Carries an ATP pyrophosphate-lyase domain on its cytoplasmic segment. Likely acts as a receptor for some unknown extracellular stimulus. Extremely expanded kinetoplastid protein family.. Expressed in the insect stage (promastigote) but not in the mammalian host stage of the parasite life cycle.. Localization: Cell surface (by feature)
Receptors, Receptor-type adenylate cyclase b (Fragment) RAC-B1
| 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. | yes | yes: 55 |
| 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 | yes | yes: 38, no: 28 |
| NetGPI | no | yes: 0, no: 66 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0016020 | membrane | 2 | 60 |
| GO:0110165 | cellular anatomical entity | 1 | 64 |
Related structures:
AlphaFold database: A4HX88
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006139 | nucleobase-containing compound metabolic process | 3 | 59 |
| GO:0006163 | purine nucleotide metabolic process | 5 | 59 |
| GO:0006164 | purine nucleotide biosynthetic process | 6 | 59 |
| GO:0006171 | cAMP biosynthetic process | 8 | 59 |
| GO:0006725 | cellular aromatic compound metabolic process | 3 | 59 |
| GO:0006753 | nucleoside phosphate metabolic process | 4 | 59 |
| GO:0006793 | phosphorus metabolic process | 3 | 59 |
| GO:0006796 | phosphate-containing compound metabolic process | 4 | 59 |
| GO:0006807 | nitrogen compound metabolic process | 2 | 59 |
| GO:0007165 | signal transduction | 2 | 59 |
| GO:0008152 | metabolic process | 1 | 59 |
| GO:0009058 | biosynthetic process | 2 | 59 |
| GO:0009117 | nucleotide metabolic process | 5 | 59 |
| GO:0009150 | purine ribonucleotide metabolic process | 6 | 59 |
| GO:0009152 | purine ribonucleotide biosynthetic process | 7 | 59 |
| GO:0009165 | nucleotide biosynthetic process | 6 | 59 |
| GO:0009187 | cyclic nucleotide metabolic process | 6 | 59 |
| GO:0009190 | cyclic nucleotide biosynthetic process | 7 | 59 |
| GO:0009259 | ribonucleotide metabolic process | 5 | 59 |
| GO:0009260 | ribonucleotide biosynthetic process | 6 | 59 |
| GO:0009987 | cellular process | 1 | 59 |
| GO:0018130 | heterocycle biosynthetic process | 4 | 59 |
| GO:0019438 | aromatic compound biosynthetic process | 4 | 59 |
| GO:0019637 | organophosphate metabolic process | 3 | 59 |
| GO:0019693 | ribose phosphate metabolic process | 4 | 59 |
| GO:0034641 | cellular nitrogen compound metabolic process | 3 | 59 |
| GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 59 |
| GO:0035556 | intracellular signal transduction | 3 | 59 |
| GO:0044237 | cellular metabolic process | 2 | 59 |
| GO:0044238 | primary metabolic process | 2 | 59 |
| GO:0044249 | cellular biosynthetic process | 3 | 59 |
| GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 59 |
| GO:0044281 | small molecule metabolic process | 2 | 59 |
| GO:0046058 | cAMP metabolic process | 7 | 59 |
| GO:0046390 | ribose phosphate biosynthetic process | 5 | 59 |
| GO:0046483 | heterocycle metabolic process | 3 | 59 |
| GO:0050789 | regulation of biological process | 2 | 59 |
| GO:0050794 | regulation of cellular process | 3 | 59 |
| GO:0052652 | cyclic purine nucleotide metabolic process | 6 | 59 |
| GO:0055086 | nucleobase-containing small molecule metabolic process | 3 | 59 |
| GO:0065007 | biological regulation | 1 | 59 |
| GO:0071704 | organic substance metabolic process | 2 | 59 |
| GO:0072521 | purine-containing compound metabolic process | 4 | 59 |
| GO:0072522 | purine-containing compound biosynthetic process | 5 | 59 |
| GO:0090407 | organophosphate biosynthetic process | 4 | 59 |
| GO:1901135 | carbohydrate derivative metabolic process | 3 | 59 |
| GO:1901137 | carbohydrate derivative biosynthetic process | 4 | 59 |
| GO:1901293 | nucleoside phosphate biosynthetic process | 5 | 59 |
| GO:1901360 | organic cyclic compound metabolic process | 3 | 59 |
| GO:1901362 | organic cyclic compound biosynthetic process | 4 | 59 |
| GO:1901564 | organonitrogen compound metabolic process | 3 | 59 |
| GO:1901566 | organonitrogen compound biosynthetic process | 4 | 59 |
| GO:1901576 | organic substance biosynthetic process | 3 | 59 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0003824 | catalytic activity | 1 | 53 |
| GO:0004016 | adenylate cyclase activity | 3 | 4 |
| GO:0009975 | cyclase activity | 2 | 4 |
| GO:0016829 | lyase activity | 2 | 53 |
| GO:0016849 | phosphorus-oxygen lyase activity | 3 | 4 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 383 | 387 | PF00656 | 0.485 |
| CLV_NRD_NRD_1 | 207 | 209 | PF00675 | 0.596 |
| CLV_NRD_NRD_1 | 660 | 662 | PF00675 | 0.522 |
| CLV_NRD_NRD_1 | 9 | 11 | PF00675 | 0.752 |
| CLV_PCSK_FUR_1 | 205 | 209 | PF00082 | 0.589 |
| CLV_PCSK_KEX2_1 | 207 | 209 | PF00082 | 0.597 |
| CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.748 |
| CLV_PCSK_SKI1_1 | 107 | 111 | PF00082 | 0.638 |
| CLV_PCSK_SKI1_1 | 129 | 133 | PF00082 | 0.572 |
| CLV_PCSK_SKI1_1 | 208 | 212 | PF00082 | 0.581 |
| CLV_PCSK_SKI1_1 | 283 | 287 | PF00082 | 0.511 |
| CLV_PCSK_SKI1_1 | 527 | 531 | PF00082 | 0.431 |
| CLV_PCSK_SKI1_1 | 548 | 552 | PF00082 | 0.450 |
| CLV_PCSK_SKI1_1 | 632 | 636 | PF00082 | 0.560 |
| CLV_PCSK_SKI1_1 | 746 | 750 | PF00082 | 0.480 |
| CLV_PCSK_SKI1_1 | 83 | 87 | PF00082 | 0.604 |
| CLV_Separin_Metazoa | 605 | 609 | PF03568 | 0.313 |
| DEG_APCC_DBOX_1 | 599 | 607 | PF00400 | 0.430 |
| DEG_COP1_1 | 587 | 596 | PF00400 | 0.201 |
| DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.742 |
| DEG_SCF_FBW7_2 | 874 | 880 | PF00400 | 0.463 |
| DEG_SPOP_SBC_1 | 289 | 293 | PF00917 | 0.433 |
| DOC_CDC14_PxL_1 | 131 | 139 | PF14671 | 0.430 |
| DOC_CDC14_PxL_1 | 519 | 527 | PF14671 | 0.250 |
| DOC_CKS1_1 | 874 | 879 | PF01111 | 0.401 |
| DOC_CYCLIN_RxL_1 | 507 | 518 | PF00134 | 0.299 |
| DOC_CYCLIN_RxL_1 | 83 | 94 | PF00134 | 0.406 |
| DOC_CYCLIN_yCln2_LP_2 | 236 | 242 | PF00134 | 0.399 |
| DOC_CYCLIN_yCln2_LP_2 | 335 | 341 | PF00134 | 0.320 |
| DOC_CYCLIN_yCln2_LP_2 | 508 | 514 | PF00134 | 0.399 |
| DOC_CYCLIN_yCln2_LP_2 | 871 | 877 | PF00134 | 0.399 |
| DOC_MAPK_gen_1 | 205 | 214 | PF00069 | 0.300 |
| DOC_MAPK_gen_1 | 30 | 40 | PF00069 | 0.645 |
| DOC_MAPK_gen_1 | 83 | 92 | PF00069 | 0.404 |
| DOC_MAPK_MEF2A_6 | 186 | 193 | PF00069 | 0.342 |
| DOC_MAPK_MEF2A_6 | 33 | 42 | PF00069 | 0.537 |
| DOC_MAPK_MEF2A_6 | 714 | 722 | PF00069 | 0.283 |
| DOC_MAPK_MEF2A_6 | 83 | 92 | PF00069 | 0.409 |
| DOC_PP1_RVXF_1 | 508 | 515 | PF00149 | 0.300 |
| DOC_PP1_RVXF_1 | 525 | 531 | PF00149 | 0.195 |
| DOC_PP1_RVXF_1 | 546 | 553 | PF00149 | 0.325 |
| DOC_PP1_RVXF_1 | 744 | 751 | PF00149 | 0.268 |
| DOC_PP1_RVXF_1 | 823 | 830 | PF00149 | 0.212 |
| DOC_PP2B_LxvP_1 | 236 | 239 | PF13499 | 0.350 |
| DOC_PP4_FxxP_1 | 165 | 168 | PF00568 | 0.415 |
| DOC_SPAK_OSR1_1 | 843 | 847 | PF12202 | 0.268 |
| DOC_USP7_MATH_1 | 289 | 293 | PF00917 | 0.430 |
| DOC_USP7_MATH_1 | 382 | 386 | PF00917 | 0.379 |
| DOC_USP7_MATH_1 | 60 | 64 | PF00917 | 0.408 |
| DOC_USP7_MATH_1 | 676 | 680 | PF00917 | 0.430 |
| DOC_USP7_MATH_1 | 735 | 739 | PF00917 | 0.406 |
| DOC_WW_Pin1_4 | 152 | 157 | PF00397 | 0.403 |
| DOC_WW_Pin1_4 | 317 | 322 | PF00397 | 0.399 |
| DOC_WW_Pin1_4 | 592 | 597 | PF00397 | 0.329 |
| DOC_WW_Pin1_4 | 781 | 786 | PF00397 | 0.325 |
| DOC_WW_Pin1_4 | 801 | 806 | PF00397 | 0.296 |
| DOC_WW_Pin1_4 | 836 | 841 | PF00397 | 0.336 |
| DOC_WW_Pin1_4 | 870 | 875 | PF00397 | 0.362 |
| DOC_WW_Pin1_4 | 888 | 893 | PF00397 | 0.381 |
| LIG_14-3-3_CanoR_1 | 205 | 214 | PF00244 | 0.339 |
| LIG_14-3-3_CanoR_1 | 290 | 298 | PF00244 | 0.382 |
| LIG_14-3-3_CanoR_1 | 483 | 489 | PF00244 | 0.400 |
| LIG_14-3-3_CanoR_1 | 632 | 641 | PF00244 | 0.426 |
| LIG_14-3-3_CanoR_1 | 661 | 669 | PF00244 | 0.348 |
| LIG_14-3-3_CanoR_1 | 746 | 751 | PF00244 | 0.401 |
| LIG_14-3-3_CanoR_1 | 771 | 780 | PF00244 | 0.384 |
| LIG_14-3-3_CanoR_1 | 825 | 830 | PF00244 | 0.383 |
| LIG_14-3-3_CanoR_1 | 884 | 892 | PF00244 | 0.529 |
| LIG_APCC_ABBA_1 | 141 | 146 | PF00400 | 0.413 |
| LIG_APCC_ABBA_1 | 307 | 312 | PF00400 | 0.317 |
| LIG_APCC_ABBA_1 | 719 | 724 | PF00400 | 0.270 |
| LIG_eIF4E_1 | 29 | 35 | PF01652 | 0.671 |
| LIG_FHA_1 | 115 | 121 | PF00498 | 0.371 |
| LIG_FHA_1 | 304 | 310 | PF00498 | 0.365 |
| LIG_FHA_1 | 355 | 361 | PF00498 | 0.430 |
| LIG_FHA_1 | 44 | 50 | PF00498 | 0.629 |
| LIG_FHA_1 | 552 | 558 | PF00498 | 0.359 |
| LIG_FHA_1 | 655 | 661 | PF00498 | 0.335 |
| LIG_FHA_1 | 678 | 684 | PF00498 | 0.383 |
| LIG_FHA_1 | 713 | 719 | PF00498 | 0.399 |
| LIG_FHA_1 | 782 | 788 | PF00498 | 0.353 |
| LIG_FHA_1 | 817 | 823 | PF00498 | 0.352 |
| LIG_FHA_1 | 900 | 906 | PF00498 | 0.388 |
| LIG_FHA_2 | 253 | 259 | PF00498 | 0.414 |
| LIG_FHA_2 | 318 | 324 | PF00498 | 0.409 |
| LIG_FHA_2 | 416 | 422 | PF00498 | 0.403 |
| LIG_FHA_2 | 697 | 703 | PF00498 | 0.335 |
| LIG_FHA_2 | 837 | 843 | PF00498 | 0.453 |
| LIG_GBD_Chelix_1 | 406 | 414 | PF00786 | 0.505 |
| LIG_LIR_Apic_2 | 292 | 298 | PF02991 | 0.253 |
| LIG_LIR_Apic_2 | 451 | 455 | PF02991 | 0.389 |
| LIG_LIR_Apic_2 | 589 | 594 | PF02991 | 0.320 |
| LIG_LIR_Apic_2 | 666 | 672 | PF02991 | 0.439 |
| LIG_LIR_Gen_1 | 209 | 219 | PF02991 | 0.427 |
| LIG_LIR_Gen_1 | 255 | 265 | PF02991 | 0.320 |
| LIG_LIR_Gen_1 | 749 | 755 | PF02991 | 0.342 |
| LIG_LIR_Nem_3 | 133 | 137 | PF02991 | 0.390 |
| LIG_LIR_Nem_3 | 209 | 214 | PF02991 | 0.399 |
| LIG_LIR_Nem_3 | 217 | 222 | PF02991 | 0.409 |
| LIG_LIR_Nem_3 | 306 | 310 | PF02991 | 0.351 |
| LIG_LIR_Nem_3 | 429 | 434 | PF02991 | 0.410 |
| LIG_LIR_Nem_3 | 516 | 522 | PF02991 | 0.344 |
| LIG_LIR_Nem_3 | 549 | 555 | PF02991 | 0.386 |
| LIG_LIR_Nem_3 | 749 | 753 | PF02991 | 0.335 |
| LIG_LIR_Nem_3 | 828 | 832 | PF02991 | 0.248 |
| LIG_LIR_Nem_3 | 841 | 847 | PF02991 | 0.470 |
| LIG_LYPXL_yS_3 | 134 | 137 | PF13949 | 0.332 |
| LIG_LYPXL_yS_3 | 522 | 525 | PF13949 | 0.419 |
| LIG_LYPXL_yS_3 | 729 | 732 | PF13949 | 0.412 |
| LIG_MYND_3 | 614 | 618 | PF01753 | 0.380 |
| LIG_NRBOX | 602 | 608 | PF00104 | 0.243 |
| LIG_PCNA_yPIPBox_3 | 527 | 540 | PF02747 | 0.415 |
| LIG_PDZ_Class_2 | 904 | 909 | PF00595 | 0.153 |
| LIG_Pex14_2 | 165 | 169 | PF04695 | 0.409 |
| LIG_PTB_Apo_2 | 389 | 396 | PF02174 | 0.313 |
| LIG_PTB_Apo_2 | 606 | 613 | PF02174 | 0.422 |
| LIG_PTB_Apo_2 | 69 | 76 | PF02174 | 0.347 |
| LIG_PTB_Phospho_1 | 606 | 612 | PF10480 | 0.430 |
| LIG_PTB_Phospho_1 | 69 | 75 | PF10480 | 0.351 |
| LIG_SH2_CRK | 452 | 456 | PF00017 | 0.390 |
| LIG_SH2_CRK | 625 | 629 | PF00017 | 0.412 |
| LIG_SH2_CRK | 669 | 673 | PF00017 | 0.459 |
| LIG_SH2_GRB2like | 390 | 393 | PF00017 | 0.442 |
| LIG_SH2_GRB2like | 542 | 545 | PF00017 | 0.388 |
| LIG_SH2_GRB2like | 669 | 672 | PF00017 | 0.456 |
| LIG_SH2_GRB2like | 847 | 850 | PF00017 | 0.287 |
| LIG_SH2_NCK_1 | 2 | 6 | PF00017 | 0.449 |
| LIG_SH2_NCK_1 | 669 | 673 | PF00017 | 0.317 |
| LIG_SH2_PTP2 | 295 | 298 | PF00017 | 0.371 |
| LIG_SH2_PTP2 | 610 | 613 | PF00017 | 0.395 |
| LIG_SH2_SRC | 2 | 5 | PF00017 | 0.450 |
| LIG_SH2_SRC | 669 | 672 | PF00017 | 0.442 |
| LIG_SH2_STAP1 | 242 | 246 | PF00017 | 0.412 |
| LIG_SH2_STAP1 | 311 | 315 | PF00017 | 0.410 |
| LIG_SH2_STAP1 | 534 | 538 | PF00017 | 0.341 |
| LIG_SH2_STAP1 | 542 | 546 | PF00017 | 0.320 |
| LIG_SH2_STAT3 | 468 | 471 | PF00017 | 0.401 |
| LIG_SH2_STAT3 | 534 | 537 | PF00017 | 0.411 |
| LIG_SH2_STAT3 | 850 | 853 | PF00017 | 0.312 |
| LIG_SH2_STAT5 | 101 | 104 | PF00017 | 0.394 |
| LIG_SH2_STAT5 | 183 | 186 | PF00017 | 0.290 |
| LIG_SH2_STAT5 | 213 | 216 | PF00017 | 0.315 |
| LIG_SH2_STAT5 | 295 | 298 | PF00017 | 0.297 |
| LIG_SH2_STAT5 | 390 | 393 | PF00017 | 0.397 |
| LIG_SH2_STAT5 | 441 | 444 | PF00017 | 0.291 |
| LIG_SH2_STAT5 | 468 | 471 | PF00017 | 0.379 |
| LIG_SH2_STAT5 | 519 | 522 | PF00017 | 0.280 |
| LIG_SH2_STAT5 | 591 | 594 | PF00017 | 0.419 |
| LIG_SH2_STAT5 | 610 | 613 | PF00017 | 0.298 |
| LIG_SH2_STAT5 | 69 | 72 | PF00017 | 0.374 |
| LIG_SH2_STAT5 | 783 | 786 | PF00017 | 0.332 |
| LIG_SH3_3 | 137 | 143 | PF00018 | 0.306 |
| LIG_SH3_3 | 590 | 596 | PF00018 | 0.345 |
| LIG_SH3_3 | 863 | 869 | PF00018 | 0.361 |
| LIG_SH3_3 | 871 | 877 | PF00018 | 0.349 |
| LIG_SUMO_SIM_anti_2 | 121 | 128 | PF11976 | 0.408 |
| LIG_SUMO_SIM_anti_2 | 226 | 233 | PF11976 | 0.440 |
| LIG_SUMO_SIM_anti_2 | 715 | 724 | PF11976 | 0.316 |
| LIG_SUMO_SIM_par_1 | 226 | 233 | PF11976 | 0.439 |
| LIG_SUMO_SIM_par_1 | 45 | 51 | PF11976 | 0.605 |
| LIG_SUMO_SIM_par_1 | 694 | 699 | PF11976 | 0.362 |
| LIG_SUMO_SIM_par_1 | 715 | 724 | PF11976 | 0.372 |
| LIG_SUMO_SIM_par_1 | 854 | 859 | PF11976 | 0.412 |
| LIG_TYR_ITIM | 623 | 628 | PF00017 | 0.374 |
| LIG_TYR_ITIM | 727 | 732 | PF00017 | 0.321 |
| LIG_UBA3_1 | 193 | 198 | PF00899 | 0.412 |
| LIG_UBA3_1 | 621 | 627 | PF00899 | 0.373 |
| LIG_Vh1_VBS_1 | 241 | 259 | PF01044 | 0.255 |
| LIG_WRC_WIRS_1 | 219 | 224 | PF05994 | 0.321 |
| LIG_WRC_WIRS_1 | 297 | 302 | PF05994 | 0.398 |
| LIG_WRC_WIRS_1 | 747 | 752 | PF05994 | 0.412 |
| MOD_CDK_SPxxK_3 | 836 | 843 | PF00069 | 0.322 |
| MOD_CDK_SPxxK_3 | 888 | 895 | PF00069 | 0.514 |
| MOD_CK1_1 | 245 | 251 | PF00069 | 0.397 |
| MOD_CK1_1 | 328 | 334 | PF00069 | 0.417 |
| MOD_CK1_1 | 384 | 390 | PF00069 | 0.465 |
| MOD_CK1_1 | 492 | 498 | PF00069 | 0.365 |
| MOD_CK1_1 | 500 | 506 | PF00069 | 0.360 |
| MOD_CK1_1 | 636 | 642 | PF00069 | 0.315 |
| MOD_CK1_1 | 663 | 669 | PF00069 | 0.321 |
| MOD_CK1_1 | 679 | 685 | PF00069 | 0.378 |
| MOD_CK1_1 | 757 | 763 | PF00069 | 0.402 |
| MOD_CK1_1 | 873 | 879 | PF00069 | 0.455 |
| MOD_CK2_1 | 151 | 157 | PF00069 | 0.373 |
| MOD_CK2_1 | 223 | 229 | PF00069 | 0.401 |
| MOD_CK2_1 | 415 | 421 | PF00069 | 0.349 |
| MOD_CK2_1 | 60 | 66 | PF00069 | 0.493 |
| MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.606 |
| MOD_GlcNHglycan | 19 | 22 | PF01048 | 0.708 |
| MOD_GlcNHglycan | 242 | 245 | PF01048 | 0.569 |
| MOD_GlcNHglycan | 292 | 295 | PF01048 | 0.597 |
| MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.615 |
| MOD_GlcNHglycan | 386 | 389 | PF01048 | 0.658 |
| MOD_GlcNHglycan | 410 | 413 | PF01048 | 0.572 |
| MOD_GlcNHglycan | 474 | 477 | PF01048 | 0.581 |
| MOD_GlcNHglycan | 491 | 494 | PF01048 | 0.575 |
| MOD_GlcNHglycan | 628 | 631 | PF01048 | 0.536 |
| MOD_GlcNHglycan | 638 | 641 | PF01048 | 0.537 |
| MOD_GlcNHglycan | 662 | 665 | PF01048 | 0.590 |
| MOD_GlcNHglycan | 684 | 687 | PF01048 | 0.543 |
| MOD_GlcNHglycan | 761 | 764 | PF01048 | 0.646 |
| MOD_GlcNHglycan | 774 | 777 | PF01048 | 0.540 |
| MOD_GlcNHglycan | 809 | 812 | PF01048 | 0.618 |
| MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.536 |
| MOD_GSK3_1 | 114 | 121 | PF00069 | 0.353 |
| MOD_GSK3_1 | 167 | 174 | PF00069 | 0.326 |
| MOD_GSK3_1 | 240 | 247 | PF00069 | 0.361 |
| MOD_GSK3_1 | 284 | 291 | PF00069 | 0.370 |
| MOD_GSK3_1 | 325 | 332 | PF00069 | 0.398 |
| MOD_GSK3_1 | 333 | 340 | PF00069 | 0.427 |
| MOD_GSK3_1 | 380 | 387 | PF00069 | 0.491 |
| MOD_GSK3_1 | 43 | 50 | PF00069 | 0.623 |
| MOD_GSK3_1 | 472 | 479 | PF00069 | 0.399 |
| MOD_GSK3_1 | 492 | 499 | PF00069 | 0.318 |
| MOD_GSK3_1 | 500 | 507 | PF00069 | 0.368 |
| MOD_GSK3_1 | 513 | 520 | PF00069 | 0.322 |
| MOD_GSK3_1 | 551 | 558 | PF00069 | 0.310 |
| MOD_GSK3_1 | 632 | 639 | PF00069 | 0.352 |
| MOD_GSK3_1 | 672 | 679 | PF00069 | 0.379 |
| MOD_GSK3_1 | 731 | 738 | PF00069 | 0.397 |
| MOD_GSK3_1 | 786 | 793 | PF00069 | 0.370 |
| MOD_GSK3_1 | 812 | 819 | PF00069 | 0.382 |
| MOD_GSK3_1 | 821 | 828 | PF00069 | 0.309 |
| MOD_GSK3_1 | 834 | 841 | PF00069 | 0.427 |
| MOD_GSK3_1 | 869 | 876 | PF00069 | 0.381 |
| MOD_GSK3_1 | 884 | 891 | PF00069 | 0.450 |
| MOD_GSK3_1 | 899 | 906 | PF00069 | 0.325 |
| MOD_N-GLC_1 | 252 | 257 | PF02516 | 0.619 |
| MOD_N-GLC_1 | 426 | 431 | PF02516 | 0.531 |
| MOD_N-GLC_1 | 555 | 560 | PF02516 | 0.564 |
| MOD_N-GLC_1 | 654 | 659 | PF02516 | 0.570 |
| MOD_N-GLC_1 | 781 | 786 | PF02516 | 0.547 |
| MOD_N-GLC_1 | 807 | 812 | PF02516 | 0.590 |
| MOD_NEK2_1 | 169 | 174 | PF00069 | 0.359 |
| MOD_NEK2_1 | 230 | 235 | PF00069 | 0.364 |
| MOD_NEK2_1 | 260 | 265 | PF00069 | 0.308 |
| MOD_NEK2_1 | 354 | 359 | PF00069 | 0.399 |
| MOD_NEK2_1 | 47 | 52 | PF00069 | 0.541 |
| MOD_NEK2_1 | 496 | 501 | PF00069 | 0.281 |
| MOD_NEK2_1 | 515 | 520 | PF00069 | 0.212 |
| MOD_NEK2_1 | 577 | 582 | PF00069 | 0.266 |
| MOD_NEK2_1 | 660 | 665 | PF00069 | 0.301 |
| MOD_NEK2_1 | 696 | 701 | PF00069 | 0.380 |
| MOD_NEK2_1 | 812 | 817 | PF00069 | 0.327 |
| MOD_NEK2_2 | 171 | 176 | PF00069 | 0.386 |
| MOD_PIKK_1 | 399 | 405 | PF00454 | 0.360 |
| MOD_PIKK_1 | 434 | 440 | PF00454 | 0.395 |
| MOD_PIKK_1 | 494 | 500 | PF00454 | 0.386 |
| MOD_PK_1 | 739 | 745 | PF00069 | 0.300 |
| MOD_PKA_2 | 206 | 212 | PF00069 | 0.413 |
| MOD_PKA_2 | 289 | 295 | PF00069 | 0.397 |
| MOD_PKA_2 | 29 | 35 | PF00069 | 0.605 |
| MOD_PKA_2 | 660 | 666 | PF00069 | 0.342 |
| MOD_PKB_1 | 882 | 890 | PF00069 | 0.379 |
| MOD_Plk_1 | 252 | 258 | PF00069 | 0.377 |
| MOD_Plk_1 | 360 | 366 | PF00069 | 0.440 |
| MOD_Plk_1 | 426 | 432 | PF00069 | 0.329 |
| MOD_Plk_1 | 503 | 509 | PF00069 | 0.368 |
| MOD_Plk_1 | 548 | 554 | PF00069 | 0.355 |
| MOD_Plk_1 | 571 | 577 | PF00069 | 0.391 |
| MOD_Plk_1 | 654 | 660 | PF00069 | 0.339 |
| MOD_Plk_1 | 712 | 718 | PF00069 | 0.386 |
| MOD_Plk_1 | 807 | 813 | PF00069 | 0.365 |
| MOD_Plk_2-3 | 223 | 229 | PF00069 | 0.406 |
| MOD_Plk_2-3 | 571 | 577 | PF00069 | 0.413 |
| MOD_Plk_4 | 133 | 139 | PF00069 | 0.385 |
| MOD_Plk_4 | 223 | 229 | PF00069 | 0.384 |
| MOD_Plk_4 | 360 | 366 | PF00069 | 0.394 |
| MOD_Plk_4 | 410 | 416 | PF00069 | 0.393 |
| MOD_Plk_4 | 578 | 584 | PF00069 | 0.274 |
| MOD_Plk_4 | 713 | 719 | PF00069 | 0.380 |
| MOD_Plk_4 | 728 | 734 | PF00069 | 0.361 |
| MOD_Plk_4 | 812 | 818 | PF00069 | 0.294 |
| MOD_Plk_4 | 903 | 909 | PF00069 | 0.283 |
| MOD_ProDKin_1 | 152 | 158 | PF00069 | 0.397 |
| MOD_ProDKin_1 | 317 | 323 | PF00069 | 0.401 |
| MOD_ProDKin_1 | 592 | 598 | PF00069 | 0.328 |
| MOD_ProDKin_1 | 781 | 787 | PF00069 | 0.322 |
| MOD_ProDKin_1 | 801 | 807 | PF00069 | 0.295 |
| MOD_ProDKin_1 | 836 | 842 | PF00069 | 0.337 |
| MOD_ProDKin_1 | 870 | 876 | PF00069 | 0.365 |
| MOD_ProDKin_1 | 888 | 894 | PF00069 | 0.377 |
| MOD_SUMO_rev_2 | 217 | 227 | PF00179 | 0.355 |
| MOD_SUMO_rev_2 | 363 | 372 | PF00179 | 0.422 |
| MOD_SUMO_rev_2 | 708 | 716 | PF00179 | 0.430 |
| TRG_DiLeu_BaEn_1 | 223 | 228 | PF01217 | 0.415 |
| TRG_DiLeu_BaEn_1 | 66 | 71 | PF01217 | 0.397 |
| TRG_DiLeu_BaEn_2 | 179 | 185 | PF01217 | 0.415 |
| TRG_DiLeu_BaEn_2 | 617 | 623 | PF01217 | 0.287 |
| TRG_DiLeu_BaEn_3 | 712 | 718 | PF01217 | 0.420 |
| TRG_DiLeu_BaLyEn_6 | 30 | 35 | PF01217 | 0.666 |
| TRG_DiLeu_BaLyEn_6 | 561 | 566 | PF01217 | 0.239 |
| TRG_ENDOCYTIC_2 | 134 | 137 | PF00928 | 0.421 |
| TRG_ENDOCYTIC_2 | 219 | 222 | PF00928 | 0.389 |
| TRG_ENDOCYTIC_2 | 310 | 313 | PF00928 | 0.387 |
| TRG_ENDOCYTIC_2 | 522 | 525 | PF00928 | 0.329 |
| TRG_ENDOCYTIC_2 | 542 | 545 | PF00928 | 0.228 |
| TRG_ENDOCYTIC_2 | 610 | 613 | PF00928 | 0.398 |
| TRG_ENDOCYTIC_2 | 625 | 628 | PF00928 | 0.370 |
| TRG_ENDOCYTIC_2 | 729 | 732 | PF00928 | 0.304 |
| TRG_ER_diArg_1 | 105 | 108 | PF00400 | 0.419 |
| TRG_ER_diArg_1 | 204 | 207 | PF00400 | 0.381 |
| TRG_ER_diArg_1 | 23 | 26 | PF00400 | 0.671 |
| TRG_ER_diArg_1 | 8 | 10 | PF00400 | 0.736 |
| TRG_ER_diArg_1 | 881 | 884 | PF00400 | 0.449 |
| TRG_Pf-PMV_PEXEL_1 | 225 | 229 | PF00026 | 0.486 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N0P457 | Leptomonas seymouri | 21% | 69% |
| A0A1X0NPQ6 | Trypanosomatidae | 26% | 100% |
| A0A1X0P171 | Trypanosomatidae | 23% | 71% |
| A0A3Q8IJB0 | Leishmania donovani | 87% | 68% |
| A0A3R7KBB6 | Trypanosoma rangeli | 27% | 100% |
| A0A3R7R8G4 | Trypanosoma rangeli | 27% | 89% |
| A0A3S5H6Z8 | Leishmania donovani | 86% | 68% |
| A4H8U6 | Leishmania braziliensis | 42% | 100% |
| A4H8V6 | Leishmania braziliensis | 52% | 99% |
| A4H8V7 | Leishmania braziliensis | 62% | 79% |
| A4HX87 | Leishmania infantum | 52% | 69% |
| C9ZM79 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 73% |
| C9ZM80 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 73% |
| C9ZM81 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 73% |
| C9ZM82 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 73% |
| C9ZM83 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 71% |
| C9ZM86 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 74% |
| C9ZN26 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 71% |
| C9ZN41 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 74% |
| C9ZN43 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 75% |
| C9ZN44 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 74% |
| C9ZN45 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 74% |
| C9ZN46 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 74% |
| C9ZN86 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 23% | 100% |
| C9ZNA5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 23% | 74% |
| C9ZNA6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 23% | 75% |
| C9ZNH3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 71% |
| C9ZNT1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 73% |
| C9ZPZ6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 73% |
| C9ZQ51 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 73% |
| C9ZQ89 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 71% |
| C9ZQ90 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 94% |
| C9ZQ91 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 98% |
| C9ZQ92 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 75% |
| C9ZTS4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 72% |
| C9ZTS5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 72% |
| C9ZTS6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 76% |
| C9ZUE6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 75% |
| C9ZWQ5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 72% |
| C9ZWU1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 67% |
| C9ZWU2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 75% |
| C9ZWU3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 82% |
| C9ZWY7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 73% |
| C9ZZQ4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 73% |
| D0A0U3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 74% |
| D0A0W7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 72% |
| D0A0X5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 72% |
| D0A1S1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 73% |
| D0A5D2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 75% |
| D0A5D5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 23% | 73% |
| D0A5U0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 73% |
| D0A5U1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 73% |
| D0A7A0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 73% |
| D0A9R3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 75% |
| D0AAV3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 73% |
| E8NHJ6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 50% | 100% |
| E9AQY4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 77% | 100% |
| E9ARD7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 42% | 66% |
| Q25263 | Leishmania donovani | 88% | 68% |
| Q26721 | Trypanosoma brucei brucei | 25% | 74% |
| Q4QEH9 | Leishmania major | 80% | 100% |
| Q4QEI0 | Leishmania major | 80% | 100% |
| Q4QEI1 | Leishmania major | 80% | 100% |
| Q4QEI3 | Leishmania major | 42% | 66% |
| Q99279 | Trypanosoma brucei brucei | 22% | 73% |
| Q99280 | Trypanosoma brucei brucei | 24% | 74% |
| V5AW53 | Trypanosoma cruzi | 29% | 100% |
| V5AYH7 | Trypanosoma cruzi | 27% | 71% |
| V5BBK5 | Trypanosoma cruzi | 28% | 76% |