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: A4H930
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 | 285 | 289 | PF00656 | 0.526 |
CLV_C14_Caspase3-7 | 591 | 595 | PF00656 | 0.319 |
CLV_C14_Caspase3-7 | 597 | 601 | PF00656 | 0.276 |
CLV_NRD_NRD_1 | 210 | 212 | PF00675 | 0.324 |
CLV_NRD_NRD_1 | 235 | 237 | PF00675 | 0.537 |
CLV_NRD_NRD_1 | 551 | 553 | PF00675 | 0.318 |
CLV_NRD_NRD_1 | 585 | 587 | PF00675 | 0.281 |
CLV_PCSK_KEX2_1 | 235 | 237 | PF00082 | 0.472 |
CLV_PCSK_KEX2_1 | 551 | 553 | PF00082 | 0.318 |
CLV_PCSK_KEX2_1 | 587 | 589 | PF00082 | 0.281 |
CLV_PCSK_KEX2_1 | 617 | 619 | PF00082 | 0.569 |
CLV_PCSK_PC1ET2_1 | 587 | 589 | PF00082 | 0.281 |
CLV_PCSK_PC7_1 | 613 | 619 | PF00082 | 0.429 |
CLV_PCSK_SKI1_1 | 247 | 251 | PF00082 | 0.331 |
CLV_PCSK_SKI1_1 | 39 | 43 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 406 | 410 | PF00082 | 0.384 |
CLV_PCSK_SKI1_1 | 458 | 462 | PF00082 | 0.603 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.633 |
DEG_SPOP_SBC_1 | 303 | 307 | PF00917 | 0.777 |
DOC_CYCLIN_RxL_1 | 34 | 46 | PF00134 | 0.466 |
DOC_CYCLIN_RxL_1 | 403 | 413 | PF00134 | 0.382 |
DOC_CYCLIN_yClb1_LxF_4 | 187 | 192 | PF00134 | 0.503 |
DOC_MAPK_DCC_7 | 235 | 245 | PF00069 | 0.286 |
DOC_MAPK_DCC_7 | 338 | 347 | PF00069 | 0.494 |
DOC_MAPK_gen_1 | 34 | 42 | PF00069 | 0.264 |
DOC_MAPK_MEF2A_6 | 197 | 204 | PF00069 | 0.468 |
DOC_PP1_RVXF_1 | 187 | 193 | PF00149 | 0.501 |
DOC_PP1_RVXF_1 | 210 | 217 | PF00149 | 0.456 |
DOC_PP2B_LxvP_1 | 115 | 118 | PF13499 | 0.501 |
DOC_PP2B_LxvP_1 | 327 | 330 | PF13499 | 0.396 |
DOC_USP7_MATH_1 | 161 | 165 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 275 | 279 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 303 | 307 | PF00917 | 0.799 |
DOC_USP7_MATH_1 | 367 | 371 | PF00917 | 0.625 |
DOC_WW_Pin1_4 | 77 | 82 | PF00397 | 0.549 |
LIG_14-3-3_CanoR_1 | 145 | 152 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 235 | 239 | PF00244 | 0.260 |
LIG_14-3-3_CanoR_1 | 438 | 445 | PF00244 | 0.448 |
LIG_14-3-3_CanoR_1 | 54 | 61 | PF00244 | 0.438 |
LIG_14-3-3_CanoR_1 | 552 | 562 | PF00244 | 0.229 |
LIG_14-3-3_CanoR_1 | 577 | 585 | PF00244 | 0.199 |
LIG_Actin_WH2_2 | 442 | 460 | PF00022 | 0.492 |
LIG_APCC_ABBA_1 | 61 | 66 | PF00400 | 0.405 |
LIG_BIR_III_4 | 288 | 292 | PF00653 | 0.537 |
LIG_BIR_III_4 | 600 | 604 | PF00653 | 0.300 |
LIG_CtBP_PxDLS_1 | 330 | 334 | PF00389 | 0.478 |
LIG_eIF4E_1 | 55 | 61 | PF01652 | 0.272 |
LIG_FHA_1 | 1 | 7 | PF00498 | 0.528 |
LIG_FHA_1 | 151 | 157 | PF00498 | 0.493 |
LIG_FHA_1 | 194 | 200 | PF00498 | 0.469 |
LIG_FHA_1 | 235 | 241 | PF00498 | 0.422 |
LIG_FHA_1 | 473 | 479 | PF00498 | 0.678 |
LIG_FHA_1 | 554 | 560 | PF00498 | 0.193 |
LIG_FHA_2 | 102 | 108 | PF00498 | 0.346 |
LIG_FHA_2 | 126 | 132 | PF00498 | 0.412 |
LIG_FHA_2 | 226 | 232 | PF00498 | 0.243 |
LIG_FHA_2 | 248 | 254 | PF00498 | 0.341 |
LIG_FHA_2 | 397 | 403 | PF00498 | 0.400 |
LIG_FHA_2 | 413 | 419 | PF00498 | 0.345 |
LIG_FHA_2 | 484 | 490 | PF00498 | 0.596 |
LIG_FHA_2 | 577 | 583 | PF00498 | 0.342 |
LIG_FHA_2 | 591 | 597 | PF00498 | 0.362 |
LIG_FHA_2 | 605 | 611 | PF00498 | 0.213 |
LIG_KLC1_Yacidic_2 | 62 | 66 | PF13176 | 0.405 |
LIG_LIR_Apic_2 | 341 | 346 | PF02991 | 0.426 |
LIG_LIR_Gen_1 | 257 | 268 | PF02991 | 0.383 |
LIG_LIR_Gen_1 | 395 | 402 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 104 | 108 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 140 | 146 | PF02991 | 0.334 |
LIG_LIR_Nem_3 | 147 | 152 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 191 | 195 | PF02991 | 0.367 |
LIG_LIR_Nem_3 | 257 | 263 | PF02991 | 0.372 |
LIG_LIR_Nem_3 | 395 | 401 | PF02991 | 0.363 |
LIG_LIR_Nem_3 | 561 | 565 | PF02991 | 0.300 |
LIG_LIR_Nem_3 | 610 | 614 | PF02991 | 0.362 |
LIG_NRBOX | 392 | 398 | PF00104 | 0.326 |
LIG_NRP_CendR_1 | 617 | 619 | PF00754 | 0.638 |
LIG_Pex14_2 | 537 | 541 | PF04695 | 0.281 |
LIG_PTAP_UEV_1 | 484 | 489 | PF05743 | 0.495 |
LIG_RPA_C_Fungi | 206 | 218 | PF08784 | 0.391 |
LIG_SH2_CRK | 531 | 535 | PF00017 | 0.413 |
LIG_SH2_STAP1 | 146 | 150 | PF00017 | 0.321 |
LIG_SH2_STAP1 | 152 | 156 | PF00017 | 0.361 |
LIG_SH2_STAP1 | 412 | 416 | PF00017 | 0.440 |
LIG_SH2_STAT5 | 152 | 155 | PF00017 | 0.281 |
LIG_SH2_STAT5 | 229 | 232 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 398 | 401 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 55 | 58 | PF00017 | 0.370 |
LIG_SH2_STAT5 | 611 | 614 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 64 | 67 | PF00017 | 0.428 |
LIG_SH3_1 | 236 | 242 | PF00018 | 0.441 |
LIG_SH3_3 | 114 | 120 | PF00018 | 0.465 |
LIG_SH3_3 | 170 | 176 | PF00018 | 0.580 |
LIG_SH3_3 | 236 | 242 | PF00018 | 0.441 |
LIG_SH3_3 | 477 | 483 | PF00018 | 0.727 |
LIG_SUMO_SIM_par_1 | 241 | 246 | PF11976 | 0.422 |
LIG_TRAF2_1 | 128 | 131 | PF00917 | 0.280 |
LIG_TRAF2_1 | 415 | 418 | PF00917 | 0.454 |
LIG_TRAF2_1 | 426 | 429 | PF00917 | 0.421 |
LIG_TRFH_1 | 340 | 344 | PF08558 | 0.337 |
LIG_TYR_ITIM | 396 | 401 | PF00017 | 0.377 |
LIG_WRC_WIRS_1 | 192 | 197 | PF05994 | 0.422 |
LIG_WRC_WIRS_1 | 219 | 224 | PF05994 | 0.238 |
MOD_CK1_1 | 164 | 170 | PF00069 | 0.660 |
MOD_CK1_1 | 359 | 365 | PF00069 | 0.684 |
MOD_CK1_1 | 441 | 447 | PF00069 | 0.482 |
MOD_CK1_1 | 464 | 470 | PF00069 | 0.674 |
MOD_CK2_1 | 125 | 131 | PF00069 | 0.368 |
MOD_CK2_1 | 152 | 158 | PF00069 | 0.471 |
MOD_CK2_1 | 225 | 231 | PF00069 | 0.381 |
MOD_CK2_1 | 247 | 253 | PF00069 | 0.401 |
MOD_CK2_1 | 259 | 265 | PF00069 | 0.430 |
MOD_CK2_1 | 396 | 402 | PF00069 | 0.398 |
MOD_CK2_1 | 412 | 418 | PF00069 | 0.353 |
MOD_CK2_1 | 430 | 436 | PF00069 | 0.398 |
MOD_CK2_1 | 483 | 489 | PF00069 | 0.733 |
MOD_CK2_1 | 576 | 582 | PF00069 | 0.475 |
MOD_CK2_1 | 590 | 596 | PF00069 | 0.362 |
MOD_CK2_1 | 604 | 610 | PF00069 | 0.213 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.467 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.633 |
MOD_GlcNHglycan | 367 | 370 | PF01048 | 0.670 |
MOD_GlcNHglycan | 440 | 443 | PF01048 | 0.460 |
MOD_GlcNHglycan | 466 | 469 | PF01048 | 0.627 |
MOD_GlcNHglycan | 475 | 478 | PF01048 | 0.731 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.295 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.487 |
MOD_GSK3_1 | 299 | 306 | PF00069 | 0.807 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.394 |
MOD_GSK3_1 | 358 | 365 | PF00069 | 0.575 |
MOD_GSK3_1 | 392 | 399 | PF00069 | 0.428 |
MOD_GSK3_1 | 400 | 407 | PF00069 | 0.375 |
MOD_GSK3_1 | 441 | 448 | PF00069 | 0.419 |
MOD_N-GLC_1 | 404 | 409 | PF02516 | 0.461 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.360 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.480 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.473 |
MOD_NEK2_1 | 218 | 223 | PF00069 | 0.241 |
MOD_NEK2_1 | 263 | 268 | PF00069 | 0.502 |
MOD_NEK2_1 | 29 | 34 | PF00069 | 0.420 |
MOD_NEK2_1 | 392 | 397 | PF00069 | 0.347 |
MOD_NEK2_1 | 401 | 406 | PF00069 | 0.364 |
MOD_NEK2_1 | 430 | 435 | PF00069 | 0.567 |
MOD_NEK2_1 | 445 | 450 | PF00069 | 0.552 |
MOD_NEK2_1 | 461 | 466 | PF00069 | 0.622 |
MOD_NEK2_1 | 472 | 477 | PF00069 | 0.561 |
MOD_NEK2_1 | 553 | 558 | PF00069 | 0.193 |
MOD_NEK2_2 | 367 | 372 | PF00069 | 0.389 |
MOD_NEK2_2 | 564 | 569 | PF00069 | 0.281 |
MOD_NEK2_2 | 581 | 586 | PF00069 | 0.199 |
MOD_PKA_1 | 338 | 344 | PF00069 | 0.424 |
MOD_PKA_2 | 144 | 150 | PF00069 | 0.350 |
MOD_PKA_2 | 234 | 240 | PF00069 | 0.262 |
MOD_PKA_2 | 53 | 59 | PF00069 | 0.434 |
MOD_PKA_2 | 576 | 582 | PF00069 | 0.274 |
MOD_PKB_1 | 588 | 596 | PF00069 | 0.468 |
MOD_Plk_1 | 268 | 274 | PF00069 | 0.557 |
MOD_Plk_1 | 404 | 410 | PF00069 | 0.516 |
MOD_Plk_2-3 | 125 | 131 | PF00069 | 0.493 |
MOD_Plk_2-3 | 225 | 231 | PF00069 | 0.241 |
MOD_Plk_2-3 | 251 | 257 | PF00069 | 0.447 |
MOD_Plk_2-3 | 576 | 582 | PF00069 | 0.199 |
MOD_Plk_4 | 175 | 181 | PF00069 | 0.544 |
MOD_Plk_4 | 19 | 25 | PF00069 | 0.423 |
MOD_Plk_4 | 225 | 231 | PF00069 | 0.346 |
MOD_Plk_4 | 259 | 265 | PF00069 | 0.532 |
MOD_Plk_4 | 367 | 373 | PF00069 | 0.537 |
MOD_Plk_4 | 392 | 398 | PF00069 | 0.378 |
MOD_Plk_4 | 404 | 410 | PF00069 | 0.364 |
MOD_ProDKin_1 | 77 | 83 | PF00069 | 0.544 |
MOD_SUMO_for_1 | 33 | 36 | PF00179 | 0.292 |
MOD_SUMO_rev_2 | 262 | 268 | PF00179 | 0.434 |
MOD_SUMO_rev_2 | 375 | 382 | PF00179 | 0.383 |
MOD_SUMO_rev_2 | 90 | 96 | PF00179 | 0.521 |
TRG_DiLeu_BaEn_1 | 495 | 500 | PF01217 | 0.648 |
TRG_DiLeu_BaLyEn_6 | 118 | 123 | PF01217 | 0.452 |
TRG_DiLeu_BaLyEn_6 | 343 | 348 | PF01217 | 0.434 |
TRG_ENDOCYTIC_2 | 105 | 108 | PF00928 | 0.553 |
TRG_ENDOCYTIC_2 | 146 | 149 | PF00928 | 0.323 |
TRG_ENDOCYTIC_2 | 219 | 222 | PF00928 | 0.337 |
TRG_ENDOCYTIC_2 | 398 | 401 | PF00928 | 0.446 |
TRG_ENDOCYTIC_2 | 562 | 565 | PF00928 | 0.300 |
TRG_ENDOCYTIC_2 | 611 | 614 | PF00928 | 0.300 |
TRG_ER_diArg_1 | 234 | 236 | PF00400 | 0.420 |
TRG_ER_diArg_1 | 37 | 40 | PF00400 | 0.460 |
TRG_ER_diArg_1 | 550 | 552 | PF00400 | 0.318 |
TRG_ER_diArg_1 | 585 | 588 | PF00400 | 0.281 |
TRG_ER_diArg_1 | 617 | 619 | PF00400 | 0.669 |
TRG_NES_CRM1_1 | 563 | 576 | PF08389 | 0.371 |
TRG_NLS_MonoExtC_3 | 585 | 590 | PF00514 | 0.300 |
TRG_Pf-PMV_PEXEL_1 | 10 | 15 | PF00026 | 0.497 |
TRG_Pf-PMV_PEXEL_1 | 121 | 125 | PF00026 | 0.464 |
TRG_Pf-PMV_PEXEL_1 | 154 | 158 | PF00026 | 0.458 |
TRG_Pf-PMV_PEXEL_1 | 39 | 43 | PF00026 | 0.437 |
TRG_Pf-PMV_PEXEL_1 | 414 | 418 | PF00026 | 0.550 |
TRG_Pf-PMV_PEXEL_1 | 509 | 513 | PF00026 | 0.360 |
TRG_PTS2 | 1 | 45 | PF00400 | 0.390 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5M4 | Leptomonas seymouri | 62% | 97% |
A0A1X0P1R3 | Trypanosomatidae | 42% | 100% |
A0A3S7X3F0 | Leishmania donovani | 84% | 100% |
A0A422P3I2 | Trypanosoma rangeli | 44% | 100% |
A4I5K9 | Leishmania infantum | 84% | 100% |
C9ZQY7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
E9B0V4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
Q4Q7B2 | Leishmania major | 84% | 100% |
V5DQL3 | Trypanosoma cruzi | 43% | 100% |