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:0005654 | nucleoplasm | 2 | 1 |
GO:0005681 | spliceosomal complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
GO:1990904 | ribonucleoprotein complex | 2 | 1 |
Related structures:
AlphaFold database: A4HNU7
Term | Name | Level | Count |
---|---|---|---|
GO:0000375 | RNA splicing, via transesterification reactions | 8 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 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:0008380 | RNA splicing | 7 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004386 | helicase activity | 2 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0016787 | hydrolase activity | 2 | 10 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0030554 | adenyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032559 | adenyl 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:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
GO:0140657 | ATP-dependent activity | 1 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0003723 | RNA binding | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 130 | 134 | PF00656 | 0.526 |
CLV_C14_Caspase3-7 | 612 | 616 | PF00656 | 0.306 |
CLV_C14_Caspase3-7 | 772 | 776 | PF00656 | 0.607 |
CLV_NRD_NRD_1 | 18 | 20 | PF00675 | 0.488 |
CLV_NRD_NRD_1 | 189 | 191 | PF00675 | 0.384 |
CLV_NRD_NRD_1 | 286 | 288 | PF00675 | 0.216 |
CLV_NRD_NRD_1 | 373 | 375 | PF00675 | 0.216 |
CLV_NRD_NRD_1 | 500 | 502 | PF00675 | 0.210 |
CLV_NRD_NRD_1 | 646 | 648 | PF00675 | 0.229 |
CLV_NRD_NRD_1 | 7 | 9 | PF00675 | 0.517 |
CLV_NRD_NRD_1 | 74 | 76 | PF00675 | 0.595 |
CLV_NRD_NRD_1 | 865 | 867 | PF00675 | 0.566 |
CLV_NRD_NRD_1 | 900 | 902 | PF00675 | 0.424 |
CLV_NRD_NRD_1 | 937 | 939 | PF00675 | 0.510 |
CLV_PCSK_KEX2_1 | 189 | 191 | PF00082 | 0.413 |
CLV_PCSK_KEX2_1 | 286 | 288 | PF00082 | 0.232 |
CLV_PCSK_KEX2_1 | 373 | 375 | PF00082 | 0.216 |
CLV_PCSK_KEX2_1 | 646 | 648 | PF00082 | 0.229 |
CLV_PCSK_KEX2_1 | 7 | 9 | PF00082 | 0.595 |
CLV_PCSK_KEX2_1 | 73 | 75 | PF00082 | 0.573 |
CLV_PCSK_KEX2_1 | 839 | 841 | PF00082 | 0.588 |
CLV_PCSK_KEX2_1 | 865 | 867 | PF00082 | 0.351 |
CLV_PCSK_KEX2_1 | 900 | 902 | PF00082 | 0.442 |
CLV_PCSK_KEX2_1 | 904 | 906 | PF00082 | 0.323 |
CLV_PCSK_KEX2_1 | 939 | 941 | PF00082 | 0.574 |
CLV_PCSK_PC1ET2_1 | 839 | 841 | PF00082 | 0.602 |
CLV_PCSK_PC1ET2_1 | 904 | 906 | PF00082 | 0.357 |
CLV_PCSK_PC1ET2_1 | 939 | 941 | PF00082 | 0.574 |
CLV_PCSK_PC7_1 | 369 | 375 | PF00082 | 0.309 |
CLV_PCSK_PC7_1 | 900 | 906 | PF00082 | 0.389 |
CLV_PCSK_SKI1_1 | 14 | 18 | PF00082 | 0.495 |
CLV_PCSK_SKI1_1 | 155 | 159 | PF00082 | 0.483 |
CLV_PCSK_SKI1_1 | 3 | 7 | PF00082 | 0.602 |
CLV_PCSK_SKI1_1 | 335 | 339 | PF00082 | 0.231 |
CLV_PCSK_SKI1_1 | 473 | 477 | PF00082 | 0.223 |
CLV_PCSK_SKI1_1 | 569 | 573 | PF00082 | 0.394 |
CLV_PCSK_SKI1_1 | 690 | 694 | PF00082 | 0.331 |
CLV_PCSK_SKI1_1 | 742 | 746 | PF00082 | 0.332 |
CLV_PCSK_SKI1_1 | 748 | 752 | PF00082 | 0.303 |
CLV_PCSK_SKI1_1 | 75 | 79 | PF00082 | 0.633 |
CLV_PCSK_SKI1_1 | 804 | 808 | PF00082 | 0.303 |
CLV_PCSK_SKI1_1 | 871 | 875 | PF00082 | 0.533 |
CLV_PCSK_SKI1_1 | 890 | 894 | PF00082 | 0.309 |
CLV_PCSK_SKI1_1 | 905 | 909 | PF00082 | 0.520 |
CLV_Separin_Metazoa | 587 | 591 | PF03568 | 0.325 |
DEG_APCC_DBOX_1 | 197 | 205 | PF00400 | 0.254 |
DEG_APCC_DBOX_1 | 747 | 755 | PF00400 | 0.338 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.549 |
DEG_SCF_FBW7_1 | 245 | 251 | PF00400 | 0.364 |
DOC_AGCK_PIF_1 | 571 | 576 | PF00069 | 0.447 |
DOC_CKS1_1 | 245 | 250 | PF01111 | 0.451 |
DOC_CYCLIN_RxL_1 | 801 | 808 | PF00134 | 0.365 |
DOC_MAPK_gen_1 | 206 | 214 | PF00069 | 0.426 |
DOC_MAPK_gen_1 | 286 | 293 | PF00069 | 0.416 |
DOC_MAPK_gen_1 | 373 | 380 | PF00069 | 0.405 |
DOC_MAPK_gen_1 | 888 | 897 | PF00069 | 0.315 |
DOC_MAPK_HePTP_8 | 887 | 899 | PF00069 | 0.404 |
DOC_MAPK_MEF2A_6 | 206 | 214 | PF00069 | 0.405 |
DOC_MAPK_MEF2A_6 | 373 | 382 | PF00069 | 0.405 |
DOC_MAPK_MEF2A_6 | 469 | 478 | PF00069 | 0.416 |
DOC_MAPK_MEF2A_6 | 756 | 765 | PF00069 | 0.397 |
DOC_MAPK_MEF2A_6 | 888 | 897 | PF00069 | 0.321 |
DOC_PP1_RVXF_1 | 310 | 316 | PF00149 | 0.405 |
DOC_PP2B_LxvP_1 | 476 | 479 | PF13499 | 0.416 |
DOC_PP2B_LxvP_1 | 614 | 617 | PF13499 | 0.362 |
DOC_USP7_MATH_1 | 125 | 129 | PF00917 | 0.575 |
DOC_USP7_MATH_1 | 138 | 142 | PF00917 | 0.547 |
DOC_USP7_MATH_1 | 248 | 252 | PF00917 | 0.425 |
DOC_USP7_MATH_1 | 304 | 308 | PF00917 | 0.534 |
DOC_USP7_MATH_1 | 510 | 514 | PF00917 | 0.417 |
DOC_USP7_MATH_1 | 60 | 64 | PF00917 | 0.517 |
DOC_USP7_MATH_1 | 829 | 833 | PF00917 | 0.458 |
DOC_USP7_MATH_1 | 912 | 916 | PF00917 | 0.374 |
DOC_WW_Pin1_4 | 101 | 106 | PF00397 | 0.612 |
DOC_WW_Pin1_4 | 244 | 249 | PF00397 | 0.492 |
DOC_WW_Pin1_4 | 482 | 487 | PF00397 | 0.443 |
DOC_WW_Pin1_4 | 493 | 498 | PF00397 | 0.407 |
LIG_14-3-3_CanoR_1 | 137 | 147 | PF00244 | 0.726 |
LIG_14-3-3_CanoR_1 | 279 | 285 | PF00244 | 0.429 |
LIG_14-3-3_CanoR_1 | 357 | 367 | PF00244 | 0.412 |
LIG_14-3-3_CanoR_1 | 558 | 564 | PF00244 | 0.445 |
LIG_14-3-3_CanoR_1 | 569 | 576 | PF00244 | 0.327 |
LIG_14-3-3_CanoR_1 | 590 | 600 | PF00244 | 0.283 |
LIG_14-3-3_CanoR_1 | 640 | 644 | PF00244 | 0.413 |
LIG_14-3-3_CanoR_1 | 865 | 874 | PF00244 | 0.407 |
LIG_14-3-3_CanoR_1 | 87 | 95 | PF00244 | 0.632 |
LIG_14-3-3_CanoR_1 | 900 | 907 | PF00244 | 0.405 |
LIG_14-3-3_CanoR_1 | 97 | 105 | PF00244 | 0.451 |
LIG_Actin_WH2_2 | 356 | 371 | PF00022 | 0.405 |
LIG_Actin_WH2_2 | 710 | 727 | PF00022 | 0.374 |
LIG_AP2alpha_1 | 392 | 396 | PF02296 | 0.433 |
LIG_BRCT_BRCA1_1 | 392 | 396 | PF00533 | 0.322 |
LIG_BRCT_BRCA1_1 | 65 | 69 | PF00533 | 0.533 |
LIG_BRCT_BRCA1_1 | 807 | 811 | PF00533 | 0.327 |
LIG_BRCT_BRCA1_1 | 857 | 861 | PF00533 | 0.348 |
LIG_BRCT_BRCA1_2 | 392 | 398 | PF00533 | 0.373 |
LIG_Clathr_ClatBox_1 | 608 | 612 | PF01394 | 0.319 |
LIG_FHA_1 | 220 | 226 | PF00498 | 0.413 |
LIG_FHA_1 | 317 | 323 | PF00498 | 0.420 |
LIG_FHA_1 | 359 | 365 | PF00498 | 0.429 |
LIG_FHA_1 | 406 | 412 | PF00498 | 0.360 |
LIG_FHA_1 | 617 | 623 | PF00498 | 0.360 |
LIG_FHA_1 | 712 | 718 | PF00498 | 0.423 |
LIG_FHA_1 | 801 | 807 | PF00498 | 0.271 |
LIG_FHA_2 | 164 | 170 | PF00498 | 0.478 |
LIG_FHA_2 | 29 | 35 | PF00498 | 0.623 |
LIG_FHA_2 | 454 | 460 | PF00498 | 0.491 |
LIG_FHA_2 | 582 | 588 | PF00498 | 0.329 |
LIG_FHA_2 | 62 | 68 | PF00498 | 0.590 |
LIG_FHA_2 | 875 | 881 | PF00498 | 0.619 |
LIG_LIR_Apic_2 | 531 | 535 | PF02991 | 0.447 |
LIG_LIR_Gen_1 | 141 | 152 | PF02991 | 0.539 |
LIG_LIR_Gen_1 | 164 | 175 | PF02991 | 0.616 |
LIG_LIR_Gen_1 | 390 | 400 | PF02991 | 0.466 |
LIG_LIR_Gen_1 | 714 | 724 | PF02991 | 0.442 |
LIG_LIR_Gen_1 | 736 | 745 | PF02991 | 0.434 |
LIG_LIR_Gen_1 | 757 | 765 | PF02991 | 0.499 |
LIG_LIR_Gen_1 | 823 | 830 | PF02991 | 0.357 |
LIG_LIR_Gen_1 | 86 | 95 | PF02991 | 0.524 |
LIG_LIR_Nem_3 | 164 | 170 | PF02991 | 0.625 |
LIG_LIR_Nem_3 | 390 | 395 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 566 | 571 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 714 | 719 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 736 | 741 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 757 | 761 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 808 | 814 | PF02991 | 0.293 |
LIG_LIR_Nem_3 | 823 | 827 | PF02991 | 0.283 |
LIG_LIR_Nem_3 | 86 | 91 | PF02991 | 0.552 |
LIG_MLH1_MIPbox_1 | 392 | 396 | PF16413 | 0.322 |
LIG_MLH1_MIPbox_1 | 807 | 811 | PF16413 | 0.327 |
LIG_NRBOX | 363 | 369 | PF00104 | 0.405 |
LIG_NRBOX | 627 | 633 | PF00104 | 0.350 |
LIG_PCNA_yPIPBox_3 | 710 | 718 | PF02747 | 0.299 |
LIG_Pex14_2 | 392 | 396 | PF04695 | 0.288 |
LIG_REV1ctd_RIR_1 | 393 | 399 | PF16727 | 0.454 |
LIG_SH2_CRK | 824 | 828 | PF00017 | 0.251 |
LIG_SH2_GRB2like | 532 | 535 | PF00017 | 0.447 |
LIG_SH2_GRB2like | 738 | 741 | PF00017 | 0.322 |
LIG_SH2_PTP2 | 716 | 719 | PF00017 | 0.285 |
LIG_SH2_PTP2 | 738 | 741 | PF00017 | 0.229 |
LIG_SH2_SRC | 230 | 233 | PF00017 | 0.472 |
LIG_SH2_SRC | 738 | 741 | PF00017 | 0.322 |
LIG_SH2_STAT3 | 533 | 536 | PF00017 | 0.472 |
LIG_SH2_STAT5 | 144 | 147 | PF00017 | 0.545 |
LIG_SH2_STAT5 | 161 | 164 | PF00017 | 0.428 |
LIG_SH2_STAT5 | 228 | 231 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 327 | 330 | PF00017 | 0.425 |
LIG_SH2_STAT5 | 423 | 426 | PF00017 | 0.324 |
LIG_SH2_STAT5 | 464 | 467 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 521 | 524 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 574 | 577 | PF00017 | 0.397 |
LIG_SH2_STAT5 | 716 | 719 | PF00017 | 0.285 |
LIG_SH2_STAT5 | 738 | 741 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 927 | 930 | PF00017 | 0.373 |
LIG_SH3_2 | 835 | 840 | PF14604 | 0.442 |
LIG_SH3_3 | 298 | 304 | PF00018 | 0.509 |
LIG_SH3_3 | 443 | 449 | PF00018 | 0.445 |
LIG_SH3_3 | 649 | 655 | PF00018 | 0.420 |
LIG_SH3_3 | 823 | 829 | PF00018 | 0.426 |
LIG_SH3_3 | 832 | 838 | PF00018 | 0.590 |
LIG_SH3_5 | 419 | 423 | PF00018 | 0.343 |
LIG_SUMO_SIM_anti_2 | 764 | 769 | PF11976 | 0.352 |
LIG_SUMO_SIM_par_1 | 210 | 217 | PF11976 | 0.406 |
LIG_SUMO_SIM_par_1 | 678 | 684 | PF11976 | 0.429 |
LIG_TRFH_1 | 234 | 238 | PF08558 | 0.509 |
LIG_TRFH_1 | 651 | 655 | PF08558 | 0.472 |
LIG_UBA3_1 | 628 | 636 | PF00899 | 0.410 |
LIG_WRC_WIRS_1 | 755 | 760 | PF05994 | 0.413 |
MOD_CDK_SPK_2 | 482 | 487 | PF00069 | 0.432 |
MOD_CDK_SPxK_1 | 244 | 250 | PF00069 | 0.350 |
MOD_CK1_1 | 219 | 225 | PF00069 | 0.405 |
MOD_CK1_1 | 251 | 257 | PF00069 | 0.429 |
MOD_CK1_1 | 358 | 364 | PF00069 | 0.413 |
MOD_CK1_1 | 405 | 411 | PF00069 | 0.472 |
MOD_CK1_1 | 427 | 433 | PF00069 | 0.388 |
MOD_CK1_1 | 482 | 488 | PF00069 | 0.350 |
MOD_CK1_1 | 548 | 554 | PF00069 | 0.405 |
MOD_CK1_1 | 618 | 624 | PF00069 | 0.350 |
MOD_CK1_1 | 63 | 69 | PF00069 | 0.618 |
MOD_CK1_1 | 769 | 775 | PF00069 | 0.477 |
MOD_CK1_1 | 867 | 873 | PF00069 | 0.566 |
MOD_CK2_1 | 145 | 151 | PF00069 | 0.506 |
MOD_CK2_1 | 163 | 169 | PF00069 | 0.402 |
MOD_CK2_1 | 28 | 34 | PF00069 | 0.561 |
MOD_CK2_1 | 289 | 295 | PF00069 | 0.405 |
MOD_CK2_1 | 45 | 51 | PF00069 | 0.355 |
MOD_CK2_1 | 453 | 459 | PF00069 | 0.468 |
MOD_CK2_1 | 482 | 488 | PF00069 | 0.457 |
MOD_CK2_1 | 581 | 587 | PF00069 | 0.335 |
MOD_CK2_1 | 697 | 703 | PF00069 | 0.421 |
MOD_CK2_1 | 847 | 853 | PF00069 | 0.453 |
MOD_CK2_1 | 874 | 880 | PF00069 | 0.656 |
MOD_Cter_Amidation | 644 | 647 | PF01082 | 0.229 |
MOD_Cter_Amidation | 863 | 866 | PF01082 | 0.519 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.698 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.668 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.579 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.205 |
MOD_GlcNHglycan | 250 | 253 | PF01048 | 0.205 |
MOD_GlcNHglycan | 383 | 386 | PF01048 | 0.205 |
MOD_GlcNHglycan | 404 | 407 | PF01048 | 0.422 |
MOD_GlcNHglycan | 426 | 429 | PF01048 | 0.359 |
MOD_GlcNHglycan | 550 | 553 | PF01048 | 0.205 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.569 |
MOD_GlcNHglycan | 593 | 596 | PF01048 | 0.425 |
MOD_GlcNHglycan | 699 | 702 | PF01048 | 0.390 |
MOD_GlcNHglycan | 768 | 771 | PF01048 | 0.627 |
MOD_GlcNHglycan | 790 | 793 | PF01048 | 0.597 |
MOD_GlcNHglycan | 807 | 810 | PF01048 | 0.210 |
MOD_GlcNHglycan | 831 | 834 | PF01048 | 0.562 |
MOD_GlcNHglycan | 914 | 917 | PF01048 | 0.409 |
MOD_GlcNHglycan | 921 | 924 | PF01048 | 0.365 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.683 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.631 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.405 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.421 |
MOD_GSK3_1 | 252 | 259 | PF00069 | 0.390 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.436 |
MOD_GSK3_1 | 453 | 460 | PF00069 | 0.491 |
MOD_GSK3_1 | 544 | 551 | PF00069 | 0.465 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.366 |
MOD_GSK3_1 | 693 | 700 | PF00069 | 0.513 |
MOD_GSK3_1 | 769 | 776 | PF00069 | 0.647 |
MOD_GSK3_1 | 908 | 915 | PF00069 | 0.326 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.683 |
MOD_LATS_1 | 355 | 361 | PF00433 | 0.451 |
MOD_N-GLC_1 | 773 | 778 | PF02516 | 0.436 |
MOD_NEK2_1 | 280 | 285 | PF00069 | 0.405 |
MOD_NEK2_1 | 402 | 407 | PF00069 | 0.435 |
MOD_NEK2_1 | 434 | 439 | PF00069 | 0.334 |
MOD_NEK2_1 | 589 | 594 | PF00069 | 0.329 |
MOD_NEK2_1 | 641 | 646 | PF00069 | 0.405 |
MOD_NEK2_1 | 733 | 738 | PF00069 | 0.343 |
MOD_NEK2_1 | 874 | 879 | PF00069 | 0.582 |
MOD_NEK2_1 | 899 | 904 | PF00069 | 0.405 |
MOD_PIKK_1 | 220 | 226 | PF00454 | 0.405 |
MOD_PIKK_1 | 280 | 286 | PF00454 | 0.418 |
MOD_PIKK_1 | 545 | 551 | PF00454 | 0.459 |
MOD_PIKK_1 | 559 | 565 | PF00454 | 0.416 |
MOD_PK_1 | 840 | 846 | PF00069 | 0.702 |
MOD_PKA_1 | 865 | 871 | PF00069 | 0.392 |
MOD_PKA_1 | 900 | 906 | PF00069 | 0.409 |
MOD_PKA_2 | 589 | 595 | PF00069 | 0.313 |
MOD_PKA_2 | 639 | 645 | PF00069 | 0.413 |
MOD_PKA_2 | 86 | 92 | PF00069 | 0.636 |
MOD_PKA_2 | 864 | 870 | PF00069 | 0.621 |
MOD_PKA_2 | 899 | 905 | PF00069 | 0.372 |
MOD_PKA_2 | 96 | 102 | PF00069 | 0.450 |
MOD_PKB_1 | 163 | 171 | PF00069 | 0.371 |
MOD_Plk_1 | 163 | 169 | PF00069 | 0.576 |
MOD_Plk_1 | 341 | 347 | PF00069 | 0.458 |
MOD_Plk_1 | 355 | 361 | PF00069 | 0.356 |
MOD_Plk_1 | 510 | 516 | PF00069 | 0.416 |
MOD_Plk_1 | 693 | 699 | PF00069 | 0.457 |
MOD_Plk_1 | 847 | 853 | PF00069 | 0.532 |
MOD_Plk_2-3 | 847 | 853 | PF00069 | 0.311 |
MOD_Plk_4 | 252 | 258 | PF00069 | 0.350 |
MOD_Plk_4 | 28 | 34 | PF00069 | 0.603 |
MOD_Plk_4 | 304 | 310 | PF00069 | 0.447 |
MOD_Plk_4 | 427 | 433 | PF00069 | 0.408 |
MOD_Plk_4 | 45 | 51 | PF00069 | 0.636 |
MOD_Plk_4 | 460 | 466 | PF00069 | 0.451 |
MOD_Plk_4 | 681 | 687 | PF00069 | 0.438 |
MOD_Plk_4 | 822 | 828 | PF00069 | 0.315 |
MOD_Plk_4 | 855 | 861 | PF00069 | 0.321 |
MOD_ProDKin_1 | 101 | 107 | PF00069 | 0.612 |
MOD_ProDKin_1 | 244 | 250 | PF00069 | 0.492 |
MOD_ProDKin_1 | 482 | 488 | PF00069 | 0.443 |
MOD_ProDKin_1 | 493 | 499 | PF00069 | 0.407 |
MOD_SUMO_for_1 | 257 | 260 | PF00179 | 0.412 |
MOD_SUMO_for_1 | 815 | 818 | PF00179 | 0.355 |
MOD_SUMO_rev_2 | 769 | 779 | PF00179 | 0.650 |
TRG_AP2beta_CARGO_1 | 164 | 174 | PF09066 | 0.502 |
TRG_DiLeu_BaEn_1 | 276 | 281 | PF01217 | 0.491 |
TRG_DiLeu_BaEn_1 | 51 | 56 | PF01217 | 0.579 |
TRG_DiLeu_BaEn_1 | 889 | 894 | PF01217 | 0.310 |
TRG_DiLeu_BaEn_4 | 231 | 237 | PF01217 | 0.509 |
TRG_DiLeu_BaLyEn_6 | 471 | 476 | PF01217 | 0.447 |
TRG_DiLeu_LyEn_5 | 276 | 281 | PF01217 | 0.491 |
TRG_ENDOCYTIC_2 | 144 | 147 | PF00928 | 0.554 |
TRG_ENDOCYTIC_2 | 481 | 484 | PF00928 | 0.405 |
TRG_ENDOCYTIC_2 | 568 | 571 | PF00928 | 0.434 |
TRG_ENDOCYTIC_2 | 716 | 719 | PF00928 | 0.285 |
TRG_ENDOCYTIC_2 | 738 | 741 | PF00928 | 0.343 |
TRG_ENDOCYTIC_2 | 824 | 827 | PF00928 | 0.330 |
TRG_ER_diArg_1 | 285 | 287 | PF00400 | 0.416 |
TRG_ER_diArg_1 | 372 | 374 | PF00400 | 0.429 |
TRG_ER_diArg_1 | 6 | 8 | PF00400 | 0.615 |
TRG_ER_diArg_1 | 646 | 648 | PF00400 | 0.429 |
TRG_ER_diArg_1 | 73 | 75 | PF00400 | 0.598 |
TRG_ER_diArg_1 | 745 | 748 | PF00400 | 0.340 |
TRG_ER_diArg_1 | 899 | 901 | PF00400 | 0.524 |
TRG_ER_diArg_1 | 937 | 940 | PF00400 | 0.544 |
TRG_NES_CRM1_1 | 587 | 599 | PF08389 | 0.307 |
TRG_NLS_MonoExtC_3 | 937 | 942 | PF00514 | 0.556 |
TRG_NLS_MonoExtN_4 | 938 | 943 | PF00514 | 0.612 |
TRG_Pf-PMV_PEXEL_1 | 357 | 362 | PF00026 | 0.216 |
TRG_Pf-PMV_PEXEL_1 | 38 | 42 | PF00026 | 0.520 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5V0 | Leptomonas seymouri | 36% | 100% |
A0A0N0P8Y1 | Leptomonas seymouri | 35% | 100% |
A0A0N0P9D2 | Leptomonas seymouri | 36% | 100% |
A0A0N1I0Z0 | Leptomonas seymouri | 35% | 87% |
A0A0N1IKA7 | Leptomonas seymouri | 34% | 100% |
A0A0N1PEU4 | Leptomonas seymouri | 72% | 99% |
A0A0S4IQ76 | Bodo saltans | 33% | 100% |
A0A0S4IR78 | Bodo saltans | 48% | 100% |
A0A0S4IS51 | Bodo saltans | 35% | 100% |
A0A0S4ITR4 | Bodo saltans | 37% | 88% |
A0A0S4IWU8 | Bodo saltans | 48% | 100% |
A0A0S4J157 | Bodo saltans | 37% | 100% |
A0A0S4JCY8 | Bodo saltans | 35% | 92% |
A0A1X0NJ46 | Trypanosomatidae | 36% | 100% |
A0A1X0NKY7 | Trypanosomatidae | 35% | 88% |
A0A1X0NUZ7 | Trypanosomatidae | 31% | 72% |
A0A1X0P0D7 | Trypanosomatidae | 37% | 100% |
A0A1X0P872 | Trypanosomatidae | 59% | 100% |
A0A1X0P9K6 | Trypanosomatidae | 37% | 100% |
A0A3Q8IEC9 | Leishmania donovani | 30% | 87% |
A0A3Q8II71 | Leishmania donovani | 36% | 100% |
A0A3Q8IJ24 | Leishmania donovani | 86% | 100% |
A0A3Q8IWG4 | Leishmania donovani | 35% | 100% |
A0A3R7MA90 | Trypanosoma rangeli | 36% | 100% |
A0A3R7MLF0 | Trypanosoma rangeli | 29% | 67% |
A0A3R7NT42 | Trypanosoma rangeli | 37% | 100% |
A0A3S7WYA1 | Leishmania donovani | 34% | 87% |
A0A3S7X8Z5 | Leishmania donovani | 36% | 100% |
A0A3S7XB01 | Leishmania donovani | 35% | 87% |
A0A422MXB1 | Trypanosoma rangeli | 36% | 89% |
A0A422N8L3 | Trypanosoma rangeli | 34% | 93% |
A1Z9L3 | Drosophila melanogaster | 39% | 76% |
A2A4P0 | Mus musculus | 39% | 76% |
A4HAT8 | Leishmania braziliensis | 34% | 98% |
A4HDG6 | Leishmania braziliensis | 33% | 100% |
A4HME2 | Leishmania braziliensis | 36% | 93% |
A4HPE9 | Leishmania braziliensis | 35% | 87% |
A4HQ83 | Leishmania braziliensis | 36% | 100% |
A4I009 | Leishmania infantum | 29% | 87% |
A4I0U7 | Leishmania infantum | 34% | 87% |
A4IA06 | Leishmania infantum | 36% | 100% |
A4IB14 | Leishmania infantum | 36% | 100% |
A4ICJ0 | Leishmania infantum | 35% | 87% |
A4ICP7 | Leishmania infantum | 87% | 100% |
A4IDY1 | Leishmania infantum | 35% | 100% |
B0XDC4 | Culex quinquefasciatus | 29% | 68% |
B8A4F4 | Danio rerio | 29% | 70% |
C9ZMN0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
C9ZNP6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
C9ZQ85 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 75% |
D0A2R5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 58% | 100% |
D0A3F8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 89% |
D0A429 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
D0A778 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 90% |
E9AEU3 | Leishmania major | 36% | 92% |
E9ASK7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
E9AT60 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 87% |
E9AU01 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
E9AVY2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 87% |
E9AWV1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 76% |
E9B512 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
E9B5Z9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
F4IE66 | Arabidopsis thaliana | 34% | 100% |
F4IJV4 | Arabidopsis thaliana | 42% | 90% |
F4JMJ3 | Arabidopsis thaliana | 37% | 100% |
F4JRJ6 | Arabidopsis thaliana | 35% | 100% |
F4K2E9 | Arabidopsis thaliana | 35% | 75% |
O22899 | Arabidopsis thaliana | 36% | 100% |
O35286 | Mus musculus | 36% | 100% |
O42643 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 38% | 81% |
O42945 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 37% | 100% |
O43143 | Homo sapiens | 36% | 100% |
O45244 | Caenorhabditis elegans | 38% | 94% |
O60114 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 29% | 66% |
O60231 | Homo sapiens | 37% | 91% |
O70133 | Mus musculus | 28% | 68% |
P20095 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 35% | 100% |
P24384 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 38% | 82% |
P34498 | Caenorhabditis elegans | 38% | 83% |
P36009 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 32% | 100% |
P45018 | Haemophilus influenzae (strain ATCC 51907 / DSM 11121 / KW20 / Rd) | 33% | 72% |
P53131 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 37% | 100% |
Q03319 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 34% | 100% |
Q09530 | Caenorhabditis elegans | 40% | 79% |
Q10752 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 39% | 89% |
Q14562 | Homo sapiens | 39% | 77% |
Q14BI7 | Mus musculus | 28% | 68% |
Q17R09 | Bos taurus | 36% | 77% |
Q20875 | Caenorhabditis elegans | 35% | 100% |
Q28141 | Bos taurus | 28% | 73% |
Q2NKY8 | Bos taurus | 32% | 77% |
Q38953 | Arabidopsis thaliana | 39% | 81% |
Q3MHU3 | Rattus norvegicus | 29% | 68% |
Q3ZBE0 | Bos taurus | 30% | 100% |
Q4Q0J4 | Leishmania major | 35% | 90% |
Q4Q1D7 | Leishmania major | 35% | 100% |
Q4Q1Y9 | Leishmania major | 85% | 100% |
Q4Q2X4 | Leishmania major | 36% | 100% |
Q4QAM3 | Leishmania major | 34% | 83% |
Q4QBJ7 | Leishmania major | 30% | 87% |
Q54F05 | Dictyostelium discoideum | 37% | 81% |
Q54MH3 | Dictyostelium discoideum | 40% | 85% |
Q54NJ4 | Dictyostelium discoideum | 35% | 100% |
Q5BJS0 | Rattus norvegicus | 31% | 79% |
Q5R864 | Pongo abelii | 38% | 100% |
Q5RAZ4 | Pongo abelii | 36% | 100% |
Q5RBD4 | Pongo abelii | 37% | 100% |
Q5XH12 | Xenopus laevis | 27% | 100% |
Q5XI69 | Rattus norvegicus | 38% | 100% |
Q5ZI74 | Gallus gallus | 32% | 77% |
Q68FK8 | Xenopus laevis | 29% | 75% |
Q6PE54 | Mus musculus | 38% | 100% |
Q767K6 | Sus scrofa | 40% | 90% |
Q7K3M5 | Drosophila melanogaster | 36% | 100% |
Q7L7V1 | Homo sapiens | 28% | 100% |
Q7YR39 | Pan troglodytes | 37% | 90% |
Q80VY9 | Mus musculus | 33% | 100% |
Q8BZS9 | Mus musculus | 29% | 100% |
Q8IX18 | Homo sapiens | 38% | 100% |
Q8NDG6 | Homo sapiens | 29% | 68% |
Q8TE96 | Homo sapiens | 30% | 100% |
Q8VY00 | Arabidopsis thaliana | 40% | 90% |
Q924H9 | Mus musculus | 30% | 100% |
Q92620 | Homo sapiens | 36% | 77% |
Q99PU8 | Mus musculus | 31% | 77% |
Q9BKQ8 | Caenorhabditis elegans | 37% | 100% |
Q9C6G0 | Arabidopsis thaliana | 29% | 67% |
Q9H5Z1 | Homo sapiens | 37% | 100% |
Q9H6R0 | Homo sapiens | 33% | 100% |
Q9HDY4 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 32% | 80% |
Q9HE06 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 34% | 100% |
Q9LZQ9 | Arabidopsis thaliana | 36% | 100% |
V5B3L7 | Trypanosoma cruzi | 36% | 100% |
V5BKH2 | Trypanosoma cruzi | 37% | 100% |
V5BND8 | Trypanosoma cruzi | 28% | 67% |
V5BPV3 | Trypanosoma cruzi | 36% | 89% |
V5BV22 | Trypanosoma cruzi | 56% | 100% |
V5C0I9 | Trypanosoma cruzi | 35% | 100% |
V5D886 | Trypanosoma cruzi | 35% | 100% |