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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005681 | spliceosomal complex | 3 | 11 |
GO:0032991 | protein-containing complex | 1 | 11 |
GO:0140513 | nuclear protein-containing complex | 2 | 11 |
GO:1990904 | ribonucleoprotein complex | 2 | 11 |
Related structures:
AlphaFold database: A0A3S7X3F0
Term | Name | Level | Count |
---|---|---|---|
GO:0000375 | RNA splicing, via transesterification reactions | 8 | 11 |
GO:0000377 | RNA splicing, via transesterification reactions with bulged adenosine as nucleophile | 9 | 11 |
GO:0000398 | mRNA splicing, via spliceosome | 8 | 11 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 11 |
GO:0006396 | RNA processing | 6 | 11 |
GO:0006397 | mRNA processing | 7 | 11 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0008380 | RNA splicing | 7 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016070 | RNA metabolic process | 5 | 11 |
GO:0016071 | mRNA metabolic process | 6 | 11 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0046483 | heterocycle metabolic process | 3 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:0090304 | nucleic acid metabolic process | 4 | 11 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 11 |
GO:0003723 | RNA binding | 4 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0008270 | zinc ion binding | 6 | 10 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043169 | cation binding | 3 | 11 |
GO:0046872 | metal ion binding | 4 | 11 |
GO:0046914 | transition metal ion binding | 5 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 431 | 435 | PF00656 | 0.522 |
CLV_C14_Caspase3-7 | 593 | 597 | PF00656 | 0.366 |
CLV_C14_Caspase3-7 | 599 | 603 | PF00656 | 0.304 |
CLV_NRD_NRD_1 | 210 | 212 | PF00675 | 0.412 |
CLV_NRD_NRD_1 | 235 | 237 | PF00675 | 0.537 |
CLV_NRD_NRD_1 | 439 | 441 | PF00675 | 0.588 |
CLV_NRD_NRD_1 | 470 | 472 | PF00675 | 0.676 |
CLV_NRD_NRD_1 | 553 | 555 | PF00675 | 0.335 |
CLV_NRD_NRD_1 | 587 | 589 | PF00675 | 0.394 |
CLV_PCSK_KEX2_1 | 235 | 237 | PF00082 | 0.504 |
CLV_PCSK_KEX2_1 | 470 | 472 | PF00082 | 0.676 |
CLV_PCSK_KEX2_1 | 553 | 555 | PF00082 | 0.335 |
CLV_PCSK_KEX2_1 | 589 | 591 | PF00082 | 0.335 |
CLV_PCSK_KEX2_1 | 619 | 621 | PF00082 | 0.593 |
CLV_PCSK_PC1ET2_1 | 589 | 591 | PF00082 | 0.335 |
CLV_PCSK_PC7_1 | 615 | 621 | PF00082 | 0.449 |
CLV_PCSK_SKI1_1 | 39 | 43 | PF00082 | 0.432 |
CLV_PCSK_SKI1_1 | 408 | 412 | PF00082 | 0.440 |
CLV_PCSK_SKI1_1 | 460 | 464 | PF00082 | 0.628 |
DEG_COP1_1 | 113 | 120 | PF00400 | 0.579 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.656 |
DEG_SPOP_SBC_1 | 305 | 309 | PF00917 | 0.805 |
DEG_SPOP_SBC_1 | 368 | 372 | PF00917 | 0.680 |
DOC_CYCLIN_RxL_1 | 36 | 46 | PF00134 | 0.485 |
DOC_CYCLIN_RxL_1 | 405 | 415 | PF00134 | 0.442 |
DOC_CYCLIN_yClb1_LxF_4 | 187 | 192 | PF00134 | 0.545 |
DOC_CYCLIN_yCln2_LP_2 | 218 | 224 | PF00134 | 0.452 |
DOC_MAPK_DCC_7 | 340 | 349 | PF00069 | 0.596 |
DOC_MAPK_MEF2A_6 | 197 | 204 | PF00069 | 0.510 |
DOC_PP1_RVXF_1 | 187 | 193 | PF00149 | 0.542 |
DOC_PP1_RVXF_1 | 210 | 217 | PF00149 | 0.515 |
DOC_PP2B_LxvP_1 | 115 | 118 | PF13499 | 0.540 |
DOC_PP2B_LxvP_1 | 329 | 332 | PF13499 | 0.572 |
DOC_USP7_MATH_1 | 161 | 165 | PF00917 | 0.627 |
DOC_USP7_MATH_1 | 277 | 281 | PF00917 | 0.657 |
DOC_USP7_MATH_1 | 304 | 308 | PF00917 | 0.808 |
DOC_USP7_MATH_1 | 367 | 371 | PF00917 | 0.751 |
DOC_WW_Pin1_4 | 116 | 121 | PF00397 | 0.546 |
DOC_WW_Pin1_4 | 172 | 177 | PF00397 | 0.601 |
DOC_WW_Pin1_4 | 481 | 486 | PF00397 | 0.584 |
DOC_WW_Pin1_4 | 77 | 82 | PF00397 | 0.668 |
LIG_14-3-3_CanoR_1 | 145 | 151 | PF00244 | 0.508 |
LIG_14-3-3_CanoR_1 | 440 | 447 | PF00244 | 0.503 |
LIG_14-3-3_CanoR_1 | 54 | 61 | PF00244 | 0.558 |
LIG_14-3-3_CanoR_1 | 560 | 565 | PF00244 | 0.309 |
LIG_Actin_WH2_2 | 444 | 462 | PF00022 | 0.615 |
LIG_APCC_ABBA_1 | 61 | 66 | PF00400 | 0.458 |
LIG_BIR_III_4 | 602 | 606 | PF00653 | 0.355 |
LIG_CtBP_PxDLS_1 | 332 | 336 | PF00389 | 0.605 |
LIG_FHA_1 | 1 | 7 | PF00498 | 0.633 |
LIG_FHA_1 | 151 | 157 | PF00498 | 0.546 |
LIG_FHA_1 | 194 | 200 | PF00498 | 0.496 |
LIG_FHA_1 | 381 | 387 | PF00498 | 0.441 |
LIG_FHA_2 | 126 | 132 | PF00498 | 0.481 |
LIG_FHA_2 | 153 | 159 | PF00498 | 0.547 |
LIG_FHA_2 | 279 | 285 | PF00498 | 0.671 |
LIG_FHA_2 | 399 | 405 | PF00498 | 0.461 |
LIG_FHA_2 | 415 | 421 | PF00498 | 0.394 |
LIG_FHA_2 | 579 | 585 | PF00498 | 0.453 |
LIG_FHA_2 | 593 | 599 | PF00498 | 0.276 |
LIG_FHA_2 | 607 | 613 | PF00498 | 0.249 |
LIG_KLC1_Yacidic_2 | 62 | 66 | PF13176 | 0.458 |
LIG_LIR_Apic_2 | 343 | 348 | PF02991 | 0.610 |
LIG_LIR_Apic_2 | 531 | 536 | PF02991 | 0.312 |
LIG_LIR_Gen_1 | 100 | 109 | PF02991 | 0.580 |
LIG_LIR_Gen_1 | 257 | 268 | PF02991 | 0.469 |
LIG_LIR_Gen_1 | 397 | 404 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 100 | 104 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 140 | 146 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 191 | 195 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 231 | 237 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 257 | 263 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 397 | 403 | PF02991 | 0.427 |
LIG_LIR_Nem_3 | 563 | 567 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 612 | 616 | PF02991 | 0.480 |
LIG_NRBOX | 394 | 400 | PF00104 | 0.387 |
LIG_NRP_CendR_1 | 619 | 621 | PF00754 | 0.671 |
LIG_Pex14_2 | 539 | 543 | PF04695 | 0.335 |
LIG_RPA_C_Fungi | 206 | 218 | PF08784 | 0.525 |
LIG_SH2_CRK | 234 | 238 | PF00017 | 0.390 |
LIG_SH2_CRK | 533 | 537 | PF00017 | 0.447 |
LIG_SH2_SRC | 229 | 232 | PF00017 | 0.467 |
LIG_SH2_STAP1 | 146 | 150 | PF00017 | 0.387 |
LIG_SH2_STAP1 | 414 | 418 | PF00017 | 0.507 |
LIG_SH2_STAT5 | 229 | 232 | PF00017 | 0.357 |
LIG_SH2_STAT5 | 400 | 403 | PF00017 | 0.573 |
LIG_SH2_STAT5 | 613 | 616 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 64 | 67 | PF00017 | 0.464 |
LIG_SH3_1 | 236 | 242 | PF00018 | 0.554 |
LIG_SH3_3 | 114 | 120 | PF00018 | 0.565 |
LIG_SH3_3 | 170 | 176 | PF00018 | 0.623 |
LIG_SH3_3 | 236 | 242 | PF00018 | 0.554 |
LIG_SH3_3 | 479 | 485 | PF00018 | 0.772 |
LIG_SH3_3 | 487 | 493 | PF00018 | 0.789 |
LIG_TRAF2_1 | 417 | 420 | PF00917 | 0.515 |
LIG_TRAF2_1 | 428 | 431 | PF00917 | 0.479 |
LIG_TRAF2_1 | 435 | 438 | PF00917 | 0.453 |
LIG_TRAF2_1 | 493 | 496 | PF00917 | 0.693 |
LIG_TRFH_1 | 342 | 346 | PF08558 | 0.471 |
LIG_TYR_ITIM | 398 | 403 | PF00017 | 0.470 |
LIG_WRC_WIRS_1 | 192 | 197 | PF05994 | 0.470 |
LIG_WRPW_2 | 219 | 222 | PF00400 | 0.449 |
MOD_CDK_SPK_2 | 116 | 121 | PF00069 | 0.509 |
MOD_CK1_1 | 175 | 181 | PF00069 | 0.589 |
MOD_CK1_1 | 361 | 367 | PF00069 | 0.745 |
MOD_CK1_1 | 443 | 449 | PF00069 | 0.524 |
MOD_CK1_1 | 466 | 472 | PF00069 | 0.696 |
MOD_CK2_1 | 125 | 131 | PF00069 | 0.409 |
MOD_CK2_1 | 152 | 158 | PF00069 | 0.534 |
MOD_CK2_1 | 251 | 257 | PF00069 | 0.473 |
MOD_CK2_1 | 259 | 265 | PF00069 | 0.520 |
MOD_CK2_1 | 278 | 284 | PF00069 | 0.410 |
MOD_CK2_1 | 398 | 404 | PF00069 | 0.461 |
MOD_CK2_1 | 414 | 420 | PF00069 | 0.404 |
MOD_CK2_1 | 432 | 438 | PF00069 | 0.454 |
MOD_CK2_1 | 52 | 58 | PF00069 | 0.496 |
MOD_CK2_1 | 578 | 584 | PF00069 | 0.474 |
MOD_CK2_1 | 592 | 598 | PF00069 | 0.457 |
MOD_CK2_1 | 606 | 612 | PF00069 | 0.249 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.499 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.638 |
MOD_GlcNHglycan | 360 | 363 | PF01048 | 0.704 |
MOD_GlcNHglycan | 442 | 445 | PF01048 | 0.517 |
MOD_GlcNHglycan | 477 | 480 | PF01048 | 0.769 |
MOD_GlcNHglycan | 584 | 587 | PF01048 | 0.397 |
MOD_GSK3_1 | 306 | 313 | PF00069 | 0.770 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.619 |
MOD_GSK3_1 | 394 | 401 | PF00069 | 0.488 |
MOD_GSK3_1 | 402 | 409 | PF00069 | 0.435 |
MOD_GSK3_1 | 443 | 450 | PF00069 | 0.474 |
MOD_GSK3_1 | 578 | 585 | PF00069 | 0.378 |
MOD_N-GLC_1 | 406 | 411 | PF02516 | 0.584 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.427 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.622 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.397 |
MOD_NEK2_1 | 394 | 399 | PF00069 | 0.412 |
MOD_NEK2_1 | 403 | 408 | PF00069 | 0.424 |
MOD_NEK2_1 | 447 | 452 | PF00069 | 0.568 |
MOD_NEK2_1 | 463 | 468 | PF00069 | 0.632 |
MOD_NEK2_2 | 528 | 533 | PF00069 | 0.312 |
MOD_NEK2_2 | 566 | 571 | PF00069 | 0.335 |
MOD_PKA_1 | 340 | 346 | PF00069 | 0.552 |
MOD_PKA_1 | 440 | 446 | PF00069 | 0.539 |
MOD_PKA_2 | 144 | 150 | PF00069 | 0.415 |
MOD_PKA_2 | 298 | 304 | PF00069 | 0.779 |
MOD_PKA_2 | 53 | 59 | PF00069 | 0.553 |
MOD_PKA_2 | 578 | 584 | PF00069 | 0.344 |
MOD_PKB_1 | 590 | 598 | PF00069 | 0.482 |
MOD_Plk_1 | 268 | 274 | PF00069 | 0.628 |
MOD_Plk_1 | 406 | 412 | PF00069 | 0.555 |
MOD_Plk_2-3 | 125 | 131 | PF00069 | 0.529 |
MOD_Plk_2-3 | 251 | 257 | PF00069 | 0.512 |
MOD_Plk_4 | 175 | 181 | PF00069 | 0.629 |
MOD_Plk_4 | 19 | 25 | PF00069 | 0.464 |
MOD_Plk_4 | 259 | 265 | PF00069 | 0.595 |
MOD_Plk_4 | 394 | 400 | PF00069 | 0.443 |
MOD_Plk_4 | 406 | 412 | PF00069 | 0.420 |
MOD_Plk_4 | 528 | 534 | PF00069 | 0.312 |
MOD_ProDKin_1 | 116 | 122 | PF00069 | 0.541 |
MOD_ProDKin_1 | 172 | 178 | PF00069 | 0.607 |
MOD_ProDKin_1 | 481 | 487 | PF00069 | 0.583 |
MOD_ProDKin_1 | 77 | 83 | PF00069 | 0.663 |
MOD_SUMO_for_1 | 111 | 114 | PF00179 | 0.561 |
MOD_SUMO_for_1 | 167 | 170 | PF00179 | 0.607 |
MOD_SUMO_for_1 | 266 | 269 | PF00179 | 0.569 |
MOD_SUMO_rev_2 | 262 | 268 | PF00179 | 0.522 |
MOD_SUMO_rev_2 | 377 | 384 | PF00179 | 0.472 |
MOD_SUMO_rev_2 | 464 | 469 | PF00179 | 0.598 |
MOD_SUMO_rev_2 | 90 | 96 | PF00179 | 0.552 |
TRG_DiLeu_BaEn_1 | 497 | 502 | PF01217 | 0.695 |
TRG_DiLeu_BaLyEn_6 | 118 | 123 | PF01217 | 0.582 |
TRG_DiLeu_BaLyEn_6 | 345 | 350 | PF01217 | 0.595 |
TRG_ENDOCYTIC_2 | 101 | 104 | PF00928 | 0.534 |
TRG_ENDOCYTIC_2 | 105 | 108 | PF00928 | 0.545 |
TRG_ENDOCYTIC_2 | 146 | 149 | PF00928 | 0.388 |
TRG_ENDOCYTIC_2 | 219 | 222 | PF00928 | 0.384 |
TRG_ENDOCYTIC_2 | 234 | 237 | PF00928 | 0.388 |
TRG_ENDOCYTIC_2 | 400 | 403 | PF00928 | 0.573 |
TRG_ENDOCYTIC_2 | 564 | 567 | PF00928 | 0.355 |
TRG_ENDOCYTIC_2 | 613 | 616 | PF00928 | 0.355 |
TRG_ER_diArg_1 | 234 | 236 | PF00400 | 0.535 |
TRG_ER_diArg_1 | 37 | 40 | PF00400 | 0.455 |
TRG_ER_diArg_1 | 470 | 473 | PF00400 | 0.688 |
TRG_ER_diArg_1 | 552 | 554 | PF00400 | 0.335 |
TRG_ER_diArg_1 | 587 | 590 | PF00400 | 0.335 |
TRG_ER_diArg_1 | 619 | 621 | PF00400 | 0.669 |
TRG_NES_CRM1_1 | 565 | 578 | PF08389 | 0.417 |
TRG_NLS_MonoExtC_3 | 587 | 592 | PF00514 | 0.355 |
TRG_Pf-PMV_PEXEL_1 | 10 | 15 | PF00026 | 0.526 |
TRG_Pf-PMV_PEXEL_1 | 121 | 125 | PF00026 | 0.578 |
TRG_Pf-PMV_PEXEL_1 | 154 | 158 | PF00026 | 0.599 |
TRG_Pf-PMV_PEXEL_1 | 39 | 43 | PF00026 | 0.472 |
TRG_Pf-PMV_PEXEL_1 | 416 | 420 | PF00026 | 0.592 |
TRG_Pf-PMV_PEXEL_1 | 511 | 515 | PF00026 | 0.408 |
TRG_PTS2 | 1 | 45 | PF00400 | 0.437 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5M4 | Leptomonas seymouri | 62% | 97% |
A0A1X0P1R3 | Trypanosomatidae | 42% | 100% |
A0A422P3I2 | Trypanosoma rangeli | 44% | 100% |
A4H930 | Leishmania braziliensis | 84% | 100% |
A4I5K9 | Leishmania infantum | 100% | 100% |
C9ZQY7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
E9B0V4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
Q4Q7B2 | Leishmania major | 95% | 100% |
V5DQL3 | Trypanosoma cruzi | 43% | 100% |