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 | yes | yes: 1, no: 9 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: A4I8G2
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 |
GO:0006396 | RNA processing | 6 | 3 |
GO:0006399 | tRNA metabolic process | 7 | 3 |
GO:0008033 | tRNA processing | 8 | 3 |
GO:0034470 | ncRNA processing | 7 | 3 |
GO:0034660 | ncRNA metabolic process | 6 | 3 |
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 |
GO:0016829 | lyase activity | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 249 | 253 | PF00656 | 0.607 |
CLV_C14_Caspase3-7 | 398 | 402 | PF00656 | 0.591 |
CLV_MEL_PAP_1 | 153 | 159 | PF00089 | 0.321 |
CLV_NRD_NRD_1 | 344 | 346 | PF00675 | 0.526 |
CLV_NRD_NRD_1 | 353 | 355 | PF00675 | 0.668 |
CLV_NRD_NRD_1 | 369 | 371 | PF00675 | 0.373 |
CLV_NRD_NRD_1 | 377 | 379 | PF00675 | 0.403 |
CLV_NRD_NRD_1 | 416 | 418 | PF00675 | 0.694 |
CLV_NRD_NRD_1 | 426 | 428 | PF00675 | 0.622 |
CLV_NRD_NRD_1 | 460 | 462 | PF00675 | 0.341 |
CLV_NRD_NRD_1 | 579 | 581 | PF00675 | 0.290 |
CLV_NRD_NRD_1 | 857 | 859 | PF00675 | 0.441 |
CLV_NRD_NRD_1 | 892 | 894 | PF00675 | 0.532 |
CLV_PCSK_FUR_1 | 414 | 418 | PF00082 | 0.579 |
CLV_PCSK_KEX2_1 | 215 | 217 | PF00082 | 0.524 |
CLV_PCSK_KEX2_1 | 344 | 346 | PF00082 | 0.526 |
CLV_PCSK_KEX2_1 | 353 | 355 | PF00082 | 0.679 |
CLV_PCSK_KEX2_1 | 369 | 371 | PF00082 | 0.417 |
CLV_PCSK_KEX2_1 | 377 | 379 | PF00082 | 0.442 |
CLV_PCSK_KEX2_1 | 416 | 418 | PF00082 | 0.630 |
CLV_PCSK_KEX2_1 | 426 | 428 | PF00082 | 0.568 |
CLV_PCSK_KEX2_1 | 462 | 464 | PF00082 | 0.282 |
CLV_PCSK_KEX2_1 | 493 | 495 | PF00082 | 0.433 |
CLV_PCSK_KEX2_1 | 579 | 581 | PF00082 | 0.323 |
CLV_PCSK_KEX2_1 | 857 | 859 | PF00082 | 0.512 |
CLV_PCSK_KEX2_1 | 892 | 894 | PF00082 | 0.531 |
CLV_PCSK_PC1ET2_1 | 215 | 217 | PF00082 | 0.422 |
CLV_PCSK_PC1ET2_1 | 462 | 464 | PF00082 | 0.282 |
CLV_PCSK_PC1ET2_1 | 493 | 495 | PF00082 | 0.433 |
CLV_PCSK_SKI1_1 | 306 | 310 | PF00082 | 0.491 |
CLV_PCSK_SKI1_1 | 43 | 47 | PF00082 | 0.355 |
CLV_PCSK_SKI1_1 | 471 | 475 | PF00082 | 0.338 |
CLV_PCSK_SKI1_1 | 517 | 521 | PF00082 | 0.324 |
CLV_PCSK_SKI1_1 | 603 | 607 | PF00082 | 0.324 |
CLV_PCSK_SKI1_1 | 719 | 723 | PF00082 | 0.287 |
CLV_PCSK_SKI1_1 | 814 | 818 | PF00082 | 0.434 |
CLV_PCSK_SKI1_1 | 929 | 933 | PF00082 | 0.314 |
CLV_Separin_Metazoa | 374 | 378 | PF03568 | 0.417 |
DEG_APCC_DBOX_1 | 301 | 309 | PF00400 | 0.475 |
DEG_APCC_DBOX_1 | 813 | 821 | PF00400 | 0.399 |
DEG_MDM2_SWIB_1 | 643 | 651 | PF02201 | 0.338 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.343 |
DEG_ODPH_VHL_1 | 792 | 805 | PF01847 | 0.319 |
DEG_SPOP_SBC_1 | 779 | 783 | PF00917 | 0.582 |
DOC_CDC14_PxL_1 | 11 | 19 | PF14671 | 0.460 |
DOC_CKS1_1 | 10 | 15 | PF01111 | 0.462 |
DOC_CKS1_1 | 20 | 25 | PF01111 | 0.540 |
DOC_CKS1_1 | 38 | 43 | PF01111 | 0.470 |
DOC_CYCLIN_RxL_1 | 513 | 522 | PF00134 | 0.322 |
DOC_CYCLIN_yCln2_LP_2 | 110 | 113 | PF00134 | 0.532 |
DOC_CYCLIN_yCln2_LP_2 | 531 | 537 | PF00134 | 0.309 |
DOC_CYCLIN_yCln2_LP_2 | 822 | 828 | PF00134 | 0.398 |
DOC_MAPK_gen_1 | 215 | 225 | PF00069 | 0.357 |
DOC_MAPK_gen_1 | 491 | 498 | PF00069 | 0.427 |
DOC_MAPK_gen_1 | 857 | 864 | PF00069 | 0.405 |
DOC_MAPK_MEF2A_6 | 216 | 225 | PF00069 | 0.349 |
DOC_MAPK_MEF2A_6 | 909 | 916 | PF00069 | 0.304 |
DOC_MAPK_NFAT4_5 | 218 | 226 | PF00069 | 0.315 |
DOC_MAPK_NFAT4_5 | 909 | 917 | PF00069 | 0.301 |
DOC_PP1_RVXF_1 | 567 | 574 | PF00149 | 0.338 |
DOC_PP1_RVXF_1 | 842 | 849 | PF00149 | 0.394 |
DOC_PP2B_LxvP_1 | 110 | 113 | PF13499 | 0.532 |
DOC_PP4_FxxP_1 | 10 | 13 | PF00568 | 0.491 |
DOC_PP4_FxxP_1 | 916 | 919 | PF00568 | 0.358 |
DOC_USP7_MATH_1 | 131 | 135 | PF00917 | 0.407 |
DOC_USP7_MATH_1 | 177 | 181 | PF00917 | 0.525 |
DOC_USP7_MATH_1 | 18 | 22 | PF00917 | 0.579 |
DOC_USP7_MATH_1 | 195 | 199 | PF00917 | 0.454 |
DOC_USP7_MATH_1 | 356 | 360 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 361 | 365 | PF00917 | 0.584 |
DOC_USP7_MATH_1 | 412 | 416 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 537 | 541 | PF00917 | 0.334 |
DOC_USP7_MATH_1 | 547 | 551 | PF00917 | 0.475 |
DOC_USP7_MATH_1 | 650 | 654 | PF00917 | 0.365 |
DOC_USP7_MATH_1 | 700 | 704 | PF00917 | 0.324 |
DOC_USP7_MATH_1 | 736 | 740 | PF00917 | 0.338 |
DOC_USP7_MATH_1 | 766 | 770 | PF00917 | 0.757 |
DOC_USP7_MATH_1 | 774 | 778 | PF00917 | 0.676 |
DOC_USP7_MATH_1 | 779 | 783 | PF00917 | 0.614 |
DOC_USP7_MATH_1 | 78 | 82 | PF00917 | 0.502 |
DOC_USP7_MATH_1 | 816 | 820 | PF00917 | 0.536 |
DOC_USP7_MATH_2 | 184 | 190 | PF00917 | 0.485 |
DOC_WW_Pin1_4 | 118 | 123 | PF00397 | 0.581 |
DOC_WW_Pin1_4 | 137 | 142 | PF00397 | 0.378 |
DOC_WW_Pin1_4 | 16 | 21 | PF00397 | 0.527 |
DOC_WW_Pin1_4 | 37 | 42 | PF00397 | 0.483 |
DOC_WW_Pin1_4 | 437 | 442 | PF00397 | 0.646 |
DOC_WW_Pin1_4 | 581 | 586 | PF00397 | 0.335 |
DOC_WW_Pin1_4 | 9 | 14 | PF00397 | 0.451 |
LIG_14-3-3_CanoR_1 | 133 | 143 | PF00244 | 0.338 |
LIG_14-3-3_CanoR_1 | 283 | 287 | PF00244 | 0.388 |
LIG_14-3-3_CanoR_1 | 37 | 41 | PF00244 | 0.544 |
LIG_14-3-3_CanoR_1 | 494 | 499 | PF00244 | 0.414 |
LIG_14-3-3_CanoR_1 | 500 | 504 | PF00244 | 0.361 |
LIG_14-3-3_CanoR_1 | 517 | 526 | PF00244 | 0.293 |
LIG_14-3-3_CanoR_1 | 546 | 556 | PF00244 | 0.336 |
LIG_14-3-3_CanoR_1 | 626 | 634 | PF00244 | 0.365 |
LIG_14-3-3_CanoR_1 | 689 | 693 | PF00244 | 0.268 |
LIG_14-3-3_CanoR_1 | 847 | 854 | PF00244 | 0.426 |
LIG_14-3-3_CanoR_1 | 909 | 913 | PF00244 | 0.382 |
LIG_BIR_III_2 | 237 | 241 | PF00653 | 0.480 |
LIG_BIR_III_2 | 438 | 442 | PF00653 | 0.584 |
LIG_BRCT_BRCA1_1 | 157 | 161 | PF00533 | 0.355 |
LIG_BRCT_BRCA1_1 | 332 | 336 | PF00533 | 0.356 |
LIG_BRCT_BRCA1_1 | 738 | 742 | PF00533 | 0.282 |
LIG_deltaCOP1_diTrp_1 | 845 | 854 | PF00928 | 0.410 |
LIG_FHA_1 | 138 | 144 | PF00498 | 0.363 |
LIG_FHA_1 | 33 | 39 | PF00498 | 0.660 |
LIG_FHA_1 | 44 | 50 | PF00498 | 0.359 |
LIG_FHA_1 | 6 | 12 | PF00498 | 0.438 |
LIG_FHA_1 | 683 | 689 | PF00498 | 0.364 |
LIG_FHA_1 | 720 | 726 | PF00498 | 0.446 |
LIG_FHA_1 | 909 | 915 | PF00498 | 0.493 |
LIG_FHA_1 | 923 | 929 | PF00498 | 0.282 |
LIG_FHA_2 | 147 | 153 | PF00498 | 0.357 |
LIG_FHA_2 | 332 | 338 | PF00498 | 0.516 |
LIG_FHA_2 | 396 | 402 | PF00498 | 0.612 |
LIG_FHA_2 | 426 | 432 | PF00498 | 0.681 |
LIG_FHA_2 | 506 | 512 | PF00498 | 0.398 |
LIG_FHA_2 | 585 | 591 | PF00498 | 0.481 |
LIG_FHA_2 | 66 | 72 | PF00498 | 0.393 |
LIG_LIR_Apic_2 | 8 | 13 | PF02991 | 0.455 |
LIG_LIR_Apic_2 | 915 | 919 | PF02991 | 0.362 |
LIG_LIR_Gen_1 | 263 | 273 | PF02991 | 0.363 |
LIG_LIR_Gen_1 | 333 | 343 | PF02991 | 0.425 |
LIG_LIR_Gen_1 | 54 | 63 | PF02991 | 0.388 |
LIG_LIR_Gen_1 | 540 | 549 | PF02991 | 0.285 |
LIG_LIR_Gen_1 | 660 | 669 | PF02991 | 0.275 |
LIG_LIR_Gen_1 | 71 | 78 | PF02991 | 0.470 |
LIG_LIR_Gen_1 | 710 | 721 | PF02991 | 0.322 |
LIG_LIR_Gen_1 | 796 | 805 | PF02991 | 0.337 |
LIG_LIR_Gen_1 | 921 | 931 | PF02991 | 0.308 |
LIG_LIR_Nem_3 | 263 | 269 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 314 | 320 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 333 | 339 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 476 | 480 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 54 | 59 | PF02991 | 0.383 |
LIG_LIR_Nem_3 | 540 | 544 | PF02991 | 0.285 |
LIG_LIR_Nem_3 | 560 | 566 | PF02991 | 0.351 |
LIG_LIR_Nem_3 | 615 | 621 | PF02991 | 0.293 |
LIG_LIR_Nem_3 | 660 | 665 | PF02991 | 0.275 |
LIG_LIR_Nem_3 | 691 | 695 | PF02991 | 0.365 |
LIG_LIR_Nem_3 | 71 | 76 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 710 | 716 | PF02991 | 0.203 |
LIG_LIR_Nem_3 | 739 | 744 | PF02991 | 0.324 |
LIG_LIR_Nem_3 | 796 | 800 | PF02991 | 0.376 |
LIG_LIR_Nem_3 | 867 | 871 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 921 | 926 | PF02991 | 0.317 |
LIG_LYPXL_S_1 | 379 | 383 | PF13949 | 0.419 |
LIG_LYPXL_yS_3 | 380 | 383 | PF13949 | 0.357 |
LIG_MLH1_MIPbox_1 | 738 | 742 | PF16413 | 0.338 |
LIG_MYND_1 | 113 | 117 | PF01753 | 0.527 |
LIG_NRBOX | 165 | 171 | PF00104 | 0.325 |
LIG_NRBOX | 304 | 310 | PF00104 | 0.432 |
LIG_Pex14_2 | 618 | 622 | PF04695 | 0.282 |
LIG_Pex14_2 | 643 | 647 | PF04695 | 0.338 |
LIG_SH2_CRK | 541 | 545 | PF00017 | 0.338 |
LIG_SH2_CRK | 73 | 77 | PF00017 | 0.454 |
LIG_SH2_CRK | 797 | 801 | PF00017 | 0.439 |
LIG_SH2_CRK | 923 | 927 | PF00017 | 0.300 |
LIG_SH2_NCK_1 | 923 | 927 | PF00017 | 0.313 |
LIG_SH2_PTP2 | 455 | 458 | PF00017 | 0.324 |
LIG_SH2_SRC | 455 | 458 | PF00017 | 0.324 |
LIG_SH2_STAP1 | 541 | 545 | PF00017 | 0.338 |
LIG_SH2_STAP1 | 797 | 801 | PF00017 | 0.313 |
LIG_SH2_STAP1 | 923 | 927 | PF00017 | 0.344 |
LIG_SH2_STAT3 | 621 | 624 | PF00017 | 0.282 |
LIG_SH2_STAT5 | 266 | 269 | PF00017 | 0.433 |
LIG_SH2_STAT5 | 455 | 458 | PF00017 | 0.394 |
LIG_SH2_STAT5 | 477 | 480 | PF00017 | 0.338 |
LIG_SH2_STAT5 | 621 | 624 | PF00017 | 0.324 |
LIG_SH2_STAT5 | 695 | 698 | PF00017 | 0.373 |
LIG_SH2_STAT5 | 728 | 731 | PF00017 | 0.350 |
LIG_SH2_STAT5 | 748 | 751 | PF00017 | 0.205 |
LIG_SH3_1 | 345 | 351 | PF00018 | 0.487 |
LIG_SH3_2 | 348 | 353 | PF14604 | 0.477 |
LIG_SH3_3 | 10 | 16 | PF00018 | 0.472 |
LIG_SH3_3 | 110 | 116 | PF00018 | 0.580 |
LIG_SH3_3 | 17 | 23 | PF00018 | 0.539 |
LIG_SH3_3 | 236 | 242 | PF00018 | 0.617 |
LIG_SH3_3 | 345 | 351 | PF00018 | 0.544 |
LIG_SH3_3 | 35 | 41 | PF00018 | 0.514 |
LIG_SH3_3 | 531 | 537 | PF00018 | 0.309 |
LIG_SH3_3 | 788 | 794 | PF00018 | 0.526 |
LIG_SH3_3 | 800 | 806 | PF00018 | 0.465 |
LIG_SH3_3 | 859 | 865 | PF00018 | 0.374 |
LIG_SH3_3 | 869 | 875 | PF00018 | 0.371 |
LIG_SH3_3 | 98 | 104 | PF00018 | 0.540 |
LIG_SUMO_SIM_par_1 | 57 | 62 | PF11976 | 0.383 |
LIG_TRAF2_1 | 291 | 294 | PF00917 | 0.422 |
LIG_TRFH_1 | 916 | 920 | PF08558 | 0.418 |
LIG_TYR_ITIM | 795 | 800 | PF00017 | 0.321 |
LIG_WW_2 | 239 | 242 | PF00397 | 0.508 |
MOD_CDK_SPxK_1 | 37 | 43 | PF00069 | 0.469 |
MOD_CK1_1 | 134 | 140 | PF00069 | 0.457 |
MOD_CK1_1 | 159 | 165 | PF00069 | 0.374 |
MOD_CK1_1 | 189 | 195 | PF00069 | 0.570 |
MOD_CK1_1 | 19 | 25 | PF00069 | 0.621 |
MOD_CK1_1 | 256 | 262 | PF00069 | 0.487 |
MOD_CK1_1 | 311 | 317 | PF00069 | 0.539 |
MOD_CK1_1 | 335 | 341 | PF00069 | 0.486 |
MOD_CK1_1 | 440 | 446 | PF00069 | 0.694 |
MOD_CK1_1 | 548 | 554 | PF00069 | 0.325 |
MOD_CK1_1 | 584 | 590 | PF00069 | 0.290 |
MOD_CK1_1 | 675 | 681 | PF00069 | 0.330 |
MOD_CK1_1 | 77 | 83 | PF00069 | 0.651 |
MOD_CK1_1 | 782 | 788 | PF00069 | 0.794 |
MOD_CK1_1 | 85 | 91 | PF00069 | 0.608 |
MOD_CK1_1 | 896 | 902 | PF00069 | 0.490 |
MOD_CK2_1 | 146 | 152 | PF00069 | 0.511 |
MOD_CK2_1 | 335 | 341 | PF00069 | 0.506 |
MOD_CK2_1 | 425 | 431 | PF00069 | 0.613 |
MOD_CK2_1 | 505 | 511 | PF00069 | 0.398 |
MOD_CK2_1 | 584 | 590 | PF00069 | 0.463 |
MOD_CK2_1 | 783 | 789 | PF00069 | 0.601 |
MOD_CK2_1 | 99 | 105 | PF00069 | 0.575 |
MOD_CMANNOS | 831 | 834 | PF00535 | 0.417 |
MOD_DYRK1A_RPxSP_1 | 37 | 41 | PF00069 | 0.493 |
MOD_GlcNHglycan | 101 | 104 | PF01048 | 0.654 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.431 |
MOD_GlcNHglycan | 23 | 26 | PF01048 | 0.626 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.618 |
MOD_GlcNHglycan | 30 | 33 | PF01048 | 0.679 |
MOD_GlcNHglycan | 442 | 445 | PF01048 | 0.672 |
MOD_GlcNHglycan | 449 | 452 | PF01048 | 0.349 |
MOD_GlcNHglycan | 547 | 550 | PF01048 | 0.290 |
MOD_GlcNHglycan | 559 | 562 | PF01048 | 0.289 |
MOD_GlcNHglycan | 702 | 705 | PF01048 | 0.324 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.568 |
MOD_GlcNHglycan | 767 | 771 | PF01048 | 0.705 |
MOD_GlcNHglycan | 776 | 779 | PF01048 | 0.616 |
MOD_GlcNHglycan | 782 | 785 | PF01048 | 0.547 |
MOD_GlcNHglycan | 826 | 829 | PF01048 | 0.490 |
MOD_GlcNHglycan | 849 | 852 | PF01048 | 0.459 |
MOD_GlcNHglycan | 895 | 898 | PF01048 | 0.646 |
MOD_GlcNHglycan | 901 | 905 | PF01048 | 0.608 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.358 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.658 |
MOD_GSK3_1 | 331 | 338 | PF00069 | 0.484 |
MOD_GSK3_1 | 443 | 450 | PF00069 | 0.574 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.429 |
MOD_GSK3_1 | 61 | 68 | PF00069 | 0.369 |
MOD_GSK3_1 | 707 | 714 | PF00069 | 0.340 |
MOD_GSK3_1 | 74 | 81 | PF00069 | 0.448 |
MOD_GSK3_1 | 744 | 751 | PF00069 | 0.427 |
MOD_GSK3_1 | 774 | 781 | PF00069 | 0.674 |
MOD_GSK3_1 | 816 | 823 | PF00069 | 0.587 |
MOD_GSK3_1 | 896 | 903 | PF00069 | 0.620 |
MOD_GSK3_1 | 908 | 915 | PF00069 | 0.446 |
MOD_GSK3_1 | 918 | 925 | PF00069 | 0.362 |
MOD_N-GLC_1 | 253 | 258 | PF02516 | 0.445 |
MOD_N-GLC_1 | 403 | 408 | PF02516 | 0.618 |
MOD_N-GLC_1 | 707 | 712 | PF02516 | 0.290 |
MOD_NEK2_1 | 132 | 137 | PF00069 | 0.368 |
MOD_NEK2_1 | 269 | 274 | PF00069 | 0.310 |
MOD_NEK2_1 | 331 | 336 | PF00069 | 0.451 |
MOD_NEK2_1 | 545 | 550 | PF00069 | 0.284 |
MOD_NEK2_1 | 627 | 632 | PF00069 | 0.375 |
MOD_NEK2_1 | 673 | 678 | PF00069 | 0.480 |
MOD_NEK2_1 | 688 | 693 | PF00069 | 0.279 |
MOD_NEK2_1 | 744 | 749 | PF00069 | 0.381 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.452 |
MOD_NEK2_1 | 846 | 851 | PF00069 | 0.433 |
MOD_NEK2_1 | 912 | 917 | PF00069 | 0.326 |
MOD_NEK2_2 | 390 | 395 | PF00069 | 0.589 |
MOD_NEK2_2 | 650 | 655 | PF00069 | 0.339 |
MOD_NEK2_2 | 736 | 741 | PF00069 | 0.338 |
MOD_NEK2_2 | 816 | 821 | PF00069 | 0.406 |
MOD_NEK2_2 | 922 | 927 | PF00069 | 0.336 |
MOD_PIKK_1 | 159 | 165 | PF00454 | 0.374 |
MOD_PIKK_1 | 887 | 893 | PF00454 | 0.456 |
MOD_PK_1 | 481 | 487 | PF00069 | 0.291 |
MOD_PK_1 | 494 | 500 | PF00069 | 0.264 |
MOD_PKA_2 | 132 | 138 | PF00069 | 0.343 |
MOD_PKA_2 | 155 | 161 | PF00069 | 0.362 |
MOD_PKA_2 | 28 | 34 | PF00069 | 0.587 |
MOD_PKA_2 | 282 | 288 | PF00069 | 0.400 |
MOD_PKA_2 | 36 | 42 | PF00069 | 0.508 |
MOD_PKA_2 | 425 | 431 | PF00069 | 0.594 |
MOD_PKA_2 | 499 | 505 | PF00069 | 0.317 |
MOD_PKA_2 | 545 | 551 | PF00069 | 0.336 |
MOD_PKA_2 | 625 | 631 | PF00069 | 0.338 |
MOD_PKA_2 | 688 | 694 | PF00069 | 0.289 |
MOD_PKA_2 | 846 | 852 | PF00069 | 0.427 |
MOD_PKA_2 | 873 | 879 | PF00069 | 0.462 |
MOD_PKA_2 | 908 | 914 | PF00069 | 0.422 |
MOD_Plk_1 | 253 | 259 | PF00069 | 0.433 |
MOD_Plk_1 | 293 | 299 | PF00069 | 0.520 |
MOD_Plk_1 | 403 | 409 | PF00069 | 0.603 |
MOD_Plk_1 | 481 | 487 | PF00069 | 0.273 |
MOD_Plk_1 | 876 | 882 | PF00069 | 0.485 |
MOD_Plk_4 | 164 | 170 | PF00069 | 0.319 |
MOD_Plk_4 | 253 | 259 | PF00069 | 0.504 |
MOD_Plk_4 | 736 | 742 | PF00069 | 0.324 |
MOD_Plk_4 | 744 | 750 | PF00069 | 0.324 |
MOD_Plk_4 | 922 | 928 | PF00069 | 0.368 |
MOD_ProDKin_1 | 118 | 124 | PF00069 | 0.576 |
MOD_ProDKin_1 | 137 | 143 | PF00069 | 0.371 |
MOD_ProDKin_1 | 16 | 22 | PF00069 | 0.531 |
MOD_ProDKin_1 | 37 | 43 | PF00069 | 0.472 |
MOD_ProDKin_1 | 437 | 443 | PF00069 | 0.646 |
MOD_ProDKin_1 | 581 | 587 | PF00069 | 0.335 |
MOD_ProDKin_1 | 9 | 15 | PF00069 | 0.457 |
TRG_DiLeu_BaEn_1 | 304 | 309 | PF01217 | 0.425 |
TRG_DiLeu_BaEn_1 | 469 | 474 | PF01217 | 0.282 |
TRG_DiLeu_BaEn_3 | 600 | 606 | PF01217 | 0.273 |
TRG_DiLeu_BaEn_4 | 597 | 603 | PF01217 | 0.245 |
TRG_ENDOCYTIC_2 | 266 | 269 | PF00928 | 0.368 |
TRG_ENDOCYTIC_2 | 380 | 383 | PF00928 | 0.357 |
TRG_ENDOCYTIC_2 | 455 | 458 | PF00928 | 0.427 |
TRG_ENDOCYTIC_2 | 477 | 480 | PF00928 | 0.338 |
TRG_ENDOCYTIC_2 | 541 | 544 | PF00928 | 0.284 |
TRG_ENDOCYTIC_2 | 662 | 665 | PF00928 | 0.282 |
TRG_ENDOCYTIC_2 | 73 | 76 | PF00928 | 0.409 |
TRG_ENDOCYTIC_2 | 797 | 800 | PF00928 | 0.423 |
TRG_ENDOCYTIC_2 | 923 | 926 | PF00928 | 0.303 |
TRG_ER_diArg_1 | 320 | 323 | PF00400 | 0.534 |
TRG_ER_diArg_1 | 343 | 345 | PF00400 | 0.500 |
TRG_ER_diArg_1 | 353 | 355 | PF00400 | 0.633 |
TRG_ER_diArg_1 | 368 | 370 | PF00400 | 0.366 |
TRG_ER_diArg_1 | 376 | 378 | PF00400 | 0.382 |
TRG_ER_diArg_1 | 414 | 417 | PF00400 | 0.643 |
TRG_ER_diArg_1 | 426 | 429 | PF00400 | 0.553 |
TRG_ER_diArg_1 | 460 | 463 | PF00400 | 0.338 |
TRG_ER_diArg_1 | 566 | 569 | PF00400 | 0.338 |
TRG_ER_diArg_1 | 579 | 581 | PF00400 | 0.338 |
TRG_ER_diArg_1 | 857 | 859 | PF00400 | 0.512 |
TRG_ER_diArg_1 | 892 | 894 | PF00400 | 0.488 |
TRG_NES_CRM1_1 | 469 | 482 | PF08389 | 0.338 |
TRG_NLS_MonoExtC_3 | 460 | 466 | PF00514 | 0.282 |
TRG_Pf-PMV_PEXEL_1 | 295 | 299 | PF00026 | 0.493 |
TRG_Pf-PMV_PEXEL_1 | 471 | 476 | PF00026 | 0.282 |
TRG_Pf-PMV_PEXEL_1 | 517 | 522 | PF00026 | 0.288 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4F4 | Leptomonas seymouri | 48% | 98% |
A0A3Q8IJ87 | Leishmania donovani | 22% | 100% |
A0A3S7X658 | Leishmania donovani | 100% | 100% |
A4HKY3 | Leishmania braziliensis | 74% | 99% |
A4IDY9 | Leishmania infantum | 22% | 100% |
D0AAQ9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
E9B3C1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q4Q0I6 | Leishmania major | 23% | 100% |
Q4Q4T4 | Leishmania major | 92% | 99% |