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: 4 |
NetGPI | no | yes: 0, no: 4 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 5 |
GO:0031499 | TRAMP complex | 3 | 5 |
GO:0032991 | protein-containing complex | 1 | 5 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
GO:0140513 | nuclear protein-containing complex | 2 | 5 |
Related structures:
AlphaFold database: A4ICZ6
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 5 |
GO:0006396 | RNA processing | 6 | 5 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 5 |
GO:0006807 | nitrogen compound metabolic process | 2 | 5 |
GO:0008152 | metabolic process | 1 | 5 |
GO:0009987 | cellular process | 1 | 5 |
GO:0016070 | RNA metabolic process | 5 | 5 |
GO:0031123 | RNA 3'-end processing | 7 | 5 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 5 |
GO:0043170 | macromolecule metabolic process | 3 | 5 |
GO:0043631 | RNA polyadenylation | 6 | 5 |
GO:0044237 | cellular metabolic process | 2 | 5 |
GO:0044238 | primary metabolic process | 2 | 5 |
GO:0046483 | heterocycle metabolic process | 3 | 5 |
GO:0071076 | RNA 3' uridylation | 8 | 5 |
GO:0071704 | organic substance metabolic process | 2 | 5 |
GO:0090304 | nucleic acid metabolic process | 4 | 5 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 5 |
GO:0004652 | obsolete polynucleotide adenylyltransferase activity | 6 | 5 |
GO:0016740 | transferase activity | 2 | 5 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 5 |
GO:0016779 | nucleotidyltransferase activity | 4 | 5 |
GO:0050265 | RNA uridylyltransferase activity | 4 | 5 |
GO:0070566 | adenylyltransferase activity | 5 | 5 |
GO:0070569 | uridylyltransferase activity | 5 | 5 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 5 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 5 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 535 | 539 | PF00656 | 0.747 |
CLV_C14_Caspase3-7 | 657 | 661 | PF00656 | 0.742 |
CLV_NRD_NRD_1 | 142 | 144 | PF00675 | 0.696 |
CLV_NRD_NRD_1 | 487 | 489 | PF00675 | 0.751 |
CLV_NRD_NRD_1 | 719 | 721 | PF00675 | 0.590 |
CLV_PCSK_KEX2_1 | 142 | 144 | PF00082 | 0.696 |
CLV_PCSK_KEX2_1 | 278 | 280 | PF00082 | 0.516 |
CLV_PCSK_KEX2_1 | 719 | 721 | PF00082 | 0.590 |
CLV_PCSK_PC1ET2_1 | 278 | 280 | PF00082 | 0.516 |
CLV_PCSK_SKI1_1 | 268 | 272 | PF00082 | 0.622 |
CLV_PCSK_SKI1_1 | 279 | 283 | PF00082 | 0.404 |
CLV_PCSK_SKI1_1 | 622 | 626 | PF00082 | 0.433 |
DEG_ODPH_VHL_1 | 271 | 284 | PF01847 | 0.535 |
DOC_CKS1_1 | 145 | 150 | PF01111 | 0.721 |
DOC_CYCLIN_RxL_1 | 663 | 673 | PF00134 | 0.618 |
DOC_CYCLIN_yCln2_LP_2 | 586 | 592 | PF00134 | 0.754 |
DOC_MAPK_DCC_7 | 503 | 512 | PF00069 | 0.751 |
DOC_MAPK_gen_1 | 277 | 284 | PF00069 | 0.504 |
DOC_PP2B_LxvP_1 | 235 | 238 | PF13499 | 0.535 |
DOC_PP2B_LxvP_1 | 270 | 273 | PF13499 | 0.592 |
DOC_PP2B_LxvP_1 | 409 | 412 | PF13499 | 0.708 |
DOC_PP2B_LxvP_1 | 440 | 443 | PF13499 | 0.762 |
DOC_PP2B_LxvP_1 | 586 | 589 | PF13499 | 0.771 |
DOC_PP4_FxxP_1 | 692 | 695 | PF00568 | 0.473 |
DOC_PP4_FxxP_1 | 730 | 733 | PF00568 | 0.494 |
DOC_USP7_MATH_1 | 128 | 132 | PF00917 | 0.691 |
DOC_USP7_MATH_1 | 20 | 24 | PF00917 | 0.782 |
DOC_USP7_MATH_1 | 273 | 277 | PF00917 | 0.526 |
DOC_USP7_MATH_1 | 446 | 450 | PF00917 | 0.720 |
DOC_USP7_MATH_1 | 475 | 479 | PF00917 | 0.646 |
DOC_USP7_MATH_1 | 569 | 573 | PF00917 | 0.808 |
DOC_USP7_MATH_1 | 580 | 584 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 658 | 662 | PF00917 | 0.657 |
DOC_USP7_MATH_1 | 680 | 684 | PF00917 | 0.513 |
DOC_USP7_UBL2_3 | 364 | 368 | PF12436 | 0.513 |
DOC_WW_Pin1_4 | 11 | 16 | PF00397 | 0.731 |
DOC_WW_Pin1_4 | 144 | 149 | PF00397 | 0.738 |
DOC_WW_Pin1_4 | 350 | 355 | PF00397 | 0.448 |
DOC_WW_Pin1_4 | 407 | 412 | PF00397 | 0.613 |
DOC_WW_Pin1_4 | 430 | 435 | PF00397 | 0.659 |
DOC_WW_Pin1_4 | 451 | 456 | PF00397 | 0.698 |
DOC_WW_Pin1_4 | 554 | 559 | PF00397 | 0.715 |
DOC_WW_Pin1_4 | 563 | 568 | PF00397 | 0.717 |
DOC_WW_Pin1_4 | 616 | 621 | PF00397 | 0.442 |
DOC_WW_Pin1_4 | 88 | 93 | PF00397 | 0.798 |
LIG_14-3-3_CanoR_1 | 160 | 169 | PF00244 | 0.583 |
LIG_14-3-3_CanoR_1 | 295 | 301 | PF00244 | 0.510 |
LIG_14-3-3_CanoR_1 | 469 | 477 | PF00244 | 0.756 |
LIG_14-3-3_CanoR_1 | 561 | 567 | PF00244 | 0.806 |
LIG_14-3-3_CanoR_1 | 702 | 712 | PF00244 | 0.544 |
LIG_14-3-3_CanoR_1 | 719 | 723 | PF00244 | 0.602 |
LIG_Actin_WH2_2 | 280 | 297 | PF00022 | 0.478 |
LIG_Actin_WH2_2 | 477 | 495 | PF00022 | 0.495 |
LIG_APCC_ABBAyCdc20_2 | 279 | 285 | PF00400 | 0.581 |
LIG_BIR_III_4 | 644 | 648 | PF00653 | 0.427 |
LIG_BRCT_BRCA1_1 | 296 | 300 | PF00533 | 0.592 |
LIG_BRCT_BRCA1_1 | 726 | 730 | PF00533 | 0.480 |
LIG_CtBP_PxDLS_1 | 509 | 513 | PF00389 | 0.516 |
LIG_EVH1_1 | 144 | 148 | PF00568 | 0.660 |
LIG_FHA_1 | 173 | 179 | PF00498 | 0.443 |
LIG_FHA_1 | 220 | 226 | PF00498 | 0.535 |
LIG_FHA_1 | 256 | 262 | PF00498 | 0.561 |
LIG_FHA_1 | 29 | 35 | PF00498 | 0.716 |
LIG_FHA_1 | 554 | 560 | PF00498 | 0.724 |
LIG_FHA_1 | 726 | 732 | PF00498 | 0.582 |
LIG_FHA_2 | 186 | 192 | PF00498 | 0.479 |
LIG_FHA_2 | 297 | 303 | PF00498 | 0.586 |
LIG_FHA_2 | 524 | 530 | PF00498 | 0.715 |
LIG_FHA_2 | 704 | 710 | PF00498 | 0.536 |
LIG_FHA_2 | 99 | 105 | PF00498 | 0.814 |
LIG_LIR_Apic_2 | 691 | 695 | PF02991 | 0.467 |
LIG_LIR_Apic_2 | 727 | 733 | PF02991 | 0.492 |
LIG_LIR_Gen_1 | 383 | 394 | PF02991 | 0.417 |
LIG_LIR_Gen_1 | 448 | 458 | PF02991 | 0.683 |
LIG_LIR_Nem_3 | 131 | 136 | PF02991 | 0.762 |
LIG_LIR_Nem_3 | 147 | 153 | PF02991 | 0.663 |
LIG_LIR_Nem_3 | 180 | 185 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 297 | 303 | PF02991 | 0.586 |
LIG_LIR_Nem_3 | 374 | 380 | PF02991 | 0.501 |
LIG_LIR_Nem_3 | 383 | 389 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 448 | 453 | PF02991 | 0.689 |
LIG_PCNA_PIPBox_1 | 203 | 212 | PF02747 | 0.565 |
LIG_PCNA_yPIPBox_3 | 197 | 210 | PF02747 | 0.546 |
LIG_PCNA_yPIPBox_3 | 364 | 376 | PF02747 | 0.447 |
LIG_RPA_C_Fungi | 336 | 348 | PF08784 | 0.542 |
LIG_SH2_CRK | 386 | 390 | PF00017 | 0.414 |
LIG_SH2_NCK_1 | 414 | 418 | PF00017 | 0.622 |
LIG_SH2_NCK_1 | 540 | 544 | PF00017 | 0.688 |
LIG_SH2_SRC | 414 | 417 | PF00017 | 0.627 |
LIG_SH2_SRC | 479 | 482 | PF00017 | 0.581 |
LIG_SH2_STAP1 | 414 | 418 | PF00017 | 0.709 |
LIG_SH2_STAT3 | 183 | 186 | PF00017 | 0.477 |
LIG_SH2_STAT5 | 184 | 187 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 201 | 204 | PF00017 | 0.229 |
LIG_SH2_STAT5 | 386 | 389 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 479 | 482 | PF00017 | 0.680 |
LIG_SH2_STAT5 | 540 | 543 | PF00017 | 0.689 |
LIG_SH3_1 | 142 | 148 | PF00018 | 0.745 |
LIG_SH3_3 | 134 | 140 | PF00018 | 0.655 |
LIG_SH3_3 | 142 | 148 | PF00018 | 0.703 |
LIG_SH3_3 | 150 | 156 | PF00018 | 0.593 |
LIG_SH3_3 | 209 | 215 | PF00018 | 0.557 |
LIG_SH3_3 | 730 | 736 | PF00018 | 0.494 |
LIG_SUMO_SIM_par_1 | 257 | 263 | PF11976 | 0.474 |
LIG_SUMO_SIM_par_1 | 508 | 513 | PF11976 | 0.672 |
LIG_SUMO_SIM_par_1 | 588 | 594 | PF11976 | 0.656 |
LIG_TRAF2_1 | 189 | 192 | PF00917 | 0.567 |
LIG_TRAF2_1 | 249 | 252 | PF00917 | 0.399 |
LIG_TRAF2_1 | 260 | 263 | PF00917 | 0.408 |
LIG_UBA3_1 | 623 | 629 | PF00899 | 0.435 |
LIG_WRC_WIRS_1 | 133 | 138 | PF05994 | 0.760 |
LIG_WW_1 | 411 | 414 | PF00397 | 0.644 |
LIG_WW_3 | 410 | 414 | PF00397 | 0.614 |
MOD_CDC14_SPxK_1 | 410 | 413 | PF00782 | 0.612 |
MOD_CDC14_SPxK_1 | 619 | 622 | PF00782 | 0.431 |
MOD_CDK_SPxK_1 | 11 | 17 | PF00069 | 0.681 |
MOD_CDK_SPxK_1 | 407 | 413 | PF00069 | 0.595 |
MOD_CDK_SPxK_1 | 616 | 622 | PF00069 | 0.445 |
MOD_CDK_SPxxK_3 | 554 | 561 | PF00069 | 0.716 |
MOD_CK1_1 | 236 | 242 | PF00069 | 0.380 |
MOD_CK1_1 | 333 | 339 | PF00069 | 0.467 |
MOD_CK1_1 | 433 | 439 | PF00069 | 0.666 |
MOD_CK1_1 | 518 | 524 | PF00069 | 0.725 |
MOD_CK1_1 | 549 | 555 | PF00069 | 0.661 |
MOD_CK1_1 | 591 | 597 | PF00069 | 0.623 |
MOD_CK1_1 | 688 | 694 | PF00069 | 0.503 |
MOD_CK1_1 | 704 | 710 | PF00069 | 0.450 |
MOD_CK1_1 | 87 | 93 | PF00069 | 0.795 |
MOD_CK2_1 | 185 | 191 | PF00069 | 0.475 |
MOD_CK2_1 | 214 | 220 | PF00069 | 0.727 |
MOD_CK2_1 | 296 | 302 | PF00069 | 0.600 |
MOD_CK2_1 | 523 | 529 | PF00069 | 0.710 |
MOD_CK2_1 | 703 | 709 | PF00069 | 0.535 |
MOD_CK2_1 | 98 | 104 | PF00069 | 0.817 |
MOD_GlcNHglycan | 130 | 133 | PF01048 | 0.705 |
MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.591 |
MOD_GlcNHglycan | 262 | 267 | PF01048 | 0.662 |
MOD_GlcNHglycan | 296 | 299 | PF01048 | 0.607 |
MOD_GlcNHglycan | 335 | 338 | PF01048 | 0.553 |
MOD_GlcNHglycan | 470 | 473 | PF01048 | 0.708 |
MOD_GlcNHglycan | 504 | 507 | PF01048 | 0.769 |
MOD_GlcNHglycan | 548 | 551 | PF01048 | 0.719 |
MOD_GlcNHglycan | 583 | 586 | PF01048 | 0.714 |
MOD_GlcNHglycan | 593 | 596 | PF01048 | 0.696 |
MOD_GlcNHglycan | 603 | 606 | PF01048 | 0.438 |
MOD_GlcNHglycan | 63 | 66 | PF01048 | 0.727 |
MOD_GlcNHglycan | 631 | 634 | PF01048 | 0.449 |
MOD_GlcNHglycan | 660 | 663 | PF01048 | 0.657 |
MOD_GlcNHglycan | 683 | 686 | PF01048 | 0.635 |
MOD_GlcNHglycan | 687 | 690 | PF01048 | 0.466 |
MOD_GlcNHglycan | 86 | 89 | PF01048 | 0.786 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.731 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.659 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.600 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.370 |
MOD_GSK3_1 | 329 | 336 | PF00069 | 0.445 |
MOD_GSK3_1 | 421 | 428 | PF00069 | 0.624 |
MOD_GSK3_1 | 429 | 436 | PF00069 | 0.704 |
MOD_GSK3_1 | 475 | 482 | PF00069 | 0.721 |
MOD_GSK3_1 | 515 | 522 | PF00069 | 0.676 |
MOD_GSK3_1 | 545 | 552 | PF00069 | 0.636 |
MOD_GSK3_1 | 553 | 560 | PF00069 | 0.715 |
MOD_GSK3_1 | 576 | 583 | PF00069 | 0.773 |
MOD_GSK3_1 | 681 | 688 | PF00069 | 0.516 |
MOD_GSK3_1 | 703 | 710 | PF00069 | 0.361 |
MOD_GSK3_1 | 721 | 728 | PF00069 | 0.633 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.789 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.760 |
MOD_LATS_1 | 317 | 323 | PF00433 | 0.559 |
MOD_N-GLC_1 | 330 | 335 | PF02516 | 0.430 |
MOD_N-GLC_1 | 407 | 412 | PF02516 | 0.613 |
MOD_N-GLC_1 | 446 | 451 | PF02516 | 0.685 |
MOD_N-GLC_1 | 492 | 497 | PF02516 | 0.550 |
MOD_N-GLC_2 | 125 | 127 | PF02516 | 0.758 |
MOD_NEK2_1 | 185 | 190 | PF00069 | 0.490 |
MOD_NEK2_1 | 227 | 232 | PF00069 | 0.353 |
MOD_NEK2_1 | 233 | 238 | PF00069 | 0.322 |
MOD_NEK2_1 | 244 | 249 | PF00069 | 0.339 |
MOD_NEK2_1 | 294 | 299 | PF00069 | 0.502 |
MOD_NEK2_1 | 429 | 434 | PF00069 | 0.649 |
MOD_NEK2_1 | 492 | 497 | PF00069 | 0.705 |
MOD_NEK2_1 | 545 | 550 | PF00069 | 0.618 |
MOD_NEK2_1 | 59 | 64 | PF00069 | 0.562 |
MOD_NEK2_1 | 701 | 706 | PF00069 | 0.450 |
MOD_NEK2_1 | 725 | 730 | PF00069 | 0.583 |
MOD_OFUCOSY | 323 | 328 | PF10250 | 0.485 |
MOD_PIKK_1 | 421 | 427 | PF00454 | 0.621 |
MOD_PIKK_1 | 538 | 544 | PF00454 | 0.611 |
MOD_PIKK_1 | 606 | 612 | PF00454 | 0.388 |
MOD_PKA_2 | 114 | 120 | PF00069 | 0.757 |
MOD_PKA_2 | 294 | 300 | PF00069 | 0.494 |
MOD_PKA_2 | 360 | 366 | PF00069 | 0.506 |
MOD_PKA_2 | 468 | 474 | PF00069 | 0.766 |
MOD_PKA_2 | 546 | 552 | PF00069 | 0.644 |
MOD_PKA_2 | 701 | 707 | PF00069 | 0.537 |
MOD_PKA_2 | 718 | 724 | PF00069 | 0.599 |
MOD_Plk_1 | 330 | 336 | PF00069 | 0.429 |
MOD_Plk_1 | 4 | 10 | PF00069 | 0.762 |
MOD_Plk_1 | 446 | 452 | PF00069 | 0.685 |
MOD_Plk_1 | 518 | 524 | PF00069 | 0.689 |
MOD_Plk_4 | 132 | 138 | PF00069 | 0.758 |
MOD_Plk_4 | 475 | 481 | PF00069 | 0.616 |
MOD_Plk_4 | 707 | 713 | PF00069 | 0.504 |
MOD_Plk_4 | 721 | 727 | PF00069 | 0.529 |
MOD_ProDKin_1 | 11 | 17 | PF00069 | 0.732 |
MOD_ProDKin_1 | 144 | 150 | PF00069 | 0.731 |
MOD_ProDKin_1 | 350 | 356 | PF00069 | 0.443 |
MOD_ProDKin_1 | 407 | 413 | PF00069 | 0.619 |
MOD_ProDKin_1 | 430 | 436 | PF00069 | 0.662 |
MOD_ProDKin_1 | 451 | 457 | PF00069 | 0.694 |
MOD_ProDKin_1 | 554 | 560 | PF00069 | 0.715 |
MOD_ProDKin_1 | 563 | 569 | PF00069 | 0.717 |
MOD_ProDKin_1 | 616 | 622 | PF00069 | 0.445 |
MOD_ProDKin_1 | 88 | 94 | PF00069 | 0.800 |
TRG_DiLeu_BaLyEn_6 | 194 | 199 | PF01217 | 0.541 |
TRG_DiLeu_BaLyEn_6 | 619 | 624 | PF01217 | 0.424 |
TRG_ENDOCYTIC_2 | 133 | 136 | PF00928 | 0.679 |
TRG_ENDOCYTIC_2 | 184 | 187 | PF00928 | 0.402 |
TRG_ENDOCYTIC_2 | 386 | 389 | PF00928 | 0.415 |
TRG_ER_diArg_1 | 141 | 143 | PF00400 | 0.698 |
TRG_ER_diArg_1 | 345 | 348 | PF00400 | 0.445 |
TRG_ER_diArg_1 | 53 | 56 | PF00400 | 0.762 |
TRG_ER_diArg_1 | 613 | 616 | PF00400 | 0.577 |
TRG_ER_diArg_1 | 718 | 720 | PF00400 | 0.593 |
TRG_NES_CRM1_1 | 177 | 191 | PF08389 | 0.547 |
TRG_Pf-PMV_PEXEL_1 | 391 | 395 | PF00026 | 0.418 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P668 | Leptomonas seymouri | 52% | 96% |
A0A3Q8IPC3 | Leishmania donovani | 98% | 100% |
E9ATI2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |