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: A4HP30
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 7 |
GO:0006364 | rRNA processing | 8 | 3 |
GO:0006396 | RNA processing | 6 | 3 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 7 |
GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0016070 | RNA metabolic process | 5 | 7 |
GO:0016072 | rRNA metabolic process | 7 | 3 |
GO:0034470 | ncRNA processing | 7 | 3 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 7 |
GO:0034660 | ncRNA metabolic process | 6 | 3 |
GO:0043170 | macromolecule metabolic process | 3 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0046483 | heterocycle metabolic process | 3 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:0090304 | nucleic acid metabolic process | 4 | 7 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 7 |
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 | 602 | 606 | PF00656 | 0.479 |
CLV_NRD_NRD_1 | 108 | 110 | PF00675 | 0.711 |
CLV_NRD_NRD_1 | 214 | 216 | PF00675 | 0.822 |
CLV_NRD_NRD_1 | 295 | 297 | PF00675 | 0.665 |
CLV_NRD_NRD_1 | 31 | 33 | PF00675 | 0.587 |
CLV_NRD_NRD_1 | 344 | 346 | PF00675 | 0.276 |
CLV_NRD_NRD_1 | 489 | 491 | PF00675 | 0.344 |
CLV_NRD_NRD_1 | 56 | 58 | PF00675 | 0.652 |
CLV_NRD_NRD_1 | 580 | 582 | PF00675 | 0.475 |
CLV_NRD_NRD_1 | 588 | 590 | PF00675 | 0.461 |
CLV_PCSK_FUR_1 | 29 | 33 | PF00082 | 0.607 |
CLV_PCSK_FUR_1 | 54 | 58 | PF00082 | 0.696 |
CLV_PCSK_FUR_1 | 586 | 590 | PF00082 | 0.467 |
CLV_PCSK_KEX2_1 | 108 | 110 | PF00082 | 0.711 |
CLV_PCSK_KEX2_1 | 295 | 297 | PF00082 | 0.671 |
CLV_PCSK_KEX2_1 | 31 | 33 | PF00082 | 0.579 |
CLV_PCSK_KEX2_1 | 344 | 346 | PF00082 | 0.276 |
CLV_PCSK_KEX2_1 | 489 | 491 | PF00082 | 0.385 |
CLV_PCSK_KEX2_1 | 50 | 52 | PF00082 | 0.671 |
CLV_PCSK_KEX2_1 | 56 | 58 | PF00082 | 0.607 |
CLV_PCSK_KEX2_1 | 580 | 582 | PF00082 | 0.475 |
CLV_PCSK_KEX2_1 | 588 | 590 | PF00082 | 0.461 |
CLV_PCSK_PC1ET2_1 | 50 | 52 | PF00082 | 0.671 |
CLV_PCSK_SKI1_1 | 259 | 263 | PF00082 | 0.651 |
CLV_PCSK_SKI1_1 | 468 | 472 | PF00082 | 0.560 |
CLV_PCSK_SKI1_1 | 552 | 556 | PF00082 | 0.432 |
CLV_PCSK_SKI1_1 | 594 | 598 | PF00082 | 0.477 |
CLV_PCSK_SKI1_1 | 613 | 617 | PF00082 | 0.388 |
DEG_APCC_DBOX_1 | 152 | 160 | PF00400 | 0.630 |
DEG_SCF_FBW7_2 | 668 | 674 | PF00400 | 0.502 |
DEG_SPOP_SBC_1 | 225 | 229 | PF00917 | 0.533 |
DOC_CKS1_1 | 45 | 50 | PF01111 | 0.680 |
DOC_CKS1_1 | 668 | 673 | PF01111 | 0.500 |
DOC_MAPK_DCC_7 | 205 | 213 | PF00069 | 0.668 |
DOC_MAPK_DCC_7 | 384 | 394 | PF00069 | 0.450 |
DOC_MAPK_gen_1 | 108 | 115 | PF00069 | 0.734 |
DOC_MAPK_gen_1 | 503 | 512 | PF00069 | 0.475 |
DOC_MAPK_MEF2A_6 | 386 | 394 | PF00069 | 0.447 |
DOC_MAPK_MEF2A_6 | 503 | 512 | PF00069 | 0.438 |
DOC_MAPK_RevD_3 | 474 | 490 | PF00069 | 0.336 |
DOC_MIT_MIM_1 | 150 | 160 | PF04212 | 0.511 |
DOC_PP1_RVXF_1 | 382 | 388 | PF00149 | 0.482 |
DOC_PP1_RVXF_1 | 533 | 539 | PF00149 | 0.407 |
DOC_PP2B_LxvP_1 | 645 | 648 | PF13499 | 0.658 |
DOC_PP4_FxxP_1 | 387 | 390 | PF00568 | 0.458 |
DOC_PP4_FxxP_1 | 497 | 500 | PF00568 | 0.498 |
DOC_USP7_MATH_1 | 217 | 221 | PF00917 | 0.722 |
DOC_USP7_MATH_1 | 248 | 252 | PF00917 | 0.752 |
DOC_USP7_MATH_1 | 25 | 29 | PF00917 | 0.538 |
DOC_USP7_MATH_1 | 286 | 290 | PF00917 | 0.561 |
DOC_USP7_MATH_1 | 310 | 314 | PF00917 | 0.708 |
DOC_USP7_MATH_1 | 317 | 321 | PF00917 | 0.729 |
DOC_USP7_MATH_1 | 428 | 432 | PF00917 | 0.402 |
DOC_USP7_MATH_1 | 501 | 505 | PF00917 | 0.520 |
DOC_USP7_MATH_1 | 547 | 551 | PF00917 | 0.440 |
DOC_USP7_MATH_1 | 652 | 656 | PF00917 | 0.741 |
DOC_USP7_MATH_1 | 84 | 88 | PF00917 | 0.732 |
DOC_WW_Pin1_4 | 141 | 146 | PF00397 | 0.564 |
DOC_WW_Pin1_4 | 264 | 269 | PF00397 | 0.688 |
DOC_WW_Pin1_4 | 44 | 49 | PF00397 | 0.687 |
DOC_WW_Pin1_4 | 451 | 456 | PF00397 | 0.546 |
DOC_WW_Pin1_4 | 594 | 599 | PF00397 | 0.484 |
DOC_WW_Pin1_4 | 667 | 672 | PF00397 | 0.500 |
DOC_WW_Pin1_4 | 93 | 98 | PF00397 | 0.628 |
LIG_14-3-3_CanoR_1 | 180 | 188 | PF00244 | 0.482 |
LIG_14-3-3_CanoR_1 | 254 | 262 | PF00244 | 0.730 |
LIG_14-3-3_CanoR_1 | 490 | 500 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 505 | 509 | PF00244 | 0.438 |
LIG_14-3-3_CanoR_1 | 535 | 539 | PF00244 | 0.395 |
LIG_14-3-3_CanoR_1 | 635 | 644 | PF00244 | 0.503 |
LIG_Actin_WH2_2 | 619 | 637 | PF00022 | 0.604 |
LIG_BRCT_BRCA1_1 | 168 | 172 | PF00533 | 0.725 |
LIG_deltaCOP1_diTrp_1 | 573 | 579 | PF00928 | 0.497 |
LIG_EH_1 | 364 | 368 | PF12763 | 0.476 |
LIG_FHA_1 | 147 | 153 | PF00498 | 0.525 |
LIG_FHA_1 | 225 | 231 | PF00498 | 0.542 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.594 |
LIG_FHA_1 | 460 | 466 | PF00498 | 0.413 |
LIG_FHA_1 | 479 | 485 | PF00498 | 0.320 |
LIG_FHA_2 | 227 | 233 | PF00498 | 0.673 |
LIG_FHA_2 | 595 | 601 | PF00498 | 0.476 |
LIG_FHA_2 | 606 | 612 | PF00498 | 0.469 |
LIG_Integrin_isoDGR_2 | 487 | 489 | PF01839 | 0.608 |
LIG_Integrin_RGD_1 | 132 | 134 | PF01839 | 0.745 |
LIG_LIR_Apic_2 | 494 | 500 | PF02991 | 0.474 |
LIG_LIR_Gen_1 | 608 | 616 | PF02991 | 0.497 |
LIG_LIR_Gen_1 | 670 | 679 | PF02991 | 0.503 |
LIG_LIR_Nem_3 | 537 | 541 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 573 | 579 | PF02991 | 0.503 |
LIG_LIR_Nem_3 | 608 | 612 | PF02991 | 0.539 |
LIG_LIR_Nem_3 | 670 | 675 | PF02991 | 0.504 |
LIG_PCNA_PIPBox_1 | 1 | 10 | PF02747 | 0.570 |
LIG_PCNA_yPIPBox_3 | 355 | 368 | PF02747 | 0.404 |
LIG_PTB_Apo_2 | 490 | 497 | PF02174 | 0.487 |
LIG_PTB_Apo_2 | 603 | 610 | PF02174 | 0.512 |
LIG_PTB_Phospho_1 | 603 | 609 | PF10480 | 0.510 |
LIG_RPA_C_Fungi | 340 | 352 | PF08784 | 0.449 |
LIG_SH2_CRK | 395 | 399 | PF00017 | 0.389 |
LIG_SH2_NCK_1 | 395 | 399 | PF00017 | 0.283 |
LIG_SH2_SRC | 609 | 612 | PF00017 | 0.556 |
LIG_SH2_STAP1 | 506 | 510 | PF00017 | 0.503 |
LIG_SH2_STAP1 | 560 | 564 | PF00017 | 0.580 |
LIG_SH2_STAT5 | 578 | 581 | PF00017 | 0.591 |
LIG_SH2_STAT5 | 607 | 610 | PF00017 | 0.600 |
LIG_SH2_STAT5 | 7 | 10 | PF00017 | 0.692 |
LIG_SH3_3 | 551 | 557 | PF00018 | 0.427 |
LIG_SH3_3 | 665 | 671 | PF00018 | 0.631 |
LIG_SUMO_SIM_par_1 | 183 | 190 | PF11976 | 0.430 |
LIG_SUMO_SIM_par_1 | 438 | 443 | PF11976 | 0.372 |
LIG_SUMO_SIM_par_1 | 614 | 622 | PF11976 | 0.384 |
LIG_TRAF2_1 | 608 | 611 | PF00917 | 0.506 |
LIG_TRAF2_2 | 145 | 150 | PF00917 | 0.552 |
LIG_UBA3_1 | 156 | 163 | PF00899 | 0.509 |
LIG_WRC_WIRS_1 | 61 | 66 | PF05994 | 0.726 |
LIG_WRPW_2 | 568 | 571 | PF00400 | 0.506 |
LIG_WW_1 | 557 | 560 | PF00397 | 0.452 |
LIG_WW_3 | 388 | 392 | PF00397 | 0.448 |
MOD_CDK_SPK_2 | 451 | 456 | PF00069 | 0.330 |
MOD_CDK_SPK_2 | 594 | 599 | PF00069 | 0.484 |
MOD_CDK_SPxK_1 | 44 | 50 | PF00069 | 0.683 |
MOD_CDK_SPxxK_3 | 44 | 51 | PF00069 | 0.685 |
MOD_CK1_1 | 116 | 122 | PF00069 | 0.539 |
MOD_CK1_1 | 454 | 460 | PF00069 | 0.325 |
MOD_CK1_1 | 504 | 510 | PF00069 | 0.436 |
MOD_CK2_1 | 178 | 184 | PF00069 | 0.465 |
MOD_CK2_1 | 192 | 198 | PF00069 | 0.468 |
MOD_CK2_1 | 340 | 346 | PF00069 | 0.328 |
MOD_CK2_1 | 547 | 553 | PF00069 | 0.447 |
MOD_CK2_1 | 594 | 600 | PF00069 | 0.473 |
MOD_CK2_1 | 605 | 611 | PF00069 | 0.468 |
MOD_Cter_Amidation | 487 | 490 | PF01082 | 0.417 |
MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.436 |
MOD_GlcNHglycan | 193 | 197 | PF01048 | 0.410 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.630 |
MOD_GlcNHglycan | 221 | 224 | PF01048 | 0.687 |
MOD_GlcNHglycan | 272 | 275 | PF01048 | 0.593 |
MOD_GlcNHglycan | 308 | 311 | PF01048 | 0.693 |
MOD_GlcNHglycan | 312 | 315 | PF01048 | 0.712 |
MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.695 |
MOD_GlcNHglycan | 352 | 355 | PF01048 | 0.339 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.659 |
MOD_GlcNHglycan | 81 | 84 | PF01048 | 0.618 |
MOD_GlcNHglycan | 86 | 89 | PF01048 | 0.631 |
MOD_GSK3_1 | 306 | 313 | PF00069 | 0.700 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.672 |
MOD_GSK3_1 | 652 | 659 | PF00069 | 0.714 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.513 |
MOD_N-GLC_1 | 605 | 610 | PF02516 | 0.519 |
MOD_N-GLC_1 | 652 | 657 | PF02516 | 0.493 |
MOD_NEK2_1 | 100 | 105 | PF00069 | 0.617 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.567 |
MOD_NEK2_1 | 332 | 337 | PF00069 | 0.482 |
MOD_NEK2_1 | 541 | 546 | PF00069 | 0.440 |
MOD_NEK2_2 | 547 | 552 | PF00069 | 0.445 |
MOD_NEK2_2 | 60 | 65 | PF00069 | 0.638 |
MOD_NEK2_2 | 652 | 657 | PF00069 | 0.746 |
MOD_PIKK_1 | 286 | 292 | PF00454 | 0.628 |
MOD_PIKK_1 | 558 | 564 | PF00454 | 0.587 |
MOD_PKA_1 | 56 | 62 | PF00069 | 0.713 |
MOD_PKA_2 | 201 | 207 | PF00069 | 0.523 |
MOD_PKA_2 | 248 | 254 | PF00069 | 0.746 |
MOD_PKA_2 | 491 | 497 | PF00069 | 0.471 |
MOD_PKA_2 | 504 | 510 | PF00069 | 0.435 |
MOD_PKA_2 | 534 | 540 | PF00069 | 0.399 |
MOD_PKA_2 | 56 | 62 | PF00069 | 0.719 |
MOD_PKA_2 | 582 | 588 | PF00069 | 0.458 |
MOD_PKA_2 | 656 | 662 | PF00069 | 0.733 |
MOD_PKA_2 | 88 | 94 | PF00069 | 0.585 |
MOD_PKB_1 | 54 | 62 | PF00069 | 0.706 |
MOD_Plk_1 | 124 | 130 | PF00069 | 0.705 |
MOD_Plk_1 | 192 | 198 | PF00069 | 0.646 |
MOD_Plk_1 | 238 | 244 | PF00069 | 0.542 |
MOD_Plk_1 | 281 | 287 | PF00069 | 0.738 |
MOD_Plk_1 | 446 | 452 | PF00069 | 0.432 |
MOD_Plk_1 | 552 | 558 | PF00069 | 0.433 |
MOD_Plk_1 | 605 | 611 | PF00069 | 0.519 |
MOD_Plk_2-3 | 605 | 611 | PF00069 | 0.484 |
MOD_Plk_2-3 | 66 | 72 | PF00069 | 0.587 |
MOD_Plk_4 | 168 | 174 | PF00069 | 0.581 |
MOD_Plk_4 | 248 | 254 | PF00069 | 0.584 |
MOD_Plk_4 | 454 | 460 | PF00069 | 0.451 |
MOD_Plk_4 | 60 | 66 | PF00069 | 0.595 |
MOD_ProDKin_1 | 141 | 147 | PF00069 | 0.560 |
MOD_ProDKin_1 | 264 | 270 | PF00069 | 0.686 |
MOD_ProDKin_1 | 44 | 50 | PF00069 | 0.683 |
MOD_ProDKin_1 | 451 | 457 | PF00069 | 0.542 |
MOD_ProDKin_1 | 594 | 600 | PF00069 | 0.480 |
MOD_ProDKin_1 | 667 | 673 | PF00069 | 0.500 |
MOD_ProDKin_1 | 93 | 99 | PF00069 | 0.630 |
MOD_SUMO_for_1 | 159 | 162 | PF00179 | 0.408 |
MOD_SUMO_rev_2 | 154 | 161 | PF00179 | 0.469 |
MOD_SUMO_rev_2 | 605 | 615 | PF00179 | 0.490 |
TRG_DiLeu_BaEn_2 | 446 | 452 | PF01217 | 0.474 |
TRG_DiLeu_BaEn_3 | 324 | 330 | PF01217 | 0.412 |
TRG_DiLeu_BaEn_4 | 238 | 244 | PF01217 | 0.542 |
TRG_DiLeu_BaEn_4 | 642 | 648 | PF01217 | 0.438 |
TRG_ENDOCYTIC_2 | 138 | 141 | PF00928 | 0.755 |
TRG_ENDOCYTIC_2 | 609 | 612 | PF00928 | 0.619 |
TRG_ER_diArg_1 | 200 | 203 | PF00400 | 0.732 |
TRG_ER_diArg_1 | 29 | 32 | PF00400 | 0.633 |
TRG_ER_diArg_1 | 294 | 296 | PF00400 | 0.678 |
TRG_ER_diArg_1 | 384 | 387 | PF00400 | 0.477 |
TRG_ER_diArg_1 | 465 | 468 | PF00400 | 0.420 |
TRG_ER_diArg_1 | 489 | 491 | PF00400 | 0.559 |
TRG_ER_diArg_1 | 579 | 581 | PF00400 | 0.488 |
TRG_ER_diArg_1 | 586 | 589 | PF00400 | 0.470 |
TRG_Pf-PMV_PEXEL_1 | 259 | 263 | PF00026 | 0.753 |
TRG_Pf-PMV_PEXEL_1 | 419 | 424 | PF00026 | 0.511 |
TRG_Pf-PMV_PEXEL_1 | 588 | 592 | PF00026 | 0.521 |
TRG_Pf-PMV_PEXEL_1 | 599 | 603 | PF00026 | 0.435 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I5W9 | Leptomonas seymouri | 69% | 85% |
A0A0S4IST3 | Bodo saltans | 40% | 100% |
A0A1X0P7U6 | Trypanosomatidae | 53% | 100% |
A0A3R7R867 | Trypanosoma rangeli | 54% | 100% |
A0A3S7XAP2 | Leishmania donovani | 84% | 79% |
A4IDD7 | Leishmania infantum | 84% | 79% |
D0A313 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 54% | 100% |
E9AST8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
Q4Q1Q8 | Leishmania major | 84% | 100% |
V5BPI0 | Trypanosoma cruzi | 56% | 100% |