Highly conserved Eukaryotic protein. Involved in N-linked oligosaccharide assembly.. Localization: ER (by homology)
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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005635 | nuclear envelope | 4 | 2 |
GO:0005783 | endoplasmic reticulum | 5 | 2 |
GO:0005789 | endoplasmic reticulum membrane | 4 | 2 |
GO:0016020 | membrane | 2 | 11 |
GO:0031090 | organelle membrane | 3 | 2 |
GO:0031967 | organelle envelope | 3 | 2 |
GO:0031975 | envelope | 2 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
Related structures:
AlphaFold database: Q4Q823
Term | Name | Level | Count |
---|---|---|---|
GO:0006488 | dolichol-linked oligosaccharide biosynthetic process | 5 | 11 |
GO:0006490 | oligosaccharide-lipid intermediate biosynthetic process | 4 | 11 |
GO:0006629 | lipid metabolic process | 3 | 11 |
GO:0006810 | transport | 3 | 2 |
GO:0006869 | lipid transport | 5 | 2 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009058 | biosynthetic process | 2 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0034203 | glycolipid translocation | 5 | 2 |
GO:0034204 | lipid translocation | 4 | 2 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0044255 | cellular lipid metabolic process | 3 | 11 |
GO:0046836 | glycolipid transport | 6 | 2 |
GO:0051179 | localization | 1 | 2 |
GO:0051234 | establishment of localization | 2 | 2 |
GO:0061024 | membrane organization | 4 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0065008 | regulation of biological quality | 2 | 2 |
GO:0071702 | organic substance transport | 4 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
GO:0097035 | regulation of membrane lipid distribution | 3 | 2 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 11 |
GO:1901137 | carbohydrate derivative biosynthetic process | 4 | 11 |
GO:1901264 | carbohydrate derivative transport | 5 | 2 |
GO:1901576 | organic substance biosynthetic process | 3 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 180 | 184 | PF00656 | 0.535 |
CLV_C14_Caspase3-7 | 341 | 345 | PF00656 | 0.502 |
CLV_C14_Caspase3-7 | 373 | 377 | PF00656 | 0.567 |
CLV_NRD_NRD_1 | 173 | 175 | PF00675 | 0.674 |
CLV_NRD_NRD_1 | 382 | 384 | PF00675 | 0.386 |
CLV_PCSK_KEX2_1 | 382 | 384 | PF00082 | 0.397 |
CLV_PCSK_SKI1_1 | 24 | 28 | PF00082 | 0.355 |
CLV_PCSK_SKI1_1 | 277 | 281 | PF00082 | 0.553 |
CLV_PCSK_SKI1_1 | 36 | 40 | PF00082 | 0.325 |
CLV_PCSK_SKI1_1 | 361 | 365 | PF00082 | 0.359 |
CLV_PCSK_SKI1_1 | 398 | 402 | PF00082 | 0.289 |
CLV_PCSK_SKI1_1 | 433 | 437 | PF00082 | 0.282 |
CLV_PCSK_SKI1_1 | 464 | 468 | PF00082 | 0.386 |
CLV_PCSK_SKI1_1 | 486 | 490 | PF00082 | 0.528 |
CLV_PCSK_SKI1_1 | 496 | 500 | PF00082 | 0.490 |
CLV_PCSK_SKI1_1 | 61 | 65 | PF00082 | 0.392 |
CLV_PCSK_SKI1_1 | 644 | 648 | PF00082 | 0.311 |
CLV_PCSK_SKI1_1 | 687 | 691 | PF00082 | 0.619 |
CLV_PCSK_SKI1_1 | 699 | 703 | PF00082 | 0.653 |
DEG_APCC_DBOX_1 | 392 | 400 | PF00400 | 0.562 |
DEG_MDM2_SWIB_1 | 579 | 587 | PF02201 | 0.480 |
DEG_ODPH_VHL_1 | 4 | 17 | PF01847 | 0.455 |
DEG_SCF_FBW7_1 | 689 | 696 | PF00400 | 0.484 |
DEG_SPOP_SBC_1 | 605 | 609 | PF00917 | 0.586 |
DOC_CDC14_PxL_1 | 188 | 196 | PF14671 | 0.442 |
DOC_CKS1_1 | 497 | 502 | PF01111 | 0.362 |
DOC_CKS1_1 | 690 | 695 | PF01111 | 0.462 |
DOC_CYCLIN_RxL_1 | 430 | 440 | PF00134 | 0.562 |
DOC_CYCLIN_yCln2_LP_2 | 194 | 200 | PF00134 | 0.369 |
DOC_CYCLIN_yCln2_LP_2 | 353 | 359 | PF00134 | 0.530 |
DOC_MAPK_FxFP_2 | 365 | 368 | PF00069 | 0.562 |
DOC_MAPK_gen_1 | 658 | 668 | PF00069 | 0.585 |
DOC_MAPK_MEF2A_6 | 10 | 19 | PF00069 | 0.354 |
DOC_MAPK_MEF2A_6 | 126 | 133 | PF00069 | 0.562 |
DOC_MAPK_MEF2A_6 | 393 | 401 | PF00069 | 0.513 |
DOC_MAPK_MEF2A_6 | 464 | 471 | PF00069 | 0.543 |
DOC_MAPK_MEF2A_6 | 584 | 593 | PF00069 | 0.355 |
DOC_MAPK_NFAT4_5 | 10 | 18 | PF00069 | 0.362 |
DOC_MAPK_NFAT4_5 | 464 | 472 | PF00069 | 0.586 |
DOC_PP1_RVXF_1 | 22 | 29 | PF00149 | 0.346 |
DOC_PP1_RVXF_1 | 431 | 437 | PF00149 | 0.482 |
DOC_PP1_RVXF_1 | 466 | 472 | PF00149 | 0.408 |
DOC_PP2B_LxvP_1 | 194 | 197 | PF13499 | 0.443 |
DOC_PP2B_LxvP_1 | 353 | 356 | PF13499 | 0.530 |
DOC_PP2B_LxvP_1 | 37 | 40 | PF13499 | 0.609 |
DOC_PP2B_LxvP_1 | 480 | 483 | PF13499 | 0.357 |
DOC_PP2B_LxvP_1 | 626 | 629 | PF13499 | 0.687 |
DOC_PP2B_LxvP_1 | 703 | 706 | PF13499 | 0.360 |
DOC_PP4_FxxP_1 | 365 | 368 | PF00568 | 0.562 |
DOC_USP7_MATH_1 | 108 | 112 | PF00917 | 0.803 |
DOC_USP7_MATH_1 | 127 | 131 | PF00917 | 0.396 |
DOC_USP7_MATH_1 | 132 | 136 | PF00917 | 0.361 |
DOC_USP7_MATH_1 | 166 | 170 | PF00917 | 0.461 |
DOC_USP7_MATH_1 | 338 | 342 | PF00917 | 0.585 |
DOC_USP7_MATH_1 | 347 | 351 | PF00917 | 0.474 |
DOC_USP7_MATH_1 | 500 | 504 | PF00917 | 0.386 |
DOC_USP7_MATH_1 | 606 | 610 | PF00917 | 0.746 |
DOC_USP7_MATH_1 | 622 | 626 | PF00917 | 0.747 |
DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.753 |
DOC_WW_Pin1_4 | 112 | 117 | PF00397 | 0.740 |
DOC_WW_Pin1_4 | 258 | 263 | PF00397 | 0.391 |
DOC_WW_Pin1_4 | 496 | 501 | PF00397 | 0.313 |
DOC_WW_Pin1_4 | 528 | 533 | PF00397 | 0.562 |
DOC_WW_Pin1_4 | 592 | 597 | PF00397 | 0.569 |
DOC_WW_Pin1_4 | 627 | 632 | PF00397 | 0.692 |
DOC_WW_Pin1_4 | 689 | 694 | PF00397 | 0.457 |
DOC_WW_Pin1_4 | 94 | 99 | PF00397 | 0.797 |
LIG_14-3-3_CanoR_1 | 114 | 120 | PF00244 | 0.716 |
LIG_14-3-3_CanoR_1 | 167 | 173 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 254 | 262 | PF00244 | 0.337 |
LIG_14-3-3_CanoR_1 | 361 | 366 | PF00244 | 0.539 |
LIG_14-3-3_CanoR_1 | 398 | 407 | PF00244 | 0.511 |
LIG_14-3-3_CanoR_1 | 456 | 463 | PF00244 | 0.524 |
LIG_Actin_WH2_2 | 385 | 400 | PF00022 | 0.534 |
LIG_APCC_ABBA_1 | 49 | 54 | PF00400 | 0.609 |
LIG_BRCT_BRCA1_1 | 129 | 133 | PF00533 | 0.363 |
LIG_BRCT_BRCA1_1 | 473 | 477 | PF00533 | 0.405 |
LIG_eIF4E_1 | 52 | 58 | PF01652 | 0.522 |
LIG_FHA_1 | 201 | 207 | PF00498 | 0.479 |
LIG_FHA_1 | 25 | 31 | PF00498 | 0.330 |
LIG_FHA_1 | 288 | 294 | PF00498 | 0.415 |
LIG_FHA_1 | 33 | 39 | PF00498 | 0.360 |
LIG_FHA_1 | 46 | 52 | PF00498 | 0.478 |
LIG_FHA_1 | 497 | 503 | PF00498 | 0.349 |
LIG_FHA_1 | 62 | 68 | PF00498 | 0.572 |
LIG_FHA_2 | 270 | 276 | PF00498 | 0.356 |
LIG_FHA_2 | 310 | 316 | PF00498 | 0.530 |
LIG_GBD_Chelix_1 | 15 | 23 | PF00786 | 0.447 |
LIG_LIR_Apic_2 | 364 | 368 | PF02991 | 0.563 |
LIG_LIR_Apic_2 | 494 | 500 | PF02991 | 0.313 |
LIG_LIR_Gen_1 | 130 | 141 | PF02991 | 0.363 |
LIG_LIR_Gen_1 | 474 | 485 | PF02991 | 0.433 |
LIG_LIR_Gen_1 | 588 | 598 | PF02991 | 0.475 |
LIG_LIR_Gen_1 | 637 | 646 | PF02991 | 0.591 |
LIG_LIR_Gen_1 | 692 | 703 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 130 | 136 | PF02991 | 0.363 |
LIG_LIR_Nem_3 | 474 | 480 | PF02991 | 0.406 |
LIG_LIR_Nem_3 | 48 | 52 | PF02991 | 0.531 |
LIG_LIR_Nem_3 | 588 | 593 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 637 | 641 | PF02991 | 0.591 |
LIG_MYND_1 | 624 | 628 | PF01753 | 0.703 |
LIG_NRBOX | 33 | 39 | PF00104 | 0.412 |
LIG_PCNA_yPIPBox_3 | 519 | 527 | PF02747 | 0.408 |
LIG_PDZ_Class_1 | 707 | 712 | PF00595 | 0.391 |
LIG_Pex14_2 | 365 | 369 | PF04695 | 0.562 |
LIG_Pex14_2 | 471 | 475 | PF04695 | 0.447 |
LIG_Pex14_2 | 579 | 583 | PF04695 | 0.480 |
LIG_Pex14_2 | 638 | 642 | PF04695 | 0.579 |
LIG_PTAP_UEV_1 | 104 | 109 | PF05743 | 0.798 |
LIG_PTB_Apo_2 | 40 | 47 | PF02174 | 0.564 |
LIG_PTB_Phospho_1 | 40 | 46 | PF10480 | 0.564 |
LIG_SH2_CRK | 295 | 299 | PF00017 | 0.441 |
LIG_SH2_CRK | 384 | 388 | PF00017 | 0.571 |
LIG_SH2_CRK | 421 | 425 | PF00017 | 0.482 |
LIG_SH2_CRK | 511 | 515 | PF00017 | 0.341 |
LIG_SH2_CRK | 675 | 679 | PF00017 | 0.332 |
LIG_SH2_GRB2like | 41 | 44 | PF00017 | 0.541 |
LIG_SH2_NCK_1 | 372 | 376 | PF00017 | 0.530 |
LIG_SH2_PTP2 | 554 | 557 | PF00017 | 0.378 |
LIG_SH2_SRC | 41 | 44 | PF00017 | 0.586 |
LIG_SH2_STAP1 | 295 | 299 | PF00017 | 0.441 |
LIG_SH2_STAP1 | 384 | 388 | PF00017 | 0.534 |
LIG_SH2_STAP1 | 493 | 497 | PF00017 | 0.356 |
LIG_SH2_STAP1 | 675 | 679 | PF00017 | 0.480 |
LIG_SH2_STAT3 | 250 | 253 | PF00017 | 0.362 |
LIG_SH2_STAT5 | 46 | 49 | PF00017 | 0.520 |
LIG_SH2_STAT5 | 472 | 475 | PF00017 | 0.324 |
LIG_SH2_STAT5 | 493 | 496 | PF00017 | 0.339 |
LIG_SH2_STAT5 | 509 | 512 | PF00017 | 0.224 |
LIG_SH2_STAT5 | 549 | 552 | PF00017 | 0.342 |
LIG_SH2_STAT5 | 554 | 557 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 590 | 593 | PF00017 | 0.495 |
LIG_SH3_3 | 102 | 108 | PF00018 | 0.787 |
LIG_SH3_3 | 194 | 200 | PF00018 | 0.400 |
LIG_SH3_3 | 526 | 532 | PF00018 | 0.586 |
LIG_SH3_3 | 590 | 596 | PF00018 | 0.445 |
LIG_SH3_3 | 615 | 621 | PF00018 | 0.772 |
LIG_SH3_3 | 625 | 631 | PF00018 | 0.602 |
LIG_Sin3_3 | 319 | 326 | PF02671 | 0.586 |
LIG_SUMO_SIM_anti_2 | 568 | 574 | PF11976 | 0.364 |
LIG_SUMO_SIM_par_1 | 217 | 223 | PF11976 | 0.391 |
LIG_SUMO_SIM_par_1 | 228 | 234 | PF11976 | 0.513 |
LIG_SUMO_SIM_par_1 | 664 | 669 | PF11976 | 0.246 |
LIG_TRFH_1 | 193 | 197 | PF08558 | 0.493 |
LIG_TYR_ITIM | 292 | 297 | PF00017 | 0.447 |
LIG_TYR_ITIM | 673 | 678 | PF00017 | 0.402 |
LIG_UBA3_1 | 17 | 24 | PF00899 | 0.402 |
LIG_Vh1_VBS_1 | 138 | 156 | PF01044 | 0.440 |
LIG_WRC_WIRS_1 | 155 | 160 | PF05994 | 0.495 |
LIG_WRC_WIRS_1 | 25 | 30 | PF05994 | 0.354 |
LIG_WRC_WIRS_1 | 388 | 393 | PF05994 | 0.480 |
LIG_WRC_WIRS_1 | 46 | 51 | PF05994 | 0.504 |
LIG_WRC_WIRS_1 | 472 | 477 | PF05994 | 0.484 |
MOD_CDK_SPxxK_3 | 94 | 101 | PF00069 | 0.774 |
MOD_CK1_1 | 106 | 112 | PF00069 | 0.727 |
MOD_CK1_1 | 186 | 192 | PF00069 | 0.594 |
MOD_CK1_1 | 29 | 35 | PF00069 | 0.447 |
MOD_CK1_1 | 411 | 417 | PF00069 | 0.415 |
MOD_CK1_1 | 426 | 432 | PF00069 | 0.264 |
MOD_CK1_1 | 664 | 670 | PF00069 | 0.405 |
MOD_CK2_1 | 269 | 275 | PF00069 | 0.440 |
MOD_CK2_1 | 309 | 315 | PF00069 | 0.448 |
MOD_CK2_1 | 399 | 405 | PF00069 | 0.355 |
MOD_CK2_1 | 562 | 568 | PF00069 | 0.439 |
MOD_CK2_1 | 94 | 100 | PF00069 | 0.768 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.762 |
MOD_GlcNHglycan | 111 | 114 | PF01048 | 0.720 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.600 |
MOD_GlcNHglycan | 255 | 258 | PF01048 | 0.416 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.447 |
MOD_GlcNHglycan | 340 | 343 | PF01048 | 0.427 |
MOD_GlcNHglycan | 350 | 353 | PF01048 | 0.353 |
MOD_GlcNHglycan | 608 | 611 | PF01048 | 0.713 |
MOD_GlcNHglycan | 75 | 79 | PF01048 | 0.626 |
MOD_GlcNHglycan | 81 | 85 | PF01048 | 0.697 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.772 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.495 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.335 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.446 |
MOD_GSK3_1 | 329 | 336 | PF00069 | 0.460 |
MOD_GSK3_1 | 370 | 377 | PF00069 | 0.425 |
MOD_GSK3_1 | 399 | 406 | PF00069 | 0.447 |
MOD_GSK3_1 | 407 | 414 | PF00069 | 0.414 |
MOD_GSK3_1 | 422 | 429 | PF00069 | 0.285 |
MOD_GSK3_1 | 445 | 452 | PF00069 | 0.432 |
MOD_GSK3_1 | 471 | 478 | PF00069 | 0.453 |
MOD_GSK3_1 | 484 | 491 | PF00069 | 0.338 |
MOD_GSK3_1 | 492 | 499 | PF00069 | 0.354 |
MOD_GSK3_1 | 562 | 569 | PF00069 | 0.473 |
MOD_GSK3_1 | 601 | 608 | PF00069 | 0.677 |
MOD_GSK3_1 | 689 | 696 | PF00069 | 0.594 |
MOD_N-GLC_1 | 177 | 182 | PF02516 | 0.602 |
MOD_N-GLC_2 | 441 | 443 | PF02516 | 0.378 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.408 |
MOD_NEK2_1 | 220 | 225 | PF00069 | 0.490 |
MOD_NEK2_1 | 26 | 31 | PF00069 | 0.250 |
MOD_NEK2_1 | 297 | 302 | PF00069 | 0.413 |
MOD_NEK2_1 | 308 | 313 | PF00069 | 0.391 |
MOD_NEK2_1 | 387 | 392 | PF00069 | 0.360 |
MOD_NEK2_1 | 407 | 412 | PF00069 | 0.150 |
MOD_NEK2_1 | 423 | 428 | PF00069 | 0.319 |
MOD_NEK2_1 | 471 | 476 | PF00069 | 0.362 |
MOD_NEK2_1 | 484 | 489 | PF00069 | 0.388 |
MOD_NEK2_1 | 492 | 497 | PF00069 | 0.338 |
MOD_NEK2_1 | 591 | 596 | PF00069 | 0.537 |
MOD_NEK2_1 | 654 | 659 | PF00069 | 0.424 |
MOD_NEK2_1 | 707 | 712 | PF00069 | 0.686 |
MOD_NEK2_2 | 585 | 590 | PF00069 | 0.447 |
MOD_PIKK_1 | 166 | 172 | PF00454 | 0.635 |
MOD_PIKK_1 | 562 | 568 | PF00454 | 0.402 |
MOD_PK_1 | 661 | 667 | PF00069 | 0.480 |
MOD_PKA_2 | 166 | 172 | PF00069 | 0.574 |
MOD_PKA_2 | 253 | 259 | PF00069 | 0.477 |
MOD_PKA_2 | 329 | 335 | PF00069 | 0.246 |
MOD_PKA_2 | 392 | 398 | PF00069 | 0.378 |
MOD_PKA_2 | 455 | 461 | PF00069 | 0.434 |
MOD_PKB_1 | 101 | 109 | PF00069 | 0.673 |
MOD_Plk_1 | 200 | 206 | PF00069 | 0.428 |
MOD_Plk_1 | 449 | 455 | PF00069 | 0.422 |
MOD_Plk_1 | 661 | 667 | PF00069 | 0.246 |
MOD_Plk_4 | 115 | 121 | PF00069 | 0.596 |
MOD_Plk_4 | 154 | 160 | PF00069 | 0.550 |
MOD_Plk_4 | 200 | 206 | PF00069 | 0.368 |
MOD_Plk_4 | 234 | 240 | PF00069 | 0.428 |
MOD_Plk_4 | 241 | 247 | PF00069 | 0.358 |
MOD_Plk_4 | 29 | 35 | PF00069 | 0.355 |
MOD_Plk_4 | 293 | 299 | PF00069 | 0.417 |
MOD_Plk_4 | 370 | 376 | PF00069 | 0.435 |
MOD_Plk_4 | 387 | 393 | PF00069 | 0.390 |
MOD_Plk_4 | 426 | 432 | PF00069 | 0.369 |
MOD_Plk_4 | 484 | 490 | PF00069 | 0.462 |
MOD_Plk_4 | 543 | 549 | PF00069 | 0.394 |
MOD_Plk_4 | 553 | 559 | PF00069 | 0.426 |
MOD_Plk_4 | 568 | 574 | PF00069 | 0.440 |
MOD_Plk_4 | 578 | 584 | PF00069 | 0.398 |
MOD_Plk_4 | 585 | 591 | PF00069 | 0.298 |
MOD_Plk_4 | 637 | 643 | PF00069 | 0.490 |
MOD_Plk_4 | 646 | 652 | PF00069 | 0.424 |
MOD_Plk_4 | 661 | 667 | PF00069 | 0.395 |
MOD_ProDKin_1 | 112 | 118 | PF00069 | 0.681 |
MOD_ProDKin_1 | 258 | 264 | PF00069 | 0.488 |
MOD_ProDKin_1 | 496 | 502 | PF00069 | 0.378 |
MOD_ProDKin_1 | 528 | 534 | PF00069 | 0.447 |
MOD_ProDKin_1 | 592 | 598 | PF00069 | 0.463 |
MOD_ProDKin_1 | 627 | 633 | PF00069 | 0.613 |
MOD_ProDKin_1 | 689 | 695 | PF00069 | 0.584 |
MOD_ProDKin_1 | 94 | 100 | PF00069 | 0.774 |
MOD_SUMO_rev_2 | 341 | 348 | PF00179 | 0.363 |
TRG_DiLeu_BaEn_1 | 234 | 239 | PF01217 | 0.355 |
TRG_DiLeu_BaEn_1 | 685 | 690 | PF01217 | 0.550 |
TRG_DiLeu_BaEn_2 | 439 | 445 | PF01217 | 0.378 |
TRG_DiLeu_BaLyEn_6 | 33 | 38 | PF01217 | 0.526 |
TRG_DiLeu_BaLyEn_6 | 430 | 435 | PF01217 | 0.408 |
TRG_DiLeu_BaLyEn_6 | 697 | 702 | PF01217 | 0.641 |
TRG_ENDOCYTIC_2 | 294 | 297 | PF00928 | 0.447 |
TRG_ENDOCYTIC_2 | 372 | 375 | PF00928 | 0.403 |
TRG_ENDOCYTIC_2 | 384 | 387 | PF00928 | 0.356 |
TRG_ENDOCYTIC_2 | 420 | 423 | PF00928 | 0.339 |
TRG_ENDOCYTIC_2 | 46 | 49 | PF00928 | 0.486 |
TRG_ENDOCYTIC_2 | 472 | 475 | PF00928 | 0.447 |
TRG_ENDOCYTIC_2 | 554 | 557 | PF00928 | 0.360 |
TRG_ENDOCYTIC_2 | 590 | 593 | PF00928 | 0.495 |
TRG_ENDOCYTIC_2 | 675 | 678 | PF00928 | 0.415 |
TRG_ER_diArg_1 | 382 | 384 | PF00400 | 0.402 |
TRG_ER_diArg_1 | 697 | 700 | PF00400 | 0.525 |
TRG_NES_CRM1_1 | 201 | 215 | PF08389 | 0.307 |
TRG_NES_CRM1_1 | 222 | 234 | PF08389 | 0.447 |
TRG_Pf-PMV_PEXEL_1 | 658 | 662 | PF00026 | 0.376 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IHL6 | Leptomonas seymouri | 60% | 99% |
A0A1X0NQN5 | Trypanosomatidae | 34% | 100% |
A0A3Q8IDZ2 | Leishmania donovani | 96% | 98% |
A0A3S5IQL5 | Trypanosoma rangeli | 33% | 100% |
A4HGU4 | Leishmania braziliensis | 79% | 98% |
A4I3X2 | Leishmania infantum | 95% | 98% |
D0A939 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
E9B062 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 98% |
V5AWN8 | Trypanosoma cruzi | 34% | 100% |