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 | 11 |
GO:0043226 | organelle | 2 | 11 |
GO:0043228 | non-membrane-bounded organelle | 3 | 11 |
GO:0043229 | intracellular organelle | 3 | 11 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
GO:0030684 | preribosome | 3 | 1 |
GO:0032040 | small-subunit processome | 4 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:1990904 | ribonucleoprotein complex | 2 | 1 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pescher et al. (upgregulation) | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Lahav et al. - mRNA
- Protein
|
Related structures:
AlphaFold database: A4I0B3
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 | 547 | 551 | PF00656 | 0.448 |
CLV_C14_Caspase3-7 | 650 | 654 | PF00656 | 0.529 |
CLV_MEL_PAP_1 | 109 | 115 | PF00089 | 0.315 |
CLV_NRD_NRD_1 | 26 | 28 | PF00675 | 0.585 |
CLV_NRD_NRD_1 | 440 | 442 | PF00675 | 0.243 |
CLV_NRD_NRD_1 | 482 | 484 | PF00675 | 0.427 |
CLV_NRD_NRD_1 | 494 | 496 | PF00675 | 0.439 |
CLV_NRD_NRD_1 | 540 | 542 | PF00675 | 0.440 |
CLV_NRD_NRD_1 | 610 | 612 | PF00675 | 0.453 |
CLV_NRD_NRD_1 | 641 | 643 | PF00675 | 0.679 |
CLV_NRD_NRD_1 | 74 | 76 | PF00675 | 0.398 |
CLV_PCSK_KEX2_1 | 129 | 131 | PF00082 | 0.447 |
CLV_PCSK_KEX2_1 | 39 | 41 | PF00082 | 0.473 |
CLV_PCSK_KEX2_1 | 470 | 472 | PF00082 | 0.534 |
CLV_PCSK_KEX2_1 | 494 | 496 | PF00082 | 0.472 |
CLV_PCSK_KEX2_1 | 640 | 642 | PF00082 | 0.674 |
CLV_PCSK_KEX2_1 | 676 | 678 | PF00082 | 0.487 |
CLV_PCSK_KEX2_1 | 73 | 75 | PF00082 | 0.423 |
CLV_PCSK_KEX2_1 | 84 | 86 | PF00082 | 0.401 |
CLV_PCSK_PC1ET2_1 | 129 | 131 | PF00082 | 0.447 |
CLV_PCSK_PC1ET2_1 | 39 | 41 | PF00082 | 0.495 |
CLV_PCSK_PC1ET2_1 | 470 | 472 | PF00082 | 0.553 |
CLV_PCSK_PC1ET2_1 | 676 | 678 | PF00082 | 0.578 |
CLV_PCSK_PC1ET2_1 | 84 | 86 | PF00082 | 0.461 |
CLV_PCSK_PC7_1 | 70 | 76 | PF00082 | 0.453 |
CLV_PCSK_PC7_1 | 80 | 86 | PF00082 | 0.344 |
CLV_PCSK_SKI1_1 | 228 | 232 | PF00082 | 0.301 |
CLV_PCSK_SKI1_1 | 317 | 321 | PF00082 | 0.299 |
CLV_PCSK_SKI1_1 | 371 | 375 | PF00082 | 0.338 |
CLV_PCSK_SKI1_1 | 412 | 416 | PF00082 | 0.322 |
CLV_PCSK_SKI1_1 | 444 | 448 | PF00082 | 0.299 |
CLV_PCSK_SKI1_1 | 529 | 533 | PF00082 | 0.506 |
CLV_PCSK_SKI1_1 | 542 | 546 | PF00082 | 0.472 |
CLV_PCSK_SKI1_1 | 59 | 63 | PF00082 | 0.424 |
CLV_PCSK_SKI1_1 | 601 | 605 | PF00082 | 0.524 |
CLV_PCSK_SKI1_1 | 612 | 616 | PF00082 | 0.460 |
CLV_PCSK_SKI1_1 | 676 | 680 | PF00082 | 0.577 |
CLV_PCSK_SKI1_1 | 85 | 89 | PF00082 | 0.494 |
DEG_SPOP_SBC_1 | 2 | 6 | PF00917 | 0.648 |
DEG_SPOP_SBC_1 | 233 | 237 | PF00917 | 0.351 |
DOC_MAPK_gen_1 | 129 | 135 | PF00069 | 0.333 |
DOC_MAPK_gen_1 | 178 | 187 | PF00069 | 0.381 |
DOC_MAPK_gen_1 | 607 | 617 | PF00069 | 0.430 |
DOC_PP1_RVXF_1 | 140 | 146 | PF00149 | 0.278 |
DOC_PP2B_LxvP_1 | 417 | 420 | PF13499 | 0.269 |
DOC_PP2B_LxvP_1 | 633 | 636 | PF13499 | 0.573 |
DOC_PP4_FxxP_1 | 288 | 291 | PF00568 | 0.343 |
DOC_USP7_MATH_1 | 233 | 237 | PF00917 | 0.316 |
DOC_USP7_MATH_1 | 3 | 7 | PF00917 | 0.749 |
DOC_USP7_MATH_1 | 377 | 381 | PF00917 | 0.435 |
DOC_USP7_MATH_1 | 496 | 500 | PF00917 | 0.496 |
DOC_USP7_MATH_1 | 597 | 601 | PF00917 | 0.613 |
DOC_USP7_UBL2_3 | 523 | 527 | PF12436 | 0.587 |
DOC_USP7_UBL2_3 | 545 | 549 | PF12436 | 0.486 |
DOC_USP7_UBL2_3 | 554 | 558 | PF12436 | 0.464 |
DOC_USP7_UBL2_3 | 604 | 608 | PF12436 | 0.556 |
DOC_USP7_UBL2_3 | 84 | 88 | PF12436 | 0.501 |
DOC_WW_Pin1_4 | 287 | 292 | PF00397 | 0.276 |
DOC_WW_Pin1_4 | 378 | 383 | PF00397 | 0.412 |
LIG_14-3-3_CanoR_1 | 10 | 14 | PF00244 | 0.497 |
LIG_14-3-3_CanoR_1 | 112 | 118 | PF00244 | 0.367 |
LIG_14-3-3_CanoR_1 | 130 | 134 | PF00244 | 0.337 |
LIG_14-3-3_CanoR_1 | 165 | 170 | PF00244 | 0.456 |
LIG_14-3-3_CanoR_1 | 180 | 188 | PF00244 | 0.445 |
LIG_14-3-3_CanoR_1 | 317 | 323 | PF00244 | 0.402 |
LIG_14-3-3_CanoR_1 | 334 | 340 | PF00244 | 0.342 |
LIG_14-3-3_CanoR_1 | 412 | 418 | PF00244 | 0.262 |
LIG_14-3-3_CanoR_1 | 495 | 501 | PF00244 | 0.606 |
LIG_14-3-3_CanoR_1 | 556 | 562 | PF00244 | 0.454 |
LIG_14-3-3_CanoR_1 | 59 | 67 | PF00244 | 0.428 |
LIG_14-3-3_CanoR_1 | 642 | 648 | PF00244 | 0.730 |
LIG_APCC_ABBA_1 | 399 | 404 | PF00400 | 0.243 |
LIG_APCC_ABBAyCdc20_2 | 579 | 585 | PF00400 | 0.599 |
LIG_BRCT_BRCA1_1 | 410 | 414 | PF00533 | 0.243 |
LIG_CSL_BTD_1 | 288 | 291 | PF09270 | 0.264 |
LIG_FHA_1 | 148 | 154 | PF00498 | 0.304 |
LIG_FHA_1 | 263 | 269 | PF00498 | 0.385 |
LIG_FHA_1 | 277 | 283 | PF00498 | 0.233 |
LIG_FHA_1 | 3 | 9 | PF00498 | 0.562 |
LIG_FHA_1 | 348 | 354 | PF00498 | 0.277 |
LIG_FHA_1 | 39 | 45 | PF00498 | 0.427 |
LIG_FHA_1 | 413 | 419 | PF00498 | 0.322 |
LIG_FHA_1 | 445 | 451 | PF00498 | 0.264 |
LIG_FHA_1 | 504 | 510 | PF00498 | 0.612 |
LIG_FHA_1 | 526 | 532 | PF00498 | 0.518 |
LIG_FHA_1 | 591 | 597 | PF00498 | 0.446 |
LIG_FHA_1 | 62 | 68 | PF00498 | 0.545 |
LIG_FHA_1 | 98 | 104 | PF00498 | 0.530 |
LIG_FHA_2 | 247 | 253 | PF00498 | 0.341 |
LIG_FHA_2 | 290 | 296 | PF00498 | 0.423 |
LIG_FHA_2 | 336 | 342 | PF00498 | 0.467 |
LIG_GBD_Chelix_1 | 445 | 453 | PF00786 | 0.243 |
LIG_GBD_Chelix_1 | 617 | 625 | PF00786 | 0.524 |
LIG_Integrin_isoDGR_2 | 315 | 317 | PF01839 | 0.202 |
LIG_IRF3_LxIS_1 | 348 | 354 | PF10401 | 0.380 |
LIG_LIR_Apic_2 | 428 | 434 | PF02991 | 0.262 |
LIG_LIR_Gen_1 | 236 | 247 | PF02991 | 0.299 |
LIG_LIR_Gen_1 | 345 | 353 | PF02991 | 0.302 |
LIG_LIR_Gen_1 | 380 | 390 | PF02991 | 0.324 |
LIG_LIR_Gen_1 | 411 | 420 | PF02991 | 0.243 |
LIG_LIR_Nem_3 | 241 | 247 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 345 | 351 | PF02991 | 0.330 |
LIG_LIR_Nem_3 | 380 | 386 | PF02991 | 0.324 |
LIG_LIR_Nem_3 | 411 | 417 | PF02991 | 0.262 |
LIG_NRP_CendR_1 | 677 | 680 | PF00754 | 0.580 |
LIG_Pex14_1 | 370 | 374 | PF04695 | 0.325 |
LIG_PTB_Apo_2 | 423 | 430 | PF02174 | 0.243 |
LIG_PTB_Apo_2 | 669 | 676 | PF02174 | 0.363 |
LIG_SH2_CRK | 131 | 135 | PF00017 | 0.462 |
LIG_SH2_CRK | 390 | 394 | PF00017 | 0.243 |
LIG_SH2_CRK | 431 | 435 | PF00017 | 0.262 |
LIG_SH2_GRB2like | 431 | 434 | PF00017 | 0.262 |
LIG_SH2_SRC | 244 | 247 | PF00017 | 0.371 |
LIG_SH2_SRC | 431 | 434 | PF00017 | 0.262 |
LIG_SH2_STAP1 | 131 | 135 | PF00017 | 0.353 |
LIG_SH2_STAP1 | 342 | 346 | PF00017 | 0.348 |
LIG_SH2_STAP1 | 583 | 587 | PF00017 | 0.601 |
LIG_SH2_STAP1 | 631 | 635 | PF00017 | 0.633 |
LIG_SH2_STAT5 | 204 | 207 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 225 | 228 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 244 | 247 | PF00017 | 0.425 |
LIG_SH3_3 | 290 | 296 | PF00018 | 0.312 |
LIG_SH3_3 | 376 | 382 | PF00018 | 0.354 |
LIG_SUMO_SIM_par_1 | 349 | 357 | PF11976 | 0.288 |
LIG_TRAF2_1 | 249 | 252 | PF00917 | 0.371 |
LIG_TRAF2_1 | 338 | 341 | PF00917 | 0.348 |
LIG_TRAF2_1 | 533 | 536 | PF00917 | 0.582 |
LIG_TYR_ITIM | 388 | 393 | PF00017 | 0.243 |
LIG_UBA3_1 | 297 | 304 | PF00899 | 0.493 |
MOD_CDK_SPxxK_3 | 378 | 385 | PF00069 | 0.408 |
MOD_CK1_1 | 237 | 243 | PF00069 | 0.352 |
MOD_CK1_1 | 347 | 353 | PF00069 | 0.413 |
MOD_CK1_1 | 354 | 360 | PF00069 | 0.421 |
MOD_CK1_1 | 557 | 563 | PF00069 | 0.451 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.754 |
MOD_CK2_1 | 246 | 252 | PF00069 | 0.335 |
MOD_CK2_1 | 335 | 341 | PF00069 | 0.508 |
MOD_CK2_1 | 496 | 502 | PF00069 | 0.587 |
MOD_CK2_1 | 530 | 536 | PF00069 | 0.476 |
MOD_CK2_1 | 660 | 666 | PF00069 | 0.748 |
MOD_GlcNHglycan | 119 | 122 | PF01048 | 0.473 |
MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.307 |
MOD_GlcNHglycan | 550 | 553 | PF01048 | 0.465 |
MOD_GlcNHglycan | 662 | 665 | PF01048 | 0.613 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.298 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.644 |
MOD_GSK3_1 | 202 | 209 | PF00069 | 0.369 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.306 |
MOD_GSK3_1 | 347 | 354 | PF00069 | 0.304 |
MOD_GSK3_1 | 408 | 415 | PF00069 | 0.334 |
MOD_GSK3_1 | 557 | 564 | PF00069 | 0.449 |
MOD_GSK3_1 | 643 | 650 | PF00069 | 0.738 |
MOD_LATS_1 | 410 | 416 | PF00433 | 0.322 |
MOD_N-GLC_1 | 147 | 152 | PF02516 | 0.284 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.304 |
MOD_NEK2_1 | 232 | 237 | PF00069 | 0.346 |
MOD_NEK2_1 | 245 | 250 | PF00069 | 0.271 |
MOD_NEK2_1 | 318 | 323 | PF00069 | 0.407 |
MOD_NEK2_1 | 351 | 356 | PF00069 | 0.409 |
MOD_NEK2_1 | 561 | 566 | PF00069 | 0.437 |
MOD_NEK2_1 | 643 | 648 | PF00069 | 0.613 |
MOD_PIKK_1 | 111 | 117 | PF00454 | 0.378 |
MOD_PIKK_1 | 123 | 129 | PF00454 | 0.351 |
MOD_PIKK_1 | 172 | 178 | PF00454 | 0.346 |
MOD_PIKK_1 | 9 | 15 | PF00454 | 0.495 |
MOD_PKA_1 | 129 | 135 | PF00069 | 0.459 |
MOD_PKA_1 | 27 | 33 | PF00069 | 0.549 |
MOD_PKA_1 | 494 | 500 | PF00069 | 0.585 |
MOD_PKA_1 | 548 | 554 | PF00069 | 0.459 |
MOD_PKA_2 | 111 | 117 | PF00069 | 0.378 |
MOD_PKA_2 | 129 | 135 | PF00069 | 0.332 |
MOD_PKA_2 | 179 | 185 | PF00069 | 0.427 |
MOD_PKA_2 | 494 | 500 | PF00069 | 0.585 |
MOD_PKA_2 | 561 | 567 | PF00069 | 0.434 |
MOD_PKA_2 | 659 | 665 | PF00069 | 0.646 |
MOD_PKA_2 | 9 | 15 | PF00069 | 0.720 |
MOD_Plk_1 | 143 | 149 | PF00069 | 0.342 |
MOD_Plk_1 | 188 | 194 | PF00069 | 0.277 |
MOD_Plk_2-3 | 38 | 44 | PF00069 | 0.441 |
MOD_Plk_2-3 | 456 | 462 | PF00069 | 0.243 |
MOD_Plk_4 | 129 | 135 | PF00069 | 0.459 |
MOD_Plk_4 | 289 | 295 | PF00069 | 0.331 |
MOD_Plk_4 | 354 | 360 | PF00069 | 0.236 |
MOD_Plk_4 | 413 | 419 | PF00069 | 0.243 |
MOD_ProDKin_1 | 287 | 293 | PF00069 | 0.283 |
MOD_ProDKin_1 | 378 | 384 | PF00069 | 0.406 |
MOD_SUMO_for_1 | 44 | 47 | PF00179 | 0.509 |
MOD_SUMO_rev_2 | 47 | 56 | PF00179 | 0.560 |
MOD_SUMO_rev_2 | 524 | 533 | PF00179 | 0.509 |
MOD_SUMO_rev_2 | 536 | 544 | PF00179 | 0.435 |
TRG_DiLeu_BaEn_1 | 32 | 37 | PF01217 | 0.475 |
TRG_DiLeu_BaEn_4 | 591 | 597 | PF01217 | 0.565 |
TRG_DiLeu_BaLyEn_6 | 293 | 298 | PF01217 | 0.451 |
TRG_ENDOCYTIC_2 | 131 | 134 | PF00928 | 0.356 |
TRG_ENDOCYTIC_2 | 239 | 242 | PF00928 | 0.304 |
TRG_ENDOCYTIC_2 | 244 | 247 | PF00928 | 0.287 |
TRG_ENDOCYTIC_2 | 383 | 386 | PF00928 | 0.249 |
TRG_ENDOCYTIC_2 | 390 | 393 | PF00928 | 0.235 |
TRG_ENDOCYTIC_2 | 92 | 95 | PF00928 | 0.551 |
TRG_ER_diArg_1 | 493 | 495 | PF00400 | 0.544 |
TRG_ER_diArg_1 | 640 | 642 | PF00400 | 0.690 |
TRG_ER_diArg_1 | 67 | 70 | PF00400 | 0.464 |
TRG_ER_diArg_1 | 73 | 75 | PF00400 | 0.477 |
TRG_Pf-PMV_PEXEL_1 | 27 | 32 | PF00026 | 0.594 |
TRG_Pf-PMV_PEXEL_1 | 337 | 341 | PF00026 | 0.335 |
TRG_Pf-PMV_PEXEL_1 | 470 | 474 | PF00026 | 0.516 |
TRG_Pf-PMV_PEXEL_1 | 498 | 502 | PF00026 | 0.529 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1ILJ4 | Leptomonas seymouri | 81% | 100% |
A0A0S4IXY1 | Bodo saltans | 68% | 100% |
A0A1X0NYJ7 | Trypanosomatidae | 71% | 100% |
A0A3Q8IM25 | Leishmania donovani | 99% | 100% |
A0A3S5IR25 | Trypanosoma rangeli | 69% | 100% |
A4H6H1 | Leishmania braziliensis | 89% | 100% |
C9ZV23 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 69% | 100% |
E9AW77 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
Q9NF84 | Leishmania major | 96% | 100% |