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:0016020 | membrane | 2 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
GO:0005635 | nuclear envelope | 4 | 1 |
GO:0005783 | endoplasmic reticulum | 5 | 1 |
GO:0005789 | endoplasmic reticulum membrane | 4 | 1 |
GO:0031090 | organelle membrane | 3 | 1 |
GO:0031967 | organelle envelope | 3 | 1 |
GO:0031975 | envelope | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
Related structures:
AlphaFold database: E9B062
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:0008152 | metabolic process | 1 | 11 |
GO:0009058 | biosynthetic process | 2 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0044255 | cellular lipid metabolic process | 3 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 11 |
GO:1901137 | carbohydrate derivative biosynthetic process | 4 | 11 |
GO:1901576 | organic substance biosynthetic process | 3 | 11 |
GO:0006810 | transport | 3 | 1 |
GO:0006869 | lipid transport | 5 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0034203 | glycolipid translocation | 5 | 1 |
GO:0034204 | lipid translocation | 4 | 1 |
GO:0046836 | glycolipid transport | 6 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0061024 | membrane organization | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0065008 | regulation of biological quality | 2 | 1 |
GO:0071702 | organic substance transport | 4 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0097035 | regulation of membrane lipid distribution | 3 | 1 |
GO:1901264 | carbohydrate derivative transport | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 180 | 184 | PF00656 | 0.533 |
CLV_C14_Caspase3-7 | 372 | 376 | PF00656 | 0.567 |
CLV_NRD_NRD_1 | 173 | 175 | PF00675 | 0.671 |
CLV_NRD_NRD_1 | 381 | 383 | PF00675 | 0.386 |
CLV_NRD_NRD_1 | 704 | 706 | PF00675 | 0.641 |
CLV_NRD_NRD_1 | 718 | 720 | PF00675 | 0.667 |
CLV_PCSK_KEX2_1 | 381 | 383 | PF00082 | 0.386 |
CLV_PCSK_KEX2_1 | 703 | 705 | PF00082 | 0.610 |
CLV_PCSK_KEX2_1 | 718 | 720 | PF00082 | 0.656 |
CLV_PCSK_SKI1_1 | 24 | 28 | PF00082 | 0.355 |
CLV_PCSK_SKI1_1 | 276 | 280 | PF00082 | 0.529 |
CLV_PCSK_SKI1_1 | 36 | 40 | PF00082 | 0.396 |
CLV_PCSK_SKI1_1 | 360 | 364 | PF00082 | 0.359 |
CLV_PCSK_SKI1_1 | 382 | 386 | PF00082 | 0.250 |
CLV_PCSK_SKI1_1 | 397 | 401 | PF00082 | 0.304 |
CLV_PCSK_SKI1_1 | 432 | 436 | PF00082 | 0.282 |
CLV_PCSK_SKI1_1 | 463 | 467 | PF00082 | 0.386 |
CLV_PCSK_SKI1_1 | 485 | 489 | PF00082 | 0.528 |
CLV_PCSK_SKI1_1 | 495 | 499 | PF00082 | 0.490 |
CLV_PCSK_SKI1_1 | 61 | 65 | PF00082 | 0.393 |
CLV_PCSK_SKI1_1 | 643 | 647 | PF00082 | 0.313 |
CLV_PCSK_SKI1_1 | 686 | 690 | PF00082 | 0.623 |
CLV_PCSK_SKI1_1 | 698 | 702 | PF00082 | 0.653 |
DEG_APCC_DBOX_1 | 391 | 399 | PF00400 | 0.562 |
DEG_MDM2_SWIB_1 | 578 | 586 | PF02201 | 0.480 |
DEG_ODPH_VHL_1 | 4 | 17 | PF01847 | 0.453 |
DEG_SCF_FBW7_1 | 688 | 695 | PF00400 | 0.486 |
DOC_CKS1_1 | 496 | 501 | PF01111 | 0.362 |
DOC_CKS1_1 | 689 | 694 | PF01111 | 0.462 |
DOC_CYCLIN_RxL_1 | 429 | 439 | PF00134 | 0.562 |
DOC_CYCLIN_yCln2_LP_2 | 352 | 358 | PF00134 | 0.530 |
DOC_CYCLIN_yCln2_LP_2 | 627 | 633 | PF00134 | 0.473 |
DOC_MAPK_FxFP_2 | 364 | 367 | PF00069 | 0.562 |
DOC_MAPK_MEF2A_6 | 10 | 19 | PF00069 | 0.346 |
DOC_MAPK_MEF2A_6 | 126 | 133 | PF00069 | 0.562 |
DOC_MAPK_MEF2A_6 | 392 | 400 | PF00069 | 0.523 |
DOC_MAPK_MEF2A_6 | 463 | 470 | PF00069 | 0.543 |
DOC_MAPK_MEF2A_6 | 583 | 592 | PF00069 | 0.355 |
DOC_MAPK_NFAT4_5 | 10 | 18 | PF00069 | 0.362 |
DOC_MAPK_NFAT4_5 | 463 | 471 | PF00069 | 0.586 |
DOC_MAPK_RevD_3 | 688 | 704 | PF00069 | 0.363 |
DOC_PP1_RVXF_1 | 22 | 29 | PF00149 | 0.355 |
DOC_PP1_RVXF_1 | 430 | 436 | PF00149 | 0.482 |
DOC_PP1_RVXF_1 | 465 | 471 | PF00149 | 0.408 |
DOC_PP2B_LxvP_1 | 352 | 355 | PF13499 | 0.530 |
DOC_PP2B_LxvP_1 | 37 | 40 | PF13499 | 0.614 |
DOC_PP2B_LxvP_1 | 479 | 482 | PF13499 | 0.357 |
DOC_PP2B_LxvP_1 | 625 | 628 | PF13499 | 0.692 |
DOC_PP4_FxxP_1 | 193 | 196 | PF00568 | 0.264 |
DOC_PP4_FxxP_1 | 364 | 367 | PF00568 | 0.562 |
DOC_USP7_MATH_1 | 108 | 112 | PF00917 | 0.786 |
DOC_USP7_MATH_1 | 127 | 131 | PF00917 | 0.272 |
DOC_USP7_MATH_1 | 132 | 136 | PF00917 | 0.361 |
DOC_USP7_MATH_1 | 166 | 170 | PF00917 | 0.435 |
DOC_USP7_MATH_1 | 337 | 341 | PF00917 | 0.585 |
DOC_USP7_MATH_1 | 346 | 350 | PF00917 | 0.474 |
DOC_USP7_MATH_1 | 499 | 503 | PF00917 | 0.386 |
DOC_USP7_MATH_1 | 621 | 625 | PF00917 | 0.743 |
DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.762 |
DOC_WW_Pin1_4 | 112 | 117 | PF00397 | 0.591 |
DOC_WW_Pin1_4 | 257 | 262 | PF00397 | 0.330 |
DOC_WW_Pin1_4 | 495 | 500 | PF00397 | 0.313 |
DOC_WW_Pin1_4 | 527 | 532 | PF00397 | 0.562 |
DOC_WW_Pin1_4 | 591 | 596 | PF00397 | 0.571 |
DOC_WW_Pin1_4 | 626 | 631 | PF00397 | 0.698 |
DOC_WW_Pin1_4 | 688 | 693 | PF00397 | 0.459 |
DOC_WW_Pin1_4 | 719 | 724 | PF00397 | 0.446 |
DOC_WW_Pin1_4 | 94 | 99 | PF00397 | 0.754 |
LIG_14-3-3_CanoR_1 | 167 | 173 | PF00244 | 0.489 |
LIG_14-3-3_CanoR_1 | 190 | 194 | PF00244 | 0.381 |
LIG_14-3-3_CanoR_1 | 253 | 261 | PF00244 | 0.337 |
LIG_14-3-3_CanoR_1 | 360 | 365 | PF00244 | 0.539 |
LIG_14-3-3_CanoR_1 | 381 | 387 | PF00244 | 0.528 |
LIG_14-3-3_CanoR_1 | 397 | 406 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 455 | 462 | PF00244 | 0.524 |
LIG_14-3-3_CanoR_1 | 583 | 589 | PF00244 | 0.199 |
LIG_14-3-3_CanoR_1 | 660 | 665 | PF00244 | 0.454 |
LIG_Actin_WH2_2 | 384 | 399 | PF00022 | 0.534 |
LIG_APCC_ABBA_1 | 49 | 54 | PF00400 | 0.609 |
LIG_BRCT_BRCA1_1 | 472 | 476 | PF00533 | 0.405 |
LIG_eIF4E_1 | 52 | 58 | PF01652 | 0.522 |
LIG_FHA_1 | 200 | 206 | PF00498 | 0.479 |
LIG_FHA_1 | 25 | 31 | PF00498 | 0.339 |
LIG_FHA_1 | 287 | 293 | PF00498 | 0.385 |
LIG_FHA_1 | 33 | 39 | PF00498 | 0.369 |
LIG_FHA_1 | 46 | 52 | PF00498 | 0.493 |
LIG_FHA_1 | 496 | 502 | PF00498 | 0.349 |
LIG_FHA_1 | 62 | 68 | PF00498 | 0.597 |
LIG_FHA_1 | 712 | 718 | PF00498 | 0.381 |
LIG_FHA_2 | 269 | 275 | PF00498 | 0.343 |
LIG_FHA_2 | 309 | 315 | PF00498 | 0.530 |
LIG_FHA_2 | 76 | 82 | PF00498 | 0.577 |
LIG_GBD_Chelix_1 | 15 | 23 | PF00786 | 0.447 |
LIG_LIR_Apic_2 | 192 | 196 | PF02991 | 0.472 |
LIG_LIR_Apic_2 | 363 | 367 | PF02991 | 0.563 |
LIG_LIR_Apic_2 | 493 | 499 | PF02991 | 0.313 |
LIG_LIR_Gen_1 | 385 | 395 | PF02991 | 0.570 |
LIG_LIR_Gen_1 | 473 | 484 | PF02991 | 0.433 |
LIG_LIR_Gen_1 | 587 | 597 | PF02991 | 0.477 |
LIG_LIR_Gen_1 | 636 | 645 | PF02991 | 0.595 |
LIG_LIR_Gen_1 | 691 | 702 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 385 | 390 | PF02991 | 0.520 |
LIG_LIR_Nem_3 | 473 | 479 | PF02991 | 0.406 |
LIG_LIR_Nem_3 | 48 | 52 | PF02991 | 0.531 |
LIG_LIR_Nem_3 | 587 | 592 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 636 | 640 | PF02991 | 0.596 |
LIG_LIR_Nem_3 | 691 | 697 | PF02991 | 0.422 |
LIG_NRBOX | 33 | 39 | PF00104 | 0.449 |
LIG_PCNA_yPIPBox_3 | 518 | 526 | PF02747 | 0.408 |
LIG_Pex14_2 | 364 | 368 | PF04695 | 0.562 |
LIG_Pex14_2 | 470 | 474 | PF04695 | 0.447 |
LIG_Pex14_2 | 578 | 582 | PF04695 | 0.480 |
LIG_Pex14_2 | 637 | 641 | PF04695 | 0.583 |
LIG_PTAP_UEV_1 | 104 | 109 | PF05743 | 0.791 |
LIG_PTB_Apo_2 | 40 | 47 | PF02174 | 0.565 |
LIG_PTB_Phospho_1 | 40 | 46 | PF10480 | 0.566 |
LIG_SH2_CRK | 383 | 387 | PF00017 | 0.565 |
LIG_SH2_CRK | 420 | 424 | PF00017 | 0.482 |
LIG_SH2_CRK | 510 | 514 | PF00017 | 0.341 |
LIG_SH2_CRK | 674 | 678 | PF00017 | 0.332 |
LIG_SH2_GRB2like | 41 | 44 | PF00017 | 0.542 |
LIG_SH2_NCK_1 | 371 | 375 | PF00017 | 0.530 |
LIG_SH2_PTP2 | 294 | 297 | PF00017 | 0.188 |
LIG_SH2_PTP2 | 553 | 556 | PF00017 | 0.378 |
LIG_SH2_SRC | 41 | 44 | PF00017 | 0.588 |
LIG_SH2_STAP1 | 383 | 387 | PF00017 | 0.565 |
LIG_SH2_STAP1 | 492 | 496 | PF00017 | 0.356 |
LIG_SH2_STAP1 | 674 | 678 | PF00017 | 0.480 |
LIG_SH2_STAT3 | 249 | 252 | PF00017 | 0.362 |
LIG_SH2_STAT5 | 294 | 297 | PF00017 | 0.253 |
LIG_SH2_STAT5 | 46 | 49 | PF00017 | 0.505 |
LIG_SH2_STAT5 | 492 | 495 | PF00017 | 0.339 |
LIG_SH2_STAT5 | 508 | 511 | PF00017 | 0.224 |
LIG_SH2_STAT5 | 553 | 556 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 589 | 592 | PF00017 | 0.496 |
LIG_SH3_3 | 102 | 108 | PF00018 | 0.792 |
LIG_SH3_3 | 193 | 199 | PF00018 | 0.379 |
LIG_SH3_3 | 525 | 531 | PF00018 | 0.586 |
LIG_SH3_3 | 589 | 595 | PF00018 | 0.447 |
LIG_SH3_3 | 614 | 620 | PF00018 | 0.772 |
LIG_SH3_3 | 717 | 723 | PF00018 | 0.458 |
LIG_Sin3_3 | 318 | 325 | PF02671 | 0.586 |
LIG_SUMO_SIM_anti_2 | 567 | 573 | PF11976 | 0.364 |
LIG_SUMO_SIM_par_1 | 216 | 222 | PF11976 | 0.391 |
LIG_SUMO_SIM_par_1 | 227 | 233 | PF11976 | 0.517 |
LIG_SUMO_SIM_par_1 | 294 | 299 | PF11976 | 0.266 |
LIG_TYR_ITIM | 291 | 296 | PF00017 | 0.447 |
LIG_TYR_ITIM | 672 | 677 | PF00017 | 0.402 |
LIG_UBA3_1 | 17 | 24 | PF00899 | 0.402 |
LIG_WRC_WIRS_1 | 25 | 30 | PF05994 | 0.335 |
LIG_WRC_WIRS_1 | 387 | 392 | PF05994 | 0.480 |
LIG_WRC_WIRS_1 | 46 | 51 | PF05994 | 0.504 |
LIG_WRC_WIRS_1 | 471 | 476 | PF05994 | 0.484 |
MOD_CDK_SPK_2 | 719 | 724 | PF00069 | 0.459 |
MOD_CDK_SPxxK_3 | 94 | 101 | PF00069 | 0.708 |
MOD_CK1_1 | 106 | 112 | PF00069 | 0.739 |
MOD_CK1_1 | 29 | 35 | PF00069 | 0.447 |
MOD_CK1_1 | 410 | 416 | PF00069 | 0.415 |
MOD_CK1_1 | 425 | 431 | PF00069 | 0.264 |
MOD_CK1_1 | 663 | 669 | PF00069 | 0.405 |
MOD_CK1_1 | 722 | 728 | PF00069 | 0.513 |
MOD_CK2_1 | 268 | 274 | PF00069 | 0.421 |
MOD_CK2_1 | 308 | 314 | PF00069 | 0.448 |
MOD_CK2_1 | 398 | 404 | PF00069 | 0.355 |
MOD_CK2_1 | 561 | 567 | PF00069 | 0.439 |
MOD_CK2_1 | 75 | 81 | PF00069 | 0.518 |
MOD_CK2_1 | 94 | 100 | PF00069 | 0.707 |
MOD_DYRK1A_RPxSP_1 | 719 | 723 | PF00069 | 0.458 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.752 |
MOD_GlcNHglycan | 111 | 114 | PF01048 | 0.705 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.416 |
MOD_GlcNHglycan | 298 | 301 | PF01048 | 0.432 |
MOD_GlcNHglycan | 339 | 342 | PF01048 | 0.437 |
MOD_GlcNHglycan | 349 | 352 | PF01048 | 0.392 |
MOD_GlcNHglycan | 81 | 85 | PF01048 | 0.711 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.661 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.485 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.332 |
MOD_GSK3_1 | 328 | 335 | PF00069 | 0.466 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.425 |
MOD_GSK3_1 | 382 | 389 | PF00069 | 0.467 |
MOD_GSK3_1 | 398 | 405 | PF00069 | 0.422 |
MOD_GSK3_1 | 406 | 413 | PF00069 | 0.414 |
MOD_GSK3_1 | 421 | 428 | PF00069 | 0.285 |
MOD_GSK3_1 | 444 | 451 | PF00069 | 0.432 |
MOD_GSK3_1 | 470 | 477 | PF00069 | 0.453 |
MOD_GSK3_1 | 483 | 490 | PF00069 | 0.338 |
MOD_GSK3_1 | 491 | 498 | PF00069 | 0.354 |
MOD_GSK3_1 | 561 | 568 | PF00069 | 0.473 |
MOD_GSK3_1 | 688 | 695 | PF00069 | 0.597 |
MOD_N-GLC_2 | 440 | 442 | PF02516 | 0.378 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.480 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.554 |
MOD_NEK2_1 | 219 | 224 | PF00069 | 0.442 |
MOD_NEK2_1 | 26 | 31 | PF00069 | 0.343 |
MOD_NEK2_1 | 296 | 301 | PF00069 | 0.422 |
MOD_NEK2_1 | 307 | 312 | PF00069 | 0.403 |
MOD_NEK2_1 | 386 | 391 | PF00069 | 0.372 |
MOD_NEK2_1 | 406 | 411 | PF00069 | 0.150 |
MOD_NEK2_1 | 422 | 427 | PF00069 | 0.319 |
MOD_NEK2_1 | 470 | 475 | PF00069 | 0.362 |
MOD_NEK2_1 | 483 | 488 | PF00069 | 0.388 |
MOD_NEK2_1 | 491 | 496 | PF00069 | 0.338 |
MOD_NEK2_1 | 590 | 595 | PF00069 | 0.539 |
MOD_NEK2_1 | 653 | 658 | PF00069 | 0.421 |
MOD_NEK2_2 | 154 | 159 | PF00069 | 0.501 |
MOD_NEK2_2 | 584 | 589 | PF00069 | 0.447 |
MOD_PIKK_1 | 166 | 172 | PF00454 | 0.632 |
MOD_PIKK_1 | 561 | 567 | PF00454 | 0.402 |
MOD_PK_1 | 660 | 666 | PF00069 | 0.480 |
MOD_PKA_2 | 166 | 172 | PF00069 | 0.571 |
MOD_PKA_2 | 189 | 195 | PF00069 | 0.351 |
MOD_PKA_2 | 252 | 258 | PF00069 | 0.477 |
MOD_PKA_2 | 391 | 397 | PF00069 | 0.405 |
MOD_PKA_2 | 454 | 460 | PF00069 | 0.434 |
MOD_PKB_1 | 703 | 711 | PF00069 | 0.502 |
MOD_Plk_1 | 199 | 205 | PF00069 | 0.432 |
MOD_Plk_1 | 448 | 454 | PF00069 | 0.422 |
MOD_Plk_2-3 | 75 | 81 | PF00069 | 0.448 |
MOD_Plk_4 | 154 | 160 | PF00069 | 0.539 |
MOD_Plk_4 | 184 | 190 | PF00069 | 0.610 |
MOD_Plk_4 | 199 | 205 | PF00069 | 0.368 |
MOD_Plk_4 | 233 | 239 | PF00069 | 0.428 |
MOD_Plk_4 | 240 | 246 | PF00069 | 0.358 |
MOD_Plk_4 | 29 | 35 | PF00069 | 0.355 |
MOD_Plk_4 | 369 | 375 | PF00069 | 0.428 |
MOD_Plk_4 | 382 | 388 | PF00069 | 0.326 |
MOD_Plk_4 | 391 | 397 | PF00069 | 0.366 |
MOD_Plk_4 | 425 | 431 | PF00069 | 0.369 |
MOD_Plk_4 | 483 | 489 | PF00069 | 0.462 |
MOD_Plk_4 | 542 | 548 | PF00069 | 0.394 |
MOD_Plk_4 | 567 | 573 | PF00069 | 0.440 |
MOD_Plk_4 | 577 | 583 | PF00069 | 0.398 |
MOD_Plk_4 | 584 | 590 | PF00069 | 0.298 |
MOD_Plk_4 | 636 | 642 | PF00069 | 0.498 |
MOD_Plk_4 | 645 | 651 | PF00069 | 0.425 |
MOD_ProDKin_1 | 112 | 118 | PF00069 | 0.482 |
MOD_ProDKin_1 | 257 | 263 | PF00069 | 0.402 |
MOD_ProDKin_1 | 495 | 501 | PF00069 | 0.378 |
MOD_ProDKin_1 | 527 | 533 | PF00069 | 0.447 |
MOD_ProDKin_1 | 591 | 597 | PF00069 | 0.467 |
MOD_ProDKin_1 | 626 | 632 | PF00069 | 0.620 |
MOD_ProDKin_1 | 688 | 694 | PF00069 | 0.586 |
MOD_ProDKin_1 | 719 | 725 | PF00069 | 0.563 |
MOD_ProDKin_1 | 94 | 100 | PF00069 | 0.715 |
TRG_DiLeu_BaEn_1 | 233 | 238 | PF01217 | 0.355 |
TRG_DiLeu_BaEn_1 | 684 | 689 | PF01217 | 0.558 |
TRG_DiLeu_BaEn_2 | 438 | 444 | PF01217 | 0.378 |
TRG_DiLeu_BaLyEn_6 | 33 | 38 | PF01217 | 0.528 |
TRG_DiLeu_BaLyEn_6 | 429 | 434 | PF01217 | 0.408 |
TRG_DiLeu_BaLyEn_6 | 696 | 701 | PF01217 | 0.635 |
TRG_ENDOCYTIC_2 | 293 | 296 | PF00928 | 0.408 |
TRG_ENDOCYTIC_2 | 371 | 374 | PF00928 | 0.403 |
TRG_ENDOCYTIC_2 | 383 | 386 | PF00928 | 0.367 |
TRG_ENDOCYTIC_2 | 419 | 422 | PF00928 | 0.339 |
TRG_ENDOCYTIC_2 | 46 | 49 | PF00928 | 0.486 |
TRG_ENDOCYTIC_2 | 471 | 474 | PF00928 | 0.447 |
TRG_ENDOCYTIC_2 | 553 | 556 | PF00928 | 0.360 |
TRG_ENDOCYTIC_2 | 589 | 592 | PF00928 | 0.496 |
TRG_ENDOCYTIC_2 | 674 | 677 | PF00928 | 0.415 |
TRG_ER_diArg_1 | 381 | 383 | PF00400 | 0.402 |
TRG_ER_diArg_1 | 696 | 699 | PF00400 | 0.519 |
TRG_ER_diArg_1 | 702 | 705 | PF00400 | 0.591 |
TRG_ER_diArg_1 | 717 | 719 | PF00400 | 0.473 |
TRG_NES_CRM1_1 | 200 | 214 | PF08389 | 0.307 |
TRG_NES_CRM1_1 | 221 | 233 | PF08389 | 0.442 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IHL6 | Leptomonas seymouri | 59% | 100% |
A0A1X0NQN5 | Trypanosomatidae | 33% | 100% |
A0A3Q8IDZ2 | Leishmania donovani | 91% | 100% |
A0A3S5IQL5 | Trypanosoma rangeli | 33% | 100% |
A4HGU4 | Leishmania braziliensis | 77% | 100% |
A4I3X2 | Leishmania infantum | 91% | 100% |
D0A939 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
Q4Q823 | Leishmania major | 92% | 100% |
V5AWN8 | Trypanosoma cruzi | 32% | 100% |