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: 9 |
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 | 2 |
GO:0005874 | microtubule | 6 | 7 |
GO:0005929 | cilium | 4 | 8 |
GO:0042995 | cell projection | 2 | 8 |
GO:0043226 | organelle | 2 | 8 |
GO:0043227 | membrane-bounded organelle | 3 | 8 |
GO:0099080 | supramolecular complex | 2 | 7 |
GO:0099081 | supramolecular polymer | 3 | 7 |
GO:0099512 | supramolecular fiber | 4 | 7 |
GO:0099513 | polymeric cytoskeletal fiber | 5 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 8 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 8 |
Related structures:
AlphaFold database: Q4QEY2
Term | Name | Level | Count |
---|---|---|---|
GO:0000226 | microtubule cytoskeleton organization | 3 | 3 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0006996 | organelle organization | 4 | 3 |
GO:0007010 | cytoskeleton organization | 5 | 3 |
GO:0007017 | microtubule-based process | 2 | 3 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009987 | cellular process | 1 | 3 |
GO:0016043 | cellular component organization | 3 | 3 |
GO:0018095 | protein polyglutamylation | 7 | 8 |
GO:0018193 | peptidyl-amino acid modification | 5 | 8 |
GO:0018200 | peptidyl-glutamic acid modification | 6 | 8 |
GO:0019538 | protein metabolic process | 3 | 11 |
GO:0036211 | protein modification process | 4 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0043412 | macromolecule modification | 4 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:0071840 | cellular component organization or biogenesis | 2 | 3 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 7 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004835 | tubulin-tyrosine ligase activity | 3 | 8 |
GO:0005488 | binding | 1 | 8 |
GO:0005515 | protein binding | 2 | 3 |
GO:0005524 | ATP binding | 5 | 7 |
GO:0008092 | cytoskeletal protein binding | 3 | 3 |
GO:0015631 | tubulin binding | 4 | 3 |
GO:0016874 | ligase activity | 2 | 11 |
GO:0016879 | ligase activity, forming carbon-nitrogen bonds | 3 | 8 |
GO:0016881 | acid-amino acid ligase activity | 4 | 8 |
GO:0017076 | purine nucleotide binding | 4 | 7 |
GO:0030554 | adenyl nucleotide binding | 5 | 7 |
GO:0032553 | ribonucleotide binding | 3 | 7 |
GO:0032555 | purine ribonucleotide binding | 4 | 7 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 7 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 7 |
GO:0036094 | small molecule binding | 2 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043168 | anion binding | 3 | 7 |
GO:0070739 | protein-glutamic acid ligase activity | 3 | 3 |
GO:0070740 | tubulin-glutamic acid ligase activity | 4 | 3 |
GO:0097159 | organic cyclic compound binding | 2 | 7 |
GO:0097367 | carbohydrate derivative binding | 2 | 7 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 8 |
GO:1901265 | nucleoside phosphate binding | 3 | 7 |
GO:1901363 | heterocyclic compound binding | 2 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 100 | 102 | PF00675 | 0.796 |
CLV_NRD_NRD_1 | 323 | 325 | PF00675 | 0.638 |
CLV_NRD_NRD_1 | 356 | 358 | PF00675 | 0.510 |
CLV_NRD_NRD_1 | 385 | 387 | PF00675 | 0.341 |
CLV_NRD_NRD_1 | 395 | 397 | PF00675 | 0.353 |
CLV_NRD_NRD_1 | 443 | 445 | PF00675 | 0.244 |
CLV_NRD_NRD_1 | 478 | 480 | PF00675 | 0.322 |
CLV_NRD_NRD_1 | 55 | 57 | PF00675 | 0.664 |
CLV_NRD_NRD_1 | 62 | 64 | PF00675 | 0.664 |
CLV_NRD_NRD_1 | 71 | 73 | PF00675 | 0.770 |
CLV_PCSK_FUR_1 | 321 | 325 | PF00082 | 0.629 |
CLV_PCSK_KEX2_1 | 100 | 102 | PF00082 | 0.705 |
CLV_PCSK_KEX2_1 | 145 | 147 | PF00082 | 0.590 |
CLV_PCSK_KEX2_1 | 196 | 198 | PF00082 | 0.653 |
CLV_PCSK_KEX2_1 | 323 | 325 | PF00082 | 0.638 |
CLV_PCSK_KEX2_1 | 356 | 358 | PF00082 | 0.495 |
CLV_PCSK_KEX2_1 | 395 | 397 | PF00082 | 0.353 |
CLV_PCSK_KEX2_1 | 443 | 445 | PF00082 | 0.244 |
CLV_PCSK_KEX2_1 | 477 | 479 | PF00082 | 0.322 |
CLV_PCSK_PC1ET2_1 | 100 | 102 | PF00082 | 0.690 |
CLV_PCSK_PC1ET2_1 | 145 | 147 | PF00082 | 0.590 |
CLV_PCSK_PC1ET2_1 | 196 | 198 | PF00082 | 0.642 |
CLV_PCSK_SKI1_1 | 14 | 18 | PF00082 | 0.662 |
CLV_PCSK_SKI1_1 | 494 | 498 | PF00082 | 0.318 |
CLV_PCSK_SKI1_1 | 58 | 62 | PF00082 | 0.580 |
CLV_PCSK_SKI1_1 | 760 | 764 | PF00082 | 0.295 |
CLV_PCSK_SKI1_1 | 772 | 776 | PF00082 | 0.309 |
CLV_PCSK_SKI1_1 | 97 | 101 | PF00082 | 0.646 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.657 |
DEG_SCF_FBW7_1 | 83 | 89 | PF00400 | 0.701 |
DEG_SPOP_SBC_1 | 283 | 287 | PF00917 | 0.626 |
DEG_SPOP_SBC_1 | 362 | 366 | PF00917 | 0.407 |
DOC_CKS1_1 | 83 | 88 | PF01111 | 0.701 |
DOC_MAPK_gen_1 | 196 | 204 | PF00069 | 0.620 |
DOC_MAPK_gen_1 | 443 | 449 | PF00069 | 0.444 |
DOC_MAPK_gen_1 | 56 | 62 | PF00069 | 0.562 |
DOC_MAPK_gen_1 | 612 | 620 | PF00069 | 0.552 |
DOC_MAPK_MEF2A_6 | 612 | 620 | PF00069 | 0.552 |
DOC_MAPK_NFAT4_5 | 613 | 621 | PF00069 | 0.552 |
DOC_MAPK_RevD_3 | 184 | 197 | PF00069 | 0.610 |
DOC_PP1_RVXF_1 | 700 | 707 | PF00149 | 0.518 |
DOC_PP1_RVXF_1 | 770 | 776 | PF00149 | 0.518 |
DOC_USP7_MATH_1 | 165 | 169 | PF00917 | 0.728 |
DOC_USP7_MATH_1 | 189 | 193 | PF00917 | 0.721 |
DOC_USP7_MATH_1 | 208 | 212 | PF00917 | 0.579 |
DOC_USP7_MATH_1 | 216 | 220 | PF00917 | 0.691 |
DOC_USP7_MATH_1 | 229 | 233 | PF00917 | 0.742 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.682 |
DOC_USP7_MATH_1 | 303 | 307 | PF00917 | 0.674 |
DOC_USP7_MATH_1 | 313 | 317 | PF00917 | 0.754 |
DOC_USP7_MATH_1 | 41 | 45 | PF00917 | 0.606 |
DOC_USP7_MATH_1 | 431 | 435 | PF00917 | 0.534 |
DOC_USP7_MATH_1 | 544 | 548 | PF00917 | 0.482 |
DOC_USP7_MATH_1 | 577 | 581 | PF00917 | 0.616 |
DOC_USP7_MATH_1 | 586 | 590 | PF00917 | 0.584 |
DOC_USP7_MATH_1 | 646 | 650 | PF00917 | 0.584 |
DOC_USP7_MATH_1 | 748 | 752 | PF00917 | 0.527 |
DOC_USP7_UBL2_3 | 196 | 200 | PF12436 | 0.530 |
DOC_USP7_UBL2_3 | 802 | 806 | PF12436 | 0.396 |
DOC_WW_Pin1_4 | 21 | 26 | PF00397 | 0.668 |
DOC_WW_Pin1_4 | 279 | 284 | PF00397 | 0.705 |
DOC_WW_Pin1_4 | 44 | 49 | PF00397 | 0.647 |
DOC_WW_Pin1_4 | 522 | 527 | PF00397 | 0.550 |
DOC_WW_Pin1_4 | 563 | 568 | PF00397 | 0.528 |
DOC_WW_Pin1_4 | 746 | 751 | PF00397 | 0.491 |
DOC_WW_Pin1_4 | 82 | 87 | PF00397 | 0.708 |
DOC_WW_Pin1_4 | 92 | 97 | PF00397 | 0.597 |
LIG_14-3-3_CanoR_1 | 250 | 259 | PF00244 | 0.587 |
LIG_14-3-3_CanoR_1 | 357 | 363 | PF00244 | 0.370 |
LIG_14-3-3_CanoR_1 | 408 | 412 | PF00244 | 0.518 |
LIG_14-3-3_CanoR_1 | 444 | 450 | PF00244 | 0.516 |
LIG_14-3-3_CanoR_1 | 529 | 533 | PF00244 | 0.444 |
LIG_14-3-3_CanoR_1 | 81 | 86 | PF00244 | 0.688 |
LIG_Actin_WH2_2 | 697 | 715 | PF00022 | 0.518 |
LIG_APCC_ABBA_1 | 468 | 473 | PF00400 | 0.518 |
LIG_BIR_III_4 | 174 | 178 | PF00653 | 0.661 |
LIG_BIR_III_4 | 426 | 430 | PF00653 | 0.475 |
LIG_BRCT_BRCA1_1 | 363 | 367 | PF00533 | 0.542 |
LIG_BRCT_BRCA1_1 | 450 | 454 | PF00533 | 0.522 |
LIG_BRCT_BRCA1_1 | 568 | 572 | PF00533 | 0.522 |
LIG_deltaCOP1_diTrp_1 | 347 | 352 | PF00928 | 0.482 |
LIG_eIF4E_1 | 602 | 608 | PF01652 | 0.518 |
LIG_eIF4E_1 | 729 | 735 | PF01652 | 0.476 |
LIG_FHA_1 | 145 | 151 | PF00498 | 0.589 |
LIG_FHA_1 | 197 | 203 | PF00498 | 0.656 |
LIG_FHA_1 | 413 | 419 | PF00498 | 0.491 |
LIG_FHA_1 | 459 | 465 | PF00498 | 0.497 |
LIG_FHA_1 | 479 | 485 | PF00498 | 0.518 |
LIG_FHA_1 | 573 | 579 | PF00498 | 0.475 |
LIG_FHA_1 | 752 | 758 | PF00498 | 0.592 |
LIG_FHA_1 | 768 | 774 | PF00498 | 0.487 |
LIG_FHA_1 | 87 | 93 | PF00498 | 0.792 |
LIG_FHA_2 | 251 | 257 | PF00498 | 0.600 |
LIG_FHA_2 | 383 | 389 | PF00498 | 0.518 |
LIG_FHA_2 | 411 | 417 | PF00498 | 0.518 |
LIG_FHA_2 | 754 | 760 | PF00498 | 0.518 |
LIG_LIR_Apic_2 | 461 | 465 | PF02991 | 0.543 |
LIG_LIR_Apic_2 | 531 | 535 | PF02991 | 0.444 |
LIG_LIR_Gen_1 | 347 | 355 | PF02991 | 0.477 |
LIG_LIR_Gen_1 | 404 | 414 | PF02991 | 0.522 |
LIG_LIR_Gen_1 | 634 | 645 | PF02991 | 0.486 |
LIG_LIR_Gen_1 | 680 | 688 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 347 | 351 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 388 | 394 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 404 | 409 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 623 | 628 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 634 | 640 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 668 | 674 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 680 | 684 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 691 | 695 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 725 | 729 | PF02991 | 0.572 |
LIG_LIR_Nem_3 | 803 | 808 | PF02991 | 0.471 |
LIG_MAD2 | 772 | 780 | PF02301 | 0.518 |
LIG_PCNA_PIPBox_1 | 652 | 661 | PF02747 | 0.518 |
LIG_PDZ_Class_2 | 805 | 810 | PF00595 | 0.450 |
LIG_Pex14_2 | 471 | 475 | PF04695 | 0.522 |
LIG_Pex14_2 | 681 | 685 | PF04695 | 0.502 |
LIG_PTB_Apo_2 | 700 | 707 | PF02174 | 0.518 |
LIG_SH2_CRK | 391 | 395 | PF00017 | 0.521 |
LIG_SH2_CRK | 406 | 410 | PF00017 | 0.518 |
LIG_SH2_CRK | 462 | 466 | PF00017 | 0.518 |
LIG_SH2_CRK | 625 | 629 | PF00017 | 0.517 |
LIG_SH2_CRK | 671 | 675 | PF00017 | 0.486 |
LIG_SH2_CRK | 709 | 713 | PF00017 | 0.510 |
LIG_SH2_CRK | 731 | 735 | PF00017 | 0.518 |
LIG_SH2_NCK_1 | 462 | 466 | PF00017 | 0.518 |
LIG_SH2_PTP2 | 619 | 622 | PF00017 | 0.518 |
LIG_SH2_SRC | 597 | 600 | PF00017 | 0.491 |
LIG_SH2_STAP1 | 731 | 735 | PF00017 | 0.518 |
LIG_SH2_STAT5 | 397 | 400 | PF00017 | 0.518 |
LIG_SH2_STAT5 | 597 | 600 | PF00017 | 0.552 |
LIG_SH2_STAT5 | 602 | 605 | PF00017 | 0.552 |
LIG_SH2_STAT5 | 619 | 622 | PF00017 | 0.547 |
LIG_SH2_STAT5 | 631 | 634 | PF00017 | 0.457 |
LIG_SH2_STAT5 | 687 | 690 | PF00017 | 0.550 |
LIG_SH2_STAT5 | 695 | 698 | PF00017 | 0.552 |
LIG_SH3_3 | 132 | 138 | PF00018 | 0.573 |
LIG_SH3_3 | 183 | 189 | PF00018 | 0.813 |
LIG_SH3_3 | 201 | 207 | PF00018 | 0.514 |
LIG_SH3_3 | 564 | 570 | PF00018 | 0.516 |
LIG_SH3_3 | 771 | 777 | PF00018 | 0.518 |
LIG_SH3_3 | 85 | 91 | PF00018 | 0.668 |
LIG_SH3_4 | 137 | 144 | PF00018 | 0.569 |
LIG_SUMO_SIM_anti_2 | 199 | 205 | PF11976 | 0.624 |
LIG_SUMO_SIM_par_1 | 445 | 451 | PF11976 | 0.491 |
LIG_TRAF2_1 | 139 | 142 | PF00917 | 0.581 |
LIG_TYR_ITAM | 388 | 409 | PF00017 | 0.518 |
LIG_TYR_ITIM | 389 | 394 | PF00017 | 0.518 |
LIG_TYR_ITIM | 707 | 712 | PF00017 | 0.518 |
LIG_WRC_WIRS_1 | 449 | 454 | PF05994 | 0.522 |
LIG_WRC_WIRS_1 | 518 | 523 | PF05994 | 0.522 |
LIG_WW_1 | 776 | 779 | PF00397 | 0.522 |
LIG_WW_2 | 90 | 93 | PF00397 | 0.604 |
MOD_CDK_SPK_2 | 92 | 97 | PF00069 | 0.568 |
MOD_CDK_SPxxK_3 | 522 | 529 | PF00069 | 0.491 |
MOD_CK1_1 | 234 | 240 | PF00069 | 0.776 |
MOD_CK1_1 | 282 | 288 | PF00069 | 0.694 |
MOD_CK1_1 | 306 | 312 | PF00069 | 0.749 |
MOD_CK1_1 | 44 | 50 | PF00069 | 0.611 |
MOD_CK1_1 | 448 | 454 | PF00069 | 0.491 |
MOD_CK1_1 | 548 | 554 | PF00069 | 0.572 |
MOD_CK1_1 | 563 | 569 | PF00069 | 0.535 |
MOD_CK1_1 | 576 | 582 | PF00069 | 0.498 |
MOD_CK1_1 | 593 | 599 | PF00069 | 0.426 |
MOD_CK1_1 | 648 | 654 | PF00069 | 0.522 |
MOD_CK1_1 | 657 | 663 | PF00069 | 0.498 |
MOD_CK1_1 | 751 | 757 | PF00069 | 0.527 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.697 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.700 |
MOD_CK2_1 | 544 | 550 | PF00069 | 0.597 |
MOD_Cter_Amidation | 194 | 197 | PF01082 | 0.651 |
MOD_Cter_Amidation | 610 | 613 | PF01082 | 0.353 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.689 |
MOD_GlcNHglycan | 119 | 122 | PF01048 | 0.612 |
MOD_GlcNHglycan | 18 | 21 | PF01048 | 0.673 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.651 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.713 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.760 |
MOD_GlcNHglycan | 237 | 240 | PF01048 | 0.761 |
MOD_GlcNHglycan | 276 | 279 | PF01048 | 0.796 |
MOD_GlcNHglycan | 295 | 298 | PF01048 | 0.784 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.661 |
MOD_GlcNHglycan | 418 | 421 | PF01048 | 0.293 |
MOD_GlcNHglycan | 433 | 436 | PF01048 | 0.369 |
MOD_GlcNHglycan | 550 | 553 | PF01048 | 0.391 |
MOD_GlcNHglycan | 556 | 559 | PF01048 | 0.333 |
MOD_GlcNHglycan | 575 | 578 | PF01048 | 0.346 |
MOD_GlcNHglycan | 588 | 591 | PF01048 | 0.299 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.828 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.793 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.766 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.654 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.748 |
MOD_GSK3_1 | 269 | 276 | PF00069 | 0.720 |
MOD_GSK3_1 | 278 | 285 | PF00069 | 0.741 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.674 |
MOD_GSK3_1 | 358 | 365 | PF00069 | 0.503 |
MOD_GSK3_1 | 412 | 419 | PF00069 | 0.536 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.696 |
MOD_GSK3_1 | 454 | 461 | PF00069 | 0.518 |
MOD_GSK3_1 | 517 | 524 | PF00069 | 0.520 |
MOD_GSK3_1 | 544 | 551 | PF00069 | 0.560 |
MOD_GSK3_1 | 572 | 579 | PF00069 | 0.567 |
MOD_GSK3_1 | 586 | 593 | PF00069 | 0.528 |
MOD_GSK3_1 | 597 | 604 | PF00069 | 0.486 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.689 |
MOD_GSK3_1 | 746 | 753 | PF00069 | 0.518 |
MOD_GSK3_1 | 792 | 799 | PF00069 | 0.463 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.738 |
MOD_N-GLC_1 | 208 | 213 | PF02516 | 0.652 |
MOD_N-GLC_1 | 21 | 26 | PF02516 | 0.569 |
MOD_N-GLC_1 | 572 | 577 | PF02516 | 0.275 |
MOD_N-GLC_1 | 746 | 751 | PF02516 | 0.318 |
MOD_N-GLC_2 | 560 | 562 | PF02516 | 0.291 |
MOD_NEK2_1 | 235 | 240 | PF00069 | 0.578 |
MOD_NEK2_1 | 284 | 289 | PF00069 | 0.648 |
MOD_NEK2_1 | 454 | 459 | PF00069 | 0.518 |
MOD_NEK2_1 | 521 | 526 | PF00069 | 0.525 |
MOD_NEK2_1 | 572 | 577 | PF00069 | 0.532 |
MOD_NEK2_1 | 621 | 626 | PF00069 | 0.481 |
MOD_NEK2_1 | 640 | 645 | PF00069 | 0.518 |
MOD_NEK2_1 | 752 | 757 | PF00069 | 0.518 |
MOD_NEK2_1 | 767 | 772 | PF00069 | 0.518 |
MOD_NEK2_2 | 245 | 250 | PF00069 | 0.608 |
MOD_NEK2_2 | 363 | 368 | PF00069 | 0.485 |
MOD_NEK2_2 | 407 | 412 | PF00069 | 0.518 |
MOD_PIKK_1 | 315 | 321 | PF00454 | 0.676 |
MOD_PIKK_1 | 478 | 484 | PF00454 | 0.482 |
MOD_PIKK_1 | 488 | 494 | PF00454 | 0.489 |
MOD_PIKK_1 | 577 | 583 | PF00454 | 0.491 |
MOD_PIKK_1 | 648 | 654 | PF00454 | 0.429 |
MOD_PKA_1 | 196 | 202 | PF00069 | 0.653 |
MOD_PKA_1 | 478 | 484 | PF00069 | 0.522 |
MOD_PKA_1 | 512 | 518 | PF00069 | 0.502 |
MOD_PKA_1 | 58 | 64 | PF00069 | 0.652 |
MOD_PKA_2 | 196 | 202 | PF00069 | 0.653 |
MOD_PKA_2 | 306 | 312 | PF00069 | 0.703 |
MOD_PKA_2 | 358 | 364 | PF00069 | 0.433 |
MOD_PKA_2 | 407 | 413 | PF00069 | 0.518 |
MOD_PKA_2 | 478 | 484 | PF00069 | 0.518 |
MOD_PKA_2 | 528 | 534 | PF00069 | 0.465 |
MOD_PKA_2 | 71 | 77 | PF00069 | 0.831 |
MOD_PKB_1 | 77 | 85 | PF00069 | 0.663 |
MOD_Plk_1 | 245 | 251 | PF00069 | 0.622 |
MOD_Plk_1 | 466 | 472 | PF00069 | 0.466 |
MOD_Plk_1 | 79 | 85 | PF00069 | 0.644 |
MOD_Plk_2-3 | 131 | 137 | PF00069 | 0.646 |
MOD_Plk_2-3 | 722 | 728 | PF00069 | 0.523 |
MOD_Plk_4 | 466 | 472 | PF00069 | 0.491 |
MOD_Plk_4 | 517 | 523 | PF00069 | 0.522 |
MOD_Plk_4 | 528 | 534 | PF00069 | 0.442 |
MOD_Plk_4 | 593 | 599 | PF00069 | 0.526 |
MOD_ProDKin_1 | 21 | 27 | PF00069 | 0.665 |
MOD_ProDKin_1 | 279 | 285 | PF00069 | 0.702 |
MOD_ProDKin_1 | 44 | 50 | PF00069 | 0.648 |
MOD_ProDKin_1 | 522 | 528 | PF00069 | 0.550 |
MOD_ProDKin_1 | 563 | 569 | PF00069 | 0.528 |
MOD_ProDKin_1 | 746 | 752 | PF00069 | 0.491 |
MOD_ProDKin_1 | 82 | 88 | PF00069 | 0.701 |
MOD_ProDKin_1 | 92 | 98 | PF00069 | 0.599 |
MOD_SUMO_for_1 | 126 | 129 | PF00179 | 0.620 |
MOD_SUMO_rev_2 | 337 | 343 | PF00179 | 0.643 |
MOD_SUMO_rev_2 | 510 | 515 | PF00179 | 0.475 |
TRG_AP2beta_CARGO_1 | 634 | 644 | PF09066 | 0.518 |
TRG_DiLeu_BaLyEn_6 | 603 | 608 | PF01217 | 0.518 |
TRG_DiLeu_BaLyEn_6 | 757 | 762 | PF01217 | 0.518 |
TRG_ENDOCYTIC_2 | 391 | 394 | PF00928 | 0.521 |
TRG_ENDOCYTIC_2 | 406 | 409 | PF00928 | 0.476 |
TRG_ENDOCYTIC_2 | 619 | 622 | PF00928 | 0.521 |
TRG_ENDOCYTIC_2 | 625 | 628 | PF00928 | 0.517 |
TRG_ENDOCYTIC_2 | 671 | 674 | PF00928 | 0.486 |
TRG_ENDOCYTIC_2 | 709 | 712 | PF00928 | 0.510 |
TRG_ENDOCYTIC_2 | 731 | 734 | PF00928 | 0.493 |
TRG_ER_diArg_1 | 320 | 323 | PF00400 | 0.660 |
TRG_ER_diArg_1 | 355 | 357 | PF00400 | 0.502 |
TRG_ER_diArg_1 | 394 | 396 | PF00400 | 0.546 |
TRG_ER_diArg_1 | 443 | 445 | PF00400 | 0.475 |
TRG_ER_diArg_1 | 477 | 479 | PF00400 | 0.522 |
TRG_ER_diArg_1 | 791 | 794 | PF00400 | 0.447 |
TRG_NES_CRM1_1 | 653 | 668 | PF08389 | 0.518 |
TRG_NLS_MonoCore_2 | 55 | 60 | PF00514 | 0.632 |
TRG_NLS_MonoExtN_4 | 56 | 61 | PF00514 | 0.629 |
TRG_NLS_MonoExtN_4 | 97 | 104 | PF00514 | 0.692 |
TRG_Pf-PMV_PEXEL_1 | 161 | 166 | PF00026 | 0.700 |
TRG_Pf-PMV_PEXEL_1 | 396 | 400 | PF00026 | 0.318 |
TRG_Pf-PMV_PEXEL_1 | 760 | 764 | PF00026 | 0.318 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDX5 | Leptomonas seymouri | 59% | 100% |
A0A3Q8IDL7 | Leishmania donovani | 23% | 100% |
A0A3S5H6X0 | Leishmania donovani | 89% | 99% |
A4H8G3 | Leishmania braziliensis | 71% | 100% |
A4HWT7 | Leishmania infantum | 90% | 99% |
A4HYN9 | Leishmania infantum | 23% | 100% |
E9AQJ5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 99% |
E9AUL7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
Q4QCW7 | Leishmania major | 24% | 100% |