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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000151 | ubiquitin ligase complex | 3 | 1 |
GO:0000152 | nuclear ubiquitin ligase complex | 3 | 1 |
GO:0005680 | anaphase-promoting complex | 4 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0031461 | cullin-RING ubiquitin ligase complex | 4 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0051286 | cell tip | 3 | 1 |
GO:0060187 | cell pole | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
GO:0140535 | intracellular protein-containing complex | 2 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1990234 | transferase complex | 3 | 1 |
Related structures:
AlphaFold database: A4H487
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 1 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0007088 | regulation of mitotic nuclear division | 6 | 1 |
GO:0007091 | metaphase/anaphase transition of mitotic cell cycle | 5 | 1 |
GO:0007346 | regulation of mitotic cell cycle | 5 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009057 | macromolecule catabolic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010498 | proteasomal protein catabolic process | 5 | 1 |
GO:0010564 | regulation of cell cycle process | 5 | 1 |
GO:0010638 | positive regulation of organelle organization | 6 | 1 |
GO:0010965 | regulation of mitotic sister chromatid separation | 6 | 1 |
GO:0016567 | protein ubiquitination | 7 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 1 |
GO:0022402 | cell cycle process | 2 | 1 |
GO:0030071 | regulation of mitotic metaphase/anaphase transition | 7 | 1 |
GO:0030163 | protein catabolic process | 4 | 1 |
GO:0031145 | anaphase-promoting complex-dependent catabolic process | 7 | 1 |
GO:0032446 | protein modification by small protein conjugation | 6 | 1 |
GO:0033043 | regulation of organelle organization | 5 | 1 |
GO:0033044 | regulation of chromosome organization | 6 | 1 |
GO:0033045 | regulation of sister chromatid segregation | 5 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043161 | proteasome-mediated ubiquitin-dependent protein catabolic process | 6 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044248 | cellular catabolic process | 3 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 1 |
GO:0044770 | cell cycle phase transition | 3 | 1 |
GO:0044772 | mitotic cell cycle phase transition | 4 | 1 |
GO:0044784 | metaphase/anaphase transition of cell cycle | 4 | 1 |
GO:0045787 | positive regulation of cell cycle | 5 | 1 |
GO:0045840 | positive regulation of mitotic nuclear division | 7 | 1 |
GO:0045842 | positive regulation of mitotic metaphase/anaphase transition | 8 | 1 |
GO:0045931 | positive regulation of mitotic cell cycle | 6 | 1 |
GO:0048518 | positive regulation of biological process | 3 | 1 |
GO:0048522 | positive regulation of cellular process | 4 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051128 | regulation of cellular component organization | 4 | 1 |
GO:0051130 | positive regulation of cellular component organization | 5 | 1 |
GO:0051301 | cell division | 2 | 1 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 1 |
GO:0051726 | regulation of cell cycle | 4 | 1 |
GO:0051783 | regulation of nuclear division | 6 | 1 |
GO:0051785 | positive regulation of nuclear division | 7 | 1 |
GO:0051983 | regulation of chromosome segregation | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090068 | positive regulation of cell cycle process | 6 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
GO:1901565 | organonitrogen compound catabolic process | 4 | 1 |
GO:1901575 | organic substance catabolic process | 3 | 1 |
GO:1901970 | positive regulation of mitotic sister chromatid separation | 7 | 1 |
GO:1901987 | regulation of cell cycle phase transition | 6 | 1 |
GO:1901989 | positive regulation of cell cycle phase transition | 7 | 1 |
GO:1901990 | regulation of mitotic cell cycle phase transition | 6 | 1 |
GO:1901992 | positive regulation of mitotic cell cycle phase transition | 7 | 1 |
GO:1902099 | regulation of metaphase/anaphase transition of cell cycle | 6 | 1 |
GO:1902101 | positive regulation of metaphase/anaphase transition of cell cycle | 7 | 1 |
GO:1903047 | mitotic cell cycle process | 3 | 1 |
GO:1905818 | regulation of chromosome separation | 5 | 1 |
GO:1905820 | positive regulation of chromosome separation | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 308 | 312 | PF00656 | 0.429 |
CLV_C14_Caspase3-7 | 539 | 543 | PF00656 | 0.443 |
CLV_NRD_NRD_1 | 134 | 136 | PF00675 | 0.555 |
CLV_NRD_NRD_1 | 232 | 234 | PF00675 | 0.473 |
CLV_NRD_NRD_1 | 300 | 302 | PF00675 | 0.467 |
CLV_NRD_NRD_1 | 361 | 363 | PF00675 | 0.640 |
CLV_NRD_NRD_1 | 424 | 426 | PF00675 | 0.559 |
CLV_NRD_NRD_1 | 733 | 735 | PF00675 | 0.304 |
CLV_NRD_NRD_1 | 778 | 780 | PF00675 | 0.477 |
CLV_NRD_NRD_1 | 796 | 798 | PF00675 | 0.330 |
CLV_PCSK_KEX2_1 | 134 | 136 | PF00082 | 0.555 |
CLV_PCSK_KEX2_1 | 231 | 233 | PF00082 | 0.486 |
CLV_PCSK_KEX2_1 | 300 | 302 | PF00082 | 0.467 |
CLV_PCSK_KEX2_1 | 361 | 363 | PF00082 | 0.640 |
CLV_PCSK_KEX2_1 | 424 | 426 | PF00082 | 0.559 |
CLV_PCSK_KEX2_1 | 615 | 617 | PF00082 | 0.371 |
CLV_PCSK_KEX2_1 | 733 | 735 | PF00082 | 0.304 |
CLV_PCSK_KEX2_1 | 778 | 780 | PF00082 | 0.304 |
CLV_PCSK_KEX2_1 | 796 | 798 | PF00082 | 0.433 |
CLV_PCSK_PC1ET2_1 | 615 | 617 | PF00082 | 0.371 |
CLV_PCSK_PC7_1 | 357 | 363 | PF00082 | 0.644 |
CLV_PCSK_SKI1_1 | 432 | 436 | PF00082 | 0.518 |
CLV_PCSK_SKI1_1 | 608 | 612 | PF00082 | 0.373 |
CLV_PCSK_SKI1_1 | 649 | 653 | PF00082 | 0.317 |
CLV_PCSK_SKI1_1 | 697 | 701 | PF00082 | 0.371 |
CLV_PCSK_SKI1_1 | 713 | 717 | PF00082 | 0.304 |
CLV_PCSK_SKI1_1 | 747 | 751 | PF00082 | 0.281 |
CLV_PCSK_SKI1_1 | 754 | 758 | PF00082 | 0.333 |
DEG_APCC_DBOX_1 | 607 | 615 | PF00400 | 0.369 |
DEG_SPOP_SBC_1 | 492 | 496 | PF00917 | 0.561 |
DOC_CYCLIN_yCln2_LP_2 | 481 | 487 | PF00134 | 0.524 |
DOC_CYCLIN_yCln2_LP_2 | 555 | 561 | PF00134 | 0.419 |
DOC_MAPK_DCC_7 | 406 | 414 | PF00069 | 0.557 |
DOC_MAPK_gen_1 | 605 | 614 | PF00069 | 0.374 |
DOC_MAPK_gen_1 | 704 | 714 | PF00069 | 0.227 |
DOC_MAPK_gen_1 | 733 | 743 | PF00069 | 0.304 |
DOC_MAPK_MEF2A_6 | 707 | 716 | PF00069 | 0.227 |
DOC_MAPK_MEF2A_6 | 734 | 743 | PF00069 | 0.304 |
DOC_MAPK_RevD_3 | 764 | 779 | PF00069 | 0.304 |
DOC_MIT_MIM_1 | 59 | 67 | PF04212 | 0.443 |
DOC_PP2B_LxvP_1 | 414 | 417 | PF13499 | 0.609 |
DOC_PP2B_LxvP_1 | 419 | 422 | PF13499 | 0.544 |
DOC_PP4_FxxP_1 | 100 | 103 | PF00568 | 0.443 |
DOC_USP7_MATH_1 | 111 | 115 | PF00917 | 0.664 |
DOC_USP7_MATH_1 | 273 | 277 | PF00917 | 0.407 |
DOC_USP7_MATH_1 | 320 | 324 | PF00917 | 0.540 |
DOC_USP7_MATH_1 | 393 | 397 | PF00917 | 0.824 |
DOC_USP7_MATH_1 | 472 | 476 | PF00917 | 0.632 |
DOC_USP7_MATH_1 | 492 | 496 | PF00917 | 0.589 |
DOC_USP7_MATH_1 | 514 | 518 | PF00917 | 0.726 |
DOC_USP7_MATH_1 | 575 | 579 | PF00917 | 0.371 |
DOC_USP7_UBL2_3 | 683 | 687 | PF12436 | 0.304 |
DOC_WW_Pin1_4 | 348 | 353 | PF00397 | 0.570 |
DOC_WW_Pin1_4 | 4 | 9 | PF00397 | 0.691 |
DOC_WW_Pin1_4 | 407 | 412 | PF00397 | 0.807 |
DOC_WW_Pin1_4 | 517 | 522 | PF00397 | 0.415 |
DOC_WW_Pin1_4 | 554 | 559 | PF00397 | 0.353 |
DOC_WW_Pin1_4 | 688 | 693 | PF00397 | 0.379 |
LIG_14-3-3_CanoR_1 | 107 | 115 | PF00244 | 0.518 |
LIG_14-3-3_CanoR_1 | 134 | 138 | PF00244 | 0.554 |
LIG_14-3-3_CanoR_1 | 258 | 264 | PF00244 | 0.471 |
LIG_14-3-3_CanoR_1 | 274 | 282 | PF00244 | 0.348 |
LIG_14-3-3_CanoR_1 | 383 | 392 | PF00244 | 0.685 |
LIG_14-3-3_CanoR_1 | 418 | 422 | PF00244 | 0.478 |
LIG_14-3-3_CanoR_1 | 465 | 471 | PF00244 | 0.517 |
LIG_14-3-3_CanoR_1 | 582 | 589 | PF00244 | 0.419 |
LIG_14-3-3_CanoR_1 | 697 | 703 | PF00244 | 0.370 |
LIG_14-3-3_CanoR_1 | 704 | 710 | PF00244 | 0.304 |
LIG_APCC_ABBA_1 | 371 | 376 | PF00400 | 0.545 |
LIG_APCC_ABBA_1 | 716 | 721 | PF00400 | 0.304 |
LIG_BIR_III_2 | 585 | 589 | PF00653 | 0.414 |
LIG_BRCT_BRCA1_1 | 159 | 163 | PF00533 | 0.549 |
LIG_Clathr_ClatBox_1 | 64 | 68 | PF01394 | 0.391 |
LIG_Clathr_ClatBox_1 | 740 | 744 | PF01394 | 0.304 |
LIG_CtBP_PxDLS_1 | 151 | 155 | PF00389 | 0.525 |
LIG_eIF4E_1 | 71 | 77 | PF01652 | 0.416 |
LIG_FHA_1 | 141 | 147 | PF00498 | 0.560 |
LIG_FHA_1 | 181 | 187 | PF00498 | 0.492 |
LIG_FHA_1 | 273 | 279 | PF00498 | 0.465 |
LIG_FHA_1 | 5 | 11 | PF00498 | 0.721 |
LIG_FHA_1 | 510 | 516 | PF00498 | 0.687 |
LIG_FHA_1 | 591 | 597 | PF00498 | 0.357 |
LIG_FHA_1 | 689 | 695 | PF00498 | 0.369 |
LIG_FHA_1 | 718 | 724 | PF00498 | 0.455 |
LIG_FHA_2 | 224 | 230 | PF00498 | 0.389 |
LIG_FHA_2 | 242 | 248 | PF00498 | 0.675 |
LIG_FHA_2 | 306 | 312 | PF00498 | 0.418 |
LIG_FHA_2 | 330 | 336 | PF00498 | 0.437 |
LIG_FHA_2 | 342 | 348 | PF00498 | 0.529 |
LIG_FHA_2 | 367 | 373 | PF00498 | 0.688 |
LIG_FHA_2 | 400 | 406 | PF00498 | 0.568 |
LIG_FHA_2 | 582 | 588 | PF00498 | 0.402 |
LIG_FHA_2 | 767 | 773 | PF00498 | 0.304 |
LIG_KLC1_Yacidic_2 | 372 | 376 | PF13176 | 0.545 |
LIG_LIR_Apic_2 | 372 | 377 | PF02991 | 0.538 |
LIG_LIR_Apic_2 | 443 | 447 | PF02991 | 0.451 |
LIG_LIR_Gen_1 | 178 | 186 | PF02991 | 0.512 |
LIG_LIR_Gen_1 | 315 | 322 | PF02991 | 0.478 |
LIG_LIR_Gen_1 | 542 | 552 | PF02991 | 0.376 |
LIG_LIR_Gen_1 | 68 | 78 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 178 | 184 | PF02991 | 0.540 |
LIG_LIR_Nem_3 | 311 | 316 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 542 | 547 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 657 | 662 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 68 | 74 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 89 | 94 | PF02991 | 0.354 |
LIG_LYPXL_yS_3 | 98 | 101 | PF13949 | 0.535 |
LIG_MYND_1 | 99 | 103 | PF01753 | 0.437 |
LIG_NRBOX | 212 | 218 | PF00104 | 0.415 |
LIG_NRBOX | 452 | 458 | PF00104 | 0.424 |
LIG_NRBOX | 752 | 758 | PF00104 | 0.304 |
LIG_PCNA_PIPBox_1 | 46 | 55 | PF02747 | 0.483 |
LIG_PCNA_yPIPBox_3 | 796 | 809 | PF02747 | 0.397 |
LIG_Pex14_1 | 137 | 141 | PF04695 | 0.637 |
LIG_Pex14_1 | 190 | 194 | PF04695 | 0.370 |
LIG_RPA_C_Fungi | 729 | 741 | PF08784 | 0.369 |
LIG_SH2_CRK | 601 | 605 | PF00017 | 0.385 |
LIG_SH2_CRK | 662 | 666 | PF00017 | 0.304 |
LIG_SH2_CRK | 91 | 95 | PF00017 | 0.361 |
LIG_SH2_NCK_1 | 181 | 185 | PF00017 | 0.503 |
LIG_SH2_PTP2 | 316 | 319 | PF00017 | 0.478 |
LIG_SH2_PTP2 | 374 | 377 | PF00017 | 0.536 |
LIG_SH2_PTP2 | 767 | 770 | PF00017 | 0.369 |
LIG_SH2_SRC | 206 | 209 | PF00017 | 0.384 |
LIG_SH2_SRC | 374 | 377 | PF00017 | 0.536 |
LIG_SH2_SRC | 52 | 55 | PF00017 | 0.364 |
LIG_SH2_SRC | 626 | 629 | PF00017 | 0.331 |
LIG_SH2_STAP1 | 436 | 440 | PF00017 | 0.352 |
LIG_SH2_STAP1 | 54 | 58 | PF00017 | 0.460 |
LIG_SH2_STAP1 | 563 | 567 | PF00017 | 0.323 |
LIG_SH2_STAP1 | 626 | 630 | PF00017 | 0.333 |
LIG_SH2_STAP1 | 719 | 723 | PF00017 | 0.304 |
LIG_SH2_STAT3 | 201 | 204 | PF00017 | 0.397 |
LIG_SH2_STAT3 | 702 | 705 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 194 | 197 | PF00017 | 0.384 |
LIG_SH2_STAT5 | 218 | 221 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 303 | 306 | PF00017 | 0.525 |
LIG_SH2_STAT5 | 316 | 319 | PF00017 | 0.641 |
LIG_SH2_STAT5 | 374 | 377 | PF00017 | 0.536 |
LIG_SH2_STAT5 | 52 | 55 | PF00017 | 0.428 |
LIG_SH2_STAT5 | 659 | 662 | PF00017 | 0.304 |
LIG_SH2_STAT5 | 719 | 722 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 767 | 770 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 800 | 803 | PF00017 | 0.388 |
LIG_SH3_2 | 352 | 357 | PF14604 | 0.571 |
LIG_SH3_3 | 102 | 108 | PF00018 | 0.562 |
LIG_SH3_3 | 301 | 307 | PF00018 | 0.534 |
LIG_SH3_3 | 349 | 355 | PF00018 | 0.620 |
LIG_SH3_3 | 409 | 415 | PF00018 | 0.769 |
LIG_SH3_3 | 465 | 471 | PF00018 | 0.468 |
LIG_SH3_3 | 486 | 492 | PF00018 | 0.554 |
LIG_SUMO_SIM_par_1 | 182 | 188 | PF11976 | 0.505 |
LIG_SUMO_SIM_par_1 | 329 | 335 | PF11976 | 0.506 |
LIG_TRAF2_1 | 244 | 247 | PF00917 | 0.626 |
LIG_TRAF2_1 | 312 | 315 | PF00917 | 0.453 |
LIG_TRAF2_1 | 44 | 47 | PF00917 | 0.488 |
LIG_TRAF2_1 | 749 | 752 | PF00917 | 0.304 |
LIG_TYR_ITIM | 179 | 184 | PF00017 | 0.535 |
LIG_TYR_ITIM | 660 | 665 | PF00017 | 0.304 |
LIG_TYR_ITIM | 765 | 770 | PF00017 | 0.369 |
LIG_UBA3_1 | 330 | 334 | PF00899 | 0.417 |
LIG_UBA3_1 | 740 | 747 | PF00899 | 0.222 |
MOD_CK1_1 | 140 | 146 | PF00069 | 0.662 |
MOD_CK1_1 | 153 | 159 | PF00069 | 0.621 |
MOD_CK1_1 | 20 | 26 | PF00069 | 0.649 |
MOD_CK1_1 | 239 | 245 | PF00069 | 0.540 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.482 |
MOD_CK1_1 | 329 | 335 | PF00069 | 0.446 |
MOD_CK1_1 | 398 | 404 | PF00069 | 0.664 |
MOD_CK1_1 | 40 | 46 | PF00069 | 0.367 |
MOD_CK1_1 | 473 | 479 | PF00069 | 0.641 |
MOD_CK1_1 | 493 | 499 | PF00069 | 0.680 |
MOD_CK1_1 | 509 | 515 | PF00069 | 0.616 |
MOD_CK1_1 | 517 | 523 | PF00069 | 0.406 |
MOD_CK1_1 | 590 | 596 | PF00069 | 0.388 |
MOD_CK1_1 | 728 | 734 | PF00069 | 0.227 |
MOD_CK1_1 | 84 | 90 | PF00069 | 0.381 |
MOD_CK2_1 | 223 | 229 | PF00069 | 0.392 |
MOD_CK2_1 | 241 | 247 | PF00069 | 0.532 |
MOD_CK2_1 | 329 | 335 | PF00069 | 0.508 |
MOD_CK2_1 | 399 | 405 | PF00069 | 0.564 |
MOD_CK2_1 | 41 | 47 | PF00069 | 0.482 |
MOD_CK2_1 | 581 | 587 | PF00069 | 0.404 |
MOD_CK2_1 | 766 | 772 | PF00069 | 0.304 |
MOD_GlcNHglycan | 115 | 118 | PF01048 | 0.661 |
MOD_GlcNHglycan | 159 | 162 | PF01048 | 0.601 |
MOD_GlcNHglycan | 165 | 168 | PF01048 | 0.544 |
MOD_GlcNHglycan | 23 | 26 | PF01048 | 0.627 |
MOD_GlcNHglycan | 241 | 244 | PF01048 | 0.512 |
MOD_GlcNHglycan | 386 | 389 | PF01048 | 0.690 |
MOD_GlcNHglycan | 395 | 398 | PF01048 | 0.585 |
MOD_GlcNHglycan | 472 | 475 | PF01048 | 0.636 |
MOD_GlcNHglycan | 508 | 511 | PF01048 | 0.562 |
MOD_GlcNHglycan | 516 | 519 | PF01048 | 0.381 |
MOD_GlcNHglycan | 539 | 542 | PF01048 | 0.383 |
MOD_GlcNHglycan | 573 | 576 | PF01048 | 0.443 |
MOD_GlcNHglycan | 589 | 592 | PF01048 | 0.583 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.406 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.572 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.563 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.600 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.625 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.498 |
MOD_GSK3_1 | 268 | 275 | PF00069 | 0.512 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.490 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.302 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.712 |
MOD_GSK3_1 | 466 | 473 | PF00069 | 0.549 |
MOD_GSK3_1 | 490 | 497 | PF00069 | 0.630 |
MOD_GSK3_1 | 571 | 578 | PF00069 | 0.452 |
MOD_GSK3_1 | 650 | 657 | PF00069 | 0.312 |
MOD_LATS_1 | 569 | 575 | PF00433 | 0.453 |
MOD_N-GLC_1 | 41 | 46 | PF02516 | 0.437 |
MOD_N-GLC_1 | 728 | 733 | PF02516 | 0.304 |
MOD_NEK2_1 | 152 | 157 | PF00069 | 0.625 |
MOD_NEK2_1 | 163 | 168 | PF00069 | 0.580 |
MOD_NEK2_1 | 217 | 222 | PF00069 | 0.382 |
MOD_NEK2_1 | 223 | 228 | PF00069 | 0.379 |
MOD_NEK2_1 | 41 | 46 | PF00069 | 0.420 |
MOD_NEK2_1 | 440 | 445 | PF00069 | 0.475 |
MOD_NEK2_1 | 477 | 482 | PF00069 | 0.670 |
MOD_NEK2_1 | 562 | 567 | PF00069 | 0.296 |
MOD_NEK2_1 | 589 | 594 | PF00069 | 0.426 |
MOD_NEK2_1 | 67 | 72 | PF00069 | 0.403 |
MOD_NEK2_1 | 698 | 703 | PF00069 | 0.362 |
MOD_PIKK_1 | 185 | 191 | PF00454 | 0.527 |
MOD_PIKK_1 | 200 | 206 | PF00454 | 0.306 |
MOD_PIKK_1 | 211 | 217 | PF00454 | 0.408 |
MOD_PIKK_1 | 273 | 279 | PF00454 | 0.400 |
MOD_PIKK_1 | 341 | 347 | PF00454 | 0.646 |
MOD_PIKK_1 | 399 | 405 | PF00454 | 0.706 |
MOD_PKA_1 | 796 | 802 | PF00069 | 0.415 |
MOD_PKA_2 | 133 | 139 | PF00069 | 0.558 |
MOD_PKA_2 | 257 | 263 | PF00069 | 0.587 |
MOD_PKA_2 | 273 | 279 | PF00069 | 0.388 |
MOD_PKA_2 | 417 | 423 | PF00069 | 0.552 |
MOD_PKA_2 | 581 | 587 | PF00069 | 0.416 |
MOD_PKA_2 | 796 | 802 | PF00069 | 0.429 |
MOD_Plk_1 | 41 | 47 | PF00069 | 0.443 |
MOD_Plk_1 | 67 | 73 | PF00069 | 0.397 |
MOD_Plk_4 | 28 | 34 | PF00069 | 0.612 |
MOD_Plk_4 | 326 | 332 | PF00069 | 0.534 |
MOD_Plk_4 | 473 | 479 | PF00069 | 0.546 |
MOD_Plk_4 | 496 | 502 | PF00069 | 0.534 |
MOD_Plk_4 | 599 | 605 | PF00069 | 0.402 |
MOD_Plk_4 | 654 | 660 | PF00069 | 0.333 |
MOD_Plk_4 | 796 | 802 | PF00069 | 0.415 |
MOD_ProDKin_1 | 348 | 354 | PF00069 | 0.569 |
MOD_ProDKin_1 | 4 | 10 | PF00069 | 0.690 |
MOD_ProDKin_1 | 407 | 413 | PF00069 | 0.805 |
MOD_ProDKin_1 | 517 | 523 | PF00069 | 0.406 |
MOD_ProDKin_1 | 554 | 560 | PF00069 | 0.347 |
MOD_ProDKin_1 | 688 | 694 | PF00069 | 0.376 |
MOD_SUMO_for_1 | 570 | 573 | PF00179 | 0.389 |
MOD_SUMO_rev_2 | 634 | 642 | PF00179 | 0.369 |
MOD_SUMO_rev_2 | 708 | 715 | PF00179 | 0.304 |
MOD_SUMO_rev_2 | 751 | 756 | PF00179 | 0.329 |
TRG_DiLeu_BaEn_1 | 752 | 757 | PF01217 | 0.304 |
TRG_DiLeu_BaLyEn_6 | 333 | 338 | PF01217 | 0.474 |
TRG_DiLeu_BaLyEn_6 | 543 | 548 | PF01217 | 0.294 |
TRG_DiLeu_BaLyEn_6 | 89 | 94 | PF01217 | 0.356 |
TRG_ENDOCYTIC_2 | 181 | 184 | PF00928 | 0.527 |
TRG_ENDOCYTIC_2 | 316 | 319 | PF00928 | 0.512 |
TRG_ENDOCYTIC_2 | 436 | 439 | PF00928 | 0.355 |
TRG_ENDOCYTIC_2 | 601 | 604 | PF00928 | 0.374 |
TRG_ENDOCYTIC_2 | 633 | 636 | PF00928 | 0.318 |
TRG_ENDOCYTIC_2 | 662 | 665 | PF00928 | 0.304 |
TRG_ENDOCYTIC_2 | 71 | 74 | PF00928 | 0.419 |
TRG_ENDOCYTIC_2 | 767 | 770 | PF00928 | 0.304 |
TRG_ENDOCYTIC_2 | 91 | 94 | PF00928 | 0.229 |
TRG_ENDOCYTIC_2 | 97 | 100 | PF00928 | 0.451 |
TRG_ER_diArg_1 | 230 | 233 | PF00400 | 0.478 |
TRG_ER_diArg_1 | 299 | 301 | PF00400 | 0.524 |
TRG_ER_diArg_1 | 361 | 364 | PF00400 | 0.647 |
TRG_ER_diArg_1 | 733 | 736 | PF00400 | 0.304 |
TRG_ER_diArg_1 | 777 | 779 | PF00400 | 0.477 |
TRG_ER_diArg_1 | 795 | 797 | PF00400 | 0.333 |
TRG_Pf-PMV_PEXEL_1 | 232 | 236 | PF00026 | 0.545 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HU62 | Leptomonas seymouri | 59% | 88% |
A0A3S5H5H6 | Leishmania donovani | 79% | 88% |
A4HSG3 | Leishmania infantum | 79% | 88% |
E9AKE7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 89% |
Q4QJG1 | Leishmania major | 81% | 100% |