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: 51 |
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: 42, no: 26 |
NetGPI | no | yes: 0, no: 68 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 65 |
GO:0110165 | cellular anatomical entity | 1 | 69 |
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 69 |
GO:0006163 | purine nucleotide metabolic process | 5 | 69 |
GO:0006164 | purine nucleotide biosynthetic process | 6 | 69 |
GO:0006171 | cAMP biosynthetic process | 8 | 69 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 69 |
GO:0006753 | nucleoside phosphate metabolic process | 4 | 69 |
GO:0006793 | phosphorus metabolic process | 3 | 69 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 69 |
GO:0006807 | nitrogen compound metabolic process | 2 | 69 |
GO:0007165 | signal transduction | 2 | 69 |
GO:0008152 | metabolic process | 1 | 69 |
GO:0009058 | biosynthetic process | 2 | 69 |
GO:0009117 | nucleotide metabolic process | 5 | 69 |
GO:0009150 | purine ribonucleotide metabolic process | 6 | 69 |
GO:0009152 | purine ribonucleotide biosynthetic process | 7 | 69 |
GO:0009165 | nucleotide biosynthetic process | 6 | 69 |
GO:0009187 | cyclic nucleotide metabolic process | 6 | 69 |
GO:0009190 | cyclic nucleotide biosynthetic process | 7 | 69 |
GO:0009259 | ribonucleotide metabolic process | 5 | 69 |
GO:0009260 | ribonucleotide biosynthetic process | 6 | 69 |
GO:0009987 | cellular process | 1 | 69 |
GO:0018130 | heterocycle biosynthetic process | 4 | 69 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 69 |
GO:0019637 | organophosphate metabolic process | 3 | 69 |
GO:0019693 | ribose phosphate metabolic process | 4 | 69 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 69 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 69 |
GO:0035556 | intracellular signal transduction | 3 | 69 |
GO:0044237 | cellular metabolic process | 2 | 69 |
GO:0044238 | primary metabolic process | 2 | 69 |
GO:0044249 | cellular biosynthetic process | 3 | 69 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 69 |
GO:0044281 | small molecule metabolic process | 2 | 69 |
GO:0046058 | cAMP metabolic process | 7 | 69 |
GO:0046390 | ribose phosphate biosynthetic process | 5 | 69 |
GO:0046483 | heterocycle metabolic process | 3 | 69 |
GO:0050789 | regulation of biological process | 2 | 69 |
GO:0050794 | regulation of cellular process | 3 | 69 |
GO:0052652 | cyclic purine nucleotide metabolic process | 6 | 69 |
GO:0055086 | nucleobase-containing small molecule metabolic process | 3 | 69 |
GO:0065007 | biological regulation | 1 | 69 |
GO:0071704 | organic substance metabolic process | 2 | 69 |
GO:0072521 | purine-containing compound metabolic process | 4 | 69 |
GO:0072522 | purine-containing compound biosynthetic process | 5 | 69 |
GO:0090407 | organophosphate biosynthetic process | 4 | 69 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 69 |
GO:1901137 | carbohydrate derivative biosynthetic process | 4 | 69 |
GO:1901293 | nucleoside phosphate biosynthetic process | 5 | 69 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 69 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 69 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 69 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 69 |
GO:1901576 | organic substance biosynthetic process | 3 | 69 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 60 |
GO:0016829 | lyase activity | 2 | 60 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 395 | 399 | PF00656 | 0.503 |
CLV_C14_Caspase3-7 | 769 | 773 | PF00656 | 0.406 |
CLV_C14_Caspase3-7 | 91 | 95 | PF00656 | 0.425 |
CLV_C14_Caspase3-7 | 933 | 937 | PF00656 | 0.605 |
CLV_C14_Caspase3-7 | 994 | 998 | PF00656 | 0.504 |
CLV_MEL_PAP_1 | 1067 | 1073 | PF00089 | 0.307 |
CLV_NRD_NRD_1 | 1157 | 1159 | PF00675 | 0.461 |
CLV_NRD_NRD_1 | 1325 | 1327 | PF00675 | 0.523 |
CLV_NRD_NRD_1 | 1365 | 1367 | PF00675 | 0.601 |
CLV_NRD_NRD_1 | 1395 | 1397 | PF00675 | 0.551 |
CLV_NRD_NRD_1 | 217 | 219 | PF00675 | 0.608 |
CLV_NRD_NRD_1 | 26 | 28 | PF00675 | 0.345 |
CLV_NRD_NRD_1 | 41 | 43 | PF00675 | 0.358 |
CLV_NRD_NRD_1 | 437 | 439 | PF00675 | 0.488 |
CLV_NRD_NRD_1 | 535 | 537 | PF00675 | 0.577 |
CLV_NRD_NRD_1 | 670 | 672 | PF00675 | 0.540 |
CLV_PCSK_FUR_1 | 215 | 219 | PF00082 | 0.610 |
CLV_PCSK_FUR_1 | 27 | 31 | PF00082 | 0.241 |
CLV_PCSK_KEX2_1 | 1157 | 1159 | PF00082 | 0.461 |
CLV_PCSK_KEX2_1 | 1325 | 1327 | PF00082 | 0.519 |
CLV_PCSK_KEX2_1 | 1365 | 1367 | PF00082 | 0.608 |
CLV_PCSK_KEX2_1 | 1394 | 1396 | PF00082 | 0.547 |
CLV_PCSK_KEX2_1 | 217 | 219 | PF00082 | 0.610 |
CLV_PCSK_KEX2_1 | 26 | 28 | PF00082 | 0.362 |
CLV_PCSK_KEX2_1 | 29 | 31 | PF00082 | 0.383 |
CLV_PCSK_KEX2_1 | 41 | 43 | PF00082 | 0.353 |
CLV_PCSK_PC1ET2_1 | 29 | 31 | PF00082 | 0.457 |
CLV_PCSK_SKI1_1 | 117 | 121 | PF00082 | 0.725 |
CLV_PCSK_SKI1_1 | 218 | 222 | PF00082 | 0.602 |
CLV_PCSK_SKI1_1 | 265 | 269 | PF00082 | 0.544 |
CLV_PCSK_SKI1_1 | 29 | 33 | PF00082 | 0.352 |
CLV_PCSK_SKI1_1 | 315 | 319 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 515 | 519 | PF00082 | 0.590 |
CLV_PCSK_SKI1_1 | 664 | 668 | PF00082 | 0.535 |
CLV_PCSK_SKI1_1 | 799 | 803 | PF00082 | 0.573 |
CLV_PCSK_SKI1_1 | 93 | 97 | PF00082 | 0.669 |
DEG_APCC_DBOX_1 | 1325 | 1333 | PF00400 | 0.720 |
DEG_APCC_DBOX_1 | 40 | 48 | PF00400 | 0.606 |
DEG_APCC_DBOX_1 | 721 | 729 | PF00400 | 0.274 |
DEG_APCC_DBOX_1 | 798 | 806 | PF00400 | 0.324 |
DEG_APCC_DBOX_1 | 894 | 902 | PF00400 | 0.360 |
DEG_APCC_KENBOX_2 | 616 | 620 | PF00400 | 0.237 |
DEG_MDM2_SWIB_1 | 492 | 499 | PF02201 | 0.217 |
DEG_ODPH_VHL_1 | 697 | 708 | PF01847 | 0.240 |
DEG_SCF_FBW7_2 | 885 | 891 | PF00400 | 0.527 |
DEG_SPOP_SBC_1 | 300 | 304 | PF00917 | 0.438 |
DOC_CDC14_PxL_1 | 529 | 537 | PF14671 | 0.243 |
DOC_CDC14_PxL_1 | 774 | 782 | PF14671 | 0.240 |
DOC_CKS1_1 | 885 | 890 | PF01111 | 0.471 |
DOC_CYCLIN_RxL_1 | 1032 | 1043 | PF00134 | 0.391 |
DOC_CYCLIN_yCln2_LP_2 | 246 | 252 | PF00134 | 0.404 |
DOC_CYCLIN_yCln2_LP_2 | 518 | 524 | PF00134 | 0.397 |
DOC_MAPK_FxFP_2 | 504 | 507 | PF00069 | 0.254 |
DOC_MAPK_gen_1 | 1341 | 1347 | PF00069 | 0.743 |
DOC_MAPK_gen_1 | 169 | 176 | PF00069 | 0.233 |
DOC_MAPK_gen_1 | 215 | 224 | PF00069 | 0.316 |
DOC_MAPK_gen_1 | 26 | 37 | PF00069 | 0.673 |
DOC_MAPK_gen_1 | 41 | 51 | PF00069 | 0.604 |
DOC_MAPK_gen_1 | 616 | 623 | PF00069 | 0.264 |
DOC_MAPK_gen_1 | 93 | 102 | PF00069 | 0.463 |
DOC_MAPK_MEF2A_6 | 42 | 51 | PF00069 | 0.512 |
DOC_MAPK_MEF2A_6 | 520 | 529 | PF00069 | 0.433 |
DOC_MAPK_MEF2A_6 | 722 | 729 | PF00069 | 0.292 |
DOC_MAPK_MEF2A_6 | 799 | 806 | PF00069 | 0.342 |
DOC_MAPK_MEF2A_6 | 906 | 915 | PF00069 | 0.250 |
DOC_MAPK_MEF2A_6 | 93 | 102 | PF00069 | 0.460 |
DOC_MAPK_RevD_3 | 1144 | 1158 | PF00069 | 0.592 |
DOC_MAPK_RevD_3 | 203 | 218 | PF00069 | 0.282 |
DOC_MAPK_RevD_3 | 601 | 617 | PF00069 | 0.208 |
DOC_PP1_RVXF_1 | 169 | 176 | PF00149 | 0.345 |
DOC_PP1_RVXF_1 | 313 | 319 | PF00149 | 0.430 |
DOC_PP1_RVXF_1 | 552 | 558 | PF00149 | 0.334 |
DOC_PP2B_LxvP_1 | 246 | 249 | PF13499 | 0.346 |
DOC_PP2B_PxIxI_1 | 610 | 616 | PF00149 | 0.201 |
DOC_PP4_FxxP_1 | 175 | 178 | PF00568 | 0.459 |
DOC_PP4_FxxP_1 | 504 | 507 | PF00568 | 0.254 |
DOC_PP4_FxxP_1 | 608 | 611 | PF00568 | 0.261 |
DOC_PP4_FxxP_1 | 622 | 625 | PF00568 | 0.349 |
DOC_PP4_FxxP_1 | 677 | 680 | PF00568 | 0.451 |
DOC_PP4_FxxP_1 | 787 | 790 | PF00568 | 0.461 |
DOC_PP4_FxxP_1 | 817 | 820 | PF00568 | 0.275 |
DOC_USP7_MATH_1 | 1002 | 1006 | PF00917 | 0.582 |
DOC_USP7_MATH_1 | 1029 | 1033 | PF00917 | 0.614 |
DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.356 |
DOC_USP7_MATH_1 | 1270 | 1274 | PF00917 | 0.679 |
DOC_USP7_MATH_1 | 1301 | 1305 | PF00917 | 0.734 |
DOC_USP7_MATH_1 | 1313 | 1317 | PF00917 | 0.752 |
DOC_USP7_MATH_1 | 1361 | 1365 | PF00917 | 0.635 |
DOC_USP7_MATH_1 | 1376 | 1380 | PF00917 | 0.561 |
DOC_USP7_MATH_1 | 240 | 244 | PF00917 | 0.281 |
DOC_USP7_MATH_1 | 300 | 304 | PF00917 | 0.436 |
DOC_USP7_MATH_1 | 394 | 398 | PF00917 | 0.398 |
DOC_USP7_MATH_1 | 643 | 647 | PF00917 | 0.390 |
DOC_USP7_MATH_1 | 686 | 690 | PF00917 | 0.451 |
DOC_USP7_MATH_1 | 880 | 884 | PF00917 | 0.440 |
DOC_USP7_UBL2_3 | 380 | 384 | PF12436 | 0.483 |
DOC_WW_Pin1_4 | 328 | 333 | PF00397 | 0.415 |
DOC_WW_Pin1_4 | 602 | 607 | PF00397 | 0.337 |
DOC_WW_Pin1_4 | 767 | 772 | PF00397 | 0.452 |
DOC_WW_Pin1_4 | 791 | 796 | PF00397 | 0.363 |
DOC_WW_Pin1_4 | 881 | 886 | PF00397 | 0.456 |
DOC_WW_Pin1_4 | 899 | 904 | PF00397 | 0.464 |
LIG_14-3-3_CanoR_1 | 1236 | 1243 | PF00244 | 0.672 |
LIG_14-3-3_CanoR_1 | 1254 | 1259 | PF00244 | 0.709 |
LIG_14-3-3_CanoR_1 | 1325 | 1330 | PF00244 | 0.694 |
LIG_14-3-3_CanoR_1 | 1336 | 1345 | PF00244 | 0.672 |
LIG_14-3-3_CanoR_1 | 1374 | 1379 | PF00244 | 0.554 |
LIG_14-3-3_CanoR_1 | 215 | 224 | PF00244 | 0.354 |
LIG_14-3-3_CanoR_1 | 301 | 308 | PF00244 | 0.403 |
LIG_14-3-3_CanoR_1 | 36 | 44 | PF00244 | 0.505 |
LIG_14-3-3_CanoR_1 | 438 | 442 | PF00244 | 0.340 |
LIG_14-3-3_CanoR_1 | 484 | 488 | PF00244 | 0.240 |
LIG_14-3-3_CanoR_1 | 671 | 679 | PF00244 | 0.386 |
LIG_14-3-3_CanoR_1 | 694 | 698 | PF00244 | 0.405 |
LIG_14-3-3_CanoR_1 | 756 | 761 | PF00244 | 0.448 |
LIG_14-3-3_CanoR_1 | 842 | 846 | PF00244 | 0.461 |
LIG_Actin_WH2_2 | 1009 | 1024 | PF00022 | 0.400 |
LIG_Actin_WH2_2 | 199 | 214 | PF00022 | 0.265 |
LIG_Actin_WH2_2 | 221 | 237 | PF00022 | 0.224 |
LIG_Actin_WH2_2 | 520 | 538 | PF00022 | 0.321 |
LIG_Actin_WH2_2 | 578 | 596 | PF00022 | 0.237 |
LIG_AP2alpha_2 | 198 | 200 | PF02296 | 0.246 |
LIG_APCC_ABBA_1 | 151 | 156 | PF00400 | 0.449 |
LIG_APCC_ABBA_1 | 318 | 323 | PF00400 | 0.319 |
LIG_APCC_ABBA_1 | 354 | 359 | PF00400 | 0.236 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.561 |
LIG_BIR_III_2 | 938 | 942 | PF00653 | 0.715 |
LIG_BRCT_BRCA1_1 | 164 | 168 | PF00533 | 0.428 |
LIG_BRCT_BRCA1_1 | 604 | 608 | PF00533 | 0.237 |
LIG_BRCT_BRCA1_1 | 746 | 750 | PF00533 | 0.223 |
LIG_BRCT_BRCA1_1 | 802 | 806 | PF00533 | 0.414 |
LIG_DLG_GKlike_1 | 756 | 763 | PF00625 | 0.285 |
LIG_EH_1 | 1285 | 1289 | PF12763 | 0.462 |
LIG_EH1_1 | 310 | 318 | PF00400 | 0.195 |
LIG_eIF4E_1 | 223 | 229 | PF01652 | 0.203 |
LIG_eIF4E_1 | 777 | 783 | PF01652 | 0.248 |
LIG_FHA_1 | 1016 | 1022 | PF00498 | 0.579 |
LIG_FHA_1 | 1025 | 1031 | PF00498 | 0.520 |
LIG_FHA_1 | 1050 | 1056 | PF00498 | 0.525 |
LIG_FHA_1 | 1100 | 1106 | PF00498 | 0.510 |
LIG_FHA_1 | 206 | 212 | PF00498 | 0.318 |
LIG_FHA_1 | 223 | 229 | PF00498 | 0.236 |
LIG_FHA_1 | 349 | 355 | PF00498 | 0.348 |
LIG_FHA_1 | 409 | 415 | PF00498 | 0.365 |
LIG_FHA_1 | 587 | 593 | PF00498 | 0.321 |
LIG_FHA_1 | 674 | 680 | PF00498 | 0.364 |
LIG_FHA_1 | 73 | 79 | PF00498 | 0.276 |
LIG_FHA_1 | 792 | 798 | PF00498 | 0.397 |
LIG_FHA_1 | 8 | 14 | PF00498 | 0.424 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.298 |
LIG_FHA_1 | 849 | 855 | PF00498 | 0.446 |
LIG_FHA_1 | 968 | 974 | PF00498 | 0.562 |
LIG_FHA_2 | 1042 | 1048 | PF00498 | 0.604 |
LIG_FHA_2 | 1162 | 1168 | PF00498 | 0.736 |
LIG_FHA_2 | 1172 | 1178 | PF00498 | 0.720 |
LIG_FHA_2 | 193 | 199 | PF00498 | 0.461 |
LIG_FHA_2 | 329 | 335 | PF00498 | 0.432 |
LIG_FHA_2 | 347 | 353 | PF00498 | 0.362 |
LIG_FHA_2 | 569 | 575 | PF00498 | 0.251 |
LIG_FHA_2 | 657 | 663 | PF00498 | 0.360 |
LIG_FHA_2 | 707 | 713 | PF00498 | 0.352 |
LIG_FHA_2 | 767 | 773 | PF00498 | 0.283 |
LIG_FHA_2 | 850 | 856 | PF00498 | 0.430 |
LIG_FHA_2 | 89 | 95 | PF00498 | 0.437 |
LIG_FHA_2 | 951 | 957 | PF00498 | 0.504 |
LIG_FHA_2 | 992 | 998 | PF00498 | 0.509 |
LIG_GBD_Chelix_1 | 1012 | 1020 | PF00786 | 0.413 |
LIG_GBD_Chelix_1 | 289 | 297 | PF00786 | 0.546 |
LIG_GBD_Chelix_1 | 416 | 424 | PF00786 | 0.530 |
LIG_GBD_Chelix_1 | 425 | 433 | PF00786 | 0.473 |
LIG_Integrin_isoDGR_2 | 115 | 117 | PF01839 | 0.484 |
LIG_Integrin_RGD_1 | 196 | 198 | PF01839 | 0.456 |
LIG_IRF3_LxIS_1 | 598 | 605 | PF10401 | 0.236 |
LIG_LIR_Apic_2 | 1046 | 1051 | PF02991 | 0.505 |
LIG_LIR_Apic_2 | 172 | 178 | PF02991 | 0.452 |
LIG_LIR_Apic_2 | 461 | 465 | PF02991 | 0.397 |
LIG_LIR_Apic_2 | 605 | 611 | PF02991 | 0.335 |
LIG_LIR_Apic_2 | 676 | 680 | PF02991 | 0.455 |
LIG_LIR_Apic_2 | 814 | 820 | PF02991 | 0.365 |
LIG_LIR_Gen_1 | 1057 | 1067 | PF02991 | 0.567 |
LIG_LIR_Gen_1 | 1079 | 1089 | PF02991 | 0.600 |
LIG_LIR_Gen_1 | 198 | 207 | PF02991 | 0.429 |
LIG_LIR_Gen_1 | 219 | 229 | PF02991 | 0.426 |
LIG_LIR_Gen_1 | 526 | 535 | PF02991 | 0.339 |
LIG_LIR_Gen_1 | 556 | 565 | PF02991 | 0.369 |
LIG_LIR_Gen_1 | 577 | 585 | PF02991 | 0.362 |
LIG_LIR_Gen_1 | 618 | 627 | PF02991 | 0.435 |
LIG_LIR_Gen_1 | 731 | 739 | PF02991 | 0.275 |
LIG_LIR_Gen_1 | 747 | 758 | PF02991 | 0.299 |
LIG_LIR_Gen_1 | 759 | 765 | PF02991 | 0.418 |
LIG_LIR_Gen_1 | 917 | 928 | PF02991 | 0.278 |
LIG_LIR_Gen_1 | 949 | 960 | PF02991 | 0.506 |
LIG_LIR_Nem_3 | 1031 | 1037 | PF02991 | 0.506 |
LIG_LIR_Nem_3 | 1057 | 1063 | PF02991 | 0.512 |
LIG_LIR_Nem_3 | 1079 | 1085 | PF02991 | 0.526 |
LIG_LIR_Nem_3 | 1086 | 1092 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 1115 | 1121 | PF02991 | 0.524 |
LIG_LIR_Nem_3 | 1206 | 1211 | PF02991 | 0.639 |
LIG_LIR_Nem_3 | 198 | 203 | PF02991 | 0.313 |
LIG_LIR_Nem_3 | 219 | 224 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 273 | 278 | PF02991 | 0.237 |
LIG_LIR_Nem_3 | 526 | 532 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 556 | 560 | PF02991 | 0.375 |
LIG_LIR_Nem_3 | 577 | 583 | PF02991 | 0.288 |
LIG_LIR_Nem_3 | 618 | 623 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 630 | 635 | PF02991 | 0.353 |
LIG_LIR_Nem_3 | 731 | 735 | PF02991 | 0.288 |
LIG_LIR_Nem_3 | 736 | 742 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 747 | 753 | PF02991 | 0.311 |
LIG_LIR_Nem_3 | 759 | 763 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 775 | 780 | PF02991 | 0.330 |
LIG_LIR_Nem_3 | 855 | 861 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 917 | 923 | PF02991 | 0.278 |
LIG_LIR_Nem_3 | 949 | 955 | PF02991 | 0.506 |
LIG_LIR_Nem_3 | 959 | 965 | PF02991 | 0.615 |
LIG_LYPXL_yS_3 | 275 | 278 | PF13949 | 0.224 |
LIG_LYPXL_yS_3 | 777 | 780 | PF13949 | 0.246 |
LIG_MYND_3 | 624 | 628 | PF01753 | 0.399 |
LIG_NRBOX | 597 | 603 | PF00104 | 0.232 |
LIG_NRBOX | 797 | 803 | PF00104 | 0.244 |
LIG_PCNA_TLS_4 | 358 | 366 | PF02747 | 0.215 |
LIG_PCNA_yPIPBox_3 | 406 | 420 | PF02747 | 0.251 |
LIG_PCNA_yPIPBox_3 | 900 | 914 | PF02747 | 0.316 |
LIG_PDZ_Class_3 | 1406 | 1411 | PF00595 | 0.602 |
LIG_Pex14_2 | 175 | 179 | PF04695 | 0.451 |
LIG_Pex14_2 | 492 | 496 | PF04695 | 0.221 |
LIG_Pex14_2 | 746 | 750 | PF04695 | 0.236 |
LIG_Pex14_2 | 783 | 787 | PF04695 | 0.301 |
LIG_PTB_Apo_2 | 399 | 406 | PF02174 | 0.370 |
LIG_PTB_Apo_2 | 73 | 80 | PF02174 | 0.422 |
LIG_PTB_Apo_2 | 781 | 788 | PF02174 | 0.251 |
LIG_PTB_Phospho_1 | 399 | 405 | PF10480 | 0.282 |
LIG_PTB_Phospho_1 | 73 | 79 | PF10480 | 0.427 |
LIG_SH2_CRK | 252 | 256 | PF00017 | 0.485 |
LIG_SH2_CRK | 462 | 466 | PF00017 | 0.396 |
LIG_SH2_GRB2like | 400 | 403 | PF00017 | 0.385 |
LIG_SH2_GRB2like | 580 | 583 | PF00017 | 0.206 |
LIG_SH2_NCK_1 | 1082 | 1086 | PF00017 | 0.600 |
LIG_SH2_NCK_1 | 252 | 256 | PF00017 | 0.486 |
LIG_SH2_NCK_1 | 658 | 662 | PF00017 | 0.451 |
LIG_SH2_PTP2 | 1048 | 1051 | PF00017 | 0.551 |
LIG_SH2_SRC | 1048 | 1051 | PF00017 | 0.562 |
LIG_SH2_SRC | 1082 | 1085 | PF00017 | 0.600 |
LIG_SH2_SRC | 369 | 372 | PF00017 | 0.345 |
LIG_SH2_SRC | 451 | 454 | PF00017 | 0.409 |
LIG_SH2_STAP1 | 1060 | 1064 | PF00017 | 0.567 |
LIG_SH2_STAP1 | 322 | 326 | PF00017 | 0.434 |
LIG_SH2_STAP1 | 583 | 587 | PF00017 | 0.379 |
LIG_SH2_STAP1 | 836 | 840 | PF00017 | 0.394 |
LIG_SH2_STAT3 | 478 | 481 | PF00017 | 0.432 |
LIG_SH2_STAT3 | 861 | 864 | PF00017 | 0.342 |
LIG_SH2_STAT5 | 1048 | 1051 | PF00017 | 0.496 |
LIG_SH2_STAT5 | 107 | 110 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 111 | 114 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 1243 | 1246 | PF00017 | 0.617 |
LIG_SH2_STAT5 | 193 | 196 | PF00017 | 0.364 |
LIG_SH2_STAT5 | 223 | 226 | PF00017 | 0.303 |
LIG_SH2_STAT5 | 306 | 309 | PF00017 | 0.318 |
LIG_SH2_STAT5 | 364 | 367 | PF00017 | 0.261 |
LIG_SH2_STAT5 | 369 | 372 | PF00017 | 0.270 |
LIG_SH2_STAT5 | 400 | 403 | PF00017 | 0.481 |
LIG_SH2_STAT5 | 451 | 454 | PF00017 | 0.306 |
LIG_SH2_STAT5 | 478 | 481 | PF00017 | 0.401 |
LIG_SH2_STAT5 | 512 | 515 | PF00017 | 0.318 |
LIG_SH2_STAT5 | 580 | 583 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 620 | 623 | PF00017 | 0.345 |
LIG_SH2_STAT5 | 632 | 635 | PF00017 | 0.282 |
LIG_SH2_STAT5 | 658 | 661 | PF00017 | 0.381 |
LIG_SH2_STAT5 | 79 | 82 | PF00017 | 0.464 |
LIG_SH2_STAT5 | 929 | 932 | PF00017 | 0.559 |
LIG_SH3_3 | 1226 | 1232 | PF00018 | 0.617 |
LIG_SH3_3 | 1382 | 1388 | PF00018 | 0.555 |
LIG_SH3_3 | 147 | 153 | PF00018 | 0.355 |
LIG_SH3_3 | 494 | 500 | PF00018 | 0.363 |
LIG_SH3_3 | 585 | 591 | PF00018 | 0.393 |
LIG_SH3_3 | 600 | 606 | PF00018 | 0.351 |
LIG_SH3_3 | 676 | 682 | PF00018 | 0.390 |
LIG_SH3_3 | 874 | 880 | PF00018 | 0.414 |
LIG_SH3_3 | 882 | 888 | PF00018 | 0.438 |
LIG_SH3_3 | 919 | 925 | PF00018 | 0.475 |
LIG_SUMO_SIM_anti_2 | 131 | 138 | PF11976 | 0.461 |
LIG_SUMO_SIM_anti_2 | 1381 | 1386 | PF11976 | 0.590 |
LIG_SUMO_SIM_anti_2 | 201 | 208 | PF11976 | 0.232 |
LIG_SUMO_SIM_anti_2 | 584 | 589 | PF11976 | 0.293 |
LIG_SUMO_SIM_anti_2 | 599 | 605 | PF11976 | 0.316 |
LIG_SUMO_SIM_anti_2 | 709 | 718 | PF11976 | 0.328 |
LIG_SUMO_SIM_anti_2 | 800 | 806 | PF11976 | 0.280 |
LIG_SUMO_SIM_anti_2 | 865 | 870 | PF11976 | 0.424 |
LIG_SUMO_SIM_anti_2 | 945 | 954 | PF11976 | 0.506 |
LIG_SUMO_SIM_par_1 | 546 | 551 | PF11976 | 0.350 |
LIG_SUMO_SIM_par_1 | 599 | 605 | PF11976 | 0.283 |
LIG_SUMO_SIM_par_1 | 726 | 731 | PF11976 | 0.399 |
LIG_SUMO_SIM_par_1 | 865 | 870 | PF11976 | 0.349 |
LIG_SUMO_SIM_par_1 | 912 | 917 | PF11976 | 0.469 |
LIG_TRAF2_1 | 1056 | 1059 | PF00917 | 0.627 |
LIG_TRAF2_1 | 1367 | 1370 | PF00917 | 0.604 |
LIG_TRFH_1 | 244 | 248 | PF08558 | 0.243 |
LIG_TRFH_1 | 85 | 89 | PF08558 | 0.295 |
LIG_TYR_ITIM | 1080 | 1085 | PF00017 | 0.486 |
LIG_TYR_ITIM | 633 | 638 | PF00017 | 0.478 |
LIG_UBA3_1 | 206 | 213 | PF00899 | 0.401 |
LIG_WRC_WIRS_1 | 241 | 246 | PF05994 | 0.300 |
LIG_WRC_WIRS_1 | 716 | 721 | PF05994 | 0.477 |
LIG_WRC_WIRS_1 | 729 | 734 | PF05994 | 0.343 |
LIG_WRC_WIRS_1 | 757 | 762 | PF05994 | 0.497 |
LIG_WW_3 | 1231 | 1235 | PF00397 | 0.682 |
MOD_CDK_SPxxK_3 | 899 | 906 | PF00069 | 0.493 |
MOD_CK1_1 | 1005 | 1011 | PF00069 | 0.508 |
MOD_CK1_1 | 1189 | 1195 | PF00069 | 0.526 |
MOD_CK1_1 | 1304 | 1310 | PF00069 | 0.690 |
MOD_CK1_1 | 1335 | 1341 | PF00069 | 0.645 |
MOD_CK1_1 | 1346 | 1352 | PF00069 | 0.631 |
MOD_CK1_1 | 239 | 245 | PF00069 | 0.478 |
MOD_CK1_1 | 339 | 345 | PF00069 | 0.625 |
MOD_CK1_1 | 432 | 438 | PF00069 | 0.334 |
MOD_CK1_1 | 688 | 694 | PF00069 | 0.489 |
MOD_CK1_1 | 718 | 724 | PF00069 | 0.456 |
MOD_CK1_1 | 767 | 773 | PF00069 | 0.505 |
MOD_CK1_1 | 883 | 889 | PF00069 | 0.653 |
MOD_CK2_1 | 1053 | 1059 | PF00069 | 0.527 |
MOD_CK2_1 | 1119 | 1125 | PF00069 | 0.363 |
MOD_CK2_1 | 1161 | 1167 | PF00069 | 0.665 |
MOD_CK2_1 | 1171 | 1177 | PF00069 | 0.614 |
MOD_CK2_1 | 1395 | 1401 | PF00069 | 0.707 |
MOD_CK2_1 | 346 | 352 | PF00069 | 0.508 |
MOD_CK2_1 | 483 | 489 | PF00069 | 0.212 |
MOD_CK2_1 | 643 | 649 | PF00069 | 0.403 |
MOD_CK2_1 | 819 | 825 | PF00069 | 0.529 |
MOD_CK2_1 | 849 | 855 | PF00069 | 0.433 |
MOD_CK2_1 | 950 | 956 | PF00069 | 0.354 |
MOD_Cter_Amidation | 1155 | 1158 | PF01082 | 0.566 |
MOD_GlcNHglycan | 1004 | 1007 | PF01048 | 0.458 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.474 |
MOD_GlcNHglycan | 1031 | 1034 | PF01048 | 0.500 |
MOD_GlcNHglycan | 1180 | 1183 | PF01048 | 0.604 |
MOD_GlcNHglycan | 1272 | 1275 | PF01048 | 0.547 |
MOD_GlcNHglycan | 1281 | 1284 | PF01048 | 0.470 |
MOD_GlcNHglycan | 1303 | 1306 | PF01048 | 0.678 |
MOD_GlcNHglycan | 1311 | 1314 | PF01048 | 0.510 |
MOD_GlcNHglycan | 1315 | 1318 | PF01048 | 0.703 |
MOD_GlcNHglycan | 1374 | 1377 | PF01048 | 0.709 |
MOD_GlcNHglycan | 238 | 241 | PF01048 | 0.457 |
MOD_GlcNHglycan | 303 | 306 | PF01048 | 0.487 |
MOD_GlcNHglycan | 339 | 342 | PF01048 | 0.632 |
MOD_GlcNHglycan | 37 | 40 | PF01048 | 0.430 |
MOD_GlcNHglycan | 420 | 423 | PF01048 | 0.492 |
MOD_GlcNHglycan | 508 | 511 | PF01048 | 0.403 |
MOD_GlcNHglycan | 556 | 560 | PF01048 | 0.421 |
MOD_GlcNHglycan | 597 | 601 | PF01048 | 0.440 |
MOD_GlcNHglycan | 659 | 662 | PF01048 | 0.459 |
MOD_GlcNHglycan | 688 | 691 | PF01048 | 0.414 |
MOD_GlcNHglycan | 825 | 828 | PF01048 | 0.528 |
MOD_GSK3_1 | 1049 | 1056 | PF00069 | 0.517 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.394 |
MOD_GSK3_1 | 1171 | 1178 | PF00069 | 0.539 |
MOD_GSK3_1 | 1185 | 1192 | PF00069 | 0.317 |
MOD_GSK3_1 | 1232 | 1239 | PF00069 | 0.627 |
MOD_GSK3_1 | 1309 | 1316 | PF00069 | 0.707 |
MOD_GSK3_1 | 1332 | 1339 | PF00069 | 0.654 |
MOD_GSK3_1 | 1357 | 1364 | PF00069 | 0.730 |
MOD_GSK3_1 | 1370 | 1377 | PF00069 | 0.717 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.401 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.396 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.484 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.556 |
MOD_GSK3_1 | 236 | 243 | PF00069 | 0.458 |
MOD_GSK3_1 | 250 | 257 | PF00069 | 0.474 |
MOD_GSK3_1 | 295 | 302 | PF00069 | 0.480 |
MOD_GSK3_1 | 336 | 343 | PF00069 | 0.607 |
MOD_GSK3_1 | 425 | 432 | PF00069 | 0.331 |
MOD_GSK3_1 | 523 | 530 | PF00069 | 0.409 |
MOD_GSK3_1 | 592 | 599 | PF00069 | 0.373 |
MOD_GSK3_1 | 643 | 650 | PF00069 | 0.406 |
MOD_GSK3_1 | 685 | 692 | PF00069 | 0.487 |
MOD_GSK3_1 | 740 | 747 | PF00069 | 0.520 |
MOD_GSK3_1 | 766 | 773 | PF00069 | 0.411 |
MOD_GSK3_1 | 819 | 826 | PF00069 | 0.512 |
MOD_GSK3_1 | 83 | 90 | PF00069 | 0.419 |
MOD_GSK3_1 | 841 | 848 | PF00069 | 0.519 |
MOD_GSK3_1 | 880 | 887 | PF00069 | 0.576 |
MOD_GSK3_1 | 946 | 953 | PF00069 | 0.368 |
MOD_GSK3_1 | 991 | 998 | PF00069 | 0.364 |
MOD_N-GLC_1 | 109 | 114 | PF02516 | 0.282 |
MOD_N-GLC_1 | 527 | 532 | PF02516 | 0.480 |
MOD_N-GLC_1 | 565 | 570 | PF02516 | 0.423 |
MOD_N-GLC_1 | 581 | 586 | PF02516 | 0.472 |
MOD_N-GLC_1 | 791 | 796 | PF02516 | 0.456 |
MOD_N-GLC_1 | 81 | 86 | PF02516 | 0.433 |
MOD_N-GLC_1 | 845 | 850 | PF02516 | 0.476 |
MOD_NEK2_1 | 106 | 111 | PF00069 | 0.370 |
MOD_NEK2_1 | 1186 | 1191 | PF00069 | 0.571 |
MOD_NEK2_1 | 1279 | 1284 | PF00069 | 0.580 |
MOD_NEK2_1 | 1318 | 1323 | PF00069 | 0.725 |
MOD_NEK2_1 | 1332 | 1337 | PF00069 | 0.462 |
MOD_NEK2_1 | 157 | 162 | PF00069 | 0.454 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.478 |
MOD_NEK2_1 | 222 | 227 | PF00069 | 0.445 |
MOD_NEK2_1 | 236 | 241 | PF00069 | 0.459 |
MOD_NEK2_1 | 271 | 276 | PF00069 | 0.386 |
MOD_NEK2_1 | 35 | 40 | PF00069 | 0.514 |
MOD_NEK2_1 | 420 | 425 | PF00069 | 0.388 |
MOD_NEK2_1 | 429 | 434 | PF00069 | 0.316 |
MOD_NEK2_1 | 446 | 451 | PF00069 | 0.261 |
MOD_NEK2_1 | 548 | 553 | PF00069 | 0.423 |
MOD_NEK2_1 | 555 | 560 | PF00069 | 0.405 |
MOD_NEK2_1 | 758 | 763 | PF00069 | 0.323 |
MOD_NEK2_1 | 81 | 86 | PF00069 | 0.387 |
MOD_NEK2_1 | 823 | 828 | PF00069 | 0.389 |
MOD_NEK2_2 | 306 | 311 | PF00069 | 0.301 |
MOD_NEK2_2 | 7 | 12 | PF00069 | 0.209 |
MOD_PIKK_1 | 1256 | 1262 | PF00454 | 0.673 |
MOD_PIKK_1 | 901 | 907 | PF00454 | 0.300 |
MOD_PK_1 | 1374 | 1380 | PF00069 | 0.458 |
MOD_PKA_1 | 1325 | 1331 | PF00069 | 0.661 |
MOD_PKA_1 | 1341 | 1347 | PF00069 | 0.704 |
MOD_PKA_1 | 1365 | 1371 | PF00069 | 0.558 |
MOD_PKA_1 | 1395 | 1401 | PF00069 | 0.464 |
MOD_PKA_2 | 11 | 17 | PF00069 | 0.480 |
MOD_PKA_2 | 1253 | 1259 | PF00069 | 0.552 |
MOD_PKA_2 | 1301 | 1307 | PF00069 | 0.691 |
MOD_PKA_2 | 1318 | 1324 | PF00069 | 0.706 |
MOD_PKA_2 | 1325 | 1331 | PF00069 | 0.678 |
MOD_PKA_2 | 1335 | 1341 | PF00069 | 0.665 |
MOD_PKA_2 | 1365 | 1371 | PF00069 | 0.765 |
MOD_PKA_2 | 1395 | 1401 | PF00069 | 0.501 |
MOD_PKA_2 | 216 | 222 | PF00069 | 0.533 |
MOD_PKA_2 | 300 | 306 | PF00069 | 0.488 |
MOD_PKA_2 | 35 | 41 | PF00069 | 0.480 |
MOD_PKA_2 | 437 | 443 | PF00069 | 0.381 |
MOD_PKA_2 | 483 | 489 | PF00069 | 0.252 |
MOD_PKA_2 | 568 | 574 | PF00069 | 0.446 |
MOD_PKA_2 | 670 | 676 | PF00069 | 0.470 |
MOD_PKA_2 | 693 | 699 | PF00069 | 0.394 |
MOD_PKA_2 | 740 | 746 | PF00069 | 0.300 |
MOD_PKA_2 | 841 | 847 | PF00069 | 0.536 |
MOD_PKB_1 | 1234 | 1242 | PF00069 | 0.683 |
MOD_Plk_1 | 201 | 207 | PF00069 | 0.280 |
MOD_Plk_1 | 370 | 376 | PF00069 | 0.386 |
MOD_Plk_1 | 446 | 452 | PF00069 | 0.412 |
MOD_Plk_1 | 555 | 561 | PF00069 | 0.458 |
MOD_Plk_1 | 581 | 587 | PF00069 | 0.455 |
MOD_Plk_1 | 643 | 649 | PF00069 | 0.472 |
MOD_Plk_1 | 664 | 670 | PF00069 | 0.470 |
MOD_Plk_1 | 81 | 87 | PF00069 | 0.452 |
MOD_Plk_2-3 | 1405 | 1411 | PF00069 | 0.444 |
MOD_Plk_2-3 | 88 | 94 | PF00069 | 0.304 |
MOD_Plk_2-3 | 991 | 997 | PF00069 | 0.353 |
MOD_Plk_4 | 1290 | 1296 | PF00069 | 0.434 |
MOD_Plk_4 | 1395 | 1401 | PF00069 | 0.464 |
MOD_Plk_4 | 143 | 149 | PF00069 | 0.507 |
MOD_Plk_4 | 158 | 164 | PF00069 | 0.393 |
MOD_Plk_4 | 201 | 207 | PF00069 | 0.440 |
MOD_Plk_4 | 370 | 376 | PF00069 | 0.472 |
MOD_Plk_4 | 420 | 426 | PF00069 | 0.533 |
MOD_Plk_4 | 429 | 435 | PF00069 | 0.427 |
MOD_Plk_4 | 483 | 489 | PF00069 | 0.438 |
MOD_Plk_4 | 715 | 721 | PF00069 | 0.454 |
MOD_Plk_4 | 800 | 806 | PF00069 | 0.344 |
MOD_Plk_4 | 862 | 868 | PF00069 | 0.411 |
MOD_Plk_4 | 914 | 920 | PF00069 | 0.329 |
MOD_Plk_4 | 946 | 952 | PF00069 | 0.352 |
MOD_Plk_4 | 995 | 1001 | PF00069 | 0.354 |
MOD_ProDKin_1 | 328 | 334 | PF00069 | 0.513 |
MOD_ProDKin_1 | 602 | 608 | PF00069 | 0.399 |
MOD_ProDKin_1 | 767 | 773 | PF00069 | 0.557 |
MOD_ProDKin_1 | 791 | 797 | PF00069 | 0.433 |
MOD_ProDKin_1 | 881 | 887 | PF00069 | 0.562 |
MOD_ProDKin_1 | 899 | 905 | PF00069 | 0.569 |
MOD_SUMO_for_1 | 615 | 618 | PF00179 | 0.215 |
MOD_SUMO_rev_2 | 231 | 237 | PF00179 | 0.398 |
MOD_SUMO_rev_2 | 373 | 382 | PF00179 | 0.561 |
MOD_SUMO_rev_2 | 432 | 440 | PF00179 | 0.470 |
MOD_SUMO_rev_2 | 88 | 98 | PF00179 | 0.381 |
TRG_DiLeu_BaEn_1 | 946 | 951 | PF01217 | 0.480 |
TRG_DiLeu_BaEn_2 | 617 | 623 | PF01217 | 0.417 |
TRG_DiLeu_BaEn_2 | 648 | 654 | PF01217 | 0.240 |
TRG_DiLeu_BaEn_4 | 1058 | 1064 | PF01217 | 0.436 |
TRG_DiLeu_BaLyEn_6 | 588 | 593 | PF01217 | 0.528 |
TRG_DiLeu_LyEn_5 | 1219 | 1224 | PF01217 | 0.590 |
TRG_DiLeu_LyEn_5 | 775 | 780 | PF01217 | 0.259 |
TRG_ENDOCYTIC_2 | 1034 | 1037 | PF00928 | 0.361 |
TRG_ENDOCYTIC_2 | 1060 | 1063 | PF00928 | 0.355 |
TRG_ENDOCYTIC_2 | 1082 | 1085 | PF00928 | 0.481 |
TRG_ENDOCYTIC_2 | 275 | 278 | PF00928 | 0.240 |
TRG_ENDOCYTIC_2 | 321 | 324 | PF00928 | 0.501 |
TRG_ENDOCYTIC_2 | 620 | 623 | PF00928 | 0.528 |
TRG_ENDOCYTIC_2 | 635 | 638 | PF00928 | 0.468 |
TRG_ENDOCYTIC_2 | 739 | 742 | PF00928 | 0.387 |
TRG_ENDOCYTIC_2 | 777 | 780 | PF00928 | 0.535 |
TRG_ER_diArg_1 | 1067 | 1070 | PF00400 | 0.354 |
TRG_ER_diArg_1 | 1233 | 1236 | PF00400 | 0.631 |
TRG_ER_diArg_1 | 1324 | 1326 | PF00400 | 0.529 |
TRG_ER_diArg_1 | 1365 | 1367 | PF00400 | 0.539 |
TRG_ER_diArg_1 | 1394 | 1396 | PF00400 | 0.691 |
TRG_ER_diArg_1 | 214 | 217 | PF00400 | 0.487 |
TRG_ER_diArg_1 | 40 | 42 | PF00400 | 0.443 |
TRG_ER_diArg_1 | 892 | 895 | PF00400 | 0.624 |
TRG_Pf-PMV_PEXEL_1 | 315 | 319 | PF00026 | 0.436 |
TRG_Pf-PMV_PEXEL_1 | 978 | 982 | PF00026 | 0.440 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A1X0P171 | Trypanosomatidae | 33% | 100% |
A0A3Q8IJB0 | Leishmania donovani | 61% | 100% |
A0A3R7R8G4 | Trypanosoma rangeli | 30% | 100% |
A0A3S5H6Z8 | Leishmania donovani | 61% | 100% |
A0A3S7WU91 | Leishmania donovani | 83% | 100% |
A0A3S7WU94 | Leishmania donovani | 54% | 100% |
A0A3S7WU95 | Leishmania donovani | 62% | 100% |
A4H8U6 | Leishmania braziliensis | 56% | 100% |
A4H8V5 | Leishmania braziliensis | 67% | 100% |
A4H8V7 | Leishmania braziliensis | 60% | 100% |
A4H8V8 | Leishmania braziliensis | 59% | 100% |
A4HPI4 | Leishmania braziliensis | 27% | 100% |
A4HX84 | Leishmania infantum | 54% | 100% |
A4HX85 | Leishmania infantum | 63% | 100% |
A4HX87 | Leishmania infantum | 84% | 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) | 33% | 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) | 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) | 30% | 100% |
C9ZNA6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
C9ZNH3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
C9ZNT1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZPZ6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
C9ZQ51 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 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) | 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) | 32% | 100% |
C9ZWQ5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZWU1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
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) | 32% | 100% |
C9ZZQ4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
D0A0U3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
D0A0W7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
D0A0X5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
D0A1S1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
D0A5D2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
D0A5D5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
D0A5U0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
D0A5U1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
D0A7A0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
D0A9R3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
D0AAV3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
E9AQY1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 62% | 100% |
E9AQY2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 66% | 100% |
E9AQY4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 65% | 100% |
E9ARD7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 57% | 100% |
Q25263 | Leishmania donovani | 62% | 100% |
Q26721 | Trypanosoma brucei brucei | 35% | 100% |
Q27675 | Leishmania donovani | 54% | 100% |
Q4QEH9 | Leishmania major | 64% | 100% |
Q4QEI0 | Leishmania major | 64% | 100% |
Q4QEI1 | Leishmania major | 64% | 100% |
Q4QEI2 | Leishmania major | 81% | 100% |
Q4QEI3 | Leishmania major | 56% | 100% |
Q99279 | Trypanosoma brucei brucei | 29% | 100% |
Q99280 | Trypanosoma brucei brucei | 32% | 100% |
V5AYH7 | Trypanosoma cruzi | 34% | 100% |