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: 36 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 26 |
NetGPI | no | yes: 0, no: 26 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 27 |
GO:0110165 | cellular anatomical entity | 1 | 27 |
GO:0005635 | nuclear envelope | 4 | 4 |
GO:0005783 | endoplasmic reticulum | 5 | 4 |
GO:0031967 | organelle envelope | 3 | 4 |
GO:0031975 | envelope | 2 | 4 |
GO:0043226 | organelle | 2 | 4 |
GO:0043227 | membrane-bounded organelle | 3 | 4 |
GO:0043229 | intracellular organelle | 3 | 4 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 4 |
Related structures:
AlphaFold database: E9B5Z5
Term | Name | Level | Count |
---|---|---|---|
GO:0006486 | protein glycosylation | 4 | 27 |
GO:0006807 | nitrogen compound metabolic process | 2 | 27 |
GO:0008152 | metabolic process | 1 | 27 |
GO:0019538 | protein metabolic process | 3 | 27 |
GO:0036211 | protein modification process | 4 | 27 |
GO:0043170 | macromolecule metabolic process | 3 | 27 |
GO:0043412 | macromolecule modification | 4 | 27 |
GO:0043413 | macromolecule glycosylation | 3 | 27 |
GO:0044238 | primary metabolic process | 2 | 27 |
GO:0070085 | glycosylation | 2 | 27 |
GO:0071704 | organic substance metabolic process | 2 | 27 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 27 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 27 |
GO:0004576 | oligosaccharyl transferase activity | 5 | 27 |
GO:0004579 | dolichyl-diphosphooligosaccharide-protein glycotransferase activity | 6 | 27 |
GO:0005488 | binding | 1 | 27 |
GO:0016740 | transferase activity | 2 | 27 |
GO:0016757 | glycosyltransferase activity | 3 | 27 |
GO:0016758 | hexosyltransferase activity | 4 | 27 |
GO:0043167 | ion binding | 2 | 27 |
GO:0043169 | cation binding | 3 | 27 |
GO:0046872 | metal ion binding | 4 | 27 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 651 | 655 | PF00656 | 0.312 |
CLV_C14_Caspase3-7 | 8 | 12 | PF00656 | 0.582 |
CLV_MEL_PAP_1 | 820 | 826 | PF00089 | 0.483 |
CLV_NRD_NRD_1 | 523 | 525 | PF00675 | 0.582 |
CLV_NRD_NRD_1 | 834 | 836 | PF00675 | 0.619 |
CLV_NRD_NRD_1 | 845 | 847 | PF00675 | 0.514 |
CLV_PCSK_KEX2_1 | 528 | 530 | PF00082 | 0.530 |
CLV_PCSK_KEX2_1 | 834 | 836 | PF00082 | 0.612 |
CLV_PCSK_KEX2_1 | 845 | 847 | PF00082 | 0.558 |
CLV_PCSK_PC1ET2_1 | 528 | 530 | PF00082 | 0.524 |
CLV_PCSK_PC1ET2_1 | 834 | 836 | PF00082 | 0.573 |
CLV_PCSK_PC7_1 | 524 | 530 | PF00082 | 0.389 |
CLV_PCSK_SKI1_1 | 396 | 400 | PF00082 | 0.447 |
CLV_PCSK_SKI1_1 | 42 | 46 | PF00082 | 0.440 |
CLV_PCSK_SKI1_1 | 47 | 51 | PF00082 | 0.390 |
CLV_PCSK_SKI1_1 | 473 | 477 | PF00082 | 0.408 |
CLV_PCSK_SKI1_1 | 555 | 559 | PF00082 | 0.354 |
CLV_PCSK_SKI1_1 | 668 | 672 | PF00082 | 0.499 |
CLV_PCSK_SKI1_1 | 775 | 779 | PF00082 | 0.602 |
CLV_PCSK_SKI1_1 | 835 | 839 | PF00082 | 0.551 |
CLV_Separin_Metazoa | 345 | 349 | PF03568 | 0.284 |
DEG_SCF_TRCP1_1 | 11 | 17 | PF00400 | 0.602 |
DEG_SPOP_SBC_1 | 139 | 143 | PF00917 | 0.473 |
DOC_AGCK_PIF_2 | 124 | 129 | PF00069 | 0.293 |
DOC_CYCLIN_RxL_1 | 39 | 48 | PF00134 | 0.570 |
DOC_CYCLIN_RxL_1 | 393 | 403 | PF00134 | 0.254 |
DOC_CYCLIN_RxL_1 | 470 | 478 | PF00134 | 0.254 |
DOC_MAPK_FxFP_2 | 59 | 62 | PF00069 | 0.489 |
DOC_MAPK_gen_1 | 244 | 253 | PF00069 | 0.359 |
DOC_MAPK_gen_1 | 348 | 355 | PF00069 | 0.484 |
DOC_MAPK_MEF2A_6 | 555 | 562 | PF00069 | 0.555 |
DOC_PP1_RVXF_1 | 452 | 458 | PF00149 | 0.496 |
DOC_PP1_RVXF_1 | 630 | 637 | PF00149 | 0.301 |
DOC_PP1_RVXF_1 | 821 | 827 | PF00149 | 0.299 |
DOC_PP2B_LxvP_1 | 381 | 384 | PF13499 | 0.206 |
DOC_PP4_FxxP_1 | 59 | 62 | PF00568 | 0.495 |
DOC_SPAK_OSR1_1 | 67 | 71 | PF12202 | 0.385 |
DOC_USP7_MATH_1 | 138 | 142 | PF00917 | 0.338 |
DOC_USP7_MATH_1 | 193 | 197 | PF00917 | 0.266 |
DOC_USP7_MATH_1 | 322 | 326 | PF00917 | 0.279 |
DOC_USP7_MATH_1 | 579 | 583 | PF00917 | 0.389 |
DOC_USP7_MATH_1 | 586 | 590 | PF00917 | 0.397 |
DOC_USP7_MATH_1 | 692 | 696 | PF00917 | 0.360 |
DOC_WW_Pin1_4 | 318 | 323 | PF00397 | 0.279 |
DOC_WW_Pin1_4 | 34 | 39 | PF00397 | 0.625 |
DOC_WW_Pin1_4 | 417 | 422 | PF00397 | 0.232 |
DOC_WW_Pin1_4 | 448 | 453 | PF00397 | 0.401 |
DOC_WW_Pin1_4 | 624 | 629 | PF00397 | 0.324 |
DOC_WW_Pin1_4 | 669 | 674 | PF00397 | 0.306 |
DOC_WW_Pin1_4 | 698 | 703 | PF00397 | 0.341 |
DOC_WW_Pin1_4 | 733 | 738 | PF00397 | 0.324 |
LIG_14-3-3_CanoR_1 | 244 | 250 | PF00244 | 0.303 |
LIG_14-3-3_CanoR_1 | 290 | 294 | PF00244 | 0.531 |
LIG_14-3-3_CanoR_1 | 299 | 304 | PF00244 | 0.405 |
LIG_14-3-3_CanoR_1 | 649 | 653 | PF00244 | 0.331 |
LIG_14-3-3_CanoR_1 | 67 | 73 | PF00244 | 0.584 |
LIG_14-3-3_CanoR_1 | 706 | 712 | PF00244 | 0.318 |
LIG_14-3-3_CanoR_1 | 740 | 744 | PF00244 | 0.370 |
LIG_14-3-3_CanoR_1 | 823 | 827 | PF00244 | 0.434 |
LIG_14-3-3_CanoR_1 | 835 | 840 | PF00244 | 0.390 |
LIG_14-3-3_CanoR_1 | 89 | 94 | PF00244 | 0.313 |
LIG_AP2alpha_2 | 104 | 106 | PF02296 | 0.279 |
LIG_BIR_III_2 | 28 | 32 | PF00653 | 0.585 |
LIG_BRCT_BRCA1_1 | 120 | 124 | PF00533 | 0.380 |
LIG_BRCT_BRCA1_1 | 452 | 456 | PF00533 | 0.430 |
LIG_BRCT_BRCA1_1 | 574 | 578 | PF00533 | 0.288 |
LIG_BRCT_BRCA1_1 | 581 | 585 | PF00533 | 0.289 |
LIG_deltaCOP1_diTrp_1 | 422 | 427 | PF00928 | 0.224 |
LIG_FHA_1 | 181 | 187 | PF00498 | 0.366 |
LIG_FHA_1 | 432 | 438 | PF00498 | 0.427 |
LIG_FHA_1 | 51 | 57 | PF00498 | 0.573 |
LIG_FHA_1 | 565 | 571 | PF00498 | 0.402 |
LIG_FHA_1 | 669 | 675 | PF00498 | 0.312 |
LIG_FHA_1 | 751 | 757 | PF00498 | 0.392 |
LIG_FHA_2 | 46 | 52 | PF00498 | 0.582 |
LIG_FHA_2 | 836 | 842 | PF00498 | 0.340 |
LIG_LIR_Apic_2 | 731 | 735 | PF02991 | 0.376 |
LIG_LIR_Apic_2 | 803 | 807 | PF02991 | 0.458 |
LIG_LIR_Gen_1 | 117 | 127 | PF02991 | 0.340 |
LIG_LIR_Gen_1 | 206 | 215 | PF02991 | 0.432 |
LIG_LIR_Gen_1 | 235 | 243 | PF02991 | 0.332 |
LIG_LIR_Gen_1 | 422 | 433 | PF02991 | 0.228 |
LIG_LIR_Gen_1 | 619 | 628 | PF02991 | 0.288 |
LIG_LIR_Gen_1 | 686 | 692 | PF02991 | 0.350 |
LIG_LIR_Gen_1 | 710 | 720 | PF02991 | 0.396 |
LIG_LIR_Gen_1 | 761 | 771 | PF02991 | 0.414 |
LIG_LIR_Gen_1 | 825 | 832 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 104 | 109 | PF02991 | 0.280 |
LIG_LIR_Nem_3 | 117 | 123 | PF02991 | 0.277 |
LIG_LIR_Nem_3 | 125 | 129 | PF02991 | 0.281 |
LIG_LIR_Nem_3 | 131 | 135 | PF02991 | 0.262 |
LIG_LIR_Nem_3 | 141 | 147 | PF02991 | 0.250 |
LIG_LIR_Nem_3 | 206 | 210 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 235 | 240 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 302 | 307 | PF02991 | 0.300 |
LIG_LIR_Nem_3 | 321 | 326 | PF02991 | 0.273 |
LIG_LIR_Nem_3 | 422 | 428 | PF02991 | 0.216 |
LIG_LIR_Nem_3 | 445 | 450 | PF02991 | 0.427 |
LIG_LIR_Nem_3 | 453 | 459 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 52 | 58 | PF02991 | 0.620 |
LIG_LIR_Nem_3 | 619 | 623 | PF02991 | 0.294 |
LIG_LIR_Nem_3 | 686 | 690 | PF02991 | 0.284 |
LIG_LIR_Nem_3 | 710 | 715 | PF02991 | 0.323 |
LIG_LIR_Nem_3 | 761 | 766 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 768 | 774 | PF02991 | 0.305 |
LIG_LIR_Nem_3 | 825 | 829 | PF02991 | 0.365 |
LIG_LYPXL_yS_3 | 144 | 147 | PF13949 | 0.375 |
LIG_MLH1_MIPbox_1 | 120 | 124 | PF16413 | 0.380 |
LIG_NRBOX | 328 | 334 | PF00104 | 0.377 |
LIG_PCNA_PIPBox_1 | 610 | 619 | PF02747 | 0.289 |
LIG_Pex14_1 | 120 | 124 | PF04695 | 0.279 |
LIG_Pex14_1 | 435 | 439 | PF04695 | 0.257 |
LIG_Pex14_1 | 637 | 641 | PF04695 | 0.291 |
LIG_Pex14_1 | 64 | 68 | PF04695 | 0.478 |
LIG_Pex14_2 | 103 | 107 | PF04695 | 0.258 |
LIG_Pex14_2 | 123 | 127 | PF04695 | 0.215 |
LIG_Pex14_2 | 55 | 59 | PF04695 | 0.627 |
LIG_PTB_Apo_2 | 706 | 713 | PF02174 | 0.322 |
LIG_PTB_Phospho_1 | 706 | 712 | PF10480 | 0.318 |
LIG_SH2_CRK | 732 | 736 | PF00017 | 0.377 |
LIG_SH2_CRK | 771 | 775 | PF00017 | 0.294 |
LIG_SH2_CRK | 96 | 100 | PF00017 | 0.293 |
LIG_SH2_PTP2 | 269 | 272 | PF00017 | 0.351 |
LIG_SH2_PTP2 | 687 | 690 | PF00017 | 0.283 |
LIG_SH2_SRC | 616 | 619 | PF00017 | 0.289 |
LIG_SH2_SRC | 98 | 101 | PF00017 | 0.313 |
LIG_SH2_STAP1 | 301 | 305 | PF00017 | 0.351 |
LIG_SH2_STAP1 | 767 | 771 | PF00017 | 0.365 |
LIG_SH2_STAT3 | 639 | 642 | PF00017 | 0.283 |
LIG_SH2_STAT5 | 237 | 240 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 269 | 272 | PF00017 | 0.351 |
LIG_SH2_STAT5 | 301 | 304 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 305 | 308 | PF00017 | 0.435 |
LIG_SH2_STAT5 | 387 | 390 | PF00017 | 0.266 |
LIG_SH2_STAT5 | 466 | 469 | PF00017 | 0.323 |
LIG_SH2_STAT5 | 616 | 619 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 620 | 623 | PF00017 | 0.302 |
LIG_SH2_STAT5 | 687 | 690 | PF00017 | 0.283 |
LIG_SH2_STAT5 | 98 | 101 | PF00017 | 0.345 |
LIG_SH3_2 | 62 | 67 | PF14604 | 0.462 |
LIG_SH3_3 | 169 | 175 | PF00018 | 0.375 |
LIG_SH3_3 | 310 | 316 | PF00018 | 0.414 |
LIG_SH3_3 | 415 | 421 | PF00018 | 0.202 |
LIG_SH3_3 | 59 | 65 | PF00018 | 0.478 |
LIG_SH3_3 | 714 | 720 | PF00018 | 0.401 |
LIG_SH3_3 | 787 | 793 | PF00018 | 0.361 |
LIG_SH3_3 | 794 | 800 | PF00018 | 0.365 |
LIG_SH3_4 | 511 | 518 | PF00018 | 0.587 |
LIG_SUMO_SIM_par_1 | 183 | 190 | PF11976 | 0.259 |
LIG_SUMO_SIM_par_1 | 440 | 446 | PF11976 | 0.221 |
LIG_SUMO_SIM_par_1 | 473 | 478 | PF11976 | 0.211 |
LIG_SUMO_SIM_par_1 | 609 | 615 | PF11976 | 0.248 |
LIG_SxIP_EBH_1 | 203 | 216 | PF03271 | 0.349 |
LIG_TRAF2_2 | 23 | 28 | PF00917 | 0.574 |
LIG_TYR_ITSM | 233 | 240 | PF00017 | 0.316 |
LIG_UBA3_1 | 743 | 752 | PF00899 | 0.394 |
LIG_WRC_WIRS_1 | 233 | 238 | PF05994 | 0.316 |
LIG_WRC_WIRS_1 | 424 | 429 | PF05994 | 0.185 |
LIG_WRC_WIRS_1 | 444 | 449 | PF05994 | 0.199 |
LIG_WRC_WIRS_1 | 570 | 575 | PF05994 | 0.159 |
MOD_CDC14_SPxK_1 | 321 | 324 | PF00782 | 0.380 |
MOD_CDC14_SPxK_1 | 451 | 454 | PF00782 | 0.452 |
MOD_CDK_SPK_2 | 624 | 629 | PF00069 | 0.241 |
MOD_CDK_SPxK_1 | 318 | 324 | PF00069 | 0.279 |
MOD_CDK_SPxK_1 | 448 | 454 | PF00069 | 0.455 |
MOD_CDK_SPxxK_3 | 34 | 41 | PF00069 | 0.591 |
MOD_CDK_SPxxK_3 | 733 | 740 | PF00069 | 0.372 |
MOD_CK1_1 | 14 | 20 | PF00069 | 0.741 |
MOD_CK1_1 | 194 | 200 | PF00069 | 0.298 |
MOD_CK1_1 | 242 | 248 | PF00069 | 0.351 |
MOD_CK1_1 | 505 | 511 | PF00069 | 0.657 |
MOD_CK1_1 | 534 | 540 | PF00069 | 0.597 |
MOD_CK1_1 | 546 | 552 | PF00069 | 0.595 |
MOD_CK1_1 | 783 | 789 | PF00069 | 0.333 |
MOD_CK2_1 | 409 | 415 | PF00069 | 0.247 |
MOD_CK2_1 | 835 | 841 | PF00069 | 0.393 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.447 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.570 |
MOD_GlcNHglycan | 192 | 196 | PF01048 | 0.497 |
MOD_GlcNHglycan | 368 | 371 | PF01048 | 0.349 |
MOD_GlcNHglycan | 391 | 394 | PF01048 | 0.504 |
MOD_GlcNHglycan | 460 | 463 | PF01048 | 0.302 |
MOD_GlcNHglycan | 477 | 480 | PF01048 | 0.167 |
MOD_GlcNHglycan | 533 | 536 | PF01048 | 0.392 |
MOD_GlcNHglycan | 545 | 548 | PF01048 | 0.286 |
MOD_GlcNHglycan | 575 | 578 | PF01048 | 0.416 |
MOD_GlcNHglycan | 629 | 632 | PF01048 | 0.419 |
MOD_GlcNHglycan | 694 | 697 | PF01048 | 0.580 |
MOD_GlcNHglycan | 782 | 785 | PF01048 | 0.567 |
MOD_GSK3_1 | 114 | 121 | PF00069 | 0.343 |
MOD_GSK3_1 | 187 | 194 | PF00069 | 0.342 |
MOD_GSK3_1 | 289 | 296 | PF00069 | 0.521 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.297 |
MOD_GSK3_1 | 498 | 505 | PF00069 | 0.624 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.701 |
MOD_GSK3_1 | 565 | 572 | PF00069 | 0.354 |
MOD_GSK3_1 | 573 | 580 | PF00069 | 0.380 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.370 |
MOD_N-GLC_1 | 448 | 453 | PF02516 | 0.211 |
MOD_N-GLC_1 | 647 | 652 | PF02516 | 0.505 |
MOD_N-GLC_1 | 780 | 785 | PF02516 | 0.529 |
MOD_N-GLC_2 | 224 | 226 | PF02516 | 0.279 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.332 |
MOD_NEK2_1 | 205 | 210 | PF00069 | 0.362 |
MOD_NEK2_1 | 214 | 219 | PF00069 | 0.355 |
MOD_NEK2_1 | 232 | 237 | PF00069 | 0.213 |
MOD_NEK2_1 | 409 | 414 | PF00069 | 0.249 |
MOD_NEK2_1 | 442 | 447 | PF00069 | 0.296 |
MOD_NEK2_1 | 475 | 480 | PF00069 | 0.205 |
MOD_NEK2_1 | 565 | 570 | PF00069 | 0.381 |
MOD_NEK2_1 | 573 | 578 | PF00069 | 0.306 |
MOD_NEK2_1 | 596 | 601 | PF00069 | 0.301 |
MOD_NEK2_1 | 68 | 73 | PF00069 | 0.409 |
MOD_NEK2_1 | 739 | 744 | PF00069 | 0.319 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.305 |
MOD_NEK2_2 | 239 | 244 | PF00069 | 0.316 |
MOD_NEK2_2 | 579 | 584 | PF00069 | 0.227 |
MOD_PIKK_1 | 513 | 519 | PF00454 | 0.698 |
MOD_PK_1 | 5 | 11 | PF00069 | 0.563 |
MOD_PK_1 | 89 | 95 | PF00069 | 0.314 |
MOD_PKA_1 | 835 | 841 | PF00069 | 0.325 |
MOD_PKA_2 | 245 | 251 | PF00069 | 0.315 |
MOD_PKA_2 | 289 | 295 | PF00069 | 0.531 |
MOD_PKA_2 | 602 | 608 | PF00069 | 0.402 |
MOD_PKA_2 | 648 | 654 | PF00069 | 0.310 |
MOD_PKA_2 | 739 | 745 | PF00069 | 0.365 |
MOD_PKA_2 | 822 | 828 | PF00069 | 0.331 |
MOD_PKA_2 | 88 | 94 | PF00069 | 0.249 |
MOD_PKB_1 | 364 | 372 | PF00069 | 0.513 |
MOD_Plk_1 | 647 | 653 | PF00069 | 0.317 |
MOD_Plk_4 | 128 | 134 | PF00069 | 0.279 |
MOD_Plk_4 | 232 | 238 | PF00069 | 0.316 |
MOD_Plk_4 | 281 | 287 | PF00069 | 0.423 |
MOD_Plk_4 | 293 | 299 | PF00069 | 0.423 |
MOD_Plk_4 | 40 | 46 | PF00069 | 0.691 |
MOD_Plk_4 | 443 | 449 | PF00069 | 0.317 |
MOD_Plk_4 | 498 | 504 | PF00069 | 0.567 |
MOD_Plk_4 | 566 | 572 | PF00069 | 0.252 |
MOD_Plk_4 | 616 | 622 | PF00069 | 0.199 |
MOD_Plk_4 | 676 | 682 | PF00069 | 0.363 |
MOD_Plk_4 | 68 | 74 | PF00069 | 0.269 |
MOD_Plk_4 | 707 | 713 | PF00069 | 0.308 |
MOD_Plk_4 | 739 | 745 | PF00069 | 0.358 |
MOD_Plk_4 | 758 | 764 | PF00069 | 0.268 |
MOD_Plk_4 | 800 | 806 | PF00069 | 0.369 |
MOD_ProDKin_1 | 318 | 324 | PF00069 | 0.279 |
MOD_ProDKin_1 | 34 | 40 | PF00069 | 0.625 |
MOD_ProDKin_1 | 417 | 423 | PF00069 | 0.232 |
MOD_ProDKin_1 | 448 | 454 | PF00069 | 0.401 |
MOD_ProDKin_1 | 624 | 630 | PF00069 | 0.325 |
MOD_ProDKin_1 | 669 | 675 | PF00069 | 0.312 |
MOD_ProDKin_1 | 698 | 704 | PF00069 | 0.338 |
MOD_ProDKin_1 | 733 | 739 | PF00069 | 0.318 |
TRG_DiLeu_BaEn_1 | 676 | 681 | PF01217 | 0.321 |
TRG_DiLeu_BaLyEn_6 | 470 | 475 | PF01217 | 0.282 |
TRG_ENDOCYTIC_2 | 144 | 147 | PF00928 | 0.419 |
TRG_ENDOCYTIC_2 | 237 | 240 | PF00928 | 0.316 |
TRG_ENDOCYTIC_2 | 259 | 262 | PF00928 | 0.316 |
TRG_ENDOCYTIC_2 | 269 | 272 | PF00928 | 0.316 |
TRG_ENDOCYTIC_2 | 301 | 304 | PF00928 | 0.316 |
TRG_ENDOCYTIC_2 | 620 | 623 | PF00928 | 0.292 |
TRG_ENDOCYTIC_2 | 687 | 690 | PF00928 | 0.283 |
TRG_ENDOCYTIC_2 | 712 | 715 | PF00928 | 0.333 |
TRG_ENDOCYTIC_2 | 771 | 774 | PF00928 | 0.290 |
TRG_ENDOCYTIC_2 | 96 | 99 | PF00928 | 0.293 |
TRG_ER_diArg_1 | 243 | 246 | PF00400 | 0.376 |
TRG_ER_diArg_1 | 347 | 350 | PF00400 | 0.497 |
TRG_ER_diArg_1 | 355 | 358 | PF00400 | 0.468 |
TRG_ER_diArg_1 | 363 | 366 | PF00400 | 0.411 |
TRG_ER_diArg_1 | 844 | 846 | PF00400 | 0.367 |
TRG_NES_CRM1_1 | 327 | 342 | PF08389 | 0.380 |
TRG_NLS_MonoExtN_4 | 831 | 838 | PF00514 | 0.344 |
TRG_Pf-PMV_PEXEL_1 | 396 | 401 | PF00026 | 0.468 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4IZ72 | Bodo saltans | 50% | 100% |
A0A1X0NFU7 | Trypanosomatidae | 55% | 100% |
A0A3Q8IHT0 | Leishmania donovani | 73% | 99% |
A0A3Q8II34 | Leishmania donovani | 55% | 100% |
A0A3Q8ILY7 | Leishmania donovani | 72% | 100% |
A0A3Q8IV37 | Leishmania donovani | 87% | 100% |
A0A422MX14 | Trypanosoma rangeli | 56% | 100% |
A4HFF9 | Leishmania braziliensis | 69% | 100% |
A4HMD5 | Leishmania braziliensis | 69% | 99% |
A4HMD6 | Leishmania braziliensis | 56% | 100% |
A4HMD7 | Leishmania braziliensis | 80% | 100% |
A4IB08 | Leishmania infantum | 73% | 99% |
A4IB09 | Leishmania infantum | 73% | 100% |
A4IB10 | Leishmania infantum | 55% | 100% |
C9ZNL1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 56% | 100% |
C9ZQ40 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 55% | 100% |
E2RG47 | Canis lupus familiaris | 31% | 100% |
E9AET6 | Leishmania major | 67% | 99% |
E9AET7 | Leishmania major | 74% | 100% |
E9AET8 | Leishmania major | 56% | 100% |
E9AET9 | Leishmania major | 89% | 100% |
E9AHU4 | Leishmania infantum | 87% | 100% |
E9B5Z2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 71% | 99% |
E9B5Z3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 77% | 100% |
E9B5Z4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 57% | 100% |
F1PJP5 | Canis lupus familiaris | 29% | 100% |
O94335 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 32% | 100% |
P39007 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 30% | 100% |
P46975 | Caenorhabditis elegans | 31% | 100% |
P46977 | Homo sapiens | 29% | 100% |
P46978 | Mus musculus | 30% | 100% |
Q2KJI2 | Bos taurus | 29% | 100% |
Q3TDQ1 | Mus musculus | 31% | 100% |
Q54NM9 | Dictyostelium discoideum | 30% | 100% |
Q5RCE2 | Pongo abelii | 29% | 100% |
Q6F2Z1 | Oryza sativa subsp. japonica | 30% | 100% |
Q7XQ88 | Oryza sativa subsp. japonica | 31% | 100% |
Q8TCJ2 | Homo sapiens | 30% | 100% |
Q93ZY3 | Arabidopsis thaliana | 31% | 100% |
Q9FX21 | Arabidopsis thaliana | 31% | 100% |
V5BDM6 | Trypanosoma cruzi | 58% | 100% |