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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005654 | nucleoplasm | 2 | 2 |
GO:0005681 | spliceosomal complex | 3 | 2 |
GO:0005684 | U2-type spliceosomal complex | 4 | 2 |
GO:0030532 | small nuclear ribonucleoprotein complex | 3 | 2 |
GO:0032991 | protein-containing complex | 1 | 11 |
GO:0046540 | U4/U6 x U5 tri-snRNP complex | 6 | 2 |
GO:0071007 | U2-type catalytic step 2 spliceosome | 4 | 2 |
GO:0071013 | catalytic step 2 spliceosome | 3 | 2 |
GO:0097525 | spliceosomal snRNP complex | 4 | 2 |
GO:0097526 | spliceosomal tri-snRNP complex | 5 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
GO:0120114 | Sm-like protein family complex | 2 | 2 |
GO:0140513 | nuclear protein-containing complex | 2 | 2 |
GO:1902494 | catalytic complex | 2 | 2 |
GO:1990904 | ribonucleoprotein complex | 2 | 11 |
Related structures:
AlphaFold database: Q4Q555
Term | Name | Level | Count |
---|---|---|---|
GO:0000375 | RNA splicing, via transesterification reactions | 8 | 2 |
GO:0000377 | RNA splicing, via transesterification reactions with bulged adenosine as nucleophile | 9 | 2 |
GO:0000398 | mRNA splicing, via spliceosome | 8 | 2 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 2 |
GO:0006396 | RNA processing | 6 | 2 |
GO:0006397 | mRNA processing | 7 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0008380 | RNA splicing | 7 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016070 | RNA metabolic process | 5 | 2 |
GO:0016071 | mRNA metabolic process | 6 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0090304 | nucleic acid metabolic process | 4 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003676 | nucleic acid binding | 3 | 2 |
GO:0003723 | RNA binding | 4 | 2 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0003924 | GTPase activity | 7 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005525 | GTP binding | 5 | 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:0017069 | snRNA binding | 5 | 2 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 12 |
GO:0019001 | guanyl nucleotide binding | 5 | 12 |
GO:0030623 | U5 snRNA binding | 6 | 2 |
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: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 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 15 | 19 | PF00656 | 0.592 |
CLV_C14_Caspase3-7 | 438 | 442 | PF00656 | 0.329 |
CLV_C14_Caspase3-7 | 468 | 472 | PF00656 | 0.333 |
CLV_C14_Caspase3-7 | 56 | 60 | PF00656 | 0.627 |
CLV_C14_Caspase3-7 | 662 | 666 | PF00656 | 0.408 |
CLV_C14_Caspase3-7 | 726 | 730 | PF00656 | 0.480 |
CLV_C14_Caspase3-7 | 791 | 795 | PF00656 | 0.409 |
CLV_C14_Caspase3-7 | 866 | 870 | PF00656 | 0.509 |
CLV_NRD_NRD_1 | 1003 | 1005 | PF00675 | 0.364 |
CLV_NRD_NRD_1 | 293 | 295 | PF00675 | 0.209 |
CLV_NRD_NRD_1 | 777 | 779 | PF00675 | 0.517 |
CLV_NRD_NRD_1 | 785 | 787 | PF00675 | 0.234 |
CLV_NRD_NRD_1 | 917 | 919 | PF00675 | 0.209 |
CLV_NRD_NRD_1 | 97 | 99 | PF00675 | 0.654 |
CLV_PCSK_KEX2_1 | 185 | 187 | PF00082 | 0.313 |
CLV_PCSK_KEX2_1 | 785 | 787 | PF00082 | 0.268 |
CLV_PCSK_KEX2_1 | 917 | 919 | PF00082 | 0.209 |
CLV_PCSK_KEX2_1 | 97 | 99 | PF00082 | 0.662 |
CLV_PCSK_PC1ET2_1 | 185 | 187 | PF00082 | 0.313 |
CLV_PCSK_PC7_1 | 181 | 187 | PF00082 | 0.224 |
CLV_PCSK_SKI1_1 | 192 | 196 | PF00082 | 0.313 |
CLV_PCSK_SKI1_1 | 215 | 219 | PF00082 | 0.313 |
CLV_PCSK_SKI1_1 | 371 | 375 | PF00082 | 0.428 |
CLV_PCSK_SKI1_1 | 753 | 757 | PF00082 | 0.430 |
CLV_PCSK_SKI1_1 | 857 | 861 | PF00082 | 0.220 |
CLV_PCSK_SKI1_1 | 877 | 881 | PF00082 | 0.340 |
CLV_PCSK_SKI1_1 | 952 | 956 | PF00082 | 0.251 |
CLV_Separin_Metazoa | 849 | 853 | PF03568 | 0.460 |
DEG_APCC_DBOX_1 | 417 | 425 | PF00400 | 0.505 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.595 |
DEG_SCF_TRCP1_1 | 59 | 64 | PF00400 | 0.469 |
DOC_CKS1_1 | 220 | 225 | PF01111 | 0.468 |
DOC_CYCLIN_yCln2_LP_2 | 891 | 897 | PF00134 | 0.417 |
DOC_MAPK_gen_1 | 277 | 287 | PF00069 | 0.403 |
DOC_MAPK_gen_1 | 294 | 300 | PF00069 | 0.440 |
DOC_MAPK_gen_1 | 370 | 379 | PF00069 | 0.528 |
DOC_MAPK_gen_1 | 380 | 388 | PF00069 | 0.336 |
DOC_MAPK_MEF2A_6 | 170 | 178 | PF00069 | 0.451 |
DOC_MAPK_MEF2A_6 | 277 | 285 | PF00069 | 0.421 |
DOC_MAPK_MEF2A_6 | 488 | 496 | PF00069 | 0.401 |
DOC_MAPK_MEF2A_6 | 672 | 679 | PF00069 | 0.513 |
DOC_MAPK_MEF2A_6 | 705 | 714 | PF00069 | 0.609 |
DOC_PP1_RVXF_1 | 373 | 380 | PF00149 | 0.366 |
DOC_PP1_RVXF_1 | 543 | 550 | PF00149 | 0.478 |
DOC_PP1_RVXF_1 | 637 | 644 | PF00149 | 0.425 |
DOC_PP1_RVXF_1 | 855 | 861 | PF00149 | 0.420 |
DOC_PP1_RVXF_1 | 96 | 103 | PF00149 | 0.574 |
DOC_PP2B_LxvP_1 | 447 | 450 | PF13499 | 0.458 |
DOC_PP2B_LxvP_1 | 901 | 904 | PF13499 | 0.416 |
DOC_PP2B_PxIxI_1 | 808 | 814 | PF00149 | 0.476 |
DOC_PP4_FxxP_1 | 643 | 646 | PF00568 | 0.455 |
DOC_USP7_MATH_1 | 140 | 144 | PF00917 | 0.503 |
DOC_USP7_MATH_1 | 248 | 252 | PF00917 | 0.415 |
DOC_USP7_MATH_1 | 451 | 455 | PF00917 | 0.377 |
DOC_USP7_MATH_1 | 465 | 469 | PF00917 | 0.329 |
DOC_USP7_MATH_1 | 495 | 499 | PF00917 | 0.488 |
DOC_USP7_MATH_1 | 531 | 535 | PF00917 | 0.542 |
DOC_USP7_MATH_1 | 594 | 598 | PF00917 | 0.483 |
DOC_USP7_MATH_1 | 658 | 662 | PF00917 | 0.454 |
DOC_USP7_MATH_1 | 832 | 836 | PF00917 | 0.461 |
DOC_USP7_MATH_1 | 941 | 945 | PF00917 | 0.420 |
DOC_USP7_UBL2_3 | 370 | 374 | PF12436 | 0.519 |
DOC_WW_Pin1_4 | 219 | 224 | PF00397 | 0.452 |
DOC_WW_Pin1_4 | 317 | 322 | PF00397 | 0.420 |
DOC_WW_Pin1_4 | 407 | 412 | PF00397 | 0.491 |
DOC_WW_Pin1_4 | 416 | 421 | PF00397 | 0.483 |
DOC_WW_Pin1_4 | 671 | 676 | PF00397 | 0.409 |
LIG_14-3-3_CanoR_1 | 215 | 220 | PF00244 | 0.513 |
LIG_14-3-3_CanoR_1 | 418 | 428 | PF00244 | 0.430 |
LIG_14-3-3_CanoR_1 | 514 | 518 | PF00244 | 0.499 |
LIG_14-3-3_CanoR_1 | 581 | 589 | PF00244 | 0.450 |
LIG_14-3-3_CanoR_1 | 740 | 745 | PF00244 | 0.519 |
LIG_14-3-3_CanoR_1 | 753 | 761 | PF00244 | 0.343 |
LIG_14-3-3_CanoR_1 | 831 | 841 | PF00244 | 0.487 |
LIG_14-3-3_CanoR_1 | 881 | 885 | PF00244 | 0.317 |
LIG_14-3-3_CanoR_1 | 952 | 961 | PF00244 | 0.409 |
LIG_Actin_WH2_2 | 810 | 828 | PF00022 | 0.513 |
LIG_AP2alpha_2 | 974 | 976 | PF02296 | 0.420 |
LIG_APCC_ABBA_1 | 677 | 682 | PF00400 | 0.513 |
LIG_BIR_III_2 | 555 | 559 | PF00653 | 0.377 |
LIG_BIR_III_4 | 49 | 53 | PF00653 | 0.593 |
LIG_BIR_III_4 | 729 | 733 | PF00653 | 0.517 |
LIG_BRCT_BRCA1_1 | 639 | 643 | PF00533 | 0.415 |
LIG_BRCT_BRCA1_1 | 716 | 720 | PF00533 | 0.385 |
LIG_BRCT_BRCA1_1 | 742 | 746 | PF00533 | 0.460 |
LIG_Clathr_ClatBox_1 | 125 | 129 | PF01394 | 0.626 |
LIG_Clathr_ClatBox_1 | 243 | 247 | PF01394 | 0.433 |
LIG_Clathr_ClatBox_1 | 546 | 550 | PF01394 | 0.344 |
LIG_eIF4E_1 | 761 | 767 | PF01652 | 0.415 |
LIG_EVH1_1 | 447 | 451 | PF00568 | 0.340 |
LIG_FHA_1 | 169 | 175 | PF00498 | 0.409 |
LIG_FHA_1 | 461 | 467 | PF00498 | 0.393 |
LIG_FHA_1 | 517 | 523 | PF00498 | 0.445 |
LIG_FHA_1 | 754 | 760 | PF00498 | 0.362 |
LIG_FHA_1 | 77 | 83 | PF00498 | 0.569 |
LIG_FHA_1 | 928 | 934 | PF00498 | 0.420 |
LIG_FHA_2 | 150 | 156 | PF00498 | 0.385 |
LIG_FHA_2 | 216 | 222 | PF00498 | 0.476 |
LIG_FHA_2 | 274 | 280 | PF00498 | 0.409 |
LIG_FHA_2 | 310 | 316 | PF00498 | 0.551 |
LIG_FHA_2 | 364 | 370 | PF00498 | 0.379 |
LIG_FHA_2 | 569 | 575 | PF00498 | 0.470 |
LIG_FHA_2 | 720 | 726 | PF00498 | 0.330 |
LIG_FHA_2 | 767 | 773 | PF00498 | 0.620 |
LIG_FHA_2 | 814 | 820 | PF00498 | 0.420 |
LIG_LIR_Apic_2 | 629 | 635 | PF02991 | 0.460 |
LIG_LIR_Apic_2 | 640 | 646 | PF02991 | 0.310 |
LIG_LIR_Gen_1 | 143 | 154 | PF02991 | 0.427 |
LIG_LIR_Gen_1 | 312 | 321 | PF02991 | 0.455 |
LIG_LIR_Gen_1 | 325 | 335 | PF02991 | 0.369 |
LIG_LIR_Gen_1 | 384 | 393 | PF02991 | 0.334 |
LIG_LIR_Gen_1 | 717 | 727 | PF02991 | 0.315 |
LIG_LIR_Gen_1 | 760 | 767 | PF02991 | 0.438 |
LIG_LIR_Gen_1 | 787 | 798 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 143 | 149 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 2 | 8 | PF02991 | 0.654 |
LIG_LIR_Nem_3 | 27 | 32 | PF02991 | 0.543 |
LIG_LIR_Nem_3 | 291 | 296 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 312 | 317 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 325 | 331 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 372 | 376 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 384 | 388 | PF02991 | 0.291 |
LIG_LIR_Nem_3 | 391 | 397 | PF02991 | 0.273 |
LIG_LIR_Nem_3 | 516 | 520 | PF02991 | 0.286 |
LIG_LIR_Nem_3 | 557 | 562 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 573 | 579 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 690 | 695 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 717 | 723 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 760 | 764 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 787 | 793 | PF02991 | 0.513 |
LIG_LYPXL_yS_3 | 350 | 353 | PF13949 | 0.368 |
LIG_MAD2 | 375 | 383 | PF02301 | 0.352 |
LIG_NRBOX | 172 | 178 | PF00104 | 0.435 |
LIG_NRBOX | 666 | 672 | PF00104 | 0.476 |
LIG_PDZ_Class_1 | 1010 | 1015 | PF00595 | 0.575 |
LIG_SH2_CRK | 293 | 297 | PF00017 | 0.409 |
LIG_SH2_CRK | 394 | 398 | PF00017 | 0.353 |
LIG_SH2_CRK | 517 | 521 | PF00017 | 0.337 |
LIG_SH2_NCK_1 | 346 | 350 | PF00017 | 0.450 |
LIG_SH2_SRC | 146 | 149 | PF00017 | 0.462 |
LIG_SH2_STAP1 | 314 | 318 | PF00017 | 0.455 |
LIG_SH2_STAP1 | 346 | 350 | PF00017 | 0.338 |
LIG_SH2_STAP1 | 560 | 564 | PF00017 | 0.326 |
LIG_SH2_STAT5 | 146 | 149 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 430 | 433 | PF00017 | 0.402 |
LIG_SH2_STAT5 | 568 | 571 | PF00017 | 0.393 |
LIG_SH2_STAT5 | 687 | 690 | PF00017 | 0.535 |
LIG_SH3_2 | 448 | 453 | PF14604 | 0.348 |
LIG_SH3_2 | 984 | 989 | PF14604 | 0.403 |
LIG_SH3_3 | 220 | 226 | PF00018 | 0.428 |
LIG_SH3_3 | 386 | 392 | PF00018 | 0.316 |
LIG_SH3_3 | 414 | 420 | PF00018 | 0.416 |
LIG_SH3_3 | 445 | 451 | PF00018 | 0.463 |
LIG_SH3_3 | 617 | 623 | PF00018 | 0.464 |
LIG_SH3_3 | 651 | 657 | PF00018 | 0.535 |
LIG_SH3_3 | 707 | 713 | PF00018 | 0.520 |
LIG_SH3_3 | 969 | 975 | PF00018 | 0.409 |
LIG_SH3_3 | 981 | 987 | PF00018 | 0.390 |
LIG_Sin3_3 | 935 | 942 | PF02671 | 0.455 |
LIG_SUMO_SIM_anti_2 | 122 | 129 | PF11976 | 0.543 |
LIG_SUMO_SIM_anti_2 | 171 | 178 | PF11976 | 0.465 |
LIG_SUMO_SIM_anti_2 | 599 | 605 | PF11976 | 0.343 |
LIG_SUMO_SIM_anti_2 | 67 | 74 | PF11976 | 0.469 |
LIG_SUMO_SIM_par_1 | 122 | 129 | PF11976 | 0.549 |
LIG_SUMO_SIM_par_1 | 198 | 205 | PF11976 | 0.361 |
LIG_SUMO_SIM_par_1 | 270 | 276 | PF11976 | 0.450 |
LIG_SUMO_SIM_par_1 | 490 | 498 | PF11976 | 0.471 |
LIG_TRAF2_1 | 31 | 34 | PF00917 | 0.584 |
LIG_TRAF2_1 | 423 | 426 | PF00917 | 0.433 |
LIG_TRAF2_1 | 45 | 48 | PF00917 | 0.591 |
LIG_TRFH_1 | 388 | 392 | PF08558 | 0.339 |
LIG_TYR_ITIM | 515 | 520 | PF00017 | 0.361 |
LIG_TYR_ITIM | 759 | 764 | PF00017 | 0.402 |
LIG_UBA3_1 | 281 | 286 | PF00899 | 0.439 |
LIG_WRC_WIRS_1 | 339 | 344 | PF05994 | 0.371 |
LIG_WRC_WIRS_1 | 720 | 725 | PF05994 | 0.280 |
LIG_WRC_WIRS_1 | 942 | 947 | PF05994 | 0.409 |
MOD_CDC14_SPxK_1 | 320 | 323 | PF00782 | 0.513 |
MOD_CDK_SPxK_1 | 317 | 323 | PF00069 | 0.513 |
MOD_CK1_1 | 253 | 259 | PF00069 | 0.466 |
MOD_CK1_1 | 309 | 315 | PF00069 | 0.461 |
MOD_CK1_1 | 338 | 344 | PF00069 | 0.352 |
MOD_CK1_1 | 35 | 41 | PF00069 | 0.687 |
MOD_CK1_1 | 419 | 425 | PF00069 | 0.512 |
MOD_CK1_1 | 64 | 70 | PF00069 | 0.483 |
MOD_CK2_1 | 169 | 175 | PF00069 | 0.455 |
MOD_CK2_1 | 28 | 34 | PF00069 | 0.635 |
MOD_CK2_1 | 363 | 369 | PF00069 | 0.382 |
MOD_CK2_1 | 42 | 48 | PF00069 | 0.615 |
MOD_CK2_1 | 719 | 725 | PF00069 | 0.306 |
MOD_CK2_1 | 813 | 819 | PF00069 | 0.420 |
MOD_Cter_Amidation | 95 | 98 | PF01082 | 0.610 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.701 |
MOD_GlcNHglycan | 138 | 141 | PF01048 | 0.661 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.296 |
MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.417 |
MOD_GlcNHglycan | 44 | 47 | PF01048 | 0.702 |
MOD_GlcNHglycan | 463 | 466 | PF01048 | 0.526 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.463 |
MOD_GlcNHglycan | 596 | 599 | PF01048 | 0.520 |
MOD_GlcNHglycan | 689 | 692 | PF01048 | 0.276 |
MOD_GlcNHglycan | 747 | 750 | PF01048 | 0.450 |
MOD_GlcNHglycan | 834 | 837 | PF01048 | 0.223 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.535 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.432 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.444 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.730 |
MOD_GSK3_1 | 306 | 313 | PF00069 | 0.463 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.703 |
MOD_GSK3_1 | 322 | 329 | PF00069 | 0.494 |
MOD_GSK3_1 | 451 | 458 | PF00069 | 0.387 |
MOD_GSK3_1 | 461 | 468 | PF00069 | 0.425 |
MOD_GSK3_1 | 521 | 528 | PF00069 | 0.596 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.567 |
MOD_GSK3_1 | 580 | 587 | PF00069 | 0.388 |
MOD_GSK3_1 | 681 | 688 | PF00069 | 0.409 |
MOD_GSK3_1 | 719 | 726 | PF00069 | 0.305 |
MOD_GSK3_1 | 736 | 743 | PF00069 | 0.378 |
MOD_GSK3_1 | 803 | 810 | PF00069 | 0.415 |
MOD_GSK3_1 | 832 | 839 | PF00069 | 0.418 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.651 |
MOD_GSK3_1 | 871 | 878 | PF00069 | 0.361 |
MOD_LATS_1 | 134 | 140 | PF00433 | 0.595 |
MOD_N-GLC_1 | 740 | 745 | PF02516 | 0.493 |
MOD_N-GLC_1 | 9 | 14 | PF02516 | 0.671 |
MOD_NEK2_1 | 273 | 278 | PF00069 | 0.416 |
MOD_NEK2_1 | 670 | 675 | PF00069 | 0.442 |
MOD_NEK2_1 | 723 | 728 | PF00069 | 0.323 |
MOD_NEK2_1 | 734 | 739 | PF00069 | 0.384 |
MOD_NEK2_1 | 837 | 842 | PF00069 | 0.513 |
MOD_NEK2_1 | 880 | 885 | PF00069 | 0.431 |
MOD_NEK2_1 | 976 | 981 | PF00069 | 0.494 |
MOD_NEK2_2 | 327 | 332 | PF00069 | 0.377 |
MOD_NEK2_2 | 465 | 470 | PF00069 | 0.298 |
MOD_NEK2_2 | 584 | 589 | PF00069 | 0.465 |
MOD_PIKK_1 | 120 | 126 | PF00454 | 0.525 |
MOD_PIKK_1 | 140 | 146 | PF00454 | 0.594 |
MOD_PIKK_1 | 714 | 720 | PF00454 | 0.371 |
MOD_PIKK_1 | 753 | 759 | PF00454 | 0.456 |
MOD_PIKK_1 | 76 | 82 | PF00454 | 0.609 |
MOD_PIKK_1 | 946 | 952 | PF00454 | 0.409 |
MOD_PK_1 | 659 | 665 | PF00069 | 0.455 |
MOD_PK_1 | 740 | 746 | PF00069 | 0.482 |
MOD_PK_1 | 807 | 813 | PF00069 | 0.443 |
MOD_PKA_2 | 10 | 16 | PF00069 | 0.639 |
MOD_PKA_2 | 322 | 328 | PF00069 | 0.526 |
MOD_PKA_2 | 35 | 41 | PF00069 | 0.731 |
MOD_PKA_2 | 381 | 387 | PF00069 | 0.415 |
MOD_PKA_2 | 513 | 519 | PF00069 | 0.371 |
MOD_PKA_2 | 580 | 586 | PF00069 | 0.451 |
MOD_PKA_2 | 837 | 843 | PF00069 | 0.498 |
MOD_PKA_2 | 880 | 886 | PF00069 | 0.331 |
MOD_PKB_1 | 453 | 461 | PF00069 | 0.422 |
MOD_Plk_1 | 179 | 185 | PF00069 | 0.455 |
MOD_Plk_1 | 192 | 198 | PF00069 | 0.516 |
MOD_Plk_1 | 685 | 691 | PF00069 | 0.409 |
MOD_Plk_1 | 740 | 746 | PF00069 | 0.561 |
MOD_Plk_1 | 813 | 819 | PF00069 | 0.416 |
MOD_Plk_1 | 976 | 982 | PF00069 | 0.492 |
MOD_Plk_2-3 | 28 | 34 | PF00069 | 0.627 |
MOD_Plk_2-3 | 551 | 557 | PF00069 | 0.408 |
MOD_Plk_4 | 169 | 175 | PF00069 | 0.409 |
MOD_Plk_4 | 199 | 205 | PF00069 | 0.447 |
MOD_Plk_4 | 381 | 387 | PF00069 | 0.319 |
MOD_Plk_4 | 442 | 448 | PF00069 | 0.405 |
MOD_Plk_4 | 584 | 590 | PF00069 | 0.478 |
MOD_Plk_4 | 807 | 813 | PF00069 | 0.412 |
MOD_Plk_4 | 880 | 886 | PF00069 | 0.377 |
MOD_Plk_4 | 928 | 934 | PF00069 | 0.482 |
MOD_ProDKin_1 | 219 | 225 | PF00069 | 0.452 |
MOD_ProDKin_1 | 317 | 323 | PF00069 | 0.420 |
MOD_ProDKin_1 | 407 | 413 | PF00069 | 0.484 |
MOD_ProDKin_1 | 416 | 422 | PF00069 | 0.473 |
MOD_ProDKin_1 | 671 | 677 | PF00069 | 0.409 |
MOD_SUMO_rev_2 | 279 | 288 | PF00179 | 0.420 |
MOD_SUMO_rev_2 | 369 | 376 | PF00179 | 0.435 |
MOD_SUMO_rev_2 | 498 | 508 | PF00179 | 0.441 |
TRG_DiLeu_BaEn_1 | 105 | 110 | PF01217 | 0.655 |
TRG_DiLeu_BaLyEn_6 | 255 | 260 | PF01217 | 0.459 |
TRG_DiLeu_BaLyEn_6 | 542 | 547 | PF01217 | 0.503 |
TRG_DiLeu_BaLyEn_6 | 643 | 648 | PF01217 | 0.491 |
TRG_ENDOCYTIC_2 | 146 | 149 | PF00928 | 0.476 |
TRG_ENDOCYTIC_2 | 293 | 296 | PF00928 | 0.409 |
TRG_ENDOCYTIC_2 | 314 | 317 | PF00928 | 0.455 |
TRG_ENDOCYTIC_2 | 350 | 353 | PF00928 | 0.320 |
TRG_ENDOCYTIC_2 | 394 | 397 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 517 | 520 | PF00928 | 0.329 |
TRG_ENDOCYTIC_2 | 559 | 562 | PF00928 | 0.363 |
TRG_ENDOCYTIC_2 | 761 | 764 | PF00928 | 0.418 |
TRG_ER_diArg_1 | 379 | 382 | PF00400 | 0.434 |
TRG_ER_diArg_1 | 453 | 456 | PF00400 | 0.400 |
TRG_ER_diArg_1 | 543 | 546 | PF00400 | 0.418 |
TRG_ER_diArg_1 | 784 | 786 | PF00400 | 0.466 |
TRG_ER_diArg_1 | 888 | 891 | PF00400 | 0.443 |
TRG_Pf-PMV_PEXEL_1 | 455 | 459 | PF00026 | 0.281 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IJN8 | Leptomonas seymouri | 74% | 100% |
A0A0N1PBS6 | Leptomonas seymouri | 27% | 100% |
A0A0S4JNU7 | Bodo saltans | 40% | 100% |
A0A1X0NU75 | Trypanosomatidae | 50% | 100% |
A0A1X0P8P3 | Trypanosomatidae | 26% | 100% |
A0A3Q8IFJ7 | Leishmania donovani | 94% | 100% |
A0A3Q8IIX7 | Leishmania donovani | 27% | 100% |
A0A3R7NHC0 | Trypanosoma rangeli | 26% | 100% |
A0A422N8J1 | Trypanosoma rangeli | 48% | 100% |
A3DMV6 | Staphylothermus marinus (strain ATCC 43588 / DSM 3639 / JCM 9404 / F1) | 24% | 100% |
A4FUD3 | Bos taurus | 31% | 100% |
A4HKL0 | Leishmania braziliensis | 85% | 100% |
A4HNM7 | Leishmania braziliensis | 27% | 100% |
A4I843 | Leishmania infantum | 95% | 100% |
A4ICW8 | Leishmania infantum | 27% | 100% |
C4YJQ8 | Candida albicans (strain WO-1) | 25% | 100% |
D0A2I0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 100% |
D0AAB0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 100% |
E9ASD6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9B301 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
O08810 | Mus musculus | 31% | 100% |
O14460 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 25% | 100% |
O94316 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 29% | 100% |
P32324 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 26% | 100% |
Q06193 | Entamoeba histolytica | 26% | 100% |
Q15029 | Homo sapiens | 31% | 100% |
Q23716 | Cryptosporidium parvum | 27% | 100% |
Q4Q259 | Leishmania major | 27% | 100% |
Q5A0M4 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 25% | 100% |
Q5F3X4 | Gallus gallus | 32% | 100% |
Q5R6E0 | Pongo abelii | 31% | 100% |
Q6FYA7 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 26% | 100% |
Q74M52 | Nanoarchaeum equitans (strain Kin4-M) | 23% | 100% |
Q754C8 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 26% | 100% |
Q875Z2 | Naumovozyma castellii (strain ATCC 76901 / BCRC 22586 / CBS 4309 / NBRC 1992 / NRRL Y-12630) | 25% | 100% |
Q9YC19 | Aeropyrum pernix (strain ATCC 700893 / DSM 11879 / JCM 9820 / NBRC 100138 / K1) | 26% | 100% |
V5AW74 | Trypanosoma cruzi | 48% | 100% |
V5DRS6 | Trypanosoma cruzi | 26% | 100% |