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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0005730 | nucleolus | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4H9M1
Term | Name | Level | Count |
---|---|---|---|
GO:0001510 | RNA methylation | 4 | 12 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009451 | RNA modification | 5 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016070 | RNA metabolic process | 5 | 12 |
GO:0032259 | methylation | 2 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043412 | macromolecule modification | 4 | 12 |
GO:0043414 | macromolecule methylation | 3 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0090304 | nucleic acid metabolic process | 4 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003723 | RNA binding | 4 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0008168 | methyltransferase activity | 4 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 28 | 32 | PF00656 | 0.350 |
CLV_C14_Caspase3-7 | 59 | 63 | PF00656 | 0.643 |
CLV_C14_Caspase3-7 | 64 | 68 | PF00656 | 0.551 |
CLV_MEL_PAP_1 | 677 | 683 | PF00089 | 0.447 |
CLV_NRD_NRD_1 | 11 | 13 | PF00675 | 0.570 |
CLV_NRD_NRD_1 | 133 | 135 | PF00675 | 0.567 |
CLV_NRD_NRD_1 | 186 | 188 | PF00675 | 0.659 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.635 |
CLV_NRD_NRD_1 | 399 | 401 | PF00675 | 0.240 |
CLV_NRD_NRD_1 | 527 | 529 | PF00675 | 0.248 |
CLV_NRD_NRD_1 | 609 | 611 | PF00675 | 0.380 |
CLV_NRD_NRD_1 | 674 | 676 | PF00675 | 0.374 |
CLV_NRD_NRD_1 | 7 | 9 | PF00675 | 0.602 |
CLV_NRD_NRD_1 | 99 | 101 | PF00675 | 0.477 |
CLV_PCSK_FUR_1 | 345 | 349 | PF00082 | 0.260 |
CLV_PCSK_KEX2_1 | 132 | 134 | PF00082 | 0.562 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.636 |
CLV_PCSK_KEX2_1 | 347 | 349 | PF00082 | 0.260 |
CLV_PCSK_KEX2_1 | 609 | 611 | PF00082 | 0.380 |
CLV_PCSK_KEX2_1 | 7 | 9 | PF00082 | 0.581 |
CLV_PCSK_KEX2_1 | 99 | 101 | PF00082 | 0.477 |
CLV_PCSK_PC1ET2_1 | 2 | 4 | PF00082 | 0.655 |
CLV_PCSK_PC1ET2_1 | 347 | 349 | PF00082 | 0.260 |
CLV_PCSK_PC7_1 | 3 | 9 | PF00082 | 0.657 |
CLV_PCSK_SKI1_1 | 224 | 228 | PF00082 | 0.477 |
CLV_PCSK_SKI1_1 | 325 | 329 | PF00082 | 0.335 |
CLV_PCSK_SKI1_1 | 422 | 426 | PF00082 | 0.268 |
CLV_PCSK_SKI1_1 | 497 | 501 | PF00082 | 0.220 |
CLV_PCSK_SKI1_1 | 528 | 532 | PF00082 | 0.499 |
CLV_PCSK_SKI1_1 | 610 | 614 | PF00082 | 0.357 |
CLV_PCSK_SKI1_1 | 704 | 708 | PF00082 | 0.500 |
CLV_PCSK_SKI1_1 | 77 | 81 | PF00082 | 0.400 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.685 |
DEG_ODPH_VHL_1 | 668 | 681 | PF01847 | 0.463 |
DOC_CKS1_1 | 201 | 206 | PF01111 | 0.466 |
DOC_CKS1_1 | 226 | 231 | PF01111 | 0.540 |
DOC_CKS1_1 | 553 | 558 | PF01111 | 0.280 |
DOC_CKS1_1 | 613 | 618 | PF01111 | 0.458 |
DOC_CYCLIN_RxL_1 | 422 | 434 | PF00134 | 0.473 |
DOC_CYCLIN_RxL_1 | 671 | 682 | PF00134 | 0.489 |
DOC_CYCLIN_RxL_1 | 74 | 84 | PF00134 | 0.278 |
DOC_CYCLIN_yCln2_LP_2 | 495 | 501 | PF00134 | 0.493 |
DOC_CYCLIN_yCln2_LP_2 | 553 | 559 | PF00134 | 0.504 |
DOC_CYCLIN_yCln2_LP_2 | 613 | 619 | PF00134 | 0.465 |
DOC_MAPK_gen_1 | 550 | 559 | PF00069 | 0.547 |
DOC_MAPK_gen_1 | 626 | 635 | PF00069 | 0.513 |
DOC_MAPK_HePTP_8 | 623 | 635 | PF00069 | 0.554 |
DOC_MAPK_MEF2A_6 | 626 | 635 | PF00069 | 0.492 |
DOC_PP1_RVXF_1 | 673 | 680 | PF00149 | 0.505 |
DOC_PP4_FxxP_1 | 667 | 670 | PF00568 | 0.515 |
DOC_USP7_MATH_1 | 178 | 182 | PF00917 | 0.621 |
DOC_USP7_MATH_1 | 240 | 244 | PF00917 | 0.493 |
DOC_USP7_MATH_1 | 56 | 60 | PF00917 | 0.750 |
DOC_USP7_MATH_1 | 586 | 590 | PF00917 | 0.546 |
DOC_USP7_MATH_1 | 63 | 67 | PF00917 | 0.504 |
DOC_USP7_UBL2_3 | 184 | 188 | PF12436 | 0.413 |
DOC_USP7_UBL2_3 | 333 | 337 | PF12436 | 0.449 |
DOC_USP7_UBL2_3 | 721 | 725 | PF12436 | 0.615 |
DOC_WW_Pin1_4 | 165 | 170 | PF00397 | 0.542 |
DOC_WW_Pin1_4 | 200 | 205 | PF00397 | 0.377 |
DOC_WW_Pin1_4 | 225 | 230 | PF00397 | 0.512 |
DOC_WW_Pin1_4 | 486 | 491 | PF00397 | 0.450 |
DOC_WW_Pin1_4 | 552 | 557 | PF00397 | 0.300 |
DOC_WW_Pin1_4 | 612 | 617 | PF00397 | 0.438 |
DOC_WW_Pin1_4 | 826 | 831 | PF00397 | 0.759 |
LIG_14-3-3_CanoR_1 | 100 | 108 | PF00244 | 0.451 |
LIG_14-3-3_CanoR_1 | 132 | 141 | PF00244 | 0.611 |
LIG_14-3-3_CanoR_1 | 210 | 218 | PF00244 | 0.454 |
LIG_14-3-3_CanoR_1 | 224 | 229 | PF00244 | 0.476 |
LIG_14-3-3_CanoR_1 | 266 | 276 | PF00244 | 0.444 |
LIG_14-3-3_CanoR_1 | 335 | 343 | PF00244 | 0.449 |
LIG_14-3-3_CanoR_1 | 403 | 413 | PF00244 | 0.484 |
LIG_14-3-3_CanoR_1 | 575 | 583 | PF00244 | 0.453 |
LIG_14-3-3_CanoR_1 | 813 | 817 | PF00244 | 0.609 |
LIG_Actin_WH2_2 | 467 | 484 | PF00022 | 0.427 |
LIG_Actin_WH2_2 | 594 | 611 | PF00022 | 0.290 |
LIG_APCC_ABBA_1 | 458 | 463 | PF00400 | 0.377 |
LIG_APCC_ABBA_1 | 512 | 517 | PF00400 | 0.449 |
LIG_BRCT_BRCA1_1 | 663 | 667 | PF00533 | 0.486 |
LIG_CSL_BTD_1 | 553 | 556 | PF09270 | 0.290 |
LIG_deltaCOP1_diTrp_1 | 191 | 197 | PF00928 | 0.400 |
LIG_deltaCOP1_diTrp_1 | 560 | 570 | PF00928 | 0.366 |
LIG_deltaCOP1_diTrp_1 | 67 | 71 | PF00928 | 0.303 |
LIG_Dynein_DLC8_1 | 335 | 341 | PF01221 | 0.489 |
LIG_FAT_LD_1 | 75 | 83 | PF03623 | 0.501 |
LIG_FHA_1 | 143 | 149 | PF00498 | 0.480 |
LIG_FHA_1 | 206 | 212 | PF00498 | 0.369 |
LIG_FHA_1 | 221 | 227 | PF00498 | 0.409 |
LIG_FHA_1 | 337 | 343 | PF00498 | 0.483 |
LIG_FHA_1 | 432 | 438 | PF00498 | 0.519 |
LIG_FHA_1 | 613 | 619 | PF00498 | 0.432 |
LIG_FHA_1 | 737 | 743 | PF00498 | 0.511 |
LIG_FHA_1 | 96 | 102 | PF00498 | 0.566 |
LIG_FHA_2 | 225 | 231 | PF00498 | 0.539 |
LIG_FHA_2 | 257 | 263 | PF00498 | 0.312 |
LIG_FHA_2 | 293 | 299 | PF00498 | 0.509 |
LIG_FHA_2 | 355 | 361 | PF00498 | 0.473 |
LIG_FHA_2 | 41 | 47 | PF00498 | 0.623 |
LIG_LIR_Apic_2 | 625 | 631 | PF02991 | 0.461 |
LIG_LIR_Apic_2 | 664 | 670 | PF02991 | 0.454 |
LIG_LIR_Gen_1 | 191 | 202 | PF02991 | 0.363 |
LIG_LIR_Gen_1 | 275 | 284 | PF02991 | 0.412 |
LIG_LIR_Gen_1 | 381 | 392 | PF02991 | 0.449 |
LIG_LIR_Gen_1 | 561 | 571 | PF02991 | 0.393 |
LIG_LIR_Gen_1 | 89 | 97 | PF02991 | 0.560 |
LIG_LIR_Nem_3 | 155 | 160 | PF02991 | 0.423 |
LIG_LIR_Nem_3 | 191 | 197 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 275 | 279 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 362 | 367 | PF02991 | 0.427 |
LIG_LIR_Nem_3 | 381 | 387 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 561 | 567 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 569 | 573 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 578 | 584 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 655 | 661 | PF02991 | 0.351 |
LIG_LIR_Nem_3 | 701 | 706 | PF02991 | 0.496 |
LIG_LIR_Nem_3 | 804 | 808 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 89 | 95 | PF02991 | 0.554 |
LIG_MYND_1 | 498 | 502 | PF01753 | 0.554 |
LIG_NRBOX | 729 | 735 | PF00104 | 0.613 |
LIG_NRBOX | 74 | 80 | PF00104 | 0.499 |
LIG_Pex14_1 | 364 | 368 | PF04695 | 0.473 |
LIG_Pex14_1 | 409 | 413 | PF04695 | 0.449 |
LIG_SH2_CRK | 349 | 353 | PF00017 | 0.473 |
LIG_SH2_CRK | 628 | 632 | PF00017 | 0.479 |
LIG_SH2_NCK_1 | 584 | 588 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 263 | 266 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 35 | 38 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 368 | 371 | PF00017 | 0.524 |
LIG_SH2_STAT5 | 413 | 416 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 696 | 699 | PF00017 | 0.528 |
LIG_SH3_3 | 231 | 237 | PF00018 | 0.434 |
LIG_SH3_3 | 369 | 375 | PF00018 | 0.500 |
LIG_SH3_3 | 495 | 501 | PF00018 | 0.512 |
LIG_SH3_3 | 527 | 533 | PF00018 | 0.509 |
LIG_SUMO_SIM_anti_2 | 462 | 469 | PF11976 | 0.449 |
LIG_SUMO_SIM_anti_2 | 710 | 715 | PF11976 | 0.390 |
LIG_SUMO_SIM_anti_2 | 738 | 744 | PF11976 | 0.536 |
LIG_SUMO_SIM_anti_2 | 76 | 82 | PF11976 | 0.521 |
LIG_SUMO_SIM_par_1 | 283 | 289 | PF11976 | 0.270 |
LIG_SUMO_SIM_par_1 | 610 | 615 | PF11976 | 0.280 |
LIG_SUMO_SIM_par_1 | 738 | 744 | PF11976 | 0.567 |
LIG_SUMO_SIM_par_1 | 78 | 85 | PF11976 | 0.444 |
LIG_TRAF2_1 | 180 | 183 | PF00917 | 0.440 |
LIG_TRAF2_1 | 275 | 278 | PF00917 | 0.364 |
LIG_TRAF2_1 | 744 | 747 | PF00917 | 0.614 |
LIG_TRAF2_1 | 830 | 833 | PF00917 | 0.788 |
LIG_TRFH_1 | 599 | 603 | PF08558 | 0.423 |
LIG_UBA3_1 | 22 | 30 | PF00899 | 0.324 |
LIG_WRC_WIRS_1 | 567 | 572 | PF05994 | 0.474 |
LIG_WRC_WIRS_1 | 802 | 807 | PF05994 | 0.459 |
LIG_WW_1 | 501 | 504 | PF00397 | 0.554 |
MOD_CDK_SPxxK_3 | 165 | 172 | PF00069 | 0.584 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.415 |
MOD_CK1_1 | 121 | 127 | PF00069 | 0.496 |
MOD_CK1_1 | 272 | 278 | PF00069 | 0.363 |
MOD_CK1_1 | 404 | 410 | PF00069 | 0.475 |
MOD_CK1_1 | 441 | 447 | PF00069 | 0.449 |
MOD_CK1_1 | 577 | 583 | PF00069 | 0.436 |
MOD_CK1_1 | 738 | 744 | PF00069 | 0.620 |
MOD_CK2_1 | 256 | 262 | PF00069 | 0.400 |
MOD_CK2_1 | 272 | 278 | PF00069 | 0.372 |
MOD_CK2_1 | 41 | 47 | PF00069 | 0.618 |
MOD_CK2_1 | 70 | 76 | PF00069 | 0.519 |
MOD_CK2_1 | 725 | 731 | PF00069 | 0.631 |
MOD_CK2_1 | 741 | 747 | PF00069 | 0.503 |
MOD_CK2_1 | 751 | 757 | PF00069 | 0.485 |
MOD_CK2_1 | 820 | 826 | PF00069 | 0.668 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.606 |
MOD_GlcNHglycan | 244 | 247 | PF01048 | 0.507 |
MOD_GlcNHglycan | 269 | 272 | PF01048 | 0.433 |
MOD_GlcNHglycan | 280 | 283 | PF01048 | 0.342 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.307 |
MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.283 |
MOD_GlcNHglycan | 393 | 396 | PF01048 | 0.249 |
MOD_GlcNHglycan | 409 | 412 | PF01048 | 0.249 |
MOD_GlcNHglycan | 57 | 61 | PF01048 | 0.693 |
MOD_GlcNHglycan | 590 | 593 | PF01048 | 0.522 |
MOD_GlcNHglycan | 663 | 666 | PF01048 | 0.374 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.334 |
MOD_GlcNHglycan | 725 | 728 | PF01048 | 0.393 |
MOD_GlcNHglycan | 780 | 783 | PF01048 | 0.363 |
MOD_GlcNHglycan | 784 | 787 | PF01048 | 0.407 |
MOD_GlcNHglycan | 822 | 825 | PF01048 | 0.726 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.410 |
MOD_GSK3_1 | 220 | 227 | PF00069 | 0.528 |
MOD_GSK3_1 | 242 | 249 | PF00069 | 0.512 |
MOD_GSK3_1 | 313 | 320 | PF00069 | 0.504 |
MOD_GSK3_1 | 370 | 377 | PF00069 | 0.536 |
MOD_GSK3_1 | 391 | 398 | PF00069 | 0.449 |
MOD_GSK3_1 | 401 | 408 | PF00069 | 0.449 |
MOD_GSK3_1 | 409 | 416 | PF00069 | 0.449 |
MOD_GSK3_1 | 732 | 739 | PF00069 | 0.564 |
MOD_GSK3_1 | 778 | 785 | PF00069 | 0.338 |
MOD_LATS_1 | 130 | 136 | PF00433 | 0.675 |
MOD_N-GLC_1 | 470 | 475 | PF02516 | 0.235 |
MOD_N-GLC_1 | 533 | 538 | PF02516 | 0.343 |
MOD_NEK2_1 | 118 | 123 | PF00069 | 0.549 |
MOD_NEK2_1 | 142 | 147 | PF00069 | 0.546 |
MOD_NEK2_1 | 40 | 45 | PF00069 | 0.486 |
MOD_NEK2_1 | 431 | 436 | PF00069 | 0.491 |
MOD_NEK2_1 | 438 | 443 | PF00069 | 0.433 |
MOD_NEK2_1 | 650 | 655 | PF00069 | 0.547 |
MOD_NEK2_1 | 679 | 684 | PF00069 | 0.497 |
MOD_NEK2_1 | 723 | 728 | PF00069 | 0.452 |
MOD_NEK2_1 | 780 | 785 | PF00069 | 0.354 |
MOD_NEK2_2 | 395 | 400 | PF00069 | 0.449 |
MOD_NEK2_2 | 652 | 657 | PF00069 | 0.423 |
MOD_NEK2_2 | 801 | 806 | PF00069 | 0.512 |
MOD_PIKK_1 | 101 | 107 | PF00454 | 0.480 |
MOD_PIKK_1 | 118 | 124 | PF00454 | 0.475 |
MOD_PIKK_1 | 336 | 342 | PF00454 | 0.477 |
MOD_PIKK_1 | 359 | 365 | PF00454 | 0.394 |
MOD_PIKK_1 | 417 | 423 | PF00454 | 0.449 |
MOD_PIKK_1 | 732 | 738 | PF00454 | 0.629 |
MOD_PIKK_1 | 751 | 757 | PF00454 | 0.556 |
MOD_PK_1 | 401 | 407 | PF00069 | 0.509 |
MOD_PKA_1 | 132 | 138 | PF00069 | 0.677 |
MOD_PKA_2 | 132 | 138 | PF00069 | 0.677 |
MOD_PKA_2 | 152 | 158 | PF00069 | 0.554 |
MOD_PKA_2 | 574 | 580 | PF00069 | 0.281 |
MOD_PKA_2 | 679 | 685 | PF00069 | 0.436 |
MOD_PKA_2 | 812 | 818 | PF00069 | 0.707 |
MOD_PKA_2 | 95 | 101 | PF00069 | 0.548 |
MOD_Plk_1 | 401 | 407 | PF00069 | 0.509 |
MOD_Plk_1 | 470 | 476 | PF00069 | 0.410 |
MOD_Plk_1 | 577 | 583 | PF00069 | 0.472 |
MOD_Plk_4 | 283 | 289 | PF00069 | 0.306 |
MOD_Plk_4 | 292 | 298 | PF00069 | 0.458 |
MOD_Plk_4 | 409 | 415 | PF00069 | 0.460 |
MOD_Plk_4 | 536 | 542 | PF00069 | 0.569 |
MOD_Plk_4 | 566 | 572 | PF00069 | 0.435 |
MOD_Plk_4 | 663 | 669 | PF00069 | 0.394 |
MOD_Plk_4 | 738 | 744 | PF00069 | 0.504 |
MOD_Plk_4 | 801 | 807 | PF00069 | 0.485 |
MOD_ProDKin_1 | 165 | 171 | PF00069 | 0.539 |
MOD_ProDKin_1 | 200 | 206 | PF00069 | 0.377 |
MOD_ProDKin_1 | 225 | 231 | PF00069 | 0.505 |
MOD_ProDKin_1 | 486 | 492 | PF00069 | 0.450 |
MOD_ProDKin_1 | 552 | 558 | PF00069 | 0.298 |
MOD_ProDKin_1 | 612 | 618 | PF00069 | 0.436 |
MOD_ProDKin_1 | 826 | 832 | PF00069 | 0.760 |
MOD_SUMO_rev_2 | 181 | 186 | PF00179 | 0.666 |
MOD_SUMO_rev_2 | 5 | 15 | PF00179 | 0.457 |
MOD_SUMO_rev_2 | 644 | 651 | PF00179 | 0.410 |
MOD_SUMO_rev_2 | 827 | 837 | PF00179 | 0.534 |
TRG_DiLeu_BaEn_1 | 747 | 752 | PF01217 | 0.608 |
TRG_DiLeu_BaEn_1 | 76 | 81 | PF01217 | 0.444 |
TRG_DiLeu_BaEn_2 | 192 | 198 | PF01217 | 0.419 |
TRG_DiLeu_BaEn_2 | 662 | 668 | PF01217 | 0.484 |
TRG_DiLeu_LyEn_5 | 144 | 149 | PF01217 | 0.411 |
TRG_ER_diArg_1 | 132 | 134 | PF00400 | 0.562 |
TRG_ER_diArg_1 | 608 | 610 | PF00400 | 0.398 |
TRG_ER_diArg_1 | 623 | 626 | PF00400 | 0.393 |
TRG_ER_diArg_1 | 7 | 10 | PF00400 | 0.612 |
TRG_ER_diArg_1 | 99 | 101 | PF00400 | 0.497 |
TRG_Pf-PMV_PEXEL_1 | 386 | 390 | PF00026 | 0.273 |
TRG_Pf-PMV_PEXEL_1 | 685 | 689 | PF00026 | 0.488 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8H1 | Leptomonas seymouri | 69% | 97% |
A0A0S4KJ12 | Bodo saltans | 42% | 100% |
A0A1X0P6Y3 | Trypanosomatidae | 54% | 100% |
A0A3R7M922 | Trypanosoma rangeli | 52% | 100% |
A0A3S7WV22 | Leishmania donovani | 83% | 99% |
A4HXY5 | Leishmania infantum | 84% | 99% |
D0A386 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 100% |
D0A5C2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 50% | 100% |
E9ARP8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 99% |
O13935 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 27% | 100% |
P38205 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 28% | 100% |
Q4QDT1 | Leishmania major | 83% | 100% |
V5DFH6 | Trypanosoma cruzi | 52% | 100% |