | 0.534 |
LIG_FHA_2 | 327 | 333 | PF00498 | 0.461 |
LIG_FHA_2 | 338 | 344 | PF00498 | 0.414 |
LIG_FHA_2 | 394 | 400 | PF00498 | 0.686 |
LIG_FHA_2 | 577 | 583 | PF00498 | 0.471 |
LIG_FHA_2 | 67 | 73 | PF00498 | 0.580 |
LIG_FHA_2 | 76 | 82 | PF00498 | 0.524 |
LIG_LIR_Apic_2 | 12 | 16 | PF02991 | 0.538 |
LIG_LIR_Gen_1 | 207 | 218 | PF02991 | 0.499 |
LIG_LIR_Gen_1 | 245 | 256 | PF02991 | 0.459 |
LIG_LIR_Gen_1 | 271 | 281 | PF02991 | 0.507 |
LIG_LIR_Gen_1 | 501 | 511 | PF02991 | 0.509 |
LIG_LIR_Gen_1 | 599 | 608 | PF02991 | 0.472 |
LIG_LIR_Gen_1 | 620 | 629 | PF02991 | 0.419 |
LIG_LIR_Gen_1 | 662 | 667 | PF02991 | 0.415 |
LIG_LIR_Gen_1 | 677 | 685 | PF02991 | 0.348 |
LIG_LIR_Gen_1 | 731 | 737 | PF02991 | 0.499 |
LIG_LIR_Nem_3 | 178 | 182 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 245 | 251 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 271 | 277 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 299 | 304 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 361 | 365 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 377 | 382 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 456 | 461 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 501 | 507 | PF02991 | 0.509 |
LIG_LIR_Nem_3 | 595 | 600 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 620 | 624 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 662 | 666 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 677 | 681 | PF02991 | 0.278 |
LIG_LIR_Nem_3 | 731 | 736 | PF02991 | 0.503 |
LIG_Pex14_1 | 621 | 625 | PF04695 | 0.536 |
LIG_Pex14_2 | 301 | 305 | PF04695 | 0.374 |
LIG_Pex14_2 | 674 | 678 | PF04695 | 0.416 |
LIG_REV1ctd_RIR_1 | 302 | 311 | PF16727 | 0.399 |
LIG_SH2_CRK | 379 | 383 | PF00017 | 0.501 |
LIG_SH2_NCK_1 | 600 | 604 | PF00017 | 0.586 |
LIG_SH2_SRC | 600 | 603 | PF00017 | 0.593 |
LIG_SH2_SRC | 625 | 628 | PF00017 | 0.592 |
LIG_SH2_STAP1 | 365 | 369 | PF00017 | 0.504 |
LIG_SH2_STAP1 | 600 | 604 | PF00017 | 0.474 |
LIG_SH2_STAP1 | 743 | 747 | PF00017 | 0.533 |
LIG_SH2_STAT3 | 353 | 356 | PF00017 | 0.558 |
LIG_SH2_STAT5 | 101 | 104 | PF00017 | 0.468 |
LIG_SH2_STAT5 | 124 | 127 | PF00017 | 0.534 |
LIG_SH2_STAT5 | 210 | 213 | PF00017 | 0.525 |
LIG_SH2_STAT5 | 279 | 282 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 339 | 342 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 365 | 368 | PF00017 | 0.550 |
LIG_SH2_STAT5 | 485 | 488 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 492 | 495 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 589 | 592 | PF00017 | 0.421 |
LIG_SH3_3 | 129 | 135 | PF00018 | 0.534 |
LIG_SH3_3 | 13 | 19 | PF00018 | 0.526 |
LIG_SH3_3 | 150 | 156 | PF00018 | 0.507 |
LIG_SH3_3 | 165 | 171 | PF00018 | 0.488 |
LIG_SH3_3 | 386 | 392 | PF00018 | 0.497 |
LIG_SH3_3 | 46 | 52 | PF00018 | 0.451 |
LIG_SUMO_SIM_anti_2 | 285 | 290 | PF11976 | 0.376 |
LIG_SUMO_SIM_anti_2 | 582 | 588 | PF11976 | 0.400 |
LIG_SUMO_SIM_par_1 | 452 | 459 | PF11976 | 0.384 |
LIG_TRAF2_1 | 109 | 112 | PF00917 | 0.405 |
LIG_TRAF2_1 | 401 | 404 | PF00917 | 0.410 |
LIG_TRAF2_1 | 579 | 582 | PF00917 | 0.370 |
LIG_TRAF2_1 | 599 | 602 | PF00917 | 0.300 |
LIG_TRAF2_1 | 643 | 646 | PF00917 | 0.403 |
LIG_TRAF2_1 | 729 | 732 | PF00917 | 0.398 |
LIG_TYR_ITSM | 375 | 382 | PF00017 | 0.444 |
LIG_UBA3_1 | 570 | 575 | PF00899 | 0.403 |
LIG_UBA3_1 | 583 | 592 | PF00899 | 0.412 |
MOD_CK1_1 | 212 | 218 | PF00069 | 0.550 |
MOD_CK1_1 | 282 | 288 | PF00069 | 0.507 |
MOD_CK1_1 | 313 | 319 | PF00069 | 0.377 |
MOD_CK1_1 | 542 | 548 | PF00069 | 0.419 |
MOD_CK1_1 | 596 | 602 | PF00069 | 0.482 |
MOD_CK1_1 | 739 | 745 | PF00069 | 0.446 |
MOD_CK2_1 | 106 | 112 | PF00069 | 0.457 |
MOD_CK2_1 | 128 | 134 | PF00069 | 0.455 |
MOD_CK2_1 | 19 | 25 | PF00069 | 0.516 |
MOD_CK2_1 | 326 | 332 | PF00069 | 0.482 |
MOD_CK2_1 | 393 | 399 | PF00069 | 0.641 |
MOD_CK2_1 | 453 | 459 | PF00069 | 0.485 |
MOD_CK2_1 | 576 | 582 | PF00069 | 0.373 |
MOD_CK2_1 | 596 | 602 | PF00069 | 0.296 |
MOD_CK2_1 | 726 | 732 | PF00069 | 0.395 |
MOD_GlcNHglycan | 108 | 111 | PF01048 | 0.291 |
MOD_GlcNHglycan | 138 | 142 | PF01048 | 0.244 |
MOD_GlcNHglycan | 237 | 240 | PF01048 | 0.432 |
MOD_GlcNHglycan | 295 | 298 | PF01048 | 0.255 |
MOD_GlcNHglycan | 315 | 319 | PF01048 | 0.322 |
MOD_GlcNHglycan | 43 | 46 | PF01048 | 0.452 |
MOD_GlcNHglycan | 464 | 467 | PF01048 | 0.257 |
MOD_GlcNHglycan | 627 | 630 | PF01048 | 0.384 |
MOD_GlcNHglycan | 652 | 655 | PF01048 | 0.484 |
MOD_GlcNHglycan | 753 | 756 | PF01048 | 0.414 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.389 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.517 |
MOD_GSK3_1 | 223 | 230 | PF00069 | 0.402 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.534 |
MOD_GSK3_1 | 310 | 317 | PF00069 | 0.504 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.500 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.468 |
MOD_GSK3_1 | 506 | 513 | PF00069 | 0.450 |
MOD_GSK3_1 | 61 | 68 | PF00069 | 0.667 |
MOD_GSK3_1 | 739 | 746 | PF00069 | 0.504 |
MOD_GSK3_1 | 749 | 756 | PF00069 | 0.603 |
MOD_N-GLC_1 | 593 | 598 | PF02516 | 0.494 |
MOD_N-GLC_1 | 617 | 622 | PF02516 | 0.501 |
MOD_N-GLC_1 | 737 | 742 | PF02516 | 0.414 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.573 |
MOD_NEK2_1 | 142 | 147 | PF00069 | 0.490 |
MOD_NEK2_1 | 268 | 273 | PF00069 | 0.507 |
MOD_NEK2_1 | 320 | 325 | PF00069 | 0.534 |
MOD_NEK2_1 | 374 | 379 | PF00069 | 0.466 |
MOD_NEK2_1 | 421 | 426 | PF00069 | 0.517 |
MOD_NEK2_1 | 539 | 544 | PF00069 | 0.413 |
MOD_NEK2_1 | 703 | 708 | PF00069 | 0.448 |
MOD_NEK2_1 | 736 | 741 | PF00069 | 0.418 |
MOD_NEK2_2 | 209 | 214 | PF00069 | 0.547 |
MOD_NEK2_2 | 326 | 331 | PF00069 | 0.473 |
MOD_NEK2_2 | 66 | 71 | PF00069 | 0.750 |
MOD_PIKK_1 | 1 | 7 | PF00454 | 0.604 |
MOD_PKA_1 | 650 | 656 | PF00069 | 0.331 |
MOD_PKA_2 | 242 | 248 | PF00069 | 0.438 |
MOD_PKA_2 | 311 | 317 | PF00069 | 0.377 |
MOD_PKA_2 | 462 | 468 | PF00069 | 0.468 |
MOD_PKA_2 | 650 | 656 | PF00069 | 0.546 |
MOD_PKA_2 | 66 | 72 | PF00069 | 0.681 |
MOD_PKA_2 | 726 | 732 | PF00069 | 0.437 |
MOD_Plk_1 | 258 | 264 | PF00069 | 0.534 |
MOD_Plk_1 | 320 | 326 | PF00069 | 0.517 |
MOD_Plk_1 | 451 | 457 | PF00069 | 0.455 |
MOD_Plk_1 | 510 | 516 | PF00069 | 0.536 |
MOD_Plk_1 | 53 | 59 | PF00069 | 0.649 |
MOD_Plk_1 | 593 | 599 | PF00069 | 0.472 |
MOD_Plk_1 | 617 | 623 | PF00069 | 0.499 |
MOD_Plk_1 | 84 | 90 | PF00069 | 0.575 |
MOD_Plk_2-3 | 617 | 623 | PF00069 | 0.485 |
MOD_Plk_4 | 170 | 176 | PF00069 | 0.534 |
MOD_Plk_4 | 232 | 238 | PF00069 | 0.630 |
MOD_Plk_4 | 264 | 270 | PF00069 | 0.515 |
MOD_Plk_4 | 273 | 279 | PF00069 | 0.449 |
MOD_Plk_4 | 333 | 339 | PF00069 | 0.465 |
MOD_Plk_4 | 421 | 427 | PF00069 | 0.534 |
MOD_Plk_4 | 43 | 49 | PF00069 | 0.574 |
MOD_Plk_4 | 453 | 459 | PF00069 | 0.504 |
MOD_Plk_4 | 566 | 572 | PF00069 | 0.459 |
MOD_Plk_4 | 582 | 588 | PF00069 | 0.266 |
MOD_Plk_4 | 632 | 638 | PF00069 | 0.644 |
MOD_Plk_4 | 685 | 691 | PF00069 | 0.420 |
MOD_ProDKin_1 | 156 | 162 | PF00069 | 0.443 |
MOD_ProDKin_1 | 228 | 234 | PF00069 | 0.559 |
MOD_ProDKin_1 | 383 | 389 | PF00069 | 0.605 |
MOD_SUMO_rev_2 | 250 | 256 | PF00179 | 0.534 |
MOD_SUMO_rev_2 | 433 | 441 | PF00179 | 0.558 |
MOD_SUMO_rev_2 | 569 | 576 | PF00179 | 0.308 |
MOD_SUMO_rev_2 | 635 | 643 | PF00179 | 0.569 |
MOD_SUMO_rev_2 | 688 | 697 | PF00179 | 0.426 |
TRG_DiLeu_BaEn_1 | 732 | 737 | PF01217 | 0.490 |
TRG_DiLeu_BaEn_4 | 711 | 717 | PF01217 | 0.484 |
TRG_DiLeu_LyEn_5 | 732 | 737 | PF01217 | 0.523 |
TRG_ENDOCYTIC_2 | 210 | 213 | PF00928 | 0.495 |
TRG_ENDOCYTIC_2 | 278 | 281 | PF00928 | 0.460 |
TRG_ENDOCYTIC_2 | 379 | 382 | PF00928 | 0.448 |
TRG_ENDOCYTIC_2 | 600 | 603 | PF00928 | 0.481 |
TRG_ER_diArg_1 | 213 | 216 | PF00400 | 0.537 |
TRG_ER_diArg_1 | 28 | 30 | PF00400 | 0.545 |
TRG_ER_diArg_1 | 307 | 310 | PF00400 | 0.460 |
TRG_ER_diArg_1 | 416 | 418 | PF00400 | 0.581 |
TRG_ER_diArg_1 | 441 | 443 | PF00400 | 0.455 |
TRG_ER_diArg_1 | 478 | 480 | PF00400 | 0.508 |
TRG_ER_diArg_1 | 699 | 701 | PF00400 | 0.396 |
TRG_Pf-PMV_PEXEL_1 | 189 | 194 | PF00026 | 0.531 |
TRG_Pf-PMV_PEXEL_1 | 398 | 402 | PF00026 | 0.641 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5H4 | Leptomonas seymouri | 22% | 90% |
A0A0N1HZ98 | Leptomonas seymouri | 26% | 98% |
A0A0N1I3M2 | Leptomonas seymouri | 76% | 99% |
A0A0N1PBW1 | Leptomonas seymouri | 27% | 100% |
A0A0S4IJW8 | Bodo saltans | 26% | 92% |
A0A0S4IQM0 | Bodo saltans | 25% | 100% |
A0A0S4J8J7 | Bodo saltans | 26% | 83% |
A0A1X0NEV8 | Trypanosomatidae | 24% | 95% |
A0A1X0NLI2 | Trypanosomatidae | 27% | 100% |
A0A1X0NMQ3 | Trypanosomatidae | 24% | 97% |
A0A1X0P419 | Trypanosomatidae | 62% | 100% |
A0A3Q1N1R0 | Bos taurus | 30% | 100% |
A0A3Q8IDH4 | Leishmania donovani | 26% | 98% |
A0A3Q8IPU3 | Leishmania donovani | 87% | 100% |
A0A3R7KM50 | Trypanosoma rangeli | 27% | 95% |
A0A3R7L048 | Trypanosoma rangeli | 58% | 100% |
A0A3S5H688 | Leishmania donovani | 23% | 100% |
A0A3S7XC76 | Leishmania donovani | 26% | 100% |
A0A422N0Z6 | Trypanosoma rangeli | 24% | 97% |
A0A422NK00 | Trypanosoma rangeli | 28% | 100% |
A4HE78 | Leishmania braziliensis | 26% | 100% |
A4HQF8 | Leishmania braziliensis | 25% | 100% |
A4I1J2 | Leishmania infantum | 26% | 98% |
A4IC94 | Leishmania infantum | 26% | 100% |
C9ZJX4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 23% | 94% |
C9ZPE7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 97% |
D0A3K7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
D0A5T5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 55% | 100% |
E1BKH1 | Bos taurus | 29% | 100% |
E9AD64 | Leishmania major | 88% | 100% |
E9AHF6 | Leishmania infantum | 88% | 100% |
E9AI34 | Leishmania braziliensis | 23% | 88% |
E9AMI2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 88% |
E9AU74 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9AXM7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 98% |
E9AYY9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q32TF8 | Danio rerio | 30% | 100% |
Q32TG3 | Gallus gallus | 28% | 100% |
Q4Q0C0 | Leishmania major | 26% | 96% |
Q4Q9U5 | Leishmania major | 27% | 100% |
Q4QI57 | Leishmania major | 23% | 100% |
Q5JST6 | Homo sapiens | 29% | 100% |
Q5JVL4 | Homo sapiens | 30% | 100% |
Q9D485 | Mus musculus | 30% | 100% |
Q9D9T8 | Mus musculus | 30% | 100% |
V5ASV2 | Trypanosoma cruzi | 26% | 100% |
V5D3X9 | Trypanosoma cruzi | 24% | 97% |
V5DA42 | Trypanosoma cruzi | 59% | 100% |