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:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3S7WWH4
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 5 |
GO:0006793 | phosphorus metabolic process | 3 | 5 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 5 |
GO:0006807 | nitrogen compound metabolic process | 2 | 5 |
GO:0008152 | metabolic process | 1 | 5 |
GO:0009987 | cellular process | 1 | 5 |
GO:0016310 | phosphorylation | 5 | 5 |
GO:0019538 | protein metabolic process | 3 | 5 |
GO:0036211 | protein modification process | 4 | 5 |
GO:0043170 | macromolecule metabolic process | 3 | 5 |
GO:0043412 | macromolecule modification | 4 | 5 |
GO:0044237 | cellular metabolic process | 2 | 5 |
GO:0044238 | primary metabolic process | 2 | 5 |
GO:0071704 | organic substance metabolic process | 2 | 5 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 5 |
GO:0003824 | catalytic activity | 1 | 5 |
GO:0004672 | protein kinase activity | 3 | 5 |
GO:0005488 | binding | 1 | 5 |
GO:0005524 | ATP binding | 5 | 5 |
GO:0016301 | kinase activity | 4 | 5 |
GO:0016740 | transferase activity | 2 | 5 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 5 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 5 |
GO:0017076 | purine nucleotide binding | 4 | 5 |
GO:0030554 | adenyl nucleotide binding | 5 | 5 |
GO:0032553 | ribonucleotide binding | 3 | 5 |
GO:0032555 | purine ribonucleotide binding | 4 | 5 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 5 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 5 |
GO:0036094 | small molecule binding | 2 | 5 |
GO:0043167 | ion binding | 2 | 5 |
GO:0043168 | anion binding | 3 | 5 |
GO:0097159 | organic cyclic compound binding | 2 | 5 |
GO:0097367 | carbohydrate derivative binding | 2 | 5 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 5 |
GO:1901265 | nucleoside phosphate binding | 3 | 5 |
GO:1901363 | heterocyclic compound binding | 2 | 5 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 127 | 129 | PF00675 | 0.506 |
CLV_NRD_NRD_1 | 207 | 209 | PF00675 | 0.373 |
CLV_NRD_NRD_1 | 301 | 303 | PF00675 | 0.461 |
CLV_NRD_NRD_1 | 84 | 86 | PF00675 | 0.432 |
CLV_NRD_NRD_1 | 844 | 846 | PF00675 | 0.639 |
CLV_PCSK_KEX2_1 | 127 | 129 | PF00082 | 0.495 |
CLV_PCSK_KEX2_1 | 207 | 209 | PF00082 | 0.373 |
CLV_PCSK_KEX2_1 | 84 | 86 | PF00082 | 0.335 |
CLV_PCSK_KEX2_1 | 844 | 846 | PF00082 | 0.744 |
CLV_PCSK_PC7_1 | 80 | 86 | PF00082 | 0.301 |
CLV_PCSK_SKI1_1 | 118 | 122 | PF00082 | 0.412 |
CLV_PCSK_SKI1_1 | 317 | 321 | PF00082 | 0.283 |
CLV_PCSK_SKI1_1 | 428 | 432 | PF00082 | 0.440 |
CLV_PCSK_SKI1_1 | 533 | 537 | PF00082 | 0.345 |
CLV_PCSK_SKI1_1 | 84 | 88 | PF00082 | 0.339 |
CLV_Separin_Metazoa | 367 | 371 | PF03568 | 0.338 |
DEG_APCC_DBOX_1 | 354 | 362 | PF00400 | 0.426 |
DEG_SCF_FBW7_1 | 683 | 690 | PF00400 | 0.622 |
DEG_SIAH_1 | 686 | 694 | PF03145 | 0.542 |
DEG_SPOP_SBC_1 | 626 | 630 | PF00917 | 0.723 |
DEG_SPOP_SBC_1 | 674 | 678 | PF00917 | 0.583 |
DOC_CKS1_1 | 18 | 23 | PF01111 | 0.461 |
DOC_CKS1_1 | 294 | 299 | PF01111 | 0.465 |
DOC_CKS1_1 | 409 | 414 | PF01111 | 0.397 |
DOC_CKS1_1 | 692 | 697 | PF01111 | 0.587 |
DOC_CYCLIN_RxL_1 | 3 | 13 | PF00134 | 0.501 |
DOC_CYCLIN_RxL_1 | 425 | 435 | PF00134 | 0.323 |
DOC_MAPK_gen_1 | 207 | 213 | PF00069 | 0.418 |
DOC_MAPK_gen_1 | 426 | 433 | PF00069 | 0.430 |
DOC_MAPK_gen_1 | 84 | 91 | PF00069 | 0.337 |
DOC_MAPK_MEF2A_6 | 426 | 433 | PF00069 | 0.413 |
DOC_MAPK_MEF2A_6 | 504 | 513 | PF00069 | 0.294 |
DOC_MAPK_NFAT4_5 | 426 | 434 | PF00069 | 0.324 |
DOC_MAPK_RevD_3 | 113 | 128 | PF00069 | 0.339 |
DOC_PP2B_LxvP_1 | 796 | 799 | PF13499 | 0.602 |
DOC_PP2B_LxvP_1 | 89 | 92 | PF13499 | 0.347 |
DOC_PP4_FxxP_1 | 360 | 363 | PF00568 | 0.364 |
DOC_USP7_MATH_1 | 155 | 159 | PF00917 | 0.444 |
DOC_USP7_MATH_1 | 373 | 377 | PF00917 | 0.437 |
DOC_USP7_MATH_1 | 477 | 481 | PF00917 | 0.483 |
DOC_USP7_MATH_1 | 547 | 551 | PF00917 | 0.308 |
DOC_USP7_MATH_1 | 620 | 624 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 66 | 70 | PF00917 | 0.530 |
DOC_USP7_MATH_1 | 674 | 678 | PF00917 | 0.667 |
DOC_USP7_MATH_1 | 699 | 703 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 717 | 721 | PF00917 | 0.585 |
DOC_USP7_MATH_1 | 776 | 780 | PF00917 | 0.632 |
DOC_USP7_MATH_1 | 799 | 803 | PF00917 | 0.693 |
DOC_USP7_MATH_2 | 218 | 224 | PF00917 | 0.463 |
DOC_USP7_UBL2_3 | 842 | 846 | PF12436 | 0.579 |
DOC_WW_Pin1_4 | 17 | 22 | PF00397 | 0.441 |
DOC_WW_Pin1_4 | 195 | 200 | PF00397 | 0.586 |
DOC_WW_Pin1_4 | 293 | 298 | PF00397 | 0.471 |
DOC_WW_Pin1_4 | 30 | 35 | PF00397 | 0.408 |
DOC_WW_Pin1_4 | 408 | 413 | PF00397 | 0.415 |
DOC_WW_Pin1_4 | 516 | 521 | PF00397 | 0.484 |
DOC_WW_Pin1_4 | 569 | 574 | PF00397 | 0.461 |
DOC_WW_Pin1_4 | 628 | 633 | PF00397 | 0.608 |
DOC_WW_Pin1_4 | 678 | 683 | PF00397 | 0.766 |
DOC_WW_Pin1_4 | 691 | 696 | PF00397 | 0.585 |
DOC_WW_Pin1_4 | 765 | 770 | PF00397 | 0.725 |
DOC_WW_Pin1_4 | 786 | 791 | PF00397 | 0.642 |
LIG_14-3-3_CanoR_1 | 262 | 267 | PF00244 | 0.517 |
LIG_14-3-3_CanoR_1 | 28 | 34 | PF00244 | 0.434 |
LIG_14-3-3_CanoR_1 | 280 | 284 | PF00244 | 0.360 |
LIG_14-3-3_CanoR_1 | 35 | 41 | PF00244 | 0.523 |
LIG_14-3-3_CanoR_1 | 80 | 84 | PF00244 | 0.343 |
LIG_14-3-3_CanoR_1 | 85 | 90 | PF00244 | 0.322 |
LIG_Actin_WH2_2 | 263 | 278 | PF00022 | 0.491 |
LIG_Actin_WH2_2 | 379 | 397 | PF00022 | 0.475 |
LIG_Actin_WH2_2 | 522 | 539 | PF00022 | 0.505 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.454 |
LIG_BIR_III_4 | 239 | 243 | PF00653 | 0.356 |
LIG_BRCT_BRCA1_1 | 733 | 737 | PF00533 | 0.640 |
LIG_BRCT_BRCA1_2 | 733 | 739 | PF00533 | 0.639 |
LIG_Clathr_ClatBox_1 | 182 | 186 | PF01394 | 0.272 |
LIG_Clathr_ClatBox_1 | 330 | 334 | PF01394 | 0.417 |
LIG_Clathr_ClatBox_1 | 430 | 434 | PF01394 | 0.333 |
LIG_CtBP_PxDLS_1 | 218 | 222 | PF00389 | 0.485 |
LIG_eIF4E_1 | 409 | 415 | PF01652 | 0.339 |
LIG_eIF4E_1 | 467 | 473 | PF01652 | 0.345 |
LIG_FHA_1 | 104 | 110 | PF00498 | 0.334 |
LIG_FHA_1 | 248 | 254 | PF00498 | 0.413 |
LIG_FHA_1 | 409 | 415 | PF00498 | 0.395 |
LIG_FHA_1 | 506 | 512 | PF00498 | 0.288 |
LIG_FHA_1 | 55 | 61 | PF00498 | 0.409 |
LIG_FHA_1 | 583 | 589 | PF00498 | 0.521 |
LIG_FHA_1 | 778 | 784 | PF00498 | 0.680 |
LIG_FHA_1 | 827 | 833 | PF00498 | 0.718 |
LIG_FHA_2 | 252 | 258 | PF00498 | 0.458 |
LIG_FHA_2 | 42 | 48 | PF00498 | 0.453 |
LIG_FHA_2 | 577 | 583 | PF00498 | 0.505 |
LIG_Integrin_isoDGR_2 | 260 | 262 | PF01839 | 0.457 |
LIG_IRF3_LxIS_1 | 392 | 397 | PF10401 | 0.324 |
LIG_LIR_Apic_2 | 29 | 34 | PF02991 | 0.526 |
LIG_LIR_Apic_2 | 407 | 412 | PF02991 | 0.363 |
LIG_LIR_Nem_3 | 177 | 183 | PF02991 | 0.282 |
LIG_LIR_Nem_3 | 318 | 323 | PF02991 | 0.427 |
LIG_LIR_Nem_3 | 404 | 409 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 643 | 649 | PF02991 | 0.689 |
LIG_NRBOX | 326 | 332 | PF00104 | 0.399 |
LIG_Pex14_2 | 179 | 183 | PF04695 | 0.350 |
LIG_PTAP_UEV_1 | 744 | 749 | PF05743 | 0.585 |
LIG_PTB_Apo_2 | 308 | 315 | PF02174 | 0.380 |
LIG_REV1ctd_RIR_1 | 1 | 10 | PF16727 | 0.512 |
LIG_SH2_CRK | 215 | 219 | PF00017 | 0.350 |
LIG_SH2_CRK | 31 | 35 | PF00017 | 0.456 |
LIG_SH2_CRK | 427 | 431 | PF00017 | 0.329 |
LIG_SH2_CRK | 459 | 463 | PF00017 | 0.469 |
LIG_SH2_CRK | 531 | 535 | PF00017 | 0.393 |
LIG_SH2_NCK_1 | 248 | 252 | PF00017 | 0.393 |
LIG_SH2_PTP2 | 409 | 412 | PF00017 | 0.313 |
LIG_SH2_STAP1 | 138 | 142 | PF00017 | 0.434 |
LIG_SH2_STAP1 | 467 | 471 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 108 | 111 | PF00017 | 0.286 |
LIG_SH2_STAT5 | 130 | 133 | PF00017 | 0.531 |
LIG_SH2_STAT5 | 31 | 34 | PF00017 | 0.501 |
LIG_SH2_STAT5 | 409 | 412 | PF00017 | 0.359 |
LIG_SH2_STAT5 | 531 | 534 | PF00017 | 0.399 |
LIG_SH3_2 | 837 | 842 | PF14604 | 0.507 |
LIG_SH3_3 | 12 | 18 | PF00018 | 0.414 |
LIG_SH3_3 | 607 | 613 | PF00018 | 0.563 |
LIG_SH3_3 | 668 | 674 | PF00018 | 0.594 |
LIG_SH3_3 | 679 | 685 | PF00018 | 0.505 |
LIG_SH3_3 | 742 | 748 | PF00018 | 0.763 |
LIG_SH3_3 | 788 | 794 | PF00018 | 0.751 |
LIG_SH3_3 | 834 | 840 | PF00018 | 0.769 |
LIG_Sin3_3 | 469 | 476 | PF02671 | 0.384 |
LIG_SUMO_SIM_anti_2 | 328 | 334 | PF11976 | 0.414 |
LIG_SUMO_SIM_par_1 | 233 | 239 | PF11976 | 0.376 |
LIG_SUMO_SIM_par_1 | 572 | 577 | PF11976 | 0.383 |
LIG_SUMO_SIM_par_1 | 794 | 800 | PF11976 | 0.511 |
LIG_SUMO_SIM_par_1 | 821 | 826 | PF11976 | 0.502 |
LIG_TRAF2_1 | 254 | 257 | PF00917 | 0.479 |
LIG_TYR_ITIM | 246 | 251 | PF00017 | 0.269 |
LIG_TYR_ITIM | 425 | 430 | PF00017 | 0.364 |
MOD_CDC14_SPxK_1 | 681 | 684 | PF00782 | 0.575 |
MOD_CDK_SPK_2 | 30 | 35 | PF00069 | 0.392 |
MOD_CDK_SPxK_1 | 678 | 684 | PF00069 | 0.576 |
MOD_CDK_SPxxK_3 | 293 | 300 | PF00069 | 0.352 |
MOD_CK1_1 | 174 | 180 | PF00069 | 0.372 |
MOD_CK1_1 | 376 | 382 | PF00069 | 0.517 |
MOD_CK1_1 | 397 | 403 | PF00069 | 0.368 |
MOD_CK1_1 | 54 | 60 | PF00069 | 0.385 |
MOD_CK1_1 | 572 | 578 | PF00069 | 0.474 |
MOD_CK1_1 | 580 | 586 | PF00069 | 0.401 |
MOD_CK1_1 | 61 | 67 | PF00069 | 0.513 |
MOD_CK1_1 | 627 | 633 | PF00069 | 0.685 |
MOD_CK1_1 | 656 | 662 | PF00069 | 0.607 |
MOD_CK1_1 | 677 | 683 | PF00069 | 0.598 |
MOD_CK1_1 | 708 | 714 | PF00069 | 0.689 |
MOD_CK1_1 | 746 | 752 | PF00069 | 0.631 |
MOD_CK1_1 | 758 | 764 | PF00069 | 0.698 |
MOD_CK1_1 | 779 | 785 | PF00069 | 0.700 |
MOD_CK1_1 | 789 | 795 | PF00069 | 0.739 |
MOD_CK1_1 | 802 | 808 | PF00069 | 0.598 |
MOD_CK1_1 | 826 | 832 | PF00069 | 0.662 |
MOD_CK1_1 | 835 | 841 | PF00069 | 0.589 |
MOD_CK2_1 | 251 | 257 | PF00069 | 0.457 |
MOD_CK2_1 | 268 | 274 | PF00069 | 0.500 |
MOD_CK2_1 | 341 | 347 | PF00069 | 0.525 |
MOD_CK2_1 | 576 | 582 | PF00069 | 0.467 |
MOD_GlcNHglycan | 173 | 176 | PF01048 | 0.355 |
MOD_GlcNHglycan | 188 | 191 | PF01048 | 0.295 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.415 |
MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.528 |
MOD_GlcNHglycan | 270 | 273 | PF01048 | 0.467 |
MOD_GlcNHglycan | 317 | 320 | PF01048 | 0.394 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.464 |
MOD_GlcNHglycan | 375 | 378 | PF01048 | 0.516 |
MOD_GlcNHglycan | 419 | 422 | PF01048 | 0.496 |
MOD_GlcNHglycan | 459 | 462 | PF01048 | 0.375 |
MOD_GlcNHglycan | 466 | 470 | PF01048 | 0.339 |
MOD_GlcNHglycan | 558 | 561 | PF01048 | 0.353 |
MOD_GlcNHglycan | 579 | 582 | PF01048 | 0.532 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.511 |
MOD_GlcNHglycan | 605 | 608 | PF01048 | 0.623 |
MOD_GlcNHglycan | 613 | 616 | PF01048 | 0.671 |
MOD_GlcNHglycan | 655 | 658 | PF01048 | 0.567 |
MOD_GlcNHglycan | 671 | 674 | PF01048 | 0.648 |
MOD_GlcNHglycan | 677 | 680 | PF01048 | 0.635 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.543 |
MOD_GlcNHglycan | 707 | 710 | PF01048 | 0.685 |
MOD_GlcNHglycan | 745 | 748 | PF01048 | 0.639 |
MOD_GlcNHglycan | 757 | 760 | PF01048 | 0.594 |
MOD_GlcNHglycan | 825 | 828 | PF01048 | 0.667 |
MOD_GlcNHglycan | 834 | 837 | PF01048 | 0.560 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.404 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.388 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.428 |
MOD_GSK3_1 | 279 | 286 | PF00069 | 0.415 |
MOD_GSK3_1 | 341 | 348 | PF00069 | 0.437 |
MOD_GSK3_1 | 512 | 519 | PF00069 | 0.450 |
MOD_GSK3_1 | 54 | 61 | PF00069 | 0.382 |
MOD_GSK3_1 | 547 | 554 | PF00069 | 0.362 |
MOD_GSK3_1 | 572 | 579 | PF00069 | 0.514 |
MOD_GSK3_1 | 582 | 589 | PF00069 | 0.491 |
MOD_GSK3_1 | 616 | 623 | PF00069 | 0.617 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.494 |
MOD_GSK3_1 | 624 | 631 | PF00069 | 0.678 |
MOD_GSK3_1 | 652 | 659 | PF00069 | 0.583 |
MOD_GSK3_1 | 669 | 676 | PF00069 | 0.678 |
MOD_GSK3_1 | 683 | 690 | PF00069 | 0.701 |
MOD_GSK3_1 | 761 | 768 | PF00069 | 0.687 |
MOD_GSK3_1 | 777 | 784 | PF00069 | 0.599 |
MOD_GSK3_1 | 785 | 792 | PF00069 | 0.695 |
MOD_GSK3_1 | 826 | 833 | PF00069 | 0.732 |
MOD_LATS_1 | 601 | 607 | PF00433 | 0.457 |
MOD_N-GLC_1 | 268 | 273 | PF02516 | 0.397 |
MOD_N-GLC_1 | 505 | 510 | PF02516 | 0.282 |
MOD_N-GLC_1 | 591 | 596 | PF02516 | 0.297 |
MOD_N-GLC_1 | 620 | 625 | PF02516 | 0.653 |
MOD_N-GLC_2 | 277 | 279 | PF02516 | 0.460 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.425 |
MOD_NEK2_1 | 202 | 207 | PF00069 | 0.349 |
MOD_NEK2_1 | 221 | 226 | PF00069 | 0.543 |
MOD_NEK2_1 | 247 | 252 | PF00069 | 0.341 |
MOD_NEK2_1 | 301 | 306 | PF00069 | 0.383 |
MOD_NEK2_1 | 333 | 338 | PF00069 | 0.485 |
MOD_NEK2_1 | 341 | 346 | PF00069 | 0.474 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.384 |
MOD_NEK2_1 | 368 | 373 | PF00069 | 0.370 |
MOD_NEK2_1 | 440 | 445 | PF00069 | 0.477 |
MOD_NEK2_1 | 457 | 462 | PF00069 | 0.354 |
MOD_NEK2_1 | 479 | 484 | PF00069 | 0.419 |
MOD_NEK2_1 | 56 | 61 | PF00069 | 0.483 |
MOD_NEK2_1 | 563 | 568 | PF00069 | 0.405 |
MOD_NEK2_1 | 591 | 596 | PF00069 | 0.430 |
MOD_NEK2_1 | 652 | 657 | PF00069 | 0.639 |
MOD_NEK2_1 | 731 | 736 | PF00069 | 0.705 |
MOD_NEK2_1 | 737 | 742 | PF00069 | 0.682 |
MOD_NEK2_1 | 753 | 758 | PF00069 | 0.546 |
MOD_NEK2_2 | 26 | 31 | PF00069 | 0.409 |
MOD_NEK2_2 | 547 | 552 | PF00069 | 0.357 |
MOD_NEK2_2 | 79 | 84 | PF00069 | 0.445 |
MOD_PIKK_1 | 333 | 339 | PF00454 | 0.395 |
MOD_PIKK_1 | 41 | 47 | PF00454 | 0.500 |
MOD_PIKK_1 | 519 | 525 | PF00454 | 0.471 |
MOD_PIKK_1 | 732 | 738 | PF00454 | 0.614 |
MOD_PIKK_1 | 789 | 795 | PF00454 | 0.606 |
MOD_PK_1 | 262 | 268 | PF00069 | 0.492 |
MOD_PKA_2 | 279 | 285 | PF00069 | 0.423 |
MOD_PKA_2 | 301 | 307 | PF00069 | 0.387 |
MOD_PKA_2 | 51 | 57 | PF00069 | 0.403 |
MOD_PKA_2 | 731 | 737 | PF00069 | 0.681 |
MOD_PKA_2 | 79 | 85 | PF00069 | 0.423 |
MOD_PKA_2 | 802 | 808 | PF00069 | 0.524 |
MOD_PKB_1 | 463 | 471 | PF00069 | 0.246 |
MOD_Plk_1 | 505 | 511 | PF00069 | 0.282 |
MOD_Plk_1 | 591 | 597 | PF00069 | 0.374 |
MOD_Plk_1 | 732 | 738 | PF00069 | 0.727 |
MOD_Plk_4 | 103 | 109 | PF00069 | 0.315 |
MOD_Plk_4 | 167 | 173 | PF00069 | 0.295 |
MOD_Plk_4 | 405 | 411 | PF00069 | 0.357 |
MOD_Plk_4 | 479 | 485 | PF00069 | 0.460 |
MOD_Plk_4 | 51 | 57 | PF00069 | 0.335 |
MOD_Plk_4 | 563 | 569 | PF00069 | 0.363 |
MOD_Plk_4 | 586 | 592 | PF00069 | 0.503 |
MOD_Plk_4 | 687 | 693 | PF00069 | 0.656 |
MOD_Plk_4 | 809 | 815 | PF00069 | 0.717 |
MOD_Plk_4 | 85 | 91 | PF00069 | 0.333 |
MOD_ProDKin_1 | 17 | 23 | PF00069 | 0.452 |
MOD_ProDKin_1 | 195 | 201 | PF00069 | 0.574 |
MOD_ProDKin_1 | 293 | 299 | PF00069 | 0.468 |
MOD_ProDKin_1 | 30 | 36 | PF00069 | 0.404 |
MOD_ProDKin_1 | 408 | 414 | PF00069 | 0.411 |
MOD_ProDKin_1 | 516 | 522 | PF00069 | 0.486 |
MOD_ProDKin_1 | 569 | 575 | PF00069 | 0.462 |
MOD_ProDKin_1 | 628 | 634 | PF00069 | 0.607 |
MOD_ProDKin_1 | 678 | 684 | PF00069 | 0.768 |
MOD_ProDKin_1 | 691 | 697 | PF00069 | 0.592 |
MOD_ProDKin_1 | 765 | 771 | PF00069 | 0.726 |
MOD_ProDKin_1 | 786 | 792 | PF00069 | 0.642 |
MOD_SUMO_for_1 | 596 | 599 | PF00179 | 0.355 |
TRG_DiLeu_BaEn_2 | 309 | 315 | PF01217 | 0.389 |
TRG_ENDOCYTIC_2 | 248 | 251 | PF00928 | 0.263 |
TRG_ENDOCYTIC_2 | 427 | 430 | PF00928 | 0.318 |
TRG_ER_diArg_1 | 126 | 128 | PF00400 | 0.407 |
TRG_ER_diArg_1 | 299 | 302 | PF00400 | 0.484 |
TRG_ER_diArg_1 | 462 | 465 | PF00400 | 0.261 |
TRG_ER_diArg_1 | 83 | 85 | PF00400 | 0.433 |
TRG_ER_diArg_1 | 843 | 845 | PF00400 | 0.637 |
TRG_NES_CRM1_1 | 322 | 334 | PF08389 | 0.398 |
TRG_Pf-PMV_PEXEL_1 | 561 | 565 | PF00026 | 0.451 |
TRG_Pf-PMV_PEXEL_1 | 72 | 77 | PF00026 | 0.404 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PER2 | Leptomonas seymouri | 54% | 96% |
A0A0S4KHN7 | Bodo saltans | 33% | 100% |
A0A1X0NY37 | Trypanosomatidae | 38% | 100% |
A0A3S5IS35 | Trypanosoma rangeli | 37% | 100% |
A4HBU3 | Leishmania braziliensis | 78% | 99% |
D0A1C9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
E9AGU9 | Leishmania infantum | 100% | 100% |
E9AV65 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 99% |
O13733 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 21% | 100% |
Q4QCB6 | Leishmania major | 93% | 100% |
Q55GS2 | Dictyostelium discoideum | 25% | 100% |
Q96KG9 | Homo sapiens | 27% | 100% |
Q9EQC5 | Mus musculus | 26% | 100% |