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: A4H5H9
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 | 168 | 172 | PF00656 | 0.404 |
CLV_C14_Caspase3-7 | 43 | 47 | PF00656 | 0.319 |
CLV_C14_Caspase3-7 | 71 | 75 | PF00656 | 0.289 |
CLV_NRD_NRD_1 | 137 | 139 | PF00675 | 0.336 |
CLV_NRD_NRD_1 | 161 | 163 | PF00675 | 0.434 |
CLV_NRD_NRD_1 | 179 | 181 | PF00675 | 0.395 |
CLV_NRD_NRD_1 | 207 | 209 | PF00675 | 0.288 |
CLV_NRD_NRD_1 | 233 | 235 | PF00675 | 0.315 |
CLV_NRD_NRD_1 | 322 | 324 | PF00675 | 0.498 |
CLV_NRD_NRD_1 | 458 | 460 | PF00675 | 0.381 |
CLV_NRD_NRD_1 | 611 | 613 | PF00675 | 0.711 |
CLV_PCSK_KEX2_1 | 161 | 163 | PF00082 | 0.542 |
CLV_PCSK_KEX2_1 | 179 | 181 | PF00082 | 0.379 |
CLV_PCSK_KEX2_1 | 207 | 209 | PF00082 | 0.326 |
CLV_PCSK_KEX2_1 | 233 | 235 | PF00082 | 0.315 |
CLV_PCSK_KEX2_1 | 322 | 324 | PF00082 | 0.482 |
CLV_PCSK_KEX2_1 | 457 | 459 | PF00082 | 0.384 |
CLV_PCSK_KEX2_1 | 523 | 525 | PF00082 | 0.711 |
CLV_PCSK_KEX2_1 | 611 | 613 | PF00082 | 0.659 |
CLV_PCSK_KEX2_1 | 624 | 626 | PF00082 | 0.482 |
CLV_PCSK_PC1ET2_1 | 457 | 459 | PF00082 | 0.469 |
CLV_PCSK_PC1ET2_1 | 523 | 525 | PF00082 | 0.606 |
CLV_PCSK_PC1ET2_1 | 624 | 626 | PF00082 | 0.660 |
CLV_PCSK_SKI1_1 | 412 | 416 | PF00082 | 0.435 |
CLV_PCSK_SKI1_1 | 454 | 458 | PF00082 | 0.447 |
CLV_PCSK_SKI1_1 | 467 | 471 | PF00082 | 0.457 |
CLV_PCSK_SKI1_1 | 485 | 489 | PF00082 | 0.262 |
CLV_PCSK_SKI1_1 | 56 | 60 | PF00082 | 0.398 |
CLV_PCSK_SKI1_1 | 647 | 651 | PF00082 | 0.651 |
DEG_APCC_DBOX_1 | 207 | 215 | PF00400 | 0.353 |
DOC_CYCLIN_yCln2_LP_2 | 120 | 126 | PF00134 | 0.365 |
DOC_CYCLIN_yCln2_LP_2 | 31 | 37 | PF00134 | 0.407 |
DOC_CYCLIN_yCln2_LP_2 | 541 | 544 | PF00134 | 0.588 |
DOC_MAPK_gen_1 | 19 | 27 | PF00069 | 0.422 |
DOC_MAPK_gen_1 | 207 | 213 | PF00069 | 0.317 |
DOC_MAPK_gen_1 | 566 | 575 | PF00069 | 0.498 |
DOC_MAPK_gen_1 | 611 | 620 | PF00069 | 0.567 |
DOC_MAPK_JIP1_4 | 614 | 620 | PF00069 | 0.478 |
DOC_MAPK_MEF2A_6 | 21 | 29 | PF00069 | 0.421 |
DOC_MAPK_MEF2A_6 | 443 | 452 | PF00069 | 0.526 |
DOC_MAPK_MEF2A_6 | 611 | 620 | PF00069 | 0.545 |
DOC_PP2B_LxvP_1 | 120 | 123 | PF13499 | 0.372 |
DOC_PP2B_LxvP_1 | 146 | 149 | PF13499 | 0.310 |
DOC_PP2B_LxvP_1 | 31 | 34 | PF13499 | 0.411 |
DOC_PP2B_LxvP_1 | 541 | 544 | PF13499 | 0.462 |
DOC_USP7_MATH_1 | 340 | 344 | PF00917 | 0.489 |
DOC_USP7_MATH_1 | 533 | 537 | PF00917 | 0.567 |
DOC_WW_Pin1_4 | 504 | 509 | PF00397 | 0.558 |
DOC_WW_Pin1_4 | 529 | 534 | PF00397 | 0.563 |
LIG_14-3-3_CanoR_1 | 138 | 142 | PF00244 | 0.530 |
LIG_14-3-3_CanoR_1 | 339 | 345 | PF00244 | 0.563 |
LIG_14-3-3_CanoR_1 | 36 | 42 | PF00244 | 0.543 |
LIG_14-3-3_CanoR_1 | 467 | 472 | PF00244 | 0.498 |
LIG_14-3-3_CanoR_1 | 625 | 630 | PF00244 | 0.517 |
LIG_BIR_III_4 | 266 | 270 | PF00653 | 0.271 |
LIG_Clathr_ClatBox_1 | 441 | 445 | PF01394 | 0.423 |
LIG_CtBP_PxDLS_1 | 615 | 619 | PF00389 | 0.539 |
LIG_deltaCOP1_diTrp_1 | 188 | 197 | PF00928 | 0.293 |
LIG_deltaCOP1_diTrp_1 | 249 | 259 | PF00928 | 0.320 |
LIG_deltaCOP1_diTrp_1 | 355 | 362 | PF00928 | 0.341 |
LIG_deltaCOP1_diTrp_1 | 87 | 95 | PF00928 | 0.317 |
LIG_eIF4E_1 | 151 | 157 | PF01652 | 0.245 |
LIG_FHA_1 | 102 | 108 | PF00498 | 0.402 |
LIG_FHA_1 | 306 | 312 | PF00498 | 0.499 |
LIG_FHA_1 | 313 | 319 | PF00498 | 0.429 |
LIG_FHA_1 | 621 | 627 | PF00498 | 0.623 |
LIG_FHA_2 | 197 | 203 | PF00498 | 0.473 |
LIG_FHA_2 | 311 | 317 | PF00498 | 0.460 |
LIG_FHA_2 | 362 | 368 | PF00498 | 0.378 |
LIG_FHA_2 | 468 | 474 | PF00498 | 0.510 |
LIG_FHA_2 | 530 | 536 | PF00498 | 0.579 |
LIG_FHA_2 | 593 | 599 | PF00498 | 0.452 |
LIG_FHA_2 | 637 | 643 | PF00498 | 0.496 |
LIG_LIR_Gen_1 | 192 | 201 | PF02991 | 0.451 |
LIG_LIR_Gen_1 | 437 | 444 | PF02991 | 0.346 |
LIG_LIR_Gen_1 | 486 | 494 | PF02991 | 0.447 |
LIG_LIR_Gen_1 | 8 | 18 | PF02991 | 0.425 |
LIG_LIR_Nem_3 | 192 | 197 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 355 | 359 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 437 | 441 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 445 | 450 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 486 | 491 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 506 | 512 | PF02991 | 0.503 |
LIG_LIR_Nem_3 | 535 | 541 | PF02991 | 0.541 |
LIG_LIR_Nem_3 | 8 | 14 | PF02991 | 0.425 |
LIG_LIR_Nem_3 | 87 | 92 | PF02991 | 0.363 |
LIG_NRBOX | 26 | 32 | PF00104 | 0.419 |
LIG_PCNA_yPIPBox_3 | 458 | 472 | PF02747 | 0.530 |
LIG_Pex14_1 | 153 | 157 | PF04695 | 0.460 |
LIG_Pex14_1 | 190 | 194 | PF04695 | 0.367 |
LIG_Pex14_1 | 89 | 93 | PF04695 | 0.316 |
LIG_Pex14_2 | 50 | 54 | PF04695 | 0.517 |
LIG_SH2_CRK | 11 | 15 | PF00017 | 0.426 |
LIG_SH2_CRK | 404 | 408 | PF00017 | 0.497 |
LIG_SH2_SRC | 254 | 257 | PF00017 | 0.251 |
LIG_SH2_STAT3 | 151 | 154 | PF00017 | 0.357 |
LIG_SH2_STAT3 | 417 | 420 | PF00017 | 0.512 |
LIG_SH2_STAT5 | 480 | 483 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 85 | 88 | PF00017 | 0.371 |
LIG_SH2_STAT5 | 92 | 95 | PF00017 | 0.354 |
LIG_SH3_3 | 537 | 543 | PF00018 | 0.617 |
LIG_SUMO_SIM_anti_2 | 74 | 82 | PF11976 | 0.273 |
LIG_SUMO_SIM_par_1 | 295 | 301 | PF11976 | 0.436 |
LIG_SUMO_SIM_par_1 | 636 | 642 | PF11976 | 0.527 |
LIG_SUMO_SIM_par_1 | 74 | 82 | PF11976 | 0.456 |
LIG_TRAF2_1 | 324 | 327 | PF00917 | 0.465 |
LIG_TRAF2_1 | 503 | 506 | PF00917 | 0.574 |
LIG_TRAF2_1 | 550 | 553 | PF00917 | 0.628 |
LIG_TRAF2_1 | 595 | 598 | PF00917 | 0.450 |
LIG_WRC_WIRS_1 | 468 | 473 | PF05994 | 0.479 |
LIG_WW_3 | 513 | 517 | PF00397 | 0.590 |
MOD_CK1_1 | 134 | 140 | PF00069 | 0.496 |
MOD_CK1_1 | 301 | 307 | PF00069 | 0.604 |
MOD_CK1_1 | 437 | 443 | PF00069 | 0.477 |
MOD_CK1_1 | 57 | 63 | PF00069 | 0.347 |
MOD_CK1_1 | 66 | 72 | PF00069 | 0.412 |
MOD_CK1_1 | 75 | 81 | PF00069 | 0.328 |
MOD_CK2_1 | 137 | 143 | PF00069 | 0.424 |
MOD_CK2_1 | 171 | 177 | PF00069 | 0.503 |
MOD_CK2_1 | 196 | 202 | PF00069 | 0.554 |
MOD_CK2_1 | 310 | 316 | PF00069 | 0.424 |
MOD_CK2_1 | 37 | 43 | PF00069 | 0.567 |
MOD_CK2_1 | 467 | 473 | PF00069 | 0.399 |
MOD_CK2_1 | 500 | 506 | PF00069 | 0.544 |
MOD_CK2_1 | 547 | 553 | PF00069 | 0.598 |
MOD_CK2_1 | 592 | 598 | PF00069 | 0.446 |
MOD_CK2_1 | 62 | 68 | PF00069 | 0.397 |
MOD_CK2_1 | 636 | 642 | PF00069 | 0.494 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.322 |
MOD_GlcNHglycan | 21 | 24 | PF01048 | 0.423 |
MOD_GlcNHglycan | 275 | 278 | PF01048 | 0.455 |
MOD_GlcNHglycan | 304 | 307 | PF01048 | 0.702 |
MOD_GlcNHglycan | 484 | 488 | PF01048 | 0.302 |
MOD_GlcNHglycan | 56 | 59 | PF01048 | 0.340 |
MOD_GlcNHglycan | 629 | 632 | PF01048 | 0.539 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.404 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.432 |
MOD_GSK3_1 | 327 | 334 | PF00069 | 0.447 |
MOD_GSK3_1 | 357 | 364 | PF00069 | 0.322 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.510 |
MOD_GSK3_1 | 385 | 392 | PF00069 | 0.588 |
MOD_GSK3_1 | 467 | 474 | PF00069 | 0.407 |
MOD_GSK3_1 | 500 | 507 | PF00069 | 0.595 |
MOD_GSK3_1 | 529 | 536 | PF00069 | 0.580 |
MOD_GSK3_1 | 543 | 550 | PF00069 | 0.572 |
MOD_GSK3_1 | 586 | 593 | PF00069 | 0.687 |
MOD_GSK3_1 | 616 | 623 | PF00069 | 0.612 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.467 |
MOD_N-GLC_1 | 301 | 306 | PF02516 | 0.549 |
MOD_N-GLC_1 | 616 | 621 | PF02516 | 0.541 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.434 |
MOD_NEK2_1 | 213 | 218 | PF00069 | 0.333 |
MOD_NEK2_1 | 221 | 226 | PF00069 | 0.407 |
MOD_NEK2_1 | 298 | 303 | PF00069 | 0.414 |
MOD_NEK2_1 | 448 | 453 | PF00069 | 0.504 |
MOD_NEK2_1 | 471 | 476 | PF00069 | 0.477 |
MOD_NEK2_1 | 5 | 10 | PF00069 | 0.543 |
MOD_PIKK_1 | 357 | 363 | PF00454 | 0.517 |
MOD_PIKK_1 | 533 | 539 | PF00454 | 0.582 |
MOD_PK_1 | 625 | 631 | PF00069 | 0.604 |
MOD_PKA_1 | 161 | 167 | PF00069 | 0.475 |
MOD_PKA_1 | 179 | 185 | PF00069 | 0.271 |
MOD_PKA_2 | 137 | 143 | PF00069 | 0.326 |
MOD_PKA_2 | 161 | 167 | PF00069 | 0.475 |
MOD_PKA_2 | 179 | 185 | PF00069 | 0.555 |
MOD_PKA_2 | 72 | 78 | PF00069 | 0.282 |
MOD_Plk_1 | 221 | 227 | PF00069 | 0.339 |
MOD_Plk_1 | 248 | 254 | PF00069 | 0.473 |
MOD_Plk_1 | 483 | 489 | PF00069 | 0.553 |
MOD_Plk_1 | 533 | 539 | PF00069 | 0.637 |
MOD_Plk_1 | 616 | 622 | PF00069 | 0.508 |
MOD_Plk_2-3 | 171 | 177 | PF00069 | 0.332 |
MOD_Plk_2-3 | 196 | 202 | PF00069 | 0.381 |
MOD_Plk_2-3 | 500 | 506 | PF00069 | 0.598 |
MOD_Plk_4 | 137 | 143 | PF00069 | 0.526 |
MOD_Plk_4 | 213 | 219 | PF00069 | 0.336 |
MOD_Plk_4 | 437 | 443 | PF00069 | 0.370 |
MOD_Plk_4 | 467 | 473 | PF00069 | 0.382 |
MOD_Plk_4 | 6 | 12 | PF00069 | 0.426 |
MOD_Plk_4 | 72 | 78 | PF00069 | 0.433 |
MOD_ProDKin_1 | 504 | 510 | PF00069 | 0.562 |
MOD_ProDKin_1 | 529 | 535 | PF00069 | 0.560 |
MOD_SUMO_rev_2 | 40 | 50 | PF00179 | 0.325 |
TRG_DiLeu_BaEn_1 | 423 | 428 | PF01217 | 0.326 |
TRG_ENDOCYTIC_2 | 11 | 14 | PF00928 | 0.429 |
TRG_ENDOCYTIC_2 | 194 | 197 | PF00928 | 0.505 |
TRG_ENDOCYTIC_2 | 404 | 407 | PF00928 | 0.445 |
TRG_ENDOCYTIC_2 | 92 | 95 | PF00928 | 0.454 |
TRG_ER_diArg_1 | 160 | 162 | PF00400 | 0.420 |
TRG_ER_diArg_1 | 179 | 181 | PF00400 | 0.395 |
TRG_ER_diArg_1 | 206 | 208 | PF00400 | 0.367 |
TRG_ER_diArg_1 | 232 | 234 | PF00400 | 0.320 |
TRG_ER_diArg_1 | 610 | 612 | PF00400 | 0.716 |
TRG_NES_CRM1_1 | 564 | 576 | PF08389 | 0.658 |
TRG_Pf-PMV_PEXEL_1 | 139 | 143 | PF00026 | 0.397 |
TRG_Pf-PMV_PEXEL_1 | 262 | 266 | PF00026 | 0.411 |
TRG_Pf-PMV_PEXEL_1 | 524 | 529 | PF00026 | 0.461 |
TRG_Pf-PMV_PEXEL_1 | 647 | 651 | PF00026 | 0.611 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1P9R7 | Leptomonas seymouri | 65% | 100% |
A0A0S4IQN5 | Bodo saltans | 27% | 100% |
A0A1X0NMW7 | Trypanosomatidae | 34% | 100% |
A0A3S7WQJ2 | Leishmania donovani | 86% | 100% |
A0A422NEC5 | Trypanosoma rangeli | 36% | 100% |
A4HTS0 | Leishmania infantum | 85% | 100% |
D0A979 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
E9AMK3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
Q4QI33 | Leishmania major | 85% | 100% |
V5BN50 | Trypanosoma cruzi | 36% | 100% |