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: 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: A0A3Q8ILW9
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 | 0.611 |
CLV_MEL_PAP_1 | 458 | 464 | PF00089 | 0.735 |
CLV_NRD_NRD_1 | 171 | 173 | PF00675 | 0.497 |
CLV_NRD_NRD_1 | 180 | 182 | PF00675 | 0.432 |
CLV_NRD_NRD_1 | 221 | 223 | PF00675 | 0.670 |
CLV_NRD_NRD_1 | 709 | 711 | PF00675 | 0.693 |
CLV_NRD_NRD_1 | 723 | 725 | PF00675 | 0.501 |
CLV_NRD_NRD_1 | 820 | 822 | PF00675 | 0.421 |
CLV_NRD_NRD_1 | 844 | 846 | PF00675 | 0.605 |
CLV_PCSK_KEX2_1 | 171 | 173 | PF00082 | 0.491 |
CLV_PCSK_KEX2_1 | 180 | 182 | PF00082 | 0.432 |
CLV_PCSK_KEX2_1 | 221 | 223 | PF00082 | 0.622 |
CLV_PCSK_KEX2_1 | 242 | 244 | PF00082 | 0.550 |
CLV_PCSK_KEX2_1 | 723 | 725 | PF00082 | 0.598 |
CLV_PCSK_KEX2_1 | 844 | 846 | PF00082 | 0.605 |
CLV_PCSK_PC1ET2_1 | 242 | 244 | PF00082 | 0.550 |
CLV_PCSK_SKI1_1 | 115 | 119 | PF00082 | 0.569 |
CLV_PCSK_SKI1_1 | 156 | 160 | PF00082 | 0.514 |
CLV_PCSK_SKI1_1 | 187 | 191 | PF00082 | 0.480 |
CLV_PCSK_SKI1_1 | 20 | 24 | PF00082 | 0.544 |
CLV_PCSK_SKI1_1 | 297 | 301 | PF00082 | 0.428 |
CLV_PCSK_SKI1_1 | 520 | 524 | PF00082 | 0.653 |
CLV_PCSK_SKI1_1 | 72 | 76 | PF00082 | 0.549 |
CLV_PCSK_SKI1_1 | 9 | 13 | PF00082 | 0.415 |
CLV_Separin_Metazoa | 830 | 834 | PF03568 | 0.362 |
DEG_APCC_DBOX_1 | 8 | 16 | PF00400 | 0.552 |
DEG_MDM2_SWIB_1 | 864 | 872 | PF02201 | 0.472 |
DOC_CKS1_1 | 773 | 778 | PF01111 | 0.481 |
DOC_CYCLIN_RxL_1 | 181 | 193 | PF00134 | 0.547 |
DOC_CYCLIN_RxL_1 | 208 | 219 | PF00134 | 0.433 |
DOC_CYCLIN_RxL_1 | 854 | 867 | PF00134 | 0.551 |
DOC_CYCLIN_yCln2_LP_2 | 345 | 351 | PF00134 | 0.472 |
DOC_CYCLIN_yCln2_LP_2 | 631 | 637 | PF00134 | 0.541 |
DOC_MAPK_DCC_7 | 833 | 843 | PF00069 | 0.515 |
DOC_MAPK_gen_1 | 160 | 170 | PF00069 | 0.379 |
DOC_MAPK_gen_1 | 171 | 179 | PF00069 | 0.462 |
DOC_MAPK_gen_1 | 43 | 52 | PF00069 | 0.568 |
DOC_MAPK_gen_1 | 449 | 458 | PF00069 | 0.704 |
DOC_MAPK_gen_1 | 710 | 716 | PF00069 | 0.763 |
DOC_MAPK_HePTP_8 | 618 | 630 | PF00069 | 0.496 |
DOC_MAPK_MEF2A_6 | 160 | 169 | PF00069 | 0.307 |
DOC_MAPK_MEF2A_6 | 449 | 458 | PF00069 | 0.643 |
DOC_MAPK_MEF2A_6 | 45 | 54 | PF00069 | 0.527 |
DOC_MAPK_MEF2A_6 | 589 | 597 | PF00069 | 0.525 |
DOC_MAPK_MEF2A_6 | 621 | 630 | PF00069 | 0.402 |
DOC_MAPK_RevD_3 | 165 | 181 | PF00069 | 0.529 |
DOC_PP1_RVXF_1 | 209 | 216 | PF00149 | 0.415 |
DOC_PP1_RVXF_1 | 858 | 865 | PF00149 | 0.543 |
DOC_PP2B_LxvP_1 | 631 | 634 | PF13499 | 0.541 |
DOC_PP2B_PxIxI_1 | 711 | 717 | PF00149 | 0.658 |
DOC_PP4_FxxP_1 | 480 | 483 | PF00568 | 0.728 |
DOC_USP7_MATH_1 | 223 | 227 | PF00917 | 0.540 |
DOC_USP7_MATH_1 | 361 | 365 | PF00917 | 0.573 |
DOC_USP7_MATH_1 | 433 | 437 | PF00917 | 0.666 |
DOC_USP7_MATH_1 | 481 | 485 | PF00917 | 0.739 |
DOC_USP7_MATH_1 | 512 | 516 | PF00917 | 0.757 |
DOC_USP7_MATH_1 | 560 | 564 | PF00917 | 0.469 |
DOC_USP7_MATH_1 | 824 | 828 | PF00917 | 0.490 |
DOC_USP7_MATH_1 | 858 | 862 | PF00917 | 0.608 |
DOC_USP7_MATH_1 | 896 | 900 | PF00917 | 0.490 |
DOC_USP7_UBL2_3 | 152 | 156 | PF12436 | 0.360 |
DOC_USP7_UBL2_3 | 327 | 331 | PF12436 | 0.540 |
DOC_WW_Pin1_4 | 546 | 551 | PF00397 | 0.602 |
DOC_WW_Pin1_4 | 65 | 70 | PF00397 | 0.442 |
DOC_WW_Pin1_4 | 772 | 777 | PF00397 | 0.487 |
LIG_14-3-3_CanoR_1 | 115 | 120 | PF00244 | 0.608 |
LIG_14-3-3_CanoR_1 | 171 | 179 | PF00244 | 0.551 |
LIG_14-3-3_CanoR_1 | 231 | 236 | PF00244 | 0.510 |
LIG_14-3-3_CanoR_1 | 461 | 466 | PF00244 | 0.665 |
LIG_14-3-3_CanoR_1 | 566 | 575 | PF00244 | 0.507 |
LIG_Actin_WH2_2 | 155 | 173 | PF00022 | 0.538 |
LIG_ActinCP_TwfCPI_2 | 480 | 490 | PF01115 | 0.662 |
LIG_AP2alpha_1 | 195 | 199 | PF02296 | 0.340 |
LIG_AP2alpha_1 | 366 | 370 | PF02296 | 0.580 |
LIG_BIR_III_4 | 570 | 574 | PF00653 | 0.478 |
LIG_BRCT_BRCA1_1 | 233 | 237 | PF00533 | 0.479 |
LIG_BRCT_BRCA1_1 | 321 | 325 | PF00533 | 0.519 |
LIG_BRCT_BRCA1_1 | 568 | 572 | PF00533 | 0.565 |
LIG_BRCT_BRCA1_1 | 580 | 584 | PF00533 | 0.540 |
LIG_BRCT_BRCA1_1 | 860 | 864 | PF00533 | 0.456 |
LIG_BRCT_BRCA1_2 | 321 | 327 | PF00533 | 0.543 |
LIG_BRCT_BRCA1_2 | 568 | 574 | PF00533 | 0.575 |
LIG_BRCT_BRCA1_2 | 860 | 866 | PF00533 | 0.564 |
LIG_eIF4E_1 | 652 | 658 | PF01652 | 0.525 |
LIG_EVH1_1 | 698 | 702 | PF00568 | 0.646 |
LIG_FHA_1 | 131 | 137 | PF00498 | 0.481 |
LIG_FHA_1 | 153 | 159 | PF00498 | 0.478 |
LIG_FHA_1 | 274 | 280 | PF00498 | 0.461 |
LIG_FHA_1 | 286 | 292 | PF00498 | 0.500 |
LIG_FHA_1 | 377 | 383 | PF00498 | 0.566 |
LIG_FHA_1 | 401 | 407 | PF00498 | 0.444 |
LIG_FHA_1 | 589 | 595 | PF00498 | 0.586 |
LIG_FHA_1 | 621 | 627 | PF00498 | 0.534 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.427 |
LIG_FHA_1 | 653 | 659 | PF00498 | 0.548 |
LIG_FHA_1 | 689 | 695 | PF00498 | 0.715 |
LIG_FHA_1 | 701 | 707 | PF00498 | 0.648 |
LIG_FHA_1 | 890 | 896 | PF00498 | 0.510 |
LIG_FHA_2 | 312 | 318 | PF00498 | 0.514 |
LIG_FHA_2 | 333 | 339 | PF00498 | 0.544 |
LIG_FHA_2 | 405 | 411 | PF00498 | 0.564 |
LIG_FHA_2 | 681 | 687 | PF00498 | 0.679 |
LIG_FHA_2 | 876 | 882 | PF00498 | 0.511 |
LIG_LIR_Gen_1 | 124 | 135 | PF02991 | 0.504 |
LIG_LIR_Gen_1 | 197 | 207 | PF02991 | 0.501 |
LIG_LIR_Gen_1 | 234 | 244 | PF02991 | 0.475 |
LIG_LIR_Gen_1 | 3 | 12 | PF02991 | 0.516 |
LIG_LIR_Gen_1 | 319 | 325 | PF02991 | 0.466 |
LIG_LIR_Gen_1 | 474 | 483 | PF02991 | 0.599 |
LIG_LIR_Gen_1 | 538 | 546 | PF02991 | 0.451 |
LIG_LIR_Gen_1 | 581 | 590 | PF02991 | 0.604 |
LIG_LIR_Gen_1 | 763 | 773 | PF02991 | 0.473 |
LIG_LIR_Gen_1 | 802 | 811 | PF02991 | 0.453 |
LIG_LIR_Gen_1 | 908 | 917 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 124 | 130 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 197 | 202 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 234 | 240 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 3 | 7 | PF02991 | 0.508 |
LIG_LIR_Nem_3 | 319 | 324 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 474 | 480 | PF02991 | 0.605 |
LIG_LIR_Nem_3 | 538 | 543 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 569 | 575 | PF02991 | 0.545 |
LIG_LIR_Nem_3 | 58 | 64 | PF02991 | 0.602 |
LIG_LIR_Nem_3 | 581 | 587 | PF02991 | 0.579 |
LIG_LIR_Nem_3 | 647 | 652 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 763 | 768 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 784 | 790 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 802 | 808 | PF02991 | 0.306 |
LIG_LIR_Nem_3 | 834 | 838 | PF02991 | 0.494 |
LIG_LIR_Nem_3 | 908 | 914 | PF02991 | 0.607 |
LIG_LYPXL_S_1 | 697 | 701 | PF13949 | 0.600 |
LIG_LYPXL_yS_3 | 698 | 701 | PF13949 | 0.602 |
LIG_NRBOX | 164 | 170 | PF00104 | 0.464 |
LIG_PCNA_yPIPBox_3 | 231 | 240 | PF02747 | 0.523 |
LIG_Pex14_2 | 195 | 199 | PF04695 | 0.509 |
LIG_Pex14_2 | 321 | 325 | PF04695 | 0.407 |
LIG_Pex14_2 | 366 | 370 | PF04695 | 0.580 |
LIG_Pex14_2 | 752 | 756 | PF04695 | 0.490 |
LIG_Pex14_2 | 805 | 809 | PF04695 | 0.504 |
LIG_Pex14_2 | 864 | 868 | PF04695 | 0.408 |
LIG_PTB_Apo_2 | 268 | 275 | PF02174 | 0.483 |
LIG_REV1ctd_RIR_1 | 477 | 482 | PF16727 | 0.651 |
LIG_SH2_CRK | 401 | 405 | PF00017 | 0.552 |
LIG_SH2_CRK | 540 | 544 | PF00017 | 0.441 |
LIG_SH2_CRK | 622 | 626 | PF00017 | 0.489 |
LIG_SH2_CRK | 741 | 745 | PF00017 | 0.523 |
LIG_SH2_CRK | 859 | 863 | PF00017 | 0.558 |
LIG_SH2_CRK | 911 | 915 | PF00017 | 0.540 |
LIG_SH2_GRB2like | 741 | 744 | PF00017 | 0.617 |
LIG_SH2_PTP2 | 351 | 354 | PF00017 | 0.295 |
LIG_SH2_SRC | 438 | 441 | PF00017 | 0.528 |
LIG_SH2_STAP1 | 401 | 405 | PF00017 | 0.552 |
LIG_SH2_STAP1 | 438 | 442 | PF00017 | 0.732 |
LIG_SH2_STAP1 | 622 | 626 | PF00017 | 0.336 |
LIG_SH2_STAP1 | 741 | 745 | PF00017 | 0.513 |
LIG_SH2_STAP1 | 911 | 915 | PF00017 | 0.540 |
LIG_SH2_STAT3 | 616 | 619 | PF00017 | 0.362 |
LIG_SH2_STAT5 | 188 | 191 | PF00017 | 0.563 |
LIG_SH2_STAT5 | 351 | 354 | PF00017 | 0.332 |
LIG_SH2_STAT5 | 355 | 358 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 616 | 619 | PF00017 | 0.502 |
LIG_SH2_STAT5 | 622 | 625 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 774 | 777 | PF00017 | 0.440 |
LIG_SH3_1 | 696 | 702 | PF00018 | 0.627 |
LIG_SH3_3 | 467 | 473 | PF00018 | 0.586 |
LIG_SH3_3 | 594 | 600 | PF00018 | 0.451 |
LIG_SH3_3 | 627 | 633 | PF00018 | 0.483 |
LIG_SH3_3 | 696 | 702 | PF00018 | 0.642 |
LIG_SH3_3 | 770 | 776 | PF00018 | 0.447 |
LIG_SH3_3 | 98 | 104 | PF00018 | 0.504 |
LIG_SUMO_SIM_anti_2 | 528 | 535 | PF11976 | 0.470 |
LIG_SUMO_SIM_anti_2 | 627 | 632 | PF11976 | 0.371 |
LIG_SUMO_SIM_anti_2 | 827 | 834 | PF11976 | 0.476 |
LIG_SUMO_SIM_anti_2 | 870 | 876 | PF11976 | 0.475 |
LIG_SUMO_SIM_par_1 | 601 | 606 | PF11976 | 0.500 |
LIG_SUMO_SIM_par_1 | 622 | 627 | PF11976 | 0.354 |
LIG_SUMO_SIM_par_1 | 892 | 899 | PF11976 | 0.428 |
LIG_TRAF2_1 | 473 | 476 | PF00917 | 0.726 |
LIG_TRAF2_1 | 486 | 489 | PF00917 | 0.547 |
LIG_TRAF2_1 | 921 | 924 | PF00917 | 0.591 |
LIG_TRFH_1 | 469 | 473 | PF08558 | 0.570 |
LIG_TYR_ITIM | 349 | 354 | PF00017 | 0.365 |
LIG_TYR_ITIM | 620 | 625 | PF00017 | 0.426 |
LIG_TYR_ITIM | 857 | 862 | PF00017 | 0.569 |
LIG_UBA3_1 | 158 | 163 | PF00899 | 0.520 |
LIG_UBA3_1 | 178 | 187 | PF00899 | 0.207 |
LIG_UBA3_1 | 235 | 242 | PF00899 | 0.494 |
LIG_UBA3_1 | 353 | 359 | PF00899 | 0.457 |
LIG_WRC_WIRS_1 | 513 | 518 | PF05994 | 0.612 |
MOD_CDK_SPxxK_3 | 65 | 72 | PF00069 | 0.398 |
MOD_CK1_1 | 216 | 222 | PF00069 | 0.641 |
MOD_CK1_1 | 252 | 258 | PF00069 | 0.547 |
MOD_CK1_1 | 443 | 449 | PF00069 | 0.630 |
MOD_CK1_1 | 531 | 537 | PF00069 | 0.533 |
MOD_CK1_1 | 588 | 594 | PF00069 | 0.553 |
MOD_CK1_1 | 677 | 683 | PF00069 | 0.688 |
MOD_CK1_1 | 782 | 788 | PF00069 | 0.477 |
MOD_CK2_1 | 23 | 29 | PF00069 | 0.569 |
MOD_CK2_1 | 311 | 317 | PF00069 | 0.473 |
MOD_CK2_1 | 461 | 467 | PF00069 | 0.736 |
MOD_CK2_1 | 483 | 489 | PF00069 | 0.657 |
MOD_CK2_1 | 532 | 538 | PF00069 | 0.504 |
MOD_CK2_1 | 666 | 672 | PF00069 | 0.424 |
MOD_CK2_1 | 680 | 686 | PF00069 | 0.680 |
MOD_CK2_1 | 824 | 830 | PF00069 | 0.487 |
MOD_CK2_1 | 867 | 873 | PF00069 | 0.537 |
MOD_CK2_1 | 99 | 105 | PF00069 | 0.453 |
MOD_CMANNOS | 229 | 232 | PF00535 | 0.414 |
MOD_Cter_Amidation | 708 | 711 | PF01082 | 0.719 |
MOD_GlcNHglycan | 251 | 254 | PF01048 | 0.524 |
MOD_GlcNHglycan | 321 | 324 | PF01048 | 0.541 |
MOD_GlcNHglycan | 335 | 338 | PF01048 | 0.496 |
MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.597 |
MOD_GlcNHglycan | 442 | 445 | PF01048 | 0.663 |
MOD_GlcNHglycan | 562 | 565 | PF01048 | 0.426 |
MOD_GlcNHglycan | 676 | 679 | PF01048 | 0.716 |
MOD_GlcNHglycan | 707 | 710 | PF01048 | 0.762 |
MOD_GlcNHglycan | 82 | 86 | PF01048 | 0.646 |
MOD_GlcNHglycan | 869 | 872 | PF01048 | 0.548 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.484 |
MOD_GSK3_1 | 400 | 407 | PF00069 | 0.395 |
MOD_GSK3_1 | 528 | 535 | PF00069 | 0.598 |
MOD_GSK3_1 | 674 | 681 | PF00069 | 0.635 |
MOD_GSK3_1 | 700 | 707 | PF00069 | 0.668 |
MOD_GSK3_1 | 710 | 717 | PF00069 | 0.635 |
MOD_GSK3_1 | 858 | 865 | PF00069 | 0.491 |
MOD_N-GLC_1 | 115 | 120 | PF02516 | 0.602 |
MOD_N-GLC_1 | 419 | 424 | PF02516 | 0.561 |
MOD_N-GLC_1 | 733 | 738 | PF02516 | 0.723 |
MOD_N-GLC_1 | 816 | 821 | PF02516 | 0.460 |
MOD_N-GLC_2 | 95 | 97 | PF02516 | 0.467 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.476 |
MOD_NEK2_1 | 130 | 135 | PF00069 | 0.361 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.355 |
MOD_NEK2_1 | 15 | 20 | PF00069 | 0.593 |
MOD_NEK2_1 | 207 | 212 | PF00069 | 0.465 |
MOD_NEK2_1 | 213 | 218 | PF00069 | 0.608 |
MOD_NEK2_1 | 382 | 387 | PF00069 | 0.588 |
MOD_NEK2_1 | 404 | 409 | PF00069 | 0.564 |
MOD_NEK2_1 | 460 | 465 | PF00069 | 0.734 |
MOD_NEK2_1 | 620 | 625 | PF00069 | 0.470 |
MOD_NEK2_1 | 666 | 671 | PF00069 | 0.515 |
MOD_NEK2_1 | 862 | 867 | PF00069 | 0.455 |
MOD_NEK2_1 | 875 | 880 | PF00069 | 0.512 |
MOD_NEK2_1 | 99 | 104 | PF00069 | 0.404 |
MOD_NEK2_2 | 400 | 405 | PF00069 | 0.429 |
MOD_NEK2_2 | 816 | 821 | PF00069 | 0.460 |
MOD_NEK2_2 | 896 | 901 | PF00069 | 0.508 |
MOD_PIKK_1 | 109 | 115 | PF00454 | 0.550 |
MOD_PIKK_1 | 216 | 222 | PF00454 | 0.690 |
MOD_PIKK_1 | 433 | 439 | PF00454 | 0.707 |
MOD_PIKK_1 | 443 | 449 | PF00454 | 0.610 |
MOD_PIKK_1 | 666 | 672 | PF00454 | 0.466 |
MOD_PK_1 | 710 | 716 | PF00069 | 0.731 |
MOD_PKA_1 | 710 | 716 | PF00069 | 0.763 |
MOD_PKA_2 | 15 | 21 | PF00069 | 0.573 |
MOD_PKA_2 | 460 | 466 | PF00069 | 0.635 |
MOD_PKA_2 | 481 | 487 | PF00069 | 0.730 |
MOD_PKA_2 | 588 | 594 | PF00069 | 0.574 |
MOD_PKA_2 | 620 | 626 | PF00069 | 0.374 |
MOD_PKB_1 | 576 | 584 | PF00069 | 0.557 |
MOD_PKB_1 | 737 | 745 | PF00069 | 0.548 |
MOD_Plk_1 | 115 | 121 | PF00069 | 0.580 |
MOD_Plk_1 | 223 | 229 | PF00069 | 0.512 |
MOD_Plk_1 | 337 | 343 | PF00069 | 0.456 |
MOD_Plk_1 | 488 | 494 | PF00069 | 0.706 |
MOD_Plk_1 | 816 | 822 | PF00069 | 0.565 |
MOD_Plk_2-3 | 3 | 9 | PF00069 | 0.482 |
MOD_Plk_4 | 115 | 121 | PF00069 | 0.562 |
MOD_Plk_4 | 130 | 136 | PF00069 | 0.340 |
MOD_Plk_4 | 224 | 230 | PF00069 | 0.488 |
MOD_Plk_4 | 231 | 237 | PF00069 | 0.409 |
MOD_Plk_4 | 400 | 406 | PF00069 | 0.413 |
MOD_Plk_4 | 461 | 467 | PF00069 | 0.739 |
MOD_Plk_4 | 528 | 534 | PF00069 | 0.516 |
MOD_Plk_4 | 598 | 604 | PF00069 | 0.445 |
MOD_Plk_4 | 620 | 626 | PF00069 | 0.324 |
MOD_Plk_4 | 710 | 716 | PF00069 | 0.664 |
MOD_Plk_4 | 782 | 788 | PF00069 | 0.393 |
MOD_Plk_4 | 824 | 830 | PF00069 | 0.427 |
MOD_Plk_4 | 83 | 89 | PF00069 | 0.573 |
MOD_Plk_4 | 864 | 870 | PF00069 | 0.441 |
MOD_Plk_4 | 909 | 915 | PF00069 | 0.567 |
MOD_ProDKin_1 | 546 | 552 | PF00069 | 0.596 |
MOD_ProDKin_1 | 65 | 71 | PF00069 | 0.438 |
MOD_ProDKin_1 | 772 | 778 | PF00069 | 0.483 |
MOD_SUMO_for_1 | 429 | 432 | PF00179 | 0.505 |
MOD_SUMO_for_1 | 522 | 525 | PF00179 | 0.564 |
MOD_SUMO_rev_2 | 149 | 158 | PF00179 | 0.564 |
MOD_SUMO_rev_2 | 241 | 249 | PF00179 | 0.529 |
MOD_SUMO_rev_2 | 484 | 492 | PF00179 | 0.750 |
MOD_SUMO_rev_2 | 713 | 722 | PF00179 | 0.669 |
TRG_DiLeu_BaEn_2 | 328 | 334 | PF01217 | 0.553 |
TRG_DiLeu_BaLyEn_6 | 341 | 346 | PF01217 | 0.474 |
TRG_DiLeu_BaLyEn_6 | 411 | 416 | PF01217 | 0.628 |
TRG_ENDOCYTIC_2 | 351 | 354 | PF00928 | 0.369 |
TRG_ENDOCYTIC_2 | 401 | 404 | PF00928 | 0.554 |
TRG_ENDOCYTIC_2 | 477 | 480 | PF00928 | 0.734 |
TRG_ENDOCYTIC_2 | 540 | 543 | PF00928 | 0.433 |
TRG_ENDOCYTIC_2 | 622 | 625 | PF00928 | 0.401 |
TRG_ENDOCYTIC_2 | 698 | 701 | PF00928 | 0.602 |
TRG_ENDOCYTIC_2 | 741 | 744 | PF00928 | 0.546 |
TRG_ENDOCYTIC_2 | 859 | 862 | PF00928 | 0.561 |
TRG_ENDOCYTIC_2 | 911 | 914 | PF00928 | 0.542 |
TRG_ER_diArg_1 | 170 | 172 | PF00400 | 0.444 |
TRG_ER_diArg_1 | 179 | 181 | PF00400 | 0.433 |
TRG_ER_diArg_1 | 575 | 578 | PF00400 | 0.588 |
TRG_ER_diArg_1 | 723 | 725 | PF00400 | 0.598 |
TRG_ER_diArg_1 | 735 | 738 | PF00400 | 0.588 |
TRG_ER_diArg_1 | 843 | 845 | PF00400 | 0.549 |
TRG_NES_CRM1_1 | 35 | 48 | PF08389 | 0.469 |
TRG_NES_CRM1_1 | 495 | 510 | PF08389 | 0.666 |
TRG_Pf-PMV_PEXEL_1 | 566 | 570 | PF00026 | 0.557 |
TRG_Pf-PMV_PEXEL_1 | 901 | 906 | PF00026 | 0.519 |
TRG_Pf-PMV_PEXEL_1 | 920 | 924 | PF00026 | 0.446 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P438 | Leptomonas seymouri | 53% | 100% |
A0A1X0NJ45 | Trypanosomatidae | 32% | 95% |
A0A3R7MMH0 | Trypanosoma rangeli | 33% | 95% |
A4HMB8 | Leishmania braziliensis | 77% | 100% |
A4IAY4 | Leishmania infantum | 99% | 100% |
C9ZNI1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 96% |
E9AER2 | Leishmania major | 92% | 100% |
E9B5W7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
V5BAN0 | Trypanosoma cruzi | 30% | 94% |