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: E9AMK3
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 3 |
GO:0006396 | RNA processing | 6 | 3 |
GO:0006397 | mRNA processing | 7 | 3 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 3 |
GO:0006807 | nitrogen compound metabolic process | 2 | 3 |
GO:0008152 | metabolic process | 1 | 3 |
GO:0009987 | cellular process | 1 | 3 |
GO:0016070 | RNA metabolic process | 5 | 3 |
GO:0016071 | mRNA metabolic process | 6 | 3 |
GO:0031123 | RNA 3'-end processing | 7 | 3 |
GO:0031124 | mRNA 3'-end processing | 8 | 3 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 3 |
GO:0043170 | macromolecule metabolic process | 3 | 3 |
GO:0044237 | cellular metabolic process | 2 | 3 |
GO:0044238 | primary metabolic process | 2 | 3 |
GO:0046483 | heterocycle metabolic process | 3 | 3 |
GO:0071704 | organic substance metabolic process | 2 | 3 |
GO:0090304 | nucleic acid metabolic process | 4 | 3 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 248 | 252 | PF00656 | 0.510 |
CLV_C14_Caspase3-7 | 263 | 267 | PF00656 | 0.409 |
CLV_NRD_NRD_1 | 117 | 119 | PF00675 | 0.434 |
CLV_NRD_NRD_1 | 189 | 191 | PF00675 | 0.309 |
CLV_NRD_NRD_1 | 227 | 229 | PF00675 | 0.537 |
CLV_NRD_NRD_1 | 278 | 280 | PF00675 | 0.494 |
CLV_NRD_NRD_1 | 414 | 416 | PF00675 | 0.391 |
CLV_NRD_NRD_1 | 567 | 569 | PF00675 | 0.675 |
CLV_NRD_NRD_1 | 93 | 95 | PF00675 | 0.331 |
CLV_PCSK_KEX2_1 | 117 | 119 | PF00082 | 0.542 |
CLV_PCSK_KEX2_1 | 189 | 191 | PF00082 | 0.309 |
CLV_PCSK_KEX2_1 | 227 | 229 | PF00082 | 0.350 |
CLV_PCSK_KEX2_1 | 278 | 280 | PF00082 | 0.477 |
CLV_PCSK_KEX2_1 | 413 | 415 | PF00082 | 0.397 |
CLV_PCSK_KEX2_1 | 479 | 481 | PF00082 | 0.721 |
CLV_PCSK_KEX2_1 | 567 | 569 | PF00082 | 0.623 |
CLV_PCSK_KEX2_1 | 580 | 582 | PF00082 | 0.476 |
CLV_PCSK_PC1ET2_1 | 413 | 415 | PF00082 | 0.481 |
CLV_PCSK_PC1ET2_1 | 479 | 481 | PF00082 | 0.616 |
CLV_PCSK_PC1ET2_1 | 580 | 582 | PF00082 | 0.654 |
CLV_PCSK_SKI1_1 | 12 | 16 | PF00082 | 0.398 |
CLV_PCSK_SKI1_1 | 149 | 153 | PF00082 | 0.480 |
CLV_PCSK_SKI1_1 | 18 | 22 | PF00082 | 0.394 |
CLV_PCSK_SKI1_1 | 368 | 372 | PF00082 | 0.442 |
CLV_PCSK_SKI1_1 | 410 | 414 | PF00082 | 0.458 |
CLV_PCSK_SKI1_1 | 603 | 607 | PF00082 | 0.666 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.497 |
DOC_CYCLIN_yCln2_LP_2 | 76 | 82 | PF00134 | 0.367 |
DOC_MAPK_gen_1 | 522 | 531 | PF00069 | 0.497 |
DOC_MAPK_gen_1 | 567 | 574 | PF00069 | 0.544 |
DOC_MAPK_MEF2A_6 | 399 | 408 | PF00069 | 0.539 |
DOC_PP2B_LxvP_1 | 102 | 105 | PF13499 | 0.313 |
DOC_PP2B_LxvP_1 | 76 | 79 | PF13499 | 0.375 |
DOC_PP4_FxxP_1 | 497 | 500 | PF00568 | 0.558 |
DOC_USP7_MATH_1 | 237 | 241 | PF00917 | 0.362 |
DOC_USP7_MATH_1 | 296 | 300 | PF00917 | 0.490 |
DOC_USP7_MATH_1 | 489 | 493 | PF00917 | 0.585 |
DOC_USP7_UBL2_3 | 330 | 334 | PF12436 | 0.489 |
DOC_USP7_UBL2_3 | 550 | 554 | PF12436 | 0.724 |
DOC_WW_Pin1_4 | 343 | 348 | PF00397 | 0.449 |
DOC_WW_Pin1_4 | 460 | 465 | PF00397 | 0.578 |
DOC_WW_Pin1_4 | 485 | 490 | PF00397 | 0.581 |
LIG_14-3-3_CanoR_1 | 227 | 231 | PF00244 | 0.504 |
LIG_14-3-3_CanoR_1 | 295 | 301 | PF00244 | 0.564 |
LIG_14-3-3_CanoR_1 | 423 | 428 | PF00244 | 0.503 |
LIG_14-3-3_CanoR_1 | 567 | 573 | PF00244 | 0.497 |
LIG_14-3-3_CanoR_1 | 581 | 586 | PF00244 | 0.516 |
LIG_14-3-3_CanoR_1 | 9 | 19 | PF00244 | 0.417 |
LIG_14-3-3_CanoR_1 | 94 | 98 | PF00244 | 0.529 |
LIG_Actin_WH2_2 | 174 | 191 | PF00022 | 0.374 |
LIG_Clathr_ClatBox_1 | 397 | 401 | PF01394 | 0.432 |
LIG_deltaCOP1_diTrp_1 | 205 | 215 | PF00928 | 0.310 |
LIG_deltaCOP1_diTrp_1 | 311 | 318 | PF00928 | 0.334 |
LIG_deltaCOP1_diTrp_1 | 43 | 51 | PF00928 | 0.316 |
LIG_deltaCOP1_diTrp_1 | 490 | 497 | PF00928 | 0.607 |
LIG_DLG_GKlike_1 | 399 | 406 | PF00625 | 0.475 |
LIG_FHA_1 | 269 | 275 | PF00498 | 0.435 |
LIG_FHA_1 | 346 | 352 | PF00498 | 0.489 |
LIG_FHA_1 | 577 | 583 | PF00498 | 0.618 |
LIG_FHA_1 | 58 | 64 | PF00498 | 0.407 |
LIG_FHA_2 | 153 | 159 | PF00498 | 0.468 |
LIG_FHA_2 | 424 | 430 | PF00498 | 0.526 |
LIG_FHA_2 | 486 | 492 | PF00498 | 0.597 |
LIG_FHA_2 | 593 | 599 | PF00498 | 0.506 |
LIG_FHA_2 | 602 | 608 | PF00498 | 0.520 |
LIG_LIR_Apic_2 | 495 | 500 | PF02991 | 0.690 |
LIG_LIR_Gen_1 | 148 | 157 | PF02991 | 0.447 |
LIG_LIR_Gen_1 | 168 | 178 | PF02991 | 0.421 |
LIG_LIR_Gen_1 | 393 | 400 | PF02991 | 0.361 |
LIG_LIR_Gen_1 | 442 | 450 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 148 | 153 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 206 | 212 | PF02991 | 0.334 |
LIG_LIR_Nem_3 | 311 | 315 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 393 | 397 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 43 | 48 | PF02991 | 0.363 |
LIG_LIR_Nem_3 | 442 | 447 | PF02991 | 0.397 |
LIG_LIR_Nem_3 | 462 | 468 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 491 | 497 | PF02991 | 0.549 |
LIG_PCNA_yPIPBox_3 | 414 | 428 | PF02747 | 0.541 |
LIG_PCNA_yPIPBox_3 | 430 | 441 | PF02747 | 0.621 |
LIG_Pex14_1 | 109 | 113 | PF04695 | 0.466 |
LIG_Pex14_1 | 146 | 150 | PF04695 | 0.361 |
LIG_Pex14_1 | 166 | 170 | PF04695 | 0.325 |
LIG_Pex14_1 | 45 | 49 | PF04695 | 0.316 |
LIG_Pex14_2 | 6 | 10 | PF04695 | 0.523 |
LIG_SH2_CRK | 360 | 364 | PF00017 | 0.504 |
LIG_SH2_STAT3 | 373 | 376 | PF00017 | 0.524 |
LIG_SH2_STAT5 | 41 | 44 | PF00017 | 0.372 |
LIG_SH2_STAT5 | 436 | 439 | PF00017 | 0.428 |
LIG_SH2_STAT5 | 48 | 51 | PF00017 | 0.353 |
LIG_SH3_3 | 493 | 499 | PF00018 | 0.620 |
LIG_SUMO_SIM_par_1 | 19 | 27 | PF11976 | 0.545 |
LIG_SUMO_SIM_par_1 | 30 | 38 | PF11976 | 0.456 |
LIG_SUMO_SIM_par_1 | 592 | 598 | PF11976 | 0.537 |
LIG_TRAF2_1 | 280 | 283 | PF00917 | 0.462 |
LIG_TRAF2_1 | 459 | 462 | PF00917 | 0.593 |
LIG_TRAF2_1 | 506 | 509 | PF00917 | 0.628 |
LIG_UBA3_1 | 403 | 410 | PF00899 | 0.429 |
LIG_WRC_WIRS_1 | 424 | 429 | PF05994 | 0.498 |
LIG_WW_3 | 469 | 473 | PF00397 | 0.607 |
MOD_CK1_1 | 13 | 19 | PF00069 | 0.351 |
MOD_CK1_1 | 22 | 28 | PF00069 | 0.406 |
MOD_CK1_1 | 257 | 263 | PF00069 | 0.620 |
MOD_CK1_1 | 393 | 399 | PF00069 | 0.493 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.494 |
MOD_CK2_1 | 127 | 133 | PF00069 | 0.479 |
MOD_CK2_1 | 152 | 158 | PF00069 | 0.550 |
MOD_CK2_1 | 423 | 429 | PF00069 | 0.409 |
MOD_CK2_1 | 456 | 462 | PF00069 | 0.568 |
MOD_CK2_1 | 489 | 495 | PF00069 | 0.604 |
MOD_CK2_1 | 503 | 509 | PF00069 | 0.601 |
MOD_CK2_1 | 592 | 598 | PF00069 | 0.504 |
MOD_CK2_1 | 601 | 607 | PF00069 | 0.516 |
MOD_CK2_1 | 93 | 99 | PF00069 | 0.424 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.339 |
MOD_GlcNHglycan | 231 | 234 | PF01048 | 0.452 |
MOD_GlcNHglycan | 263 | 266 | PF01048 | 0.692 |
MOD_GlcNHglycan | 268 | 271 | PF01048 | 0.613 |
MOD_GlcNHglycan | 585 | 588 | PF01048 | 0.540 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.325 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.461 |
MOD_GSK3_1 | 168 | 175 | PF00069 | 0.414 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.480 |
MOD_GSK3_1 | 254 | 261 | PF00069 | 0.564 |
MOD_GSK3_1 | 283 | 290 | PF00069 | 0.447 |
MOD_GSK3_1 | 341 | 348 | PF00069 | 0.596 |
MOD_GSK3_1 | 456 | 463 | PF00069 | 0.618 |
MOD_GSK3_1 | 485 | 492 | PF00069 | 0.598 |
MOD_GSK3_1 | 499 | 506 | PF00069 | 0.572 |
MOD_GSK3_1 | 542 | 549 | PF00069 | 0.692 |
MOD_GSK3_1 | 568 | 575 | PF00069 | 0.553 |
MOD_GSK3_1 | 611 | 618 | PF00069 | 0.605 |
MOD_N-GLC_1 | 572 | 577 | PF02516 | 0.525 |
MOD_NEK2_1 | 100 | 105 | PF00069 | 0.436 |
MOD_NEK2_1 | 177 | 182 | PF00069 | 0.416 |
MOD_NEK2_1 | 268 | 273 | PF00069 | 0.600 |
MOD_NEK2_1 | 404 | 409 | PF00069 | 0.513 |
MOD_NEK2_1 | 601 | 606 | PF00069 | 0.550 |
MOD_PIKK_1 | 197 | 203 | PF00454 | 0.293 |
MOD_PIKK_1 | 313 | 319 | PF00454 | 0.510 |
MOD_PIKK_1 | 489 | 495 | PF00454 | 0.596 |
MOD_PK_1 | 568 | 574 | PF00069 | 0.528 |
MOD_PK_1 | 581 | 587 | PF00069 | 0.605 |
MOD_PKA_1 | 117 | 123 | PF00069 | 0.472 |
MOD_PKA_2 | 117 | 123 | PF00069 | 0.472 |
MOD_PKA_2 | 226 | 232 | PF00069 | 0.508 |
MOD_PKA_2 | 422 | 428 | PF00069 | 0.482 |
MOD_PKA_2 | 93 | 99 | PF00069 | 0.325 |
MOD_PKB_1 | 546 | 554 | PF00069 | 0.547 |
MOD_Plk_1 | 204 | 210 | PF00069 | 0.470 |
MOD_Plk_1 | 439 | 445 | PF00069 | 0.573 |
MOD_Plk_1 | 489 | 495 | PF00069 | 0.651 |
MOD_Plk_1 | 601 | 607 | PF00069 | 0.697 |
MOD_Plk_2-3 | 456 | 462 | PF00069 | 0.622 |
MOD_Plk_4 | 177 | 183 | PF00069 | 0.448 |
MOD_Plk_4 | 245 | 251 | PF00069 | 0.364 |
MOD_Plk_4 | 31 | 37 | PF00069 | 0.395 |
MOD_Plk_4 | 393 | 399 | PF00069 | 0.386 |
MOD_Plk_4 | 423 | 429 | PF00069 | 0.392 |
MOD_Plk_4 | 93 | 99 | PF00069 | 0.526 |
MOD_ProDKin_1 | 343 | 349 | PF00069 | 0.447 |
MOD_ProDKin_1 | 460 | 466 | PF00069 | 0.583 |
MOD_ProDKin_1 | 485 | 491 | PF00069 | 0.578 |
MOD_SUMO_rev_2 | 322 | 332 | PF00179 | 0.448 |
TRG_ENDOCYTIC_2 | 150 | 153 | PF00928 | 0.502 |
TRG_ENDOCYTIC_2 | 360 | 363 | PF00928 | 0.453 |
TRG_ENDOCYTIC_2 | 48 | 51 | PF00928 | 0.453 |
TRG_ER_diArg_1 | 116 | 118 | PF00400 | 0.420 |
TRG_ER_diArg_1 | 188 | 190 | PF00400 | 0.313 |
TRG_ER_diArg_1 | 566 | 568 | PF00400 | 0.685 |
TRG_NES_CRM1_1 | 244 | 258 | PF08389 | 0.369 |
TRG_NES_CRM1_1 | 520 | 532 | PF08389 | 0.654 |
TRG_Pf-PMV_PEXEL_1 | 218 | 222 | PF00026 | 0.392 |
TRG_Pf-PMV_PEXEL_1 | 603 | 607 | PF00026 | 0.626 |
TRG_Pf-PMV_PEXEL_1 | 95 | 99 | PF00026 | 0.396 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1P9R7 | Leptomonas seymouri | 65% | 99% |
A0A0S4IQN5 | Bodo saltans | 29% | 100% |
A0A1X0NMW7 | Trypanosomatidae | 33% | 98% |
A0A3S7WQJ2 | Leishmania donovani | 95% | 100% |
A0A422NEC5 | Trypanosoma rangeli | 35% | 99% |
A4H5H9 | Leishmania braziliensis | 86% | 100% |
A4HTS0 | Leishmania infantum | 95% | 100% |
D0A979 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 97% |
Q4QI33 | Leishmania major | 94% | 100% |
V5BN50 | Trypanosoma cruzi | 36% | 100% |