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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0030684 | preribosome | 3 | 1 |
GO:0032040 | small-subunit processome | 4 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:1990904 | ribonucleoprotein complex | 2 | 1 |
Related structures:
AlphaFold database: A0A3S7X7G1
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 11 |
GO:0006364 | rRNA processing | 8 | 11 |
GO:0006396 | RNA processing | 6 | 11 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016070 | RNA metabolic process | 5 | 11 |
GO:0016072 | rRNA metabolic process | 7 | 11 |
GO:0034470 | ncRNA processing | 7 | 11 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 11 |
GO:0034660 | ncRNA metabolic process | 6 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0046483 | heterocycle metabolic process | 3 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:0090304 | nucleic acid metabolic process | 4 | 11 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 11 |
GO:0003723 | RNA binding | 4 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0030515 | snoRNA binding | 5 | 11 |
GO:0034511 | U3 snoRNA binding | 6 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 102 | 106 | PF00656 | 0.496 |
CLV_C14_Caspase3-7 | 630 | 634 | PF00656 | 0.736 |
CLV_NRD_NRD_1 | 112 | 114 | PF00675 | 0.607 |
CLV_NRD_NRD_1 | 18 | 20 | PF00675 | 0.541 |
CLV_NRD_NRD_1 | 205 | 207 | PF00675 | 0.516 |
CLV_NRD_NRD_1 | 276 | 278 | PF00675 | 0.291 |
CLV_NRD_NRD_1 | 328 | 330 | PF00675 | 0.499 |
CLV_NRD_NRD_1 | 37 | 39 | PF00675 | 0.473 |
CLV_NRD_NRD_1 | 412 | 414 | PF00675 | 0.418 |
CLV_NRD_NRD_1 | 467 | 469 | PF00675 | 0.558 |
CLV_NRD_NRD_1 | 525 | 527 | PF00675 | 0.729 |
CLV_NRD_NRD_1 | 566 | 568 | PF00675 | 0.520 |
CLV_NRD_NRD_1 | 589 | 591 | PF00675 | 0.495 |
CLV_NRD_NRD_1 | 692 | 694 | PF00675 | 0.707 |
CLV_PCSK_KEX2_1 | 112 | 114 | PF00082 | 0.607 |
CLV_PCSK_KEX2_1 | 18 | 20 | PF00082 | 0.596 |
CLV_PCSK_KEX2_1 | 204 | 206 | PF00082 | 0.595 |
CLV_PCSK_KEX2_1 | 412 | 414 | PF00082 | 0.418 |
CLV_PCSK_KEX2_1 | 467 | 469 | PF00082 | 0.558 |
CLV_PCSK_KEX2_1 | 511 | 513 | PF00082 | 0.741 |
CLV_PCSK_KEX2_1 | 566 | 568 | PF00082 | 0.486 |
CLV_PCSK_KEX2_1 | 692 | 694 | PF00082 | 0.686 |
CLV_PCSK_KEX2_1 | 734 | 736 | PF00082 | 0.675 |
CLV_PCSK_KEX2_1 | 758 | 760 | PF00082 | 0.704 |
CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.562 |
CLV_PCSK_PC1ET2_1 | 511 | 513 | PF00082 | 0.705 |
CLV_PCSK_PC1ET2_1 | 692 | 694 | PF00082 | 0.712 |
CLV_PCSK_PC1ET2_1 | 734 | 736 | PF00082 | 0.671 |
CLV_PCSK_PC1ET2_1 | 758 | 760 | PF00082 | 0.673 |
CLV_PCSK_PC1ET2_1 | 9 | 11 | PF00082 | 0.641 |
CLV_PCSK_SKI1_1 | 206 | 210 | PF00082 | 0.414 |
CLV_PCSK_SKI1_1 | 234 | 238 | PF00082 | 0.529 |
CLV_PCSK_SKI1_1 | 270 | 274 | PF00082 | 0.505 |
CLV_PCSK_SKI1_1 | 278 | 282 | PF00082 | 0.342 |
CLV_PCSK_SKI1_1 | 365 | 369 | PF00082 | 0.628 |
CLV_PCSK_SKI1_1 | 6 | 10 | PF00082 | 0.637 |
CLV_PCSK_SKI1_1 | 61 | 65 | PF00082 | 0.716 |
CLV_PCSK_SKI1_1 | 725 | 729 | PF00082 | 0.686 |
CLV_PCSK_SKI1_1 | 731 | 735 | PF00082 | 0.675 |
CLV_PCSK_SKI1_1 | 755 | 759 | PF00082 | 0.637 |
DEG_APCC_DBOX_1 | 412 | 420 | PF00400 | 0.468 |
DEG_APCC_DBOX_1 | 589 | 597 | PF00400 | 0.646 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.560 |
DEG_SPOP_SBC_1 | 44 | 48 | PF00917 | 0.555 |
DOC_CYCLIN_RxL_1 | 204 | 211 | PF00134 | 0.499 |
DOC_CYCLIN_yCln2_LP_2 | 209 | 215 | PF00134 | 0.439 |
DOC_MAPK_gen_1 | 176 | 185 | PF00069 | 0.460 |
DOC_MAPK_gen_1 | 204 | 210 | PF00069 | 0.549 |
DOC_MAPK_gen_1 | 277 | 285 | PF00069 | 0.526 |
DOC_MAPK_gen_1 | 412 | 419 | PF00069 | 0.386 |
DOC_MAPK_gen_1 | 675 | 682 | PF00069 | 0.673 |
DOC_MAPK_gen_1 | 705 | 715 | PF00069 | 0.687 |
DOC_MAPK_MEF2A_6 | 179 | 187 | PF00069 | 0.483 |
DOC_MAPK_MEF2A_6 | 412 | 419 | PF00069 | 0.479 |
DOC_MAPK_MEF2A_6 | 526 | 535 | PF00069 | 0.591 |
DOC_MAPK_MEF2A_6 | 577 | 585 | PF00069 | 0.498 |
DOC_PP2B_LxvP_1 | 581 | 584 | PF13499 | 0.492 |
DOC_PP4_FxxP_1 | 54 | 57 | PF00568 | 0.584 |
DOC_USP7_MATH_1 | 192 | 196 | PF00917 | 0.609 |
DOC_USP7_MATH_1 | 363 | 367 | PF00917 | 0.629 |
DOC_USP7_MATH_1 | 42 | 46 | PF00917 | 0.643 |
DOC_USP7_MATH_1 | 486 | 490 | PF00917 | 0.467 |
DOC_USP7_MATH_1 | 521 | 525 | PF00917 | 0.811 |
DOC_USP7_MATH_1 | 57 | 61 | PF00917 | 0.524 |
DOC_USP7_MATH_1 | 627 | 631 | PF00917 | 0.746 |
DOC_USP7_MATH_1 | 632 | 636 | PF00917 | 0.748 |
DOC_USP7_MATH_1 | 687 | 691 | PF00917 | 0.733 |
DOC_USP7_MATH_1 | 716 | 720 | PF00917 | 0.724 |
DOC_USP7_MATH_1 | 72 | 76 | PF00917 | 0.502 |
DOC_USP7_UBL2_3 | 5 | 9 | PF12436 | 0.617 |
DOC_USP7_UBL2_3 | 691 | 695 | PF12436 | 0.594 |
DOC_USP7_UBL2_3 | 754 | 758 | PF12436 | 0.645 |
DOC_WW_Pin1_4 | 365 | 370 | PF00397 | 0.703 |
DOC_WW_Pin1_4 | 372 | 377 | PF00397 | 0.742 |
LIG_BIR_III_2 | 520 | 524 | PF00653 | 0.651 |
LIG_BIR_III_4 | 618 | 622 | PF00653 | 0.773 |
LIG_BIR_III_4 | 640 | 644 | PF00653 | 0.726 |
LIG_BRCT_BRCA1_1 | 546 | 550 | PF00533 | 0.323 |
LIG_Clathr_ClatBox_1 | 607 | 611 | PF01394 | 0.686 |
LIG_FHA_1 | 143 | 149 | PF00498 | 0.473 |
LIG_FHA_1 | 166 | 172 | PF00498 | 0.512 |
LIG_FHA_1 | 287 | 293 | PF00498 | 0.526 |
LIG_FHA_1 | 298 | 304 | PF00498 | 0.421 |
LIG_FHA_1 | 320 | 326 | PF00498 | 0.460 |
LIG_FHA_2 | 230 | 236 | PF00498 | 0.624 |
LIG_FHA_2 | 238 | 244 | PF00498 | 0.608 |
LIG_FHA_2 | 333 | 339 | PF00498 | 0.350 |
LIG_FHA_2 | 430 | 436 | PF00498 | 0.498 |
LIG_FHA_2 | 97 | 103 | PF00498 | 0.482 |
LIG_LIR_Apic_2 | 52 | 57 | PF02991 | 0.591 |
LIG_LIR_Gen_1 | 260 | 268 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 260 | 265 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 459 | 463 | PF02991 | 0.537 |
LIG_LIR_Nem_3 | 487 | 493 | PF02991 | 0.471 |
LIG_MAD2 | 207 | 215 | PF02301 | 0.522 |
LIG_PCNA_PIPBox_1 | 309 | 318 | PF02747 | 0.517 |
LIG_Rb_pABgroove_1 | 660 | 668 | PF01858 | 0.637 |
LIG_RPA_C_Fungi | 116 | 128 | PF08784 | 0.612 |
LIG_SH2_CRK | 425 | 429 | PF00017 | 0.435 |
LIG_SH2_CRK | 490 | 494 | PF00017 | 0.334 |
LIG_SH2_SRC | 357 | 360 | PF00017 | 0.525 |
LIG_SH2_SRC | 481 | 484 | PF00017 | 0.419 |
LIG_SH2_STAP1 | 481 | 485 | PF00017 | 0.308 |
LIG_SH2_STAT5 | 138 | 141 | PF00017 | 0.512 |
LIG_SH2_STAT5 | 181 | 184 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 249 | 252 | PF00017 | 0.322 |
LIG_SH3_3 | 209 | 215 | PF00018 | 0.418 |
LIG_SH3_3 | 373 | 379 | PF00018 | 0.736 |
LIG_SH3_3 | 414 | 420 | PF00018 | 0.551 |
LIG_SUMO_SIM_anti_2 | 555 | 560 | PF11976 | 0.405 |
LIG_SUMO_SIM_par_1 | 181 | 186 | PF11976 | 0.506 |
LIG_SUMO_SIM_par_1 | 308 | 313 | PF11976 | 0.478 |
LIG_SUMO_SIM_par_1 | 532 | 538 | PF11976 | 0.431 |
LIG_TRAF2_1 | 614 | 617 | PF00917 | 0.700 |
LIG_TRAF2_1 | 620 | 623 | PF00917 | 0.743 |
LIG_TYR_ITIM | 479 | 484 | PF00017 | 0.334 |
LIG_UBA3_1 | 272 | 278 | PF00899 | 0.516 |
LIG_ULM_U2AF65_1 | 566 | 571 | PF00076 | 0.540 |
MOD_CK1_1 | 186 | 192 | PF00069 | 0.636 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.511 |
MOD_CK1_1 | 245 | 251 | PF00069 | 0.389 |
MOD_CK1_1 | 45 | 51 | PF00069 | 0.678 |
MOD_CK1_1 | 459 | 465 | PF00069 | 0.732 |
MOD_CK1_1 | 711 | 717 | PF00069 | 0.670 |
MOD_CK2_1 | 257 | 263 | PF00069 | 0.457 |
MOD_CK2_1 | 291 | 297 | PF00069 | 0.315 |
MOD_CK2_1 | 332 | 338 | PF00069 | 0.366 |
MOD_CK2_1 | 429 | 435 | PF00069 | 0.488 |
MOD_CK2_1 | 645 | 651 | PF00069 | 0.654 |
MOD_Cter_Amidation | 509 | 512 | PF01082 | 0.665 |
MOD_Cter_Amidation | 588 | 591 | PF01082 | 0.530 |
MOD_GlcNHglycan | 13 | 16 | PF01048 | 0.559 |
MOD_GlcNHglycan | 175 | 179 | PF01048 | 0.376 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.582 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.444 |
MOD_GlcNHglycan | 574 | 577 | PF01048 | 0.414 |
MOD_GlcNHglycan | 587 | 590 | PF01048 | 0.435 |
MOD_GlcNHglycan | 640 | 644 | PF01048 | 0.702 |
MOD_GlcNHglycan | 65 | 68 | PF01048 | 0.716 |
MOD_GlcNHglycan | 697 | 700 | PF01048 | 0.735 |
MOD_GlcNHglycan | 718 | 721 | PF01048 | 0.760 |
MOD_GlcNHglycan | 728 | 731 | PF01048 | 0.771 |
MOD_GlcNHglycan | 74 | 77 | PF01048 | 0.562 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.544 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.402 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.545 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.555 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.374 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.357 |
MOD_GSK3_1 | 522 | 529 | PF00069 | 0.674 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.722 |
MOD_GSK3_1 | 704 | 711 | PF00069 | 0.679 |
MOD_LATS_1 | 276 | 282 | PF00433 | 0.419 |
MOD_N-GLC_1 | 391 | 396 | PF02516 | 0.439 |
MOD_NEK2_1 | 131 | 136 | PF00069 | 0.468 |
MOD_NEK2_1 | 187 | 192 | PF00069 | 0.593 |
MOD_NEK2_1 | 237 | 242 | PF00069 | 0.532 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.565 |
MOD_NEK2_1 | 391 | 396 | PF00069 | 0.439 |
MOD_NEK2_1 | 585 | 590 | PF00069 | 0.491 |
MOD_NEK2_1 | 704 | 709 | PF00069 | 0.545 |
MOD_NEK2_1 | 743 | 748 | PF00069 | 0.650 |
MOD_NEK2_1 | 750 | 755 | PF00069 | 0.617 |
MOD_NEK2_1 | 83 | 88 | PF00069 | 0.495 |
MOD_OFUCOSY | 157 | 162 | PF10250 | 0.441 |
MOD_PIKK_1 | 25 | 31 | PF00454 | 0.591 |
MOD_PIKK_1 | 348 | 354 | PF00454 | 0.400 |
MOD_PKA_1 | 329 | 335 | PF00069 | 0.512 |
MOD_PKA_1 | 526 | 532 | PF00069 | 0.452 |
MOD_PKA_1 | 708 | 714 | PF00069 | 0.632 |
MOD_PKA_2 | 229 | 235 | PF00069 | 0.520 |
MOD_PKA_2 | 704 | 710 | PF00069 | 0.702 |
MOD_PKA_2 | 716 | 722 | PF00069 | 0.651 |
MOD_Plk_1 | 183 | 189 | PF00069 | 0.568 |
MOD_Plk_1 | 237 | 243 | PF00069 | 0.543 |
MOD_Plk_1 | 363 | 369 | PF00069 | 0.564 |
MOD_Plk_1 | 391 | 397 | PF00069 | 0.435 |
MOD_Plk_1 | 711 | 717 | PF00069 | 0.693 |
MOD_Plk_1 | 96 | 102 | PF00069 | 0.482 |
MOD_Plk_2-3 | 238 | 244 | PF00069 | 0.569 |
MOD_Plk_4 | 245 | 251 | PF00069 | 0.400 |
MOD_Plk_4 | 288 | 294 | PF00069 | 0.276 |
MOD_Plk_4 | 379 | 385 | PF00069 | 0.564 |
MOD_Plk_4 | 391 | 397 | PF00069 | 0.393 |
MOD_ProDKin_1 | 365 | 371 | PF00069 | 0.701 |
MOD_ProDKin_1 | 372 | 378 | PF00069 | 0.740 |
MOD_SUMO_for_1 | 738 | 741 | PF00179 | 0.690 |
MOD_SUMO_rev_2 | 52 | 60 | PF00179 | 0.561 |
TRG_ENDOCYTIC_2 | 425 | 428 | PF00928 | 0.435 |
TRG_ENDOCYTIC_2 | 481 | 484 | PF00928 | 0.319 |
TRG_ENDOCYTIC_2 | 490 | 493 | PF00928 | 0.292 |
TRG_ER_diArg_1 | 17 | 19 | PF00400 | 0.639 |
TRG_ER_diArg_1 | 204 | 206 | PF00400 | 0.595 |
TRG_ER_diArg_1 | 565 | 567 | PF00400 | 0.508 |
TRG_NES_CRM1_1 | 671 | 685 | PF08389 | 0.489 |
TRG_NLS_MonoCore_2 | 690 | 695 | PF00514 | 0.634 |
TRG_NLS_MonoExtC_3 | 37 | 43 | PF00514 | 0.687 |
TRG_NLS_MonoExtC_3 | 690 | 695 | PF00514 | 0.591 |
TRG_NLS_MonoExtC_3 | 730 | 735 | PF00514 | 0.681 |
TRG_NLS_MonoExtN_4 | 57 | 62 | PF00514 | 0.613 |
TRG_NLS_MonoExtN_4 | 691 | 698 | PF00514 | 0.616 |
TRG_NLS_MonoExtN_4 | 755 | 762 | PF00514 | 0.582 |
TRG_Pf-PMV_PEXEL_1 | 207 | 211 | PF00026 | 0.522 |
TRG_Pf-PMV_PEXEL_1 | 85 | 89 | PF00026 | 0.440 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5A4 | Leptomonas seymouri | 68% | 100% |
A0A1X0P8I5 | Trypanosomatidae | 43% | 100% |
A0A3S5IQN4 | Trypanosoma rangeli | 44% | 100% |
A4H7E0 | Leishmania braziliensis | 79% | 99% |
A4I9K0 | Leishmania infantum | 100% | 100% |
D0A1V8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
E9B4J8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
Q4Q3H8 | Leishmania major | 91% | 99% |
V5BRS0 | Trypanosoma cruzi | 42% | 100% |