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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0035869 | ciliary transition zone | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3Q8IJN1
Term | Name | Level | Count |
---|---|---|---|
GO:0006996 | organelle organization | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0030030 | cell projection organization | 4 | 1 |
GO:0044782 | cilium organization | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0120036 | plasma membrane bounded cell projection organization | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 198 | 202 | PF00656 | 0.588 |
CLV_C14_Caspase3-7 | 472 | 476 | PF00656 | 0.581 |
CLV_C14_Caspase3-7 | 673 | 677 | PF00656 | 0.686 |
CLV_C14_Caspase3-7 | 738 | 742 | PF00656 | 0.641 |
CLV_C14_Caspase3-7 | 800 | 804 | PF00656 | 0.673 |
CLV_NRD_NRD_1 | 144 | 146 | PF00675 | 0.658 |
CLV_NRD_NRD_1 | 17 | 19 | PF00675 | 0.519 |
CLV_NRD_NRD_1 | 185 | 187 | PF00675 | 0.635 |
CLV_NRD_NRD_1 | 195 | 197 | PF00675 | 0.471 |
CLV_NRD_NRD_1 | 422 | 424 | PF00675 | 0.361 |
CLV_NRD_NRD_1 | 481 | 483 | PF00675 | 0.381 |
CLV_NRD_NRD_1 | 494 | 496 | PF00675 | 0.253 |
CLV_NRD_NRD_1 | 504 | 506 | PF00675 | 0.315 |
CLV_NRD_NRD_1 | 574 | 576 | PF00675 | 0.313 |
CLV_NRD_NRD_1 | 765 | 767 | PF00675 | 0.663 |
CLV_NRD_NRD_1 | 88 | 90 | PF00675 | 0.460 |
CLV_PCSK_FUR_1 | 183 | 187 | PF00082 | 0.585 |
CLV_PCSK_KEX2_1 | 143 | 145 | PF00082 | 0.652 |
CLV_PCSK_KEX2_1 | 17 | 19 | PF00082 | 0.519 |
CLV_PCSK_KEX2_1 | 185 | 187 | PF00082 | 0.635 |
CLV_PCSK_KEX2_1 | 23 | 25 | PF00082 | 0.513 |
CLV_PCSK_KEX2_1 | 259 | 261 | PF00082 | 0.585 |
CLV_PCSK_KEX2_1 | 422 | 424 | PF00082 | 0.361 |
CLV_PCSK_KEX2_1 | 481 | 483 | PF00082 | 0.381 |
CLV_PCSK_KEX2_1 | 494 | 496 | PF00082 | 0.269 |
CLV_PCSK_KEX2_1 | 503 | 505 | PF00082 | 0.358 |
CLV_PCSK_KEX2_1 | 576 | 578 | PF00082 | 0.322 |
CLV_PCSK_KEX2_1 | 664 | 666 | PF00082 | 0.612 |
CLV_PCSK_KEX2_1 | 765 | 767 | PF00082 | 0.708 |
CLV_PCSK_PC1ET2_1 | 23 | 25 | PF00082 | 0.467 |
CLV_PCSK_PC1ET2_1 | 259 | 261 | PF00082 | 0.585 |
CLV_PCSK_PC1ET2_1 | 503 | 505 | PF00082 | 0.415 |
CLV_PCSK_PC1ET2_1 | 576 | 578 | PF00082 | 0.381 |
CLV_PCSK_PC1ET2_1 | 664 | 666 | PF00082 | 0.612 |
CLV_PCSK_PC7_1 | 139 | 145 | PF00082 | 0.724 |
CLV_PCSK_PC7_1 | 572 | 578 | PF00082 | 0.337 |
CLV_PCSK_SKI1_1 | 102 | 106 | PF00082 | 0.512 |
CLV_PCSK_SKI1_1 | 135 | 139 | PF00082 | 0.624 |
CLV_PCSK_SKI1_1 | 20 | 24 | PF00082 | 0.704 |
CLV_PCSK_SKI1_1 | 407 | 411 | PF00082 | 0.381 |
CLV_PCSK_SKI1_1 | 417 | 421 | PF00082 | 0.283 |
CLV_PCSK_SKI1_1 | 591 | 595 | PF00082 | 0.348 |
CLV_PCSK_SKI1_1 | 609 | 613 | PF00082 | 0.359 |
CLV_PCSK_SKI1_1 | 647 | 651 | PF00082 | 0.580 |
CLV_PCSK_SKI1_1 | 664 | 668 | PF00082 | 0.584 |
DEG_APCC_DBOX_1 | 121 | 129 | PF00400 | 0.632 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.558 |
DEG_SPOP_SBC_1 | 484 | 488 | PF00917 | 0.505 |
DOC_ANK_TNKS_1 | 690 | 697 | PF00023 | 0.660 |
DOC_CKS1_1 | 304 | 309 | PF01111 | 0.739 |
DOC_CYCLIN_yCln2_LP_2 | 775 | 781 | PF00134 | 0.589 |
DOC_MAPK_gen_1 | 119 | 128 | PF00069 | 0.504 |
DOC_MAPK_gen_1 | 183 | 191 | PF00069 | 0.640 |
DOC_MAPK_gen_1 | 422 | 430 | PF00069 | 0.537 |
DOC_MAPK_MEF2A_6 | 164 | 172 | PF00069 | 0.522 |
DOC_MAPK_MEF2A_6 | 422 | 430 | PF00069 | 0.581 |
DOC_MAPK_RevD_3 | 467 | 482 | PF00069 | 0.526 |
DOC_PP1_RVXF_1 | 186 | 192 | PF00149 | 0.593 |
DOC_PP2B_LxvP_1 | 775 | 778 | PF13499 | 0.642 |
DOC_PP4_FxxP_1 | 629 | 632 | PF00568 | 0.573 |
DOC_USP7_MATH_1 | 285 | 289 | PF00917 | 0.725 |
DOC_USP7_MATH_1 | 29 | 33 | PF00917 | 0.624 |
DOC_USP7_MATH_1 | 292 | 296 | PF00917 | 0.626 |
DOC_USP7_MATH_1 | 320 | 324 | PF00917 | 0.668 |
DOC_USP7_MATH_1 | 357 | 361 | PF00917 | 0.693 |
DOC_USP7_MATH_1 | 378 | 382 | PF00917 | 0.733 |
DOC_USP7_MATH_1 | 393 | 397 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 403 | 407 | PF00917 | 0.316 |
DOC_USP7_MATH_1 | 409 | 413 | PF00917 | 0.433 |
DOC_USP7_MATH_1 | 483 | 487 | PF00917 | 0.521 |
DOC_USP7_MATH_1 | 687 | 691 | PF00917 | 0.652 |
DOC_USP7_MATH_1 | 726 | 730 | PF00917 | 0.598 |
DOC_USP7_MATH_1 | 744 | 748 | PF00917 | 0.512 |
DOC_USP7_MATH_1 | 759 | 763 | PF00917 | 0.707 |
DOC_USP7_MATH_1 | 770 | 774 | PF00917 | 0.594 |
DOC_WW_Pin1_4 | 210 | 215 | PF00397 | 0.700 |
DOC_WW_Pin1_4 | 221 | 226 | PF00397 | 0.491 |
DOC_WW_Pin1_4 | 258 | 263 | PF00397 | 0.710 |
DOC_WW_Pin1_4 | 273 | 278 | PF00397 | 0.531 |
DOC_WW_Pin1_4 | 288 | 293 | PF00397 | 0.609 |
DOC_WW_Pin1_4 | 303 | 308 | PF00397 | 0.692 |
DOC_WW_Pin1_4 | 381 | 386 | PF00397 | 0.681 |
DOC_WW_Pin1_4 | 467 | 472 | PF00397 | 0.548 |
DOC_WW_Pin1_4 | 495 | 500 | PF00397 | 0.552 |
DOC_WW_Pin1_4 | 507 | 512 | PF00397 | 0.510 |
DOC_WW_Pin1_4 | 520 | 525 | PF00397 | 0.472 |
DOC_WW_Pin1_4 | 65 | 70 | PF00397 | 0.582 |
DOC_WW_Pin1_4 | 666 | 671 | PF00397 | 0.565 |
DOC_WW_Pin1_4 | 695 | 700 | PF00397 | 0.681 |
DOC_WW_Pin1_4 | 717 | 722 | PF00397 | 0.707 |
DOC_WW_Pin1_4 | 754 | 759 | PF00397 | 0.706 |
LIG_14-3-3_CanoR_1 | 112 | 118 | PF00244 | 0.476 |
LIG_14-3-3_CanoR_1 | 144 | 152 | PF00244 | 0.544 |
LIG_14-3-3_CanoR_1 | 155 | 163 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 196 | 204 | PF00244 | 0.600 |
LIG_14-3-3_CanoR_1 | 293 | 297 | PF00244 | 0.590 |
LIG_14-3-3_CanoR_1 | 482 | 492 | PF00244 | 0.581 |
LIG_14-3-3_CanoR_1 | 575 | 583 | PF00244 | 0.544 |
LIG_14-3-3_CanoR_1 | 591 | 600 | PF00244 | 0.428 |
LIG_14-3-3_CanoR_1 | 665 | 670 | PF00244 | 0.599 |
LIG_14-3-3_CanoR_1 | 748 | 754 | PF00244 | 0.671 |
LIG_14-3-3_CanoR_1 | 765 | 770 | PF00244 | 0.510 |
LIG_14-3-3_CanoR_1 | 788 | 794 | PF00244 | 0.673 |
LIG_Actin_WH2_2 | 106 | 121 | PF00022 | 0.593 |
LIG_BIR_III_4 | 680 | 684 | PF00653 | 0.657 |
LIG_EVH1_1 | 338 | 342 | PF00568 | 0.656 |
LIG_EVH1_2 | 352 | 356 | PF00568 | 0.643 |
LIG_EVH1_2 | 71 | 75 | PF00568 | 0.684 |
LIG_FHA_1 | 537 | 543 | PF00498 | 0.501 |
LIG_FHA_1 | 592 | 598 | PF00498 | 0.501 |
LIG_FHA_1 | 666 | 672 | PF00498 | 0.535 |
LIG_FHA_1 | 677 | 683 | PF00498 | 0.647 |
LIG_FHA_1 | 687 | 693 | PF00498 | 0.565 |
LIG_FHA_1 | 772 | 778 | PF00498 | 0.672 |
LIG_FHA_2 | 136 | 142 | PF00498 | 0.651 |
LIG_FHA_2 | 411 | 417 | PF00498 | 0.574 |
LIG_LIR_Gen_1 | 107 | 118 | PF02991 | 0.631 |
LIG_LIR_Nem_3 | 107 | 113 | PF02991 | 0.630 |
LIG_LIR_Nem_3 | 418 | 424 | PF02991 | 0.581 |
LIG_LIR_Nem_3 | 561 | 567 | PF02991 | 0.589 |
LIG_LIR_Nem_3 | 59 | 65 | PF02991 | 0.518 |
LIG_Pex14_2 | 441 | 445 | PF04695 | 0.495 |
LIG_PTAP_UEV_1 | 341 | 346 | PF05743 | 0.598 |
LIG_PTAP_UEV_1 | 348 | 353 | PF05743 | 0.572 |
LIG_RPA_C_Plants | 40 | 51 | PF08784 | 0.600 |
LIG_SH2_NCK_1 | 220 | 224 | PF00017 | 0.739 |
LIG_SH2_STAP1 | 543 | 547 | PF00017 | 0.620 |
LIG_SH2_STAP1 | 79 | 83 | PF00017 | 0.479 |
LIG_SH2_STAT3 | 424 | 427 | PF00017 | 0.581 |
LIG_SH2_STAT3 | 546 | 549 | PF00017 | 0.526 |
LIG_SH2_STAT5 | 4 | 7 | PF00017 | 0.563 |
LIG_SH2_STAT5 | 546 | 549 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 581 | 584 | PF00017 | 0.495 |
LIG_SH3_1 | 346 | 352 | PF00018 | 0.530 |
LIG_SH3_1 | 66 | 72 | PF00018 | 0.576 |
LIG_SH3_2 | 490 | 495 | PF14604 | 0.450 |
LIG_SH3_3 | 126 | 132 | PF00018 | 0.599 |
LIG_SH3_3 | 277 | 283 | PF00018 | 0.731 |
LIG_SH3_3 | 293 | 299 | PF00018 | 0.579 |
LIG_SH3_3 | 301 | 307 | PF00018 | 0.728 |
LIG_SH3_3 | 314 | 320 | PF00018 | 0.601 |
LIG_SH3_3 | 325 | 331 | PF00018 | 0.686 |
LIG_SH3_3 | 33 | 39 | PF00018 | 0.635 |
LIG_SH3_3 | 333 | 339 | PF00018 | 0.611 |
LIG_SH3_3 | 346 | 352 | PF00018 | 0.653 |
LIG_SH3_3 | 359 | 365 | PF00018 | 0.768 |
LIG_SH3_3 | 367 | 373 | PF00018 | 0.603 |
LIG_SH3_3 | 433 | 439 | PF00018 | 0.581 |
LIG_SH3_3 | 460 | 466 | PF00018 | 0.581 |
LIG_SH3_3 | 487 | 493 | PF00018 | 0.450 |
LIG_SH3_3 | 508 | 514 | PF00018 | 0.548 |
LIG_SH3_3 | 66 | 72 | PF00018 | 0.593 |
LIG_SH3_3 | 774 | 780 | PF00018 | 0.714 |
LIG_TRAF2_1 | 702 | 705 | PF00917 | 0.726 |
LIG_TRFH_1 | 467 | 471 | PF08558 | 0.548 |
LIG_WW_2 | 339 | 342 | PF00397 | 0.697 |
LIG_WW_3 | 37 | 41 | PF00397 | 0.616 |
LIG_WW_3 | 491 | 495 | PF00397 | 0.505 |
MOD_CDC14_SPxK_1 | 215 | 218 | PF00782 | 0.730 |
MOD_CDK_SPK_2 | 288 | 293 | PF00069 | 0.597 |
MOD_CDK_SPK_2 | 520 | 525 | PF00069 | 0.494 |
MOD_CDK_SPxK_1 | 212 | 218 | PF00069 | 0.713 |
MOD_CDK_SPxxK_3 | 467 | 474 | PF00069 | 0.526 |
MOD_CDK_SPxxK_3 | 717 | 724 | PF00069 | 0.670 |
MOD_CK1_1 | 114 | 120 | PF00069 | 0.547 |
MOD_CK1_1 | 258 | 264 | PF00069 | 0.704 |
MOD_CK1_1 | 276 | 282 | PF00069 | 0.484 |
MOD_CK1_1 | 288 | 294 | PF00069 | 0.643 |
MOD_CK1_1 | 381 | 387 | PF00069 | 0.701 |
MOD_CK1_1 | 396 | 402 | PF00069 | 0.609 |
MOD_CK1_1 | 523 | 529 | PF00069 | 0.531 |
MOD_CK1_1 | 720 | 726 | PF00069 | 0.710 |
MOD_CK1_1 | 733 | 739 | PF00069 | 0.563 |
MOD_CK1_1 | 742 | 748 | PF00069 | 0.643 |
MOD_CK1_1 | 750 | 756 | PF00069 | 0.662 |
MOD_CK1_1 | 761 | 767 | PF00069 | 0.774 |
MOD_CK1_1 | 768 | 774 | PF00069 | 0.772 |
MOD_CK1_1 | 795 | 801 | PF00069 | 0.713 |
MOD_CK2_1 | 117 | 123 | PF00069 | 0.660 |
MOD_CK2_1 | 135 | 141 | PF00069 | 0.442 |
MOD_CK2_1 | 176 | 182 | PF00069 | 0.606 |
MOD_CK2_1 | 649 | 655 | PF00069 | 0.514 |
MOD_CK2_1 | 687 | 693 | PF00069 | 0.644 |
MOD_CK2_1 | 787 | 793 | PF00069 | 0.675 |
MOD_Cter_Amidation | 479 | 482 | PF01082 | 0.381 |
MOD_Cter_Amidation | 501 | 504 | PF01082 | 0.337 |
MOD_GlcNHglycan | 113 | 116 | PF01048 | 0.587 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.533 |
MOD_GlcNHglycan | 287 | 290 | PF01048 | 0.739 |
MOD_GlcNHglycan | 359 | 362 | PF01048 | 0.805 |
MOD_GlcNHglycan | 366 | 369 | PF01048 | 0.768 |
MOD_GlcNHglycan | 380 | 383 | PF01048 | 0.619 |
MOD_GlcNHglycan | 396 | 399 | PF01048 | 0.625 |
MOD_GlcNHglycan | 471 | 474 | PF01048 | 0.338 |
MOD_GlcNHglycan | 487 | 490 | PF01048 | 0.244 |
MOD_GlcNHglycan | 499 | 502 | PF01048 | 0.389 |
MOD_GlcNHglycan | 525 | 528 | PF01048 | 0.359 |
MOD_GlcNHglycan | 578 | 581 | PF01048 | 0.381 |
MOD_GlcNHglycan | 714 | 717 | PF01048 | 0.689 |
MOD_GlcNHglycan | 732 | 736 | PF01048 | 0.522 |
MOD_GlcNHglycan | 770 | 773 | PF01048 | 0.663 |
MOD_GlcNHglycan | 789 | 792 | PF01048 | 0.511 |
MOD_GSK3_1 | 114 | 121 | PF00069 | 0.458 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.682 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.589 |
MOD_GSK3_1 | 254 | 261 | PF00069 | 0.703 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.695 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.637 |
MOD_GSK3_1 | 381 | 388 | PF00069 | 0.680 |
MOD_GSK3_1 | 547 | 554 | PF00069 | 0.501 |
MOD_GSK3_1 | 672 | 679 | PF00069 | 0.632 |
MOD_GSK3_1 | 726 | 733 | PF00069 | 0.636 |
MOD_GSK3_1 | 735 | 742 | PF00069 | 0.648 |
MOD_GSK3_1 | 743 | 750 | PF00069 | 0.641 |
MOD_GSK3_1 | 754 | 761 | PF00069 | 0.753 |
MOD_GSK3_1 | 764 | 771 | PF00069 | 0.570 |
MOD_GSK3_1 | 795 | 802 | PF00069 | 0.642 |
MOD_LATS_1 | 589 | 595 | PF00433 | 0.548 |
MOD_NEK2_1 | 191 | 196 | PF00069 | 0.644 |
MOD_NEK2_2 | 426 | 431 | PF00069 | 0.581 |
MOD_PIKK_1 | 410 | 416 | PF00454 | 0.517 |
MOD_PIKK_1 | 536 | 542 | PF00454 | 0.495 |
MOD_PKA_1 | 576 | 582 | PF00069 | 0.581 |
MOD_PKA_1 | 765 | 771 | PF00069 | 0.675 |
MOD_PKA_2 | 111 | 117 | PF00069 | 0.515 |
MOD_PKA_2 | 118 | 124 | PF00069 | 0.444 |
MOD_PKA_2 | 195 | 201 | PF00069 | 0.587 |
MOD_PKA_2 | 292 | 298 | PF00069 | 0.585 |
MOD_PKA_2 | 484 | 490 | PF00069 | 0.519 |
MOD_PKA_2 | 529 | 535 | PF00069 | 0.581 |
MOD_PKA_2 | 576 | 582 | PF00069 | 0.581 |
MOD_PKA_2 | 604 | 610 | PF00069 | 0.505 |
MOD_PKA_2 | 747 | 753 | PF00069 | 0.636 |
MOD_PKA_2 | 764 | 770 | PF00069 | 0.560 |
MOD_PKA_2 | 787 | 793 | PF00069 | 0.675 |
MOD_PKB_1 | 143 | 151 | PF00069 | 0.665 |
MOD_PKB_1 | 153 | 161 | PF00069 | 0.525 |
MOD_Plk_1 | 551 | 557 | PF00069 | 0.537 |
MOD_Plk_1 | 687 | 693 | PF00069 | 0.728 |
MOD_Plk_1 | 795 | 801 | PF00069 | 0.713 |
MOD_Plk_4 | 71 | 77 | PF00069 | 0.559 |
MOD_ProDKin_1 | 210 | 216 | PF00069 | 0.703 |
MOD_ProDKin_1 | 221 | 227 | PF00069 | 0.489 |
MOD_ProDKin_1 | 258 | 264 | PF00069 | 0.704 |
MOD_ProDKin_1 | 273 | 279 | PF00069 | 0.531 |
MOD_ProDKin_1 | 288 | 294 | PF00069 | 0.608 |
MOD_ProDKin_1 | 303 | 309 | PF00069 | 0.689 |
MOD_ProDKin_1 | 381 | 387 | PF00069 | 0.681 |
MOD_ProDKin_1 | 467 | 473 | PF00069 | 0.548 |
MOD_ProDKin_1 | 495 | 501 | PF00069 | 0.552 |
MOD_ProDKin_1 | 507 | 513 | PF00069 | 0.510 |
MOD_ProDKin_1 | 520 | 526 | PF00069 | 0.472 |
MOD_ProDKin_1 | 65 | 71 | PF00069 | 0.579 |
MOD_ProDKin_1 | 666 | 672 | PF00069 | 0.571 |
MOD_ProDKin_1 | 695 | 701 | PF00069 | 0.681 |
MOD_ProDKin_1 | 717 | 723 | PF00069 | 0.704 |
MOD_ProDKin_1 | 754 | 760 | PF00069 | 0.708 |
MOD_SUMO_rev_2 | 472 | 479 | PF00179 | 0.559 |
MOD_SUMO_rev_2 | 704 | 709 | PF00179 | 0.674 |
TRG_DiLeu_BaEn_1 | 31 | 36 | PF01217 | 0.687 |
TRG_DiLeu_BaEn_2 | 186 | 192 | PF01217 | 0.593 |
TRG_DiLeu_BaLyEn_6 | 206 | 211 | PF01217 | 0.686 |
TRG_ENDOCYTIC_2 | 79 | 82 | PF00928 | 0.484 |
TRG_ER_diArg_1 | 100 | 103 | PF00400 | 0.565 |
TRG_ER_diArg_1 | 142 | 145 | PF00400 | 0.654 |
TRG_ER_diArg_1 | 152 | 155 | PF00400 | 0.634 |
TRG_ER_diArg_1 | 183 | 186 | PF00400 | 0.644 |
TRG_ER_diArg_1 | 39 | 42 | PF00400 | 0.547 |
TRG_ER_diArg_1 | 421 | 423 | PF00400 | 0.537 |
TRG_ER_diArg_1 | 481 | 483 | PF00400 | 0.505 |
TRG_ER_diArg_1 | 493 | 495 | PF00400 | 0.524 |
TRG_ER_diArg_1 | 574 | 577 | PF00400 | 0.517 |
TRG_NLS_MonoExtC_3 | 22 | 27 | PF00514 | 0.470 |
TRG_NLS_MonoExtN_4 | 20 | 27 | PF00514 | 0.466 |
TRG_NLS_MonoExtN_4 | 572 | 579 | PF00514 | 0.537 |
TRG_Pf-PMV_PEXEL_1 | 591 | 595 | PF00026 | 0.381 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A1X0NTK5 | Trypanosomatidae | 34% | 98% |
A4HKY6 | Leishmania braziliensis | 73% | 100% |
A4I8G7 | Leishmania infantum | 99% | 100% |
E9B3C6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
E9B3C7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4Q4S9 | Leishmania major | 91% | 100% |