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:0005737 | cytoplasm | 2 | 1 |
GO:0031974 | membrane-enclosed lumen | 2 | 1 |
GO:0031981 | nuclear lumen | 5 | 1 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0043233 | organelle lumen | 3 | 1 |
GO:0070013 | intracellular organelle lumen | 4 | 1 |
GO:0097014 | ciliary plasm | 5 | 1 |
GO:0099568 | cytoplasmic region | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:1990904 | ribonucleoprotein complex | 2 | 1 |
Related structures:
AlphaFold database: A4HEB0
Term | Name | Level | Count |
---|---|---|---|
GO:0006996 | organelle organization | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022607 | cellular component assembly | 4 | 1 |
GO:0042255 | ribosome assembly | 7 | 1 |
GO:0042256 | cytosolic ribosome assembly | 8 | 1 |
GO:0070925 | organelle assembly | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0140694 | non-membrane-bounded organelle assembly | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003746 | translation elongation factor activity | 4 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0003924 | GTPase activity | 7 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005525 | GTP binding | 5 | 12 |
GO:0008135 | translation factor activity, RNA binding | 3 | 12 |
GO:0016462 | pyrophosphatase activity | 5 | 12 |
GO:0016787 | hydrolase activity | 2 | 12 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 12 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 12 |
GO:0019001 | guanyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032561 | guanyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0045182 | translation regulator activity | 1 | 12 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0043021 | ribonucleoprotein complex binding | 3 | 1 |
GO:0043022 | ribosome binding | 4 | 1 |
GO:0044877 | protein-containing complex binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 118 | 122 | PF00656 | 0.453 |
CLV_C14_Caspase3-7 | 826 | 830 | PF00656 | 0.493 |
CLV_NRD_NRD_1 | 313 | 315 | PF00675 | 0.467 |
CLV_NRD_NRD_1 | 351 | 353 | PF00675 | 0.400 |
CLV_NRD_NRD_1 | 746 | 748 | PF00675 | 0.361 |
CLV_NRD_NRD_1 | 774 | 776 | PF00675 | 0.253 |
CLV_NRD_NRD_1 | 864 | 866 | PF00675 | 0.430 |
CLV_PCSK_FUR_1 | 861 | 865 | PF00082 | 0.383 |
CLV_PCSK_KEX2_1 | 313 | 315 | PF00082 | 0.457 |
CLV_PCSK_KEX2_1 | 350 | 352 | PF00082 | 0.422 |
CLV_PCSK_KEX2_1 | 639 | 641 | PF00082 | 0.449 |
CLV_PCSK_KEX2_1 | 746 | 748 | PF00082 | 0.361 |
CLV_PCSK_KEX2_1 | 773 | 775 | PF00082 | 0.253 |
CLV_PCSK_KEX2_1 | 863 | 865 | PF00082 | 0.419 |
CLV_PCSK_PC1ET2_1 | 639 | 641 | PF00082 | 0.419 |
CLV_PCSK_PC1ET2_1 | 863 | 865 | PF00082 | 0.515 |
CLV_PCSK_SKI1_1 | 321 | 325 | PF00082 | 0.397 |
CLV_PCSK_SKI1_1 | 369 | 373 | PF00082 | 0.457 |
CLV_PCSK_SKI1_1 | 475 | 479 | PF00082 | 0.345 |
CLV_PCSK_SKI1_1 | 550 | 554 | PF00082 | 0.386 |
CLV_PCSK_SKI1_1 | 66 | 70 | PF00082 | 0.253 |
DEG_APCC_DBOX_1 | 316 | 324 | PF00400 | 0.381 |
DEG_APCC_DBOX_1 | 349 | 357 | PF00400 | 0.445 |
DEG_APCC_DBOX_1 | 792 | 800 | PF00400 | 0.477 |
DEG_SCF_FBW7_1 | 469 | 474 | PF00400 | 0.390 |
DEG_SPOP_SBC_1 | 587 | 591 | PF00917 | 0.312 |
DOC_CYCLIN_RxL_1 | 317 | 326 | PF00134 | 0.411 |
DOC_CYCLIN_yClb1_LxF_4 | 654 | 659 | PF00134 | 0.432 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 235 | 244 | PF00134 | 0.434 |
DOC_CYCLIN_yCln2_LP_2 | 342 | 348 | PF00134 | 0.396 |
DOC_MAPK_gen_1 | 165 | 172 | PF00069 | 0.539 |
DOC_MAPK_gen_1 | 229 | 237 | PF00069 | 0.526 |
DOC_MAPK_gen_1 | 262 | 269 | PF00069 | 0.529 |
DOC_MAPK_gen_1 | 421 | 430 | PF00069 | 0.402 |
DOC_MAPK_HePTP_8 | 520 | 532 | PF00069 | 0.384 |
DOC_MAPK_MEF2A_6 | 136 | 145 | PF00069 | 0.373 |
DOC_MAPK_MEF2A_6 | 262 | 271 | PF00069 | 0.537 |
DOC_MAPK_MEF2A_6 | 523 | 532 | PF00069 | 0.387 |
DOC_PP1_RVXF_1 | 654 | 660 | PF00149 | 0.424 |
DOC_PP1_SILK_1 | 128 | 133 | PF00149 | 0.493 |
DOC_USP7_MATH_1 | 569 | 573 | PF00917 | 0.396 |
DOC_USP7_MATH_1 | 695 | 699 | PF00917 | 0.403 |
DOC_USP7_MATH_1 | 82 | 86 | PF00917 | 0.554 |
DOC_USP7_MATH_1 | 847 | 851 | PF00917 | 0.425 |
DOC_USP7_UBL2_3 | 615 | 619 | PF12436 | 0.589 |
DOC_USP7_UBL2_3 | 881 | 885 | PF12436 | 0.567 |
DOC_WW_Pin1_4 | 255 | 260 | PF00397 | 0.501 |
DOC_WW_Pin1_4 | 341 | 346 | PF00397 | 0.362 |
DOC_WW_Pin1_4 | 361 | 366 | PF00397 | 0.245 |
DOC_WW_Pin1_4 | 375 | 380 | PF00397 | 0.337 |
DOC_WW_Pin1_4 | 44 | 49 | PF00397 | 0.477 |
DOC_WW_Pin1_4 | 467 | 472 | PF00397 | 0.363 |
DOC_WW_Pin1_4 | 90 | 95 | PF00397 | 0.453 |
LIG_14-3-3_CanoR_1 | 132 | 136 | PF00244 | 0.539 |
LIG_14-3-3_CanoR_1 | 351 | 357 | PF00244 | 0.458 |
LIG_14-3-3_CanoR_1 | 500 | 504 | PF00244 | 0.392 |
LIG_14-3-3_CanoR_1 | 66 | 71 | PF00244 | 0.453 |
LIG_14-3-3_CanoR_1 | 773 | 782 | PF00244 | 0.477 |
LIG_Actin_WH2_2 | 116 | 134 | PF00022 | 0.453 |
LIG_Actin_WH2_2 | 410 | 425 | PF00022 | 0.414 |
LIG_APCC_ABBA_1 | 428 | 433 | PF00400 | 0.403 |
LIG_APCC_ABBAyCdc20_2 | 865 | 871 | PF00400 | 0.464 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.556 |
LIG_BIR_III_2 | 829 | 833 | PF00653 | 0.453 |
LIG_BRCT_BRCA1_1 | 222 | 226 | PF00533 | 0.509 |
LIG_BRCT_BRCA1_1 | 458 | 462 | PF00533 | 0.485 |
LIG_BRCT_BRCA1_1 | 758 | 762 | PF00533 | 0.558 |
LIG_BRCT_BRCA1_1 | 786 | 790 | PF00533 | 0.464 |
LIG_CSK_EPIYA_1 | 704 | 708 | PF00017 | 0.465 |
LIG_CSL_BTD_1 | 326 | 329 | PF09270 | 0.446 |
LIG_deltaCOP1_diTrp_1 | 218 | 227 | PF00928 | 0.453 |
LIG_deltaCOP1_diTrp_1 | 242 | 250 | PF00928 | 0.436 |
LIG_deltaCOP1_diTrp_1 | 276 | 285 | PF00928 | 0.351 |
LIG_deltaCOP1_diTrp_1 | 453 | 462 | PF00928 | 0.254 |
LIG_deltaCOP1_diTrp_1 | 675 | 684 | PF00928 | 0.427 |
LIG_EH1_1 | 394 | 402 | PF00400 | 0.509 |
LIG_FHA_1 | 125 | 131 | PF00498 | 0.513 |
LIG_FHA_1 | 252 | 258 | PF00498 | 0.458 |
LIG_FHA_1 | 391 | 397 | PF00498 | 0.417 |
LIG_FHA_1 | 4 | 10 | PF00498 | 0.344 |
LIG_FHA_1 | 453 | 459 | PF00498 | 0.489 |
LIG_FHA_1 | 468 | 474 | PF00498 | 0.358 |
LIG_FHA_1 | 494 | 500 | PF00498 | 0.420 |
LIG_FHA_1 | 587 | 593 | PF00498 | 0.520 |
LIG_FHA_1 | 815 | 821 | PF00498 | 0.445 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.561 |
LIG_FHA_1 | 849 | 855 | PF00498 | 0.497 |
LIG_FHA_2 | 132 | 138 | PF00498 | 0.539 |
LIG_FHA_2 | 156 | 162 | PF00498 | 0.477 |
LIG_FHA_2 | 32 | 38 | PF00498 | 0.453 |
LIG_FHA_2 | 362 | 368 | PF00498 | 0.566 |
LIG_FHA_2 | 540 | 546 | PF00498 | 0.410 |
LIG_FHA_2 | 835 | 841 | PF00498 | 0.481 |
LIG_LIR_Apic_2 | 200 | 206 | PF02991 | 0.453 |
LIG_LIR_Apic_2 | 247 | 252 | PF02991 | 0.493 |
LIG_LIR_Apic_2 | 306 | 312 | PF02991 | 0.459 |
LIG_LIR_Apic_2 | 831 | 836 | PF02991 | 0.530 |
LIG_LIR_Gen_1 | 160 | 170 | PF02991 | 0.527 |
LIG_LIR_Gen_1 | 225 | 235 | PF02991 | 0.389 |
LIG_LIR_Gen_1 | 474 | 483 | PF02991 | 0.403 |
LIG_LIR_Gen_1 | 557 | 566 | PF02991 | 0.372 |
LIG_LIR_Gen_1 | 675 | 683 | PF02991 | 0.430 |
LIG_LIR_Gen_1 | 823 | 833 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 160 | 166 | PF02991 | 0.527 |
LIG_LIR_Nem_3 | 225 | 230 | PF02991 | 0.374 |
LIG_LIR_Nem_3 | 276 | 282 | PF02991 | 0.363 |
LIG_LIR_Nem_3 | 325 | 330 | PF02991 | 0.375 |
LIG_LIR_Nem_3 | 408 | 414 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 474 | 479 | PF02991 | 0.396 |
LIG_LIR_Nem_3 | 487 | 491 | PF02991 | 0.427 |
LIG_LIR_Nem_3 | 557 | 562 | PF02991 | 0.367 |
LIG_LIR_Nem_3 | 675 | 681 | PF02991 | 0.365 |
LIG_LIR_Nem_3 | 823 | 828 | PF02991 | 0.464 |
LIG_NRBOX | 319 | 325 | PF00104 | 0.383 |
LIG_Pex14_1 | 245 | 249 | PF04695 | 0.386 |
LIG_REV1ctd_RIR_1 | 224 | 233 | PF16727 | 0.463 |
LIG_SH2_CRK | 476 | 480 | PF00017 | 0.364 |
LIG_SH2_CRK | 768 | 772 | PF00017 | 0.461 |
LIG_SH2_GRB2like | 180 | 183 | PF00017 | 0.513 |
LIG_SH2_NCK_1 | 476 | 480 | PF00017 | 0.495 |
LIG_SH2_SRC | 429 | 432 | PF00017 | 0.445 |
LIG_SH2_STAP1 | 180 | 184 | PF00017 | 0.513 |
LIG_SH2_STAP1 | 282 | 286 | PF00017 | 0.447 |
LIG_SH2_STAP1 | 753 | 757 | PF00017 | 0.464 |
LIG_SH2_STAT3 | 180 | 183 | PF00017 | 0.513 |
LIG_SH2_STAT5 | 157 | 160 | PF00017 | 0.538 |
LIG_SH2_STAT5 | 163 | 166 | PF00017 | 0.540 |
LIG_SH2_STAT5 | 249 | 252 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 38 | 41 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 386 | 389 | PF00017 | 0.332 |
LIG_SH2_STAT5 | 395 | 398 | PF00017 | 0.468 |
LIG_SH2_STAT5 | 429 | 432 | PF00017 | 0.395 |
LIG_SH2_STAT5 | 472 | 475 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 791 | 794 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 833 | 836 | PF00017 | 0.445 |
LIG_SH3_3 | 326 | 332 | PF00018 | 0.489 |
LIG_SH3_3 | 376 | 382 | PF00018 | 0.402 |
LIG_SH3_3 | 480 | 486 | PF00018 | 0.387 |
LIG_SH3_3 | 502 | 508 | PF00018 | 0.530 |
LIG_SH3_3 | 88 | 94 | PF00018 | 0.453 |
LIG_SUMO_SIM_anti_2 | 529 | 535 | PF11976 | 0.349 |
LIG_SUMO_SIM_anti_2 | 609 | 618 | PF11976 | 0.536 |
LIG_SUMO_SIM_par_1 | 113 | 118 | PF11976 | 0.453 |
LIG_SUMO_SIM_par_1 | 489 | 497 | PF11976 | 0.424 |
LIG_TRAF2_1 | 158 | 161 | PF00917 | 0.453 |
LIG_TRAF2_1 | 290 | 293 | PF00917 | 0.573 |
LIG_TRAF2_1 | 838 | 841 | PF00917 | 0.507 |
LIG_TYR_ITSM | 472 | 479 | PF00017 | 0.484 |
LIG_UBA3_1 | 858 | 866 | PF00899 | 0.460 |
LIG_WRC_WIRS_1 | 485 | 490 | PF05994 | 0.278 |
LIG_WRC_WIRS_1 | 556 | 561 | PF05994 | 0.395 |
LIG_WRC_WIRS_1 | 570 | 575 | PF05994 | 0.347 |
MOD_CDK_SPxxK_3 | 255 | 262 | PF00069 | 0.582 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.405 |
MOD_CK1_1 | 481 | 487 | PF00069 | 0.478 |
MOD_CK1_1 | 579 | 585 | PF00069 | 0.572 |
MOD_CK1_1 | 652 | 658 | PF00069 | 0.521 |
MOD_CK1_1 | 722 | 728 | PF00069 | 0.456 |
MOD_CK1_1 | 760 | 766 | PF00069 | 0.479 |
MOD_CK2_1 | 131 | 137 | PF00069 | 0.539 |
MOD_CK2_1 | 155 | 161 | PF00069 | 0.453 |
MOD_CK2_1 | 165 | 171 | PF00069 | 0.453 |
MOD_CK2_1 | 286 | 292 | PF00069 | 0.502 |
MOD_CK2_1 | 361 | 367 | PF00069 | 0.578 |
MOD_CK2_1 | 539 | 545 | PF00069 | 0.408 |
MOD_CK2_1 | 569 | 575 | PF00069 | 0.382 |
MOD_CK2_1 | 588 | 594 | PF00069 | 0.321 |
MOD_CK2_1 | 729 | 735 | PF00069 | 0.514 |
MOD_CK2_1 | 820 | 826 | PF00069 | 0.561 |
MOD_CK2_1 | 834 | 840 | PF00069 | 0.313 |
MOD_GlcNHglycan | 11 | 15 | PF01048 | 0.500 |
MOD_GlcNHglycan | 282 | 285 | PF01048 | 0.313 |
MOD_GlcNHglycan | 288 | 291 | PF01048 | 0.431 |
MOD_GlcNHglycan | 418 | 421 | PF01048 | 0.324 |
MOD_GlcNHglycan | 457 | 461 | PF01048 | 0.334 |
MOD_GlcNHglycan | 480 | 483 | PF01048 | 0.273 |
MOD_GlcNHglycan | 581 | 584 | PF01048 | 0.619 |
MOD_GlcNHglycan | 620 | 623 | PF01048 | 0.535 |
MOD_GlcNHglycan | 641 | 644 | PF01048 | 0.498 |
MOD_GlcNHglycan | 651 | 654 | PF01048 | 0.342 |
MOD_GlcNHglycan | 697 | 700 | PF01048 | 0.377 |
MOD_GlcNHglycan | 721 | 724 | PF01048 | 0.394 |
MOD_GlcNHglycan | 759 | 762 | PF01048 | 0.277 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.457 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.509 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.526 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.457 |
MOD_GSK3_1 | 452 | 459 | PF00069 | 0.431 |
MOD_GSK3_1 | 467 | 474 | PF00069 | 0.367 |
MOD_GSK3_1 | 477 | 484 | PF00069 | 0.372 |
MOD_GSK3_1 | 528 | 535 | PF00069 | 0.437 |
MOD_GSK3_1 | 569 | 576 | PF00069 | 0.372 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.453 |
MOD_GSK3_1 | 753 | 760 | PF00069 | 0.457 |
MOD_GSK3_1 | 769 | 776 | PF00069 | 0.433 |
MOD_GSK3_1 | 809 | 816 | PF00069 | 0.456 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.453 |
MOD_N-GLC_1 | 238 | 243 | PF02516 | 0.413 |
MOD_N-GLC_1 | 579 | 584 | PF02516 | 0.649 |
MOD_N-GLC_2 | 21 | 23 | PF02516 | 0.253 |
MOD_NEK2_1 | 131 | 136 | PF00069 | 0.512 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.356 |
MOD_NEK2_1 | 212 | 217 | PF00069 | 0.477 |
MOD_NEK2_1 | 286 | 291 | PF00069 | 0.506 |
MOD_NEK2_1 | 323 | 328 | PF00069 | 0.291 |
MOD_NEK2_1 | 39 | 44 | PF00069 | 0.453 |
MOD_NEK2_1 | 390 | 395 | PF00069 | 0.436 |
MOD_NEK2_1 | 493 | 498 | PF00069 | 0.496 |
MOD_NEK2_1 | 555 | 560 | PF00069 | 0.372 |
MOD_NEK2_1 | 56 | 61 | PF00069 | 0.453 |
MOD_NEK2_1 | 573 | 578 | PF00069 | 0.373 |
MOD_NEK2_1 | 597 | 602 | PF00069 | 0.358 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.453 |
MOD_NEK2_1 | 711 | 716 | PF00069 | 0.499 |
MOD_NEK2_1 | 820 | 825 | PF00069 | 0.464 |
MOD_NEK2_2 | 569 | 574 | PF00069 | 0.402 |
MOD_NEK2_2 | 753 | 758 | PF00069 | 0.464 |
MOD_PIKK_1 | 121 | 127 | PF00454 | 0.453 |
MOD_PIKK_1 | 151 | 157 | PF00454 | 0.539 |
MOD_PIKK_1 | 390 | 396 | PF00454 | 0.394 |
MOD_PIKK_1 | 760 | 766 | PF00454 | 0.464 |
MOD_PIKK_1 | 809 | 815 | PF00454 | 0.464 |
MOD_PK_1 | 165 | 171 | PF00069 | 0.477 |
MOD_PK_1 | 71 | 77 | PF00069 | 0.453 |
MOD_PKA_1 | 313 | 319 | PF00069 | 0.323 |
MOD_PKA_1 | 639 | 645 | PF00069 | 0.488 |
MOD_PKA_1 | 773 | 779 | PF00069 | 0.477 |
MOD_PKA_2 | 131 | 137 | PF00069 | 0.539 |
MOD_PKA_2 | 313 | 319 | PF00069 | 0.323 |
MOD_PKA_2 | 499 | 505 | PF00069 | 0.375 |
MOD_PKA_2 | 573 | 579 | PF00069 | 0.384 |
MOD_PKA_2 | 639 | 645 | PF00069 | 0.480 |
MOD_PKA_2 | 773 | 779 | PF00069 | 0.477 |
MOD_PKB_1 | 350 | 358 | PF00069 | 0.520 |
MOD_Plk_1 | 437 | 443 | PF00069 | 0.474 |
MOD_Plk_1 | 452 | 458 | PF00069 | 0.496 |
MOD_Plk_1 | 528 | 534 | PF00069 | 0.431 |
MOD_Plk_1 | 753 | 759 | PF00069 | 0.464 |
MOD_Plk_2-3 | 196 | 202 | PF00069 | 0.493 |
MOD_Plk_2-3 | 288 | 294 | PF00069 | 0.577 |
MOD_Plk_4 | 126 | 132 | PF00069 | 0.464 |
MOD_Plk_4 | 323 | 329 | PF00069 | 0.390 |
MOD_Plk_4 | 352 | 358 | PF00069 | 0.503 |
MOD_Plk_4 | 440 | 446 | PF00069 | 0.510 |
MOD_Plk_4 | 494 | 500 | PF00069 | 0.410 |
MOD_Plk_4 | 528 | 534 | PF00069 | 0.445 |
MOD_Plk_4 | 573 | 579 | PF00069 | 0.426 |
MOD_Plk_4 | 588 | 594 | PF00069 | 0.487 |
MOD_Plk_4 | 684 | 690 | PF00069 | 0.389 |
MOD_Plk_4 | 753 | 759 | PF00069 | 0.464 |
MOD_ProDKin_1 | 255 | 261 | PF00069 | 0.501 |
MOD_ProDKin_1 | 341 | 347 | PF00069 | 0.368 |
MOD_ProDKin_1 | 361 | 367 | PF00069 | 0.247 |
MOD_ProDKin_1 | 375 | 381 | PF00069 | 0.331 |
MOD_ProDKin_1 | 44 | 50 | PF00069 | 0.477 |
MOD_ProDKin_1 | 467 | 473 | PF00069 | 0.359 |
MOD_ProDKin_1 | 90 | 96 | PF00069 | 0.453 |
MOD_SUMO_rev_2 | 247 | 254 | PF00179 | 0.502 |
MOD_SUMO_rev_2 | 361 | 371 | PF00179 | 0.566 |
MOD_SUMO_rev_2 | 612 | 621 | PF00179 | 0.557 |
TRG_DiLeu_BaEn_1 | 392 | 397 | PF01217 | 0.319 |
TRG_DiLeu_BaEn_1 | 609 | 614 | PF01217 | 0.504 |
TRG_DiLeu_BaLyEn_6 | 516 | 521 | PF01217 | 0.416 |
TRG_DiLeu_BaLyEn_6 | 52 | 57 | PF01217 | 0.453 |
TRG_ENDOCYTIC_2 | 163 | 166 | PF00928 | 0.453 |
TRG_ENDOCYTIC_2 | 282 | 285 | PF00928 | 0.367 |
TRG_ENDOCYTIC_2 | 476 | 479 | PF00928 | 0.367 |
TRG_ENDOCYTIC_2 | 768 | 771 | PF00928 | 0.461 |
TRG_ER_diArg_1 | 164 | 167 | PF00400 | 0.453 |
TRG_ER_diArg_1 | 312 | 314 | PF00400 | 0.452 |
TRG_ER_diArg_1 | 350 | 352 | PF00400 | 0.422 |
TRG_ER_diArg_1 | 745 | 747 | PF00400 | 0.377 |
TRG_ER_diArg_1 | 773 | 775 | PF00400 | 0.453 |
TRG_NES_CRM1_1 | 554 | 568 | PF08389 | 0.387 |
TRG_NLS_MonoCore_2 | 862 | 867 | PF00514 | 0.516 |
TRG_NLS_MonoExtN_4 | 861 | 867 | PF00514 | 0.519 |
TRG_Pf-PMV_PEXEL_1 | 167 | 171 | PF00026 | 0.264 |
TRG_Pf-PMV_PEXEL_1 | 296 | 300 | PF00026 | 0.544 |
TRG_Pf-PMV_PEXEL_1 | 509 | 513 | PF00026 | 0.557 |
TRG_Pf-PMV_PEXEL_1 | 550 | 554 | PF00026 | 0.386 |
TRG_Pf-PMV_PEXEL_1 | 604 | 609 | PF00026 | 0.416 |
TRG_Pf-PMV_PEXEL_1 | 746 | 750 | PF00026 | 0.305 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I9M7 | Leptomonas seymouri | 85% | 100% |
A0A0N1PBS6 | Leptomonas seymouri | 31% | 100% |
A0A0S4JM05 | Bodo saltans | 31% | 100% |
A0A0S4JP20 | Bodo saltans | 55% | 90% |
A0A1X0NY54 | Trypanosomatidae | 71% | 99% |
A0A1X0P8P3 | Trypanosomatidae | 31% | 100% |
A0A3Q8IIX7 | Leishmania donovani | 31% | 100% |
A0A3R7MX75 | Trypanosoma rangeli | 68% | 100% |
A0A3R7NHC0 | Trypanosoma rangeli | 31% | 100% |
A0A3S7WZE0 | Leishmania donovani | 92% | 100% |
A0A422N8J1 | Trypanosoma rangeli | 25% | 93% |
A0B7D5 | Methanothrix thermoacetophila (strain DSM 6194 / JCM 14653 / NBRC 101360 / PT) | 27% | 100% |
A0SXL6 | Callithrix jacchus | 31% | 100% |
A3CXM8 | Methanoculleus marisnigri (strain ATCC 35101 / DSM 1498 / JR1) | 27% | 100% |
A4FUD3 | Bos taurus | 26% | 91% |
A4HNM7 | Leishmania braziliensis | 31% | 100% |
A4I1Q6 | Leishmania infantum | 92% | 100% |
A4ICW8 | Leishmania infantum | 31% | 100% |
A5DI11 | Meyerozyma guilliermondii (strain ATCC 6260 / CBS 566 / DSM 6381 / JCM 1539 / NBRC 10279 / NRRL Y-324) | 31% | 100% |
A5ULM6 | Methanobrevibacter smithii (strain ATCC 35061 / DSM 861 / OCM 144 / PS) | 27% | 100% |
A6UV44 | Methanococcus aeolicus (strain ATCC BAA-1280 / DSM 17508 / OCM 812 / Nankai-3) | 27% | 100% |
B0R8C8 | Halobacterium salinarum (strain ATCC 29341 / DSM 671 / R1) | 28% | 100% |
C3MQ53 | Sulfolobus islandicus (strain L.S.2.15 / Lassen #1) | 27% | 100% |
C3MVH1 | Sulfolobus islandicus (strain M.14.25 / Kamchatka #1) | 27% | 100% |
C3N5S0 | Sulfolobus islandicus (strain M.16.27) | 27% | 100% |
C3NED6 | Sulfolobus islandicus (strain Y.G.57.14 / Yellowstone #1) | 27% | 100% |
C3NHB6 | Sulfolobus islandicus (strain Y.N.15.51 / Yellowstone #2) | 27% | 100% |
C4KHE9 | Sulfolobus islandicus (strain M.16.4 / Kamchatka #3) | 27% | 100% |
C4YJQ8 | Candida albicans (strain WO-1) | 31% | 100% |
C7NYH7 | Halomicrobium mukohataei (strain ATCC 700874 / DSM 12286 / JCM 9738 / NCIMB 13541) | 28% | 100% |
C9ZKB0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 69% | 100% |
D0A2I0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
E9ASD6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E9AXU0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
F4JWP9 | Arabidopsis thaliana | 28% | 91% |
O08810 | Mus musculus | 26% | 91% |
O14460 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 31% | 100% |
O23755 | Beta vulgaris | 32% | 100% |
O27131 | Methanothermobacter thermautotrophicus (strain ATCC 29096 / DSM 1053 / JCM 10044 / NBRC 100330 / Delta H) | 27% | 100% |
O74945 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 34% | 89% |
O94316 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 26% | 90% |
P05197 | Rattus norvegicus | 31% | 100% |
P09445 | Cricetulus griseus | 30% | 100% |
P13060 | Drosophila melanogaster | 32% | 100% |
P13639 | Homo sapiens | 31% | 100% |
P15112 | Dictyostelium discoideum | 32% | 100% |
P23112 | Sulfolobus acidocaldarius (strain ATCC 33909 / DSM 639 / JCM 8929 / NBRC 15157 / NCIMB 11770) | 26% | 100% |
P28996 | Parachlorella kessleri | 32% | 100% |
P29691 | Caenorhabditis elegans | 31% | 100% |
P30925 | Saccharolobus solfataricus (strain ATCC 35092 / DSM 1617 / JCM 11322 / P2) | 27% | 100% |
P32324 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 31% | 100% |
P36048 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 23% | 88% |
P58252 | Mus musculus | 31% | 100% |
Q06193 | Entamoeba histolytica | 31% | 100% |
Q15029 | Homo sapiens | 26% | 91% |
Q17152 | Blastocystis hominis | 31% | 100% |
Q1HPK6 | Bombyx mori | 32% | 100% |
Q23716 | Cryptosporidium parvum | 32% | 100% |
Q2NEL0 | Methanosphaera stadtmanae (strain ATCC 43021 / DSM 3091 / JCM 11832 / MCB-3) | 26% | 100% |
Q3SYU2 | Bos taurus | 31% | 100% |
Q4Q259 | Leishmania major | 31% | 93% |
Q4Q9N1 | Leishmania major | 92% | 100% |
Q5A0M4 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 31% | 100% |
Q5F3X4 | Gallus gallus | 26% | 91% |
Q5R6E0 | Pongo abelii | 26% | 91% |
Q5R8Z3 | Pongo abelii | 31% | 100% |
Q6BJ25 | Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / BCRC 21394 / JCM 1990 / NBRC 0083 / IGC 2968) | 31% | 100% |
Q6CPQ9 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 31% | 100% |
Q6FYA7 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 30% | 100% |
Q6L200 | Picrophilus torridus (strain ATCC 700027 / DSM 9790 / JCM 10055 / NBRC 100828) | 28% | 100% |
Q754C8 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 31% | 100% |
Q7Z2Z2 | Homo sapiens | 30% | 79% |
Q874B9 | Komagataella pastoris | 30% | 100% |
Q875S0 | Lachancea kluyveri (strain ATCC 58438 / CBS 3082 / BCRC 21498 / NBRC 1685 / JCM 7257 / NCYC 543 / NRRL Y-12651) | 31% | 100% |
Q875Z2 | Naumovozyma castellii (strain ATCC 76901 / BCRC 22586 / CBS 4309 / NBRC 1992 / NRRL Y-12630) | 31% | 100% |
Q8SQT7 | Encephalitozoon cuniculi (strain GB-M1) | 28% | 100% |
Q90705 | Gallus gallus | 31% | 100% |
Q96X45 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 31% | 100% |
Q975H5 | Sulfurisphaera tokodaii (strain DSM 16993 / JCM 10545 / NBRC 100140 / 7) | 27% | 100% |
Q9ASR1 | Arabidopsis thaliana | 32% | 100% |
Q9HM85 | Halobacterium salinarum (strain ATCC 700922 / JCM 11081 / NRC-1) | 28% | 100% |
Q9LNC5 | Arabidopsis thaliana | 28% | 90% |
Q9YC19 | Aeropyrum pernix (strain ATCC 700893 / DSM 11879 / JCM 9820 / NBRC 100138 / K1) | 28% | 100% |
V5AW74 | Trypanosoma cruzi | 25% | 93% |
V5BI00 | Trypanosoma cruzi | 69% | 100% |
V5DRS6 | Trypanosoma cruzi | 31% | 100% |