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:0005794 | Golgi apparatus | 5 | 9 |
GO:0043226 | organelle | 2 | 9 |
GO:0043227 | membrane-bounded organelle | 3 | 9 |
GO:0043229 | intracellular organelle | 3 | 9 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
GO:0000938 | GARP complex | 3 | 1 |
GO:0005829 | cytosol | 2 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0099023 | vesicle tethering complex | 2 | 1 |
Related structures:
AlphaFold database: A4HAY3
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 10 |
GO:0008104 | protein localization | 4 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0015031 | protein transport | 4 | 10 |
GO:0033036 | macromolecule localization | 2 | 10 |
GO:0045184 | establishment of protein localization | 3 | 10 |
GO:0051179 | localization | 1 | 10 |
GO:0051234 | establishment of localization | 2 | 10 |
GO:0051641 | cellular localization | 2 | 10 |
GO:0070727 | cellular macromolecule localization | 3 | 10 |
GO:0071702 | organic substance transport | 4 | 10 |
GO:0071705 | nitrogen compound transport | 4 | 10 |
GO:0006892 | post-Golgi vesicle-mediated transport | 6 | 1 |
GO:0006896 | Golgi to vacuole transport | 5 | 1 |
GO:0007034 | vacuolar transport | 4 | 1 |
GO:0016192 | vesicle-mediated transport | 4 | 1 |
GO:0016197 | endosomal transport | 4 | 1 |
GO:0016482 | cytosolic transport | 4 | 1 |
GO:0032456 | endocytic recycling | 5 | 1 |
GO:0042147 | retrograde transport, endosome to Golgi | 5 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0048193 | Golgi vesicle transport | 5 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
GO:0051668 | localization within membrane | 3 | 1 |
GO:0098876 | vesicle-mediated transport to the plasma membrane | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000149 | SNARE binding | 3 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0005515 | protein binding | 2 | 1 |
GO:0019905 | syntaxin binding | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 187 | 191 | PF00656 | 0.279 |
CLV_C14_Caspase3-7 | 364 | 368 | PF00656 | 0.350 |
CLV_C14_Caspase3-7 | 457 | 461 | PF00656 | 0.266 |
CLV_NRD_NRD_1 | 104 | 106 | PF00675 | 0.282 |
CLV_NRD_NRD_1 | 125 | 127 | PF00675 | 0.355 |
CLV_NRD_NRD_1 | 131 | 133 | PF00675 | 0.264 |
CLV_NRD_NRD_1 | 173 | 175 | PF00675 | 0.392 |
CLV_NRD_NRD_1 | 329 | 331 | PF00675 | 0.460 |
CLV_NRD_NRD_1 | 45 | 47 | PF00675 | 0.406 |
CLV_NRD_NRD_1 | 618 | 620 | PF00675 | 0.442 |
CLV_NRD_NRD_1 | 674 | 676 | PF00675 | 0.555 |
CLV_NRD_NRD_1 | 816 | 818 | PF00675 | 0.492 |
CLV_NRD_NRD_1 | 866 | 868 | PF00675 | 0.426 |
CLV_PCSK_KEX2_1 | 131 | 133 | PF00082 | 0.308 |
CLV_PCSK_KEX2_1 | 173 | 175 | PF00082 | 0.430 |
CLV_PCSK_KEX2_1 | 329 | 331 | PF00082 | 0.460 |
CLV_PCSK_KEX2_1 | 45 | 47 | PF00082 | 0.406 |
CLV_PCSK_KEX2_1 | 617 | 619 | PF00082 | 0.399 |
CLV_PCSK_KEX2_1 | 674 | 676 | PF00082 | 0.555 |
CLV_PCSK_PC1ET2_1 | 617 | 619 | PF00082 | 0.399 |
CLV_PCSK_PC7_1 | 169 | 175 | PF00082 | 0.400 |
CLV_PCSK_PC7_1 | 325 | 331 | PF00082 | 0.553 |
CLV_PCSK_SKI1_1 | 210 | 214 | PF00082 | 0.344 |
CLV_PCSK_SKI1_1 | 215 | 219 | PF00082 | 0.344 |
CLV_PCSK_SKI1_1 | 269 | 273 | PF00082 | 0.270 |
CLV_PCSK_SKI1_1 | 339 | 343 | PF00082 | 0.562 |
CLV_PCSK_SKI1_1 | 361 | 365 | PF00082 | 0.433 |
CLV_PCSK_SKI1_1 | 444 | 448 | PF00082 | 0.341 |
CLV_PCSK_SKI1_1 | 505 | 509 | PF00082 | 0.403 |
CLV_PCSK_SKI1_1 | 513 | 517 | PF00082 | 0.401 |
CLV_PCSK_SKI1_1 | 736 | 740 | PF00082 | 0.312 |
CLV_Separin_Metazoa | 814 | 818 | PF03568 | 0.459 |
DEG_SCF_FBW7_1 | 652 | 659 | PF00400 | 0.516 |
DEG_SCF_FBW7_1 | 778 | 784 | PF00400 | 0.477 |
DOC_CDC14_PxL_1 | 489 | 497 | PF14671 | 0.452 |
DOC_CDC14_PxL_1 | 523 | 531 | PF14671 | 0.462 |
DOC_CKS1_1 | 778 | 783 | PF01111 | 0.594 |
DOC_CYCLIN_RxL_1 | 169 | 179 | PF00134 | 0.348 |
DOC_CYCLIN_RxL_1 | 210 | 222 | PF00134 | 0.400 |
DOC_CYCLIN_RxL_1 | 733 | 743 | PF00134 | 0.344 |
DOC_MAPK_gen_1 | 867 | 873 | PF00069 | 0.523 |
DOC_MIT_MIM_1 | 170 | 178 | PF04212 | 0.400 |
DOC_PP1_RVXF_1 | 171 | 178 | PF00149 | 0.285 |
DOC_PP1_RVXF_1 | 180 | 187 | PF00149 | 0.282 |
DOC_PP1_RVXF_1 | 240 | 247 | PF00149 | 0.203 |
DOC_PP1_RVXF_1 | 672 | 679 | PF00149 | 0.509 |
DOC_PP2B_LxvP_1 | 900 | 903 | PF13499 | 0.332 |
DOC_PP4_FxxP_1 | 246 | 249 | PF00568 | 0.203 |
DOC_USP7_MATH_1 | 27 | 31 | PF00917 | 0.520 |
DOC_USP7_MATH_1 | 291 | 295 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 349 | 353 | PF00917 | 0.648 |
DOC_USP7_MATH_1 | 539 | 543 | PF00917 | 0.466 |
DOC_USP7_MATH_1 | 656 | 660 | PF00917 | 0.715 |
DOC_USP7_MATH_1 | 680 | 684 | PF00917 | 0.616 |
DOC_USP7_MATH_1 | 71 | 75 | PF00917 | 0.360 |
DOC_USP7_MATH_1 | 734 | 738 | PF00917 | 0.471 |
DOC_USP7_MATH_1 | 757 | 761 | PF00917 | 0.538 |
DOC_USP7_UBL2_3 | 203 | 207 | PF12436 | 0.400 |
DOC_WW_Pin1_4 | 619 | 624 | PF00397 | 0.428 |
DOC_WW_Pin1_4 | 652 | 657 | PF00397 | 0.709 |
DOC_WW_Pin1_4 | 660 | 665 | PF00397 | 0.700 |
DOC_WW_Pin1_4 | 686 | 691 | PF00397 | 0.762 |
DOC_WW_Pin1_4 | 767 | 772 | PF00397 | 0.647 |
DOC_WW_Pin1_4 | 777 | 782 | PF00397 | 0.627 |
LIG_14-3-3_CanoR_1 | 194 | 202 | PF00244 | 0.336 |
LIG_14-3-3_CanoR_1 | 261 | 268 | PF00244 | 0.348 |
LIG_14-3-3_CanoR_1 | 332 | 341 | PF00244 | 0.503 |
LIG_14-3-3_CanoR_1 | 361 | 366 | PF00244 | 0.439 |
LIG_14-3-3_CanoR_1 | 509 | 513 | PF00244 | 0.412 |
LIG_14-3-3_CanoR_1 | 530 | 535 | PF00244 | 0.429 |
LIG_14-3-3_CanoR_1 | 582 | 586 | PF00244 | 0.500 |
LIG_14-3-3_CanoR_1 | 703 | 708 | PF00244 | 0.375 |
LIG_14-3-3_CanoR_1 | 867 | 872 | PF00244 | 0.384 |
LIG_Actin_WH2_2 | 493 | 511 | PF00022 | 0.450 |
LIG_Actin_WH2_2 | 566 | 584 | PF00022 | 0.262 |
LIG_AP2alpha_2 | 595 | 597 | PF02296 | 0.277 |
LIG_APCC_ABBA_1 | 54 | 59 | PF00400 | 0.379 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.675 |
LIG_BRCT_BRCA1_1 | 235 | 239 | PF00533 | 0.400 |
LIG_BRCT_BRCA1_1 | 582 | 586 | PF00533 | 0.394 |
LIG_BRCT_BRCA1_1 | 855 | 859 | PF00533 | 0.323 |
LIG_Clathr_ClatBox_1 | 15 | 19 | PF01394 | 0.374 |
LIG_Clathr_ClatBox_1 | 739 | 743 | PF01394 | 0.306 |
LIG_eIF4E_1 | 267 | 273 | PF01652 | 0.203 |
LIG_FHA_1 | 211 | 217 | PF00498 | 0.344 |
LIG_FHA_1 | 352 | 358 | PF00498 | 0.587 |
LIG_FHA_1 | 454 | 460 | PF00498 | 0.476 |
LIG_FHA_1 | 467 | 473 | PF00498 | 0.309 |
LIG_FHA_1 | 526 | 532 | PF00498 | 0.414 |
LIG_FHA_1 | 576 | 582 | PF00498 | 0.449 |
LIG_FHA_1 | 744 | 750 | PF00498 | 0.472 |
LIG_FHA_1 | 8 | 14 | PF00498 | 0.606 |
LIG_FHA_1 | 850 | 856 | PF00498 | 0.287 |
LIG_FHA_1 | 889 | 895 | PF00498 | 0.469 |
LIG_FHA_2 | 216 | 222 | PF00498 | 0.448 |
LIG_FHA_2 | 362 | 368 | PF00498 | 0.364 |
LIG_FHA_2 | 435 | 441 | PF00498 | 0.494 |
LIG_FHA_2 | 485 | 491 | PF00498 | 0.478 |
LIG_FHA_2 | 512 | 518 | PF00498 | 0.411 |
LIG_FHA_2 | 609 | 615 | PF00498 | 0.317 |
LIG_FHA_2 | 638 | 644 | PF00498 | 0.418 |
LIG_FHA_2 | 859 | 865 | PF00498 | 0.423 |
LIG_GBD_Chelix_1 | 854 | 862 | PF00786 | 0.265 |
LIG_Integrin_isoDGR_2 | 672 | 674 | PF01839 | 0.515 |
LIG_LIR_Gen_1 | 140 | 149 | PF02991 | 0.285 |
LIG_LIR_Gen_1 | 150 | 155 | PF02991 | 0.286 |
LIG_LIR_Gen_1 | 397 | 408 | PF02991 | 0.393 |
LIG_LIR_Gen_1 | 632 | 639 | PF02991 | 0.462 |
LIG_LIR_Gen_1 | 856 | 865 | PF02991 | 0.328 |
LIG_LIR_LC3C_4 | 851 | 855 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 140 | 145 | PF02991 | 0.285 |
LIG_LIR_Nem_3 | 149 | 154 | PF02991 | 0.286 |
LIG_LIR_Nem_3 | 256 | 262 | PF02991 | 0.296 |
LIG_LIR_Nem_3 | 397 | 403 | PF02991 | 0.384 |
LIG_LIR_Nem_3 | 541 | 547 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 591 | 597 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 632 | 638 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 640 | 644 | PF02991 | 0.506 |
LIG_LIR_Nem_3 | 732 | 738 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 856 | 862 | PF02991 | 0.546 |
LIG_LRP6_Inhibitor_1 | 188 | 194 | PF00058 | 0.400 |
LIG_MAD2 | 215 | 223 | PF02301 | 0.400 |
LIG_NRBOX | 896 | 902 | PF00104 | 0.393 |
LIG_PCNA_yPIPBox_3 | 717 | 725 | PF02747 | 0.498 |
LIG_Pex14_1 | 398 | 402 | PF04695 | 0.328 |
LIG_Pex14_2 | 239 | 243 | PF04695 | 0.400 |
LIG_Pex14_2 | 402 | 406 | PF04695 | 0.432 |
LIG_Pex14_2 | 419 | 423 | PF04695 | 0.263 |
LIG_Pex14_2 | 597 | 601 | PF04695 | 0.251 |
LIG_PTB_Apo_2 | 547 | 554 | PF02174 | 0.489 |
LIG_PTB_Phospho_1 | 547 | 553 | PF10480 | 0.495 |
LIG_SH2_CRK | 142 | 146 | PF00017 | 0.308 |
LIG_SH2_CRK | 635 | 639 | PF00017 | 0.256 |
LIG_SH2_GRB2like | 575 | 578 | PF00017 | 0.436 |
LIG_SH2_SRC | 711 | 714 | PF00017 | 0.480 |
LIG_SH2_STAP1 | 635 | 639 | PF00017 | 0.370 |
LIG_SH2_STAT3 | 247 | 250 | PF00017 | 0.203 |
LIG_SH2_STAT3 | 262 | 265 | PF00017 | 0.368 |
LIG_SH2_STAT3 | 267 | 270 | PF00017 | 0.319 |
LIG_SH2_STAT3 | 707 | 710 | PF00017 | 0.338 |
LIG_SH2_STAT5 | 164 | 167 | PF00017 | 0.284 |
LIG_SH2_STAT5 | 267 | 270 | PF00017 | 0.321 |
LIG_SH2_STAT5 | 43 | 46 | PF00017 | 0.536 |
LIG_SH2_STAT5 | 553 | 556 | PF00017 | 0.410 |
LIG_SH2_STAT5 | 575 | 578 | PF00017 | 0.464 |
LIG_SH2_STAT5 | 635 | 638 | PF00017 | 0.355 |
LIG_SH2_STAT5 | 711 | 714 | PF00017 | 0.454 |
LIG_SH3_1 | 776 | 782 | PF00018 | 0.493 |
LIG_SH3_2 | 771 | 776 | PF14604 | 0.526 |
LIG_SH3_3 | 285 | 291 | PF00018 | 0.527 |
LIG_SH3_3 | 304 | 310 | PF00018 | 0.609 |
LIG_SH3_3 | 317 | 323 | PF00018 | 0.541 |
LIG_SH3_3 | 590 | 596 | PF00018 | 0.333 |
LIG_SH3_3 | 658 | 664 | PF00018 | 0.700 |
LIG_SH3_3 | 768 | 774 | PF00018 | 0.707 |
LIG_SH3_3 | 775 | 781 | PF00018 | 0.721 |
LIG_Sin3_3 | 443 | 450 | PF02671 | 0.455 |
LIG_SUMO_SIM_anti_2 | 460 | 467 | PF11976 | 0.403 |
LIG_SUMO_SIM_anti_2 | 737 | 744 | PF11976 | 0.377 |
LIG_SUMO_SIM_par_1 | 215 | 222 | PF11976 | 0.399 |
LIG_SUMO_SIM_par_1 | 492 | 498 | PF11976 | 0.351 |
LIG_SUMO_SIM_par_1 | 737 | 744 | PF11976 | 0.549 |
LIG_SUMO_SIM_par_1 | 851 | 856 | PF11976 | 0.270 |
LIG_TRAF2_1 | 232 | 235 | PF00917 | 0.429 |
LIG_TRAF2_1 | 294 | 297 | PF00917 | 0.515 |
LIG_TRAF2_1 | 726 | 729 | PF00917 | 0.317 |
LIG_UBA3_1 | 609 | 617 | PF00899 | 0.392 |
LIG_WRC_WIRS_1 | 100 | 105 | PF05994 | 0.355 |
LIG_WRC_WIRS_1 | 598 | 603 | PF05994 | 0.446 |
MOD_CK1_1 | 156 | 162 | PF00069 | 0.463 |
MOD_CK1_1 | 279 | 285 | PF00069 | 0.360 |
MOD_CK1_1 | 35 | 41 | PF00069 | 0.426 |
MOD_CK1_1 | 511 | 517 | PF00069 | 0.453 |
MOD_CK1_1 | 648 | 654 | PF00069 | 0.674 |
MOD_CK1_1 | 657 | 663 | PF00069 | 0.729 |
MOD_CK1_1 | 756 | 762 | PF00069 | 0.484 |
MOD_CK1_1 | 807 | 813 | PF00069 | 0.336 |
MOD_CK1_1 | 829 | 835 | PF00069 | 0.667 |
MOD_CK1_1 | 860 | 866 | PF00069 | 0.421 |
MOD_CK1_1 | 889 | 895 | PF00069 | 0.421 |
MOD_CK2_1 | 156 | 162 | PF00069 | 0.351 |
MOD_CK2_1 | 215 | 221 | PF00069 | 0.401 |
MOD_CK2_1 | 229 | 235 | PF00069 | 0.249 |
MOD_CK2_1 | 291 | 297 | PF00069 | 0.487 |
MOD_CK2_1 | 3 | 9 | PF00069 | 0.617 |
MOD_CK2_1 | 349 | 355 | PF00069 | 0.627 |
MOD_CK2_1 | 434 | 440 | PF00069 | 0.447 |
MOD_CK2_1 | 449 | 455 | PF00069 | 0.339 |
MOD_CK2_1 | 511 | 517 | PF00069 | 0.523 |
MOD_CK2_1 | 637 | 643 | PF00069 | 0.428 |
MOD_CK2_1 | 686 | 692 | PF00069 | 0.818 |
MOD_CK2_1 | 84 | 90 | PF00069 | 0.257 |
MOD_CK2_1 | 858 | 864 | PF00069 | 0.536 |
MOD_Cter_Amidation | 672 | 675 | PF01082 | 0.514 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.677 |
MOD_GlcNHglycan | 142 | 145 | PF01048 | 0.338 |
MOD_GlcNHglycan | 178 | 181 | PF01048 | 0.335 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.285 |
MOD_GlcNHglycan | 234 | 238 | PF01048 | 0.407 |
MOD_GlcNHglycan | 280 | 284 | PF01048 | 0.406 |
MOD_GlcNHglycan | 293 | 296 | PF01048 | 0.485 |
MOD_GlcNHglycan | 437 | 440 | PF01048 | 0.513 |
MOD_GlcNHglycan | 497 | 500 | PF01048 | 0.347 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.496 |
MOD_GlcNHglycan | 541 | 544 | PF01048 | 0.370 |
MOD_GlcNHglycan | 647 | 650 | PF01048 | 0.548 |
MOD_GlcNHglycan | 652 | 655 | PF01048 | 0.650 |
MOD_GlcNHglycan | 656 | 659 | PF01048 | 0.681 |
MOD_GlcNHglycan | 669 | 672 | PF01048 | 0.805 |
MOD_GlcNHglycan | 755 | 758 | PF01048 | 0.532 |
MOD_GlcNHglycan | 759 | 762 | PF01048 | 0.581 |
MOD_GlcNHglycan | 831 | 834 | PF01048 | 0.732 |
MOD_GlcNHglycan | 85 | 89 | PF01048 | 0.313 |
MOD_GlcNHglycan | 855 | 858 | PF01048 | 0.266 |
MOD_GlcNHglycan | 877 | 880 | PF01048 | 0.510 |
MOD_GSK3_1 | 229 | 236 | PF00069 | 0.422 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.627 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.614 |
MOD_GSK3_1 | 339 | 346 | PF00069 | 0.712 |
MOD_GSK3_1 | 349 | 356 | PF00069 | 0.519 |
MOD_GSK3_1 | 361 | 368 | PF00069 | 0.364 |
MOD_GSK3_1 | 449 | 456 | PF00069 | 0.483 |
MOD_GSK3_1 | 525 | 532 | PF00069 | 0.386 |
MOD_GSK3_1 | 577 | 584 | PF00069 | 0.404 |
MOD_GSK3_1 | 629 | 636 | PF00069 | 0.401 |
MOD_GSK3_1 | 648 | 655 | PF00069 | 0.639 |
MOD_GSK3_1 | 656 | 663 | PF00069 | 0.705 |
MOD_GSK3_1 | 753 | 760 | PF00069 | 0.517 |
MOD_GSK3_1 | 777 | 784 | PF00069 | 0.646 |
MOD_GSK3_1 | 800 | 807 | PF00069 | 0.504 |
MOD_GSK3_1 | 820 | 827 | PF00069 | 0.536 |
MOD_GSK3_1 | 829 | 836 | PF00069 | 0.709 |
MOD_GSK3_1 | 849 | 856 | PF00069 | 0.448 |
MOD_GSK3_1 | 882 | 889 | PF00069 | 0.473 |
MOD_LATS_1 | 337 | 343 | PF00433 | 0.572 |
MOD_N-GLC_1 | 156 | 161 | PF02516 | 0.484 |
MOD_N-GLC_1 | 460 | 465 | PF02516 | 0.251 |
MOD_N-GLC_1 | 767 | 772 | PF02516 | 0.722 |
MOD_N-GLC_1 | 829 | 834 | PF02516 | 0.648 |
MOD_N-GLC_1 | 889 | 894 | PF02516 | 0.387 |
MOD_N-GLC_2 | 411 | 413 | PF02516 | 0.368 |
MOD_NEK2_1 | 184 | 189 | PF00069 | 0.300 |
MOD_NEK2_1 | 233 | 238 | PF00069 | 0.332 |
MOD_NEK2_1 | 263 | 268 | PF00069 | 0.425 |
MOD_NEK2_1 | 365 | 370 | PF00069 | 0.443 |
MOD_NEK2_1 | 495 | 500 | PF00069 | 0.328 |
MOD_NEK2_1 | 501 | 506 | PF00069 | 0.337 |
MOD_NEK2_1 | 508 | 513 | PF00069 | 0.346 |
MOD_NEK2_1 | 529 | 534 | PF00069 | 0.327 |
MOD_NEK2_1 | 581 | 586 | PF00069 | 0.482 |
MOD_NEK2_1 | 597 | 602 | PF00069 | 0.228 |
MOD_NEK2_1 | 629 | 634 | PF00069 | 0.473 |
MOD_NEK2_1 | 753 | 758 | PF00069 | 0.566 |
MOD_NEK2_1 | 789 | 794 | PF00069 | 0.445 |
MOD_NEK2_1 | 824 | 829 | PF00069 | 0.627 |
MOD_NEK2_1 | 853 | 858 | PF00069 | 0.462 |
MOD_PIKK_1 | 261 | 267 | PF00454 | 0.454 |
MOD_PIKK_1 | 32 | 38 | PF00454 | 0.616 |
MOD_PIKK_1 | 332 | 338 | PF00454 | 0.524 |
MOD_PIKK_1 | 711 | 717 | PF00454 | 0.486 |
MOD_PIKK_1 | 800 | 806 | PF00454 | 0.436 |
MOD_PK_1 | 330 | 336 | PF00069 | 0.510 |
MOD_PK_1 | 867 | 873 | PF00069 | 0.265 |
MOD_PKA_1 | 867 | 873 | PF00069 | 0.324 |
MOD_PKA_2 | 508 | 514 | PF00069 | 0.408 |
MOD_PKA_2 | 529 | 535 | PF00069 | 0.422 |
MOD_PKA_2 | 581 | 587 | PF00069 | 0.526 |
MOD_PKB_1 | 330 | 338 | PF00069 | 0.517 |
MOD_Plk_1 | 156 | 162 | PF00069 | 0.448 |
MOD_Plk_1 | 279 | 285 | PF00069 | 0.360 |
MOD_Plk_1 | 330 | 336 | PF00069 | 0.410 |
MOD_Plk_1 | 454 | 460 | PF00069 | 0.417 |
MOD_Plk_1 | 743 | 749 | PF00069 | 0.394 |
MOD_Plk_1 | 790 | 796 | PF00069 | 0.366 |
MOD_Plk_1 | 848 | 854 | PF00069 | 0.470 |
MOD_Plk_1 | 889 | 895 | PF00069 | 0.392 |
MOD_Plk_4 | 263 | 269 | PF00069 | 0.434 |
MOD_Plk_4 | 454 | 460 | PF00069 | 0.366 |
MOD_Plk_4 | 503 | 509 | PF00069 | 0.362 |
MOD_Plk_4 | 581 | 587 | PF00069 | 0.528 |
MOD_Plk_4 | 597 | 603 | PF00069 | 0.432 |
MOD_Plk_4 | 608 | 614 | PF00069 | 0.322 |
MOD_Plk_4 | 633 | 639 | PF00069 | 0.434 |
MOD_Plk_4 | 734 | 740 | PF00069 | 0.399 |
MOD_Plk_4 | 790 | 796 | PF00069 | 0.570 |
MOD_Plk_4 | 849 | 855 | PF00069 | 0.422 |
MOD_Plk_4 | 867 | 873 | PF00069 | 0.360 |
MOD_Plk_4 | 889 | 895 | PF00069 | 0.418 |
MOD_ProDKin_1 | 619 | 625 | PF00069 | 0.425 |
MOD_ProDKin_1 | 652 | 658 | PF00069 | 0.711 |
MOD_ProDKin_1 | 660 | 666 | PF00069 | 0.699 |
MOD_ProDKin_1 | 686 | 692 | PF00069 | 0.764 |
MOD_ProDKin_1 | 767 | 773 | PF00069 | 0.648 |
MOD_ProDKin_1 | 777 | 783 | PF00069 | 0.627 |
TRG_DiLeu_BaEn_1 | 20 | 25 | PF01217 | 0.447 |
TRG_DiLeu_BaEn_1 | 355 | 360 | PF01217 | 0.500 |
TRG_DiLeu_BaEn_1 | 849 | 854 | PF01217 | 0.373 |
TRG_DiLeu_BaEn_1 | 896 | 901 | PF01217 | 0.339 |
TRG_DiLeu_BaEn_1 | 9 | 14 | PF01217 | 0.604 |
TRG_DiLeu_BaLyEn_6 | 490 | 495 | PF01217 | 0.331 |
TRG_DiLeu_LyEn_5 | 355 | 360 | PF01217 | 0.500 |
TRG_DiLeu_LyEn_5 | 896 | 901 | PF01217 | 0.302 |
TRG_ENDOCYTIC_2 | 142 | 145 | PF00928 | 0.324 |
TRG_ENDOCYTIC_2 | 635 | 638 | PF00928 | 0.373 |
TRG_ENDOCYTIC_2 | 83 | 86 | PF00928 | 0.296 |
TRG_ER_diArg_1 | 173 | 175 | PF00400 | 0.428 |
TRG_ER_diArg_1 | 44 | 46 | PF00400 | 0.403 |
TRG_ER_diArg_1 | 674 | 676 | PF00400 | 0.555 |
TRG_Pf-PMV_PEXEL_1 | 231 | 235 | PF00026 | 0.284 |
TRG_Pf-PMV_PEXEL_1 | 62 | 66 | PF00026 | 0.343 |
TRG_Pf-PMV_PEXEL_1 | 674 | 679 | PF00026 | 0.507 |
TRG_Pf-PMV_PEXEL_1 | 91 | 95 | PF00026 | 0.434 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P609 | Leptomonas seymouri | 64% | 100% |
A0A0S4JX74 | Bodo saltans | 33% | 100% |
A0A1X0PA29 | Trypanosomatidae | 36% | 100% |
A0A3Q8IHM2 | Leishmania donovani | 77% | 100% |
A0A422NRZ3 | Trypanosoma rangeli | 36% | 100% |
A4IA42 | Leishmania infantum | 77% | 100% |
E9B556 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 99% |
Q4Q2S9 | Leishmania major | 79% | 100% |