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: 10 |
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: 14 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005654 | nucleoplasm | 2 | 1 |
GO:0010494 | cytoplasmic stress granule | 5 | 1 |
GO:0035770 | ribonucleoprotein granule | 3 | 1 |
GO:0036464 | cytoplasmic ribonucleoprotein granule | 4 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0099080 | supramolecular complex | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9B2K9
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006396 | RNA processing | 6 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 9 |
GO:0003723 | RNA binding | 4 | 7 |
GO:0005488 | binding | 1 | 9 |
GO:0097159 | organic cyclic compound binding | 2 | 9 |
GO:1901363 | heterocyclic compound binding | 2 | 9 |
GO:0003729 | mRNA binding | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 245 | 249 | PF00656 | 0.485 |
CLV_C14_Caspase3-7 | 390 | 394 | PF00656 | 0.603 |
CLV_C14_Caspase3-7 | 638 | 642 | PF00656 | 0.534 |
CLV_C14_Caspase3-7 | 681 | 685 | PF00656 | 0.695 |
CLV_NRD_NRD_1 | 200 | 202 | PF00675 | 0.542 |
CLV_NRD_NRD_1 | 56 | 58 | PF00675 | 0.564 |
CLV_NRD_NRD_1 | 623 | 625 | PF00675 | 0.328 |
CLV_PCSK_FUR_1 | 538 | 542 | PF00082 | 0.429 |
CLV_PCSK_KEX2_1 | 200 | 202 | PF00082 | 0.542 |
CLV_PCSK_KEX2_1 | 501 | 503 | PF00082 | 0.453 |
CLV_PCSK_KEX2_1 | 540 | 542 | PF00082 | 0.447 |
CLV_PCSK_KEX2_1 | 56 | 58 | PF00082 | 0.564 |
CLV_PCSK_KEX2_1 | 623 | 625 | PF00082 | 0.328 |
CLV_PCSK_PC1ET2_1 | 501 | 503 | PF00082 | 0.413 |
CLV_PCSK_PC1ET2_1 | 540 | 542 | PF00082 | 0.447 |
CLV_PCSK_SKI1_1 | 20 | 24 | PF00082 | 0.444 |
CLV_PCSK_SKI1_1 | 215 | 219 | PF00082 | 0.453 |
CLV_PCSK_SKI1_1 | 272 | 276 | PF00082 | 0.492 |
CLV_PCSK_SKI1_1 | 555 | 559 | PF00082 | 0.582 |
CLV_PCSK_SKI1_1 | 752 | 756 | PF00082 | 0.670 |
CLV_PCSK_SKI1_1 | 759 | 763 | PF00082 | 0.598 |
DEG_APCC_DBOX_1 | 214 | 222 | PF00400 | 0.421 |
DEG_COP1_1 | 741 | 749 | PF00400 | 0.665 |
DEG_MDM2_SWIB_1 | 275 | 282 | PF02201 | 0.419 |
DOC_ANK_TNKS_1 | 407 | 414 | PF00023 | 0.736 |
DOC_CYCLIN_RxL_1 | 17 | 27 | PF00134 | 0.432 |
DOC_MAPK_gen_1 | 200 | 206 | PF00069 | 0.528 |
DOC_MAPK_gen_1 | 649 | 658 | PF00069 | 0.534 |
DOC_MAPK_MEF2A_6 | 652 | 660 | PF00069 | 0.534 |
DOC_PP1_RVXF_1 | 270 | 276 | PF00149 | 0.396 |
DOC_PP1_RVXF_1 | 655 | 661 | PF00149 | 0.611 |
DOC_PP4_FxxP_1 | 514 | 517 | PF00568 | 0.499 |
DOC_USP7_MATH_1 | 143 | 147 | PF00917 | 0.620 |
DOC_USP7_MATH_1 | 153 | 157 | PF00917 | 0.746 |
DOC_USP7_MATH_1 | 178 | 182 | PF00917 | 0.801 |
DOC_USP7_MATH_1 | 196 | 200 | PF00917 | 0.449 |
DOC_USP7_MATH_1 | 288 | 292 | PF00917 | 0.785 |
DOC_USP7_MATH_1 | 327 | 331 | PF00917 | 0.600 |
DOC_USP7_MATH_1 | 373 | 377 | PF00917 | 0.635 |
DOC_USP7_MATH_1 | 667 | 671 | PF00917 | 0.638 |
DOC_USP7_MATH_1 | 706 | 710 | PF00917 | 0.721 |
DOC_USP7_MATH_1 | 716 | 720 | PF00917 | 0.639 |
DOC_USP7_MATH_1 | 97 | 101 | PF00917 | 0.521 |
DOC_USP7_UBL2_3 | 608 | 612 | PF12436 | 0.534 |
DOC_USP7_UBL2_3 | 755 | 759 | PF12436 | 0.645 |
DOC_WW_Pin1_4 | 165 | 170 | PF00397 | 0.694 |
DOC_WW_Pin1_4 | 350 | 355 | PF00397 | 0.595 |
DOC_WW_Pin1_4 | 440 | 445 | PF00397 | 0.667 |
LIG_14-3-3_CanoR_1 | 56 | 60 | PF00244 | 0.545 |
LIG_14-3-3_CanoR_1 | 657 | 661 | PF00244 | 0.502 |
LIG_Actin_WH2_2 | 595 | 610 | PF00022 | 0.534 |
LIG_APCC_ABBA_1 | 271 | 276 | PF00400 | 0.472 |
LIG_APCC_ABBAyCdc20_2 | 584 | 590 | PF00400 | 0.485 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.451 |
LIG_BIR_III_4 | 334 | 338 | PF00653 | 0.636 |
LIG_deltaCOP1_diTrp_1 | 486 | 494 | PF00928 | 0.433 |
LIG_eIF4E_1 | 485 | 491 | PF01652 | 0.344 |
LIG_FHA_1 | 1 | 7 | PF00498 | 0.424 |
LIG_FHA_1 | 212 | 218 | PF00498 | 0.436 |
LIG_FHA_1 | 239 | 245 | PF00498 | 0.480 |
LIG_FHA_1 | 470 | 476 | PF00498 | 0.537 |
LIG_FHA_1 | 506 | 512 | PF00498 | 0.417 |
LIG_FHA_1 | 518 | 524 | PF00498 | 0.394 |
LIG_FHA_1 | 597 | 603 | PF00498 | 0.479 |
LIG_FHA_2 | 44 | 50 | PF00498 | 0.469 |
LIG_FHA_2 | 548 | 554 | PF00498 | 0.571 |
LIG_FHA_2 | 636 | 642 | PF00498 | 0.551 |
LIG_IBAR_NPY_1 | 321 | 323 | PF08397 | 0.692 |
LIG_Integrin_RGD_1 | 381 | 383 | PF01839 | 0.522 |
LIG_LIR_Apic_2 | 302 | 307 | PF02991 | 0.709 |
LIG_LIR_Gen_1 | 276 | 287 | PF02991 | 0.620 |
LIG_LIR_Gen_1 | 486 | 494 | PF02991 | 0.367 |
LIG_LIR_Gen_1 | 653 | 663 | PF02991 | 0.579 |
LIG_LIR_Nem_3 | 110 | 114 | PF02991 | 0.523 |
LIG_LIR_Nem_3 | 276 | 282 | PF02991 | 0.594 |
LIG_LIR_Nem_3 | 440 | 445 | PF02991 | 0.667 |
LIG_LIR_Nem_3 | 486 | 491 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 492 | 497 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 653 | 658 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 659 | 663 | PF02991 | 0.457 |
LIG_NRBOX | 486 | 492 | PF00104 | 0.356 |
LIG_NRP_CendR_1 | 762 | 763 | PF00754 | 0.698 |
LIG_Pex14_2 | 275 | 279 | PF04695 | 0.494 |
LIG_PTB_Apo_2 | 264 | 271 | PF02174 | 0.495 |
LIG_PTB_Phospho_1 | 264 | 270 | PF10480 | 0.504 |
LIG_REV1ctd_RIR_1 | 619 | 628 | PF16727 | 0.499 |
LIG_SH2_CRK | 111 | 115 | PF00017 | 0.523 |
LIG_SH2_CRK | 304 | 308 | PF00017 | 0.707 |
LIG_SH2_PTP2 | 150 | 153 | PF00017 | 0.540 |
LIG_SH2_PTP2 | 270 | 273 | PF00017 | 0.379 |
LIG_SH2_STAP1 | 485 | 489 | PF00017 | 0.346 |
LIG_SH2_STAT3 | 157 | 160 | PF00017 | 0.716 |
LIG_SH2_STAT3 | 306 | 309 | PF00017 | 0.627 |
LIG_SH2_STAT5 | 113 | 116 | PF00017 | 0.517 |
LIG_SH2_STAT5 | 150 | 153 | PF00017 | 0.540 |
LIG_SH2_STAT5 | 270 | 273 | PF00017 | 0.410 |
LIG_SH2_STAT5 | 526 | 529 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 594 | 597 | PF00017 | 0.551 |
LIG_SH3_1 | 281 | 287 | PF00018 | 0.565 |
LIG_SH3_1 | 574 | 580 | PF00018 | 0.523 |
LIG_SH3_2 | 195 | 200 | PF14604 | 0.611 |
LIG_SH3_2 | 727 | 732 | PF14604 | 0.584 |
LIG_SH3_3 | 155 | 161 | PF00018 | 0.694 |
LIG_SH3_3 | 190 | 196 | PF00018 | 0.612 |
LIG_SH3_3 | 232 | 238 | PF00018 | 0.503 |
LIG_SH3_3 | 281 | 287 | PF00018 | 0.611 |
LIG_SH3_3 | 366 | 372 | PF00018 | 0.699 |
LIG_SH3_3 | 441 | 447 | PF00018 | 0.659 |
LIG_SH3_3 | 574 | 580 | PF00018 | 0.523 |
LIG_SH3_3 | 661 | 667 | PF00018 | 0.539 |
LIG_SH3_3 | 719 | 725 | PF00018 | 0.595 |
LIG_SH3_3 | 72 | 78 | PF00018 | 0.618 |
LIG_SH3_3 | 741 | 747 | PF00018 | 0.532 |
LIG_SH3_3 | 83 | 89 | PF00018 | 0.613 |
LIG_SH3_CIN85_PxpxPR_1 | 747 | 752 | PF14604 | 0.586 |
LIG_SUMO_SIM_anti_2 | 519 | 525 | PF11976 | 0.414 |
LIG_SUMO_SIM_par_1 | 2 | 7 | PF11976 | 0.482 |
LIG_SUMO_SIM_par_1 | 227 | 232 | PF11976 | 0.426 |
LIG_SUMO_SIM_par_1 | 471 | 476 | PF11976 | 0.467 |
LIG_TRAF2_1 | 46 | 49 | PF00917 | 0.485 |
LIG_TRAF2_1 | 715 | 718 | PF00917 | 0.714 |
LIG_TRAF2_1 | 726 | 729 | PF00917 | 0.578 |
LIG_TRAF2_1 | 733 | 736 | PF00917 | 0.520 |
LIG_UBA3_1 | 643 | 649 | PF00899 | 0.464 |
MOD_CK1_1 | 172 | 178 | PF00069 | 0.731 |
MOD_CK1_1 | 35 | 41 | PF00069 | 0.564 |
MOD_CK1_1 | 352 | 358 | PF00069 | 0.685 |
MOD_CK1_1 | 404 | 410 | PF00069 | 0.664 |
MOD_CK1_1 | 466 | 472 | PF00069 | 0.432 |
MOD_CK1_1 | 55 | 61 | PF00069 | 0.336 |
MOD_CK2_1 | 429 | 435 | PF00069 | 0.581 |
MOD_CK2_1 | 43 | 49 | PF00069 | 0.472 |
MOD_CK2_1 | 440 | 446 | PF00069 | 0.653 |
MOD_CK2_1 | 547 | 553 | PF00069 | 0.564 |
MOD_CK2_1 | 600 | 606 | PF00069 | 0.483 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.695 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.629 |
MOD_GlcNHglycan | 250 | 253 | PF01048 | 0.352 |
MOD_GlcNHglycan | 301 | 304 | PF01048 | 0.823 |
MOD_GlcNHglycan | 329 | 332 | PF01048 | 0.597 |
MOD_GlcNHglycan | 355 | 358 | PF01048 | 0.729 |
MOD_GlcNHglycan | 389 | 392 | PF01048 | 0.666 |
MOD_GlcNHglycan | 431 | 434 | PF01048 | 0.689 |
MOD_GlcNHglycan | 446 | 450 | PF01048 | 0.774 |
MOD_GlcNHglycan | 467 | 471 | PF01048 | 0.482 |
MOD_GlcNHglycan | 555 | 558 | PF01048 | 0.478 |
MOD_GlcNHglycan | 718 | 721 | PF01048 | 0.690 |
MOD_GlcNHglycan | 759 | 762 | PF01048 | 0.559 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.518 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.719 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.701 |
MOD_GSK3_1 | 349 | 356 | PF00069 | 0.668 |
MOD_GSK3_1 | 465 | 472 | PF00069 | 0.636 |
MOD_GSK3_1 | 547 | 554 | PF00069 | 0.576 |
MOD_GSK3_1 | 555 | 562 | PF00069 | 0.479 |
MOD_GSK3_1 | 596 | 603 | PF00069 | 0.491 |
MOD_N-GLC_1 | 178 | 183 | PF02516 | 0.658 |
MOD_N-GLC_1 | 478 | 483 | PF02516 | 0.470 |
MOD_N-GLC_1 | 596 | 601 | PF02516 | 0.279 |
MOD_N-GLC_2 | 267 | 269 | PF02516 | 0.504 |
MOD_NEK2_1 | 24 | 29 | PF00069 | 0.520 |
MOD_NEK2_1 | 532 | 537 | PF00069 | 0.378 |
MOD_NEK2_1 | 566 | 571 | PF00069 | 0.635 |
MOD_NEK2_1 | 593 | 598 | PF00069 | 0.479 |
MOD_NEK2_1 | 656 | 661 | PF00069 | 0.423 |
MOD_NEK2_2 | 40 | 45 | PF00069 | 0.445 |
MOD_OFUCOSY | 471 | 477 | PF10250 | 0.422 |
MOD_PIKK_1 | 143 | 149 | PF00454 | 0.586 |
MOD_PIKK_1 | 35 | 41 | PF00454 | 0.490 |
MOD_PIKK_1 | 358 | 364 | PF00454 | 0.765 |
MOD_PIKK_1 | 559 | 565 | PF00454 | 0.344 |
MOD_PIKK_1 | 706 | 712 | PF00454 | 0.575 |
MOD_PIKK_1 | 97 | 103 | PF00454 | 0.748 |
MOD_PKA_2 | 404 | 410 | PF00069 | 0.695 |
MOD_PKA_2 | 429 | 435 | PF00069 | 0.681 |
MOD_PKA_2 | 532 | 538 | PF00069 | 0.396 |
MOD_PKA_2 | 547 | 553 | PF00069 | 0.563 |
MOD_PKA_2 | 55 | 61 | PF00069 | 0.539 |
MOD_PKA_2 | 656 | 662 | PF00069 | 0.512 |
MOD_PKA_2 | 667 | 673 | PF00069 | 0.581 |
MOD_Plk_1 | 478 | 484 | PF00069 | 0.416 |
MOD_Plk_2-3 | 547 | 553 | PF00069 | 0.564 |
MOD_Plk_2-3 | 600 | 606 | PF00069 | 0.464 |
MOD_Plk_4 | 121 | 127 | PF00069 | 0.516 |
MOD_Plk_4 | 172 | 178 | PF00069 | 0.670 |
MOD_Plk_4 | 469 | 475 | PF00069 | 0.555 |
MOD_Plk_4 | 519 | 525 | PF00069 | 0.399 |
MOD_Plk_4 | 532 | 538 | PF00069 | 0.518 |
MOD_ProDKin_1 | 165 | 171 | PF00069 | 0.696 |
MOD_ProDKin_1 | 350 | 356 | PF00069 | 0.596 |
MOD_ProDKin_1 | 440 | 446 | PF00069 | 0.668 |
MOD_SUMO_rev_2 | 547 | 557 | PF00179 | 0.606 |
MOD_SUMO_rev_2 | 600 | 610 | PF00179 | 0.534 |
TRG_DiLeu_BaEn_1 | 49 | 54 | PF01217 | 0.451 |
TRG_ENDOCYTIC_2 | 111 | 114 | PF00928 | 0.572 |
TRG_ENDOCYTIC_2 | 126 | 129 | PF00928 | 0.693 |
TRG_ENDOCYTIC_2 | 270 | 273 | PF00928 | 0.379 |
TRG_ER_diArg_1 | 200 | 203 | PF00400 | 0.553 |
TRG_ER_diArg_1 | 583 | 586 | PF00400 | 0.571 |
TRG_ER_diArg_1 | 622 | 624 | PF00400 | 0.528 |
TRG_Pf-PMV_PEXEL_1 | 203 | 207 | PF00026 | 0.517 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1I1 | Leptomonas seymouri | 45% | 100% |
A0A3Q8IFS5 | Leishmania donovani | 23% | 100% |
A0A3Q8IJ43 | Leishmania donovani | 90% | 100% |
A4HK66 | Leishmania braziliensis | 72% | 98% |
A4I7Q0 | Leishmania infantum | 23% | 100% |
A4I7Q1 | Leishmania infantum | 90% | 100% |
Q4Q5J7 | Leishmania major | 90% | 100% |