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 |
Related structures:
AlphaFold database: Q9NE58
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 10 |
GO:0006508 | proteolysis | 4 | 2 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 2 |
GO:0006793 | phosphorus metabolic process | 3 | 10 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 10 |
GO:0006807 | nitrogen compound metabolic process | 2 | 10 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0009056 | catabolic process | 2 | 2 |
GO:0009057 | macromolecule catabolic process | 4 | 2 |
GO:0009987 | cellular process | 1 | 10 |
GO:0010941 | regulation of cell death | 4 | 2 |
GO:0016310 | phosphorylation | 5 | 10 |
GO:0016567 | protein ubiquitination | 7 | 2 |
GO:0019538 | protein metabolic process | 3 | 10 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 2 |
GO:0032446 | protein modification by small protein conjugation | 6 | 2 |
GO:0036211 | protein modification process | 4 | 10 |
GO:0042981 | regulation of apoptotic process | 6 | 2 |
GO:0043067 | regulation of programmed cell death | 5 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 10 |
GO:0043412 | macromolecule modification | 4 | 10 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 2 |
GO:0044237 | cellular metabolic process | 2 | 10 |
GO:0044238 | primary metabolic process | 2 | 10 |
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:0050789 | regulation of biological process | 2 | 2 |
GO:0050794 | regulation of cellular process | 3 | 2 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 10 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 10 |
GO:1901575 | organic substance catabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 10 |
GO:0003824 | catalytic activity | 1 | 10 |
GO:0004672 | protein kinase activity | 3 | 10 |
GO:0005488 | binding | 1 | 10 |
GO:0005524 | ATP binding | 5 | 10 |
GO:0008270 | zinc ion binding | 6 | 9 |
GO:0016301 | kinase activity | 4 | 10 |
GO:0016740 | transferase activity | 2 | 10 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 10 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 10 |
GO:0017076 | purine nucleotide binding | 4 | 10 |
GO:0030554 | adenyl nucleotide binding | 5 | 10 |
GO:0032553 | ribonucleotide binding | 3 | 10 |
GO:0032555 | purine ribonucleotide binding | 4 | 10 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 10 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 10 |
GO:0036094 | small molecule binding | 2 | 10 |
GO:0043167 | ion binding | 2 | 10 |
GO:0043168 | anion binding | 3 | 10 |
GO:0043169 | cation binding | 3 | 9 |
GO:0046872 | metal ion binding | 4 | 9 |
GO:0046914 | transition metal ion binding | 5 | 9 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:0097367 | carbohydrate derivative binding | 2 | 10 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 10 |
GO:1901265 | nucleoside phosphate binding | 3 | 10 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 604 | 608 | PF00656 | 0.565 |
CLV_NRD_NRD_1 | 567 | 569 | PF00675 | 0.447 |
CLV_NRD_NRD_1 | 7 | 9 | PF00675 | 0.444 |
CLV_NRD_NRD_1 | 77 | 79 | PF00675 | 0.408 |
CLV_NRD_NRD_1 | 785 | 787 | PF00675 | 0.408 |
CLV_NRD_NRD_1 | 839 | 841 | PF00675 | 0.444 |
CLV_PCSK_KEX2_1 | 7 | 9 | PF00082 | 0.444 |
CLV_PCSK_KEX2_1 | 77 | 79 | PF00082 | 0.408 |
CLV_PCSK_PC1ET2_1 | 7 | 9 | PF00082 | 0.444 |
CLV_PCSK_SKI1_1 | 225 | 229 | PF00082 | 0.356 |
CLV_PCSK_SKI1_1 | 230 | 234 | PF00082 | 0.331 |
CLV_PCSK_SKI1_1 | 243 | 247 | PF00082 | 0.275 |
CLV_PCSK_SKI1_1 | 330 | 334 | PF00082 | 0.365 |
CLV_PCSK_SKI1_1 | 336 | 340 | PF00082 | 0.326 |
CLV_PCSK_SKI1_1 | 402 | 406 | PF00082 | 0.657 |
CLV_PCSK_SKI1_1 | 48 | 52 | PF00082 | 0.348 |
CLV_PCSK_SKI1_1 | 502 | 506 | PF00082 | 0.762 |
CLV_PCSK_SKI1_1 | 568 | 572 | PF00082 | 0.579 |
CLV_PCSK_SKI1_1 | 635 | 639 | PF00082 | 0.662 |
CLV_PCSK_SKI1_1 | 787 | 791 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 964 | 968 | PF00082 | 0.444 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.509 |
DOC_ANK_TNKS_1 | 7 | 14 | PF00023 | 0.444 |
DOC_CKS1_1 | 264 | 269 | PF01111 | 0.344 |
DOC_CYCLIN_RxL_1 | 452 | 460 | PF00134 | 0.727 |
DOC_CYCLIN_RxL_1 | 631 | 641 | PF00134 | 0.601 |
DOC_MAPK_gen_1 | 230 | 239 | PF00069 | 0.344 |
DOC_MAPK_gen_1 | 24 | 34 | PF00069 | 0.408 |
DOC_MAPK_gen_1 | 48 | 56 | PF00069 | 0.351 |
DOC_MAPK_gen_1 | 657 | 667 | PF00069 | 0.522 |
DOC_MAPK_MEF2A_6 | 48 | 56 | PF00069 | 0.348 |
DOC_PP1_RVXF_1 | 453 | 460 | PF00149 | 0.729 |
DOC_PP1_RVXF_1 | 972 | 978 | PF00149 | 0.565 |
DOC_PP2B_LxvP_1 | 509 | 512 | PF13499 | 0.728 |
DOC_PP2B_LxvP_1 | 545 | 548 | PF13499 | 0.521 |
DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.731 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.672 |
DOC_USP7_MATH_1 | 303 | 307 | PF00917 | 0.344 |
DOC_USP7_MATH_1 | 347 | 351 | PF00917 | 0.485 |
DOC_USP7_MATH_1 | 366 | 370 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 374 | 378 | PF00917 | 0.639 |
DOC_USP7_MATH_1 | 466 | 470 | PF00917 | 0.810 |
DOC_USP7_MATH_1 | 512 | 516 | PF00917 | 0.674 |
DOC_USP7_MATH_1 | 650 | 654 | PF00917 | 0.742 |
DOC_USP7_MATH_1 | 710 | 714 | PF00917 | 0.407 |
DOC_USP7_MATH_1 | 723 | 727 | PF00917 | 0.449 |
DOC_USP7_MATH_1 | 81 | 85 | PF00917 | 0.683 |
DOC_USP7_MATH_1 | 860 | 864 | PF00917 | 0.444 |
DOC_USP7_MATH_1 | 87 | 91 | PF00917 | 0.656 |
DOC_WW_Pin1_4 | 263 | 268 | PF00397 | 0.344 |
DOC_WW_Pin1_4 | 345 | 350 | PF00397 | 0.343 |
DOC_WW_Pin1_4 | 360 | 365 | PF00397 | 0.577 |
DOC_WW_Pin1_4 | 442 | 447 | PF00397 | 0.757 |
DOC_WW_Pin1_4 | 461 | 466 | PF00397 | 0.573 |
DOC_WW_Pin1_4 | 595 | 600 | PF00397 | 0.480 |
DOC_WW_Pin1_4 | 605 | 610 | PF00397 | 0.573 |
DOC_WW_Pin1_4 | 692 | 697 | PF00397 | 0.291 |
DOC_WW_Pin1_4 | 715 | 720 | PF00397 | 0.485 |
DOC_WW_Pin1_4 | 787 | 792 | PF00397 | 0.444 |
LIG_14-3-3_CanoR_1 | 24 | 34 | PF00244 | 0.498 |
LIG_14-3-3_CanoR_1 | 260 | 268 | PF00244 | 0.444 |
LIG_14-3-3_CanoR_1 | 419 | 427 | PF00244 | 0.691 |
LIG_14-3-3_CanoR_1 | 473 | 477 | PF00244 | 0.793 |
LIG_14-3-3_CanoR_1 | 514 | 519 | PF00244 | 0.720 |
LIG_14-3-3_CanoR_1 | 724 | 728 | PF00244 | 0.460 |
LIG_14-3-3_CanoR_1 | 974 | 978 | PF00244 | 0.547 |
LIG_Actin_WH2_2 | 544 | 561 | PF00022 | 0.389 |
LIG_APCC_ABBAyCdc20_2 | 225 | 231 | PF00400 | 0.401 |
LIG_BIR_III_2 | 788 | 792 | PF00653 | 0.408 |
LIG_BIR_III_4 | 810 | 814 | PF00653 | 0.344 |
LIG_BRCT_BRCA1_1 | 500 | 504 | PF00533 | 0.676 |
LIG_Clathr_ClatBox_1 | 636 | 640 | PF01394 | 0.627 |
LIG_eIF4E_1 | 64 | 70 | PF01652 | 0.344 |
LIG_FHA_1 | 143 | 149 | PF00498 | 0.754 |
LIG_FHA_1 | 253 | 259 | PF00498 | 0.401 |
LIG_FHA_1 | 380 | 386 | PF00498 | 0.660 |
LIG_FHA_1 | 522 | 528 | PF00498 | 0.701 |
LIG_FHA_1 | 575 | 581 | PF00498 | 0.552 |
LIG_FHA_1 | 583 | 589 | PF00498 | 0.483 |
LIG_FHA_1 | 788 | 794 | PF00498 | 0.444 |
LIG_FHA_1 | 884 | 890 | PF00498 | 0.408 |
LIG_FHA_2 | 189 | 195 | PF00498 | 0.362 |
LIG_FHA_2 | 296 | 302 | PF00498 | 0.344 |
LIG_FHA_2 | 36 | 42 | PF00498 | 0.477 |
LIG_FHA_2 | 666 | 672 | PF00498 | 0.410 |
LIG_FHA_2 | 951 | 957 | PF00498 | 0.401 |
LIG_GBD_Chelix_1 | 170 | 178 | PF00786 | 0.444 |
LIG_GBD_Chelix_1 | 331 | 339 | PF00786 | 0.485 |
LIG_LIR_Apic_2 | 266 | 272 | PF02991 | 0.344 |
LIG_LIR_Gen_1 | 501 | 512 | PF02991 | 0.701 |
LIG_LIR_Gen_1 | 63 | 71 | PF02991 | 0.344 |
LIG_LIR_Gen_1 | 751 | 760 | PF02991 | 0.444 |
LIG_LIR_Gen_1 | 816 | 824 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 240 | 245 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 501 | 507 | PF02991 | 0.706 |
LIG_LIR_Nem_3 | 63 | 67 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 751 | 755 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 816 | 820 | PF02991 | 0.444 |
LIG_LRP6_Inhibitor_1 | 862 | 868 | PF00058 | 0.344 |
LIG_LRP6_Inhibitor_1 | 908 | 914 | PF00058 | 0.444 |
LIG_MAD2 | 51 | 59 | PF02301 | 0.401 |
LIG_NRBOX | 292 | 298 | PF00104 | 0.444 |
LIG_NRBOX | 330 | 336 | PF00104 | 0.369 |
LIG_PCNA_yPIPBox_3 | 181 | 192 | PF02747 | 0.446 |
LIG_Pex14_2 | 67 | 71 | PF04695 | 0.344 |
LIG_PTB_Apo_2 | 221 | 228 | PF02174 | 0.252 |
LIG_SH2_CRK | 242 | 246 | PF00017 | 0.485 |
LIG_SH2_CRK | 817 | 821 | PF00017 | 0.444 |
LIG_SH2_NCK_1 | 817 | 821 | PF00017 | 0.444 |
LIG_SH2_STAP1 | 30 | 34 | PF00017 | 0.444 |
LIG_SH2_STAP1 | 327 | 331 | PF00017 | 0.485 |
LIG_SH2_STAT5 | 269 | 272 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 4 | 7 | PF00017 | 0.289 |
LIG_SH2_STAT5 | 64 | 67 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 899 | 902 | PF00017 | 0.327 |
LIG_SH3_3 | 261 | 267 | PF00018 | 0.344 |
LIG_SH3_3 | 477 | 483 | PF00018 | 0.715 |
LIG_SH3_3 | 656 | 662 | PF00018 | 0.661 |
LIG_SH3_3 | 713 | 719 | PF00018 | 0.441 |
LIG_SUMO_SIM_par_1 | 290 | 295 | PF11976 | 0.344 |
LIG_SUMO_SIM_par_1 | 579 | 586 | PF11976 | 0.463 |
LIG_SUMO_SIM_par_1 | 601 | 608 | PF11976 | 0.479 |
LIG_TRAF2_1 | 191 | 194 | PF00917 | 0.408 |
LIG_TRAF2_1 | 38 | 41 | PF00917 | 0.416 |
LIG_TRFH_1 | 268 | 272 | PF08558 | 0.401 |
LIG_UBA3_1 | 372 | 380 | PF00899 | 0.711 |
MOD_CDK_SPK_2 | 787 | 792 | PF00069 | 0.444 |
MOD_CDK_SPxxK_3 | 787 | 794 | PF00069 | 0.444 |
MOD_CK1_1 | 142 | 148 | PF00069 | 0.691 |
MOD_CK1_1 | 151 | 157 | PF00069 | 0.721 |
MOD_CK1_1 | 26 | 32 | PF00069 | 0.485 |
MOD_CK1_1 | 418 | 424 | PF00069 | 0.745 |
MOD_CK1_1 | 469 | 475 | PF00069 | 0.751 |
MOD_CK1_1 | 484 | 490 | PF00069 | 0.736 |
MOD_CK1_1 | 519 | 525 | PF00069 | 0.723 |
MOD_CK1_1 | 60 | 66 | PF00069 | 0.444 |
MOD_CK1_1 | 660 | 666 | PF00069 | 0.580 |
MOD_CK1_1 | 685 | 691 | PF00069 | 0.344 |
MOD_CK1_1 | 692 | 698 | PF00069 | 0.333 |
MOD_CK1_1 | 973 | 979 | PF00069 | 0.585 |
MOD_CK2_1 | 107 | 113 | PF00069 | 0.668 |
MOD_CK2_1 | 188 | 194 | PF00069 | 0.425 |
MOD_CK2_1 | 199 | 205 | PF00069 | 0.379 |
MOD_CK2_1 | 207 | 213 | PF00069 | 0.262 |
MOD_CK2_1 | 295 | 301 | PF00069 | 0.441 |
MOD_CK2_1 | 35 | 41 | PF00069 | 0.477 |
MOD_CK2_1 | 665 | 671 | PF00069 | 0.436 |
MOD_CK2_1 | 677 | 683 | PF00069 | 0.342 |
MOD_CK2_1 | 860 | 866 | PF00069 | 0.369 |
MOD_CK2_1 | 889 | 895 | PF00069 | 0.419 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.702 |
MOD_GlcNHglycan | 141 | 144 | PF01048 | 0.471 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.444 |
MOD_GlcNHglycan | 368 | 371 | PF01048 | 0.729 |
MOD_GlcNHglycan | 442 | 445 | PF01048 | 0.740 |
MOD_GlcNHglycan | 532 | 536 | PF01048 | 0.742 |
MOD_GlcNHglycan | 615 | 618 | PF01048 | 0.461 |
MOD_GlcNHglycan | 652 | 655 | PF01048 | 0.781 |
MOD_GlcNHglycan | 683 | 687 | PF01048 | 0.339 |
MOD_GlcNHglycan | 697 | 700 | PF01048 | 0.356 |
MOD_GlcNHglycan | 705 | 708 | PF01048 | 0.364 |
MOD_GlcNHglycan | 775 | 778 | PF01048 | 0.405 |
MOD_GlcNHglycan | 810 | 814 | PF01048 | 0.344 |
MOD_GlcNHglycan | 833 | 836 | PF01048 | 0.444 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.778 |
MOD_GlcNHglycan | 891 | 894 | PF01048 | 0.405 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.700 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.814 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.640 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.408 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.477 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.344 |
MOD_GSK3_1 | 326 | 333 | PF00069 | 0.331 |
MOD_GSK3_1 | 355 | 362 | PF00069 | 0.524 |
MOD_GSK3_1 | 418 | 425 | PF00069 | 0.705 |
MOD_GSK3_1 | 426 | 433 | PF00069 | 0.659 |
MOD_GSK3_1 | 436 | 443 | PF00069 | 0.587 |
MOD_GSK3_1 | 453 | 460 | PF00069 | 0.745 |
MOD_GSK3_1 | 461 | 468 | PF00069 | 0.768 |
MOD_GSK3_1 | 481 | 488 | PF00069 | 0.460 |
MOD_GSK3_1 | 498 | 505 | PF00069 | 0.609 |
MOD_GSK3_1 | 512 | 519 | PF00069 | 0.668 |
MOD_GSK3_1 | 613 | 620 | PF00069 | 0.440 |
MOD_GSK3_1 | 685 | 692 | PF00069 | 0.464 |
MOD_GSK3_1 | 705 | 712 | PF00069 | 0.462 |
MOD_N-GLC_1 | 425 | 430 | PF02516 | 0.804 |
MOD_N-GLC_1 | 466 | 471 | PF02516 | 0.754 |
MOD_N-GLC_1 | 485 | 490 | PF02516 | 0.648 |
MOD_N-GLC_1 | 574 | 579 | PF02516 | 0.625 |
MOD_NEK2_1 | 105 | 110 | PF00069 | 0.653 |
MOD_NEK2_1 | 195 | 200 | PF00069 | 0.474 |
MOD_NEK2_1 | 252 | 257 | PF00069 | 0.369 |
MOD_NEK2_1 | 325 | 330 | PF00069 | 0.344 |
MOD_NEK2_1 | 368 | 373 | PF00069 | 0.733 |
MOD_NEK2_1 | 397 | 402 | PF00069 | 0.654 |
MOD_NEK2_1 | 457 | 462 | PF00069 | 0.781 |
MOD_NEK2_1 | 521 | 526 | PF00069 | 0.602 |
MOD_NEK2_1 | 582 | 587 | PF00069 | 0.556 |
MOD_NEK2_1 | 763 | 768 | PF00069 | 0.444 |
MOD_NEK2_1 | 876 | 881 | PF00069 | 0.344 |
MOD_NEK2_1 | 921 | 926 | PF00069 | 0.348 |
MOD_PIKK_1 | 521 | 527 | PF00454 | 0.691 |
MOD_PK_1 | 355 | 361 | PF00069 | 0.624 |
MOD_PK_1 | 57 | 63 | PF00069 | 0.444 |
MOD_PKA_1 | 657 | 663 | PF00069 | 0.599 |
MOD_PKA_2 | 188 | 194 | PF00069 | 0.386 |
MOD_PKA_2 | 23 | 29 | PF00069 | 0.485 |
MOD_PKA_2 | 259 | 265 | PF00069 | 0.344 |
MOD_PKA_2 | 418 | 424 | PF00069 | 0.693 |
MOD_PKA_2 | 472 | 478 | PF00069 | 0.794 |
MOD_PKA_2 | 617 | 623 | PF00069 | 0.401 |
MOD_PKA_2 | 660 | 666 | PF00069 | 0.580 |
MOD_PKA_2 | 677 | 683 | PF00069 | 0.344 |
MOD_PKA_2 | 710 | 716 | PF00069 | 0.431 |
MOD_PKA_2 | 723 | 729 | PF00069 | 0.460 |
MOD_PKA_2 | 973 | 979 | PF00069 | 0.546 |
MOD_PKB_1 | 413 | 421 | PF00069 | 0.723 |
MOD_Plk_1 | 2 | 8 | PF00069 | 0.289 |
MOD_Plk_1 | 425 | 431 | PF00069 | 0.728 |
MOD_Plk_1 | 519 | 525 | PF00069 | 0.723 |
MOD_Plk_2-3 | 295 | 301 | PF00069 | 0.344 |
MOD_Plk_2-3 | 739 | 745 | PF00069 | 0.408 |
MOD_Plk_4 | 100 | 106 | PF00069 | 0.750 |
MOD_Plk_4 | 148 | 154 | PF00069 | 0.772 |
MOD_Plk_4 | 207 | 213 | PF00069 | 0.344 |
MOD_Plk_4 | 303 | 309 | PF00069 | 0.405 |
MOD_Plk_4 | 314 | 320 | PF00069 | 0.317 |
MOD_Plk_4 | 330 | 336 | PF00069 | 0.442 |
MOD_Plk_4 | 348 | 354 | PF00069 | 0.293 |
MOD_Plk_4 | 368 | 374 | PF00069 | 0.709 |
MOD_Plk_4 | 426 | 432 | PF00069 | 0.722 |
MOD_Plk_4 | 540 | 546 | PF00069 | 0.531 |
MOD_Plk_4 | 57 | 63 | PF00069 | 0.355 |
MOD_Plk_4 | 717 | 723 | PF00069 | 0.466 |
MOD_Plk_4 | 748 | 754 | PF00069 | 0.401 |
MOD_Plk_4 | 973 | 979 | PF00069 | 0.516 |
MOD_ProDKin_1 | 263 | 269 | PF00069 | 0.344 |
MOD_ProDKin_1 | 345 | 351 | PF00069 | 0.343 |
MOD_ProDKin_1 | 360 | 366 | PF00069 | 0.582 |
MOD_ProDKin_1 | 442 | 448 | PF00069 | 0.754 |
MOD_ProDKin_1 | 461 | 467 | PF00069 | 0.573 |
MOD_ProDKin_1 | 595 | 601 | PF00069 | 0.473 |
MOD_ProDKin_1 | 605 | 611 | PF00069 | 0.566 |
MOD_ProDKin_1 | 692 | 698 | PF00069 | 0.291 |
MOD_ProDKin_1 | 715 | 721 | PF00069 | 0.485 |
MOD_ProDKin_1 | 787 | 793 | PF00069 | 0.444 |
MOD_SUMO_rev_2 | 240 | 245 | PF00179 | 0.344 |
TRG_DiLeu_BaEn_1 | 49 | 54 | PF01217 | 0.344 |
TRG_ENDOCYTIC_2 | 242 | 245 | PF00928 | 0.401 |
TRG_ENDOCYTIC_2 | 64 | 67 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 817 | 820 | PF00928 | 0.444 |
TRG_ENDOCYTIC_2 | 941 | 944 | PF00928 | 0.344 |
TRG_ER_diArg_1 | 76 | 78 | PF00400 | 0.408 |
TRG_ER_diArg_1 | 791 | 794 | PF00400 | 0.444 |
TRG_NES_CRM1_1 | 285 | 295 | PF08389 | 0.478 |
TRG_NLS_MonoExtC_3 | 6 | 12 | PF00514 | 0.444 |
TRG_NLS_MonoExtN_4 | 837 | 844 | PF00514 | 0.444 |
TRG_Pf-PMV_PEXEL_1 | 274 | 278 | PF00026 | 0.344 |
TRG_Pf-PMV_PEXEL_1 | 491 | 496 | PF00026 | 0.755 |
TRG_Pf-PMV_PEXEL_1 | 767 | 771 | PF00026 | 0.401 |
TRG_Pf-PMV_PEXEL_1 | 8 | 12 | PF00026 | 0.444 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PFF2 | Leptomonas seymouri | 72% | 99% |
A0A1X0P1U2 | Trypanosomatidae | 46% | 100% |
A0A3Q8IEB1 | Leishmania donovani | 95% | 99% |
A0A422N709 | Trypanosoma rangeli | 47% | 100% |
A4HIE5 | Leishmania braziliensis | 84% | 100% |
A4I5P2 | Leishmania infantum | 95% | 99% |
E9B0Y6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 99% |
V5DCX1 | Trypanosoma cruzi | 47% | 100% |