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: A0A3Q8IBE5
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 | 496 | 500 | PF00656 | 0.652 |
CLV_NRD_NRD_1 | 337 | 339 | PF00675 | 0.436 |
CLV_NRD_NRD_1 | 511 | 513 | PF00675 | 0.572 |
CLV_NRD_NRD_1 | 585 | 587 | PF00675 | 0.667 |
CLV_NRD_NRD_1 | 768 | 770 | PF00675 | 0.662 |
CLV_NRD_NRD_1 | 802 | 804 | PF00675 | 0.628 |
CLV_PCSK_KEX2_1 | 337 | 339 | PF00082 | 0.451 |
CLV_PCSK_KEX2_1 | 484 | 486 | PF00082 | 0.559 |
CLV_PCSK_KEX2_1 | 511 | 513 | PF00082 | 0.542 |
CLV_PCSK_KEX2_1 | 580 | 582 | PF00082 | 0.606 |
CLV_PCSK_KEX2_1 | 585 | 587 | PF00082 | 0.638 |
CLV_PCSK_KEX2_1 | 802 | 804 | PF00082 | 0.603 |
CLV_PCSK_PC1ET2_1 | 484 | 486 | PF00082 | 0.559 |
CLV_PCSK_PC1ET2_1 | 580 | 582 | PF00082 | 0.641 |
CLV_PCSK_PC7_1 | 581 | 587 | PF00082 | 0.685 |
CLV_PCSK_SKI1_1 | 312 | 316 | PF00082 | 0.453 |
CLV_PCSK_SKI1_1 | 422 | 426 | PF00082 | 0.282 |
CLV_PCSK_SKI1_1 | 560 | 564 | PF00082 | 0.620 |
CLV_PCSK_SKI1_1 | 61 | 65 | PF00082 | 0.511 |
CLV_PCSK_SKI1_1 | 753 | 757 | PF00082 | 0.570 |
DEG_APCC_DBOX_1 | 421 | 429 | PF00400 | 0.582 |
DEG_SCF_FBW7_1 | 196 | 202 | PF00400 | 0.456 |
DEG_SPOP_SBC_1 | 201 | 205 | PF00917 | 0.456 |
DEG_SPOP_SBC_1 | 682 | 686 | PF00917 | 0.471 |
DOC_ANK_TNKS_1 | 353 | 360 | PF00023 | 0.770 |
DOC_CDC14_PxL_1 | 563 | 571 | PF14671 | 0.389 |
DOC_CKS1_1 | 196 | 201 | PF01111 | 0.456 |
DOC_CKS1_1 | 655 | 660 | PF01111 | 0.431 |
DOC_CYCLIN_RxL_1 | 750 | 759 | PF00134 | 0.393 |
DOC_CYCLIN_RxL_1 | 802 | 814 | PF00134 | 0.315 |
DOC_CYCLIN_yCln2_LP_2 | 247 | 253 | PF00134 | 0.520 |
DOC_CYCLIN_yCln2_LP_2 | 794 | 800 | PF00134 | 0.390 |
DOC_MAPK_gen_1 | 417 | 427 | PF00069 | 0.524 |
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 | 208 | 215 | PF00149 | 0.582 |
DOC_PP1_RVXF_1 | 88 | 94 | PF00149 | 0.424 |
DOC_PP2B_LxvP_1 | 333 | 336 | PF13499 | 0.450 |
DOC_PP2B_LxvP_1 | 667 | 670 | PF13499 | 0.512 |
DOC_PP2B_LxvP_1 | 727 | 730 | PF13499 | 0.451 |
DOC_PP4_FxxP_1 | 40 | 43 | PF00568 | 0.301 |
DOC_PP4_FxxP_1 | 447 | 450 | PF00568 | 0.293 |
DOC_PP4_FxxP_1 | 655 | 658 | PF00568 | 0.445 |
DOC_USP7_MATH_1 | 139 | 143 | PF00917 | 0.345 |
DOC_USP7_MATH_1 | 172 | 176 | PF00917 | 0.517 |
DOC_USP7_MATH_1 | 199 | 203 | PF00917 | 0.590 |
DOC_USP7_MATH_1 | 341 | 345 | PF00917 | 0.716 |
DOC_USP7_MATH_1 | 349 | 353 | PF00917 | 0.736 |
DOC_USP7_MATH_1 | 364 | 368 | PF00917 | 0.800 |
DOC_USP7_MATH_1 | 371 | 375 | PF00917 | 0.746 |
DOC_USP7_MATH_1 | 413 | 417 | PF00917 | 0.514 |
DOC_USP7_MATH_1 | 594 | 598 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 63 | 67 | PF00917 | 0.284 |
DOC_USP7_MATH_1 | 676 | 680 | PF00917 | 0.570 |
DOC_USP7_MATH_1 | 682 | 686 | PF00917 | 0.605 |
DOC_USP7_MATH_1 | 690 | 694 | PF00917 | 0.500 |
DOC_USP7_UBL2_3 | 766 | 770 | PF12436 | 0.382 |
DOC_WW_Pin1_4 | 167 | 172 | PF00397 | 0.493 |
DOC_WW_Pin1_4 | 195 | 200 | PF00397 | 0.550 |
DOC_WW_Pin1_4 | 367 | 372 | PF00397 | 0.736 |
DOC_WW_Pin1_4 | 446 | 451 | PF00397 | 0.355 |
DOC_WW_Pin1_4 | 479 | 484 | PF00397 | 0.745 |
DOC_WW_Pin1_4 | 486 | 491 | PF00397 | 0.755 |
DOC_WW_Pin1_4 | 519 | 524 | PF00397 | 0.661 |
DOC_WW_Pin1_4 | 592 | 597 | PF00397 | 0.541 |
DOC_WW_Pin1_4 | 654 | 659 | PF00397 | 0.415 |
DOC_WW_Pin1_4 | 678 | 683 | PF00397 | 0.604 |
DOC_WW_Pin1_4 | 725 | 730 | PF00397 | 0.359 |
DOC_WW_Pin1_4 | 784 | 789 | PF00397 | 0.373 |
LIG_14-3-3_CanoR_1 | 183 | 193 | PF00244 | 0.507 |
LIG_14-3-3_CanoR_1 | 195 | 199 | PF00244 | 0.520 |
LIG_14-3-3_CanoR_1 | 278 | 287 | PF00244 | 0.334 |
LIG_14-3-3_CanoR_1 | 4 | 11 | PF00244 | 0.644 |
LIG_14-3-3_CanoR_1 | 612 | 618 | PF00244 | 0.395 |
LIG_14-3-3_CanoR_1 | 625 | 631 | PF00244 | 0.283 |
LIG_14-3-3_CanoR_1 | 691 | 701 | PF00244 | 0.493 |
LIG_14-3-3_CanoR_1 | 81 | 87 | PF00244 | 0.437 |
LIG_Actin_WH2_2 | 751 | 768 | PF00022 | 0.330 |
LIG_BRCT_BRCA1_1 | 521 | 525 | PF00533 | 0.678 |
LIG_BRCT_BRCA1_1 | 627 | 631 | PF00533 | 0.323 |
LIG_BRCT_BRCA1_1 | 65 | 69 | PF00533 | 0.301 |
LIG_CaM_IQ_9 | 758 | 774 | PF13499 | 0.365 |
LIG_Clathr_ClatBox_1 | 240 | 244 | PF01394 | 0.474 |
LIG_Clathr_ClatBox_1 | 301 | 305 | PF01394 | 0.382 |
LIG_deltaCOP1_diTrp_1 | 622 | 630 | PF00928 | 0.320 |
LIG_deltaCOP1_diTrp_1 | 633 | 641 | PF00928 | 0.314 |
LIG_FHA_1 | 286 | 292 | PF00498 | 0.257 |
LIG_FHA_1 | 370 | 376 | PF00498 | 0.769 |
LIG_FHA_1 | 4 | 10 | PF00498 | 0.649 |
LIG_FHA_1 | 458 | 464 | PF00498 | 0.437 |
LIG_FHA_1 | 487 | 493 | PF00498 | 0.764 |
LIG_FHA_1 | 606 | 612 | PF00498 | 0.433 |
LIG_FHA_1 | 614 | 620 | PF00498 | 0.301 |
LIG_FHA_1 | 750 | 756 | PF00498 | 0.376 |
LIG_FHA_1 | 769 | 775 | PF00498 | 0.360 |
LIG_FHA_2 | 494 | 500 | PF00498 | 0.748 |
LIG_GBD_Chelix_1 | 254 | 262 | PF00786 | 0.474 |
LIG_GBD_Chelix_1 | 534 | 542 | PF00786 | 0.424 |
LIG_HP1_1 | 329 | 333 | PF01393 | 0.474 |
LIG_LIR_Apic_2 | 37 | 43 | PF02991 | 0.313 |
LIG_LIR_Apic_2 | 423 | 429 | PF02991 | 0.456 |
LIG_LIR_Apic_2 | 444 | 450 | PF02991 | 0.284 |
LIG_LIR_Apic_2 | 622 | 627 | PF02991 | 0.329 |
LIG_LIR_Apic_2 | 654 | 658 | PF02991 | 0.443 |
LIG_LIR_Gen_1 | 113 | 123 | PF02991 | 0.330 |
LIG_LIR_Gen_1 | 146 | 156 | PF02991 | 0.327 |
LIG_LIR_Gen_1 | 282 | 292 | PF02991 | 0.304 |
LIG_LIR_Gen_1 | 35 | 46 | PF02991 | 0.302 |
LIG_LIR_Gen_1 | 6 | 16 | PF02991 | 0.546 |
LIG_LIR_Gen_1 | 66 | 77 | PF02991 | 0.284 |
LIG_LIR_Gen_1 | 721 | 730 | PF02991 | 0.359 |
LIG_LIR_Gen_1 | 777 | 784 | PF02991 | 0.407 |
LIG_LIR_Gen_1 | 787 | 798 | PF02991 | 0.356 |
LIG_LIR_LC3C_4 | 260 | 264 | PF02991 | 0.349 |
LIG_LIR_Nem_3 | 113 | 118 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 146 | 151 | PF02991 | 0.285 |
LIG_LIR_Nem_3 | 163 | 169 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 26 | 31 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 282 | 287 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 288 | 292 | PF02991 | 0.299 |
LIG_LIR_Nem_3 | 35 | 41 | PF02991 | 0.290 |
LIG_LIR_Nem_3 | 564 | 569 | PF02991 | 0.348 |
LIG_LIR_Nem_3 | 622 | 626 | PF02991 | 0.330 |
LIG_LIR_Nem_3 | 633 | 639 | PF02991 | 0.315 |
LIG_LIR_Nem_3 | 66 | 72 | PF02991 | 0.281 |
LIG_LIR_Nem_3 | 710 | 715 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 721 | 727 | PF02991 | 0.276 |
LIG_LIR_Nem_3 | 777 | 782 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 787 | 793 | PF02991 | 0.315 |
LIG_LYPXL_yS_3 | 452 | 455 | PF13949 | 0.337 |
LIG_LYPXL_yS_3 | 566 | 569 | PF13949 | 0.380 |
LIG_MLH1_MIPbox_1 | 627 | 631 | PF16413 | 0.323 |
LIG_MYND_1 | 513 | 517 | PF01753 | 0.654 |
LIG_NRBOX | 126 | 132 | PF00104 | 0.362 |
LIG_NRBOX | 242 | 248 | PF00104 | 0.474 |
LIG_NRBOX | 257 | 263 | PF00104 | 0.474 |
LIG_Pex14_2 | 24 | 28 | PF04695 | 0.420 |
LIG_Pex14_2 | 318 | 322 | PF04695 | 0.437 |
LIG_Pex14_2 | 430 | 434 | PF04695 | 0.323 |
LIG_Pex14_2 | 536 | 540 | PF04695 | 0.437 |
LIG_Pex14_2 | 626 | 630 | PF04695 | 0.312 |
LIG_PTB_Apo_2 | 773 | 780 | PF02174 | 0.392 |
LIG_PTB_Phospho_1 | 773 | 779 | PF10480 | 0.401 |
LIG_REV1ctd_RIR_1 | 306 | 316 | PF16727 | 0.318 |
LIG_SH2_CRK | 624 | 628 | PF00017 | 0.329 |
LIG_SH2_NCK_1 | 169 | 173 | PF00017 | 0.456 |
LIG_SH2_PTP2 | 426 | 429 | PF00017 | 0.388 |
LIG_SH2_STAP1 | 545 | 549 | PF00017 | 0.402 |
LIG_SH2_STAP1 | 615 | 619 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 23 | 26 | PF00017 | 0.281 |
LIG_SH2_STAT5 | 276 | 279 | PF00017 | 0.289 |
LIG_SH2_STAT5 | 426 | 429 | PF00017 | 0.330 |
LIG_SH2_STAT5 | 46 | 49 | PF00017 | 0.353 |
LIG_SH2_STAT5 | 552 | 555 | PF00017 | 0.363 |
LIG_SH2_STAT5 | 615 | 618 | PF00017 | 0.323 |
LIG_SH2_STAT5 | 712 | 715 | PF00017 | 0.422 |
LIG_SH2_STAT5 | 8 | 11 | PF00017 | 0.629 |
LIG_SH2_STAT5 | 92 | 95 | PF00017 | 0.337 |
LIG_SH3_2 | 171 | 176 | PF14604 | 0.456 |
LIG_SH3_3 | 168 | 174 | PF00018 | 0.456 |
LIG_SH3_3 | 447 | 453 | PF00018 | 0.284 |
LIG_SH3_3 | 507 | 513 | PF00018 | 0.718 |
LIG_SH3_3 | 653 | 659 | PF00018 | 0.471 |
LIG_SH3_3 | 710 | 716 | PF00018 | 0.424 |
LIG_SH3_3 | 803 | 809 | PF00018 | 0.443 |
LIG_Sin3_3 | 328 | 335 | PF02671 | 0.349 |
LIG_SUMO_SIM_anti_2 | 260 | 265 | PF11976 | 0.349 |
LIG_SUMO_SIM_par_1 | 126 | 132 | PF11976 | 0.299 |
LIG_SUMO_SIM_par_1 | 14 | 19 | PF11976 | 0.396 |
LIG_SUMO_SIM_par_1 | 491 | 496 | PF11976 | 0.746 |
LIG_SUMO_SIM_par_1 | 780 | 785 | PF11976 | 0.442 |
LIG_SUMO_SIM_par_1 | 808 | 814 | PF11976 | 0.362 |
LIG_TRAF2_1 | 360 | 363 | PF00917 | 0.691 |
LIG_TRAF2_1 | 660 | 663 | PF00917 | 0.501 |
LIG_TYR_ITIM | 637 | 642 | PF00017 | 0.282 |
LIG_UBA3_1 | 435 | 443 | PF00899 | 0.472 |
LIG_WW_3 | 207 | 211 | PF00397 | 0.582 |
LIG_WW_3 | 508 | 512 | PF00397 | 0.757 |
MOD_CDC14_SPxK_1 | 173 | 176 | PF00782 | 0.456 |
MOD_CDK_SPK_2 | 479 | 484 | PF00069 | 0.797 |
MOD_CDK_SPxK_1 | 170 | 176 | PF00069 | 0.520 |
MOD_CDK_SPxK_1 | 479 | 485 | PF00069 | 0.771 |
MOD_CK1_1 | 170 | 176 | PF00069 | 0.532 |
MOD_CK1_1 | 202 | 208 | PF00069 | 0.541 |
MOD_CK1_1 | 344 | 350 | PF00069 | 0.736 |
MOD_CK1_1 | 367 | 373 | PF00069 | 0.729 |
MOD_CK1_1 | 416 | 422 | PF00069 | 0.546 |
MOD_CK1_1 | 595 | 601 | PF00069 | 0.560 |
MOD_CK1_1 | 654 | 660 | PF00069 | 0.447 |
MOD_CK1_1 | 681 | 687 | PF00069 | 0.584 |
MOD_CK1_1 | 728 | 734 | PF00069 | 0.420 |
MOD_CK1_1 | 85 | 91 | PF00069 | 0.436 |
MOD_CK2_1 | 553 | 559 | PF00069 | 0.369 |
MOD_Cter_Amidation | 767 | 770 | PF01082 | 0.583 |
MOD_GlcNHglycan | 118 | 121 | PF01048 | 0.400 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.353 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.288 |
MOD_GlcNHglycan | 222 | 225 | PF01048 | 0.413 |
MOD_GlcNHglycan | 237 | 240 | PF01048 | 0.413 |
MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.571 |
MOD_GlcNHglycan | 343 | 346 | PF01048 | 0.546 |
MOD_GlcNHglycan | 351 | 354 | PF01048 | 0.560 |
MOD_GlcNHglycan | 366 | 369 | PF01048 | 0.581 |
MOD_GlcNHglycan | 382 | 385 | PF01048 | 0.382 |
MOD_GlcNHglycan | 477 | 480 | PF01048 | 0.564 |
MOD_GlcNHglycan | 50 | 53 | PF01048 | 0.501 |
MOD_GlcNHglycan | 555 | 558 | PF01048 | 0.590 |
MOD_GlcNHglycan | 663 | 666 | PF01048 | 0.658 |
MOD_GlcNHglycan | 733 | 736 | PF01048 | 0.571 |
MOD_GlcNHglycan | 758 | 761 | PF01048 | 0.624 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.337 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.370 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.550 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.702 |
MOD_GSK3_1 | 367 | 374 | PF00069 | 0.770 |
MOD_GSK3_1 | 375 | 382 | PF00069 | 0.752 |
MOD_GSK3_1 | 475 | 482 | PF00069 | 0.720 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.301 |
MOD_GSK3_1 | 601 | 608 | PF00069 | 0.478 |
MOD_GSK3_1 | 676 | 683 | PF00069 | 0.588 |
MOD_GSK3_1 | 686 | 693 | PF00069 | 0.581 |
MOD_N-GLC_1 | 364 | 369 | PF02516 | 0.572 |
MOD_N-GLC_1 | 756 | 761 | PF02516 | 0.622 |
MOD_N-GLC_2 | 99 | 101 | PF02516 | 0.382 |
MOD_NEK2_1 | 110 | 115 | PF00069 | 0.394 |
MOD_NEK2_1 | 116 | 121 | PF00069 | 0.394 |
MOD_NEK2_1 | 129 | 134 | PF00069 | 0.491 |
MOD_NEK2_1 | 16 | 21 | PF00069 | 0.402 |
MOD_NEK2_1 | 220 | 225 | PF00069 | 0.437 |
MOD_NEK2_1 | 254 | 259 | PF00069 | 0.425 |
MOD_NEK2_1 | 292 | 297 | PF00069 | 0.382 |
MOD_NEK2_1 | 340 | 345 | PF00069 | 0.708 |
MOD_NEK2_1 | 375 | 380 | PF00069 | 0.754 |
MOD_NEK2_1 | 392 | 397 | PF00069 | 0.657 |
MOD_NEK2_1 | 436 | 441 | PF00069 | 0.430 |
MOD_NEK2_1 | 457 | 462 | PF00069 | 0.374 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.301 |
MOD_NEK2_1 | 541 | 546 | PF00069 | 0.351 |
MOD_NEK2_1 | 641 | 646 | PF00069 | 0.331 |
MOD_NEK2_1 | 751 | 756 | PF00069 | 0.356 |
MOD_NEK2_1 | 798 | 803 | PF00069 | 0.472 |
MOD_NEK2_2 | 23 | 28 | PF00069 | 0.299 |
MOD_PIKK_1 | 160 | 166 | PF00454 | 0.492 |
MOD_PIKK_1 | 605 | 611 | PF00454 | 0.503 |
MOD_PIKK_1 | 768 | 774 | PF00454 | 0.509 |
MOD_PKA_1 | 511 | 517 | PF00069 | 0.784 |
MOD_PKA_2 | 194 | 200 | PF00069 | 0.563 |
MOD_PKA_2 | 277 | 283 | PF00069 | 0.355 |
MOD_PKA_2 | 3 | 9 | PF00069 | 0.655 |
MOD_PKA_2 | 380 | 386 | PF00069 | 0.745 |
MOD_PKA_2 | 416 | 422 | PF00069 | 0.582 |
MOD_PKA_2 | 511 | 517 | PF00069 | 0.784 |
MOD_PKA_2 | 690 | 696 | PF00069 | 0.511 |
MOD_PKA_2 | 768 | 774 | PF00069 | 0.528 |
MOD_PKB_1 | 377 | 385 | PF00069 | 0.750 |
MOD_Plk_1 | 34 | 40 | PF00069 | 0.324 |
MOD_Plk_1 | 364 | 370 | PF00069 | 0.795 |
MOD_Plk_1 | 756 | 762 | PF00069 | 0.423 |
MOD_Plk_4 | 110 | 116 | PF00069 | 0.377 |
MOD_Plk_4 | 139 | 145 | PF00069 | 0.396 |
MOD_Plk_4 | 257 | 263 | PF00069 | 0.488 |
MOD_Plk_4 | 265 | 271 | PF00069 | 0.353 |
MOD_Plk_4 | 371 | 377 | PF00069 | 0.782 |
MOD_Plk_4 | 392 | 398 | PF00069 | 0.667 |
MOD_Plk_4 | 626 | 632 | PF00069 | 0.344 |
MOD_Plk_4 | 651 | 657 | PF00069 | 0.453 |
MOD_Plk_4 | 746 | 752 | PF00069 | 0.422 |
MOD_ProDKin_1 | 167 | 173 | PF00069 | 0.493 |
MOD_ProDKin_1 | 195 | 201 | PF00069 | 0.550 |
MOD_ProDKin_1 | 367 | 373 | PF00069 | 0.736 |
MOD_ProDKin_1 | 446 | 452 | PF00069 | 0.355 |
MOD_ProDKin_1 | 479 | 485 | PF00069 | 0.745 |
MOD_ProDKin_1 | 486 | 492 | PF00069 | 0.754 |
MOD_ProDKin_1 | 519 | 525 | PF00069 | 0.655 |
MOD_ProDKin_1 | 592 | 598 | PF00069 | 0.542 |
MOD_ProDKin_1 | 654 | 660 | PF00069 | 0.414 |
MOD_ProDKin_1 | 678 | 684 | PF00069 | 0.603 |
MOD_ProDKin_1 | 725 | 731 | PF00069 | 0.365 |
MOD_ProDKin_1 | 784 | 790 | PF00069 | 0.376 |
MOD_SUMO_for_1 | 483 | 486 | PF00179 | 0.760 |
TRG_DiLeu_BaEn_2 | 35 | 41 | PF01217 | 0.301 |
TRG_ENDOCYTIC_2 | 289 | 292 | PF00928 | 0.324 |
TRG_ENDOCYTIC_2 | 452 | 455 | PF00928 | 0.337 |
TRG_ENDOCYTIC_2 | 566 | 569 | PF00928 | 0.335 |
TRG_ENDOCYTIC_2 | 614 | 617 | PF00928 | 0.382 |
TRG_ENDOCYTIC_2 | 639 | 642 | PF00928 | 0.335 |
TRG_ENDOCYTIC_2 | 779 | 782 | PF00928 | 0.400 |
TRG_ENDOCYTIC_2 | 795 | 798 | PF00928 | 0.324 |
TRG_ENDOCYTIC_2 | 8 | 11 | PF00928 | 0.622 |
TRG_ENDOCYTIC_2 | 92 | 95 | PF00928 | 0.359 |
TRG_ER_diArg_1 | 336 | 338 | PF00400 | 0.670 |
TRG_ER_diArg_1 | 376 | 379 | PF00400 | 0.753 |
TRG_ER_diArg_1 | 510 | 512 | PF00400 | 0.798 |
TRG_ER_diArg_1 | 584 | 586 | PF00400 | 0.516 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I3C3 | Leptomonas seymouri | 53% | 100% |
A0A0S4ITY5 | Bodo saltans | 27% | 100% |
A0A422NUF2 | Trypanosoma rangeli | 40% | 100% |
C9ZQC6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
E9AGA5 | Leishmania infantum | 99% | 100% |
E9ANU3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 98% |
Q4QGS7 | Leishmania major | 80% | 99% |