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: Q4QI33
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 | 0.577 |
CLV_NRD_NRD_1 | 117 | 119 | PF00675 | 0.578 |
CLV_NRD_NRD_1 | 189 | 191 | PF00675 | 0.378 |
CLV_NRD_NRD_1 | 226 | 228 | PF00675 | 0.537 |
CLV_NRD_NRD_1 | 278 | 280 | PF00675 | 0.524 |
CLV_NRD_NRD_1 | 414 | 416 | PF00675 | 0.454 |
CLV_NRD_NRD_1 | 567 | 569 | PF00675 | 0.714 |
CLV_NRD_NRD_1 | 93 | 95 | PF00675 | 0.529 |
CLV_PCSK_KEX2_1 | 117 | 119 | PF00082 | 0.551 |
CLV_PCSK_KEX2_1 | 189 | 191 | PF00082 | 0.378 |
CLV_PCSK_KEX2_1 | 278 | 280 | PF00082 | 0.511 |
CLV_PCSK_KEX2_1 | 413 | 415 | PF00082 | 0.461 |
CLV_PCSK_KEX2_1 | 479 | 481 | PF00082 | 0.759 |
CLV_PCSK_KEX2_1 | 567 | 569 | PF00082 | 0.685 |
CLV_PCSK_KEX2_1 | 580 | 582 | PF00082 | 0.539 |
CLV_PCSK_PC1ET2_1 | 413 | 415 | PF00082 | 0.536 |
CLV_PCSK_PC1ET2_1 | 479 | 481 | PF00082 | 0.771 |
CLV_PCSK_PC1ET2_1 | 580 | 582 | PF00082 | 0.682 |
CLV_PCSK_SKI1_1 | 12 | 16 | PF00082 | 0.447 |
CLV_PCSK_SKI1_1 | 149 | 153 | PF00082 | 0.537 |
CLV_PCSK_SKI1_1 | 18 | 22 | PF00082 | 0.415 |
CLV_PCSK_SKI1_1 | 368 | 372 | PF00082 | 0.487 |
CLV_PCSK_SKI1_1 | 410 | 414 | PF00082 | 0.522 |
CLV_PCSK_SKI1_1 | 548 | 552 | PF00082 | 0.602 |
CLV_PCSK_SKI1_1 | 603 | 607 | PF00082 | 0.688 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.560 |
DOC_CYCLIN_yCln2_LP_2 | 76 | 82 | PF00134 | 0.513 |
DOC_MAPK_gen_1 | 278 | 286 | PF00069 | 0.533 |
DOC_MAPK_gen_1 | 567 | 576 | PF00069 | 0.703 |
DOC_MAPK_JIP1_4 | 570 | 576 | PF00069 | 0.545 |
DOC_MAPK_MEF2A_6 | 18 | 25 | PF00069 | 0.334 |
DOC_MAPK_MEF2A_6 | 399 | 408 | PF00069 | 0.566 |
DOC_MAPK_MEF2A_6 | 567 | 576 | PF00069 | 0.664 |
DOC_MAPK_NFAT4_5 | 18 | 26 | PF00069 | 0.340 |
DOC_PP2B_LxvP_1 | 102 | 105 | PF13499 | 0.376 |
DOC_PP2B_LxvP_1 | 76 | 79 | PF13499 | 0.522 |
DOC_PP4_FxxP_1 | 497 | 500 | PF00568 | 0.649 |
DOC_USP7_MATH_1 | 236 | 240 | PF00917 | 0.417 |
DOC_USP7_MATH_1 | 296 | 300 | PF00917 | 0.531 |
DOC_USP7_MATH_1 | 489 | 493 | PF00917 | 0.632 |
DOC_USP7_UBL2_3 | 330 | 334 | PF12436 | 0.536 |
DOC_WW_Pin1_4 | 343 | 348 | PF00397 | 0.504 |
DOC_WW_Pin1_4 | 460 | 465 | PF00397 | 0.636 |
DOC_WW_Pin1_4 | 485 | 490 | PF00397 | 0.630 |
LIG_14-3-3_CanoR_1 | 227 | 231 | PF00244 | 0.525 |
LIG_14-3-3_CanoR_1 | 295 | 301 | PF00244 | 0.576 |
LIG_14-3-3_CanoR_1 | 423 | 428 | PF00244 | 0.536 |
LIG_14-3-3_CanoR_1 | 546 | 551 | PF00244 | 0.493 |
LIG_14-3-3_CanoR_1 | 581 | 586 | PF00244 | 0.576 |
LIG_14-3-3_CanoR_1 | 9 | 19 | PF00244 | 0.476 |
LIG_14-3-3_CanoR_1 | 94 | 98 | PF00244 | 0.542 |
LIG_Actin_WH2_2 | 282 | 300 | PF00022 | 0.552 |
LIG_Clathr_ClatBox_1 | 397 | 401 | PF01394 | 0.481 |
LIG_CtBP_PxDLS_1 | 571 | 575 | PF00389 | 0.655 |
LIG_deltaCOP1_diTrp_1 | 205 | 215 | PF00928 | 0.373 |
LIG_deltaCOP1_diTrp_1 | 311 | 318 | PF00928 | 0.395 |
LIG_deltaCOP1_diTrp_1 | 43 | 51 | PF00928 | 0.380 |
LIG_deltaCOP1_diTrp_1 | 490 | 497 | PF00928 | 0.649 |
LIG_FHA_1 | 269 | 275 | PF00498 | 0.561 |
LIG_FHA_1 | 577 | 583 | PF00498 | 0.657 |
LIG_FHA_1 | 58 | 64 | PF00498 | 0.468 |
LIG_FHA_2 | 153 | 159 | PF00498 | 0.531 |
LIG_FHA_2 | 424 | 430 | PF00498 | 0.566 |
LIG_FHA_2 | 486 | 492 | PF00498 | 0.730 |
LIG_FHA_2 | 593 | 599 | PF00498 | 0.567 |
LIG_FHA_2 | 602 | 608 | PF00498 | 0.584 |
LIG_LIR_Apic_2 | 495 | 500 | PF02991 | 0.706 |
LIG_LIR_Gen_1 | 148 | 156 | PF02991 | 0.512 |
LIG_LIR_Gen_1 | 168 | 178 | PF02991 | 0.475 |
LIG_LIR_Gen_1 | 393 | 400 | PF02991 | 0.407 |
LIG_LIR_Gen_1 | 443 | 453 | PF02991 | 0.518 |
LIG_LIR_Nem_3 | 148 | 153 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 206 | 212 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 311 | 315 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 393 | 397 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 43 | 48 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 443 | 449 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 462 | 468 | PF02991 | 0.581 |
LIG_LIR_Nem_3 | 491 | 497 | PF02991 | 0.596 |
LIG_PCNA_yPIPBox_3 | 414 | 428 | PF02747 | 0.577 |
LIG_PCNA_yPIPBox_3 | 430 | 441 | PF02747 | 0.635 |
LIG_Pex14_1 | 109 | 113 | PF04695 | 0.503 |
LIG_Pex14_1 | 146 | 150 | PF04695 | 0.410 |
LIG_Pex14_1 | 166 | 170 | PF04695 | 0.435 |
LIG_Pex14_1 | 45 | 49 | PF04695 | 0.379 |
LIG_Pex14_2 | 6 | 10 | PF04695 | 0.547 |
LIG_SH2_CRK | 360 | 364 | PF00017 | 0.542 |
LIG_SH2_STAT3 | 373 | 376 | PF00017 | 0.561 |
LIG_SH2_STAT5 | 41 | 44 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 436 | 439 | PF00017 | 0.484 |
LIG_SH2_STAT5 | 48 | 51 | PF00017 | 0.341 |
LIG_SH3_3 | 493 | 499 | PF00018 | 0.653 |
LIG_SUMO_SIM_par_1 | 19 | 24 | PF11976 | 0.553 |
LIG_SUMO_SIM_par_1 | 30 | 38 | PF11976 | 0.500 |
LIG_SUMO_SIM_par_1 | 592 | 598 | PF11976 | 0.678 |
LIG_TRAF2_1 | 280 | 283 | PF00917 | 0.592 |
LIG_TRAF2_1 | 459 | 462 | PF00917 | 0.641 |
LIG_TRAF2_1 | 506 | 509 | PF00917 | 0.760 |
LIG_UBA3_1 | 403 | 410 | PF00899 | 0.476 |
LIG_WRC_WIRS_1 | 424 | 429 | PF05994 | 0.544 |
LIG_WW_3 | 469 | 473 | PF00397 | 0.748 |
MOD_CK1_1 | 13 | 19 | PF00069 | 0.412 |
MOD_CK1_1 | 257 | 263 | PF00069 | 0.665 |
MOD_CK1_1 | 393 | 399 | PF00069 | 0.520 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.532 |
MOD_CK2_1 | 127 | 133 | PF00069 | 0.528 |
MOD_CK2_1 | 152 | 158 | PF00069 | 0.593 |
MOD_CK2_1 | 423 | 429 | PF00069 | 0.463 |
MOD_CK2_1 | 456 | 462 | PF00069 | 0.615 |
MOD_CK2_1 | 489 | 495 | PF00069 | 0.645 |
MOD_CK2_1 | 503 | 509 | PF00069 | 0.647 |
MOD_CK2_1 | 592 | 598 | PF00069 | 0.564 |
MOD_CK2_1 | 601 | 607 | PF00069 | 0.581 |
MOD_CK2_1 | 93 | 99 | PF00069 | 0.478 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.403 |
MOD_GlcNHglycan | 258 | 262 | PF01048 | 0.715 |
MOD_GlcNHglycan | 263 | 266 | PF01048 | 0.708 |
MOD_GlcNHglycan | 268 | 271 | PF01048 | 0.613 |
MOD_GlcNHglycan | 585 | 588 | PF01048 | 0.600 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.390 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.502 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.539 |
MOD_GSK3_1 | 256 | 263 | PF00069 | 0.670 |
MOD_GSK3_1 | 456 | 463 | PF00069 | 0.653 |
MOD_GSK3_1 | 485 | 492 | PF00069 | 0.648 |
MOD_GSK3_1 | 499 | 506 | PF00069 | 0.624 |
MOD_GSK3_1 | 542 | 549 | PF00069 | 0.708 |
MOD_GSK3_1 | 572 | 579 | PF00069 | 0.647 |
MOD_GSK3_1 | 611 | 618 | PF00069 | 0.660 |
MOD_N-GLC_1 | 572 | 577 | PF02516 | 0.593 |
MOD_NEK2_1 | 100 | 105 | PF00069 | 0.479 |
MOD_NEK2_1 | 177 | 182 | PF00069 | 0.475 |
MOD_NEK2_1 | 268 | 273 | PF00069 | 0.603 |
MOD_NEK2_1 | 31 | 36 | PF00069 | 0.432 |
MOD_NEK2_1 | 404 | 409 | PF00069 | 0.551 |
MOD_NEK2_1 | 601 | 606 | PF00069 | 0.612 |
MOD_PIKK_1 | 197 | 203 | PF00454 | 0.349 |
MOD_PIKK_1 | 313 | 319 | PF00454 | 0.532 |
MOD_PIKK_1 | 489 | 495 | PF00454 | 0.724 |
MOD_PK_1 | 581 | 587 | PF00069 | 0.646 |
MOD_PKA_1 | 117 | 123 | PF00069 | 0.608 |
MOD_PKA_2 | 117 | 123 | PF00069 | 0.617 |
MOD_PKA_2 | 226 | 232 | PF00069 | 0.526 |
MOD_PKA_2 | 422 | 428 | PF00069 | 0.530 |
MOD_PKA_2 | 93 | 99 | PF00069 | 0.419 |
MOD_PKB_1 | 546 | 554 | PF00069 | 0.657 |
MOD_Plk_1 | 204 | 210 | PF00069 | 0.509 |
MOD_Plk_1 | 439 | 445 | PF00069 | 0.593 |
MOD_Plk_1 | 489 | 495 | PF00069 | 0.680 |
MOD_Plk_1 | 572 | 578 | PF00069 | 0.563 |
MOD_Plk_1 | 601 | 607 | PF00069 | 0.706 |
MOD_Plk_2-3 | 154 | 160 | PF00069 | 0.441 |
MOD_Plk_2-3 | 456 | 462 | PF00069 | 0.652 |
MOD_Plk_4 | 31 | 37 | PF00069 | 0.452 |
MOD_Plk_4 | 393 | 399 | PF00069 | 0.439 |
MOD_Plk_4 | 423 | 429 | PF00069 | 0.432 |
MOD_Plk_4 | 93 | 99 | PF00069 | 0.506 |
MOD_ProDKin_1 | 343 | 349 | PF00069 | 0.501 |
MOD_ProDKin_1 | 460 | 466 | PF00069 | 0.642 |
MOD_ProDKin_1 | 485 | 491 | PF00069 | 0.629 |
MOD_SUMO_rev_2 | 322 | 332 | PF00179 | 0.504 |
TRG_DiLeu_BaEn_2 | 26 | 32 | PF01217 | 0.446 |
TRG_ENDOCYTIC_2 | 150 | 153 | PF00928 | 0.542 |
TRG_ENDOCYTIC_2 | 360 | 363 | PF00928 | 0.479 |
TRG_ENDOCYTIC_2 | 48 | 51 | PF00928 | 0.491 |
TRG_ER_diArg_1 | 116 | 118 | PF00400 | 0.562 |
TRG_ER_diArg_1 | 188 | 190 | PF00400 | 0.383 |
TRG_ER_diArg_1 | 566 | 568 | PF00400 | 0.714 |
TRG_NES_CRM1_1 | 520 | 532 | PF08389 | 0.673 |
TRG_Pf-PMV_PEXEL_1 | 603 | 607 | PF00026 | 0.664 |
TRG_Pf-PMV_PEXEL_1 | 95 | 99 | PF00026 | 0.455 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1P9R7 | Leptomonas seymouri | 63% | 99% |
A0A0S4IQN5 | Bodo saltans | 28% | 100% |
A0A1X0NMW7 | Trypanosomatidae | 34% | 98% |
A0A3S7WQJ2 | Leishmania donovani | 94% | 100% |
A0A422NEC5 | Trypanosoma rangeli | 35% | 99% |
A4H5H9 | Leishmania braziliensis | 85% | 93% |
A4HTS0 | Leishmania infantum | 94% | 100% |
D0A979 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 97% |
E9AMK3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
V5BN50 | Trypanosoma cruzi | 36% | 100% |