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: 60 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 5 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | yes | yes: 47, no: 28 |
NetGPI | no | yes: 0, no: 75 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 70 |
GO:0110165 | cellular anatomical entity | 1 | 76 |
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 75 |
GO:0006163 | purine nucleotide metabolic process | 5 | 75 |
GO:0006164 | purine nucleotide biosynthetic process | 6 | 75 |
GO:0006171 | cAMP biosynthetic process | 8 | 75 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 75 |
GO:0006753 | nucleoside phosphate metabolic process | 4 | 75 |
GO:0006793 | phosphorus metabolic process | 3 | 75 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 75 |
GO:0006807 | nitrogen compound metabolic process | 2 | 75 |
GO:0007165 | signal transduction | 2 | 75 |
GO:0008152 | metabolic process | 1 | 75 |
GO:0009058 | biosynthetic process | 2 | 75 |
GO:0009117 | nucleotide metabolic process | 5 | 75 |
GO:0009150 | purine ribonucleotide metabolic process | 6 | 75 |
GO:0009152 | purine ribonucleotide biosynthetic process | 7 | 75 |
GO:0009165 | nucleotide biosynthetic process | 6 | 75 |
GO:0009187 | cyclic nucleotide metabolic process | 6 | 75 |
GO:0009190 | cyclic nucleotide biosynthetic process | 7 | 75 |
GO:0009259 | ribonucleotide metabolic process | 5 | 75 |
GO:0009260 | ribonucleotide biosynthetic process | 6 | 75 |
GO:0009987 | cellular process | 1 | 75 |
GO:0018130 | heterocycle biosynthetic process | 4 | 75 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 75 |
GO:0019637 | organophosphate metabolic process | 3 | 75 |
GO:0019693 | ribose phosphate metabolic process | 4 | 75 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 75 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 75 |
GO:0035556 | intracellular signal transduction | 3 | 75 |
GO:0044237 | cellular metabolic process | 2 | 75 |
GO:0044238 | primary metabolic process | 2 | 75 |
GO:0044249 | cellular biosynthetic process | 3 | 75 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 75 |
GO:0044281 | small molecule metabolic process | 2 | 75 |
GO:0046058 | cAMP metabolic process | 7 | 75 |
GO:0046390 | ribose phosphate biosynthetic process | 5 | 75 |
GO:0046483 | heterocycle metabolic process | 3 | 75 |
GO:0050789 | regulation of biological process | 2 | 75 |
GO:0050794 | regulation of cellular process | 3 | 75 |
GO:0052652 | cyclic purine nucleotide metabolic process | 6 | 75 |
GO:0055086 | nucleobase-containing small molecule metabolic process | 3 | 75 |
GO:0065007 | biological regulation | 1 | 75 |
GO:0071704 | organic substance metabolic process | 2 | 75 |
GO:0072521 | purine-containing compound metabolic process | 4 | 75 |
GO:0072522 | purine-containing compound biosynthetic process | 5 | 75 |
GO:0090407 | organophosphate biosynthetic process | 4 | 75 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 75 |
GO:1901137 | carbohydrate derivative biosynthetic process | 4 | 75 |
GO:1901293 | nucleoside phosphate biosynthetic process | 5 | 75 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 75 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 75 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 75 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 75 |
GO:1901576 | organic substance biosynthetic process | 3 | 75 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 64 |
GO:0016829 | lyase activity | 2 | 64 |
GO:0004016 | adenylate cyclase activity | 3 | 1 |
GO:0009975 | cyclase activity | 2 | 1 |
GO:0016849 | phosphorus-oxygen lyase activity | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 383 | 387 | PF00656 | 0.412 |
CLV_C14_Caspase3-7 | 635 | 639 | PF00656 | 0.352 |
CLV_C14_Caspase3-7 | 983 | 987 | PF00656 | 0.450 |
CLV_MEL_PAP_1 | 1056 | 1062 | PF00089 | 0.238 |
CLV_NRD_NRD_1 | 1146 | 1148 | PF00675 | 0.344 |
CLV_NRD_NRD_1 | 1310 | 1312 | PF00675 | 0.547 |
CLV_NRD_NRD_1 | 207 | 209 | PF00675 | 0.560 |
CLV_NRD_NRD_1 | 660 | 662 | PF00675 | 0.454 |
CLV_NRD_NRD_1 | 801 | 803 | PF00675 | 0.563 |
CLV_NRD_NRD_1 | 886 | 888 | PF00675 | 0.518 |
CLV_NRD_NRD_1 | 9 | 11 | PF00675 | 0.591 |
CLV_PCSK_FUR_1 | 1308 | 1312 | PF00082 | 0.343 |
CLV_PCSK_FUR_1 | 205 | 209 | PF00082 | 0.558 |
CLV_PCSK_FUR_1 | 884 | 888 | PF00082 | 0.492 |
CLV_PCSK_KEX2_1 | 1146 | 1148 | PF00082 | 0.344 |
CLV_PCSK_KEX2_1 | 1310 | 1312 | PF00082 | 0.544 |
CLV_PCSK_KEX2_1 | 207 | 209 | PF00082 | 0.561 |
CLV_PCSK_KEX2_1 | 801 | 803 | PF00082 | 0.577 |
CLV_PCSK_KEX2_1 | 886 | 888 | PF00082 | 0.488 |
CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.592 |
CLV_PCSK_PC7_1 | 882 | 888 | PF00082 | 0.493 |
CLV_PCSK_SKI1_1 | 1008 | 1012 | PF00082 | 0.239 |
CLV_PCSK_SKI1_1 | 107 | 111 | PF00082 | 0.649 |
CLV_PCSK_SKI1_1 | 1243 | 1247 | PF00082 | 0.384 |
CLV_PCSK_SKI1_1 | 129 | 133 | PF00082 | 0.499 |
CLV_PCSK_SKI1_1 | 208 | 212 | PF00082 | 0.558 |
CLV_PCSK_SKI1_1 | 283 | 287 | PF00082 | 0.497 |
CLV_PCSK_SKI1_1 | 632 | 636 | PF00082 | 0.458 |
CLV_PCSK_SKI1_1 | 746 | 750 | PF00082 | 0.490 |
CLV_PCSK_SKI1_1 | 768 | 772 | PF00082 | 0.611 |
CLV_PCSK_SKI1_1 | 83 | 87 | PF00082 | 0.579 |
CLV_PCSK_SKI1_1 | 887 | 891 | PF00082 | 0.549 |
CLV_Separin_Metazoa | 605 | 609 | PF03568 | 0.240 |
DEG_APCC_DBOX_1 | 599 | 607 | PF00400 | 0.195 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.520 |
DEG_SCF_FBW7_2 | 874 | 880 | PF00400 | 0.496 |
DEG_SPOP_SBC_1 | 289 | 293 | PF00917 | 0.402 |
DEG_SPOP_SBC_1 | 807 | 811 | PF00917 | 0.446 |
DOC_CDC14_PxL_1 | 131 | 139 | PF14671 | 0.389 |
DOC_CKS1_1 | 782 | 787 | PF01111 | 0.343 |
DOC_CKS1_1 | 874 | 879 | PF01111 | 0.426 |
DOC_CYCLIN_RxL_1 | 507 | 516 | PF00134 | 0.237 |
DOC_CYCLIN_RxL_1 | 83 | 94 | PF00134 | 0.213 |
DOC_CYCLIN_yCln2_LP_2 | 236 | 242 | PF00134 | 0.305 |
DOC_CYCLIN_yCln2_LP_2 | 335 | 341 | PF00134 | 0.246 |
DOC_CYCLIN_yCln2_LP_2 | 871 | 877 | PF00134 | 0.423 |
DOC_MAPK_gen_1 | 205 | 214 | PF00069 | 0.261 |
DOC_MAPK_gen_1 | 30 | 40 | PF00069 | 0.423 |
DOC_MAPK_gen_1 | 83 | 92 | PF00069 | 0.378 |
DOC_MAPK_MEF2A_6 | 186 | 193 | PF00069 | 0.303 |
DOC_MAPK_MEF2A_6 | 33 | 42 | PF00069 | 0.298 |
DOC_MAPK_MEF2A_6 | 510 | 519 | PF00069 | 0.391 |
DOC_MAPK_MEF2A_6 | 714 | 722 | PF00069 | 0.235 |
DOC_MAPK_MEF2A_6 | 83 | 92 | PF00069 | 0.373 |
DOC_MAPK_RevD_3 | 1133 | 1147 | PF00069 | 0.478 |
DOC_PP1_RVXF_1 | 508 | 515 | PF00149 | 0.237 |
DOC_PP1_RVXF_1 | 744 | 751 | PF00149 | 0.268 |
DOC_PP2B_LxvP_1 | 236 | 239 | PF13499 | 0.264 |
DOC_PP4_FxxP_1 | 165 | 168 | PF00568 | 0.263 |
DOC_PP4_FxxP_1 | 825 | 828 | PF00568 | 0.188 |
DOC_SPAK_OSR1_1 | 843 | 847 | PF12202 | 0.206 |
DOC_USP7_MATH_1 | 1245 | 1249 | PF00917 | 0.609 |
DOC_USP7_MATH_1 | 1290 | 1294 | PF00917 | 0.670 |
DOC_USP7_MATH_1 | 289 | 293 | PF00917 | 0.407 |
DOC_USP7_MATH_1 | 382 | 386 | PF00917 | 0.286 |
DOC_USP7_MATH_1 | 60 | 64 | PF00917 | 0.280 |
DOC_USP7_MATH_1 | 676 | 680 | PF00917 | 0.408 |
DOC_USP7_MATH_1 | 735 | 739 | PF00917 | 0.378 |
DOC_USP7_MATH_1 | 778 | 782 | PF00917 | 0.374 |
DOC_USP7_MATH_1 | 991 | 995 | PF00917 | 0.519 |
DOC_WW_Pin1_4 | 152 | 157 | PF00397 | 0.368 |
DOC_WW_Pin1_4 | 317 | 322 | PF00397 | 0.351 |
DOC_WW_Pin1_4 | 545 | 550 | PF00397 | 0.362 |
DOC_WW_Pin1_4 | 558 | 563 | PF00397 | 0.398 |
DOC_WW_Pin1_4 | 592 | 597 | PF00397 | 0.342 |
DOC_WW_Pin1_4 | 781 | 786 | PF00397 | 0.332 |
DOC_WW_Pin1_4 | 836 | 841 | PF00397 | 0.253 |
DOC_WW_Pin1_4 | 870 | 875 | PF00397 | 0.381 |
DOC_WW_Pin1_4 | 888 | 893 | PF00397 | 0.358 |
LIG_14-3-3_CanoR_1 | 1043 | 1049 | PF00244 | 0.583 |
LIG_14-3-3_CanoR_1 | 1225 | 1232 | PF00244 | 0.599 |
LIG_14-3-3_CanoR_1 | 1243 | 1248 | PF00244 | 0.567 |
LIG_14-3-3_CanoR_1 | 1314 | 1322 | PF00244 | 0.687 |
LIG_14-3-3_CanoR_1 | 205 | 214 | PF00244 | 0.303 |
LIG_14-3-3_CanoR_1 | 290 | 297 | PF00244 | 0.359 |
LIG_14-3-3_CanoR_1 | 483 | 489 | PF00244 | 0.370 |
LIG_14-3-3_CanoR_1 | 632 | 637 | PF00244 | 0.366 |
LIG_14-3-3_CanoR_1 | 661 | 669 | PF00244 | 0.326 |
LIG_14-3-3_CanoR_1 | 746 | 751 | PF00244 | 0.403 |
LIG_14-3-3_CanoR_1 | 993 | 1001 | PF00244 | 0.561 |
LIG_APCC_ABBA_1 | 141 | 146 | PF00400 | 0.399 |
LIG_APCC_ABBA_1 | 307 | 312 | PF00400 | 0.239 |
LIG_APCC_ABBA_1 | 719 | 724 | PF00400 | 0.254 |
LIG_APCC_ABBA_1 | 770 | 775 | PF00400 | 0.225 |
LIG_BIR_III_2 | 775 | 779 | PF00653 | 0.222 |
LIG_BIR_III_2 | 927 | 931 | PF00653 | 0.588 |
LIG_BRCT_BRCA1_1 | 510 | 514 | PF00533 | 0.235 |
LIG_eIF4E_1 | 29 | 35 | PF01652 | 0.401 |
LIG_FHA_1 | 1005 | 1011 | PF00498 | 0.513 |
LIG_FHA_1 | 1014 | 1020 | PF00498 | 0.447 |
LIG_FHA_1 | 1039 | 1045 | PF00498 | 0.456 |
LIG_FHA_1 | 1089 | 1095 | PF00498 | 0.452 |
LIG_FHA_1 | 1268 | 1274 | PF00498 | 0.577 |
LIG_FHA_1 | 304 | 310 | PF00498 | 0.352 |
LIG_FHA_1 | 355 | 361 | PF00498 | 0.382 |
LIG_FHA_1 | 44 | 50 | PF00498 | 0.430 |
LIG_FHA_1 | 552 | 558 | PF00498 | 0.370 |
LIG_FHA_1 | 572 | 578 | PF00498 | 0.328 |
LIG_FHA_1 | 655 | 661 | PF00498 | 0.307 |
LIG_FHA_1 | 678 | 684 | PF00498 | 0.361 |
LIG_FHA_1 | 713 | 719 | PF00498 | 0.376 |
LIG_FHA_1 | 811 | 817 | PF00498 | 0.369 |
LIG_FHA_1 | 904 | 910 | PF00498 | 0.357 |
LIG_FHA_2 | 1031 | 1037 | PF00498 | 0.547 |
LIG_FHA_2 | 1151 | 1157 | PF00498 | 0.681 |
LIG_FHA_2 | 1161 | 1167 | PF00498 | 0.687 |
LIG_FHA_2 | 253 | 259 | PF00498 | 0.381 |
LIG_FHA_2 | 318 | 324 | PF00498 | 0.390 |
LIG_FHA_2 | 416 | 422 | PF00498 | 0.380 |
LIG_FHA_2 | 633 | 639 | PF00498 | 0.382 |
LIG_FHA_2 | 697 | 703 | PF00498 | 0.280 |
LIG_FHA_2 | 822 | 828 | PF00498 | 0.222 |
LIG_FHA_2 | 837 | 843 | PF00498 | 0.367 |
LIG_FHA_2 | 940 | 946 | PF00498 | 0.445 |
LIG_FHA_2 | 981 | 987 | PF00498 | 0.453 |
LIG_GBD_Chelix_1 | 1001 | 1009 | PF00786 | 0.328 |
LIG_GBD_Chelix_1 | 406 | 414 | PF00786 | 0.444 |
LIG_HCF-1_HBM_1 | 1020 | 1023 | PF13415 | 0.345 |
LIG_LIR_Apic_2 | 1035 | 1040 | PF02991 | 0.443 |
LIG_LIR_Apic_2 | 451 | 455 | PF02991 | 0.298 |
LIG_LIR_Apic_2 | 589 | 594 | PF02991 | 0.330 |
LIG_LIR_Apic_2 | 824 | 828 | PF02991 | 0.282 |
LIG_LIR_Gen_1 | 1020 | 1031 | PF02991 | 0.424 |
LIG_LIR_Gen_1 | 1046 | 1056 | PF02991 | 0.510 |
LIG_LIR_Gen_1 | 1068 | 1078 | PF02991 | 0.550 |
LIG_LIR_Gen_1 | 209 | 219 | PF02991 | 0.397 |
LIG_LIR_Gen_1 | 255 | 265 | PF02991 | 0.297 |
LIG_LIR_Gen_1 | 511 | 520 | PF02991 | 0.263 |
LIG_LIR_Gen_1 | 749 | 755 | PF02991 | 0.299 |
LIG_LIR_Gen_1 | 938 | 949 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 1020 | 1026 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 1046 | 1052 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 1068 | 1074 | PF02991 | 0.545 |
LIG_LIR_Nem_3 | 1075 | 1081 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 1104 | 1110 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 1195 | 1200 | PF02991 | 0.581 |
LIG_LIR_Nem_3 | 133 | 137 | PF02991 | 0.322 |
LIG_LIR_Nem_3 | 209 | 214 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 217 | 222 | PF02991 | 0.323 |
LIG_LIR_Nem_3 | 306 | 310 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 429 | 434 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 511 | 517 | PF02991 | 0.276 |
LIG_LIR_Nem_3 | 749 | 753 | PF02991 | 0.292 |
LIG_LIR_Nem_3 | 827 | 832 | PF02991 | 0.215 |
LIG_LIR_Nem_3 | 841 | 847 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 938 | 944 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 948 | 954 | PF02991 | 0.556 |
LIG_LYPXL_yS_3 | 134 | 137 | PF13949 | 0.239 |
LIG_LYPXL_yS_3 | 729 | 732 | PF13949 | 0.379 |
LIG_MYND_3 | 614 | 618 | PF01753 | 0.287 |
LIG_NRBOX | 602 | 608 | PF00104 | 0.191 |
LIG_PCNA_yPIPBox_3 | 895 | 903 | PF02747 | 0.202 |
LIG_Pex14_2 | 165 | 169 | PF04695 | 0.407 |
LIG_Pex14_2 | 825 | 829 | PF04695 | 0.393 |
LIG_PTB_Apo_2 | 389 | 396 | PF02174 | 0.255 |
LIG_PTB_Apo_2 | 606 | 613 | PF02174 | 0.238 |
LIG_PTB_Apo_2 | 69 | 76 | PF02174 | 0.313 |
LIG_PTB_Phospho_1 | 606 | 612 | PF10480 | 0.240 |
LIG_PTB_Phospho_1 | 69 | 75 | PF10480 | 0.321 |
LIG_SH2_CRK | 452 | 456 | PF00017 | 0.296 |
LIG_SH2_CRK | 625 | 629 | PF00017 | 0.383 |
LIG_SH2_CRK | 669 | 673 | PF00017 | 0.442 |
LIG_SH2_GRB2like | 390 | 393 | PF00017 | 0.427 |
LIG_SH2_GRB2like | 669 | 672 | PF00017 | 0.436 |
LIG_SH2_GRB2like | 847 | 850 | PF00017 | 0.233 |
LIG_SH2_NCK_1 | 1037 | 1041 | PF00017 | 0.417 |
LIG_SH2_NCK_1 | 1071 | 1075 | PF00017 | 0.541 |
LIG_SH2_NCK_1 | 2 | 6 | PF00017 | 0.206 |
LIG_SH2_NCK_1 | 669 | 673 | PF00017 | 0.268 |
LIG_SH2_PTP2 | 610 | 613 | PF00017 | 0.381 |
LIG_SH2_SRC | 1037 | 1040 | PF00017 | 0.502 |
LIG_SH2_SRC | 1071 | 1074 | PF00017 | 0.541 |
LIG_SH2_SRC | 2 | 5 | PF00017 | 0.208 |
LIG_SH2_SRC | 669 | 672 | PF00017 | 0.417 |
LIG_SH2_STAP1 | 1049 | 1053 | PF00017 | 0.502 |
LIG_SH2_STAP1 | 242 | 246 | PF00017 | 0.383 |
LIG_SH2_STAP1 | 311 | 315 | PF00017 | 0.256 |
LIG_SH2_STAP1 | 573 | 577 | PF00017 | 0.312 |
LIG_SH2_STAT3 | 468 | 471 | PF00017 | 0.385 |
LIG_SH2_STAT3 | 850 | 853 | PF00017 | 0.254 |
LIG_SH2_STAT5 | 101 | 104 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 1023 | 1026 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 1232 | 1235 | PF00017 | 0.569 |
LIG_SH2_STAT5 | 183 | 186 | PF00017 | 0.282 |
LIG_SH2_STAT5 | 213 | 216 | PF00017 | 0.257 |
LIG_SH2_STAT5 | 295 | 298 | PF00017 | 0.275 |
LIG_SH2_STAT5 | 390 | 393 | PF00017 | 0.371 |
LIG_SH2_STAT5 | 441 | 444 | PF00017 | 0.247 |
LIG_SH2_STAT5 | 468 | 471 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 542 | 545 | PF00017 | 0.304 |
LIG_SH2_STAT5 | 573 | 576 | PF00017 | 0.418 |
LIG_SH2_STAT5 | 591 | 594 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 610 | 613 | PF00017 | 0.323 |
LIG_SH2_STAT5 | 69 | 72 | PF00017 | 0.360 |
LIG_SH2_STAT5 | 918 | 921 | PF00017 | 0.493 |
LIG_SH3_3 | 1215 | 1221 | PF00018 | 0.553 |
LIG_SH3_3 | 1270 | 1276 | PF00018 | 0.635 |
LIG_SH3_3 | 137 | 143 | PF00018 | 0.273 |
LIG_SH3_3 | 590 | 596 | PF00018 | 0.366 |
LIG_SH3_3 | 863 | 869 | PF00018 | 0.348 |
LIG_SH3_3 | 871 | 877 | PF00018 | 0.379 |
LIG_SUMO_SIM_anti_2 | 121 | 128 | PF11976 | 0.373 |
LIG_SUMO_SIM_anti_2 | 226 | 233 | PF11976 | 0.235 |
LIG_SUMO_SIM_anti_2 | 715 | 724 | PF11976 | 0.289 |
LIG_SUMO_SIM_anti_2 | 906 | 911 | PF11976 | 0.337 |
LIG_SUMO_SIM_anti_2 | 934 | 943 | PF11976 | 0.449 |
LIG_SUMO_SIM_par_1 | 226 | 233 | PF11976 | 0.234 |
LIG_SUMO_SIM_par_1 | 45 | 51 | PF11976 | 0.368 |
LIG_SUMO_SIM_par_1 | 694 | 699 | PF11976 | 0.339 |
LIG_SUMO_SIM_par_1 | 715 | 724 | PF11976 | 0.358 |
LIG_SUMO_SIM_par_1 | 854 | 859 | PF11976 | 0.269 |
LIG_SUMO_SIM_par_1 | 905 | 911 | PF11976 | 0.383 |
LIG_TRAF2_1 | 1045 | 1048 | PF00917 | 0.578 |
LIG_TYR_ITIM | 1069 | 1074 | PF00017 | 0.426 |
LIG_TYR_ITIM | 623 | 628 | PF00017 | 0.346 |
LIG_TYR_ITIM | 727 | 732 | PF00017 | 0.313 |
LIG_UBA3_1 | 193 | 198 | PF00899 | 0.522 |
LIG_UBA3_1 | 621 | 627 | PF00899 | 0.418 |
LIG_Vh1_VBS_1 | 241 | 259 | PF01044 | 0.248 |
LIG_WRC_WIRS_1 | 219 | 224 | PF05994 | 0.276 |
LIG_WRC_WIRS_1 | 297 | 302 | PF05994 | 0.481 |
LIG_WRC_WIRS_1 | 747 | 752 | PF05994 | 0.536 |
LIG_WRC_WIRS_1 | 822 | 827 | PF05994 | 0.479 |
LIG_WW_3 | 1220 | 1224 | PF00397 | 0.537 |
MOD_CDK_SPxxK_3 | 836 | 843 | PF00069 | 0.254 |
MOD_CDK_SPxxK_3 | 888 | 895 | PF00069 | 0.426 |
MOD_CK1_1 | 1178 | 1184 | PF00069 | 0.400 |
MOD_CK1_1 | 1282 | 1288 | PF00069 | 0.538 |
MOD_CK1_1 | 1293 | 1299 | PF00069 | 0.649 |
MOD_CK1_1 | 245 | 251 | PF00069 | 0.409 |
MOD_CK1_1 | 328 | 334 | PF00069 | 0.559 |
MOD_CK1_1 | 384 | 390 | PF00069 | 0.521 |
MOD_CK1_1 | 492 | 498 | PF00069 | 0.411 |
MOD_CK1_1 | 503 | 509 | PF00069 | 0.373 |
MOD_CK1_1 | 535 | 541 | PF00069 | 0.328 |
MOD_CK1_1 | 679 | 685 | PF00069 | 0.473 |
MOD_CK1_1 | 757 | 763 | PF00069 | 0.473 |
MOD_CK1_1 | 781 | 787 | PF00069 | 0.395 |
MOD_CK1_1 | 806 | 812 | PF00069 | 0.479 |
MOD_CK1_1 | 821 | 827 | PF00069 | 0.326 |
MOD_CK1_1 | 873 | 879 | PF00069 | 0.670 |
MOD_CK1_1 | 994 | 1000 | PF00069 | 0.452 |
MOD_CK2_1 | 1042 | 1048 | PF00069 | 0.478 |
MOD_CK2_1 | 1108 | 1114 | PF00069 | 0.318 |
MOD_CK2_1 | 1150 | 1156 | PF00069 | 0.608 |
MOD_CK2_1 | 151 | 157 | PF00069 | 0.414 |
MOD_CK2_1 | 223 | 229 | PF00069 | 0.474 |
MOD_CK2_1 | 415 | 421 | PF00069 | 0.404 |
MOD_CK2_1 | 60 | 66 | PF00069 | 0.489 |
MOD_CK2_1 | 821 | 827 | PF00069 | 0.310 |
MOD_CK2_1 | 939 | 945 | PF00069 | 0.290 |
MOD_Cter_Amidation | 1144 | 1147 | PF01082 | 0.422 |
MOD_GlcNHglycan | 1169 | 1172 | PF01048 | 0.498 |
MOD_GlcNHglycan | 1292 | 1295 | PF01048 | 0.654 |
MOD_GlcNHglycan | 1300 | 1303 | PF01048 | 0.657 |
MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.507 |
MOD_GlcNHglycan | 19 | 22 | PF01048 | 0.403 |
MOD_GlcNHglycan | 242 | 245 | PF01048 | 0.445 |
MOD_GlcNHglycan | 292 | 295 | PF01048 | 0.441 |
MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.563 |
MOD_GlcNHglycan | 386 | 389 | PF01048 | 0.538 |
MOD_GlcNHglycan | 410 | 413 | PF01048 | 0.436 |
MOD_GlcNHglycan | 474 | 477 | PF01048 | 0.443 |
MOD_GlcNHglycan | 491 | 494 | PF01048 | 0.411 |
MOD_GlcNHglycan | 628 | 631 | PF01048 | 0.387 |
MOD_GlcNHglycan | 638 | 641 | PF01048 | 0.377 |
MOD_GlcNHglycan | 662 | 665 | PF01048 | 0.475 |
MOD_GlcNHglycan | 684 | 687 | PF01048 | 0.399 |
MOD_GlcNHglycan | 761 | 764 | PF01048 | 0.350 |
MOD_GlcNHglycan | 788 | 791 | PF01048 | 0.446 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.384 |
MOD_GlcNHglycan | 993 | 996 | PF01048 | 0.388 |
MOD_GSK3_1 | 1038 | 1045 | PF00069 | 0.459 |
MOD_GSK3_1 | 1160 | 1167 | PF00069 | 0.456 |
MOD_GSK3_1 | 1174 | 1181 | PF00069 | 0.491 |
MOD_GSK3_1 | 1221 | 1228 | PF00069 | 0.549 |
MOD_GSK3_1 | 1314 | 1321 | PF00069 | 0.610 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.411 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.440 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.541 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.460 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.525 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.418 |
MOD_GSK3_1 | 472 | 479 | PF00069 | 0.493 |
MOD_GSK3_1 | 500 | 507 | PF00069 | 0.420 |
MOD_GSK3_1 | 528 | 535 | PF00069 | 0.344 |
MOD_GSK3_1 | 551 | 558 | PF00069 | 0.398 |
MOD_GSK3_1 | 567 | 574 | PF00069 | 0.402 |
MOD_GSK3_1 | 632 | 639 | PF00069 | 0.331 |
MOD_GSK3_1 | 672 | 679 | PF00069 | 0.444 |
MOD_GSK3_1 | 731 | 738 | PF00069 | 0.445 |
MOD_GSK3_1 | 764 | 771 | PF00069 | 0.383 |
MOD_GSK3_1 | 786 | 793 | PF00069 | 0.473 |
MOD_GSK3_1 | 803 | 810 | PF00069 | 0.427 |
MOD_GSK3_1 | 834 | 841 | PF00069 | 0.462 |
MOD_GSK3_1 | 869 | 876 | PF00069 | 0.496 |
MOD_GSK3_1 | 935 | 942 | PF00069 | 0.314 |
MOD_GSK3_1 | 980 | 987 | PF00069 | 0.292 |
MOD_N-GLC_1 | 1314 | 1319 | PF02516 | 0.549 |
MOD_N-GLC_1 | 178 | 183 | PF02516 | 0.180 |
MOD_N-GLC_1 | 252 | 257 | PF02516 | 0.513 |
MOD_N-GLC_1 | 426 | 431 | PF02516 | 0.355 |
MOD_N-GLC_1 | 545 | 550 | PF02516 | 0.358 |
MOD_N-GLC_1 | 555 | 560 | PF02516 | 0.454 |
MOD_N-GLC_1 | 571 | 576 | PF02516 | 0.462 |
MOD_N-GLC_1 | 654 | 659 | PF02516 | 0.413 |
MOD_NEK2_1 | 1175 | 1180 | PF00069 | 0.422 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.397 |
MOD_NEK2_1 | 230 | 235 | PF00069 | 0.439 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.324 |
MOD_NEK2_1 | 354 | 359 | PF00069 | 0.451 |
MOD_NEK2_1 | 47 | 52 | PF00069 | 0.282 |
MOD_NEK2_1 | 532 | 537 | PF00069 | 0.358 |
MOD_NEK2_1 | 636 | 641 | PF00069 | 0.356 |
MOD_NEK2_1 | 660 | 665 | PF00069 | 0.334 |
MOD_NEK2_1 | 696 | 701 | PF00069 | 0.419 |
MOD_NEK2_1 | 792 | 797 | PF00069 | 0.346 |
MOD_NEK2_1 | 803 | 808 | PF00069 | 0.406 |
MOD_NEK2_2 | 178 | 183 | PF00069 | 0.422 |
MOD_PIKK_1 | 1245 | 1251 | PF00454 | 0.552 |
MOD_PIKK_1 | 399 | 405 | PF00454 | 0.413 |
MOD_PIKK_1 | 434 | 440 | PF00454 | 0.447 |
MOD_PIKK_1 | 494 | 500 | PF00454 | 0.423 |
MOD_PIKK_1 | 778 | 784 | PF00454 | 0.490 |
MOD_PK_1 | 739 | 745 | PF00069 | 0.275 |
MOD_PK_1 | 818 | 824 | PF00069 | 0.248 |
MOD_PKA_2 | 1042 | 1048 | PF00069 | 0.482 |
MOD_PKA_2 | 1290 | 1296 | PF00069 | 0.655 |
MOD_PKA_2 | 1318 | 1324 | PF00069 | 0.647 |
MOD_PKA_2 | 206 | 212 | PF00069 | 0.506 |
MOD_PKA_2 | 289 | 295 | PF00069 | 0.439 |
MOD_PKA_2 | 29 | 35 | PF00069 | 0.384 |
MOD_PKA_2 | 660 | 666 | PF00069 | 0.384 |
MOD_PKB_1 | 1223 | 1231 | PF00069 | 0.622 |
MOD_Plk_1 | 178 | 184 | PF00069 | 0.459 |
MOD_Plk_1 | 252 | 258 | PF00069 | 0.437 |
MOD_Plk_1 | 360 | 366 | PF00069 | 0.324 |
MOD_Plk_1 | 426 | 432 | PF00069 | 0.355 |
MOD_Plk_1 | 654 | 660 | PF00069 | 0.366 |
MOD_Plk_1 | 712 | 718 | PF00069 | 0.426 |
MOD_Plk_2-3 | 223 | 229 | PF00069 | 0.492 |
MOD_Plk_2-3 | 980 | 986 | PF00069 | 0.290 |
MOD_Plk_4 | 133 | 139 | PF00069 | 0.431 |
MOD_Plk_4 | 170 | 176 | PF00069 | 0.302 |
MOD_Plk_4 | 178 | 184 | PF00069 | 0.339 |
MOD_Plk_4 | 223 | 229 | PF00069 | 0.439 |
MOD_Plk_4 | 360 | 366 | PF00069 | 0.436 |
MOD_Plk_4 | 410 | 416 | PF00069 | 0.491 |
MOD_Plk_4 | 513 | 519 | PF00069 | 0.368 |
MOD_Plk_4 | 535 | 541 | PF00069 | 0.256 |
MOD_Plk_4 | 632 | 638 | PF00069 | 0.355 |
MOD_Plk_4 | 713 | 719 | PF00069 | 0.424 |
MOD_Plk_4 | 728 | 734 | PF00069 | 0.357 |
MOD_Plk_4 | 768 | 774 | PF00069 | 0.461 |
MOD_Plk_4 | 818 | 824 | PF00069 | 0.300 |
MOD_Plk_4 | 935 | 941 | PF00069 | 0.288 |
MOD_Plk_4 | 984 | 990 | PF00069 | 0.292 |
MOD_ProDKin_1 | 152 | 158 | PF00069 | 0.454 |
MOD_ProDKin_1 | 317 | 323 | PF00069 | 0.440 |
MOD_ProDKin_1 | 545 | 551 | PF00069 | 0.458 |
MOD_ProDKin_1 | 558 | 564 | PF00069 | 0.503 |
MOD_ProDKin_1 | 592 | 598 | PF00069 | 0.420 |
MOD_ProDKin_1 | 781 | 787 | PF00069 | 0.410 |
MOD_ProDKin_1 | 836 | 842 | PF00069 | 0.300 |
MOD_ProDKin_1 | 870 | 876 | PF00069 | 0.482 |
MOD_ProDKin_1 | 888 | 894 | PF00069 | 0.437 |
MOD_SUMO_rev_2 | 217 | 227 | PF00179 | 0.349 |
MOD_SUMO_rev_2 | 363 | 372 | PF00179 | 0.517 |
MOD_SUMO_rev_2 | 708 | 716 | PF00179 | 0.476 |
TRG_DiLeu_BaEn_1 | 223 | 228 | PF01217 | 0.509 |
TRG_DiLeu_BaEn_1 | 66 | 71 | PF01217 | 0.452 |
TRG_DiLeu_BaEn_1 | 935 | 940 | PF01217 | 0.427 |
TRG_DiLeu_BaEn_2 | 179 | 185 | PF01217 | 0.497 |
TRG_DiLeu_BaEn_2 | 617 | 623 | PF01217 | 0.282 |
TRG_DiLeu_BaEn_3 | 712 | 718 | PF01217 | 0.465 |
TRG_DiLeu_BaEn_4 | 1047 | 1053 | PF01217 | 0.308 |
TRG_DiLeu_BaLyEn_6 | 1273 | 1278 | PF01217 | 0.568 |
TRG_DiLeu_BaLyEn_6 | 30 | 35 | PF01217 | 0.444 |
TRG_DiLeu_BaLyEn_6 | 520 | 525 | PF01217 | 0.412 |
TRG_DiLeu_BaLyEn_6 | 911 | 916 | PF01217 | 0.156 |
TRG_DiLeu_LyEn_5 | 1208 | 1213 | PF01217 | 0.450 |
TRG_ENDOCYTIC_2 | 1023 | 1026 | PF00928 | 0.302 |
TRG_ENDOCYTIC_2 | 1049 | 1052 | PF00928 | 0.287 |
TRG_ENDOCYTIC_2 | 1071 | 1074 | PF00928 | 0.426 |
TRG_ENDOCYTIC_2 | 134 | 137 | PF00928 | 0.459 |
TRG_ENDOCYTIC_2 | 219 | 222 | PF00928 | 0.435 |
TRG_ENDOCYTIC_2 | 310 | 313 | PF00928 | 0.443 |
TRG_ENDOCYTIC_2 | 610 | 613 | PF00928 | 0.494 |
TRG_ENDOCYTIC_2 | 625 | 628 | PF00928 | 0.443 |
TRG_ENDOCYTIC_2 | 729 | 732 | PF00928 | 0.324 |
TRG_ENDOCYTIC_2 | 918 | 921 | PF00928 | 0.430 |
TRG_ER_diArg_1 | 105 | 108 | PF00400 | 0.519 |
TRG_ER_diArg_1 | 1056 | 1059 | PF00400 | 0.292 |
TRG_ER_diArg_1 | 1222 | 1225 | PF00400 | 0.551 |
TRG_ER_diArg_1 | 1307 | 1310 | PF00400 | 0.499 |
TRG_ER_diArg_1 | 204 | 207 | PF00400 | 0.426 |
TRG_ER_diArg_1 | 23 | 26 | PF00400 | 0.417 |
TRG_ER_diArg_1 | 8 | 10 | PF00400 | 0.500 |
TRG_ER_diArg_1 | 800 | 802 | PF00400 | 0.505 |
TRG_ER_diArg_1 | 881 | 884 | PF00400 | 0.538 |
TRG_Pf-PMV_PEXEL_1 | 225 | 229 | PF00026 | 0.268 |
TRG_Pf-PMV_PEXEL_1 | 801 | 805 | PF00026 | 0.279 |
TRG_Pf-PMV_PEXEL_1 | 967 | 971 | PF00026 | 0.433 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P457 | Leptomonas seymouri | 26% | 100% |
A0A1X0NPQ6 | Trypanosomatidae | 29% | 100% |
A0A1X0P171 | Trypanosomatidae | 33% | 100% |
A0A3R7R8G4 | Trypanosoma rangeli | 30% | 100% |
A0A3S5H6Z8 | Leishmania donovani | 99% | 100% |
A0A3S7WU91 | Leishmania donovani | 66% | 94% |
A0A3S7WU94 | Leishmania donovani | 55% | 96% |
A0A3S7WU95 | Leishmania donovani | 91% | 95% |
A0A3S7XB85 | Leishmania donovani | 27% | 94% |
A4H8U6 | Leishmania braziliensis | 54% | 100% |
A4H8V5 | Leishmania braziliensis | 62% | 100% |
A4H8V7 | Leishmania braziliensis | 68% | 100% |
A4H8V8 | Leishmania braziliensis | 70% | 100% |
A4HPI4 | Leishmania braziliensis | 26% | 100% |
A4HX84 | Leishmania infantum | 55% | 100% |
A4HX85 | Leishmania infantum | 97% | 100% |
A4HX87 | Leishmania infantum | 66% | 100% |
A4HX88 | Leishmania infantum | 87% | 100% |
A4IDA6 | Leishmania infantum | 28% | 100% |
C9ZM79 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZM80 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 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) | 35% | 100% |
C9ZN41 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
C9ZN43 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
C9ZN44 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
C9ZN45 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
C9ZN46 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
C9ZNA5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
C9ZNA6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZNH3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
C9ZNT1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZPZ6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 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) | 32% | 100% |
C9ZTS4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZTS5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZTS6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZUE6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
C9ZWQ5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
C9ZWU1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 98% |
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) | 31% | 100% |
D0A0U3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
D0A0W7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
D0A0X5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 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) | 31% | 100% |
D0A5U0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
D0A5U1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
D0A7A0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
D0A9R3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
D0AAV3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
E9AQY0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 61% | 100% |
E9AQY1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 55% | 100% |
E9AQY2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 100% |
E9AQY4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
E9ARD7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 54% | 100% |
E9AT96 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
Q25263 | Leishmania donovani | 97% | 100% |
Q26721 | Trypanosoma brucei brucei | 33% | 100% |
Q27675 | Leishmania donovani | 55% | 96% |
Q4Q1A1 | Leishmania major | 27% | 100% |
Q4QEH9 | Leishmania major | 88% | 100% |
Q4QEI0 | Leishmania major | 88% | 100% |
Q4QEI1 | Leishmania major | 89% | 100% |
Q4QEI2 | Leishmania major | 63% | 100% |
Q4QEI3 | Leishmania major | 55% | 100% |
Q99279 | Trypanosoma brucei brucei | 29% | 100% |
Q99280 | Trypanosoma brucei brucei | 32% | 100% |
V5AYH7 | Trypanosoma cruzi | 34% | 100% |