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 |
Related structures:
AlphaFold database: Q4Q419
Term | Name | Level | Count |
---|---|---|---|
GO:0006790 | sulfur compound metabolic process | 3 | 8 |
GO:0008152 | metabolic process | 1 | 8 |
GO:0009987 | cellular process | 1 | 8 |
GO:0016043 | cellular component organization | 3 | 8 |
GO:0016226 | iron-sulfur cluster assembly | 4 | 8 |
GO:0022607 | cellular component assembly | 4 | 8 |
GO:0031163 | metallo-sulfur cluster assembly | 5 | 8 |
GO:0044237 | cellular metabolic process | 2 | 8 |
GO:0044571 | [2Fe-2S] cluster assembly | 5 | 8 |
GO:0071840 | cellular component organization or biogenesis | 2 | 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 8 |
GO:0003824 | catalytic activity | 1 | 8 |
GO:0004652 | obsolete polynucleotide adenylyltransferase activity | 6 | 8 |
GO:0004810 | CCA tRNA nucleotidyltransferase activity | 8 | 8 |
GO:0005488 | binding | 1 | 8 |
GO:0005524 | ATP binding | 5 | 8 |
GO:0016740 | transferase activity | 2 | 8 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 8 |
GO:0016779 | nucleotidyltransferase activity | 4 | 8 |
GO:0016782 | transferase activity, transferring sulphur-containing groups | 3 | 8 |
GO:0016783 | sulfurtransferase activity | 4 | 8 |
GO:0017076 | purine nucleotide binding | 4 | 8 |
GO:0019842 | vitamin binding | 3 | 8 |
GO:0030170 | pyridoxal phosphate binding | 4 | 8 |
GO:0030554 | adenyl nucleotide binding | 5 | 8 |
GO:0031071 | cysteine desulfurase activity | 5 | 8 |
GO:0032553 | ribonucleotide binding | 3 | 8 |
GO:0032555 | purine ribonucleotide binding | 4 | 8 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 8 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 8 |
GO:0036094 | small molecule binding | 2 | 8 |
GO:0043167 | ion binding | 2 | 8 |
GO:0043168 | anion binding | 3 | 8 |
GO:0043169 | cation binding | 3 | 8 |
GO:0046872 | metal ion binding | 4 | 8 |
GO:0051536 | iron-sulfur cluster binding | 3 | 8 |
GO:0051540 | metal cluster binding | 2 | 8 |
GO:0070279 | vitamin B6 binding | 3 | 8 |
GO:0070566 | adenylyltransferase activity | 5 | 8 |
GO:0097159 | organic cyclic compound binding | 2 | 8 |
GO:0097367 | carbohydrate derivative binding | 2 | 8 |
GO:1901265 | nucleoside phosphate binding | 3 | 8 |
GO:1901363 | heterocyclic compound binding | 2 | 8 |
GO:1990817 | poly(A) RNA polymerase activity | 7 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 614 | 618 | PF00656 | 0.556 |
CLV_NRD_NRD_1 | 139 | 141 | PF00675 | 0.526 |
CLV_NRD_NRD_1 | 152 | 154 | PF00675 | 0.400 |
CLV_NRD_NRD_1 | 170 | 172 | PF00675 | 0.493 |
CLV_NRD_NRD_1 | 201 | 203 | PF00675 | 0.680 |
CLV_NRD_NRD_1 | 270 | 272 | PF00675 | 0.319 |
CLV_NRD_NRD_1 | 371 | 373 | PF00675 | 0.407 |
CLV_NRD_NRD_1 | 403 | 405 | PF00675 | 0.559 |
CLV_NRD_NRD_1 | 411 | 413 | PF00675 | 0.542 |
CLV_NRD_NRD_1 | 701 | 703 | PF00675 | 0.317 |
CLV_NRD_NRD_1 | 71 | 73 | PF00675 | 0.715 |
CLV_PCSK_KEX2_1 | 113 | 115 | PF00082 | 0.695 |
CLV_PCSK_KEX2_1 | 141 | 143 | PF00082 | 0.477 |
CLV_PCSK_KEX2_1 | 152 | 154 | PF00082 | 0.457 |
CLV_PCSK_KEX2_1 | 270 | 272 | PF00082 | 0.324 |
CLV_PCSK_KEX2_1 | 403 | 405 | PF00082 | 0.559 |
CLV_PCSK_KEX2_1 | 411 | 413 | PF00082 | 0.542 |
CLV_PCSK_KEX2_1 | 701 | 703 | PF00082 | 0.317 |
CLV_PCSK_KEX2_1 | 71 | 73 | PF00082 | 0.680 |
CLV_PCSK_KEX2_1 | 85 | 87 | PF00082 | 0.723 |
CLV_PCSK_PC1ET2_1 | 113 | 115 | PF00082 | 0.740 |
CLV_PCSK_PC1ET2_1 | 141 | 143 | PF00082 | 0.477 |
CLV_PCSK_PC1ET2_1 | 85 | 87 | PF00082 | 0.678 |
CLV_PCSK_PC7_1 | 67 | 73 | PF00082 | 0.709 |
CLV_PCSK_SKI1_1 | 152 | 156 | PF00082 | 0.447 |
CLV_PCSK_SKI1_1 | 207 | 211 | PF00082 | 0.611 |
CLV_PCSK_SKI1_1 | 242 | 246 | PF00082 | 0.356 |
CLV_PCSK_SKI1_1 | 411 | 415 | PF00082 | 0.552 |
CLV_PCSK_SKI1_1 | 419 | 423 | PF00082 | 0.500 |
CLV_PCSK_SKI1_1 | 585 | 589 | PF00082 | 0.558 |
CLV_PCSK_SKI1_1 | 638 | 642 | PF00082 | 0.325 |
CLV_PCSK_SKI1_1 | 785 | 789 | PF00082 | 0.432 |
DEG_APCC_DBOX_1 | 139 | 147 | PF00400 | 0.446 |
DEG_APCC_DBOX_1 | 411 | 419 | PF00400 | 0.616 |
DEG_APCC_DBOX_1 | 513 | 521 | PF00400 | 0.556 |
DEG_ODPH_VHL_1 | 356 | 368 | PF01847 | 0.556 |
DEG_SCF_FBW7_1 | 754 | 761 | PF00400 | 0.607 |
DOC_CDC14_PxL_1 | 56 | 64 | PF14671 | 0.664 |
DOC_CKS1_1 | 219 | 224 | PF01111 | 0.518 |
DOC_MAPK_gen_1 | 140 | 146 | PF00069 | 0.446 |
DOC_MAPK_gen_1 | 411 | 420 | PF00069 | 0.537 |
DOC_MAPK_MEF2A_6 | 140 | 148 | PF00069 | 0.440 |
DOC_MAPK_MEF2A_6 | 353 | 362 | PF00069 | 0.556 |
DOC_MAPK_RevD_3 | 127 | 142 | PF00069 | 0.492 |
DOC_MAPK_RevD_3 | 57 | 72 | PF00069 | 0.708 |
DOC_PP1_RVXF_1 | 603 | 609 | PF00149 | 0.556 |
DOC_PP1_RVXF_1 | 763 | 769 | PF00149 | 0.517 |
DOC_PP2B_PxIxI_1 | 357 | 363 | PF00149 | 0.607 |
DOC_USP7_MATH_1 | 41 | 45 | PF00917 | 0.662 |
DOC_USP7_MATH_1 | 760 | 764 | PF00917 | 0.556 |
DOC_USP7_UBL2_3 | 177 | 181 | PF12436 | 0.615 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.777 |
DOC_WW_Pin1_4 | 218 | 223 | PF00397 | 0.484 |
DOC_WW_Pin1_4 | 233 | 238 | PF00397 | 0.517 |
DOC_WW_Pin1_4 | 447 | 452 | PF00397 | 0.696 |
DOC_WW_Pin1_4 | 754 | 759 | PF00397 | 0.607 |
LIG_14-3-3_CanoR_1 | 275 | 280 | PF00244 | 0.519 |
LIG_14-3-3_CanoR_1 | 372 | 378 | PF00244 | 0.556 |
LIG_14-3-3_CanoR_1 | 403 | 407 | PF00244 | 0.542 |
LIG_14-3-3_CanoR_1 | 412 | 421 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 676 | 681 | PF00244 | 0.551 |
LIG_14-3-3_CanoR_1 | 72 | 81 | PF00244 | 0.696 |
LIG_14-3-3_CanoR_1 | 726 | 733 | PF00244 | 0.574 |
LIG_14-3-3_CanoR_1 | 765 | 769 | PF00244 | 0.517 |
LIG_14-3-3_CanoR_1 | 779 | 788 | PF00244 | 0.491 |
LIG_Actin_WH2_2 | 119 | 137 | PF00022 | 0.508 |
LIG_BRCT_BRCA1_1 | 432 | 436 | PF00533 | 0.515 |
LIG_Clathr_ClatBox_1 | 603 | 607 | PF01394 | 0.556 |
LIG_FHA_1 | 122 | 128 | PF00498 | 0.446 |
LIG_FHA_1 | 260 | 266 | PF00498 | 0.522 |
LIG_FHA_1 | 578 | 584 | PF00498 | 0.469 |
LIG_FHA_1 | 657 | 663 | PF00498 | 0.511 |
LIG_FHA_1 | 687 | 693 | PF00498 | 0.549 |
LIG_FHA_1 | 719 | 725 | PF00498 | 0.556 |
LIG_FHA_1 | 741 | 747 | PF00498 | 0.517 |
LIG_FHA_1 | 759 | 765 | PF00498 | 0.517 |
LIG_FHA_2 | 164 | 170 | PF00498 | 0.532 |
LIG_FHA_2 | 586 | 592 | PF00498 | 0.609 |
LIG_FHA_2 | 747 | 753 | PF00498 | 0.556 |
LIG_FHA_2 | 771 | 777 | PF00498 | 0.506 |
LIG_FHA_2 | 90 | 96 | PF00498 | 0.708 |
LIG_IRF3_LxIS_1 | 123 | 128 | PF10401 | 0.543 |
LIG_LIR_Apic_2 | 437 | 442 | PF02991 | 0.442 |
LIG_LIR_Apic_2 | 550 | 555 | PF02991 | 0.400 |
LIG_LIR_Gen_1 | 748 | 759 | PF02991 | 0.519 |
LIG_LIR_Gen_1 | 767 | 774 | PF02991 | 0.556 |
LIG_LIR_Gen_1 | 95 | 103 | PF02991 | 0.602 |
LIG_LIR_Nem_3 | 307 | 313 | PF02991 | 0.492 |
LIG_LIR_Nem_3 | 345 | 351 | PF02991 | 0.510 |
LIG_LIR_Nem_3 | 433 | 439 | PF02991 | 0.553 |
LIG_LIR_Nem_3 | 44 | 50 | PF02991 | 0.595 |
LIG_LIR_Nem_3 | 607 | 611 | PF02991 | 0.556 |
LIG_LIR_Nem_3 | 748 | 754 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 767 | 771 | PF02991 | 0.553 |
LIG_LIR_Nem_3 | 95 | 100 | PF02991 | 0.612 |
LIG_LYPXL_S_1 | 347 | 351 | PF13949 | 0.317 |
LIG_MYND_3 | 59 | 63 | PF01753 | 0.737 |
LIG_NRP_CendR_1 | 792 | 795 | PF00754 | 0.529 |
LIG_PCNA_yPIPBox_3 | 172 | 186 | PF02747 | 0.527 |
LIG_SH2_CRK | 545 | 549 | PF00017 | 0.579 |
LIG_SH2_CRK | 751 | 755 | PF00017 | 0.517 |
LIG_SH2_GRB2like | 718 | 721 | PF00017 | 0.607 |
LIG_SH2_PTP2 | 287 | 290 | PF00017 | 0.556 |
LIG_SH2_PTP2 | 97 | 100 | PF00017 | 0.638 |
LIG_SH2_SRC | 287 | 290 | PF00017 | 0.556 |
LIG_SH2_STAT3 | 438 | 441 | PF00017 | 0.661 |
LIG_SH2_STAT5 | 133 | 136 | PF00017 | 0.535 |
LIG_SH2_STAT5 | 287 | 290 | PF00017 | 0.556 |
LIG_SH2_STAT5 | 47 | 50 | PF00017 | 0.603 |
LIG_SH2_STAT5 | 471 | 474 | PF00017 | 0.556 |
LIG_SH2_STAT5 | 636 | 639 | PF00017 | 0.492 |
LIG_SH2_STAT5 | 708 | 711 | PF00017 | 0.607 |
LIG_SH2_STAT5 | 97 | 100 | PF00017 | 0.638 |
LIG_SH3_3 | 216 | 222 | PF00018 | 0.501 |
LIG_SH3_3 | 352 | 358 | PF00018 | 0.524 |
LIG_SH3_3 | 54 | 60 | PF00018 | 0.692 |
LIG_SH3_3 | 545 | 551 | PF00018 | 0.696 |
LIG_SH3_3 | 8 | 14 | PF00018 | 0.736 |
LIG_SUMO_SIM_anti_2 | 121 | 128 | PF11976 | 0.527 |
LIG_SUMO_SIM_par_1 | 123 | 128 | PF11976 | 0.454 |
LIG_SUMO_SIM_par_1 | 225 | 231 | PF11976 | 0.556 |
LIG_TRAF2_1 | 195 | 198 | PF00917 | 0.629 |
LIG_TRAF2_1 | 380 | 383 | PF00917 | 0.556 |
LIG_UBA3_1 | 182 | 191 | PF00899 | 0.541 |
LIG_WRC_WIRS_1 | 348 | 353 | PF05994 | 0.440 |
LIG_WRC_WIRS_1 | 374 | 379 | PF05994 | 0.517 |
LIG_WW_1 | 715 | 718 | PF00397 | 0.524 |
MOD_CDK_SPxxK_3 | 218 | 225 | PF00069 | 0.519 |
MOD_CK1_1 | 434 | 440 | PF00069 | 0.538 |
MOD_CK1_1 | 447 | 453 | PF00069 | 0.706 |
MOD_CK1_1 | 532 | 538 | PF00069 | 0.556 |
MOD_CK1_1 | 553 | 559 | PF00069 | 0.551 |
MOD_CK1_1 | 647 | 653 | PF00069 | 0.607 |
MOD_CK1_1 | 725 | 731 | PF00069 | 0.556 |
MOD_CK1_1 | 767 | 773 | PF00069 | 0.556 |
MOD_CK2_1 | 125 | 131 | PF00069 | 0.444 |
MOD_CK2_1 | 163 | 169 | PF00069 | 0.519 |
MOD_CK2_1 | 261 | 267 | PF00069 | 0.527 |
MOD_CK2_1 | 377 | 383 | PF00069 | 0.522 |
MOD_CK2_1 | 499 | 505 | PF00069 | 0.556 |
MOD_CK2_1 | 553 | 559 | PF00069 | 0.565 |
MOD_CK2_1 | 585 | 591 | PF00069 | 0.615 |
MOD_CK2_1 | 89 | 95 | PF00069 | 0.707 |
MOD_Cter_Amidation | 111 | 114 | PF01082 | 0.704 |
MOD_Cter_Amidation | 401 | 404 | PF01082 | 0.538 |
MOD_Cter_Amidation | 69 | 72 | PF01082 | 0.707 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.581 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.527 |
MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.317 |
MOD_GlcNHglycan | 250 | 253 | PF01048 | 0.284 |
MOD_GlcNHglycan | 331 | 334 | PF01048 | 0.356 |
MOD_GlcNHglycan | 394 | 397 | PF01048 | 0.670 |
MOD_GlcNHglycan | 501 | 504 | PF01048 | 0.317 |
MOD_GlcNHglycan | 531 | 534 | PF01048 | 0.356 |
MOD_GlcNHglycan | 646 | 649 | PF01048 | 0.407 |
MOD_GlcNHglycan | 704 | 708 | PF01048 | 0.319 |
MOD_GlcNHglycan | 738 | 741 | PF01048 | 0.336 |
MOD_GlcNHglycan | 781 | 784 | PF01048 | 0.483 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.459 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.553 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.556 |
MOD_GSK3_1 | 313 | 320 | PF00069 | 0.565 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.556 |
MOD_GSK3_1 | 373 | 380 | PF00069 | 0.517 |
MOD_GSK3_1 | 430 | 437 | PF00069 | 0.525 |
MOD_GSK3_1 | 495 | 502 | PF00069 | 0.517 |
MOD_GSK3_1 | 528 | 535 | PF00069 | 0.517 |
MOD_GSK3_1 | 550 | 557 | PF00069 | 0.567 |
MOD_GSK3_1 | 607 | 614 | PF00069 | 0.542 |
MOD_GSK3_1 | 615 | 622 | PF00069 | 0.517 |
MOD_GSK3_1 | 718 | 725 | PF00069 | 0.551 |
MOD_GSK3_1 | 736 | 743 | PF00069 | 0.422 |
MOD_GSK3_1 | 746 | 753 | PF00069 | 0.511 |
MOD_GSK3_1 | 754 | 761 | PF00069 | 0.415 |
MOD_N-GLC_1 | 256 | 261 | PF02516 | 0.317 |
MOD_N-GLC_1 | 304 | 309 | PF02516 | 0.317 |
MOD_N-GLC_1 | 342 | 347 | PF02516 | 0.317 |
MOD_N-GLC_1 | 447 | 452 | PF02516 | 0.774 |
MOD_N-GLC_1 | 585 | 590 | PF02516 | 0.598 |
MOD_N-GLC_1 | 746 | 751 | PF02516 | 0.317 |
MOD_NEK2_1 | 125 | 130 | PF00069 | 0.435 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.537 |
MOD_NEK2_1 | 255 | 260 | PF00069 | 0.531 |
MOD_NEK2_1 | 313 | 318 | PF00069 | 0.506 |
MOD_NEK2_1 | 321 | 326 | PF00069 | 0.470 |
MOD_NEK2_1 | 377 | 382 | PF00069 | 0.517 |
MOD_NEK2_1 | 392 | 397 | PF00069 | 0.632 |
MOD_NEK2_1 | 499 | 504 | PF00069 | 0.517 |
MOD_NEK2_1 | 611 | 616 | PF00069 | 0.502 |
MOD_NEK2_1 | 674 | 679 | PF00069 | 0.540 |
MOD_NEK2_2 | 337 | 342 | PF00069 | 0.556 |
MOD_NEK2_2 | 760 | 765 | PF00069 | 0.556 |
MOD_PIKK_1 | 193 | 199 | PF00454 | 0.637 |
MOD_PIKK_1 | 292 | 298 | PF00454 | 0.556 |
MOD_PIKK_1 | 335 | 341 | PF00454 | 0.517 |
MOD_PIKK_1 | 597 | 603 | PF00454 | 0.556 |
MOD_PIKK_1 | 611 | 617 | PF00454 | 0.556 |
MOD_PIKK_1 | 647 | 653 | PF00454 | 0.527 |
MOD_PKA_2 | 274 | 280 | PF00069 | 0.517 |
MOD_PKA_2 | 402 | 408 | PF00069 | 0.543 |
MOD_PKA_2 | 444 | 450 | PF00069 | 0.660 |
MOD_PKA_2 | 725 | 731 | PF00069 | 0.574 |
MOD_PKA_2 | 764 | 770 | PF00069 | 0.517 |
MOD_Plk_1 | 288 | 294 | PF00069 | 0.553 |
MOD_Plk_1 | 304 | 310 | PF00069 | 0.400 |
MOD_Plk_1 | 321 | 327 | PF00069 | 0.371 |
MOD_Plk_1 | 342 | 348 | PF00069 | 0.517 |
MOD_Plk_1 | 377 | 383 | PF00069 | 0.517 |
MOD_Plk_1 | 434 | 440 | PF00069 | 0.538 |
MOD_Plk_1 | 611 | 617 | PF00069 | 0.460 |
MOD_Plk_1 | 746 | 752 | PF00069 | 0.556 |
MOD_Plk_2-3 | 261 | 267 | PF00069 | 0.556 |
MOD_Plk_2-3 | 459 | 465 | PF00069 | 0.664 |
MOD_Plk_2-3 | 579 | 585 | PF00069 | 0.475 |
MOD_Plk_2-3 | 607 | 613 | PF00069 | 0.556 |
MOD_Plk_4 | 121 | 127 | PF00069 | 0.464 |
MOD_Plk_4 | 163 | 169 | PF00069 | 0.519 |
MOD_Plk_4 | 261 | 267 | PF00069 | 0.540 |
MOD_Plk_4 | 343 | 349 | PF00069 | 0.496 |
MOD_Plk_4 | 565 | 571 | PF00069 | 0.511 |
MOD_Plk_4 | 746 | 752 | PF00069 | 0.556 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.774 |
MOD_ProDKin_1 | 218 | 224 | PF00069 | 0.490 |
MOD_ProDKin_1 | 233 | 239 | PF00069 | 0.517 |
MOD_ProDKin_1 | 447 | 453 | PF00069 | 0.700 |
MOD_ProDKin_1 | 754 | 760 | PF00069 | 0.607 |
MOD_SUMO_rev_2 | 3 | 11 | PF00179 | 0.755 |
MOD_SUMO_rev_2 | 423 | 430 | PF00179 | 0.505 |
MOD_SUMO_rev_2 | 52 | 57 | PF00179 | 0.668 |
TRG_DiLeu_BaEn_1 | 121 | 126 | PF01217 | 0.553 |
TRG_DiLeu_BaEn_1 | 178 | 183 | PF01217 | 0.588 |
TRG_DiLeu_BaEn_1 | 683 | 688 | PF01217 | 0.542 |
TRG_DiLeu_BaLyEn_6 | 355 | 360 | PF01217 | 0.556 |
TRG_ENDOCYTIC_2 | 241 | 244 | PF00928 | 0.499 |
TRG_ENDOCYTIC_2 | 287 | 290 | PF00928 | 0.556 |
TRG_ENDOCYTIC_2 | 310 | 313 | PF00928 | 0.492 |
TRG_ENDOCYTIC_2 | 348 | 351 | PF00928 | 0.511 |
TRG_ENDOCYTIC_2 | 545 | 548 | PF00928 | 0.593 |
TRG_ENDOCYTIC_2 | 751 | 754 | PF00928 | 0.492 |
TRG_ENDOCYTIC_2 | 97 | 100 | PF00928 | 0.638 |
TRG_ER_diArg_1 | 140 | 143 | PF00400 | 0.501 |
TRG_ER_diArg_1 | 151 | 153 | PF00400 | 0.406 |
TRG_ER_diArg_1 | 270 | 272 | PF00400 | 0.524 |
TRG_ER_diArg_1 | 410 | 412 | PF00400 | 0.616 |
TRG_ER_diArg_1 | 71 | 73 | PF00400 | 0.715 |
TRG_NES_CRM1_1 | 274 | 289 | PF08389 | 0.556 |
TRG_Pf-PMV_PEXEL_1 | 145 | 149 | PF00026 | 0.441 |
TRG_Pf-PMV_PEXEL_1 | 270 | 274 | PF00026 | 0.324 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IM59 | Leptomonas seymouri | 82% | 100% |
A0A0S4JKY0 | Bodo saltans | 43% | 85% |
A0A3S7X6Q8 | Leishmania donovani | 96% | 100% |
A4HLM9 | Leishmania braziliensis | 91% | 100% |
A4I940 | Leishmania infantum | 96% | 100% |
E9B405 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |