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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0005654 | nucleoplasm | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4H3M1
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 5 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 5 |
GO:0006807 | nitrogen compound metabolic process | 2 | 5 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0008152 | metabolic process | 1 | 5 |
GO:0009987 | cellular process | 1 | 5 |
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:0034085 | establishment of sister chromatid cohesion | 3 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 5 |
GO:0044237 | cellular metabolic process | 2 | 5 |
GO:0044238 | primary metabolic process | 2 | 5 |
GO:0046483 | heterocycle metabolic process | 3 | 5 |
GO:0051276 | chromosome organization | 5 | 1 |
GO:0071103 | DNA conformation change | 6 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 5 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 7 |
GO:0003676 | nucleic acid binding | 3 | 7 |
GO:0003677 | DNA binding | 4 | 7 |
GO:0003678 | DNA helicase activity | 3 | 7 |
GO:0003824 | catalytic activity | 1 | 7 |
GO:0004386 | helicase activity | 2 | 7 |
GO:0005488 | binding | 1 | 7 |
GO:0005524 | ATP binding | 5 | 7 |
GO:0008094 | ATP-dependent activity, acting on DNA | 2 | 7 |
GO:0016787 | hydrolase activity | 2 | 7 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 7 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 7 |
GO:0017076 | purine nucleotide binding | 4 | 7 |
GO:0030554 | adenyl nucleotide binding | 5 | 7 |
GO:0032553 | ribonucleotide binding | 3 | 7 |
GO:0032555 | purine ribonucleotide binding | 4 | 7 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 7 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 7 |
GO:0036094 | small molecule binding | 2 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043168 | anion binding | 3 | 7 |
GO:0097159 | organic cyclic compound binding | 2 | 7 |
GO:0097367 | carbohydrate derivative binding | 2 | 7 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 7 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 7 |
GO:0140657 | ATP-dependent activity | 1 | 7 |
GO:1901265 | nucleoside phosphate binding | 3 | 7 |
GO:1901363 | heterocyclic compound binding | 2 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 659 | 663 | PF00656 | 0.439 |
CLV_C14_Caspase3-7 | 747 | 751 | PF00656 | 0.579 |
CLV_C14_Caspase3-7 | 862 | 866 | PF00656 | 0.790 |
CLV_NRD_NRD_1 | 172 | 174 | PF00675 | 0.677 |
CLV_NRD_NRD_1 | 175 | 177 | PF00675 | 0.704 |
CLV_NRD_NRD_1 | 183 | 185 | PF00675 | 0.581 |
CLV_NRD_NRD_1 | 189 | 191 | PF00675 | 0.576 |
CLV_NRD_NRD_1 | 283 | 285 | PF00675 | 0.637 |
CLV_NRD_NRD_1 | 397 | 399 | PF00675 | 0.356 |
CLV_NRD_NRD_1 | 427 | 429 | PF00675 | 0.585 |
CLV_NRD_NRD_1 | 516 | 518 | PF00675 | 0.398 |
CLV_NRD_NRD_1 | 616 | 618 | PF00675 | 0.714 |
CLV_NRD_NRD_1 | 629 | 631 | PF00675 | 0.571 |
CLV_NRD_NRD_1 | 649 | 651 | PF00675 | 0.506 |
CLV_NRD_NRD_1 | 710 | 712 | PF00675 | 0.480 |
CLV_NRD_NRD_1 | 897 | 899 | PF00675 | 0.807 |
CLV_PCSK_FUR_1 | 173 | 177 | PF00082 | 0.587 |
CLV_PCSK_FUR_1 | 514 | 518 | PF00082 | 0.398 |
CLV_PCSK_FUR_1 | 627 | 631 | PF00082 | 0.785 |
CLV_PCSK_FUR_1 | 895 | 899 | PF00082 | 0.806 |
CLV_PCSK_KEX2_1 | 172 | 174 | PF00082 | 0.632 |
CLV_PCSK_KEX2_1 | 175 | 177 | PF00082 | 0.630 |
CLV_PCSK_KEX2_1 | 183 | 185 | PF00082 | 0.585 |
CLV_PCSK_KEX2_1 | 191 | 193 | PF00082 | 0.564 |
CLV_PCSK_KEX2_1 | 397 | 399 | PF00082 | 0.356 |
CLV_PCSK_KEX2_1 | 427 | 429 | PF00082 | 0.650 |
CLV_PCSK_KEX2_1 | 516 | 518 | PF00082 | 0.398 |
CLV_PCSK_KEX2_1 | 616 | 618 | PF00082 | 0.714 |
CLV_PCSK_KEX2_1 | 627 | 629 | PF00082 | 0.608 |
CLV_PCSK_KEX2_1 | 649 | 651 | PF00082 | 0.555 |
CLV_PCSK_KEX2_1 | 710 | 712 | PF00082 | 0.480 |
CLV_PCSK_KEX2_1 | 875 | 877 | PF00082 | 0.772 |
CLV_PCSK_KEX2_1 | 897 | 899 | PF00082 | 0.807 |
CLV_PCSK_PC1ET2_1 | 191 | 193 | PF00082 | 0.659 |
CLV_PCSK_PC1ET2_1 | 875 | 877 | PF00082 | 0.772 |
CLV_PCSK_PC7_1 | 187 | 193 | PF00082 | 0.613 |
CLV_PCSK_SKI1_1 | 223 | 227 | PF00082 | 0.490 |
CLV_PCSK_SKI1_1 | 307 | 311 | PF00082 | 0.506 |
CLV_PCSK_SKI1_1 | 439 | 443 | PF00082 | 0.524 |
CLV_PCSK_SKI1_1 | 474 | 478 | PF00082 | 0.347 |
CLV_PCSK_SKI1_1 | 531 | 535 | PF00082 | 0.350 |
CLV_PCSK_SKI1_1 | 553 | 557 | PF00082 | 0.350 |
CLV_PCSK_SKI1_1 | 710 | 714 | PF00082 | 0.540 |
CLV_PCSK_SKI1_1 | 723 | 727 | PF00082 | 0.531 |
CLV_Separin_Metazoa | 157 | 161 | PF03568 | 0.672 |
DEG_APCC_DBOX_1 | 473 | 481 | PF00400 | 0.293 |
DEG_SPOP_SBC_1 | 246 | 250 | PF00917 | 0.625 |
DOC_CYCLIN_RxL_1 | 528 | 538 | PF00134 | 0.598 |
DOC_CYCLIN_RxL_1 | 707 | 714 | PF00134 | 0.469 |
DOC_CYCLIN_RxL_1 | 791 | 800 | PF00134 | 0.439 |
DOC_MAPK_gen_1 | 187 | 195 | PF00069 | 0.738 |
DOC_MAPK_gen_1 | 284 | 290 | PF00069 | 0.547 |
DOC_MAPK_gen_1 | 729 | 738 | PF00069 | 0.489 |
DOC_PP1_RVXF_1 | 285 | 291 | PF00149 | 0.468 |
DOC_PP2B_LxvP_1 | 358 | 361 | PF13499 | 0.552 |
DOC_PP4_FxxP_1 | 352 | 355 | PF00568 | 0.573 |
DOC_PP4_FxxP_1 | 575 | 578 | PF00568 | 0.755 |
DOC_USP7_MATH_1 | 118 | 122 | PF00917 | 0.749 |
DOC_USP7_MATH_1 | 141 | 145 | PF00917 | 0.730 |
DOC_USP7_MATH_1 | 246 | 250 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 329 | 333 | PF00917 | 0.741 |
DOC_USP7_MATH_1 | 346 | 350 | PF00917 | 0.592 |
DOC_USP7_MATH_1 | 363 | 367 | PF00917 | 0.674 |
DOC_USP7_MATH_1 | 576 | 580 | PF00917 | 0.791 |
DOC_USP7_MATH_1 | 602 | 606 | PF00917 | 0.509 |
DOC_USP7_MATH_1 | 648 | 652 | PF00917 | 0.550 |
DOC_USP7_MATH_1 | 749 | 753 | PF00917 | 0.353 |
DOC_WW_Pin1_4 | 126 | 131 | PF00397 | 0.502 |
DOC_WW_Pin1_4 | 255 | 260 | PF00397 | 0.555 |
DOC_WW_Pin1_4 | 351 | 356 | PF00397 | 0.840 |
DOC_WW_Pin1_4 | 441 | 446 | PF00397 | 0.669 |
DOC_WW_Pin1_4 | 579 | 584 | PF00397 | 0.773 |
DOC_WW_Pin1_4 | 58 | 63 | PF00397 | 0.597 |
DOC_WW_Pin1_4 | 635 | 640 | PF00397 | 0.542 |
DOC_WW_Pin1_4 | 770 | 775 | PF00397 | 0.790 |
DOC_WW_Pin1_4 | 780 | 785 | PF00397 | 0.644 |
DOC_WW_Pin1_4 | 83 | 88 | PF00397 | 0.485 |
LIG_14-3-3_CanoR_1 | 143 | 147 | PF00244 | 0.600 |
LIG_14-3-3_CanoR_1 | 223 | 229 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 236 | 244 | PF00244 | 0.768 |
LIG_14-3-3_CanoR_1 | 293 | 302 | PF00244 | 0.493 |
LIG_14-3-3_CanoR_1 | 320 | 324 | PF00244 | 0.627 |
LIG_14-3-3_CanoR_1 | 378 | 384 | PF00244 | 0.577 |
LIG_14-3-3_CanoR_1 | 45 | 54 | PF00244 | 0.796 |
LIG_14-3-3_CanoR_1 | 617 | 626 | PF00244 | 0.732 |
LIG_14-3-3_CanoR_1 | 649 | 654 | PF00244 | 0.538 |
LIG_14-3-3_CanoR_1 | 694 | 704 | PF00244 | 0.534 |
LIG_14-3-3_CanoR_1 | 778 | 784 | PF00244 | 0.525 |
LIG_14-3-3_CanoR_1 | 867 | 871 | PF00244 | 0.595 |
LIG_APCC_ABBA_1 | 680 | 685 | PF00400 | 0.508 |
LIG_APCC_ABBA_1 | 713 | 718 | PF00400 | 0.270 |
LIG_BRCT_BRCA1_1 | 101 | 105 | PF00533 | 0.512 |
LIG_BRCT_BRCA1_1 | 348 | 352 | PF00533 | 0.656 |
LIG_BRCT_BRCA1_1 | 750 | 754 | PF00533 | 0.381 |
LIG_eIF4E_1 | 527 | 533 | PF01652 | 0.598 |
LIG_FHA_1 | 225 | 231 | PF00498 | 0.507 |
LIG_FHA_1 | 239 | 245 | PF00498 | 0.484 |
LIG_FHA_1 | 37 | 43 | PF00498 | 0.533 |
LIG_FHA_1 | 49 | 55 | PF00498 | 0.494 |
LIG_FHA_1 | 528 | 534 | PF00498 | 0.550 |
LIG_FHA_1 | 641 | 647 | PF00498 | 0.550 |
LIG_FHA_1 | 696 | 702 | PF00498 | 0.486 |
LIG_FHA_1 | 791 | 797 | PF00498 | 0.556 |
LIG_FHA_1 | 815 | 821 | PF00498 | 0.474 |
LIG_FHA_1 | 869 | 875 | PF00498 | 0.569 |
LIG_FHA_2 | 152 | 158 | PF00498 | 0.721 |
LIG_FHA_2 | 489 | 495 | PF00498 | 0.570 |
LIG_FHA_2 | 564 | 570 | PF00498 | 0.712 |
LIG_FHA_2 | 783 | 789 | PF00498 | 0.623 |
LIG_GSK3_LRP6_1 | 62 | 67 | PF00069 | 0.609 |
LIG_Integrin_isoDGR_2 | 340 | 342 | PF01839 | 0.539 |
LIG_Integrin_RGD_1 | 231 | 233 | PF01839 | 0.778 |
LIG_LIR_Apic_2 | 349 | 355 | PF02991 | 0.573 |
LIG_LIR_Gen_1 | 662 | 673 | PF02991 | 0.653 |
LIG_LIR_Gen_1 | 811 | 820 | PF02991 | 0.564 |
LIG_LIR_Nem_3 | 102 | 108 | PF02991 | 0.528 |
LIG_LIR_Nem_3 | 538 | 544 | PF02991 | 0.550 |
LIG_LIR_Nem_3 | 811 | 816 | PF02991 | 0.568 |
LIG_MYND_1 | 356 | 360 | PF01753 | 0.545 |
LIG_NRBOX | 472 | 478 | PF00104 | 0.285 |
LIG_NRBOX | 702 | 708 | PF00104 | 0.288 |
LIG_PCNA_PIPBox_1 | 23 | 32 | PF02747 | 0.450 |
LIG_PCNA_yPIPBox_3 | 92 | 105 | PF02747 | 0.400 |
LIG_SH2_CRK | 544 | 548 | PF00017 | 0.512 |
LIG_SH2_CRK | 7 | 11 | PF00017 | 0.396 |
LIG_SH2_CRK | 813 | 817 | PF00017 | 0.563 |
LIG_SH2_SRC | 7 | 10 | PF00017 | 0.397 |
LIG_SH2_STAP1 | 720 | 724 | PF00017 | 0.532 |
LIG_SH2_STAP1 | 834 | 838 | PF00017 | 0.631 |
LIG_SH2_STAT3 | 16 | 19 | PF00017 | 0.428 |
LIG_SH2_STAT3 | 219 | 222 | PF00017 | 0.730 |
LIG_SH2_STAT3 | 29 | 32 | PF00017 | 0.493 |
LIG_SH2_STAT3 | 426 | 429 | PF00017 | 0.662 |
LIG_SH2_STAT5 | 289 | 292 | PF00017 | 0.445 |
LIG_SH2_STAT5 | 29 | 32 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 410 | 413 | PF00017 | 0.630 |
LIG_SH2_STAT5 | 467 | 470 | PF00017 | 0.493 |
LIG_SH2_STAT5 | 479 | 482 | PF00017 | 0.524 |
LIG_SH2_STAT5 | 510 | 513 | PF00017 | 0.598 |
LIG_SH2_STAT5 | 527 | 530 | PF00017 | 0.568 |
LIG_SH2_STAT5 | 546 | 549 | PF00017 | 0.382 |
LIG_SH2_STAT5 | 692 | 695 | PF00017 | 0.383 |
LIG_SH3_3 | 144 | 150 | PF00018 | 0.770 |
LIG_SH3_3 | 311 | 317 | PF00018 | 0.653 |
LIG_SH3_3 | 354 | 360 | PF00018 | 0.830 |
LIG_SH3_3 | 60 | 66 | PF00018 | 0.603 |
LIG_SH3_3 | 781 | 787 | PF00018 | 0.624 |
LIG_SH3_3 | 9 | 15 | PF00018 | 0.426 |
LIG_SUMO_SIM_anti_2 | 79 | 86 | PF11976 | 0.557 |
LIG_SUMO_SIM_par_1 | 51 | 58 | PF11976 | 0.525 |
LIG_TRAF2_1 | 154 | 157 | PF00917 | 0.608 |
LIG_TRAF2_1 | 17 | 20 | PF00917 | 0.422 |
LIG_TRAF2_1 | 842 | 845 | PF00917 | 0.416 |
LIG_TYR_ITIM | 542 | 547 | PF00017 | 0.370 |
LIG_UBA3_1 | 280 | 287 | PF00899 | 0.703 |
LIG_UBA3_1 | 735 | 741 | PF00899 | 0.270 |
LIG_WRC_WIRS_1 | 798 | 803 | PF05994 | 0.479 |
LIG_WRC_WIRS_1 | 815 | 820 | PF05994 | 0.443 |
MOD_CDK_SPxxK_3 | 441 | 448 | PF00069 | 0.666 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.556 |
MOD_CK1_1 | 240 | 246 | PF00069 | 0.688 |
MOD_CK1_1 | 247 | 253 | PF00069 | 0.665 |
MOD_CK1_1 | 254 | 260 | PF00069 | 0.648 |
MOD_CK1_1 | 351 | 357 | PF00069 | 0.756 |
MOD_CK1_1 | 36 | 42 | PF00069 | 0.539 |
MOD_CK1_1 | 367 | 373 | PF00069 | 0.518 |
MOD_CK1_1 | 43 | 49 | PF00069 | 0.540 |
MOD_CK1_1 | 508 | 514 | PF00069 | 0.491 |
MOD_CK1_1 | 579 | 585 | PF00069 | 0.802 |
MOD_CK1_1 | 58 | 64 | PF00069 | 0.497 |
MOD_CK1_1 | 605 | 611 | PF00069 | 0.693 |
MOD_CK1_1 | 640 | 646 | PF00069 | 0.549 |
MOD_CK1_1 | 695 | 701 | PF00069 | 0.597 |
MOD_CK1_1 | 782 | 788 | PF00069 | 0.662 |
MOD_CK1_1 | 99 | 105 | PF00069 | 0.579 |
MOD_CK2_1 | 151 | 157 | PF00069 | 0.619 |
MOD_CK2_1 | 200 | 206 | PF00069 | 0.781 |
MOD_CK2_1 | 356 | 362 | PF00069 | 0.550 |
MOD_CK2_1 | 488 | 494 | PF00069 | 0.552 |
MOD_CK2_1 | 563 | 569 | PF00069 | 0.703 |
MOD_CK2_1 | 649 | 655 | PF00069 | 0.534 |
MOD_CK2_1 | 782 | 788 | PF00069 | 0.554 |
MOD_CK2_1 | 839 | 845 | PF00069 | 0.401 |
MOD_GlcNHglycan | 118 | 121 | PF01048 | 0.763 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.793 |
MOD_GlcNHglycan | 244 | 247 | PF01048 | 0.753 |
MOD_GlcNHglycan | 330 | 334 | PF01048 | 0.753 |
MOD_GlcNHglycan | 499 | 502 | PF01048 | 0.720 |
MOD_GlcNHglycan | 57 | 60 | PF01048 | 0.570 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.565 |
MOD_GlcNHglycan | 694 | 697 | PF01048 | 0.632 |
MOD_GlcNHglycan | 861 | 864 | PF01048 | 0.762 |
MOD_GlcNHglycan | 879 | 882 | PF01048 | 0.493 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.681 |
MOD_GSK3_1 | 246 | 253 | PF00069 | 0.687 |
MOD_GSK3_1 | 254 | 261 | PF00069 | 0.689 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.629 |
MOD_GSK3_1 | 289 | 296 | PF00069 | 0.465 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.695 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.602 |
MOD_GSK3_1 | 363 | 370 | PF00069 | 0.574 |
MOD_GSK3_1 | 468 | 475 | PF00069 | 0.565 |
MOD_GSK3_1 | 504 | 511 | PF00069 | 0.312 |
MOD_GSK3_1 | 559 | 566 | PF00069 | 0.700 |
MOD_GSK3_1 | 578 | 585 | PF00069 | 0.528 |
MOD_GSK3_1 | 58 | 65 | PF00069 | 0.563 |
MOD_GSK3_1 | 635 | 642 | PF00069 | 0.555 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.708 |
MOD_GSK3_1 | 719 | 726 | PF00069 | 0.600 |
MOD_GSK3_1 | 779 | 786 | PF00069 | 0.686 |
MOD_GSK3_1 | 83 | 90 | PF00069 | 0.419 |
MOD_GSK3_1 | 851 | 858 | PF00069 | 0.680 |
MOD_GSK3_1 | 884 | 891 | PF00069 | 0.642 |
MOD_LATS_1 | 647 | 653 | PF00433 | 0.546 |
MOD_NEK2_1 | 200 | 205 | PF00069 | 0.679 |
MOD_NEK2_1 | 238 | 243 | PF00069 | 0.705 |
MOD_NEK2_1 | 244 | 249 | PF00069 | 0.672 |
MOD_NEK2_1 | 305 | 310 | PF00069 | 0.503 |
MOD_NEK2_1 | 417 | 422 | PF00069 | 0.639 |
MOD_NEK2_1 | 57 | 62 | PF00069 | 0.523 |
MOD_NEK2_1 | 620 | 625 | PF00069 | 0.459 |
MOD_NEK2_1 | 664 | 669 | PF00069 | 0.571 |
MOD_NEK2_1 | 67 | 72 | PF00069 | 0.540 |
MOD_NEK2_1 | 819 | 824 | PF00069 | 0.457 |
MOD_NEK2_1 | 96 | 101 | PF00069 | 0.564 |
MOD_NEK2_2 | 749 | 754 | PF00069 | 0.367 |
MOD_PIKK_1 | 149 | 155 | PF00454 | 0.480 |
MOD_PIKK_1 | 209 | 215 | PF00454 | 0.717 |
MOD_PIKK_1 | 293 | 299 | PF00454 | 0.496 |
MOD_PIKK_1 | 43 | 49 | PF00454 | 0.704 |
MOD_PIKK_1 | 819 | 825 | PF00454 | 0.534 |
MOD_PIKK_1 | 90 | 96 | PF00454 | 0.416 |
MOD_PK_1 | 649 | 655 | PF00069 | 0.690 |
MOD_PKA_1 | 649 | 655 | PF00069 | 0.534 |
MOD_PKA_2 | 142 | 148 | PF00069 | 0.692 |
MOD_PKA_2 | 319 | 325 | PF00069 | 0.621 |
MOD_PKA_2 | 33 | 39 | PF00069 | 0.602 |
MOD_PKA_2 | 377 | 383 | PF00069 | 0.603 |
MOD_PKA_2 | 618 | 624 | PF00069 | 0.723 |
MOD_PKA_2 | 648 | 654 | PF00069 | 0.539 |
MOD_PKA_2 | 856 | 862 | PF00069 | 0.604 |
MOD_PKA_2 | 866 | 872 | PF00069 | 0.632 |
MOD_PKA_2 | 877 | 883 | PF00069 | 0.747 |
MOD_PKB_1 | 617 | 625 | PF00069 | 0.452 |
MOD_Plk_1 | 141 | 147 | PF00069 | 0.550 |
MOD_Plk_1 | 749 | 755 | PF00069 | 0.566 |
MOD_Plk_2-3 | 839 | 845 | PF00069 | 0.401 |
MOD_Plk_4 | 142 | 148 | PF00069 | 0.549 |
MOD_Plk_4 | 276 | 282 | PF00069 | 0.727 |
MOD_Plk_4 | 505 | 511 | PF00069 | 0.491 |
MOD_Plk_4 | 749 | 755 | PF00069 | 0.378 |
MOD_Plk_4 | 797 | 803 | PF00069 | 0.480 |
MOD_Plk_4 | 814 | 820 | PF00069 | 0.443 |
MOD_Plk_4 | 96 | 102 | PF00069 | 0.564 |
MOD_ProDKin_1 | 126 | 132 | PF00069 | 0.504 |
MOD_ProDKin_1 | 255 | 261 | PF00069 | 0.554 |
MOD_ProDKin_1 | 351 | 357 | PF00069 | 0.838 |
MOD_ProDKin_1 | 441 | 447 | PF00069 | 0.665 |
MOD_ProDKin_1 | 579 | 585 | PF00069 | 0.773 |
MOD_ProDKin_1 | 58 | 64 | PF00069 | 0.599 |
MOD_ProDKin_1 | 635 | 641 | PF00069 | 0.542 |
MOD_ProDKin_1 | 770 | 776 | PF00069 | 0.793 |
MOD_ProDKin_1 | 780 | 786 | PF00069 | 0.640 |
MOD_ProDKin_1 | 83 | 89 | PF00069 | 0.490 |
MOD_SUMO_rev_2 | 264 | 273 | PF00179 | 0.500 |
MOD_SUMO_rev_2 | 839 | 849 | PF00179 | 0.427 |
TRG_DiLeu_BaEn_1 | 142 | 147 | PF01217 | 0.550 |
TRG_DiLeu_BaEn_1 | 206 | 211 | PF01217 | 0.775 |
TRG_DiLeu_BaEn_2 | 733 | 739 | PF01217 | 0.482 |
TRG_DiLeu_BaLyEn_6 | 528 | 533 | PF01217 | 0.491 |
TRG_DiLeu_BaLyEn_6 | 708 | 713 | PF01217 | 0.397 |
TRG_DiLeu_BaLyEn_6 | 720 | 725 | PF01217 | 0.499 |
TRG_DiLeu_BaLyEn_6 | 771 | 776 | PF01217 | 0.507 |
TRG_ENDOCYTIC_2 | 544 | 547 | PF00928 | 0.370 |
TRG_ENDOCYTIC_2 | 813 | 816 | PF00928 | 0.564 |
TRG_ER_diArg_1 | 159 | 162 | PF00400 | 0.684 |
TRG_ER_diArg_1 | 175 | 178 | PF00400 | 0.478 |
TRG_ER_diArg_1 | 190 | 193 | PF00400 | 0.500 |
TRG_ER_diArg_1 | 396 | 398 | PF00400 | 0.337 |
TRG_ER_diArg_1 | 426 | 428 | PF00400 | 0.628 |
TRG_ER_diArg_1 | 514 | 517 | PF00400 | 0.491 |
TRG_ER_diArg_1 | 616 | 619 | PF00400 | 0.718 |
TRG_ER_diArg_1 | 626 | 629 | PF00400 | 0.620 |
TRG_ER_diArg_1 | 648 | 650 | PF00400 | 0.559 |
TRG_ER_diArg_1 | 710 | 712 | PF00400 | 0.484 |
TRG_ER_diArg_1 | 895 | 898 | PF00400 | 0.805 |
TRG_NLS_Bipartite_1 | 172 | 194 | PF00514 | 0.444 |
TRG_NLS_MonoCore_2 | 283 | 288 | PF00514 | 0.587 |
TRG_NLS_MonoExtC_3 | 189 | 194 | PF00514 | 0.675 |
TRG_NLS_MonoExtN_4 | 187 | 194 | PF00514 | 0.670 |
TRG_NLS_MonoExtN_4 | 282 | 288 | PF00514 | 0.601 |
TRG_Pf-PMV_PEXEL_1 | 162 | 166 | PF00026 | 0.684 |
TRG_Pf-PMV_PEXEL_1 | 184 | 188 | PF00026 | 0.692 |
TRG_Pf-PMV_PEXEL_1 | 313 | 318 | PF00026 | 0.381 |
TRG_Pf-PMV_PEXEL_1 | 516 | 521 | PF00026 | 0.423 |
TRG_Pf-PMV_PEXEL_1 | 710 | 714 | PF00026 | 0.467 |
TRG_Pf-PMV_PEXEL_1 | 733 | 737 | PF00026 | 0.280 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4IWB2 | Bodo saltans | 23% | 83% |
A0A3S7WNM9 | Leishmania donovani | 69% | 67% |
D0A263 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 85% |
E9ACK4 | Leishmania major | 69% | 66% |
E9AG48 | Leishmania infantum | 70% | 67% |