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: A4HK66
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 | 235 | 239 | PF00656 | 0.571 |
CLV_C14_Caspase3-7 | 625 | 629 | PF00656 | 0.597 |
CLV_C14_Caspase3-7 | 668 | 672 | PF00656 | 0.803 |
CLV_NRD_NRD_1 | 190 | 192 | PF00675 | 0.668 |
CLV_NRD_NRD_1 | 56 | 58 | PF00675 | 0.678 |
CLV_NRD_NRD_1 | 610 | 612 | PF00675 | 0.598 |
CLV_PCSK_FUR_1 | 525 | 529 | PF00082 | 0.519 |
CLV_PCSK_KEX2_1 | 190 | 192 | PF00082 | 0.668 |
CLV_PCSK_KEX2_1 | 488 | 490 | PF00082 | 0.444 |
CLV_PCSK_KEX2_1 | 527 | 529 | PF00082 | 0.476 |
CLV_PCSK_KEX2_1 | 56 | 58 | PF00082 | 0.678 |
CLV_PCSK_KEX2_1 | 610 | 612 | PF00082 | 0.598 |
CLV_PCSK_PC1ET2_1 | 488 | 490 | PF00082 | 0.503 |
CLV_PCSK_PC1ET2_1 | 527 | 529 | PF00082 | 0.476 |
CLV_PCSK_SKI1_1 | 20 | 24 | PF00082 | 0.531 |
CLV_PCSK_SKI1_1 | 205 | 209 | PF00082 | 0.517 |
CLV_PCSK_SKI1_1 | 542 | 546 | PF00082 | 0.656 |
CLV_PCSK_SKI1_1 | 747 | 751 | PF00082 | 0.705 |
DEG_APCC_DBOX_1 | 204 | 212 | PF00400 | 0.518 |
DOC_ANK_TNKS_1 | 385 | 392 | PF00023 | 0.704 |
DOC_ANK_TNKS_1 | 394 | 401 | PF00023 | 0.811 |
DOC_ANK_TNKS_1 | 416 | 423 | PF00023 | 0.564 |
DOC_ANK_TNKS_1 | 440 | 447 | PF00023 | 0.570 |
DOC_CKS1_1 | 182 | 187 | PF01111 | 0.553 |
DOC_CKS1_1 | 679 | 684 | PF01111 | 0.605 |
DOC_CYCLIN_RxL_1 | 17 | 27 | PF00134 | 0.516 |
DOC_MAPK_gen_1 | 190 | 196 | PF00069 | 0.648 |
DOC_MAPK_gen_1 | 573 | 582 | PF00069 | 0.368 |
DOC_MAPK_gen_1 | 610 | 618 | PF00069 | 0.404 |
DOC_MAPK_gen_1 | 636 | 645 | PF00069 | 0.639 |
DOC_MAPK_MEF2A_6 | 639 | 647 | PF00069 | 0.641 |
DOC_PP1_RVXF_1 | 260 | 266 | PF00149 | 0.490 |
DOC_PP1_RVXF_1 | 597 | 604 | PF00149 | 0.390 |
DOC_PP1_RVXF_1 | 642 | 648 | PF00149 | 0.625 |
DOC_PP4_FxxP_1 | 501 | 504 | PF00568 | 0.633 |
DOC_USP7_MATH_1 | 155 | 159 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 186 | 190 | PF00917 | 0.532 |
DOC_USP7_MATH_1 | 219 | 223 | PF00917 | 0.405 |
DOC_USP7_MATH_1 | 297 | 301 | PF00917 | 0.702 |
DOC_USP7_MATH_1 | 356 | 360 | PF00917 | 0.622 |
DOC_USP7_MATH_1 | 431 | 435 | PF00917 | 0.728 |
DOC_USP7_MATH_1 | 696 | 700 | PF00917 | 0.818 |
DOC_USP7_MATH_1 | 730 | 734 | PF00917 | 0.713 |
DOC_USP7_UBL2_3 | 595 | 599 | PF12436 | 0.628 |
DOC_WW_Pin1_4 | 181 | 186 | PF00397 | 0.747 |
DOC_WW_Pin1_4 | 301 | 306 | PF00397 | 0.566 |
DOC_WW_Pin1_4 | 340 | 345 | PF00397 | 0.604 |
DOC_WW_Pin1_4 | 427 | 432 | PF00397 | 0.753 |
DOC_WW_Pin1_4 | 453 | 458 | PF00397 | 0.474 |
DOC_WW_Pin1_4 | 559 | 564 | PF00397 | 0.438 |
DOC_WW_Pin1_4 | 678 | 683 | PF00397 | 0.646 |
DOC_WW_Pin1_4 | 735 | 740 | PF00397 | 0.583 |
DOC_WW_Pin1_4 | 90 | 95 | PF00397 | 0.578 |
LIG_14-3-3_CanoR_1 | 337 | 344 | PF00244 | 0.565 |
LIG_14-3-3_CanoR_1 | 56 | 60 | PF00244 | 0.660 |
LIG_14-3-3_CanoR_1 | 644 | 648 | PF00244 | 0.627 |
LIG_Actin_WH2_2 | 582 | 597 | PF00022 | 0.630 |
LIG_APCC_ABBA_1 | 261 | 266 | PF00400 | 0.593 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.522 |
LIG_BIR_III_4 | 324 | 328 | PF00653 | 0.729 |
LIG_deltaCOP1_diTrp_1 | 266 | 272 | PF00928 | 0.493 |
LIG_deltaCOP1_diTrp_1 | 473 | 481 | PF00928 | 0.557 |
LIG_eIF4E_1 | 472 | 478 | PF01652 | 0.439 |
LIG_FHA_1 | 1 | 7 | PF00498 | 0.507 |
LIG_FHA_1 | 202 | 208 | PF00498 | 0.501 |
LIG_FHA_1 | 229 | 235 | PF00498 | 0.520 |
LIG_FHA_1 | 493 | 499 | PF00498 | 0.513 |
LIG_FHA_1 | 584 | 590 | PF00498 | 0.539 |
LIG_FHA_1 | 612 | 618 | PF00498 | 0.386 |
LIG_FHA_2 | 44 | 50 | PF00498 | 0.561 |
LIG_FHA_2 | 623 | 629 | PF00498 | 0.607 |
LIG_IBAR_NPY_1 | 311 | 313 | PF08397 | 0.833 |
LIG_LIR_Apic_2 | 292 | 297 | PF02991 | 0.728 |
LIG_LIR_Gen_1 | 266 | 277 | PF02991 | 0.713 |
LIG_LIR_Gen_1 | 473 | 481 | PF02991 | 0.440 |
LIG_LIR_Gen_1 | 646 | 654 | PF02991 | 0.570 |
LIG_LIR_Nem_3 | 266 | 272 | PF02991 | 0.686 |
LIG_LIR_Nem_3 | 427 | 432 | PF02991 | 0.731 |
LIG_LIR_Nem_3 | 473 | 478 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 479 | 484 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 646 | 650 | PF02991 | 0.550 |
LIG_MYND_1 | 75 | 79 | PF01753 | 0.585 |
LIG_NRBOX | 473 | 479 | PF00104 | 0.451 |
LIG_NRP_CendR_1 | 750 | 751 | PF00754 | 0.836 |
LIG_Pex14_2 | 265 | 269 | PF04695 | 0.585 |
LIG_PTB_Apo_2 | 254 | 261 | PF02174 | 0.610 |
LIG_PTB_Phospho_1 | 254 | 260 | PF10480 | 0.618 |
LIG_SH2_CRK | 294 | 298 | PF00017 | 0.753 |
LIG_SH2_GRB2like | 120 | 123 | PF00017 | 0.581 |
LIG_SH2_PTP2 | 260 | 263 | PF00017 | 0.471 |
LIG_SH2_STAP1 | 120 | 124 | PF00017 | 0.676 |
LIG_SH2_STAP1 | 472 | 476 | PF00017 | 0.443 |
LIG_SH2_STAT3 | 147 | 150 | PF00017 | 0.833 |
LIG_SH2_STAT3 | 296 | 299 | PF00017 | 0.724 |
LIG_SH2_STAT5 | 166 | 169 | PF00017 | 0.712 |
LIG_SH2_STAT5 | 260 | 263 | PF00017 | 0.471 |
LIG_SH2_STAT5 | 264 | 267 | PF00017 | 0.542 |
LIG_SH2_STAT5 | 513 | 516 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 581 | 584 | PF00017 | 0.596 |
LIG_SH3_1 | 561 | 567 | PF00018 | 0.627 |
LIG_SH3_2 | 185 | 190 | PF14604 | 0.743 |
LIG_SH3_2 | 712 | 717 | PF14604 | 0.609 |
LIG_SH3_3 | 145 | 151 | PF00018 | 0.806 |
LIG_SH3_3 | 180 | 186 | PF00018 | 0.717 |
LIG_SH3_3 | 222 | 228 | PF00018 | 0.605 |
LIG_SH3_3 | 271 | 277 | PF00018 | 0.657 |
LIG_SH3_3 | 317 | 323 | PF00018 | 0.711 |
LIG_SH3_3 | 444 | 450 | PF00018 | 0.642 |
LIG_SH3_3 | 561 | 567 | PF00018 | 0.627 |
LIG_SH3_3 | 648 | 654 | PF00018 | 0.586 |
LIG_SH3_3 | 65 | 71 | PF00018 | 0.584 |
LIG_SH3_3 | 707 | 713 | PF00018 | 0.663 |
LIG_SH3_3 | 73 | 79 | PF00018 | 0.709 |
LIG_SH3_3 | 88 | 94 | PF00018 | 0.800 |
LIG_SUMO_SIM_par_1 | 2 | 7 | PF11976 | 0.592 |
LIG_SUMO_SIM_par_1 | 458 | 463 | PF11976 | 0.592 |
LIG_TRAF2_1 | 46 | 49 | PF00917 | 0.578 |
LIG_TRAF2_1 | 695 | 698 | PF00917 | 0.752 |
LIG_WW_3 | 562 | 566 | PF00397 | 0.480 |
MOD_CDK_SPK_2 | 735 | 740 | PF00069 | 0.583 |
MOD_CDK_SPxK_1 | 559 | 565 | PF00069 | 0.460 |
MOD_CK1_1 | 162 | 168 | PF00069 | 0.842 |
MOD_CK1_1 | 301 | 307 | PF00069 | 0.569 |
MOD_CK1_1 | 340 | 346 | PF00069 | 0.756 |
MOD_CK1_1 | 35 | 41 | PF00069 | 0.681 |
MOD_CK1_1 | 453 | 459 | PF00069 | 0.466 |
MOD_CK1_1 | 738 | 744 | PF00069 | 0.593 |
MOD_CK2_1 | 43 | 49 | PF00069 | 0.565 |
MOD_CK2_1 | 730 | 736 | PF00069 | 0.692 |
MOD_GlcNHglycan | 108 | 111 | PF01048 | 0.821 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.728 |
MOD_GlcNHglycan | 291 | 294 | PF01048 | 0.784 |
MOD_GlcNHglycan | 306 | 309 | PF01048 | 0.617 |
MOD_GlcNHglycan | 334 | 337 | PF01048 | 0.689 |
MOD_GlcNHglycan | 374 | 377 | PF01048 | 0.688 |
MOD_GlcNHglycan | 382 | 385 | PF01048 | 0.661 |
MOD_GlcNHglycan | 418 | 421 | PF01048 | 0.797 |
MOD_GlcNHglycan | 422 | 425 | PF01048 | 0.747 |
MOD_GlcNHglycan | 433 | 437 | PF01048 | 0.798 |
MOD_GlcNHglycan | 462 | 465 | PF01048 | 0.378 |
MOD_GlcNHglycan | 467 | 470 | PF01048 | 0.390 |
MOD_GlcNHglycan | 529 | 532 | PF01048 | 0.575 |
MOD_GlcNHglycan | 542 | 545 | PF01048 | 0.683 |
MOD_GlcNHglycan | 731 | 735 | PF01048 | 0.702 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.783 |
MOD_GSK3_1 | 226 | 233 | PF00069 | 0.430 |
MOD_GSK3_1 | 295 | 302 | PF00069 | 0.675 |
MOD_GSK3_1 | 416 | 423 | PF00069 | 0.564 |
MOD_GSK3_1 | 427 | 434 | PF00069 | 0.530 |
MOD_GSK3_1 | 538 | 545 | PF00069 | 0.624 |
MOD_GSK3_1 | 735 | 742 | PF00069 | 0.586 |
MOD_N-GLC_1 | 168 | 173 | PF02516 | 0.739 |
MOD_N-GLC_1 | 465 | 470 | PF02516 | 0.592 |
MOD_N-GLC_1 | 583 | 588 | PF02516 | 0.541 |
MOD_N-GLC_2 | 257 | 259 | PF02516 | 0.615 |
MOD_NEK2_1 | 24 | 29 | PF00069 | 0.631 |
MOD_NEK2_1 | 580 | 585 | PF00069 | 0.441 |
MOD_NEK2_1 | 643 | 648 | PF00069 | 0.521 |
MOD_NEK2_2 | 40 | 45 | PF00069 | 0.537 |
MOD_NEK2_2 | 406 | 411 | PF00069 | 0.557 |
MOD_PIKK_1 | 155 | 161 | PF00454 | 0.572 |
MOD_PIKK_1 | 295 | 301 | PF00454 | 0.573 |
MOD_PIKK_1 | 348 | 354 | PF00454 | 0.746 |
MOD_PIKK_1 | 35 | 41 | PF00454 | 0.581 |
MOD_PIKK_1 | 450 | 456 | PF00454 | 0.487 |
MOD_PIKK_1 | 81 | 87 | PF00454 | 0.613 |
MOD_PKA_1 | 527 | 533 | PF00069 | 0.628 |
MOD_PKA_2 | 406 | 412 | PF00069 | 0.647 |
MOD_PKA_2 | 416 | 422 | PF00069 | 0.777 |
MOD_PKA_2 | 527 | 533 | PF00069 | 0.577 |
MOD_PKA_2 | 55 | 61 | PF00069 | 0.654 |
MOD_PKA_2 | 643 | 649 | PF00069 | 0.633 |
MOD_Plk_4 | 162 | 168 | PF00069 | 0.745 |
MOD_Plk_4 | 604 | 610 | PF00069 | 0.420 |
MOD_ProDKin_1 | 181 | 187 | PF00069 | 0.742 |
MOD_ProDKin_1 | 301 | 307 | PF00069 | 0.569 |
MOD_ProDKin_1 | 340 | 346 | PF00069 | 0.607 |
MOD_ProDKin_1 | 427 | 433 | PF00069 | 0.751 |
MOD_ProDKin_1 | 453 | 459 | PF00069 | 0.460 |
MOD_ProDKin_1 | 559 | 565 | PF00069 | 0.448 |
MOD_ProDKin_1 | 678 | 684 | PF00069 | 0.644 |
MOD_ProDKin_1 | 735 | 741 | PF00069 | 0.585 |
MOD_ProDKin_1 | 90 | 96 | PF00069 | 0.576 |
MOD_SUMO_rev_2 | 536 | 544 | PF00179 | 0.705 |
MOD_SUMO_rev_2 | 587 | 597 | PF00179 | 0.638 |
TRG_DiLeu_BaEn_1 | 49 | 54 | PF01217 | 0.538 |
TRG_ENDOCYTIC_2 | 120 | 123 | PF00928 | 0.805 |
TRG_ENDOCYTIC_2 | 260 | 263 | PF00928 | 0.471 |
TRG_ER_diArg_1 | 190 | 193 | PF00400 | 0.671 |
TRG_ER_diArg_1 | 570 | 573 | PF00400 | 0.732 |
TRG_ER_diArg_1 | 609 | 611 | PF00400 | 0.588 |
TRG_ER_diArg_1 | 638 | 641 | PF00400 | 0.401 |
TRG_Pf-PMV_PEXEL_1 | 193 | 197 | PF00026 | 0.638 |
TRG_Pf-PMV_PEXEL_1 | 655 | 659 | PF00026 | 0.553 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1I1 | Leptomonas seymouri | 44% | 100% |
A0A3Q8IJ43 | Leishmania donovani | 73% | 99% |
A4I7Q1 | Leishmania infantum | 74% | 99% |
E9B2K9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 72% | 98% |
Q4Q5J7 | Leishmania major | 75% | 100% |