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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
Related structures:
AlphaFold database: A0A3Q8IUC9
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 7 |
GO:0003824 | catalytic activity | 1 | 7 |
GO:0005488 | binding | 1 | 7 |
GO:0005524 | ATP binding | 5 | 7 |
GO:0016462 | pyrophosphatase activity | 5 | 7 |
GO:0016787 | hydrolase activity | 2 | 7 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 7 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 7 |
GO:0016887 | ATP hydrolysis activity | 7 | 7 |
GO:0017076 | purine nucleotide binding | 4 | 7 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 7 |
GO:0030554 | adenyl nucleotide binding | 5 | 7 |
GO:0032553 | ribonucleotide binding | 3 | 7 |
GO:0032555 | purine ribonucleotide binding | 4 | 7 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 7 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 7 |
GO:0036094 | small molecule binding | 2 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043168 | anion binding | 3 | 7 |
GO:0097159 | organic cyclic compound binding | 2 | 7 |
GO:0097367 | carbohydrate derivative binding | 2 | 7 |
GO:1901265 | nucleoside phosphate binding | 3 | 7 |
GO:1901363 | heterocyclic compound binding | 2 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 608 | 612 | PF00656 | 0.716 |
CLV_C14_Caspase3-7 | 643 | 647 | PF00656 | 0.707 |
CLV_C14_Caspase3-7 | 792 | 796 | PF00656 | 0.597 |
CLV_NRD_NRD_1 | 169 | 171 | PF00675 | 0.452 |
CLV_NRD_NRD_1 | 215 | 217 | PF00675 | 0.448 |
CLV_NRD_NRD_1 | 290 | 292 | PF00675 | 0.449 |
CLV_NRD_NRD_1 | 511 | 513 | PF00675 | 0.275 |
CLV_NRD_NRD_1 | 584 | 586 | PF00675 | 0.448 |
CLV_NRD_NRD_1 | 744 | 746 | PF00675 | 0.427 |
CLV_PCSK_KEX2_1 | 169 | 171 | PF00082 | 0.452 |
CLV_PCSK_KEX2_1 | 191 | 193 | PF00082 | 0.546 |
CLV_PCSK_KEX2_1 | 215 | 217 | PF00082 | 0.466 |
CLV_PCSK_KEX2_1 | 290 | 292 | PF00082 | 0.449 |
CLV_PCSK_KEX2_1 | 343 | 345 | PF00082 | 0.518 |
CLV_PCSK_KEX2_1 | 511 | 513 | PF00082 | 0.275 |
CLV_PCSK_KEX2_1 | 744 | 746 | PF00082 | 0.427 |
CLV_PCSK_PC1ET2_1 | 191 | 193 | PF00082 | 0.512 |
CLV_PCSK_PC1ET2_1 | 343 | 345 | PF00082 | 0.518 |
CLV_PCSK_SKI1_1 | 126 | 130 | PF00082 | 0.396 |
CLV_PCSK_SKI1_1 | 344 | 348 | PF00082 | 0.476 |
CLV_PCSK_SKI1_1 | 43 | 47 | PF00082 | 0.379 |
CLV_PCSK_SKI1_1 | 756 | 760 | PF00082 | 0.376 |
DEG_APCC_DBOX_1 | 343 | 351 | PF00400 | 0.684 |
DEG_APCC_DBOX_1 | 510 | 518 | PF00400 | 0.475 |
DEG_COP1_1 | 135 | 145 | PF00400 | 0.602 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.496 |
DEG_SPOP_SBC_1 | 427 | 431 | PF00917 | 0.667 |
DOC_ANK_TNKS_1 | 476 | 483 | PF00023 | 0.585 |
DOC_CDC14_PxL_1 | 348 | 356 | PF14671 | 0.678 |
DOC_MAPK_gen_1 | 343 | 350 | PF00069 | 0.665 |
DOC_MAPK_gen_1 | 449 | 458 | PF00069 | 0.610 |
DOC_MAPK_gen_1 | 508 | 517 | PF00069 | 0.485 |
DOC_MAPK_gen_1 | 546 | 555 | PF00069 | 0.665 |
DOC_MAPK_MEF2A_6 | 511 | 519 | PF00069 | 0.475 |
DOC_PP1_RVXF_1 | 484 | 490 | PF00149 | 0.530 |
DOC_PP2B_LxvP_1 | 680 | 683 | PF13499 | 0.592 |
DOC_PP4_FxxP_1 | 273 | 276 | PF00568 | 0.722 |
DOC_PP4_FxxP_1 | 478 | 481 | PF00568 | 0.609 |
DOC_SPAK_OSR1_1 | 477 | 481 | PF12202 | 0.576 |
DOC_USP7_MATH_1 | 195 | 199 | PF00917 | 0.705 |
DOC_USP7_MATH_1 | 316 | 320 | PF00917 | 0.747 |
DOC_USP7_MATH_1 | 389 | 393 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 399 | 403 | PF00917 | 0.695 |
DOC_USP7_MATH_1 | 414 | 418 | PF00917 | 0.720 |
DOC_USP7_MATH_1 | 557 | 561 | PF00917 | 0.573 |
DOC_USP7_MATH_1 | 618 | 622 | PF00917 | 0.735 |
DOC_USP7_MATH_1 | 703 | 707 | PF00917 | 0.610 |
DOC_WD40_RPTOR_TOS_1 | 535 | 541 | PF00400 | 0.634 |
DOC_WW_Pin1_4 | 616 | 621 | PF00397 | 0.745 |
LIG_14-3-3_CanoR_1 | 124 | 129 | PF00244 | 0.667 |
LIG_14-3-3_CanoR_1 | 131 | 141 | PF00244 | 0.607 |
LIG_14-3-3_CanoR_1 | 330 | 335 | PF00244 | 0.618 |
LIG_14-3-3_CanoR_1 | 43 | 53 | PF00244 | 0.619 |
LIG_14-3-3_CanoR_1 | 449 | 454 | PF00244 | 0.630 |
LIG_14-3-3_CanoR_1 | 463 | 468 | PF00244 | 0.481 |
LIG_14-3-3_CanoR_1 | 486 | 490 | PF00244 | 0.577 |
LIG_14-3-3_CanoR_1 | 556 | 562 | PF00244 | 0.525 |
LIG_14-3-3_CanoR_1 | 744 | 752 | PF00244 | 0.622 |
LIG_14-3-3_CanoR_1 | 790 | 795 | PF00244 | 0.610 |
LIG_Actin_WH2_2 | 524 | 542 | PF00022 | 0.608 |
LIG_AP2alpha_1 | 673 | 677 | PF02296 | 0.530 |
LIG_APCC_ABBA_1 | 372 | 377 | PF00400 | 0.669 |
LIG_APCC_ABBA_1 | 561 | 566 | PF00400 | 0.525 |
LIG_APCC_ABBAyCdc20_2 | 110 | 116 | PF00400 | 0.667 |
LIG_BIR_III_4 | 568 | 572 | PF00653 | 0.536 |
LIG_BRCT_BRCA1_1 | 104 | 108 | PF00533 | 0.645 |
LIG_BRCT_BRCA1_1 | 110 | 114 | PF00533 | 0.649 |
LIG_BRCT_BRCA1_1 | 121 | 125 | PF00533 | 0.576 |
LIG_BRCT_BRCA1_1 | 269 | 273 | PF00533 | 0.767 |
LIG_BRCT_BRCA1_1 | 402 | 406 | PF00533 | 0.674 |
LIG_BRCT_BRCA1_1 | 454 | 458 | PF00533 | 0.537 |
LIG_BRCT_BRCA1_2 | 104 | 110 | PF00533 | 0.625 |
LIG_CaM_IQ_9 | 577 | 593 | PF13499 | 0.619 |
LIG_CAP-Gly_1 | 795 | 803 | PF01302 | 0.648 |
LIG_CtBP_PxDLS_1 | 660 | 664 | PF00389 | 0.618 |
LIG_deltaCOP1_diTrp_1 | 115 | 125 | PF00928 | 0.678 |
LIG_eIF4E_1 | 102 | 108 | PF01652 | 0.663 |
LIG_FHA_1 | 12 | 18 | PF00498 | 0.262 |
LIG_FHA_1 | 331 | 337 | PF00498 | 0.613 |
LIG_FHA_1 | 460 | 466 | PF00498 | 0.543 |
LIG_FHA_1 | 486 | 492 | PF00498 | 0.579 |
LIG_FHA_1 | 498 | 504 | PF00498 | 0.430 |
LIG_FHA_1 | 548 | 554 | PF00498 | 0.658 |
LIG_FHA_1 | 650 | 656 | PF00498 | 0.677 |
LIG_FHA_1 | 721 | 727 | PF00498 | 0.526 |
LIG_FHA_1 | 747 | 753 | PF00498 | 0.578 |
LIG_FHA_1 | 786 | 792 | PF00498 | 0.527 |
LIG_FHA_2 | 264 | 270 | PF00498 | 0.707 |
LIG_FHA_2 | 522 | 528 | PF00498 | 0.490 |
LIG_FXI_DFP_1 | 564 | 568 | PF00024 | 0.327 |
LIG_GBD_Chelix_1 | 506 | 514 | PF00786 | 0.275 |
LIG_HCF-1_HBM_1 | 727 | 730 | PF13415 | 0.593 |
LIG_LIR_Apic_2 | 270 | 276 | PF02991 | 0.820 |
LIG_LIR_Apic_2 | 288 | 292 | PF02991 | 0.588 |
LIG_LIR_Gen_1 | 101 | 108 | PF02991 | 0.609 |
LIG_LIR_Gen_1 | 452 | 459 | PF02991 | 0.594 |
LIG_LIR_Gen_1 | 565 | 573 | PF02991 | 0.537 |
LIG_LIR_Gen_1 | 671 | 680 | PF02991 | 0.545 |
LIG_LIR_Gen_1 | 684 | 690 | PF02991 | 0.530 |
LIG_LIR_Gen_1 | 795 | 803 | PF02991 | 0.590 |
LIG_LIR_Nem_3 | 101 | 107 | PF02991 | 0.610 |
LIG_LIR_Nem_3 | 115 | 121 | PF02991 | 0.627 |
LIG_LIR_Nem_3 | 122 | 128 | PF02991 | 0.598 |
LIG_LIR_Nem_3 | 379 | 385 | PF02991 | 0.654 |
LIG_LIR_Nem_3 | 452 | 456 | PF02991 | 0.544 |
LIG_LIR_Nem_3 | 565 | 570 | PF02991 | 0.557 |
LIG_LIR_Nem_3 | 572 | 577 | PF02991 | 0.596 |
LIG_LIR_Nem_3 | 671 | 676 | PF02991 | 0.538 |
LIG_LIR_Nem_3 | 684 | 689 | PF02991 | 0.532 |
LIG_LIR_Nem_3 | 795 | 800 | PF02991 | 0.581 |
LIG_LYPXL_S_1 | 350 | 354 | PF13949 | 0.481 |
LIG_LYPXL_yS_3 | 351 | 354 | PF13949 | 0.679 |
LIG_MLH1_MIPbox_1 | 269 | 273 | PF16413 | 0.733 |
LIG_MLH1_MIPbox_1 | 454 | 458 | PF16413 | 0.537 |
LIG_NRBOX | 12 | 18 | PF00104 | 0.340 |
LIG_PDZ_Class_3 | 798 | 803 | PF00595 | 0.688 |
LIG_Pex14_2 | 114 | 118 | PF04695 | 0.629 |
LIG_Pex14_2 | 125 | 129 | PF04695 | 0.615 |
LIG_Pex14_2 | 30 | 34 | PF04695 | 0.304 |
LIG_Pex14_2 | 40 | 44 | PF04695 | 0.585 |
LIG_Pex14_2 | 453 | 457 | PF04695 | 0.551 |
LIG_Pex14_2 | 673 | 677 | PF04695 | 0.530 |
LIG_Pex14_2 | 686 | 690 | PF04695 | 0.517 |
LIG_SH2_CRK | 104 | 108 | PF00017 | 0.616 |
LIG_SH2_CRK | 289 | 293 | PF00017 | 0.640 |
LIG_SH2_SRC | 102 | 105 | PF00017 | 0.606 |
LIG_SH2_SRC | 217 | 220 | PF00017 | 0.625 |
LIG_SH2_STAP1 | 102 | 106 | PF00017 | 0.604 |
LIG_SH2_STAP1 | 121 | 125 | PF00017 | 0.621 |
LIG_SH2_STAP1 | 217 | 221 | PF00017 | 0.651 |
LIG_SH2_STAP1 | 730 | 734 | PF00017 | 0.601 |
LIG_SH2_STAT5 | 335 | 338 | PF00017 | 0.628 |
LIG_SH2_STAT5 | 383 | 386 | PF00017 | 0.583 |
LIG_SH2_STAT5 | 562 | 565 | PF00017 | 0.522 |
LIG_SH2_STAT5 | 78 | 81 | PF00017 | 0.587 |
LIG_SH2_STAT5 | 83 | 86 | PF00017 | 0.582 |
LIG_SH3_3 | 239 | 245 | PF00018 | 0.750 |
LIG_SH3_3 | 273 | 279 | PF00018 | 0.716 |
LIG_SH3_3 | 346 | 352 | PF00018 | 0.682 |
LIG_SH3_3 | 528 | 534 | PF00018 | 0.578 |
LIG_SUMO_SIM_anti_2 | 138 | 144 | PF11976 | 0.617 |
LIG_SUMO_SIM_anti_2 | 281 | 288 | PF11976 | 0.704 |
LIG_SUMO_SIM_par_1 | 281 | 288 | PF11976 | 0.704 |
LIG_SUMO_SIM_par_1 | 513 | 518 | PF11976 | 0.499 |
LIG_SUMO_SIM_par_1 | 520 | 527 | PF11976 | 0.514 |
LIG_TYR_ITIM | 349 | 354 | PF00017 | 0.679 |
LIG_WRC_WIRS_1 | 794 | 799 | PF05994 | 0.586 |
MOD_CK1_1 | 177 | 183 | PF00069 | 0.731 |
MOD_CK1_1 | 261 | 267 | PF00069 | 0.760 |
MOD_CK1_1 | 268 | 274 | PF00069 | 0.715 |
MOD_CK1_1 | 304 | 310 | PF00069 | 0.730 |
MOD_CK1_1 | 402 | 408 | PF00069 | 0.700 |
MOD_CK1_1 | 445 | 451 | PF00069 | 0.695 |
MOD_CK1_1 | 547 | 553 | PF00069 | 0.688 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.426 |
MOD_CK1_1 | 619 | 625 | PF00069 | 0.736 |
MOD_CK1_1 | 628 | 634 | PF00069 | 0.694 |
MOD_CK1_1 | 793 | 799 | PF00069 | 0.623 |
MOD_CK2_1 | 132 | 138 | PF00069 | 0.573 |
MOD_CK2_1 | 263 | 269 | PF00069 | 0.719 |
MOD_CK2_1 | 515 | 521 | PF00069 | 0.479 |
MOD_CK2_1 | 655 | 661 | PF00069 | 0.664 |
MOD_Cter_Amidation | 167 | 170 | PF01082 | 0.447 |
MOD_Cter_Amidation | 189 | 192 | PF01082 | 0.546 |
MOD_Cter_Amidation | 742 | 745 | PF01082 | 0.406 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.513 |
MOD_GlcNHglycan | 377 | 381 | PF01048 | 0.447 |
MOD_GlcNHglycan | 386 | 389 | PF01048 | 0.454 |
MOD_GlcNHglycan | 402 | 405 | PF01048 | 0.439 |
MOD_GlcNHglycan | 445 | 448 | PF01048 | 0.465 |
MOD_GlcNHglycan | 599 | 602 | PF01048 | 0.471 |
MOD_GlcNHglycan | 622 | 625 | PF01048 | 0.637 |
MOD_GlcNHglycan | 627 | 630 | PF01048 | 0.591 |
MOD_GlcNHglycan | 769 | 772 | PF01048 | 0.319 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.629 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.626 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.730 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.700 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.808 |
MOD_GSK3_1 | 357 | 364 | PF00069 | 0.688 |
MOD_GSK3_1 | 389 | 396 | PF00069 | 0.715 |
MOD_GSK3_1 | 400 | 407 | PF00069 | 0.753 |
MOD_GSK3_1 | 414 | 421 | PF00069 | 0.709 |
MOD_GSK3_1 | 425 | 432 | PF00069 | 0.710 |
MOD_GSK3_1 | 445 | 452 | PF00069 | 0.659 |
MOD_GSK3_1 | 459 | 466 | PF00069 | 0.484 |
MOD_GSK3_1 | 494 | 501 | PF00069 | 0.485 |
MOD_GSK3_1 | 517 | 524 | PF00069 | 0.547 |
MOD_GSK3_1 | 547 | 554 | PF00069 | 0.688 |
MOD_GSK3_1 | 612 | 619 | PF00069 | 0.726 |
MOD_GSK3_1 | 763 | 770 | PF00069 | 0.534 |
MOD_GSK3_1 | 785 | 792 | PF00069 | 0.574 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.394 |
MOD_N-GLC_1 | 302 | 307 | PF02516 | 0.466 |
MOD_N-GLC_1 | 762 | 767 | PF02516 | 0.307 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.627 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.686 |
MOD_NEK2_1 | 301 | 306 | PF00069 | 0.673 |
MOD_NEK2_1 | 426 | 431 | PF00069 | 0.683 |
MOD_NEK2_1 | 655 | 660 | PF00069 | 0.634 |
MOD_NEK2_1 | 701 | 706 | PF00069 | 0.592 |
MOD_NEK2_1 | 708 | 713 | PF00069 | 0.544 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.612 |
MOD_NEK2_1 | 747 | 752 | PF00069 | 0.535 |
MOD_NEK2_1 | 762 | 767 | PF00069 | 0.542 |
MOD_NEK2_2 | 44 | 49 | PF00069 | 0.567 |
MOD_NEK2_2 | 485 | 490 | PF00069 | 0.579 |
MOD_NEK2_2 | 557 | 562 | PF00069 | 0.540 |
MOD_PIKK_1 | 177 | 183 | PF00454 | 0.731 |
MOD_PIKK_1 | 244 | 250 | PF00454 | 0.659 |
MOD_PIKK_1 | 263 | 269 | PF00454 | 0.730 |
MOD_PIKK_1 | 295 | 301 | PF00454 | 0.649 |
MOD_PIKK_1 | 314 | 320 | PF00454 | 0.559 |
MOD_PIKK_1 | 612 | 618 | PF00454 | 0.738 |
MOD_PIKK_1 | 720 | 726 | PF00454 | 0.668 |
MOD_PIKK_1 | 747 | 753 | PF00454 | 0.532 |
MOD_PK_1 | 790 | 796 | PF00069 | 0.618 |
MOD_PKA_2 | 174 | 180 | PF00069 | 0.732 |
MOD_PKA_2 | 485 | 491 | PF00069 | 0.577 |
MOD_PKA_2 | 547 | 553 | PF00069 | 0.720 |
MOD_PKA_2 | 604 | 610 | PF00069 | 0.815 |
MOD_PKA_2 | 649 | 655 | PF00069 | 0.732 |
MOD_PKA_2 | 789 | 795 | PF00069 | 0.566 |
MOD_Plk_1 | 102 | 108 | PF00069 | 0.594 |
MOD_Plk_1 | 137 | 143 | PF00069 | 0.620 |
MOD_Plk_1 | 268 | 274 | PF00069 | 0.704 |
MOD_Plk_1 | 415 | 421 | PF00069 | 0.698 |
MOD_Plk_1 | 708 | 714 | PF00069 | 0.557 |
MOD_Plk_1 | 735 | 741 | PF00069 | 0.694 |
MOD_Plk_2-3 | 521 | 527 | PF00069 | 0.460 |
MOD_Plk_2-3 | 637 | 643 | PF00069 | 0.687 |
MOD_Plk_2-3 | 666 | 672 | PF00069 | 0.613 |
MOD_Plk_4 | 102 | 108 | PF00069 | 0.594 |
MOD_Plk_4 | 12 | 18 | PF00069 | 0.322 |
MOD_Plk_4 | 137 | 143 | PF00069 | 0.680 |
MOD_Plk_4 | 268 | 274 | PF00069 | 0.697 |
MOD_Plk_4 | 330 | 336 | PF00069 | 0.620 |
MOD_Plk_4 | 350 | 356 | PF00069 | 0.623 |
MOD_Plk_4 | 452 | 458 | PF00069 | 0.553 |
MOD_Plk_4 | 463 | 469 | PF00069 | 0.549 |
MOD_Plk_4 | 485 | 491 | PF00069 | 0.587 |
MOD_Plk_4 | 498 | 504 | PF00069 | 0.425 |
MOD_Plk_4 | 557 | 563 | PF00069 | 0.538 |
MOD_Plk_4 | 649 | 655 | PF00069 | 0.680 |
MOD_Plk_4 | 682 | 688 | PF00069 | 0.544 |
MOD_Plk_4 | 703 | 709 | PF00069 | 0.633 |
MOD_ProDKin_1 | 616 | 622 | PF00069 | 0.744 |
MOD_SUMO_rev_2 | 269 | 279 | PF00179 | 0.705 |
TRG_DiLeu_BaEn_2 | 151 | 157 | PF01217 | 0.629 |
TRG_DiLeu_BaLyEn_6 | 697 | 702 | PF01217 | 0.550 |
TRG_ENDOCYTIC_2 | 104 | 107 | PF00928 | 0.619 |
TRG_ENDOCYTIC_2 | 351 | 354 | PF00928 | 0.679 |
TRG_ENDOCYTIC_2 | 382 | 385 | PF00928 | 0.644 |
TRG_ENDOCYTIC_2 | 42 | 45 | PF00928 | 0.608 |
TRG_ER_diArg_1 | 214 | 216 | PF00400 | 0.662 |
TRG_ER_diArg_1 | 289 | 291 | PF00400 | 0.644 |
TRG_ER_diArg_1 | 475 | 478 | PF00400 | 0.574 |
TRG_ER_diArg_1 | 510 | 512 | PF00400 | 0.475 |
TRG_Pf-PMV_PEXEL_1 | 291 | 296 | PF00026 | 0.441 |
TRG_Pf-PMV_PEXEL_1 | 585 | 590 | PF00026 | 0.452 |
TRG_Pf-PMV_PEXEL_1 | 64 | 68 | PF00026 | 0.431 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDZ4 | Leptomonas seymouri | 51% | 97% |
A4HAE8 | Leishmania braziliensis | 69% | 99% |
A4I9K4 | Leishmania infantum | 99% | 100% |
E9B4K2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
Q4Q3H4 | Leishmania major | 91% | 100% |