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. | no | 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: 27 |
NetGPI | no | yes: 0, no: 73 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 68 |
GO:0110165 | cellular anatomical entity | 1 | 74 |
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 | 63 |
GO:0016829 | lyase activity | 2 | 63 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 396 | 400 | PF00656 | 0.450 |
CLV_C14_Caspase3-7 | 714 | 718 | PF00656 | 0.254 |
CLV_C14_Caspase3-7 | 936 | 940 | PF00656 | 0.556 |
CLV_C14_Caspase3-7 | 997 | 1001 | PF00656 | 0.457 |
CLV_MEL_PAP_1 | 1070 | 1076 | PF00089 | 0.249 |
CLV_NRD_NRD_1 | 11 | 13 | PF00675 | 0.463 |
CLV_NRD_NRD_1 | 1160 | 1162 | PF00675 | 0.372 |
CLV_NRD_NRD_1 | 1328 | 1330 | PF00675 | 0.484 |
CLV_NRD_NRD_1 | 1343 | 1345 | PF00675 | 0.495 |
CLV_NRD_NRD_1 | 1368 | 1370 | PF00675 | 0.518 |
CLV_NRD_NRD_1 | 1398 | 1400 | PF00675 | 0.334 |
CLV_NRD_NRD_1 | 219 | 221 | PF00675 | 0.564 |
CLV_NRD_NRD_1 | 440 | 442 | PF00675 | 0.441 |
CLV_NRD_NRD_1 | 538 | 540 | PF00675 | 0.558 |
CLV_PCSK_FUR_1 | 1396 | 1400 | PF00082 | 0.289 |
CLV_PCSK_FUR_1 | 217 | 221 | PF00082 | 0.563 |
CLV_PCSK_KEX2_1 | 11 | 13 | PF00082 | 0.461 |
CLV_PCSK_KEX2_1 | 1160 | 1162 | PF00082 | 0.372 |
CLV_PCSK_KEX2_1 | 1328 | 1330 | PF00082 | 0.481 |
CLV_PCSK_KEX2_1 | 1368 | 1370 | PF00082 | 0.349 |
CLV_PCSK_KEX2_1 | 1396 | 1398 | PF00082 | 0.322 |
CLV_PCSK_KEX2_1 | 214 | 216 | PF00082 | 0.565 |
CLV_PCSK_KEX2_1 | 219 | 221 | PF00082 | 0.565 |
CLV_PCSK_KEX2_1 | 29 | 31 | PF00082 | 0.558 |
CLV_PCSK_PC1ET2_1 | 214 | 216 | PF00082 | 0.362 |
CLV_PCSK_PC1ET2_1 | 29 | 31 | PF00082 | 0.614 |
CLV_PCSK_PC7_1 | 215 | 221 | PF00082 | 0.380 |
CLV_PCSK_SKI1_1 | 1022 | 1026 | PF00082 | 0.247 |
CLV_PCSK_SKI1_1 | 1257 | 1261 | PF00082 | 0.409 |
CLV_PCSK_SKI1_1 | 220 | 224 | PF00082 | 0.559 |
CLV_PCSK_SKI1_1 | 317 | 321 | PF00082 | 0.458 |
CLV_PCSK_SKI1_1 | 518 | 522 | PF00082 | 0.535 |
CLV_PCSK_SKI1_1 | 645 | 649 | PF00082 | 0.473 |
CLV_PCSK_SKI1_1 | 759 | 763 | PF00082 | 0.494 |
CLV_PCSK_SKI1_1 | 802 | 806 | PF00082 | 0.549 |
DEG_APCC_DBOX_1 | 40 | 48 | PF00400 | 0.448 |
DEG_APCC_DBOX_1 | 801 | 809 | PF00400 | 0.262 |
DEG_APCC_KENBOX_2 | 619 | 623 | PF00400 | 0.199 |
DEG_SCF_FBW7_2 | 468 | 474 | PF00400 | 0.160 |
DEG_SCF_FBW7_2 | 888 | 894 | PF00400 | 0.489 |
DEG_SPOP_SBC_1 | 302 | 306 | PF00917 | 0.396 |
DOC_CDC14_PxL_1 | 143 | 151 | PF14671 | 0.395 |
DOC_CDC14_PxL_1 | 777 | 785 | PF14671 | 0.183 |
DOC_CKS1_1 | 468 | 473 | PF01111 | 0.166 |
DOC_CKS1_1 | 888 | 893 | PF01111 | 0.425 |
DOC_CYCLIN_RxL_1 | 756 | 764 | PF00134 | 0.232 |
DOC_CYCLIN_yCln2_LP_2 | 248 | 254 | PF00134 | 0.322 |
DOC_CYCLIN_yCln2_LP_2 | 521 | 527 | PF00134 | 0.345 |
DOC_MAPK_gen_1 | 11 | 19 | PF00069 | 0.218 |
DOC_MAPK_gen_1 | 131 | 138 | PF00069 | 0.274 |
DOC_MAPK_gen_1 | 1344 | 1350 | PF00069 | 0.509 |
DOC_MAPK_gen_1 | 217 | 226 | PF00069 | 0.267 |
DOC_MAPK_gen_1 | 29 | 37 | PF00069 | 0.469 |
DOC_MAPK_HePTP_8 | 520 | 532 | PF00069 | 0.359 |
DOC_MAPK_MEF2A_6 | 523 | 532 | PF00069 | 0.391 |
DOC_MAPK_MEF2A_6 | 802 | 809 | PF00069 | 0.292 |
DOC_MAPK_RevD_3 | 1147 | 1161 | PF00069 | 0.506 |
DOC_MAPK_RevD_3 | 205 | 220 | PF00069 | 0.226 |
DOC_PP1_RVXF_1 | 171 | 178 | PF00149 | 0.303 |
DOC_PP1_RVXF_1 | 315 | 321 | PF00149 | 0.383 |
DOC_PP1_RVXF_1 | 555 | 561 | PF00149 | 0.282 |
DOC_PP1_RVXF_1 | 757 | 764 | PF00149 | 0.281 |
DOC_PP2B_LxvP_1 | 248 | 251 | PF13499 | 0.270 |
DOC_PP4_FxxP_1 | 156 | 159 | PF00568 | 0.329 |
DOC_PP4_FxxP_1 | 177 | 180 | PF00568 | 0.414 |
DOC_PP4_FxxP_1 | 611 | 614 | PF00568 | 0.247 |
DOC_PP4_FxxP_1 | 625 | 628 | PF00568 | 0.341 |
DOC_PP4_FxxP_1 | 680 | 683 | PF00568 | 0.420 |
DOC_PP4_FxxP_1 | 790 | 793 | PF00568 | 0.233 |
DOC_PP4_FxxP_1 | 820 | 823 | PF00568 | 0.242 |
DOC_USP7_MATH_1 | 1005 | 1009 | PF00917 | 0.528 |
DOC_USP7_MATH_1 | 1259 | 1263 | PF00917 | 0.643 |
DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.360 |
DOC_USP7_MATH_1 | 1304 | 1308 | PF00917 | 0.664 |
DOC_USP7_MATH_1 | 1316 | 1320 | PF00917 | 0.645 |
DOC_USP7_MATH_1 | 1364 | 1368 | PF00917 | 0.542 |
DOC_USP7_MATH_1 | 159 | 163 | PF00917 | 0.394 |
DOC_USP7_MATH_1 | 302 | 306 | PF00917 | 0.394 |
DOC_USP7_MATH_1 | 395 | 399 | PF00917 | 0.326 |
DOC_USP7_MATH_1 | 646 | 650 | PF00917 | 0.361 |
DOC_USP7_MATH_1 | 67 | 71 | PF00917 | 0.472 |
DOC_USP7_MATH_1 | 689 | 693 | PF00917 | 0.440 |
DOC_USP7_MATH_1 | 883 | 887 | PF00917 | 0.353 |
DOC_USP7_UBL2_3 | 141 | 145 | PF12436 | 0.321 |
DOC_USP7_UBL2_3 | 383 | 387 | PF12436 | 0.424 |
DOC_USP7_UBL2_3 | 73 | 77 | PF12436 | 0.300 |
DOC_WW_Pin1_4 | 330 | 335 | PF00397 | 0.370 |
DOC_WW_Pin1_4 | 467 | 472 | PF00397 | 0.350 |
DOC_WW_Pin1_4 | 605 | 610 | PF00397 | 0.294 |
DOC_WW_Pin1_4 | 770 | 775 | PF00397 | 0.403 |
DOC_WW_Pin1_4 | 794 | 799 | PF00397 | 0.305 |
DOC_WW_Pin1_4 | 884 | 889 | PF00397 | 0.379 |
DOC_WW_Pin1_4 | 902 | 907 | PF00397 | 0.371 |
LIG_14-3-3_CanoR_1 | 1007 | 1015 | PF00244 | 0.565 |
LIG_14-3-3_CanoR_1 | 1057 | 1063 | PF00244 | 0.583 |
LIG_14-3-3_CanoR_1 | 1239 | 1246 | PF00244 | 0.610 |
LIG_14-3-3_CanoR_1 | 1257 | 1262 | PF00244 | 0.600 |
LIG_14-3-3_CanoR_1 | 1328 | 1333 | PF00244 | 0.672 |
LIG_14-3-3_CanoR_1 | 217 | 226 | PF00244 | 0.306 |
LIG_14-3-3_CanoR_1 | 303 | 310 | PF00244 | 0.362 |
LIG_14-3-3_CanoR_1 | 357 | 367 | PF00244 | 0.273 |
LIG_14-3-3_CanoR_1 | 36 | 44 | PF00244 | 0.271 |
LIG_14-3-3_CanoR_1 | 441 | 445 | PF00244 | 0.286 |
LIG_14-3-3_CanoR_1 | 487 | 491 | PF00244 | 0.180 |
LIG_14-3-3_CanoR_1 | 645 | 654 | PF00244 | 0.371 |
LIG_14-3-3_CanoR_1 | 675 | 681 | PF00244 | 0.355 |
LIG_14-3-3_CanoR_1 | 759 | 764 | PF00244 | 0.407 |
LIG_14-3-3_CanoR_1 | 845 | 849 | PF00244 | 0.391 |
LIG_Actin_WH2_2 | 20 | 38 | PF00022 | 0.502 |
LIG_Actin_WH2_2 | 201 | 216 | PF00022 | 0.213 |
LIG_Actin_WH2_2 | 523 | 541 | PF00022 | 0.266 |
LIG_Actin_WH2_2 | 581 | 599 | PF00022 | 0.182 |
LIG_Actin_WH2_2 | 662 | 677 | PF00022 | 0.294 |
LIG_Actin_WH2_2 | 683 | 699 | PF00022 | 0.324 |
LIG_AP2alpha_2 | 200 | 202 | PF02296 | 0.191 |
LIG_AP2alpha_2 | 90 | 92 | PF02296 | 0.295 |
LIG_APCC_ABBA_1 | 153 | 158 | PF00400 | 0.398 |
LIG_APCC_ABBA_1 | 320 | 325 | PF00400 | 0.250 |
LIG_BIR_III_2 | 941 | 945 | PF00653 | 0.624 |
LIG_BRCT_BRCA1_1 | 1366 | 1370 | PF00533 | 0.480 |
LIG_BRCT_BRCA1_1 | 607 | 611 | PF00533 | 0.189 |
LIG_BRCT_BRCA1_1 | 805 | 809 | PF00533 | 0.363 |
LIG_deltaCOP1_diTrp_1 | 580 | 583 | PF00928 | 0.177 |
LIG_eIF4E_1 | 780 | 786 | PF01652 | 0.189 |
LIG_FHA_1 | 1019 | 1025 | PF00498 | 0.574 |
LIG_FHA_1 | 1028 | 1034 | PF00498 | 0.355 |
LIG_FHA_1 | 1053 | 1059 | PF00498 | 0.466 |
LIG_FHA_1 | 1103 | 1109 | PF00498 | 0.462 |
LIG_FHA_1 | 12 | 18 | PF00498 | 0.460 |
LIG_FHA_1 | 204 | 210 | PF00498 | 0.298 |
LIG_FHA_1 | 368 | 374 | PF00498 | 0.414 |
LIG_FHA_1 | 412 | 418 | PF00498 | 0.320 |
LIG_FHA_1 | 527 | 533 | PF00498 | 0.322 |
LIG_FHA_1 | 590 | 596 | PF00498 | 0.282 |
LIG_FHA_1 | 795 | 801 | PF00498 | 0.337 |
LIG_FHA_1 | 84 | 90 | PF00498 | 0.227 |
LIG_FHA_1 | 852 | 858 | PF00498 | 0.408 |
LIG_FHA_1 | 918 | 924 | PF00498 | 0.357 |
LIG_FHA_2 | 1045 | 1051 | PF00498 | 0.570 |
LIG_FHA_2 | 1165 | 1171 | PF00498 | 0.679 |
LIG_FHA_2 | 1175 | 1181 | PF00498 | 0.671 |
LIG_FHA_2 | 195 | 201 | PF00498 | 0.410 |
LIG_FHA_2 | 331 | 337 | PF00498 | 0.383 |
LIG_FHA_2 | 429 | 435 | PF00498 | 0.364 |
LIG_FHA_2 | 710 | 716 | PF00498 | 0.297 |
LIG_FHA_2 | 954 | 960 | PF00498 | 0.457 |
LIG_FHA_2 | 995 | 1001 | PF00498 | 0.457 |
LIG_GBD_Chelix_1 | 1015 | 1023 | PF00786 | 0.366 |
LIG_GBD_Chelix_1 | 291 | 299 | PF00786 | 0.475 |
LIG_GBD_Chelix_1 | 419 | 427 | PF00786 | 0.473 |
LIG_Integrin_isoDGR_2 | 117 | 119 | PF01839 | 0.446 |
LIG_Integrin_RGD_1 | 198 | 200 | PF01839 | 0.397 |
LIG_IRF3_LxIS_1 | 548 | 554 | PF10401 | 0.164 |
LIG_IRF3_LxIS_1 | 601 | 608 | PF10401 | 0.183 |
LIG_LIR_Apic_2 | 1049 | 1054 | PF02991 | 0.447 |
LIG_LIR_Apic_2 | 174 | 180 | PF02991 | 0.409 |
LIG_LIR_Apic_2 | 464 | 468 | PF02991 | 0.323 |
LIG_LIR_Apic_2 | 608 | 614 | PF02991 | 0.305 |
LIG_LIR_Apic_2 | 679 | 683 | PF02991 | 0.423 |
LIG_LIR_Apic_2 | 817 | 823 | PF02991 | 0.325 |
LIG_LIR_Gen_1 | 1060 | 1070 | PF02991 | 0.510 |
LIG_LIR_Gen_1 | 1082 | 1092 | PF02991 | 0.551 |
LIG_LIR_Gen_1 | 200 | 209 | PF02991 | 0.394 |
LIG_LIR_Gen_1 | 221 | 231 | PF02991 | 0.394 |
LIG_LIR_Gen_1 | 269 | 278 | PF02991 | 0.317 |
LIG_LIR_Gen_1 | 559 | 568 | PF02991 | 0.337 |
LIG_LIR_Gen_1 | 580 | 588 | PF02991 | 0.304 |
LIG_LIR_Gen_1 | 621 | 630 | PF02991 | 0.401 |
LIG_LIR_Gen_1 | 725 | 735 | PF02991 | 0.273 |
LIG_LIR_Gen_1 | 741 | 750 | PF02991 | 0.282 |
LIG_LIR_Gen_1 | 762 | 768 | PF02991 | 0.319 |
LIG_LIR_Gen_1 | 952 | 963 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 1034 | 1040 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 1060 | 1066 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 1082 | 1088 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 1089 | 1095 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 1118 | 1124 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 1209 | 1214 | PF02991 | 0.585 |
LIG_LIR_Nem_3 | 144 | 149 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 221 | 226 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 233 | 239 | PF02991 | 0.292 |
LIG_LIR_Nem_3 | 559 | 563 | PF02991 | 0.339 |
LIG_LIR_Nem_3 | 580 | 586 | PF02991 | 0.230 |
LIG_LIR_Nem_3 | 621 | 626 | PF02991 | 0.384 |
LIG_LIR_Nem_3 | 633 | 638 | PF02991 | 0.312 |
LIG_LIR_Nem_3 | 725 | 731 | PF02991 | 0.280 |
LIG_LIR_Nem_3 | 734 | 738 | PF02991 | 0.262 |
LIG_LIR_Nem_3 | 741 | 745 | PF02991 | 0.299 |
LIG_LIR_Nem_3 | 746 | 752 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 762 | 766 | PF02991 | 0.314 |
LIG_LIR_Nem_3 | 778 | 783 | PF02991 | 0.248 |
LIG_LIR_Nem_3 | 858 | 864 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 952 | 958 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 962 | 968 | PF02991 | 0.559 |
LIG_LYPXL_yS_3 | 146 | 149 | PF13949 | 0.259 |
LIG_LYPXL_yS_3 | 780 | 783 | PF13949 | 0.188 |
LIG_MYND_3 | 627 | 631 | PF01753 | 0.323 |
LIG_NRBOX | 600 | 606 | PF00104 | 0.178 |
LIG_NRBOX | 800 | 806 | PF00104 | 0.184 |
LIG_PCNA_yPIPBox_3 | 416 | 426 | PF02747 | 0.402 |
LIG_PCNA_yPIPBox_3 | 903 | 917 | PF02747 | 0.220 |
LIG_PDZ_Class_3 | 1409 | 1414 | PF00595 | 0.517 |
LIG_Pex14_2 | 177 | 181 | PF04695 | 0.402 |
LIG_Pex14_2 | 786 | 790 | PF04695 | 0.230 |
LIG_PTB_Apo_2 | 75 | 82 | PF02174 | 0.384 |
LIG_PTB_Apo_2 | 784 | 791 | PF02174 | 0.189 |
LIG_PTB_Phospho_1 | 75 | 81 | PF10480 | 0.393 |
LIG_SH2_CRK | 236 | 240 | PF00017 | 0.330 |
LIG_SH2_CRK | 254 | 258 | PF00017 | 0.438 |
LIG_SH2_CRK | 465 | 469 | PF00017 | 0.322 |
LIG_SH2_GRB2like | 515 | 518 | PF00017 | 0.238 |
LIG_SH2_NCK_1 | 1051 | 1055 | PF00017 | 0.426 |
LIG_SH2_NCK_1 | 1085 | 1089 | PF00017 | 0.547 |
LIG_SH2_NCK_1 | 254 | 258 | PF00017 | 0.451 |
LIG_SH2_NCK_1 | 661 | 665 | PF00017 | 0.410 |
LIG_SH2_SRC | 1051 | 1054 | PF00017 | 0.505 |
LIG_SH2_SRC | 1085 | 1088 | PF00017 | 0.547 |
LIG_SH2_SRC | 454 | 457 | PF00017 | 0.354 |
LIG_SH2_STAP1 | 1063 | 1067 | PF00017 | 0.511 |
LIG_SH2_STAP1 | 324 | 328 | PF00017 | 0.389 |
LIG_SH2_STAP1 | 403 | 407 | PF00017 | 0.239 |
LIG_SH2_STAP1 | 509 | 513 | PF00017 | 0.286 |
LIG_SH2_STAP1 | 586 | 590 | PF00017 | 0.297 |
LIG_SH2_STAP1 | 839 | 843 | PF00017 | 0.357 |
LIG_SH2_STAT3 | 481 | 484 | PF00017 | 0.388 |
LIG_SH2_STAT3 | 864 | 867 | PF00017 | 0.269 |
LIG_SH2_STAT5 | 1246 | 1249 | PF00017 | 0.580 |
LIG_SH2_STAT5 | 195 | 198 | PF00017 | 0.309 |
LIG_SH2_STAT5 | 225 | 228 | PF00017 | 0.262 |
LIG_SH2_STAT5 | 308 | 311 | PF00017 | 0.275 |
LIG_SH2_STAT5 | 454 | 457 | PF00017 | 0.253 |
LIG_SH2_STAT5 | 481 | 484 | PF00017 | 0.351 |
LIG_SH2_STAT5 | 515 | 518 | PF00017 | 0.267 |
LIG_SH2_STAT5 | 623 | 626 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 635 | 638 | PF00017 | 0.256 |
LIG_SH2_STAT5 | 661 | 664 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 81 | 84 | PF00017 | 0.404 |
LIG_SH3_1 | 465 | 471 | PF00018 | 0.210 |
LIG_SH3_3 | 1229 | 1235 | PF00018 | 0.557 |
LIG_SH3_3 | 1284 | 1290 | PF00018 | 0.602 |
LIG_SH3_3 | 1385 | 1391 | PF00018 | 0.500 |
LIG_SH3_3 | 149 | 155 | PF00018 | 0.285 |
LIG_SH3_3 | 465 | 471 | PF00018 | 0.210 |
LIG_SH3_3 | 588 | 594 | PF00018 | 0.337 |
LIG_SH3_3 | 603 | 609 | PF00018 | 0.293 |
LIG_SH3_3 | 877 | 883 | PF00018 | 0.336 |
LIG_SH3_3 | 885 | 891 | PF00018 | 0.373 |
LIG_SUMO_SIM_anti_2 | 133 | 140 | PF11976 | 0.395 |
LIG_SUMO_SIM_anti_2 | 1384 | 1389 | PF11976 | 0.512 |
LIG_SUMO_SIM_anti_2 | 587 | 592 | PF11976 | 0.393 |
LIG_SUMO_SIM_anti_2 | 602 | 608 | PF11976 | 0.220 |
LIG_SUMO_SIM_anti_2 | 803 | 809 | PF11976 | 0.221 |
LIG_SUMO_SIM_anti_2 | 920 | 925 | PF11976 | 0.346 |
LIG_SUMO_SIM_anti_2 | 948 | 957 | PF11976 | 0.461 |
LIG_SUMO_SIM_par_1 | 203 | 210 | PF11976 | 0.238 |
LIG_SUMO_SIM_par_1 | 238 | 245 | PF11976 | 0.223 |
LIG_SUMO_SIM_par_1 | 549 | 556 | PF11976 | 0.305 |
LIG_SUMO_SIM_par_1 | 602 | 608 | PF11976 | 0.231 |
LIG_SUMO_SIM_par_1 | 729 | 734 | PF11976 | 0.355 |
LIG_SUMO_SIM_par_1 | 868 | 873 | PF11976 | 0.272 |
LIG_SUMO_SIM_par_1 | 919 | 925 | PF11976 | 0.395 |
LIG_TRAF2_1 | 1059 | 1062 | PF00917 | 0.579 |
LIG_TRAF2_1 | 825 | 828 | PF00917 | 0.346 |
LIG_TRAF2_2 | 897 | 902 | PF00917 | 0.289 |
LIG_TRFH_1 | 246 | 250 | PF08558 | 0.180 |
LIG_TRFH_1 | 87 | 91 | PF08558 | 0.199 |
LIG_TYR_ITIM | 1083 | 1088 | PF00017 | 0.434 |
LIG_TYR_ITIM | 636 | 641 | PF00017 | 0.406 |
LIG_UBA3_1 | 208 | 214 | PF00899 | 0.524 |
LIG_UBA3_1 | 785 | 792 | PF00899 | 0.184 |
LIG_WRC_WIRS_1 | 243 | 248 | PF05994 | 0.241 |
LIG_WRC_WIRS_1 | 732 | 737 | PF05994 | 0.285 |
LIG_WRC_WIRS_1 | 760 | 765 | PF05994 | 0.539 |
LIG_WW_3 | 1234 | 1238 | PF00397 | 0.583 |
MOD_CDK_SPxxK_3 | 902 | 909 | PF00069 | 0.446 |
MOD_CK1_1 | 1008 | 1014 | PF00069 | 0.448 |
MOD_CK1_1 | 1192 | 1198 | PF00069 | 0.415 |
MOD_CK1_1 | 1270 | 1276 | PF00069 | 0.359 |
MOD_CK1_1 | 1296 | 1302 | PF00069 | 0.553 |
MOD_CK1_1 | 1307 | 1313 | PF00069 | 0.629 |
MOD_CK1_1 | 1349 | 1355 | PF00069 | 0.614 |
MOD_CK1_1 | 241 | 247 | PF00069 | 0.379 |
MOD_CK1_1 | 341 | 347 | PF00069 | 0.555 |
MOD_CK1_1 | 397 | 403 | PF00069 | 0.573 |
MOD_CK1_1 | 58 | 64 | PF00069 | 0.317 |
MOD_CK1_1 | 639 | 645 | PF00069 | 0.320 |
MOD_CK1_1 | 691 | 697 | PF00069 | 0.500 |
MOD_CK1_1 | 770 | 776 | PF00069 | 0.460 |
MOD_CK1_1 | 887 | 893 | PF00069 | 0.617 |
MOD_CK2_1 | 1056 | 1062 | PF00069 | 0.470 |
MOD_CK2_1 | 1122 | 1128 | PF00069 | 0.317 |
MOD_CK2_1 | 1164 | 1170 | PF00069 | 0.603 |
MOD_CK2_1 | 1340 | 1346 | PF00069 | 0.677 |
MOD_CK2_1 | 1398 | 1404 | PF00069 | 0.441 |
MOD_CK2_1 | 346 | 352 | PF00069 | 0.446 |
MOD_CK2_1 | 428 | 434 | PF00069 | 0.380 |
MOD_CK2_1 | 646 | 652 | PF00069 | 0.358 |
MOD_CK2_1 | 695 | 701 | PF00069 | 0.303 |
MOD_CK2_1 | 772 | 778 | PF00069 | 0.278 |
MOD_CK2_1 | 822 | 828 | PF00069 | 0.480 |
MOD_CK2_1 | 852 | 858 | PF00069 | 0.373 |
MOD_CK2_1 | 953 | 959 | PF00069 | 0.308 |
MOD_Cter_Amidation | 1158 | 1161 | PF01082 | 0.462 |
MOD_Cter_Amidation | 1394 | 1397 | PF01082 | 0.332 |
MOD_GlcNHglycan | 1007 | 1010 | PF01048 | 0.394 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.414 |
MOD_GlcNHglycan | 110 | 113 | PF01048 | 0.446 |
MOD_GlcNHglycan | 1183 | 1186 | PF01048 | 0.514 |
MOD_GlcNHglycan | 1275 | 1278 | PF01048 | 0.474 |
MOD_GlcNHglycan | 1284 | 1287 | PF01048 | 0.311 |
MOD_GlcNHglycan | 1306 | 1309 | PF01048 | 0.631 |
MOD_GlcNHglycan | 1314 | 1317 | PF01048 | 0.626 |
MOD_GlcNHglycan | 1318 | 1321 | PF01048 | 0.566 |
MOD_GlcNHglycan | 1377 | 1380 | PF01048 | 0.452 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.465 |
MOD_GlcNHglycan | 305 | 308 | PF01048 | 0.449 |
MOD_GlcNHglycan | 341 | 344 | PF01048 | 0.567 |
MOD_GlcNHglycan | 37 | 40 | PF01048 | 0.422 |
MOD_GlcNHglycan | 399 | 402 | PF01048 | 0.586 |
MOD_GlcNHglycan | 423 | 426 | PF01048 | 0.454 |
MOD_GlcNHglycan | 511 | 514 | PF01048 | 0.337 |
MOD_GlcNHglycan | 559 | 563 | PF01048 | 0.415 |
MOD_GlcNHglycan | 600 | 604 | PF01048 | 0.406 |
MOD_GlcNHglycan | 662 | 665 | PF01048 | 0.399 |
MOD_GlcNHglycan | 668 | 672 | PF01048 | 0.449 |
MOD_GlcNHglycan | 69 | 73 | PF01048 | 0.503 |
MOD_GlcNHglycan | 691 | 694 | PF01048 | 0.429 |
MOD_GlcNHglycan | 828 | 831 | PF01048 | 0.529 |
MOD_GlcNHglycan | 854 | 857 | PF01048 | 0.370 |
MOD_GSK3_1 | 1052 | 1059 | PF00069 | 0.457 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.354 |
MOD_GSK3_1 | 1174 | 1181 | PF00069 | 0.468 |
MOD_GSK3_1 | 1188 | 1195 | PF00069 | 0.503 |
MOD_GSK3_1 | 1235 | 1242 | PF00069 | 0.558 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.400 |
MOD_GSK3_1 | 1312 | 1319 | PF00069 | 0.653 |
MOD_GSK3_1 | 1335 | 1342 | PF00069 | 0.640 |
MOD_GSK3_1 | 1360 | 1367 | PF00069 | 0.638 |
MOD_GSK3_1 | 1373 | 1380 | PF00069 | 0.623 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.391 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.467 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.325 |
MOD_GSK3_1 | 203 | 210 | PF00069 | 0.503 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.380 |
MOD_GSK3_1 | 252 | 259 | PF00069 | 0.441 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.429 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.555 |
MOD_GSK3_1 | 393 | 400 | PF00069 | 0.576 |
MOD_GSK3_1 | 526 | 533 | PF00069 | 0.368 |
MOD_GSK3_1 | 564 | 571 | PF00069 | 0.363 |
MOD_GSK3_1 | 595 | 602 | PF00069 | 0.307 |
MOD_GSK3_1 | 636 | 643 | PF00069 | 0.339 |
MOD_GSK3_1 | 688 | 695 | PF00069 | 0.490 |
MOD_GSK3_1 | 696 | 703 | PF00069 | 0.415 |
MOD_GSK3_1 | 741 | 748 | PF00069 | 0.493 |
MOD_GSK3_1 | 772 | 779 | PF00069 | 0.331 |
MOD_GSK3_1 | 822 | 829 | PF00069 | 0.470 |
MOD_GSK3_1 | 844 | 851 | PF00069 | 0.451 |
MOD_GSK3_1 | 883 | 890 | PF00069 | 0.490 |
MOD_GSK3_1 | 949 | 956 | PF00069 | 0.324 |
MOD_GSK3_1 | 994 | 1001 | PF00069 | 0.308 |
MOD_N-GLC_1 | 1270 | 1275 | PF02516 | 0.458 |
MOD_N-GLC_1 | 530 | 535 | PF02516 | 0.454 |
MOD_N-GLC_1 | 568 | 573 | PF02516 | 0.390 |
MOD_N-GLC_1 | 584 | 589 | PF02516 | 0.413 |
MOD_N-GLC_1 | 83 | 88 | PF02516 | 0.333 |
MOD_N-GLC_1 | 848 | 853 | PF02516 | 0.391 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.327 |
MOD_NEK2_1 | 108 | 113 | PF00069 | 0.331 |
MOD_NEK2_1 | 1189 | 1194 | PF00069 | 0.439 |
MOD_NEK2_1 | 1321 | 1326 | PF00069 | 0.649 |
MOD_NEK2_1 | 1335 | 1340 | PF00069 | 0.670 |
MOD_NEK2_1 | 160 | 165 | PF00069 | 0.468 |
MOD_NEK2_1 | 181 | 186 | PF00069 | 0.423 |
MOD_NEK2_1 | 224 | 229 | PF00069 | 0.432 |
MOD_NEK2_1 | 238 | 243 | PF00069 | 0.382 |
MOD_NEK2_1 | 273 | 278 | PF00069 | 0.348 |
MOD_NEK2_1 | 35 | 40 | PF00069 | 0.453 |
MOD_NEK2_1 | 367 | 372 | PF00069 | 0.503 |
MOD_NEK2_1 | 558 | 563 | PF00069 | 0.378 |
MOD_NEK2_1 | 568 | 573 | PF00069 | 0.362 |
MOD_NEK2_1 | 722 | 727 | PF00069 | 0.415 |
MOD_NEK2_1 | 745 | 750 | PF00069 | 0.388 |
MOD_NEK2_1 | 761 | 766 | PF00069 | 0.283 |
MOD_NEK2_1 | 826 | 831 | PF00069 | 0.395 |
MOD_NEK2_1 | 83 | 88 | PF00069 | 0.288 |
MOD_NEK2_2 | 308 | 313 | PF00069 | 0.248 |
MOD_PIKK_1 | 1259 | 1265 | PF00454 | 0.600 |
MOD_PIKK_1 | 568 | 574 | PF00454 | 0.403 |
MOD_PK_1 | 1377 | 1383 | PF00069 | 0.359 |
MOD_PKA_1 | 11 | 17 | PF00069 | 0.346 |
MOD_PKA_1 | 1328 | 1334 | PF00069 | 0.607 |
MOD_PKA_1 | 1344 | 1350 | PF00069 | 0.646 |
MOD_PKA_1 | 1368 | 1374 | PF00069 | 0.429 |
MOD_PKA_1 | 1398 | 1404 | PF00069 | 0.409 |
MOD_PKA_2 | 1056 | 1062 | PF00069 | 0.479 |
MOD_PKA_2 | 11 | 17 | PF00069 | 0.418 |
MOD_PKA_2 | 1304 | 1310 | PF00069 | 0.638 |
MOD_PKA_2 | 1321 | 1327 | PF00069 | 0.548 |
MOD_PKA_2 | 1328 | 1334 | PF00069 | 0.624 |
MOD_PKA_2 | 1368 | 1374 | PF00069 | 0.668 |
MOD_PKA_2 | 1398 | 1404 | PF00069 | 0.416 |
MOD_PKA_2 | 218 | 224 | PF00069 | 0.500 |
MOD_PKA_2 | 302 | 308 | PF00069 | 0.444 |
MOD_PKA_2 | 35 | 41 | PF00069 | 0.427 |
MOD_PKA_2 | 440 | 446 | PF00069 | 0.326 |
MOD_PKA_2 | 486 | 492 | PF00069 | 0.212 |
MOD_PKA_2 | 844 | 850 | PF00069 | 0.495 |
MOD_PKB_1 | 1237 | 1245 | PF00069 | 0.485 |
MOD_PKB_1 | 1265 | 1273 | PF00069 | 0.405 |
MOD_PKB_1 | 1396 | 1404 | PF00069 | 0.358 |
MOD_PKB_1 | 391 | 399 | PF00069 | 0.315 |
MOD_Plk_1 | 203 | 209 | PF00069 | 0.230 |
MOD_Plk_1 | 373 | 379 | PF00069 | 0.363 |
MOD_Plk_1 | 428 | 434 | PF00069 | 0.401 |
MOD_Plk_1 | 558 | 564 | PF00069 | 0.445 |
MOD_Plk_1 | 584 | 590 | PF00069 | 0.404 |
MOD_Plk_1 | 639 | 645 | PF00069 | 0.460 |
MOD_Plk_1 | 667 | 673 | PF00069 | 0.381 |
MOD_Plk_1 | 83 | 89 | PF00069 | 0.352 |
MOD_Plk_2-3 | 741 | 747 | PF00069 | 0.201 |
MOD_Plk_2-3 | 994 | 1000 | PF00069 | 0.306 |
MOD_Plk_4 | 1293 | 1299 | PF00069 | 0.570 |
MOD_Plk_4 | 1398 | 1404 | PF00069 | 0.409 |
MOD_Plk_4 | 145 | 151 | PF00069 | 0.437 |
MOD_Plk_4 | 160 | 166 | PF00069 | 0.398 |
MOD_Plk_4 | 2 | 8 | PF00069 | 0.357 |
MOD_Plk_4 | 203 | 209 | PF00069 | 0.420 |
MOD_Plk_4 | 238 | 244 | PF00069 | 0.418 |
MOD_Plk_4 | 373 | 379 | PF00069 | 0.468 |
MOD_Plk_4 | 486 | 492 | PF00069 | 0.399 |
MOD_Plk_4 | 700 | 706 | PF00069 | 0.237 |
MOD_Plk_4 | 796 | 802 | PF00069 | 0.338 |
MOD_Plk_4 | 803 | 809 | PF00069 | 0.310 |
MOD_Plk_4 | 949 | 955 | PF00069 | 0.306 |
MOD_Plk_4 | 998 | 1004 | PF00069 | 0.308 |
MOD_ProDKin_1 | 330 | 336 | PF00069 | 0.470 |
MOD_ProDKin_1 | 467 | 473 | PF00069 | 0.435 |
MOD_ProDKin_1 | 605 | 611 | PF00069 | 0.358 |
MOD_ProDKin_1 | 770 | 776 | PF00069 | 0.508 |
MOD_ProDKin_1 | 794 | 800 | PF00069 | 0.373 |
MOD_ProDKin_1 | 884 | 890 | PF00069 | 0.479 |
MOD_ProDKin_1 | 902 | 908 | PF00069 | 0.456 |
MOD_SUMO_rev_2 | 233 | 239 | PF00179 | 0.334 |
MOD_SUMO_rev_2 | 376 | 385 | PF00179 | 0.541 |
MOD_SUMO_rev_2 | 434 | 443 | PF00179 | 0.410 |
MOD_SUMO_rev_2 | 90 | 100 | PF00179 | 0.264 |
TRG_DiLeu_BaEn_1 | 652 | 657 | PF01217 | 0.467 |
TRG_DiLeu_BaEn_1 | 756 | 761 | PF01217 | 0.199 |
TRG_DiLeu_BaEn_1 | 949 | 954 | PF01217 | 0.435 |
TRG_DiLeu_BaEn_2 | 620 | 626 | PF01217 | 0.374 |
TRG_DiLeu_BaEn_4 | 1061 | 1067 | PF01217 | 0.342 |
TRG_DiLeu_BaLyEn_6 | 1287 | 1292 | PF01217 | 0.506 |
TRG_DiLeu_BaLyEn_6 | 591 | 596 | PF01217 | 0.486 |
TRG_DiLeu_BaLyEn_6 | 925 | 930 | PF01217 | 0.160 |
TRG_DiLeu_LyEn_5 | 1222 | 1227 | PF01217 | 0.483 |
TRG_DiLeu_LyEn_5 | 756 | 761 | PF01217 | 0.199 |
TRG_DiLeu_LyEn_5 | 778 | 783 | PF01217 | 0.199 |
TRG_ENDOCYTIC_2 | 1037 | 1040 | PF00928 | 0.314 |
TRG_ENDOCYTIC_2 | 1063 | 1066 | PF00928 | 0.294 |
TRG_ENDOCYTIC_2 | 1085 | 1088 | PF00928 | 0.432 |
TRG_ENDOCYTIC_2 | 146 | 149 | PF00928 | 0.472 |
TRG_ENDOCYTIC_2 | 236 | 239 | PF00928 | 0.446 |
TRG_ENDOCYTIC_2 | 323 | 326 | PF00928 | 0.443 |
TRG_ENDOCYTIC_2 | 623 | 626 | PF00928 | 0.509 |
TRG_ENDOCYTIC_2 | 638 | 641 | PF00928 | 0.447 |
TRG_ENDOCYTIC_2 | 742 | 745 | PF00928 | 0.370 |
TRG_ENDOCYTIC_2 | 780 | 783 | PF00928 | 0.479 |
TRG_ER_diArg_1 | 1070 | 1073 | PF00400 | 0.308 |
TRG_ER_diArg_1 | 1236 | 1239 | PF00400 | 0.559 |
TRG_ER_diArg_1 | 1265 | 1268 | PF00400 | 0.577 |
TRG_ER_diArg_1 | 1327 | 1329 | PF00400 | 0.511 |
TRG_ER_diArg_1 | 1368 | 1370 | PF00400 | 0.415 |
TRG_ER_diArg_1 | 1396 | 1399 | PF00400 | 0.392 |
TRG_ER_diArg_1 | 216 | 219 | PF00400 | 0.437 |
TRG_ER_diArg_1 | 390 | 393 | PF00400 | 0.347 |
TRG_ER_diArg_1 | 895 | 898 | PF00400 | 0.563 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P457 | Leptomonas seymouri | 27% | 100% |
A0A1X0P171 | Trypanosomatidae | 33% | 100% |
A0A3Q8IJB0 | Leishmania donovani | 66% | 100% |
A0A3R7R8G4 | Trypanosoma rangeli | 30% | 100% |
A0A3S5H6Z8 | Leishmania donovani | 66% | 100% |
A0A3S7WU94 | Leishmania donovani | 55% | 100% |
A0A3S7WU95 | Leishmania donovani | 64% | 100% |
A0A3S7XB85 | Leishmania donovani | 28% | 100% |
A4H8U6 | Leishmania braziliensis | 55% | 100% |
A4H8V5 | Leishmania braziliensis | 68% | 100% |
A4H8V7 | Leishmania braziliensis | 60% | 100% |
A4H8V8 | Leishmania braziliensis | 59% | 100% |
A4HPI4 | Leishmania braziliensis | 27% | 100% |
A4HX84 | Leishmania infantum | 55% | 100% |
A4HX85 | Leishmania infantum | 66% | 100% |
A4HX87 | Leishmania infantum | 98% | 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) | 33% | 100% |
C9ZM81 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
C9ZM82 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZM83 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 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) | 35% | 100% |
C9ZN43 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
C9ZN44 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
C9ZN45 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
C9ZN46 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
C9ZNA5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
C9ZNA6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
C9ZNH3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZNT1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZPZ6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZQ51 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
C9ZQ89 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
C9ZQ90 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZQ92 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
C9ZTS4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
C9ZTS5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
C9ZTS6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
C9ZUE6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZWQ5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
C9ZWU1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 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) | 33% | 100% |
C9ZZQ4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
D0A0U3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
D0A0W7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
D0A0X5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
D0A1S1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
D0A5D2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
D0A5D5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
D0A5U0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
D0A5U1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
D0A7A0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
D0A9R3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
D0AAV3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
E9AQY0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
E9AQY1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 59% | 100% |
E9AQY2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 64% | 100% |
E9AQY4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 63% | 100% |
E9ARD7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 56% | 100% |
E9AT96 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
Q25263 | Leishmania donovani | 64% | 100% |
Q26721 | Trypanosoma brucei brucei | 34% | 100% |
Q27675 | Leishmania donovani | 55% | 100% |
Q4Q1A1 | Leishmania major | 28% | 100% |
Q4QEH9 | Leishmania major | 64% | 100% |
Q4QEI0 | Leishmania major | 64% | 100% |
Q4QEI1 | Leishmania major | 64% | 100% |
Q4QEI2 | Leishmania major | 86% | 100% |
Q4QEI3 | Leishmania major | 56% | 100% |
Q99279 | Trypanosoma brucei brucei | 30% | 100% |
Q99280 | Trypanosoma brucei brucei | 32% | 100% |
V5AYH7 | Trypanosoma cruzi | 34% | 100% |