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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005789 | endoplasmic reticulum membrane | 4 | 9 |
GO:0016020 | membrane | 2 | 9 |
GO:0031090 | organelle membrane | 3 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
Related structures:
AlphaFold database: E9ANU3
Term | Name | Level | Count |
---|---|---|---|
GO:0006486 | protein glycosylation | 4 | 9 |
GO:0006807 | nitrogen compound metabolic process | 2 | 9 |
GO:0008152 | metabolic process | 1 | 9 |
GO:0019538 | protein metabolic process | 3 | 9 |
GO:0036211 | protein modification process | 4 | 9 |
GO:0043170 | macromolecule metabolic process | 3 | 9 |
GO:0043412 | macromolecule modification | 4 | 9 |
GO:0043413 | macromolecule glycosylation | 3 | 9 |
GO:0044238 | primary metabolic process | 2 | 9 |
GO:0070085 | glycosylation | 2 | 9 |
GO:0071704 | organic substance metabolic process | 2 | 9 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 9 |
GO:0006487 | protein N-linked glycosylation | 5 | 1 |
GO:0006488 | dolichol-linked oligosaccharide biosynthetic process | 5 | 1 |
GO:0006490 | oligosaccharide-lipid intermediate biosynthetic process | 4 | 1 |
GO:0006629 | lipid metabolic process | 3 | 1 |
GO:0009058 | biosynthetic process | 2 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044255 | cellular lipid metabolic process | 3 | 1 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 1 |
GO:1901137 | carbohydrate derivative biosynthetic process | 4 | 1 |
GO:1901576 | organic substance biosynthetic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000026 | alpha-1,2-mannosyltransferase activity | 6 | 9 |
GO:0000030 | mannosyltransferase activity | 5 | 9 |
GO:0003824 | catalytic activity | 1 | 9 |
GO:0016740 | transferase activity | 2 | 9 |
GO:0016757 | glycosyltransferase activity | 3 | 9 |
GO:0016758 | hexosyltransferase activity | 4 | 9 |
GO:0052918 | dol-P-Man:Man(8)GlcNAc(2)-PP-Dol alpha-1,2-mannosyltransferase activity | 7 | 9 |
GO:0052926 | dol-P-Man:Man(6)GlcNAc(2)-PP-Dol alpha-1,2-mannosyltransferase activity | 7 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 755 | 759 | PF00656 | 0.344 |
CLV_NRD_NRD_1 | 277 | 279 | PF00675 | 0.385 |
CLV_NRD_NRD_1 | 336 | 338 | PF00675 | 0.460 |
CLV_NRD_NRD_1 | 492 | 494 | PF00675 | 0.531 |
CLV_NRD_NRD_1 | 566 | 568 | PF00675 | 0.658 |
CLV_NRD_NRD_1 | 724 | 726 | PF00675 | 0.630 |
CLV_NRD_NRD_1 | 783 | 785 | PF00675 | 0.630 |
CLV_PCSK_KEX2_1 | 277 | 279 | PF00082 | 0.385 |
CLV_PCSK_KEX2_1 | 336 | 338 | PF00082 | 0.480 |
CLV_PCSK_KEX2_1 | 492 | 494 | PF00082 | 0.506 |
CLV_PCSK_KEX2_1 | 561 | 563 | PF00082 | 0.599 |
CLV_PCSK_KEX2_1 | 566 | 568 | PF00082 | 0.630 |
CLV_PCSK_KEX2_1 | 724 | 726 | PF00082 | 0.639 |
CLV_PCSK_KEX2_1 | 783 | 785 | PF00082 | 0.605 |
CLV_PCSK_PC1ET2_1 | 561 | 563 | PF00082 | 0.635 |
CLV_PCSK_PC7_1 | 273 | 279 | PF00082 | 0.385 |
CLV_PCSK_PC7_1 | 562 | 568 | PF00082 | 0.674 |
CLV_PCSK_SKI1_1 | 337 | 341 | PF00082 | 0.403 |
CLV_PCSK_SKI1_1 | 734 | 738 | PF00082 | 0.667 |
CLV_PCSK_SKI1_1 | 754 | 758 | PF00082 | 0.671 |
DEG_APCC_DBOX_1 | 420 | 428 | PF00400 | 0.582 |
DEG_APCC_DBOX_1 | 724 | 732 | PF00400 | 0.434 |
DEG_SPOP_SBC_1 | 290 | 294 | PF00917 | 0.185 |
DOC_CKS1_1 | 623 | 628 | PF01111 | 0.442 |
DOC_CKS1_1 | 636 | 641 | PF01111 | 0.458 |
DOC_CYCLIN_RxL_1 | 731 | 741 | PF00134 | 0.496 |
DOC_CYCLIN_yCln2_LP_2 | 623 | 629 | PF00134 | 0.344 |
DOC_CYCLIN_yCln2_LP_2 | 775 | 781 | PF00134 | 0.370 |
DOC_MAPK_MEF2A_6 | 121 | 129 | PF00069 | 0.362 |
DOC_MAPK_MEF2A_6 | 65 | 72 | PF00069 | 0.382 |
DOC_MAPK_NFAT4_5 | 65 | 73 | PF00069 | 0.382 |
DOC_PP1_RVXF_1 | 207 | 214 | PF00149 | 0.582 |
DOC_PP2B_LxvP_1 | 332 | 335 | PF13499 | 0.450 |
DOC_PP2B_LxvP_1 | 648 | 651 | PF13499 | 0.518 |
DOC_PP2B_LxvP_1 | 708 | 711 | PF13499 | 0.493 |
DOC_PP4_FxxP_1 | 205 | 208 | PF00568 | 0.385 |
DOC_PP4_FxxP_1 | 40 | 43 | PF00568 | 0.301 |
DOC_PP4_FxxP_1 | 446 | 449 | PF00568 | 0.293 |
DOC_PP4_FxxP_1 | 636 | 639 | PF00568 | 0.465 |
DOC_USP7_MATH_1 | 139 | 143 | PF00917 | 0.325 |
DOC_USP7_MATH_1 | 343 | 347 | PF00917 | 0.730 |
DOC_USP7_MATH_1 | 348 | 352 | PF00917 | 0.728 |
DOC_USP7_MATH_1 | 363 | 367 | PF00917 | 0.804 |
DOC_USP7_MATH_1 | 370 | 374 | PF00917 | 0.736 |
DOC_USP7_MATH_1 | 391 | 395 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 412 | 416 | PF00917 | 0.509 |
DOC_USP7_MATH_1 | 575 | 579 | PF00917 | 0.548 |
DOC_USP7_MATH_1 | 63 | 67 | PF00917 | 0.284 |
DOC_USP7_MATH_1 | 663 | 667 | PF00917 | 0.590 |
DOC_USP7_MATH_1 | 671 | 675 | PF00917 | 0.443 |
DOC_WW_Pin1_4 | 199 | 204 | PF00397 | 0.594 |
DOC_WW_Pin1_4 | 366 | 371 | PF00397 | 0.732 |
DOC_WW_Pin1_4 | 445 | 450 | PF00397 | 0.355 |
DOC_WW_Pin1_4 | 494 | 499 | PF00397 | 0.696 |
DOC_WW_Pin1_4 | 573 | 578 | PF00397 | 0.520 |
DOC_WW_Pin1_4 | 622 | 627 | PF00397 | 0.387 |
DOC_WW_Pin1_4 | 635 | 640 | PF00397 | 0.431 |
DOC_WW_Pin1_4 | 659 | 664 | PF00397 | 0.604 |
DOC_WW_Pin1_4 | 765 | 770 | PF00397 | 0.376 |
LIG_14-3-3_CanoR_1 | 162 | 167 | PF00244 | 0.500 |
LIG_14-3-3_CanoR_1 | 277 | 286 | PF00244 | 0.355 |
LIG_14-3-3_CanoR_1 | 4 | 11 | PF00244 | 0.661 |
LIG_14-3-3_CanoR_1 | 606 | 612 | PF00244 | 0.274 |
LIG_14-3-3_CanoR_1 | 665 | 671 | PF00244 | 0.510 |
LIG_14-3-3_CanoR_1 | 81 | 87 | PF00244 | 0.437 |
LIG_BRCT_BRCA1_1 | 112 | 116 | PF00533 | 0.379 |
LIG_BRCT_BRCA1_1 | 201 | 205 | PF00533 | 0.385 |
LIG_BRCT_BRCA1_1 | 608 | 612 | PF00533 | 0.319 |
LIG_BRCT_BRCA1_1 | 65 | 69 | PF00533 | 0.301 |
LIG_Clathr_ClatBox_1 | 239 | 243 | PF01394 | 0.474 |
LIG_Clathr_ClatBox_1 | 300 | 304 | PF01394 | 0.382 |
LIG_deltaCOP1_diTrp_1 | 420 | 430 | PF00928 | 0.385 |
LIG_deltaCOP1_diTrp_1 | 603 | 611 | PF00928 | 0.315 |
LIG_EVH1_1 | 200 | 204 | PF00568 | 0.385 |
LIG_FHA_1 | 103 | 109 | PF00498 | 0.199 |
LIG_FHA_1 | 190 | 196 | PF00498 | 0.475 |
LIG_FHA_1 | 369 | 375 | PF00498 | 0.758 |
LIG_FHA_1 | 4 | 10 | PF00498 | 0.666 |
LIG_FHA_1 | 457 | 463 | PF00498 | 0.437 |
LIG_FHA_1 | 485 | 491 | PF00498 | 0.610 |
LIG_FHA_1 | 587 | 593 | PF00498 | 0.443 |
LIG_FHA_1 | 595 | 601 | PF00498 | 0.309 |
LIG_FHA_1 | 731 | 737 | PF00498 | 0.457 |
LIG_FHA_2 | 438 | 444 | PF00498 | 0.199 |
LIG_FHA_2 | 753 | 759 | PF00498 | 0.345 |
LIG_GBD_Chelix_1 | 253 | 261 | PF00786 | 0.474 |
LIG_HP1_1 | 328 | 332 | PF01393 | 0.474 |
LIG_IRF3_LxIS_1 | 26 | 32 | PF10401 | 0.199 |
LIG_LIR_Apic_2 | 202 | 208 | PF02991 | 0.385 |
LIG_LIR_Apic_2 | 37 | 43 | PF02991 | 0.313 |
LIG_LIR_Apic_2 | 443 | 449 | PF02991 | 0.284 |
LIG_LIR_Apic_2 | 603 | 608 | PF02991 | 0.321 |
LIG_LIR_Apic_2 | 635 | 639 | PF02991 | 0.462 |
LIG_LIR_Gen_1 | 146 | 156 | PF02991 | 0.345 |
LIG_LIR_Gen_1 | 281 | 291 | PF02991 | 0.304 |
LIG_LIR_Gen_1 | 35 | 46 | PF02991 | 0.302 |
LIG_LIR_Gen_1 | 420 | 431 | PF02991 | 0.417 |
LIG_LIR_Gen_1 | 66 | 77 | PF02991 | 0.284 |
LIG_LIR_Gen_1 | 702 | 711 | PF02991 | 0.378 |
LIG_LIR_Gen_1 | 758 | 767 | PF02991 | 0.406 |
LIG_LIR_Gen_1 | 768 | 779 | PF02991 | 0.331 |
LIG_LIR_LC3C_4 | 259 | 263 | PF02991 | 0.349 |
LIG_LIR_Nem_3 | 113 | 118 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 146 | 151 | PF02991 | 0.303 |
LIG_LIR_Nem_3 | 21 | 26 | PF02991 | 0.374 |
LIG_LIR_Nem_3 | 27 | 31 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 281 | 286 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 307 | 313 | PF02991 | 0.203 |
LIG_LIR_Nem_3 | 35 | 41 | PF02991 | 0.290 |
LIG_LIR_Nem_3 | 545 | 549 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 60 | 64 | PF02991 | 0.288 |
LIG_LIR_Nem_3 | 603 | 607 | PF02991 | 0.313 |
LIG_LIR_Nem_3 | 609 | 615 | PF02991 | 0.296 |
LIG_LIR_Nem_3 | 66 | 72 | PF02991 | 0.281 |
LIG_LIR_Nem_3 | 691 | 696 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 702 | 708 | PF02991 | 0.308 |
LIG_LIR_Nem_3 | 752 | 756 | PF02991 | 0.348 |
LIG_LIR_Nem_3 | 758 | 763 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 768 | 774 | PF02991 | 0.307 |
LIG_LYPXL_yS_3 | 451 | 454 | PF13949 | 0.362 |
LIG_MLH1_MIPbox_1 | 608 | 612 | PF16413 | 0.319 |
LIG_NRBOX | 126 | 132 | PF00104 | 0.362 |
LIG_NRBOX | 241 | 247 | PF00104 | 0.474 |
LIG_NRBOX | 256 | 262 | PF00104 | 0.231 |
LIG_Pex14_2 | 24 | 28 | PF04695 | 0.420 |
LIG_Pex14_2 | 317 | 321 | PF04695 | 0.437 |
LIG_Pex14_2 | 517 | 521 | PF04695 | 0.437 |
LIG_Pex14_2 | 607 | 611 | PF04695 | 0.306 |
LIG_SH2_CRK | 605 | 609 | PF00017 | 0.309 |
LIG_SH2_CRK | 620 | 624 | PF00017 | 0.252 |
LIG_SH2_CRK | 753 | 757 | PF00017 | 0.347 |
LIG_SH2_STAP1 | 526 | 530 | PF00017 | 0.402 |
LIG_SH2_STAP1 | 596 | 600 | PF00017 | 0.346 |
LIG_SH2_STAT3 | 134 | 137 | PF00017 | 0.275 |
LIG_SH2_STAT5 | 23 | 26 | PF00017 | 0.281 |
LIG_SH2_STAT5 | 275 | 278 | PF00017 | 0.289 |
LIG_SH2_STAT5 | 46 | 49 | PF00017 | 0.353 |
LIG_SH2_STAT5 | 533 | 536 | PF00017 | 0.384 |
LIG_SH2_STAT5 | 596 | 599 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 627 | 630 | PF00017 | 0.341 |
LIG_SH2_STAT5 | 693 | 696 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 92 | 95 | PF00017 | 0.337 |
LIG_SH3_2 | 204 | 209 | PF14604 | 0.475 |
LIG_SH3_2 | 491 | 496 | PF14604 | 0.572 |
LIG_SH3_3 | 198 | 204 | PF00018 | 0.470 |
LIG_SH3_3 | 446 | 452 | PF00018 | 0.284 |
LIG_SH3_3 | 488 | 494 | PF00018 | 0.699 |
LIG_SH3_3 | 634 | 640 | PF00018 | 0.483 |
LIG_SH3_3 | 691 | 697 | PF00018 | 0.423 |
LIG_SH3_3 | 784 | 790 | PF00018 | 0.462 |
LIG_SH3_CIN85_PxpxPR_1 | 204 | 209 | PF14604 | 0.475 |
LIG_Sin3_3 | 327 | 334 | PF02671 | 0.349 |
LIG_SUMO_SIM_anti_2 | 222 | 228 | PF11976 | 0.324 |
LIG_SUMO_SIM_anti_2 | 259 | 264 | PF11976 | 0.390 |
LIG_SUMO_SIM_par_1 | 16 | 21 | PF11976 | 0.392 |
LIG_SUMO_SIM_par_1 | 761 | 766 | PF11976 | 0.445 |
LIG_TRAF2_1 | 641 | 644 | PF00917 | 0.549 |
LIG_TYR_ITSM | 19 | 26 | PF00017 | 0.199 |
LIG_UBA3_1 | 433 | 442 | PF00899 | 0.461 |
LIG_WW_3 | 206 | 210 | PF00397 | 0.582 |
LIG_WW_3 | 709 | 713 | PF00397 | 0.344 |
MOD_CDC14_SPxK_1 | 662 | 665 | PF00782 | 0.493 |
MOD_CDK_SPxK_1 | 659 | 665 | PF00069 | 0.497 |
MOD_CK1_1 | 165 | 171 | PF00069 | 0.518 |
MOD_CK1_1 | 356 | 362 | PF00069 | 0.794 |
MOD_CK1_1 | 366 | 372 | PF00069 | 0.723 |
MOD_CK1_1 | 415 | 421 | PF00069 | 0.538 |
MOD_CK1_1 | 576 | 582 | PF00069 | 0.550 |
MOD_CK1_1 | 635 | 641 | PF00069 | 0.459 |
MOD_CK1_1 | 664 | 670 | PF00069 | 0.593 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.439 |
MOD_CK2_1 | 437 | 443 | PF00069 | 0.242 |
MOD_CK2_1 | 534 | 540 | PF00069 | 0.395 |
MOD_GlcNHglycan | 118 | 121 | PF01048 | 0.378 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.323 |
MOD_GlcNHglycan | 236 | 239 | PF01048 | 0.362 |
MOD_GlcNHglycan | 293 | 296 | PF01048 | 0.555 |
MOD_GlcNHglycan | 350 | 353 | PF01048 | 0.554 |
MOD_GlcNHglycan | 365 | 368 | PF01048 | 0.563 |
MOD_GlcNHglycan | 476 | 479 | PF01048 | 0.501 |
MOD_GlcNHglycan | 50 | 53 | PF01048 | 0.501 |
MOD_GlcNHglycan | 536 | 539 | PF01048 | 0.607 |
MOD_GlcNHglycan | 714 | 717 | PF01048 | 0.627 |
MOD_GlcNHglycan | 81 | 84 | PF01048 | 0.291 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.432 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.330 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.392 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.555 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.498 |
MOD_GSK3_1 | 339 | 346 | PF00069 | 0.704 |
MOD_GSK3_1 | 366 | 373 | PF00069 | 0.764 |
MOD_GSK3_1 | 374 | 381 | PF00069 | 0.737 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.301 |
MOD_GSK3_1 | 582 | 589 | PF00069 | 0.486 |
MOD_GSK3_1 | 659 | 666 | PF00069 | 0.581 |
MOD_LATS_1 | 376 | 382 | PF00433 | 0.579 |
MOD_N-GLC_1 | 363 | 368 | PF02516 | 0.509 |
MOD_N-GLC_1 | 737 | 742 | PF02516 | 0.686 |
MOD_N-GLC_2 | 99 | 101 | PF02516 | 0.382 |
MOD_NEK2_1 | 110 | 115 | PF00069 | 0.365 |
MOD_NEK2_1 | 116 | 121 | PF00069 | 0.366 |
MOD_NEK2_1 | 16 | 21 | PF00069 | 0.402 |
MOD_NEK2_1 | 219 | 224 | PF00069 | 0.396 |
MOD_NEK2_1 | 24 | 29 | PF00069 | 0.382 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.371 |
MOD_NEK2_1 | 291 | 296 | PF00069 | 0.382 |
MOD_NEK2_1 | 339 | 344 | PF00069 | 0.705 |
MOD_NEK2_1 | 374 | 379 | PF00069 | 0.744 |
MOD_NEK2_1 | 435 | 440 | PF00069 | 0.432 |
MOD_NEK2_1 | 456 | 461 | PF00069 | 0.374 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.301 |
MOD_NEK2_1 | 522 | 527 | PF00069 | 0.400 |
MOD_NEK2_1 | 732 | 737 | PF00069 | 0.466 |
MOD_NEK2_1 | 779 | 784 | PF00069 | 0.455 |
MOD_NEK2_1 | 79 | 84 | PF00069 | 0.340 |
MOD_NEK2_2 | 171 | 176 | PF00069 | 0.385 |
MOD_PIKK_1 | 160 | 166 | PF00454 | 0.474 |
MOD_PIKK_1 | 586 | 592 | PF00454 | 0.514 |
MOD_PKA_1 | 492 | 498 | PF00069 | 0.768 |
MOD_PKA_2 | 178 | 184 | PF00069 | 0.523 |
MOD_PKA_2 | 276 | 282 | PF00069 | 0.355 |
MOD_PKA_2 | 3 | 9 | PF00069 | 0.673 |
MOD_PKA_2 | 415 | 421 | PF00069 | 0.582 |
MOD_PKA_2 | 492 | 498 | PF00069 | 0.755 |
MOD_PKA_2 | 664 | 670 | PF00069 | 0.515 |
MOD_PKA_2 | 671 | 677 | PF00069 | 0.488 |
MOD_Plk_1 | 34 | 40 | PF00069 | 0.324 |
MOD_Plk_1 | 363 | 369 | PF00069 | 0.799 |
MOD_Plk_1 | 737 | 743 | PF00069 | 0.483 |
MOD_Plk_4 | 110 | 116 | PF00069 | 0.377 |
MOD_Plk_4 | 139 | 145 | PF00069 | 0.385 |
MOD_Plk_4 | 194 | 200 | PF00069 | 0.470 |
MOD_Plk_4 | 24 | 30 | PF00069 | 0.403 |
MOD_Plk_4 | 256 | 262 | PF00069 | 0.404 |
MOD_Plk_4 | 264 | 270 | PF00069 | 0.385 |
MOD_Plk_4 | 370 | 376 | PF00069 | 0.774 |
MOD_Plk_4 | 57 | 63 | PF00069 | 0.185 |
MOD_Plk_4 | 607 | 613 | PF00069 | 0.340 |
MOD_Plk_4 | 632 | 638 | PF00069 | 0.440 |
MOD_Plk_4 | 727 | 733 | PF00069 | 0.500 |
MOD_ProDKin_1 | 199 | 205 | PF00069 | 0.594 |
MOD_ProDKin_1 | 366 | 372 | PF00069 | 0.731 |
MOD_ProDKin_1 | 445 | 451 | PF00069 | 0.355 |
MOD_ProDKin_1 | 494 | 500 | PF00069 | 0.695 |
MOD_ProDKin_1 | 573 | 579 | PF00069 | 0.523 |
MOD_ProDKin_1 | 622 | 628 | PF00069 | 0.386 |
MOD_ProDKin_1 | 635 | 641 | PF00069 | 0.439 |
MOD_ProDKin_1 | 659 | 665 | PF00069 | 0.604 |
MOD_ProDKin_1 | 765 | 771 | PF00069 | 0.378 |
TRG_DiLeu_BaEn_2 | 303 | 309 | PF01217 | 0.185 |
TRG_DiLeu_BaEn_2 | 35 | 41 | PF01217 | 0.301 |
TRG_ENDOCYTIC_2 | 23 | 26 | PF00928 | 0.268 |
TRG_ENDOCYTIC_2 | 288 | 291 | PF00928 | 0.324 |
TRG_ENDOCYTIC_2 | 451 | 454 | PF00928 | 0.362 |
TRG_ENDOCYTIC_2 | 595 | 598 | PF00928 | 0.388 |
TRG_ENDOCYTIC_2 | 620 | 623 | PF00928 | 0.352 |
TRG_ENDOCYTIC_2 | 753 | 756 | PF00928 | 0.348 |
TRG_ENDOCYTIC_2 | 760 | 763 | PF00928 | 0.390 |
TRG_ENDOCYTIC_2 | 776 | 779 | PF00928 | 0.398 |
TRG_ENDOCYTIC_2 | 92 | 95 | PF00928 | 0.359 |
TRG_ER_diArg_1 | 335 | 337 | PF00400 | 0.657 |
TRG_ER_diArg_1 | 491 | 493 | PF00400 | 0.787 |
TRG_ER_diArg_1 | 565 | 567 | PF00400 | 0.501 |
TRG_ER_diArg_1 | 723 | 725 | PF00400 | 0.430 |
TRG_Pf-PMV_PEXEL_1 | 541 | 545 | PF00026 | 0.512 |
TRG_Pf-PMV_PEXEL_1 | 724 | 729 | PF00026 | 0.653 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I3C3 | Leptomonas seymouri | 53% | 100% |
A0A0S4ITY5 | Bodo saltans | 29% | 100% |
A0A3Q8IBE5 | Leishmania donovani | 81% | 98% |
A0A422NUF2 | Trypanosoma rangeli | 40% | 100% |
C9ZQC6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
E9AGA5 | Leishmania infantum | 80% | 98% |
Q4QGS7 | Leishmania major | 81% | 99% |