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)
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:0016020 | membrane | 2 | 70 |
GO:0110165 | cellular anatomical entity | 1 | 76 |
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 75 |
GO:0006163 | purine nucleotide metabolic process | 5 | 75 |
GO:0006164 | purine nucleotide biosynthetic process | 6 | 75 |
GO:0006171 | cAMP biosynthetic process | 8 | 75 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 75 |
GO:0006753 | nucleoside phosphate metabolic process | 4 | 75 |
GO:0006793 | phosphorus metabolic process | 3 | 75 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 75 |
GO:0006807 | nitrogen compound metabolic process | 2 | 75 |
GO:0007165 | signal transduction | 2 | 75 |
GO:0008152 | metabolic process | 1 | 75 |
GO:0009058 | biosynthetic process | 2 | 75 |
GO:0009117 | nucleotide metabolic process | 5 | 75 |
GO:0009150 | purine ribonucleotide metabolic process | 6 | 75 |
GO:0009152 | purine ribonucleotide biosynthetic process | 7 | 75 |
GO:0009165 | nucleotide biosynthetic process | 6 | 75 |
GO:0009187 | cyclic nucleotide metabolic process | 6 | 75 |
GO:0009190 | cyclic nucleotide biosynthetic process | 7 | 75 |
GO:0009259 | ribonucleotide metabolic process | 5 | 75 |
GO:0009260 | ribonucleotide biosynthetic process | 6 | 75 |
GO:0009987 | cellular process | 1 | 75 |
GO:0018130 | heterocycle biosynthetic process | 4 | 75 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 75 |
GO:0019637 | organophosphate metabolic process | 3 | 75 |
GO:0019693 | ribose phosphate metabolic process | 4 | 75 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 75 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 75 |
GO:0035556 | intracellular signal transduction | 3 | 75 |
GO:0044237 | cellular metabolic process | 2 | 75 |
GO:0044238 | primary metabolic process | 2 | 75 |
GO:0044249 | cellular biosynthetic process | 3 | 75 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 75 |
GO:0044281 | small molecule metabolic process | 2 | 75 |
GO:0046058 | cAMP metabolic process | 7 | 75 |
GO:0046390 | ribose phosphate biosynthetic process | 5 | 75 |
GO:0046483 | heterocycle metabolic process | 3 | 75 |
GO:0050789 | regulation of biological process | 2 | 75 |
GO:0050794 | regulation of cellular process | 3 | 75 |
GO:0052652 | cyclic purine nucleotide metabolic process | 6 | 75 |
GO:0055086 | nucleobase-containing small molecule metabolic process | 3 | 75 |
GO:0065007 | biological regulation | 1 | 75 |
GO:0071704 | organic substance metabolic process | 2 | 75 |
GO:0072521 | purine-containing compound metabolic process | 4 | 75 |
GO:0072522 | purine-containing compound biosynthetic process | 5 | 75 |
GO:0090407 | organophosphate biosynthetic process | 4 | 75 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 75 |
GO:1901137 | carbohydrate derivative biosynthetic process | 4 | 75 |
GO:1901293 | nucleoside phosphate biosynthetic process | 5 | 75 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 75 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 75 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 75 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 75 |
GO:1901576 | organic substance biosynthetic process | 3 | 75 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 65 |
GO:0016829 | lyase activity | 2 | 65 |
GO:0004016 | adenylate cyclase activity | 3 | 2 |
GO:0009975 | cyclase activity | 2 | 2 |
GO:0016849 | phosphorus-oxygen lyase activity | 3 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 172 | 176 | PF00656 | 0.458 |
CLV_C14_Caspase3-7 | 692 | 696 | PF00656 | 0.362 |
CLV_C14_Caspase3-7 | 915 | 919 | PF00656 | 0.592 |
CLV_C14_Caspase3-7 | 976 | 980 | PF00656 | 0.509 |
CLV_MEL_PAP_1 | 1049 | 1055 | PF00089 | 0.301 |
CLV_NRD_NRD_1 | 11 | 13 | PF00675 | 0.361 |
CLV_NRD_NRD_1 | 1139 | 1141 | PF00675 | 0.436 |
CLV_NRD_NRD_1 | 202 | 204 | PF00675 | 0.610 |
CLV_NRD_NRD_1 | 576 | 578 | PF00675 | 0.507 |
CLV_NRD_NRD_1 | 768 | 770 | PF00675 | 0.522 |
CLV_PCSK_FUR_1 | 200 | 204 | PF00082 | 0.608 |
CLV_PCSK_KEX2_1 | 11 | 13 | PF00082 | 0.389 |
CLV_PCSK_KEX2_1 | 1139 | 1141 | PF00082 | 0.436 |
CLV_PCSK_KEX2_1 | 202 | 204 | PF00082 | 0.611 |
CLV_PCSK_KEX2_1 | 307 | 309 | PF00082 | 0.608 |
CLV_PCSK_KEX2_1 | 539 | 541 | PF00082 | 0.509 |
CLV_PCSK_KEX2_1 | 576 | 578 | PF00082 | 0.483 |
CLV_PCSK_KEX2_1 | 600 | 602 | PF00082 | 0.505 |
CLV_PCSK_KEX2_1 | 768 | 770 | PF00082 | 0.549 |
CLV_PCSK_PC1ET2_1 | 307 | 309 | PF00082 | 0.633 |
CLV_PCSK_PC1ET2_1 | 539 | 541 | PF00082 | 0.528 |
CLV_PCSK_PC1ET2_1 | 600 | 602 | PF00082 | 0.567 |
CLV_PCSK_SKI1_1 | 101 | 105 | PF00082 | 0.695 |
CLV_PCSK_SKI1_1 | 1232 | 1236 | PF00082 | 0.417 |
CLV_PCSK_SKI1_1 | 203 | 207 | PF00082 | 0.617 |
CLV_PCSK_SKI1_1 | 280 | 284 | PF00082 | 0.567 |
CLV_PCSK_SKI1_1 | 300 | 304 | PF00082 | 0.520 |
CLV_PCSK_SKI1_1 | 307 | 311 | PF00082 | 0.502 |
CLV_PCSK_SKI1_1 | 337 | 341 | PF00082 | 0.469 |
CLV_PCSK_SKI1_1 | 380 | 384 | PF00082 | 0.606 |
CLV_PCSK_SKI1_1 | 503 | 507 | PF00082 | 0.600 |
CLV_PCSK_SKI1_1 | 698 | 702 | PF00082 | 0.668 |
DEG_APCC_DBOX_1 | 1117 | 1125 | PF00400 | 0.413 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.482 |
DOC_CKS1_1 | 867 | 872 | PF01111 | 0.415 |
DOC_CYCLIN_RxL_1 | 304 | 314 | PF00134 | 0.263 |
DOC_CYCLIN_yCln2_LP_2 | 230 | 236 | PF00134 | 0.351 |
DOC_CYCLIN_yCln2_LP_2 | 662 | 668 | PF00134 | 0.218 |
DOC_CYCLIN_yCln2_LP_2 | 864 | 870 | PF00134 | 0.424 |
DOC_MAPK_FxFP_2 | 487 | 490 | PF00069 | 0.454 |
DOC_MAPK_gen_1 | 200 | 209 | PF00069 | 0.322 |
DOC_MAPK_gen_1 | 599 | 606 | PF00069 | 0.281 |
DOC_MAPK_MEF2A_6 | 181 | 190 | PF00069 | 0.370 |
DOC_MAPK_MEF2A_6 | 503 | 511 | PF00069 | 0.445 |
DOC_MAPK_MEF2A_6 | 683 | 691 | PF00069 | 0.485 |
DOC_MAPK_RevD_3 | 1126 | 1140 | PF00069 | 0.626 |
DOC_MAPK_RevD_3 | 188 | 203 | PF00069 | 0.263 |
DOC_MAPK_RevD_3 | 585 | 601 | PF00069 | 0.238 |
DOC_PP1_RVXF_1 | 200 | 207 | PF00149 | 0.283 |
DOC_PP1_RVXF_1 | 298 | 304 | PF00149 | 0.438 |
DOC_PP1_RVXF_1 | 737 | 744 | PF00149 | 0.328 |
DOC_PP2B_LxvP_1 | 864 | 867 | PF13499 | 0.492 |
DOC_PP4_FxxP_1 | 43 | 46 | PF00568 | 0.408 |
DOC_PP4_FxxP_1 | 487 | 490 | PF00568 | 0.448 |
DOC_PP4_FxxP_1 | 660 | 663 | PF00568 | 0.422 |
DOC_PP4_FxxP_1 | 770 | 773 | PF00568 | 0.495 |
DOC_SPAK_OSR1_1 | 433 | 437 | PF12202 | 0.249 |
DOC_USP7_MATH_1 | 1238 | 1242 | PF00917 | 0.694 |
DOC_USP7_MATH_1 | 1283 | 1287 | PF00917 | 0.796 |
DOC_USP7_MATH_1 | 147 | 151 | PF00917 | 0.410 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.426 |
DOC_USP7_MATH_1 | 493 | 497 | PF00917 | 0.363 |
DOC_USP7_MATH_1 | 5 | 9 | PF00917 | 0.460 |
DOC_USP7_MATH_1 | 626 | 630 | PF00917 | 0.415 |
DOC_USP7_MATH_1 | 771 | 775 | PF00917 | 0.396 |
DOC_USP7_MATH_1 | 795 | 799 | PF00917 | 0.409 |
DOC_USP7_MATH_1 | 984 | 988 | PF00917 | 0.574 |
DOC_USP7_UBL2_3 | 80 | 84 | PF12436 | 0.312 |
DOC_WW_Pin1_4 | 326 | 331 | PF00397 | 0.416 |
DOC_WW_Pin1_4 | 356 | 361 | PF00397 | 0.442 |
DOC_WW_Pin1_4 | 42 | 47 | PF00397 | 0.436 |
DOC_WW_Pin1_4 | 512 | 517 | PF00397 | 0.267 |
DOC_WW_Pin1_4 | 585 | 590 | PF00397 | 0.379 |
DOC_WW_Pin1_4 | 678 | 683 | PF00397 | 0.385 |
DOC_WW_Pin1_4 | 750 | 755 | PF00397 | 0.474 |
DOC_WW_Pin1_4 | 757 | 762 | PF00397 | 0.453 |
DOC_WW_Pin1_4 | 774 | 779 | PF00397 | 0.411 |
DOC_WW_Pin1_4 | 866 | 871 | PF00397 | 0.375 |
DOC_WW_Pin1_4 | 881 | 886 | PF00397 | 0.459 |
LIG_14-3-3_CanoR_1 | 1036 | 1042 | PF00244 | 0.634 |
LIG_14-3-3_CanoR_1 | 1218 | 1225 | PF00244 | 0.679 |
LIG_14-3-3_CanoR_1 | 1236 | 1241 | PF00244 | 0.699 |
LIG_14-3-3_CanoR_1 | 171 | 179 | PF00244 | 0.439 |
LIG_14-3-3_CanoR_1 | 286 | 293 | PF00244 | 0.420 |
LIG_14-3-3_CanoR_1 | 380 | 385 | PF00244 | 0.469 |
LIG_14-3-3_CanoR_1 | 540 | 544 | PF00244 | 0.356 |
LIG_14-3-3_CanoR_1 | 545 | 551 | PF00244 | 0.324 |
LIG_14-3-3_CanoR_1 | 576 | 580 | PF00244 | 0.245 |
LIG_14-3-3_CanoR_1 | 635 | 639 | PF00244 | 0.451 |
LIG_14-3-3_CanoR_1 | 669 | 679 | PF00244 | 0.365 |
LIG_14-3-3_CanoR_1 | 698 | 703 | PF00244 | 0.274 |
LIG_14-3-3_CanoR_1 | 739 | 744 | PF00244 | 0.456 |
LIG_14-3-3_CanoR_1 | 812 | 822 | PF00244 | 0.314 |
LIG_14-3-3_CanoR_1 | 877 | 885 | PF00244 | 0.483 |
LIG_14-3-3_CterR_2 | 1304 | 1308 | PF00244 | 0.669 |
LIG_AP2alpha_2 | 664 | 666 | PF02296 | 0.221 |
LIG_APCC_ABBA_1 | 136 | 141 | PF00400 | 0.441 |
LIG_APCC_ABBA_1 | 509 | 514 | PF00400 | 0.306 |
LIG_BIR_III_2 | 1134 | 1138 | PF00653 | 0.601 |
LIG_BIR_III_2 | 920 | 924 | PF00653 | 0.667 |
LIG_BRCT_BRCA1_1 | 175 | 179 | PF00533 | 0.399 |
LIG_BRCT_BRCA1_1 | 352 | 356 | PF00533 | 0.526 |
LIG_BRCT_BRCA1_1 | 39 | 43 | PF00533 | 0.195 |
LIG_BRCT_BRCA1_1 | 649 | 653 | PF00533 | 0.342 |
LIG_BRCT_BRCA1_2 | 649 | 655 | PF00533 | 0.232 |
LIG_Clathr_ClatBox_1 | 510 | 514 | PF01394 | 0.369 |
LIG_DLG_GKlike_1 | 739 | 746 | PF00625 | 0.284 |
LIG_eIF4E_1 | 591 | 597 | PF01652 | 0.253 |
LIG_FHA_1 | 1007 | 1013 | PF00498 | 0.506 |
LIG_FHA_1 | 1032 | 1038 | PF00498 | 0.518 |
LIG_FHA_1 | 1082 | 1088 | PF00498 | 0.515 |
LIG_FHA_1 | 116 | 122 | PF00498 | 0.454 |
LIG_FHA_1 | 143 | 149 | PF00498 | 0.309 |
LIG_FHA_1 | 27 | 33 | PF00498 | 0.555 |
LIG_FHA_1 | 37 | 43 | PF00498 | 0.446 |
LIG_FHA_1 | 504 | 510 | PF00498 | 0.376 |
LIG_FHA_1 | 576 | 582 | PF00498 | 0.337 |
LIG_FHA_1 | 657 | 663 | PF00498 | 0.332 |
LIG_FHA_1 | 671 | 677 | PF00498 | 0.376 |
LIG_FHA_1 | 721 | 727 | PF00498 | 0.384 |
LIG_FHA_1 | 775 | 781 | PF00498 | 0.437 |
LIG_FHA_1 | 800 | 806 | PF00498 | 0.399 |
LIG_FHA_1 | 867 | 873 | PF00498 | 0.346 |
LIG_FHA_1 | 998 | 1004 | PF00498 | 0.571 |
LIG_FHA_2 | 1144 | 1150 | PF00498 | 0.741 |
LIG_FHA_2 | 1154 | 1160 | PF00498 | 0.739 |
LIG_FHA_2 | 170 | 176 | PF00498 | 0.449 |
LIG_FHA_2 | 178 | 184 | PF00498 | 0.448 |
LIG_FHA_2 | 384 | 390 | PF00498 | 0.338 |
LIG_FHA_2 | 646 | 652 | PF00498 | 0.300 |
LIG_FHA_2 | 690 | 696 | PF00498 | 0.383 |
LIG_FHA_2 | 882 | 888 | PF00498 | 0.421 |
LIG_FHA_2 | 933 | 939 | PF00498 | 0.508 |
LIG_FHA_2 | 974 | 980 | PF00498 | 0.513 |
LIG_GBD_Chelix_1 | 274 | 282 | PF00786 | 0.545 |
LIG_GBD_Chelix_1 | 994 | 1002 | PF00786 | 0.413 |
LIG_LIR_Apic_2 | 1027 | 1033 | PF02991 | 0.494 |
LIG_LIR_Apic_2 | 40 | 46 | PF02991 | 0.357 |
LIG_LIR_Apic_2 | 484 | 490 | PF02991 | 0.441 |
LIG_LIR_Apic_2 | 588 | 594 | PF02991 | 0.384 |
LIG_LIR_Apic_2 | 659 | 663 | PF02991 | 0.424 |
LIG_LIR_Gen_1 | 1039 | 1049 | PF02991 | 0.565 |
LIG_LIR_Gen_1 | 1061 | 1071 | PF02991 | 0.605 |
LIG_LIR_Gen_1 | 218 | 229 | PF02991 | 0.295 |
LIG_LIR_Gen_1 | 336 | 346 | PF02991 | 0.265 |
LIG_LIR_Gen_1 | 35 | 46 | PF02991 | 0.249 |
LIG_LIR_Gen_1 | 476 | 487 | PF02991 | 0.437 |
LIG_LIR_Gen_1 | 742 | 748 | PF02991 | 0.471 |
LIG_LIR_Gen_1 | 931 | 942 | PF02991 | 0.509 |
LIG_LIR_Nem_3 | 1006 | 1010 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 1013 | 1019 | PF02991 | 0.511 |
LIG_LIR_Nem_3 | 1039 | 1045 | PF02991 | 0.510 |
LIG_LIR_Nem_3 | 1061 | 1067 | PF02991 | 0.534 |
LIG_LIR_Nem_3 | 1068 | 1074 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 1097 | 1103 | PF02991 | 0.541 |
LIG_LIR_Nem_3 | 1187 | 1193 | PF02991 | 0.646 |
LIG_LIR_Nem_3 | 218 | 224 | PF02991 | 0.315 |
LIG_LIR_Nem_3 | 336 | 341 | PF02991 | 0.274 |
LIG_LIR_Nem_3 | 35 | 41 | PF02991 | 0.241 |
LIG_LIR_Nem_3 | 476 | 482 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 742 | 746 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 837 | 843 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 931 | 937 | PF02991 | 0.509 |
LIG_LIR_Nem_3 | 941 | 947 | PF02991 | 0.610 |
LIG_MLH1_MIPbox_1 | 175 | 179 | PF16413 | 0.418 |
LIG_MYND_3 | 607 | 611 | PF01753 | 0.368 |
LIG_NRBOX | 225 | 231 | PF00104 | 0.243 |
LIG_PCNA_yPIPBox_3 | 128 | 136 | PF02747 | 0.246 |
LIG_PCNA_yPIPBox_3 | 223 | 231 | PF02747 | 0.234 |
LIG_PCNA_yPIPBox_3 | 378 | 388 | PF02747 | 0.276 |
LIG_PCNA_yPIPBox_3 | 888 | 896 | PF02747 | 0.237 |
LIG_Pex14_2 | 44 | 48 | PF04695 | 0.207 |
LIG_Pex14_2 | 615 | 619 | PF04695 | 0.199 |
LIG_Pex14_2 | 766 | 770 | PF04695 | 0.344 |
LIG_PTB_Apo_2 | 63 | 70 | PF02174 | 0.371 |
LIG_PTB_Apo_2 | 89 | 96 | PF02174 | 0.247 |
LIG_PTB_Phospho_1 | 63 | 69 | PF10480 | 0.379 |
LIG_PTB_Phospho_1 | 89 | 95 | PF10480 | 0.247 |
LIG_RPA_C_Fungi | 281 | 293 | PF08784 | 0.439 |
LIG_SH2_CRK | 221 | 225 | PF00017 | 0.475 |
LIG_SH2_CRK | 237 | 241 | PF00017 | 0.560 |
LIG_SH2_CRK | 591 | 595 | PF00017 | 0.574 |
LIG_SH2_GRB2like | 840 | 843 | PF00017 | 0.360 |
LIG_SH2_NCK_1 | 1064 | 1068 | PF00017 | 0.482 |
LIG_SH2_PTP2 | 1030 | 1033 | PF00017 | 0.408 |
LIG_SH2_PTP2 | 2 | 5 | PF00017 | 0.223 |
LIG_SH2_PTP2 | 338 | 341 | PF00017 | 0.321 |
LIG_SH2_PTP2 | 603 | 606 | PF00017 | 0.565 |
LIG_SH2_SRC | 1030 | 1033 | PF00017 | 0.425 |
LIG_SH2_SRC | 1064 | 1067 | PF00017 | 0.476 |
LIG_SH2_SRC | 291 | 294 | PF00017 | 0.558 |
LIG_SH2_STAP1 | 1042 | 1046 | PF00017 | 0.438 |
LIG_SH2_STAP1 | 566 | 570 | PF00017 | 0.456 |
LIG_SH2_STAP1 | 69 | 73 | PF00017 | 0.315 |
LIG_SH2_STAP1 | 722 | 726 | PF00017 | 0.309 |
LIG_SH2_STAT3 | 461 | 464 | PF00017 | 0.541 |
LIG_SH2_STAT3 | 843 | 846 | PF00017 | 0.396 |
LIG_SH2_STAT5 | 1030 | 1033 | PF00017 | 0.331 |
LIG_SH2_STAT5 | 1225 | 1228 | PF00017 | 0.520 |
LIG_SH2_STAT5 | 178 | 181 | PF00017 | 0.416 |
LIG_SH2_STAT5 | 2 | 5 | PF00017 | 0.223 |
LIG_SH2_STAT5 | 291 | 294 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 338 | 341 | PF00017 | 0.324 |
LIG_SH2_STAT5 | 349 | 352 | PF00017 | 0.347 |
LIG_SH2_STAT5 | 440 | 443 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 455 | 458 | PF00017 | 0.504 |
LIG_SH2_STAT5 | 461 | 464 | PF00017 | 0.485 |
LIG_SH2_STAT5 | 591 | 594 | PF00017 | 0.534 |
LIG_SH2_STAT5 | 603 | 606 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 618 | 621 | PF00017 | 0.303 |
LIG_SH2_STAT5 | 63 | 66 | PF00017 | 0.502 |
LIG_SH2_STAT5 | 722 | 725 | PF00017 | 0.372 |
LIG_SH2_STAT5 | 911 | 914 | PF00017 | 0.412 |
LIG_SH3_3 | 1208 | 1214 | PF00018 | 0.532 |
LIG_SH3_3 | 132 | 138 | PF00018 | 0.388 |
LIG_SH3_3 | 568 | 574 | PF00018 | 0.514 |
LIG_SH3_3 | 583 | 589 | PF00018 | 0.460 |
LIG_SH3_3 | 794 | 800 | PF00018 | 0.426 |
LIG_SH3_3 | 818 | 824 | PF00018 | 0.428 |
LIG_SH3_3 | 856 | 862 | PF00018 | 0.476 |
LIG_SH3_3 | 864 | 870 | PF00018 | 0.452 |
LIG_Sin3_3 | 30 | 37 | PF02671 | 0.509 |
LIG_SUMO_SIM_anti_2 | 150 | 157 | PF11976 | 0.389 |
LIG_SUMO_SIM_anti_2 | 506 | 512 | PF11976 | 0.433 |
LIG_SUMO_SIM_anti_2 | 567 | 572 | PF11976 | 0.599 |
LIG_SUMO_SIM_anti_2 | 927 | 936 | PF11976 | 0.361 |
LIG_SUMO_SIM_par_1 | 1008 | 1013 | PF11976 | 0.223 |
LIG_SUMO_SIM_par_1 | 144 | 150 | PF11976 | 0.338 |
LIG_SUMO_SIM_par_1 | 262 | 268 | PF11976 | 0.345 |
LIG_SUMO_SIM_par_1 | 896 | 902 | PF11976 | 0.453 |
LIG_TRAF2_1 | 1038 | 1041 | PF00917 | 0.525 |
LIG_TRAF2_1 | 1104 | 1107 | PF00917 | 0.402 |
LIG_TYR_ITIM | 1062 | 1067 | PF00017 | 0.485 |
LIG_TYR_ITIM | 219 | 224 | PF00017 | 0.422 |
LIG_TYR_ITIM | 616 | 621 | PF00017 | 0.431 |
LIG_UBA3_1 | 122 | 131 | PF00899 | 0.435 |
LIG_UBA3_1 | 185 | 189 | PF00899 | 0.549 |
LIG_UBA3_1 | 301 | 307 | PF00899 | 0.426 |
LIG_UBA3_1 | 470 | 475 | PF00899 | 0.544 |
LIG_UBA3_1 | 509 | 517 | PF00899 | 0.278 |
LIG_UBA3_1 | 614 | 620 | PF00899 | 0.478 |
LIG_WRC_WIRS_1 | 384 | 389 | PF05994 | 0.301 |
LIG_WRC_WIRS_1 | 699 | 704 | PF05994 | 0.511 |
LIG_WRC_WIRS_1 | 740 | 745 | PF05994 | 0.587 |
LIG_WW_3 | 1213 | 1217 | PF00397 | 0.663 |
LIG_WW_3 | 1290 | 1294 | PF00397 | 0.499 |
MOD_CDK_SPK_2 | 512 | 517 | PF00069 | 0.222 |
MOD_CDK_SPK_2 | 678 | 683 | PF00069 | 0.269 |
MOD_CDK_SPxxK_3 | 757 | 764 | PF00069 | 0.556 |
MOD_CDK_SPxxK_3 | 881 | 888 | PF00069 | 0.440 |
MOD_CK1_1 | 1171 | 1177 | PF00069 | 0.483 |
MOD_CK1_1 | 1286 | 1292 | PF00069 | 0.679 |
MOD_CK1_1 | 285 | 291 | PF00069 | 0.391 |
MOD_CK1_1 | 314 | 320 | PF00069 | 0.530 |
MOD_CK1_1 | 329 | 335 | PF00069 | 0.579 |
MOD_CK1_1 | 485 | 491 | PF00069 | 0.467 |
MOD_CK1_1 | 629 | 635 | PF00069 | 0.431 |
MOD_CK1_1 | 735 | 741 | PF00069 | 0.413 |
MOD_CK1_1 | 742 | 748 | PF00069 | 0.506 |
MOD_CK1_1 | 750 | 756 | PF00069 | 0.562 |
MOD_CK1_1 | 774 | 780 | PF00069 | 0.478 |
MOD_CK1_1 | 813 | 819 | PF00069 | 0.384 |
MOD_CK1_1 | 881 | 887 | PF00069 | 0.485 |
MOD_CK1_1 | 987 | 993 | PF00069 | 0.507 |
MOD_CK2_1 | 1035 | 1041 | PF00069 | 0.527 |
MOD_CK2_1 | 1101 | 1107 | PF00069 | 0.366 |
MOD_CK2_1 | 1143 | 1149 | PF00069 | 0.666 |
MOD_CK2_1 | 1153 | 1159 | PF00069 | 0.618 |
MOD_CK2_1 | 177 | 183 | PF00069 | 0.542 |
MOD_CK2_1 | 322 | 328 | PF00069 | 0.503 |
MOD_CK2_1 | 383 | 389 | PF00069 | 0.423 |
MOD_CK2_1 | 494 | 500 | PF00069 | 0.313 |
MOD_CK2_1 | 639 | 645 | PF00069 | 0.455 |
MOD_CK2_1 | 881 | 887 | PF00069 | 0.558 |
MOD_CK2_1 | 932 | 938 | PF00069 | 0.358 |
MOD_Cter_Amidation | 1137 | 1140 | PF01082 | 0.531 |
MOD_GlcNHglycan | 1162 | 1165 | PF01048 | 0.574 |
MOD_GlcNHglycan | 1175 | 1178 | PF01048 | 0.369 |
MOD_GlcNHglycan | 1285 | 1288 | PF01048 | 0.677 |
MOD_GlcNHglycan | 1293 | 1296 | PF01048 | 0.719 |
MOD_GlcNHglycan | 1297 | 1300 | PF01048 | 0.737 |
MOD_GlcNHglycan | 241 | 244 | PF01048 | 0.448 |
MOD_GlcNHglycan | 288 | 291 | PF01048 | 0.518 |
MOD_GlcNHglycan | 311 | 314 | PF01048 | 0.517 |
MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.633 |
MOD_GlcNHglycan | 351 | 355 | PF01048 | 0.403 |
MOD_GlcNHglycan | 373 | 376 | PF01048 | 0.629 |
MOD_GlcNHglycan | 403 | 406 | PF01048 | 0.504 |
MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.557 |
MOD_GlcNHglycan | 491 | 494 | PF01048 | 0.443 |
MOD_GlcNHglycan | 628 | 631 | PF01048 | 0.459 |
MOD_GlcNHglycan | 641 | 644 | PF01048 | 0.479 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.427 |
MOD_GlcNHglycan | 833 | 836 | PF01048 | 0.429 |
MOD_GlcNHglycan | 880 | 883 | PF01048 | 0.593 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.396 |
MOD_GlcNHglycan | 986 | 989 | PF01048 | 0.452 |
MOD_GSK3_1 | 1031 | 1038 | PF00069 | 0.511 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.471 |
MOD_GSK3_1 | 1153 | 1160 | PF00069 | 0.535 |
MOD_GSK3_1 | 1167 | 1174 | PF00069 | 0.579 |
MOD_GSK3_1 | 1214 | 1221 | PF00069 | 0.635 |
MOD_GSK3_1 | 1291 | 1298 | PF00069 | 0.754 |
MOD_GSK3_1 | 162 | 169 | PF00069 | 0.407 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.480 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.496 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.504 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.465 |
MOD_GSK3_1 | 322 | 329 | PF00069 | 0.609 |
MOD_GSK3_1 | 352 | 359 | PF00069 | 0.584 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.657 |
MOD_GSK3_1 | 376 | 383 | PF00069 | 0.562 |
MOD_GSK3_1 | 485 | 492 | PF00069 | 0.388 |
MOD_GSK3_1 | 544 | 551 | PF00069 | 0.399 |
MOD_GSK3_1 | 581 | 588 | PF00069 | 0.382 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.378 |
MOD_GSK3_1 | 670 | 677 | PF00069 | 0.443 |
MOD_GSK3_1 | 694 | 701 | PF00069 | 0.516 |
MOD_GSK3_1 | 727 | 734 | PF00069 | 0.489 |
MOD_GSK3_1 | 735 | 742 | PF00069 | 0.440 |
MOD_GSK3_1 | 795 | 802 | PF00069 | 0.457 |
MOD_GSK3_1 | 810 | 817 | PF00069 | 0.413 |
MOD_GSK3_1 | 827 | 834 | PF00069 | 0.464 |
MOD_GSK3_1 | 862 | 869 | PF00069 | 0.491 |
MOD_GSK3_1 | 877 | 884 | PF00069 | 0.485 |
MOD_GSK3_1 | 928 | 935 | PF00069 | 0.375 |
MOD_GSK3_1 | 973 | 980 | PF00069 | 0.360 |
MOD_N-GLC_1 | 115 | 120 | PF02516 | 0.330 |
MOD_N-GLC_1 | 380 | 385 | PF02516 | 0.372 |
MOD_N-GLC_1 | 494 | 499 | PF02516 | 0.551 |
MOD_N-GLC_1 | 564 | 569 | PF02516 | 0.500 |
MOD_N-GLC_1 | 774 | 779 | PF02516 | 0.509 |
MOD_NEK2_1 | 1168 | 1173 | PF00069 | 0.522 |
MOD_NEK2_1 | 1184 | 1189 | PF00069 | 0.312 |
MOD_NEK2_1 | 164 | 169 | PF00069 | 0.491 |
MOD_NEK2_1 | 207 | 212 | PF00069 | 0.486 |
MOD_NEK2_1 | 222 | 227 | PF00069 | 0.428 |
MOD_NEK2_1 | 256 | 261 | PF00069 | 0.413 |
MOD_NEK2_1 | 282 | 287 | PF00069 | 0.428 |
MOD_NEK2_1 | 309 | 314 | PF00069 | 0.358 |
MOD_NEK2_1 | 32 | 37 | PF00069 | 0.460 |
MOD_NEK2_1 | 456 | 461 | PF00069 | 0.498 |
MOD_NEK2_1 | 546 | 551 | PF00069 | 0.409 |
MOD_NEK2_1 | 64 | 69 | PF00069 | 0.333 |
MOD_NEK2_1 | 653 | 658 | PF00069 | 0.389 |
MOD_NEK2_1 | 672 | 677 | PF00069 | 0.289 |
MOD_NEK2_1 | 811 | 816 | PF00069 | 0.331 |
MOD_NEK2_1 | 90 | 95 | PF00069 | 0.352 |
MOD_NEK2_2 | 166 | 171 | PF00069 | 0.508 |
MOD_NEK2_2 | 173 | 178 | PF00069 | 0.536 |
MOD_PIKK_1 | 1238 | 1244 | PF00454 | 0.641 |
MOD_PIKK_1 | 22 | 28 | PF00454 | 0.247 |
MOD_PIKK_1 | 341 | 347 | PF00454 | 0.449 |
MOD_PIKK_1 | 799 | 805 | PF00454 | 0.384 |
MOD_PK_1 | 539 | 545 | PF00069 | 0.317 |
MOD_PKA_1 | 539 | 545 | PF00069 | 0.514 |
MOD_PKA_2 | 1035 | 1041 | PF00069 | 0.528 |
MOD_PKA_2 | 1283 | 1289 | PF00069 | 0.739 |
MOD_PKA_2 | 285 | 291 | PF00069 | 0.508 |
MOD_PKA_2 | 539 | 545 | PF00069 | 0.455 |
MOD_PKA_2 | 575 | 581 | PF00069 | 0.410 |
MOD_PKA_2 | 634 | 640 | PF00069 | 0.504 |
MOD_PKA_2 | 811 | 817 | PF00069 | 0.258 |
MOD_PKB_1 | 1216 | 1224 | PF00069 | 0.699 |
MOD_PKB_1 | 378 | 386 | PF00069 | 0.317 |
MOD_PKB_1 | 875 | 883 | PF00069 | 0.396 |
MOD_Plk_1 | 361 | 367 | PF00069 | 0.438 |
MOD_Plk_1 | 380 | 386 | PF00069 | 0.311 |
MOD_Plk_1 | 475 | 481 | PF00069 | 0.462 |
MOD_Plk_1 | 564 | 570 | PF00069 | 0.490 |
MOD_Plk_2-3 | 361 | 367 | PF00069 | 0.607 |
MOD_Plk_2-3 | 645 | 651 | PF00069 | 0.515 |
MOD_Plk_2-3 | 973 | 979 | PF00069 | 0.358 |
MOD_Plk_4 | 173 | 179 | PF00069 | 0.445 |
MOD_Plk_4 | 225 | 231 | PF00069 | 0.457 |
MOD_Plk_4 | 293 | 299 | PF00069 | 0.443 |
MOD_Plk_4 | 311 | 317 | PF00069 | 0.384 |
MOD_Plk_4 | 368 | 374 | PF00069 | 0.632 |
MOD_Plk_4 | 37 | 43 | PF00069 | 0.277 |
MOD_Plk_4 | 383 | 389 | PF00069 | 0.554 |
MOD_Plk_4 | 403 | 409 | PF00069 | 0.555 |
MOD_Plk_4 | 44 | 50 | PF00069 | 0.252 |
MOD_Plk_4 | 469 | 475 | PF00069 | 0.464 |
MOD_Plk_4 | 482 | 488 | PF00069 | 0.399 |
MOD_Plk_4 | 503 | 509 | PF00069 | 0.465 |
MOD_Plk_4 | 581 | 587 | PF00069 | 0.361 |
MOD_Plk_4 | 64 | 70 | PF00069 | 0.209 |
MOD_Plk_4 | 698 | 704 | PF00069 | 0.495 |
MOD_Plk_4 | 776 | 782 | PF00069 | 0.458 |
MOD_Plk_4 | 785 | 791 | PF00069 | 0.370 |
MOD_Plk_4 | 868 | 874 | PF00069 | 0.441 |
MOD_Plk_4 | 928 | 934 | PF00069 | 0.356 |
MOD_Plk_4 | 977 | 983 | PF00069 | 0.360 |
MOD_ProDKin_1 | 326 | 332 | PF00069 | 0.503 |
MOD_ProDKin_1 | 356 | 362 | PF00069 | 0.543 |
MOD_ProDKin_1 | 42 | 48 | PF00069 | 0.436 |
MOD_ProDKin_1 | 512 | 518 | PF00069 | 0.301 |
MOD_ProDKin_1 | 585 | 591 | PF00069 | 0.455 |
MOD_ProDKin_1 | 678 | 684 | PF00069 | 0.467 |
MOD_ProDKin_1 | 750 | 756 | PF00069 | 0.589 |
MOD_ProDKin_1 | 757 | 763 | PF00069 | 0.564 |
MOD_ProDKin_1 | 774 | 780 | PF00069 | 0.501 |
MOD_ProDKin_1 | 866 | 872 | PF00069 | 0.448 |
MOD_ProDKin_1 | 881 | 887 | PF00069 | 0.564 |
MOD_SUMO_for_1 | 154 | 157 | PF00179 | 0.294 |
MOD_SUMO_rev_2 | 183 | 191 | PF00179 | 0.526 |
MOD_SUMO_rev_2 | 72 | 82 | PF00179 | 0.319 |
TRG_DiLeu_BaEn_1 | 60 | 65 | PF01217 | 0.521 |
TRG_DiLeu_BaEn_1 | 928 | 933 | PF01217 | 0.486 |
TRG_DiLeu_BaEn_2 | 610 | 616 | PF01217 | 0.360 |
TRG_DiLeu_BaLyEn_6 | 305 | 310 | PF01217 | 0.513 |
TRG_DiLeu_BaLyEn_6 | 736 | 741 | PF01217 | 0.314 |
TRG_DiLeu_LyEn_5 | 1201 | 1206 | PF01217 | 0.548 |
TRG_ENDOCYTIC_2 | 1016 | 1019 | PF00928 | 0.366 |
TRG_ENDOCYTIC_2 | 1042 | 1045 | PF00928 | 0.346 |
TRG_ENDOCYTIC_2 | 1064 | 1067 | PF00928 | 0.482 |
TRG_ENDOCYTIC_2 | 221 | 224 | PF00928 | 0.491 |
TRG_ENDOCYTIC_2 | 338 | 341 | PF00928 | 0.324 |
TRG_ENDOCYTIC_2 | 603 | 606 | PF00928 | 0.560 |
TRG_ENDOCYTIC_2 | 618 | 621 | PF00928 | 0.464 |
TRG_ENDOCYTIC_2 | 722 | 725 | PF00928 | 0.387 |
TRG_ENDOCYTIC_2 | 911 | 914 | PF00928 | 0.482 |
TRG_ER_diArg_1 | 1049 | 1052 | PF00400 | 0.359 |
TRG_ER_diArg_1 | 1215 | 1218 | PF00400 | 0.689 |
TRG_ER_diArg_1 | 1244 | 1247 | PF00400 | 0.668 |
TRG_ER_diArg_1 | 199 | 202 | PF00400 | 0.479 |
TRG_ER_diArg_1 | 377 | 380 | PF00400 | 0.326 |
TRG_ER_diArg_1 | 575 | 577 | PF00400 | 0.390 |
TRG_ER_diArg_1 | 768 | 770 | PF00400 | 0.423 |
TRG_ER_diArg_1 | 874 | 877 | PF00400 | 0.514 |
TRG_Pf-PMV_PEXEL_1 | 960 | 964 | PF00026 | 0.431 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P457 | Leptomonas seymouri | 26% | 99% |
A0A1X0NPQ6 | Trypanosomatidae | 30% | 100% |
A0A1X0P171 | Trypanosomatidae | 33% | 100% |
A0A3Q8IJB0 | Leishmania donovani | 54% | 98% |
A0A3R7M6J4 | Trypanosoma rangeli | 37% | 100% |
A0A3R7R8G4 | Trypanosoma rangeli | 31% | 100% |
A0A3S5H6Z8 | Leishmania donovani | 54% | 98% |
A0A3S7WU91 | Leishmania donovani | 55% | 93% |
A0A3S7WU94 | Leishmania donovani | 68% | 95% |
A0A3S7WU95 | Leishmania donovani | 54% | 93% |
A0A3S7XB85 | Leishmania donovani | 30% | 93% |
A4H8V5 | Leishmania braziliensis | 68% | 100% |
A4H8V7 | Leishmania braziliensis | 65% | 100% |
A4H8V8 | Leishmania braziliensis | 64% | 93% |
A4HPI4 | Leishmania braziliensis | 27% | 93% |
A4HX84 | Leishmania infantum | 68% | 95% |
A4HX85 | Leishmania infantum | 55% | 93% |
A4HX87 | Leishmania infantum | 56% | 99% |
A4HX88 | Leishmania infantum | 42% | 100% |
A4IDA6 | Leishmania infantum | 30% | 93% |
C9ZM79 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
C9ZM80 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
C9ZM81 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
C9ZM82 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
C9ZM83 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZM86 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZN26 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
C9ZN41 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
C9ZN43 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZN44 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
C9ZN45 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
C9ZN46 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
C9ZNA5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
C9ZNA6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
C9ZNH3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 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) | 33% | 100% |
C9ZQ89 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
C9ZQ90 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZQ91 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 100% |
C9ZQ92 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
C9ZTS4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZTS5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
C9ZTS6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZUE6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
C9ZWQ5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
C9ZWU2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 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) | 34% | 100% |
D0A0U3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
D0A0W7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
D0A0X5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
D0A1S1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
D0A5D2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
D0A5D5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 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) | 56% | 93% |
E9AQY1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 66% | 94% |
E9AQY2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 54% | 93% |
E9AQY4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 54% | 98% |
E9ARD7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 66% | 95% |
E9AT96 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 93% |
Q25263 | Leishmania donovani | 55% | 98% |
Q26721 | Trypanosoma brucei brucei | 34% | 100% |
Q27675 | Leishmania donovani | 68% | 95% |
Q4Q1A1 | Leishmania major | 29% | 100% |
Q4QEH9 | Leishmania major | 54% | 100% |
Q4QEI0 | Leishmania major | 54% | 100% |
Q4QEI1 | Leishmania major | 55% | 100% |
Q4QEI2 | Leishmania major | 55% | 100% |
Q4QEI3 | Leishmania major | 66% | 100% |
Q99279 | Trypanosoma brucei brucei | 29% | 100% |
Q99280 | Trypanosoma brucei brucei | 31% | 100% |
V5AYH7 | Trypanosoma cruzi | 34% | 100% |