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:0005635 | nuclear envelope | 4 | 5 |
GO:0005783 | endoplasmic reticulum | 5 | 5 |
GO:0016020 | membrane | 2 | 27 |
GO:0031967 | organelle envelope | 3 | 5 |
GO:0031975 | envelope | 2 | 5 |
GO:0043226 | organelle | 2 | 5 |
GO:0043227 | membrane-bounded organelle | 3 | 5 |
GO:0043229 | intracellular organelle | 3 | 5 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 5 |
GO:0110165 | cellular anatomical entity | 1 | 27 |
Related structures:
AlphaFold database: E9AET9
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 | 652 | 656 | PF00656 | 0.267 |
CLV_C14_Caspase3-7 | 8 | 12 | PF00656 | 0.575 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.378 |
CLV_NRD_NRD_1 | 753 | 755 | PF00675 | 0.598 |
CLV_NRD_NRD_1 | 834 | 836 | PF00675 | 0.645 |
CLV_NRD_NRD_1 | 848 | 850 | PF00675 | 0.517 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.513 |
CLV_PCSK_KEX2_1 | 753 | 755 | PF00082 | 0.598 |
CLV_PCSK_KEX2_1 | 848 | 850 | PF00082 | 0.561 |
CLV_PCSK_PC1ET2_1 | 3 | 5 | PF00082 | 0.513 |
CLV_PCSK_PC1ET2_1 | 753 | 755 | PF00082 | 0.479 |
CLV_PCSK_SKI1_1 | 396 | 400 | PF00082 | 0.447 |
CLV_PCSK_SKI1_1 | 41 | 45 | PF00082 | 0.415 |
CLV_PCSK_SKI1_1 | 47 | 51 | PF00082 | 0.359 |
CLV_PCSK_SKI1_1 | 473 | 477 | PF00082 | 0.408 |
CLV_PCSK_SKI1_1 | 534 | 538 | PF00082 | 0.305 |
CLV_PCSK_SKI1_1 | 556 | 560 | PF00082 | 0.295 |
CLV_PCSK_SKI1_1 | 669 | 673 | PF00082 | 0.499 |
CLV_PCSK_SKI1_1 | 755 | 759 | PF00082 | 0.626 |
CLV_PCSK_SKI1_1 | 776 | 780 | PF00082 | 0.604 |
CLV_Separin_Metazoa | 345 | 349 | PF03568 | 0.284 |
DEG_ODPH_VHL_1 | 382 | 395 | PF01847 | 0.367 |
DEG_SCF_TRCP1_1 | 11 | 17 | PF00400 | 0.592 |
DEG_SPOP_SBC_1 | 139 | 143 | PF00917 | 0.474 |
DOC_AGCK_PIF_2 | 124 | 129 | PF00069 | 0.293 |
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 | 0.491 |
DOC_MAPK_gen_1 | 244 | 253 | PF00069 | 0.359 |
DOC_MAPK_gen_1 | 348 | 355 | PF00069 | 0.484 |
DOC_MAPK_gen_1 | 356 | 365 | PF00069 | 0.498 |
DOC_MAPK_gen_1 | 753 | 759 | PF00069 | 0.379 |
DOC_MAPK_HePTP_8 | 355 | 367 | PF00069 | 0.457 |
DOC_MAPK_JIP1_4 | 608 | 614 | PF00069 | 0.160 |
DOC_MAPK_MEF2A_6 | 358 | 367 | PF00069 | 0.508 |
DOC_MAPK_MEF2A_6 | 556 | 563 | PF00069 | 0.494 |
DOC_PP1_RVXF_1 | 452 | 458 | PF00149 | 0.496 |
DOC_PP1_RVXF_1 | 631 | 638 | PF00149 | 0.279 |
DOC_PP4_FxxP_1 | 59 | 62 | PF00568 | 0.497 |
DOC_USP7_MATH_1 | 138 | 142 | PF00917 | 0.338 |
DOC_USP7_MATH_1 | 16 | 20 | PF00917 | 0.690 |
DOC_USP7_MATH_1 | 193 | 197 | PF00917 | 0.266 |
DOC_USP7_MATH_1 | 322 | 326 | PF00917 | 0.279 |
DOC_USP7_MATH_1 | 547 | 551 | PF00917 | 0.403 |
DOC_USP7_MATH_1 | 580 | 584 | PF00917 | 0.328 |
DOC_USP7_MATH_1 | 587 | 591 | PF00917 | 0.332 |
DOC_USP7_MATH_1 | 693 | 697 | PF00917 | 0.364 |
DOC_USP7_UBL2_3 | 511 | 515 | PF12436 | 0.379 |
DOC_WW_Pin1_4 | 318 | 323 | PF00397 | 0.279 |
DOC_WW_Pin1_4 | 34 | 39 | PF00397 | 0.606 |
DOC_WW_Pin1_4 | 417 | 422 | PF00397 | 0.232 |
DOC_WW_Pin1_4 | 448 | 453 | PF00397 | 0.401 |
DOC_WW_Pin1_4 | 625 | 630 | PF00397 | 0.268 |
DOC_WW_Pin1_4 | 670 | 675 | PF00397 | 0.307 |
DOC_WW_Pin1_4 | 699 | 704 | PF00397 | 0.346 |
DOC_WW_Pin1_4 | 734 | 739 | PF00397 | 0.329 |
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 | 366 | 371 | PF00244 | 0.453 |
LIG_14-3-3_CanoR_1 | 4 | 10 | PF00244 | 0.569 |
LIG_14-3-3_CanoR_1 | 650 | 654 | PF00244 | 0.294 |
LIG_14-3-3_CanoR_1 | 707 | 713 | PF00244 | 0.313 |
LIG_14-3-3_CanoR_1 | 741 | 745 | PF00244 | 0.372 |
LIG_14-3-3_CanoR_1 | 89 | 94 | PF00244 | 0.279 |
LIG_Actin_WH2_2 | 611 | 627 | PF00022 | 0.219 |
LIG_AP2alpha_1 | 542 | 546 | PF02296 | 0.364 |
LIG_AP2alpha_2 | 104 | 106 | PF02296 | 0.279 |
LIG_BRCT_BRCA1_1 | 120 | 124 | PF00533 | 0.380 |
LIG_BRCT_BRCA1_1 | 452 | 456 | PF00533 | 0.430 |
LIG_BRCT_BRCA1_1 | 575 | 579 | PF00533 | 0.288 |
LIG_BRCT_BRCA1_1 | 582 | 586 | PF00533 | 0.230 |
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 | 567 | 573 | PF00498 | 0.416 |
LIG_FHA_1 | 670 | 676 | PF00498 | 0.313 |
LIG_FHA_2 | 46 | 52 | PF00498 | 0.554 |
LIG_FHA_2 | 490 | 496 | PF00498 | 0.278 |
LIG_FHA_2 | 626 | 632 | PF00498 | 0.257 |
LIG_FHA_2 | 829 | 835 | PF00498 | 0.362 |
LIG_IRF3_LxIS_1 | 374 | 380 | PF10401 | 0.224 |
LIG_LIR_Apic_2 | 385 | 390 | PF02991 | 0.305 |
LIG_LIR_Apic_2 | 732 | 736 | PF02991 | 0.382 |
LIG_LIR_Apic_2 | 804 | 808 | PF02991 | 0.461 |
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 | 687 | 693 | PF02991 | 0.351 |
LIG_LIR_Gen_1 | 711 | 721 | PF02991 | 0.394 |
LIG_LIR_Gen_1 | 762 | 772 | PF02991 | 0.416 |
LIG_LIR_Gen_1 | 81 | 91 | PF02991 | 0.418 |
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 | 185 | 191 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 206 | 210 | PF02991 | 0.380 |
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 | 385 | 391 | PF02991 | 0.279 |
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 | 0.617 |
LIG_LIR_Nem_3 | 687 | 691 | PF02991 | 0.284 |
LIG_LIR_Nem_3 | 711 | 716 | PF02991 | 0.318 |
LIG_LIR_Nem_3 | 762 | 767 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 769 | 775 | PF02991 | 0.305 |
LIG_LIR_Nem_3 | 81 | 86 | PF02991 | 0.370 |
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_NRP_CendR_1 | 856 | 857 | PF00754 | 0.572 |
LIG_PCNA_yPIPBox_3 | 604 | 618 | PF02747 | 0.249 |
LIG_Pex14_1 | 120 | 124 | PF04695 | 0.279 |
LIG_Pex14_1 | 638 | 642 | PF04695 | 0.268 |
LIG_Pex14_1 | 64 | 68 | PF04695 | 0.475 |
LIG_Pex14_2 | 103 | 107 | PF04695 | 0.258 |
LIG_Pex14_2 | 123 | 127 | PF04695 | 0.215 |
LIG_Pex14_2 | 542 | 546 | PF04695 | 0.401 |
LIG_Pex14_2 | 55 | 59 | PF04695 | 0.624 |
LIG_Pex14_2 | 575 | 579 | PF04695 | 0.232 |
LIG_PTB_Apo_2 | 707 | 714 | PF02174 | 0.317 |
LIG_PTB_Phospho_1 | 707 | 713 | PF10480 | 0.313 |
LIG_RPA_C_Insects | 743 | 758 | PF08784 | 0.282 |
LIG_SH2_CRK | 733 | 737 | PF00017 | 0.476 |
LIG_SH2_CRK | 772 | 776 | PF00017 | 0.354 |
LIG_SH2_CRK | 96 | 100 | PF00017 | 0.352 |
LIG_SH2_NCK_1 | 733 | 737 | PF00017 | 0.416 |
LIG_SH2_PTP2 | 269 | 272 | PF00017 | 0.352 |
LIG_SH2_PTP2 | 688 | 691 | PF00017 | 0.338 |
LIG_SH2_SRC | 98 | 101 | PF00017 | 0.379 |
LIG_SH2_STAP1 | 301 | 305 | PF00017 | 0.352 |
LIG_SH2_STAP1 | 768 | 772 | PF00017 | 0.453 |
LIG_SH2_STAT3 | 640 | 643 | PF00017 | 0.316 |
LIG_SH2_STAT5 | 237 | 240 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 269 | 272 | PF00017 | 0.352 |
LIG_SH2_STAT5 | 301 | 304 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 305 | 308 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 387 | 390 | PF00017 | 0.313 |
LIG_SH2_STAT5 | 466 | 469 | PF00017 | 0.323 |
LIG_SH2_STAT5 | 617 | 620 | PF00017 | 0.334 |
LIG_SH2_STAT5 | 688 | 691 | PF00017 | 0.338 |
LIG_SH2_STAT5 | 98 | 101 | PF00017 | 0.425 |
LIG_SH3_3 | 169 | 175 | PF00018 | 0.375 |
LIG_SH3_3 | 310 | 316 | PF00018 | 0.414 |
LIG_SH3_3 | 378 | 384 | PF00018 | 0.343 |
LIG_SH3_3 | 415 | 421 | PF00018 | 0.224 |
LIG_SH3_3 | 59 | 65 | PF00018 | 0.331 |
LIG_SH3_3 | 715 | 721 | PF00018 | 0.503 |
LIG_SH3_3 | 788 | 794 | PF00018 | 0.450 |
LIG_SH3_3 | 795 | 801 | PF00018 | 0.454 |
LIG_SUMO_SIM_par_1 | 439 | 446 | PF11976 | 0.224 |
LIG_SUMO_SIM_par_1 | 473 | 478 | PF11976 | 0.236 |
LIG_SxIP_EBH_1 | 203 | 216 | PF03271 | 0.349 |
LIG_TRAF2_1 | 841 | 844 | PF00917 | 0.364 |
LIG_TYR_ITSM | 233 | 240 | PF00017 | 0.316 |
LIG_UBA3_1 | 744 | 753 | PF00899 | 0.498 |
LIG_WRC_WIRS_1 | 233 | 238 | PF05994 | 0.316 |
LIG_WRC_WIRS_1 | 444 | 449 | PF05994 | 0.199 |
MOD_CDC14_SPxK_1 | 321 | 324 | PF00782 | 0.474 |
MOD_CDC14_SPxK_1 | 451 | 454 | PF00782 | 0.293 |
MOD_CDK_SPxK_1 | 318 | 324 | PF00069 | 0.332 |
MOD_CDK_SPxK_1 | 448 | 454 | PF00069 | 0.299 |
MOD_CDK_SPxxK_3 | 34 | 41 | PF00069 | 0.460 |
MOD_CDK_SPxxK_3 | 734 | 741 | PF00069 | 0.468 |
MOD_CK1_1 | 14 | 20 | PF00069 | 0.689 |
MOD_CK1_1 | 194 | 200 | PF00069 | 0.358 |
MOD_CK1_1 | 242 | 248 | PF00069 | 0.352 |
MOD_CK1_1 | 505 | 511 | PF00069 | 0.350 |
MOD_CK1_1 | 573 | 579 | PF00069 | 0.374 |
MOD_CK1_1 | 581 | 587 | PF00069 | 0.356 |
MOD_CK1_1 | 734 | 740 | PF00069 | 0.408 |
MOD_CK1_1 | 784 | 790 | PF00069 | 0.411 |
MOD_CK2_1 | 409 | 415 | PF00069 | 0.286 |
MOD_CK2_1 | 489 | 495 | PF00069 | 0.406 |
MOD_CK2_1 | 624 | 630 | PF00069 | 0.254 |
MOD_CK2_1 | 838 | 844 | PF00069 | 0.490 |
MOD_Cter_Amidation | 1 | 4 | PF01082 | 0.696 |
MOD_Cter_Amidation | 751 | 754 | PF01082 | 0.302 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.551 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.459 |
MOD_GlcNHglycan | 192 | 196 | PF01048 | 0.357 |
MOD_GlcNHglycan | 21 | 25 | PF01048 | 0.573 |
MOD_GlcNHglycan | 460 | 463 | PF01048 | 0.302 |
MOD_GlcNHglycan | 477 | 480 | PF01048 | 0.167 |
MOD_GlcNHglycan | 527 | 530 | PF01048 | 0.450 |
MOD_GlcNHglycan | 695 | 698 | PF01048 | 0.480 |
MOD_GlcNHglycan | 783 | 786 | PF01048 | 0.459 |
MOD_GSK3_1 | 114 | 121 | PF00069 | 0.421 |
MOD_GSK3_1 | 16 | 23 | PF00069 | 0.622 |
MOD_GSK3_1 | 187 | 194 | PF00069 | 0.342 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.647 |
MOD_GSK3_1 | 289 | 296 | PF00069 | 0.391 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.357 |
MOD_GSK3_1 | 498 | 505 | PF00069 | 0.438 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.637 |
MOD_GSK3_1 | 566 | 573 | PF00069 | 0.354 |
MOD_GSK3_1 | 574 | 581 | PF00069 | 0.288 |
MOD_N-GLC_1 | 534 | 539 | PF02516 | 0.171 |
MOD_N-GLC_1 | 648 | 653 | PF02516 | 0.314 |
MOD_N-GLC_1 | 781 | 786 | PF02516 | 0.405 |
MOD_N-GLC_2 | 169 | 171 | PF02516 | 0.436 |
MOD_N-GLC_2 | 224 | 226 | PF02516 | 0.332 |
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 | 0.214 |
MOD_NEK2_1 | 377 | 382 | PF00069 | 0.290 |
MOD_NEK2_1 | 409 | 414 | PF00069 | 0.290 |
MOD_NEK2_1 | 442 | 447 | PF00069 | 0.297 |
MOD_NEK2_1 | 458 | 463 | PF00069 | 0.324 |
MOD_NEK2_1 | 475 | 480 | PF00069 | 0.206 |
MOD_NEK2_1 | 489 | 494 | PF00069 | 0.389 |
MOD_NEK2_1 | 546 | 551 | PF00069 | 0.199 |
MOD_NEK2_1 | 557 | 562 | PF00069 | 0.192 |
MOD_NEK2_1 | 566 | 571 | PF00069 | 0.381 |
MOD_NEK2_1 | 624 | 629 | PF00069 | 0.278 |
MOD_NEK2_1 | 68 | 73 | PF00069 | 0.409 |
MOD_NEK2_1 | 740 | 745 | PF00069 | 0.391 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.305 |
MOD_NEK2_1 | 9 | 14 | PF00069 | 0.482 |
MOD_NEK2_2 | 239 | 244 | PF00069 | 0.316 |
MOD_PIKK_1 | 28 | 34 | PF00454 | 0.734 |
MOD_PK_1 | 366 | 372 | PF00069 | 0.417 |
MOD_PK_1 | 89 | 95 | PF00069 | 0.381 |
MOD_PKA_2 | 245 | 251 | PF00069 | 0.382 |
MOD_PKA_2 | 289 | 295 | PF00069 | 0.405 |
MOD_PKA_2 | 603 | 609 | PF00069 | 0.354 |
MOD_PKA_2 | 624 | 630 | PF00069 | 0.278 |
MOD_PKA_2 | 649 | 655 | PF00069 | 0.316 |
MOD_PKA_2 | 740 | 746 | PF00069 | 0.456 |
MOD_PKA_2 | 850 | 856 | PF00069 | 0.376 |
MOD_PKB_1 | 364 | 372 | PF00069 | 0.379 |
MOD_Plk_1 | 648 | 654 | PF00069 | 0.329 |
MOD_Plk_4 | 128 | 134 | PF00069 | 0.332 |
MOD_Plk_4 | 232 | 238 | PF00069 | 0.316 |
MOD_Plk_4 | 281 | 287 | PF00069 | 0.423 |
MOD_Plk_4 | 293 | 299 | PF00069 | 0.254 |
MOD_Plk_4 | 436 | 442 | PF00069 | 0.342 |
MOD_Plk_4 | 443 | 449 | PF00069 | 0.318 |
MOD_Plk_4 | 489 | 495 | PF00069 | 0.340 |
MOD_Plk_4 | 498 | 504 | PF00069 | 0.364 |
MOD_Plk_4 | 570 | 576 | PF00069 | 0.269 |
MOD_Plk_4 | 677 | 683 | PF00069 | 0.449 |
MOD_Plk_4 | 68 | 74 | PF00069 | 0.269 |
MOD_Plk_4 | 708 | 714 | PF00069 | 0.367 |
MOD_Plk_4 | 740 | 746 | PF00069 | 0.445 |
MOD_Plk_4 | 759 | 765 | PF00069 | 0.325 |
MOD_Plk_4 | 801 | 807 | PF00069 | 0.459 |
MOD_ProDKin_1 | 318 | 324 | PF00069 | 0.332 |
MOD_ProDKin_1 | 34 | 40 | PF00069 | 0.508 |
MOD_ProDKin_1 | 417 | 423 | PF00069 | 0.266 |
MOD_ProDKin_1 | 448 | 454 | PF00069 | 0.222 |
MOD_ProDKin_1 | 625 | 631 | PF00069 | 0.316 |
MOD_ProDKin_1 | 670 | 676 | PF00069 | 0.380 |
MOD_ProDKin_1 | 699 | 705 | PF00069 | 0.420 |
MOD_ProDKin_1 | 734 | 740 | PF00069 | 0.394 |
MOD_SUMO_rev_2 | 528 | 536 | PF00179 | 0.171 |
TRG_DiLeu_BaEn_1 | 677 | 682 | PF01217 | 0.391 |
TRG_DiLeu_BaLyEn_6 | 470 | 475 | PF01217 | 0.283 |
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 | 621 | 624 | PF00928 | 0.316 |
TRG_ENDOCYTIC_2 | 688 | 691 | PF00928 | 0.338 |
TRG_ENDOCYTIC_2 | 713 | 716 | PF00928 | 0.404 |
TRG_ENDOCYTIC_2 | 772 | 775 | PF00928 | 0.347 |
TRG_ENDOCYTIC_2 | 96 | 99 | PF00928 | 0.352 |
TRG_ER_diArg_1 | 243 | 246 | PF00400 | 0.468 |
TRG_ER_diArg_1 | 347 | 350 | PF00400 | 0.357 |
TRG_ER_diArg_1 | 355 | 358 | PF00400 | 0.316 |
TRG_ER_diArg_1 | 363 | 366 | PF00400 | 0.237 |
TRG_ER_diArg_1 | 393 | 396 | PF00400 | 0.301 |
TRG_ER_diArg_1 | 847 | 849 | PF00400 | 0.463 |
TRG_NES_CRM1_1 | 327 | 342 | PF08389 | 0.474 |
TRG_Pf-PMV_PEXEL_1 | 396 | 401 | PF00026 | 0.317 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4IZ72 | Bodo saltans | 51% | 100% |
A0A1X0NFU7 | Trypanosomatidae | 56% | 100% |
A0A3Q8IHT0 | Leishmania donovani | 73% | 99% |
A0A3Q8II34 | Leishmania donovani | 55% | 100% |
A0A3Q8ILY7 | Leishmania donovani | 73% | 100% |
A0A3Q8IV37 | Leishmania donovani | 91% | 100% |
A0A422MX14 | Trypanosoma rangeli | 55% | 100% |
A4HFF9 | Leishmania braziliensis | 65% | 100% |
A4HMD5 | Leishmania braziliensis | 71% | 100% |
A4HMD6 | Leishmania braziliensis | 55% | 100% |
A4HMD7 | Leishmania braziliensis | 80% | 100% |
A4IB08 | Leishmania infantum | 73% | 99% |
A4IB09 | Leishmania infantum | 73% | 100% |
A4IB10 | Leishmania infantum | 56% | 100% |
C9ZNL1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 55% | 100% |
C9ZQ40 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 54% | 100% |
E2RG47 | Canis lupus familiaris | 29% | 100% |
E9AET6 | Leishmania major | 69% | 99% |
E9AET7 | Leishmania major | 76% | 100% |
E9AET8 | Leishmania major | 57% | 100% |
E9AHU4 | Leishmania infantum | 91% | 100% |
E9B5Z2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 68% | 99% |
E9B5Z3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 74% | 100% |
E9B5Z4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 55% | 100% |
E9B5Z5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
F1PJP5 | Canis lupus familiaris | 29% | 100% |
O94335 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 31% | 100% |
P39007 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 29% | 100% |
P46975 | Caenorhabditis elegans | 30% | 100% |
P46977 | Homo sapiens | 30% | 100% |
P46978 | Mus musculus | 30% | 100% |
Q2KJI2 | Bos taurus | 30% | 100% |
Q3TDQ1 | Mus musculus | 30% | 100% |
Q54NM9 | Dictyostelium discoideum | 31% | 100% |
Q5RCE2 | Pongo abelii | 30% | 100% |
Q6F2Z1 | Oryza sativa subsp. japonica | 29% | 100% |
Q7XQ88 | Oryza sativa subsp. japonica | 32% | 100% |
Q8TCJ2 | Homo sapiens | 29% | 100% |
Q93ZY3 | Arabidopsis thaliana | 32% | 100% |
Q9FX21 | Arabidopsis thaliana | 31% | 100% |
V5BDM6 | Trypanosoma cruzi | 56% | 100% |