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 |
Related structures:
AlphaFold database: E9AST8
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 8 |
GO:0006364 | rRNA processing | 8 | 4 |
GO:0006396 | RNA processing | 6 | 4 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 8 |
GO:0006807 | nitrogen compound metabolic process | 2 | 8 |
GO:0008152 | metabolic process | 1 | 8 |
GO:0009987 | cellular process | 1 | 8 |
GO:0016070 | RNA metabolic process | 5 | 8 |
GO:0016072 | rRNA metabolic process | 7 | 4 |
GO:0034470 | ncRNA processing | 7 | 4 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 8 |
GO:0034660 | ncRNA metabolic process | 6 | 4 |
GO:0043170 | macromolecule metabolic process | 3 | 8 |
GO:0044237 | cellular metabolic process | 2 | 8 |
GO:0044238 | primary metabolic process | 2 | 8 |
GO:0046483 | heterocycle metabolic process | 3 | 8 |
GO:0071704 | organic substance metabolic process | 2 | 8 |
GO:0090304 | nucleic acid metabolic process | 4 | 8 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 8 |
GO:0001522 | pseudouridine synthesis | 6 | 4 |
GO:0009451 | RNA modification | 5 | 4 |
GO:0043412 | macromolecule modification | 4 | 4 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003723 | RNA binding | 4 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004730 | pseudouridylate synthase activity | 5 | 8 |
GO:0005488 | binding | 1 | 12 |
GO:0009982 | pseudouridine synthase activity | 4 | 12 |
GO:0016829 | lyase activity | 2 | 8 |
GO:0016835 | carbon-oxygen lyase activity | 3 | 8 |
GO:0016836 | hydro-lyase activity | 4 | 8 |
GO:0016853 | isomerase activity | 2 | 12 |
GO:0016866 | intramolecular transferase activity | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0106029 | tRNA pseudouridine synthase activity | 5 | 1 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 1 |
GO:0140101 | catalytic activity, acting on a tRNA | 4 | 1 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 131 | 135 | PF00656 | 0.700 |
CLV_C14_Caspase3-7 | 406 | 410 | PF00656 | 0.456 |
CLV_C14_Caspase3-7 | 604 | 608 | PF00656 | 0.500 |
CLV_C14_Caspase3-7 | 613 | 617 | PF00656 | 0.466 |
CLV_NRD_NRD_1 | 108 | 110 | PF00675 | 0.727 |
CLV_NRD_NRD_1 | 214 | 216 | PF00675 | 0.810 |
CLV_NRD_NRD_1 | 255 | 257 | PF00675 | 0.763 |
CLV_NRD_NRD_1 | 297 | 299 | PF00675 | 0.693 |
CLV_NRD_NRD_1 | 308 | 310 | PF00675 | 0.713 |
CLV_NRD_NRD_1 | 346 | 348 | PF00675 | 0.276 |
CLV_NRD_NRD_1 | 48 | 50 | PF00675 | 0.683 |
CLV_NRD_NRD_1 | 529 | 531 | PF00675 | 0.296 |
CLV_NRD_NRD_1 | 56 | 58 | PF00675 | 0.671 |
CLV_NRD_NRD_1 | 582 | 584 | PF00675 | 0.483 |
CLV_NRD_NRD_1 | 590 | 592 | PF00675 | 0.470 |
CLV_NRD_NRD_1 | 637 | 639 | PF00675 | 0.586 |
CLV_NRD_NRD_1 | 659 | 661 | PF00675 | 0.684 |
CLV_PCSK_FUR_1 | 54 | 58 | PF00082 | 0.721 |
CLV_PCSK_FUR_1 | 588 | 592 | PF00082 | 0.476 |
CLV_PCSK_KEX2_1 | 108 | 110 | PF00082 | 0.727 |
CLV_PCSK_KEX2_1 | 255 | 257 | PF00082 | 0.763 |
CLV_PCSK_KEX2_1 | 297 | 299 | PF00082 | 0.698 |
CLV_PCSK_KEX2_1 | 308 | 310 | PF00082 | 0.713 |
CLV_PCSK_KEX2_1 | 346 | 348 | PF00082 | 0.276 |
CLV_PCSK_KEX2_1 | 50 | 52 | PF00082 | 0.731 |
CLV_PCSK_KEX2_1 | 56 | 58 | PF00082 | 0.627 |
CLV_PCSK_KEX2_1 | 582 | 584 | PF00082 | 0.483 |
CLV_PCSK_KEX2_1 | 590 | 592 | PF00082 | 0.470 |
CLV_PCSK_KEX2_1 | 631 | 633 | PF00082 | 0.545 |
CLV_PCSK_KEX2_1 | 637 | 639 | PF00082 | 0.582 |
CLV_PCSK_KEX2_1 | 659 | 661 | PF00082 | 0.684 |
CLV_PCSK_PC1ET2_1 | 50 | 52 | PF00082 | 0.731 |
CLV_PCSK_PC1ET2_1 | 631 | 633 | PF00082 | 0.336 |
CLV_PCSK_PC7_1 | 251 | 257 | PF00082 | 0.643 |
CLV_PCSK_SKI1_1 | 215 | 219 | PF00082 | 0.639 |
CLV_PCSK_SKI1_1 | 256 | 260 | PF00082 | 0.630 |
CLV_PCSK_SKI1_1 | 261 | 265 | PF00082 | 0.628 |
CLV_PCSK_SKI1_1 | 470 | 474 | PF00082 | 0.381 |
CLV_PCSK_SKI1_1 | 554 | 558 | PF00082 | 0.425 |
CLV_PCSK_SKI1_1 | 596 | 600 | PF00082 | 0.487 |
CLV_PCSK_SKI1_1 | 615 | 619 | PF00082 | 0.364 |
DEG_APCC_DBOX_1 | 152 | 160 | PF00400 | 0.635 |
DEG_APCC_DBOX_1 | 462 | 470 | PF00400 | 0.524 |
DOC_CKS1_1 | 45 | 50 | PF01111 | 0.755 |
DOC_MAPK_DCC_7 | 386 | 396 | PF00069 | 0.448 |
DOC_MAPK_gen_1 | 108 | 115 | PF00069 | 0.748 |
DOC_MAPK_gen_1 | 505 | 514 | PF00069 | 0.471 |
DOC_MAPK_gen_1 | 530 | 540 | PF00069 | 0.260 |
DOC_MAPK_gen_1 | 659 | 667 | PF00069 | 0.563 |
DOC_MAPK_MEF2A_6 | 388 | 396 | PF00069 | 0.445 |
DOC_MAPK_MEF2A_6 | 505 | 514 | PF00069 | 0.435 |
DOC_MIT_MIM_1 | 150 | 160 | PF04212 | 0.516 |
DOC_PP1_RVXF_1 | 384 | 390 | PF00149 | 0.480 |
DOC_PP1_RVXF_1 | 535 | 541 | PF00149 | 0.401 |
DOC_PP4_FxxP_1 | 389 | 392 | PF00568 | 0.456 |
DOC_PP4_FxxP_1 | 499 | 502 | PF00568 | 0.479 |
DOC_PP4_FxxP_1 | 647 | 650 | PF00568 | 0.432 |
DOC_USP7_MATH_1 | 116 | 120 | PF00917 | 0.632 |
DOC_USP7_MATH_1 | 25 | 29 | PF00917 | 0.564 |
DOC_USP7_MATH_1 | 319 | 323 | PF00917 | 0.684 |
DOC_USP7_MATH_1 | 430 | 434 | PF00917 | 0.476 |
DOC_USP7_MATH_1 | 503 | 507 | PF00917 | 0.505 |
DOC_USP7_MATH_1 | 549 | 553 | PF00917 | 0.437 |
DOC_USP7_MATH_1 | 654 | 658 | PF00917 | 0.748 |
DOC_USP7_MATH_1 | 84 | 88 | PF00917 | 0.762 |
DOC_WW_Pin1_4 | 141 | 146 | PF00397 | 0.578 |
DOC_WW_Pin1_4 | 203 | 208 | PF00397 | 0.746 |
DOC_WW_Pin1_4 | 266 | 271 | PF00397 | 0.668 |
DOC_WW_Pin1_4 | 288 | 293 | PF00397 | 0.699 |
DOC_WW_Pin1_4 | 44 | 49 | PF00397 | 0.756 |
DOC_WW_Pin1_4 | 596 | 601 | PF00397 | 0.498 |
DOC_WW_Pin1_4 | 93 | 98 | PF00397 | 0.644 |
LIG_14-3-3_CanoR_1 | 215 | 224 | PF00244 | 0.598 |
LIG_14-3-3_CanoR_1 | 308 | 313 | PF00244 | 0.680 |
LIG_14-3-3_CanoR_1 | 507 | 511 | PF00244 | 0.434 |
LIG_14-3-3_CanoR_1 | 537 | 541 | PF00244 | 0.387 |
LIG_14-3-3_CanoR_1 | 637 | 646 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 659 | 663 | PF00244 | 0.684 |
LIG_Actin_WH2_2 | 144 | 162 | PF00022 | 0.596 |
LIG_Actin_WH2_2 | 621 | 639 | PF00022 | 0.609 |
LIG_BIR_III_4 | 409 | 413 | PF00653 | 0.456 |
LIG_BRCT_BRCA1_1 | 168 | 172 | PF00533 | 0.749 |
LIG_deltaCOP1_diTrp_1 | 575 | 581 | PF00928 | 0.522 |
LIG_EH_1 | 366 | 370 | PF12763 | 0.476 |
LIG_FHA_1 | 147 | 153 | PF00498 | 0.530 |
LIG_FHA_1 | 240 | 246 | PF00498 | 0.528 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.673 |
LIG_FHA_1 | 462 | 468 | PF00498 | 0.486 |
LIG_FHA_1 | 481 | 487 | PF00498 | 0.306 |
LIG_FHA_2 | 226 | 232 | PF00498 | 0.688 |
LIG_FHA_2 | 34 | 40 | PF00498 | 0.660 |
LIG_FHA_2 | 597 | 603 | PF00498 | 0.487 |
LIG_FHA_2 | 608 | 614 | PF00498 | 0.467 |
LIG_Integrin_isoDGR_2 | 489 | 491 | PF01839 | 0.581 |
LIG_Integrin_RGD_1 | 132 | 134 | PF01839 | 0.756 |
LIG_LIR_Apic_2 | 497 | 502 | PF02991 | 0.460 |
LIG_LIR_Apic_2 | 644 | 650 | PF02991 | 0.430 |
LIG_LIR_Gen_1 | 610 | 618 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 539 | 543 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 575 | 581 | PF02991 | 0.528 |
LIG_LIR_Nem_3 | 610 | 614 | PF02991 | 0.531 |
LIG_PCNA_PIPBox_1 | 1 | 10 | PF02747 | 0.550 |
LIG_PTB_Apo_2 | 492 | 499 | PF02174 | 0.467 |
LIG_PTB_Apo_2 | 605 | 612 | PF02174 | 0.526 |
LIG_PTB_Phospho_1 | 605 | 611 | PF10480 | 0.524 |
LIG_RPA_C_Fungi | 342 | 354 | PF08784 | 0.449 |
LIG_SH2_CRK | 397 | 401 | PF00017 | 0.328 |
LIG_SH2_SRC | 611 | 614 | PF00017 | 0.543 |
LIG_SH2_STAP1 | 508 | 512 | PF00017 | 0.503 |
LIG_SH2_STAP1 | 562 | 566 | PF00017 | 0.584 |
LIG_SH2_STAT5 | 465 | 468 | PF00017 | 0.321 |
LIG_SH2_STAT5 | 580 | 583 | PF00017 | 0.603 |
LIG_SH2_STAT5 | 609 | 612 | PF00017 | 0.606 |
LIG_SH2_STAT5 | 7 | 10 | PF00017 | 0.673 |
LIG_SH3_2 | 292 | 297 | PF14604 | 0.553 |
LIG_SH3_3 | 204 | 210 | PF00018 | 0.488 |
LIG_SH3_3 | 289 | 295 | PF00018 | 0.680 |
LIG_SH3_3 | 553 | 559 | PF00018 | 0.423 |
LIG_SH3_3 | 566 | 572 | PF00018 | 0.462 |
LIG_SUMO_SIM_par_1 | 440 | 445 | PF11976 | 0.328 |
LIG_TRAF2_1 | 234 | 237 | PF00917 | 0.743 |
LIG_TRAF2_1 | 24 | 27 | PF00917 | 0.602 |
LIG_TRAF2_1 | 610 | 613 | PF00917 | 0.503 |
LIG_TRAF2_1 | 677 | 680 | PF00917 | 0.675 |
LIG_TRAF2_2 | 145 | 150 | PF00917 | 0.558 |
LIG_UBA3_1 | 156 | 163 | PF00899 | 0.510 |
LIG_UBA3_1 | 524 | 531 | PF00899 | 0.286 |
LIG_WRC_WIRS_1 | 61 | 66 | PF05994 | 0.729 |
LIG_WW_1 | 559 | 562 | PF00397 | 0.461 |
LIG_WW_3 | 390 | 394 | PF00397 | 0.447 |
MOD_CDC14_SPxK_1 | 269 | 272 | PF00782 | 0.506 |
MOD_CDK_SPK_2 | 44 | 49 | PF00069 | 0.562 |
MOD_CDK_SPK_2 | 596 | 601 | PF00069 | 0.498 |
MOD_CDK_SPxK_1 | 266 | 272 | PF00069 | 0.510 |
MOD_CDK_SPxK_1 | 44 | 50 | PF00069 | 0.756 |
MOD_CDK_SPxxK_3 | 44 | 51 | PF00069 | 0.754 |
MOD_CK1_1 | 506 | 512 | PF00069 | 0.433 |
MOD_CK2_1 | 33 | 39 | PF00069 | 0.752 |
MOD_CK2_1 | 342 | 348 | PF00069 | 0.328 |
MOD_CK2_1 | 549 | 555 | PF00069 | 0.444 |
MOD_CK2_1 | 596 | 602 | PF00069 | 0.485 |
MOD_CK2_1 | 607 | 613 | PF00069 | 0.473 |
MOD_Cter_Amidation | 306 | 309 | PF01082 | 0.656 |
MOD_Cter_Amidation | 528 | 531 | PF01082 | 0.288 |
MOD_GlcNHglycan | 221 | 224 | PF01048 | 0.672 |
MOD_GlcNHglycan | 321 | 324 | PF01048 | 0.644 |
MOD_GlcNHglycan | 354 | 357 | PF01048 | 0.339 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.673 |
MOD_GlcNHglycan | 81 | 84 | PF01048 | 0.664 |
MOD_GlcNHglycan | 86 | 89 | PF01048 | 0.651 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.568 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.687 |
MOD_GSK3_1 | 654 | 661 | PF00069 | 0.719 |
MOD_N-GLC_1 | 361 | 366 | PF02516 | 0.398 |
MOD_N-GLC_1 | 607 | 612 | PF02516 | 0.530 |
MOD_NEK2_1 | 100 | 105 | PF00069 | 0.629 |
MOD_NEK2_1 | 334 | 339 | PF00069 | 0.479 |
MOD_NEK2_1 | 543 | 548 | PF00069 | 0.439 |
MOD_NEK2_2 | 549 | 554 | PF00069 | 0.442 |
MOD_NEK2_2 | 60 | 65 | PF00069 | 0.643 |
MOD_NEK2_2 | 654 | 659 | PF00069 | 0.750 |
MOD_PIKK_1 | 215 | 221 | PF00454 | 0.501 |
MOD_PIKK_1 | 560 | 566 | PF00454 | 0.595 |
MOD_PK_1 | 308 | 314 | PF00069 | 0.684 |
MOD_PKA_1 | 215 | 221 | PF00069 | 0.660 |
MOD_PKA_1 | 308 | 314 | PF00069 | 0.742 |
MOD_PKA_1 | 56 | 62 | PF00069 | 0.728 |
MOD_PKA_1 | 637 | 643 | PF00069 | 0.510 |
MOD_PKA_2 | 280 | 286 | PF00069 | 0.496 |
MOD_PKA_2 | 308 | 314 | PF00069 | 0.655 |
MOD_PKA_2 | 506 | 512 | PF00069 | 0.432 |
MOD_PKA_2 | 536 | 542 | PF00069 | 0.395 |
MOD_PKA_2 | 56 | 62 | PF00069 | 0.735 |
MOD_PKA_2 | 584 | 590 | PF00069 | 0.466 |
MOD_PKA_2 | 637 | 643 | PF00069 | 0.407 |
MOD_PKA_2 | 658 | 664 | PF00069 | 0.737 |
MOD_PKB_1 | 54 | 62 | PF00069 | 0.725 |
MOD_Plk_1 | 124 | 130 | PF00069 | 0.708 |
MOD_Plk_1 | 283 | 289 | PF00069 | 0.770 |
MOD_Plk_1 | 317 | 323 | PF00069 | 0.530 |
MOD_Plk_1 | 448 | 454 | PF00069 | 0.344 |
MOD_Plk_1 | 554 | 560 | PF00069 | 0.434 |
MOD_Plk_1 | 607 | 613 | PF00069 | 0.524 |
MOD_Plk_1 | 688 | 694 | PF00069 | 0.630 |
MOD_Plk_2-3 | 607 | 613 | PF00069 | 0.490 |
MOD_Plk_4 | 168 | 174 | PF00069 | 0.606 |
MOD_Plk_4 | 308 | 314 | PF00069 | 0.739 |
MOD_Plk_4 | 456 | 462 | PF00069 | 0.348 |
MOD_Plk_4 | 60 | 66 | PF00069 | 0.599 |
MOD_ProDKin_1 | 141 | 147 | PF00069 | 0.572 |
MOD_ProDKin_1 | 203 | 209 | PF00069 | 0.746 |
MOD_ProDKin_1 | 266 | 272 | PF00069 | 0.669 |
MOD_ProDKin_1 | 288 | 294 | PF00069 | 0.690 |
MOD_ProDKin_1 | 44 | 50 | PF00069 | 0.756 |
MOD_ProDKin_1 | 596 | 602 | PF00069 | 0.492 |
MOD_ProDKin_1 | 93 | 99 | PF00069 | 0.644 |
MOD_SUMO_for_1 | 234 | 237 | PF00179 | 0.719 |
MOD_SUMO_rev_2 | 154 | 161 | PF00179 | 0.474 |
MOD_SUMO_rev_2 | 607 | 617 | PF00179 | 0.482 |
TRG_DiLeu_BaEn_1 | 241 | 246 | PF01217 | 0.727 |
TRG_DiLeu_BaEn_1 | 624 | 629 | PF01217 | 0.346 |
TRG_DiLeu_BaEn_2 | 326 | 332 | PF01217 | 0.555 |
TRG_DiLeu_BaEn_2 | 448 | 454 | PF01217 | 0.385 |
TRG_ENDOCYTIC_2 | 138 | 141 | PF00928 | 0.770 |
TRG_ENDOCYTIC_2 | 611 | 614 | PF00928 | 0.606 |
TRG_ER_diArg_1 | 177 | 180 | PF00400 | 0.553 |
TRG_ER_diArg_1 | 296 | 298 | PF00400 | 0.703 |
TRG_ER_diArg_1 | 384 | 387 | PF00400 | 0.496 |
TRG_ER_diArg_1 | 467 | 470 | PF00400 | 0.344 |
TRG_ER_diArg_1 | 48 | 51 | PF00400 | 0.561 |
TRG_ER_diArg_1 | 581 | 583 | PF00400 | 0.494 |
TRG_ER_diArg_1 | 588 | 591 | PF00400 | 0.478 |
TRG_ER_diArg_1 | 636 | 638 | PF00400 | 0.624 |
TRG_Pf-PMV_PEXEL_1 | 261 | 265 | PF00026 | 0.731 |
TRG_Pf-PMV_PEXEL_1 | 421 | 426 | PF00026 | 0.344 |
TRG_Pf-PMV_PEXEL_1 | 590 | 594 | PF00026 | 0.529 |
TRG_Pf-PMV_PEXEL_1 | 601 | 605 | PF00026 | 0.448 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I5W9 | Leptomonas seymouri | 69% | 85% |
A0A0S4IST3 | Bodo saltans | 40% | 100% |
A0A1X0P7U6 | Trypanosomatidae | 55% | 100% |
A0A3R7R867 | Trypanosoma rangeli | 54% | 100% |
A0A3S7XAP2 | Leishmania donovani | 92% | 79% |
A4HP30 | Leishmania braziliensis | 83% | 100% |
A4IDD7 | Leishmania infantum | 92% | 79% |
D0A313 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 53% | 100% |
Q4Q1Q8 | Leishmania major | 92% | 100% |
V5BPI0 | Trypanosoma cruzi | 55% | 100% |