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:0000938 | GARP complex | 3 | 2 |
GO:0005829 | cytosol | 2 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0099023 | vesicle tethering complex | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
GO:0005794 | Golgi apparatus | 5 | 8 |
GO:0043226 | organelle | 2 | 8 |
GO:0043227 | membrane-bounded organelle | 3 | 8 |
GO:0043229 | intracellular organelle | 3 | 8 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 8 |
Related structures:
AlphaFold database: Q4Q2S9
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 10 |
GO:0006892 | post-Golgi vesicle-mediated transport | 6 | 2 |
GO:0006896 | Golgi to vacuole transport | 5 | 2 |
GO:0007034 | vacuolar transport | 4 | 2 |
GO:0008104 | protein localization | 4 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0015031 | protein transport | 4 | 10 |
GO:0016192 | vesicle-mediated transport | 4 | 2 |
GO:0016197 | endosomal transport | 4 | 2 |
GO:0016482 | cytosolic transport | 4 | 2 |
GO:0032456 | endocytic recycling | 5 | 2 |
GO:0033036 | macromolecule localization | 2 | 10 |
GO:0042147 | retrograde transport, endosome to Golgi | 5 | 2 |
GO:0045184 | establishment of protein localization | 3 | 10 |
GO:0046907 | intracellular transport | 3 | 2 |
GO:0048193 | Golgi vesicle transport | 5 | 2 |
GO:0051179 | localization | 1 | 10 |
GO:0051234 | establishment of localization | 2 | 10 |
GO:0051641 | cellular localization | 2 | 10 |
GO:0051649 | establishment of localization in cell | 3 | 2 |
GO:0051668 | localization within membrane | 3 | 2 |
GO:0070727 | cellular macromolecule localization | 3 | 10 |
GO:0071702 | organic substance transport | 4 | 10 |
GO:0071705 | nitrogen compound transport | 4 | 10 |
GO:0098876 | vesicle-mediated transport to the plasma membrane | 4 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000149 | SNARE binding | 3 | 2 |
GO:0005488 | binding | 1 | 2 |
GO:0005515 | protein binding | 2 | 2 |
GO:0019905 | syntaxin binding | 4 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 125 | 127 | PF00675 | 0.410 |
CLV_NRD_NRD_1 | 131 | 133 | PF00675 | 0.321 |
CLV_NRD_NRD_1 | 173 | 175 | PF00675 | 0.410 |
CLV_NRD_NRD_1 | 329 | 331 | PF00675 | 0.521 |
CLV_NRD_NRD_1 | 618 | 620 | PF00675 | 0.562 |
CLV_NRD_NRD_1 | 816 | 818 | PF00675 | 0.535 |
CLV_NRD_NRD_1 | 871 | 873 | PF00675 | 0.465 |
CLV_PCSK_KEX2_1 | 131 | 133 | PF00082 | 0.351 |
CLV_PCSK_KEX2_1 | 173 | 175 | PF00082 | 0.444 |
CLV_PCSK_KEX2_1 | 329 | 331 | PF00082 | 0.521 |
CLV_PCSK_KEX2_1 | 617 | 619 | PF00082 | 0.454 |
CLV_PCSK_PC1ET2_1 | 617 | 619 | PF00082 | 0.454 |
CLV_PCSK_PC7_1 | 169 | 175 | PF00082 | 0.444 |
CLV_PCSK_PC7_1 | 325 | 331 | PF00082 | 0.595 |
CLV_PCSK_SKI1_1 | 210 | 214 | PF00082 | 0.401 |
CLV_PCSK_SKI1_1 | 299 | 303 | PF00082 | 0.530 |
CLV_PCSK_SKI1_1 | 339 | 343 | PF00082 | 0.579 |
CLV_PCSK_SKI1_1 | 361 | 365 | PF00082 | 0.490 |
CLV_PCSK_SKI1_1 | 444 | 448 | PF00082 | 0.386 |
CLV_PCSK_SKI1_1 | 505 | 509 | PF00082 | 0.459 |
CLV_PCSK_SKI1_1 | 513 | 517 | PF00082 | 0.462 |
CLV_PCSK_SKI1_1 | 796 | 800 | PF00082 | 0.518 |
CLV_PCSK_SKI1_1 | 886 | 890 | PF00082 | 0.508 |
CLV_Separin_Metazoa | 814 | 818 | PF03568 | 0.585 |
DEG_APCC_DBOX_1 | 885 | 893 | PF00400 | 0.344 |
DEG_SPOP_SBC_1 | 653 | 657 | PF00917 | 0.571 |
DEG_SPOP_SBC_1 | 700 | 704 | PF00917 | 0.539 |
DEG_SPOP_SBC_1 | 760 | 764 | PF00917 | 0.554 |
DEG_SPOP_SBC_1 | 767 | 771 | PF00917 | 0.544 |
DOC_CDC14_PxL_1 | 489 | 497 | PF14671 | 0.499 |
DOC_CDC14_PxL_1 | 523 | 531 | PF14671 | 0.490 |
DOC_CYCLIN_RxL_1 | 169 | 179 | PF00134 | 0.405 |
DOC_CYCLIN_RxL_1 | 210 | 222 | PF00134 | 0.441 |
DOC_MAPK_gen_1 | 376 | 384 | PF00069 | 0.587 |
DOC_MAPK_gen_1 | 872 | 878 | PF00069 | 0.530 |
DOC_MIT_MIM_1 | 170 | 178 | PF04212 | 0.444 |
DOC_PP1_RVXF_1 | 171 | 178 | PF00149 | 0.345 |
DOC_PP1_RVXF_1 | 180 | 187 | PF00149 | 0.327 |
DOC_PP4_FxxP_1 | 783 | 786 | PF00568 | 0.430 |
DOC_USP7_MATH_1 | 291 | 295 | PF00917 | 0.565 |
DOC_USP7_MATH_1 | 349 | 353 | PF00917 | 0.688 |
DOC_USP7_MATH_1 | 450 | 454 | PF00917 | 0.469 |
DOC_USP7_MATH_1 | 539 | 543 | PF00917 | 0.516 |
DOC_USP7_MATH_1 | 653 | 657 | PF00917 | 0.744 |
DOC_USP7_MATH_1 | 686 | 690 | PF00917 | 0.769 |
DOC_USP7_MATH_1 | 700 | 704 | PF00917 | 0.601 |
DOC_USP7_MATH_1 | 71 | 75 | PF00917 | 0.485 |
DOC_USP7_MATH_1 | 838 | 842 | PF00917 | 0.577 |
DOC_USP7_UBL2_3 | 203 | 207 | PF12436 | 0.444 |
DOC_WW_Pin1_4 | 529 | 534 | PF00397 | 0.415 |
DOC_WW_Pin1_4 | 619 | 624 | PF00397 | 0.555 |
DOC_WW_Pin1_4 | 660 | 665 | PF00397 | 0.734 |
DOC_WW_Pin1_4 | 730 | 735 | PF00397 | 0.634 |
LIG_14-3-3_CanoR_1 | 194 | 202 | PF00244 | 0.481 |
LIG_14-3-3_CanoR_1 | 261 | 268 | PF00244 | 0.405 |
LIG_14-3-3_CanoR_1 | 329 | 335 | PF00244 | 0.542 |
LIG_14-3-3_CanoR_1 | 361 | 366 | PF00244 | 0.463 |
LIG_14-3-3_CanoR_1 | 404 | 410 | PF00244 | 0.497 |
LIG_14-3-3_CanoR_1 | 509 | 513 | PF00244 | 0.446 |
LIG_14-3-3_CanoR_1 | 618 | 623 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 796 | 805 | PF00244 | 0.497 |
LIG_Actin_WH2_2 | 493 | 511 | PF00022 | 0.493 |
LIG_Actin_WH2_2 | 782 | 798 | PF00022 | 0.552 |
LIG_AP2alpha_1 | 64 | 68 | PF02296 | 0.548 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.693 |
LIG_BRCT_BRCA1_1 | 235 | 239 | PF00533 | 0.444 |
LIG_BRCT_BRCA1_1 | 860 | 864 | PF00533 | 0.396 |
LIG_DLG_GKlike_1 | 353 | 360 | PF00625 | 0.548 |
LIG_EVH1_2 | 779 | 783 | PF00568 | 0.473 |
LIG_FHA_1 | 211 | 217 | PF00498 | 0.401 |
LIG_FHA_1 | 352 | 358 | PF00498 | 0.628 |
LIG_FHA_1 | 467 | 473 | PF00498 | 0.360 |
LIG_FHA_1 | 526 | 532 | PF00498 | 0.460 |
LIG_FHA_1 | 576 | 582 | PF00498 | 0.478 |
LIG_FHA_1 | 619 | 625 | PF00498 | 0.474 |
LIG_FHA_1 | 700 | 706 | PF00498 | 0.639 |
LIG_FHA_1 | 707 | 713 | PF00498 | 0.460 |
LIG_FHA_1 | 8 | 14 | PF00498 | 0.638 |
LIG_FHA_1 | 894 | 900 | PF00498 | 0.487 |
LIG_FHA_2 | 224 | 230 | PF00498 | 0.410 |
LIG_FHA_2 | 362 | 368 | PF00498 | 0.428 |
LIG_FHA_2 | 435 | 441 | PF00498 | 0.552 |
LIG_FHA_2 | 485 | 491 | PF00498 | 0.526 |
LIG_FHA_2 | 512 | 518 | PF00498 | 0.539 |
LIG_FHA_2 | 638 | 644 | PF00498 | 0.553 |
LIG_FHA_2 | 864 | 870 | PF00498 | 0.548 |
LIG_LIR_Gen_1 | 140 | 150 | PF02991 | 0.345 |
LIG_LIR_Gen_1 | 397 | 406 | PF02991 | 0.425 |
LIG_LIR_Gen_1 | 632 | 639 | PF02991 | 0.437 |
LIG_LIR_Gen_1 | 733 | 742 | PF02991 | 0.527 |
LIG_LIR_Gen_1 | 861 | 869 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 140 | 145 | PF02991 | 0.345 |
LIG_LIR_Nem_3 | 149 | 154 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 256 | 262 | PF02991 | 0.349 |
LIG_LIR_Nem_3 | 397 | 403 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 542 | 547 | PF02991 | 0.514 |
LIG_LIR_Nem_3 | 640 | 644 | PF02991 | 0.499 |
LIG_LIR_Nem_3 | 733 | 738 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 861 | 867 | PF02991 | 0.551 |
LIG_LRP6_Inhibitor_1 | 188 | 194 | PF00058 | 0.444 |
LIG_MAD2 | 215 | 223 | PF02301 | 0.444 |
LIG_NRBOX | 901 | 907 | PF00104 | 0.460 |
LIG_PCNA_yPIPBox_3 | 717 | 729 | PF02747 | 0.554 |
LIG_PCNA_yPIPBox_3 | 891 | 902 | PF02747 | 0.336 |
LIG_Pex14_1 | 398 | 402 | PF04695 | 0.389 |
LIG_Pex14_2 | 239 | 243 | PF04695 | 0.444 |
LIG_Pex14_2 | 402 | 406 | PF04695 | 0.449 |
LIG_Pex14_2 | 419 | 423 | PF04695 | 0.259 |
LIG_Pex14_2 | 64 | 68 | PF04695 | 0.548 |
LIG_PROFILIN_1 | 774 | 780 | PF00235 | 0.518 |
LIG_PTB_Apo_2 | 547 | 554 | PF02174 | 0.531 |
LIG_PTB_Phospho_1 | 547 | 553 | PF10480 | 0.536 |
LIG_RPA_C_Fungi | 348 | 360 | PF08784 | 0.578 |
LIG_SH2_CRK | 142 | 146 | PF00017 | 0.369 |
LIG_SH2_CRK | 247 | 251 | PF00017 | 0.321 |
LIG_SH2_GRB2like | 575 | 578 | PF00017 | 0.488 |
LIG_SH2_SRC | 711 | 714 | PF00017 | 0.544 |
LIG_SH2_SRC | 737 | 740 | PF00017 | 0.352 |
LIG_SH2_STAP1 | 635 | 639 | PF00017 | 0.429 |
LIG_SH2_STAT3 | 262 | 265 | PF00017 | 0.407 |
LIG_SH2_STAT3 | 267 | 270 | PF00017 | 0.356 |
LIG_SH2_STAT5 | 142 | 145 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 164 | 167 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 259 | 262 | PF00017 | 0.361 |
LIG_SH2_STAT5 | 267 | 270 | PF00017 | 0.381 |
LIG_SH2_STAT5 | 383 | 386 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 43 | 46 | PF00017 | 0.603 |
LIG_SH2_STAT5 | 553 | 556 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 575 | 578 | PF00017 | 0.485 |
LIG_SH2_STAT5 | 635 | 638 | PF00017 | 0.359 |
LIG_SH2_STAT5 | 711 | 714 | PF00017 | 0.487 |
LIG_SH2_STAT5 | 737 | 740 | PF00017 | 0.455 |
LIG_SH3_3 | 285 | 291 | PF00018 | 0.444 |
LIG_SH3_3 | 317 | 323 | PF00018 | 0.515 |
LIG_SH3_3 | 772 | 778 | PF00018 | 0.734 |
LIG_Sin3_3 | 443 | 450 | PF02671 | 0.498 |
LIG_SUMO_SIM_anti_2 | 460 | 467 | PF11976 | 0.463 |
LIG_SUMO_SIM_par_1 | 215 | 222 | PF11976 | 0.416 |
LIG_SUMO_SIM_par_1 | 249 | 254 | PF11976 | 0.408 |
LIG_SUMO_SIM_par_1 | 492 | 498 | PF11976 | 0.368 |
LIG_TRAF2_1 | 232 | 235 | PF00917 | 0.463 |
LIG_TRAF2_1 | 294 | 297 | PF00917 | 0.557 |
LIG_TRAF2_1 | 55 | 58 | PF00917 | 0.578 |
LIG_WRC_WIRS_1 | 598 | 603 | PF05994 | 0.497 |
MOD_CDK_SPxxK_3 | 529 | 536 | PF00069 | 0.514 |
MOD_CDK_SPxxK_3 | 660 | 667 | PF00069 | 0.624 |
MOD_CK1_1 | 156 | 162 | PF00069 | 0.485 |
MOD_CK1_1 | 279 | 285 | PF00069 | 0.414 |
MOD_CK1_1 | 453 | 459 | PF00069 | 0.486 |
MOD_CK1_1 | 511 | 517 | PF00069 | 0.498 |
MOD_CK1_1 | 52 | 58 | PF00069 | 0.579 |
MOD_CK1_1 | 584 | 590 | PF00069 | 0.644 |
MOD_CK1_1 | 597 | 603 | PF00069 | 0.374 |
MOD_CK1_1 | 654 | 660 | PF00069 | 0.768 |
MOD_CK1_1 | 703 | 709 | PF00069 | 0.634 |
MOD_CK1_1 | 829 | 835 | PF00069 | 0.698 |
MOD_CK1_1 | 865 | 871 | PF00069 | 0.545 |
MOD_CK2_1 | 223 | 229 | PF00069 | 0.386 |
MOD_CK2_1 | 291 | 297 | PF00069 | 0.507 |
MOD_CK2_1 | 3 | 9 | PF00069 | 0.639 |
MOD_CK2_1 | 349 | 355 | PF00069 | 0.632 |
MOD_CK2_1 | 434 | 440 | PF00069 | 0.522 |
MOD_CK2_1 | 511 | 517 | PF00069 | 0.542 |
MOD_CK2_1 | 52 | 58 | PF00069 | 0.568 |
MOD_CK2_1 | 637 | 643 | PF00069 | 0.485 |
MOD_CK2_1 | 686 | 692 | PF00069 | 0.795 |
MOD_CK2_1 | 71 | 77 | PF00069 | 0.312 |
MOD_CK2_1 | 863 | 869 | PF00069 | 0.552 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.776 |
MOD_GlcNHglycan | 108 | 112 | PF01048 | 0.384 |
MOD_GlcNHglycan | 178 | 181 | PF01048 | 0.394 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.337 |
MOD_GlcNHglycan | 234 | 238 | PF01048 | 0.436 |
MOD_GlcNHglycan | 280 | 284 | PF01048 | 0.485 |
MOD_GlcNHglycan | 293 | 296 | PF01048 | 0.562 |
MOD_GlcNHglycan | 310 | 313 | PF01048 | 0.368 |
MOD_GlcNHglycan | 346 | 349 | PF01048 | 0.496 |
MOD_GlcNHglycan | 437 | 440 | PF01048 | 0.526 |
MOD_GlcNHglycan | 448 | 451 | PF01048 | 0.275 |
MOD_GlcNHglycan | 497 | 500 | PF01048 | 0.408 |
MOD_GlcNHglycan | 505 | 508 | PF01048 | 0.420 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.569 |
MOD_GlcNHglycan | 583 | 586 | PF01048 | 0.554 |
MOD_GlcNHglycan | 647 | 650 | PF01048 | 0.611 |
MOD_GlcNHglycan | 669 | 672 | PF01048 | 0.814 |
MOD_GlcNHglycan | 724 | 727 | PF01048 | 0.473 |
MOD_GlcNHglycan | 755 | 758 | PF01048 | 0.627 |
MOD_GlcNHglycan | 770 | 773 | PF01048 | 0.683 |
MOD_GlcNHglycan | 831 | 834 | PF01048 | 0.727 |
MOD_GlcNHglycan | 840 | 843 | PF01048 | 0.601 |
MOD_GlcNHglycan | 860 | 863 | PF01048 | 0.522 |
MOD_GlcNHglycan | 882 | 885 | PF01048 | 0.536 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.412 |
MOD_GSK3_1 | 229 | 236 | PF00069 | 0.454 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.648 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.661 |
MOD_GSK3_1 | 339 | 346 | PF00069 | 0.664 |
MOD_GSK3_1 | 349 | 356 | PF00069 | 0.520 |
MOD_GSK3_1 | 361 | 368 | PF00069 | 0.297 |
MOD_GSK3_1 | 405 | 412 | PF00069 | 0.490 |
MOD_GSK3_1 | 446 | 453 | PF00069 | 0.541 |
MOD_GSK3_1 | 525 | 532 | PF00069 | 0.433 |
MOD_GSK3_1 | 629 | 636 | PF00069 | 0.513 |
MOD_GSK3_1 | 652 | 659 | PF00069 | 0.754 |
MOD_GSK3_1 | 669 | 676 | PF00069 | 0.764 |
MOD_GSK3_1 | 699 | 706 | PF00069 | 0.650 |
MOD_GSK3_1 | 755 | 762 | PF00069 | 0.621 |
MOD_GSK3_1 | 796 | 803 | PF00069 | 0.496 |
MOD_GSK3_1 | 820 | 827 | PF00069 | 0.527 |
MOD_GSK3_1 | 829 | 836 | PF00069 | 0.680 |
MOD_GSK3_1 | 838 | 845 | PF00069 | 0.557 |
MOD_GSK3_1 | 854 | 861 | PF00069 | 0.474 |
MOD_GSK3_1 | 863 | 870 | PF00069 | 0.490 |
MOD_GSK3_1 | 887 | 894 | PF00069 | 0.483 |
MOD_LATS_1 | 337 | 343 | PF00433 | 0.603 |
MOD_N-GLC_1 | 156 | 161 | PF02516 | 0.471 |
MOD_N-GLC_1 | 540 | 545 | PF02516 | 0.536 |
MOD_N-GLC_1 | 667 | 672 | PF02516 | 0.727 |
MOD_N-GLC_1 | 767 | 772 | PF02516 | 0.775 |
MOD_N-GLC_1 | 829 | 834 | PF02516 | 0.758 |
MOD_N-GLC_2 | 411 | 413 | PF02516 | 0.431 |
MOD_NEK2_1 | 107 | 112 | PF00069 | 0.407 |
MOD_NEK2_1 | 184 | 189 | PF00069 | 0.361 |
MOD_NEK2_1 | 233 | 238 | PF00069 | 0.376 |
MOD_NEK2_1 | 263 | 268 | PF00069 | 0.466 |
MOD_NEK2_1 | 344 | 349 | PF00069 | 0.493 |
MOD_NEK2_1 | 365 | 370 | PF00069 | 0.495 |
MOD_NEK2_1 | 495 | 500 | PF00069 | 0.382 |
MOD_NEK2_1 | 501 | 506 | PF00069 | 0.398 |
MOD_NEK2_1 | 508 | 513 | PF00069 | 0.405 |
MOD_NEK2_1 | 629 | 634 | PF00069 | 0.494 |
MOD_NEK2_1 | 64 | 69 | PF00069 | 0.608 |
MOD_NEK2_1 | 753 | 758 | PF00069 | 0.641 |
MOD_NEK2_1 | 824 | 829 | PF00069 | 0.652 |
MOD_NEK2_1 | 858 | 863 | PF00069 | 0.512 |
MOD_NEK2_1 | 867 | 872 | PF00069 | 0.492 |
MOD_NEK2_1 | 905 | 910 | PF00069 | 0.435 |
MOD_PIKK_1 | 261 | 267 | PF00454 | 0.477 |
MOD_PIKK_1 | 32 | 38 | PF00454 | 0.663 |
MOD_PIKK_1 | 332 | 338 | PF00454 | 0.568 |
MOD_PIKK_1 | 706 | 712 | PF00454 | 0.560 |
MOD_PIKK_1 | 71 | 77 | PF00454 | 0.459 |
MOD_PIKK_1 | 755 | 761 | PF00454 | 0.747 |
MOD_PIKK_1 | 796 | 802 | PF00454 | 0.507 |
MOD_PIKK_1 | 804 | 810 | PF00454 | 0.473 |
MOD_PK_1 | 330 | 336 | PF00069 | 0.561 |
MOD_PKA_1 | 126 | 132 | PF00069 | 0.408 |
MOD_PKA_1 | 618 | 624 | PF00069 | 0.485 |
MOD_PKA_2 | 508 | 514 | PF00069 | 0.463 |
MOD_PKA_2 | 581 | 587 | PF00069 | 0.657 |
MOD_PKA_2 | 618 | 624 | PF00069 | 0.485 |
MOD_PKA_2 | 64 | 70 | PF00069 | 0.547 |
MOD_PKB_1 | 330 | 338 | PF00069 | 0.565 |
MOD_PKB_1 | 667 | 675 | PF00069 | 0.611 |
MOD_Plk_1 | 156 | 162 | PF00069 | 0.454 |
MOD_Plk_1 | 279 | 285 | PF00069 | 0.485 |
MOD_Plk_1 | 365 | 371 | PF00069 | 0.383 |
MOD_Plk_1 | 454 | 460 | PF00069 | 0.510 |
MOD_Plk_1 | 539 | 545 | PF00069 | 0.519 |
MOD_Plk_1 | 853 | 859 | PF00069 | 0.510 |
MOD_Plk_2-3 | 229 | 235 | PF00069 | 0.452 |
MOD_Plk_4 | 160 | 166 | PF00069 | 0.369 |
MOD_Plk_4 | 263 | 269 | PF00069 | 0.466 |
MOD_Plk_4 | 405 | 411 | PF00069 | 0.414 |
MOD_Plk_4 | 454 | 460 | PF00069 | 0.433 |
MOD_Plk_4 | 597 | 603 | PF00069 | 0.438 |
MOD_Plk_4 | 633 | 639 | PF00069 | 0.458 |
MOD_Plk_4 | 64 | 70 | PF00069 | 0.559 |
MOD_Plk_4 | 854 | 860 | PF00069 | 0.546 |
MOD_Plk_4 | 893 | 899 | PF00069 | 0.484 |
MOD_ProDKin_1 | 529 | 535 | PF00069 | 0.424 |
MOD_ProDKin_1 | 619 | 625 | PF00069 | 0.552 |
MOD_ProDKin_1 | 660 | 666 | PF00069 | 0.730 |
MOD_ProDKin_1 | 730 | 736 | PF00069 | 0.631 |
TRG_DiLeu_BaEn_1 | 20 | 25 | PF01217 | 0.514 |
TRG_DiLeu_BaEn_1 | 355 | 360 | PF01217 | 0.625 |
TRG_DiLeu_BaEn_1 | 854 | 859 | PF01217 | 0.432 |
TRG_DiLeu_BaEn_1 | 9 | 14 | PF01217 | 0.640 |
TRG_DiLeu_BaLyEn_6 | 269 | 274 | PF01217 | 0.408 |
TRG_DiLeu_BaLyEn_6 | 490 | 495 | PF01217 | 0.397 |
TRG_DiLeu_BaLyEn_6 | 901 | 906 | PF01217 | 0.335 |
TRG_DiLeu_LyEn_5 | 355 | 360 | PF01217 | 0.625 |
TRG_ENDOCYTIC_2 | 142 | 145 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 635 | 638 | PF00928 | 0.371 |
TRG_ENDOCYTIC_2 | 83 | 86 | PF00928 | 0.344 |
TRG_ER_diArg_1 | 173 | 175 | PF00400 | 0.444 |
TRG_ER_diArg_1 | 329 | 332 | PF00400 | 0.556 |
TRG_ER_diArg_1 | 375 | 378 | PF00400 | 0.588 |
TRG_ER_diArg_1 | 847 | 850 | PF00400 | 0.517 |
TRG_NLS_Bipartite_1 | 603 | 621 | PF00514 | 0.310 |
TRG_Pf-PMV_PEXEL_1 | 272 | 277 | PF00026 | 0.402 |
TRG_Pf-PMV_PEXEL_1 | 747 | 751 | PF00026 | 0.543 |
TRG_Pf-PMV_PEXEL_1 | 91 | 95 | PF00026 | 0.466 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P609 | Leptomonas seymouri | 63% | 100% |
A0A0S4JX74 | Bodo saltans | 34% | 100% |
A0A1X0PA29 | Trypanosomatidae | 36% | 100% |
A0A3Q8IHM2 | Leishmania donovani | 92% | 100% |
A0A422NRZ3 | Trypanosoma rangeli | 35% | 100% |
A4HAY3 | Leishmania braziliensis | 79% | 100% |
A4IA42 | Leishmania infantum | 92% | 100% |
E9B556 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |