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: 26 |
NetGPI | no | yes: 0, no: 72 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 67 |
GO:0110165 | cellular anatomical entity | 1 | 73 |
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 73 |
GO:0006163 | purine nucleotide metabolic process | 5 | 73 |
GO:0006164 | purine nucleotide biosynthetic process | 6 | 73 |
GO:0006171 | cAMP biosynthetic process | 8 | 73 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 73 |
GO:0006753 | nucleoside phosphate metabolic process | 4 | 73 |
GO:0006793 | phosphorus metabolic process | 3 | 73 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 73 |
GO:0006807 | nitrogen compound metabolic process | 2 | 73 |
GO:0007165 | signal transduction | 2 | 73 |
GO:0008152 | metabolic process | 1 | 73 |
GO:0009058 | biosynthetic process | 2 | 73 |
GO:0009117 | nucleotide metabolic process | 5 | 73 |
GO:0009150 | purine ribonucleotide metabolic process | 6 | 73 |
GO:0009152 | purine ribonucleotide biosynthetic process | 7 | 73 |
GO:0009165 | nucleotide biosynthetic process | 6 | 73 |
GO:0009187 | cyclic nucleotide metabolic process | 6 | 73 |
GO:0009190 | cyclic nucleotide biosynthetic process | 7 | 73 |
GO:0009259 | ribonucleotide metabolic process | 5 | 73 |
GO:0009260 | ribonucleotide biosynthetic process | 6 | 73 |
GO:0009987 | cellular process | 1 | 73 |
GO:0018130 | heterocycle biosynthetic process | 4 | 73 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 73 |
GO:0019637 | organophosphate metabolic process | 3 | 73 |
GO:0019693 | ribose phosphate metabolic process | 4 | 73 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 73 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 73 |
GO:0035556 | intracellular signal transduction | 3 | 73 |
GO:0044237 | cellular metabolic process | 2 | 73 |
GO:0044238 | primary metabolic process | 2 | 73 |
GO:0044249 | cellular biosynthetic process | 3 | 73 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 73 |
GO:0044281 | small molecule metabolic process | 2 | 73 |
GO:0046058 | cAMP metabolic process | 7 | 73 |
GO:0046390 | ribose phosphate biosynthetic process | 5 | 73 |
GO:0046483 | heterocycle metabolic process | 3 | 73 |
GO:0050789 | regulation of biological process | 2 | 73 |
GO:0050794 | regulation of cellular process | 3 | 73 |
GO:0052652 | cyclic purine nucleotide metabolic process | 6 | 73 |
GO:0055086 | nucleobase-containing small molecule metabolic process | 3 | 73 |
GO:0065007 | biological regulation | 1 | 73 |
GO:0071704 | organic substance metabolic process | 2 | 73 |
GO:0072521 | purine-containing compound metabolic process | 4 | 73 |
GO:0072522 | purine-containing compound biosynthetic process | 5 | 73 |
GO:0090407 | organophosphate biosynthetic process | 4 | 73 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 73 |
GO:1901137 | carbohydrate derivative biosynthetic process | 4 | 73 |
GO:1901293 | nucleoside phosphate biosynthetic process | 5 | 73 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 73 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 73 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 73 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 73 |
GO:1901576 | organic substance biosynthetic process | 3 | 73 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 62 |
GO:0016829 | lyase activity | 2 | 62 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 247 | 251 | PF00656 | 0.313 |
CLV_C14_Caspase3-7 | 480 | 484 | PF00656 | 0.318 |
CLV_C14_Caspase3-7 | 811 | 815 | PF00656 | 0.263 |
CLV_C14_Caspase3-7 | 922 | 926 | PF00656 | 0.592 |
CLV_C14_Caspase3-7 | 983 | 987 | PF00656 | 0.507 |
CLV_MEL_PAP_1 | 1056 | 1062 | PF00089 | 0.299 |
CLV_NRD_NRD_1 | 1146 | 1148 | PF00675 | 0.439 |
CLV_NRD_NRD_1 | 1314 | 1316 | PF00675 | 0.524 |
CLV_NRD_NRD_1 | 1354 | 1356 | PF00675 | 0.634 |
CLV_NRD_NRD_1 | 1363 | 1365 | PF00675 | 0.601 |
CLV_NRD_NRD_1 | 207 | 209 | PF00675 | 0.620 |
CLV_NRD_NRD_1 | 30 | 32 | PF00675 | 0.561 |
CLV_NRD_NRD_1 | 393 | 395 | PF00675 | 0.524 |
CLV_NRD_NRD_1 | 440 | 442 | PF00675 | 0.428 |
CLV_NRD_NRD_1 | 632 | 634 | PF00675 | 0.623 |
CLV_NRD_NRD_1 | 689 | 691 | PF00675 | 0.625 |
CLV_NRD_NRD_1 | 9 | 11 | PF00675 | 0.570 |
CLV_PCSK_FUR_1 | 205 | 209 | PF00082 | 0.617 |
CLV_PCSK_KEX2_1 | 1146 | 1148 | PF00082 | 0.439 |
CLV_PCSK_KEX2_1 | 1314 | 1316 | PF00082 | 0.523 |
CLV_PCSK_KEX2_1 | 1354 | 1356 | PF00082 | 0.634 |
CLV_PCSK_KEX2_1 | 1363 | 1365 | PF00082 | 0.601 |
CLV_PCSK_KEX2_1 | 207 | 209 | PF00082 | 0.620 |
CLV_PCSK_KEX2_1 | 24 | 26 | PF00082 | 0.615 |
CLV_PCSK_KEX2_1 | 30 | 32 | PF00082 | 0.550 |
CLV_PCSK_KEX2_1 | 393 | 395 | PF00082 | 0.512 |
CLV_PCSK_KEX2_1 | 440 | 442 | PF00082 | 0.408 |
CLV_PCSK_KEX2_1 | 632 | 634 | PF00082 | 0.561 |
CLV_PCSK_KEX2_1 | 689 | 691 | PF00082 | 0.559 |
CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.570 |
CLV_PCSK_PC1ET2_1 | 24 | 26 | PF00082 | 0.683 |
CLV_PCSK_SKI1_1 | 1239 | 1243 | PF00082 | 0.444 |
CLV_PCSK_SKI1_1 | 129 | 133 | PF00082 | 0.557 |
CLV_PCSK_SKI1_1 | 208 | 212 | PF00082 | 0.618 |
CLV_PCSK_SKI1_1 | 284 | 288 | PF00082 | 0.555 |
CLV_PCSK_SKI1_1 | 305 | 309 | PF00082 | 0.506 |
CLV_PCSK_SKI1_1 | 393 | 397 | PF00082 | 0.624 |
CLV_PCSK_SKI1_1 | 541 | 545 | PF00082 | 0.449 |
CLV_PCSK_SKI1_1 | 632 | 636 | PF00082 | 0.515 |
CLV_PCSK_SKI1_1 | 642 | 646 | PF00082 | 0.634 |
CLV_PCSK_SKI1_1 | 746 | 750 | PF00082 | 0.536 |
CLV_PCSK_SKI1_1 | 802 | 806 | PF00082 | 0.551 |
CLV_PCSK_SKI1_1 | 808 | 812 | PF00082 | 0.533 |
CLV_Separin_Metazoa | 605 | 609 | PF03568 | 0.317 |
DEG_APCC_DBOX_1 | 1124 | 1132 | PF00400 | 0.414 |
DEG_APCC_DBOX_1 | 1314 | 1322 | PF00400 | 0.548 |
DEG_APCC_DBOX_1 | 189 | 197 | PF00400 | 0.257 |
DEG_SPOP_SBC_1 | 290 | 294 | PF00917 | 0.447 |
DEG_SPOP_SBC_1 | 735 | 739 | PF00917 | 0.306 |
DOC_CDC14_PxL_1 | 131 | 139 | PF14671 | 0.444 |
DOC_CKS1_1 | 230 | 235 | PF01111 | 0.228 |
DOC_CKS1_1 | 782 | 787 | PF01111 | 0.386 |
DOC_CKS1_1 | 874 | 879 | PF01111 | 0.413 |
DOC_CYCLIN_RxL_1 | 507 | 516 | PF00134 | 0.289 |
DOC_CYCLIN_yCln2_LP_2 | 230 | 236 | PF00134 | 0.337 |
DOC_CYCLIN_yCln2_LP_2 | 508 | 514 | PF00134 | 0.398 |
DOC_CYCLIN_yCln2_LP_2 | 871 | 877 | PF00134 | 0.419 |
DOC_MAPK_gen_1 | 1311 | 1320 | PF00069 | 0.642 |
DOC_MAPK_gen_1 | 205 | 214 | PF00069 | 0.323 |
DOC_MAPK_MEF2A_6 | 510 | 519 | PF00069 | 0.441 |
DOC_MAPK_MEF2A_6 | 714 | 722 | PF00069 | 0.290 |
DOC_MAPK_RevD_3 | 1133 | 1147 | PF00069 | 0.629 |
DOC_PP1_RVXF_1 | 1378 | 1385 | PF00149 | 0.544 |
DOC_PP1_RVXF_1 | 303 | 309 | PF00149 | 0.435 |
DOC_PP1_RVXF_1 | 508 | 515 | PF00149 | 0.290 |
DOC_PP1_RVXF_1 | 688 | 695 | PF00149 | 0.246 |
DOC_PP1_RVXF_1 | 744 | 751 | PF00149 | 0.323 |
DOC_PP2B_LxvP_1 | 236 | 239 | PF13499 | 0.342 |
DOC_PP2B_LxvP_1 | 871 | 874 | PF13499 | 0.494 |
DOC_PP4_FxxP_1 | 1348 | 1351 | PF00568 | 0.579 |
DOC_PP4_FxxP_1 | 50 | 53 | PF00568 | 0.414 |
DOC_USP7_MATH_1 | 1245 | 1249 | PF00917 | 0.703 |
DOC_USP7_MATH_1 | 1290 | 1294 | PF00917 | 0.819 |
DOC_USP7_MATH_1 | 1365 | 1369 | PF00917 | 0.795 |
DOC_USP7_MATH_1 | 290 | 294 | PF00917 | 0.445 |
DOC_USP7_MATH_1 | 477 | 481 | PF00917 | 0.441 |
DOC_USP7_MATH_1 | 712 | 716 | PF00917 | 0.397 |
DOC_USP7_MATH_1 | 735 | 739 | PF00917 | 0.420 |
DOC_USP7_MATH_1 | 778 | 782 | PF00917 | 0.432 |
DOC_USP7_MATH_1 | 991 | 995 | PF00917 | 0.576 |
DOC_WW_Pin1_4 | 152 | 157 | PF00397 | 0.392 |
DOC_WW_Pin1_4 | 2 | 7 | PF00397 | 0.346 |
DOC_WW_Pin1_4 | 229 | 234 | PF00397 | 0.395 |
DOC_WW_Pin1_4 | 29 | 34 | PF00397 | 0.452 |
DOC_WW_Pin1_4 | 318 | 323 | PF00397 | 0.424 |
DOC_WW_Pin1_4 | 736 | 741 | PF00397 | 0.377 |
DOC_WW_Pin1_4 | 764 | 769 | PF00397 | 0.440 |
DOC_WW_Pin1_4 | 781 | 786 | PF00397 | 0.380 |
DOC_WW_Pin1_4 | 873 | 878 | PF00397 | 0.375 |
DOC_WW_Pin1_4 | 888 | 893 | PF00397 | 0.454 |
LIG_14-3-3_CanoR_1 | 1043 | 1049 | PF00244 | 0.634 |
LIG_14-3-3_CanoR_1 | 1225 | 1232 | PF00244 | 0.683 |
LIG_14-3-3_CanoR_1 | 1243 | 1248 | PF00244 | 0.662 |
LIG_14-3-3_CanoR_1 | 205 | 214 | PF00244 | 0.363 |
LIG_14-3-3_CanoR_1 | 25 | 30 | PF00244 | 0.454 |
LIG_14-3-3_CanoR_1 | 284 | 290 | PF00244 | 0.427 |
LIG_14-3-3_CanoR_1 | 291 | 298 | PF00244 | 0.413 |
LIG_14-3-3_CanoR_1 | 559 | 566 | PF00244 | 0.287 |
LIG_14-3-3_CanoR_1 | 632 | 641 | PF00244 | 0.416 |
LIG_14-3-3_CanoR_1 | 662 | 668 | PF00244 | 0.371 |
LIG_14-3-3_CanoR_1 | 746 | 751 | PF00244 | 0.449 |
LIG_14-3-3_CanoR_1 | 789 | 798 | PF00244 | 0.319 |
LIG_14-3-3_CanoR_1 | 802 | 808 | PF00244 | 0.334 |
LIG_14-3-3_CanoR_1 | 884 | 892 | PF00244 | 0.484 |
LIG_Actin_WH2_2 | 529 | 546 | PF00022 | 0.419 |
LIG_Actin_WH2_2 | 617 | 634 | PF00022 | 0.227 |
LIG_APCC_ABBA_1 | 141 | 146 | PF00400 | 0.444 |
LIG_APCC_ABBA_1 | 308 | 313 | PF00400 | 0.303 |
LIG_APCC_ABBA_1 | 719 | 724 | PF00400 | 0.311 |
LIG_BIR_III_2 | 1141 | 1145 | PF00653 | 0.614 |
LIG_BIR_III_2 | 765 | 769 | PF00653 | 0.266 |
LIG_BIR_III_2 | 927 | 931 | PF00653 | 0.671 |
LIG_BRCT_BRCA1_1 | 1309 | 1313 | PF00533 | 0.741 |
LIG_eIF4E_1 | 29 | 35 | PF01652 | 0.501 |
LIG_eIF4E_1 | 598 | 604 | PF01652 | 0.263 |
LIG_FHA_1 | 1005 | 1011 | PF00498 | 0.570 |
LIG_FHA_1 | 1014 | 1020 | PF00498 | 0.506 |
LIG_FHA_1 | 1039 | 1045 | PF00498 | 0.517 |
LIG_FHA_1 | 1089 | 1095 | PF00498 | 0.512 |
LIG_FHA_1 | 126 | 132 | PF00498 | 0.414 |
LIG_FHA_1 | 339 | 345 | PF00498 | 0.372 |
LIG_FHA_1 | 356 | 362 | PF00498 | 0.464 |
LIG_FHA_1 | 406 | 412 | PF00498 | 0.350 |
LIG_FHA_1 | 44 | 50 | PF00498 | 0.441 |
LIG_FHA_1 | 522 | 528 | PF00498 | 0.329 |
LIG_FHA_1 | 552 | 558 | PF00498 | 0.401 |
LIG_FHA_1 | 572 | 578 | PF00498 | 0.339 |
LIG_FHA_1 | 655 | 661 | PF00498 | 0.353 |
LIG_FHA_1 | 678 | 684 | PF00498 | 0.400 |
LIG_FHA_1 | 728 | 734 | PF00498 | 0.378 |
LIG_FHA_1 | 791 | 797 | PF00498 | 0.298 |
LIG_FHA_1 | 874 | 880 | PF00498 | 0.345 |
LIG_FHA_2 | 1151 | 1157 | PF00498 | 0.741 |
LIG_FHA_2 | 1161 | 1167 | PF00498 | 0.724 |
LIG_FHA_2 | 213 | 219 | PF00498 | 0.359 |
LIG_FHA_2 | 254 | 260 | PF00498 | 0.430 |
LIG_FHA_2 | 319 | 325 | PF00498 | 0.433 |
LIG_FHA_2 | 417 | 423 | PF00498 | 0.397 |
LIG_FHA_2 | 487 | 493 | PF00498 | 0.334 |
LIG_FHA_2 | 697 | 703 | PF00498 | 0.341 |
LIG_FHA_2 | 809 | 815 | PF00498 | 0.301 |
LIG_FHA_2 | 889 | 895 | PF00498 | 0.415 |
LIG_FHA_2 | 940 | 946 | PF00498 | 0.507 |
LIG_FHA_2 | 981 | 987 | PF00498 | 0.511 |
LIG_GBD_Chelix_1 | 1001 | 1009 | PF00786 | 0.417 |
LIG_GBD_Chelix_1 | 279 | 287 | PF00786 | 0.535 |
LIG_GBD_Chelix_1 | 578 | 586 | PF00786 | 0.429 |
LIG_LIR_Apic_2 | 1034 | 1040 | PF02991 | 0.491 |
LIG_LIR_Apic_2 | 452 | 456 | PF02991 | 0.368 |
LIG_LIR_Apic_2 | 589 | 594 | PF02991 | 0.364 |
LIG_LIR_Apic_2 | 666 | 672 | PF02991 | 0.443 |
LIG_LIR_Gen_1 | 1046 | 1056 | PF02991 | 0.562 |
LIG_LIR_Gen_1 | 1068 | 1078 | PF02991 | 0.603 |
LIG_LIR_Gen_1 | 209 | 219 | PF02991 | 0.451 |
LIG_LIR_Gen_1 | 221 | 231 | PF02991 | 0.338 |
LIG_LIR_Gen_1 | 256 | 266 | PF02991 | 0.343 |
LIG_LIR_Gen_1 | 281 | 290 | PF02991 | 0.426 |
LIG_LIR_Gen_1 | 484 | 495 | PF02991 | 0.439 |
LIG_LIR_Gen_1 | 504 | 512 | PF02991 | 0.311 |
LIG_LIR_Gen_1 | 749 | 755 | PF02991 | 0.362 |
LIG_LIR_Gen_1 | 938 | 949 | PF02991 | 0.508 |
LIG_LIR_Nem_3 | 1013 | 1017 | PF02991 | 0.526 |
LIG_LIR_Nem_3 | 1020 | 1026 | PF02991 | 0.509 |
LIG_LIR_Nem_3 | 1046 | 1052 | PF02991 | 0.507 |
LIG_LIR_Nem_3 | 1068 | 1074 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 1075 | 1081 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 1104 | 1110 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 1194 | 1200 | PF02991 | 0.647 |
LIG_LIR_Nem_3 | 133 | 137 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 209 | 214 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 221 | 227 | PF02991 | 0.352 |
LIG_LIR_Nem_3 | 264 | 268 | PF02991 | 0.257 |
LIG_LIR_Nem_3 | 281 | 285 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 430 | 435 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 484 | 490 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 492 | 498 | PF02991 | 0.306 |
LIG_LIR_Nem_3 | 504 | 508 | PF02991 | 0.277 |
LIG_LIR_Nem_3 | 749 | 753 | PF02991 | 0.354 |
LIG_LIR_Nem_3 | 86 | 92 | PF02991 | 0.243 |
LIG_LIR_Nem_3 | 938 | 944 | PF02991 | 0.508 |
LIG_LIR_Nem_3 | 948 | 954 | PF02991 | 0.609 |
LIG_LYPXL_yS_3 | 134 | 137 | PF13949 | 0.310 |
LIG_LYPXL_yS_3 | 265 | 268 | PF13949 | 0.222 |
LIG_MYND_3 | 614 | 618 | PF01753 | 0.366 |
LIG_NRBOX | 148 | 154 | PF00104 | 0.343 |
LIG_PCNA_yPIPBox_3 | 533 | 544 | PF02747 | 0.207 |
LIG_PCNA_yPIPBox_3 | 895 | 903 | PF02747 | 0.262 |
LIG_PTB_Apo_2 | 497 | 504 | PF02174 | 0.221 |
LIG_PTB_Apo_2 | 606 | 613 | PF02174 | 0.317 |
LIG_PTB_Apo_2 | 69 | 76 | PF02174 | 0.364 |
LIG_PTB_Apo_2 | 95 | 102 | PF02174 | 0.247 |
LIG_PTB_Phospho_1 | 497 | 503 | PF10480 | 0.222 |
LIG_PTB_Phospho_1 | 606 | 612 | PF10480 | 0.320 |
LIG_PTB_Phospho_1 | 69 | 75 | PF10480 | 0.373 |
LIG_PTB_Phospho_1 | 95 | 101 | PF10480 | 0.246 |
LIG_SH2_CRK | 242 | 246 | PF00017 | 0.506 |
LIG_SH2_CRK | 453 | 457 | PF00017 | 0.366 |
LIG_SH2_CRK | 505 | 509 | PF00017 | 0.251 |
LIG_SH2_CRK | 669 | 673 | PF00017 | 0.471 |
LIG_SH2_CRK | 729 | 733 | PF00017 | 0.441 |
LIG_SH2_GRB2like | 625 | 628 | PF00017 | 0.388 |
LIG_SH2_GRB2like | 817 | 820 | PF00017 | 0.424 |
LIG_SH2_NCK_1 | 101 | 105 | PF00017 | 0.448 |
LIG_SH2_NCK_1 | 1071 | 1075 | PF00017 | 0.596 |
LIG_SH2_NCK_1 | 669 | 673 | PF00017 | 0.307 |
LIG_SH2_PTP2 | 1037 | 1040 | PF00017 | 0.546 |
LIG_SH2_PTP2 | 610 | 613 | PF00017 | 0.449 |
LIG_SH2_SRC | 1037 | 1040 | PF00017 | 0.557 |
LIG_SH2_SRC | 1071 | 1074 | PF00017 | 0.596 |
LIG_SH2_SRC | 224 | 227 | PF00017 | 0.395 |
LIG_SH2_SRC | 442 | 445 | PF00017 | 0.412 |
LIG_SH2_SRC | 84 | 87 | PF00017 | 0.218 |
LIG_SH2_STAP1 | 1049 | 1053 | PF00017 | 0.563 |
LIG_SH2_STAP1 | 224 | 228 | PF00017 | 0.266 |
LIG_SH2_STAP1 | 312 | 316 | PF00017 | 0.443 |
LIG_SH2_STAP1 | 573 | 577 | PF00017 | 0.360 |
LIG_SH2_STAP1 | 625 | 629 | PF00017 | 0.220 |
LIG_SH2_STAP1 | 729 | 733 | PF00017 | 0.266 |
LIG_SH2_STAP1 | 84 | 88 | PF00017 | 0.279 |
LIG_SH2_STAT3 | 354 | 357 | PF00017 | 0.266 |
LIG_SH2_STAT3 | 469 | 472 | PF00017 | 0.433 |
LIG_SH2_STAT3 | 850 | 853 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 101 | 104 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 1037 | 1040 | PF00017 | 0.488 |
LIG_SH2_STAT5 | 1232 | 1235 | PF00017 | 0.653 |
LIG_SH2_STAT5 | 183 | 186 | PF00017 | 0.347 |
LIG_SH2_STAT5 | 213 | 216 | PF00017 | 0.320 |
LIG_SH2_STAT5 | 296 | 299 | PF00017 | 0.331 |
LIG_SH2_STAT5 | 435 | 438 | PF00017 | 0.325 |
LIG_SH2_STAT5 | 442 | 445 | PF00017 | 0.304 |
LIG_SH2_STAT5 | 448 | 451 | PF00017 | 0.321 |
LIG_SH2_STAT5 | 469 | 472 | PF00017 | 0.395 |
LIG_SH2_STAT5 | 497 | 500 | PF00017 | 0.334 |
LIG_SH2_STAT5 | 505 | 508 | PF00017 | 0.331 |
LIG_SH2_STAT5 | 542 | 545 | PF00017 | 0.361 |
LIG_SH2_STAT5 | 573 | 576 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 591 | 594 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 610 | 613 | PF00017 | 0.370 |
LIG_SH2_STAT5 | 69 | 72 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 729 | 732 | PF00017 | 0.331 |
LIG_SH2_STAT5 | 817 | 820 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 918 | 921 | PF00017 | 0.543 |
LIG_SH3_1 | 453 | 459 | PF00018 | 0.255 |
LIG_SH3_3 | 1215 | 1221 | PF00018 | 0.636 |
LIG_SH3_3 | 137 | 143 | PF00018 | 0.335 |
LIG_SH3_3 | 1373 | 1379 | PF00018 | 0.598 |
LIG_SH3_3 | 1382 | 1388 | PF00018 | 0.557 |
LIG_SH3_3 | 453 | 459 | PF00018 | 0.255 |
LIG_SH3_3 | 590 | 596 | PF00018 | 0.380 |
LIG_SH3_3 | 672 | 678 | PF00018 | 0.374 |
LIG_SH3_3 | 863 | 869 | PF00018 | 0.388 |
LIG_SH3_3 | 871 | 877 | PF00018 | 0.374 |
LIG_Sin3_3 | 37 | 44 | PF02671 | 0.485 |
LIG_SUMO_SIM_anti_2 | 122 | 128 | PF11976 | 0.442 |
LIG_SUMO_SIM_anti_2 | 1370 | 1377 | PF11976 | 0.628 |
LIG_SUMO_SIM_anti_2 | 160 | 167 | PF11976 | 0.372 |
LIG_SUMO_SIM_anti_2 | 192 | 198 | PF11976 | 0.276 |
LIG_SUMO_SIM_anti_2 | 225 | 232 | PF11976 | 0.294 |
LIG_SUMO_SIM_anti_2 | 715 | 721 | PF11976 | 0.344 |
LIG_SUMO_SIM_anti_2 | 934 | 943 | PF11976 | 0.510 |
LIG_SUMO_SIM_par_1 | 1015 | 1020 | PF11976 | 0.414 |
LIG_SUMO_SIM_par_1 | 122 | 128 | PF11976 | 0.411 |
LIG_SUMO_SIM_par_1 | 225 | 232 | PF11976 | 0.294 |
LIG_SUMO_SIM_par_1 | 45 | 51 | PF11976 | 0.434 |
LIG_SUMO_SIM_par_1 | 546 | 554 | PF11976 | 0.387 |
LIG_SUMO_SIM_par_1 | 673 | 680 | PF11976 | 0.292 |
LIG_SUMO_SIM_par_1 | 694 | 699 | PF11976 | 0.396 |
LIG_SUMO_SIM_par_1 | 717 | 724 | PF11976 | 0.399 |
LIG_SUMO_SIM_par_1 | 854 | 859 | PF11976 | 0.337 |
LIG_SUMO_SIM_par_1 | 903 | 909 | PF11976 | 0.449 |
LIG_SxIP_EBH_1 | 337 | 348 | PF03271 | 0.293 |
LIG_TRAF2_1 | 1045 | 1048 | PF00917 | 0.629 |
LIG_TRAF2_1 | 1111 | 1114 | PF00917 | 0.537 |
LIG_TRAF2_1 | 1356 | 1359 | PF00917 | 0.835 |
LIG_TRAF2_1 | 421 | 424 | PF00917 | 0.443 |
LIG_TRAF2_1 | 489 | 492 | PF00917 | 0.225 |
LIG_TYR_ITIM | 1069 | 1074 | PF00017 | 0.482 |
LIG_TYR_ITIM | 623 | 628 | PF00017 | 0.438 |
LIG_TYR_ITIM | 727 | 732 | PF00017 | 0.374 |
LIG_UBA3_1 | 193 | 198 | PF00899 | 0.586 |
LIG_WRC_WIRS_1 | 417 | 422 | PF05994 | 0.221 |
LIG_WRC_WIRS_1 | 747 | 752 | PF05994 | 0.576 |
LIG_WW_3 | 1220 | 1224 | PF00397 | 0.673 |
LIG_WW_3 | 1297 | 1301 | PF00397 | 0.842 |
MOD_CDK_SPxxK_3 | 2 | 9 | PF00069 | 0.346 |
MOD_CDK_SPxxK_3 | 888 | 895 | PF00069 | 0.435 |
MOD_CK1_1 | 1178 | 1184 | PF00069 | 0.514 |
MOD_CK1_1 | 1293 | 1299 | PF00069 | 0.829 |
MOD_CK1_1 | 1335 | 1341 | PF00069 | 0.658 |
MOD_CK1_1 | 329 | 335 | PF00069 | 0.664 |
MOD_CK1_1 | 385 | 391 | PF00069 | 0.649 |
MOD_CK1_1 | 504 | 510 | PF00069 | 0.378 |
MOD_CK1_1 | 551 | 557 | PF00069 | 0.341 |
MOD_CK1_1 | 636 | 642 | PF00069 | 0.389 |
MOD_CK1_1 | 654 | 660 | PF00069 | 0.385 |
MOD_CK1_1 | 663 | 669 | PF00069 | 0.404 |
MOD_CK1_1 | 679 | 685 | PF00069 | 0.498 |
MOD_CK1_1 | 757 | 763 | PF00069 | 0.549 |
MOD_CK1_1 | 781 | 787 | PF00069 | 0.436 |
MOD_CK1_1 | 888 | 894 | PF00069 | 0.475 |
MOD_CK1_1 | 994 | 1000 | PF00069 | 0.506 |
MOD_CK2_1 | 1042 | 1048 | PF00069 | 0.529 |
MOD_CK2_1 | 1108 | 1114 | PF00069 | 0.367 |
MOD_CK2_1 | 1150 | 1156 | PF00069 | 0.665 |
MOD_CK2_1 | 1160 | 1166 | PF00069 | 0.612 |
MOD_CK2_1 | 1326 | 1332 | PF00069 | 0.733 |
MOD_CK2_1 | 416 | 422 | PF00069 | 0.407 |
MOD_CK2_1 | 486 | 492 | PF00069 | 0.334 |
MOD_CK2_1 | 80 | 86 | PF00069 | 0.333 |
MOD_CK2_1 | 803 | 809 | PF00069 | 0.447 |
MOD_CK2_1 | 888 | 894 | PF00069 | 0.551 |
MOD_CK2_1 | 939 | 945 | PF00069 | 0.356 |
MOD_Cter_Amidation | 1144 | 1147 | PF01082 | 0.535 |
MOD_Cter_Amidation | 205 | 208 | PF01082 | 0.220 |
MOD_GlcNHglycan | 1169 | 1172 | PF01048 | 0.593 |
MOD_GlcNHglycan | 1182 | 1185 | PF01048 | 0.348 |
MOD_GlcNHglycan | 1292 | 1295 | PF01048 | 0.804 |
MOD_GlcNHglycan | 1302 | 1307 | PF01048 | 0.728 |
MOD_GlcNHglycan | 1334 | 1337 | PF01048 | 0.706 |
MOD_GlcNHglycan | 1365 | 1368 | PF01048 | 0.774 |
MOD_GlcNHglycan | 1394 | 1397 | PF01048 | 0.729 |
MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.509 |
MOD_GlcNHglycan | 172 | 175 | PF01048 | 0.375 |
MOD_GlcNHglycan | 242 | 245 | PF01048 | 0.542 |
MOD_GlcNHglycan | 250 | 253 | PF01048 | 0.465 |
MOD_GlcNHglycan | 293 | 296 | PF01048 | 0.500 |
MOD_GlcNHglycan | 329 | 332 | PF01048 | 0.667 |
MOD_GlcNHglycan | 387 | 390 | PF01048 | 0.664 |
MOD_GlcNHglycan | 483 | 486 | PF01048 | 0.509 |
MOD_GlcNHglycan | 491 | 495 | PF01048 | 0.457 |
MOD_GlcNHglycan | 536 | 539 | PF01048 | 0.402 |
MOD_GlcNHglycan | 638 | 641 | PF01048 | 0.424 |
MOD_GlcNHglycan | 662 | 665 | PF01048 | 0.508 |
MOD_GlcNHglycan | 684 | 687 | PF01048 | 0.446 |
MOD_GlcNHglycan | 713 | 717 | PF01048 | 0.348 |
MOD_GlcNHglycan | 761 | 764 | PF01048 | 0.470 |
MOD_GlcNHglycan | 840 | 843 | PF01048 | 0.447 |
MOD_GlcNHglycan | 887 | 890 | PF01048 | 0.434 |
MOD_GlcNHglycan | 993 | 996 | PF01048 | 0.447 |
MOD_GSK3_1 | 1038 | 1045 | PF00069 | 0.510 |
MOD_GSK3_1 | 1160 | 1167 | PF00069 | 0.524 |
MOD_GSK3_1 | 1174 | 1181 | PF00069 | 0.593 |
MOD_GSK3_1 | 1221 | 1228 | PF00069 | 0.647 |
MOD_GSK3_1 | 1298 | 1305 | PF00069 | 0.797 |
MOD_GSK3_1 | 1326 | 1333 | PF00069 | 0.736 |
MOD_GSK3_1 | 1346 | 1353 | PF00069 | 0.778 |
MOD_GSK3_1 | 1363 | 1370 | PF00069 | 0.458 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.514 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.514 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.483 |
MOD_GSK3_1 | 326 | 333 | PF00069 | 0.643 |
MOD_GSK3_1 | 334 | 341 | PF00069 | 0.591 |
MOD_GSK3_1 | 477 | 484 | PF00069 | 0.549 |
MOD_GSK3_1 | 486 | 493 | PF00069 | 0.357 |
MOD_GSK3_1 | 513 | 520 | PF00069 | 0.410 |
MOD_GSK3_1 | 632 | 639 | PF00069 | 0.394 |
MOD_GSK3_1 | 727 | 734 | PF00069 | 0.490 |
MOD_GSK3_1 | 735 | 742 | PF00069 | 0.484 |
MOD_GSK3_1 | 754 | 761 | PF00069 | 0.417 |
MOD_GSK3_1 | 834 | 841 | PF00069 | 0.422 |
MOD_GSK3_1 | 869 | 876 | PF00069 | 0.489 |
MOD_GSK3_1 | 884 | 891 | PF00069 | 0.482 |
MOD_GSK3_1 | 935 | 942 | PF00069 | 0.374 |
MOD_GSK3_1 | 980 | 987 | PF00069 | 0.365 |
MOD_N-GLC_1 | 339 | 344 | PF02516 | 0.433 |
MOD_N-GLC_1 | 571 | 576 | PF02516 | 0.478 |
MOD_N-GLC_2 | 500 | 502 | PF02516 | 0.240 |
MOD_NEK2_1 | 1175 | 1180 | PF00069 | 0.549 |
MOD_NEK2_1 | 1191 | 1196 | PF00069 | 0.253 |
MOD_NEK2_1 | 1307 | 1312 | PF00069 | 0.569 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.471 |
MOD_NEK2_1 | 212 | 217 | PF00069 | 0.491 |
MOD_NEK2_1 | 248 | 253 | PF00069 | 0.449 |
MOD_NEK2_1 | 261 | 266 | PF00069 | 0.363 |
MOD_NEK2_1 | 327 | 332 | PF00069 | 0.426 |
MOD_NEK2_1 | 355 | 360 | PF00069 | 0.550 |
MOD_NEK2_1 | 405 | 410 | PF00069 | 0.398 |
MOD_NEK2_1 | 660 | 665 | PF00069 | 0.380 |
MOD_NEK2_1 | 696 | 701 | PF00069 | 0.459 |
MOD_NEK2_1 | 727 | 732 | PF00069 | 0.349 |
MOD_NEK2_1 | 800 | 805 | PF00069 | 0.421 |
MOD_NEK2_2 | 296 | 301 | PF00069 | 0.307 |
MOD_PIKK_1 | 1245 | 1251 | PF00454 | 0.657 |
MOD_PIKK_1 | 334 | 340 | PF00454 | 0.472 |
MOD_PIKK_1 | 778 | 784 | PF00454 | 0.539 |
MOD_PK_1 | 633 | 639 | PF00069 | 0.475 |
MOD_PKA_1 | 1330 | 1336 | PF00069 | 0.462 |
MOD_PKA_1 | 1354 | 1360 | PF00069 | 0.576 |
MOD_PKA_1 | 1363 | 1369 | PF00069 | 0.487 |
MOD_PKA_1 | 632 | 638 | PF00069 | 0.472 |
MOD_PKA_2 | 1042 | 1048 | PF00069 | 0.533 |
MOD_PKA_2 | 1290 | 1296 | PF00069 | 0.826 |
MOD_PKA_2 | 1307 | 1313 | PF00069 | 0.631 |
MOD_PKA_2 | 1354 | 1360 | PF00069 | 0.587 |
MOD_PKA_2 | 1363 | 1369 | PF00069 | 0.489 |
MOD_PKA_2 | 206 | 212 | PF00069 | 0.558 |
MOD_PKA_2 | 290 | 296 | PF00069 | 0.493 |
MOD_PKA_2 | 558 | 564 | PF00069 | 0.469 |
MOD_PKA_2 | 632 | 638 | PF00069 | 0.426 |
MOD_PKB_1 | 1223 | 1231 | PF00069 | 0.706 |
MOD_PKB_1 | 882 | 890 | PF00069 | 0.388 |
MOD_Plk_1 | 253 | 259 | PF00069 | 0.484 |
MOD_Plk_1 | 339 | 345 | PF00069 | 0.498 |
MOD_Plk_1 | 361 | 367 | PF00069 | 0.425 |
MOD_Plk_1 | 427 | 433 | PF00069 | 0.392 |
MOD_Plk_1 | 651 | 657 | PF00069 | 0.397 |
MOD_Plk_1 | 712 | 718 | PF00069 | 0.472 |
MOD_Plk_1 | 808 | 814 | PF00069 | 0.422 |
MOD_Plk_2-3 | 980 | 986 | PF00069 | 0.355 |
MOD_Plk_4 | 133 | 139 | PF00069 | 0.483 |
MOD_Plk_4 | 361 | 367 | PF00069 | 0.530 |
MOD_Plk_4 | 411 | 417 | PF00069 | 0.531 |
MOD_Plk_4 | 513 | 519 | PF00069 | 0.435 |
MOD_Plk_4 | 670 | 676 | PF00069 | 0.300 |
MOD_Plk_4 | 783 | 789 | PF00069 | 0.417 |
MOD_Plk_4 | 851 | 857 | PF00069 | 0.414 |
MOD_Plk_4 | 875 | 881 | PF00069 | 0.446 |
MOD_Plk_4 | 935 | 941 | PF00069 | 0.355 |
MOD_Plk_4 | 984 | 990 | PF00069 | 0.369 |
MOD_ProDKin_1 | 152 | 158 | PF00069 | 0.470 |
MOD_ProDKin_1 | 2 | 8 | PF00069 | 0.346 |
MOD_ProDKin_1 | 229 | 235 | PF00069 | 0.475 |
MOD_ProDKin_1 | 29 | 35 | PF00069 | 0.451 |
MOD_ProDKin_1 | 318 | 324 | PF00069 | 0.523 |
MOD_ProDKin_1 | 736 | 742 | PF00069 | 0.453 |
MOD_ProDKin_1 | 764 | 770 | PF00069 | 0.545 |
MOD_ProDKin_1 | 781 | 787 | PF00069 | 0.456 |
MOD_ProDKin_1 | 873 | 879 | PF00069 | 0.447 |
MOD_ProDKin_1 | 888 | 894 | PF00069 | 0.556 |
MOD_SUMO_rev_2 | 364 | 373 | PF00179 | 0.588 |
TRG_DiLeu_BaEn_1 | 66 | 71 | PF01217 | 0.509 |
TRG_DiLeu_BaEn_1 | 935 | 940 | PF01217 | 0.483 |
TRG_DiLeu_BaEn_2 | 179 | 185 | PF01217 | 0.571 |
TRG_DiLeu_BaEn_2 | 617 | 623 | PF01217 | 0.359 |
TRG_DiLeu_BaLyEn_6 | 30 | 35 | PF01217 | 0.467 |
TRG_DiLeu_LyEn_5 | 1208 | 1213 | PF01217 | 0.559 |
TRG_ENDOCYTIC_2 | 1023 | 1026 | PF00928 | 0.363 |
TRG_ENDOCYTIC_2 | 1049 | 1052 | PF00928 | 0.343 |
TRG_ENDOCYTIC_2 | 1071 | 1074 | PF00928 | 0.480 |
TRG_ENDOCYTIC_2 | 134 | 137 | PF00928 | 0.523 |
TRG_ENDOCYTIC_2 | 224 | 227 | PF00928 | 0.517 |
TRG_ENDOCYTIC_2 | 265 | 268 | PF00928 | 0.519 |
TRG_ENDOCYTIC_2 | 311 | 314 | PF00928 | 0.498 |
TRG_ENDOCYTIC_2 | 505 | 508 | PF00928 | 0.275 |
TRG_ENDOCYTIC_2 | 610 | 613 | PF00928 | 0.559 |
TRG_ENDOCYTIC_2 | 625 | 628 | PF00928 | 0.475 |
TRG_ENDOCYTIC_2 | 729 | 732 | PF00928 | 0.380 |
TRG_ENDOCYTIC_2 | 918 | 921 | PF00928 | 0.476 |
TRG_ER_diArg_1 | 1056 | 1059 | PF00400 | 0.356 |
TRG_ER_diArg_1 | 1222 | 1225 | PF00400 | 0.642 |
TRG_ER_diArg_1 | 1251 | 1254 | PF00400 | 0.599 |
TRG_ER_diArg_1 | 1313 | 1315 | PF00400 | 0.505 |
TRG_ER_diArg_1 | 204 | 207 | PF00400 | 0.490 |
TRG_ER_diArg_1 | 29 | 31 | PF00400 | 0.454 |
TRG_ER_diArg_1 | 392 | 394 | PF00400 | 0.399 |
TRG_ER_diArg_1 | 440 | 442 | PF00400 | 0.212 |
TRG_ER_diArg_1 | 631 | 633 | PF00400 | 0.241 |
TRG_ER_diArg_1 | 688 | 690 | PF00400 | 0.551 |
TRG_ER_diArg_1 | 8 | 10 | PF00400 | 0.446 |
TRG_ER_diArg_1 | 881 | 884 | PF00400 | 0.508 |
TRG_Pf-PMV_PEXEL_1 | 967 | 971 | PF00026 | 0.427 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P457 | Leptomonas seymouri | 26% | 100% |
A0A1X0P171 | Trypanosomatidae | 34% | 100% |
A0A3Q8IJB0 | Leishmania donovani | 70% | 100% |
A0A3R7R8G4 | Trypanosoma rangeli | 33% | 100% |
A0A3S5H6Z8 | Leishmania donovani | 70% | 100% |
A0A3S7WU91 | Leishmania donovani | 59% | 99% |
A0A3S7WU94 | Leishmania donovani | 53% | 100% |
A0A3S7WU95 | Leishmania donovani | 68% | 100% |
A0A3S7XB85 | Leishmania donovani | 28% | 100% |
A4H8U6 | Leishmania braziliensis | 64% | 100% |
A4H8V5 | Leishmania braziliensis | 70% | 100% |
A4H8V7 | Leishmania braziliensis | 91% | 100% |
A4HPI4 | Leishmania braziliensis | 27% | 100% |
A4HX84 | Leishmania infantum | 53% | 100% |
A4HX85 | Leishmania infantum | 70% | 100% |
A4HX87 | Leishmania infantum | 59% | 100% |
A4IDA6 | Leishmania infantum | 28% | 100% |
C9ZM79 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
C9ZM80 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
C9ZM81 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
C9ZM82 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
C9ZM83 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 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) | 36% | 100% |
C9ZN43 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
C9ZN44 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
C9ZN45 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
C9ZN46 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 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) | 32% | 100% |
C9ZNT1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
C9ZPZ6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
C9ZQ51 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 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) | 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% |
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) | 33% | 100% |
D0A0U3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
D0A0W7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
D0A0X5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
D0A1S1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
D0A5D2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
D0A5D5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
D0A5U0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
D0A5U1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
D0A7A0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
D0A9R3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
D0AAV3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
E9AQY0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 59% | 100% |
E9AQY1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 55% | 100% |
E9AQY2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 68% | 100% |
E9AQY4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 70% | 100% |
E9ARD7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 54% | 100% |
E9AT96 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
Q25263 | Leishmania donovani | 71% | 100% |
Q26721 | Trypanosoma brucei brucei | 35% | 100% |
Q27675 | Leishmania donovani | 53% | 100% |
Q4Q1A1 | Leishmania major | 28% | 100% |
Q4QEH9 | Leishmania major | 70% | 100% |
Q4QEI0 | Leishmania major | 70% | 100% |
Q4QEI1 | Leishmania major | 71% | 100% |
Q4QEI2 | Leishmania major | 58% | 100% |
Q4QEI3 | Leishmania major | 52% | 100% |
Q99279 | Trypanosoma brucei brucei | 30% | 100% |
Q99280 | Trypanosoma brucei brucei | 33% | 100% |
V5AYH7 | Trypanosoma cruzi | 36% | 100% |