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: A4HFF9
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 | 661 | 665 | PF00656 | 0.319 |
CLV_NRD_NRD_1 | 527 | 529 | PF00675 | 0.597 |
CLV_NRD_NRD_1 | 550 | 552 | PF00675 | 0.464 |
CLV_NRD_NRD_1 | 560 | 562 | PF00675 | 0.453 |
CLV_NRD_NRD_1 | 6 | 8 | PF00675 | 0.390 |
CLV_PCSK_FUR_1 | 525 | 529 | PF00082 | 0.397 |
CLV_PCSK_KEX2_1 | 527 | 529 | PF00082 | 0.551 |
CLV_PCSK_KEX2_1 | 550 | 552 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 391 | 395 | PF00082 | 0.456 |
CLV_PCSK_SKI1_1 | 467 | 471 | PF00082 | 0.415 |
CLV_PCSK_SKI1_1 | 562 | 566 | PF00082 | 0.473 |
CLV_PCSK_SKI1_1 | 574 | 578 | PF00082 | 0.195 |
CLV_PCSK_SKI1_1 | 678 | 682 | PF00082 | 0.504 |
CLV_PCSK_SKI1_1 | 784 | 788 | PF00082 | 0.604 |
DEG_SCF_FBW7_2 | 17 | 24 | PF00400 | 0.597 |
DEG_SPOP_SBC_1 | 134 | 138 | PF00917 | 0.473 |
DOC_AGCK_PIF_2 | 119 | 124 | PF00069 | 0.302 |
DOC_ANK_TNKS_1 | 33 | 40 | PF00023 | 0.587 |
DOC_CKS1_1 | 440 | 445 | PF01111 | 0.158 |
DOC_CYCLIN_RxL_1 | 388 | 398 | PF00134 | 0.263 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 440 | 449 | PF00134 | 0.158 |
DOC_MAPK_gen_1 | 239 | 248 | PF00069 | 0.363 |
DOC_MAPK_gen_1 | 343 | 350 | PF00069 | 0.493 |
DOC_MAPK_gen_1 | 550 | 558 | PF00069 | 0.720 |
DOC_PP1_RVXF_1 | 64 | 71 | PF00149 | 0.158 |
DOC_PP1_RVXF_1 | 640 | 647 | PF00149 | 0.310 |
DOC_PP2B_LxvP_1 | 438 | 441 | PF13499 | 0.224 |
DOC_PP4_FxxP_1 | 432 | 435 | PF00568 | 0.404 |
DOC_PP4_MxPP_1 | 42 | 45 | PF00568 | 0.564 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.710 |
DOC_USP7_MATH_1 | 317 | 321 | PF00917 | 0.288 |
DOC_USP7_MATH_1 | 540 | 544 | PF00917 | 0.662 |
DOC_USP7_MATH_1 | 759 | 763 | PF00917 | 0.404 |
DOC_USP7_UBL2_3 | 4 | 8 | PF12436 | 0.624 |
DOC_WW_Pin1_4 | 17 | 22 | PF00397 | 0.624 |
DOC_WW_Pin1_4 | 313 | 318 | PF00397 | 0.288 |
DOC_WW_Pin1_4 | 37 | 42 | PF00397 | 0.630 |
DOC_WW_Pin1_4 | 375 | 380 | PF00397 | 0.188 |
DOC_WW_Pin1_4 | 439 | 444 | PF00397 | 0.230 |
DOC_WW_Pin1_4 | 509 | 514 | PF00397 | 0.571 |
DOC_WW_Pin1_4 | 604 | 609 | PF00397 | 0.266 |
DOC_WW_Pin1_4 | 634 | 639 | PF00397 | 0.329 |
DOC_WW_Pin1_4 | 679 | 684 | PF00397 | 0.312 |
DOC_WW_Pin1_4 | 708 | 713 | PF00397 | 0.339 |
LIG_14-3-3_CanoR_1 | 239 | 245 | PF00244 | 0.311 |
LIG_14-3-3_CanoR_1 | 285 | 289 | PF00244 | 0.538 |
LIG_14-3-3_CanoR_1 | 361 | 366 | PF00244 | 0.458 |
LIG_14-3-3_CanoR_1 | 550 | 556 | PF00244 | 0.710 |
LIG_14-3-3_CanoR_1 | 642 | 647 | PF00244 | 0.256 |
LIG_14-3-3_CanoR_1 | 659 | 663 | PF00244 | 0.324 |
LIG_14-3-3_CanoR_1 | 716 | 722 | PF00244 | 0.324 |
LIG_14-3-3_CanoR_1 | 749 | 753 | PF00244 | 0.375 |
LIG_14-3-3_CanoR_1 | 84 | 89 | PF00244 | 0.288 |
LIG_14-3-3_CanoR_1 | 852 | 857 | PF00244 | 0.520 |
LIG_Actin_WH2_2 | 488 | 504 | PF00022 | 0.453 |
LIG_AP2alpha_2 | 99 | 101 | PF02296 | 0.288 |
LIG_BRCT_BRCA1_1 | 115 | 119 | PF00533 | 0.380 |
LIG_Clathr_ClatBox_1 | 183 | 187 | PF01394 | 0.218 |
LIG_Clathr_ClatBox_1 | 555 | 559 | PF01394 | 0.586 |
LIG_eIF4E_1 | 446 | 452 | PF01652 | 0.382 |
LIG_FHA_1 | 187 | 193 | PF00498 | 0.291 |
LIG_FHA_1 | 228 | 234 | PF00498 | 0.289 |
LIG_FHA_1 | 385 | 391 | PF00498 | 0.385 |
LIG_FHA_1 | 440 | 446 | PF00498 | 0.401 |
LIG_FHA_1 | 461 | 467 | PF00498 | 0.406 |
LIG_FHA_1 | 551 | 557 | PF00498 | 0.715 |
LIG_FHA_1 | 575 | 581 | PF00498 | 0.440 |
LIG_FHA_1 | 618 | 624 | PF00498 | 0.266 |
LIG_FHA_1 | 679 | 685 | PF00498 | 0.313 |
LIG_FHA_1 | 69 | 75 | PF00498 | 0.404 |
LIG_FHA_1 | 81 | 87 | PF00498 | 0.153 |
LIG_FHA_2 | 30 | 36 | PF00498 | 0.592 |
LIG_FHA_2 | 38 | 44 | PF00498 | 0.611 |
LIG_FHA_2 | 543 | 549 | PF00498 | 0.652 |
LIG_FHA_2 | 635 | 641 | PF00498 | 0.309 |
LIG_FHA_2 | 853 | 859 | PF00498 | 0.394 |
LIG_GBD_Chelix_1 | 176 | 184 | PF00786 | 0.266 |
LIG_LIR_Apic_2 | 380 | 385 | PF02991 | 0.314 |
LIG_LIR_Apic_2 | 739 | 744 | PF02991 | 0.383 |
LIG_LIR_Apic_2 | 812 | 816 | PF02991 | 0.456 |
LIG_LIR_Gen_1 | 116 | 125 | PF02991 | 0.340 |
LIG_LIR_Gen_1 | 195 | 205 | PF02991 | 0.439 |
LIG_LIR_Gen_1 | 230 | 238 | PF02991 | 0.345 |
LIG_LIR_Gen_1 | 549 | 560 | PF02991 | 0.548 |
LIG_LIR_Gen_1 | 628 | 638 | PF02991 | 0.310 |
LIG_LIR_Gen_1 | 696 | 702 | PF02991 | 0.356 |
LIG_LIR_Gen_1 | 720 | 730 | PF02991 | 0.440 |
LIG_LIR_Gen_1 | 770 | 780 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 116 | 122 | PF02991 | 0.283 |
LIG_LIR_Nem_3 | 126 | 130 | PF02991 | 0.272 |
LIG_LIR_Nem_3 | 136 | 142 | PF02991 | 0.261 |
LIG_LIR_Nem_3 | 195 | 200 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 230 | 235 | PF02991 | 0.330 |
LIG_LIR_Nem_3 | 316 | 321 | PF02991 | 0.282 |
LIG_LIR_Nem_3 | 380 | 386 | PF02991 | 0.288 |
LIG_LIR_Nem_3 | 549 | 555 | PF02991 | 0.602 |
LIG_LIR_Nem_3 | 628 | 633 | PF02991 | 0.316 |
LIG_LIR_Nem_3 | 645 | 649 | PF02991 | 0.263 |
LIG_LIR_Nem_3 | 696 | 700 | PF02991 | 0.292 |
LIG_LIR_Nem_3 | 720 | 725 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 770 | 775 | PF02991 | 0.365 |
LIG_LIR_Nem_3 | 777 | 783 | PF02991 | 0.309 |
LIG_LIR_Nem_3 | 90 | 94 | PF02991 | 0.291 |
LIG_LIR_Nem_3 | 99 | 104 | PF02991 | 0.289 |
LIG_LYPXL_yS_3 | 139 | 142 | PF13949 | 0.387 |
LIG_MLH1_MIPbox_1 | 115 | 119 | PF16413 | 0.380 |
LIG_NRBOX | 326 | 332 | PF00104 | 0.393 |
LIG_PAM2_1 | 441 | 453 | PF00658 | 0.355 |
LIG_Pex14_1 | 115 | 119 | PF04695 | 0.288 |
LIG_Pex14_1 | 647 | 651 | PF04695 | 0.300 |
LIG_Pex14_2 | 118 | 122 | PF04695 | 0.215 |
LIG_Pex14_2 | 492 | 496 | PF04695 | 0.592 |
LIG_Pex14_2 | 592 | 596 | PF04695 | 0.314 |
LIG_Pex14_2 | 98 | 102 | PF04695 | 0.267 |
LIG_PTB_Apo_2 | 421 | 428 | PF02174 | 0.155 |
LIG_PTB_Apo_2 | 716 | 723 | PF02174 | 0.329 |
LIG_PTB_Phospho_1 | 421 | 427 | PF10480 | 0.155 |
LIG_PTB_Phospho_1 | 716 | 722 | PF10480 | 0.324 |
LIG_SH2_CRK | 173 | 177 | PF00017 | 0.188 |
LIG_SH2_CRK | 446 | 450 | PF00017 | 0.496 |
LIG_SH2_CRK | 552 | 556 | PF00017 | 0.594 |
LIG_SH2_CRK | 58 | 62 | PF00017 | 0.487 |
LIG_SH2_CRK | 65 | 69 | PF00017 | 0.197 |
LIG_SH2_CRK | 741 | 745 | PF00017 | 0.376 |
LIG_SH2_CRK | 780 | 784 | PF00017 | 0.299 |
LIG_SH2_CRK | 91 | 95 | PF00017 | 0.302 |
LIG_SH2_GRB2like | 422 | 425 | PF00017 | 0.347 |
LIG_SH2_PTP2 | 264 | 267 | PF00017 | 0.363 |
LIG_SH2_PTP2 | 697 | 700 | PF00017 | 0.291 |
LIG_SH2_SRC | 422 | 425 | PF00017 | 0.265 |
LIG_SH2_SRC | 626 | 629 | PF00017 | 0.296 |
LIG_SH2_SRC | 93 | 96 | PF00017 | 0.312 |
LIG_SH2_STAP1 | 296 | 300 | PF00017 | 0.363 |
LIG_SH2_STAP1 | 446 | 450 | PF00017 | 0.511 |
LIG_SH2_STAP1 | 454 | 458 | PF00017 | 0.289 |
LIG_SH2_STAP1 | 552 | 556 | PF00017 | 0.548 |
LIG_SH2_STAP1 | 58 | 62 | PF00017 | 0.635 |
LIG_SH2_STAP1 | 75 | 79 | PF00017 | 0.242 |
LIG_SH2_STAP1 | 776 | 780 | PF00017 | 0.409 |
LIG_SH2_STAT3 | 649 | 652 | PF00017 | 0.292 |
LIG_SH2_STAT5 | 232 | 235 | PF00017 | 0.387 |
LIG_SH2_STAT5 | 264 | 267 | PF00017 | 0.363 |
LIG_SH2_STAT5 | 300 | 303 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 382 | 385 | PF00017 | 0.275 |
LIG_SH2_STAT5 | 419 | 422 | PF00017 | 0.232 |
LIG_SH2_STAT5 | 427 | 430 | PF00017 | 0.244 |
LIG_SH2_STAT5 | 460 | 463 | PF00017 | 0.336 |
LIG_SH2_STAT5 | 49 | 52 | PF00017 | 0.643 |
LIG_SH2_STAT5 | 552 | 555 | PF00017 | 0.600 |
LIG_SH2_STAT5 | 595 | 598 | PF00017 | 0.346 |
LIG_SH2_STAT5 | 626 | 629 | PF00017 | 0.320 |
LIG_SH2_STAT5 | 63 | 66 | PF00017 | 0.282 |
LIG_SH2_STAT5 | 697 | 700 | PF00017 | 0.291 |
LIG_SH2_STAT5 | 93 | 96 | PF00017 | 0.351 |
LIG_SH3_3 | 164 | 170 | PF00018 | 0.387 |
LIG_SH3_3 | 373 | 379 | PF00018 | 0.342 |
LIG_SH3_3 | 38 | 44 | PF00018 | 0.607 |
LIG_SH3_3 | 724 | 730 | PF00018 | 0.392 |
LIG_SH3_3 | 796 | 802 | PF00018 | 0.358 |
LIG_SH3_3 | 803 | 809 | PF00018 | 0.364 |
LIG_SUMO_SIM_par_1 | 619 | 625 | PF11976 | 0.248 |
LIG_SUMO_SIM_par_1 | 83 | 90 | PF11976 | 0.312 |
LIG_SxIP_EBH_1 | 198 | 211 | PF03271 | 0.348 |
LIG_TYR_ITIM | 420 | 425 | PF00017 | 0.202 |
LIG_TYR_ITSM | 228 | 235 | PF00017 | 0.329 |
LIG_WRC_WIRS_1 | 228 | 233 | PF05994 | 0.329 |
MOD_CDC14_SPxK_1 | 316 | 319 | PF00782 | 0.380 |
MOD_CDK_SPxK_1 | 313 | 319 | PF00069 | 0.288 |
MOD_CK1_1 | 237 | 243 | PF00069 | 0.363 |
MOD_CK1_1 | 481 | 487 | PF00069 | 0.186 |
MOD_CK1_1 | 597 | 603 | PF00069 | 0.352 |
MOD_CK1_1 | 604 | 610 | PF00069 | 0.341 |
MOD_CK1_1 | 792 | 798 | PF00069 | 0.341 |
MOD_CK1_1 | 87 | 93 | PF00069 | 0.292 |
MOD_CK2_1 | 37 | 43 | PF00069 | 0.592 |
MOD_CK2_1 | 404 | 410 | PF00069 | 0.256 |
MOD_CK2_1 | 542 | 548 | PF00069 | 0.628 |
MOD_CK2_1 | 852 | 858 | PF00069 | 0.412 |
MOD_Cter_Amidation | 571 | 574 | PF01082 | 0.365 |
MOD_Cter_Amidation | 838 | 841 | PF01082 | 0.587 |
MOD_GlcNHglycan | 110 | 113 | PF01048 | 0.532 |
MOD_GlcNHglycan | 115 | 118 | PF01048 | 0.569 |
MOD_GlcNHglycan | 194 | 197 | PF01048 | 0.322 |
MOD_GlcNHglycan | 478 | 481 | PF01048 | 0.227 |
MOD_GlcNHglycan | 483 | 486 | PF01048 | 0.233 |
MOD_GlcNHglycan | 521 | 524 | PF01048 | 0.543 |
MOD_GlcNHglycan | 580 | 583 | PF01048 | 0.331 |
MOD_GlcNHglycan | 761 | 764 | PF01048 | 0.623 |
MOD_GlcNHglycan | 791 | 794 | PF01048 | 0.575 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.355 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.282 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.529 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.726 |
MOD_GSK3_1 | 301 | 308 | PF00069 | 0.219 |
MOD_GSK3_1 | 313 | 320 | PF00069 | 0.306 |
MOD_GSK3_1 | 481 | 488 | PF00069 | 0.224 |
MOD_GSK3_1 | 574 | 581 | PF00069 | 0.492 |
MOD_GSK3_1 | 597 | 604 | PF00069 | 0.352 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.333 |
MOD_N-GLC_1 | 657 | 662 | PF02516 | 0.514 |
MOD_N-GLC_1 | 789 | 794 | PF02516 | 0.537 |
MOD_N-GLC_2 | 164 | 166 | PF02516 | 0.443 |
MOD_N-GLC_2 | 219 | 221 | PF02516 | 0.288 |
MOD_NEK2_1 | 142 | 147 | PF00069 | 0.345 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.303 |
MOD_NEK2_1 | 200 | 205 | PF00069 | 0.374 |
MOD_NEK2_1 | 209 | 214 | PF00069 | 0.367 |
MOD_NEK2_1 | 227 | 232 | PF00069 | 0.221 |
MOD_NEK2_1 | 395 | 400 | PF00069 | 0.285 |
MOD_NEK2_1 | 404 | 409 | PF00069 | 0.258 |
MOD_NEK2_1 | 452 | 457 | PF00069 | 0.336 |
MOD_NEK2_1 | 478 | 483 | PF00069 | 0.320 |
MOD_NEK2_1 | 578 | 583 | PF00069 | 0.334 |
MOD_NEK2_1 | 596 | 601 | PF00069 | 0.320 |
MOD_NEK2_1 | 611 | 616 | PF00069 | 0.277 |
MOD_NEK2_1 | 748 | 753 | PF00069 | 0.323 |
MOD_NEK2_1 | 850 | 855 | PF00069 | 0.403 |
MOD_NEK2_2 | 234 | 239 | PF00069 | 0.329 |
MOD_PIKK_1 | 29 | 35 | PF00454 | 0.792 |
MOD_PIKK_1 | 512 | 518 | PF00454 | 0.688 |
MOD_PIKK_1 | 533 | 539 | PF00454 | 0.618 |
MOD_PK_1 | 361 | 367 | PF00069 | 0.425 |
MOD_PK_1 | 84 | 90 | PF00069 | 0.322 |
MOD_PKA_1 | 550 | 556 | PF00069 | 0.604 |
MOD_PKA_2 | 240 | 246 | PF00069 | 0.323 |
MOD_PKA_2 | 284 | 290 | PF00069 | 0.538 |
MOD_PKA_2 | 33 | 39 | PF00069 | 0.599 |
MOD_PKA_2 | 540 | 546 | PF00069 | 0.768 |
MOD_PKA_2 | 550 | 556 | PF00069 | 0.669 |
MOD_PKA_2 | 658 | 664 | PF00069 | 0.318 |
MOD_PKA_2 | 748 | 754 | PF00069 | 0.371 |
MOD_PKB_1 | 359 | 367 | PF00069 | 0.512 |
MOD_Plk_1 | 657 | 663 | PF00069 | 0.314 |
MOD_Plk_4 | 123 | 129 | PF00069 | 0.288 |
MOD_Plk_4 | 227 | 233 | PF00069 | 0.329 |
MOD_Plk_4 | 276 | 282 | PF00069 | 0.431 |
MOD_Plk_4 | 288 | 294 | PF00069 | 0.431 |
MOD_Plk_4 | 45 | 51 | PF00069 | 0.708 |
MOD_Plk_4 | 478 | 484 | PF00069 | 0.325 |
MOD_Plk_4 | 551 | 557 | PF00069 | 0.715 |
MOD_Plk_4 | 574 | 580 | PF00069 | 0.431 |
MOD_Plk_4 | 583 | 589 | PF00069 | 0.278 |
MOD_Plk_4 | 617 | 623 | PF00069 | 0.319 |
MOD_Plk_4 | 642 | 648 | PF00069 | 0.259 |
MOD_Plk_4 | 686 | 692 | PF00069 | 0.368 |
MOD_Plk_4 | 717 | 723 | PF00069 | 0.325 |
MOD_Plk_4 | 748 | 754 | PF00069 | 0.363 |
MOD_Plk_4 | 767 | 773 | PF00069 | 0.451 |
MOD_Plk_4 | 809 | 815 | PF00069 | 0.374 |
MOD_ProDKin_1 | 17 | 23 | PF00069 | 0.625 |
MOD_ProDKin_1 | 313 | 319 | PF00069 | 0.288 |
MOD_ProDKin_1 | 37 | 43 | PF00069 | 0.628 |
MOD_ProDKin_1 | 375 | 381 | PF00069 | 0.188 |
MOD_ProDKin_1 | 439 | 445 | PF00069 | 0.230 |
MOD_ProDKin_1 | 509 | 515 | PF00069 | 0.572 |
MOD_ProDKin_1 | 604 | 610 | PF00069 | 0.263 |
MOD_ProDKin_1 | 634 | 640 | PF00069 | 0.330 |
MOD_ProDKin_1 | 679 | 685 | PF00069 | 0.318 |
MOD_ProDKin_1 | 708 | 714 | PF00069 | 0.335 |
MOD_SUMO_rev_2 | 559 | 566 | PF00179 | 0.532 |
TRG_DiLeu_BaEn_1 | 686 | 691 | PF01217 | 0.328 |
TRG_DiLeu_BaLyEn_6 | 464 | 469 | PF01217 | 0.295 |
TRG_ENDOCYTIC_2 | 139 | 142 | PF00928 | 0.428 |
TRG_ENDOCYTIC_2 | 173 | 176 | PF00928 | 0.188 |
TRG_ENDOCYTIC_2 | 232 | 235 | PF00928 | 0.329 |
TRG_ENDOCYTIC_2 | 254 | 257 | PF00928 | 0.329 |
TRG_ENDOCYTIC_2 | 264 | 267 | PF00928 | 0.329 |
TRG_ENDOCYTIC_2 | 296 | 299 | PF00928 | 0.329 |
TRG_ENDOCYTIC_2 | 422 | 425 | PF00928 | 0.276 |
TRG_ENDOCYTIC_2 | 446 | 449 | PF00928 | 0.465 |
TRG_ENDOCYTIC_2 | 454 | 457 | PF00928 | 0.273 |
TRG_ENDOCYTIC_2 | 552 | 555 | PF00928 | 0.733 |
TRG_ENDOCYTIC_2 | 58 | 61 | PF00928 | 0.595 |
TRG_ENDOCYTIC_2 | 630 | 633 | PF00928 | 0.311 |
TRG_ENDOCYTIC_2 | 65 | 68 | PF00928 | 0.292 |
TRG_ENDOCYTIC_2 | 697 | 700 | PF00928 | 0.291 |
TRG_ENDOCYTIC_2 | 722 | 725 | PF00928 | 0.340 |
TRG_ENDOCYTIC_2 | 780 | 783 | PF00928 | 0.293 |
TRG_ENDOCYTIC_2 | 91 | 94 | PF00928 | 0.302 |
TRG_ER_diArg_1 | 238 | 241 | PF00400 | 0.376 |
TRG_ER_diArg_1 | 342 | 345 | PF00400 | 0.505 |
TRG_ER_diArg_1 | 350 | 353 | PF00400 | 0.477 |
TRG_ER_diArg_1 | 358 | 361 | PF00400 | 0.418 |
TRG_ER_diArg_1 | 525 | 528 | PF00400 | 0.598 |
TRG_ER_diArg_1 | 550 | 552 | PF00400 | 0.663 |
TRG_NES_CRM1_1 | 322 | 337 | PF08389 | 0.380 |
TRG_Pf-PMV_PEXEL_1 | 319 | 323 | PF00026 | 0.404 |
TRG_Pf-PMV_PEXEL_1 | 84 | 89 | PF00026 | 0.406 |
TRG_Pf-PMV_PEXEL_1 | 854 | 858 | PF00026 | 0.589 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4IZ72 | Bodo saltans | 50% | 100% |
A0A1X0NFU7 | Trypanosomatidae | 55% | 100% |
A0A3Q8IHT0 | Leishmania donovani | 78% | 100% |
A0A3Q8II34 | Leishmania donovani | 54% | 100% |
A0A3Q8ILY7 | Leishmania donovani | 69% | 100% |
A0A3Q8IV37 | Leishmania donovani | 71% | 100% |
A0A422MX14 | Trypanosoma rangeli | 55% | 100% |
A4HMD5 | Leishmania braziliensis | 76% | 100% |
A4HMD6 | Leishmania braziliensis | 57% | 100% |
A4HMD7 | Leishmania braziliensis | 70% | 100% |
A4IB08 | Leishmania infantum | 79% | 100% |
A4IB09 | Leishmania infantum | 69% | 100% |
A4IB10 | Leishmania infantum | 55% | 100% |
C9ZNL1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 54% | 100% |
C9ZQ40 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 53% | 100% |
E2RG47 | Canis lupus familiaris | 30% | 100% |
E9AET6 | Leishmania major | 78% | 100% |
E9AET7 | Leishmania major | 69% | 98% |
E9AET8 | Leishmania major | 54% | 99% |
E9AET9 | Leishmania major | 65% | 100% |
E9AHU4 | Leishmania infantum | 71% | 100% |
E9B5Z2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 76% | 100% |
E9B5Z3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 69% | 100% |
E9B5Z4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 53% | 100% |
E9B5Z5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 69% | 100% |
F1PJP5 | Canis lupus familiaris | 30% | 100% |
O94335 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 32% | 100% |
P46975 | Caenorhabditis elegans | 30% | 100% |
P46977 | Homo sapiens | 31% | 100% |
P46978 | Mus musculus | 31% | 100% |
Q2KJI2 | Bos taurus | 31% | 100% |
Q3TDQ1 | Mus musculus | 30% | 100% |
Q5RCE2 | Pongo abelii | 31% | 100% |
Q6F2Z1 | Oryza sativa subsp. japonica | 30% | 100% |
Q7XQ88 | Oryza sativa subsp. japonica | 32% | 100% |
Q8TCJ2 | Homo sapiens | 30% | 100% |
Q93ZY3 | Arabidopsis thaliana | 31% | 100% |
Q9FX21 | Arabidopsis thaliana | 32% | 100% |
V5BDM6 | Trypanosoma cruzi | 54% | 100% |