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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005730 | nucleolus | 5 | 3 |
GO:0030684 | preribosome | 3 | 1 |
GO:0032040 | small-subunit processome | 4 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0043226 | organelle | 2 | 3 |
GO:0043228 | non-membrane-bounded organelle | 3 | 3 |
GO:0043229 | intracellular organelle | 3 | 3 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
GO:1990904 | ribonucleoprotein complex | 2 | 1 |
Related structures:
AlphaFold database: A4HEY0
Term | Name | Level | Count |
---|---|---|---|
GO:0000462 | maturation of SSU-rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA) | 10 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006364 | rRNA processing | 8 | 1 |
GO:0006396 | RNA processing | 6 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0016072 | rRNA metabolic process | 7 | 1 |
GO:0030490 | maturation of SSU-rRNA | 9 | 1 |
GO:0034470 | ncRNA processing | 7 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0034660 | ncRNA metabolic process | 6 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 317 | 321 | PF00656 | 0.448 |
CLV_NRD_NRD_1 | 105 | 107 | PF00675 | 0.372 |
CLV_NRD_NRD_1 | 27 | 29 | PF00675 | 0.467 |
CLV_NRD_NRD_1 | 524 | 526 | PF00675 | 0.557 |
CLV_NRD_NRD_1 | 539 | 541 | PF00675 | 0.377 |
CLV_NRD_NRD_1 | 546 | 548 | PF00675 | 0.473 |
CLV_NRD_NRD_1 | 620 | 622 | PF00675 | 0.645 |
CLV_NRD_NRD_1 | 652 | 654 | PF00675 | 0.549 |
CLV_NRD_NRD_1 | 677 | 679 | PF00675 | 0.535 |
CLV_PCSK_FUR_1 | 617 | 621 | PF00082 | 0.700 |
CLV_PCSK_KEX2_1 | 27 | 29 | PF00082 | 0.481 |
CLV_PCSK_KEX2_1 | 31 | 33 | PF00082 | 0.471 |
CLV_PCSK_KEX2_1 | 458 | 460 | PF00082 | 0.480 |
CLV_PCSK_KEX2_1 | 524 | 526 | PF00082 | 0.566 |
CLV_PCSK_KEX2_1 | 539 | 541 | PF00082 | 0.383 |
CLV_PCSK_KEX2_1 | 546 | 548 | PF00082 | 0.474 |
CLV_PCSK_KEX2_1 | 619 | 621 | PF00082 | 0.648 |
CLV_PCSK_KEX2_1 | 652 | 654 | PF00082 | 0.549 |
CLV_PCSK_PC1ET2_1 | 31 | 33 | PF00082 | 0.501 |
CLV_PCSK_PC1ET2_1 | 458 | 460 | PF00082 | 0.480 |
CLV_PCSK_PC1ET2_1 | 619 | 621 | PF00082 | 0.703 |
CLV_PCSK_PC7_1 | 27 | 33 | PF00082 | 0.523 |
CLV_PCSK_SKI1_1 | 107 | 111 | PF00082 | 0.336 |
CLV_PCSK_SKI1_1 | 115 | 119 | PF00082 | 0.356 |
CLV_PCSK_SKI1_1 | 265 | 269 | PF00082 | 0.498 |
CLV_PCSK_SKI1_1 | 303 | 307 | PF00082 | 0.363 |
CLV_PCSK_SKI1_1 | 386 | 390 | PF00082 | 0.371 |
CLV_PCSK_SKI1_1 | 455 | 459 | PF00082 | 0.353 |
CLV_PCSK_SKI1_1 | 539 | 543 | PF00082 | 0.518 |
CLV_PCSK_SKI1_1 | 54 | 58 | PF00082 | 0.323 |
CLV_PCSK_SKI1_1 | 644 | 648 | PF00082 | 0.682 |
CLV_PCSK_SKI1_1 | 652 | 656 | PF00082 | 0.565 |
DEG_APCC_DBOX_1 | 605 | 613 | PF00400 | 0.644 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.403 |
DOC_CYCLIN_RxL_1 | 262 | 271 | PF00134 | 0.503 |
DOC_CYCLIN_yCln2_LP_2 | 263 | 269 | PF00134 | 0.401 |
DOC_MAPK_gen_1 | 368 | 378 | PF00069 | 0.289 |
DOC_MAPK_gen_1 | 678 | 688 | PF00069 | 0.544 |
DOC_PP4_FxxP_1 | 657 | 660 | PF00568 | 0.465 |
DOC_USP7_MATH_1 | 16 | 20 | PF00917 | 0.462 |
DOC_USP7_MATH_1 | 205 | 209 | PF00917 | 0.378 |
DOC_USP7_MATH_1 | 516 | 520 | PF00917 | 0.639 |
DOC_USP7_MATH_1 | 541 | 545 | PF00917 | 0.496 |
DOC_USP7_MATH_1 | 632 | 636 | PF00917 | 0.679 |
DOC_USP7_UBL2_3 | 306 | 310 | PF12436 | 0.364 |
DOC_WW_Pin1_4 | 150 | 155 | PF00397 | 0.471 |
DOC_WW_Pin1_4 | 619 | 624 | PF00397 | 0.579 |
DOC_WW_Pin1_4 | 99 | 104 | PF00397 | 0.365 |
LIG_14-3-3_CanoR_1 | 158 | 162 | PF00244 | 0.280 |
LIG_14-3-3_CanoR_1 | 235 | 245 | PF00244 | 0.503 |
LIG_14-3-3_CanoR_1 | 371 | 376 | PF00244 | 0.391 |
LIG_14-3-3_CanoR_1 | 459 | 467 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 540 | 550 | PF00244 | 0.589 |
LIG_14-3-3_CanoR_1 | 588 | 596 | PF00244 | 0.503 |
LIG_14-3-3_CanoR_1 | 652 | 657 | PF00244 | 0.508 |
LIG_BRCT_BRCA1_1 | 83 | 87 | PF00533 | 0.430 |
LIG_FHA_1 | 120 | 126 | PF00498 | 0.509 |
LIG_FHA_1 | 246 | 252 | PF00498 | 0.413 |
LIG_FHA_1 | 300 | 306 | PF00498 | 0.385 |
LIG_FHA_1 | 378 | 384 | PF00498 | 0.398 |
LIG_FHA_1 | 468 | 474 | PF00498 | 0.449 |
LIG_FHA_1 | 641 | 647 | PF00498 | 0.516 |
LIG_FHA_1 | 9 | 15 | PF00498 | 0.368 |
LIG_FHA_2 | 315 | 321 | PF00498 | 0.365 |
LIG_FHA_2 | 388 | 394 | PF00498 | 0.487 |
LIG_FHA_2 | 533 | 539 | PF00498 | 0.571 |
LIG_FHA_2 | 653 | 659 | PF00498 | 0.606 |
LIG_FHA_2 | 685 | 691 | PF00498 | 0.589 |
LIG_LIR_Apic_2 | 655 | 660 | PF02991 | 0.470 |
LIG_LIR_Gen_1 | 137 | 148 | PF02991 | 0.460 |
LIG_LIR_Gen_1 | 314 | 323 | PF02991 | 0.374 |
LIG_LIR_Gen_1 | 374 | 383 | PF02991 | 0.410 |
LIG_LIR_Gen_1 | 389 | 398 | PF02991 | 0.449 |
LIG_LIR_Gen_1 | 528 | 536 | PF02991 | 0.444 |
LIG_LIR_Gen_1 | 553 | 561 | PF02991 | 0.584 |
LIG_LIR_Nem_3 | 102 | 108 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 137 | 143 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 314 | 319 | PF02991 | 0.365 |
LIG_LIR_Nem_3 | 326 | 331 | PF02991 | 0.390 |
LIG_LIR_Nem_3 | 374 | 378 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 389 | 395 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 442 | 447 | PF02991 | 0.543 |
LIG_LIR_Nem_3 | 528 | 532 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 553 | 558 | PF02991 | 0.529 |
LIG_Pex14_2 | 505 | 509 | PF04695 | 0.510 |
LIG_PTB_Apo_2 | 426 | 433 | PF02174 | 0.400 |
LIG_PTB_Apo_2 | 523 | 530 | PF02174 | 0.536 |
LIG_PTB_Phospho_1 | 426 | 432 | PF10480 | 0.393 |
LIG_PTB_Phospho_1 | 523 | 529 | PF10480 | 0.585 |
LIG_REV1ctd_RIR_1 | 281 | 291 | PF16727 | 0.423 |
LIG_RPA_C_Fungi | 535 | 547 | PF08784 | 0.501 |
LIG_SH2_CRK | 529 | 533 | PF00017 | 0.459 |
LIG_SH2_SRC | 570 | 573 | PF00017 | 0.535 |
LIG_SH2_STAP1 | 259 | 263 | PF00017 | 0.367 |
LIG_SH2_STAP1 | 529 | 533 | PF00017 | 0.459 |
LIG_SH2_STAP1 | 550 | 554 | PF00017 | 0.489 |
LIG_SH2_STAT5 | 282 | 285 | PF00017 | 0.341 |
LIG_SH2_STAT5 | 447 | 450 | PF00017 | 0.440 |
LIG_SH3_3 | 126 | 132 | PF00018 | 0.378 |
LIG_SH3_3 | 435 | 441 | PF00018 | 0.409 |
LIG_SUMO_SIM_anti_2 | 374 | 382 | PF11976 | 0.411 |
LIG_SUMO_SIM_par_1 | 265 | 271 | PF11976 | 0.393 |
LIG_TRAF2_1 | 238 | 241 | PF00917 | 0.479 |
LIG_TRAF2_1 | 35 | 38 | PF00917 | 0.632 |
MOD_CDK_SPxK_1 | 619 | 625 | PF00069 | 0.520 |
MOD_CDK_SPxxK_3 | 99 | 106 | PF00069 | 0.366 |
MOD_CK1_1 | 150 | 156 | PF00069 | 0.244 |
MOD_CK1_1 | 160 | 166 | PF00069 | 0.378 |
MOD_CK1_1 | 222 | 228 | PF00069 | 0.573 |
MOD_CK1_1 | 288 | 294 | PF00069 | 0.439 |
MOD_CK1_1 | 299 | 305 | PF00069 | 0.329 |
MOD_CK1_1 | 314 | 320 | PF00069 | 0.405 |
MOD_CK1_1 | 587 | 593 | PF00069 | 0.685 |
MOD_CK2_1 | 16 | 22 | PF00069 | 0.450 |
MOD_CK2_1 | 371 | 377 | PF00069 | 0.377 |
MOD_CK2_1 | 396 | 402 | PF00069 | 0.432 |
MOD_CK2_1 | 532 | 538 | PF00069 | 0.525 |
MOD_CK2_1 | 652 | 658 | PF00069 | 0.614 |
MOD_CK2_1 | 678 | 684 | PF00069 | 0.588 |
MOD_Cter_Amidation | 650 | 653 | PF01082 | 0.501 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.410 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.335 |
MOD_GlcNHglycan | 173 | 176 | PF01048 | 0.507 |
MOD_GlcNHglycan | 190 | 193 | PF01048 | 0.378 |
MOD_GlcNHglycan | 221 | 224 | PF01048 | 0.455 |
MOD_GlcNHglycan | 225 | 228 | PF01048 | 0.406 |
MOD_GlcNHglycan | 240 | 244 | PF01048 | 0.299 |
MOD_GlcNHglycan | 252 | 255 | PF01048 | 0.414 |
MOD_GlcNHglycan | 298 | 301 | PF01048 | 0.330 |
MOD_GlcNHglycan | 33 | 36 | PF01048 | 0.678 |
MOD_GlcNHglycan | 344 | 348 | PF01048 | 0.340 |
MOD_GlcNHglycan | 493 | 496 | PF01048 | 0.576 |
MOD_GlcNHglycan | 543 | 546 | PF01048 | 0.593 |
MOD_GlcNHglycan | 591 | 594 | PF01048 | 0.761 |
MOD_GlcNHglycan | 614 | 617 | PF01048 | 0.641 |
MOD_GlcNHglycan | 638 | 641 | PF01048 | 0.692 |
MOD_GlcNHglycan | 648 | 651 | PF01048 | 0.548 |
MOD_GlcNHglycan | 696 | 699 | PF01048 | 0.675 |
MOD_GlcNHglycan | 96 | 99 | PF01048 | 0.453 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.441 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.363 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.360 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.330 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.475 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.283 |
MOD_GSK3_1 | 219 | 226 | PF00069 | 0.496 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.432 |
MOD_GSK3_1 | 311 | 318 | PF00069 | 0.383 |
MOD_GSK3_1 | 458 | 465 | PF00069 | 0.494 |
MOD_GSK3_1 | 491 | 498 | PF00069 | 0.588 |
MOD_GSK3_1 | 632 | 639 | PF00069 | 0.725 |
MOD_GSK3_1 | 640 | 647 | PF00069 | 0.692 |
MOD_GSK3_1 | 674 | 681 | PF00069 | 0.493 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.366 |
MOD_N-GLC_1 | 12 | 17 | PF02516 | 0.377 |
MOD_N-GLC_1 | 314 | 319 | PF02516 | 0.363 |
MOD_N-GLC_1 | 60 | 65 | PF02516 | 0.324 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.418 |
MOD_NEK2_1 | 134 | 139 | PF00069 | 0.404 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.262 |
MOD_NEK2_1 | 245 | 250 | PF00069 | 0.348 |
MOD_NEK2_1 | 674 | 679 | PF00069 | 0.670 |
MOD_NEK2_1 | 694 | 699 | PF00069 | 0.566 |
MOD_NEK2_1 | 85 | 90 | PF00069 | 0.361 |
MOD_PKA_1 | 31 | 37 | PF00069 | 0.630 |
MOD_PKA_1 | 458 | 464 | PF00069 | 0.444 |
MOD_PKA_1 | 652 | 658 | PF00069 | 0.593 |
MOD_PKA_1 | 678 | 684 | PF00069 | 0.630 |
MOD_PKA_2 | 157 | 163 | PF00069 | 0.285 |
MOD_PKA_2 | 31 | 37 | PF00069 | 0.630 |
MOD_PKA_2 | 458 | 464 | PF00069 | 0.481 |
MOD_PKA_2 | 587 | 593 | PF00069 | 0.618 |
MOD_PKA_2 | 636 | 642 | PF00069 | 0.775 |
MOD_PKA_2 | 652 | 658 | PF00069 | 0.544 |
MOD_Plk_1 | 292 | 298 | PF00069 | 0.391 |
MOD_Plk_1 | 314 | 320 | PF00069 | 0.369 |
MOD_Plk_1 | 326 | 332 | PF00069 | 0.337 |
MOD_Plk_1 | 386 | 392 | PF00069 | 0.469 |
MOD_Plk_1 | 393 | 399 | PF00069 | 0.402 |
MOD_Plk_1 | 81 | 87 | PF00069 | 0.442 |
MOD_Plk_2-3 | 377 | 383 | PF00069 | 0.395 |
MOD_Plk_2-3 | 387 | 393 | PF00069 | 0.467 |
MOD_Plk_2-3 | 684 | 690 | PF00069 | 0.557 |
MOD_Plk_4 | 278 | 284 | PF00069 | 0.339 |
MOD_Plk_4 | 292 | 298 | PF00069 | 0.393 |
MOD_Plk_4 | 371 | 377 | PF00069 | 0.378 |
MOD_Plk_4 | 387 | 393 | PF00069 | 0.475 |
MOD_Plk_4 | 652 | 658 | PF00069 | 0.623 |
MOD_ProDKin_1 | 150 | 156 | PF00069 | 0.467 |
MOD_ProDKin_1 | 619 | 625 | PF00069 | 0.577 |
MOD_ProDKin_1 | 99 | 105 | PF00069 | 0.366 |
MOD_SUMO_rev_2 | 381 | 388 | PF00179 | 0.428 |
MOD_SUMO_rev_2 | 474 | 482 | PF00179 | 0.475 |
TRG_DiLeu_BaEn_1 | 241 | 246 | PF01217 | 0.528 |
TRG_DiLeu_BaEn_1 | 528 | 533 | PF01217 | 0.443 |
TRG_DiLeu_BaEn_2 | 161 | 167 | PF01217 | 0.411 |
TRG_DiLeu_BaLyEn_6 | 263 | 268 | PF01217 | 0.402 |
TRG_ENDOCYTIC_2 | 105 | 108 | PF00928 | 0.484 |
TRG_ENDOCYTIC_2 | 140 | 143 | PF00928 | 0.481 |
TRG_ENDOCYTIC_2 | 392 | 395 | PF00928 | 0.455 |
TRG_ENDOCYTIC_2 | 432 | 435 | PF00928 | 0.415 |
TRG_ENDOCYTIC_2 | 529 | 532 | PF00928 | 0.458 |
TRG_ER_diArg_1 | 128 | 131 | PF00400 | 0.364 |
TRG_ER_diArg_1 | 652 | 654 | PF00400 | 0.605 |
TRG_NES_CRM1_1 | 92 | 104 | PF08389 | 0.339 |
TRG_NLS_MonoExtC_3 | 27 | 32 | PF00514 | 0.474 |
TRG_NLS_MonoExtC_3 | 618 | 623 | PF00514 | 0.733 |
TRG_NLS_MonoExtC_3 | 677 | 682 | PF00514 | 0.559 |
TRG_NLS_MonoExtN_4 | 27 | 32 | PF00514 | 0.474 |
TRG_NLS_MonoExtN_4 | 617 | 623 | PF00514 | 0.732 |
TRG_NLS_MonoExtN_4 | 678 | 683 | PF00514 | 0.557 |
TRG_Pf-PMV_PEXEL_1 | 18 | 22 | PF00026 | 0.459 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3D9 | Leptomonas seymouri | 79% | 100% |
A0A0S4JNM6 | Bodo saltans | 53% | 100% |
A0A1X0NSW1 | Trypanosomatidae | 63% | 100% |
A0A3R7KNJ7 | Trypanosoma rangeli | 70% | 100% |
A0A3S7WZS4 | Leishmania donovani | 88% | 100% |
A4I254 | Leishmania infantum | 89% | 100% |
C9ZRU9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 60% | 100% |
E9AYA4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
G0S902 | Chaetomium thermophilum (strain DSM 1495 / CBS 144.50 / IMI 039719) | 26% | 100% |
O74879 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 30% | 100% |
Q4Q969 | Leishmania major | 88% | 99% |
Q802W4 | Danio rerio | 32% | 97% |