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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: Q4Q7Z8
Term | Name | Level | Count |
---|---|---|---|
GO:0006777 | Mo-molybdopterin cofactor biosynthetic process | 5 | 6 |
GO:0006793 | phosphorus metabolic process | 3 | 6 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 6 |
GO:0006807 | nitrogen compound metabolic process | 2 | 6 |
GO:0008152 | metabolic process | 1 | 6 |
GO:0009058 | biosynthetic process | 2 | 6 |
GO:0009987 | cellular process | 1 | 6 |
GO:0018130 | heterocycle biosynthetic process | 4 | 6 |
GO:0019637 | organophosphate metabolic process | 3 | 6 |
GO:0019720 | Mo-molybdopterin cofactor metabolic process | 4 | 6 |
GO:0032324 | molybdopterin cofactor biosynthetic process | 4 | 6 |
GO:0043545 | molybdopterin cofactor metabolic process | 3 | 6 |
GO:0044237 | cellular metabolic process | 2 | 6 |
GO:0044249 | cellular biosynthetic process | 3 | 6 |
GO:0046483 | heterocycle metabolic process | 3 | 6 |
GO:0051189 | prosthetic group metabolic process | 2 | 6 |
GO:0071704 | organic substance metabolic process | 2 | 6 |
GO:0090407 | organophosphate biosynthetic process | 4 | 6 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 6 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 6 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 6 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 6 |
GO:1901576 | organic substance biosynthetic process | 3 | 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 2 |
GO:0016829 | lyase activity | 2 | 2 |
GO:0016830 | carbon-carbon lyase activity | 3 | 2 |
GO:0016849 | phosphorus-oxygen lyase activity | 3 | 2 |
GO:0061798 | GTP 3',8'-cyclase activity | 4 | 2 |
GO:0061799 | cyclic pyranopterin monophosphate synthase activity | 4 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 288 | 292 | PF00656 | 0.796 |
CLV_C14_Caspase3-7 | 556 | 560 | PF00656 | 0.624 |
CLV_C14_Caspase3-7 | 588 | 592 | PF00656 | 0.623 |
CLV_C14_Caspase3-7 | 651 | 655 | PF00656 | 0.657 |
CLV_C14_Caspase3-7 | 703 | 707 | PF00656 | 0.765 |
CLV_NRD_NRD_1 | 277 | 279 | PF00675 | 0.684 |
CLV_NRD_NRD_1 | 318 | 320 | PF00675 | 0.820 |
CLV_NRD_NRD_1 | 404 | 406 | PF00675 | 0.840 |
CLV_NRD_NRD_1 | 428 | 430 | PF00675 | 0.786 |
CLV_NRD_NRD_1 | 499 | 501 | PF00675 | 0.840 |
CLV_NRD_NRD_1 | 574 | 576 | PF00675 | 0.850 |
CLV_NRD_NRD_1 | 586 | 588 | PF00675 | 0.661 |
CLV_NRD_NRD_1 | 604 | 606 | PF00675 | 0.647 |
CLV_NRD_NRD_1 | 614 | 616 | PF00675 | 0.682 |
CLV_NRD_NRD_1 | 664 | 666 | PF00675 | 0.847 |
CLV_NRD_NRD_1 | 746 | 748 | PF00675 | 0.847 |
CLV_NRD_NRD_1 | 76 | 78 | PF00675 | 0.529 |
CLV_NRD_NRD_1 | 96 | 98 | PF00675 | 0.199 |
CLV_PCSK_KEX2_1 | 167 | 169 | PF00082 | 0.529 |
CLV_PCSK_KEX2_1 | 273 | 275 | PF00082 | 0.700 |
CLV_PCSK_KEX2_1 | 277 | 279 | PF00082 | 0.665 |
CLV_PCSK_KEX2_1 | 310 | 312 | PF00082 | 0.661 |
CLV_PCSK_KEX2_1 | 318 | 320 | PF00082 | 0.801 |
CLV_PCSK_KEX2_1 | 404 | 406 | PF00082 | 0.834 |
CLV_PCSK_KEX2_1 | 428 | 430 | PF00082 | 0.786 |
CLV_PCSK_KEX2_1 | 498 | 500 | PF00082 | 0.854 |
CLV_PCSK_KEX2_1 | 525 | 527 | PF00082 | 0.853 |
CLV_PCSK_KEX2_1 | 532 | 534 | PF00082 | 0.726 |
CLV_PCSK_KEX2_1 | 586 | 588 | PF00082 | 0.822 |
CLV_PCSK_KEX2_1 | 663 | 665 | PF00082 | 0.849 |
CLV_PCSK_KEX2_1 | 679 | 681 | PF00082 | 0.601 |
CLV_PCSK_KEX2_1 | 75 | 77 | PF00082 | 0.529 |
CLV_PCSK_KEX2_1 | 755 | 757 | PF00082 | 0.827 |
CLV_PCSK_KEX2_1 | 760 | 762 | PF00082 | 0.736 |
CLV_PCSK_KEX2_1 | 95 | 97 | PF00082 | 0.199 |
CLV_PCSK_PC1ET2_1 | 167 | 169 | PF00082 | 0.529 |
CLV_PCSK_PC1ET2_1 | 273 | 275 | PF00082 | 0.840 |
CLV_PCSK_PC1ET2_1 | 310 | 312 | PF00082 | 0.762 |
CLV_PCSK_PC1ET2_1 | 498 | 500 | PF00082 | 0.854 |
CLV_PCSK_PC1ET2_1 | 525 | 527 | PF00082 | 0.853 |
CLV_PCSK_PC1ET2_1 | 532 | 534 | PF00082 | 0.726 |
CLV_PCSK_PC1ET2_1 | 679 | 681 | PF00082 | 0.638 |
CLV_PCSK_PC1ET2_1 | 755 | 757 | PF00082 | 0.827 |
CLV_PCSK_PC1ET2_1 | 760 | 762 | PF00082 | 0.736 |
CLV_PCSK_PC7_1 | 756 | 762 | PF00082 | 0.821 |
CLV_PCSK_PC7_1 | 91 | 97 | PF00082 | 0.529 |
CLV_PCSK_SKI1_1 | 2 | 6 | PF00082 | 0.699 |
CLV_PCSK_SKI1_1 | 234 | 238 | PF00082 | 0.660 |
CLV_PCSK_SKI1_1 | 435 | 439 | PF00082 | 0.846 |
CLV_PCSK_SKI1_1 | 748 | 752 | PF00082 | 0.846 |
CLV_PCSK_SKI1_1 | 77 | 81 | PF00082 | 0.529 |
CLV_PCSK_SKI1_1 | 91 | 95 | PF00082 | 0.298 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.720 |
DEG_SCF_FBW7_1 | 7 | 13 | PF00400 | 0.817 |
DEG_SPOP_SBC_1 | 473 | 477 | PF00917 | 0.862 |
DOC_CKS1_1 | 334 | 339 | PF01111 | 0.743 |
DOC_CKS1_1 | 4 | 9 | PF01111 | 0.828 |
DOC_CKS1_1 | 63 | 68 | PF01111 | 0.467 |
DOC_CYCLIN_yCln2_LP_2 | 327 | 330 | PF00134 | 0.785 |
DOC_CYCLIN_yCln2_LP_2 | 4 | 10 | PF00134 | 0.825 |
DOC_MAPK_DCC_7 | 19 | 28 | PF00069 | 0.510 |
DOC_MAPK_FxFP_2 | 61 | 64 | PF00069 | 0.467 |
DOC_MAPK_MEF2A_6 | 19 | 28 | PF00069 | 0.510 |
DOC_PP2B_LxvP_1 | 327 | 330 | PF13499 | 0.785 |
DOC_PP2B_LxvP_1 | 80 | 83 | PF13499 | 0.529 |
DOC_PP4_FxxP_1 | 61 | 64 | PF00568 | 0.467 |
DOC_USP7_MATH_1 | 103 | 107 | PF00917 | 0.492 |
DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.688 |
DOC_USP7_MATH_1 | 222 | 226 | PF00917 | 0.787 |
DOC_USP7_MATH_1 | 350 | 354 | PF00917 | 0.771 |
DOC_USP7_MATH_1 | 408 | 412 | PF00917 | 0.728 |
DOC_USP7_MATH_1 | 437 | 441 | PF00917 | 0.784 |
DOC_USP7_MATH_1 | 443 | 447 | PF00917 | 0.688 |
DOC_USP7_MATH_1 | 596 | 600 | PF00917 | 0.706 |
DOC_USP7_UBL2_3 | 373 | 377 | PF12436 | 0.705 |
DOC_USP7_UBL2_3 | 667 | 671 | PF12436 | 0.859 |
DOC_USP7_UBL2_3 | 748 | 752 | PF12436 | 0.859 |
DOC_WW_Pin1_4 | 199 | 204 | PF00397 | 0.640 |
DOC_WW_Pin1_4 | 220 | 225 | PF00397 | 0.735 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.833 |
DOC_WW_Pin1_4 | 328 | 333 | PF00397 | 0.833 |
DOC_WW_Pin1_4 | 336 | 341 | PF00397 | 0.722 |
DOC_WW_Pin1_4 | 610 | 615 | PF00397 | 0.791 |
DOC_WW_Pin1_4 | 62 | 67 | PF00397 | 0.526 |
DOC_WW_Pin1_4 | 738 | 743 | PF00397 | 0.666 |
LIG_14-3-3_CanoR_1 | 234 | 239 | PF00244 | 0.742 |
LIG_14-3-3_CanoR_1 | 384 | 393 | PF00244 | 0.699 |
LIG_14-3-3_CanoR_1 | 428 | 436 | PF00244 | 0.677 |
LIG_14-3-3_CanoR_1 | 499 | 509 | PF00244 | 0.748 |
LIG_14-3-3_CanoR_1 | 595 | 601 | PF00244 | 0.660 |
LIG_14-3-3_CanoR_1 | 618 | 626 | PF00244 | 0.789 |
LIG_14-3-3_CanoR_1 | 69 | 75 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 95 | 101 | PF00244 | 0.529 |
LIG_BIR_III_4 | 239 | 243 | PF00653 | 0.784 |
LIG_BRCT_BRCA1_1 | 12 | 16 | PF00533 | 0.654 |
LIG_BRCT_BRCA1_1 | 596 | 600 | PF00533 | 0.745 |
LIG_BRCT_BRCA1_1 | 70 | 74 | PF00533 | 0.454 |
LIG_deltaCOP1_diTrp_1 | 690 | 696 | PF00928 | 0.855 |
LIG_Dynein_DLC8_1 | 523 | 529 | PF01221 | 0.786 |
LIG_FHA_1 | 173 | 179 | PF00498 | 0.738 |
LIG_FHA_1 | 362 | 368 | PF00498 | 0.594 |
LIG_FHA_1 | 394 | 400 | PF00498 | 0.848 |
LIG_FHA_1 | 407 | 413 | PF00498 | 0.630 |
LIG_FHA_1 | 41 | 47 | PF00498 | 0.389 |
LIG_FHA_2 | 139 | 145 | PF00498 | 0.529 |
LIG_FHA_2 | 283 | 289 | PF00498 | 0.792 |
LIG_FHA_2 | 477 | 483 | PF00498 | 0.763 |
LIG_FHA_2 | 586 | 592 | PF00498 | 0.624 |
LIG_FHA_2 | 725 | 731 | PF00498 | 0.839 |
LIG_LIR_Gen_1 | 109 | 116 | PF02991 | 0.529 |
LIG_LIR_Gen_1 | 141 | 150 | PF02991 | 0.529 |
LIG_LIR_Gen_1 | 173 | 182 | PF02991 | 0.756 |
LIG_LIR_Nem_3 | 109 | 113 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 141 | 146 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 173 | 177 | PF02991 | 0.715 |
LIG_NRP_CendR_1 | 760 | 762 | PF00754 | 0.840 |
LIG_Pex14_1 | 692 | 696 | PF04695 | 0.858 |
LIG_RPA_C_Fungi | 660 | 672 | PF08784 | 0.794 |
LIG_SH2_CRK | 110 | 114 | PF00017 | 0.529 |
LIG_SH2_CRK | 143 | 147 | PF00017 | 0.529 |
LIG_SH2_STAP1 | 110 | 114 | PF00017 | 0.529 |
LIG_SH2_STAT5 | 114 | 117 | PF00017 | 0.529 |
LIG_SH2_STAT5 | 33 | 36 | PF00017 | 0.529 |
LIG_SH2_STAT5 | 534 | 537 | PF00017 | 0.833 |
LIG_SH3_1 | 326 | 332 | PF00018 | 0.786 |
LIG_SH3_2 | 675 | 680 | PF14604 | 0.783 |
LIG_SH3_2 | 742 | 747 | PF14604 | 0.824 |
LIG_SH3_3 | 179 | 185 | PF00018 | 0.810 |
LIG_SH3_3 | 18 | 24 | PF00018 | 0.563 |
LIG_SH3_3 | 210 | 216 | PF00018 | 0.778 |
LIG_SH3_3 | 326 | 332 | PF00018 | 0.689 |
LIG_SH3_3 | 334 | 340 | PF00018 | 0.642 |
LIG_SH3_3 | 4 | 10 | PF00018 | 0.825 |
LIG_SH3_3 | 672 | 678 | PF00018 | 0.783 |
LIG_SH3_3 | 737 | 743 | PF00018 | 0.830 |
LIG_SH3_3 | 76 | 82 | PF00018 | 0.529 |
LIG_SH3_CIN85_PxpxPR_1 | 742 | 747 | PF14604 | 0.601 |
LIG_SUMO_SIM_anti_2 | 25 | 31 | PF11976 | 0.758 |
LIG_TRAF2_1 | 258 | 261 | PF00917 | 0.857 |
LIG_TRAF2_1 | 263 | 266 | PF00917 | 0.760 |
LIG_TRAF2_1 | 418 | 421 | PF00917 | 0.794 |
LIG_TRAF2_1 | 462 | 465 | PF00917 | 0.803 |
LIG_TRAF2_1 | 469 | 472 | PF00917 | 0.708 |
LIG_TRAF2_1 | 544 | 547 | PF00917 | 0.784 |
LIG_TRAF2_1 | 634 | 637 | PF00917 | 0.786 |
LIG_TRAF2_1 | 716 | 719 | PF00917 | 0.739 |
LIG_WW_3 | 744 | 748 | PF00397 | 0.790 |
LIG_WW_3 | 81 | 85 | PF00397 | 0.529 |
MOD_CDK_SPK_2 | 610 | 615 | PF00069 | 0.791 |
MOD_CDK_SPxK_1 | 610 | 616 | PF00069 | 0.792 |
MOD_CDK_SPxxK_3 | 336 | 343 | PF00069 | 0.747 |
MOD_CDK_SPxxK_3 | 62 | 69 | PF00069 | 0.467 |
MOD_CK1_1 | 202 | 208 | PF00069 | 0.601 |
MOD_CK1_1 | 225 | 231 | PF00069 | 0.817 |
MOD_CK1_1 | 339 | 345 | PF00069 | 0.826 |
MOD_CK1_1 | 351 | 357 | PF00069 | 0.624 |
MOD_CK1_1 | 376 | 382 | PF00069 | 0.834 |
MOD_CK1_1 | 431 | 437 | PF00069 | 0.621 |
MOD_CK1_1 | 520 | 526 | PF00069 | 0.714 |
MOD_CK1_1 | 697 | 703 | PF00069 | 0.840 |
MOD_CK2_1 | 103 | 109 | PF00069 | 0.467 |
MOD_CK2_1 | 155 | 161 | PF00069 | 0.529 |
MOD_CK2_1 | 177 | 183 | PF00069 | 0.736 |
MOD_CK2_1 | 24 | 30 | PF00069 | 0.759 |
MOD_CK2_1 | 303 | 309 | PF00069 | 0.779 |
MOD_CK2_1 | 353 | 359 | PF00069 | 0.680 |
MOD_CK2_1 | 408 | 414 | PF00069 | 0.669 |
MOD_CK2_1 | 443 | 449 | PF00069 | 0.783 |
MOD_CK2_1 | 630 | 636 | PF00069 | 0.792 |
MOD_CK2_1 | 724 | 730 | PF00069 | 0.839 |
MOD_Cter_Amidation | 523 | 526 | PF01082 | 0.851 |
MOD_Cter_Amidation | 584 | 587 | PF01082 | 0.855 |
MOD_Cter_Amidation | 603 | 606 | PF01082 | 0.539 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.731 |
MOD_GlcNHglycan | 188 | 191 | PF01048 | 0.826 |
MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.792 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.755 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.515 |
MOD_GlcNHglycan | 244 | 247 | PF01048 | 0.548 |
MOD_GlcNHglycan | 269 | 272 | PF01048 | 0.761 |
MOD_GlcNHglycan | 291 | 295 | PF01048 | 0.840 |
MOD_GlcNHglycan | 350 | 353 | PF01048 | 0.804 |
MOD_GlcNHglycan | 355 | 358 | PF01048 | 0.730 |
MOD_GlcNHglycan | 387 | 390 | PF01048 | 0.779 |
MOD_GlcNHglycan | 439 | 442 | PF01048 | 0.842 |
MOD_GlcNHglycan | 445 | 448 | PF01048 | 0.741 |
MOD_GlcNHglycan | 522 | 525 | PF01048 | 0.799 |
MOD_GlcNHglycan | 568 | 571 | PF01048 | 0.730 |
MOD_GlcNHglycan | 602 | 605 | PF01048 | 0.815 |
MOD_GlcNHglycan | 619 | 622 | PF01048 | 0.577 |
MOD_GlcNHglycan | 629 | 635 | PF01048 | 0.689 |
MOD_GlcNHglycan | 657 | 660 | PF01048 | 0.756 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.302 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.828 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.795 |
MOD_GSK3_1 | 339 | 346 | PF00069 | 0.800 |
MOD_GSK3_1 | 427 | 434 | PF00069 | 0.807 |
MOD_GSK3_1 | 472 | 479 | PF00069 | 0.863 |
MOD_GSK3_1 | 499 | 506 | PF00069 | 0.833 |
MOD_GSK3_1 | 508 | 515 | PF00069 | 0.712 |
MOD_GSK3_1 | 520 | 527 | PF00069 | 0.627 |
MOD_GSK3_1 | 581 | 588 | PF00069 | 0.779 |
MOD_GSK3_1 | 596 | 603 | PF00069 | 0.680 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.735 |
MOD_N-GLC_1 | 431 | 436 | PF02516 | 0.850 |
MOD_NEK2_1 | 136 | 141 | PF00069 | 0.411 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.826 |
MOD_NEK2_1 | 40 | 45 | PF00069 | 0.389 |
MOD_NEK2_1 | 600 | 605 | PF00069 | 0.752 |
MOD_NEK2_2 | 138 | 143 | PF00069 | 0.529 |
MOD_NEK2_2 | 408 | 413 | PF00069 | 0.627 |
MOD_NEK2_2 | 70 | 75 | PF00069 | 0.378 |
MOD_PIKK_1 | 524 | 530 | PF00454 | 0.782 |
MOD_PIKK_1 | 694 | 700 | PF00454 | 0.630 |
MOD_PKA_1 | 428 | 434 | PF00069 | 0.622 |
MOD_PKA_1 | 499 | 505 | PF00069 | 0.849 |
MOD_PKA_1 | 95 | 101 | PF00069 | 0.529 |
MOD_PKA_2 | 303 | 309 | PF00069 | 0.717 |
MOD_PKA_2 | 427 | 433 | PF00069 | 0.665 |
MOD_PKA_2 | 499 | 505 | PF00069 | 0.849 |
MOD_PKA_2 | 585 | 591 | PF00069 | 0.683 |
MOD_PKA_2 | 594 | 600 | PF00069 | 0.578 |
MOD_PKA_2 | 617 | 623 | PF00069 | 0.845 |
MOD_PKA_2 | 68 | 74 | PF00069 | 0.529 |
MOD_PKA_2 | 95 | 101 | PF00069 | 0.529 |
MOD_PKB_1 | 343 | 351 | PF00069 | 0.790 |
MOD_PKB_1 | 382 | 390 | PF00069 | 0.615 |
MOD_Plk_1 | 108 | 114 | PF00069 | 0.529 |
MOD_Plk_1 | 431 | 437 | PF00069 | 0.847 |
MOD_Plk_2-3 | 155 | 161 | PF00069 | 0.529 |
MOD_Plk_2-3 | 549 | 555 | PF00069 | 0.623 |
MOD_Plk_4 | 108 | 114 | PF00069 | 0.529 |
MOD_Plk_4 | 138 | 144 | PF00069 | 0.529 |
MOD_Plk_4 | 24 | 30 | PF00069 | 0.759 |
MOD_Plk_4 | 376 | 382 | PF00069 | 0.834 |
MOD_Plk_4 | 517 | 523 | PF00069 | 0.625 |
MOD_Plk_4 | 54 | 60 | PF00069 | 0.465 |
MOD_ProDKin_1 | 199 | 205 | PF00069 | 0.642 |
MOD_ProDKin_1 | 220 | 226 | PF00069 | 0.734 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.831 |
MOD_ProDKin_1 | 328 | 334 | PF00069 | 0.832 |
MOD_ProDKin_1 | 336 | 342 | PF00069 | 0.725 |
MOD_ProDKin_1 | 610 | 616 | PF00069 | 0.792 |
MOD_ProDKin_1 | 62 | 68 | PF00069 | 0.526 |
MOD_ProDKin_1 | 738 | 744 | PF00069 | 0.664 |
TRG_ENDOCYTIC_2 | 110 | 113 | PF00928 | 0.529 |
TRG_ENDOCYTIC_2 | 143 | 146 | PF00928 | 0.529 |
TRG_ER_diArg_1 | 276 | 278 | PF00400 | 0.698 |
TRG_ER_diArg_1 | 317 | 319 | PF00400 | 0.808 |
TRG_ER_diArg_1 | 404 | 406 | PF00400 | 0.834 |
TRG_ER_diArg_1 | 433 | 436 | PF00400 | 0.838 |
TRG_ER_diArg_1 | 663 | 665 | PF00400 | 0.787 |
TRG_ER_diArg_1 | 74 | 77 | PF00400 | 0.529 |
TRG_ER_diArg_1 | 94 | 97 | PF00400 | 0.199 |
TRG_NES_CRM1_1 | 130 | 144 | PF08389 | 0.529 |
TRG_NLS_Bipartite_1 | 605 | 619 | PF00514 | 0.855 |
TRG_NLS_MonoCore_2 | 496 | 501 | PF00514 | 0.854 |
TRG_NLS_MonoExtC_3 | 746 | 751 | PF00514 | 0.853 |
TRG_NLS_MonoExtN_4 | 497 | 502 | PF00514 | 0.849 |
TRG_NLS_MonoExtN_4 | 614 | 619 | PF00514 | 0.852 |
TRG_NLS_MonoExtN_4 | 744 | 751 | PF00514 | 0.836 |
TRG_Pf-PMV_PEXEL_1 | 184 | 188 | PF00026 | 0.781 |
TRG_Pf-PMV_PEXEL_1 | 310 | 314 | PF00026 | 0.764 |
TRG_Pf-PMV_PEXEL_1 | 533 | 537 | PF00026 | 0.715 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IDC7 | Leishmania donovani | 90% | 100% |
A4HGW7 | Leishmania braziliensis | 67% | 100% |
A4I3Z7 | Leishmania infantum | 90% | 85% |
E9B087 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |