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: 6 |
NetGPI | no | yes: 0, no: 6 |
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: A0A3Q8IJ43
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 | 7 |
GO:0003723 | RNA binding | 4 | 7 |
GO:0005488 | binding | 1 | 7 |
GO:0097159 | organic cyclic compound binding | 2 | 7 |
GO:1901363 | heterocyclic compound binding | 2 | 7 |
GO:0003729 | mRNA binding | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 245 | 249 | PF00656 | 0.478 |
CLV_C14_Caspase3-7 | 384 | 388 | PF00656 | 0.601 |
CLV_C14_Caspase3-7 | 632 | 636 | PF00656 | 0.529 |
CLV_C14_Caspase3-7 | 675 | 679 | PF00656 | 0.693 |
CLV_C14_Caspase3-7 | 680 | 684 | PF00656 | 0.667 |
CLV_C14_Caspase3-7 | 729 | 733 | PF00656 | 0.659 |
CLV_NRD_NRD_1 | 200 | 202 | PF00675 | 0.649 |
CLV_NRD_NRD_1 | 374 | 376 | PF00675 | 0.669 |
CLV_NRD_NRD_1 | 56 | 58 | PF00675 | 0.560 |
CLV_NRD_NRD_1 | 617 | 619 | PF00675 | 0.324 |
CLV_PCSK_FUR_1 | 532 | 536 | PF00082 | 0.426 |
CLV_PCSK_KEX2_1 | 200 | 202 | PF00082 | 0.649 |
CLV_PCSK_KEX2_1 | 373 | 375 | PF00082 | 0.690 |
CLV_PCSK_KEX2_1 | 495 | 497 | PF00082 | 0.403 |
CLV_PCSK_KEX2_1 | 534 | 536 | PF00082 | 0.443 |
CLV_PCSK_KEX2_1 | 56 | 58 | PF00082 | 0.560 |
CLV_PCSK_KEX2_1 | 617 | 619 | PF00082 | 0.324 |
CLV_PCSK_PC1ET2_1 | 495 | 497 | PF00082 | 0.403 |
CLV_PCSK_PC1ET2_1 | 534 | 536 | PF00082 | 0.443 |
CLV_PCSK_SKI1_1 | 20 | 24 | PF00082 | 0.442 |
CLV_PCSK_SKI1_1 | 215 | 219 | PF00082 | 0.415 |
CLV_PCSK_SKI1_1 | 272 | 276 | PF00082 | 0.431 |
CLV_PCSK_SKI1_1 | 746 | 750 | PF00082 | 0.669 |
DEG_APCC_DBOX_1 | 214 | 222 | PF00400 | 0.415 |
DEG_COP1_1 | 735 | 743 | PF00400 | 0.667 |
DOC_ANK_TNKS_1 | 401 | 408 | PF00023 | 0.730 |
DOC_CYCLIN_RxL_1 | 17 | 27 | PF00134 | 0.429 |
DOC_MAPK_gen_1 | 200 | 206 | PF00069 | 0.514 |
DOC_MAPK_gen_1 | 643 | 652 | PF00069 | 0.529 |
DOC_MAPK_MEF2A_6 | 646 | 654 | PF00069 | 0.529 |
DOC_PP1_RVXF_1 | 270 | 276 | PF00149 | 0.398 |
DOC_PP1_RVXF_1 | 649 | 655 | PF00149 | 0.611 |
DOC_PP4_FxxP_1 | 274 | 277 | PF00568 | 0.445 |
DOC_PP4_FxxP_1 | 508 | 511 | PF00568 | 0.507 |
DOC_USP7_MATH_1 | 153 | 157 | PF00917 | 0.732 |
DOC_USP7_MATH_1 | 178 | 182 | PF00917 | 0.656 |
DOC_USP7_MATH_1 | 196 | 200 | PF00917 | 0.515 |
DOC_USP7_MATH_1 | 288 | 292 | PF00917 | 0.668 |
DOC_USP7_MATH_1 | 330 | 334 | PF00917 | 0.619 |
DOC_USP7_MATH_1 | 661 | 665 | PF00917 | 0.699 |
DOC_USP7_MATH_1 | 700 | 704 | PF00917 | 0.724 |
DOC_USP7_MATH_1 | 710 | 714 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 752 | 756 | PF00917 | 0.574 |
DOC_USP7_UBL2_3 | 602 | 606 | PF12436 | 0.529 |
DOC_USP7_UBL2_3 | 749 | 753 | PF12436 | 0.648 |
DOC_WW_Pin1_4 | 165 | 170 | PF00397 | 0.688 |
DOC_WW_Pin1_4 | 434 | 439 | PF00397 | 0.651 |
LIG_14-3-3_CanoR_1 | 183 | 192 | PF00244 | 0.507 |
LIG_14-3-3_CanoR_1 | 56 | 60 | PF00244 | 0.542 |
LIG_14-3-3_CanoR_1 | 651 | 655 | PF00244 | 0.500 |
LIG_Actin_WH2_2 | 589 | 604 | PF00022 | 0.529 |
LIG_AP2alpha_2 | 369 | 371 | PF02296 | 0.633 |
LIG_APCC_ABBA_1 | 271 | 276 | PF00400 | 0.471 |
LIG_APCC_ABBAyCdc20_2 | 578 | 584 | PF00400 | 0.482 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.447 |
LIG_BIR_III_4 | 334 | 338 | PF00653 | 0.637 |
LIG_deltaCOP1_diTrp_1 | 480 | 488 | PF00928 | 0.430 |
LIG_eIF4E_1 | 479 | 485 | PF01652 | 0.341 |
LIG_FHA_1 | 1 | 7 | PF00498 | 0.420 |
LIG_FHA_1 | 212 | 218 | PF00498 | 0.418 |
LIG_FHA_1 | 239 | 245 | PF00498 | 0.448 |
LIG_FHA_1 | 464 | 470 | PF00498 | 0.424 |
LIG_FHA_1 | 500 | 506 | PF00498 | 0.439 |
LIG_FHA_1 | 591 | 597 | PF00498 | 0.478 |
LIG_FHA_2 | 44 | 50 | PF00498 | 0.468 |
LIG_FHA_2 | 542 | 548 | PF00498 | 0.564 |
LIG_FHA_2 | 630 | 636 | PF00498 | 0.529 |
LIG_FHA_2 | 686 | 692 | PF00498 | 0.665 |
LIG_IBAR_NPY_1 | 321 | 323 | PF08397 | 0.707 |
LIG_LIR_Apic_2 | 302 | 307 | PF02991 | 0.738 |
LIG_LIR_Gen_1 | 276 | 287 | PF02991 | 0.616 |
LIG_LIR_Gen_1 | 480 | 488 | PF02991 | 0.354 |
LIG_LIR_Gen_1 | 647 | 657 | PF02991 | 0.573 |
LIG_LIR_Nem_3 | 276 | 282 | PF02991 | 0.583 |
LIG_LIR_Nem_3 | 434 | 439 | PF02991 | 0.625 |
LIG_LIR_Nem_3 | 480 | 485 | PF02991 | 0.351 |
LIG_LIR_Nem_3 | 486 | 491 | PF02991 | 0.363 |
LIG_LIR_Nem_3 | 647 | 652 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 653 | 657 | PF02991 | 0.459 |
LIG_LYPXL_yS_3 | 457 | 460 | PF13949 | 0.526 |
LIG_NRBOX | 480 | 486 | PF00104 | 0.352 |
LIG_NRP_CendR_1 | 756 | 757 | PF00754 | 0.692 |
LIG_Pex14_2 | 275 | 279 | PF04695 | 0.483 |
LIG_PTB_Apo_2 | 264 | 271 | PF02174 | 0.491 |
LIG_PTB_Phospho_1 | 264 | 270 | PF10480 | 0.500 |
LIG_REV1ctd_RIR_1 | 613 | 619 | PF16727 | 0.495 |
LIG_SH2_CRK | 150 | 154 | PF00017 | 0.641 |
LIG_SH2_CRK | 304 | 308 | PF00017 | 0.698 |
LIG_SH2_NCK_1 | 150 | 154 | PF00017 | 0.641 |
LIG_SH2_NCK_1 | 323 | 327 | PF00017 | 0.565 |
LIG_SH2_PTP2 | 270 | 273 | PF00017 | 0.382 |
LIG_SH2_STAP1 | 479 | 483 | PF00017 | 0.343 |
LIG_SH2_STAT3 | 157 | 160 | PF00017 | 0.708 |
LIG_SH2_STAT3 | 306 | 309 | PF00017 | 0.619 |
LIG_SH2_STAT5 | 176 | 179 | PF00017 | 0.623 |
LIG_SH2_STAT5 | 270 | 273 | PF00017 | 0.382 |
LIG_SH2_STAT5 | 520 | 523 | PF00017 | 0.412 |
LIG_SH2_STAT5 | 588 | 591 | PF00017 | 0.529 |
LIG_SH3_1 | 281 | 287 | PF00018 | 0.570 |
LIG_SH3_1 | 568 | 574 | PF00018 | 0.556 |
LIG_SH3_2 | 195 | 200 | PF14604 | 0.600 |
LIG_SH3_3 | 152 | 158 | PF00018 | 0.696 |
LIG_SH3_3 | 190 | 196 | PF00018 | 0.594 |
LIG_SH3_3 | 232 | 238 | PF00018 | 0.496 |
LIG_SH3_3 | 281 | 287 | PF00018 | 0.616 |
LIG_SH3_3 | 324 | 330 | PF00018 | 0.585 |
LIG_SH3_3 | 357 | 363 | PF00018 | 0.608 |
LIG_SH3_3 | 435 | 441 | PF00018 | 0.643 |
LIG_SH3_3 | 568 | 574 | PF00018 | 0.556 |
LIG_SH3_3 | 655 | 661 | PF00018 | 0.498 |
LIG_SH3_3 | 69 | 75 | PF00018 | 0.572 |
LIG_SH3_3 | 696 | 702 | PF00018 | 0.701 |
LIG_SH3_3 | 713 | 719 | PF00018 | 0.652 |
LIG_SH3_3 | 93 | 99 | PF00018 | 0.657 |
LIG_SUMO_SIM_par_1 | 2 | 7 | PF11976 | 0.479 |
LIG_SUMO_SIM_par_1 | 227 | 232 | PF11976 | 0.422 |
LIG_SUMO_SIM_par_1 | 465 | 470 | PF11976 | 0.461 |
LIG_TRAF2_1 | 46 | 49 | PF00917 | 0.484 |
LIG_TRAF2_1 | 709 | 712 | PF00917 | 0.743 |
LIG_TRAF2_1 | 720 | 723 | PF00917 | 0.649 |
LIG_TRAF2_1 | 727 | 730 | PF00917 | 0.574 |
LIG_UBA3_1 | 637 | 643 | PF00899 | 0.460 |
MOD_CK1_1 | 172 | 178 | PF00069 | 0.816 |
MOD_CK1_1 | 181 | 187 | PF00069 | 0.543 |
MOD_CK1_1 | 35 | 41 | PF00069 | 0.564 |
MOD_CK1_1 | 352 | 358 | PF00069 | 0.665 |
MOD_CK1_1 | 398 | 404 | PF00069 | 0.661 |
MOD_CK2_1 | 43 | 49 | PF00069 | 0.472 |
MOD_CK2_1 | 434 | 440 | PF00069 | 0.635 |
MOD_CK2_1 | 541 | 547 | PF00069 | 0.555 |
MOD_CK2_1 | 594 | 600 | PF00069 | 0.473 |
MOD_CK2_1 | 685 | 691 | PF00069 | 0.669 |
MOD_Cter_Amidation | 371 | 374 | PF01082 | 0.590 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.693 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.612 |
MOD_GlcNHglycan | 301 | 304 | PF01048 | 0.718 |
MOD_GlcNHglycan | 355 | 358 | PF01048 | 0.726 |
MOD_GlcNHglycan | 383 | 386 | PF01048 | 0.647 |
MOD_GlcNHglycan | 425 | 428 | PF01048 | 0.682 |
MOD_GlcNHglycan | 440 | 444 | PF01048 | 0.758 |
MOD_GlcNHglycan | 536 | 539 | PF01048 | 0.531 |
MOD_GlcNHglycan | 712 | 715 | PF01048 | 0.745 |
MOD_GlcNHglycan | 737 | 740 | PF01048 | 0.634 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.734 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.584 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.669 |
MOD_GSK3_1 | 349 | 356 | PF00069 | 0.653 |
MOD_GSK3_1 | 459 | 466 | PF00069 | 0.523 |
MOD_GSK3_1 | 541 | 548 | PF00069 | 0.602 |
MOD_GSK3_1 | 549 | 556 | PF00069 | 0.491 |
MOD_GSK3_1 | 590 | 597 | PF00069 | 0.490 |
MOD_N-GLC_1 | 178 | 183 | PF02516 | 0.635 |
MOD_N-GLC_1 | 472 | 477 | PF02516 | 0.465 |
MOD_N-GLC_1 | 590 | 595 | PF02516 | 0.275 |
MOD_N-GLC_2 | 267 | 269 | PF02516 | 0.494 |
MOD_N-GLC_2 | 463 | 465 | PF02516 | 0.462 |
MOD_NEK2_1 | 24 | 29 | PF00069 | 0.518 |
MOD_NEK2_1 | 526 | 531 | PF00069 | 0.377 |
MOD_NEK2_1 | 560 | 565 | PF00069 | 0.529 |
MOD_NEK2_1 | 587 | 592 | PF00069 | 0.496 |
MOD_NEK2_1 | 650 | 655 | PF00069 | 0.442 |
MOD_NEK2_2 | 40 | 45 | PF00069 | 0.444 |
MOD_OFUCOSY | 465 | 471 | PF10250 | 0.417 |
MOD_PIKK_1 | 35 | 41 | PF00454 | 0.489 |
MOD_PIKK_1 | 358 | 364 | PF00454 | 0.710 |
MOD_PIKK_1 | 685 | 691 | PF00454 | 0.674 |
MOD_PIKK_1 | 700 | 706 | PF00454 | 0.578 |
MOD_PKA_1 | 534 | 540 | PF00069 | 0.524 |
MOD_PKA_2 | 398 | 404 | PF00069 | 0.658 |
MOD_PKA_2 | 423 | 429 | PF00069 | 0.668 |
MOD_PKA_2 | 526 | 532 | PF00069 | 0.396 |
MOD_PKA_2 | 534 | 540 | PF00069 | 0.485 |
MOD_PKA_2 | 541 | 547 | PF00069 | 0.555 |
MOD_PKA_2 | 55 | 61 | PF00069 | 0.535 |
MOD_PKA_2 | 650 | 656 | PF00069 | 0.510 |
MOD_PKA_2 | 661 | 667 | PF00069 | 0.521 |
MOD_Plk_1 | 472 | 478 | PF00069 | 0.411 |
MOD_Plk_2-3 | 541 | 547 | PF00069 | 0.555 |
MOD_Plk_2-3 | 594 | 600 | PF00069 | 0.460 |
MOD_Plk_4 | 172 | 178 | PF00069 | 0.653 |
MOD_Plk_4 | 463 | 469 | PF00069 | 0.440 |
MOD_Plk_4 | 526 | 532 | PF00069 | 0.485 |
MOD_ProDKin_1 | 165 | 171 | PF00069 | 0.690 |
MOD_ProDKin_1 | 434 | 440 | PF00069 | 0.650 |
MOD_SUMO_rev_2 | 541 | 551 | PF00179 | 0.599 |
MOD_SUMO_rev_2 | 594 | 604 | PF00179 | 0.529 |
TRG_DiLeu_BaEn_1 | 49 | 54 | PF01217 | 0.444 |
TRG_ENDOCYTIC_2 | 126 | 129 | PF00928 | 0.685 |
TRG_ENDOCYTIC_2 | 270 | 273 | PF00928 | 0.382 |
TRG_ENDOCYTIC_2 | 457 | 460 | PF00928 | 0.544 |
TRG_ER_diArg_1 | 200 | 203 | PF00400 | 0.654 |
TRG_ER_diArg_1 | 373 | 375 | PF00400 | 0.585 |
TRG_ER_diArg_1 | 577 | 580 | PF00400 | 0.600 |
TRG_ER_diArg_1 | 616 | 618 | PF00400 | 0.524 |
TRG_Pf-PMV_PEXEL_1 | 203 | 207 | PF00026 | 0.559 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1I1 | Leptomonas seymouri | 42% | 100% |
A4HK66 | Leishmania braziliensis | 73% | 99% |
A4I7Q1 | Leishmania infantum | 99% | 100% |
E9B2K9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4Q5J7 | Leishmania major | 92% | 100% |