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: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005730 | nucleolus | 5 | 11 |
GO:0005840 | ribosome | 5 | 12 |
GO:0032991 | protein-containing complex | 1 | 12 |
GO:0043226 | organelle | 2 | 12 |
GO:0043228 | non-membrane-bounded organelle | 3 | 12 |
GO:0043229 | intracellular organelle | 3 | 12 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:1990904 | ribonucleoprotein complex | 2 | 12 |
GO:0030684 | preribosome | 3 | 1 |
GO:0032040 | small-subunit processome | 4 | 1 |
GO:0034388 | Pwp2p-containing subcomplex of 90S preribosome | 3 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
Related structures:
AlphaFold database: E9ARM0
Term | Name | Level | Count |
---|---|---|---|
GO:0000028 | ribosomal small subunit assembly | 7 | 1 |
GO:0000462 | maturation of SSU-rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA) | 10 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006364 | rRNA processing | 8 | 1 |
GO:0006396 | RNA processing | 6 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0016072 | rRNA metabolic process | 7 | 1 |
GO:0022607 | cellular component assembly | 4 | 1 |
GO:0022618 | ribonucleoprotein complex assembly | 6 | 1 |
GO:0030490 | maturation of SSU-rRNA | 9 | 1 |
GO:0034470 | ncRNA processing | 7 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0034660 | ncRNA metabolic process | 6 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043933 | protein-containing complex organization | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0065003 | protein-containing complex assembly | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0071826 | ribonucleoprotein complex subunit organization | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 205 | 209 | PF00656 | 0.248 |
CLV_C14_Caspase3-7 | 465 | 469 | PF00656 | 0.437 |
CLV_MEL_PAP_1 | 243 | 249 | PF00089 | 0.350 |
CLV_NRD_NRD_1 | 231 | 233 | PF00675 | 0.454 |
CLV_NRD_NRD_1 | 274 | 276 | PF00675 | 0.522 |
CLV_NRD_NRD_1 | 595 | 597 | PF00675 | 0.331 |
CLV_NRD_NRD_1 | 633 | 635 | PF00675 | 0.495 |
CLV_NRD_NRD_1 | 723 | 725 | PF00675 | 0.503 |
CLV_NRD_NRD_1 | 741 | 743 | PF00675 | 0.403 |
CLV_NRD_NRD_1 | 826 | 828 | PF00675 | 0.242 |
CLV_PCSK_KEX2_1 | 128 | 130 | PF00082 | 0.476 |
CLV_PCSK_KEX2_1 | 231 | 233 | PF00082 | 0.474 |
CLV_PCSK_KEX2_1 | 276 | 278 | PF00082 | 0.515 |
CLV_PCSK_KEX2_1 | 595 | 597 | PF00082 | 0.311 |
CLV_PCSK_KEX2_1 | 723 | 725 | PF00082 | 0.503 |
CLV_PCSK_KEX2_1 | 741 | 743 | PF00082 | 0.403 |
CLV_PCSK_KEX2_1 | 826 | 828 | PF00082 | 0.242 |
CLV_PCSK_PC1ET2_1 | 128 | 130 | PF00082 | 0.476 |
CLV_PCSK_PC1ET2_1 | 276 | 278 | PF00082 | 0.515 |
CLV_PCSK_PC1ET2_1 | 741 | 743 | PF00082 | 0.457 |
CLV_PCSK_SKI1_1 | 148 | 152 | PF00082 | 0.394 |
CLV_PCSK_SKI1_1 | 232 | 236 | PF00082 | 0.410 |
CLV_PCSK_SKI1_1 | 270 | 274 | PF00082 | 0.475 |
CLV_PCSK_SKI1_1 | 301 | 305 | PF00082 | 0.343 |
CLV_PCSK_SKI1_1 | 309 | 313 | PF00082 | 0.308 |
CLV_PCSK_SKI1_1 | 327 | 331 | PF00082 | 0.285 |
CLV_PCSK_SKI1_1 | 385 | 389 | PF00082 | 0.280 |
CLV_PCSK_SKI1_1 | 621 | 625 | PF00082 | 0.477 |
CLV_PCSK_SKI1_1 | 724 | 728 | PF00082 | 0.606 |
CLV_PCSK_SKI1_1 | 86 | 90 | PF00082 | 0.372 |
CLV_PCSK_SKI1_1 | 900 | 904 | PF00082 | 0.360 |
CLV_PCSK_SKI1_1 | 906 | 910 | PF00082 | 0.280 |
DEG_APCC_DBOX_1 | 231 | 239 | PF00400 | 0.436 |
DEG_APCC_DBOX_1 | 274 | 282 | PF00400 | 0.590 |
DEG_APCC_DBOX_1 | 722 | 730 | PF00400 | 0.549 |
DEG_APCC_DBOX_1 | 85 | 93 | PF00400 | 0.410 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.390 |
DOC_ANK_TNKS_1 | 570 | 577 | PF00023 | 0.490 |
DOC_CYCLIN_RxL_1 | 382 | 391 | PF00134 | 0.314 |
DOC_MAPK_gen_1 | 275 | 283 | PF00069 | 0.462 |
DOC_MAPK_gen_1 | 325 | 332 | PF00069 | 0.299 |
DOC_MAPK_gen_1 | 779 | 787 | PF00069 | 0.387 |
DOC_MAPK_gen_1 | 826 | 837 | PF00069 | 0.301 |
DOC_MAPK_MEF2A_6 | 781 | 789 | PF00069 | 0.454 |
DOC_MAPK_MEF2A_6 | 830 | 837 | PF00069 | 0.301 |
DOC_MAPK_MEF2A_6 | 890 | 897 | PF00069 | 0.161 |
DOC_PP1_RVXF_1 | 127 | 134 | PF00149 | 0.445 |
DOC_PP1_RVXF_1 | 648 | 654 | PF00149 | 0.455 |
DOC_PP1_RVXF_1 | 73 | 80 | PF00149 | 0.290 |
DOC_PP2B_LxvP_1 | 727 | 730 | PF13499 | 0.469 |
DOC_PP4_FxxP_1 | 323 | 326 | PF00568 | 0.408 |
DOC_PP4_FxxP_1 | 485 | 488 | PF00568 | 0.458 |
DOC_USP7_MATH_1 | 378 | 382 | PF00917 | 0.269 |
DOC_USP7_MATH_1 | 506 | 510 | PF00917 | 0.280 |
DOC_USP7_MATH_1 | 757 | 761 | PF00917 | 0.372 |
DOC_USP7_MATH_1 | 829 | 833 | PF00917 | 0.277 |
DOC_USP7_MATH_1 | 839 | 843 | PF00917 | 0.228 |
DOC_USP7_UBL2_3 | 179 | 183 | PF12436 | 0.608 |
DOC_WW_Pin1_4 | 103 | 108 | PF00397 | 0.280 |
DOC_WW_Pin1_4 | 20 | 25 | PF00397 | 0.341 |
DOC_WW_Pin1_4 | 263 | 268 | PF00397 | 0.677 |
DOC_WW_Pin1_4 | 28 | 33 | PF00397 | 0.323 |
DOC_WW_Pin1_4 | 483 | 488 | PF00397 | 0.417 |
DOC_WW_Pin1_4 | 60 | 65 | PF00397 | 0.358 |
DOC_WW_Pin1_4 | 651 | 656 | PF00397 | 0.323 |
DOC_WW_Pin1_4 | 97 | 102 | PF00397 | 0.348 |
LIG_14-3-3_CanoR_1 | 129 | 134 | PF00244 | 0.439 |
LIG_14-3-3_CanoR_1 | 287 | 295 | PF00244 | 0.474 |
LIG_14-3-3_CanoR_1 | 650 | 654 | PF00244 | 0.359 |
LIG_14-3-3_CanoR_1 | 701 | 709 | PF00244 | 0.377 |
LIG_14-3-3_CanoR_1 | 790 | 796 | PF00244 | 0.430 |
LIG_14-3-3_CanoR_1 | 927 | 936 | PF00244 | 0.572 |
LIG_AP2alpha_1 | 559 | 563 | PF02296 | 0.432 |
LIG_BIR_III_4 | 628 | 632 | PF00653 | 0.315 |
LIG_BRCT_BRCA1_1 | 335 | 339 | PF00533 | 0.301 |
LIG_BRCT_BRCA1_1 | 841 | 845 | PF00533 | 0.256 |
LIG_deltaCOP1_diTrp_1 | 375 | 379 | PF00928 | 0.366 |
LIG_eIF4E_2 | 295 | 301 | PF01652 | 0.433 |
LIG_FHA_1 | 117 | 123 | PF00498 | 0.210 |
LIG_FHA_1 | 145 | 151 | PF00498 | 0.312 |
LIG_FHA_1 | 208 | 214 | PF00498 | 0.241 |
LIG_FHA_1 | 336 | 342 | PF00498 | 0.368 |
LIG_FHA_1 | 416 | 422 | PF00498 | 0.455 |
LIG_FHA_1 | 445 | 451 | PF00498 | 0.331 |
LIG_FHA_1 | 462 | 468 | PF00498 | 0.301 |
LIG_FHA_1 | 520 | 526 | PF00498 | 0.356 |
LIG_FHA_1 | 581 | 587 | PF00498 | 0.374 |
LIG_FHA_1 | 684 | 690 | PF00498 | 0.355 |
LIG_FHA_1 | 765 | 771 | PF00498 | 0.400 |
LIG_FHA_1 | 791 | 797 | PF00498 | 0.404 |
LIG_FHA_1 | 817 | 823 | PF00498 | 0.454 |
LIG_FHA_1 | 886 | 892 | PF00498 | 0.208 |
LIG_FHA_1 | 98 | 104 | PF00498 | 0.500 |
LIG_FHA_2 | 149 | 155 | PF00498 | 0.396 |
LIG_FHA_2 | 203 | 209 | PF00498 | 0.444 |
LIG_FHA_2 | 228 | 234 | PF00498 | 0.383 |
LIG_FHA_2 | 341 | 347 | PF00498 | 0.319 |
LIG_FHA_2 | 440 | 446 | PF00498 | 0.311 |
LIG_FHA_2 | 56 | 62 | PF00498 | 0.174 |
LIG_FHA_2 | 623 | 629 | PF00498 | 0.358 |
LIG_FHA_2 | 756 | 762 | PF00498 | 0.310 |
LIG_FHA_2 | 790 | 796 | PF00498 | 0.499 |
LIG_GBD_Chelix_1 | 112 | 120 | PF00786 | 0.258 |
LIG_Integrin_RGD_1 | 373 | 375 | PF01839 | 0.333 |
LIG_Integrin_RGDW_4 | 373 | 376 | PF00362 | 0.327 |
LIG_IRF3_LxIS_1 | 354 | 361 | PF10401 | 0.332 |
LIG_LIR_Apic_2 | 292 | 298 | PF02991 | 0.491 |
LIG_LIR_Apic_2 | 321 | 326 | PF02991 | 0.398 |
LIG_LIR_Gen_1 | 375 | 384 | PF02991 | 0.287 |
LIG_LIR_Gen_1 | 646 | 655 | PF02991 | 0.447 |
LIG_LIR_Gen_1 | 665 | 674 | PF02991 | 0.165 |
LIG_LIR_Nem_3 | 27 | 33 | PF02991 | 0.425 |
LIG_LIR_Nem_3 | 375 | 379 | PF02991 | 0.278 |
LIG_LIR_Nem_3 | 646 | 651 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 665 | 671 | PF02991 | 0.177 |
LIG_LIR_Nem_3 | 842 | 848 | PF02991 | 0.275 |
LIG_LIR_Nem_3 | 878 | 883 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 914 | 919 | PF02991 | 0.242 |
LIG_NRBOX | 353 | 359 | PF00104 | 0.340 |
LIG_NRBOX | 383 | 389 | PF00104 | 0.313 |
LIG_Pex14_1 | 668 | 672 | PF04695 | 0.269 |
LIG_Pex14_2 | 559 | 563 | PF04695 | 0.432 |
LIG_Pex14_2 | 623 | 627 | PF04695 | 0.340 |
LIG_SH2_CRK | 123 | 127 | PF00017 | 0.356 |
LIG_SH2_CRK | 30 | 34 | PF00017 | 0.290 |
LIG_SH2_CRK | 81 | 85 | PF00017 | 0.197 |
LIG_SH2_NCK_1 | 123 | 127 | PF00017 | 0.325 |
LIG_SH2_NCK_1 | 30 | 34 | PF00017 | 0.217 |
LIG_SH2_NCK_1 | 81 | 85 | PF00017 | 0.197 |
LIG_SH2_PTP2 | 111 | 114 | PF00017 | 0.282 |
LIG_SH2_SRC | 295 | 298 | PF00017 | 0.489 |
LIG_SH2_SRC | 406 | 409 | PF00017 | 0.417 |
LIG_SH2_STAP1 | 302 | 306 | PF00017 | 0.358 |
LIG_SH2_STAP1 | 609 | 613 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 111 | 114 | PF00017 | 0.300 |
LIG_SH2_STAT5 | 123 | 126 | PF00017 | 0.381 |
LIG_SH2_STAT5 | 15 | 18 | PF00017 | 0.293 |
LIG_SH2_STAT5 | 295 | 298 | PF00017 | 0.374 |
LIG_SH2_STAT5 | 36 | 39 | PF00017 | 0.271 |
LIG_SH2_STAT5 | 397 | 400 | PF00017 | 0.332 |
LIG_SH2_STAT5 | 678 | 681 | PF00017 | 0.410 |
LIG_SH2_STAT5 | 916 | 919 | PF00017 | 0.245 |
LIG_SH2_STAT5 | 921 | 924 | PF00017 | 0.237 |
LIG_SH3_3 | 18 | 24 | PF00018 | 0.384 |
LIG_SH3_3 | 481 | 487 | PF00018 | 0.461 |
LIG_SH3_3 | 774 | 780 | PF00018 | 0.368 |
LIG_SUMO_SIM_anti_2 | 218 | 224 | PF11976 | 0.319 |
LIG_SUMO_SIM_anti_2 | 351 | 356 | PF11976 | 0.353 |
LIG_SUMO_SIM_par_1 | 356 | 361 | PF11976 | 0.312 |
LIG_SUMO_SIM_par_1 | 503 | 510 | PF11976 | 0.290 |
LIG_SUMO_SIM_par_1 | 577 | 584 | PF11976 | 0.284 |
LIG_SUMO_SIM_par_1 | 832 | 838 | PF11976 | 0.224 |
LIG_TRAF2_1 | 602 | 605 | PF00917 | 0.473 |
LIG_TRAF2_1 | 792 | 795 | PF00917 | 0.428 |
LIG_TRFH_1 | 60 | 64 | PF08558 | 0.368 |
LIG_UBA3_1 | 234 | 242 | PF00899 | 0.409 |
LIG_WRC_WIRS_1 | 130 | 135 | PF05994 | 0.469 |
LIG_WRC_WIRS_1 | 440 | 445 | PF05994 | 0.315 |
LIG_WRC_WIRS_1 | 620 | 625 | PF05994 | 0.336 |
MOD_CDK_SPK_2 | 265 | 270 | PF00069 | 0.661 |
MOD_CDK_SPxxK_3 | 263 | 270 | PF00069 | 0.668 |
MOD_CDK_SPxxK_3 | 97 | 104 | PF00069 | 0.336 |
MOD_CK1_1 | 268 | 274 | PF00069 | 0.629 |
MOD_CK1_1 | 335 | 341 | PF00069 | 0.357 |
MOD_CK1_1 | 451 | 457 | PF00069 | 0.398 |
MOD_CK1_1 | 53 | 59 | PF00069 | 0.327 |
MOD_CK1_1 | 544 | 550 | PF00069 | 0.509 |
MOD_CK2_1 | 154 | 160 | PF00069 | 0.318 |
MOD_CK2_1 | 227 | 233 | PF00069 | 0.359 |
MOD_CK2_1 | 268 | 274 | PF00069 | 0.494 |
MOD_CK2_1 | 340 | 346 | PF00069 | 0.303 |
MOD_CK2_1 | 419 | 425 | PF00069 | 0.509 |
MOD_CK2_1 | 439 | 445 | PF00069 | 0.187 |
MOD_CK2_1 | 483 | 489 | PF00069 | 0.359 |
MOD_CK2_1 | 604 | 610 | PF00069 | 0.347 |
MOD_CK2_1 | 755 | 761 | PF00069 | 0.312 |
MOD_CK2_1 | 789 | 795 | PF00069 | 0.485 |
MOD_CK2_1 | 928 | 934 | PF00069 | 0.489 |
MOD_Cter_Amidation | 593 | 596 | PF01082 | 0.329 |
MOD_Cter_Amidation | 739 | 742 | PF01082 | 0.430 |
MOD_DYRK1A_RPxSP_1 | 483 | 487 | PF00069 | 0.456 |
MOD_GlcNHglycan | 196 | 199 | PF01048 | 0.439 |
MOD_GlcNHglycan | 288 | 291 | PF01048 | 0.474 |
MOD_GlcNHglycan | 335 | 338 | PF01048 | 0.308 |
MOD_GlcNHglycan | 360 | 363 | PF01048 | 0.349 |
MOD_GlcNHglycan | 380 | 383 | PF01048 | 0.164 |
MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.213 |
MOD_GlcNHglycan | 435 | 438 | PF01048 | 0.292 |
MOD_GlcNHglycan | 450 | 453 | PF01048 | 0.274 |
MOD_GlcNHglycan | 455 | 458 | PF01048 | 0.419 |
MOD_GlcNHglycan | 499 | 503 | PF01048 | 0.334 |
MOD_GlcNHglycan | 543 | 546 | PF01048 | 0.214 |
MOD_GlcNHglycan | 549 | 552 | PF01048 | 0.206 |
MOD_GlcNHglycan | 567 | 570 | PF01048 | 0.442 |
MOD_GlcNHglycan | 592 | 595 | PF01048 | 0.323 |
MOD_GlcNHglycan | 640 | 643 | PF01048 | 0.455 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.363 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.469 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.346 |
MOD_GSK3_1 | 310 | 317 | PF00069 | 0.461 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.337 |
MOD_GSK3_1 | 411 | 418 | PF00069 | 0.419 |
MOD_GSK3_1 | 444 | 451 | PF00069 | 0.349 |
MOD_GSK3_1 | 452 | 459 | PF00069 | 0.395 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.312 |
MOD_GSK3_1 | 463 | 470 | PF00069 | 0.334 |
MOD_GSK3_1 | 543 | 550 | PF00069 | 0.399 |
MOD_GSK3_1 | 586 | 593 | PF00069 | 0.357 |
MOD_GSK3_1 | 604 | 611 | PF00069 | 0.195 |
MOD_GSK3_1 | 619 | 626 | PF00069 | 0.325 |
MOD_GSK3_1 | 835 | 842 | PF00069 | 0.246 |
MOD_N-GLC_1 | 53 | 58 | PF02516 | 0.330 |
MOD_N-GLC_1 | 565 | 570 | PF02516 | 0.588 |
MOD_N-GLC_1 | 701 | 706 | PF02516 | 0.511 |
MOD_N-GLC_1 | 928 | 933 | PF02516 | 0.604 |
MOD_NEK2_1 | 116 | 121 | PF00069 | 0.291 |
MOD_NEK2_1 | 13 | 18 | PF00069 | 0.303 |
MOD_NEK2_1 | 310 | 315 | PF00069 | 0.484 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.324 |
MOD_NEK2_1 | 462 | 467 | PF00069 | 0.453 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.380 |
MOD_NEK2_1 | 586 | 591 | PF00069 | 0.303 |
MOD_NEK2_1 | 619 | 624 | PF00069 | 0.476 |
MOD_NEK2_1 | 755 | 760 | PF00069 | 0.299 |
MOD_NEK2_1 | 771 | 776 | PF00069 | 0.300 |
MOD_NEK2_1 | 79 | 84 | PF00069 | 0.341 |
MOD_NEK2_1 | 898 | 903 | PF00069 | 0.297 |
MOD_NEK2_1 | 928 | 933 | PF00069 | 0.518 |
MOD_NEK2_2 | 36 | 41 | PF00069 | 0.357 |
MOD_OFUCOSY | 52 | 59 | PF10250 | 0.429 |
MOD_PIKK_1 | 24 | 30 | PF00454 | 0.374 |
MOD_PIKK_1 | 488 | 494 | PF00454 | 0.370 |
MOD_PIKK_1 | 507 | 513 | PF00454 | 0.172 |
MOD_PIKK_1 | 672 | 678 | PF00454 | 0.308 |
MOD_PKA_1 | 741 | 747 | PF00069 | 0.415 |
MOD_PKA_2 | 286 | 292 | PF00069 | 0.429 |
MOD_PKA_2 | 649 | 655 | PF00069 | 0.386 |
MOD_PKA_2 | 741 | 747 | PF00069 | 0.415 |
MOD_PKA_2 | 789 | 795 | PF00069 | 0.560 |
MOD_PKA_2 | 829 | 835 | PF00069 | 0.425 |
MOD_Plk_1 | 116 | 122 | PF00069 | 0.320 |
MOD_Plk_1 | 291 | 297 | PF00069 | 0.403 |
MOD_Plk_1 | 350 | 356 | PF00069 | 0.323 |
MOD_Plk_1 | 488 | 494 | PF00069 | 0.370 |
MOD_Plk_1 | 53 | 59 | PF00069 | 0.327 |
MOD_Plk_1 | 604 | 610 | PF00069 | 0.297 |
MOD_Plk_1 | 816 | 822 | PF00069 | 0.349 |
MOD_Plk_2-3 | 154 | 160 | PF00069 | 0.291 |
MOD_Plk_4 | 141 | 147 | PF00069 | 0.267 |
MOD_Plk_4 | 188 | 194 | PF00069 | 0.502 |
MOD_Plk_4 | 268 | 274 | PF00069 | 0.484 |
MOD_Plk_4 | 291 | 297 | PF00069 | 0.403 |
MOD_Plk_4 | 350 | 356 | PF00069 | 0.323 |
MOD_Plk_4 | 46 | 52 | PF00069 | 0.323 |
MOD_Plk_4 | 619 | 625 | PF00069 | 0.469 |
MOD_Plk_4 | 840 | 846 | PF00069 | 0.260 |
MOD_Plk_4 | 868 | 874 | PF00069 | 0.250 |
MOD_ProDKin_1 | 20 | 26 | PF00069 | 0.341 |
MOD_ProDKin_1 | 263 | 269 | PF00069 | 0.674 |
MOD_ProDKin_1 | 28 | 34 | PF00069 | 0.326 |
MOD_ProDKin_1 | 483 | 489 | PF00069 | 0.421 |
MOD_ProDKin_1 | 60 | 66 | PF00069 | 0.359 |
MOD_ProDKin_1 | 651 | 657 | PF00069 | 0.322 |
MOD_ProDKin_1 | 97 | 103 | PF00069 | 0.338 |
MOD_SUMO_for_1 | 241 | 244 | PF00179 | 0.569 |
MOD_SUMO_for_1 | 602 | 605 | PF00179 | 0.363 |
MOD_SUMO_rev_2 | 268 | 278 | PF00179 | 0.606 |
MOD_SUMO_rev_2 | 422 | 429 | PF00179 | 0.406 |
TRG_DiLeu_BaEn_1 | 656 | 661 | PF01217 | 0.433 |
TRG_DiLeu_BaLyEn_6 | 903 | 908 | PF01217 | 0.386 |
TRG_ENDOCYTIC_2 | 111 | 114 | PF00928 | 0.282 |
TRG_ENDOCYTIC_2 | 30 | 33 | PF00928 | 0.285 |
TRG_ENDOCYTIC_2 | 405 | 408 | PF00928 | 0.410 |
TRG_ENDOCYTIC_2 | 474 | 477 | PF00928 | 0.305 |
TRG_ENDOCYTIC_2 | 479 | 482 | PF00928 | 0.332 |
TRG_ENDOCYTIC_2 | 916 | 919 | PF00928 | 0.254 |
TRG_ER_diArg_1 | 275 | 278 | PF00400 | 0.518 |
TRG_ER_diArg_1 | 595 | 597 | PF00400 | 0.331 |
TRG_ER_diArg_1 | 779 | 782 | PF00400 | 0.487 |
TRG_ER_diArg_1 | 825 | 827 | PF00400 | 0.287 |
TRG_NES_CRM1_1 | 351 | 363 | PF08389 | 0.341 |
TRG_Pf-PMV_PEXEL_1 | 232 | 236 | PF00026 | 0.275 |
TRG_Pf-PMV_PEXEL_1 | 724 | 728 | PF00026 | 0.606 |
TRG_Pf-PMV_PEXEL_1 | 900 | 904 | PF00026 | 0.270 |
TRG_Pf-PMV_PEXEL_1 | 906 | 910 | PF00026 | 0.255 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PE02 | Leptomonas seymouri | 88% | 100% |
A0A0S4J1U6 | Bodo saltans | 63% | 99% |
A0A1X0P754 | Trypanosomatidae | 71% | 100% |
A0A3S5H735 | Leishmania donovani | 96% | 100% |
A0A422P1S2 | Trypanosoma rangeli | 70% | 100% |
A4H9J4 | Leishmania braziliensis | 91% | 100% |
A4HXV7 | Leishmania infantum | 96% | 100% |
C9ZZU6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 68% | 100% |
P25635 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 29% | 100% |
P91341 | Caenorhabditis elegans | 28% | 100% |
Q15269 | Homo sapiens | 31% | 100% |
Q4QDV9 | Leishmania major | 95% | 100% |
Q54PE0 | Dictyostelium discoideum | 27% | 100% |
Q5RFQ3 | Pongo abelii | 31% | 100% |
Q8BU03 | Mus musculus | 31% | 100% |
Q8VYZ5 | Arabidopsis thaliana | 30% | 100% |
Q9C1X1 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 29% | 100% |
Q9C270 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 33% | 100% |
V5B6K0 | Trypanosoma cruzi | 69% | 100% |