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: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HC09
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 13 |
GO:0006793 | phosphorus metabolic process | 3 | 13 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 13 |
GO:0006807 | nitrogen compound metabolic process | 2 | 13 |
GO:0008152 | metabolic process | 1 | 13 |
GO:0009987 | cellular process | 1 | 13 |
GO:0016310 | phosphorylation | 5 | 13 |
GO:0019538 | protein metabolic process | 3 | 13 |
GO:0036211 | protein modification process | 4 | 13 |
GO:0043170 | macromolecule metabolic process | 3 | 13 |
GO:0043412 | macromolecule modification | 4 | 13 |
GO:0044237 | cellular metabolic process | 2 | 13 |
GO:0044238 | primary metabolic process | 2 | 13 |
GO:0071704 | organic substance metabolic process | 2 | 13 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 13 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 13 |
GO:0003824 | catalytic activity | 1 | 13 |
GO:0004672 | protein kinase activity | 3 | 13 |
GO:0005488 | binding | 1 | 13 |
GO:0005524 | ATP binding | 5 | 13 |
GO:0016301 | kinase activity | 4 | 13 |
GO:0016740 | transferase activity | 2 | 13 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 13 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 13 |
GO:0017076 | purine nucleotide binding | 4 | 13 |
GO:0030554 | adenyl nucleotide binding | 5 | 13 |
GO:0032553 | ribonucleotide binding | 3 | 13 |
GO:0032555 | purine ribonucleotide binding | 4 | 13 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 13 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 13 |
GO:0036094 | small molecule binding | 2 | 13 |
GO:0043167 | ion binding | 2 | 13 |
GO:0043168 | anion binding | 3 | 13 |
GO:0097159 | organic cyclic compound binding | 2 | 13 |
GO:0097367 | carbohydrate derivative binding | 2 | 13 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 13 |
GO:1901265 | nucleoside phosphate binding | 3 | 13 |
GO:1901363 | heterocyclic compound binding | 2 | 13 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 515 | 519 | PF00656 | 0.706 |
CLV_C14_Caspase3-7 | 701 | 705 | PF00656 | 0.513 |
CLV_NRD_NRD_1 | 276 | 278 | PF00675 | 0.642 |
CLV_NRD_NRD_1 | 294 | 296 | PF00675 | 0.538 |
CLV_NRD_NRD_1 | 332 | 334 | PF00675 | 0.566 |
CLV_NRD_NRD_1 | 340 | 342 | PF00675 | 0.447 |
CLV_NRD_NRD_1 | 352 | 354 | PF00675 | 0.384 |
CLV_NRD_NRD_1 | 364 | 366 | PF00675 | 0.473 |
CLV_NRD_NRD_1 | 381 | 383 | PF00675 | 0.441 |
CLV_NRD_NRD_1 | 439 | 441 | PF00675 | 0.503 |
CLV_NRD_NRD_1 | 493 | 495 | PF00675 | 0.621 |
CLV_NRD_NRD_1 | 513 | 515 | PF00675 | 0.404 |
CLV_NRD_NRD_1 | 519 | 521 | PF00675 | 0.557 |
CLV_NRD_NRD_1 | 588 | 590 | PF00675 | 0.625 |
CLV_PCSK_KEX2_1 | 245 | 247 | PF00082 | 0.370 |
CLV_PCSK_KEX2_1 | 276 | 278 | PF00082 | 0.670 |
CLV_PCSK_KEX2_1 | 294 | 296 | PF00082 | 0.503 |
CLV_PCSK_KEX2_1 | 331 | 333 | PF00082 | 0.566 |
CLV_PCSK_KEX2_1 | 340 | 342 | PF00082 | 0.510 |
CLV_PCSK_KEX2_1 | 354 | 356 | PF00082 | 0.432 |
CLV_PCSK_KEX2_1 | 380 | 382 | PF00082 | 0.472 |
CLV_PCSK_KEX2_1 | 439 | 441 | PF00082 | 0.503 |
CLV_PCSK_KEX2_1 | 513 | 515 | PF00082 | 0.534 |
CLV_PCSK_PC1ET2_1 | 245 | 247 | PF00082 | 0.396 |
CLV_PCSK_PC1ET2_1 | 354 | 356 | PF00082 | 0.511 |
CLV_PCSK_SKI1_1 | 103 | 107 | PF00082 | 0.281 |
CLV_PCSK_SKI1_1 | 127 | 131 | PF00082 | 0.293 |
CLV_PCSK_SKI1_1 | 214 | 218 | PF00082 | 0.256 |
CLV_PCSK_SKI1_1 | 285 | 289 | PF00082 | 0.376 |
CLV_PCSK_SKI1_1 | 318 | 322 | PF00082 | 0.422 |
CLV_PCSK_SKI1_1 | 354 | 358 | PF00082 | 0.523 |
CLV_PCSK_SKI1_1 | 494 | 498 | PF00082 | 0.666 |
CLV_PCSK_SKI1_1 | 521 | 525 | PF00082 | 0.574 |
CLV_PCSK_SKI1_1 | 636 | 640 | PF00082 | 0.671 |
CLV_PCSK_SKI1_1 | 647 | 651 | PF00082 | 0.510 |
CLV_PCSK_SKI1_1 | 688 | 692 | PF00082 | 0.674 |
CLV_PCSK_SKI1_1 | 707 | 711 | PF00082 | 0.456 |
CLV_PCSK_SKI1_1 | 734 | 738 | PF00082 | 0.360 |
DEG_APCC_DBOX_1 | 258 | 266 | PF00400 | 0.330 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.398 |
DEG_SCF_FBW7_1 | 481 | 488 | PF00400 | 0.725 |
DEG_SCF_FBW7_2 | 638 | 643 | PF00400 | 0.599 |
DEG_SPOP_SBC_1 | 485 | 489 | PF00917 | 0.621 |
DOC_CKS1_1 | 482 | 487 | PF01111 | 0.727 |
DOC_CYCLIN_RxL_1 | 519 | 529 | PF00134 | 0.473 |
DOC_CYCLIN_yCln2_LP_2 | 476 | 482 | PF00134 | 0.504 |
DOC_CYCLIN_yCln2_LP_2 | 559 | 565 | PF00134 | 0.474 |
DOC_CYCLIN_yCln2_LP_2 | 573 | 579 | PF00134 | 0.472 |
DOC_MAPK_gen_1 | 127 | 136 | PF00069 | 0.284 |
DOC_MAPK_gen_1 | 273 | 282 | PF00069 | 0.629 |
DOC_MAPK_gen_1 | 340 | 350 | PF00069 | 0.435 |
DOC_MAPK_gen_1 | 520 | 526 | PF00069 | 0.461 |
DOC_MAPK_MEF2A_6 | 553 | 561 | PF00069 | 0.494 |
DOC_MAPK_MEF2A_6 | 729 | 737 | PF00069 | 0.381 |
DOC_MAPK_MEF2A_6 | 73 | 80 | PF00069 | 0.264 |
DOC_PP2B_LxvP_1 | 472 | 475 | PF13499 | 0.773 |
DOC_PP2B_LxvP_1 | 559 | 562 | PF13499 | 0.533 |
DOC_PP2B_LxvP_1 | 573 | 576 | PF13499 | 0.555 |
DOC_PP4_FxxP_1 | 715 | 718 | PF00568 | 0.569 |
DOC_USP7_MATH_1 | 247 | 251 | PF00917 | 0.288 |
DOC_USP7_MATH_1 | 486 | 490 | PF00917 | 0.709 |
DOC_USP7_MATH_1 | 536 | 540 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 565 | 569 | PF00917 | 0.507 |
DOC_USP7_MATH_1 | 579 | 583 | PF00917 | 0.518 |
DOC_USP7_MATH_1 | 702 | 706 | PF00917 | 0.614 |
DOC_USP7_MATH_1 | 718 | 722 | PF00917 | 0.450 |
DOC_USP7_MATH_2 | 42 | 48 | PF00917 | 0.249 |
DOC_USP7_UBL2_3 | 373 | 377 | PF12436 | 0.613 |
DOC_USP7_UBL2_3 | 581 | 585 | PF12436 | 0.624 |
DOC_USP7_UBL2_3 | 8 | 12 | PF12436 | 0.339 |
DOC_WW_Pin1_4 | 163 | 168 | PF00397 | 0.284 |
DOC_WW_Pin1_4 | 411 | 416 | PF00397 | 0.682 |
DOC_WW_Pin1_4 | 481 | 486 | PF00397 | 0.603 |
DOC_WW_Pin1_4 | 544 | 549 | PF00397 | 0.667 |
DOC_WW_Pin1_4 | 571 | 576 | PF00397 | 0.545 |
DOC_WW_Pin1_4 | 591 | 596 | PF00397 | 0.662 |
DOC_WW_Pin1_4 | 636 | 641 | PF00397 | 0.616 |
DOC_WW_Pin1_4 | 655 | 660 | PF00397 | 0.666 |
LIG_14-3-3_CanoR_1 | 154 | 158 | PF00244 | 0.256 |
LIG_14-3-3_CanoR_1 | 233 | 241 | PF00244 | 0.337 |
LIG_14-3-3_CanoR_1 | 246 | 255 | PF00244 | 0.206 |
LIG_14-3-3_CanoR_1 | 276 | 280 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 45 | 52 | PF00244 | 0.182 |
LIG_14-3-3_CanoR_1 | 494 | 501 | PF00244 | 0.566 |
LIG_14-3-3_CanoR_1 | 553 | 557 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 686 | 691 | PF00244 | 0.623 |
LIG_Actin_WH2_2 | 145 | 162 | PF00022 | 0.249 |
LIG_Actin_WH2_2 | 204 | 219 | PF00022 | 0.262 |
LIG_Actin_WH2_2 | 28 | 43 | PF00022 | 0.339 |
LIG_AP2alpha_1 | 690 | 694 | PF02296 | 0.523 |
LIG_APCC_ABBA_1 | 733 | 738 | PF00400 | 0.358 |
LIG_BRCT_BRCA1_1 | 505 | 509 | PF00533 | 0.659 |
LIG_BRCT_BRCA1_1 | 554 | 558 | PF00533 | 0.506 |
LIG_FHA_1 | 129 | 135 | PF00498 | 0.280 |
LIG_FHA_1 | 154 | 160 | PF00498 | 0.272 |
LIG_FHA_1 | 62 | 68 | PF00498 | 0.281 |
LIG_FHA_1 | 712 | 718 | PF00498 | 0.458 |
LIG_FHA_1 | 721 | 727 | PF00498 | 0.446 |
LIG_FHA_2 | 495 | 501 | PF00498 | 0.617 |
LIG_FHA_2 | 658 | 664 | PF00498 | 0.589 |
LIG_FHA_2 | 687 | 693 | PF00498 | 0.499 |
LIG_FHA_2 | 696 | 702 | PF00498 | 0.418 |
LIG_LIR_Apic_2 | 166 | 172 | PF02991 | 0.311 |
LIG_LIR_Apic_2 | 714 | 718 | PF02991 | 0.468 |
LIG_LIR_Gen_1 | 2 | 10 | PF02991 | 0.270 |
LIG_LIR_Gen_1 | 555 | 565 | PF02991 | 0.479 |
LIG_LIR_Gen_1 | 668 | 678 | PF02991 | 0.394 |
LIG_LIR_Gen_1 | 75 | 83 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 2 | 7 | PF02991 | 0.281 |
LIG_LIR_Nem_3 | 555 | 561 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 668 | 674 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 87 | 92 | PF02991 | 0.249 |
LIG_LYPXL_S_1 | 219 | 223 | PF13949 | 0.262 |
LIG_LYPXL_yS_3 | 220 | 223 | PF13949 | 0.249 |
LIG_MAD2 | 214 | 222 | PF02301 | 0.249 |
LIG_PCNA_yPIPBox_3 | 209 | 220 | PF02747 | 0.267 |
LIG_PDZ_Class_2 | 801 | 806 | PF00595 | 0.577 |
LIG_Pex14_2 | 15 | 19 | PF04695 | 0.249 |
LIG_Pex14_2 | 690 | 694 | PF04695 | 0.523 |
LIG_PTAP_UEV_1 | 608 | 613 | PF05743 | 0.476 |
LIG_RPA_C_Plants | 285 | 296 | PF08784 | 0.375 |
LIG_SH2_CRK | 4 | 8 | PF00017 | 0.304 |
LIG_SH2_CRK | 89 | 93 | PF00017 | 0.249 |
LIG_SH2_GRB2like | 82 | 85 | PF00017 | 0.280 |
LIG_SH2_SRC | 66 | 69 | PF00017 | 0.284 |
LIG_SH2_SRC | 82 | 85 | PF00017 | 0.260 |
LIG_SH2_STAP1 | 227 | 231 | PF00017 | 0.300 |
LIG_SH2_STAT5 | 169 | 172 | PF00017 | 0.249 |
LIG_SH2_STAT5 | 4 | 7 | PF00017 | 0.253 |
LIG_SH2_STAT5 | 454 | 457 | PF00017 | 0.706 |
LIG_SH2_STAT5 | 66 | 69 | PF00017 | 0.318 |
LIG_SH3_3 | 216 | 222 | PF00018 | 0.328 |
LIG_SH3_3 | 476 | 482 | PF00018 | 0.610 |
LIG_SH3_3 | 558 | 564 | PF00018 | 0.629 |
LIG_SH3_3 | 569 | 575 | PF00018 | 0.584 |
LIG_SH3_3 | 602 | 608 | PF00018 | 0.613 |
LIG_SH3_3 | 613 | 619 | PF00018 | 0.727 |
LIG_SUMO_SIM_par_1 | 250 | 256 | PF11976 | 0.253 |
LIG_SUMO_SIM_par_1 | 278 | 284 | PF11976 | 0.509 |
LIG_TRAF2_1 | 281 | 284 | PF00917 | 0.510 |
LIG_TRAF2_1 | 349 | 352 | PF00917 | 0.521 |
LIG_TRAF2_1 | 497 | 500 | PF00917 | 0.606 |
LIG_UBA3_1 | 238 | 245 | PF00899 | 0.304 |
LIG_WW_3 | 480 | 484 | PF00397 | 0.719 |
MOD_CK1_1 | 14 | 20 | PF00069 | 0.292 |
MOD_CK1_1 | 229 | 235 | PF00069 | 0.334 |
MOD_CK1_1 | 278 | 284 | PF00069 | 0.598 |
MOD_CK1_1 | 489 | 495 | PF00069 | 0.505 |
MOD_CK1_1 | 534 | 540 | PF00069 | 0.602 |
MOD_CK1_1 | 544 | 550 | PF00069 | 0.690 |
MOD_CK1_1 | 610 | 616 | PF00069 | 0.785 |
MOD_CK1_1 | 799 | 805 | PF00069 | 0.557 |
MOD_CK2_1 | 278 | 284 | PF00069 | 0.595 |
MOD_CK2_1 | 427 | 433 | PF00069 | 0.575 |
MOD_CK2_1 | 494 | 500 | PF00069 | 0.626 |
MOD_CK2_1 | 590 | 596 | PF00069 | 0.571 |
MOD_CK2_1 | 655 | 661 | PF00069 | 0.583 |
MOD_CK2_1 | 695 | 701 | PF00069 | 0.414 |
MOD_CK2_1 | 756 | 762 | PF00069 | 0.604 |
MOD_GlcNHglycan | 16 | 19 | PF01048 | 0.249 |
MOD_GlcNHglycan | 235 | 238 | PF01048 | 0.308 |
MOD_GlcNHglycan | 428 | 432 | PF01048 | 0.545 |
MOD_GlcNHglycan | 46 | 49 | PF01048 | 0.249 |
MOD_GlcNHglycan | 543 | 546 | PF01048 | 0.695 |
MOD_GlcNHglycan | 554 | 557 | PF01048 | 0.657 |
MOD_GlcNHglycan | 585 | 588 | PF01048 | 0.544 |
MOD_GlcNHglycan | 609 | 612 | PF01048 | 0.676 |
MOD_GlcNHglycan | 613 | 616 | PF01048 | 0.630 |
MOD_GlcNHglycan | 720 | 723 | PF01048 | 0.600 |
MOD_GlcNHglycan | 756 | 759 | PF01048 | 0.568 |
MOD_GlcNHglycan | 768 | 771 | PF01048 | 0.557 |
MOD_GlcNHglycan | 801 | 804 | PF01048 | 0.696 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.266 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.313 |
MOD_GSK3_1 | 407 | 414 | PF00069 | 0.745 |
MOD_GSK3_1 | 481 | 488 | PF00069 | 0.725 |
MOD_GSK3_1 | 490 | 497 | PF00069 | 0.708 |
MOD_GSK3_1 | 537 | 544 | PF00069 | 0.735 |
MOD_GSK3_1 | 579 | 586 | PF00069 | 0.716 |
MOD_GSK3_1 | 590 | 597 | PF00069 | 0.680 |
MOD_GSK3_1 | 607 | 614 | PF00069 | 0.750 |
MOD_N-GLC_1 | 181 | 186 | PF02516 | 0.249 |
MOD_N-GLC_1 | 229 | 234 | PF02516 | 0.319 |
MOD_N-GLC_1 | 247 | 252 | PF02516 | 0.409 |
MOD_N-GLC_1 | 551 | 556 | PF02516 | 0.650 |
MOD_N-GLC_1 | 583 | 588 | PF02516 | 0.524 |
MOD_N-GLC_1 | 61 | 66 | PF02516 | 0.279 |
MOD_N-GLC_1 | 686 | 691 | PF02516 | 0.431 |
MOD_N-GLC_1 | 718 | 723 | PF02516 | 0.552 |
MOD_N-GLC_1 | 754 | 759 | PF02516 | 0.540 |
MOD_NEK2_1 | 114 | 119 | PF00069 | 0.288 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.284 |
MOD_NEK2_1 | 159 | 164 | PF00069 | 0.284 |
MOD_NEK2_1 | 226 | 231 | PF00069 | 0.348 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.439 |
MOD_NEK2_1 | 526 | 531 | PF00069 | 0.595 |
MOD_NEK2_1 | 54 | 59 | PF00069 | 0.414 |
MOD_PIKK_1 | 107 | 113 | PF00454 | 0.262 |
MOD_PIKK_1 | 128 | 134 | PF00454 | 0.249 |
MOD_PIKK_1 | 2 | 8 | PF00454 | 0.328 |
MOD_PIKK_1 | 247 | 253 | PF00454 | 0.280 |
MOD_PIKK_1 | 459 | 465 | PF00454 | 0.586 |
MOD_PIKK_1 | 531 | 537 | PF00454 | 0.528 |
MOD_PKA_1 | 494 | 500 | PF00069 | 0.469 |
MOD_PKA_2 | 153 | 159 | PF00069 | 0.249 |
MOD_PKA_2 | 258 | 264 | PF00069 | 0.294 |
MOD_PKA_2 | 275 | 281 | PF00069 | 0.613 |
MOD_PKA_2 | 44 | 50 | PF00069 | 0.256 |
MOD_PKA_2 | 552 | 558 | PF00069 | 0.491 |
MOD_Plk_1 | 194 | 200 | PF00069 | 0.249 |
MOD_Plk_1 | 229 | 235 | PF00069 | 0.331 |
MOD_Plk_1 | 247 | 253 | PF00069 | 0.183 |
MOD_Plk_1 | 61 | 67 | PF00069 | 0.272 |
MOD_Plk_1 | 686 | 692 | PF00069 | 0.629 |
MOD_Plk_1 | 695 | 701 | PF00069 | 0.631 |
MOD_Plk_2-3 | 695 | 701 | PF00069 | 0.521 |
MOD_Plk_4 | 114 | 120 | PF00069 | 0.328 |
MOD_Plk_4 | 148 | 154 | PF00069 | 0.262 |
MOD_Plk_4 | 253 | 259 | PF00069 | 0.328 |
MOD_Plk_4 | 450 | 456 | PF00069 | 0.578 |
MOD_Plk_4 | 566 | 572 | PF00069 | 0.498 |
MOD_Plk_4 | 673 | 679 | PF00069 | 0.414 |
MOD_Plk_4 | 72 | 78 | PF00069 | 0.309 |
MOD_ProDKin_1 | 163 | 169 | PF00069 | 0.284 |
MOD_ProDKin_1 | 411 | 417 | PF00069 | 0.681 |
MOD_ProDKin_1 | 481 | 487 | PF00069 | 0.605 |
MOD_ProDKin_1 | 544 | 550 | PF00069 | 0.659 |
MOD_ProDKin_1 | 571 | 577 | PF00069 | 0.547 |
MOD_ProDKin_1 | 591 | 597 | PF00069 | 0.659 |
MOD_ProDKin_1 | 636 | 642 | PF00069 | 0.611 |
MOD_ProDKin_1 | 655 | 661 | PF00069 | 0.659 |
MOD_SUMO_rev_2 | 347 | 356 | PF00179 | 0.549 |
MOD_SUMO_rev_2 | 68 | 75 | PF00179 | 0.288 |
MOD_SUMO_rev_2 | 705 | 715 | PF00179 | 0.671 |
TRG_DiLeu_BaEn_1 | 283 | 288 | PF01217 | 0.378 |
TRG_DiLeu_BaEn_4 | 283 | 289 | PF01217 | 0.541 |
TRG_DiLeu_BaLyEn_6 | 230 | 235 | PF01217 | 0.396 |
TRG_ENDOCYTIC_2 | 220 | 223 | PF00928 | 0.249 |
TRG_ENDOCYTIC_2 | 4 | 7 | PF00928 | 0.249 |
TRG_ENDOCYTIC_2 | 435 | 438 | PF00928 | 0.506 |
TRG_ENDOCYTIC_2 | 671 | 674 | PF00928 | 0.375 |
TRG_ENDOCYTIC_2 | 750 | 753 | PF00928 | 0.389 |
TRG_ENDOCYTIC_2 | 89 | 92 | PF00928 | 0.276 |
TRG_ER_diArg_1 | 331 | 333 | PF00400 | 0.570 |
TRG_ER_diArg_1 | 340 | 342 | PF00400 | 0.558 |
TRG_ER_diArg_1 | 380 | 382 | PF00400 | 0.574 |
TRG_ER_diArg_1 | 438 | 440 | PF00400 | 0.509 |
TRG_ER_diArg_1 | 512 | 514 | PF00400 | 0.520 |
TRG_NES_CRM1_1 | 724 | 738 | PF08389 | 0.388 |
TRG_NES_CRM1_1 | 762 | 776 | PF08389 | 0.421 |
TRG_Pf-PMV_PEXEL_1 | 123 | 128 | PF00026 | 0.259 |
TRG_Pf-PMV_PEXEL_1 | 285 | 289 | PF00026 | 0.375 |
TRG_Pf-PMV_PEXEL_1 | 333 | 337 | PF00026 | 0.513 |
TRG_Pf-PMV_PEXEL_1 | 340 | 345 | PF00026 | 0.450 |
TRG_Pf-PMV_PEXEL_1 | 355 | 359 | PF00026 | 0.386 |
TRG_Pf-PMV_PEXEL_1 | 365 | 370 | PF00026 | 0.461 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1P9W7 | Leptomonas seymouri | 64% | 100% |
A0A0S4JKY4 | Bodo saltans | 44% | 100% |
A0A1X0NHD4 | Trypanosomatidae | 48% | 100% |
A0A3Q8IBZ9 | Leishmania donovani | 84% | 100% |
A0A3R7M6Z7 | Trypanosoma rangeli | 47% | 100% |
A4HZM2 | Leishmania infantum | 84% | 100% |
D0A118 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 100% |
E9AJJ2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E9AVE6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |
Q4QC33 | Leishmania major | 84% | 99% |
V5BLW4 | Trypanosoma cruzi | 47% | 100% |