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. | yes | yes: 5 |
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:0005829 | cytosol | 2 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0070209 | ASTRA complex | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
Related structures:
AlphaFold database: A4HMB8
Term | Name | Level | Count |
---|---|---|---|
GO:0000723 | telomere maintenance | 5 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006259 | DNA metabolic process | 4 | 1 |
GO:0006278 | RNA-templated DNA biosynthetic process | 6 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007004 | telomere maintenance via telomerase | 7 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009058 | biosynthetic process | 2 | 1 |
GO:0009059 | macromolecule biosynthetic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010833 | telomere maintenance via telomere lengthening | 6 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0018130 | heterocycle biosynthetic process | 4 | 1 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 1 |
GO:0031647 | regulation of protein stability | 3 | 1 |
GO:0032200 | telomere organization | 6 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044249 | cellular biosynthetic process | 3 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0050821 | protein stabilization | 4 | 1 |
GO:0051276 | chromosome organization | 5 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0065008 | regulation of biological quality | 2 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0071897 | DNA biosynthetic process | 5 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 1 |
GO:1901576 | organic substance biosynthetic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003677 | DNA binding | 4 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0005515 | protein binding | 2 | 1 |
GO:0031072 | heat shock protein binding | 3 | 1 |
GO:0042162 | telomeric DNA binding | 6 | 1 |
GO:0043565 | sequence-specific DNA binding | 5 | 1 |
GO:0051879 | Hsp90 protein binding | 4 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 407 | 411 | PF00656 | 0.614 |
CLV_MEL_PAP_1 | 458 | 464 | PF00089 | 0.812 |
CLV_NRD_NRD_1 | 171 | 173 | PF00675 | 0.566 |
CLV_NRD_NRD_1 | 180 | 182 | PF00675 | 0.487 |
CLV_NRD_NRD_1 | 221 | 223 | PF00675 | 0.737 |
CLV_NRD_NRD_1 | 325 | 327 | PF00675 | 0.332 |
CLV_NRD_NRD_1 | 709 | 711 | PF00675 | 0.748 |
CLV_NRD_NRD_1 | 723 | 725 | PF00675 | 0.554 |
CLV_NRD_NRD_1 | 820 | 822 | PF00675 | 0.475 |
CLV_NRD_NRD_1 | 844 | 846 | PF00675 | 0.635 |
CLV_NRD_NRD_1 | 883 | 885 | PF00675 | 0.387 |
CLV_PCSK_KEX2_1 | 171 | 173 | PF00082 | 0.560 |
CLV_PCSK_KEX2_1 | 180 | 182 | PF00082 | 0.487 |
CLV_PCSK_KEX2_1 | 221 | 223 | PF00082 | 0.689 |
CLV_PCSK_KEX2_1 | 242 | 244 | PF00082 | 0.602 |
CLV_PCSK_KEX2_1 | 723 | 725 | PF00082 | 0.651 |
CLV_PCSK_KEX2_1 | 844 | 846 | PF00082 | 0.635 |
CLV_PCSK_PC1ET2_1 | 242 | 244 | PF00082 | 0.602 |
CLV_PCSK_PC7_1 | 238 | 244 | PF00082 | 0.347 |
CLV_PCSK_SKI1_1 | 156 | 160 | PF00082 | 0.563 |
CLV_PCSK_SKI1_1 | 163 | 167 | PF00082 | 0.499 |
CLV_PCSK_SKI1_1 | 187 | 191 | PF00082 | 0.524 |
CLV_PCSK_SKI1_1 | 520 | 524 | PF00082 | 0.692 |
CLV_PCSK_SKI1_1 | 72 | 76 | PF00082 | 0.603 |
CLV_PCSK_SKI1_1 | 891 | 895 | PF00082 | 0.462 |
CLV_Separin_Metazoa | 48 | 52 | PF03568 | 0.380 |
CLV_Separin_Metazoa | 830 | 834 | PF03568 | 0.413 |
CLV_Separin_Metazoa | 881 | 885 | PF03568 | 0.368 |
DEG_APCC_DBOX_1 | 8 | 16 | PF00400 | 0.616 |
DEG_APCC_DBOX_1 | 890 | 898 | PF00400 | 0.460 |
DEG_MDM2_SWIB_1 | 864 | 872 | PF02201 | 0.522 |
DEG_SCF_FBW7_1 | 448 | 455 | PF00400 | 0.697 |
DEG_SIAH_1 | 366 | 374 | PF03145 | 0.358 |
DEG_SPOP_SBC_1 | 857 | 861 | PF00917 | 0.449 |
DOC_CKS1_1 | 433 | 438 | PF01111 | 0.666 |
DOC_CKS1_1 | 773 | 778 | PF01111 | 0.528 |
DOC_CYCLIN_RxL_1 | 181 | 193 | PF00134 | 0.598 |
DOC_CYCLIN_yCln2_LP_2 | 345 | 351 | PF00134 | 0.522 |
DOC_CYCLIN_yCln2_LP_2 | 631 | 637 | PF00134 | 0.588 |
DOC_MAPK_DCC_7 | 589 | 599 | PF00069 | 0.355 |
DOC_MAPK_DCC_7 | 833 | 843 | PF00069 | 0.569 |
DOC_MAPK_gen_1 | 43 | 52 | PF00069 | 0.639 |
DOC_MAPK_gen_1 | 621 | 630 | PF00069 | 0.435 |
DOC_MAPK_gen_1 | 710 | 716 | PF00069 | 0.795 |
DOC_MAPK_gen_1 | 96 | 103 | PF00069 | 0.324 |
DOC_MAPK_HePTP_8 | 618 | 630 | PF00069 | 0.545 |
DOC_MAPK_MEF2A_6 | 45 | 54 | PF00069 | 0.599 |
DOC_MAPK_MEF2A_6 | 589 | 597 | PF00069 | 0.571 |
DOC_MAPK_MEF2A_6 | 621 | 630 | PF00069 | 0.452 |
DOC_MAPK_MEF2A_6 | 96 | 103 | PF00069 | 0.324 |
DOC_MAPK_RevD_3 | 165 | 181 | PF00069 | 0.588 |
DOC_PP2B_LxvP_1 | 631 | 634 | PF13499 | 0.589 |
DOC_PP4_FxxP_1 | 370 | 373 | PF00568 | 0.343 |
DOC_PP4_FxxP_1 | 480 | 483 | PF00568 | 0.770 |
DOC_USP7_MATH_1 | 512 | 516 | PF00917 | 0.788 |
DOC_USP7_MATH_1 | 824 | 828 | PF00917 | 0.539 |
DOC_USP7_MATH_1 | 856 | 860 | PF00917 | 0.681 |
DOC_USP7_UBL2_3 | 327 | 331 | PF12436 | 0.589 |
DOC_WW_Pin1_4 | 405 | 410 | PF00397 | 0.481 |
DOC_WW_Pin1_4 | 432 | 437 | PF00397 | 0.552 |
DOC_WW_Pin1_4 | 448 | 453 | PF00397 | 0.547 |
DOC_WW_Pin1_4 | 496 | 501 | PF00397 | 0.636 |
DOC_WW_Pin1_4 | 606 | 611 | PF00397 | 0.381 |
DOC_WW_Pin1_4 | 65 | 70 | PF00397 | 0.492 |
DOC_WW_Pin1_4 | 772 | 777 | PF00397 | 0.535 |
LIG_14-3-3_CanoR_1 | 171 | 179 | PF00244 | 0.612 |
LIG_14-3-3_CanoR_1 | 289 | 296 | PF00244 | 0.535 |
LIG_14-3-3_CanoR_1 | 461 | 466 | PF00244 | 0.738 |
LIG_14-3-3_CanoR_1 | 51 | 55 | PF00244 | 0.639 |
LIG_14-3-3_CanoR_1 | 566 | 575 | PF00244 | 0.558 |
LIG_14-3-3_CanoR_1 | 710 | 716 | PF00244 | 0.568 |
LIG_14-3-3_CanoR_1 | 9 | 13 | PF00244 | 0.461 |
LIG_Actin_WH2_2 | 155 | 173 | PF00022 | 0.594 |
LIG_AP2alpha_1 | 366 | 370 | PF02296 | 0.643 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.404 |
LIG_BRCT_BRCA1_1 | 115 | 119 | PF00533 | 0.422 |
LIG_BRCT_BRCA1_1 | 233 | 237 | PF00533 | 0.528 |
LIG_BRCT_BRCA1_1 | 270 | 274 | PF00533 | 0.329 |
LIG_BRCT_BRCA1_1 | 321 | 325 | PF00533 | 0.569 |
LIG_BRCT_BRCA1_1 | 568 | 572 | PF00533 | 0.615 |
LIG_BRCT_BRCA1_1 | 580 | 584 | PF00533 | 0.574 |
LIG_BRCT_BRCA1_1 | 860 | 864 | PF00533 | 0.515 |
LIG_BRCT_BRCA1_2 | 321 | 327 | PF00533 | 0.593 |
LIG_BRCT_BRCA1_2 | 568 | 574 | PF00533 | 0.626 |
LIG_BRCT_BRCA1_2 | 860 | 866 | PF00533 | 0.620 |
LIG_Clathr_ClatBox_1 | 503 | 507 | PF01394 | 0.502 |
LIG_eIF4E_1 | 652 | 658 | PF01652 | 0.568 |
LIG_EVH1_1 | 698 | 702 | PF00568 | 0.697 |
LIG_FHA_1 | 131 | 137 | PF00498 | 0.526 |
LIG_FHA_1 | 153 | 159 | PF00498 | 0.525 |
LIG_FHA_1 | 164 | 170 | PF00498 | 0.541 |
LIG_FHA_1 | 246 | 252 | PF00498 | 0.375 |
LIG_FHA_1 | 274 | 280 | PF00498 | 0.517 |
LIG_FHA_1 | 377 | 383 | PF00498 | 0.624 |
LIG_FHA_1 | 453 | 459 | PF00498 | 0.614 |
LIG_FHA_1 | 589 | 595 | PF00498 | 0.627 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.475 |
LIG_FHA_1 | 653 | 659 | PF00498 | 0.592 |
LIG_FHA_1 | 701 | 707 | PF00498 | 0.698 |
LIG_FHA_1 | 710 | 716 | PF00498 | 0.668 |
LIG_FHA_1 | 748 | 754 | PF00498 | 0.369 |
LIG_FHA_1 | 824 | 830 | PF00498 | 0.418 |
LIG_FHA_1 | 878 | 884 | PF00498 | 0.539 |
LIG_FHA_1 | 890 | 896 | PF00498 | 0.569 |
LIG_FHA_1 | 9 | 15 | PF00498 | 0.611 |
LIG_FHA_2 | 24 | 30 | PF00498 | 0.756 |
LIG_FHA_2 | 3 | 9 | PF00498 | 0.472 |
LIG_FHA_2 | 312 | 318 | PF00498 | 0.562 |
LIG_FHA_2 | 333 | 339 | PF00498 | 0.595 |
LIG_FHA_2 | 405 | 411 | PF00498 | 0.674 |
LIG_FHA_2 | 462 | 468 | PF00498 | 0.785 |
LIG_FHA_2 | 876 | 882 | PF00498 | 0.576 |
LIG_FHA_2 | 897 | 903 | PF00498 | 0.579 |
LIG_LIR_Apic_2 | 368 | 373 | PF02991 | 0.369 |
LIG_LIR_Gen_1 | 197 | 207 | PF02991 | 0.552 |
LIG_LIR_Gen_1 | 271 | 282 | PF02991 | 0.320 |
LIG_LIR_Gen_1 | 3 | 12 | PF02991 | 0.580 |
LIG_LIR_Gen_1 | 319 | 325 | PF02991 | 0.517 |
LIG_LIR_Gen_1 | 474 | 483 | PF02991 | 0.647 |
LIG_LIR_Gen_1 | 538 | 546 | PF02991 | 0.509 |
LIG_LIR_Gen_1 | 569 | 579 | PF02991 | 0.578 |
LIG_LIR_Gen_1 | 581 | 590 | PF02991 | 0.637 |
LIG_LIR_Gen_1 | 750 | 760 | PF02991 | 0.460 |
LIG_LIR_Gen_1 | 763 | 773 | PF02991 | 0.508 |
LIG_LIR_Gen_1 | 802 | 811 | PF02991 | 0.506 |
LIG_LIR_Gen_1 | 908 | 917 | PF02991 | 0.609 |
LIG_LIR_Nem_3 | 197 | 202 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 219 | 223 | PF02991 | 0.667 |
LIG_LIR_Nem_3 | 234 | 240 | PF02991 | 0.515 |
LIG_LIR_Nem_3 | 271 | 277 | PF02991 | 0.321 |
LIG_LIR_Nem_3 | 3 | 7 | PF02991 | 0.573 |
LIG_LIR_Nem_3 | 319 | 324 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 474 | 480 | PF02991 | 0.657 |
LIG_LIR_Nem_3 | 538 | 543 | PF02991 | 0.496 |
LIG_LIR_Nem_3 | 569 | 575 | PF02991 | 0.595 |
LIG_LIR_Nem_3 | 58 | 64 | PF02991 | 0.680 |
LIG_LIR_Nem_3 | 581 | 587 | PF02991 | 0.611 |
LIG_LIR_Nem_3 | 647 | 652 | PF02991 | 0.523 |
LIG_LIR_Nem_3 | 750 | 755 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 763 | 768 | PF02991 | 0.507 |
LIG_LIR_Nem_3 | 784 | 790 | PF02991 | 0.533 |
LIG_LIR_Nem_3 | 802 | 808 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 834 | 838 | PF02991 | 0.548 |
LIG_LYPXL_S_1 | 697 | 701 | PF13949 | 0.654 |
LIG_LYPXL_yS_3 | 698 | 701 | PF13949 | 0.660 |
LIG_MYND_1 | 596 | 600 | PF01753 | 0.352 |
LIG_PCNA_yPIPBox_3 | 233 | 247 | PF02747 | 0.568 |
LIG_Pex14_2 | 139 | 143 | PF04695 | 0.342 |
LIG_Pex14_2 | 195 | 199 | PF04695 | 0.546 |
LIG_Pex14_2 | 321 | 325 | PF04695 | 0.458 |
LIG_Pex14_2 | 366 | 370 | PF04695 | 0.643 |
LIG_Pex14_2 | 752 | 756 | PF04695 | 0.542 |
LIG_Pex14_2 | 805 | 809 | PF04695 | 0.553 |
LIG_Pex14_2 | 864 | 868 | PF04695 | 0.457 |
LIG_SH2_CRK | 351 | 355 | PF00017 | 0.525 |
LIG_SH2_CRK | 401 | 405 | PF00017 | 0.599 |
LIG_SH2_CRK | 540 | 544 | PF00017 | 0.498 |
LIG_SH2_CRK | 622 | 626 | PF00017 | 0.543 |
LIG_SH2_CRK | 741 | 745 | PF00017 | 0.521 |
LIG_SH2_GRB2like | 741 | 744 | PF00017 | 0.640 |
LIG_SH2_STAP1 | 351 | 355 | PF00017 | 0.525 |
LIG_SH2_STAP1 | 401 | 405 | PF00017 | 0.599 |
LIG_SH2_STAP1 | 438 | 442 | PF00017 | 0.794 |
LIG_SH2_STAT5 | 138 | 141 | PF00017 | 0.593 |
LIG_SH2_STAT5 | 188 | 191 | PF00017 | 0.602 |
LIG_SH2_STAT5 | 401 | 404 | PF00017 | 0.332 |
LIG_SH2_STAT5 | 73 | 76 | PF00017 | 0.336 |
LIG_SH2_STAT5 | 774 | 777 | PF00017 | 0.488 |
LIG_SH3_1 | 430 | 436 | PF00018 | 0.458 |
LIG_SH3_3 | 281 | 287 | PF00018 | 0.455 |
LIG_SH3_3 | 403 | 409 | PF00018 | 0.453 |
LIG_SH3_3 | 430 | 436 | PF00018 | 0.520 |
LIG_SH3_3 | 467 | 473 | PF00018 | 0.646 |
LIG_SH3_3 | 590 | 596 | PF00018 | 0.484 |
LIG_SH3_3 | 627 | 633 | PF00018 | 0.533 |
LIG_SH3_3 | 671 | 677 | PF00018 | 0.451 |
LIG_SH3_3 | 696 | 702 | PF00018 | 0.690 |
LIG_SH3_3 | 770 | 776 | PF00018 | 0.493 |
LIG_SH3_3 | 98 | 104 | PF00018 | 0.557 |
LIG_SUMO_SIM_anti_2 | 166 | 171 | PF11976 | 0.413 |
LIG_SUMO_SIM_anti_2 | 499 | 505 | PF11976 | 0.481 |
LIG_SUMO_SIM_anti_2 | 669 | 676 | PF11976 | 0.425 |
LIG_SUMO_SIM_anti_2 | 826 | 834 | PF11976 | 0.529 |
LIG_SUMO_SIM_par_1 | 163 | 168 | PF11976 | 0.573 |
LIG_SUMO_SIM_par_1 | 595 | 601 | PF11976 | 0.526 |
LIG_SUMO_SIM_par_1 | 892 | 899 | PF11976 | 0.480 |
LIG_TRAF2_1 | 26 | 29 | PF00917 | 0.694 |
LIG_TRAF2_1 | 473 | 476 | PF00917 | 0.789 |
LIG_TRAF2_1 | 609 | 612 | PF00917 | 0.453 |
LIG_TRFH_1 | 469 | 473 | PF08558 | 0.627 |
LIG_TYR_ITIM | 349 | 354 | PF00017 | 0.418 |
LIG_TYR_ITIM | 620 | 625 | PF00017 | 0.477 |
LIG_UBA3_1 | 158 | 163 | PF00899 | 0.572 |
LIG_UBA3_1 | 235 | 242 | PF00899 | 0.551 |
LIG_UBA3_1 | 349 | 358 | PF00899 | 0.477 |
LIG_UBA3_1 | 36 | 45 | PF00899 | 0.380 |
LIG_UBA3_1 | 617 | 623 | PF00899 | 0.371 |
LIG_WRC_WIRS_1 | 513 | 518 | PF05994 | 0.643 |
MOD_CDK_SPxxK_3 | 65 | 72 | PF00069 | 0.447 |
MOD_CK1_1 | 216 | 222 | PF00069 | 0.698 |
MOD_CK1_1 | 252 | 258 | PF00069 | 0.600 |
MOD_CK1_1 | 268 | 274 | PF00069 | 0.476 |
MOD_CK1_1 | 481 | 487 | PF00069 | 0.633 |
MOD_CK1_1 | 499 | 505 | PF00069 | 0.447 |
MOD_CK1_1 | 588 | 594 | PF00069 | 0.594 |
MOD_CK1_1 | 606 | 612 | PF00069 | 0.353 |
MOD_CK1_1 | 666 | 672 | PF00069 | 0.592 |
MOD_CK1_1 | 782 | 788 | PF00069 | 0.527 |
MOD_CK2_1 | 2 | 8 | PF00069 | 0.500 |
MOD_CK2_1 | 23 | 29 | PF00069 | 0.651 |
MOD_CK2_1 | 311 | 317 | PF00069 | 0.519 |
MOD_CK2_1 | 461 | 467 | PF00069 | 0.780 |
MOD_CK2_1 | 532 | 538 | PF00069 | 0.501 |
MOD_CK2_1 | 606 | 612 | PF00069 | 0.386 |
MOD_CK2_1 | 666 | 672 | PF00069 | 0.482 |
MOD_CK2_1 | 824 | 830 | PF00069 | 0.520 |
MOD_CK2_1 | 867 | 873 | PF00069 | 0.587 |
MOD_CK2_1 | 875 | 881 | PF00069 | 0.528 |
MOD_CK2_1 | 99 | 105 | PF00069 | 0.505 |
MOD_CMANNOS | 229 | 232 | PF00535 | 0.459 |
MOD_GlcNHglycan | 115 | 118 | PF01048 | 0.427 |
MOD_GlcNHglycan | 251 | 254 | PF01048 | 0.576 |
MOD_GlcNHglycan | 321 | 324 | PF01048 | 0.591 |
MOD_GlcNHglycan | 335 | 338 | PF01048 | 0.523 |
MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.489 |
MOD_GlcNHglycan | 56 | 61 | PF01048 | 0.519 |
MOD_GlcNHglycan | 82 | 86 | PF01048 | 0.706 |
MOD_GlcNHglycan | 869 | 872 | PF01048 | 0.582 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.586 |
MOD_GSK3_1 | 245 | 252 | PF00069 | 0.426 |
MOD_GSK3_1 | 264 | 271 | PF00069 | 0.447 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.566 |
MOD_GSK3_1 | 381 | 388 | PF00069 | 0.515 |
MOD_GSK3_1 | 448 | 455 | PF00069 | 0.680 |
MOD_GSK3_1 | 478 | 485 | PF00069 | 0.617 |
MOD_GSK3_1 | 566 | 573 | PF00069 | 0.362 |
MOD_GSK3_1 | 678 | 685 | PF00069 | 0.676 |
MOD_GSK3_1 | 705 | 712 | PF00069 | 0.701 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.566 |
MOD_GSK3_1 | 858 | 865 | PF00069 | 0.555 |
MOD_N-GLC_1 | 113 | 118 | PF02516 | 0.647 |
MOD_N-GLC_1 | 264 | 269 | PF02516 | 0.516 |
MOD_N-GLC_1 | 733 | 738 | PF02516 | 0.750 |
MOD_N-GLC_1 | 816 | 821 | PF02516 | 0.511 |
MOD_N-GLC_2 | 146 | 148 | PF02516 | 0.472 |
MOD_NEK2_1 | 130 | 135 | PF00069 | 0.408 |
MOD_NEK2_1 | 15 | 20 | PF00069 | 0.661 |
MOD_NEK2_1 | 165 | 170 | PF00069 | 0.322 |
MOD_NEK2_1 | 207 | 212 | PF00069 | 0.523 |
MOD_NEK2_1 | 257 | 262 | PF00069 | 0.449 |
MOD_NEK2_1 | 382 | 387 | PF00069 | 0.640 |
MOD_NEK2_1 | 404 | 409 | PF00069 | 0.612 |
MOD_NEK2_1 | 460 | 465 | PF00069 | 0.809 |
MOD_NEK2_1 | 807 | 812 | PF00069 | 0.468 |
MOD_NEK2_1 | 862 | 867 | PF00069 | 0.509 |
MOD_NEK2_1 | 875 | 880 | PF00069 | 0.603 |
MOD_NEK2_1 | 99 | 104 | PF00069 | 0.457 |
MOD_NEK2_2 | 213 | 218 | PF00069 | 0.698 |
MOD_NEK2_2 | 816 | 821 | PF00069 | 0.511 |
MOD_NEK2_2 | 896 | 901 | PF00069 | 0.561 |
MOD_PIKK_1 | 666 | 672 | PF00454 | 0.524 |
MOD_PK_1 | 710 | 716 | PF00069 | 0.763 |
MOD_PKA_1 | 710 | 716 | PF00069 | 0.795 |
MOD_PKA_2 | 288 | 294 | PF00069 | 0.548 |
MOD_PKA_2 | 385 | 391 | PF00069 | 0.393 |
MOD_PKA_2 | 460 | 466 | PF00069 | 0.685 |
MOD_PKA_2 | 50 | 56 | PF00069 | 0.637 |
MOD_PKA_2 | 588 | 594 | PF00069 | 0.615 |
MOD_PKA_2 | 709 | 715 | PF00069 | 0.644 |
MOD_PKA_2 | 8 | 14 | PF00069 | 0.566 |
MOD_Plk_1 | 2 | 8 | PF00069 | 0.500 |
MOD_Plk_1 | 264 | 270 | PF00069 | 0.539 |
MOD_Plk_1 | 337 | 343 | PF00069 | 0.515 |
MOD_Plk_1 | 733 | 739 | PF00069 | 0.493 |
MOD_Plk_1 | 816 | 822 | PF00069 | 0.616 |
MOD_Plk_4 | 130 | 136 | PF00069 | 0.387 |
MOD_Plk_4 | 165 | 171 | PF00069 | 0.414 |
MOD_Plk_4 | 231 | 237 | PF00069 | 0.456 |
MOD_Plk_4 | 252 | 258 | PF00069 | 0.342 |
MOD_Plk_4 | 461 | 467 | PF00069 | 0.813 |
MOD_Plk_4 | 499 | 505 | PF00069 | 0.512 |
MOD_Plk_4 | 598 | 604 | PF00069 | 0.487 |
MOD_Plk_4 | 663 | 669 | PF00069 | 0.325 |
MOD_Plk_4 | 710 | 716 | PF00069 | 0.695 |
MOD_Plk_4 | 782 | 788 | PF00069 | 0.443 |
MOD_Plk_4 | 824 | 830 | PF00069 | 0.476 |
MOD_Plk_4 | 858 | 864 | PF00069 | 0.518 |
MOD_Plk_4 | 909 | 915 | PF00069 | 0.642 |
MOD_ProDKin_1 | 405 | 411 | PF00069 | 0.481 |
MOD_ProDKin_1 | 432 | 438 | PF00069 | 0.556 |
MOD_ProDKin_1 | 448 | 454 | PF00069 | 0.546 |
MOD_ProDKin_1 | 496 | 502 | PF00069 | 0.635 |
MOD_ProDKin_1 | 606 | 612 | PF00069 | 0.386 |
MOD_ProDKin_1 | 65 | 71 | PF00069 | 0.487 |
MOD_ProDKin_1 | 772 | 778 | PF00069 | 0.531 |
MOD_SUMO_for_1 | 429 | 432 | PF00179 | 0.552 |
MOD_SUMO_for_1 | 522 | 525 | PF00179 | 0.585 |
MOD_SUMO_rev_2 | 149 | 158 | PF00179 | 0.603 |
MOD_SUMO_rev_2 | 241 | 249 | PF00179 | 0.582 |
MOD_SUMO_rev_2 | 705 | 713 | PF00179 | 0.742 |
TRG_DiLeu_BaEn_1 | 590 | 595 | PF01217 | 0.455 |
TRG_DiLeu_BaEn_2 | 328 | 334 | PF01217 | 0.602 |
TRG_DiLeu_BaLyEn_6 | 370 | 375 | PF01217 | 0.338 |
TRG_DiLeu_BaLyEn_6 | 411 | 416 | PF01217 | 0.672 |
TRG_DiLeu_BaLyEn_6 | 613 | 618 | PF01217 | 0.629 |
TRG_ENDOCYTIC_2 | 351 | 354 | PF00928 | 0.424 |
TRG_ENDOCYTIC_2 | 401 | 404 | PF00928 | 0.600 |
TRG_ENDOCYTIC_2 | 477 | 480 | PF00928 | 0.777 |
TRG_ENDOCYTIC_2 | 540 | 543 | PF00928 | 0.491 |
TRG_ENDOCYTIC_2 | 622 | 625 | PF00928 | 0.455 |
TRG_ENDOCYTIC_2 | 698 | 701 | PF00928 | 0.660 |
TRG_ENDOCYTIC_2 | 741 | 744 | PF00928 | 0.540 |
TRG_ER_diArg_1 | 170 | 172 | PF00400 | 0.511 |
TRG_ER_diArg_1 | 179 | 181 | PF00400 | 0.488 |
TRG_ER_diArg_1 | 220 | 222 | PF00400 | 0.606 |
TRG_ER_diArg_1 | 723 | 725 | PF00400 | 0.651 |
TRG_ER_diArg_1 | 735 | 738 | PF00400 | 0.617 |
TRG_ER_diArg_1 | 843 | 845 | PF00400 | 0.586 |
TRG_NES_CRM1_1 | 35 | 48 | PF08389 | 0.532 |
TRG_NES_CRM1_1 | 788 | 802 | PF08389 | 0.344 |
TRG_NES_CRM1_1 | 90 | 105 | PF08389 | 0.492 |
TRG_NLS_MonoExtC_3 | 357 | 363 | PF00514 | 0.409 |
TRG_Pf-PMV_PEXEL_1 | 566 | 570 | PF00026 | 0.606 |
TRG_Pf-PMV_PEXEL_1 | 850 | 855 | PF00026 | 0.538 |
TRG_Pf-PMV_PEXEL_1 | 901 | 906 | PF00026 | 0.582 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P438 | Leptomonas seymouri | 52% | 100% |
A0A1X0NJ45 | Trypanosomatidae | 30% | 95% |
A0A3Q8ILW9 | Leishmania donovani | 77% | 100% |
A0A3R7MMH0 | Trypanosoma rangeli | 31% | 95% |
A4IAY4 | Leishmania infantum | 77% | 100% |
C9ZNI1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 96% |
E9AER2 | Leishmania major | 77% | 100% |
E9B5W7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 100% |
V5BAN0 | Trypanosoma cruzi | 30% | 94% |