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: A4IAY4
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 | 13 | 17 | PF00656 | 0.548 |
CLV_C14_Caspase3-7 | 406 | 410 | PF00656 | 0.558 |
CLV_MEL_PAP_1 | 457 | 463 | PF00089 | 0.742 |
CLV_NRD_NRD_1 | 170 | 172 | PF00675 | 0.486 |
CLV_NRD_NRD_1 | 179 | 181 | PF00675 | 0.425 |
CLV_NRD_NRD_1 | 220 | 222 | PF00675 | 0.699 |
CLV_NRD_NRD_1 | 708 | 710 | PF00675 | 0.674 |
CLV_NRD_NRD_1 | 722 | 724 | PF00675 | 0.516 |
CLV_NRD_NRD_1 | 819 | 821 | PF00675 | 0.420 |
CLV_NRD_NRD_1 | 843 | 845 | PF00675 | 0.577 |
CLV_PCSK_KEX2_1 | 170 | 172 | PF00082 | 0.480 |
CLV_PCSK_KEX2_1 | 179 | 181 | PF00082 | 0.425 |
CLV_PCSK_KEX2_1 | 220 | 222 | PF00082 | 0.651 |
CLV_PCSK_KEX2_1 | 241 | 243 | PF00082 | 0.540 |
CLV_PCSK_KEX2_1 | 722 | 724 | PF00082 | 0.613 |
CLV_PCSK_KEX2_1 | 843 | 845 | PF00082 | 0.577 |
CLV_PCSK_PC1ET2_1 | 241 | 243 | PF00082 | 0.540 |
CLV_PCSK_SKI1_1 | 114 | 118 | PF00082 | 0.564 |
CLV_PCSK_SKI1_1 | 155 | 159 | PF00082 | 0.509 |
CLV_PCSK_SKI1_1 | 186 | 190 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 19 | 23 | PF00082 | 0.551 |
CLV_PCSK_SKI1_1 | 296 | 300 | PF00082 | 0.422 |
CLV_PCSK_SKI1_1 | 519 | 523 | PF00082 | 0.653 |
CLV_PCSK_SKI1_1 | 71 | 75 | PF00082 | 0.546 |
CLV_PCSK_SKI1_1 | 8 | 12 | PF00082 | 0.417 |
CLV_Separin_Metazoa | 829 | 833 | PF03568 | 0.361 |
DEG_APCC_DBOX_1 | 7 | 15 | PF00400 | 0.550 |
DEG_MDM2_SWIB_1 | 863 | 871 | PF02201 | 0.470 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.443 |
DOC_CKS1_1 | 772 | 777 | PF01111 | 0.484 |
DOC_CYCLIN_RxL_1 | 180 | 192 | PF00134 | 0.538 |
DOC_CYCLIN_RxL_1 | 207 | 218 | PF00134 | 0.437 |
DOC_CYCLIN_RxL_1 | 853 | 866 | PF00134 | 0.556 |
DOC_CYCLIN_yCln2_LP_2 | 344 | 350 | PF00134 | 0.467 |
DOC_CYCLIN_yCln2_LP_2 | 630 | 636 | PF00134 | 0.534 |
DOC_MAPK_DCC_7 | 832 | 842 | PF00069 | 0.514 |
DOC_MAPK_gen_1 | 159 | 169 | PF00069 | 0.374 |
DOC_MAPK_gen_1 | 170 | 178 | PF00069 | 0.449 |
DOC_MAPK_gen_1 | 42 | 51 | PF00069 | 0.564 |
DOC_MAPK_gen_1 | 448 | 457 | PF00069 | 0.703 |
DOC_MAPK_gen_1 | 709 | 715 | PF00069 | 0.723 |
DOC_MAPK_HePTP_8 | 617 | 629 | PF00069 | 0.489 |
DOC_MAPK_MEF2A_6 | 159 | 168 | PF00069 | 0.301 |
DOC_MAPK_MEF2A_6 | 44 | 53 | PF00069 | 0.523 |
DOC_MAPK_MEF2A_6 | 448 | 457 | PF00069 | 0.643 |
DOC_MAPK_MEF2A_6 | 588 | 596 | PF00069 | 0.512 |
DOC_MAPK_MEF2A_6 | 620 | 629 | PF00069 | 0.395 |
DOC_MAPK_RevD_3 | 164 | 180 | PF00069 | 0.519 |
DOC_PP1_RVXF_1 | 208 | 215 | PF00149 | 0.418 |
DOC_PP1_RVXF_1 | 857 | 864 | PF00149 | 0.550 |
DOC_PP2B_LxvP_1 | 630 | 633 | PF13499 | 0.536 |
DOC_PP2B_PxIxI_1 | 710 | 716 | PF00149 | 0.617 |
DOC_PP4_FxxP_1 | 479 | 482 | PF00568 | 0.732 |
DOC_USP7_MATH_1 | 222 | 226 | PF00917 | 0.552 |
DOC_USP7_MATH_1 | 360 | 364 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 432 | 436 | PF00917 | 0.660 |
DOC_USP7_MATH_1 | 480 | 484 | PF00917 | 0.741 |
DOC_USP7_MATH_1 | 511 | 515 | PF00917 | 0.763 |
DOC_USP7_MATH_1 | 559 | 563 | PF00917 | 0.464 |
DOC_USP7_MATH_1 | 823 | 827 | PF00917 | 0.491 |
DOC_USP7_MATH_1 | 895 | 899 | PF00917 | 0.478 |
DOC_USP7_UBL2_3 | 151 | 155 | PF12436 | 0.354 |
DOC_USP7_UBL2_3 | 326 | 330 | PF12436 | 0.534 |
DOC_WW_Pin1_4 | 545 | 550 | PF00397 | 0.594 |
DOC_WW_Pin1_4 | 64 | 69 | PF00397 | 0.434 |
DOC_WW_Pin1_4 | 771 | 776 | PF00397 | 0.489 |
LIG_14-3-3_CanoR_1 | 114 | 119 | PF00244 | 0.603 |
LIG_14-3-3_CanoR_1 | 170 | 178 | PF00244 | 0.538 |
LIG_14-3-3_CanoR_1 | 230 | 235 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 460 | 465 | PF00244 | 0.670 |
LIG_14-3-3_CanoR_1 | 565 | 574 | PF00244 | 0.504 |
LIG_Actin_WH2_2 | 154 | 172 | PF00022 | 0.532 |
LIG_ActinCP_TwfCPI_2 | 479 | 489 | PF01115 | 0.665 |
LIG_AP2alpha_1 | 194 | 198 | PF02296 | 0.330 |
LIG_AP2alpha_1 | 365 | 369 | PF02296 | 0.573 |
LIG_BIR_III_4 | 569 | 573 | PF00653 | 0.476 |
LIG_BRCT_BRCA1_1 | 232 | 236 | PF00533 | 0.468 |
LIG_BRCT_BRCA1_1 | 320 | 324 | PF00533 | 0.516 |
LIG_BRCT_BRCA1_1 | 567 | 571 | PF00533 | 0.562 |
LIG_BRCT_BRCA1_1 | 579 | 583 | PF00533 | 0.516 |
LIG_BRCT_BRCA1_1 | 859 | 863 | PF00533 | 0.460 |
LIG_BRCT_BRCA1_2 | 320 | 326 | PF00533 | 0.539 |
LIG_BRCT_BRCA1_2 | 567 | 573 | PF00533 | 0.573 |
LIG_BRCT_BRCA1_2 | 859 | 865 | PF00533 | 0.565 |
LIG_eIF4E_1 | 651 | 657 | PF01652 | 0.512 |
LIG_EVH1_1 | 697 | 701 | PF00568 | 0.641 |
LIG_FHA_1 | 130 | 136 | PF00498 | 0.477 |
LIG_FHA_1 | 152 | 158 | PF00498 | 0.472 |
LIG_FHA_1 | 285 | 291 | PF00498 | 0.493 |
LIG_FHA_1 | 376 | 382 | PF00498 | 0.561 |
LIG_FHA_1 | 400 | 406 | PF00498 | 0.430 |
LIG_FHA_1 | 588 | 594 | PF00498 | 0.570 |
LIG_FHA_1 | 620 | 626 | PF00498 | 0.525 |
LIG_FHA_1 | 64 | 70 | PF00498 | 0.418 |
LIG_FHA_1 | 652 | 658 | PF00498 | 0.537 |
LIG_FHA_1 | 688 | 694 | PF00498 | 0.722 |
LIG_FHA_1 | 700 | 706 | PF00498 | 0.642 |
LIG_FHA_1 | 889 | 895 | PF00498 | 0.513 |
LIG_FHA_2 | 311 | 317 | PF00498 | 0.514 |
LIG_FHA_2 | 332 | 338 | PF00498 | 0.522 |
LIG_FHA_2 | 404 | 410 | PF00498 | 0.617 |
LIG_FHA_2 | 680 | 686 | PF00498 | 0.689 |
LIG_FHA_2 | 875 | 881 | PF00498 | 0.515 |
LIG_LIR_Gen_1 | 123 | 134 | PF02991 | 0.498 |
LIG_LIR_Gen_1 | 196 | 206 | PF02991 | 0.496 |
LIG_LIR_Gen_1 | 2 | 11 | PF02991 | 0.513 |
LIG_LIR_Gen_1 | 233 | 243 | PF02991 | 0.464 |
LIG_LIR_Gen_1 | 318 | 324 | PF02991 | 0.464 |
LIG_LIR_Gen_1 | 473 | 482 | PF02991 | 0.606 |
LIG_LIR_Gen_1 | 537 | 545 | PF02991 | 0.445 |
LIG_LIR_Gen_1 | 580 | 589 | PF02991 | 0.578 |
LIG_LIR_Gen_1 | 762 | 772 | PF02991 | 0.445 |
LIG_LIR_Gen_1 | 801 | 810 | PF02991 | 0.448 |
LIG_LIR_Gen_1 | 907 | 916 | PF02991 | 0.537 |
LIG_LIR_Nem_3 | 123 | 129 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 196 | 201 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 2 | 6 | PF02991 | 0.503 |
LIG_LIR_Nem_3 | 233 | 239 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 318 | 323 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 473 | 479 | PF02991 | 0.610 |
LIG_LIR_Nem_3 | 537 | 542 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 568 | 574 | PF02991 | 0.542 |
LIG_LIR_Nem_3 | 57 | 63 | PF02991 | 0.595 |
LIG_LIR_Nem_3 | 580 | 586 | PF02991 | 0.550 |
LIG_LIR_Nem_3 | 646 | 651 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 762 | 767 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 783 | 789 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 801 | 807 | PF02991 | 0.303 |
LIG_LIR_Nem_3 | 833 | 837 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 857 | 861 | PF02991 | 0.548 |
LIG_LIR_Nem_3 | 907 | 913 | PF02991 | 0.539 |
LIG_LYPXL_S_1 | 696 | 700 | PF13949 | 0.597 |
LIG_LYPXL_yS_3 | 697 | 700 | PF13949 | 0.600 |
LIG_NRBOX | 163 | 169 | PF00104 | 0.458 |
LIG_PCNA_yPIPBox_3 | 230 | 239 | PF02747 | 0.514 |
LIG_Pex14_2 | 194 | 198 | PF04695 | 0.500 |
LIG_Pex14_2 | 320 | 324 | PF04695 | 0.405 |
LIG_Pex14_2 | 365 | 369 | PF04695 | 0.573 |
LIG_Pex14_2 | 751 | 755 | PF04695 | 0.486 |
LIG_Pex14_2 | 804 | 808 | PF04695 | 0.501 |
LIG_Pex14_2 | 863 | 867 | PF04695 | 0.407 |
LIG_PTB_Apo_2 | 267 | 274 | PF02174 | 0.483 |
LIG_REV1ctd_RIR_1 | 476 | 481 | PF16727 | 0.653 |
LIG_SH2_CRK | 350 | 354 | PF00017 | 0.469 |
LIG_SH2_CRK | 400 | 404 | PF00017 | 0.541 |
LIG_SH2_CRK | 539 | 543 | PF00017 | 0.433 |
LIG_SH2_CRK | 621 | 625 | PF00017 | 0.481 |
LIG_SH2_CRK | 740 | 744 | PF00017 | 0.475 |
LIG_SH2_CRK | 858 | 862 | PF00017 | 0.564 |
LIG_SH2_CRK | 910 | 914 | PF00017 | 0.541 |
LIG_SH2_GRB2like | 740 | 743 | PF00017 | 0.596 |
LIG_SH2_SRC | 437 | 440 | PF00017 | 0.531 |
LIG_SH2_STAP1 | 350 | 354 | PF00017 | 0.469 |
LIG_SH2_STAP1 | 400 | 404 | PF00017 | 0.541 |
LIG_SH2_STAP1 | 437 | 441 | PF00017 | 0.732 |
LIG_SH2_STAP1 | 621 | 625 | PF00017 | 0.329 |
LIG_SH2_STAP1 | 740 | 744 | PF00017 | 0.496 |
LIG_SH2_STAP1 | 910 | 914 | PF00017 | 0.541 |
LIG_SH2_STAT3 | 615 | 618 | PF00017 | 0.354 |
LIG_SH2_STAT5 | 187 | 190 | PF00017 | 0.550 |
LIG_SH2_STAT5 | 354 | 357 | PF00017 | 0.401 |
LIG_SH2_STAT5 | 615 | 618 | PF00017 | 0.494 |
LIG_SH2_STAT5 | 621 | 624 | PF00017 | 0.397 |
LIG_SH2_STAT5 | 773 | 776 | PF00017 | 0.436 |
LIG_SH3_1 | 695 | 701 | PF00018 | 0.624 |
LIG_SH3_3 | 466 | 472 | PF00018 | 0.589 |
LIG_SH3_3 | 593 | 599 | PF00018 | 0.442 |
LIG_SH3_3 | 626 | 632 | PF00018 | 0.480 |
LIG_SH3_3 | 695 | 701 | PF00018 | 0.639 |
LIG_SH3_3 | 769 | 775 | PF00018 | 0.448 |
LIG_SH3_3 | 97 | 103 | PF00018 | 0.498 |
LIG_SUMO_SIM_anti_2 | 527 | 534 | PF11976 | 0.453 |
LIG_SUMO_SIM_anti_2 | 626 | 631 | PF11976 | 0.367 |
LIG_SUMO_SIM_anti_2 | 826 | 833 | PF11976 | 0.476 |
LIG_SUMO_SIM_anti_2 | 869 | 875 | PF11976 | 0.473 |
LIG_SUMO_SIM_par_1 | 600 | 605 | PF11976 | 0.491 |
LIG_SUMO_SIM_par_1 | 621 | 626 | PF11976 | 0.347 |
LIG_SUMO_SIM_par_1 | 891 | 898 | PF11976 | 0.427 |
LIG_TRAF2_1 | 472 | 475 | PF00917 | 0.736 |
LIG_TRAF2_1 | 485 | 488 | PF00917 | 0.550 |
LIG_TRAF2_1 | 920 | 923 | PF00917 | 0.587 |
LIG_TRFH_1 | 468 | 472 | PF08558 | 0.576 |
LIG_TYR_ITIM | 348 | 353 | PF00017 | 0.363 |
LIG_TYR_ITIM | 619 | 624 | PF00017 | 0.417 |
LIG_TYR_ITIM | 856 | 861 | PF00017 | 0.576 |
LIG_UBA3_1 | 157 | 162 | PF00899 | 0.515 |
LIG_UBA3_1 | 177 | 186 | PF00899 | 0.201 |
LIG_UBA3_1 | 234 | 241 | PF00899 | 0.483 |
LIG_UBA3_1 | 352 | 358 | PF00899 | 0.454 |
LIG_WRC_WIRS_1 | 512 | 517 | PF05994 | 0.620 |
MOD_CDK_SPxxK_3 | 64 | 71 | PF00069 | 0.392 |
MOD_CK1_1 | 215 | 221 | PF00069 | 0.654 |
MOD_CK1_1 | 251 | 257 | PF00069 | 0.542 |
MOD_CK1_1 | 442 | 448 | PF00069 | 0.664 |
MOD_CK1_1 | 530 | 536 | PF00069 | 0.531 |
MOD_CK1_1 | 587 | 593 | PF00069 | 0.536 |
MOD_CK1_1 | 676 | 682 | PF00069 | 0.692 |
MOD_CK1_1 | 781 | 787 | PF00069 | 0.477 |
MOD_CK2_1 | 22 | 28 | PF00069 | 0.600 |
MOD_CK2_1 | 310 | 316 | PF00069 | 0.476 |
MOD_CK2_1 | 460 | 466 | PF00069 | 0.710 |
MOD_CK2_1 | 482 | 488 | PF00069 | 0.658 |
MOD_CK2_1 | 531 | 537 | PF00069 | 0.448 |
MOD_CK2_1 | 665 | 671 | PF00069 | 0.423 |
MOD_CK2_1 | 679 | 685 | PF00069 | 0.687 |
MOD_CK2_1 | 823 | 829 | PF00069 | 0.472 |
MOD_CK2_1 | 866 | 872 | PF00069 | 0.534 |
MOD_CK2_1 | 98 | 104 | PF00069 | 0.446 |
MOD_CMANNOS | 228 | 231 | PF00535 | 0.407 |
MOD_Cter_Amidation | 707 | 710 | PF01082 | 0.710 |
MOD_GlcNHglycan | 250 | 253 | PF01048 | 0.520 |
MOD_GlcNHglycan | 320 | 323 | PF01048 | 0.533 |
MOD_GlcNHglycan | 334 | 337 | PF01048 | 0.413 |
MOD_GlcNHglycan | 406 | 409 | PF01048 | 0.591 |
MOD_GlcNHglycan | 420 | 423 | PF01048 | 0.428 |
MOD_GlcNHglycan | 441 | 444 | PF01048 | 0.715 |
MOD_GlcNHglycan | 561 | 564 | PF01048 | 0.422 |
MOD_GlcNHglycan | 675 | 678 | PF01048 | 0.715 |
MOD_GlcNHglycan | 706 | 709 | PF01048 | 0.761 |
MOD_GlcNHglycan | 81 | 85 | PF01048 | 0.642 |
MOD_GlcNHglycan | 868 | 871 | PF01048 | 0.528 |
MOD_GSK3_1 | 332 | 339 | PF00069 | 0.490 |
MOD_GSK3_1 | 399 | 406 | PF00069 | 0.400 |
MOD_GSK3_1 | 527 | 534 | PF00069 | 0.453 |
MOD_GSK3_1 | 673 | 680 | PF00069 | 0.631 |
MOD_GSK3_1 | 699 | 706 | PF00069 | 0.663 |
MOD_GSK3_1 | 709 | 716 | PF00069 | 0.596 |
MOD_GSK3_1 | 857 | 864 | PF00069 | 0.498 |
MOD_N-GLC_1 | 114 | 119 | PF02516 | 0.597 |
MOD_N-GLC_1 | 418 | 423 | PF02516 | 0.544 |
MOD_N-GLC_1 | 732 | 737 | PF02516 | 0.706 |
MOD_N-GLC_1 | 815 | 820 | PF02516 | 0.460 |
MOD_N-GLC_2 | 94 | 96 | PF02516 | 0.461 |
MOD_NEK2_1 | 120 | 125 | PF00069 | 0.465 |
MOD_NEK2_1 | 129 | 134 | PF00069 | 0.355 |
MOD_NEK2_1 | 136 | 141 | PF00069 | 0.347 |
MOD_NEK2_1 | 14 | 19 | PF00069 | 0.591 |
MOD_NEK2_1 | 206 | 211 | PF00069 | 0.466 |
MOD_NEK2_1 | 212 | 217 | PF00069 | 0.616 |
MOD_NEK2_1 | 381 | 386 | PF00069 | 0.569 |
MOD_NEK2_1 | 403 | 408 | PF00069 | 0.552 |
MOD_NEK2_1 | 459 | 464 | PF00069 | 0.739 |
MOD_NEK2_1 | 619 | 624 | PF00069 | 0.461 |
MOD_NEK2_1 | 665 | 670 | PF00069 | 0.516 |
MOD_NEK2_1 | 861 | 866 | PF00069 | 0.457 |
MOD_NEK2_1 | 874 | 879 | PF00069 | 0.543 |
MOD_NEK2_1 | 98 | 103 | PF00069 | 0.398 |
MOD_NEK2_2 | 399 | 404 | PF00069 | 0.418 |
MOD_NEK2_2 | 815 | 820 | PF00069 | 0.460 |
MOD_NEK2_2 | 895 | 900 | PF00069 | 0.507 |
MOD_PIKK_1 | 108 | 114 | PF00454 | 0.542 |
MOD_PIKK_1 | 215 | 221 | PF00454 | 0.703 |
MOD_PIKK_1 | 432 | 438 | PF00454 | 0.709 |
MOD_PIKK_1 | 442 | 448 | PF00454 | 0.614 |
MOD_PIKK_1 | 513 | 519 | PF00454 | 0.641 |
MOD_PIKK_1 | 665 | 671 | PF00454 | 0.465 |
MOD_PK_1 | 709 | 715 | PF00069 | 0.691 |
MOD_PKA_1 | 709 | 715 | PF00069 | 0.723 |
MOD_PKA_2 | 14 | 20 | PF00069 | 0.573 |
MOD_PKA_2 | 459 | 465 | PF00069 | 0.616 |
MOD_PKA_2 | 480 | 486 | PF00069 | 0.733 |
MOD_PKA_2 | 587 | 593 | PF00069 | 0.557 |
MOD_PKA_2 | 619 | 625 | PF00069 | 0.365 |
MOD_PKB_1 | 575 | 583 | PF00069 | 0.541 |
MOD_PKB_1 | 736 | 744 | PF00069 | 0.528 |
MOD_Plk_1 | 114 | 120 | PF00069 | 0.574 |
MOD_Plk_1 | 222 | 228 | PF00069 | 0.519 |
MOD_Plk_1 | 336 | 342 | PF00069 | 0.441 |
MOD_Plk_1 | 487 | 493 | PF00069 | 0.717 |
MOD_Plk_1 | 815 | 821 | PF00069 | 0.564 |
MOD_Plk_4 | 114 | 120 | PF00069 | 0.556 |
MOD_Plk_4 | 129 | 135 | PF00069 | 0.337 |
MOD_Plk_4 | 223 | 229 | PF00069 | 0.489 |
MOD_Plk_4 | 230 | 236 | PF00069 | 0.399 |
MOD_Plk_4 | 399 | 405 | PF00069 | 0.404 |
MOD_Plk_4 | 460 | 466 | PF00069 | 0.743 |
MOD_Plk_4 | 527 | 533 | PF00069 | 0.496 |
MOD_Plk_4 | 597 | 603 | PF00069 | 0.433 |
MOD_Plk_4 | 619 | 625 | PF00069 | 0.315 |
MOD_Plk_4 | 709 | 715 | PF00069 | 0.623 |
MOD_Plk_4 | 781 | 787 | PF00069 | 0.393 |
MOD_Plk_4 | 82 | 88 | PF00069 | 0.568 |
MOD_Plk_4 | 823 | 829 | PF00069 | 0.428 |
MOD_Plk_4 | 863 | 869 | PF00069 | 0.440 |
MOD_Plk_4 | 908 | 914 | PF00069 | 0.571 |
MOD_ProDKin_1 | 545 | 551 | PF00069 | 0.588 |
MOD_ProDKin_1 | 64 | 70 | PF00069 | 0.430 |
MOD_ProDKin_1 | 771 | 777 | PF00069 | 0.484 |
MOD_SUMO_for_1 | 428 | 431 | PF00179 | 0.495 |
MOD_SUMO_for_1 | 521 | 524 | PF00179 | 0.551 |
MOD_SUMO_rev_2 | 148 | 157 | PF00179 | 0.557 |
MOD_SUMO_rev_2 | 240 | 248 | PF00179 | 0.518 |
MOD_SUMO_rev_2 | 483 | 491 | PF00179 | 0.755 |
MOD_SUMO_rev_2 | 712 | 721 | PF00179 | 0.649 |
TRG_DiLeu_BaEn_2 | 327 | 333 | PF01217 | 0.546 |
TRG_DiLeu_BaLyEn_6 | 340 | 345 | PF01217 | 0.467 |
TRG_DiLeu_BaLyEn_6 | 410 | 415 | PF01217 | 0.612 |
TRG_ENDOCYTIC_2 | 350 | 353 | PF00928 | 0.369 |
TRG_ENDOCYTIC_2 | 400 | 403 | PF00928 | 0.544 |
TRG_ENDOCYTIC_2 | 476 | 479 | PF00928 | 0.732 |
TRG_ENDOCYTIC_2 | 539 | 542 | PF00928 | 0.426 |
TRG_ENDOCYTIC_2 | 621 | 624 | PF00928 | 0.392 |
TRG_ENDOCYTIC_2 | 697 | 700 | PF00928 | 0.600 |
TRG_ENDOCYTIC_2 | 740 | 743 | PF00928 | 0.495 |
TRG_ENDOCYTIC_2 | 858 | 861 | PF00928 | 0.568 |
TRG_ENDOCYTIC_2 | 910 | 913 | PF00928 | 0.543 |
TRG_ER_diArg_1 | 169 | 171 | PF00400 | 0.435 |
TRG_ER_diArg_1 | 178 | 180 | PF00400 | 0.425 |
TRG_ER_diArg_1 | 574 | 577 | PF00400 | 0.581 |
TRG_ER_diArg_1 | 722 | 724 | PF00400 | 0.613 |
TRG_ER_diArg_1 | 734 | 737 | PF00400 | 0.568 |
TRG_ER_diArg_1 | 842 | 844 | PF00400 | 0.530 |
TRG_NES_CRM1_1 | 34 | 47 | PF08389 | 0.459 |
TRG_NES_CRM1_1 | 494 | 509 | PF08389 | 0.691 |
TRG_Pf-PMV_PEXEL_1 | 565 | 569 | PF00026 | 0.554 |
TRG_Pf-PMV_PEXEL_1 | 900 | 905 | PF00026 | 0.522 |
TRG_Pf-PMV_PEXEL_1 | 919 | 923 | PF00026 | 0.441 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P438 | Leptomonas seymouri | 53% | 100% |
A0A1X0NJ45 | Trypanosomatidae | 32% | 95% |
A0A3Q8ILW9 | Leishmania donovani | 99% | 100% |
A0A3R7MMH0 | Trypanosoma rangeli | 33% | 95% |
A4HMB8 | Leishmania braziliensis | 77% | 100% |
C9ZNI1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 96% |
E9AER2 | Leishmania major | 92% | 100% |
E9B5W7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
V5BAN0 | Trypanosoma cruzi | 30% | 94% |