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: 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: 48, no: 32 |
NetGPI | no | yes: 0, no: 80 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 74 |
GO:0110165 | cellular anatomical entity | 1 | 80 |
Related structures:
AlphaFold database: Q4QEI1
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 77 |
GO:0006163 | purine nucleotide metabolic process | 5 | 77 |
GO:0006164 | purine nucleotide biosynthetic process | 6 | 77 |
GO:0006171 | cAMP biosynthetic process | 8 | 77 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 77 |
GO:0006753 | nucleoside phosphate metabolic process | 4 | 77 |
GO:0006793 | phosphorus metabolic process | 3 | 77 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 77 |
GO:0006807 | nitrogen compound metabolic process | 2 | 77 |
GO:0007165 | signal transduction | 2 | 77 |
GO:0008152 | metabolic process | 1 | 77 |
GO:0009058 | biosynthetic process | 2 | 77 |
GO:0009117 | nucleotide metabolic process | 5 | 77 |
GO:0009150 | purine ribonucleotide metabolic process | 6 | 77 |
GO:0009152 | purine ribonucleotide biosynthetic process | 7 | 77 |
GO:0009165 | nucleotide biosynthetic process | 6 | 77 |
GO:0009187 | cyclic nucleotide metabolic process | 6 | 77 |
GO:0009190 | cyclic nucleotide biosynthetic process | 7 | 77 |
GO:0009259 | ribonucleotide metabolic process | 5 | 77 |
GO:0009260 | ribonucleotide biosynthetic process | 6 | 77 |
GO:0009987 | cellular process | 1 | 77 |
GO:0018130 | heterocycle biosynthetic process | 4 | 77 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 77 |
GO:0019637 | organophosphate metabolic process | 3 | 77 |
GO:0019693 | ribose phosphate metabolic process | 4 | 77 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 77 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 77 |
GO:0035556 | intracellular signal transduction | 3 | 77 |
GO:0044237 | cellular metabolic process | 2 | 77 |
GO:0044238 | primary metabolic process | 2 | 77 |
GO:0044249 | cellular biosynthetic process | 3 | 77 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 77 |
GO:0044281 | small molecule metabolic process | 2 | 77 |
GO:0046058 | cAMP metabolic process | 7 | 77 |
GO:0046390 | ribose phosphate biosynthetic process | 5 | 77 |
GO:0046483 | heterocycle metabolic process | 3 | 77 |
GO:0050789 | regulation of biological process | 2 | 77 |
GO:0050794 | regulation of cellular process | 3 | 77 |
GO:0052652 | cyclic purine nucleotide metabolic process | 6 | 77 |
GO:0055086 | nucleobase-containing small molecule metabolic process | 3 | 77 |
GO:0065007 | biological regulation | 1 | 77 |
GO:0071704 | organic substance metabolic process | 2 | 77 |
GO:0072521 | purine-containing compound metabolic process | 4 | 77 |
GO:0072522 | purine-containing compound biosynthetic process | 5 | 77 |
GO:0090407 | organophosphate biosynthetic process | 4 | 77 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 77 |
GO:1901137 | carbohydrate derivative biosynthetic process | 4 | 77 |
GO:1901293 | nucleoside phosphate biosynthetic process | 5 | 77 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 77 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 77 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 77 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 77 |
GO:1901576 | organic substance biosynthetic process | 3 | 77 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 66 |
GO:0016829 | lyase activity | 2 | 66 |
GO:0004016 | adenylate cyclase activity | 3 | 2 |
GO:0009975 | cyclase activity | 2 | 2 |
GO:0016849 | phosphorus-oxygen lyase activity | 3 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 1016 | 1020 | PF00656 | 0.559 |
CLV_C14_Caspase3-7 | 634 | 638 | PF00656 | 0.455 |
CLV_C14_Caspase3-7 | 982 | 986 | PF00656 | 0.490 |
CLV_MEL_PAP_1 | 1055 | 1061 | PF00089 | 0.282 |
CLV_NRD_NRD_1 | 1145 | 1147 | PF00675 | 0.404 |
CLV_NRD_NRD_1 | 207 | 209 | PF00675 | 0.631 |
CLV_NRD_NRD_1 | 659 | 661 | PF00675 | 0.527 |
CLV_NRD_NRD_1 | 800 | 802 | PF00675 | 0.642 |
CLV_NRD_NRD_1 | 882 | 884 | PF00675 | 0.548 |
CLV_NRD_NRD_1 | 9 | 11 | PF00675 | 0.776 |
CLV_PCSK_FUR_1 | 205 | 209 | PF00082 | 0.631 |
CLV_PCSK_KEX2_1 | 1145 | 1147 | PF00082 | 0.404 |
CLV_PCSK_KEX2_1 | 207 | 209 | PF00082 | 0.631 |
CLV_PCSK_KEX2_1 | 800 | 802 | PF00082 | 0.664 |
CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.787 |
CLV_PCSK_SKI1_1 | 1007 | 1011 | PF00082 | 0.284 |
CLV_PCSK_SKI1_1 | 107 | 111 | PF00082 | 0.666 |
CLV_PCSK_SKI1_1 | 1242 | 1246 | PF00082 | 0.457 |
CLV_PCSK_SKI1_1 | 129 | 133 | PF00082 | 0.589 |
CLV_PCSK_SKI1_1 | 208 | 212 | PF00082 | 0.599 |
CLV_PCSK_SKI1_1 | 631 | 635 | PF00082 | 0.560 |
CLV_PCSK_SKI1_1 | 745 | 749 | PF00082 | 0.511 |
CLV_PCSK_SKI1_1 | 767 | 771 | PF00082 | 0.632 |
CLV_PCSK_SKI1_1 | 83 | 87 | PF00082 | 0.624 |
CLV_PCSK_SKI1_1 | 969 | 973 | PF00082 | 0.223 |
CLV_Separin_Metazoa | 604 | 608 | PF03568 | 0.326 |
DEG_APCC_DBOX_1 | 882 | 890 | PF00400 | 0.389 |
DEG_Nend_UBRbox_4 | 1 | 3 | PF02207 | 0.722 |
DEG_SCF_FBW7_2 | 873 | 879 | PF00400 | 0.465 |
DEG_SPOP_SBC_1 | 245 | 249 | PF00917 | 0.290 |
DEG_SPOP_SBC_1 | 289 | 293 | PF00917 | 0.459 |
DEG_SPOP_SBC_1 | 806 | 810 | PF00917 | 0.550 |
DOC_CDC14_PxL_1 | 131 | 139 | PF14671 | 0.320 |
DOC_CKS1_1 | 781 | 786 | PF01111 | 0.358 |
DOC_CKS1_1 | 873 | 878 | PF01111 | 0.409 |
DOC_CYCLIN_RxL_1 | 506 | 515 | PF00134 | 0.306 |
DOC_CYCLIN_RxL_1 | 83 | 94 | PF00134 | 0.428 |
DOC_CYCLIN_yCln2_LP_2 | 236 | 242 | PF00134 | 0.376 |
DOC_CYCLIN_yCln2_LP_2 | 335 | 341 | PF00134 | 0.318 |
DOC_CYCLIN_yCln2_LP_2 | 507 | 513 | PF00134 | 0.422 |
DOC_CYCLIN_yCln2_LP_2 | 870 | 876 | PF00134 | 0.413 |
DOC_MAPK_gen_1 | 1053 | 1061 | PF00069 | 0.513 |
DOC_MAPK_gen_1 | 30 | 40 | PF00069 | 0.717 |
DOC_MAPK_gen_1 | 688 | 697 | PF00069 | 0.239 |
DOC_MAPK_gen_1 | 83 | 92 | PF00069 | 0.431 |
DOC_MAPK_MEF2A_6 | 1053 | 1061 | PF00069 | 0.440 |
DOC_MAPK_MEF2A_6 | 120 | 128 | PF00069 | 0.386 |
DOC_MAPK_MEF2A_6 | 186 | 193 | PF00069 | 0.351 |
DOC_MAPK_MEF2A_6 | 33 | 42 | PF00069 | 0.588 |
DOC_MAPK_MEF2A_6 | 509 | 518 | PF00069 | 0.441 |
DOC_MAPK_MEF2A_6 | 688 | 697 | PF00069 | 0.430 |
DOC_MAPK_MEF2A_6 | 713 | 721 | PF00069 | 0.296 |
DOC_MAPK_MEF2A_6 | 83 | 92 | PF00069 | 0.431 |
DOC_MAPK_RevD_3 | 1132 | 1146 | PF00069 | 0.532 |
DOC_PP1_RVXF_1 | 507 | 514 | PF00149 | 0.303 |
DOC_PP1_RVXF_1 | 743 | 750 | PF00149 | 0.303 |
DOC_PP2B_LxvP_1 | 236 | 239 | PF13499 | 0.342 |
DOC_PP4_FxxP_1 | 165 | 168 | PF00568 | 0.435 |
DOC_USP7_MATH_1 | 1017 | 1021 | PF00917 | 0.606 |
DOC_USP7_MATH_1 | 1244 | 1248 | PF00917 | 0.690 |
DOC_USP7_MATH_1 | 1258 | 1262 | PF00917 | 0.745 |
DOC_USP7_MATH_1 | 151 | 155 | PF00917 | 0.442 |
DOC_USP7_MATH_1 | 289 | 293 | PF00917 | 0.455 |
DOC_USP7_MATH_1 | 675 | 679 | PF00917 | 0.454 |
DOC_USP7_MATH_1 | 734 | 738 | PF00917 | 0.440 |
DOC_USP7_MATH_1 | 777 | 781 | PF00917 | 0.444 |
DOC_USP7_MATH_1 | 990 | 994 | PF00917 | 0.554 |
DOC_USP7_UBL2_3 | 370 | 374 | PF12436 | 0.435 |
DOC_USP7_UBL2_3 | 884 | 888 | PF12436 | 0.573 |
DOC_WW_Pin1_4 | 1080 | 1085 | PF00397 | 0.535 |
DOC_WW_Pin1_4 | 152 | 157 | PF00397 | 0.409 |
DOC_WW_Pin1_4 | 317 | 322 | PF00397 | 0.422 |
DOC_WW_Pin1_4 | 544 | 549 | PF00397 | 0.454 |
DOC_WW_Pin1_4 | 557 | 562 | PF00397 | 0.447 |
DOC_WW_Pin1_4 | 591 | 596 | PF00397 | 0.357 |
DOC_WW_Pin1_4 | 60 | 65 | PF00397 | 0.483 |
DOC_WW_Pin1_4 | 780 | 785 | PF00397 | 0.368 |
DOC_WW_Pin1_4 | 835 | 840 | PF00397 | 0.405 |
DOC_WW_Pin1_4 | 869 | 874 | PF00397 | 0.376 |
LIG_14-3-3_CanoR_1 | 1042 | 1048 | PF00244 | 0.616 |
LIG_14-3-3_CanoR_1 | 1224 | 1231 | PF00244 | 0.667 |
LIG_14-3-3_CanoR_1 | 1242 | 1247 | PF00244 | 0.649 |
LIG_14-3-3_CanoR_1 | 205 | 214 | PF00244 | 0.360 |
LIG_14-3-3_CanoR_1 | 290 | 298 | PF00244 | 0.402 |
LIG_14-3-3_CanoR_1 | 660 | 668 | PF00244 | 0.377 |
LIG_14-3-3_CanoR_1 | 745 | 750 | PF00244 | 0.428 |
LIG_14-3-3_CanoR_1 | 767 | 772 | PF00244 | 0.437 |
LIG_14-3-3_CanoR_1 | 992 | 1000 | PF00244 | 0.598 |
LIG_Actin_WH2_2 | 528 | 545 | PF00022 | 0.255 |
LIG_APCC_ABBA_1 | 141 | 146 | PF00400 | 0.435 |
LIG_APCC_ABBA_1 | 307 | 312 | PF00400 | 0.303 |
LIG_APCC_ABBA_1 | 718 | 723 | PF00400 | 0.303 |
LIG_BIR_III_2 | 926 | 930 | PF00653 | 0.618 |
LIG_deltaCOP1_diTrp_1 | 217 | 222 | PF00928 | 0.265 |
LIG_deltaCOP1_diTrp_1 | 79 | 89 | PF00928 | 0.233 |
LIG_eIF4E_1 | 29 | 35 | PF01652 | 0.667 |
LIG_FHA_1 | 1004 | 1010 | PF00498 | 0.552 |
LIG_FHA_1 | 1013 | 1019 | PF00498 | 0.487 |
LIG_FHA_1 | 1038 | 1044 | PF00498 | 0.498 |
LIG_FHA_1 | 1088 | 1094 | PF00498 | 0.495 |
LIG_FHA_1 | 304 | 310 | PF00498 | 0.382 |
LIG_FHA_1 | 355 | 361 | PF00498 | 0.449 |
LIG_FHA_1 | 44 | 50 | PF00498 | 0.697 |
LIG_FHA_1 | 571 | 577 | PF00498 | 0.372 |
LIG_FHA_1 | 654 | 660 | PF00498 | 0.351 |
LIG_FHA_1 | 677 | 683 | PF00498 | 0.415 |
LIG_FHA_1 | 712 | 718 | PF00498 | 0.422 |
LIG_FHA_1 | 810 | 816 | PF00498 | 0.419 |
LIG_FHA_1 | 821 | 827 | PF00498 | 0.398 |
LIG_FHA_1 | 838 | 844 | PF00498 | 0.532 |
LIG_FHA_1 | 903 | 909 | PF00498 | 0.392 |
LIG_FHA_2 | 1030 | 1036 | PF00498 | 0.586 |
LIG_FHA_2 | 1150 | 1156 | PF00498 | 0.762 |
LIG_FHA_2 | 1160 | 1166 | PF00498 | 0.795 |
LIG_FHA_2 | 253 | 259 | PF00498 | 0.427 |
LIG_FHA_2 | 318 | 324 | PF00498 | 0.424 |
LIG_FHA_2 | 415 | 421 | PF00498 | 0.421 |
LIG_FHA_2 | 632 | 638 | PF00498 | 0.474 |
LIG_FHA_2 | 696 | 702 | PF00498 | 0.355 |
LIG_FHA_2 | 836 | 842 | PF00498 | 0.519 |
LIG_FHA_2 | 888 | 894 | PF00498 | 0.532 |
LIG_FHA_2 | 939 | 945 | PF00498 | 0.489 |
LIG_FHA_2 | 980 | 986 | PF00498 | 0.494 |
LIG_GBD_Chelix_1 | 1000 | 1008 | PF00786 | 0.390 |
LIG_GBD_Chelix_1 | 278 | 286 | PF00786 | 0.503 |
LIG_GBD_Chelix_1 | 405 | 413 | PF00786 | 0.497 |
LIG_LIR_Apic_2 | 1034 | 1039 | PF02991 | 0.479 |
LIG_LIR_Apic_2 | 292 | 298 | PF02991 | 0.255 |
LIG_LIR_Apic_2 | 450 | 454 | PF02991 | 0.372 |
LIG_LIR_Apic_2 | 665 | 671 | PF02991 | 0.463 |
LIG_LIR_Gen_1 | 1045 | 1055 | PF02991 | 0.545 |
LIG_LIR_Gen_1 | 1067 | 1077 | PF02991 | 0.588 |
LIG_LIR_Gen_1 | 209 | 219 | PF02991 | 0.449 |
LIG_LIR_Gen_1 | 255 | 265 | PF02991 | 0.348 |
LIG_LIR_Gen_1 | 588 | 598 | PF02991 | 0.412 |
LIG_LIR_Gen_1 | 748 | 754 | PF02991 | 0.342 |
LIG_LIR_Gen_1 | 937 | 948 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 1019 | 1025 | PF02991 | 0.492 |
LIG_LIR_Nem_3 | 1045 | 1051 | PF02991 | 0.492 |
LIG_LIR_Nem_3 | 1067 | 1073 | PF02991 | 0.508 |
LIG_LIR_Nem_3 | 1074 | 1080 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 1103 | 1109 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 1193 | 1199 | PF02991 | 0.674 |
LIG_LIR_Nem_3 | 133 | 137 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 209 | 214 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 217 | 222 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 306 | 310 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 588 | 593 | PF02991 | 0.351 |
LIG_LIR_Nem_3 | 748 | 752 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 937 | 943 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 947 | 953 | PF02991 | 0.593 |
LIG_LYPXL_yS_3 | 134 | 137 | PF13949 | 0.326 |
LIG_MYND_3 | 613 | 617 | PF01753 | 0.427 |
LIG_PCNA_yPIPBox_3 | 888 | 902 | PF02747 | 0.389 |
LIG_Pex14_1 | 218 | 222 | PF04695 | 0.264 |
LIG_Pex14_2 | 165 | 169 | PF04695 | 0.427 |
LIG_PTB_Apo_2 | 388 | 395 | PF02174 | 0.300 |
LIG_PTB_Apo_2 | 605 | 612 | PF02174 | 0.462 |
LIG_PTB_Apo_2 | 69 | 76 | PF02174 | 0.356 |
LIG_PTB_Phospho_1 | 605 | 611 | PF10480 | 0.467 |
LIG_PTB_Phospho_1 | 69 | 75 | PF10480 | 0.361 |
LIG_SH2_CRK | 242 | 246 | PF00017 | 0.465 |
LIG_SH2_CRK | 451 | 455 | PF00017 | 0.375 |
LIG_SH2_CRK | 624 | 628 | PF00017 | 0.437 |
LIG_SH2_CRK | 668 | 672 | PF00017 | 0.485 |
LIG_SH2_CRK | 728 | 732 | PF00017 | 0.434 |
LIG_SH2_GRB2like | 389 | 392 | PF00017 | 0.458 |
LIG_SH2_GRB2like | 668 | 671 | PF00017 | 0.481 |
LIG_SH2_GRB2like | 846 | 849 | PF00017 | 0.295 |
LIG_SH2_NCK_1 | 101 | 105 | PF00017 | 0.446 |
LIG_SH2_NCK_1 | 1070 | 1074 | PF00017 | 0.581 |
LIG_SH2_NCK_1 | 242 | 246 | PF00017 | 0.475 |
LIG_SH2_NCK_1 | 668 | 672 | PF00017 | 0.320 |
LIG_SH2_PTP2 | 1036 | 1039 | PF00017 | 0.520 |
LIG_SH2_PTP2 | 295 | 298 | PF00017 | 0.375 |
LIG_SH2_PTP2 | 609 | 612 | PF00017 | 0.426 |
LIG_SH2_SRC | 1036 | 1039 | PF00017 | 0.533 |
LIG_SH2_SRC | 1070 | 1073 | PF00017 | 0.581 |
LIG_SH2_SRC | 668 | 671 | PF00017 | 0.464 |
LIG_SH2_STAP1 | 1048 | 1052 | PF00017 | 0.546 |
LIG_SH2_STAP1 | 311 | 315 | PF00017 | 0.442 |
LIG_SH2_STAP1 | 572 | 576 | PF00017 | 0.387 |
LIG_SH2_STAP1 | 728 | 732 | PF00017 | 0.275 |
LIG_SH2_STAT3 | 467 | 470 | PF00017 | 0.425 |
LIG_SH2_STAT3 | 849 | 852 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 101 | 104 | PF00017 | 0.416 |
LIG_SH2_STAT5 | 1036 | 1039 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 1231 | 1234 | PF00017 | 0.616 |
LIG_SH2_STAT5 | 183 | 186 | PF00017 | 0.325 |
LIG_SH2_STAT5 | 213 | 216 | PF00017 | 0.331 |
LIG_SH2_STAT5 | 295 | 298 | PF00017 | 0.309 |
LIG_SH2_STAT5 | 389 | 392 | PF00017 | 0.407 |
LIG_SH2_STAT5 | 440 | 443 | PF00017 | 0.313 |
LIG_SH2_STAT5 | 467 | 470 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 541 | 544 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 572 | 575 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 590 | 593 | PF00017 | 0.445 |
LIG_SH2_STAT5 | 609 | 612 | PF00017 | 0.346 |
LIG_SH2_STAT5 | 69 | 72 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 917 | 920 | PF00017 | 0.658 |
LIG_SH3_3 | 1214 | 1220 | PF00018 | 0.616 |
LIG_SH3_3 | 137 | 143 | PF00018 | 0.314 |
LIG_SH3_3 | 516 | 522 | PF00018 | 0.348 |
LIG_SH3_3 | 589 | 595 | PF00018 | 0.369 |
LIG_SH3_3 | 61 | 67 | PF00018 | 0.469 |
LIG_SH3_3 | 862 | 868 | PF00018 | 0.373 |
LIG_SH3_3 | 870 | 876 | PF00018 | 0.361 |
LIG_Sin3_3 | 1171 | 1178 | PF02671 | 0.558 |
LIG_SUMO_SIM_anti_2 | 121 | 128 | PF11976 | 0.444 |
LIG_SUMO_SIM_anti_2 | 226 | 233 | PF11976 | 0.462 |
LIG_SUMO_SIM_anti_2 | 714 | 723 | PF11976 | 0.345 |
LIG_SUMO_SIM_anti_2 | 905 | 910 | PF11976 | 0.382 |
LIG_SUMO_SIM_anti_2 | 933 | 942 | PF11976 | 0.490 |
LIG_SUMO_SIM_par_1 | 45 | 51 | PF11976 | 0.650 |
LIG_SUMO_SIM_par_1 | 693 | 698 | PF11976 | 0.394 |
LIG_SUMO_SIM_par_1 | 714 | 723 | PF11976 | 0.399 |
LIG_SUMO_SIM_par_1 | 853 | 858 | PF11976 | 0.438 |
LIG_TRAF2_1 | 1044 | 1047 | PF00917 | 0.612 |
LIG_TYR_ITIM | 1068 | 1073 | PF00017 | 0.468 |
LIG_TYR_ITIM | 622 | 627 | PF00017 | 0.434 |
LIG_TYR_ITIM | 726 | 731 | PF00017 | 0.393 |
LIG_UBA3_1 | 193 | 198 | PF00899 | 0.550 |
LIG_UBA3_1 | 538 | 543 | PF00899 | 0.293 |
LIG_UBA3_1 | 620 | 626 | PF00899 | 0.476 |
LIG_WRC_WIRS_1 | 219 | 224 | PF05994 | 0.348 |
LIG_WRC_WIRS_1 | 297 | 302 | PF05994 | 0.514 |
LIG_WRC_WIRS_1 | 746 | 751 | PF05994 | 0.550 |
LIG_WW_3 | 1219 | 1223 | PF00397 | 0.660 |
MOD_CDK_SPxxK_3 | 835 | 842 | PF00069 | 0.450 |
MOD_CK1_1 | 1177 | 1183 | PF00069 | 0.566 |
MOD_CK1_1 | 247 | 253 | PF00069 | 0.495 |
MOD_CK1_1 | 328 | 334 | PF00069 | 0.558 |
MOD_CK1_1 | 383 | 389 | PF00069 | 0.596 |
MOD_CK1_1 | 491 | 497 | PF00069 | 0.472 |
MOD_CK1_1 | 499 | 505 | PF00069 | 0.438 |
MOD_CK1_1 | 635 | 641 | PF00069 | 0.408 |
MOD_CK1_1 | 662 | 668 | PF00069 | 0.413 |
MOD_CK1_1 | 678 | 684 | PF00069 | 0.528 |
MOD_CK1_1 | 756 | 762 | PF00069 | 0.541 |
MOD_CK1_1 | 78 | 84 | PF00069 | 0.462 |
MOD_CK1_1 | 780 | 786 | PF00069 | 0.423 |
MOD_CK1_1 | 805 | 811 | PF00069 | 0.586 |
MOD_CK1_1 | 819 | 825 | PF00069 | 0.375 |
MOD_CK1_1 | 872 | 878 | PF00069 | 0.585 |
MOD_CK1_1 | 993 | 999 | PF00069 | 0.490 |
MOD_CK2_1 | 1041 | 1047 | PF00069 | 0.512 |
MOD_CK2_1 | 1107 | 1113 | PF00069 | 0.350 |
MOD_CK2_1 | 1149 | 1155 | PF00069 | 0.691 |
MOD_CK2_1 | 1159 | 1165 | PF00069 | 0.709 |
MOD_CK2_1 | 151 | 157 | PF00069 | 0.472 |
MOD_CK2_1 | 223 | 229 | PF00069 | 0.506 |
MOD_CK2_1 | 414 | 420 | PF00069 | 0.427 |
MOD_CK2_1 | 60 | 66 | PF00069 | 0.684 |
MOD_CK2_1 | 887 | 893 | PF00069 | 0.727 |
MOD_CK2_1 | 938 | 944 | PF00069 | 0.338 |
MOD_Cter_Amidation | 1143 | 1146 | PF01082 | 0.522 |
MOD_GlcNHglycan | 1019 | 1022 | PF01048 | 0.489 |
MOD_GlcNHglycan | 104 | 107 | PF01048 | 0.430 |
MOD_GlcNHglycan | 1168 | 1171 | PF01048 | 0.628 |
MOD_GlcNHglycan | 1176 | 1179 | PF01048 | 0.549 |
MOD_GlcNHglycan | 1260 | 1263 | PF01048 | 0.627 |
MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.527 |
MOD_GlcNHglycan | 172 | 175 | PF01048 | 0.366 |
MOD_GlcNHglycan | 242 | 245 | PF01048 | 0.477 |
MOD_GlcNHglycan | 292 | 295 | PF01048 | 0.516 |
MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.551 |
MOD_GlcNHglycan | 385 | 388 | PF01048 | 0.590 |
MOD_GlcNHglycan | 409 | 412 | PF01048 | 0.477 |
MOD_GlcNHglycan | 473 | 476 | PF01048 | 0.508 |
MOD_GlcNHglycan | 490 | 493 | PF01048 | 0.482 |
MOD_GlcNHglycan | 544 | 547 | PF01048 | 0.546 |
MOD_GlcNHglycan | 627 | 630 | PF01048 | 0.477 |
MOD_GlcNHglycan | 637 | 640 | PF01048 | 0.448 |
MOD_GlcNHglycan | 661 | 664 | PF01048 | 0.506 |
MOD_GlcNHglycan | 683 | 686 | PF01048 | 0.471 |
MOD_GlcNHglycan | 760 | 763 | PF01048 | 0.611 |
MOD_GlcNHglycan | 787 | 790 | PF01048 | 0.463 |
MOD_GlcNHglycan | 795 | 798 | PF01048 | 0.483 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.415 |
MOD_GlcNHglycan | 992 | 995 | PF01048 | 0.435 |
MOD_GSK3_1 | 1037 | 1044 | PF00069 | 0.495 |
MOD_GSK3_1 | 114 | 121 | PF00069 | 0.463 |
MOD_GSK3_1 | 1159 | 1166 | PF00069 | 0.632 |
MOD_GSK3_1 | 1173 | 1180 | PF00069 | 0.646 |
MOD_GSK3_1 | 1220 | 1227 | PF00069 | 0.649 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.470 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.470 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.537 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.531 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.702 |
MOD_GSK3_1 | 471 | 478 | PF00069 | 0.538 |
MOD_GSK3_1 | 499 | 506 | PF00069 | 0.459 |
MOD_GSK3_1 | 566 | 573 | PF00069 | 0.495 |
MOD_GSK3_1 | 631 | 638 | PF00069 | 0.456 |
MOD_GSK3_1 | 671 | 678 | PF00069 | 0.482 |
MOD_GSK3_1 | 726 | 733 | PF00069 | 0.512 |
MOD_GSK3_1 | 734 | 741 | PF00069 | 0.525 |
MOD_GSK3_1 | 763 | 770 | PF00069 | 0.446 |
MOD_GSK3_1 | 791 | 798 | PF00069 | 0.511 |
MOD_GSK3_1 | 802 | 809 | PF00069 | 0.587 |
MOD_GSK3_1 | 816 | 823 | PF00069 | 0.460 |
MOD_GSK3_1 | 833 | 840 | PF00069 | 0.612 |
MOD_GSK3_1 | 868 | 875 | PF00069 | 0.486 |
MOD_GSK3_1 | 934 | 941 | PF00069 | 0.354 |
MOD_GSK3_1 | 979 | 986 | PF00069 | 0.348 |
MOD_N-GLC_1 | 252 | 257 | PF02516 | 0.543 |
MOD_N-GLC_1 | 531 | 536 | PF02516 | 0.527 |
MOD_N-GLC_1 | 554 | 559 | PF02516 | 0.496 |
MOD_N-GLC_1 | 570 | 575 | PF02516 | 0.557 |
MOD_N-GLC_1 | 60 | 65 | PF02516 | 0.524 |
MOD_N-GLC_1 | 653 | 658 | PF02516 | 0.481 |
MOD_NEK2_1 | 1174 | 1179 | PF00069 | 0.588 |
MOD_NEK2_1 | 1190 | 1195 | PF00069 | 0.376 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.463 |
MOD_NEK2_1 | 230 | 235 | PF00069 | 0.517 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.384 |
MOD_NEK2_1 | 354 | 359 | PF00069 | 0.519 |
MOD_NEK2_1 | 47 | 52 | PF00069 | 0.551 |
MOD_NEK2_1 | 542 | 547 | PF00069 | 0.502 |
MOD_NEK2_1 | 659 | 664 | PF00069 | 0.385 |
MOD_NEK2_1 | 695 | 700 | PF00069 | 0.493 |
MOD_NEK2_1 | 795 | 800 | PF00069 | 0.421 |
MOD_NEK2_1 | 802 | 807 | PF00069 | 0.538 |
MOD_PIKK_1 | 1244 | 1250 | PF00454 | 0.660 |
MOD_PIKK_1 | 398 | 404 | PF00454 | 0.459 |
MOD_PIKK_1 | 433 | 439 | PF00454 | 0.522 |
MOD_PIKK_1 | 493 | 499 | PF00454 | 0.500 |
MOD_PIKK_1 | 777 | 783 | PF00454 | 0.537 |
MOD_PK_1 | 738 | 744 | PF00069 | 0.351 |
MOD_PK_1 | 817 | 823 | PF00069 | 0.346 |
MOD_PKA_2 | 1041 | 1047 | PF00069 | 0.515 |
MOD_PKA_2 | 206 | 212 | PF00069 | 0.553 |
MOD_PKA_2 | 289 | 295 | PF00069 | 0.509 |
MOD_PKA_2 | 29 | 35 | PF00069 | 0.719 |
MOD_PKA_2 | 659 | 665 | PF00069 | 0.423 |
MOD_PKA_2 | 816 | 822 | PF00069 | 0.575 |
MOD_PKB_1 | 1222 | 1230 | PF00069 | 0.695 |
MOD_PKB_1 | 1250 | 1258 | PF00069 | 0.489 |
MOD_Plk_1 | 1102 | 1108 | PF00069 | 0.367 |
MOD_Plk_1 | 252 | 258 | PF00069 | 0.475 |
MOD_Plk_1 | 502 | 508 | PF00069 | 0.497 |
MOD_Plk_1 | 531 | 537 | PF00069 | 0.512 |
MOD_Plk_1 | 631 | 637 | PF00069 | 0.536 |
MOD_Plk_1 | 653 | 659 | PF00069 | 0.431 |
MOD_Plk_1 | 711 | 717 | PF00069 | 0.506 |
MOD_Plk_1 | 78 | 84 | PF00069 | 0.431 |
MOD_Plk_1 | 817 | 823 | PF00069 | 0.479 |
MOD_Plk_2-3 | 223 | 229 | PF00069 | 0.514 |
MOD_Plk_2-3 | 632 | 638 | PF00069 | 0.610 |
MOD_Plk_2-3 | 646 | 652 | PF00069 | 0.509 |
MOD_Plk_2-3 | 979 | 985 | PF00069 | 0.338 |
MOD_Plk_4 | 1102 | 1108 | PF00069 | 0.310 |
MOD_Plk_4 | 133 | 139 | PF00069 | 0.518 |
MOD_Plk_4 | 223 | 229 | PF00069 | 0.488 |
MOD_Plk_4 | 360 | 366 | PF00069 | 0.502 |
MOD_Plk_4 | 409 | 415 | PF00069 | 0.526 |
MOD_Plk_4 | 512 | 518 | PF00069 | 0.428 |
MOD_Plk_4 | 712 | 718 | PF00069 | 0.491 |
MOD_Plk_4 | 727 | 733 | PF00069 | 0.471 |
MOD_Plk_4 | 767 | 773 | PF00069 | 0.485 |
MOD_Plk_4 | 934 | 940 | PF00069 | 0.335 |
MOD_Plk_4 | 983 | 989 | PF00069 | 0.352 |
MOD_ProDKin_1 | 1080 | 1086 | PF00069 | 0.401 |
MOD_ProDKin_1 | 152 | 158 | PF00069 | 0.497 |
MOD_ProDKin_1 | 317 | 323 | PF00069 | 0.525 |
MOD_ProDKin_1 | 544 | 550 | PF00069 | 0.560 |
MOD_ProDKin_1 | 557 | 563 | PF00069 | 0.557 |
MOD_ProDKin_1 | 591 | 597 | PF00069 | 0.432 |
MOD_ProDKin_1 | 60 | 66 | PF00069 | 0.595 |
MOD_ProDKin_1 | 780 | 786 | PF00069 | 0.444 |
MOD_ProDKin_1 | 835 | 841 | PF00069 | 0.499 |
MOD_ProDKin_1 | 869 | 875 | PF00069 | 0.461 |
MOD_SUMO_rev_2 | 217 | 227 | PF00179 | 0.428 |
MOD_SUMO_rev_2 | 363 | 372 | PF00179 | 0.553 |
MOD_SUMO_rev_2 | 707 | 715 | PF00179 | 0.566 |
TRG_DiLeu_BaEn_1 | 223 | 228 | PF01217 | 0.543 |
TRG_DiLeu_BaEn_1 | 66 | 71 | PF01217 | 0.524 |
TRG_DiLeu_BaEn_1 | 893 | 898 | PF01217 | 0.419 |
TRG_DiLeu_BaEn_1 | 934 | 939 | PF01217 | 0.469 |
TRG_DiLeu_BaEn_2 | 179 | 185 | PF01217 | 0.542 |
TRG_DiLeu_BaEn_2 | 616 | 622 | PF01217 | 0.347 |
TRG_DiLeu_BaEn_3 | 711 | 717 | PF01217 | 0.552 |
TRG_DiLeu_BaEn_4 | 1046 | 1052 | PF01217 | 0.366 |
TRG_DiLeu_BaLyEn_6 | 30 | 35 | PF01217 | 0.639 |
TRG_DiLeu_BaLyEn_6 | 519 | 524 | PF01217 | 0.528 |
TRG_DiLeu_BaLyEn_6 | 764 | 769 | PF01217 | 0.310 |
TRG_DiLeu_LyEn_5 | 1207 | 1212 | PF01217 | 0.523 |
TRG_ENDOCYTIC_2 | 1022 | 1025 | PF00928 | 0.346 |
TRG_ENDOCYTIC_2 | 1048 | 1051 | PF00928 | 0.330 |
TRG_ENDOCYTIC_2 | 1070 | 1073 | PF00928 | 0.466 |
TRG_ENDOCYTIC_2 | 134 | 137 | PF00928 | 0.563 |
TRG_ENDOCYTIC_2 | 310 | 313 | PF00928 | 0.498 |
TRG_ENDOCYTIC_2 | 590 | 593 | PF00928 | 0.568 |
TRG_ENDOCYTIC_2 | 609 | 612 | PF00928 | 0.533 |
TRG_ENDOCYTIC_2 | 624 | 627 | PF00928 | 0.480 |
TRG_ENDOCYTIC_2 | 728 | 731 | PF00928 | 0.400 |
TRG_ENDOCYTIC_2 | 917 | 920 | PF00928 | 0.643 |
TRG_ER_diArg_1 | 1055 | 1058 | PF00400 | 0.340 |
TRG_ER_diArg_1 | 1221 | 1224 | PF00400 | 0.667 |
TRG_ER_diArg_1 | 1250 | 1253 | PF00400 | 0.665 |
TRG_ER_diArg_1 | 204 | 207 | PF00400 | 0.529 |
TRG_ER_diArg_1 | 688 | 691 | PF00400 | 0.585 |
TRG_ER_diArg_1 | 799 | 801 | PF00400 | 0.560 |
TRG_ER_diArg_1 | 8 | 10 | PF00400 | 0.513 |
TRG_ER_diArg_1 | 880 | 883 | PF00400 | 0.545 |
TRG_Pf-PMV_PEXEL_1 | 225 | 229 | PF00026 | 0.320 |
TRG_Pf-PMV_PEXEL_1 | 800 | 804 | PF00026 | 0.387 |
TRG_Pf-PMV_PEXEL_1 | 966 | 970 | PF00026 | 0.415 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P457 | Leptomonas seymouri | 26% | 95% |
A0A1X0NPQ6 | Trypanosomatidae | 28% | 100% |
A0A1X0P171 | Trypanosomatidae | 33% | 99% |
A0A3Q8IJB0 | Leishmania donovani | 89% | 95% |
A0A3R7KBB6 | Trypanosoma rangeli | 28% | 100% |
A0A3R7M6J4 | Trypanosoma rangeli | 38% | 100% |
A0A3R7R8G4 | Trypanosoma rangeli | 31% | 100% |
A0A3S5H6Z8 | Leishmania donovani | 89% | 95% |
A0A3S7WU91 | Leishmania donovani | 64% | 89% |
A0A3S7WU94 | Leishmania donovani | 56% | 92% |
A0A3S7WU95 | Leishmania donovani | 83% | 90% |
A0A3S7XB85 | Leishmania donovani | 27% | 90% |
A4H8U6 | Leishmania braziliensis | 55% | 97% |
A4H8V5 | Leishmania braziliensis | 62% | 100% |
A4H8V7 | Leishmania braziliensis | 69% | 100% |
A4H8V8 | Leishmania braziliensis | 71% | 90% |
A4HPI4 | Leishmania braziliensis | 26% | 90% |
A4HX84 | Leishmania infantum | 56% | 92% |
A4HX85 | Leishmania infantum | 90% | 90% |
A4HX87 | Leishmania infantum | 64% | 96% |
A4HX88 | Leishmania infantum | 80% | 100% |
A4IDA6 | Leishmania infantum | 28% | 90% |
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) | 33% | 100% |
C9ZM82 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZM83 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 98% |
C9ZM86 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
C9ZN26 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 99% |
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) | 33% | 100% |
C9ZN46 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 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) | 31% | 99% |
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) | 31% | 99% |
C9ZQ90 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZQ91 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 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) | 32% | 100% |
C9ZWU1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 93% |
C9ZWU2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZWU3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 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) | 31% | 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) | 30% | 100% |
D0A9R3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
D0AAV3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
E8NHJ6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 49% | 100% |
E9AQY0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 64% | 90% |
E9AQY1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 56% | 91% |
E9AQY2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 90% |
E9AQY4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 95% |
E9ARD7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 55% | 92% |
E9AT96 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 90% |
Q25263 | Leishmania donovani | 89% | 95% |
Q26721 | Trypanosoma brucei brucei | 33% | 100% |
Q27675 | Leishmania donovani | 56% | 92% |
Q4Q1A1 | Leishmania major | 28% | 100% |
Q4QEH9 | Leishmania major | 99% | 100% |
Q4QEI0 | Leishmania major | 100% | 100% |
Q4QEI2 | Leishmania major | 67% | 89% |
Q4QEI3 | Leishmania major | 57% | 92% |
Q99279 | Trypanosoma brucei brucei | 29% | 100% |
Q99280 | Trypanosoma brucei brucei | 31% | 100% |
V5AYH7 | Trypanosoma cruzi | 33% | 99% |
V5B1C8 | Trypanosoma cruzi | 38% | 100% |