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
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 2 |
Forrest at al. (procyclic) | no | yes: 2 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 60 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 5 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 47, no: 29 |
NetGPI | no | yes: 0, no: 76 |
Term | Name | Level | Count |
---|---|---|---|
GO:0110165 | cellular anatomical entity | 1 | 77 |
GO:0016020 | membrane | 2 | 70 |
Related structures:
AlphaFold database: A4HX87
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 76 |
GO:0006163 | purine nucleotide metabolic process | 5 | 76 |
GO:0006164 | purine nucleotide biosynthetic process | 6 | 76 |
GO:0006171 | cAMP biosynthetic process | 8 | 76 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 76 |
GO:0006753 | nucleoside phosphate metabolic process | 4 | 76 |
GO:0006793 | phosphorus metabolic process | 3 | 76 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 76 |
GO:0006807 | nitrogen compound metabolic process | 2 | 76 |
GO:0007165 | signal transduction | 2 | 76 |
GO:0008152 | metabolic process | 1 | 76 |
GO:0009058 | biosynthetic process | 2 | 76 |
GO:0009117 | nucleotide metabolic process | 5 | 76 |
GO:0009150 | purine ribonucleotide metabolic process | 6 | 76 |
GO:0009152 | purine ribonucleotide biosynthetic process | 7 | 76 |
GO:0009165 | nucleotide biosynthetic process | 6 | 76 |
GO:0009187 | cyclic nucleotide metabolic process | 6 | 76 |
GO:0009190 | cyclic nucleotide biosynthetic process | 7 | 76 |
GO:0009259 | ribonucleotide metabolic process | 5 | 76 |
GO:0009260 | ribonucleotide biosynthetic process | 6 | 76 |
GO:0009987 | cellular process | 1 | 76 |
GO:0018130 | heterocycle biosynthetic process | 4 | 76 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 76 |
GO:0019637 | organophosphate metabolic process | 3 | 76 |
GO:0019693 | ribose phosphate metabolic process | 4 | 76 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 76 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 76 |
GO:0035556 | intracellular signal transduction | 3 | 76 |
GO:0044237 | cellular metabolic process | 2 | 76 |
GO:0044238 | primary metabolic process | 2 | 76 |
GO:0044249 | cellular biosynthetic process | 3 | 76 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 76 |
GO:0044281 | small molecule metabolic process | 2 | 76 |
GO:0046058 | cAMP metabolic process | 7 | 76 |
GO:0046390 | ribose phosphate biosynthetic process | 5 | 76 |
GO:0046483 | heterocycle metabolic process | 3 | 76 |
GO:0050789 | regulation of biological process | 2 | 76 |
GO:0050794 | regulation of cellular process | 3 | 76 |
GO:0052652 | cyclic purine nucleotide metabolic process | 6 | 76 |
GO:0055086 | nucleobase-containing small molecule metabolic process | 3 | 76 |
GO:0065007 | biological regulation | 1 | 76 |
GO:0071704 | organic substance metabolic process | 2 | 76 |
GO:0072521 | purine-containing compound metabolic process | 4 | 76 |
GO:0072522 | purine-containing compound biosynthetic process | 5 | 76 |
GO:0090407 | organophosphate biosynthetic process | 4 | 76 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 76 |
GO:1901137 | carbohydrate derivative biosynthetic process | 4 | 76 |
GO:1901293 | nucleoside phosphate biosynthetic process | 5 | 76 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 76 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 76 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 76 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 76 |
GO:1901576 | organic substance biosynthetic process | 3 | 76 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 65 |
GO:0016829 | lyase activity | 2 | 65 |
GO:0004016 | adenylate cyclase activity | 3 | 1 |
GO:0009975 | cyclase activity | 2 | 1 |
GO:0016849 | phosphorus-oxygen lyase activity | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 304 | 308 | PF00656 | 0.538 |
CLV_C14_Caspase3-7 | 622 | 626 | PF00656 | 0.310 |
CLV_C14_Caspase3-7 | 844 | 848 | PF00656 | 0.632 |
CLV_C14_Caspase3-7 | 905 | 909 | PF00656 | 0.482 |
CLV_MEL_PAP_1 | 978 | 984 | PF00089 | 0.273 |
CLV_NRD_NRD_1 | 1068 | 1070 | PF00675 | 0.397 |
CLV_NRD_NRD_1 | 1236 | 1238 | PF00675 | 0.609 |
CLV_NRD_NRD_1 | 1251 | 1253 | PF00675 | 0.580 |
CLV_NRD_NRD_1 | 127 | 129 | PF00675 | 0.613 |
CLV_NRD_NRD_1 | 1276 | 1278 | PF00675 | 0.631 |
CLV_NRD_NRD_1 | 1306 | 1308 | PF00675 | 0.440 |
CLV_NRD_NRD_1 | 348 | 350 | PF00675 | 0.502 |
CLV_NRD_NRD_1 | 446 | 448 | PF00675 | 0.580 |
CLV_PCSK_FUR_1 | 125 | 129 | PF00082 | 0.605 |
CLV_PCSK_FUR_1 | 1304 | 1308 | PF00082 | 0.400 |
CLV_PCSK_KEX2_1 | 1068 | 1070 | PF00082 | 0.397 |
CLV_PCSK_KEX2_1 | 122 | 124 | PF00082 | 0.623 |
CLV_PCSK_KEX2_1 | 1236 | 1238 | PF00082 | 0.605 |
CLV_PCSK_KEX2_1 | 127 | 129 | PF00082 | 0.613 |
CLV_PCSK_KEX2_1 | 1276 | 1278 | PF00082 | 0.634 |
CLV_PCSK_KEX2_1 | 1304 | 1306 | PF00082 | 0.440 |
CLV_PCSK_PC1ET2_1 | 122 | 124 | PF00082 | 0.425 |
CLV_PCSK_PC7_1 | 123 | 129 | PF00082 | 0.431 |
CLV_PCSK_SKI1_1 | 1165 | 1169 | PF00082 | 0.435 |
CLV_PCSK_SKI1_1 | 128 | 132 | PF00082 | 0.583 |
CLV_PCSK_SKI1_1 | 225 | 229 | PF00082 | 0.496 |
CLV_PCSK_SKI1_1 | 426 | 430 | PF00082 | 0.635 |
CLV_PCSK_SKI1_1 | 553 | 557 | PF00082 | 0.540 |
CLV_PCSK_SKI1_1 | 667 | 671 | PF00082 | 0.498 |
CLV_PCSK_SKI1_1 | 710 | 714 | PF00082 | 0.566 |
CLV_PCSK_SKI1_1 | 930 | 934 | PF00082 | 0.275 |
DEG_APCC_DBOX_1 | 709 | 717 | PF00400 | 0.279 |
DEG_APCC_KENBOX_2 | 527 | 531 | PF00400 | 0.247 |
DEG_SCF_FBW7_2 | 376 | 382 | PF00400 | 0.234 |
DEG_SCF_FBW7_2 | 796 | 802 | PF00400 | 0.469 |
DEG_SPOP_SBC_1 | 210 | 214 | PF00917 | 0.445 |
DOC_CDC14_PxL_1 | 51 | 59 | PF14671 | 0.454 |
DOC_CDC14_PxL_1 | 685 | 693 | PF14671 | 0.233 |
DOC_CKS1_1 | 376 | 381 | PF01111 | 0.239 |
DOC_CKS1_1 | 796 | 801 | PF01111 | 0.406 |
DOC_CYCLIN_RxL_1 | 664 | 672 | PF00134 | 0.241 |
DOC_CYCLIN_yCln2_LP_2 | 156 | 162 | PF00134 | 0.361 |
DOC_CYCLIN_yCln2_LP_2 | 429 | 435 | PF00134 | 0.410 |
DOC_MAPK_gen_1 | 125 | 134 | PF00069 | 0.298 |
DOC_MAPK_gen_1 | 1252 | 1258 | PF00069 | 0.613 |
DOC_MAPK_gen_1 | 39 | 46 | PF00069 | 0.323 |
DOC_MAPK_HePTP_8 | 428 | 440 | PF00069 | 0.411 |
DOC_MAPK_MEF2A_6 | 431 | 440 | PF00069 | 0.428 |
DOC_MAPK_MEF2A_6 | 710 | 717 | PF00069 | 0.314 |
DOC_MAPK_RevD_3 | 1055 | 1069 | PF00069 | 0.529 |
DOC_MAPK_RevD_3 | 113 | 128 | PF00069 | 0.259 |
DOC_PP1_RVXF_1 | 223 | 229 | PF00149 | 0.419 |
DOC_PP1_RVXF_1 | 463 | 469 | PF00149 | 0.374 |
DOC_PP1_RVXF_1 | 665 | 672 | PF00149 | 0.287 |
DOC_PP1_RVXF_1 | 79 | 86 | PF00149 | 0.343 |
DOC_PP2B_LxvP_1 | 156 | 159 | PF13499 | 0.327 |
DOC_PP4_FxxP_1 | 519 | 522 | PF00568 | 0.282 |
DOC_PP4_FxxP_1 | 533 | 536 | PF00568 | 0.360 |
DOC_PP4_FxxP_1 | 588 | 591 | PF00568 | 0.442 |
DOC_PP4_FxxP_1 | 64 | 67 | PF00568 | 0.370 |
DOC_PP4_FxxP_1 | 698 | 701 | PF00568 | 0.457 |
DOC_PP4_FxxP_1 | 728 | 731 | PF00568 | 0.348 |
DOC_PP4_FxxP_1 | 85 | 88 | PF00568 | 0.431 |
DOC_USP7_MATH_1 | 1167 | 1171 | PF00917 | 0.668 |
DOC_USP7_MATH_1 | 1212 | 1216 | PF00917 | 0.794 |
DOC_USP7_MATH_1 | 1224 | 1228 | PF00917 | 0.760 |
DOC_USP7_MATH_1 | 1272 | 1276 | PF00917 | 0.667 |
DOC_USP7_MATH_1 | 210 | 214 | PF00917 | 0.443 |
DOC_USP7_MATH_1 | 303 | 307 | PF00917 | 0.427 |
DOC_USP7_MATH_1 | 34 | 38 | PF00917 | 0.397 |
DOC_USP7_MATH_1 | 554 | 558 | PF00917 | 0.421 |
DOC_USP7_MATH_1 | 597 | 601 | PF00917 | 0.456 |
DOC_USP7_MATH_1 | 67 | 71 | PF00917 | 0.420 |
DOC_USP7_MATH_1 | 791 | 795 | PF00917 | 0.355 |
DOC_USP7_MATH_1 | 913 | 917 | PF00917 | 0.549 |
DOC_USP7_UBL2_3 | 291 | 295 | PF12436 | 0.442 |
DOC_USP7_UBL2_3 | 49 | 53 | PF12436 | 0.390 |
DOC_WW_Pin1_4 | 238 | 243 | PF00397 | 0.418 |
DOC_WW_Pin1_4 | 375 | 380 | PF00397 | 0.419 |
DOC_WW_Pin1_4 | 513 | 518 | PF00397 | 0.324 |
DOC_WW_Pin1_4 | 678 | 683 | PF00397 | 0.452 |
DOC_WW_Pin1_4 | 702 | 707 | PF00397 | 0.334 |
DOC_WW_Pin1_4 | 792 | 797 | PF00397 | 0.366 |
LIG_14-3-3_CanoR_1 | 1147 | 1154 | PF00244 | 0.648 |
LIG_14-3-3_CanoR_1 | 1165 | 1170 | PF00244 | 0.627 |
LIG_14-3-3_CanoR_1 | 1236 | 1241 | PF00244 | 0.794 |
LIG_14-3-3_CanoR_1 | 125 | 134 | PF00244 | 0.340 |
LIG_14-3-3_CanoR_1 | 211 | 218 | PF00244 | 0.385 |
LIG_14-3-3_CanoR_1 | 265 | 275 | PF00244 | 0.289 |
LIG_14-3-3_CanoR_1 | 349 | 353 | PF00244 | 0.336 |
LIG_14-3-3_CanoR_1 | 553 | 562 | PF00244 | 0.425 |
LIG_14-3-3_CanoR_1 | 583 | 589 | PF00244 | 0.370 |
LIG_14-3-3_CanoR_1 | 667 | 672 | PF00244 | 0.412 |
LIG_14-3-3_CanoR_1 | 753 | 757 | PF00244 | 0.445 |
LIG_14-3-3_CanoR_1 | 915 | 923 | PF00244 | 0.590 |
LIG_14-3-3_CanoR_1 | 965 | 971 | PF00244 | 0.608 |
LIG_Actin_WH2_2 | 109 | 124 | PF00022 | 0.240 |
LIG_Actin_WH2_2 | 431 | 449 | PF00022 | 0.310 |
LIG_Actin_WH2_2 | 489 | 507 | PF00022 | 0.230 |
LIG_Actin_WH2_2 | 570 | 585 | PF00022 | 0.334 |
LIG_Actin_WH2_2 | 591 | 607 | PF00022 | 0.344 |
LIG_AP2alpha_2 | 108 | 110 | PF02296 | 0.217 |
LIG_APCC_ABBA_1 | 228 | 233 | PF00400 | 0.290 |
LIG_APCC_ABBA_1 | 61 | 66 | PF00400 | 0.435 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.221 |
LIG_BIR_III_2 | 849 | 853 | PF00653 | 0.614 |
LIG_BRCT_BRCA1_1 | 515 | 519 | PF00533 | 0.216 |
LIG_BRCT_BRCA1_1 | 713 | 717 | PF00533 | 0.389 |
LIG_deltaCOP1_diTrp_1 | 488 | 491 | PF00928 | 0.232 |
LIG_eIF4E_1 | 688 | 694 | PF01652 | 0.228 |
LIG_FHA_1 | 1011 | 1017 | PF00498 | 0.487 |
LIG_FHA_1 | 112 | 118 | PF00498 | 0.308 |
LIG_FHA_1 | 276 | 282 | PF00498 | 0.449 |
LIG_FHA_1 | 320 | 326 | PF00498 | 0.335 |
LIG_FHA_1 | 358 | 364 | PF00498 | 0.391 |
LIG_FHA_1 | 435 | 441 | PF00498 | 0.338 |
LIG_FHA_1 | 498 | 504 | PF00498 | 0.312 |
LIG_FHA_1 | 631 | 637 | PF00498 | 0.435 |
LIG_FHA_1 | 703 | 709 | PF00498 | 0.351 |
LIG_FHA_1 | 760 | 766 | PF00498 | 0.487 |
LIG_FHA_1 | 826 | 832 | PF00498 | 0.387 |
LIG_FHA_1 | 927 | 933 | PF00498 | 0.545 |
LIG_FHA_1 | 936 | 942 | PF00498 | 0.480 |
LIG_FHA_1 | 961 | 967 | PF00498 | 0.490 |
LIG_FHA_2 | 103 | 109 | PF00498 | 0.424 |
LIG_FHA_2 | 1073 | 1079 | PF00498 | 0.741 |
LIG_FHA_2 | 1083 | 1089 | PF00498 | 0.780 |
LIG_FHA_2 | 239 | 245 | PF00498 | 0.419 |
LIG_FHA_2 | 337 | 343 | PF00498 | 0.404 |
LIG_FHA_2 | 618 | 624 | PF00498 | 0.348 |
LIG_FHA_2 | 862 | 868 | PF00498 | 0.480 |
LIG_FHA_2 | 903 | 909 | PF00498 | 0.485 |
LIG_FHA_2 | 953 | 959 | PF00498 | 0.578 |
LIG_GBD_Chelix_1 | 199 | 207 | PF00786 | 0.485 |
LIG_GBD_Chelix_1 | 327 | 335 | PF00786 | 0.491 |
LIG_GBD_Chelix_1 | 923 | 931 | PF00786 | 0.388 |
LIG_Integrin_isoDGR_2 | 25 | 27 | PF01839 | 0.469 |
LIG_Integrin_RGD_1 | 106 | 108 | PF01839 | 0.416 |
LIG_IRF3_LxIS_1 | 456 | 462 | PF10401 | 0.214 |
LIG_IRF3_LxIS_1 | 509 | 516 | PF10401 | 0.233 |
LIG_LIR_Apic_2 | 372 | 376 | PF02991 | 0.360 |
LIG_LIR_Apic_2 | 516 | 522 | PF02991 | 0.339 |
LIG_LIR_Apic_2 | 587 | 591 | PF02991 | 0.440 |
LIG_LIR_Apic_2 | 725 | 731 | PF02991 | 0.447 |
LIG_LIR_Apic_2 | 82 | 88 | PF02991 | 0.416 |
LIG_LIR_Apic_2 | 957 | 962 | PF02991 | 0.471 |
LIG_LIR_Gen_1 | 108 | 117 | PF02991 | 0.394 |
LIG_LIR_Gen_1 | 129 | 139 | PF02991 | 0.429 |
LIG_LIR_Gen_1 | 177 | 186 | PF02991 | 0.334 |
LIG_LIR_Gen_1 | 467 | 476 | PF02991 | 0.374 |
LIG_LIR_Gen_1 | 488 | 496 | PF02991 | 0.362 |
LIG_LIR_Gen_1 | 529 | 538 | PF02991 | 0.427 |
LIG_LIR_Gen_1 | 649 | 658 | PF02991 | 0.293 |
LIG_LIR_Gen_1 | 670 | 676 | PF02991 | 0.327 |
LIG_LIR_Gen_1 | 714 | 723 | PF02991 | 0.261 |
LIG_LIR_Gen_1 | 860 | 871 | PF02991 | 0.482 |
LIG_LIR_Gen_1 | 968 | 978 | PF02991 | 0.536 |
LIG_LIR_Gen_1 | 990 | 1000 | PF02991 | 0.579 |
LIG_LIR_Nem_3 | 1026 | 1032 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 1117 | 1122 | PF02991 | 0.653 |
LIG_LIR_Nem_3 | 129 | 134 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 141 | 147 | PF02991 | 0.336 |
LIG_LIR_Nem_3 | 467 | 471 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 488 | 494 | PF02991 | 0.288 |
LIG_LIR_Nem_3 | 52 | 57 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 529 | 534 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 541 | 546 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 642 | 646 | PF02991 | 0.286 |
LIG_LIR_Nem_3 | 649 | 653 | PF02991 | 0.323 |
LIG_LIR_Nem_3 | 654 | 660 | PF02991 | 0.337 |
LIG_LIR_Nem_3 | 670 | 674 | PF02991 | 0.318 |
LIG_LIR_Nem_3 | 686 | 691 | PF02991 | 0.299 |
LIG_LIR_Nem_3 | 714 | 720 | PF02991 | 0.199 |
LIG_LIR_Nem_3 | 766 | 772 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 860 | 866 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 870 | 876 | PF02991 | 0.584 |
LIG_LIR_Nem_3 | 942 | 948 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 968 | 974 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 990 | 996 | PF02991 | 0.499 |
LIG_LIR_Nem_3 | 997 | 1003 | PF02991 | 0.460 |
LIG_LYPXL_yS_3 | 54 | 57 | PF13949 | 0.321 |
LIG_LYPXL_yS_3 | 688 | 691 | PF13949 | 0.228 |
LIG_MYND_3 | 535 | 539 | PF01753 | 0.353 |
LIG_NRBOX | 508 | 514 | PF00104 | 0.239 |
LIG_NRBOX | 708 | 714 | PF00104 | 0.201 |
LIG_PCNA_yPIPBox_3 | 324 | 334 | PF02747 | 0.417 |
LIG_PCNA_yPIPBox_3 | 811 | 825 | PF02747 | 0.357 |
LIG_PDZ_Class_3 | 1317 | 1322 | PF00595 | 0.634 |
LIG_Pex14_2 | 694 | 698 | PF04695 | 0.263 |
LIG_Pex14_2 | 85 | 89 | PF04695 | 0.421 |
LIG_PTB_Apo_2 | 692 | 699 | PF02174 | 0.232 |
LIG_SH2_CRK | 144 | 148 | PF00017 | 0.377 |
LIG_SH2_CRK | 162 | 166 | PF00017 | 0.453 |
LIG_SH2_CRK | 373 | 377 | PF00017 | 0.362 |
LIG_SH2_GRB2like | 423 | 426 | PF00017 | 0.321 |
LIG_SH2_NCK_1 | 162 | 166 | PF00017 | 0.465 |
LIG_SH2_NCK_1 | 569 | 573 | PF00017 | 0.467 |
LIG_SH2_NCK_1 | 959 | 963 | PF00017 | 0.452 |
LIG_SH2_NCK_1 | 993 | 997 | PF00017 | 0.572 |
LIG_SH2_SRC | 362 | 365 | PF00017 | 0.408 |
LIG_SH2_SRC | 959 | 962 | PF00017 | 0.527 |
LIG_SH2_SRC | 993 | 996 | PF00017 | 0.572 |
LIG_SH2_STAP1 | 232 | 236 | PF00017 | 0.430 |
LIG_SH2_STAP1 | 311 | 315 | PF00017 | 0.247 |
LIG_SH2_STAP1 | 417 | 421 | PF00017 | 0.367 |
LIG_SH2_STAP1 | 494 | 498 | PF00017 | 0.346 |
LIG_SH2_STAP1 | 747 | 751 | PF00017 | 0.398 |
LIG_SH2_STAP1 | 971 | 975 | PF00017 | 0.537 |
LIG_SH2_STAT3 | 389 | 392 | PF00017 | 0.424 |
LIG_SH2_STAT3 | 772 | 775 | PF00017 | 0.307 |
LIG_SH2_STAT5 | 103 | 106 | PF00017 | 0.320 |
LIG_SH2_STAT5 | 1154 | 1157 | PF00017 | 0.597 |
LIG_SH2_STAT5 | 133 | 136 | PF00017 | 0.309 |
LIG_SH2_STAT5 | 216 | 219 | PF00017 | 0.288 |
LIG_SH2_STAT5 | 362 | 365 | PF00017 | 0.308 |
LIG_SH2_STAT5 | 389 | 392 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 423 | 426 | PF00017 | 0.351 |
LIG_SH2_STAT5 | 531 | 534 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 543 | 546 | PF00017 | 0.273 |
LIG_SH2_STAT5 | 569 | 572 | PF00017 | 0.382 |
LIG_SH2_STAT5 | 615 | 618 | PF00017 | 0.240 |
LIG_SH3_1 | 373 | 379 | PF00018 | 0.261 |
LIG_SH3_3 | 1137 | 1143 | PF00018 | 0.590 |
LIG_SH3_3 | 1192 | 1198 | PF00018 | 0.753 |
LIG_SH3_3 | 1293 | 1299 | PF00018 | 0.511 |
LIG_SH3_3 | 373 | 379 | PF00018 | 0.261 |
LIG_SH3_3 | 496 | 502 | PF00018 | 0.364 |
LIG_SH3_3 | 511 | 517 | PF00018 | 0.335 |
LIG_SH3_3 | 57 | 63 | PF00018 | 0.317 |
LIG_SH3_3 | 785 | 791 | PF00018 | 0.360 |
LIG_SH3_3 | 793 | 799 | PF00018 | 0.354 |
LIG_SUMO_SIM_anti_2 | 1292 | 1297 | PF11976 | 0.535 |
LIG_SUMO_SIM_anti_2 | 41 | 48 | PF11976 | 0.434 |
LIG_SUMO_SIM_anti_2 | 495 | 500 | PF11976 | 0.434 |
LIG_SUMO_SIM_anti_2 | 510 | 516 | PF11976 | 0.272 |
LIG_SUMO_SIM_anti_2 | 711 | 717 | PF11976 | 0.243 |
LIG_SUMO_SIM_anti_2 | 828 | 833 | PF11976 | 0.378 |
LIG_SUMO_SIM_anti_2 | 856 | 865 | PF11976 | 0.483 |
LIG_SUMO_SIM_par_1 | 111 | 118 | PF11976 | 0.251 |
LIG_SUMO_SIM_par_1 | 146 | 153 | PF11976 | 0.276 |
LIG_SUMO_SIM_par_1 | 457 | 464 | PF11976 | 0.380 |
LIG_SUMO_SIM_par_1 | 510 | 516 | PF11976 | 0.280 |
LIG_SUMO_SIM_par_1 | 637 | 642 | PF11976 | 0.380 |
LIG_SUMO_SIM_par_1 | 776 | 781 | PF11976 | 0.299 |
LIG_SUMO_SIM_par_1 | 827 | 833 | PF11976 | 0.421 |
LIG_TRAF2_1 | 733 | 736 | PF00917 | 0.381 |
LIG_TRAF2_1 | 967 | 970 | PF00917 | 0.604 |
LIG_TRAF2_2 | 805 | 810 | PF00917 | 0.326 |
LIG_TRFH_1 | 154 | 158 | PF08558 | 0.272 |
LIG_TYR_ITIM | 544 | 549 | PF00017 | 0.434 |
LIG_TYR_ITIM | 991 | 996 | PF00017 | 0.459 |
LIG_UBA3_1 | 116 | 122 | PF00899 | 0.549 |
LIG_UBA3_1 | 398 | 404 | PF00899 | 0.524 |
LIG_UBA3_1 | 693 | 700 | PF00899 | 0.234 |
LIG_WRC_WIRS_1 | 151 | 156 | PF05994 | 0.325 |
LIG_WRC_WIRS_1 | 640 | 645 | PF05994 | 0.311 |
LIG_WRC_WIRS_1 | 668 | 673 | PF05994 | 0.533 |
LIG_WW_3 | 1142 | 1146 | PF00397 | 0.633 |
MOD_CK1_1 | 1100 | 1106 | PF00069 | 0.530 |
MOD_CK1_1 | 1178 | 1184 | PF00069 | 0.477 |
MOD_CK1_1 | 1204 | 1210 | PF00069 | 0.724 |
MOD_CK1_1 | 1215 | 1221 | PF00069 | 0.766 |
MOD_CK1_1 | 1257 | 1263 | PF00069 | 0.759 |
MOD_CK1_1 | 149 | 155 | PF00069 | 0.461 |
MOD_CK1_1 | 249 | 255 | PF00069 | 0.540 |
MOD_CK1_1 | 305 | 311 | PF00069 | 0.659 |
MOD_CK1_1 | 547 | 553 | PF00069 | 0.370 |
MOD_CK1_1 | 599 | 605 | PF00069 | 0.526 |
MOD_CK1_1 | 678 | 684 | PF00069 | 0.515 |
MOD_CK1_1 | 794 | 800 | PF00069 | 0.566 |
MOD_CK1_1 | 916 | 922 | PF00069 | 0.482 |
MOD_CK2_1 | 1030 | 1036 | PF00069 | 0.341 |
MOD_CK2_1 | 1072 | 1078 | PF00069 | 0.672 |
MOD_CK2_1 | 1248 | 1254 | PF00069 | 0.790 |
MOD_CK2_1 | 1306 | 1312 | PF00069 | 0.605 |
MOD_CK2_1 | 254 | 260 | PF00069 | 0.486 |
MOD_CK2_1 | 336 | 342 | PF00069 | 0.416 |
MOD_CK2_1 | 554 | 560 | PF00069 | 0.420 |
MOD_CK2_1 | 603 | 609 | PF00069 | 0.343 |
MOD_CK2_1 | 680 | 686 | PF00069 | 0.339 |
MOD_CK2_1 | 730 | 736 | PF00069 | 0.551 |
MOD_CK2_1 | 760 | 766 | PF00069 | 0.497 |
MOD_CK2_1 | 861 | 867 | PF00069 | 0.330 |
MOD_CK2_1 | 964 | 970 | PF00069 | 0.504 |
MOD_Cter_Amidation | 1066 | 1069 | PF01082 | 0.518 |
MOD_Cter_Amidation | 1302 | 1305 | PF01082 | 0.473 |
MOD_GlcNHglycan | 1091 | 1094 | PF01048 | 0.602 |
MOD_GlcNHglycan | 1183 | 1186 | PF01048 | 0.611 |
MOD_GlcNHglycan | 1192 | 1195 | PF01048 | 0.559 |
MOD_GlcNHglycan | 1214 | 1217 | PF01048 | 0.795 |
MOD_GlcNHglycan | 1222 | 1225 | PF01048 | 0.759 |
MOD_GlcNHglycan | 1226 | 1229 | PF01048 | 0.706 |
MOD_GlcNHglycan | 1285 | 1288 | PF01048 | 0.584 |
MOD_GlcNHglycan | 13 | 16 | PF01048 | 0.430 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.475 |
MOD_GlcNHglycan | 18 | 21 | PF01048 | 0.490 |
MOD_GlcNHglycan | 213 | 216 | PF01048 | 0.489 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.537 |
MOD_GlcNHglycan | 307 | 310 | PF01048 | 0.661 |
MOD_GlcNHglycan | 331 | 334 | PF01048 | 0.471 |
MOD_GlcNHglycan | 419 | 422 | PF01048 | 0.437 |
MOD_GlcNHglycan | 467 | 471 | PF01048 | 0.489 |
MOD_GlcNHglycan | 508 | 512 | PF01048 | 0.481 |
MOD_GlcNHglycan | 570 | 573 | PF01048 | 0.478 |
MOD_GlcNHglycan | 576 | 580 | PF01048 | 0.483 |
MOD_GlcNHglycan | 599 | 602 | PF01048 | 0.461 |
MOD_GlcNHglycan | 736 | 739 | PF01048 | 0.561 |
MOD_GlcNHglycan | 762 | 765 | PF01048 | 0.490 |
MOD_GlcNHglycan | 813 | 816 | PF01048 | 0.405 |
MOD_GlcNHglycan | 915 | 918 | PF01048 | 0.425 |
MOD_GSK3_1 | 1082 | 1089 | PF00069 | 0.614 |
MOD_GSK3_1 | 1096 | 1103 | PF00069 | 0.614 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.493 |
MOD_GSK3_1 | 1143 | 1150 | PF00069 | 0.618 |
MOD_GSK3_1 | 1220 | 1227 | PF00069 | 0.783 |
MOD_GSK3_1 | 1243 | 1250 | PF00069 | 0.772 |
MOD_GSK3_1 | 1268 | 1275 | PF00069 | 0.792 |
MOD_GSK3_1 | 1281 | 1288 | PF00069 | 0.789 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.438 |
MOD_GSK3_1 | 16 | 23 | PF00069 | 0.384 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.453 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.458 |
MOD_GSK3_1 | 246 | 253 | PF00069 | 0.527 |
MOD_GSK3_1 | 301 | 308 | PF00069 | 0.692 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.469 |
MOD_GSK3_1 | 434 | 441 | PF00069 | 0.399 |
MOD_GSK3_1 | 472 | 479 | PF00069 | 0.379 |
MOD_GSK3_1 | 503 | 510 | PF00069 | 0.381 |
MOD_GSK3_1 | 544 | 551 | PF00069 | 0.376 |
MOD_GSK3_1 | 596 | 603 | PF00069 | 0.507 |
MOD_GSK3_1 | 604 | 611 | PF00069 | 0.464 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.427 |
MOD_GSK3_1 | 680 | 687 | PF00069 | 0.396 |
MOD_GSK3_1 | 730 | 737 | PF00069 | 0.531 |
MOD_GSK3_1 | 752 | 759 | PF00069 | 0.512 |
MOD_GSK3_1 | 791 | 798 | PF00069 | 0.476 |
MOD_GSK3_1 | 857 | 864 | PF00069 | 0.347 |
MOD_GSK3_1 | 902 | 909 | PF00069 | 0.339 |
MOD_GSK3_1 | 960 | 967 | PF00069 | 0.486 |
MOD_N-GLC_1 | 1178 | 1183 | PF02516 | 0.569 |
MOD_N-GLC_1 | 438 | 443 | PF02516 | 0.477 |
MOD_N-GLC_1 | 476 | 481 | PF02516 | 0.426 |
MOD_N-GLC_1 | 492 | 497 | PF02516 | 0.484 |
MOD_N-GLC_1 | 756 | 761 | PF02516 | 0.489 |
MOD_NEK2_1 | 1097 | 1102 | PF00069 | 0.549 |
MOD_NEK2_1 | 1229 | 1234 | PF00069 | 0.795 |
MOD_NEK2_1 | 1243 | 1248 | PF00069 | 0.819 |
MOD_NEK2_1 | 132 | 137 | PF00069 | 0.477 |
MOD_NEK2_1 | 146 | 151 | PF00069 | 0.430 |
MOD_NEK2_1 | 16 | 21 | PF00069 | 0.376 |
MOD_NEK2_1 | 181 | 186 | PF00069 | 0.382 |
MOD_NEK2_1 | 275 | 280 | PF00069 | 0.531 |
MOD_NEK2_1 | 357 | 362 | PF00069 | 0.269 |
MOD_NEK2_1 | 466 | 471 | PF00069 | 0.439 |
MOD_NEK2_1 | 476 | 481 | PF00069 | 0.398 |
MOD_NEK2_1 | 630 | 635 | PF00069 | 0.488 |
MOD_NEK2_1 | 653 | 658 | PF00069 | 0.377 |
MOD_NEK2_1 | 669 | 674 | PF00069 | 0.273 |
MOD_NEK2_1 | 68 | 73 | PF00069 | 0.495 |
MOD_NEK2_1 | 734 | 739 | PF00069 | 0.418 |
MOD_NEK2_1 | 89 | 94 | PF00069 | 0.462 |
MOD_NEK2_2 | 216 | 221 | PF00069 | 0.260 |
MOD_PIKK_1 | 1167 | 1173 | PF00454 | 0.633 |
MOD_PIKK_1 | 476 | 482 | PF00454 | 0.434 |
MOD_PK_1 | 1285 | 1291 | PF00069 | 0.485 |
MOD_PKA_1 | 1236 | 1242 | PF00069 | 0.759 |
MOD_PKA_1 | 1252 | 1258 | PF00069 | 0.753 |
MOD_PKA_1 | 1276 | 1282 | PF00069 | 0.572 |
MOD_PKA_1 | 1306 | 1312 | PF00069 | 0.543 |
MOD_PKA_2 | 1212 | 1218 | PF00069 | 0.803 |
MOD_PKA_2 | 1229 | 1235 | PF00069 | 0.658 |
MOD_PKA_2 | 1236 | 1242 | PF00069 | 0.784 |
MOD_PKA_2 | 126 | 132 | PF00069 | 0.535 |
MOD_PKA_2 | 1276 | 1282 | PF00069 | 0.820 |
MOD_PKA_2 | 1306 | 1312 | PF00069 | 0.566 |
MOD_PKA_2 | 210 | 216 | PF00069 | 0.484 |
MOD_PKA_2 | 348 | 354 | PF00069 | 0.395 |
MOD_PKA_2 | 394 | 400 | PF00069 | 0.237 |
MOD_PKA_2 | 752 | 758 | PF00069 | 0.561 |
MOD_PKA_2 | 964 | 970 | PF00069 | 0.507 |
MOD_PKB_1 | 1145 | 1153 | PF00069 | 0.675 |
MOD_PKB_1 | 1173 | 1181 | PF00069 | 0.488 |
MOD_PKB_1 | 1304 | 1312 | PF00069 | 0.496 |
MOD_PKB_1 | 299 | 307 | PF00069 | 0.430 |
MOD_Plk_1 | 111 | 117 | PF00069 | 0.236 |
MOD_Plk_1 | 281 | 287 | PF00069 | 0.389 |
MOD_Plk_1 | 336 | 342 | PF00069 | 0.440 |
MOD_Plk_1 | 357 | 363 | PF00069 | 0.414 |
MOD_Plk_1 | 466 | 472 | PF00069 | 0.484 |
MOD_Plk_1 | 492 | 498 | PF00069 | 0.475 |
MOD_Plk_1 | 547 | 553 | PF00069 | 0.495 |
MOD_Plk_1 | 575 | 581 | PF00069 | 0.423 |
MOD_Plk_2-3 | 902 | 908 | PF00069 | 0.330 |
MOD_Plk_4 | 111 | 117 | PF00069 | 0.426 |
MOD_Plk_4 | 1201 | 1207 | PF00069 | 0.755 |
MOD_Plk_4 | 1306 | 1312 | PF00069 | 0.554 |
MOD_Plk_4 | 146 | 152 | PF00069 | 0.474 |
MOD_Plk_4 | 281 | 287 | PF00069 | 0.492 |
MOD_Plk_4 | 394 | 400 | PF00069 | 0.426 |
MOD_Plk_4 | 53 | 59 | PF00069 | 0.507 |
MOD_Plk_4 | 608 | 614 | PF00069 | 0.271 |
MOD_Plk_4 | 68 | 74 | PF00069 | 0.434 |
MOD_Plk_4 | 704 | 710 | PF00069 | 0.345 |
MOD_Plk_4 | 711 | 717 | PF00069 | 0.329 |
MOD_Plk_4 | 857 | 863 | PF00069 | 0.328 |
MOD_Plk_4 | 906 | 912 | PF00069 | 0.344 |
MOD_ProDKin_1 | 238 | 244 | PF00069 | 0.523 |
MOD_ProDKin_1 | 375 | 381 | PF00069 | 0.519 |
MOD_ProDKin_1 | 513 | 519 | PF00069 | 0.392 |
MOD_ProDKin_1 | 678 | 684 | PF00069 | 0.562 |
MOD_ProDKin_1 | 702 | 708 | PF00069 | 0.399 |
MOD_ProDKin_1 | 792 | 798 | PF00069 | 0.453 |
MOD_SUMO_rev_2 | 141 | 147 | PF00179 | 0.394 |
MOD_SUMO_rev_2 | 284 | 293 | PF00179 | 0.554 |
MOD_SUMO_rev_2 | 3 | 8 | PF00179 | 0.292 |
MOD_SUMO_rev_2 | 342 | 351 | PF00179 | 0.455 |
TRG_DiLeu_BaEn_1 | 560 | 565 | PF01217 | 0.489 |
TRG_DiLeu_BaEn_1 | 664 | 669 | PF01217 | 0.208 |
TRG_DiLeu_BaEn_1 | 857 | 862 | PF01217 | 0.460 |
TRG_DiLeu_BaEn_2 | 528 | 534 | PF01217 | 0.407 |
TRG_DiLeu_BaEn_4 | 969 | 975 | PF01217 | 0.364 |
TRG_DiLeu_BaLyEn_6 | 1195 | 1200 | PF01217 | 0.717 |
TRG_DiLeu_BaLyEn_6 | 499 | 504 | PF01217 | 0.508 |
TRG_DiLeu_BaLyEn_6 | 833 | 838 | PF01217 | 0.184 |
TRG_DiLeu_LyEn_5 | 1130 | 1135 | PF01217 | 0.503 |
TRG_DiLeu_LyEn_5 | 664 | 669 | PF01217 | 0.208 |
TRG_DiLeu_LyEn_5 | 686 | 691 | PF01217 | 0.263 |
TRG_ENDOCYTIC_2 | 144 | 147 | PF00928 | 0.495 |
TRG_ENDOCYTIC_2 | 231 | 234 | PF00928 | 0.483 |
TRG_ENDOCYTIC_2 | 531 | 534 | PF00928 | 0.523 |
TRG_ENDOCYTIC_2 | 54 | 57 | PF00928 | 0.547 |
TRG_ENDOCYTIC_2 | 546 | 549 | PF00928 | 0.482 |
TRG_ENDOCYTIC_2 | 650 | 653 | PF00928 | 0.396 |
TRG_ENDOCYTIC_2 | 688 | 691 | PF00928 | 0.502 |
TRG_ENDOCYTIC_2 | 945 | 948 | PF00928 | 0.337 |
TRG_ENDOCYTIC_2 | 971 | 974 | PF00928 | 0.320 |
TRG_ENDOCYTIC_2 | 993 | 996 | PF00928 | 0.457 |
TRG_ER_diArg_1 | 1144 | 1147 | PF00400 | 0.639 |
TRG_ER_diArg_1 | 1173 | 1176 | PF00400 | 0.646 |
TRG_ER_diArg_1 | 1235 | 1237 | PF00400 | 0.686 |
TRG_ER_diArg_1 | 124 | 127 | PF00400 | 0.490 |
TRG_ER_diArg_1 | 1276 | 1278 | PF00400 | 0.822 |
TRG_ER_diArg_1 | 1304 | 1307 | PF00400 | 0.540 |
TRG_ER_diArg_1 | 298 | 301 | PF00400 | 0.420 |
TRG_ER_diArg_1 | 803 | 806 | PF00400 | 0.554 |
TRG_ER_diArg_1 | 978 | 981 | PF00400 | 0.331 |
TRG_Pf-PMV_PEXEL_1 | 1276 | 1280 | PF00026 | 0.511 |
TRG_Pf-PMV_PEXEL_1 | 889 | 893 | PF00026 | 0.405 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P457 | Leptomonas seymouri | 27% | 100% |
A0A1X0NPQ6 | Trypanosomatidae | 29% | 100% |
A0A1X0P171 | Trypanosomatidae | 33% | 100% |
A0A3Q8IJB0 | Leishmania donovani | 66% | 99% |
A0A3R7M6J4 | Trypanosoma rangeli | 36% | 100% |
A0A3R7R8G4 | Trypanosoma rangeli | 30% | 100% |
A0A3S5H6Z8 | Leishmania donovani | 66% | 99% |
A0A3S7WU91 | Leishmania donovani | 98% | 93% |
A0A3S7WU94 | Leishmania donovani | 56% | 96% |
A0A3S7WU95 | Leishmania donovani | 65% | 94% |
A0A3S7XB85 | Leishmania donovani | 28% | 94% |
A4H8U6 | Leishmania braziliensis | 56% | 100% |
A4H8V5 | Leishmania braziliensis | 68% | 100% |
A4H8V7 | Leishmania braziliensis | 60% | 100% |
A4H8V8 | Leishmania braziliensis | 59% | 100% |
A4HPI4 | Leishmania braziliensis | 27% | 100% |
A4HX84 | Leishmania infantum | 56% | 100% |
A4HX85 | Leishmania infantum | 67% | 100% |
A4HX88 | Leishmania infantum | 52% | 100% |
A4IDA6 | Leishmania infantum | 28% | 94% |
C9ZM79 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZM80 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZM81 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
C9ZM82 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZM83 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
C9ZM86 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZN26 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
C9ZN41 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
C9ZN43 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
C9ZN44 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
C9ZN45 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
C9ZN46 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
C9ZNA5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
C9ZNA6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
C9ZNH3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZNT1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZPZ6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZQ51 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
C9ZQ89 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
C9ZQ90 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZQ92 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
C9ZTS4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
C9ZTS5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
C9ZTS6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
C9ZUE6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZWQ5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
C9ZWU1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 97% |
C9ZWU2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
C9ZWU3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
C9ZWY7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZZQ4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
D0A0U3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
D0A0W7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
D0A0X5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
D0A1S1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
D0A5D2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
D0A5D5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
D0A5U0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
D0A5U1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
D0A7A0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
D0A9R3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
D0AAV3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
E9AQY0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
E9AQY1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 59% | 100% |
E9AQY2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 64% | 100% |
E9AQY4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 63% | 100% |
E9ARD7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 56% | 100% |
E9AT96 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 94% |
Q25263 | Leishmania donovani | 65% | 99% |
Q26721 | Trypanosoma brucei brucei | 34% | 100% |
Q27675 | Leishmania donovani | 56% | 96% |
Q4Q1A1 | Leishmania major | 28% | 100% |
Q4QEH9 | Leishmania major | 65% | 100% |
Q4QEI0 | Leishmania major | 65% | 100% |
Q4QEI1 | Leishmania major | 64% | 100% |
Q4QEI2 | Leishmania major | 87% | 100% |
Q4QEI3 | Leishmania major | 57% | 100% |
Q99279 | Trypanosoma brucei brucei | 30% | 100% |
Q99280 | Trypanosoma brucei brucei | 32% | 100% |
V5AYH7 | Trypanosoma cruzi | 34% | 100% |