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:0000974 | Prp19 complex | 2 | 1 |
GO:0005654 | nucleoplasm | 2 | 1 |
GO:0005681 | spliceosomal complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
GO:1990904 | ribonucleoprotein complex | 2 | 1 |
Related structures:
AlphaFold database: A4H921
Term | Name | Level | Count |
---|---|---|---|
GO:0000375 | RNA splicing, via transesterification reactions | 8 | 1 |
GO:0000377 | RNA splicing, via transesterification reactions with bulged adenosine as nucleophile | 9 | 1 |
GO:0000398 | mRNA splicing, via spliceosome | 8 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006396 | RNA processing | 6 | 1 |
GO:0006397 | mRNA processing | 7 | 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:0008380 | RNA splicing | 7 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0016071 | mRNA metabolic process | 6 | 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 | 1 |
GO:0003677 | DNA 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 | 260 | 264 | PF00656 | 0.712 |
CLV_C14_Caspase3-7 | 313 | 317 | PF00656 | 0.587 |
CLV_C14_Caspase3-7 | 450 | 454 | PF00656 | 0.720 |
CLV_C14_Caspase3-7 | 535 | 539 | PF00656 | 0.626 |
CLV_C14_Caspase3-7 | 545 | 549 | PF00656 | 0.612 |
CLV_C14_Caspase3-7 | 723 | 727 | PF00656 | 0.644 |
CLV_NRD_NRD_1 | 151 | 153 | PF00675 | 0.462 |
CLV_NRD_NRD_1 | 154 | 156 | PF00675 | 0.487 |
CLV_NRD_NRD_1 | 194 | 196 | PF00675 | 0.492 |
CLV_NRD_NRD_1 | 228 | 230 | PF00675 | 0.532 |
CLV_NRD_NRD_1 | 500 | 502 | PF00675 | 0.578 |
CLV_NRD_NRD_1 | 522 | 524 | PF00675 | 0.555 |
CLV_NRD_NRD_1 | 568 | 570 | PF00675 | 0.693 |
CLV_NRD_NRD_1 | 775 | 777 | PF00675 | 0.504 |
CLV_NRD_NRD_1 | 92 | 94 | PF00675 | 0.277 |
CLV_PCSK_FUR_1 | 148 | 152 | PF00082 | 0.448 |
CLV_PCSK_KEX2_1 | 148 | 150 | PF00082 | 0.444 |
CLV_PCSK_KEX2_1 | 151 | 153 | PF00082 | 0.462 |
CLV_PCSK_KEX2_1 | 435 | 437 | PF00082 | 0.631 |
CLV_PCSK_KEX2_1 | 481 | 483 | PF00082 | 0.634 |
CLV_PCSK_KEX2_1 | 522 | 524 | PF00082 | 0.555 |
CLV_PCSK_KEX2_1 | 568 | 570 | PF00082 | 0.584 |
CLV_PCSK_KEX2_1 | 629 | 631 | PF00082 | 0.560 |
CLV_PCSK_KEX2_1 | 775 | 777 | PF00082 | 0.504 |
CLV_PCSK_KEX2_1 | 92 | 94 | PF00082 | 0.277 |
CLV_PCSK_PC1ET2_1 | 435 | 437 | PF00082 | 0.628 |
CLV_PCSK_PC1ET2_1 | 481 | 483 | PF00082 | 0.559 |
CLV_PCSK_PC1ET2_1 | 629 | 631 | PF00082 | 0.560 |
CLV_PCSK_SKI1_1 | 20 | 24 | PF00082 | 0.277 |
CLV_PCSK_SKI1_1 | 229 | 233 | PF00082 | 0.528 |
CLV_PCSK_SKI1_1 | 297 | 301 | PF00082 | 0.475 |
CLV_PCSK_SKI1_1 | 334 | 338 | PF00082 | 0.625 |
CLV_PCSK_SKI1_1 | 346 | 350 | PF00082 | 0.504 |
CLV_PCSK_SKI1_1 | 41 | 45 | PF00082 | 0.281 |
CLV_PCSK_SKI1_1 | 438 | 442 | PF00082 | 0.647 |
CLV_PCSK_SKI1_1 | 761 | 765 | PF00082 | 0.491 |
CLV_PCSK_SKI1_1 | 769 | 773 | PF00082 | 0.542 |
DEG_APCC_DBOX_1 | 333 | 341 | PF00400 | 0.538 |
DEG_APCC_DBOX_1 | 437 | 445 | PF00400 | 0.640 |
DEG_APCC_DBOX_1 | 774 | 782 | PF00400 | 0.507 |
DEG_SCF_TRCP1_1 | 484 | 489 | PF00400 | 0.538 |
DEG_SPOP_SBC_1 | 473 | 477 | PF00917 | 0.682 |
DEG_SPOP_SBC_1 | 540 | 544 | PF00917 | 0.778 |
DEG_SPOP_SBC_1 | 582 | 586 | PF00917 | 0.567 |
DOC_CKS1_1 | 353 | 358 | PF01111 | 0.548 |
DOC_CKS1_1 | 495 | 500 | PF01111 | 0.527 |
DOC_MAPK_DCC_7 | 436 | 446 | PF00069 | 0.720 |
DOC_MAPK_gen_1 | 501 | 508 | PF00069 | 0.547 |
DOC_PP1_RVXF_1 | 1 | 7 | PF00149 | 0.545 |
DOC_PP1_RVXF_1 | 69 | 76 | PF00149 | 0.418 |
DOC_PP2B_LxvP_1 | 736 | 739 | PF13499 | 0.647 |
DOC_USP7_MATH_1 | 261 | 265 | PF00917 | 0.725 |
DOC_USP7_MATH_1 | 325 | 329 | PF00917 | 0.661 |
DOC_USP7_MATH_1 | 373 | 377 | PF00917 | 0.543 |
DOC_USP7_MATH_1 | 378 | 382 | PF00917 | 0.505 |
DOC_USP7_MATH_1 | 473 | 477 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 480 | 484 | PF00917 | 0.711 |
DOC_USP7_MATH_1 | 514 | 518 | PF00917 | 0.707 |
DOC_USP7_MATH_1 | 534 | 538 | PF00917 | 0.596 |
DOC_USP7_MATH_1 | 549 | 553 | PF00917 | 0.533 |
DOC_USP7_MATH_1 | 582 | 586 | PF00917 | 0.704 |
DOC_USP7_MATH_1 | 616 | 620 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 724 | 728 | PF00917 | 0.587 |
DOC_USP7_MATH_1 | 737 | 741 | PF00917 | 0.544 |
DOC_USP7_UBL2_3 | 192 | 196 | PF12436 | 0.494 |
DOC_USP7_UBL2_3 | 392 | 396 | PF12436 | 0.630 |
DOC_WW_Pin1_4 | 352 | 357 | PF00397 | 0.699 |
DOC_WW_Pin1_4 | 417 | 422 | PF00397 | 0.632 |
DOC_WW_Pin1_4 | 494 | 499 | PF00397 | 0.604 |
DOC_WW_Pin1_4 | 584 | 589 | PF00397 | 0.692 |
DOC_WW_Pin1_4 | 591 | 596 | PF00397 | 0.633 |
DOC_WW_Pin1_4 | 634 | 639 | PF00397 | 0.541 |
DOC_WW_Pin1_4 | 698 | 703 | PF00397 | 0.611 |
DOC_WW_Pin1_4 | 718 | 723 | PF00397 | 0.677 |
DOC_WW_Pin1_4 | 91 | 96 | PF00397 | 0.477 |
LIG_14-3-3_CanoR_1 | 33 | 38 | PF00244 | 0.477 |
LIG_14-3-3_CanoR_1 | 645 | 653 | PF00244 | 0.655 |
LIG_Actin_WH2_2 | 705 | 721 | PF00022 | 0.458 |
LIG_APCC_ABBA_1 | 277 | 282 | PF00400 | 0.541 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.554 |
LIG_BIR_III_4 | 256 | 260 | PF00653 | 0.541 |
LIG_BIR_III_4 | 316 | 320 | PF00653 | 0.615 |
LIG_BRCT_BRCA1_1 | 551 | 555 | PF00533 | 0.537 |
LIG_FHA_1 | 180 | 186 | PF00498 | 0.453 |
LIG_FHA_1 | 220 | 226 | PF00498 | 0.529 |
LIG_FHA_1 | 239 | 245 | PF00498 | 0.562 |
LIG_FHA_1 | 353 | 359 | PF00498 | 0.597 |
LIG_FHA_1 | 695 | 701 | PF00498 | 0.587 |
LIG_FHA_2 | 10 | 16 | PF00498 | 0.477 |
LIG_FHA_2 | 155 | 161 | PF00498 | 0.465 |
LIG_FHA_2 | 313 | 319 | PF00498 | 0.510 |
LIG_FHA_2 | 396 | 402 | PF00498 | 0.467 |
LIG_FHA_2 | 445 | 451 | PF00498 | 0.751 |
LIG_FHA_2 | 552 | 558 | PF00498 | 0.616 |
LIG_FHA_2 | 584 | 590 | PF00498 | 0.698 |
LIG_FHA_2 | 592 | 598 | PF00498 | 0.669 |
LIG_FHA_2 | 646 | 652 | PF00498 | 0.487 |
LIG_FHA_2 | 721 | 727 | PF00498 | 0.638 |
LIG_LIR_Apic_2 | 51 | 56 | PF02991 | 0.477 |
LIG_LIR_Gen_1 | 106 | 115 | PF02991 | 0.382 |
LIG_LIR_Gen_1 | 271 | 280 | PF02991 | 0.584 |
LIG_LIR_Gen_1 | 30 | 38 | PF02991 | 0.477 |
LIG_LIR_Gen_1 | 401 | 410 | PF02991 | 0.554 |
LIG_LIR_Gen_1 | 552 | 562 | PF02991 | 0.590 |
LIG_LIR_Gen_1 | 690 | 699 | PF02991 | 0.520 |
LIG_LIR_Gen_1 | 74 | 80 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 106 | 112 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 271 | 277 | PF02991 | 0.595 |
LIG_LIR_Nem_3 | 30 | 34 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 401 | 406 | PF02991 | 0.541 |
LIG_LIR_Nem_3 | 48 | 53 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 489 | 495 | PF02991 | 0.583 |
LIG_LIR_Nem_3 | 552 | 558 | PF02991 | 0.609 |
LIG_LIR_Nem_3 | 690 | 694 | PF02991 | 0.511 |
LIG_LIR_Nem_3 | 74 | 78 | PF02991 | 0.418 |
LIG_MYND_1 | 429 | 433 | PF01753 | 0.545 |
LIG_Pex14_2 | 75 | 79 | PF04695 | 0.481 |
LIG_PROFILIN_1 | 426 | 432 | PF00235 | 0.539 |
LIG_Rb_pABgroove_1 | 486 | 494 | PF01858 | 0.534 |
LIG_SH2_PTP2 | 98 | 101 | PF00017 | 0.413 |
LIG_SH2_SRC | 472 | 475 | PF00017 | 0.552 |
LIG_SH2_SRC | 53 | 56 | PF00017 | 0.539 |
LIG_SH2_STAP1 | 656 | 660 | PF00017 | 0.451 |
LIG_SH2_STAT3 | 280 | 283 | PF00017 | 0.521 |
LIG_SH2_STAT3 | 656 | 659 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 109 | 112 | PF00017 | 0.370 |
LIG_SH2_STAT5 | 119 | 122 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 53 | 56 | PF00017 | 0.539 |
LIG_SH2_STAT5 | 711 | 714 | PF00017 | 0.539 |
LIG_SH2_STAT5 | 744 | 747 | PF00017 | 0.571 |
LIG_SH2_STAT5 | 98 | 101 | PF00017 | 0.413 |
LIG_SH3_2 | 430 | 435 | PF14604 | 0.651 |
LIG_SH3_2 | 466 | 471 | PF14604 | 0.648 |
LIG_SH3_3 | 353 | 359 | PF00018 | 0.605 |
LIG_SH3_3 | 409 | 415 | PF00018 | 0.533 |
LIG_SH3_3 | 422 | 428 | PF00018 | 0.597 |
LIG_SH3_3 | 463 | 469 | PF00018 | 0.749 |
LIG_SUMO_SIM_par_1 | 442 | 447 | PF11976 | 0.720 |
LIG_TRAF2_1 | 157 | 160 | PF00917 | 0.458 |
LIG_TRAF2_1 | 234 | 237 | PF00917 | 0.509 |
LIG_TRAF2_1 | 391 | 394 | PF00917 | 0.629 |
LIG_TRAF2_1 | 447 | 450 | PF00917 | 0.718 |
LIG_TRAF2_1 | 65 | 68 | PF00917 | 0.477 |
LIG_WRC_WIRS_1 | 141 | 146 | PF05994 | 0.513 |
LIG_WW_2 | 356 | 359 | PF00397 | 0.543 |
LIG_WW_2 | 429 | 432 | PF00397 | 0.697 |
MOD_CDK_SPK_2 | 698 | 703 | PF00069 | 0.448 |
MOD_CDK_SPxxK_3 | 494 | 501 | PF00069 | 0.524 |
MOD_CK1_1 | 140 | 146 | PF00069 | 0.519 |
MOD_CK1_1 | 327 | 333 | PF00069 | 0.604 |
MOD_CK1_1 | 36 | 42 | PF00069 | 0.315 |
MOD_CK1_1 | 420 | 426 | PF00069 | 0.609 |
MOD_CK1_1 | 455 | 461 | PF00069 | 0.597 |
MOD_CK2_1 | 154 | 160 | PF00069 | 0.470 |
MOD_CK2_1 | 210 | 216 | PF00069 | 0.473 |
MOD_CK2_1 | 379 | 385 | PF00069 | 0.513 |
MOD_CK2_1 | 444 | 450 | PF00069 | 0.720 |
MOD_CK2_1 | 551 | 557 | PF00069 | 0.621 |
MOD_CK2_1 | 583 | 589 | PF00069 | 0.717 |
MOD_CK2_1 | 591 | 597 | PF00069 | 0.660 |
MOD_CK2_1 | 62 | 68 | PF00069 | 0.315 |
MOD_CK2_1 | 645 | 651 | PF00069 | 0.502 |
MOD_CK2_1 | 9 | 15 | PF00069 | 0.315 |
MOD_GlcNHglycan | 168 | 171 | PF01048 | 0.518 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.518 |
MOD_GlcNHglycan | 241 | 244 | PF01048 | 0.504 |
MOD_GlcNHglycan | 254 | 260 | PF01048 | 0.604 |
MOD_GlcNHglycan | 263 | 266 | PF01048 | 0.589 |
MOD_GlcNHglycan | 312 | 315 | PF01048 | 0.723 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.517 |
MOD_GlcNHglycan | 364 | 367 | PF01048 | 0.670 |
MOD_GlcNHglycan | 407 | 410 | PF01048 | 0.772 |
MOD_GlcNHglycan | 484 | 487 | PF01048 | 0.639 |
MOD_GlcNHglycan | 544 | 547 | PF01048 | 0.672 |
MOD_GlcNHglycan | 618 | 621 | PF01048 | 0.653 |
MOD_GlcNHglycan | 648 | 651 | PF01048 | 0.477 |
MOD_GlcNHglycan | 656 | 659 | PF01048 | 0.443 |
MOD_GlcNHglycan | 726 | 729 | PF01048 | 0.688 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.553 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.503 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.631 |
MOD_GSK3_1 | 347 | 354 | PF00069 | 0.622 |
MOD_GSK3_1 | 413 | 420 | PF00069 | 0.655 |
MOD_GSK3_1 | 482 | 489 | PF00069 | 0.616 |
MOD_GSK3_1 | 514 | 521 | PF00069 | 0.626 |
MOD_GSK3_1 | 549 | 556 | PF00069 | 0.635 |
MOD_GSK3_1 | 694 | 701 | PF00069 | 0.582 |
MOD_GSK3_1 | 720 | 727 | PF00069 | 0.638 |
MOD_N-GLC_1 | 362 | 367 | PF02516 | 0.535 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.447 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.532 |
MOD_NEK2_1 | 395 | 400 | PF00069 | 0.530 |
MOD_NEK2_1 | 402 | 407 | PF00069 | 0.595 |
MOD_NEK2_2 | 221 | 226 | PF00069 | 0.535 |
MOD_PIKK_1 | 41 | 47 | PF00454 | 0.320 |
MOD_PIKK_1 | 629 | 635 | PF00454 | 0.717 |
MOD_PIKK_1 | 667 | 673 | PF00454 | 0.578 |
MOD_PK_1 | 442 | 448 | PF00069 | 0.693 |
MOD_PKA_1 | 629 | 635 | PF00069 | 0.555 |
MOD_PKA_2 | 154 | 160 | PF00069 | 0.470 |
MOD_PKA_2 | 225 | 231 | PF00069 | 0.530 |
MOD_PKA_2 | 261 | 267 | PF00069 | 0.705 |
MOD_PKA_2 | 576 | 582 | PF00069 | 0.604 |
MOD_PKA_2 | 629 | 635 | PF00069 | 0.555 |
MOD_PKA_2 | 799 | 805 | PF00069 | 0.430 |
MOD_PKB_1 | 755 | 763 | PF00069 | 0.505 |
MOD_Plk_1 | 321 | 327 | PF00069 | 0.534 |
MOD_Plk_1 | 473 | 479 | PF00069 | 0.570 |
MOD_Plk_1 | 791 | 797 | PF00069 | 0.501 |
MOD_Plk_2-3 | 137 | 143 | PF00069 | 0.566 |
MOD_Plk_2-3 | 312 | 318 | PF00069 | 0.500 |
MOD_Plk_2-3 | 608 | 614 | PF00069 | 0.489 |
MOD_Plk_2-3 | 62 | 68 | PF00069 | 0.315 |
MOD_Plk_4 | 140 | 146 | PF00069 | 0.519 |
MOD_Plk_4 | 33 | 39 | PF00069 | 0.315 |
MOD_ProDKin_1 | 352 | 358 | PF00069 | 0.700 |
MOD_ProDKin_1 | 417 | 423 | PF00069 | 0.634 |
MOD_ProDKin_1 | 494 | 500 | PF00069 | 0.598 |
MOD_ProDKin_1 | 584 | 590 | PF00069 | 0.693 |
MOD_ProDKin_1 | 591 | 597 | PF00069 | 0.630 |
MOD_ProDKin_1 | 634 | 640 | PF00069 | 0.541 |
MOD_ProDKin_1 | 698 | 704 | PF00069 | 0.611 |
MOD_ProDKin_1 | 718 | 724 | PF00069 | 0.684 |
MOD_ProDKin_1 | 91 | 97 | PF00069 | 0.315 |
MOD_SUMO_for_1 | 112 | 115 | PF00179 | 0.385 |
MOD_SUMO_for_1 | 209 | 212 | PF00179 | 0.476 |
MOD_SUMO_for_1 | 391 | 394 | PF00179 | 0.629 |
MOD_SUMO_rev_2 | 390 | 398 | PF00179 | 0.548 |
MOD_SUMO_rev_2 | 65 | 73 | PF00179 | 0.315 |
TRG_DiLeu_BaEn_1 | 301 | 306 | PF01217 | 0.436 |
TRG_DiLeu_BaEn_1 | 68 | 73 | PF01217 | 0.315 |
TRG_DiLeu_BaLyEn_6 | 81 | 86 | PF01217 | 0.315 |
TRG_DiLeu_LyEn_5 | 301 | 306 | PF01217 | 0.436 |
TRG_ENDOCYTIC_2 | 109 | 112 | PF00928 | 0.370 |
TRG_ER_diArg_1 | 148 | 151 | PF00400 | 0.452 |
TRG_ER_diArg_1 | 568 | 570 | PF00400 | 0.584 |
TRG_ER_diArg_1 | 755 | 758 | PF00400 | 0.670 |
TRG_ER_diArg_1 | 774 | 776 | PF00400 | 0.387 |
TRG_NLS_MonoExtC_3 | 228 | 233 | PF00514 | 0.515 |
TRG_NLS_MonoExtN_4 | 226 | 233 | PF00514 | 0.522 |
TRG_Pf-PMV_PEXEL_1 | 233 | 237 | PF00026 | 0.508 |
TRG_Pf-PMV_PEXEL_1 | 293 | 298 | PF00026 | 0.482 |
TRG_Pf-PMV_PEXEL_1 | 304 | 308 | PF00026 | 0.508 |
TRG_Pf-PMV_PEXEL_1 | 84 | 88 | PF00026 | 0.315 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IKC2 | Leptomonas seymouri | 54% | 100% |
A0A3S7WUG8 | Leishmania donovani | 82% | 100% |
A4HXF3 | Leishmania infantum | 82% | 100% |
E9AR48 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
Q4QEB5 | Leishmania major | 81% | 100% |