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: E9B5W7
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 | 14 | 18 | PF00656 | 0.559 |
CLV_MEL_PAP_1 | 458 | 464 | PF00089 | 0.742 |
CLV_NRD_NRD_1 | 171 | 173 | PF00675 | 0.491 |
CLV_NRD_NRD_1 | 180 | 182 | PF00675 | 0.431 |
CLV_NRD_NRD_1 | 221 | 223 | PF00675 | 0.672 |
CLV_NRD_NRD_1 | 708 | 710 | PF00675 | 0.656 |
CLV_NRD_NRD_1 | 722 | 724 | PF00675 | 0.520 |
CLV_NRD_NRD_1 | 819 | 821 | PF00675 | 0.423 |
CLV_NRD_NRD_1 | 843 | 845 | PF00675 | 0.577 |
CLV_PCSK_KEX2_1 | 171 | 173 | PF00082 | 0.485 |
CLV_PCSK_KEX2_1 | 180 | 182 | PF00082 | 0.431 |
CLV_PCSK_KEX2_1 | 221 | 223 | PF00082 | 0.624 |
CLV_PCSK_KEX2_1 | 242 | 244 | PF00082 | 0.544 |
CLV_PCSK_KEX2_1 | 722 | 724 | PF00082 | 0.617 |
CLV_PCSK_KEX2_1 | 843 | 845 | PF00082 | 0.577 |
CLV_PCSK_PC1ET2_1 | 242 | 244 | PF00082 | 0.544 |
CLV_PCSK_SKI1_1 | 115 | 119 | PF00082 | 0.562 |
CLV_PCSK_SKI1_1 | 156 | 160 | PF00082 | 0.508 |
CLV_PCSK_SKI1_1 | 187 | 191 | PF00082 | 0.480 |
CLV_PCSK_SKI1_1 | 297 | 301 | PF00082 | 0.428 |
CLV_PCSK_SKI1_1 | 9 | 13 | PF00082 | 0.426 |
CLV_Separin_Metazoa | 829 | 833 | PF03568 | 0.361 |
DEG_APCC_DBOX_1 | 296 | 304 | PF00400 | 0.396 |
DEG_APCC_DBOX_1 | 8 | 16 | PF00400 | 0.562 |
DEG_MDM2_SWIB_1 | 863 | 871 | PF02201 | 0.470 |
DEG_SCF_FBW7_1 | 65 | 72 | PF00400 | 0.242 |
DOC_CKS1_1 | 258 | 263 | PF01111 | 0.417 |
DOC_CKS1_1 | 772 | 777 | PF01111 | 0.481 |
DOC_CYCLIN_RxL_1 | 181 | 193 | PF00134 | 0.547 |
DOC_CYCLIN_RxL_1 | 853 | 864 | PF00134 | 0.551 |
DOC_CYCLIN_yCln2_LP_2 | 345 | 351 | PF00134 | 0.473 |
DOC_CYCLIN_yCln2_LP_2 | 630 | 636 | PF00134 | 0.540 |
DOC_MAPK_DCC_7 | 832 | 842 | PF00069 | 0.506 |
DOC_MAPK_gen_1 | 171 | 179 | PF00069 | 0.454 |
DOC_MAPK_gen_1 | 43 | 52 | PF00069 | 0.565 |
DOC_MAPK_gen_1 | 620 | 629 | PF00069 | 0.382 |
DOC_MAPK_gen_1 | 709 | 715 | PF00069 | 0.735 |
DOC_MAPK_HePTP_8 | 617 | 629 | PF00069 | 0.493 |
DOC_MAPK_MEF2A_6 | 45 | 54 | PF00069 | 0.523 |
DOC_MAPK_MEF2A_6 | 620 | 629 | PF00069 | 0.398 |
DOC_MAPK_RevD_3 | 165 | 181 | PF00069 | 0.524 |
DOC_PP1_RVXF_1 | 857 | 864 | PF00149 | 0.539 |
DOC_PP2B_LxvP_1 | 630 | 633 | PF13499 | 0.541 |
DOC_USP7_MATH_1 | 223 | 227 | PF00917 | 0.535 |
DOC_USP7_MATH_1 | 361 | 365 | PF00917 | 0.646 |
DOC_USP7_MATH_1 | 433 | 437 | PF00917 | 0.659 |
DOC_USP7_MATH_1 | 511 | 515 | PF00917 | 0.747 |
DOC_USP7_MATH_1 | 559 | 563 | PF00917 | 0.468 |
DOC_USP7_MATH_1 | 823 | 827 | PF00917 | 0.490 |
DOC_USP7_MATH_1 | 895 | 899 | PF00917 | 0.480 |
DOC_USP7_UBL2_3 | 327 | 331 | PF12436 | 0.535 |
DOC_WW_Pin1_4 | 257 | 262 | PF00397 | 0.406 |
DOC_WW_Pin1_4 | 357 | 362 | PF00397 | 0.320 |
DOC_WW_Pin1_4 | 545 | 550 | PF00397 | 0.601 |
DOC_WW_Pin1_4 | 65 | 70 | PF00397 | 0.432 |
DOC_WW_Pin1_4 | 771 | 776 | PF00397 | 0.487 |
LIG_14-3-3_CanoR_1 | 115 | 120 | PF00244 | 0.601 |
LIG_14-3-3_CanoR_1 | 171 | 179 | PF00244 | 0.543 |
LIG_14-3-3_CanoR_1 | 231 | 236 | PF00244 | 0.507 |
LIG_14-3-3_CanoR_1 | 289 | 296 | PF00244 | 0.474 |
LIG_14-3-3_CanoR_1 | 461 | 466 | PF00244 | 0.664 |
LIG_14-3-3_CanoR_1 | 482 | 490 | PF00244 | 0.583 |
LIG_14-3-3_CanoR_1 | 565 | 574 | PF00244 | 0.498 |
LIG_14-3-3_CanoR_1 | 709 | 715 | PF00244 | 0.509 |
LIG_Actin_WH2_2 | 155 | 173 | PF00022 | 0.535 |
LIG_AP2alpha_1 | 366 | 370 | PF02296 | 0.586 |
LIG_BRCT_BRCA1_1 | 321 | 325 | PF00533 | 0.517 |
LIG_BRCT_BRCA1_1 | 567 | 571 | PF00533 | 0.555 |
LIG_BRCT_BRCA1_1 | 579 | 583 | PF00533 | 0.521 |
LIG_BRCT_BRCA1_1 | 859 | 863 | PF00533 | 0.453 |
LIG_BRCT_BRCA1_2 | 321 | 327 | PF00533 | 0.540 |
LIG_BRCT_BRCA1_2 | 567 | 573 | PF00533 | 0.567 |
LIG_BRCT_BRCA1_2 | 859 | 865 | PF00533 | 0.561 |
LIG_CaM_IQ_9 | 234 | 249 | PF13499 | 0.258 |
LIG_eIF4E_1 | 651 | 657 | PF01652 | 0.518 |
LIG_EVH1_1 | 697 | 701 | PF00568 | 0.615 |
LIG_FHA_1 | 131 | 137 | PF00498 | 0.478 |
LIG_FHA_1 | 153 | 159 | PF00498 | 0.474 |
LIG_FHA_1 | 274 | 280 | PF00498 | 0.456 |
LIG_FHA_1 | 289 | 295 | PF00498 | 0.484 |
LIG_FHA_1 | 377 | 383 | PF00498 | 0.565 |
LIG_FHA_1 | 401 | 407 | PF00498 | 0.432 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.417 |
LIG_FHA_1 | 652 | 658 | PF00498 | 0.541 |
LIG_FHA_1 | 700 | 706 | PF00498 | 0.592 |
LIG_FHA_1 | 709 | 715 | PF00498 | 0.609 |
LIG_FHA_1 | 889 | 895 | PF00498 | 0.517 |
LIG_FHA_2 | 312 | 318 | PF00498 | 0.518 |
LIG_FHA_2 | 333 | 339 | PF00498 | 0.534 |
LIG_FHA_2 | 358 | 364 | PF00498 | 0.331 |
LIG_FHA_2 | 519 | 525 | PF00498 | 0.571 |
LIG_FHA_2 | 686 | 692 | PF00498 | 0.570 |
LIG_FHA_2 | 875 | 881 | PF00498 | 0.516 |
LIG_LIR_Gen_1 | 124 | 135 | PF02991 | 0.501 |
LIG_LIR_Gen_1 | 234 | 244 | PF02991 | 0.474 |
LIG_LIR_Gen_1 | 3 | 12 | PF02991 | 0.524 |
LIG_LIR_Gen_1 | 319 | 325 | PF02991 | 0.463 |
LIG_LIR_Gen_1 | 537 | 545 | PF02991 | 0.445 |
LIG_LIR_Gen_1 | 568 | 578 | PF02991 | 0.521 |
LIG_LIR_Gen_1 | 580 | 589 | PF02991 | 0.582 |
LIG_LIR_Gen_1 | 590 | 601 | PF02991 | 0.269 |
LIG_LIR_Gen_1 | 762 | 772 | PF02991 | 0.461 |
LIG_LIR_Gen_1 | 801 | 810 | PF02991 | 0.454 |
LIG_LIR_Gen_1 | 907 | 916 | PF02991 | 0.542 |
LIG_LIR_Nem_3 | 124 | 130 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 197 | 202 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 234 | 240 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 3 | 7 | PF02991 | 0.514 |
LIG_LIR_Nem_3 | 319 | 324 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 474 | 480 | PF02991 | 0.598 |
LIG_LIR_Nem_3 | 537 | 542 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 568 | 574 | PF02991 | 0.536 |
LIG_LIR_Nem_3 | 58 | 64 | PF02991 | 0.595 |
LIG_LIR_Nem_3 | 580 | 586 | PF02991 | 0.557 |
LIG_LIR_Nem_3 | 590 | 596 | PF02991 | 0.284 |
LIG_LIR_Nem_3 | 646 | 651 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 762 | 767 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 783 | 789 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 801 | 807 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 833 | 837 | PF02991 | 0.489 |
LIG_LIR_Nem_3 | 857 | 861 | PF02991 | 0.532 |
LIG_LIR_Nem_3 | 907 | 913 | PF02991 | 0.542 |
LIG_LYPXL_S_1 | 696 | 700 | PF13949 | 0.568 |
LIG_LYPXL_yS_3 | 697 | 700 | PF13949 | 0.567 |
LIG_NRBOX | 164 | 170 | PF00104 | 0.462 |
LIG_PCNA_yPIPBox_3 | 231 | 240 | PF02747 | 0.521 |
LIG_Pex14_2 | 195 | 199 | PF04695 | 0.495 |
LIG_Pex14_2 | 321 | 325 | PF04695 | 0.406 |
LIG_Pex14_2 | 366 | 370 | PF04695 | 0.586 |
LIG_Pex14_2 | 751 | 755 | PF04695 | 0.493 |
LIG_Pex14_2 | 804 | 808 | PF04695 | 0.505 |
LIG_Pex14_2 | 863 | 867 | PF04695 | 0.405 |
LIG_PTB_Apo_2 | 268 | 275 | PF02174 | 0.472 |
LIG_REV1ctd_RIR_1 | 477 | 486 | PF16727 | 0.634 |
LIG_SH2_CRK | 351 | 355 | PF00017 | 0.480 |
LIG_SH2_CRK | 401 | 405 | PF00017 | 0.543 |
LIG_SH2_CRK | 539 | 543 | PF00017 | 0.432 |
LIG_SH2_CRK | 621 | 625 | PF00017 | 0.487 |
LIG_SH2_CRK | 740 | 744 | PF00017 | 0.485 |
LIG_SH2_CRK | 858 | 862 | PF00017 | 0.553 |
LIG_SH2_CRK | 910 | 914 | PF00017 | 0.549 |
LIG_SH2_GRB2like | 740 | 743 | PF00017 | 0.607 |
LIG_SH2_STAP1 | 275 | 279 | PF00017 | 0.334 |
LIG_SH2_STAP1 | 351 | 355 | PF00017 | 0.480 |
LIG_SH2_STAP1 | 401 | 405 | PF00017 | 0.543 |
LIG_SH2_STAP1 | 438 | 442 | PF00017 | 0.725 |
LIG_SH2_STAP1 | 57 | 61 | PF00017 | 0.335 |
LIG_SH2_STAP1 | 740 | 744 | PF00017 | 0.505 |
LIG_SH2_STAP1 | 910 | 914 | PF00017 | 0.549 |
LIG_SH2_STAT5 | 138 | 141 | PF00017 | 0.532 |
LIG_SH2_STAT5 | 188 | 191 | PF00017 | 0.561 |
LIG_SH2_STAT5 | 275 | 278 | PF00017 | 0.397 |
LIG_SH2_STAT5 | 520 | 523 | PF00017 | 0.554 |
LIG_SH2_STAT5 | 64 | 67 | PF00017 | 0.289 |
LIG_SH2_STAT5 | 773 | 776 | PF00017 | 0.440 |
LIG_SH3_1 | 695 | 701 | PF00018 | 0.605 |
LIG_SH3_3 | 19 | 25 | PF00018 | 0.668 |
LIG_SH3_3 | 467 | 473 | PF00018 | 0.579 |
LIG_SH3_3 | 593 | 599 | PF00018 | 0.447 |
LIG_SH3_3 | 626 | 632 | PF00018 | 0.482 |
LIG_SH3_3 | 695 | 701 | PF00018 | 0.619 |
LIG_SH3_3 | 769 | 775 | PF00018 | 0.445 |
LIG_SH3_3 | 98 | 104 | PF00018 | 0.496 |
LIG_SUMO_SIM_anti_2 | 132 | 138 | PF11976 | 0.273 |
LIG_SUMO_SIM_anti_2 | 527 | 534 | PF11976 | 0.456 |
LIG_SUMO_SIM_anti_2 | 592 | 598 | PF11976 | 0.380 |
LIG_SUMO_SIM_anti_2 | 626 | 631 | PF11976 | 0.370 |
LIG_SUMO_SIM_anti_2 | 826 | 833 | PF11976 | 0.476 |
LIG_SUMO_SIM_anti_2 | 869 | 875 | PF11976 | 0.474 |
LIG_SUMO_SIM_par_1 | 600 | 605 | PF11976 | 0.496 |
LIG_SUMO_SIM_par_1 | 891 | 898 | PF11976 | 0.430 |
LIG_TRAF2_1 | 473 | 476 | PF00917 | 0.728 |
LIG_TYR_ITIM | 349 | 354 | PF00017 | 0.372 |
LIG_TYR_ITIM | 619 | 624 | PF00017 | 0.423 |
LIG_TYR_ITIM | 856 | 861 | PF00017 | 0.562 |
LIG_UBA3_1 | 158 | 163 | PF00899 | 0.517 |
LIG_UBA3_1 | 178 | 187 | PF00899 | 0.207 |
LIG_UBA3_1 | 235 | 242 | PF00899 | 0.495 |
LIG_UBA3_1 | 353 | 359 | PF00899 | 0.461 |
LIG_UBA3_1 | 616 | 622 | PF00899 | 0.320 |
LIG_WRC_WIRS_1 | 512 | 517 | PF05994 | 0.605 |
MOD_CK1_1 | 18 | 24 | PF00069 | 0.469 |
MOD_CK1_1 | 216 | 222 | PF00069 | 0.657 |
MOD_CK1_1 | 252 | 258 | PF00069 | 0.547 |
MOD_CK1_1 | 443 | 449 | PF00069 | 0.671 |
MOD_CK1_1 | 483 | 489 | PF00069 | 0.572 |
MOD_CK1_1 | 530 | 536 | PF00069 | 0.529 |
MOD_CK1_1 | 676 | 682 | PF00069 | 0.688 |
MOD_CK1_1 | 708 | 714 | PF00069 | 0.554 |
MOD_CK1_1 | 781 | 787 | PF00069 | 0.479 |
MOD_CK2_1 | 311 | 317 | PF00069 | 0.476 |
MOD_CK2_1 | 357 | 363 | PF00069 | 0.326 |
MOD_CK2_1 | 461 | 467 | PF00069 | 0.705 |
MOD_CK2_1 | 518 | 524 | PF00069 | 0.560 |
MOD_CK2_1 | 531 | 537 | PF00069 | 0.446 |
MOD_CK2_1 | 665 | 671 | PF00069 | 0.424 |
MOD_CK2_1 | 685 | 691 | PF00069 | 0.727 |
MOD_CK2_1 | 823 | 829 | PF00069 | 0.472 |
MOD_CK2_1 | 866 | 872 | PF00069 | 0.535 |
MOD_CK2_1 | 99 | 105 | PF00069 | 0.443 |
MOD_CMANNOS | 229 | 232 | PF00535 | 0.407 |
MOD_GlcNHglycan | 251 | 254 | PF01048 | 0.527 |
MOD_GlcNHglycan | 321 | 324 | PF01048 | 0.539 |
MOD_GlcNHglycan | 335 | 338 | PF01048 | 0.462 |
MOD_GlcNHglycan | 407 | 410 | PF01048 | 0.598 |
MOD_GlcNHglycan | 561 | 564 | PF01048 | 0.423 |
MOD_GlcNHglycan | 675 | 678 | PF01048 | 0.714 |
MOD_GlcNHglycan | 82 | 86 | PF01048 | 0.648 |
MOD_GlcNHglycan | 868 | 871 | PF01048 | 0.531 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.501 |
MOD_GSK3_1 | 357 | 364 | PF00069 | 0.473 |
MOD_GSK3_1 | 527 | 534 | PF00069 | 0.456 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.491 |
MOD_GSK3_1 | 673 | 680 | PF00069 | 0.633 |
MOD_GSK3_1 | 699 | 706 | PF00069 | 0.614 |
MOD_GSK3_1 | 709 | 716 | PF00069 | 0.608 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.510 |
MOD_GSK3_1 | 857 | 864 | PF00069 | 0.488 |
MOD_N-GLC_1 | 115 | 120 | PF02516 | 0.595 |
MOD_N-GLC_1 | 419 | 424 | PF02516 | 0.548 |
MOD_N-GLC_1 | 732 | 737 | PF02516 | 0.726 |
MOD_N-GLC_1 | 815 | 820 | PF02516 | 0.461 |
MOD_N-GLC_2 | 146 | 148 | PF02516 | 0.438 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.467 |
MOD_NEK2_1 | 130 | 135 | PF00069 | 0.357 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.338 |
MOD_NEK2_1 | 15 | 20 | PF00069 | 0.595 |
MOD_NEK2_1 | 207 | 212 | PF00069 | 0.478 |
MOD_NEK2_1 | 382 | 387 | PF00069 | 0.578 |
MOD_NEK2_1 | 460 | 465 | PF00069 | 0.740 |
MOD_NEK2_1 | 480 | 485 | PF00069 | 0.426 |
MOD_NEK2_1 | 665 | 670 | PF00069 | 0.515 |
MOD_NEK2_1 | 705 | 710 | PF00069 | 0.431 |
MOD_NEK2_1 | 861 | 866 | PF00069 | 0.452 |
MOD_NEK2_1 | 874 | 879 | PF00069 | 0.544 |
MOD_NEK2_1 | 99 | 104 | PF00069 | 0.394 |
MOD_NEK2_2 | 213 | 218 | PF00069 | 0.668 |
MOD_NEK2_2 | 400 | 405 | PF00069 | 0.421 |
MOD_NEK2_2 | 815 | 820 | PF00069 | 0.461 |
MOD_NEK2_2 | 895 | 900 | PF00069 | 0.509 |
MOD_PIKK_1 | 109 | 115 | PF00454 | 0.546 |
MOD_PIKK_1 | 216 | 222 | PF00454 | 0.705 |
MOD_PIKK_1 | 433 | 439 | PF00454 | 0.703 |
MOD_PIKK_1 | 443 | 449 | PF00454 | 0.622 |
MOD_PIKK_1 | 665 | 671 | PF00454 | 0.466 |
MOD_PK_1 | 709 | 715 | PF00069 | 0.703 |
MOD_PKA_1 | 709 | 715 | PF00069 | 0.735 |
MOD_PKA_2 | 15 | 21 | PF00069 | 0.576 |
MOD_PKA_2 | 288 | 294 | PF00069 | 0.483 |
MOD_PKA_2 | 311 | 317 | PF00069 | 0.525 |
MOD_PKA_2 | 460 | 466 | PF00069 | 0.613 |
MOD_PKA_2 | 481 | 487 | PF00069 | 0.720 |
MOD_PKA_2 | 587 | 593 | PF00069 | 0.559 |
MOD_PKA_2 | 708 | 714 | PF00069 | 0.581 |
MOD_PKB_1 | 575 | 583 | PF00069 | 0.543 |
MOD_Plk_1 | 115 | 121 | PF00069 | 0.572 |
MOD_Plk_1 | 223 | 229 | PF00069 | 0.507 |
MOD_Plk_1 | 337 | 343 | PF00069 | 0.450 |
MOD_Plk_1 | 419 | 425 | PF00069 | 0.502 |
MOD_Plk_1 | 815 | 821 | PF00069 | 0.566 |
MOD_Plk_2-3 | 3 | 9 | PF00069 | 0.489 |
MOD_Plk_2-3 | 685 | 691 | PF00069 | 0.559 |
MOD_Plk_4 | 115 | 121 | PF00069 | 0.554 |
MOD_Plk_4 | 130 | 136 | PF00069 | 0.338 |
MOD_Plk_4 | 157 | 163 | PF00069 | 0.395 |
MOD_Plk_4 | 224 | 230 | PF00069 | 0.482 |
MOD_Plk_4 | 231 | 237 | PF00069 | 0.406 |
MOD_Plk_4 | 400 | 406 | PF00069 | 0.406 |
MOD_Plk_4 | 461 | 467 | PF00069 | 0.737 |
MOD_Plk_4 | 527 | 533 | PF00069 | 0.500 |
MOD_Plk_4 | 589 | 595 | PF00069 | 0.476 |
MOD_Plk_4 | 597 | 603 | PF00069 | 0.437 |
MOD_Plk_4 | 709 | 715 | PF00069 | 0.636 |
MOD_Plk_4 | 781 | 787 | PF00069 | 0.394 |
MOD_Plk_4 | 823 | 829 | PF00069 | 0.427 |
MOD_Plk_4 | 83 | 89 | PF00069 | 0.571 |
MOD_Plk_4 | 908 | 914 | PF00069 | 0.575 |
MOD_ProDKin_1 | 257 | 263 | PF00069 | 0.409 |
MOD_ProDKin_1 | 357 | 363 | PF00069 | 0.326 |
MOD_ProDKin_1 | 545 | 551 | PF00069 | 0.595 |
MOD_ProDKin_1 | 65 | 71 | PF00069 | 0.428 |
MOD_ProDKin_1 | 771 | 777 | PF00069 | 0.482 |
MOD_SUMO_for_1 | 429 | 432 | PF00179 | 0.498 |
MOD_SUMO_rev_2 | 149 | 158 | PF00179 | 0.557 |
MOD_SUMO_rev_2 | 241 | 249 | PF00179 | 0.529 |
MOD_SUMO_rev_2 | 712 | 721 | PF00179 | 0.664 |
TRG_DiLeu_BaEn_1 | 154 | 159 | PF01217 | 0.364 |
TRG_DiLeu_BaEn_2 | 328 | 334 | PF01217 | 0.547 |
TRG_DiLeu_BaEn_2 | 588 | 594 | PF01217 | 0.289 |
TRG_DiLeu_BaLyEn_6 | 341 | 346 | PF01217 | 0.472 |
TRG_DiLeu_BaLyEn_6 | 411 | 416 | PF01217 | 0.617 |
TRG_ENDOCYTIC_2 | 351 | 354 | PF00928 | 0.379 |
TRG_ENDOCYTIC_2 | 401 | 404 | PF00928 | 0.546 |
TRG_ENDOCYTIC_2 | 477 | 480 | PF00928 | 0.720 |
TRG_ENDOCYTIC_2 | 539 | 542 | PF00928 | 0.425 |
TRG_ENDOCYTIC_2 | 621 | 624 | PF00928 | 0.399 |
TRG_ENDOCYTIC_2 | 697 | 700 | PF00928 | 0.567 |
TRG_ENDOCYTIC_2 | 740 | 743 | PF00928 | 0.506 |
TRG_ENDOCYTIC_2 | 858 | 861 | PF00928 | 0.556 |
TRG_ENDOCYTIC_2 | 910 | 913 | PF00928 | 0.550 |
TRG_ER_diArg_1 | 170 | 172 | PF00400 | 0.441 |
TRG_ER_diArg_1 | 179 | 181 | PF00400 | 0.431 |
TRG_ER_diArg_1 | 574 | 577 | PF00400 | 0.577 |
TRG_ER_diArg_1 | 722 | 724 | PF00400 | 0.617 |
TRG_ER_diArg_1 | 734 | 737 | PF00400 | 0.585 |
TRG_ER_diArg_1 | 842 | 844 | PF00400 | 0.513 |
TRG_NES_CRM1_1 | 35 | 48 | PF08389 | 0.458 |
TRG_NES_CRM1_1 | 494 | 509 | PF08389 | 0.683 |
TRG_Pf-PMV_PEXEL_1 | 565 | 569 | PF00026 | 0.546 |
TRG_Pf-PMV_PEXEL_1 | 900 | 905 | PF00026 | 0.520 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P438 | Leptomonas seymouri | 52% | 100% |
A0A1X0NJ45 | Trypanosomatidae | 31% | 95% |
A0A3Q8ILW9 | Leishmania donovani | 91% | 100% |
A0A3R7MMH0 | Trypanosoma rangeli | 32% | 95% |
A4HMB8 | Leishmania braziliensis | 78% | 100% |
A4IAY4 | Leishmania infantum | 91% | 100% |
C9ZNI1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 96% |
E9AER2 | Leishmania major | 92% | 100% |
V5BAN0 | Trypanosoma cruzi | 31% | 94% |