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: A4HGU4
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 | 0.417 |
CLV_C14_Caspase3-7 | 373 | 377 | PF00656 | 0.539 |
CLV_NRD_NRD_1 | 382 | 384 | PF00675 | 0.282 |
CLV_NRD_NRD_1 | 687 | 689 | PF00675 | 0.510 |
CLV_PCSK_KEX2_1 | 382 | 384 | PF00082 | 0.282 |
CLV_PCSK_KEX2_1 | 644 | 646 | PF00082 | 0.331 |
CLV_PCSK_KEX2_1 | 687 | 689 | PF00082 | 0.491 |
CLV_PCSK_PC1ET2_1 | 644 | 646 | PF00082 | 0.251 |
CLV_PCSK_SKI1_1 | 24 | 28 | PF00082 | 0.289 |
CLV_PCSK_SKI1_1 | 36 | 40 | PF00082 | 0.285 |
CLV_PCSK_SKI1_1 | 398 | 402 | PF00082 | 0.257 |
CLV_PCSK_SKI1_1 | 433 | 437 | PF00082 | 0.236 |
CLV_PCSK_SKI1_1 | 464 | 468 | PF00082 | 0.282 |
CLV_PCSK_SKI1_1 | 487 | 491 | PF00082 | 0.511 |
CLV_PCSK_SKI1_1 | 496 | 500 | PF00082 | 0.490 |
CLV_PCSK_SKI1_1 | 61 | 65 | PF00082 | 0.363 |
CLV_PCSK_SKI1_1 | 687 | 691 | PF00082 | 0.574 |
CLV_PCSK_SKI1_1 | 699 | 703 | PF00082 | 0.602 |
DEG_APCC_DBOX_1 | 392 | 400 | PF00400 | 0.531 |
DEG_APCC_DBOX_1 | 696 | 704 | PF00400 | 0.394 |
DEG_MDM2_SWIB_1 | 579 | 587 | PF02201 | 0.335 |
DEG_SCF_FBW7_1 | 352 | 359 | PF00400 | 0.381 |
DEG_SCF_FBW7_1 | 689 | 696 | PF00400 | 0.373 |
DOC_CKS1_1 | 353 | 358 | PF01111 | 0.382 |
DOC_CKS1_1 | 497 | 502 | PF01111 | 0.331 |
DOC_CKS1_1 | 690 | 695 | PF01111 | 0.423 |
DOC_CYCLIN_RxL_1 | 430 | 440 | PF00134 | 0.531 |
DOC_MAPK_FxFP_2 | 365 | 368 | PF00069 | 0.531 |
DOC_MAPK_gen_1 | 658 | 668 | PF00069 | 0.572 |
DOC_MAPK_MEF2A_6 | 10 | 19 | PF00069 | 0.331 |
DOC_MAPK_MEF2A_6 | 126 | 133 | PF00069 | 0.531 |
DOC_MAPK_MEF2A_6 | 393 | 401 | PF00069 | 0.478 |
DOC_MAPK_MEF2A_6 | 464 | 471 | PF00069 | 0.504 |
DOC_MAPK_MEF2A_6 | 584 | 593 | PF00069 | 0.289 |
DOC_MAPK_NFAT4_5 | 10 | 18 | PF00069 | 0.331 |
DOC_MAPK_NFAT4_5 | 464 | 472 | PF00069 | 0.482 |
DOC_MAPK_RevD_3 | 631 | 645 | PF00069 | 0.478 |
DOC_PP1_RVXF_1 | 22 | 29 | PF00149 | 0.289 |
DOC_PP1_RVXF_1 | 431 | 437 | PF00149 | 0.436 |
DOC_PP1_RVXF_1 | 466 | 472 | PF00149 | 0.349 |
DOC_PP2B_LxvP_1 | 37 | 40 | PF13499 | 0.513 |
DOC_PP2B_LxvP_1 | 480 | 483 | PF13499 | 0.291 |
DOC_PP4_FxxP_1 | 365 | 368 | PF00568 | 0.531 |
DOC_USP7_MATH_1 | 132 | 136 | PF00917 | 0.295 |
DOC_USP7_MATH_1 | 166 | 170 | PF00917 | 0.416 |
DOC_USP7_MATH_1 | 336 | 340 | PF00917 | 0.590 |
DOC_USP7_MATH_1 | 354 | 358 | PF00917 | 0.373 |
DOC_USP7_MATH_1 | 500 | 504 | PF00917 | 0.282 |
DOC_USP7_MATH_1 | 622 | 626 | PF00917 | 0.715 |
DOC_USP7_MATH_1 | 63 | 67 | PF00917 | 0.510 |
DOC_USP7_MATH_1 | 714 | 718 | PF00917 | 0.436 |
DOC_WW_Pin1_4 | 112 | 117 | PF00397 | 0.582 |
DOC_WW_Pin1_4 | 308 | 313 | PF00397 | 0.532 |
DOC_WW_Pin1_4 | 352 | 357 | PF00397 | 0.480 |
DOC_WW_Pin1_4 | 496 | 501 | PF00397 | 0.267 |
DOC_WW_Pin1_4 | 528 | 533 | PF00397 | 0.556 |
DOC_WW_Pin1_4 | 592 | 597 | PF00397 | 0.528 |
DOC_WW_Pin1_4 | 624 | 629 | PF00397 | 0.693 |
DOC_WW_Pin1_4 | 689 | 694 | PF00397 | 0.419 |
LIG_14-3-3_CanoR_1 | 114 | 120 | PF00244 | 0.600 |
LIG_14-3-3_CanoR_1 | 167 | 174 | PF00244 | 0.468 |
LIG_14-3-3_CanoR_1 | 260 | 266 | PF00244 | 0.394 |
LIG_14-3-3_CanoR_1 | 361 | 366 | PF00244 | 0.499 |
LIG_14-3-3_CanoR_1 | 398 | 408 | PF00244 | 0.454 |
LIG_14-3-3_CanoR_1 | 456 | 463 | PF00244 | 0.480 |
LIG_14-3-3_CanoR_1 | 661 | 666 | PF00244 | 0.414 |
LIG_Actin_WH2_2 | 10 | 26 | PF00022 | 0.246 |
LIG_Actin_WH2_2 | 385 | 400 | PF00022 | 0.492 |
LIG_APCC_ABBA_1 | 49 | 54 | PF00400 | 0.506 |
LIG_BRCT_BRCA1_1 | 363 | 367 | PF00533 | 0.462 |
LIG_eIF4E_1 | 425 | 431 | PF01652 | 0.446 |
LIG_eIF4E_1 | 52 | 58 | PF01652 | 0.477 |
LIG_FHA_1 | 201 | 207 | PF00498 | 0.458 |
LIG_FHA_1 | 25 | 31 | PF00498 | 0.275 |
LIG_FHA_1 | 288 | 294 | PF00498 | 0.356 |
LIG_FHA_1 | 33 | 39 | PF00498 | 0.327 |
LIG_FHA_1 | 46 | 52 | PF00498 | 0.452 |
LIG_FHA_1 | 497 | 503 | PF00498 | 0.311 |
LIG_FHA_1 | 595 | 601 | PF00498 | 0.487 |
LIG_FHA_1 | 62 | 68 | PF00498 | 0.533 |
LIG_FHA_2 | 259 | 265 | PF00498 | 0.348 |
LIG_FHA_2 | 270 | 276 | PF00498 | 0.322 |
LIG_GBD_Chelix_1 | 15 | 23 | PF00786 | 0.404 |
LIG_LIR_Apic_2 | 363 | 368 | PF02991 | 0.529 |
LIG_LIR_Apic_2 | 494 | 500 | PF02991 | 0.267 |
LIG_LIR_Gen_1 | 359 | 369 | PF02991 | 0.501 |
LIG_LIR_Gen_1 | 476 | 484 | PF02991 | 0.421 |
LIG_LIR_Gen_1 | 588 | 598 | PF02991 | 0.425 |
LIG_LIR_Gen_1 | 637 | 646 | PF02991 | 0.553 |
LIG_LIR_Gen_1 | 692 | 703 | PF02991 | 0.383 |
LIG_LIR_LC3C_4 | 296 | 299 | PF02991 | 0.193 |
LIG_LIR_LC3C_4 | 429 | 432 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 225 | 230 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 359 | 365 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 476 | 480 | PF02991 | 0.406 |
LIG_LIR_Nem_3 | 48 | 52 | PF02991 | 0.485 |
LIG_LIR_Nem_3 | 588 | 593 | PF02991 | 0.351 |
LIG_LIR_Nem_3 | 637 | 641 | PF02991 | 0.580 |
LIG_LIR_Nem_3 | 692 | 698 | PF02991 | 0.337 |
LIG_MYND_1 | 624 | 628 | PF01753 | 0.633 |
LIG_NRBOX | 29 | 35 | PF00104 | 0.276 |
LIG_PCNA_yPIPBox_3 | 519 | 527 | PF02747 | 0.349 |
LIG_Pex14_2 | 365 | 369 | PF04695 | 0.531 |
LIG_Pex14_2 | 471 | 475 | PF04695 | 0.404 |
LIG_Pex14_2 | 579 | 583 | PF04695 | 0.335 |
LIG_Pex14_2 | 638 | 642 | PF04695 | 0.535 |
LIG_PTAP_UEV_1 | 107 | 112 | PF05743 | 0.682 |
LIG_PTB_Apo_2 | 40 | 47 | PF02174 | 0.523 |
LIG_PTB_Phospho_1 | 40 | 46 | PF10480 | 0.523 |
LIG_SH2_CRK | 295 | 299 | PF00017 | 0.394 |
LIG_SH2_CRK | 421 | 425 | PF00017 | 0.436 |
LIG_SH2_CRK | 511 | 515 | PF00017 | 0.276 |
LIG_SH2_GRB2like | 41 | 44 | PF00017 | 0.494 |
LIG_SH2_NCK_1 | 165 | 169 | PF00017 | 0.259 |
LIG_SH2_PTP2 | 554 | 557 | PF00017 | 0.314 |
LIG_SH2_SRC | 41 | 44 | PF00017 | 0.554 |
LIG_SH2_STAP1 | 295 | 299 | PF00017 | 0.394 |
LIG_SH2_STAP1 | 493 | 497 | PF00017 | 0.321 |
LIG_SH2_STAP1 | 675 | 679 | PF00017 | 0.335 |
LIG_SH2_STAT3 | 250 | 253 | PF00017 | 0.331 |
LIG_SH2_STAT5 | 198 | 201 | PF00017 | 0.275 |
LIG_SH2_STAT5 | 295 | 298 | PF00017 | 0.218 |
LIG_SH2_STAT5 | 46 | 49 | PF00017 | 0.472 |
LIG_SH2_STAT5 | 472 | 475 | PF00017 | 0.295 |
LIG_SH2_STAT5 | 493 | 496 | PF00017 | 0.299 |
LIG_SH2_STAT5 | 509 | 512 | PF00017 | 0.189 |
LIG_SH2_STAT5 | 549 | 552 | PF00017 | 0.277 |
LIG_SH2_STAT5 | 554 | 557 | PF00017 | 0.264 |
LIG_SH2_STAT5 | 590 | 593 | PF00017 | 0.452 |
LIG_SH3_3 | 105 | 111 | PF00018 | 0.689 |
LIG_SH3_3 | 191 | 197 | PF00018 | 0.357 |
LIG_SH3_3 | 526 | 532 | PF00018 | 0.584 |
LIG_SH3_3 | 590 | 596 | PF00018 | 0.383 |
LIG_SH3_3 | 612 | 618 | PF00018 | 0.784 |
LIG_SH3_3 | 625 | 631 | PF00018 | 0.566 |
LIG_Sin3_3 | 319 | 326 | PF02671 | 0.482 |
LIG_SUMO_SIM_anti_2 | 568 | 574 | PF11976 | 0.333 |
LIG_SUMO_SIM_anti_2 | 664 | 670 | PF11976 | 0.193 |
LIG_SUMO_SIM_par_1 | 201 | 208 | PF11976 | 0.245 |
LIG_SUMO_SIM_par_1 | 217 | 223 | PF11976 | 0.329 |
LIG_SUMO_SIM_par_1 | 228 | 234 | PF11976 | 0.472 |
LIG_SUMO_SIM_par_1 | 295 | 300 | PF11976 | 0.215 |
LIG_TRAF2_1 | 92 | 95 | PF00917 | 0.602 |
LIG_TYR_ITIM | 292 | 297 | PF00017 | 0.404 |
LIG_WRC_WIRS_1 | 25 | 30 | PF05994 | 0.288 |
LIG_WRC_WIRS_1 | 388 | 393 | PF05994 | 0.335 |
LIG_WRC_WIRS_1 | 46 | 51 | PF05994 | 0.359 |
MOD_CDK_SPxxK_3 | 627 | 634 | PF00069 | 0.353 |
MOD_CK1_1 | 109 | 115 | PF00069 | 0.679 |
MOD_CK1_1 | 29 | 35 | PF00069 | 0.404 |
MOD_CK1_1 | 341 | 347 | PF00069 | 0.289 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.393 |
MOD_CK1_1 | 411 | 417 | PF00069 | 0.358 |
MOD_CK1_1 | 594 | 600 | PF00069 | 0.326 |
MOD_CK1_1 | 66 | 72 | PF00069 | 0.335 |
MOD_CK1_1 | 717 | 723 | PF00069 | 0.521 |
MOD_CK2_1 | 259 | 265 | PF00069 | 0.423 |
MOD_CK2_1 | 269 | 275 | PF00069 | 0.393 |
MOD_CK2_1 | 307 | 313 | PF00069 | 0.402 |
MOD_CK2_1 | 399 | 405 | PF00069 | 0.289 |
MOD_CK2_1 | 723 | 729 | PF00069 | 0.439 |
MOD_CK2_1 | 73 | 79 | PF00069 | 0.363 |
MOD_GlcNHglycan | 108 | 111 | PF01048 | 0.701 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.481 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.427 |
MOD_GlcNHglycan | 338 | 341 | PF01048 | 0.433 |
MOD_GlcNHglycan | 343 | 346 | PF01048 | 0.410 |
MOD_GlcNHglycan | 722 | 725 | PF01048 | 0.685 |
MOD_GlcNHglycan | 75 | 79 | PF01048 | 0.570 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.588 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.430 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.442 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.377 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.271 |
MOD_GSK3_1 | 269 | 276 | PF00069 | 0.344 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.460 |
MOD_GSK3_1 | 348 | 355 | PF00069 | 0.226 |
MOD_GSK3_1 | 356 | 363 | PF00069 | 0.342 |
MOD_GSK3_1 | 370 | 377 | PF00069 | 0.390 |
MOD_GSK3_1 | 399 | 406 | PF00069 | 0.368 |
MOD_GSK3_1 | 407 | 414 | PF00069 | 0.356 |
MOD_GSK3_1 | 445 | 452 | PF00069 | 0.382 |
MOD_GSK3_1 | 487 | 494 | PF00069 | 0.326 |
MOD_GSK3_1 | 496 | 503 | PF00069 | 0.289 |
MOD_GSK3_1 | 601 | 608 | PF00069 | 0.656 |
MOD_GSK3_1 | 622 | 629 | PF00069 | 0.636 |
MOD_GSK3_1 | 689 | 696 | PF00069 | 0.574 |
MOD_N-GLC_2 | 441 | 443 | PF02516 | 0.314 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.321 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.371 |
MOD_NEK2_1 | 220 | 225 | PF00069 | 0.435 |
MOD_NEK2_1 | 273 | 278 | PF00069 | 0.324 |
MOD_NEK2_1 | 28 | 33 | PF00069 | 0.225 |
MOD_NEK2_1 | 297 | 302 | PF00069 | 0.412 |
MOD_NEK2_1 | 329 | 334 | PF00069 | 0.414 |
MOD_NEK2_1 | 387 | 392 | PF00069 | 0.307 |
MOD_NEK2_1 | 407 | 412 | PF00069 | 0.150 |
MOD_NEK2_1 | 449 | 454 | PF00069 | 0.284 |
MOD_NEK2_1 | 475 | 480 | PF00069 | 0.315 |
MOD_NEK2_1 | 488 | 493 | PF00069 | 0.356 |
MOD_NEK2_1 | 591 | 596 | PF00069 | 0.520 |
MOD_NEK2_1 | 654 | 659 | PF00069 | 0.355 |
MOD_NEK2_2 | 356 | 361 | PF00069 | 0.328 |
MOD_NEK2_2 | 585 | 590 | PF00069 | 0.404 |
MOD_PIKK_1 | 166 | 172 | PF00454 | 0.478 |
MOD_PIKK_1 | 354 | 360 | PF00454 | 0.314 |
MOD_PIKK_1 | 482 | 488 | PF00454 | 0.451 |
MOD_PK_1 | 175 | 181 | PF00069 | 0.414 |
MOD_PK_1 | 661 | 667 | PF00069 | 0.335 |
MOD_PKA_2 | 166 | 172 | PF00069 | 0.505 |
MOD_PKA_2 | 259 | 265 | PF00069 | 0.293 |
MOD_PKA_2 | 360 | 366 | PF00069 | 0.233 |
MOD_PKA_2 | 392 | 398 | PF00069 | 0.345 |
MOD_PKA_2 | 455 | 461 | PF00069 | 0.384 |
MOD_PKB_1 | 704 | 712 | PF00069 | 0.420 |
MOD_Plk_1 | 200 | 206 | PF00069 | 0.382 |
MOD_Plk_1 | 449 | 455 | PF00069 | 0.374 |
MOD_Plk_4 | 115 | 121 | PF00069 | 0.471 |
MOD_Plk_4 | 154 | 160 | PF00069 | 0.502 |
MOD_Plk_4 | 190 | 196 | PF00069 | 0.490 |
MOD_Plk_4 | 200 | 206 | PF00069 | 0.303 |
MOD_Plk_4 | 222 | 228 | PF00069 | 0.447 |
MOD_Plk_4 | 234 | 240 | PF00069 | 0.401 |
MOD_Plk_4 | 241 | 247 | PF00069 | 0.361 |
MOD_Plk_4 | 29 | 35 | PF00069 | 0.289 |
MOD_Plk_4 | 293 | 299 | PF00069 | 0.376 |
MOD_Plk_4 | 348 | 354 | PF00069 | 0.400 |
MOD_Plk_4 | 361 | 367 | PF00069 | 0.420 |
MOD_Plk_4 | 374 | 380 | PF00069 | 0.354 |
MOD_Plk_4 | 387 | 393 | PF00069 | 0.222 |
MOD_Plk_4 | 403 | 409 | PF00069 | 0.200 |
MOD_Plk_4 | 426 | 432 | PF00069 | 0.304 |
MOD_Plk_4 | 488 | 494 | PF00069 | 0.344 |
MOD_Plk_4 | 543 | 549 | PF00069 | 0.424 |
MOD_Plk_4 | 568 | 574 | PF00069 | 0.421 |
MOD_Plk_4 | 578 | 584 | PF00069 | 0.355 |
MOD_Plk_4 | 585 | 591 | PF00069 | 0.239 |
MOD_Plk_4 | 594 | 600 | PF00069 | 0.396 |
MOD_Plk_4 | 637 | 643 | PF00069 | 0.437 |
MOD_Plk_4 | 646 | 652 | PF00069 | 0.365 |
MOD_Plk_4 | 661 | 667 | PF00069 | 0.333 |
MOD_ProDKin_1 | 112 | 118 | PF00069 | 0.461 |
MOD_ProDKin_1 | 308 | 314 | PF00069 | 0.404 |
MOD_ProDKin_1 | 352 | 358 | PF00069 | 0.332 |
MOD_ProDKin_1 | 496 | 502 | PF00069 | 0.314 |
MOD_ProDKin_1 | 528 | 534 | PF00069 | 0.438 |
MOD_ProDKin_1 | 592 | 598 | PF00069 | 0.414 |
MOD_ProDKin_1 | 624 | 630 | PF00069 | 0.620 |
MOD_ProDKin_1 | 689 | 695 | PF00069 | 0.530 |
TRG_DiLeu_BaEn_1 | 234 | 239 | PF01217 | 0.292 |
TRG_DiLeu_BaEn_1 | 403 | 408 | PF01217 | 0.293 |
TRG_DiLeu_BaEn_1 | 685 | 690 | PF01217 | 0.499 |
TRG_DiLeu_BaEn_2 | 439 | 445 | PF01217 | 0.314 |
TRG_DiLeu_BaLyEn_6 | 33 | 38 | PF01217 | 0.383 |
TRG_DiLeu_BaLyEn_6 | 430 | 435 | PF01217 | 0.349 |
TRG_DiLeu_BaLyEn_6 | 696 | 701 | PF01217 | 0.468 |
TRG_DiLeu_LyEn_5 | 685 | 690 | PF01217 | 0.379 |
TRG_ENDOCYTIC_2 | 294 | 297 | PF00928 | 0.404 |
TRG_ENDOCYTIC_2 | 420 | 423 | PF00928 | 0.274 |
TRG_ENDOCYTIC_2 | 46 | 49 | PF00928 | 0.452 |
TRG_ENDOCYTIC_2 | 472 | 475 | PF00928 | 0.427 |
TRG_ENDOCYTIC_2 | 554 | 557 | PF00928 | 0.294 |
TRG_ENDOCYTIC_2 | 590 | 593 | PF00928 | 0.452 |
TRG_ER_diArg_1 | 686 | 688 | PF00400 | 0.361 |
TRG_ER_diArg_1 | 697 | 700 | PF00400 | 0.441 |
TRG_ER_diArg_1 | 703 | 706 | PF00400 | 0.491 |
TRG_ER_diLys_1 | 725 | 729 | PF00400 | 0.445 |
TRG_NES_CRM1_1 | 222 | 234 | PF08389 | 0.413 |
TRG_Pf-PMV_PEXEL_1 | 271 | 275 | PF00026 | 0.284 |
TRG_Pf-PMV_PEXEL_1 | 327 | 331 | PF00026 | 0.193 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IHL6 | Leptomonas seymouri | 59% | 100% |
A0A1X0NQN5 | Trypanosomatidae | 33% | 100% |
A0A3Q8IDZ2 | Leishmania donovani | 79% | 100% |
A0A3S5IQL5 | Trypanosoma rangeli | 35% | 100% |
A4I3X2 | Leishmania infantum | 79% | 100% |
D0A939 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
E9B062 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 77% | 100% |
Q4Q823 | Leishmania major | 79% | 100% |
V5AWN8 | Trypanosoma cruzi | 34% | 100% |