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:0005634 | nucleus | 5 | 2 |
GO:0005730 | nucleolus | 5 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043228 | non-membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4Q1P5
Term | Name | Level | Count |
---|---|---|---|
GO:0000956 | nuclear-transcribed mRNA catabolic process | 7 | 2 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006401 | RNA catabolic process | 5 | 2 |
GO:0006402 | mRNA catabolic process | 6 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009056 | catabolic process | 2 | 2 |
GO:0009057 | macromolecule catabolic process | 4 | 2 |
GO:0009892 | negative regulation of metabolic process | 4 | 2 |
GO:0009987 | cellular process | 1 | 12 |
GO:0010468 | regulation of gene expression | 5 | 2 |
GO:0010605 | negative regulation of macromolecule metabolic process | 5 | 2 |
GO:0010629 | negative regulation of gene expression | 6 | 2 |
GO:0016070 | RNA metabolic process | 5 | 12 |
GO:0016071 | mRNA metabolic process | 6 | 2 |
GO:0019222 | regulation of metabolic process | 3 | 2 |
GO:0019439 | aromatic compound catabolic process | 4 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0034655 | nucleobase-containing compound catabolic process | 4 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044248 | cellular catabolic process | 3 | 2 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 2 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 2 |
GO:0044270 | cellular nitrogen compound catabolic process | 4 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0046700 | heterocycle catabolic process | 4 | 2 |
GO:0048519 | negative regulation of biological process | 3 | 2 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0090304 | nucleic acid metabolic process | 4 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
GO:1901361 | organic cyclic compound catabolic process | 4 | 2 |
GO:1901575 | organic substance catabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003723 | RNA binding | 4 | 2 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004518 | nuclease activity | 4 | 12 |
GO:0004527 | exonuclease activity | 5 | 12 |
GO:0004532 | RNA exonuclease activity | 5 | 2 |
GO:0004534 | 5'-3' RNA exonuclease activity | 7 | 2 |
GO:0004540 | RNA nuclease activity | 4 | 2 |
GO:0005488 | binding | 1 | 12 |
GO:0008409 | 5'-3' exonuclease activity | 6 | 2 |
GO:0016787 | hydrolase activity | 2 | 12 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 12 |
GO:0016796 | exonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 5'-phosphomonoesters | 6 | 2 |
GO:0016896 | RNA exonuclease activity, producing 5'-phosphomonoesters | 6 | 2 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 2 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 2 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 16 | 20 | PF00656 | 0.515 |
CLV_C14_Caspase3-7 | 24 | 28 | PF00656 | 0.482 |
CLV_C14_Caspase3-7 | 407 | 411 | PF00656 | 0.523 |
CLV_C14_Caspase3-7 | 441 | 445 | PF00656 | 0.458 |
CLV_NRD_NRD_1 | 115 | 117 | PF00675 | 0.245 |
CLV_NRD_NRD_1 | 419 | 421 | PF00675 | 0.331 |
CLV_NRD_NRD_1 | 741 | 743 | PF00675 | 0.741 |
CLV_NRD_NRD_1 | 758 | 760 | PF00675 | 0.454 |
CLV_NRD_NRD_1 | 773 | 775 | PF00675 | 0.667 |
CLV_NRD_NRD_1 | 791 | 793 | PF00675 | 0.720 |
CLV_NRD_NRD_1 | 822 | 824 | PF00675 | 0.707 |
CLV_NRD_NRD_1 | 862 | 864 | PF00675 | 0.777 |
CLV_PCSK_FUR_1 | 113 | 117 | PF00082 | 0.245 |
CLV_PCSK_FUR_1 | 771 | 775 | PF00082 | 0.778 |
CLV_PCSK_KEX2_1 | 115 | 117 | PF00082 | 0.245 |
CLV_PCSK_KEX2_1 | 730 | 732 | PF00082 | 0.770 |
CLV_PCSK_KEX2_1 | 743 | 745 | PF00082 | 0.501 |
CLV_PCSK_KEX2_1 | 758 | 760 | PF00082 | 0.558 |
CLV_PCSK_KEX2_1 | 773 | 775 | PF00082 | 0.601 |
CLV_PCSK_KEX2_1 | 790 | 792 | PF00082 | 0.679 |
CLV_PCSK_KEX2_1 | 822 | 824 | PF00082 | 0.731 |
CLV_PCSK_KEX2_1 | 836 | 838 | PF00082 | 0.737 |
CLV_PCSK_KEX2_1 | 862 | 864 | PF00082 | 0.761 |
CLV_PCSK_PC1ET2_1 | 730 | 732 | PF00082 | 0.791 |
CLV_PCSK_PC1ET2_1 | 743 | 745 | PF00082 | 0.505 |
CLV_PCSK_PC1ET2_1 | 758 | 760 | PF00082 | 0.597 |
CLV_PCSK_PC1ET2_1 | 836 | 838 | PF00082 | 0.746 |
CLV_PCSK_SKI1_1 | 166 | 170 | PF00082 | 0.331 |
CLV_PCSK_SKI1_1 | 186 | 190 | PF00082 | 0.303 |
CLV_PCSK_SKI1_1 | 459 | 463 | PF00082 | 0.291 |
CLV_PCSK_SKI1_1 | 553 | 557 | PF00082 | 0.289 |
CLV_PCSK_SKI1_1 | 707 | 711 | PF00082 | 0.473 |
CLV_PCSK_SKI1_1 | 862 | 866 | PF00082 | 0.733 |
DEG_SPOP_SBC_1 | 801 | 805 | PF00917 | 0.711 |
DEG_SPOP_SBC_1 | 855 | 859 | PF00917 | 0.752 |
DOC_CDC14_PxL_1 | 497 | 505 | PF14671 | 0.456 |
DOC_CDC14_PxL_1 | 530 | 538 | PF14671 | 0.470 |
DOC_CKS1_1 | 156 | 161 | PF01111 | 0.445 |
DOC_CYCLIN_RxL_1 | 88 | 101 | PF00134 | 0.445 |
DOC_CYCLIN_yCln2_LP_2 | 637 | 643 | PF00134 | 0.579 |
DOC_MAPK_gen_1 | 315 | 323 | PF00069 | 0.456 |
DOC_MAPK_gen_1 | 591 | 599 | PF00069 | 0.550 |
DOC_MAPK_gen_1 | 88 | 98 | PF00069 | 0.445 |
DOC_MAPK_MEF2A_6 | 78 | 87 | PF00069 | 0.469 |
DOC_MAPK_MEF2A_6 | 91 | 100 | PF00069 | 0.405 |
DOC_MAPK_NFAT4_5 | 93 | 101 | PF00069 | 0.445 |
DOC_PP2B_LxvP_1 | 579 | 582 | PF13499 | 0.456 |
DOC_PP2B_LxvP_1 | 637 | 640 | PF13499 | 0.596 |
DOC_SPAK_OSR1_1 | 425 | 429 | PF12202 | 0.383 |
DOC_USP7_MATH_1 | 310 | 314 | PF00917 | 0.531 |
DOC_USP7_MATH_1 | 389 | 393 | PF00917 | 0.548 |
DOC_USP7_MATH_1 | 400 | 404 | PF00917 | 0.501 |
DOC_USP7_MATH_1 | 461 | 465 | PF00917 | 0.517 |
DOC_USP7_MATH_1 | 626 | 630 | PF00917 | 0.623 |
DOC_USP7_MATH_1 | 643 | 647 | PF00917 | 0.452 |
DOC_USP7_MATH_1 | 723 | 727 | PF00917 | 0.700 |
DOC_USP7_MATH_1 | 801 | 805 | PF00917 | 0.716 |
DOC_USP7_MATH_1 | 821 | 825 | PF00917 | 0.493 |
DOC_USP7_MATH_1 | 854 | 858 | PF00917 | 0.678 |
DOC_USP7_MATH_1 | 864 | 868 | PF00917 | 0.690 |
DOC_USP7_MATH_1 | 874 | 878 | PF00917 | 0.587 |
DOC_USP7_UBL2_3 | 357 | 361 | PF12436 | 0.503 |
DOC_USP7_UBL2_3 | 373 | 377 | PF12436 | 0.376 |
DOC_USP7_UBL2_3 | 730 | 734 | PF12436 | 0.788 |
DOC_USP7_UBL2_3 | 832 | 836 | PF12436 | 0.765 |
DOC_WW_Pin1_4 | 155 | 160 | PF00397 | 0.445 |
DOC_WW_Pin1_4 | 734 | 739 | PF00397 | 0.757 |
LIG_14-3-3_CanoR_1 | 186 | 191 | PF00244 | 0.506 |
LIG_14-3-3_CanoR_1 | 210 | 216 | PF00244 | 0.496 |
LIG_14-3-3_CanoR_1 | 249 | 258 | PF00244 | 0.536 |
LIG_14-3-3_CanoR_1 | 383 | 391 | PF00244 | 0.505 |
LIG_14-3-3_CanoR_1 | 518 | 522 | PF00244 | 0.504 |
LIG_14-3-3_CanoR_1 | 535 | 539 | PF00244 | 0.354 |
LIG_BRCT_BRCA1_1 | 113 | 117 | PF00533 | 0.445 |
LIG_BRCT_BRCA1_1 | 159 | 163 | PF00533 | 0.445 |
LIG_Clathr_ClatBox_1 | 596 | 600 | PF01394 | 0.554 |
LIG_deltaCOP1_diTrp_1 | 181 | 192 | PF00928 | 0.456 |
LIG_deltaCOP1_diTrp_1 | 492 | 495 | PF00928 | 0.456 |
LIG_EH1_1 | 523 | 531 | PF00400 | 0.445 |
LIG_eIF4E_1 | 497 | 503 | PF01652 | 0.506 |
LIG_FHA_1 | 220 | 226 | PF00498 | 0.446 |
LIG_FHA_1 | 314 | 320 | PF00498 | 0.445 |
LIG_FHA_1 | 422 | 428 | PF00498 | 0.514 |
LIG_FHA_1 | 508 | 514 | PF00498 | 0.463 |
LIG_FHA_1 | 61 | 67 | PF00498 | 0.445 |
LIG_FHA_1 | 649 | 655 | PF00498 | 0.550 |
LIG_FHA_1 | 868 | 874 | PF00498 | 0.575 |
LIG_FHA_2 | 268 | 274 | PF00498 | 0.445 |
LIG_FHA_2 | 383 | 389 | PF00498 | 0.562 |
LIG_FHA_2 | 439 | 445 | PF00498 | 0.510 |
LIG_FHA_2 | 700 | 706 | PF00498 | 0.547 |
LIG_KLC1_Yacidic_2 | 46 | 51 | PF13176 | 0.456 |
LIG_LIR_Apic_2 | 139 | 144 | PF02991 | 0.533 |
LIG_LIR_Apic_2 | 490 | 496 | PF02991 | 0.445 |
LIG_LIR_Gen_1 | 278 | 287 | PF02991 | 0.405 |
LIG_LIR_Gen_1 | 292 | 301 | PF02991 | 0.417 |
LIG_LIR_Gen_1 | 341 | 352 | PF02991 | 0.475 |
LIG_LIR_Gen_1 | 44 | 52 | PF02991 | 0.461 |
LIG_LIR_Gen_1 | 73 | 83 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 182 | 188 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 278 | 282 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 292 | 297 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 341 | 347 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 363 | 369 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 44 | 48 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 490 | 494 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 574 | 578 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 705 | 709 | PF02991 | 0.528 |
LIG_LIR_Nem_3 | 77 | 83 | PF02991 | 0.458 |
LIG_LYPXL_S_1 | 559 | 563 | PF13949 | 0.331 |
LIG_LYPXL_yS_3 | 560 | 563 | PF13949 | 0.531 |
LIG_Pex14_1 | 479 | 483 | PF04695 | 0.445 |
LIG_Pex14_1 | 491 | 495 | PF04695 | 0.445 |
LIG_Pex14_2 | 296 | 300 | PF04695 | 0.445 |
LIG_Pex14_2 | 350 | 354 | PF04695 | 0.445 |
LIG_Pex14_2 | 603 | 607 | PF04695 | 0.503 |
LIG_Pex14_2 | 76 | 80 | PF04695 | 0.456 |
LIG_Rb_LxCxE_1 | 463 | 485 | PF01857 | 0.486 |
LIG_Rb_LxCxE_1 | 605 | 624 | PF01857 | 0.435 |
LIG_SH2_CRK | 141 | 145 | PF00017 | 0.550 |
LIG_SH2_CRK | 367 | 371 | PF00017 | 0.464 |
LIG_SH2_CRK | 499 | 503 | PF00017 | 0.445 |
LIG_SH2_CRK | 575 | 579 | PF00017 | 0.445 |
LIG_SH2_CRK | 706 | 710 | PF00017 | 0.488 |
LIG_SH2_GRB2like | 265 | 268 | PF00017 | 0.409 |
LIG_SH2_GRB2like | 45 | 48 | PF00017 | 0.506 |
LIG_SH2_STAP1 | 45 | 49 | PF00017 | 0.506 |
LIG_SH2_STAP1 | 661 | 665 | PF00017 | 0.495 |
LIG_SH2_STAT3 | 335 | 338 | PF00017 | 0.523 |
LIG_SH2_STAT5 | 174 | 177 | PF00017 | 0.531 |
LIG_SH2_STAT5 | 208 | 211 | PF00017 | 0.445 |
LIG_SH2_STAT5 | 265 | 268 | PF00017 | 0.324 |
LIG_SH2_STAT5 | 326 | 329 | PF00017 | 0.445 |
LIG_SH2_STAT5 | 335 | 338 | PF00017 | 0.445 |
LIG_SH2_STAT5 | 437 | 440 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 473 | 476 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 484 | 487 | PF00017 | 0.433 |
LIG_SH2_STAT5 | 49 | 52 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 494 | 497 | PF00017 | 0.445 |
LIG_SH2_STAT5 | 609 | 612 | PF00017 | 0.446 |
LIG_SH3_3 | 153 | 159 | PF00018 | 0.440 |
LIG_SH3_3 | 304 | 310 | PF00018 | 0.445 |
LIG_SH3_3 | 519 | 525 | PF00018 | 0.445 |
LIG_SH3_3 | 546 | 552 | PF00018 | 0.445 |
LIG_SH3_3 | 637 | 643 | PF00018 | 0.528 |
LIG_SH3_3 | 86 | 92 | PF00018 | 0.470 |
LIG_SH3_3 | 870 | 876 | PF00018 | 0.613 |
LIG_SH3_5 | 216 | 220 | PF00018 | 0.550 |
LIG_SUMO_SIM_anti_2 | 81 | 87 | PF11976 | 0.506 |
LIG_SUMO_SIM_par_1 | 310 | 316 | PF11976 | 0.435 |
LIG_SUMO_SIM_par_1 | 562 | 567 | PF11976 | 0.527 |
LIG_SUMO_SIM_par_1 | 595 | 602 | PF11976 | 0.578 |
LIG_TYR_ITIM | 342 | 347 | PF00017 | 0.470 |
LIG_UBA3_1 | 349 | 357 | PF00899 | 0.550 |
LIG_UBA3_1 | 359 | 364 | PF00899 | 0.432 |
LIG_UBA3_1 | 412 | 421 | PF00899 | 0.463 |
LIG_WW_3 | 737 | 741 | PF00397 | 0.661 |
MOD_CDC14_SPxK_1 | 737 | 740 | PF00782 | 0.700 |
MOD_CDK_SPxK_1 | 734 | 740 | PF00069 | 0.708 |
MOD_CK1_1 | 136 | 142 | PF00069 | 0.431 |
MOD_CK1_1 | 313 | 319 | PF00069 | 0.445 |
MOD_CK1_1 | 38 | 44 | PF00069 | 0.480 |
MOD_CK1_1 | 647 | 653 | PF00069 | 0.545 |
MOD_CK1_1 | 726 | 732 | PF00069 | 0.757 |
MOD_CK1_1 | 802 | 808 | PF00069 | 0.713 |
MOD_CK1_1 | 845 | 851 | PF00069 | 0.736 |
MOD_CK1_1 | 857 | 863 | PF00069 | 0.699 |
MOD_CK1_1 | 867 | 873 | PF00069 | 0.796 |
MOD_CK2_1 | 236 | 242 | PF00069 | 0.445 |
MOD_CK2_1 | 267 | 273 | PF00069 | 0.446 |
MOD_CK2_1 | 382 | 388 | PF00069 | 0.530 |
MOD_CK2_1 | 776 | 782 | PF00069 | 0.757 |
MOD_CK2_1 | 845 | 851 | PF00069 | 0.723 |
MOD_Cter_Amidation | 833 | 836 | PF01082 | 0.808 |
MOD_GlcNHglycan | 40 | 43 | PF01048 | 0.298 |
MOD_GlcNHglycan | 417 | 420 | PF01048 | 0.323 |
MOD_GlcNHglycan | 519 | 522 | PF01048 | 0.330 |
MOD_GlcNHglycan | 628 | 631 | PF01048 | 0.623 |
MOD_GlcNHglycan | 814 | 817 | PF01048 | 0.645 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.470 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.506 |
MOD_GSK3_1 | 643 | 650 | PF00069 | 0.553 |
MOD_GSK3_1 | 786 | 793 | PF00069 | 0.745 |
MOD_GSK3_1 | 795 | 802 | PF00069 | 0.720 |
MOD_GSK3_1 | 808 | 815 | PF00069 | 0.570 |
MOD_GSK3_1 | 836 | 843 | PF00069 | 0.724 |
MOD_GSK3_1 | 854 | 861 | PF00069 | 0.631 |
MOD_GSK3_1 | 879 | 886 | PF00069 | 0.770 |
MOD_N-GLC_1 | 220 | 225 | PF02516 | 0.307 |
MOD_N-GLC_1 | 266 | 271 | PF02516 | 0.424 |
MOD_N-GLC_1 | 352 | 357 | PF02516 | 0.336 |
MOD_N-GLC_1 | 571 | 576 | PF02516 | 0.298 |
MOD_N-GLC_1 | 714 | 719 | PF02516 | 0.713 |
MOD_N-GLC_2 | 131 | 133 | PF02516 | 0.306 |
MOD_N-GLC_2 | 797 | 799 | PF02516 | 0.542 |
MOD_NEK2_1 | 236 | 241 | PF00069 | 0.455 |
MOD_NEK2_1 | 252 | 257 | PF00069 | 0.414 |
MOD_NEK2_1 | 266 | 271 | PF00069 | 0.301 |
MOD_NEK2_1 | 352 | 357 | PF00069 | 0.498 |
MOD_NEK2_1 | 415 | 420 | PF00069 | 0.444 |
MOD_NEK2_1 | 433 | 438 | PF00069 | 0.387 |
MOD_NEK2_1 | 509 | 514 | PF00069 | 0.543 |
MOD_NEK2_1 | 517 | 522 | PF00069 | 0.514 |
MOD_NEK2_1 | 603 | 608 | PF00069 | 0.431 |
MOD_NEK2_1 | 678 | 683 | PF00069 | 0.515 |
MOD_NEK2_1 | 880 | 885 | PF00069 | 0.801 |
MOD_NEK2_2 | 310 | 315 | PF00069 | 0.445 |
MOD_NEK2_2 | 534 | 539 | PF00069 | 0.531 |
MOD_PIKK_1 | 211 | 217 | PF00454 | 0.506 |
MOD_PIKK_1 | 334 | 340 | PF00454 | 0.523 |
MOD_PIKK_1 | 461 | 467 | PF00454 | 0.426 |
MOD_PIKK_1 | 699 | 705 | PF00454 | 0.522 |
MOD_PIKK_1 | 836 | 842 | PF00454 | 0.771 |
MOD_PKA_1 | 760 | 766 | PF00069 | 0.779 |
MOD_PKA_1 | 790 | 796 | PF00069 | 0.771 |
MOD_PKA_1 | 822 | 828 | PF00069 | 0.759 |
MOD_PKA_1 | 835 | 841 | PF00069 | 0.750 |
MOD_PKA_2 | 382 | 388 | PF00069 | 0.562 |
MOD_PKA_2 | 517 | 523 | PF00069 | 0.504 |
MOD_PKA_2 | 534 | 540 | PF00069 | 0.354 |
MOD_PKA_2 | 760 | 766 | PF00069 | 0.773 |
MOD_PKA_2 | 790 | 796 | PF00069 | 0.706 |
MOD_PKA_2 | 805 | 811 | PF00069 | 0.658 |
MOD_PKA_2 | 821 | 827 | PF00069 | 0.748 |
MOD_PKA_2 | 836 | 842 | PF00069 | 0.567 |
MOD_PKA_2 | 845 | 851 | PF00069 | 0.721 |
MOD_PKA_2 | 867 | 873 | PF00069 | 0.720 |
MOD_PKA_2 | 874 | 880 | PF00069 | 0.754 |
MOD_PKB_1 | 759 | 767 | PF00069 | 0.795 |
MOD_PKB_1 | 774 | 782 | PF00069 | 0.780 |
MOD_Plk_1 | 220 | 226 | PF00069 | 0.506 |
MOD_Plk_1 | 266 | 272 | PF00069 | 0.383 |
MOD_Plk_1 | 421 | 427 | PF00069 | 0.527 |
MOD_Plk_1 | 438 | 444 | PF00069 | 0.430 |
MOD_Plk_1 | 571 | 577 | PF00069 | 0.498 |
MOD_Plk_1 | 611 | 617 | PF00069 | 0.396 |
MOD_Plk_4 | 133 | 139 | PF00069 | 0.383 |
MOD_Plk_4 | 186 | 192 | PF00069 | 0.550 |
MOD_Plk_4 | 394 | 400 | PF00069 | 0.533 |
MOD_Plk_4 | 551 | 557 | PF00069 | 0.445 |
MOD_Plk_4 | 603 | 609 | PF00069 | 0.381 |
MOD_ProDKin_1 | 155 | 161 | PF00069 | 0.445 |
MOD_ProDKin_1 | 734 | 740 | PF00069 | 0.757 |
MOD_SUMO_rev_2 | 200 | 206 | PF00179 | 0.439 |
MOD_SUMO_rev_2 | 547 | 555 | PF00179 | 0.506 |
MOD_SUMO_rev_2 | 845 | 850 | PF00179 | 0.617 |
MOD_SUMO_rev_2 | 867 | 873 | PF00179 | 0.556 |
TRG_DiLeu_BaEn_2 | 421 | 427 | PF01217 | 0.437 |
TRG_DiLeu_BaLyEn_6 | 498 | 503 | PF01217 | 0.445 |
TRG_ENDOCYTIC_2 | 265 | 268 | PF00928 | 0.324 |
TRG_ENDOCYTIC_2 | 344 | 347 | PF00928 | 0.465 |
TRG_ENDOCYTIC_2 | 366 | 369 | PF00928 | 0.461 |
TRG_ENDOCYTIC_2 | 45 | 48 | PF00928 | 0.464 |
TRG_ENDOCYTIC_2 | 49 | 52 | PF00928 | 0.448 |
TRG_ENDOCYTIC_2 | 499 | 502 | PF00928 | 0.453 |
TRG_ENDOCYTIC_2 | 560 | 563 | PF00928 | 0.495 |
TRG_ENDOCYTIC_2 | 575 | 578 | PF00928 | 0.366 |
TRG_ENDOCYTIC_2 | 706 | 709 | PF00928 | 0.490 |
TRG_ER_diArg_1 | 113 | 116 | PF00400 | 0.445 |
TRG_ER_diArg_1 | 144 | 147 | PF00400 | 0.484 |
TRG_ER_diArg_1 | 423 | 426 | PF00400 | 0.470 |
TRG_ER_diArg_1 | 739 | 742 | PF00400 | 0.786 |
TRG_ER_diArg_1 | 790 | 792 | PF00400 | 0.704 |
TRG_ER_diArg_1 | 827 | 830 | PF00400 | 0.601 |
TRG_NES_CRM1_1 | 504 | 516 | PF08389 | 0.503 |
TRG_NLS_Bipartite_1 | 730 | 746 | PF00514 | 0.803 |
TRG_NLS_Bipartite_1 | 822 | 839 | PF00514 | 0.765 |
TRG_NLS_MonoCore_2 | 757 | 762 | PF00514 | 0.703 |
TRG_NLS_MonoExtC_3 | 741 | 746 | PF00514 | 0.745 |
TRG_NLS_MonoExtN_4 | 739 | 746 | PF00514 | 0.751 |
TRG_NLS_MonoExtN_4 | 758 | 763 | PF00514 | 0.713 |
TRG_NLS_MonoExtN_4 | 832 | 839 | PF00514 | 0.719 |
TRG_Pf-PMV_PEXEL_1 | 177 | 181 | PF00026 | 0.286 |
TRG_Pf-PMV_PEXEL_1 | 210 | 215 | PF00026 | 0.245 |
TRG_Pf-PMV_PEXEL_1 | 594 | 598 | PF00026 | 0.350 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HYA8 | Leptomonas seymouri | 87% | 98% |
A0A0S4IWC0 | Bodo saltans | 55% | 100% |
A0A1X0P7T7 | Trypanosomatidae | 58% | 100% |
A0A3Q8IH53 | Leishmania donovani | 93% | 100% |
A0A3R7LZH3 | Trypanosoma rangeli | 63% | 100% |
A4HP43 | Leishmania braziliensis | 88% | 100% |
A4IDF0 | Leishmania infantum | 93% | 100% |
D0A327 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 56% | 100% |
E9ASV1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
Q5R4L5 | Pongo abelii | 32% | 94% |
Q60SG7 | Caenorhabditis briggsae | 31% | 92% |
Q9FQ02 | Arabidopsis thaliana | 33% | 88% |
Q9FQ03 | Arabidopsis thaliana | 32% | 88% |
Q9FQ04 | Arabidopsis thaliana | 35% | 95% |
Q9H0D6 | Homo sapiens | 32% | 94% |
Q9U299 | Caenorhabditis elegans | 31% | 92% |
Q9VM71 | Drosophila melanogaster | 34% | 99% |
V5DKX1 | Trypanosoma cruzi | 61% | 100% |