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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: E9ATN8
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 6 |
GO:0006793 | phosphorus metabolic process | 3 | 6 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 6 |
GO:0006807 | nitrogen compound metabolic process | 2 | 6 |
GO:0008152 | metabolic process | 1 | 6 |
GO:0009987 | cellular process | 1 | 6 |
GO:0016310 | phosphorylation | 5 | 6 |
GO:0019538 | protein metabolic process | 3 | 6 |
GO:0036211 | protein modification process | 4 | 6 |
GO:0043170 | macromolecule metabolic process | 3 | 6 |
GO:0043412 | macromolecule modification | 4 | 6 |
GO:0044237 | cellular metabolic process | 2 | 6 |
GO:0044238 | primary metabolic process | 2 | 6 |
GO:0071704 | organic substance metabolic process | 2 | 6 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 6 |
GO:0003676 | nucleic acid binding | 3 | 5 |
GO:0003746 | translation elongation factor activity | 4 | 5 |
GO:0003824 | catalytic activity | 1 | 6 |
GO:0004672 | protein kinase activity | 3 | 6 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 6 |
GO:0005488 | binding | 1 | 6 |
GO:0005524 | ATP binding | 5 | 6 |
GO:0008135 | translation factor activity, RNA binding | 3 | 5 |
GO:0016301 | kinase activity | 4 | 6 |
GO:0016740 | transferase activity | 2 | 6 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 6 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 6 |
GO:0017076 | purine nucleotide binding | 4 | 6 |
GO:0030554 | adenyl nucleotide binding | 5 | 6 |
GO:0032553 | ribonucleotide binding | 3 | 6 |
GO:0032555 | purine ribonucleotide binding | 4 | 6 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 6 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 6 |
GO:0036094 | small molecule binding | 2 | 6 |
GO:0043167 | ion binding | 2 | 6 |
GO:0043168 | anion binding | 3 | 6 |
GO:0045182 | translation regulator activity | 1 | 5 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 5 |
GO:0097159 | organic cyclic compound binding | 2 | 6 |
GO:0097367 | carbohydrate derivative binding | 2 | 6 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 6 |
GO:1901265 | nucleoside phosphate binding | 3 | 6 |
GO:1901363 | heterocyclic compound binding | 2 | 6 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 111 | 115 | PF00656 | 0.416 |
CLV_C14_Caspase3-7 | 159 | 163 | PF00656 | 0.505 |
CLV_C14_Caspase3-7 | 325 | 329 | PF00656 | 0.391 |
CLV_C14_Caspase3-7 | 40 | 44 | PF00656 | 0.281 |
CLV_C14_Caspase3-7 | 412 | 416 | PF00656 | 0.346 |
CLV_NRD_NRD_1 | 480 | 482 | PF00675 | 0.607 |
CLV_NRD_NRD_1 | 554 | 556 | PF00675 | 0.566 |
CLV_NRD_NRD_1 | 636 | 638 | PF00675 | 0.527 |
CLV_PCSK_KEX2_1 | 480 | 482 | PF00082 | 0.607 |
CLV_PCSK_KEX2_1 | 537 | 539 | PF00082 | 0.610 |
CLV_PCSK_KEX2_1 | 554 | 556 | PF00082 | 0.441 |
CLV_PCSK_KEX2_1 | 593 | 595 | PF00082 | 0.471 |
CLV_PCSK_KEX2_1 | 636 | 638 | PF00082 | 0.527 |
CLV_PCSK_KEX2_1 | 698 | 700 | PF00082 | 0.459 |
CLV_PCSK_KEX2_1 | 97 | 99 | PF00082 | 0.317 |
CLV_PCSK_PC1ET2_1 | 537 | 539 | PF00082 | 0.604 |
CLV_PCSK_PC1ET2_1 | 593 | 595 | PF00082 | 0.471 |
CLV_PCSK_PC1ET2_1 | 698 | 700 | PF00082 | 0.459 |
CLV_PCSK_PC1ET2_1 | 97 | 99 | PF00082 | 0.290 |
CLV_PCSK_PC7_1 | 533 | 539 | PF00082 | 0.565 |
CLV_PCSK_SKI1_1 | 199 | 203 | PF00082 | 0.472 |
CLV_PCSK_SKI1_1 | 230 | 234 | PF00082 | 0.311 |
CLV_PCSK_SKI1_1 | 251 | 255 | PF00082 | 0.447 |
CLV_PCSK_SKI1_1 | 443 | 447 | PF00082 | 0.554 |
CLV_PCSK_SKI1_1 | 555 | 559 | PF00082 | 0.532 |
CLV_PCSK_SKI1_1 | 560 | 564 | PF00082 | 0.460 |
CLV_PCSK_SKI1_1 | 593 | 597 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 637 | 641 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 712 | 716 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 810 | 814 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 832 | 836 | PF00082 | 0.477 |
CLV_Separin_Metazoa | 561 | 565 | PF03568 | 0.439 |
DEG_APCC_DBOX_1 | 781 | 789 | PF00400 | 0.346 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.427 |
DEG_SPOP_SBC_1 | 402 | 406 | PF00917 | 0.222 |
DOC_AGCK_PIF_1 | 45 | 50 | PF00069 | 0.391 |
DOC_ANK_TNKS_1 | 38 | 45 | PF00023 | 0.346 |
DOC_ANK_TNKS_1 | 851 | 858 | PF00023 | 0.316 |
DOC_CYCLIN_RxL_1 | 440 | 451 | PF00134 | 0.546 |
DOC_CYCLIN_RxL_1 | 554 | 567 | PF00134 | 0.349 |
DOC_CYCLIN_RxL_1 | 816 | 828 | PF00134 | 0.331 |
DOC_CYCLIN_yCln2_LP_2 | 69 | 75 | PF00134 | 0.391 |
DOC_MAPK_gen_1 | 140 | 149 | PF00069 | 0.599 |
DOC_MAPK_gen_1 | 480 | 487 | PF00069 | 0.484 |
DOC_MAPK_gen_1 | 593 | 599 | PF00069 | 0.453 |
DOC_MAPK_gen_1 | 841 | 849 | PF00069 | 0.426 |
DOC_MAPK_MEF2A_6 | 140 | 149 | PF00069 | 0.599 |
DOC_MAPK_RevD_3 | 147 | 161 | PF00069 | 0.491 |
DOC_PP1_RVXF_1 | 289 | 296 | PF00149 | 0.391 |
DOC_PP1_RVXF_1 | 469 | 476 | PF00149 | 0.461 |
DOC_PP1_RVXF_1 | 610 | 616 | PF00149 | 0.391 |
DOC_PP1_RVXF_1 | 710 | 716 | PF00149 | 0.346 |
DOC_PP4_FxxP_1 | 475 | 478 | PF00568 | 0.461 |
DOC_PP4_FxxP_1 | 519 | 522 | PF00568 | 0.672 |
DOC_USP7_MATH_1 | 185 | 189 | PF00917 | 0.585 |
DOC_USP7_MATH_1 | 476 | 480 | PF00917 | 0.554 |
DOC_USP7_MATH_1 | 488 | 492 | PF00917 | 0.581 |
DOC_USP7_MATH_1 | 501 | 505 | PF00917 | 0.539 |
DOC_USP7_MATH_1 | 507 | 511 | PF00917 | 0.481 |
DOC_USP7_MATH_1 | 515 | 519 | PF00917 | 0.504 |
DOC_USP7_MATH_1 | 547 | 551 | PF00917 | 0.537 |
DOC_USP7_UBL2_3 | 537 | 541 | PF12436 | 0.607 |
DOC_WW_Pin1_4 | 172 | 177 | PF00397 | 0.605 |
DOC_WW_Pin1_4 | 341 | 346 | PF00397 | 0.391 |
DOC_WW_Pin1_4 | 450 | 455 | PF00397 | 0.496 |
DOC_WW_Pin1_4 | 474 | 479 | PF00397 | 0.569 |
DOC_WW_Pin1_4 | 588 | 593 | PF00397 | 0.367 |
DOC_WW_Pin1_4 | 689 | 694 | PF00397 | 0.267 |
DOC_WW_Pin1_4 | 741 | 746 | PF00397 | 0.346 |
LIG_14-3-3_CanoR_1 | 215 | 224 | PF00244 | 0.519 |
LIG_14-3-3_CanoR_1 | 324 | 332 | PF00244 | 0.391 |
LIG_14-3-3_CanoR_1 | 480 | 488 | PF00244 | 0.640 |
LIG_14-3-3_CanoR_1 | 554 | 563 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 782 | 790 | PF00244 | 0.222 |
LIG_14-3-3_CanoR_1 | 832 | 837 | PF00244 | 0.377 |
LIG_Actin_RPEL_3 | 557 | 576 | PF02755 | 0.448 |
LIG_APCC_ABBA_1 | 147 | 152 | PF00400 | 0.601 |
LIG_APCC_ABBAyCdc20_2 | 146 | 152 | PF00400 | 0.603 |
LIG_BIR_III_4 | 357 | 361 | PF00653 | 0.391 |
LIG_BRCT_BRCA1_1 | 170 | 174 | PF00533 | 0.591 |
LIG_BRCT_BRCA1_1 | 318 | 322 | PF00533 | 0.391 |
LIG_BRCT_BRCA1_1 | 656 | 660 | PF00533 | 0.391 |
LIG_BRCT_BRCA1_1 | 78 | 82 | PF00533 | 0.360 |
LIG_BRCT_BRCA1_2 | 656 | 662 | PF00533 | 0.391 |
LIG_Clathr_ClatBox_1 | 435 | 439 | PF01394 | 0.405 |
LIG_CSL_BTD_1 | 589 | 592 | PF09270 | 0.361 |
LIG_deltaCOP1_diTrp_1 | 587 | 596 | PF00928 | 0.461 |
LIG_eIF4E_1 | 68 | 74 | PF01652 | 0.391 |
LIG_FHA_1 | 134 | 140 | PF00498 | 0.634 |
LIG_FHA_1 | 298 | 304 | PF00498 | 0.267 |
LIG_FHA_1 | 509 | 515 | PF00498 | 0.600 |
LIG_FHA_1 | 570 | 576 | PF00498 | 0.495 |
LIG_FHA_1 | 708 | 714 | PF00498 | 0.470 |
LIG_FHA_1 | 835 | 841 | PF00498 | 0.498 |
LIG_FHA_2 | 165 | 171 | PF00498 | 0.641 |
LIG_FHA_2 | 224 | 230 | PF00498 | 0.378 |
LIG_FHA_2 | 323 | 329 | PF00498 | 0.391 |
LIG_FHA_2 | 410 | 416 | PF00498 | 0.346 |
LIG_FHA_2 | 556 | 562 | PF00498 | 0.524 |
LIG_FHA_2 | 577 | 583 | PF00498 | 0.442 |
LIG_FHA_2 | 616 | 622 | PF00498 | 0.374 |
LIG_FHA_2 | 75 | 81 | PF00498 | 0.391 |
LIG_FHA_2 | 784 | 790 | PF00498 | 0.391 |
LIG_FHA_2 | 833 | 839 | PF00498 | 0.462 |
LIG_Integrin_RGD_1 | 28 | 30 | PF01839 | 0.612 |
LIG_LIR_Apic_2 | 474 | 478 | PF02991 | 0.464 |
LIG_LIR_Apic_2 | 518 | 522 | PF02991 | 0.666 |
LIG_LIR_Apic_2 | 572 | 577 | PF02991 | 0.409 |
LIG_LIR_Gen_1 | 228 | 236 | PF02991 | 0.495 |
LIG_LIR_Gen_1 | 260 | 270 | PF02991 | 0.331 |
LIG_LIR_Gen_1 | 359 | 369 | PF02991 | 0.357 |
LIG_LIR_Gen_1 | 371 | 378 | PF02991 | 0.310 |
LIG_LIR_Gen_1 | 43 | 51 | PF02991 | 0.376 |
LIG_LIR_Gen_1 | 646 | 656 | PF02991 | 0.391 |
LIG_LIR_Gen_1 | 752 | 761 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 132 | 138 | PF02991 | 0.635 |
LIG_LIR_Nem_3 | 228 | 234 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 260 | 266 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 337 | 343 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 359 | 364 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 36 | 41 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 371 | 376 | PF02991 | 0.310 |
LIG_LIR_Nem_3 | 43 | 48 | PF02991 | 0.324 |
LIG_LIR_Nem_3 | 646 | 651 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 700 | 705 | PF02991 | 0.527 |
LIG_LIR_Nem_3 | 752 | 758 | PF02991 | 0.480 |
LIG_MLH1_MIPbox_1 | 318 | 322 | PF16413 | 0.391 |
LIG_NRBOX | 431 | 437 | PF00104 | 0.344 |
LIG_Pex14_2 | 660 | 664 | PF04695 | 0.527 |
LIG_Pex14_2 | 846 | 850 | PF04695 | 0.429 |
LIG_REV1ctd_RIR_1 | 319 | 328 | PF16727 | 0.391 |
LIG_REV1ctd_RIR_1 | 700 | 710 | PF16727 | 0.527 |
LIG_SH2_PTP2 | 200 | 203 | PF00017 | 0.509 |
LIG_SH2_PTP2 | 574 | 577 | PF00017 | 0.404 |
LIG_SH2_SRC | 574 | 577 | PF00017 | 0.404 |
LIG_SH2_STAP1 | 135 | 139 | PF00017 | 0.636 |
LIG_SH2_STAP1 | 231 | 235 | PF00017 | 0.429 |
LIG_SH2_STAP1 | 299 | 303 | PF00017 | 0.373 |
LIG_SH2_STAP1 | 581 | 585 | PF00017 | 0.453 |
LIG_SH2_STAT3 | 793 | 796 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 135 | 138 | PF00017 | 0.634 |
LIG_SH2_STAT5 | 200 | 203 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 270 | 273 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 299 | 302 | PF00017 | 0.281 |
LIG_SH2_STAT5 | 50 | 53 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 574 | 577 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 647 | 650 | PF00017 | 0.527 |
LIG_SH2_STAT5 | 68 | 71 | PF00017 | 0.218 |
LIG_SH3_3 | 198 | 204 | PF00018 | 0.502 |
LIG_SH3_3 | 298 | 304 | PF00018 | 0.346 |
LIG_SH3_3 | 332 | 338 | PF00018 | 0.352 |
LIG_SH3_3 | 339 | 345 | PF00018 | 0.364 |
LIG_SH3_3 | 482 | 488 | PF00018 | 0.488 |
LIG_SH3_3 | 519 | 525 | PF00018 | 0.667 |
LIG_SH3_3 | 528 | 534 | PF00018 | 0.553 |
LIG_SUMO_SIM_par_1 | 682 | 687 | PF11976 | 0.335 |
LIG_TRAF2_1 | 235 | 238 | PF00917 | 0.491 |
LIG_TRAF2_1 | 526 | 529 | PF00917 | 0.547 |
LIG_TRAF2_1 | 624 | 627 | PF00917 | 0.222 |
LIG_TRAF2_1 | 858 | 861 | PF00917 | 0.447 |
LIG_TRFH_1 | 252 | 256 | PF08558 | 0.469 |
LIG_TRFH_1 | 68 | 72 | PF08558 | 0.391 |
LIG_TYR_ITIM | 198 | 203 | PF00017 | 0.494 |
LIG_UBA3_1 | 562 | 568 | PF00899 | 0.497 |
LIG_UBA3_1 | 849 | 854 | PF00899 | 0.404 |
LIG_WRC_WIRS_1 | 516 | 521 | PF05994 | 0.617 |
MOD_CDC14_SPxK_1 | 477 | 480 | PF00782 | 0.526 |
MOD_CDK_SPK_2 | 588 | 593 | PF00069 | 0.362 |
MOD_CDK_SPxK_1 | 474 | 480 | PF00069 | 0.524 |
MOD_CDK_SPxK_1 | 588 | 594 | PF00069 | 0.361 |
MOD_CDK_SPxxK_3 | 450 | 457 | PF00069 | 0.493 |
MOD_CDK_SPxxK_3 | 474 | 481 | PF00069 | 0.571 |
MOD_CK1_1 | 14 | 20 | PF00069 | 0.613 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.684 |
MOD_CK1_1 | 374 | 380 | PF00069 | 0.391 |
MOD_CK1_1 | 46 | 52 | PF00069 | 0.391 |
MOD_CK1_1 | 704 | 710 | PF00069 | 0.527 |
MOD_CK1_1 | 762 | 768 | PF00069 | 0.527 |
MOD_CK2_1 | 164 | 170 | PF00069 | 0.660 |
MOD_CK2_1 | 493 | 499 | PF00069 | 0.589 |
MOD_CK2_1 | 523 | 529 | PF00069 | 0.547 |
MOD_CK2_1 | 555 | 561 | PF00069 | 0.531 |
MOD_CK2_1 | 74 | 80 | PF00069 | 0.391 |
MOD_CK2_1 | 783 | 789 | PF00069 | 0.391 |
MOD_CK2_1 | 855 | 861 | PF00069 | 0.404 |
MOD_CK2_1 | 87 | 93 | PF00069 | 0.266 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.498 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.620 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.491 |
MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.391 |
MOD_GlcNHglycan | 380 | 383 | PF01048 | 0.391 |
MOD_GlcNHglycan | 405 | 408 | PF01048 | 0.346 |
MOD_GlcNHglycan | 505 | 508 | PF01048 | 0.617 |
MOD_GlcNHglycan | 542 | 545 | PF01048 | 0.643 |
MOD_GlcNHglycan | 549 | 552 | PF01048 | 0.607 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.346 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.637 |
MOD_GSK3_1 | 168 | 175 | PF00069 | 0.572 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.481 |
MOD_GSK3_1 | 214 | 221 | PF00069 | 0.463 |
MOD_GSK3_1 | 322 | 329 | PF00069 | 0.374 |
MOD_GSK3_1 | 341 | 348 | PF00069 | 0.263 |
MOD_GSK3_1 | 374 | 381 | PF00069 | 0.391 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.391 |
MOD_GSK3_1 | 476 | 483 | PF00069 | 0.599 |
MOD_GSK3_1 | 493 | 500 | PF00069 | 0.517 |
MOD_GSK3_1 | 501 | 508 | PF00069 | 0.631 |
MOD_GSK3_1 | 536 | 543 | PF00069 | 0.527 |
MOD_GSK3_1 | 697 | 704 | PF00069 | 0.521 |
MOD_GSK3_1 | 762 | 769 | PF00069 | 0.527 |
MOD_N-GLC_1 | 402 | 407 | PF02516 | 0.391 |
MOD_N-GLC_1 | 448 | 453 | PF02516 | 0.385 |
MOD_N-GLC_1 | 783 | 788 | PF02516 | 0.222 |
MOD_N-GLC_2 | 739 | 741 | PF02516 | 0.391 |
MOD_NEK2_1 | 108 | 113 | PF00069 | 0.526 |
MOD_NEK2_1 | 11 | 16 | PF00069 | 0.609 |
MOD_NEK2_1 | 214 | 219 | PF00069 | 0.485 |
MOD_NEK2_1 | 24 | 29 | PF00069 | 0.503 |
MOD_NEK2_1 | 322 | 327 | PF00069 | 0.378 |
MOD_NEK2_1 | 378 | 383 | PF00069 | 0.391 |
MOD_NEK2_1 | 615 | 620 | PF00069 | 0.222 |
MOD_NEK2_2 | 101 | 106 | PF00069 | 0.391 |
MOD_NEK2_2 | 138 | 143 | PF00069 | 0.585 |
MOD_NEK2_2 | 297 | 302 | PF00069 | 0.222 |
MOD_NEK2_2 | 635 | 640 | PF00069 | 0.391 |
MOD_PIKK_1 | 493 | 499 | PF00454 | 0.578 |
MOD_PIKK_1 | 524 | 530 | PF00454 | 0.489 |
MOD_PIKK_1 | 555 | 561 | PF00454 | 0.564 |
MOD_PKA_1 | 160 | 166 | PF00069 | 0.576 |
MOD_PKA_1 | 480 | 486 | PF00069 | 0.605 |
MOD_PKA_2 | 214 | 220 | PF00069 | 0.498 |
MOD_PKA_2 | 323 | 329 | PF00069 | 0.391 |
MOD_PKA_2 | 480 | 486 | PF00069 | 0.650 |
MOD_PKA_2 | 553 | 559 | PF00069 | 0.554 |
MOD_PKA_2 | 635 | 641 | PF00069 | 0.391 |
MOD_PKA_2 | 723 | 729 | PF00069 | 0.380 |
MOD_PKA_2 | 815 | 821 | PF00069 | 0.391 |
MOD_PKB_1 | 830 | 838 | PF00069 | 0.389 |
MOD_Plk_1 | 20 | 26 | PF00069 | 0.491 |
MOD_Plk_1 | 586 | 592 | PF00069 | 0.482 |
MOD_Plk_1 | 625 | 631 | PF00069 | 0.222 |
MOD_Plk_1 | 749 | 755 | PF00069 | 0.391 |
MOD_Plk_2-3 | 789 | 795 | PF00069 | 0.391 |
MOD_Plk_4 | 28 | 34 | PF00069 | 0.463 |
MOD_Plk_4 | 490 | 496 | PF00069 | 0.506 |
MOD_Plk_4 | 515 | 521 | PF00069 | 0.658 |
MOD_Plk_4 | 570 | 576 | PF00069 | 0.303 |
MOD_Plk_4 | 625 | 631 | PF00069 | 0.346 |
MOD_Plk_4 | 655 | 661 | PF00069 | 0.319 |
MOD_ProDKin_1 | 172 | 178 | PF00069 | 0.605 |
MOD_ProDKin_1 | 341 | 347 | PF00069 | 0.391 |
MOD_ProDKin_1 | 450 | 456 | PF00069 | 0.490 |
MOD_ProDKin_1 | 474 | 480 | PF00069 | 0.569 |
MOD_ProDKin_1 | 588 | 594 | PF00069 | 0.367 |
MOD_ProDKin_1 | 689 | 695 | PF00069 | 0.267 |
MOD_ProDKin_1 | 741 | 747 | PF00069 | 0.346 |
MOD_SUMO_rev_2 | 838 | 842 | PF00179 | 0.458 |
TRG_AP2beta_CARGO_1 | 43 | 52 | PF09066 | 0.346 |
TRG_DiLeu_BaEn_1 | 770 | 775 | PF01217 | 0.346 |
TRG_ENDOCYTIC_2 | 200 | 203 | PF00928 | 0.509 |
TRG_ENDOCYTIC_2 | 231 | 234 | PF00928 | 0.465 |
TRG_ENDOCYTIC_2 | 263 | 266 | PF00928 | 0.470 |
TRG_ENDOCYTIC_2 | 38 | 41 | PF00928 | 0.391 |
TRG_ER_diArg_1 | 248 | 251 | PF00400 | 0.487 |
TRG_ER_diArg_1 | 480 | 482 | PF00400 | 0.607 |
TRG_ER_diArg_1 | 51 | 54 | PF00400 | 0.346 |
TRG_ER_diArg_1 | 635 | 637 | PF00400 | 0.527 |
TRG_ER_diArg_1 | 813 | 816 | PF00400 | 0.346 |
TRG_Pf-PMV_PEXEL_1 | 39 | 43 | PF00026 | 0.346 |
TRG_Pf-PMV_PEXEL_1 | 480 | 484 | PF00026 | 0.476 |
TRG_Pf-PMV_PEXEL_1 | 555 | 559 | PF00026 | 0.532 |
TRG_Pf-PMV_PEXEL_1 | 604 | 608 | PF00026 | 0.512 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IWB8 | Leishmania donovani | 86% | 75% |
A4HPX2 | Leishmania braziliensis | 69% | 100% |
A4IDN4 | Leishmania infantum | 86% | 75% |
Q4Q0V9 | Leishmania major | 85% | 100% |