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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 2 |
GO:0005737 | cytoplasm | 2 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: Q4Q5Z1
Term | Name | Level | Count |
---|---|---|---|
GO:0000459 | exonucleolytic trimming involved in rRNA processing | 8 | 5 |
GO:0000467 | exonucleolytic trimming to generate mature 3'-end of 5.8S rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA) | 9 | 5 |
GO:0000469 | cleavage involved in rRNA processing | 7 | 5 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 5 |
GO:0006364 | rRNA processing | 8 | 5 |
GO:0006396 | RNA processing | 6 | 5 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 5 |
GO:0006807 | nitrogen compound metabolic process | 2 | 5 |
GO:0008152 | metabolic process | 1 | 5 |
GO:0009987 | cellular process | 1 | 5 |
GO:0016070 | RNA metabolic process | 5 | 5 |
GO:0016072 | rRNA metabolic process | 7 | 5 |
GO:0031123 | RNA 3'-end processing | 7 | 5 |
GO:0031125 | rRNA 3'-end processing | 9 | 5 |
GO:0034470 | ncRNA processing | 7 | 5 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 5 |
GO:0034660 | ncRNA metabolic process | 6 | 5 |
GO:0043170 | macromolecule metabolic process | 3 | 5 |
GO:0043628 | regulatory ncRNA 3'-end processing | 8 | 5 |
GO:0044237 | cellular metabolic process | 2 | 5 |
GO:0044238 | primary metabolic process | 2 | 5 |
GO:0046483 | heterocycle metabolic process | 3 | 5 |
GO:0071704 | organic substance metabolic process | 2 | 5 |
GO:0090304 | nucleic acid metabolic process | 4 | 5 |
GO:0090305 | nucleic acid phosphodiester bond hydrolysis | 5 | 5 |
GO:0090501 | RNA phosphodiester bond hydrolysis | 6 | 5 |
GO:0090503 | RNA phosphodiester bond hydrolysis, exonucleolytic | 7 | 5 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 10 |
GO:0003824 | catalytic activity | 1 | 8 |
GO:0004518 | nuclease activity | 4 | 8 |
GO:0004527 | exonuclease activity | 5 | 8 |
GO:0005488 | binding | 1 | 10 |
GO:0008408 | 3'-5' exonuclease activity | 6 | 7 |
GO:0016787 | hydrolase activity | 2 | 8 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 8 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
GO:0000175 | 3'-5'-RNA exonuclease activity | 7 | 5 |
GO:0004532 | RNA exonuclease activity | 5 | 5 |
GO:0004540 | RNA nuclease activity | 4 | 5 |
GO:0016796 | exonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 5'-phosphomonoesters | 6 | 5 |
GO:0016896 | RNA exonuclease activity, producing 5'-phosphomonoesters | 6 | 5 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 5 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 5 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 182 | 186 | PF00656 | 0.426 |
CLV_C14_Caspase3-7 | 282 | 286 | PF00656 | 0.538 |
CLV_NRD_NRD_1 | 149 | 151 | PF00675 | 0.537 |
CLV_NRD_NRD_1 | 196 | 198 | PF00675 | 0.467 |
CLV_NRD_NRD_1 | 4 | 6 | PF00675 | 0.374 |
CLV_NRD_NRD_1 | 453 | 455 | PF00675 | 0.469 |
CLV_NRD_NRD_1 | 487 | 489 | PF00675 | 0.358 |
CLV_NRD_NRD_1 | 514 | 516 | PF00675 | 0.471 |
CLV_NRD_NRD_1 | 655 | 657 | PF00675 | 0.733 |
CLV_NRD_NRD_1 | 66 | 68 | PF00675 | 0.564 |
CLV_NRD_NRD_1 | 661 | 663 | PF00675 | 0.740 |
CLV_NRD_NRD_1 | 682 | 684 | PF00675 | 0.526 |
CLV_NRD_NRD_1 | 72 | 74 | PF00675 | 0.502 |
CLV_NRD_NRD_1 | 793 | 795 | PF00675 | 0.545 |
CLV_PCSK_FUR_1 | 791 | 795 | PF00082 | 0.485 |
CLV_PCSK_KEX2_1 | 149 | 151 | PF00082 | 0.458 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.377 |
CLV_PCSK_KEX2_1 | 453 | 455 | PF00082 | 0.469 |
CLV_PCSK_KEX2_1 | 487 | 489 | PF00082 | 0.505 |
CLV_PCSK_KEX2_1 | 514 | 516 | PF00082 | 0.471 |
CLV_PCSK_KEX2_1 | 657 | 659 | PF00082 | 0.717 |
CLV_PCSK_KEX2_1 | 661 | 663 | PF00082 | 0.705 |
CLV_PCSK_KEX2_1 | 682 | 684 | PF00082 | 0.487 |
CLV_PCSK_KEX2_1 | 72 | 74 | PF00082 | 0.510 |
CLV_PCSK_KEX2_1 | 793 | 795 | PF00082 | 0.544 |
CLV_PCSK_PC1ET2_1 | 657 | 659 | PF00082 | 0.642 |
CLV_PCSK_SKI1_1 | 149 | 153 | PF00082 | 0.414 |
CLV_PCSK_SKI1_1 | 213 | 217 | PF00082 | 0.353 |
CLV_PCSK_SKI1_1 | 302 | 306 | PF00082 | 0.450 |
CLV_PCSK_SKI1_1 | 487 | 491 | PF00082 | 0.401 |
CLV_PCSK_SKI1_1 | 603 | 607 | PF00082 | 0.320 |
CLV_PCSK_SKI1_1 | 72 | 76 | PF00082 | 0.495 |
CLV_PCSK_SKI1_1 | 734 | 738 | PF00082 | 0.414 |
CLV_PCSK_SKI1_1 | 764 | 768 | PF00082 | 0.359 |
CLV_PCSK_SKI1_1 | 839 | 843 | PF00082 | 0.382 |
DEG_APCC_DBOX_1 | 586 | 594 | PF00400 | 0.431 |
DEG_APCC_DBOX_1 | 602 | 610 | PF00400 | 0.254 |
DEG_APCC_DBOX_1 | 71 | 79 | PF00400 | 0.467 |
DEG_APCC_DBOX_1 | 733 | 741 | PF00400 | 0.428 |
DEG_APCC_KENBOX_2 | 462 | 466 | PF00400 | 0.336 |
DEG_COP1_1 | 42 | 52 | PF00400 | 0.471 |
DEG_MDM2_SWIB_1 | 39 | 47 | PF02201 | 0.422 |
DEG_SCF_FBW7_2 | 568 | 575 | PF00400 | 0.539 |
DOC_CDC14_PxL_1 | 779 | 787 | PF14671 | 0.491 |
DOC_CKS1_1 | 408 | 413 | PF01111 | 0.466 |
DOC_CKS1_1 | 569 | 574 | PF01111 | 0.587 |
DOC_CKS1_1 | 640 | 645 | PF01111 | 0.608 |
DOC_CYCLIN_RxL_1 | 833 | 846 | PF00134 | 0.392 |
DOC_CYCLIN_yCln2_LP_2 | 109 | 115 | PF00134 | 0.461 |
DOC_MAPK_gen_1 | 149 | 158 | PF00069 | 0.387 |
DOC_MAPK_gen_1 | 164 | 174 | PF00069 | 0.330 |
DOC_MAPK_gen_1 | 460 | 468 | PF00069 | 0.438 |
DOC_MAPK_MEF2A_6 | 167 | 174 | PF00069 | 0.516 |
DOC_MAPK_MEF2A_6 | 487 | 495 | PF00069 | 0.377 |
DOC_PP1_RVXF_1 | 402 | 409 | PF00149 | 0.407 |
DOC_PP2B_LxvP_1 | 47 | 50 | PF13499 | 0.568 |
DOC_PP4_FxxP_1 | 459 | 462 | PF00568 | 0.400 |
DOC_PP4_FxxP_1 | 528 | 531 | PF00568 | 0.358 |
DOC_SPAK_OSR1_1 | 478 | 482 | PF12202 | 0.329 |
DOC_USP7_MATH_1 | 193 | 197 | PF00917 | 0.478 |
DOC_USP7_MATH_1 | 257 | 261 | PF00917 | 0.295 |
DOC_USP7_MATH_1 | 281 | 285 | PF00917 | 0.583 |
DOC_USP7_MATH_1 | 344 | 348 | PF00917 | 0.657 |
DOC_USP7_MATH_1 | 629 | 633 | PF00917 | 0.618 |
DOC_USP7_MATH_1 | 667 | 671 | PF00917 | 0.632 |
DOC_USP7_MATH_1 | 795 | 799 | PF00917 | 0.590 |
DOC_USP7_MATH_1 | 809 | 813 | PF00917 | 0.700 |
DOC_WW_Pin1_4 | 243 | 248 | PF00397 | 0.385 |
DOC_WW_Pin1_4 | 308 | 313 | PF00397 | 0.582 |
DOC_WW_Pin1_4 | 407 | 412 | PF00397 | 0.494 |
DOC_WW_Pin1_4 | 568 | 573 | PF00397 | 0.714 |
DOC_WW_Pin1_4 | 639 | 644 | PF00397 | 0.699 |
DOC_WW_Pin1_4 | 649 | 654 | PF00397 | 0.718 |
DOC_WW_Pin1_4 | 804 | 809 | PF00397 | 0.686 |
DOC_WW_Pin1_4 | 810 | 815 | PF00397 | 0.706 |
DOC_WW_Pin1_4 | 881 | 886 | PF00397 | 0.480 |
LIG_14-3-3_CanoR_1 | 128 | 133 | PF00244 | 0.407 |
LIG_14-3-3_CanoR_1 | 682 | 686 | PF00244 | 0.457 |
LIG_14-3-3_CanoR_1 | 793 | 801 | PF00244 | 0.639 |
LIG_14-3-3_CanoR_1 | 865 | 871 | PF00244 | 0.330 |
LIG_Actin_WH2_2 | 131 | 146 | PF00022 | 0.350 |
LIG_AP2alpha_2 | 111 | 113 | PF02296 | 0.458 |
LIG_APCC_ABBA_1 | 156 | 161 | PF00400 | 0.415 |
LIG_APCC_ABBA_1 | 163 | 168 | PF00400 | 0.429 |
LIG_APCC_ABBA_1 | 599 | 604 | PF00400 | 0.357 |
LIG_BIR_III_4 | 745 | 749 | PF00653 | 0.525 |
LIG_BRCT_BRCA1_1 | 269 | 273 | PF00533 | 0.379 |
LIG_BRCT_BRCA1_1 | 32 | 36 | PF00533 | 0.494 |
LIG_BRCT_BRCA1_1 | 506 | 510 | PF00533 | 0.285 |
LIG_BRCT_BRCA1_1 | 831 | 835 | PF00533 | 0.354 |
LIG_BRCT_BRCA1_2 | 506 | 512 | PF00533 | 0.295 |
LIG_DLG_GKlike_1 | 208 | 215 | PF00625 | 0.433 |
LIG_EH1_1 | 834 | 842 | PF00400 | 0.429 |
LIG_FHA_1 | 138 | 144 | PF00498 | 0.460 |
LIG_FHA_1 | 207 | 213 | PF00498 | 0.516 |
LIG_FHA_1 | 286 | 292 | PF00498 | 0.422 |
LIG_FHA_1 | 318 | 324 | PF00498 | 0.537 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.463 |
LIG_FHA_1 | 682 | 688 | PF00498 | 0.494 |
LIG_FHA_1 | 78 | 84 | PF00498 | 0.342 |
LIG_FHA_1 | 87 | 93 | PF00498 | 0.274 |
LIG_FHA_2 | 198 | 204 | PF00498 | 0.615 |
LIG_FHA_2 | 221 | 227 | PF00498 | 0.400 |
LIG_FHA_2 | 280 | 286 | PF00498 | 0.648 |
LIG_FHA_2 | 293 | 299 | PF00498 | 0.379 |
LIG_FHA_2 | 351 | 357 | PF00498 | 0.587 |
LIG_FHA_2 | 389 | 395 | PF00498 | 0.531 |
LIG_FHA_2 | 784 | 790 | PF00498 | 0.586 |
LIG_FHA_2 | 882 | 888 | PF00498 | 0.457 |
LIG_LIR_Apic_2 | 457 | 462 | PF02991 | 0.400 |
LIG_LIR_Apic_2 | 526 | 531 | PF02991 | 0.351 |
LIG_LIR_Gen_1 | 22 | 32 | PF02991 | 0.382 |
LIG_LIR_Gen_1 | 445 | 452 | PF02991 | 0.424 |
LIG_LIR_Gen_1 | 499 | 505 | PF02991 | 0.320 |
LIG_LIR_Gen_1 | 541 | 548 | PF02991 | 0.434 |
LIG_LIR_Gen_1 | 595 | 601 | PF02991 | 0.372 |
LIG_LIR_Gen_1 | 832 | 842 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 117 | 123 | PF02991 | 0.539 |
LIG_LIR_Nem_3 | 168 | 172 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 22 | 27 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 33 | 39 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 445 | 450 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 499 | 503 | PF02991 | 0.325 |
LIG_LIR_Nem_3 | 541 | 546 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 595 | 599 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 695 | 700 | PF02991 | 0.485 |
LIG_LIR_Nem_3 | 832 | 838 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 9 | 15 | PF02991 | 0.329 |
LIG_LYPXL_S_1 | 696 | 700 | PF13949 | 0.384 |
LIG_LYPXL_yS_3 | 169 | 172 | PF13949 | 0.441 |
LIG_PAM2_1 | 25 | 37 | PF00658 | 0.325 |
LIG_Pex14_1 | 866 | 870 | PF04695 | 0.325 |
LIG_Pex14_2 | 39 | 43 | PF04695 | 0.407 |
LIG_Pex14_2 | 440 | 444 | PF04695 | 0.377 |
LIG_Pex14_2 | 862 | 866 | PF04695 | 0.331 |
LIG_Rb_LxCxE_1 | 295 | 314 | PF01857 | 0.542 |
LIG_REV1ctd_RIR_1 | 697 | 706 | PF16727 | 0.486 |
LIG_RPA_C_Fungi | 666 | 678 | PF08784 | 0.578 |
LIG_SH2_CRK | 34 | 38 | PF00017 | 0.397 |
LIG_SH2_CRK | 372 | 376 | PF00017 | 0.347 |
LIG_SH2_CRK | 500 | 504 | PF00017 | 0.310 |
LIG_SH2_GRB2like | 372 | 375 | PF00017 | 0.348 |
LIG_SH2_GRB2like | 396 | 399 | PF00017 | 0.461 |
LIG_SH2_NCK_1 | 372 | 376 | PF00017 | 0.370 |
LIG_SH2_NCK_1 | 845 | 849 | PF00017 | 0.444 |
LIG_SH2_SRC | 372 | 375 | PF00017 | 0.372 |
LIG_SH2_SRC | 543 | 546 | PF00017 | 0.433 |
LIG_SH2_SRC | 561 | 564 | PF00017 | 0.292 |
LIG_SH2_SRC | 829 | 832 | PF00017 | 0.469 |
LIG_SH2_STAP1 | 139 | 143 | PF00017 | 0.376 |
LIG_SH2_STAP1 | 261 | 265 | PF00017 | 0.421 |
LIG_SH2_STAP1 | 500 | 504 | PF00017 | 0.310 |
LIG_SH2_STAP1 | 543 | 547 | PF00017 | 0.475 |
LIG_SH2_STAT3 | 252 | 255 | PF00017 | 0.344 |
LIG_SH2_STAT3 | 458 | 461 | PF00017 | 0.349 |
LIG_SH2_STAT5 | 139 | 142 | PF00017 | 0.374 |
LIG_SH2_STAT5 | 396 | 399 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 458 | 461 | PF00017 | 0.349 |
LIG_SH2_STAT5 | 689 | 692 | PF00017 | 0.414 |
LIG_SH2_STAT5 | 829 | 832 | PF00017 | 0.483 |
LIG_SH3_3 | 109 | 115 | PF00018 | 0.461 |
LIG_SH3_3 | 272 | 278 | PF00018 | 0.397 |
LIG_SH3_3 | 374 | 380 | PF00018 | 0.449 |
LIG_SH3_3 | 4 | 10 | PF00018 | 0.369 |
LIG_SH3_3 | 637 | 643 | PF00018 | 0.700 |
LIG_SUMO_SIM_anti_2 | 131 | 136 | PF11976 | 0.423 |
LIG_SUMO_SIM_anti_2 | 176 | 182 | PF11976 | 0.356 |
LIG_SUMO_SIM_anti_2 | 202 | 211 | PF11976 | 0.447 |
LIG_SUMO_SIM_anti_2 | 501 | 507 | PF11976 | 0.317 |
LIG_SUMO_SIM_anti_2 | 595 | 601 | PF11976 | 0.439 |
LIG_SUMO_SIM_anti_2 | 776 | 784 | PF11976 | 0.436 |
LIG_SUMO_SIM_par_1 | 179 | 185 | PF11976 | 0.413 |
LIG_SUMO_SIM_par_1 | 501 | 507 | PF11976 | 0.256 |
LIG_TRAF2_1 | 200 | 203 | PF00917 | 0.673 |
LIG_TRAF2_1 | 560 | 563 | PF00917 | 0.462 |
LIG_TYR_ITIM | 32 | 37 | PF00017 | 0.345 |
LIG_UBA3_1 | 532 | 538 | PF00899 | 0.414 |
LIG_WRC_WIRS_1 | 609 | 614 | PF05994 | 0.415 |
MOD_CDK_SPxK_1 | 568 | 574 | PF00069 | 0.470 |
MOD_CDK_SPxxK_3 | 649 | 656 | PF00069 | 0.603 |
MOD_CDK_SPxxK_3 | 804 | 811 | PF00069 | 0.542 |
MOD_CK1_1 | 211 | 217 | PF00069 | 0.548 |
MOD_CK1_1 | 220 | 226 | PF00069 | 0.473 |
MOD_CK1_1 | 284 | 290 | PF00069 | 0.661 |
MOD_CK1_1 | 311 | 317 | PF00069 | 0.440 |
MOD_CK1_1 | 472 | 478 | PF00069 | 0.359 |
MOD_CK1_1 | 496 | 502 | PF00069 | 0.359 |
MOD_CK1_1 | 66 | 72 | PF00069 | 0.616 |
MOD_CK1_1 | 762 | 768 | PF00069 | 0.439 |
MOD_CK1_1 | 804 | 810 | PF00069 | 0.733 |
MOD_CK1_1 | 822 | 828 | PF00069 | 0.543 |
MOD_CK1_1 | 84 | 90 | PF00069 | 0.227 |
MOD_CK1_1 | 846 | 852 | PF00069 | 0.522 |
MOD_CK2_1 | 19 | 25 | PF00069 | 0.351 |
MOD_CK2_1 | 197 | 203 | PF00069 | 0.532 |
MOD_CK2_1 | 220 | 226 | PF00069 | 0.460 |
MOD_CK2_1 | 292 | 298 | PF00069 | 0.467 |
MOD_CK2_1 | 783 | 789 | PF00069 | 0.580 |
MOD_CK2_1 | 794 | 800 | PF00069 | 0.682 |
MOD_CK2_1 | 866 | 872 | PF00069 | 0.451 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.594 |
MOD_GlcNHglycan | 175 | 178 | PF01048 | 0.441 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.435 |
MOD_GlcNHglycan | 269 | 272 | PF01048 | 0.581 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.549 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.562 |
MOD_GlcNHglycan | 424 | 427 | PF01048 | 0.529 |
MOD_GlcNHglycan | 471 | 474 | PF01048 | 0.428 |
MOD_GlcNHglycan | 557 | 560 | PF01048 | 0.418 |
MOD_GlcNHglycan | 631 | 634 | PF01048 | 0.696 |
MOD_GlcNHglycan | 649 | 652 | PF01048 | 0.616 |
MOD_GlcNHglycan | 728 | 731 | PF01048 | 0.566 |
MOD_GlcNHglycan | 740 | 743 | PF01048 | 0.618 |
MOD_GlcNHglycan | 753 | 756 | PF01048 | 0.682 |
MOD_GlcNHglycan | 849 | 852 | PF01048 | 0.500 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.513 |
MOD_GSK3_1 | 202 | 209 | PF00069 | 0.420 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.500 |
MOD_GSK3_1 | 384 | 391 | PF00069 | 0.414 |
MOD_GSK3_1 | 489 | 496 | PF00069 | 0.327 |
MOD_GSK3_1 | 647 | 654 | PF00069 | 0.746 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.293 |
MOD_GSK3_1 | 773 | 780 | PF00069 | 0.433 |
MOD_GSK3_1 | 843 | 850 | PF00069 | 0.444 |
MOD_LATS_1 | 195 | 201 | PF00433 | 0.480 |
MOD_N-GLC_1 | 285 | 290 | PF02516 | 0.485 |
MOD_N-GLC_1 | 342 | 347 | PF02516 | 0.518 |
MOD_N-GLC_1 | 373 | 378 | PF02516 | 0.357 |
MOD_N-GLC_1 | 442 | 447 | PF02516 | 0.382 |
MOD_N-GLC_1 | 751 | 756 | PF02516 | 0.697 |
MOD_N-GLC_1 | 804 | 809 | PF02516 | 0.705 |
MOD_N-GLC_2 | 217 | 219 | PF02516 | 0.402 |
MOD_N-GLC_2 | 465 | 467 | PF02516 | 0.325 |
MOD_NEK2_1 | 292 | 297 | PF00069 | 0.376 |
MOD_NEK2_1 | 316 | 321 | PF00069 | 0.605 |
MOD_NEK2_1 | 323 | 328 | PF00069 | 0.770 |
MOD_NEK2_1 | 41 | 46 | PF00069 | 0.356 |
MOD_NEK2_1 | 431 | 436 | PF00069 | 0.400 |
MOD_NEK2_1 | 504 | 509 | PF00069 | 0.324 |
MOD_NEK2_1 | 510 | 515 | PF00069 | 0.397 |
MOD_NEK2_1 | 735 | 740 | PF00069 | 0.475 |
MOD_NEK2_1 | 801 | 806 | PF00069 | 0.758 |
MOD_PK_1 | 128 | 134 | PF00069 | 0.387 |
MOD_PKA_1 | 197 | 203 | PF00069 | 0.510 |
MOD_PKA_1 | 656 | 662 | PF00069 | 0.620 |
MOD_PKA_2 | 349 | 355 | PF00069 | 0.537 |
MOD_PKA_2 | 66 | 72 | PF00069 | 0.520 |
MOD_PKA_2 | 681 | 687 | PF00069 | 0.461 |
MOD_PKA_2 | 866 | 872 | PF00069 | 0.398 |
MOD_PKB_1 | 664 | 672 | PF00069 | 0.785 |
MOD_Plk_1 | 202 | 208 | PF00069 | 0.441 |
MOD_Plk_1 | 257 | 263 | PF00069 | 0.313 |
MOD_Plk_1 | 342 | 348 | PF00069 | 0.547 |
MOD_Plk_1 | 373 | 379 | PF00069 | 0.356 |
MOD_Plk_1 | 431 | 437 | PF00069 | 0.411 |
MOD_Plk_1 | 442 | 448 | PF00069 | 0.415 |
MOD_Plk_2-3 | 373 | 379 | PF00069 | 0.356 |
MOD_Plk_4 | 19 | 25 | PF00069 | 0.449 |
MOD_Plk_4 | 202 | 208 | PF00069 | 0.635 |
MOD_Plk_4 | 472 | 478 | PF00069 | 0.417 |
MOD_Plk_4 | 489 | 495 | PF00069 | 0.302 |
MOD_Plk_4 | 595 | 601 | PF00069 | 0.370 |
MOD_Plk_4 | 673 | 679 | PF00069 | 0.574 |
MOD_Plk_4 | 692 | 698 | PF00069 | 0.386 |
MOD_Plk_4 | 777 | 783 | PF00069 | 0.388 |
MOD_Plk_4 | 86 | 92 | PF00069 | 0.299 |
MOD_Plk_4 | 866 | 872 | PF00069 | 0.375 |
MOD_ProDKin_1 | 243 | 249 | PF00069 | 0.378 |
MOD_ProDKin_1 | 308 | 314 | PF00069 | 0.593 |
MOD_ProDKin_1 | 407 | 413 | PF00069 | 0.499 |
MOD_ProDKin_1 | 568 | 574 | PF00069 | 0.718 |
MOD_ProDKin_1 | 639 | 645 | PF00069 | 0.701 |
MOD_ProDKin_1 | 649 | 655 | PF00069 | 0.718 |
MOD_ProDKin_1 | 804 | 810 | PF00069 | 0.688 |
MOD_ProDKin_1 | 881 | 887 | PF00069 | 0.476 |
MOD_SUMO_for_1 | 548 | 551 | PF00179 | 0.366 |
MOD_SUMO_rev_2 | 161 | 165 | PF00179 | 0.473 |
MOD_SUMO_rev_2 | 418 | 423 | PF00179 | 0.513 |
MOD_SUMO_rev_2 | 797 | 804 | PF00179 | 0.512 |
TRG_DiLeu_BaEn_1 | 202 | 207 | PF01217 | 0.389 |
TRG_DiLeu_BaEn_1 | 774 | 779 | PF01217 | 0.407 |
TRG_DiLeu_BaEn_3 | 680 | 686 | PF01217 | 0.429 |
TRG_DiLeu_BaEn_4 | 419 | 425 | PF01217 | 0.455 |
TRG_DiLeu_BaLyEn_6 | 141 | 146 | PF01217 | 0.333 |
TRG_DiLeu_BaLyEn_6 | 70 | 75 | PF01217 | 0.530 |
TRG_DiLeu_BaLyEn_6 | 836 | 841 | PF01217 | 0.372 |
TRG_ENDOCYTIC_2 | 139 | 142 | PF00928 | 0.426 |
TRG_ENDOCYTIC_2 | 169 | 172 | PF00928 | 0.328 |
TRG_ENDOCYTIC_2 | 20 | 23 | PF00928 | 0.520 |
TRG_ENDOCYTIC_2 | 34 | 37 | PF00928 | 0.287 |
TRG_ENDOCYTIC_2 | 372 | 375 | PF00928 | 0.348 |
TRG_ENDOCYTIC_2 | 447 | 450 | PF00928 | 0.459 |
TRG_ENDOCYTIC_2 | 486 | 489 | PF00928 | 0.399 |
TRG_ENDOCYTIC_2 | 500 | 503 | PF00928 | 0.353 |
TRG_ENDOCYTIC_2 | 543 | 546 | PF00928 | 0.433 |
TRG_ENDOCYTIC_2 | 620 | 623 | PF00928 | 0.563 |
TRG_ENDOCYTIC_2 | 697 | 700 | PF00928 | 0.435 |
TRG_ER_diArg_1 | 149 | 151 | PF00400 | 0.384 |
TRG_ER_diArg_1 | 2 | 5 | PF00400 | 0.421 |
TRG_ER_diArg_1 | 452 | 454 | PF00400 | 0.457 |
TRG_ER_diArg_1 | 486 | 488 | PF00400 | 0.496 |
TRG_ER_diArg_1 | 514 | 516 | PF00400 | 0.432 |
TRG_ER_diArg_1 | 586 | 589 | PF00400 | 0.437 |
TRG_ER_diArg_1 | 661 | 664 | PF00400 | 0.633 |
TRG_ER_diArg_1 | 71 | 73 | PF00400 | 0.560 |
TRG_ER_diArg_1 | 791 | 794 | PF00400 | 0.477 |
TRG_NES_CRM1_1 | 173 | 185 | PF08389 | 0.396 |
TRG_Pf-PMV_PEXEL_1 | 144 | 148 | PF00026 | 0.282 |
TRG_Pf-PMV_PEXEL_1 | 225 | 230 | PF00026 | 0.493 |
TRG_Pf-PMV_PEXEL_1 | 4 | 9 | PF00026 | 0.379 |
TRG_Pf-PMV_PEXEL_1 | 514 | 518 | PF00026 | 0.457 |
TRG_Pf-PMV_PEXEL_1 | 603 | 607 | PF00026 | 0.499 |
TRG_Pf-PMV_PEXEL_1 | 839 | 843 | PF00026 | 0.382 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IJE4 | Leptomonas seymouri | 53% | 97% |
A0A1X0NK05 | Trypanosomatidae | 35% | 100% |
A0A3Q8ISV5 | Leishmania donovani | 93% | 100% |
A0A422NPF9 | Trypanosoma rangeli | 36% | 100% |
A4HJQ7 | Leishmania braziliensis | 76% | 98% |
A4I774 | Leishmania infantum | 93% | 100% |
E9B268 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
V5D1X6 | Trypanosoma cruzi | 36% | 100% |