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:0005634 | nucleus | 5 | 1 |
GO:0005737 | cytoplasm | 2 | 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 |
Related structures:
AlphaFold database: E9B3Z7
Term | Name | Level | Count |
---|---|---|---|
GO:0001522 | pseudouridine synthesis | 6 | 11 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 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:0009451 | RNA modification | 5 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016070 | RNA metabolic process | 5 | 11 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0043412 | macromolecule modification | 4 | 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 | 11 |
GO:0003723 | RNA binding | 4 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0009982 | pseudouridine synthase activity | 4 | 11 |
GO:0016853 | isomerase activity | 2 | 11 |
GO:0016866 | intramolecular transferase activity | 3 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 655 | 659 | PF00656 | 0.646 |
CLV_C14_Caspase3-7 | 881 | 885 | PF00656 | 0.609 |
CLV_MEL_PAP_1 | 863 | 869 | PF00089 | 0.476 |
CLV_NRD_NRD_1 | 217 | 219 | PF00675 | 0.522 |
CLV_NRD_NRD_1 | 277 | 279 | PF00675 | 0.677 |
CLV_NRD_NRD_1 | 375 | 377 | PF00675 | 0.476 |
CLV_NRD_NRD_1 | 606 | 608 | PF00675 | 0.558 |
CLV_NRD_NRD_1 | 635 | 637 | PF00675 | 0.411 |
CLV_NRD_NRD_1 | 723 | 725 | PF00675 | 0.690 |
CLV_PCSK_FUR_1 | 275 | 279 | PF00082 | 0.675 |
CLV_PCSK_KEX2_1 | 217 | 219 | PF00082 | 0.522 |
CLV_PCSK_KEX2_1 | 275 | 277 | PF00082 | 0.687 |
CLV_PCSK_KEX2_1 | 340 | 342 | PF00082 | 0.760 |
CLV_PCSK_KEX2_1 | 375 | 377 | PF00082 | 0.476 |
CLV_PCSK_KEX2_1 | 546 | 548 | PF00082 | 0.564 |
CLV_PCSK_KEX2_1 | 605 | 607 | PF00082 | 0.531 |
CLV_PCSK_KEX2_1 | 635 | 637 | PF00082 | 0.559 |
CLV_PCSK_KEX2_1 | 723 | 725 | PF00082 | 0.692 |
CLV_PCSK_KEX2_1 | 818 | 820 | PF00082 | 0.723 |
CLV_PCSK_PC1ET2_1 | 340 | 342 | PF00082 | 0.752 |
CLV_PCSK_PC1ET2_1 | 546 | 548 | PF00082 | 0.564 |
CLV_PCSK_PC1ET2_1 | 818 | 820 | PF00082 | 0.749 |
CLV_PCSK_SKI1_1 | 282 | 286 | PF00082 | 0.561 |
CLV_PCSK_SKI1_1 | 421 | 425 | PF00082 | 0.544 |
CLV_PCSK_SKI1_1 | 458 | 462 | PF00082 | 0.536 |
CLV_PCSK_SKI1_1 | 636 | 640 | PF00082 | 0.630 |
CLV_PCSK_SKI1_1 | 662 | 666 | PF00082 | 0.732 |
CLV_PCSK_SKI1_1 | 741 | 745 | PF00082 | 0.406 |
CLV_PCSK_SKI1_1 | 774 | 778 | PF00082 | 0.674 |
CLV_PCSK_SKI1_1 | 821 | 825 | PF00082 | 0.713 |
CLV_PCSK_SKI1_1 | 99 | 103 | PF00082 | 0.620 |
CLV_Separin_Metazoa | 72 | 76 | PF03568 | 0.735 |
DEG_APCC_DBOX_1 | 457 | 465 | PF00400 | 0.523 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.720 |
DEG_SIAH_1 | 808 | 816 | PF03145 | 0.700 |
DEG_SPOP_SBC_1 | 80 | 84 | PF00917 | 0.658 |
DOC_CDC14_PxL_1 | 70 | 78 | PF14671 | 0.736 |
DOC_CYCLIN_RxL_1 | 738 | 748 | PF00134 | 0.540 |
DOC_CYCLIN_yCln2_LP_2 | 671 | 677 | PF00134 | 0.549 |
DOC_MAPK_DCC_7 | 662 | 671 | PF00069 | 0.567 |
DOC_MAPK_MEF2A_6 | 445 | 452 | PF00069 | 0.407 |
DOC_MAPK_MEF2A_6 | 454 | 463 | PF00069 | 0.382 |
DOC_PP2B_LxvP_1 | 671 | 674 | PF13499 | 0.589 |
DOC_PP4_FxxP_1 | 346 | 349 | PF00568 | 0.679 |
DOC_PP4_FxxP_1 | 527 | 530 | PF00568 | 0.284 |
DOC_PP4_FxxP_1 | 761 | 764 | PF00568 | 0.574 |
DOC_PP4_FxxP_1 | 770 | 773 | PF00568 | 0.722 |
DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.701 |
DOC_USP7_MATH_1 | 150 | 154 | PF00917 | 0.488 |
DOC_USP7_MATH_1 | 247 | 251 | PF00917 | 0.601 |
DOC_USP7_MATH_1 | 252 | 256 | PF00917 | 0.463 |
DOC_USP7_MATH_1 | 330 | 334 | PF00917 | 0.748 |
DOC_USP7_MATH_1 | 39 | 43 | PF00917 | 0.700 |
DOC_USP7_MATH_1 | 443 | 447 | PF00917 | 0.357 |
DOC_USP7_MATH_1 | 565 | 569 | PF00917 | 0.663 |
DOC_USP7_MATH_1 | 656 | 660 | PF00917 | 0.742 |
DOC_USP7_MATH_1 | 762 | 766 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 776 | 780 | PF00917 | 0.593 |
DOC_USP7_MATH_1 | 803 | 807 | PF00917 | 0.600 |
DOC_USP7_MATH_1 | 837 | 841 | PF00917 | 0.643 |
DOC_USP7_MATH_1 | 865 | 869 | PF00917 | 0.497 |
DOC_USP7_MATH_2 | 311 | 317 | PF00917 | 0.603 |
DOC_WW_Pin1_4 | 234 | 239 | PF00397 | 0.719 |
DOC_WW_Pin1_4 | 339 | 344 | PF00397 | 0.680 |
DOC_WW_Pin1_4 | 360 | 365 | PF00397 | 0.514 |
DOC_WW_Pin1_4 | 41 | 46 | PF00397 | 0.676 |
DOC_WW_Pin1_4 | 453 | 458 | PF00397 | 0.546 |
DOC_WW_Pin1_4 | 481 | 486 | PF00397 | 0.649 |
DOC_WW_Pin1_4 | 520 | 525 | PF00397 | 0.419 |
DOC_WW_Pin1_4 | 882 | 887 | PF00397 | 0.432 |
LIG_14-3-3_CanoR_1 | 26 | 30 | PF00244 | 0.690 |
LIG_14-3-3_CanoR_1 | 286 | 293 | PF00244 | 0.412 |
LIG_14-3-3_CanoR_1 | 375 | 381 | PF00244 | 0.455 |
LIG_14-3-3_CanoR_1 | 662 | 667 | PF00244 | 0.590 |
LIG_14-3-3_CanoR_1 | 686 | 690 | PF00244 | 0.516 |
LIG_14-3-3_CanoR_1 | 723 | 733 | PF00244 | 0.672 |
LIG_14-3-3_CanoR_1 | 821 | 828 | PF00244 | 0.587 |
LIG_14-3-3_CanoR_1 | 866 | 870 | PF00244 | 0.532 |
LIG_Actin_WH2_2 | 163 | 179 | PF00022 | 0.455 |
LIG_Actin_WH2_2 | 869 | 885 | PF00022 | 0.559 |
LIG_BIR_III_4 | 469 | 473 | PF00653 | 0.531 |
LIG_BRCT_BRCA1_1 | 700 | 704 | PF00533 | 0.604 |
LIG_deltaCOP1_diTrp_1 | 589 | 596 | PF00928 | 0.488 |
LIG_DLG_GKlike_1 | 376 | 384 | PF00625 | 0.480 |
LIG_EVH1_1 | 131 | 135 | PF00568 | 0.736 |
LIG_FHA_1 | 173 | 179 | PF00498 | 0.486 |
LIG_FHA_1 | 286 | 292 | PF00498 | 0.486 |
LIG_FHA_1 | 454 | 460 | PF00498 | 0.521 |
LIG_FHA_1 | 535 | 541 | PF00498 | 0.477 |
LIG_FHA_1 | 8 | 14 | PF00498 | 0.653 |
LIG_FHA_1 | 822 | 828 | PF00498 | 0.661 |
LIG_FHA_2 | 307 | 313 | PF00498 | 0.521 |
LIG_FHA_2 | 707 | 713 | PF00498 | 0.413 |
LIG_FHA_2 | 786 | 792 | PF00498 | 0.406 |
LIG_FHA_2 | 98 | 104 | PF00498 | 0.675 |
LIG_HP1_1 | 457 | 461 | PF01393 | 0.531 |
LIG_LIR_Apic_2 | 44 | 50 | PF02991 | 0.715 |
LIG_LIR_Apic_2 | 760 | 764 | PF02991 | 0.569 |
LIG_LIR_Gen_1 | 614 | 625 | PF02991 | 0.403 |
LIG_LIR_LC3C_4 | 627 | 630 | PF02991 | 0.260 |
LIG_LIR_Nem_3 | 614 | 620 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 737 | 743 | PF02991 | 0.511 |
LIG_PDZ_Class_1 | 882 | 887 | PF00595 | 0.671 |
LIG_Pex14_1 | 757 | 761 | PF04695 | 0.549 |
LIG_REV1ctd_RIR_1 | 532 | 540 | PF16727 | 0.488 |
LIG_RPA_C_Fungi | 175 | 187 | PF08784 | 0.469 |
LIG_RPA_C_Fungi | 371 | 383 | PF08784 | 0.347 |
LIG_RPA_C_Fungi | 681 | 693 | PF08784 | 0.495 |
LIG_SH2_CRK | 490 | 494 | PF00017 | 0.382 |
LIG_SH2_NCK_1 | 549 | 553 | PF00017 | 0.480 |
LIG_SH2_NCK_1 | 679 | 683 | PF00017 | 0.529 |
LIG_SH2_PTP2 | 47 | 50 | PF00017 | 0.447 |
LIG_SH2_SRC | 47 | 50 | PF00017 | 0.736 |
LIG_SH2_SRC | 549 | 552 | PF00017 | 0.466 |
LIG_SH2_STAP1 | 264 | 268 | PF00017 | 0.405 |
LIG_SH2_STAP1 | 287 | 291 | PF00017 | 0.486 |
LIG_SH2_STAP1 | 490 | 494 | PF00017 | 0.382 |
LIG_SH2_STAP1 | 549 | 553 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 185 | 188 | PF00017 | 0.538 |
LIG_SH2_STAT5 | 227 | 230 | PF00017 | 0.663 |
LIG_SH2_STAT5 | 287 | 290 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 47 | 50 | PF00017 | 0.725 |
LIG_SH2_STAT5 | 521 | 524 | PF00017 | 0.513 |
LIG_SH2_STAT5 | 679 | 682 | PF00017 | 0.344 |
LIG_SH3_1 | 129 | 135 | PF00018 | 0.740 |
LIG_SH3_3 | 112 | 118 | PF00018 | 0.457 |
LIG_SH3_3 | 129 | 135 | PF00018 | 0.740 |
LIG_SH3_3 | 237 | 243 | PF00018 | 0.706 |
LIG_SH3_3 | 419 | 425 | PF00018 | 0.498 |
LIG_SH3_3 | 527 | 533 | PF00018 | 0.313 |
LIG_SH3_3 | 727 | 733 | PF00018 | 0.520 |
LIG_SH3_3 | 736 | 742 | PF00018 | 0.554 |
LIG_Sin3_3 | 212 | 219 | PF02671 | 0.446 |
LIG_SUMO_SIM_par_1 | 667 | 672 | PF11976 | 0.642 |
LIG_SUMO_SIM_par_1 | 694 | 699 | PF11976 | 0.580 |
LIG_SUMO_SIM_par_1 | 741 | 746 | PF11976 | 0.494 |
LIG_TYR_ITIM | 488 | 493 | PF00017 | 0.492 |
LIG_WRC_WIRS_1 | 106 | 111 | PF05994 | 0.637 |
LIG_WRC_WIRS_1 | 302 | 307 | PF05994 | 0.472 |
MOD_CDC14_SPxK_1 | 484 | 487 | PF00782 | 0.599 |
MOD_CDK_SPK_2 | 239 | 244 | PF00069 | 0.594 |
MOD_CDK_SPK_2 | 41 | 46 | PF00069 | 0.724 |
MOD_CDK_SPK_2 | 453 | 458 | PF00069 | 0.546 |
MOD_CDK_SPxK_1 | 481 | 487 | PF00069 | 0.631 |
MOD_CK1_1 | 105 | 111 | PF00069 | 0.646 |
MOD_CK1_1 | 355 | 361 | PF00069 | 0.555 |
MOD_CK1_1 | 362 | 368 | PF00069 | 0.564 |
MOD_CK1_1 | 779 | 785 | PF00069 | 0.563 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.723 |
MOD_CK1_1 | 847 | 853 | PF00069 | 0.487 |
MOD_CK2_1 | 119 | 125 | PF00069 | 0.491 |
MOD_CK2_1 | 306 | 312 | PF00069 | 0.608 |
MOD_CK2_1 | 348 | 354 | PF00069 | 0.636 |
MOD_CK2_1 | 66 | 72 | PF00069 | 0.795 |
MOD_CK2_1 | 699 | 705 | PF00069 | 0.597 |
MOD_CK2_1 | 757 | 763 | PF00069 | 0.520 |
MOD_CK2_1 | 97 | 103 | PF00069 | 0.650 |
MOD_CMANNOS | 592 | 595 | PF00535 | 0.512 |
MOD_Cter_Amidation | 633 | 636 | PF01082 | 0.392 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.765 |
MOD_GlcNHglycan | 188 | 191 | PF01048 | 0.585 |
MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.663 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.261 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.495 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.635 |
MOD_GlcNHglycan | 331 | 335 | PF01048 | 0.769 |
MOD_GlcNHglycan | 346 | 349 | PF01048 | 0.540 |
MOD_GlcNHglycan | 364 | 367 | PF01048 | 0.285 |
MOD_GlcNHglycan | 395 | 398 | PF01048 | 0.528 |
MOD_GlcNHglycan | 662 | 665 | PF01048 | 0.736 |
MOD_GlcNHglycan | 671 | 674 | PF01048 | 0.651 |
MOD_GlcNHglycan | 835 | 838 | PF01048 | 0.608 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.446 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.572 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.698 |
MOD_GSK3_1 | 355 | 362 | PF00069 | 0.542 |
MOD_GSK3_1 | 534 | 541 | PF00069 | 0.423 |
MOD_GSK3_1 | 656 | 663 | PF00069 | 0.757 |
MOD_GSK3_1 | 669 | 676 | PF00069 | 0.642 |
MOD_GSK3_1 | 833 | 840 | PF00069 | 0.543 |
MOD_GSK3_1 | 847 | 854 | PF00069 | 0.526 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.642 |
MOD_N-GLC_1 | 142 | 147 | PF02516 | 0.503 |
MOD_N-GLC_1 | 735 | 740 | PF02516 | 0.649 |
MOD_N-GLC_1 | 779 | 784 | PF02516 | 0.635 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.748 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.598 |
MOD_NEK2_1 | 113 | 118 | PF00069 | 0.588 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.582 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.590 |
MOD_NEK2_1 | 534 | 539 | PF00069 | 0.393 |
MOD_NEK2_1 | 81 | 86 | PF00069 | 0.620 |
MOD_NEK2_1 | 94 | 99 | PF00069 | 0.662 |
MOD_NEK2_2 | 685 | 690 | PF00069 | 0.480 |
MOD_NEK2_2 | 735 | 740 | PF00069 | 0.360 |
MOD_PIKK_1 | 113 | 119 | PF00454 | 0.753 |
MOD_PIKK_1 | 306 | 312 | PF00454 | 0.393 |
MOD_PIKK_1 | 425 | 431 | PF00454 | 0.595 |
MOD_PIKK_1 | 475 | 481 | PF00454 | 0.650 |
MOD_PIKK_1 | 677 | 683 | PF00454 | 0.467 |
MOD_PIKK_1 | 791 | 797 | PF00454 | 0.496 |
MOD_PKA_2 | 25 | 31 | PF00069 | 0.638 |
MOD_PKA_2 | 252 | 258 | PF00069 | 0.466 |
MOD_PKA_2 | 285 | 291 | PF00069 | 0.511 |
MOD_PKA_2 | 352 | 358 | PF00069 | 0.548 |
MOD_PKA_2 | 685 | 691 | PF00069 | 0.519 |
MOD_PKA_2 | 865 | 871 | PF00069 | 0.530 |
MOD_PKB_1 | 819 | 827 | PF00069 | 0.678 |
MOD_Plk_1 | 102 | 108 | PF00069 | 0.655 |
MOD_Plk_1 | 398 | 404 | PF00069 | 0.469 |
MOD_Plk_1 | 735 | 741 | PF00069 | 0.636 |
MOD_Plk_1 | 779 | 785 | PF00069 | 0.626 |
MOD_Plk_2-3 | 654 | 660 | PF00069 | 0.458 |
MOD_Plk_2-3 | 699 | 705 | PF00069 | 0.602 |
MOD_Plk_4 | 735 | 741 | PF00069 | 0.574 |
MOD_Plk_4 | 779 | 785 | PF00069 | 0.588 |
MOD_Plk_4 | 838 | 844 | PF00069 | 0.630 |
MOD_Plk_4 | 847 | 853 | PF00069 | 0.551 |
MOD_ProDKin_1 | 234 | 240 | PF00069 | 0.713 |
MOD_ProDKin_1 | 339 | 345 | PF00069 | 0.680 |
MOD_ProDKin_1 | 360 | 366 | PF00069 | 0.552 |
MOD_ProDKin_1 | 41 | 47 | PF00069 | 0.667 |
MOD_ProDKin_1 | 453 | 459 | PF00069 | 0.532 |
MOD_ProDKin_1 | 481 | 487 | PF00069 | 0.637 |
MOD_ProDKin_1 | 520 | 526 | PF00069 | 0.426 |
MOD_SUMO_rev_2 | 316 | 326 | PF00179 | 0.717 |
TRG_DiLeu_BaLyEn_6 | 739 | 744 | PF01217 | 0.527 |
TRG_ENDOCYTIC_2 | 490 | 493 | PF00928 | 0.382 |
TRG_ER_diArg_1 | 216 | 218 | PF00400 | 0.521 |
TRG_ER_diArg_1 | 275 | 278 | PF00400 | 0.678 |
TRG_ER_diArg_1 | 374 | 376 | PF00400 | 0.460 |
TRG_ER_diArg_1 | 604 | 607 | PF00400 | 0.527 |
TRG_ER_diArg_1 | 819 | 822 | PF00400 | 0.580 |
TRG_NES_CRM1_1 | 614 | 627 | PF08389 | 0.405 |
TRG_NLS_MonoExtN_4 | 815 | 822 | PF00514 | 0.698 |
TRG_Pf-PMV_PEXEL_1 | 129 | 133 | PF00026 | 0.744 |
TRG_Pf-PMV_PEXEL_1 | 160 | 164 | PF00026 | 0.515 |
TRG_Pf-PMV_PEXEL_1 | 184 | 188 | PF00026 | 0.437 |
TRG_Pf-PMV_PEXEL_1 | 445 | 449 | PF00026 | 0.531 |
TRG_Pf-PMV_PEXEL_1 | 741 | 746 | PF00026 | 0.549 |
TRG_Pf-PMV_PEXEL_1 | 821 | 825 | PF00026 | 0.681 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I0E0 | Leptomonas seymouri | 46% | 97% |
A0A1X0P134 | Trypanosomatidae | 26% | 100% |
A0A3Q8IEW6 | Leishmania donovani | 87% | 99% |
A0A3R7KAP3 | Trypanosoma rangeli | 29% | 100% |
A4HLM1 | Leishmania braziliensis | 76% | 100% |
A4I932 | Leishmania infantum | 87% | 99% |
D0A535 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
Q4Q427 | Leishmania major | 87% | 100% |
V5BLS1 | Trypanosoma cruzi | 29% | 100% |