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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 2 |
GO:0005829 | cytosol | 2 | 2 |
GO:0030684 | preribosome | 3 | 2 |
GO:0030688 | preribosome, small subunit precursor | 4 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:1990904 | ribonucleoprotein complex | 2 | 2 |
Related structures:
AlphaFold database: E9ADZ7
Term | Name | Level | Count |
---|---|---|---|
GO:0000054 | ribosomal subunit export from nucleus | 3 | 2 |
GO:0000056 | ribosomal small subunit export from nucleus | 4 | 2 |
GO:0006810 | transport | 3 | 2 |
GO:0006913 | nucleocytoplasmic transport | 5 | 2 |
GO:0009987 | cellular process | 1 | 8 |
GO:0022613 | ribonucleoprotein complex biogenesis | 4 | 8 |
GO:0031503 | protein-containing complex localization | 2 | 2 |
GO:0033750 | ribosome localization | 3 | 2 |
GO:0042274 | ribosomal small subunit biogenesis | 5 | 8 |
GO:0044085 | cellular component biogenesis | 3 | 8 |
GO:0046907 | intracellular transport | 3 | 2 |
GO:0051168 | nuclear export | 6 | 2 |
GO:0051169 | nuclear transport | 4 | 2 |
GO:0051179 | localization | 1 | 2 |
GO:0051234 | establishment of localization | 2 | 2 |
GO:0051640 | organelle localization | 2 | 2 |
GO:0051641 | cellular localization | 2 | 2 |
GO:0051649 | establishment of localization in cell | 3 | 2 |
GO:0051656 | establishment of organelle localization | 3 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 123 | 127 | PF00656 | 0.644 |
CLV_C14_Caspase3-7 | 20 | 24 | PF00656 | 0.596 |
CLV_C14_Caspase3-7 | 442 | 446 | PF00656 | 0.599 |
CLV_C14_Caspase3-7 | 509 | 513 | PF00656 | 0.544 |
CLV_C14_Caspase3-7 | 516 | 520 | PF00656 | 0.544 |
CLV_NRD_NRD_1 | 255 | 257 | PF00675 | 0.551 |
CLV_NRD_NRD_1 | 262 | 264 | PF00675 | 0.607 |
CLV_NRD_NRD_1 | 405 | 407 | PF00675 | 0.508 |
CLV_NRD_NRD_1 | 41 | 43 | PF00675 | 0.535 |
CLV_NRD_NRD_1 | 490 | 492 | PF00675 | 0.604 |
CLV_NRD_NRD_1 | 496 | 498 | PF00675 | 0.582 |
CLV_NRD_NRD_1 | 56 | 58 | PF00675 | 0.653 |
CLV_NRD_NRD_1 | 600 | 602 | PF00675 | 0.620 |
CLV_NRD_NRD_1 | 612 | 614 | PF00675 | 0.427 |
CLV_NRD_NRD_1 | 623 | 625 | PF00675 | 0.439 |
CLV_NRD_NRD_1 | 643 | 645 | PF00675 | 0.535 |
CLV_NRD_NRD_1 | 652 | 654 | PF00675 | 0.577 |
CLV_NRD_NRD_1 | 77 | 79 | PF00675 | 0.503 |
CLV_PCSK_FUR_1 | 260 | 264 | PF00082 | 0.619 |
CLV_PCSK_FUR_1 | 621 | 625 | PF00082 | 0.536 |
CLV_PCSK_FUR_1 | 74 | 78 | PF00082 | 0.508 |
CLV_PCSK_KEX2_1 | 254 | 256 | PF00082 | 0.552 |
CLV_PCSK_KEX2_1 | 260 | 262 | PF00082 | 0.599 |
CLV_PCSK_KEX2_1 | 405 | 407 | PF00082 | 0.518 |
CLV_PCSK_KEX2_1 | 41 | 43 | PF00082 | 0.522 |
CLV_PCSK_KEX2_1 | 490 | 492 | PF00082 | 0.583 |
CLV_PCSK_KEX2_1 | 496 | 498 | PF00082 | 0.550 |
CLV_PCSK_KEX2_1 | 56 | 58 | PF00082 | 0.626 |
CLV_PCSK_KEX2_1 | 600 | 602 | PF00082 | 0.605 |
CLV_PCSK_KEX2_1 | 612 | 614 | PF00082 | 0.427 |
CLV_PCSK_KEX2_1 | 623 | 625 | PF00082 | 0.439 |
CLV_PCSK_KEX2_1 | 643 | 645 | PF00082 | 0.459 |
CLV_PCSK_KEX2_1 | 652 | 654 | PF00082 | 0.577 |
CLV_PCSK_KEX2_1 | 74 | 76 | PF00082 | 0.440 |
CLV_PCSK_KEX2_1 | 77 | 79 | PF00082 | 0.507 |
CLV_PCSK_PC7_1 | 256 | 262 | PF00082 | 0.575 |
CLV_PCSK_SKI1_1 | 10 | 14 | PF00082 | 0.445 |
CLV_PCSK_SKI1_1 | 146 | 150 | PF00082 | 0.723 |
CLV_PCSK_SKI1_1 | 240 | 244 | PF00082 | 0.523 |
CLV_PCSK_SKI1_1 | 298 | 302 | PF00082 | 0.458 |
CLV_PCSK_SKI1_1 | 331 | 335 | PF00082 | 0.533 |
CLV_PCSK_SKI1_1 | 496 | 500 | PF00082 | 0.660 |
CLV_PCSK_SKI1_1 | 624 | 628 | PF00082 | 0.493 |
CLV_PCSK_SKI1_1 | 644 | 648 | PF00082 | 0.456 |
DEG_SPOP_SBC_1 | 526 | 530 | PF00917 | 0.540 |
DOC_CYCLIN_RxL_1 | 206 | 215 | PF00134 | 0.532 |
DOC_MAPK_gen_1 | 405 | 414 | PF00069 | 0.469 |
DOC_MAPK_gen_1 | 563 | 571 | PF00069 | 0.613 |
DOC_MAPK_gen_1 | 588 | 597 | PF00069 | 0.601 |
DOC_MAPK_MEF2A_6 | 405 | 414 | PF00069 | 0.372 |
DOC_MAPK_MEF2A_6 | 588 | 597 | PF00069 | 0.574 |
DOC_PP1_RVXF_1 | 207 | 214 | PF00149 | 0.478 |
DOC_PP1_RVXF_1 | 651 | 658 | PF00149 | 0.558 |
DOC_PP2B_LxvP_1 | 140 | 143 | PF13499 | 0.553 |
DOC_USP7_MATH_1 | 158 | 162 | PF00917 | 0.686 |
DOC_USP7_MATH_1 | 372 | 376 | PF00917 | 0.552 |
DOC_USP7_MATH_1 | 429 | 433 | PF00917 | 0.642 |
DOC_USP7_MATH_1 | 489 | 493 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 543 | 547 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 577 | 581 | PF00917 | 0.593 |
DOC_USP7_UBL2_3 | 247 | 251 | PF12436 | 0.476 |
DOC_USP7_UBL2_3 | 6 | 10 | PF12436 | 0.514 |
DOC_USP7_UBL2_3 | 602 | 606 | PF12436 | 0.531 |
DOC_USP7_UBL2_3 | 627 | 631 | PF12436 | 0.463 |
DOC_WW_Pin1_4 | 427 | 432 | PF00397 | 0.601 |
DOC_WW_Pin1_4 | 437 | 442 | PF00397 | 0.703 |
DOC_WW_Pin1_4 | 541 | 546 | PF00397 | 0.670 |
LIG_14-3-3_CanoR_1 | 298 | 307 | PF00244 | 0.447 |
LIG_14-3-3_CanoR_1 | 490 | 498 | PF00244 | 0.661 |
LIG_14-3-3_CanoR_1 | 624 | 634 | PF00244 | 0.522 |
LIG_14-3-3_CanoR_1 | 652 | 656 | PF00244 | 0.586 |
LIG_BIR_III_4 | 23 | 27 | PF00653 | 0.615 |
LIG_BIR_III_4 | 376 | 380 | PF00653 | 0.579 |
LIG_BIR_III_4 | 85 | 89 | PF00653 | 0.604 |
LIG_Clathr_ClatBox_1 | 455 | 459 | PF01394 | 0.659 |
LIG_deltaCOP1_diTrp_1 | 119 | 129 | PF00928 | 0.670 |
LIG_FHA_1 | 11 | 17 | PF00498 | 0.429 |
LIG_FHA_1 | 381 | 387 | PF00498 | 0.536 |
LIG_FHA_1 | 399 | 405 | PF00498 | 0.514 |
LIG_FHA_1 | 528 | 534 | PF00498 | 0.638 |
LIG_FHA_1 | 553 | 559 | PF00498 | 0.621 |
LIG_FHA_2 | 241 | 247 | PF00498 | 0.531 |
LIG_FHA_2 | 332 | 338 | PF00498 | 0.529 |
LIG_FHA_2 | 445 | 451 | PF00498 | 0.636 |
LIG_FHA_2 | 509 | 515 | PF00498 | 0.694 |
LIG_FHA_2 | 603 | 609 | PF00498 | 0.464 |
LIG_FHA_2 | 631 | 637 | PF00498 | 0.531 |
LIG_Integrin_RGD_1 | 535 | 537 | PF01839 | 0.619 |
LIG_LIR_Apic_2 | 477 | 483 | PF02991 | 0.537 |
LIG_LIR_Gen_1 | 297 | 307 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 13 | 17 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 226 | 231 | PF02991 | 0.646 |
LIG_LIR_Nem_3 | 236 | 242 | PF02991 | 0.537 |
LIG_LIR_Nem_3 | 633 | 637 | PF02991 | 0.516 |
LIG_Pex14_2 | 393 | 397 | PF04695 | 0.464 |
LIG_RPA_C_Fungi | 251 | 263 | PF08784 | 0.570 |
LIG_SH2_CRK | 14 | 18 | PF00017 | 0.493 |
LIG_SH2_CRK | 480 | 484 | PF00017 | 0.588 |
LIG_SH2_GRB2like | 479 | 482 | PF00017 | 0.521 |
LIG_SH2_NCK_1 | 480 | 484 | PF00017 | 0.588 |
LIG_SH2_NCK_1 | 62 | 66 | PF00017 | 0.508 |
LIG_SH2_SRC | 90 | 93 | PF00017 | 0.616 |
LIG_SH2_STAP1 | 102 | 106 | PF00017 | 0.569 |
LIG_SH2_STAP1 | 62 | 66 | PF00017 | 0.508 |
LIG_SH2_STAT3 | 479 | 482 | PF00017 | 0.543 |
LIG_SH2_STAT5 | 317 | 320 | PF00017 | 0.523 |
LIG_SH2_STAT5 | 332 | 335 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 365 | 368 | PF00017 | 0.522 |
LIG_SH3_3 | 132 | 138 | PF00018 | 0.637 |
LIG_SH3_3 | 425 | 431 | PF00018 | 0.503 |
LIG_SH3_3 | 568 | 574 | PF00018 | 0.614 |
LIG_SH3_4 | 6 | 13 | PF00018 | 0.512 |
LIG_SUMO_SIM_anti_2 | 432 | 440 | PF11976 | 0.500 |
LIG_SUMO_SIM_anti_2 | 450 | 459 | PF11976 | 0.657 |
LIG_TRAF2_1 | 101 | 104 | PF00917 | 0.639 |
LIG_TRAF2_1 | 185 | 188 | PF00917 | 0.700 |
LIG_TRAF2_1 | 335 | 338 | PF00917 | 0.450 |
LIG_TRAF2_1 | 448 | 451 | PF00917 | 0.659 |
LIG_TRAF2_1 | 605 | 608 | PF00917 | 0.475 |
LIG_TRFH_1 | 14 | 18 | PF08558 | 0.489 |
LIG_TYR_ITIM | 12 | 17 | PF00017 | 0.484 |
LIG_UBA3_1 | 359 | 364 | PF00899 | 0.534 |
LIG_UBA3_1 | 455 | 463 | PF00899 | 0.629 |
MOD_CK1_1 | 215 | 221 | PF00069 | 0.605 |
MOD_CK1_1 | 439 | 445 | PF00069 | 0.646 |
MOD_CK1_1 | 474 | 480 | PF00069 | 0.497 |
MOD_CK1_1 | 550 | 556 | PF00069 | 0.683 |
MOD_CK1_1 | 580 | 586 | PF00069 | 0.656 |
MOD_CK1_1 | 645 | 651 | PF00069 | 0.529 |
MOD_CK2_1 | 240 | 246 | PF00069 | 0.521 |
MOD_CK2_1 | 32 | 38 | PF00069 | 0.487 |
MOD_CK2_1 | 331 | 337 | PF00069 | 0.532 |
MOD_CK2_1 | 437 | 443 | PF00069 | 0.663 |
MOD_CK2_1 | 444 | 450 | PF00069 | 0.800 |
MOD_CK2_1 | 508 | 514 | PF00069 | 0.684 |
MOD_CK2_1 | 575 | 581 | PF00069 | 0.652 |
MOD_CK2_1 | 602 | 608 | PF00069 | 0.472 |
MOD_CK2_1 | 630 | 636 | PF00069 | 0.534 |
MOD_GlcNHglycan | 152 | 155 | PF01048 | 0.720 |
MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.585 |
MOD_GlcNHglycan | 44 | 47 | PF01048 | 0.627 |
MOD_GlcNHglycan | 473 | 476 | PF01048 | 0.508 |
MOD_GlcNHglycan | 491 | 494 | PF01048 | 0.710 |
MOD_GlcNHglycan | 539 | 542 | PF01048 | 0.687 |
MOD_GlcNHglycan | 547 | 550 | PF01048 | 0.746 |
MOD_GlcNHglycan | 560 | 563 | PF01048 | 0.596 |
MOD_GlcNHglycan | 627 | 630 | PF01048 | 0.534 |
MOD_GlcNHglycan | 644 | 647 | PF01048 | 0.555 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.601 |
MOD_GSK3_1 | 417 | 424 | PF00069 | 0.521 |
MOD_GSK3_1 | 471 | 478 | PF00069 | 0.489 |
MOD_GSK3_1 | 508 | 515 | PF00069 | 0.581 |
MOD_GSK3_1 | 525 | 532 | PF00069 | 0.692 |
MOD_GSK3_1 | 537 | 544 | PF00069 | 0.728 |
MOD_GSK3_1 | 552 | 559 | PF00069 | 0.676 |
MOD_LATS_1 | 139 | 145 | PF00433 | 0.556 |
MOD_NEK2_1 | 159 | 164 | PF00069 | 0.631 |
MOD_NEK2_1 | 275 | 280 | PF00069 | 0.630 |
MOD_NEK2_1 | 339 | 344 | PF00069 | 0.531 |
MOD_NEK2_1 | 630 | 635 | PF00069 | 0.535 |
MOD_NEK2_1 | 642 | 647 | PF00069 | 0.657 |
MOD_NEK2_2 | 651 | 656 | PF00069 | 0.482 |
MOD_PIKK_1 | 141 | 147 | PF00454 | 0.584 |
MOD_PIKK_1 | 289 | 295 | PF00454 | 0.593 |
MOD_PIKK_1 | 645 | 651 | PF00454 | 0.513 |
MOD_PKA_1 | 255 | 261 | PF00069 | 0.566 |
MOD_PKA_2 | 255 | 261 | PF00069 | 0.606 |
MOD_PKA_2 | 489 | 495 | PF00069 | 0.642 |
MOD_PKA_2 | 642 | 648 | PF00069 | 0.534 |
MOD_PKA_2 | 651 | 657 | PF00069 | 0.548 |
MOD_Plk_2-3 | 315 | 321 | PF00069 | 0.526 |
MOD_Plk_2-3 | 636 | 642 | PF00069 | 0.528 |
MOD_Plk_4 | 381 | 387 | PF00069 | 0.510 |
MOD_Plk_4 | 475 | 481 | PF00069 | 0.505 |
MOD_Plk_4 | 529 | 535 | PF00069 | 0.681 |
MOD_Plk_4 | 553 | 559 | PF00069 | 0.586 |
MOD_ProDKin_1 | 427 | 433 | PF00069 | 0.605 |
MOD_ProDKin_1 | 437 | 443 | PF00069 | 0.702 |
MOD_ProDKin_1 | 541 | 547 | PF00069 | 0.671 |
MOD_SUMO_rev_2 | 126 | 135 | PF00179 | 0.681 |
MOD_SUMO_rev_2 | 186 | 195 | PF00179 | 0.593 |
MOD_SUMO_rev_2 | 244 | 249 | PF00179 | 0.482 |
MOD_SUMO_rev_2 | 453 | 462 | PF00179 | 0.637 |
MOD_SUMO_rev_2 | 603 | 611 | PF00179 | 0.472 |
TRG_DiLeu_BaEn_1 | 237 | 242 | PF01217 | 0.539 |
TRG_DiLeu_BaEn_1 | 451 | 456 | PF01217 | 0.666 |
TRG_DiLeu_BaEn_3 | 451 | 457 | PF01217 | 0.633 |
TRG_DiLeu_LyEn_5 | 237 | 242 | PF01217 | 0.539 |
TRG_ENDOCYTIC_2 | 14 | 17 | PF00928 | 0.479 |
TRG_ENDOCYTIC_2 | 634 | 637 | PF00928 | 0.493 |
TRG_ER_diArg_1 | 254 | 256 | PF00400 | 0.552 |
TRG_ER_diArg_1 | 260 | 263 | PF00400 | 0.602 |
TRG_ER_diArg_1 | 40 | 42 | PF00400 | 0.502 |
TRG_ER_diArg_1 | 404 | 406 | PF00400 | 0.528 |
TRG_ER_diArg_1 | 409 | 412 | PF00400 | 0.482 |
TRG_ER_diArg_1 | 489 | 491 | PF00400 | 0.643 |
TRG_ER_diArg_1 | 496 | 498 | PF00400 | 0.601 |
TRG_ER_diArg_1 | 599 | 601 | PF00400 | 0.657 |
TRG_ER_diArg_1 | 642 | 644 | PF00400 | 0.543 |
TRG_ER_diArg_1 | 74 | 77 | PF00400 | 0.494 |
TRG_NLS_MonoCore_2 | 4 | 9 | PF00514 | 0.513 |
TRG_NLS_MonoExtN_4 | 2 | 9 | PF00514 | 0.528 |
TRG_Pf-PMV_PEXEL_1 | 240 | 244 | PF00026 | 0.523 |
TRG_Pf-PMV_PEXEL_1 | 294 | 299 | PF00026 | 0.489 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2D0 | Leptomonas seymouri | 50% | 93% |
A0A3Q8IHA2 | Leishmania donovani | 87% | 100% |
A4HHE8 | Leishmania braziliensis | 67% | 100% |
A4I4J8 | Leishmania infantum | 87% | 100% |
E9ALT4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
V5BH77 | Trypanosoma cruzi | 37% | 100% |