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 | 12 |
GO:0032991 | protein-containing complex | 1 | 12 |
GO:0042555 | MCM complex | 2 | 12 |
GO:0043226 | organelle | 2 | 12 |
GO:0043227 | membrane-bounded organelle | 3 | 12 |
GO:0043229 | intracellular organelle | 3 | 12 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
Related structures:
AlphaFold database: A0A3S5H7J9
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006259 | DNA metabolic process | 4 | 12 |
GO:0006270 | DNA replication initiation | 5 | 12 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0007049 | cell cycle | 2 | 11 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
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:0000724 | double-strand break repair via homologous recombination | 7 | 1 |
GO:0000725 | recombinational repair | 6 | 1 |
GO:0000727 | double-strand break repair via break-induced replication | 8 | 1 |
GO:0006260 | DNA replication | 5 | 1 |
GO:0006261 | DNA-templated DNA replication | 6 | 1 |
GO:0006268 | DNA unwinding involved in DNA replication | 9 | 1 |
GO:0006281 | DNA repair | 5 | 1 |
GO:0006302 | double-strand break repair | 6 | 1 |
GO:0006310 | DNA recombination | 5 | 1 |
GO:0006950 | response to stress | 2 | 1 |
GO:0006974 | DNA damage response | 4 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022402 | cell cycle process | 2 | 1 |
GO:0032392 | DNA geometric change | 7 | 1 |
GO:0032508 | DNA duplex unwinding | 8 | 1 |
GO:0033260 | nuclear DNA replication | 4 | 1 |
GO:0033554 | cellular response to stress | 3 | 1 |
GO:0044786 | cell cycle DNA replication | 3 | 1 |
GO:0050896 | response to stimulus | 1 | 1 |
GO:0051276 | chromosome organization | 5 | 1 |
GO:0051716 | cellular response to stimulus | 2 | 1 |
GO:0071103 | DNA conformation change | 6 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:1902969 | mitotic DNA replication | 4 | 1 |
GO:1903047 | mitotic cell cycle process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003677 | DNA binding | 4 | 12 |
GO:0003678 | DNA helicase activity | 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:0008094 | ATP-dependent activity, acting on DNA | 2 | 12 |
GO:0016787 | hydrolase activity | 2 | 12 |
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:0140097 | catalytic activity, acting on DNA | 3 | 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:0003697 | single-stranded DNA binding | 5 | 1 |
GO:0016462 | pyrophosphatase activity | 5 | 3 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 3 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 3 |
GO:0016887 | ATP hydrolysis activity | 7 | 3 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 344 | 348 | PF00656 | 0.446 |
CLV_C14_Caspase3-7 | 361 | 365 | PF00656 | 0.487 |
CLV_C14_Caspase3-7 | 722 | 726 | PF00656 | 0.602 |
CLV_NRD_NRD_1 | 299 | 301 | PF00675 | 0.527 |
CLV_NRD_NRD_1 | 352 | 354 | PF00675 | 0.497 |
CLV_NRD_NRD_1 | 386 | 388 | PF00675 | 0.309 |
CLV_NRD_NRD_1 | 558 | 560 | PF00675 | 0.250 |
CLV_NRD_NRD_1 | 784 | 786 | PF00675 | 0.385 |
CLV_PCSK_KEX2_1 | 299 | 301 | PF00082 | 0.527 |
CLV_PCSK_KEX2_1 | 386 | 388 | PF00082 | 0.308 |
CLV_PCSK_KEX2_1 | 557 | 559 | PF00082 | 0.238 |
CLV_PCSK_KEX2_1 | 784 | 786 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 153 | 157 | PF00082 | 0.464 |
CLV_PCSK_SKI1_1 | 304 | 308 | PF00082 | 0.676 |
CLV_PCSK_SKI1_1 | 353 | 357 | PF00082 | 0.517 |
CLV_PCSK_SKI1_1 | 360 | 364 | PF00082 | 0.584 |
CLV_PCSK_SKI1_1 | 393 | 397 | PF00082 | 0.259 |
CLV_PCSK_SKI1_1 | 428 | 432 | PF00082 | 0.269 |
CLV_PCSK_SKI1_1 | 625 | 629 | PF00082 | 0.271 |
CLV_PCSK_SKI1_1 | 832 | 836 | PF00082 | 0.324 |
CLV_Separin_Metazoa | 695 | 699 | PF03568 | 0.447 |
DEG_APCC_DBOX_1 | 573 | 581 | PF00400 | 0.459 |
DEG_APCC_DBOX_1 | 697 | 705 | PF00400 | 0.465 |
DEG_Kelch_Keap1_1 | 481 | 486 | PF01344 | 0.508 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.664 |
DEG_SCF_FBW7_1 | 627 | 632 | PF00400 | 0.533 |
DEG_SIAH_1 | 14 | 22 | PF03145 | 0.685 |
DOC_ANK_TNKS_1 | 276 | 283 | PF00023 | 0.552 |
DOC_CKS1_1 | 373 | 378 | PF01111 | 0.589 |
DOC_CYCLIN_RxL_1 | 828 | 838 | PF00134 | 0.533 |
DOC_MAPK_DCC_7 | 861 | 870 | PF00069 | 0.585 |
DOC_MAPK_gen_1 | 139 | 148 | PF00069 | 0.432 |
DOC_MAPK_gen_1 | 31 | 40 | PF00069 | 0.387 |
DOC_MAPK_gen_1 | 630 | 640 | PF00069 | 0.458 |
DOC_MAPK_gen_1 | 848 | 858 | PF00069 | 0.447 |
DOC_MAPK_HePTP_8 | 858 | 870 | PF00069 | 0.651 |
DOC_MAPK_MEF2A_6 | 139 | 148 | PF00069 | 0.432 |
DOC_MAPK_MEF2A_6 | 182 | 189 | PF00069 | 0.447 |
DOC_MAPK_MEF2A_6 | 31 | 40 | PF00069 | 0.442 |
DOC_MAPK_MEF2A_6 | 405 | 413 | PF00069 | 0.458 |
DOC_MAPK_MEF2A_6 | 432 | 439 | PF00069 | 0.459 |
DOC_MAPK_MEF2A_6 | 49 | 56 | PF00069 | 0.561 |
DOC_MAPK_MEF2A_6 | 574 | 582 | PF00069 | 0.459 |
DOC_MAPK_MEF2A_6 | 686 | 694 | PF00069 | 0.488 |
DOC_MAPK_MEF2A_6 | 851 | 860 | PF00069 | 0.447 |
DOC_MAPK_MEF2A_6 | 861 | 870 | PF00069 | 0.585 |
DOC_MAPK_NFAT4_5 | 410 | 418 | PF00069 | 0.447 |
DOC_MAPK_RevD_3 | 285 | 300 | PF00069 | 0.643 |
DOC_PP4_MxPP_1 | 1 | 4 | PF00568 | 0.709 |
DOC_USP7_MATH_1 | 394 | 398 | PF00917 | 0.533 |
DOC_USP7_MATH_1 | 540 | 544 | PF00917 | 0.438 |
DOC_USP7_MATH_1 | 57 | 61 | PF00917 | 0.653 |
DOC_USP7_MATH_1 | 570 | 574 | PF00917 | 0.447 |
DOC_USP7_MATH_1 | 68 | 72 | PF00917 | 0.582 |
DOC_USP7_MATH_1 | 735 | 739 | PF00917 | 0.740 |
DOC_USP7_MATH_1 | 756 | 760 | PF00917 | 0.694 |
DOC_USP7_MATH_1 | 773 | 777 | PF00917 | 0.714 |
DOC_USP7_UBL2_3 | 509 | 513 | PF12436 | 0.447 |
DOC_USP7_UBL2_3 | 531 | 535 | PF12436 | 0.447 |
DOC_USP7_UBL2_3 | 786 | 790 | PF12436 | 0.533 |
DOC_WW_Pin1_4 | 114 | 119 | PF00397 | 0.415 |
DOC_WW_Pin1_4 | 372 | 377 | PF00397 | 0.490 |
DOC_WW_Pin1_4 | 625 | 630 | PF00397 | 0.480 |
LIG_14-3-3_CanoR_1 | 161 | 165 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 177 | 185 | PF00244 | 0.416 |
LIG_14-3-3_CanoR_1 | 609 | 619 | PF00244 | 0.414 |
LIG_14-3-3_CanoR_1 | 622 | 628 | PF00244 | 0.434 |
LIG_14-3-3_CanoR_1 | 660 | 666 | PF00244 | 0.447 |
LIG_14-3-3_CanoR_1 | 671 | 679 | PF00244 | 0.447 |
LIG_14-3-3_CanoR_1 | 698 | 706 | PF00244 | 0.539 |
LIG_14-3-3_CanoR_1 | 736 | 745 | PF00244 | 0.768 |
LIG_14-3-3_CanoR_1 | 81 | 88 | PF00244 | 0.439 |
LIG_Actin_WH2_2 | 148 | 163 | PF00022 | 0.441 |
LIG_BIR_III_2 | 811 | 815 | PF00653 | 0.552 |
LIG_BIR_III_4 | 26 | 30 | PF00653 | 0.493 |
LIG_BIR_III_4 | 347 | 351 | PF00653 | 0.553 |
LIG_BRCT_BRCA1_1 | 144 | 148 | PF00533 | 0.423 |
LIG_Clathr_ClatBox_1 | 855 | 859 | PF01394 | 0.426 |
LIG_DLG_GKlike_1 | 387 | 395 | PF00625 | 0.522 |
LIG_FHA_1 | 176 | 182 | PF00498 | 0.447 |
LIG_FHA_1 | 195 | 201 | PF00498 | 0.447 |
LIG_FHA_1 | 257 | 263 | PF00498 | 0.467 |
LIG_FHA_1 | 321 | 327 | PF00498 | 0.613 |
LIG_FHA_1 | 354 | 360 | PF00498 | 0.541 |
LIG_FHA_1 | 394 | 400 | PF00498 | 0.456 |
LIG_FHA_1 | 473 | 479 | PF00498 | 0.456 |
LIG_FHA_1 | 524 | 530 | PF00498 | 0.447 |
LIG_FHA_1 | 540 | 546 | PF00498 | 0.447 |
LIG_FHA_1 | 566 | 572 | PF00498 | 0.447 |
LIG_FHA_1 | 626 | 632 | PF00498 | 0.464 |
LIG_FHA_1 | 660 | 666 | PF00498 | 0.447 |
LIG_FHA_1 | 674 | 680 | PF00498 | 0.488 |
LIG_FHA_1 | 819 | 825 | PF00498 | 0.512 |
LIG_FHA_1 | 88 | 94 | PF00498 | 0.382 |
LIG_FHA_2 | 342 | 348 | PF00498 | 0.421 |
LIG_FHA_2 | 373 | 379 | PF00498 | 0.481 |
LIG_FHA_2 | 422 | 428 | PF00498 | 0.533 |
LIG_FHA_2 | 611 | 617 | PF00498 | 0.515 |
LIG_FHA_2 | 686 | 692 | PF00498 | 0.513 |
LIG_FHA_2 | 705 | 711 | PF00498 | 0.486 |
LIG_FHA_2 | 717 | 723 | PF00498 | 0.608 |
LIG_FHA_2 | 813 | 819 | PF00498 | 0.508 |
LIG_GBD_Chelix_1 | 797 | 805 | PF00786 | 0.288 |
LIG_Integrin_RGD_1 | 432 | 434 | PF01839 | 0.247 |
LIG_LIR_Gen_1 | 110 | 120 | PF02991 | 0.368 |
LIG_LIR_Gen_1 | 145 | 155 | PF02991 | 0.465 |
LIG_LIR_Gen_1 | 238 | 244 | PF02991 | 0.456 |
LIG_LIR_Gen_1 | 505 | 512 | PF02991 | 0.447 |
LIG_LIR_Gen_1 | 573 | 582 | PF02991 | 0.447 |
LIG_LIR_Gen_1 | 792 | 803 | PF02991 | 0.488 |
LIG_LIR_Gen_1 | 838 | 849 | PF02991 | 0.448 |
LIG_LIR_Gen_1 | 97 | 106 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 110 | 116 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 145 | 151 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 238 | 242 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 576 | 582 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 614 | 620 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 792 | 798 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 838 | 844 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 97 | 101 | PF02991 | 0.396 |
LIG_NRBOX | 410 | 416 | PF00104 | 0.459 |
LIG_PCNA_yPIPBox_3 | 115 | 128 | PF02747 | 0.485 |
LIG_PCNA_yPIPBox_3 | 840 | 850 | PF02747 | 0.459 |
LIG_Pex14_2 | 575 | 579 | PF04695 | 0.447 |
LIG_SH2_GRB2like | 136 | 139 | PF00017 | 0.488 |
LIG_SH2_GRB2like | 841 | 844 | PF00017 | 0.459 |
LIG_SH2_NCK_1 | 208 | 212 | PF00017 | 0.459 |
LIG_SH2_PTP2 | 841 | 844 | PF00017 | 0.459 |
LIG_SH2_SRC | 869 | 872 | PF00017 | 0.618 |
LIG_SH2_STAP1 | 623 | 627 | PF00017 | 0.459 |
LIG_SH2_STAT3 | 823 | 826 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 208 | 211 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 463 | 466 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 620 | 623 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 74 | 77 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 794 | 797 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 823 | 826 | PF00017 | 0.528 |
LIG_SH2_STAT5 | 841 | 844 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 869 | 872 | PF00017 | 0.591 |
LIG_SH3_1 | 7 | 13 | PF00018 | 0.725 |
LIG_SH3_3 | 226 | 232 | PF00018 | 0.459 |
LIG_SH3_3 | 268 | 274 | PF00018 | 0.445 |
LIG_SH3_3 | 370 | 376 | PF00018 | 0.601 |
LIG_SH3_3 | 437 | 443 | PF00018 | 0.459 |
LIG_SH3_3 | 605 | 611 | PF00018 | 0.449 |
LIG_SH3_3 | 7 | 13 | PF00018 | 0.725 |
LIG_SUMO_SIM_anti_2 | 707 | 713 | PF11976 | 0.511 |
LIG_SUMO_SIM_par_1 | 21 | 26 | PF11976 | 0.581 |
LIG_SUMO_SIM_par_1 | 854 | 859 | PF11976 | 0.426 |
LIG_TRAF2_1 | 815 | 818 | PF00917 | 0.533 |
LIG_TRFH_1 | 225 | 229 | PF08558 | 0.438 |
LIG_TYR_ITIM | 839 | 844 | PF00017 | 0.459 |
LIG_WW_3 | 864 | 868 | PF00397 | 0.469 |
MOD_CDK_SPK_2 | 625 | 630 | PF00069 | 0.472 |
MOD_CDK_SPxxK_3 | 372 | 379 | PF00069 | 0.585 |
MOD_CK1_1 | 422 | 428 | PF00069 | 0.447 |
MOD_CK1_1 | 469 | 475 | PF00069 | 0.471 |
MOD_CK1_1 | 653 | 659 | PF00069 | 0.447 |
MOD_CK1_1 | 673 | 679 | PF00069 | 0.479 |
MOD_CK1_1 | 700 | 706 | PF00069 | 0.547 |
MOD_CK1_1 | 740 | 746 | PF00069 | 0.759 |
MOD_CK1_1 | 774 | 780 | PF00069 | 0.694 |
MOD_CK1_1 | 83 | 89 | PF00069 | 0.459 |
MOD_CK2_1 | 372 | 378 | PF00069 | 0.475 |
MOD_CK2_1 | 421 | 427 | PF00069 | 0.488 |
MOD_CK2_1 | 685 | 691 | PF00069 | 0.533 |
MOD_CK2_1 | 704 | 710 | PF00069 | 0.482 |
MOD_CK2_1 | 716 | 722 | PF00069 | 0.604 |
MOD_CK2_1 | 812 | 818 | PF00069 | 0.466 |
MOD_DYRK1A_RPxSP_1 | 625 | 629 | PF00069 | 0.472 |
MOD_GlcNHglycan | 454 | 457 | PF01048 | 0.280 |
MOD_GlcNHglycan | 464 | 467 | PF01048 | 0.210 |
MOD_GlcNHglycan | 471 | 474 | PF01048 | 0.173 |
MOD_GlcNHglycan | 583 | 587 | PF01048 | 0.333 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.661 |
MOD_GlcNHglycan | 63 | 68 | PF01048 | 0.645 |
MOD_GlcNHglycan | 725 | 728 | PF01048 | 0.740 |
MOD_GlcNHglycan | 737 | 740 | PF01048 | 0.785 |
MOD_GlcNHglycan | 757 | 761 | PF01048 | 0.433 |
MOD_GlcNHglycan | 773 | 776 | PF01048 | 0.659 |
MOD_GSK3_1 | 142 | 149 | PF00069 | 0.432 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.295 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.528 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.447 |
MOD_GSK3_1 | 441 | 448 | PF00069 | 0.447 |
MOD_GSK3_1 | 462 | 469 | PF00069 | 0.447 |
MOD_GSK3_1 | 472 | 479 | PF00069 | 0.447 |
MOD_GSK3_1 | 481 | 488 | PF00069 | 0.447 |
MOD_GSK3_1 | 625 | 632 | PF00069 | 0.512 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.682 |
MOD_GSK3_1 | 700 | 707 | PF00069 | 0.554 |
MOD_GSK3_1 | 735 | 742 | PF00069 | 0.728 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.462 |
MOD_N-GLC_1 | 653 | 658 | PF02516 | 0.259 |
MOD_N-GLC_1 | 716 | 721 | PF02516 | 0.532 |
MOD_N-GLC_2 | 436 | 438 | PF02516 | 0.247 |
MOD_NEK2_1 | 146 | 151 | PF00069 | 0.380 |
MOD_NEK2_1 | 160 | 165 | PF00069 | 0.419 |
MOD_NEK2_1 | 320 | 325 | PF00069 | 0.712 |
MOD_NEK2_1 | 340 | 345 | PF00069 | 0.247 |
MOD_NEK2_1 | 38 | 43 | PF00069 | 0.469 |
MOD_NEK2_1 | 474 | 479 | PF00069 | 0.447 |
MOD_NEK2_1 | 648 | 653 | PF00069 | 0.463 |
MOD_NEK2_1 | 665 | 670 | PF00069 | 0.447 |
MOD_NEK2_1 | 697 | 702 | PF00069 | 0.440 |
MOD_NEK2_1 | 844 | 849 | PF00069 | 0.528 |
MOD_NEK2_2 | 716 | 721 | PF00069 | 0.666 |
MOD_PIKK_1 | 176 | 182 | PF00454 | 0.447 |
MOD_PIKK_1 | 353 | 359 | PF00454 | 0.603 |
MOD_PIKK_1 | 445 | 451 | PF00454 | 0.459 |
MOD_PIKK_1 | 633 | 639 | PF00454 | 0.513 |
MOD_PK_1 | 785 | 791 | PF00069 | 0.533 |
MOD_PKA_1 | 353 | 359 | PF00069 | 0.533 |
MOD_PKA_1 | 785 | 791 | PF00069 | 0.533 |
MOD_PKA_2 | 160 | 166 | PF00069 | 0.456 |
MOD_PKA_2 | 176 | 182 | PF00069 | 0.416 |
MOD_PKA_2 | 190 | 196 | PF00069 | 0.447 |
MOD_PKA_2 | 629 | 635 | PF00069 | 0.469 |
MOD_PKA_2 | 659 | 665 | PF00069 | 0.447 |
MOD_PKA_2 | 670 | 676 | PF00069 | 0.447 |
MOD_PKA_2 | 685 | 691 | PF00069 | 0.508 |
MOD_PKA_2 | 697 | 703 | PF00069 | 0.374 |
MOD_PKA_2 | 735 | 741 | PF00069 | 0.781 |
MOD_PKA_2 | 80 | 86 | PF00069 | 0.428 |
MOD_Plk_1 | 485 | 491 | PF00069 | 0.447 |
MOD_Plk_1 | 633 | 639 | PF00069 | 0.474 |
MOD_Plk_1 | 716 | 722 | PF00069 | 0.707 |
MOD_Plk_4 | 142 | 148 | PF00069 | 0.439 |
MOD_Plk_4 | 160 | 166 | PF00069 | 0.372 |
MOD_Plk_4 | 387 | 393 | PF00069 | 0.522 |
MOD_Plk_4 | 540 | 546 | PF00069 | 0.447 |
MOD_Plk_4 | 665 | 671 | PF00069 | 0.442 |
MOD_Plk_4 | 818 | 824 | PF00069 | 0.488 |
MOD_ProDKin_1 | 114 | 120 | PF00069 | 0.408 |
MOD_ProDKin_1 | 372 | 378 | PF00069 | 0.483 |
MOD_ProDKin_1 | 625 | 631 | PF00069 | 0.480 |
MOD_SUMO_for_1 | 728 | 731 | PF00179 | 0.758 |
MOD_SUMO_rev_2 | 347 | 356 | PF00179 | 0.501 |
MOD_SUMO_rev_2 | 847 | 856 | PF00179 | 0.506 |
TRG_DiLeu_BaEn_1 | 490 | 495 | PF01217 | 0.447 |
TRG_DiLeu_BaEn_1 | 634 | 639 | PF01217 | 0.459 |
TRG_DiLeu_BaLyEn_6 | 39 | 44 | PF01217 | 0.493 |
TRG_DiLeu_BaLyEn_6 | 661 | 666 | PF01217 | 0.447 |
TRG_DiLeu_BaLyEn_6 | 830 | 835 | PF01217 | 0.533 |
TRG_ENDOCYTIC_2 | 643 | 646 | PF00928 | 0.447 |
TRG_ENDOCYTIC_2 | 794 | 797 | PF00928 | 0.447 |
TRG_ENDOCYTIC_2 | 841 | 844 | PF00928 | 0.454 |
TRG_ER_diArg_1 | 30 | 33 | PF00400 | 0.475 |
TRG_ER_diArg_1 | 379 | 382 | PF00400 | 0.526 |
TRG_ER_diArg_1 | 385 | 387 | PF00400 | 0.499 |
TRG_ER_diArg_1 | 557 | 559 | PF00400 | 0.528 |
TRG_ER_diArg_1 | 783 | 785 | PF00400 | 0.664 |
TRG_NES_CRM1_1 | 695 | 710 | PF08389 | 0.562 |
TRG_Pf-PMV_PEXEL_1 | 832 | 836 | PF00026 | 0.333 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2J6 | Leptomonas seymouri | 87% | 99% |
A0A0N1PC47 | Leptomonas seymouri | 28% | 100% |
A0A0S4IK09 | Bodo saltans | 31% | 89% |
A0A0S4IVB8 | Bodo saltans | 60% | 100% |
A0A0S4IYQ3 | Bodo saltans | 28% | 100% |
A0A1X0NQM5 | Trypanosomatidae | 70% | 99% |
A0A1X0NT66 | Trypanosomatidae | 32% | 100% |
A0A1X0NVE7 | Trypanosomatidae | 29% | 100% |
A0A3S5H7S8 | Leishmania donovani | 32% | 100% |
A0A3S7WY81 | Leishmania donovani | 28% | 100% |
A0A422N694 | Trypanosoma rangeli | 75% | 100% |
A0A422NHH5 | Trypanosoma rangeli | 29% | 100% |
A4FUD9 | Bos taurus | 31% | 100% |
A4HDE7 | Leishmania braziliensis | 29% | 100% |
A4HGU2 | Leishmania braziliensis | 94% | 100% |
A4HKT9 | Leishmania braziliensis | 33% | 100% |
A4I0T0 | Leishmania infantum | 30% | 100% |
A4I3W9 | Leishmania infantum | 100% | 100% |
A4I8B8 | Leishmania infantum | 32% | 100% |
B8AZ14 | Oryza sativa subsp. indica | 29% | 100% |
B8AZ99 | Oryza sativa subsp. indica | 33% | 100% |
B8AZX3 | Oryza sativa subsp. indica | 40% | 100% |
B9FKM7 | Oryza sativa subsp. japonica | 29% | 100% |
D0A759 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
D0A936 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 70% | 100% |
D0A999 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
D0AAI9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
D3ZVK1 | Rattus norvegicus | 31% | 100% |
E1BPX4 | Bos taurus | 31% | 100% |
E9AWT2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9B059 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 98% | 100% |
E9B377 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
F4KAB8 | Arabidopsis thaliana | 38% | 100% |
F6RIX4 | Xenopus tropicalis | 31% | 79% |
I0IUP3 | Gallus gallus | 32% | 100% |
O80786 | Arabidopsis thaliana | 32% | 100% |
P25205 | Homo sapiens | 32% | 100% |
P25206 | Mus musculus | 31% | 100% |
P29469 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 31% | 100% |
P30664 | Xenopus laevis | 33% | 100% |
P30666 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 31% | 100% |
P33991 | Homo sapiens | 31% | 100% |
P33992 | Homo sapiens | 30% | 100% |
P34647 | Caenorhabditis elegans | 38% | 100% |
P40377 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 34% | 100% |
P41389 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 31% | 100% |
P49718 | Mus musculus | 30% | 100% |
P49731 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 40% | 99% |
P49736 | Homo sapiens | 32% | 97% |
P49739 | Xenopus laevis | 31% | 100% |
P53091 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 43% | 87% |
P55861 | Xenopus laevis | 33% | 99% |
P55862 | Xenopus laevis | 29% | 100% |
P97310 | Mus musculus | 32% | 97% |
P97311 | Mus musculus | 42% | 100% |
Q0DHC4 | Oryza sativa subsp. japonica | 33% | 100% |
Q0V8B7 | Bos taurus | 31% | 100% |
Q0V9Q6 | Xenopus tropicalis | 31% | 100% |
Q14566 | Homo sapiens | 42% | 100% |
Q21902 | Caenorhabditis elegans | 30% | 100% |
Q26454 | Drosophila melanogaster | 32% | 100% |
Q28BS0 | Xenopus tropicalis | 32% | 100% |
Q28CM3 | Xenopus tropicalis | 40% | 100% |
Q29JI9 | Drosophila pseudoobscura pseudoobscura | 40% | 100% |
Q2KIZ8 | Bos taurus | 41% | 100% |
Q43704 | Zea mays | 31% | 100% |
Q498J7 | Xenopus laevis | 40% | 100% |
Q4Q826 | Leishmania major | 97% | 100% |
Q4QAP2 | Leishmania major | 30% | 100% |
Q54CP4 | Dictyostelium discoideum | 29% | 100% |
Q561P5 | Xenopus tropicalis | 29% | 100% |
Q5F310 | Xenopus laevis | 31% | 100% |
Q5FWY4 | Xenopus laevis | 44% | 100% |
Q5R8G6 | Pongo abelii | 32% | 100% |
Q5XK83 | Xenopus laevis | 31% | 100% |
Q5ZMN2 | Gallus gallus | 32% | 100% |
Q61J08 | Caenorhabditis briggsae | 36% | 100% |
Q6DIH3 | Xenopus tropicalis | 33% | 100% |
Q6F353 | Oryza sativa subsp. japonica | 40% | 100% |
Q6GL41 | Xenopus tropicalis | 31% | 100% |
Q6NRM6 | Xenopus laevis | 31% | 77% |
Q6P1V8 | Xenopus tropicalis | 40% | 100% |
Q6PCI7 | Xenopus laevis | 28% | 100% |
Q7Q0Q1 | Anopheles gambiae | 40% | 100% |
Q7ZXZ0 | Xenopus laevis | 32% | 100% |
Q7ZY18 | Xenopus laevis | 39% | 100% |
Q86B14 | Dictyostelium discoideum | 36% | 100% |
Q95XQ8 | Caenorhabditis elegans | 35% | 100% |
Q9CWV1 | Mus musculus | 31% | 100% |
Q9FL33 | Arabidopsis thaliana | 33% | 100% |
Q9SF37 | Arabidopsis thaliana | 29% | 100% |
Q9SX03 | Zea mays | 31% | 100% |
Q9SX04 | Zea mays | 31% | 100% |
Q9U1E0 | Leishmania major | 32% | 100% |
Q9UJA3 | Homo sapiens | 31% | 100% |
Q9UXG1 | Saccharolobus solfataricus (strain ATCC 35092 / DSM 1617 / JCM 11322 / P2) | 33% | 100% |
Q9V461 | Drosophila melanogaster | 39% | 100% |
Q9VGW6 | Drosophila melanogaster | 32% | 100% |
Q9XYU1 | Drosophila melanogaster | 30% | 100% |
V5BGQ5 | Trypanosoma cruzi | 71% | 100% |
V5BQA9 | Trypanosoma cruzi | 32% | 100% |
V5C0K6 | Trypanosoma cruzi | 29% | 100% |