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:0005730 | nucleolus | 5 | 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:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HQH3
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 | 1 |
GO:0003723 | RNA binding | 4 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 368 | 372 | PF00656 | 0.436 |
CLV_C14_Caspase3-7 | 393 | 397 | PF00656 | 0.683 |
CLV_C14_Caspase3-7 | 461 | 465 | PF00656 | 0.781 |
CLV_NRD_NRD_1 | 148 | 150 | PF00675 | 0.393 |
CLV_NRD_NRD_1 | 272 | 274 | PF00675 | 0.393 |
CLV_NRD_NRD_1 | 413 | 415 | PF00675 | 0.466 |
CLV_NRD_NRD_1 | 49 | 51 | PF00675 | 0.639 |
CLV_NRD_NRD_1 | 523 | 525 | PF00675 | 0.465 |
CLV_NRD_NRD_1 | 54 | 56 | PF00675 | 0.530 |
CLV_NRD_NRD_1 | 575 | 577 | PF00675 | 0.489 |
CLV_NRD_NRD_1 | 696 | 698 | PF00675 | 0.453 |
CLV_PCSK_FUR_1 | 407 | 411 | PF00082 | 0.614 |
CLV_PCSK_KEX2_1 | 147 | 149 | PF00082 | 0.385 |
CLV_PCSK_KEX2_1 | 191 | 193 | PF00082 | 0.477 |
CLV_PCSK_KEX2_1 | 272 | 274 | PF00082 | 0.469 |
CLV_PCSK_KEX2_1 | 409 | 411 | PF00082 | 0.531 |
CLV_PCSK_KEX2_1 | 413 | 415 | PF00082 | 0.520 |
CLV_PCSK_KEX2_1 | 49 | 51 | PF00082 | 0.634 |
CLV_PCSK_KEX2_1 | 523 | 525 | PF00082 | 0.465 |
CLV_PCSK_KEX2_1 | 54 | 56 | PF00082 | 0.530 |
CLV_PCSK_KEX2_1 | 575 | 577 | PF00082 | 0.489 |
CLV_PCSK_KEX2_1 | 648 | 650 | PF00082 | 0.520 |
CLV_PCSK_KEX2_1 | 668 | 670 | PF00082 | 0.571 |
CLV_PCSK_KEX2_1 | 677 | 679 | PF00082 | 0.597 |
CLV_PCSK_KEX2_1 | 695 | 697 | PF00082 | 0.395 |
CLV_PCSK_PC1ET2_1 | 191 | 193 | PF00082 | 0.477 |
CLV_PCSK_PC1ET2_1 | 409 | 411 | PF00082 | 0.568 |
CLV_PCSK_PC1ET2_1 | 648 | 650 | PF00082 | 0.545 |
CLV_PCSK_PC1ET2_1 | 668 | 670 | PF00082 | 0.624 |
CLV_PCSK_PC1ET2_1 | 677 | 679 | PF00082 | 0.645 |
CLV_PCSK_PC7_1 | 50 | 56 | PF00082 | 0.622 |
CLV_PCSK_SKI1_1 | 2 | 6 | PF00082 | 0.743 |
CLV_PCSK_SKI1_1 | 525 | 529 | PF00082 | 0.486 |
CLV_PCSK_SKI1_1 | 532 | 536 | PF00082 | 0.469 |
CLV_PCSK_SKI1_1 | 581 | 585 | PF00082 | 0.483 |
CLV_PCSK_SKI1_1 | 591 | 595 | PF00082 | 0.475 |
CLV_PCSK_SKI1_1 | 620 | 624 | PF00082 | 0.479 |
CLV_PCSK_SKI1_1 | 648 | 652 | PF00082 | 0.585 |
CLV_PCSK_SKI1_1 | 69 | 73 | PF00082 | 0.451 |
DEG_APCC_DBOX_1 | 553 | 561 | PF00400 | 0.603 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.539 |
DEG_SPOP_SBC_1 | 103 | 107 | PF00917 | 0.508 |
DOC_ANK_TNKS_1 | 681 | 688 | PF00023 | 0.484 |
DOC_MAPK_gen_1 | 198 | 206 | PF00069 | 0.482 |
DOC_MAPK_gen_1 | 646 | 656 | PF00069 | 0.452 |
DOC_MAPK_MEF2A_6 | 198 | 206 | PF00069 | 0.431 |
DOC_PP1_RVXF_1 | 353 | 359 | PF00149 | 0.423 |
DOC_PP4_FxxP_1 | 324 | 327 | PF00568 | 0.430 |
DOC_PP4_FxxP_1 | 36 | 39 | PF00568 | 0.495 |
DOC_SPAK_OSR1_1 | 40 | 44 | PF12202 | 0.498 |
DOC_USP7_MATH_1 | 103 | 107 | PF00917 | 0.596 |
DOC_USP7_MATH_1 | 340 | 344 | PF00917 | 0.462 |
DOC_USP7_MATH_1 | 388 | 392 | PF00917 | 0.559 |
DOC_USP7_MATH_1 | 434 | 438 | PF00917 | 0.764 |
DOC_USP7_MATH_1 | 681 | 685 | PF00917 | 0.620 |
DOC_USP7_UBL2_3 | 405 | 409 | PF12436 | 0.612 |
DOC_USP7_UBL2_3 | 521 | 525 | PF12436 | 0.485 |
DOC_USP7_UBL2_3 | 528 | 532 | PF12436 | 0.474 |
DOC_USP7_UBL2_3 | 573 | 577 | PF12436 | 0.505 |
DOC_WW_Pin1_4 | 323 | 328 | PF00397 | 0.506 |
LIG_14-3-3_CanoR_1 | 35 | 39 | PF00244 | 0.477 |
LIG_14-3-3_CanoR_1 | 355 | 359 | PF00244 | 0.428 |
LIG_14-3-3_CanoR_1 | 365 | 370 | PF00244 | 0.467 |
LIG_14-3-3_CanoR_1 | 454 | 460 | PF00244 | 0.575 |
LIG_14-3-3_CanoR_1 | 54 | 60 | PF00244 | 0.594 |
LIG_14-3-3_CanoR_1 | 598 | 605 | PF00244 | 0.517 |
LIG_14-3-3_CanoR_1 | 649 | 657 | PF00244 | 0.428 |
LIG_14-3-3_CanoR_1 | 682 | 686 | PF00244 | 0.647 |
LIG_14-3-3_CanoR_1 | 695 | 700 | PF00244 | 0.398 |
LIG_CaM_IQ_9 | 494 | 510 | PF13499 | 0.612 |
LIG_CSL_BTD_1 | 135 | 138 | PF09270 | 0.627 |
LIG_FHA_1 | 291 | 297 | PF00498 | 0.272 |
LIG_FHA_1 | 344 | 350 | PF00498 | 0.319 |
LIG_FHA_1 | 507 | 513 | PF00498 | 0.649 |
LIG_FHA_1 | 604 | 610 | PF00498 | 0.680 |
LIG_FHA_1 | 649 | 655 | PF00498 | 0.386 |
LIG_FHA_2 | 374 | 380 | PF00498 | 0.506 |
LIG_FHA_2 | 610 | 616 | PF00498 | 0.553 |
LIG_LIR_Apic_2 | 321 | 327 | PF02991 | 0.433 |
LIG_LIR_Gen_1 | 156 | 165 | PF02991 | 0.373 |
LIG_LIR_Nem_3 | 156 | 160 | PF02991 | 0.343 |
LIG_LIR_Nem_3 | 164 | 169 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 336 | 341 | PF02991 | 0.357 |
LIG_Pex14_2 | 32 | 36 | PF04695 | 0.505 |
LIG_Pex14_2 | 354 | 358 | PF04695 | 0.406 |
LIG_Pex14_2 | 70 | 74 | PF04695 | 0.563 |
LIG_REV1ctd_RIR_1 | 689 | 700 | PF16727 | 0.625 |
LIG_SH2_CRK | 166 | 170 | PF00017 | 0.391 |
LIG_SH2_CRK | 416 | 420 | PF00017 | 0.488 |
LIG_SH2_NCK_1 | 283 | 287 | PF00017 | 0.321 |
LIG_SH2_STAP1 | 166 | 170 | PF00017 | 0.356 |
LIG_SH2_STAP1 | 416 | 420 | PF00017 | 0.445 |
LIG_SH2_STAT5 | 317 | 320 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 385 | 388 | PF00017 | 0.527 |
LIG_SH3_3 | 237 | 243 | PF00018 | 0.745 |
LIG_SUMO_SIM_anti_2 | 651 | 660 | PF11976 | 0.372 |
LIG_SUMO_SIM_par_1 | 178 | 183 | PF11976 | 0.414 |
LIG_TRAF2_1 | 122 | 125 | PF00917 | 0.696 |
LIG_TRAF2_1 | 376 | 379 | PF00917 | 0.673 |
LIG_TYR_ITIM | 296 | 301 | PF00017 | 0.302 |
LIG_WRC_WIRS_1 | 285 | 290 | PF05994 | 0.367 |
LIG_WRC_WIRS_1 | 341 | 346 | PF05994 | 0.422 |
MOD_CDK_SPxxK_3 | 323 | 330 | PF00069 | 0.502 |
MOD_CK1_1 | 101 | 107 | PF00069 | 0.718 |
MOD_CK1_1 | 290 | 296 | PF00069 | 0.351 |
MOD_CK1_1 | 343 | 349 | PF00069 | 0.410 |
MOD_CK1_1 | 94 | 100 | PF00069 | 0.717 |
MOD_CK2_1 | 373 | 379 | PF00069 | 0.619 |
MOD_CK2_1 | 388 | 394 | PF00069 | 0.501 |
MOD_CK2_1 | 443 | 449 | PF00069 | 0.629 |
MOD_CK2_1 | 453 | 459 | PF00069 | 0.618 |
MOD_CK2_1 | 568 | 574 | PF00069 | 0.519 |
MOD_CK2_1 | 609 | 615 | PF00069 | 0.552 |
MOD_Cter_Amidation | 189 | 192 | PF01082 | 0.379 |
MOD_Cter_Amidation | 47 | 50 | PF01082 | 0.500 |
MOD_Cter_Amidation | 666 | 669 | PF01082 | 0.601 |
MOD_GlcNHglycan | 101 | 104 | PF01048 | 0.769 |
MOD_GlcNHglycan | 218 | 223 | PF01048 | 0.722 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.434 |
MOD_GlcNHglycan | 289 | 292 | PF01048 | 0.375 |
MOD_GlcNHglycan | 307 | 311 | PF01048 | 0.426 |
MOD_GlcNHglycan | 346 | 349 | PF01048 | 0.464 |
MOD_GlcNHglycan | 435 | 439 | PF01048 | 0.666 |
MOD_GlcNHglycan | 570 | 573 | PF01048 | 0.518 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.502 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.708 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.415 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.699 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.461 |
MOD_GSK3_1 | 365 | 372 | PF00069 | 0.456 |
MOD_GSK3_1 | 439 | 446 | PF00069 | 0.803 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.769 |
MOD_GSK3_1 | 628 | 635 | PF00069 | 0.530 |
MOD_GSK3_1 | 691 | 698 | PF00069 | 0.596 |
MOD_GSK3_1 | 83 | 90 | PF00069 | 0.646 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.678 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.535 |
MOD_NEK2_1 | 344 | 349 | PF00069 | 0.405 |
MOD_NEK2_1 | 369 | 374 | PF00069 | 0.592 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.537 |
MOD_NEK2_1 | 41 | 46 | PF00069 | 0.536 |
MOD_NEK2_1 | 527 | 532 | PF00069 | 0.592 |
MOD_NEK2_1 | 603 | 608 | PF00069 | 0.550 |
MOD_NEK2_1 | 641 | 646 | PF00069 | 0.624 |
MOD_NEK2_1 | 656 | 661 | PF00069 | 0.367 |
MOD_NEK2_1 | 691 | 696 | PF00069 | 0.535 |
MOD_NEK2_2 | 340 | 345 | PF00069 | 0.435 |
MOD_PIKK_1 | 347 | 353 | PF00454 | 0.420 |
MOD_PIKK_1 | 42 | 48 | PF00454 | 0.492 |
MOD_PIKK_1 | 53 | 59 | PF00454 | 0.517 |
MOD_PIKK_1 | 598 | 604 | PF00454 | 0.678 |
MOD_PIKK_1 | 609 | 615 | PF00454 | 0.591 |
MOD_PIKK_1 | 641 | 647 | PF00454 | 0.583 |
MOD_PKA_1 | 49 | 55 | PF00069 | 0.762 |
MOD_PKA_1 | 648 | 654 | PF00069 | 0.496 |
MOD_PKA_2 | 34 | 40 | PF00069 | 0.448 |
MOD_PKA_2 | 354 | 360 | PF00069 | 0.418 |
MOD_PKA_2 | 453 | 459 | PF00069 | 0.558 |
MOD_PKA_2 | 49 | 55 | PF00069 | 0.552 |
MOD_PKA_2 | 568 | 574 | PF00069 | 0.665 |
MOD_PKA_2 | 648 | 654 | PF00069 | 0.400 |
MOD_PKA_2 | 681 | 687 | PF00069 | 0.612 |
MOD_PKA_2 | 99 | 105 | PF00069 | 0.524 |
MOD_Plk_1 | 180 | 186 | PF00069 | 0.413 |
MOD_Plk_1 | 448 | 454 | PF00069 | 0.596 |
MOD_Plk_1 | 482 | 488 | PF00069 | 0.564 |
MOD_Plk_1 | 80 | 86 | PF00069 | 0.674 |
MOD_Plk_2-3 | 233 | 239 | PF00069 | 0.674 |
MOD_Plk_2-3 | 444 | 450 | PF00069 | 0.546 |
MOD_Plk_4 | 180 | 186 | PF00069 | 0.413 |
MOD_Plk_4 | 369 | 375 | PF00069 | 0.428 |
MOD_Plk_4 | 474 | 480 | PF00069 | 0.669 |
MOD_ProDKin_1 | 323 | 329 | PF00069 | 0.502 |
MOD_SUMO_rev_2 | 398 | 406 | PF00179 | 0.623 |
MOD_SUMO_rev_2 | 487 | 495 | PF00179 | 0.536 |
MOD_SUMO_rev_2 | 672 | 679 | PF00179 | 0.648 |
TRG_DiLeu_BaEn_4 | 124 | 130 | PF01217 | 0.623 |
TRG_ENDOCYTIC_2 | 166 | 169 | PF00928 | 0.382 |
TRG_ENDOCYTIC_2 | 282 | 285 | PF00928 | 0.346 |
TRG_ENDOCYTIC_2 | 298 | 301 | PF00928 | 0.391 |
TRG_ENDOCYTIC_2 | 416 | 419 | PF00928 | 0.440 |
TRG_ER_diArg_1 | 147 | 149 | PF00400 | 0.410 |
TRG_ER_diArg_1 | 17 | 20 | PF00400 | 0.579 |
TRG_ER_diArg_1 | 271 | 273 | PF00400 | 0.454 |
TRG_ER_diArg_1 | 278 | 281 | PF00400 | 0.417 |
TRG_ER_diArg_1 | 364 | 367 | PF00400 | 0.423 |
TRG_ER_diArg_1 | 412 | 414 | PF00400 | 0.484 |
TRG_ER_diArg_1 | 522 | 524 | PF00400 | 0.479 |
TRG_ER_diArg_1 | 695 | 697 | PF00400 | 0.428 |
TRG_NES_CRM1_1 | 164 | 178 | PF08389 | 0.352 |
TRG_NES_CRM1_1 | 450 | 464 | PF08389 | 0.658 |
TRG_NLS_Bipartite_1 | 576 | 598 | PF00514 | 0.493 |
TRG_NLS_MonoExtC_3 | 527 | 532 | PF00514 | 0.479 |
TRG_NLS_MonoExtC_3 | 593 | 598 | PF00514 | 0.517 |
TRG_NLS_MonoExtC_3 | 667 | 673 | PF00514 | 0.622 |
TRG_NLS_MonoExtN_4 | 525 | 532 | PF00514 | 0.503 |
TRG_NLS_MonoExtN_4 | 591 | 598 | PF00514 | 0.474 |
TRG_NLS_MonoExtN_4 | 665 | 672 | PF00514 | 0.608 |
TRG_Pf-PMV_PEXEL_1 | 110 | 114 | PF00026 | 0.623 |
TRG_Pf-PMV_PEXEL_1 | 316 | 320 | PF00026 | 0.317 |
TRG_Pf-PMV_PEXEL_1 | 367 | 371 | PF00026 | 0.368 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2Z4 | Leptomonas seymouri | 67% | 96% |
A0A0S4IQI8 | Bodo saltans | 45% | 95% |
A0A3S5IRC1 | Trypanosoma rangeli | 52% | 100% |
A0A3S7XCB2 | Leishmania donovani | 82% | 100% |
A4ICA9 | Leishmania infantum | 81% | 100% |
D0A3M2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 50% | 98% |
E9AU86 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |
Q4Q0A5 | Leishmania major | 80% | 100% |
V5AXL9 | Trypanosoma cruzi | 51% | 100% |