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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0005829 | cytosol | 2 | 1 |
GO:0030684 | preribosome | 3 | 1 |
GO:0030688 | preribosome, small subunit precursor | 4 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:1990904 | ribonucleoprotein complex | 2 | 1 |
Related structures:
AlphaFold database: E9ALT4
Term | Name | Level | Count |
---|---|---|---|
GO:0009987 | cellular process | 1 | 7 |
GO:0022613 | ribonucleoprotein complex biogenesis | 4 | 7 |
GO:0042274 | ribosomal small subunit biogenesis | 5 | 7 |
GO:0044085 | cellular component biogenesis | 3 | 7 |
GO:0071840 | cellular component organization or biogenesis | 2 | 7 |
GO:0000054 | ribosomal subunit export from nucleus | 3 | 1 |
GO:0000056 | ribosomal small subunit export from nucleus | 4 | 1 |
GO:0006810 | transport | 3 | 1 |
GO:0006913 | nucleocytoplasmic transport | 5 | 1 |
GO:0031503 | protein-containing complex localization | 2 | 1 |
GO:0033750 | ribosome localization | 3 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0051168 | nuclear export | 6 | 1 |
GO:0051169 | nuclear transport | 4 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0051640 | organelle localization | 2 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
GO:0051656 | establishment of organelle localization | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 121 | 125 | PF00656 | 0.612 |
CLV_C14_Caspase3-7 | 20 | 24 | PF00656 | 0.562 |
CLV_NRD_NRD_1 | 256 | 258 | PF00675 | 0.528 |
CLV_NRD_NRD_1 | 263 | 265 | PF00675 | 0.596 |
CLV_NRD_NRD_1 | 406 | 408 | PF00675 | 0.508 |
CLV_NRD_NRD_1 | 41 | 43 | PF00675 | 0.583 |
CLV_NRD_NRD_1 | 491 | 493 | PF00675 | 0.640 |
CLV_NRD_NRD_1 | 497 | 499 | PF00675 | 0.670 |
CLV_NRD_NRD_1 | 601 | 603 | PF00675 | 0.667 |
CLV_NRD_NRD_1 | 613 | 615 | PF00675 | 0.386 |
CLV_NRD_NRD_1 | 624 | 626 | PF00675 | 0.504 |
CLV_NRD_NRD_1 | 644 | 646 | PF00675 | 0.612 |
CLV_NRD_NRD_1 | 653 | 655 | PF00675 | 0.515 |
CLV_NRD_NRD_1 | 7 | 9 | PF00675 | 0.363 |
CLV_NRD_NRD_1 | 77 | 79 | PF00675 | 0.502 |
CLV_PCSK_FUR_1 | 261 | 265 | PF00082 | 0.710 |
CLV_PCSK_FUR_1 | 622 | 626 | PF00082 | 0.625 |
CLV_PCSK_FUR_1 | 74 | 78 | PF00082 | 0.495 |
CLV_PCSK_KEX2_1 | 255 | 257 | PF00082 | 0.524 |
CLV_PCSK_KEX2_1 | 261 | 263 | PF00082 | 0.592 |
CLV_PCSK_KEX2_1 | 406 | 408 | PF00082 | 0.519 |
CLV_PCSK_KEX2_1 | 41 | 43 | PF00082 | 0.583 |
CLV_PCSK_KEX2_1 | 491 | 493 | PF00082 | 0.646 |
CLV_PCSK_KEX2_1 | 497 | 499 | PF00082 | 0.614 |
CLV_PCSK_KEX2_1 | 601 | 603 | PF00082 | 0.667 |
CLV_PCSK_KEX2_1 | 613 | 615 | PF00082 | 0.386 |
CLV_PCSK_KEX2_1 | 624 | 626 | PF00082 | 0.504 |
CLV_PCSK_KEX2_1 | 644 | 646 | PF00082 | 0.494 |
CLV_PCSK_KEX2_1 | 653 | 655 | PF00082 | 0.515 |
CLV_PCSK_KEX2_1 | 74 | 76 | PF00082 | 0.413 |
CLV_PCSK_KEX2_1 | 77 | 79 | PF00082 | 0.504 |
CLV_PCSK_PC7_1 | 257 | 263 | PF00082 | 0.561 |
CLV_PCSK_SKI1_1 | 10 | 14 | PF00082 | 0.473 |
CLV_PCSK_SKI1_1 | 241 | 245 | PF00082 | 0.503 |
CLV_PCSK_SKI1_1 | 299 | 303 | PF00082 | 0.474 |
CLV_PCSK_SKI1_1 | 332 | 336 | PF00082 | 0.610 |
CLV_PCSK_SKI1_1 | 412 | 416 | PF00082 | 0.381 |
CLV_PCSK_SKI1_1 | 497 | 501 | PF00082 | 0.801 |
CLV_PCSK_SKI1_1 | 625 | 629 | PF00082 | 0.496 |
CLV_PCSK_SKI1_1 | 645 | 649 | PF00082 | 0.489 |
CLV_Separin_Metazoa | 303 | 307 | PF03568 | 0.450 |
DEG_SPOP_SBC_1 | 545 | 549 | PF00917 | 0.656 |
DOC_CYCLIN_RxL_1 | 204 | 215 | PF00134 | 0.600 |
DOC_MAPK_gen_1 | 406 | 413 | PF00069 | 0.550 |
DOC_MAPK_gen_1 | 564 | 572 | PF00069 | 0.699 |
DOC_PP1_RVXF_1 | 205 | 212 | PF00149 | 0.504 |
DOC_PP1_RVXF_1 | 652 | 659 | PF00149 | 0.535 |
DOC_USP7_MATH_1 | 156 | 160 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 373 | 377 | PF00917 | 0.568 |
DOC_USP7_MATH_1 | 430 | 434 | PF00917 | 0.659 |
DOC_USP7_MATH_1 | 490 | 494 | PF00917 | 0.615 |
DOC_USP7_MATH_1 | 544 | 548 | PF00917 | 0.732 |
DOC_USP7_UBL2_3 | 128 | 132 | PF12436 | 0.523 |
DOC_USP7_UBL2_3 | 248 | 252 | PF12436 | 0.444 |
DOC_USP7_UBL2_3 | 5 | 9 | PF12436 | 0.487 |
DOC_USP7_UBL2_3 | 564 | 568 | PF12436 | 0.680 |
DOC_USP7_UBL2_3 | 603 | 607 | PF12436 | 0.508 |
DOC_USP7_UBL2_3 | 628 | 632 | PF12436 | 0.493 |
DOC_WW_Pin1_4 | 583 | 588 | PF00397 | 0.544 |
LIG_14-3-3_CanoR_1 | 299 | 308 | PF00244 | 0.479 |
LIG_14-3-3_CanoR_1 | 491 | 499 | PF00244 | 0.748 |
LIG_14-3-3_CanoR_1 | 625 | 635 | PF00244 | 0.493 |
LIG_14-3-3_CanoR_1 | 653 | 657 | PF00244 | 0.540 |
LIG_BIR_III_4 | 23 | 27 | PF00653 | 0.687 |
LIG_BIR_III_4 | 377 | 381 | PF00653 | 0.690 |
LIG_BIR_III_4 | 96 | 100 | PF00653 | 0.563 |
LIG_Clathr_ClatBox_1 | 456 | 460 | PF01394 | 0.737 |
LIG_deltaCOP1_diTrp_1 | 117 | 127 | PF00928 | 0.634 |
LIG_FHA_1 | 11 | 17 | PF00498 | 0.469 |
LIG_FHA_1 | 153 | 159 | PF00498 | 0.543 |
LIG_FHA_1 | 382 | 388 | PF00498 | 0.563 |
LIG_FHA_1 | 400 | 406 | PF00498 | 0.479 |
LIG_FHA_1 | 494 | 500 | PF00498 | 0.606 |
LIG_FHA_1 | 530 | 536 | PF00498 | 0.714 |
LIG_FHA_1 | 567 | 573 | PF00498 | 0.590 |
LIG_FHA_2 | 242 | 248 | PF00498 | 0.486 |
LIG_FHA_2 | 333 | 339 | PF00498 | 0.651 |
LIG_FHA_2 | 446 | 452 | PF00498 | 0.698 |
LIG_FHA_2 | 510 | 516 | PF00498 | 0.768 |
LIG_FHA_2 | 583 | 589 | PF00498 | 0.516 |
LIG_FHA_2 | 604 | 610 | PF00498 | 0.500 |
LIG_FHA_2 | 632 | 638 | PF00498 | 0.606 |
LIG_LIR_Apic_2 | 478 | 484 | PF02991 | 0.570 |
LIG_LIR_Gen_1 | 298 | 308 | PF02991 | 0.501 |
LIG_LIR_Nem_3 | 111 | 116 | PF02991 | 0.496 |
LIG_LIR_Nem_3 | 13 | 17 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 226 | 232 | PF02991 | 0.632 |
LIG_LIR_Nem_3 | 237 | 243 | PF02991 | 0.518 |
LIG_LIR_Nem_3 | 634 | 638 | PF02991 | 0.507 |
LIG_Pex14_2 | 394 | 398 | PF04695 | 0.500 |
LIG_REV1ctd_RIR_1 | 37 | 46 | PF16727 | 0.394 |
LIG_RPA_C_Fungi | 252 | 264 | PF08784 | 0.649 |
LIG_SH2_CRK | 14 | 18 | PF00017 | 0.457 |
LIG_SH2_CRK | 481 | 485 | PF00017 | 0.592 |
LIG_SH2_GRB2like | 480 | 483 | PF00017 | 0.579 |
LIG_SH2_GRB2like | 90 | 93 | PF00017 | 0.498 |
LIG_SH2_NCK_1 | 481 | 485 | PF00017 | 0.592 |
LIG_SH2_NCK_1 | 62 | 66 | PF00017 | 0.483 |
LIG_SH2_SRC | 90 | 93 | PF00017 | 0.673 |
LIG_SH2_STAP1 | 62 | 66 | PF00017 | 0.483 |
LIG_SH2_STAT3 | 480 | 483 | PF00017 | 0.598 |
LIG_SH2_STAT5 | 105 | 108 | PF00017 | 0.595 |
LIG_SH2_STAT5 | 318 | 321 | PF00017 | 0.572 |
LIG_SH2_STAT5 | 333 | 336 | PF00017 | 0.485 |
LIG_SH2_STAT5 | 366 | 369 | PF00017 | 0.509 |
LIG_SH3_3 | 130 | 136 | PF00018 | 0.733 |
LIG_SH3_3 | 262 | 268 | PF00018 | 0.480 |
LIG_SH3_3 | 426 | 432 | PF00018 | 0.532 |
LIG_SH3_3 | 435 | 441 | PF00018 | 0.586 |
LIG_SH3_3 | 569 | 575 | PF00018 | 0.733 |
LIG_SH3_4 | 6 | 13 | PF00018 | 0.485 |
LIG_SUMO_SIM_anti_2 | 451 | 460 | PF11976 | 0.731 |
LIG_TRAF2_1 | 183 | 186 | PF00917 | 0.654 |
LIG_TRAF2_1 | 336 | 339 | PF00917 | 0.493 |
LIG_TRAF2_1 | 449 | 452 | PF00917 | 0.636 |
LIG_TRAF2_1 | 606 | 609 | PF00917 | 0.509 |
LIG_TRFH_1 | 14 | 18 | PF08558 | 0.457 |
LIG_TYR_ITIM | 12 | 17 | PF00017 | 0.452 |
LIG_UBA3_1 | 360 | 365 | PF00899 | 0.526 |
LIG_UBA3_1 | 456 | 464 | PF00899 | 0.601 |
MOD_CDK_SPxK_1 | 583 | 589 | PF00069 | 0.516 |
MOD_CK1_1 | 475 | 481 | PF00069 | 0.542 |
MOD_CK1_1 | 493 | 499 | PF00069 | 0.520 |
MOD_CK1_1 | 548 | 554 | PF00069 | 0.702 |
MOD_CK1_1 | 557 | 563 | PF00069 | 0.672 |
MOD_CK1_1 | 646 | 652 | PF00069 | 0.506 |
MOD_CK2_1 | 241 | 247 | PF00069 | 0.496 |
MOD_CK2_1 | 32 | 38 | PF00069 | 0.458 |
MOD_CK2_1 | 332 | 338 | PF00069 | 0.642 |
MOD_CK2_1 | 445 | 451 | PF00069 | 0.636 |
MOD_CK2_1 | 504 | 510 | PF00069 | 0.700 |
MOD_CK2_1 | 582 | 588 | PF00069 | 0.681 |
MOD_CK2_1 | 603 | 609 | PF00069 | 0.508 |
MOD_CK2_1 | 631 | 637 | PF00069 | 0.607 |
MOD_GlcNHglycan | 150 | 153 | PF01048 | 0.646 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.707 |
MOD_GlcNHglycan | 44 | 47 | PF01048 | 0.697 |
MOD_GlcNHglycan | 474 | 477 | PF01048 | 0.525 |
MOD_GlcNHglycan | 492 | 495 | PF01048 | 0.690 |
MOD_GlcNHglycan | 506 | 509 | PF01048 | 0.557 |
MOD_GlcNHglycan | 525 | 528 | PF01048 | 0.587 |
MOD_GlcNHglycan | 540 | 543 | PF01048 | 0.664 |
MOD_GlcNHglycan | 548 | 551 | PF01048 | 0.666 |
MOD_GlcNHglycan | 561 | 564 | PF01048 | 0.560 |
MOD_GlcNHglycan | 628 | 631 | PF01048 | 0.500 |
MOD_GlcNHglycan | 645 | 648 | PF01048 | 0.495 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.575 |
MOD_GSK3_1 | 282 | 289 | PF00069 | 0.543 |
MOD_GSK3_1 | 418 | 425 | PF00069 | 0.488 |
MOD_GSK3_1 | 472 | 479 | PF00069 | 0.525 |
MOD_GSK3_1 | 523 | 530 | PF00069 | 0.640 |
MOD_GSK3_1 | 544 | 551 | PF00069 | 0.617 |
MOD_GSK3_1 | 554 | 561 | PF00069 | 0.633 |
MOD_N-GLC_1 | 518 | 523 | PF02516 | 0.621 |
MOD_NEK2_1 | 157 | 162 | PF00069 | 0.678 |
MOD_NEK2_1 | 276 | 281 | PF00069 | 0.716 |
MOD_NEK2_1 | 340 | 345 | PF00069 | 0.669 |
MOD_NEK2_1 | 631 | 636 | PF00069 | 0.607 |
MOD_NEK2_1 | 643 | 648 | PF00069 | 0.613 |
MOD_NEK2_2 | 596 | 601 | PF00069 | 0.436 |
MOD_NEK2_2 | 652 | 657 | PF00069 | 0.517 |
MOD_PIKK_1 | 290 | 296 | PF00454 | 0.628 |
MOD_PIKK_1 | 646 | 652 | PF00454 | 0.606 |
MOD_PKA_1 | 256 | 262 | PF00069 | 0.550 |
MOD_PKA_1 | 564 | 570 | PF00069 | 0.585 |
MOD_PKA_2 | 256 | 262 | PF00069 | 0.550 |
MOD_PKA_2 | 415 | 421 | PF00069 | 0.383 |
MOD_PKA_2 | 490 | 496 | PF00069 | 0.624 |
MOD_PKA_2 | 643 | 649 | PF00069 | 0.611 |
MOD_PKA_2 | 652 | 658 | PF00069 | 0.524 |
MOD_PKB_1 | 410 | 418 | PF00069 | 0.380 |
MOD_Plk_2-3 | 223 | 229 | PF00069 | 0.517 |
MOD_Plk_2-3 | 316 | 322 | PF00069 | 0.566 |
MOD_Plk_2-3 | 637 | 643 | PF00069 | 0.606 |
MOD_Plk_4 | 382 | 388 | PF00069 | 0.583 |
MOD_Plk_4 | 476 | 482 | PF00069 | 0.553 |
MOD_Plk_4 | 530 | 536 | PF00069 | 0.749 |
MOD_ProDKin_1 | 583 | 589 | PF00069 | 0.544 |
MOD_SUMO_rev_2 | 124 | 133 | PF00179 | 0.752 |
MOD_SUMO_rev_2 | 185 | 193 | PF00179 | 0.602 |
MOD_SUMO_rev_2 | 245 | 250 | PF00179 | 0.453 |
MOD_SUMO_rev_2 | 454 | 463 | PF00179 | 0.610 |
MOD_SUMO_rev_2 | 604 | 612 | PF00179 | 0.507 |
TRG_DiLeu_BaEn_1 | 238 | 243 | PF01217 | 0.504 |
TRG_DiLeu_BaEn_1 | 452 | 457 | PF01217 | 0.742 |
TRG_DiLeu_BaEn_3 | 452 | 458 | PF01217 | 0.612 |
TRG_DiLeu_LyEn_5 | 238 | 243 | PF01217 | 0.504 |
TRG_ENDOCYTIC_2 | 14 | 17 | PF00928 | 0.446 |
TRG_ENDOCYTIC_2 | 635 | 638 | PF00928 | 0.487 |
TRG_ER_diArg_1 | 255 | 257 | PF00400 | 0.524 |
TRG_ER_diArg_1 | 261 | 264 | PF00400 | 0.602 |
TRG_ER_diArg_1 | 40 | 42 | PF00400 | 0.558 |
TRG_ER_diArg_1 | 405 | 407 | PF00400 | 0.527 |
TRG_ER_diArg_1 | 410 | 413 | PF00400 | 0.489 |
TRG_ER_diArg_1 | 490 | 492 | PF00400 | 0.742 |
TRG_ER_diArg_1 | 497 | 499 | PF00400 | 0.663 |
TRG_ER_diArg_1 | 600 | 602 | PF00400 | 0.668 |
TRG_ER_diArg_1 | 612 | 614 | PF00400 | 0.385 |
TRG_ER_diArg_1 | 643 | 645 | PF00400 | 0.621 |
TRG_ER_diArg_1 | 74 | 77 | PF00400 | 0.498 |
TRG_NLS_MonoCore_2 | 4 | 9 | PF00514 | 0.486 |
TRG_NLS_MonoExtC_3 | 4 | 9 | PF00514 | 0.366 |
TRG_NLS_MonoExtN_4 | 2 | 9 | PF00514 | 0.500 |
TRG_Pf-PMV_PEXEL_1 | 241 | 245 | PF00026 | 0.492 |
TRG_Pf-PMV_PEXEL_1 | 295 | 300 | PF00026 | 0.554 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2D0 | Leptomonas seymouri | 58% | 93% |
A0A3Q8IHA2 | Leishmania donovani | 84% | 100% |
A4HHE8 | Leishmania braziliensis | 67% | 94% |
A4I4J8 | Leishmania infantum | 84% | 100% |
E9ADZ7 | Leishmania major | 86% | 100% |