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: E9ATI2
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 | 0.793 |
CLV_C14_Caspase3-7 | 657 | 661 | PF00656 | 0.753 |
CLV_NRD_NRD_1 | 487 | 489 | PF00675 | 0.739 |
CLV_PCSK_KEX2_1 | 278 | 280 | PF00082 | 0.534 |
CLV_PCSK_PC1ET2_1 | 278 | 280 | PF00082 | 0.534 |
CLV_PCSK_SKI1_1 | 279 | 283 | PF00082 | 0.503 |
CLV_PCSK_SKI1_1 | 622 | 626 | PF00082 | 0.432 |
CLV_PCSK_SKI1_1 | 734 | 738 | PF00082 | 0.408 |
CLV_PCSK_SKI1_1 | 80 | 84 | PF00082 | 0.566 |
DOC_CKS1_1 | 145 | 150 | PF01111 | 0.722 |
DOC_CYCLIN_RxL_1 | 663 | 673 | PF00134 | 0.633 |
DOC_CYCLIN_yClb3_PxF_3 | 144 | 150 | PF00134 | 0.493 |
DOC_CYCLIN_yCln2_LP_2 | 586 | 592 | PF00134 | 0.748 |
DOC_MAPK_DCC_7 | 503 | 512 | PF00069 | 0.744 |
DOC_MAPK_gen_1 | 278 | 284 | PF00069 | 0.513 |
DOC_PP2B_LxvP_1 | 235 | 238 | PF13499 | 0.535 |
DOC_PP2B_LxvP_1 | 409 | 412 | PF13499 | 0.689 |
DOC_PP2B_LxvP_1 | 440 | 443 | PF13499 | 0.763 |
DOC_PP2B_LxvP_1 | 586 | 589 | PF13499 | 0.759 |
DOC_PP4_FxxP_1 | 450 | 453 | PF00568 | 0.550 |
DOC_PP4_FxxP_1 | 692 | 695 | PF00568 | 0.494 |
DOC_PP4_FxxP_1 | 730 | 733 | PF00568 | 0.462 |
DOC_USP7_MATH_1 | 128 | 132 | PF00917 | 0.652 |
DOC_USP7_MATH_1 | 20 | 24 | PF00917 | 0.802 |
DOC_USP7_MATH_1 | 475 | 479 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 484 | 488 | PF00917 | 0.449 |
DOC_USP7_MATH_1 | 569 | 573 | PF00917 | 0.795 |
DOC_USP7_MATH_1 | 580 | 584 | PF00917 | 0.610 |
DOC_USP7_MATH_1 | 635 | 639 | PF00917 | 0.392 |
DOC_USP7_UBL2_3 | 364 | 368 | PF12436 | 0.514 |
DOC_WW_Pin1_4 | 144 | 149 | PF00397 | 0.737 |
DOC_WW_Pin1_4 | 18 | 23 | PF00397 | 0.705 |
DOC_WW_Pin1_4 | 350 | 355 | PF00397 | 0.452 |
DOC_WW_Pin1_4 | 407 | 412 | PF00397 | 0.539 |
DOC_WW_Pin1_4 | 430 | 435 | PF00397 | 0.657 |
DOC_WW_Pin1_4 | 451 | 456 | PF00397 | 0.664 |
DOC_WW_Pin1_4 | 554 | 559 | PF00397 | 0.709 |
DOC_WW_Pin1_4 | 563 | 568 | PF00397 | 0.710 |
DOC_WW_Pin1_4 | 616 | 621 | PF00397 | 0.442 |
DOC_WW_Pin1_4 | 88 | 93 | PF00397 | 0.776 |
LIG_14-3-3_CanoR_1 | 160 | 169 | PF00244 | 0.560 |
LIG_14-3-3_CanoR_1 | 295 | 301 | PF00244 | 0.481 |
LIG_14-3-3_CanoR_1 | 469 | 477 | PF00244 | 0.747 |
LIG_14-3-3_CanoR_1 | 561 | 567 | PF00244 | 0.793 |
LIG_14-3-3_CanoR_1 | 629 | 637 | PF00244 | 0.374 |
LIG_14-3-3_CanoR_1 | 702 | 712 | PF00244 | 0.456 |
LIG_14-3-3_CanoR_1 | 84 | 93 | PF00244 | 0.586 |
LIG_14-3-3_CterR_2 | 734 | 739 | PF00244 | 0.427 |
LIG_Actin_WH2_2 | 280 | 297 | PF00022 | 0.485 |
LIG_APCC_ABBAyCdc20_2 | 279 | 285 | PF00400 | 0.594 |
LIG_BRCT_BRCA1_1 | 296 | 300 | PF00533 | 0.607 |
LIG_BRCT_BRCA1_1 | 330 | 334 | PF00533 | 0.312 |
LIG_BRCT_BRCA1_1 | 446 | 450 | PF00533 | 0.574 |
LIG_BRCT_BRCA1_1 | 726 | 730 | PF00533 | 0.474 |
LIG_FHA_1 | 173 | 179 | PF00498 | 0.450 |
LIG_FHA_1 | 220 | 226 | PF00498 | 0.399 |
LIG_FHA_1 | 256 | 262 | PF00498 | 0.550 |
LIG_FHA_1 | 726 | 732 | PF00498 | 0.565 |
LIG_FHA_2 | 186 | 192 | PF00498 | 0.488 |
LIG_FHA_2 | 213 | 219 | PF00498 | 0.552 |
LIG_FHA_2 | 27 | 33 | PF00498 | 0.572 |
LIG_FHA_2 | 297 | 303 | PF00498 | 0.602 |
LIG_FHA_2 | 670 | 676 | PF00498 | 0.540 |
LIG_FHA_2 | 704 | 710 | PF00498 | 0.448 |
LIG_FHA_2 | 99 | 105 | PF00498 | 0.726 |
LIG_LIR_Apic_2 | 447 | 453 | PF02991 | 0.732 |
LIG_LIR_Apic_2 | 691 | 695 | PF02991 | 0.492 |
LIG_LIR_Apic_2 | 727 | 733 | PF02991 | 0.477 |
LIG_LIR_Gen_1 | 131 | 141 | PF02991 | 0.531 |
LIG_LIR_Gen_1 | 180 | 187 | PF02991 | 0.312 |
LIG_LIR_Gen_1 | 383 | 394 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 131 | 136 | PF02991 | 0.765 |
LIG_LIR_Nem_3 | 147 | 153 | PF02991 | 0.597 |
LIG_LIR_Nem_3 | 180 | 185 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 297 | 303 | PF02991 | 0.602 |
LIG_LIR_Nem_3 | 374 | 380 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 383 | 389 | PF02991 | 0.341 |
LIG_PCNA_PIPBox_1 | 203 | 212 | PF02747 | 0.564 |
LIG_PCNA_yPIPBox_3 | 197 | 210 | PF02747 | 0.550 |
LIG_PCNA_yPIPBox_3 | 364 | 376 | PF02747 | 0.457 |
LIG_RPA_C_Fungi | 336 | 348 | PF08784 | 0.551 |
LIG_SH2_CRK | 386 | 390 | PF00017 | 0.421 |
LIG_SH2_NCK_1 | 414 | 418 | PF00017 | 0.622 |
LIG_SH2_NCK_1 | 540 | 544 | PF00017 | 0.796 |
LIG_SH2_SRC | 414 | 417 | PF00017 | 0.625 |
LIG_SH2_SRC | 479 | 482 | PF00017 | 0.641 |
LIG_SH2_STAP1 | 133 | 137 | PF00017 | 0.533 |
LIG_SH2_STAP1 | 414 | 418 | PF00017 | 0.709 |
LIG_SH2_STAT5 | 184 | 187 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 201 | 204 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 386 | 389 | PF00017 | 0.422 |
LIG_SH2_STAT5 | 479 | 482 | PF00017 | 0.641 |
LIG_SH2_STAT5 | 540 | 543 | PF00017 | 0.800 |
LIG_SH3_1 | 143 | 149 | PF00018 | 0.728 |
LIG_SH3_3 | 142 | 148 | PF00018 | 0.701 |
LIG_SH3_3 | 150 | 156 | PF00018 | 0.595 |
LIG_SH3_3 | 19 | 25 | PF00018 | 0.588 |
LIG_SUMO_SIM_par_1 | 257 | 262 | PF11976 | 0.485 |
LIG_SUMO_SIM_par_1 | 93 | 99 | PF11976 | 0.579 |
LIG_SxIP_EBH_1 | 469 | 482 | PF03271 | 0.508 |
LIG_TRAF2_1 | 188 | 191 | PF00917 | 0.598 |
LIG_TRAF2_1 | 249 | 252 | PF00917 | 0.399 |
LIG_TRAF2_1 | 655 | 658 | PF00917 | 0.507 |
LIG_WRC_WIRS_1 | 133 | 138 | PF05994 | 0.765 |
LIG_WRC_WIRS_1 | 676 | 681 | PF05994 | 0.364 |
LIG_WW_1 | 411 | 414 | PF00397 | 0.624 |
MOD_CDC14_SPxK_1 | 619 | 622 | PF00782 | 0.428 |
MOD_CDK_SPxK_1 | 616 | 622 | PF00069 | 0.443 |
MOD_CDK_SPxxK_3 | 554 | 561 | PF00069 | 0.708 |
MOD_CK1_1 | 236 | 242 | PF00069 | 0.399 |
MOD_CK1_1 | 273 | 279 | PF00069 | 0.406 |
MOD_CK1_1 | 30 | 36 | PF00069 | 0.571 |
MOD_CK1_1 | 333 | 339 | PF00069 | 0.488 |
MOD_CK1_1 | 433 | 439 | PF00069 | 0.666 |
MOD_CK1_1 | 471 | 477 | PF00069 | 0.524 |
MOD_CK1_1 | 688 | 694 | PF00069 | 0.479 |
MOD_CK1_1 | 704 | 710 | PF00069 | 0.433 |
MOD_CK1_1 | 87 | 93 | PF00069 | 0.787 |
MOD_CK2_1 | 128 | 134 | PF00069 | 0.526 |
MOD_CK2_1 | 185 | 191 | PF00069 | 0.485 |
MOD_CK2_1 | 212 | 218 | PF00069 | 0.649 |
MOD_CK2_1 | 296 | 302 | PF00069 | 0.612 |
MOD_CK2_1 | 30 | 36 | PF00069 | 0.571 |
MOD_CK2_1 | 652 | 658 | PF00069 | 0.460 |
MOD_CK2_1 | 669 | 675 | PF00069 | 0.327 |
MOD_CK2_1 | 703 | 709 | PF00069 | 0.454 |
MOD_CK2_1 | 98 | 104 | PF00069 | 0.768 |
MOD_GlcNHglycan | 130 | 133 | PF01048 | 0.685 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.581 |
MOD_GlcNHglycan | 264 | 267 | PF01048 | 0.642 |
MOD_GlcNHglycan | 272 | 275 | PF01048 | 0.505 |
MOD_GlcNHglycan | 296 | 299 | PF01048 | 0.620 |
MOD_GlcNHglycan | 335 | 338 | PF01048 | 0.504 |
MOD_GlcNHglycan | 470 | 473 | PF01048 | 0.689 |
MOD_GlcNHglycan | 548 | 551 | PF01048 | 0.768 |
MOD_GlcNHglycan | 582 | 585 | PF01048 | 0.698 |
MOD_GlcNHglycan | 593 | 596 | PF01048 | 0.718 |
MOD_GlcNHglycan | 603 | 606 | PF01048 | 0.444 |
MOD_GlcNHglycan | 631 | 634 | PF01048 | 0.449 |
MOD_GlcNHglycan | 637 | 640 | PF01048 | 0.414 |
MOD_GlcNHglycan | 654 | 657 | PF01048 | 0.682 |
MOD_GlcNHglycan | 660 | 663 | PF01048 | 0.667 |
MOD_GlcNHglycan | 686 | 690 | PF01048 | 0.540 |
MOD_GlcNHglycan | 86 | 89 | PF01048 | 0.784 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.659 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.635 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.606 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.474 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.588 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.387 |
MOD_GSK3_1 | 421 | 428 | PF00069 | 0.645 |
MOD_GSK3_1 | 430 | 437 | PF00069 | 0.671 |
MOD_GSK3_1 | 471 | 478 | PF00069 | 0.653 |
MOD_GSK3_1 | 515 | 522 | PF00069 | 0.672 |
MOD_GSK3_1 | 546 | 553 | PF00069 | 0.715 |
MOD_GSK3_1 | 559 | 566 | PF00069 | 0.686 |
MOD_GSK3_1 | 681 | 688 | PF00069 | 0.498 |
MOD_GSK3_1 | 721 | 728 | PF00069 | 0.612 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.759 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.784 |
MOD_LATS_1 | 317 | 323 | PF00433 | 0.574 |
MOD_N-GLC_1 | 407 | 412 | PF02516 | 0.579 |
MOD_N-GLC_1 | 658 | 663 | PF02516 | 0.563 |
MOD_N-GLC_2 | 125 | 127 | PF02516 | 0.763 |
MOD_N-GLC_2 | 525 | 527 | PF02516 | 0.564 |
MOD_NEK2_1 | 185 | 190 | PF00069 | 0.500 |
MOD_NEK2_1 | 227 | 232 | PF00069 | 0.399 |
MOD_NEK2_1 | 233 | 238 | PF00069 | 0.399 |
MOD_NEK2_1 | 244 | 249 | PF00069 | 0.175 |
MOD_NEK2_1 | 270 | 275 | PF00069 | 0.431 |
MOD_NEK2_1 | 294 | 299 | PF00069 | 0.463 |
MOD_NEK2_1 | 318 | 323 | PF00069 | 0.376 |
MOD_NEK2_1 | 515 | 520 | PF00069 | 0.521 |
MOD_NEK2_1 | 545 | 550 | PF00069 | 0.650 |
MOD_NEK2_1 | 701 | 706 | PF00069 | 0.439 |
MOD_NEK2_1 | 725 | 730 | PF00069 | 0.567 |
MOD_NEK2_1 | 82 | 87 | PF00069 | 0.618 |
MOD_PIKK_1 | 186 | 192 | PF00454 | 0.341 |
MOD_PIKK_1 | 421 | 427 | PF00454 | 0.585 |
MOD_PIKK_1 | 538 | 544 | PF00454 | 0.708 |
MOD_PIKK_1 | 82 | 88 | PF00454 | 0.612 |
MOD_PKA_2 | 114 | 120 | PF00069 | 0.831 |
MOD_PKA_2 | 294 | 300 | PF00069 | 0.485 |
MOD_PKA_2 | 318 | 324 | PF00069 | 0.382 |
MOD_PKA_2 | 360 | 366 | PF00069 | 0.420 |
MOD_PKA_2 | 468 | 474 | PF00069 | 0.749 |
MOD_PKA_2 | 519 | 525 | PF00069 | 0.539 |
MOD_PKA_2 | 546 | 552 | PF00069 | 0.699 |
MOD_PKA_2 | 701 | 707 | PF00069 | 0.453 |
MOD_Plk_1 | 4 | 10 | PF00069 | 0.771 |
MOD_Plk_2-3 | 255 | 261 | PF00069 | 0.252 |
MOD_Plk_4 | 132 | 138 | PF00069 | 0.762 |
MOD_Plk_4 | 330 | 336 | PF00069 | 0.317 |
MOD_Plk_4 | 475 | 481 | PF00069 | 0.647 |
MOD_Plk_4 | 492 | 498 | PF00069 | 0.525 |
MOD_Plk_4 | 721 | 727 | PF00069 | 0.516 |
MOD_ProDKin_1 | 144 | 150 | PF00069 | 0.730 |
MOD_ProDKin_1 | 18 | 24 | PF00069 | 0.707 |
MOD_ProDKin_1 | 350 | 356 | PF00069 | 0.447 |
MOD_ProDKin_1 | 407 | 413 | PF00069 | 0.544 |
MOD_ProDKin_1 | 430 | 436 | PF00069 | 0.659 |
MOD_ProDKin_1 | 451 | 457 | PF00069 | 0.661 |
MOD_ProDKin_1 | 554 | 560 | PF00069 | 0.708 |
MOD_ProDKin_1 | 563 | 569 | PF00069 | 0.710 |
MOD_ProDKin_1 | 616 | 622 | PF00069 | 0.443 |
MOD_ProDKin_1 | 88 | 94 | PF00069 | 0.775 |
TRG_DiLeu_BaLyEn_6 | 194 | 199 | PF01217 | 0.555 |
TRG_DiLeu_BaLyEn_6 | 619 | 624 | PF01217 | 0.423 |
TRG_DiLeu_BaLyEn_6 | 731 | 736 | PF01217 | 0.430 |
TRG_ENDOCYTIC_2 | 133 | 136 | PF00928 | 0.682 |
TRG_ENDOCYTIC_2 | 184 | 187 | PF00928 | 0.461 |
TRG_ENDOCYTIC_2 | 386 | 389 | PF00928 | 0.422 |
TRG_ER_diArg_1 | 345 | 348 | PF00400 | 0.409 |
TRG_ER_diArg_1 | 53 | 56 | PF00400 | 0.771 |
TRG_ER_diArg_1 | 613 | 616 | PF00400 | 0.580 |
TRG_NES_CRM1_1 | 177 | 191 | PF08389 | 0.552 |
TRG_Pf-PMV_PEXEL_1 | 391 | 395 | PF00026 | 0.433 |
TRG_Pf-PMV_PEXEL_1 | 629 | 634 | PF00026 | 0.353 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P668 | Leptomonas seymouri | 51% | 96% |
A0A3Q8IPC3 | Leishmania donovani | 84% | 100% |
A4ICZ6 | Leishmania infantum | 84% | 100% |