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: 57 |
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 | yes | yes: 46, no: 28 |
NetGPI | no | yes: 0, no: 74 |
Term | Name | Level | Count |
---|---|---|---|
GO:0110165 | cellular anatomical entity | 1 | 75 |
GO:0016020 | membrane | 2 | 68 |
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 74 |
GO:0006163 | purine nucleotide metabolic process | 5 | 74 |
GO:0006164 | purine nucleotide biosynthetic process | 6 | 74 |
GO:0006171 | cAMP biosynthetic process | 8 | 74 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 74 |
GO:0006753 | nucleoside phosphate metabolic process | 4 | 74 |
GO:0006793 | phosphorus metabolic process | 3 | 74 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 74 |
GO:0006807 | nitrogen compound metabolic process | 2 | 74 |
GO:0007165 | signal transduction | 2 | 74 |
GO:0008152 | metabolic process | 1 | 74 |
GO:0009058 | biosynthetic process | 2 | 74 |
GO:0009117 | nucleotide metabolic process | 5 | 74 |
GO:0009150 | purine ribonucleotide metabolic process | 6 | 74 |
GO:0009152 | purine ribonucleotide biosynthetic process | 7 | 74 |
GO:0009165 | nucleotide biosynthetic process | 6 | 74 |
GO:0009187 | cyclic nucleotide metabolic process | 6 | 74 |
GO:0009190 | cyclic nucleotide biosynthetic process | 7 | 74 |
GO:0009259 | ribonucleotide metabolic process | 5 | 74 |
GO:0009260 | ribonucleotide biosynthetic process | 6 | 74 |
GO:0009987 | cellular process | 1 | 74 |
GO:0018130 | heterocycle biosynthetic process | 4 | 74 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 74 |
GO:0019637 | organophosphate metabolic process | 3 | 74 |
GO:0019693 | ribose phosphate metabolic process | 4 | 74 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 74 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 74 |
GO:0035556 | intracellular signal transduction | 3 | 74 |
GO:0044237 | cellular metabolic process | 2 | 74 |
GO:0044238 | primary metabolic process | 2 | 74 |
GO:0044249 | cellular biosynthetic process | 3 | 74 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 74 |
GO:0044281 | small molecule metabolic process | 2 | 74 |
GO:0046058 | cAMP metabolic process | 7 | 74 |
GO:0046390 | ribose phosphate biosynthetic process | 5 | 74 |
GO:0046483 | heterocycle metabolic process | 3 | 74 |
GO:0050789 | regulation of biological process | 2 | 74 |
GO:0050794 | regulation of cellular process | 3 | 74 |
GO:0052652 | cyclic purine nucleotide metabolic process | 6 | 74 |
GO:0055086 | nucleobase-containing small molecule metabolic process | 3 | 74 |
GO:0065007 | biological regulation | 1 | 74 |
GO:0071704 | organic substance metabolic process | 2 | 74 |
GO:0072521 | purine-containing compound metabolic process | 4 | 74 |
GO:0072522 | purine-containing compound biosynthetic process | 5 | 74 |
GO:0090407 | organophosphate biosynthetic process | 4 | 74 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 74 |
GO:1901137 | carbohydrate derivative biosynthetic process | 4 | 74 |
GO:1901293 | nucleoside phosphate biosynthetic process | 5 | 74 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 74 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 74 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 74 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 74 |
GO:1901576 | organic substance biosynthetic process | 3 | 74 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 64 |
GO:0016829 | lyase activity | 2 | 64 |
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 | 1009 | 1013 | PF00656 | 0.557 |
CLV_C14_Caspase3-7 | 1250 | 1254 | PF00656 | 0.699 |
CLV_C14_Caspase3-7 | 1332 | 1336 | PF00656 | 0.704 |
CLV_C14_Caspase3-7 | 172 | 176 | PF00656 | 0.434 |
CLV_C14_Caspase3-7 | 670 | 674 | PF00656 | 0.364 |
CLV_C14_Caspase3-7 | 975 | 979 | PF00656 | 0.488 |
CLV_MEL_PAP_1 | 1361 | 1367 | PF00089 | 0.313 |
CLV_NRD_NRD_1 | 1138 | 1140 | PF00675 | 0.421 |
CLV_NRD_NRD_1 | 202 | 204 | PF00675 | 0.587 |
CLV_NRD_NRD_1 | 378 | 380 | PF00675 | 0.511 |
CLV_NRD_NRD_1 | 599 | 601 | PF00675 | 0.477 |
CLV_PCSK_FUR_1 | 200 | 204 | PF00082 | 0.587 |
CLV_PCSK_KEX2_1 | 1138 | 1140 | PF00082 | 0.421 |
CLV_PCSK_KEX2_1 | 1257 | 1259 | PF00082 | 0.452 |
CLV_PCSK_KEX2_1 | 202 | 204 | PF00082 | 0.588 |
CLV_PCSK_KEX2_1 | 307 | 309 | PF00082 | 0.581 |
CLV_PCSK_KEX2_1 | 599 | 601 | PF00082 | 0.504 |
CLV_PCSK_PC1ET2_1 | 1257 | 1259 | PF00082 | 0.557 |
CLV_PCSK_PC1ET2_1 | 307 | 309 | PF00082 | 0.606 |
CLV_PCSK_SKI1_1 | 1000 | 1004 | PF00082 | 0.283 |
CLV_PCSK_SKI1_1 | 101 | 105 | PF00082 | 0.699 |
CLV_PCSK_SKI1_1 | 1235 | 1239 | PF00082 | 0.430 |
CLV_PCSK_SKI1_1 | 1373 | 1377 | PF00082 | 0.341 |
CLV_PCSK_SKI1_1 | 203 | 207 | PF00082 | 0.579 |
CLV_PCSK_SKI1_1 | 280 | 284 | PF00082 | 0.530 |
CLV_PCSK_SKI1_1 | 300 | 304 | PF00082 | 0.492 |
CLV_PCSK_SKI1_1 | 307 | 311 | PF00082 | 0.477 |
CLV_PCSK_SKI1_1 | 802 | 806 | PF00082 | 0.534 |
CLV_PCSK_SKI1_1 | 962 | 966 | PF00082 | 0.226 |
DEG_APCC_DBOX_1 | 875 | 883 | PF00400 | 0.326 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.277 |
DEG_SCF_FBW7_2 | 865 | 872 | PF00400 | 0.489 |
DEG_SPOP_SBC_1 | 285 | 289 | PF00917 | 0.446 |
DEG_SPOP_SBC_1 | 330 | 334 | PF00917 | 0.245 |
DEG_SPOP_SBC_1 | 793 | 797 | PF00917 | 0.429 |
DOC_CDC14_PxL_1 | 589 | 597 | PF14671 | 0.391 |
DOC_CKS1_1 | 866 | 871 | PF01111 | 0.434 |
DOC_CYCLIN_RxL_1 | 304 | 314 | PF00134 | 0.239 |
DOC_CYCLIN_yClb1_LxF_4 | 196 | 201 | PF00134 | 0.186 |
DOC_CYCLIN_yCln2_LP_2 | 230 | 236 | PF00134 | 0.336 |
DOC_CYCLIN_yCln2_LP_2 | 863 | 869 | PF00134 | 0.436 |
DOC_MAPK_FxFP_2 | 486 | 489 | PF00069 | 0.259 |
DOC_MAPK_gen_1 | 1046 | 1054 | PF00069 | 0.510 |
DOC_MAPK_gen_1 | 198 | 206 | PF00069 | 0.290 |
DOC_MAPK_gen_1 | 26 | 34 | PF00069 | 0.526 |
DOC_MAPK_gen_1 | 596 | 605 | PF00069 | 0.279 |
DOC_MAPK_MEF2A_6 | 181 | 190 | PF00069 | 0.344 |
DOC_MAPK_MEF2A_6 | 497 | 506 | PF00069 | 0.421 |
DOC_MAPK_RevD_3 | 1125 | 1139 | PF00069 | 0.539 |
DOC_MAPK_RevD_3 | 188 | 203 | PF00069 | 0.240 |
DOC_PP1_RVXF_1 | 196 | 202 | PF00149 | 0.251 |
DOC_PP1_RVXF_1 | 298 | 304 | PF00149 | 0.419 |
DOC_PP2B_LxvP_1 | 1343 | 1346 | PF13499 | 0.497 |
DOC_PP2B_LxvP_1 | 160 | 163 | PF13499 | 0.419 |
DOC_PP2B_LxvP_1 | 863 | 866 | PF13499 | 0.502 |
DOC_PP4_FxxP_1 | 486 | 489 | PF00568 | 0.447 |
DOC_PP4_FxxP_1 | 659 | 662 | PF00568 | 0.413 |
DOC_PP4_FxxP_1 | 769 | 772 | PF00568 | 0.282 |
DOC_SPAK_OSR1_1 | 432 | 436 | PF12202 | 0.233 |
DOC_USP7_MATH_1 | 1010 | 1014 | PF00917 | 0.606 |
DOC_USP7_MATH_1 | 1237 | 1241 | PF00917 | 0.660 |
DOC_USP7_MATH_1 | 285 | 289 | PF00917 | 0.445 |
DOC_USP7_MATH_1 | 330 | 334 | PF00917 | 0.317 |
DOC_USP7_MATH_1 | 531 | 535 | PF00917 | 0.372 |
DOC_USP7_MATH_1 | 662 | 666 | PF00917 | 0.411 |
DOC_USP7_MATH_1 | 791 | 795 | PF00917 | 0.368 |
DOC_USP7_MATH_1 | 983 | 987 | PF00917 | 0.556 |
DOC_USP7_UBL2_3 | 189 | 193 | PF12436 | 0.195 |
DOC_WW_Pin1_4 | 1073 | 1078 | PF00397 | 0.532 |
DOC_WW_Pin1_4 | 326 | 331 | PF00397 | 0.407 |
DOC_WW_Pin1_4 | 677 | 682 | PF00397 | 0.350 |
DOC_WW_Pin1_4 | 773 | 778 | PF00397 | 0.345 |
DOC_WW_Pin1_4 | 861 | 866 | PF00397 | 0.391 |
DOC_WW_Pin1_4 | 880 | 885 | PF00397 | 0.378 |
LIG_14-3-3_CanoR_1 | 1035 | 1041 | PF00244 | 0.616 |
LIG_14-3-3_CanoR_1 | 1217 | 1224 | PF00244 | 0.648 |
LIG_14-3-3_CanoR_1 | 1235 | 1240 | PF00244 | 0.619 |
LIG_14-3-3_CanoR_1 | 1258 | 1267 | PF00244 | 0.561 |
LIG_14-3-3_CanoR_1 | 1339 | 1346 | PF00244 | 0.706 |
LIG_14-3-3_CanoR_1 | 171 | 179 | PF00244 | 0.416 |
LIG_14-3-3_CanoR_1 | 286 | 293 | PF00244 | 0.412 |
LIG_14-3-3_CanoR_1 | 308 | 317 | PF00244 | 0.448 |
LIG_14-3-3_CanoR_1 | 321 | 331 | PF00244 | 0.437 |
LIG_14-3-3_CanoR_1 | 420 | 424 | PF00244 | 0.334 |
LIG_14-3-3_CanoR_1 | 474 | 479 | PF00244 | 0.379 |
LIG_14-3-3_CanoR_1 | 624 | 628 | PF00244 | 0.395 |
LIG_14-3-3_CanoR_1 | 638 | 646 | PF00244 | 0.341 |
LIG_14-3-3_CanoR_1 | 725 | 731 | PF00244 | 0.410 |
LIG_14-3-3_CanoR_1 | 738 | 743 | PF00244 | 0.432 |
LIG_14-3-3_CanoR_1 | 985 | 993 | PF00244 | 0.598 |
LIG_Actin_WH2_2 | 609 | 626 | PF00022 | 0.211 |
LIG_Actin_WH2_2 | 710 | 727 | PF00022 | 0.383 |
LIG_APCC_ABBA_1 | 136 | 141 | PF00400 | 0.427 |
LIG_APCC_ABBA_1 | 717 | 722 | PF00400 | 0.299 |
LIG_BIR_III_2 | 919 | 923 | PF00653 | 0.643 |
LIG_BRCT_BRCA1_1 | 175 | 179 | PF00533 | 0.366 |
LIG_BRCT_BRCA1_1 | 351 | 355 | PF00533 | 0.264 |
LIG_BRCT_BRCA1_1 | 694 | 698 | PF00533 | 0.427 |
LIG_deltaCOP1_diTrp_1 | 756 | 765 | PF00928 | 0.453 |
LIG_DLG_GKlike_1 | 738 | 745 | PF00625 | 0.264 |
LIG_FHA_1 | 1006 | 1012 | PF00498 | 0.487 |
LIG_FHA_1 | 1031 | 1037 | PF00498 | 0.497 |
LIG_FHA_1 | 1081 | 1087 | PF00498 | 0.493 |
LIG_FHA_1 | 143 | 149 | PF00498 | 0.306 |
LIG_FHA_1 | 28 | 34 | PF00498 | 0.431 |
LIG_FHA_1 | 326 | 332 | PF00498 | 0.307 |
LIG_FHA_1 | 412 | 418 | PF00498 | 0.405 |
LIG_FHA_1 | 624 | 630 | PF00498 | 0.337 |
LIG_FHA_1 | 631 | 637 | PF00498 | 0.352 |
LIG_FHA_1 | 656 | 662 | PF00498 | 0.323 |
LIG_FHA_1 | 670 | 676 | PF00498 | 0.366 |
LIG_FHA_1 | 725 | 731 | PF00498 | 0.368 |
LIG_FHA_1 | 774 | 780 | PF00498 | 0.376 |
LIG_FHA_1 | 793 | 799 | PF00498 | 0.305 |
LIG_FHA_1 | 803 | 809 | PF00498 | 0.384 |
LIG_FHA_1 | 902 | 908 | PF00498 | 0.386 |
LIG_FHA_1 | 997 | 1003 | PF00498 | 0.552 |
LIG_FHA_2 | 1023 | 1029 | PF00498 | 0.585 |
LIG_FHA_2 | 1143 | 1149 | PF00498 | 0.735 |
LIG_FHA_2 | 1153 | 1159 | PF00498 | 0.725 |
LIG_FHA_2 | 1171 | 1177 | PF00498 | 0.569 |
LIG_FHA_2 | 1245 | 1251 | PF00498 | 0.679 |
LIG_FHA_2 | 170 | 176 | PF00498 | 0.424 |
LIG_FHA_2 | 178 | 184 | PF00498 | 0.428 |
LIG_FHA_2 | 380 | 386 | PF00498 | 0.372 |
LIG_FHA_2 | 478 | 484 | PF00498 | 0.305 |
LIG_FHA_2 | 73 | 79 | PF00498 | 0.413 |
LIG_FHA_2 | 749 | 755 | PF00498 | 0.283 |
LIG_FHA_2 | 795 | 801 | PF00498 | 0.307 |
LIG_FHA_2 | 82 | 88 | PF00498 | 0.365 |
LIG_FHA_2 | 830 | 836 | PF00498 | 0.413 |
LIG_FHA_2 | 932 | 938 | PF00498 | 0.488 |
LIG_FHA_2 | 973 | 979 | PF00498 | 0.492 |
LIG_GBD_Chelix_1 | 118 | 126 | PF00786 | 0.619 |
LIG_GBD_Chelix_1 | 191 | 199 | PF00786 | 0.389 |
LIG_GBD_Chelix_1 | 993 | 1001 | PF00786 | 0.396 |
LIG_LIR_Apic_2 | 1027 | 1032 | PF02991 | 0.478 |
LIG_LIR_Apic_2 | 443 | 447 | PF02991 | 0.365 |
LIG_LIR_Apic_2 | 483 | 489 | PF02991 | 0.442 |
LIG_LIR_Apic_2 | 658 | 662 | PF02991 | 0.419 |
LIG_LIR_Gen_1 | 1012 | 1023 | PF02991 | 0.462 |
LIG_LIR_Gen_1 | 1038 | 1048 | PF02991 | 0.543 |
LIG_LIR_Gen_1 | 1060 | 1070 | PF02991 | 0.586 |
LIG_LIR_Gen_1 | 238 | 248 | PF02991 | 0.348 |
LIG_LIR_Gen_1 | 250 | 261 | PF02991 | 0.329 |
LIG_LIR_Gen_1 | 477 | 486 | PF02991 | 0.391 |
LIG_LIR_Gen_1 | 544 | 554 | PF02991 | 0.346 |
LIG_LIR_Gen_1 | 695 | 706 | PF02991 | 0.383 |
LIG_LIR_Gen_1 | 718 | 728 | PF02991 | 0.281 |
LIG_LIR_Gen_1 | 741 | 747 | PF02991 | 0.361 |
LIG_LIR_Gen_1 | 930 | 941 | PF02991 | 0.489 |
LIG_LIR_Nem_3 | 1012 | 1018 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 1038 | 1044 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 1060 | 1066 | PF02991 | 0.507 |
LIG_LIR_Nem_3 | 1067 | 1073 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 1096 | 1102 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 1186 | 1192 | PF02991 | 0.631 |
LIG_LIR_Nem_3 | 238 | 244 | PF02991 | 0.286 |
LIG_LIR_Nem_3 | 304 | 309 | PF02991 | 0.370 |
LIG_LIR_Nem_3 | 352 | 358 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 477 | 482 | PF02991 | 0.322 |
LIG_LIR_Nem_3 | 512 | 517 | PF02991 | 0.339 |
LIG_LIR_Nem_3 | 544 | 549 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 695 | 701 | PF02991 | 0.372 |
LIG_LIR_Nem_3 | 718 | 724 | PF02991 | 0.310 |
LIG_LIR_Nem_3 | 741 | 745 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 756 | 762 | PF02991 | 0.349 |
LIG_LIR_Nem_3 | 836 | 842 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 930 | 936 | PF02991 | 0.489 |
LIG_LIR_Nem_3 | 940 | 946 | PF02991 | 0.592 |
LIG_LYPXL_yS_3 | 514 | 517 | PF13949 | 0.422 |
LIG_MLH1_MIPbox_1 | 175 | 179 | PF16413 | 0.382 |
LIG_MYND_1 | 861 | 865 | PF01753 | 0.385 |
LIG_MYND_3 | 606 | 610 | PF01753 | 0.358 |
LIG_NRBOX | 225 | 231 | PF00104 | 0.231 |
LIG_NRBOX | 674 | 680 | PF00104 | 0.219 |
LIG_PCNA_TLS_4 | 380 | 387 | PF02747 | 0.271 |
LIG_PCNA_yPIPBox_3 | 128 | 136 | PF02747 | 0.229 |
LIG_PCNA_yPIPBox_3 | 216 | 230 | PF02747 | 0.231 |
LIG_PCNA_yPIPBox_3 | 299 | 308 | PF02747 | 0.314 |
LIG_Pex14_1 | 478 | 482 | PF04695 | 0.197 |
LIG_Pex14_2 | 482 | 486 | PF04695 | 0.436 |
LIG_Pex14_2 | 765 | 769 | PF04695 | 0.285 |
LIG_PTB_Apo_2 | 1365 | 1372 | PF02174 | 0.490 |
LIG_PTB_Apo_2 | 63 | 70 | PF02174 | 0.391 |
LIG_PTB_Apo_2 | 803 | 810 | PF02174 | 0.264 |
LIG_PTB_Phospho_1 | 1365 | 1371 | PF10480 | 0.490 |
LIG_PTB_Phospho_1 | 63 | 69 | PF10480 | 0.400 |
LIG_PTB_Phospho_1 | 803 | 809 | PF10480 | 0.312 |
LIG_SH2_CRK | 237 | 241 | PF00017 | 0.417 |
LIG_SH2_CRK | 306 | 310 | PF00017 | 0.419 |
LIG_SH2_CRK | 444 | 448 | PF00017 | 0.363 |
LIG_SH2_GRB2like | 809 | 812 | PF00017 | 0.411 |
LIG_SH2_NCK_1 | 1063 | 1067 | PF00017 | 0.580 |
LIG_SH2_NCK_1 | 116 | 120 | PF00017 | 0.381 |
LIG_SH2_NCK_1 | 237 | 241 | PF00017 | 0.430 |
LIG_SH2_NCK_1 | 617 | 621 | PF00017 | 0.410 |
LIG_SH2_PTP2 | 1029 | 1032 | PF00017 | 0.522 |
LIG_SH2_PTP2 | 602 | 605 | PF00017 | 0.446 |
LIG_SH2_SRC | 1029 | 1032 | PF00017 | 0.535 |
LIG_SH2_SRC | 1063 | 1066 | PF00017 | 0.580 |
LIG_SH2_SRC | 116 | 119 | PF00017 | 0.363 |
LIG_SH2_SRC | 139 | 142 | PF00017 | 0.223 |
LIG_SH2_SRC | 348 | 351 | PF00017 | 0.323 |
LIG_SH2_SRC | 809 | 812 | PF00017 | 0.365 |
LIG_SH2_STAP1 | 1041 | 1045 | PF00017 | 0.544 |
LIG_SH2_STAP1 | 1371 | 1375 | PF00017 | 0.506 |
LIG_SH2_STAP1 | 565 | 569 | PF00017 | 0.341 |
LIG_SH2_STAP1 | 69 | 73 | PF00017 | 0.279 |
LIG_SH2_STAP1 | 91 | 95 | PF00017 | 0.431 |
LIG_SH2_STAT3 | 460 | 463 | PF00017 | 0.427 |
LIG_SH2_STAT3 | 91 | 94 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 1029 | 1032 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 1224 | 1227 | PF00017 | 0.623 |
LIG_SH2_STAT5 | 139 | 142 | PF00017 | 0.346 |
LIG_SH2_STAT5 | 178 | 181 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 221 | 224 | PF00017 | 0.363 |
LIG_SH2_STAT5 | 291 | 294 | PF00017 | 0.320 |
LIG_SH2_STAT5 | 348 | 351 | PF00017 | 0.257 |
LIG_SH2_STAT5 | 381 | 384 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 439 | 442 | PF00017 | 0.318 |
LIG_SH2_STAT5 | 460 | 463 | PF00017 | 0.386 |
LIG_SH2_STAT5 | 479 | 482 | PF00017 | 0.317 |
LIG_SH2_STAT5 | 602 | 605 | PF00017 | 0.367 |
LIG_SH2_STAT5 | 614 | 617 | PF00017 | 0.279 |
LIG_SH2_STAT5 | 63 | 66 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 74 | 77 | PF00017 | 0.350 |
LIG_SH2_STAT5 | 809 | 812 | PF00017 | 0.327 |
LIG_SH2_STAT5 | 910 | 913 | PF00017 | 0.527 |
LIG_SH3_1 | 370 | 376 | PF00018 | 0.323 |
LIG_SH3_1 | 444 | 450 | PF00018 | 0.248 |
LIG_SH3_3 | 1111 | 1117 | PF00018 | 0.431 |
LIG_SH3_3 | 1207 | 1213 | PF00018 | 0.596 |
LIG_SH3_3 | 132 | 138 | PF00018 | 0.316 |
LIG_SH3_3 | 370 | 376 | PF00018 | 0.325 |
LIG_SH3_3 | 444 | 450 | PF00018 | 0.248 |
LIG_SH3_3 | 567 | 573 | PF00018 | 0.383 |
LIG_SH3_3 | 582 | 588 | PF00018 | 0.348 |
LIG_SH3_3 | 855 | 861 | PF00018 | 0.367 |
LIG_SH3_3 | 863 | 869 | PF00018 | 0.388 |
LIG_SUMO_SIM_anti_2 | 1356 | 1364 | PF11976 | 0.592 |
LIG_SUMO_SIM_anti_2 | 156 | 162 | PF11976 | 0.360 |
LIG_SUMO_SIM_anti_2 | 566 | 571 | PF11976 | 0.439 |
LIG_SUMO_SIM_anti_2 | 845 | 851 | PF11976 | 0.427 |
LIG_SUMO_SIM_anti_2 | 926 | 935 | PF11976 | 0.491 |
LIG_SUMO_SIM_par_1 | 897 | 904 | PF11976 | 0.428 |
LIG_TRAF2_1 | 1037 | 1040 | PF00917 | 0.612 |
LIG_TRAF2_1 | 127 | 130 | PF00917 | 0.400 |
LIG_TRAF2_1 | 57 | 60 | PF00917 | 0.347 |
LIG_TRAF2_1 | 641 | 644 | PF00917 | 0.222 |
LIG_TRFH_1 | 584 | 588 | PF08558 | 0.277 |
LIG_TYR_ITIM | 1061 | 1066 | PF00017 | 0.466 |
LIG_TYR_ITIM | 239 | 244 | PF00017 | 0.486 |
LIG_TYR_ITIM | 615 | 620 | PF00017 | 0.429 |
LIG_UBA3_1 | 122 | 131 | PF00899 | 0.427 |
LIG_WRC_WIRS_1 | 739 | 744 | PF05994 | 0.563 |
LIG_WRC_WIRS_1 | 821 | 826 | PF05994 | 0.482 |
LIG_WW_3 | 1212 | 1216 | PF00397 | 0.622 |
MOD_CDK_SPxxK_3 | 880 | 887 | PF00069 | 0.444 |
MOD_CK1_1 | 1170 | 1176 | PF00069 | 0.473 |
MOD_CK1_1 | 1286 | 1292 | PF00069 | 0.621 |
MOD_CK1_1 | 1325 | 1331 | PF00069 | 0.681 |
MOD_CK1_1 | 1341 | 1347 | PF00069 | 0.639 |
MOD_CK1_1 | 242 | 248 | PF00069 | 0.409 |
MOD_CK1_1 | 311 | 317 | PF00069 | 0.472 |
MOD_CK1_1 | 325 | 331 | PF00069 | 0.610 |
MOD_CK1_1 | 477 | 483 | PF00069 | 0.422 |
MOD_CK1_1 | 495 | 501 | PF00069 | 0.393 |
MOD_CK1_1 | 563 | 569 | PF00069 | 0.386 |
MOD_CK1_1 | 741 | 747 | PF00069 | 0.494 |
MOD_CK1_1 | 794 | 800 | PF00069 | 0.442 |
MOD_CK1_1 | 986 | 992 | PF00069 | 0.490 |
MOD_CK2_1 | 1034 | 1040 | PF00069 | 0.512 |
MOD_CK2_1 | 1100 | 1106 | PF00069 | 0.347 |
MOD_CK2_1 | 1142 | 1148 | PF00069 | 0.668 |
MOD_CK2_1 | 1152 | 1158 | PF00069 | 0.619 |
MOD_CK2_1 | 1326 | 1332 | PF00069 | 0.702 |
MOD_CK2_1 | 1341 | 1347 | PF00069 | 0.631 |
MOD_CK2_1 | 177 | 183 | PF00069 | 0.521 |
MOD_CK2_1 | 379 | 385 | PF00069 | 0.479 |
MOD_CK2_1 | 638 | 644 | PF00069 | 0.367 |
MOD_CK2_1 | 748 | 754 | PF00069 | 0.354 |
MOD_CK2_1 | 794 | 800 | PF00069 | 0.439 |
MOD_CK2_1 | 829 | 835 | PF00069 | 0.424 |
MOD_CK2_1 | 842 | 848 | PF00069 | 0.434 |
MOD_CK2_1 | 931 | 937 | PF00069 | 0.337 |
MOD_Cter_Amidation | 1136 | 1139 | PF01082 | 0.512 |
MOD_GlcNHglycan | 1012 | 1015 | PF01048 | 0.487 |
MOD_GlcNHglycan | 1161 | 1164 | PF01048 | 0.560 |
MOD_GlcNHglycan | 1285 | 1288 | PF01048 | 0.642 |
MOD_GlcNHglycan | 1295 | 1298 | PF01048 | 0.550 |
MOD_GlcNHglycan | 1340 | 1343 | PF01048 | 0.445 |
MOD_GlcNHglycan | 1351 | 1355 | PF01048 | 0.500 |
MOD_GlcNHglycan | 155 | 158 | PF01048 | 0.489 |
MOD_GlcNHglycan | 167 | 170 | PF01048 | 0.361 |
MOD_GlcNHglycan | 288 | 291 | PF01048 | 0.510 |
MOD_GlcNHglycan | 310 | 313 | PF01048 | 0.496 |
MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.643 |
MOD_GlcNHglycan | 350 | 354 | PF01048 | 0.319 |
MOD_GlcNHglycan | 402 | 405 | PF01048 | 0.485 |
MOD_GlcNHglycan | 44 | 47 | PF01048 | 0.428 |
MOD_GlcNHglycan | 466 | 469 | PF01048 | 0.495 |
MOD_GlcNHglycan | 640 | 643 | PF01048 | 0.382 |
MOD_GlcNHglycan | 985 | 988 | PF01048 | 0.433 |
MOD_GSK3_1 | 1030 | 1037 | PF00069 | 0.494 |
MOD_GSK3_1 | 1152 | 1159 | PF00069 | 0.532 |
MOD_GSK3_1 | 1166 | 1173 | PF00069 | 0.569 |
MOD_GSK3_1 | 1213 | 1220 | PF00069 | 0.598 |
MOD_GSK3_1 | 1282 | 1289 | PF00069 | 0.654 |
MOD_GSK3_1 | 1308 | 1315 | PF00069 | 0.629 |
MOD_GSK3_1 | 1322 | 1329 | PF00069 | 0.712 |
MOD_GSK3_1 | 1341 | 1348 | PF00069 | 0.668 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.393 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.465 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.408 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.475 |
MOD_GSK3_1 | 322 | 329 | PF00069 | 0.616 |
MOD_GSK3_1 | 375 | 382 | PF00069 | 0.601 |
MOD_GSK3_1 | 407 | 414 | PF00069 | 0.366 |
MOD_GSK3_1 | 464 | 471 | PF00069 | 0.535 |
MOD_GSK3_1 | 477 | 484 | PF00069 | 0.329 |
MOD_GSK3_1 | 488 | 495 | PF00069 | 0.400 |
MOD_GSK3_1 | 667 | 674 | PF00069 | 0.443 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.387 |
MOD_GSK3_1 | 746 | 753 | PF00069 | 0.407 |
MOD_GSK3_1 | 794 | 801 | PF00069 | 0.437 |
MOD_GSK3_1 | 813 | 820 | PF00069 | 0.340 |
MOD_GSK3_1 | 829 | 836 | PF00069 | 0.354 |
MOD_GSK3_1 | 861 | 868 | PF00069 | 0.504 |
MOD_GSK3_1 | 927 | 934 | PF00069 | 0.354 |
MOD_GSK3_1 | 972 | 979 | PF00069 | 0.345 |
MOD_N-GLC_1 | 1308 | 1313 | PF02516 | 0.655 |
MOD_N-GLC_1 | 418 | 423 | PF02516 | 0.394 |
MOD_N-GLC_1 | 474 | 479 | PF02516 | 0.486 |
MOD_N-GLC_1 | 493 | 498 | PF02516 | 0.533 |
MOD_N-GLC_1 | 563 | 568 | PF02516 | 0.452 |
MOD_N-GLC_1 | 773 | 778 | PF02516 | 0.422 |
MOD_NEK2_1 | 1167 | 1172 | PF00069 | 0.513 |
MOD_NEK2_1 | 1183 | 1188 | PF00069 | 0.310 |
MOD_NEK2_1 | 1308 | 1313 | PF00069 | 0.727 |
MOD_NEK2_1 | 1338 | 1343 | PF00069 | 0.660 |
MOD_NEK2_1 | 164 | 169 | PF00069 | 0.451 |
MOD_NEK2_1 | 207 | 212 | PF00069 | 0.444 |
MOD_NEK2_1 | 256 | 261 | PF00069 | 0.358 |
MOD_NEK2_1 | 27 | 32 | PF00069 | 0.512 |
MOD_NEK2_1 | 293 | 298 | PF00069 | 0.314 |
MOD_NEK2_1 | 33 | 38 | PF00069 | 0.406 |
MOD_NEK2_1 | 402 | 407 | PF00069 | 0.389 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.303 |
MOD_NEK2_1 | 455 | 460 | PF00069 | 0.477 |
MOD_NEK2_1 | 482 | 487 | PF00069 | 0.304 |
MOD_NEK2_1 | 532 | 537 | PF00069 | 0.405 |
MOD_NEK2_1 | 623 | 628 | PF00069 | 0.361 |
MOD_NEK2_1 | 630 | 635 | PF00069 | 0.454 |
MOD_NEK2_1 | 652 | 657 | PF00069 | 0.359 |
MOD_NEK2_1 | 671 | 676 | PF00069 | 0.278 |
MOD_NEK2_1 | 724 | 729 | PF00069 | 0.362 |
MOD_NEK2_1 | 740 | 745 | PF00069 | 0.311 |
MOD_NEK2_1 | 792 | 797 | PF00069 | 0.403 |
MOD_NEK2_1 | 842 | 847 | PF00069 | 0.307 |
MOD_NEK2_1 | 90 | 95 | PF00069 | 0.340 |
MOD_NEK2_1 | 901 | 906 | PF00069 | 0.314 |
MOD_NEK2_2 | 173 | 178 | PF00069 | 0.496 |
MOD_PIKK_1 | 1237 | 1243 | PF00454 | 0.610 |
MOD_PIKK_1 | 1317 | 1323 | PF00454 | 0.478 |
MOD_PIKK_1 | 340 | 346 | PF00454 | 0.443 |
MOD_PIKK_1 | 495 | 501 | PF00454 | 0.401 |
MOD_PIKK_1 | 90 | 96 | PF00454 | 0.245 |
MOD_PKA_1 | 1257 | 1263 | PF00069 | 0.589 |
MOD_PKA_1 | 379 | 385 | PF00069 | 0.605 |
MOD_PKA_2 | 1034 | 1040 | PF00069 | 0.515 |
MOD_PKA_2 | 1257 | 1263 | PF00069 | 0.462 |
MOD_PKA_2 | 1280 | 1286 | PF00069 | 0.660 |
MOD_PKA_2 | 1312 | 1318 | PF00069 | 0.725 |
MOD_PKA_2 | 1322 | 1328 | PF00069 | 0.707 |
MOD_PKA_2 | 1338 | 1344 | PF00069 | 0.654 |
MOD_PKA_2 | 1363 | 1369 | PF00069 | 0.408 |
MOD_PKA_2 | 142 | 148 | PF00069 | 0.470 |
MOD_PKA_2 | 207 | 213 | PF00069 | 0.518 |
MOD_PKA_2 | 27 | 33 | PF00069 | 0.492 |
MOD_PKA_2 | 285 | 291 | PF00069 | 0.502 |
MOD_PKA_2 | 3 | 9 | PF00069 | 0.577 |
MOD_PKA_2 | 419 | 425 | PF00069 | 0.379 |
MOD_PKA_2 | 623 | 629 | PF00069 | 0.408 |
MOD_PKA_2 | 724 | 730 | PF00069 | 0.289 |
MOD_PKB_1 | 1215 | 1223 | PF00069 | 0.664 |
MOD_PKB_1 | 377 | 385 | PF00069 | 0.347 |
MOD_Plk_1 | 1095 | 1101 | PF00069 | 0.366 |
MOD_Plk_1 | 1346 | 1352 | PF00069 | 0.695 |
MOD_Plk_1 | 242 | 248 | PF00069 | 0.406 |
MOD_Plk_1 | 418 | 424 | PF00069 | 0.397 |
MOD_Plk_1 | 474 | 480 | PF00069 | 0.451 |
MOD_Plk_1 | 482 | 488 | PF00069 | 0.419 |
MOD_Plk_1 | 532 | 538 | PF00069 | 0.491 |
MOD_Plk_1 | 563 | 569 | PF00069 | 0.451 |
MOD_Plk_1 | 630 | 636 | PF00069 | 0.457 |
MOD_Plk_1 | 715 | 721 | PF00069 | 0.438 |
MOD_Plk_2-3 | 72 | 78 | PF00069 | 0.275 |
MOD_Plk_2-3 | 750 | 756 | PF00069 | 0.386 |
MOD_Plk_2-3 | 972 | 978 | PF00069 | 0.336 |
MOD_Plk_4 | 1095 | 1101 | PF00069 | 0.305 |
MOD_Plk_4 | 1110 | 1116 | PF00069 | 0.298 |
MOD_Plk_4 | 173 | 179 | PF00069 | 0.409 |
MOD_Plk_4 | 225 | 231 | PF00069 | 0.440 |
MOD_Plk_4 | 293 | 299 | PF00069 | 0.397 |
MOD_Plk_4 | 402 | 408 | PF00069 | 0.537 |
MOD_Plk_4 | 474 | 480 | PF00069 | 0.453 |
MOD_Plk_4 | 505 | 511 | PF00069 | 0.409 |
MOD_Plk_4 | 542 | 548 | PF00069 | 0.402 |
MOD_Plk_4 | 715 | 721 | PF00069 | 0.456 |
MOD_Plk_4 | 775 | 781 | PF00069 | 0.375 |
MOD_Plk_4 | 794 | 800 | PF00069 | 0.332 |
MOD_Plk_4 | 903 | 909 | PF00069 | 0.340 |
MOD_Plk_4 | 927 | 933 | PF00069 | 0.336 |
MOD_Plk_4 | 976 | 982 | PF00069 | 0.350 |
MOD_ProDKin_1 | 1073 | 1079 | PF00069 | 0.398 |
MOD_ProDKin_1 | 326 | 332 | PF00069 | 0.498 |
MOD_ProDKin_1 | 677 | 683 | PF00069 | 0.426 |
MOD_ProDKin_1 | 773 | 779 | PF00069 | 0.414 |
MOD_ProDKin_1 | 861 | 867 | PF00069 | 0.483 |
MOD_ProDKin_1 | 880 | 886 | PF00069 | 0.454 |
MOD_SUMO_rev_2 | 183 | 191 | PF00179 | 0.503 |
MOD_SUMO_rev_2 | 72 | 82 | PF00179 | 0.337 |
MOD_SUMO_rev_2 | 794 | 804 | PF00179 | 0.487 |
TRG_DiLeu_BaEn_1 | 927 | 932 | PF01217 | 0.467 |
TRG_DiLeu_BaEn_4 | 1039 | 1045 | PF01217 | 0.374 |
TRG_DiLeu_BaLyEn_6 | 305 | 310 | PF01217 | 0.481 |
TRG_DiLeu_LyEn_5 | 1200 | 1205 | PF01217 | 0.536 |
TRG_ENDOCYTIC_2 | 1015 | 1018 | PF00928 | 0.343 |
TRG_ENDOCYTIC_2 | 1041 | 1044 | PF00928 | 0.326 |
TRG_ENDOCYTIC_2 | 1063 | 1066 | PF00928 | 0.464 |
TRG_ENDOCYTIC_2 | 241 | 244 | PF00928 | 0.480 |
TRG_ENDOCYTIC_2 | 306 | 309 | PF00928 | 0.490 |
TRG_ENDOCYTIC_2 | 357 | 360 | PF00928 | 0.468 |
TRG_ENDOCYTIC_2 | 479 | 482 | PF00928 | 0.372 |
TRG_ENDOCYTIC_2 | 514 | 517 | PF00928 | 0.447 |
TRG_ENDOCYTIC_2 | 602 | 605 | PF00928 | 0.562 |
TRG_ENDOCYTIC_2 | 617 | 620 | PF00928 | 0.464 |
TRG_ENDOCYTIC_2 | 721 | 724 | PF00928 | 0.371 |
TRG_ENDOCYTIC_2 | 839 | 842 | PF00928 | 0.478 |
TRG_ENDOCYTIC_2 | 910 | 913 | PF00928 | 0.460 |
TRG_ER_diArg_1 | 1048 | 1051 | PF00400 | 0.337 |
TRG_ER_diArg_1 | 1214 | 1217 | PF00400 | 0.597 |
TRG_ER_diArg_1 | 1278 | 1281 | PF00400 | 0.685 |
TRG_ER_diArg_1 | 1303 | 1306 | PF00400 | 0.566 |
TRG_ER_diArg_1 | 201 | 203 | PF00400 | 0.462 |
TRG_ER_diArg_1 | 376 | 379 | PF00400 | 0.370 |
TRG_ER_diArg_1 | 873 | 876 | PF00400 | 0.536 |
TRG_NES_CRM1_1 | 499 | 512 | PF08389 | 0.352 |
TRG_Pf-PMV_PEXEL_1 | 959 | 963 | PF00026 | 0.413 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P457 | Leptomonas seymouri | 26% | 100% |
A0A1X0P171 | Trypanosomatidae | 33% | 100% |
A0A3Q8IJB0 | Leishmania donovani | 55% | 100% |
A0A3R7M6J4 | Trypanosoma rangeli | 36% | 100% |
A0A3R7R8G4 | Trypanosoma rangeli | 30% | 100% |
A0A3S5H6Z8 | Leishmania donovani | 55% | 100% |
A0A3S7WU91 | Leishmania donovani | 56% | 97% |
A0A3S7WU94 | Leishmania donovani | 86% | 100% |
A0A3S7WU95 | Leishmania donovani | 54% | 98% |
A0A3S7XB85 | Leishmania donovani | 29% | 98% |
A4H8U6 | Leishmania braziliensis | 66% | 100% |
A4H8V5 | Leishmania braziliensis | 56% | 100% |
A4H8V7 | Leishmania braziliensis | 52% | 100% |
A4H8V8 | Leishmania braziliensis | 52% | 98% |
A4HPI4 | Leishmania braziliensis | 27% | 98% |
A4HX84 | Leishmania infantum | 86% | 100% |
A4HX85 | Leishmania infantum | 55% | 98% |
A4HX87 | Leishmania infantum | 57% | 100% |
A4HX88 | Leishmania infantum | 42% | 100% |
A4IDA6 | Leishmania infantum | 30% | 98% |
C9ZM79 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZM80 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
C9ZM81 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZM82 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZM83 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZM86 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
C9ZN26 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
C9ZN41 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
C9ZN43 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZN44 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 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) | 32% | 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) | 32% | 100% |
C9ZPZ6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 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% |
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) | 33% | 100% |
C9ZTS6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZUE6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZWQ5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
C9ZWU1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
C9ZWU2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZWU3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
C9ZWY7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZZQ4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
D0A0U3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
D0A0W7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
D0A0X5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 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) | 30% | 100% |
D0A5U1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
D0A7A0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
D0A9R3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
D0AAV3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
E9AQY0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 56% | 98% |
E9AQY1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 77% | 99% |
E9AQY2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 53% | 98% |
E9AQY4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 55% | 100% |
E9ARD7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |
E9AT96 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 98% |
Q25263 | Leishmania donovani | 54% | 100% |
Q26721 | Trypanosoma brucei brucei | 33% | 100% |
Q27675 | Leishmania donovani | 86% | 100% |
Q4QEH9 | Leishmania major | 56% | 100% |
Q4QEI0 | Leishmania major | 56% | 100% |
Q4QEI1 | Leishmania major | 57% | 100% |
Q4QEI2 | Leishmania major | 57% | 100% |
Q99279 | Trypanosoma brucei brucei | 30% | 100% |
Q99280 | Trypanosoma brucei brucei | 31% | 100% |
V5AYH7 | Trypanosoma cruzi | 34% | 100% |