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:0043226 | organelle | 2 | 11 |
GO:0043227 | membrane-bounded organelle | 3 | 11 |
GO:0043229 | intracellular organelle | 3 | 11 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0005654 | nucleoplasm | 2 | 1 |
GO:0008023 | transcription elongation factor complex | 3 | 1 |
GO:0016593 | Cdc73/Paf1 complex | 4 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
Related structures:
AlphaFold database: A4HHQ3
Term | Name | Level | Count |
---|---|---|---|
GO:0006355 | regulation of DNA-templated transcription | 6 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009889 | regulation of biosynthetic process | 4 | 12 |
GO:0010468 | regulation of gene expression | 5 | 12 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 12 |
GO:0016570 | histone modification | 5 | 12 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 12 |
GO:0019222 | regulation of metabolic process | 3 | 12 |
GO:0019538 | protein metabolic process | 3 | 12 |
GO:0031323 | regulation of cellular metabolic process | 4 | 12 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 12 |
GO:0036211 | protein modification process | 4 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043412 | macromolecule modification | 4 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0050789 | regulation of biological process | 2 | 12 |
GO:0050794 | regulation of cellular process | 3 | 12 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 12 |
GO:0051252 | regulation of RNA metabolic process | 5 | 12 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 12 |
GO:0065007 | biological regulation | 1 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0080090 | regulation of primary metabolic process | 4 | 12 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 12 |
GO:1903506 | regulation of nucleic acid-templated transcription | 7 | 12 |
GO:2001141 | regulation of RNA biosynthetic process | 6 | 12 |
GO:0031056 | regulation of histone modification | 7 | 1 |
GO:0031060 | regulation of histone methylation | 5 | 1 |
GO:0031399 | regulation of protein modification process | 6 | 1 |
GO:0051246 | regulation of protein metabolic process | 5 | 1 |
GO:0051569 | regulation of histone H3-K4 methylation | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000993 | RNA polymerase II complex binding | 5 | 1 |
GO:0001098 | basal transcription machinery binding | 3 | 1 |
GO:0001099 | basal RNA polymerase II transcription machinery binding | 4 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0005515 | protein binding | 2 | 1 |
GO:0019899 | enzyme binding | 3 | 1 |
GO:0043175 | RNA polymerase core enzyme binding | 5 | 1 |
GO:0070063 | RNA polymerase binding | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 623 | 627 | PF00656 | 0.510 |
CLV_C14_Caspase3-7 | 654 | 658 | PF00656 | 0.421 |
CLV_C14_Caspase3-7 | 847 | 851 | PF00656 | 0.616 |
CLV_NRD_NRD_1 | 100 | 102 | PF00675 | 0.526 |
CLV_NRD_NRD_1 | 170 | 172 | PF00675 | 0.485 |
CLV_NRD_NRD_1 | 599 | 601 | PF00675 | 0.465 |
CLV_NRD_NRD_1 | 729 | 731 | PF00675 | 0.385 |
CLV_NRD_NRD_1 | 788 | 790 | PF00675 | 0.520 |
CLV_NRD_NRD_1 | 800 | 802 | PF00675 | 0.511 |
CLV_NRD_NRD_1 | 815 | 817 | PF00675 | 0.496 |
CLV_PCSK_FUR_1 | 747 | 751 | PF00082 | 0.435 |
CLV_PCSK_KEX2_1 | 170 | 172 | PF00082 | 0.435 |
CLV_PCSK_KEX2_1 | 383 | 385 | PF00082 | 0.367 |
CLV_PCSK_KEX2_1 | 454 | 456 | PF00082 | 0.446 |
CLV_PCSK_KEX2_1 | 599 | 601 | PF00082 | 0.465 |
CLV_PCSK_KEX2_1 | 729 | 731 | PF00082 | 0.419 |
CLV_PCSK_KEX2_1 | 749 | 751 | PF00082 | 0.463 |
CLV_PCSK_KEX2_1 | 788 | 790 | PF00082 | 0.468 |
CLV_PCSK_KEX2_1 | 800 | 802 | PF00082 | 0.459 |
CLV_PCSK_KEX2_1 | 99 | 101 | PF00082 | 0.464 |
CLV_PCSK_PC1ET2_1 | 383 | 385 | PF00082 | 0.273 |
CLV_PCSK_PC1ET2_1 | 454 | 456 | PF00082 | 0.446 |
CLV_PCSK_PC1ET2_1 | 749 | 751 | PF00082 | 0.509 |
CLV_PCSK_SKI1_1 | 170 | 174 | PF00082 | 0.468 |
CLV_PCSK_SKI1_1 | 246 | 250 | PF00082 | 0.435 |
CLV_PCSK_SKI1_1 | 270 | 274 | PF00082 | 0.364 |
CLV_PCSK_SKI1_1 | 330 | 334 | PF00082 | 0.286 |
CLV_PCSK_SKI1_1 | 526 | 530 | PF00082 | 0.473 |
CLV_PCSK_SKI1_1 | 575 | 579 | PF00082 | 0.434 |
CLV_PCSK_SKI1_1 | 583 | 587 | PF00082 | 0.497 |
CLV_PCSK_SKI1_1 | 711 | 715 | PF00082 | 0.580 |
CLV_PCSK_SKI1_1 | 730 | 734 | PF00082 | 0.452 |
CLV_PCSK_SKI1_1 | 788 | 792 | PF00082 | 0.563 |
CLV_Separin_Metazoa | 74 | 78 | PF03568 | 0.491 |
DEG_APCC_DBOX_1 | 245 | 253 | PF00400 | 0.384 |
DEG_APCC_DBOX_1 | 50 | 58 | PF00400 | 0.438 |
DEG_APCC_DBOX_1 | 825 | 833 | PF00400 | 0.530 |
DEG_SPOP_SBC_1 | 4 | 8 | PF00917 | 0.596 |
DEG_SPOP_SBC_1 | 548 | 552 | PF00917 | 0.271 |
DOC_CYCLIN_RxL_1 | 388 | 401 | PF00134 | 0.512 |
DOC_CYCLIN_RxL_1 | 775 | 785 | PF00134 | 0.342 |
DOC_CYCLIN_yCln2_LP_2 | 540 | 546 | PF00134 | 0.399 |
DOC_MAPK_gen_1 | 459 | 467 | PF00069 | 0.357 |
DOC_MAPK_MEF2A_6 | 459 | 467 | PF00069 | 0.351 |
DOC_PP1_RVXF_1 | 478 | 484 | PF00149 | 0.498 |
DOC_PP2B_LxvP_1 | 396 | 399 | PF13499 | 0.539 |
DOC_PP2B_LxvP_1 | 540 | 543 | PF13499 | 0.420 |
DOC_PP2B_LxvP_1 | 682 | 685 | PF13499 | 0.341 |
DOC_PP4_FxxP_1 | 474 | 477 | PF00568 | 0.323 |
DOC_USP7_MATH_1 | 34 | 38 | PF00917 | 0.474 |
DOC_USP7_MATH_1 | 372 | 376 | PF00917 | 0.411 |
DOC_USP7_MATH_1 | 547 | 551 | PF00917 | 0.324 |
DOC_USP7_MATH_1 | 79 | 83 | PF00917 | 0.466 |
DOC_USP7_MATH_2 | 857 | 863 | PF00917 | 0.513 |
DOC_WW_Pin1_4 | 254 | 259 | PF00397 | 0.455 |
LIG_14-3-3_CanoR_1 | 237 | 243 | PF00244 | 0.388 |
LIG_14-3-3_CanoR_1 | 244 | 249 | PF00244 | 0.377 |
LIG_14-3-3_CanoR_1 | 345 | 352 | PF00244 | 0.462 |
LIG_14-3-3_CanoR_1 | 51 | 55 | PF00244 | 0.496 |
LIG_14-3-3_CanoR_1 | 652 | 660 | PF00244 | 0.468 |
LIG_14-3-3_CanoR_1 | 669 | 677 | PF00244 | 0.496 |
LIG_14-3-3_CanoR_1 | 729 | 735 | PF00244 | 0.312 |
LIG_14-3-3_CanoR_1 | 761 | 767 | PF00244 | 0.475 |
LIG_Actin_WH2_2 | 226 | 241 | PF00022 | 0.494 |
LIG_Actin_WH2_2 | 37 | 53 | PF00022 | 0.506 |
LIG_Actin_WH2_2 | 694 | 710 | PF00022 | 0.481 |
LIG_APCC_ABBA_1 | 177 | 182 | PF00400 | 0.460 |
LIG_APCC_ABBA_1 | 191 | 196 | PF00400 | 0.246 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.560 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.505 |
LIG_CtBP_PxDLS_1 | 258 | 262 | PF00389 | 0.431 |
LIG_deltaCOP1_diTrp_1 | 784 | 791 | PF00928 | 0.527 |
LIG_EH1_1 | 38 | 46 | PF00400 | 0.480 |
LIG_eIF4E_1 | 446 | 452 | PF01652 | 0.400 |
LIG_FHA_1 | 11 | 17 | PF00498 | 0.542 |
LIG_FHA_1 | 203 | 209 | PF00498 | 0.392 |
LIG_FHA_1 | 216 | 222 | PF00498 | 0.376 |
LIG_FHA_1 | 355 | 361 | PF00498 | 0.403 |
LIG_FHA_1 | 620 | 626 | PF00498 | 0.527 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.559 |
LIG_FHA_1 | 669 | 675 | PF00498 | 0.455 |
LIG_FHA_1 | 677 | 683 | PF00498 | 0.435 |
LIG_FHA_1 | 693 | 699 | PF00498 | 0.385 |
LIG_FHA_1 | 708 | 714 | PF00498 | 0.515 |
LIG_FHA_2 | 102 | 108 | PF00498 | 0.508 |
LIG_FHA_2 | 731 | 737 | PF00498 | 0.521 |
LIG_FHA_2 | 845 | 851 | PF00498 | 0.621 |
LIG_GBD_Chelix_1 | 191 | 199 | PF00786 | 0.438 |
LIG_GBD_Chelix_1 | 844 | 852 | PF00786 | 0.595 |
LIG_Integrin_RGD_1 | 600 | 602 | PF01839 | 0.462 |
LIG_Integrin_RGD_1 | 92 | 94 | PF01839 | 0.468 |
LIG_LIR_Apic_2 | 472 | 477 | PF02991 | 0.469 |
LIG_LIR_Gen_1 | 644 | 650 | PF02991 | 0.514 |
LIG_LIR_Gen_1 | 822 | 832 | PF02991 | 0.563 |
LIG_LIR_Nem_3 | 130 | 136 | PF02991 | 0.338 |
LIG_LIR_Nem_3 | 184 | 190 | PF02991 | 0.466 |
LIG_LIR_Nem_3 | 438 | 444 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 560 | 566 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 572 | 577 | PF02991 | 0.315 |
LIG_LIR_Nem_3 | 784 | 790 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 822 | 827 | PF02991 | 0.521 |
LIG_NRBOX | 244 | 250 | PF00104 | 0.503 |
LIG_NRBOX | 447 | 453 | PF00104 | 0.340 |
LIG_NRBOX | 497 | 503 | PF00104 | 0.401 |
LIG_PCNA_PIPBox_1 | 512 | 521 | PF02747 | 0.481 |
LIG_PCNA_yPIPBox_3 | 512 | 526 | PF02747 | 0.492 |
LIG_PCNA_yPIPBox_3 | 694 | 708 | PF02747 | 0.473 |
LIG_Pex14_1 | 787 | 791 | PF04695 | 0.440 |
LIG_Rb_LxCxE_1 | 268 | 287 | PF01857 | 0.415 |
LIG_SH2_CRK | 302 | 306 | PF00017 | 0.331 |
LIG_SH2_GRB2like | 308 | 311 | PF00017 | 0.192 |
LIG_SH2_PTP2 | 194 | 197 | PF00017 | 0.408 |
LIG_SH2_PTP2 | 441 | 444 | PF00017 | 0.331 |
LIG_SH2_PTP2 | 464 | 467 | PF00017 | 0.339 |
LIG_SH2_SRC | 83 | 86 | PF00017 | 0.341 |
LIG_SH2_STAP1 | 129 | 133 | PF00017 | 0.474 |
LIG_SH2_STAP1 | 138 | 142 | PF00017 | 0.499 |
LIG_SH2_STAP1 | 302 | 306 | PF00017 | 0.286 |
LIG_SH2_STAP1 | 352 | 356 | PF00017 | 0.377 |
LIG_SH2_STAP1 | 660 | 664 | PF00017 | 0.371 |
LIG_SH2_STAP1 | 670 | 674 | PF00017 | 0.309 |
LIG_SH2_STAT3 | 251 | 254 | PF00017 | 0.500 |
LIG_SH2_STAT5 | 124 | 127 | PF00017 | 0.467 |
LIG_SH2_STAT5 | 136 | 139 | PF00017 | 0.400 |
LIG_SH2_STAT5 | 194 | 197 | PF00017 | 0.430 |
LIG_SH2_STAT5 | 229 | 232 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 251 | 254 | PF00017 | 0.500 |
LIG_SH2_STAT5 | 441 | 444 | PF00017 | 0.331 |
LIG_SH2_STAT5 | 464 | 467 | PF00017 | 0.305 |
LIG_SH2_STAT5 | 645 | 648 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 670 | 673 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 751 | 754 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 758 | 761 | PF00017 | 0.336 |
LIG_SH2_STAT5 | 83 | 86 | PF00017 | 0.341 |
LIG_SH3_2 | 72 | 77 | PF14604 | 0.582 |
LIG_SH3_3 | 69 | 75 | PF00018 | 0.589 |
LIG_SUMO_SIM_anti_2 | 671 | 679 | PF11976 | 0.456 |
LIG_TRAF2_1 | 257 | 260 | PF00917 | 0.442 |
LIG_TYR_ITIM | 300 | 305 | PF00017 | 0.331 |
LIG_TYR_ITIM | 439 | 444 | PF00017 | 0.339 |
LIG_UBA3_1 | 734 | 741 | PF00899 | 0.336 |
LIG_WRC_WIRS_1 | 659 | 664 | PF05994 | 0.260 |
MOD_CK1_1 | 569 | 575 | PF00069 | 0.451 |
MOD_CK1_1 | 612 | 618 | PF00069 | 0.606 |
MOD_CK1_1 | 9 | 15 | PF00069 | 0.550 |
MOD_CK2_1 | 101 | 107 | PF00069 | 0.434 |
MOD_CK2_1 | 124 | 130 | PF00069 | 0.413 |
MOD_CK2_1 | 254 | 260 | PF00069 | 0.411 |
MOD_CK2_1 | 607 | 613 | PF00069 | 0.515 |
MOD_CK2_1 | 730 | 736 | PF00069 | 0.422 |
MOD_CK2_1 | 79 | 85 | PF00069 | 0.425 |
MOD_CMANNOS | 497 | 500 | PF00535 | 0.475 |
MOD_Cter_Amidation | 727 | 730 | PF01082 | 0.293 |
MOD_GlcNHglycan | 286 | 289 | PF01048 | 0.324 |
MOD_GlcNHglycan | 404 | 407 | PF01048 | 0.548 |
MOD_GlcNHglycan | 411 | 414 | PF01048 | 0.500 |
MOD_GlcNHglycan | 568 | 571 | PF01048 | 0.360 |
MOD_GlcNHglycan | 685 | 688 | PF01048 | 0.518 |
MOD_GlcNHglycan | 726 | 729 | PF01048 | 0.349 |
MOD_GlcNHglycan | 755 | 758 | PF01048 | 0.489 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.602 |
MOD_GSK3_1 | 350 | 357 | PF00069 | 0.376 |
MOD_GSK3_1 | 372 | 379 | PF00069 | 0.456 |
MOD_GSK3_1 | 398 | 405 | PF00069 | 0.510 |
MOD_GSK3_1 | 57 | 64 | PF00069 | 0.516 |
MOD_GSK3_1 | 609 | 616 | PF00069 | 0.554 |
MOD_GSK3_1 | 707 | 714 | PF00069 | 0.496 |
MOD_GSK3_1 | 730 | 737 | PF00069 | 0.345 |
MOD_N-GLC_1 | 216 | 221 | PF02516 | 0.430 |
MOD_N-GLC_1 | 322 | 327 | PF02516 | 0.415 |
MOD_N-GLC_1 | 535 | 540 | PF02516 | 0.544 |
MOD_NEK2_1 | 238 | 243 | PF00069 | 0.479 |
MOD_NEK2_1 | 284 | 289 | PF00069 | 0.276 |
MOD_NEK2_1 | 350 | 355 | PF00069 | 0.373 |
MOD_NEK2_1 | 356 | 361 | PF00069 | 0.373 |
MOD_NEK2_1 | 430 | 435 | PF00069 | 0.516 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.435 |
MOD_NEK2_1 | 507 | 512 | PF00069 | 0.467 |
MOD_NEK2_1 | 520 | 525 | PF00069 | 0.405 |
MOD_NEK2_1 | 566 | 571 | PF00069 | 0.459 |
MOD_NEK2_1 | 607 | 612 | PF00069 | 0.514 |
MOD_NEK2_1 | 61 | 66 | PF00069 | 0.451 |
MOD_NEK2_1 | 676 | 681 | PF00069 | 0.485 |
MOD_NEK2_1 | 707 | 712 | PF00069 | 0.472 |
MOD_NEK2_1 | 734 | 739 | PF00069 | 0.377 |
MOD_NEK2_1 | 827 | 832 | PF00069 | 0.521 |
MOD_NEK2_1 | 844 | 849 | PF00069 | 0.476 |
MOD_NEK2_1 | 852 | 857 | PF00069 | 0.637 |
MOD_NEK2_2 | 136 | 141 | PF00069 | 0.483 |
MOD_PIKK_1 | 124 | 130 | PF00454 | 0.491 |
MOD_PIKK_1 | 558 | 564 | PF00454 | 0.455 |
MOD_PKA_2 | 344 | 350 | PF00069 | 0.484 |
MOD_PKA_2 | 50 | 56 | PF00069 | 0.391 |
MOD_PKA_2 | 651 | 657 | PF00069 | 0.446 |
MOD_PKA_2 | 668 | 674 | PF00069 | 0.492 |
MOD_PKA_2 | 827 | 833 | PF00069 | 0.540 |
MOD_PKB_1 | 99 | 107 | PF00069 | 0.441 |
MOD_Plk_1 | 129 | 135 | PF00069 | 0.476 |
MOD_Plk_1 | 216 | 222 | PF00069 | 0.425 |
MOD_Plk_1 | 322 | 328 | PF00069 | 0.415 |
MOD_Plk_1 | 437 | 443 | PF00069 | 0.415 |
MOD_Plk_1 | 61 | 67 | PF00069 | 0.446 |
MOD_Plk_1 | 612 | 618 | PF00069 | 0.435 |
MOD_Plk_4 | 147 | 153 | PF00069 | 0.270 |
MOD_Plk_4 | 216 | 222 | PF00069 | 0.413 |
MOD_Plk_4 | 314 | 320 | PF00069 | 0.343 |
MOD_Plk_4 | 437 | 443 | PF00069 | 0.415 |
MOD_Plk_4 | 730 | 736 | PF00069 | 0.503 |
MOD_Plk_4 | 79 | 85 | PF00069 | 0.449 |
MOD_ProDKin_1 | 254 | 260 | PF00069 | 0.449 |
MOD_SUMO_for_1 | 35 | 38 | PF00179 | 0.484 |
MOD_SUMO_rev_2 | 809 | 819 | PF00179 | 0.646 |
TRG_DiLeu_BaEn_1 | 259 | 264 | PF01217 | 0.489 |
TRG_DiLeu_BaEn_1 | 268 | 273 | PF01217 | 0.340 |
TRG_DiLeu_BaEn_1 | 672 | 677 | PF01217 | 0.495 |
TRG_DiLeu_BaEn_2 | 24 | 30 | PF01217 | 0.309 |
TRG_DiLeu_BaEn_4 | 867 | 873 | PF01217 | 0.507 |
TRG_DiLeu_BaLyEn_6 | 267 | 272 | PF01217 | 0.364 |
TRG_DiLeu_BaLyEn_6 | 280 | 285 | PF01217 | 0.255 |
TRG_DiLeu_BaLyEn_6 | 301 | 306 | PF01217 | 0.365 |
TRG_DiLeu_BaLyEn_6 | 440 | 445 | PF01217 | 0.425 |
TRG_ENDOCYTIC_2 | 194 | 197 | PF00928 | 0.480 |
TRG_ENDOCYTIC_2 | 302 | 305 | PF00928 | 0.306 |
TRG_ENDOCYTIC_2 | 441 | 444 | PF00928 | 0.324 |
TRG_ENDOCYTIC_2 | 464 | 467 | PF00928 | 0.314 |
TRG_ENDOCYTIC_2 | 478 | 481 | PF00928 | 0.304 |
TRG_ENDOCYTIC_2 | 574 | 577 | PF00928 | 0.370 |
TRG_ENDOCYTIC_2 | 742 | 745 | PF00928 | 0.479 |
TRG_ENDOCYTIC_2 | 824 | 827 | PF00928 | 0.552 |
TRG_ER_diArg_1 | 170 | 172 | PF00400 | 0.485 |
TRG_ER_diArg_1 | 252 | 255 | PF00400 | 0.368 |
TRG_ER_diArg_1 | 787 | 789 | PF00400 | 0.574 |
TRG_ER_diArg_1 | 99 | 101 | PF00400 | 0.464 |
TRG_NES_CRM1_1 | 183 | 196 | PF08389 | 0.302 |
TRG_Pf-PMV_PEXEL_1 | 14 | 18 | PF00026 | 0.530 |
TRG_Pf-PMV_PEXEL_1 | 170 | 174 | PF00026 | 0.477 |
TRG_Pf-PMV_PEXEL_1 | 198 | 202 | PF00026 | 0.430 |
TRG_Pf-PMV_PEXEL_1 | 231 | 235 | PF00026 | 0.472 |
TRG_Pf-PMV_PEXEL_1 | 816 | 820 | PF00026 | 0.526 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEV8 | Leptomonas seymouri | 75% | 100% |
A0A0S4IRK7 | Bodo saltans | 28% | 99% |
A0A1X0P9X2 | Trypanosomatidae | 42% | 96% |
A0A3Q8IEI0 | Leishmania donovani | 90% | 100% |
A0A3R7MIY5 | Trypanosoma rangeli | 42% | 95% |
A4I4W8 | Leishmania infantum | 90% | 100% |
C9ZKZ1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 97% |
E9AEB7 | Leishmania major | 91% | 100% |
E9ALG9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
V5BC46 | Trypanosoma cruzi | 42% | 96% |