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 | no | yes: 47, no: 29 |
NetGPI | no | yes: 0, no: 76 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 71 |
GO:0110165 | cellular anatomical entity | 1 | 77 |
Related structures:
AlphaFold database: A4H8V7
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 | 218 | 222 | PF00656 | 0.332 |
CLV_C14_Caspase3-7 | 661 | 665 | PF00656 | 0.664 |
CLV_C14_Caspase3-7 | 722 | 726 | PF00656 | 0.505 |
CLV_MEL_PAP_1 | 795 | 801 | PF00089 | 0.298 |
CLV_NRD_NRD_1 | 1053 | 1055 | PF00675 | 0.613 |
CLV_NRD_NRD_1 | 1093 | 1095 | PF00675 | 0.499 |
CLV_NRD_NRD_1 | 1102 | 1104 | PF00675 | 0.647 |
CLV_NRD_NRD_1 | 131 | 133 | PF00675 | 0.705 |
CLV_NRD_NRD_1 | 371 | 373 | PF00675 | 0.675 |
CLV_NRD_NRD_1 | 428 | 430 | PF00675 | 0.673 |
CLV_NRD_NRD_1 | 885 | 887 | PF00675 | 0.422 |
CLV_PCSK_KEX2_1 | 1053 | 1055 | PF00082 | 0.605 |
CLV_PCSK_KEX2_1 | 1093 | 1095 | PF00082 | 0.499 |
CLV_PCSK_KEX2_1 | 1102 | 1104 | PF00082 | 0.657 |
CLV_PCSK_KEX2_1 | 131 | 133 | PF00082 | 0.506 |
CLV_PCSK_KEX2_1 | 371 | 373 | PF00082 | 0.627 |
CLV_PCSK_KEX2_1 | 428 | 430 | PF00082 | 0.607 |
CLV_PCSK_KEX2_1 | 885 | 887 | PF00082 | 0.422 |
CLV_PCSK_SKI1_1 | 131 | 135 | PF00082 | 0.619 |
CLV_PCSK_SKI1_1 | 22 | 26 | PF00082 | 0.561 |
CLV_PCSK_SKI1_1 | 287 | 291 | PF00082 | 0.501 |
CLV_PCSK_SKI1_1 | 371 | 375 | PF00082 | 0.571 |
CLV_PCSK_SKI1_1 | 381 | 385 | PF00082 | 0.620 |
CLV_PCSK_SKI1_1 | 43 | 47 | PF00082 | 0.550 |
CLV_PCSK_SKI1_1 | 485 | 489 | PF00082 | 0.521 |
CLV_PCSK_SKI1_1 | 978 | 982 | PF00082 | 0.455 |
CLV_Separin_Metazoa | 344 | 348 | PF03568 | 0.337 |
DEG_APCC_DBOX_1 | 1053 | 1061 | PF00400 | 0.632 |
DEG_APCC_DBOX_1 | 863 | 871 | PF00400 | 0.413 |
DEG_Nend_UBRbox_3 | 1 | 2 | PF02207 | 0.345 |
DEG_SPOP_SBC_1 | 263 | 267 | PF00917 | 0.426 |
DEG_SPOP_SBC_1 | 28 | 32 | PF00917 | 0.500 |
DEG_SPOP_SBC_1 | 474 | 478 | PF00917 | 0.331 |
DOC_CKS1_1 | 613 | 618 | PF01111 | 0.405 |
DOC_CYCLIN_RxL_1 | 244 | 255 | PF00134 | 0.341 |
DOC_CYCLIN_yCln2_LP_2 | 247 | 253 | PF00134 | 0.454 |
DOC_CYCLIN_yCln2_LP_2 | 610 | 616 | PF00134 | 0.405 |
DOC_MAPK_gen_1 | 1050 | 1059 | PF00069 | 0.726 |
DOC_MAPK_MEF2A_6 | 249 | 258 | PF00069 | 0.459 |
DOC_MAPK_MEF2A_6 | 453 | 461 | PF00069 | 0.310 |
DOC_MAPK_RevD_3 | 872 | 886 | PF00069 | 0.618 |
DOC_PP1_RVXF_1 | 1117 | 1124 | PF00149 | 0.586 |
DOC_PP1_RVXF_1 | 247 | 254 | PF00149 | 0.335 |
DOC_PP1_RVXF_1 | 278 | 285 | PF00149 | 0.413 |
DOC_PP1_RVXF_1 | 41 | 47 | PF00149 | 0.468 |
DOC_PP1_RVXF_1 | 427 | 434 | PF00149 | 0.264 |
DOC_PP1_RVXF_1 | 483 | 490 | PF00149 | 0.312 |
DOC_PP2B_LxvP_1 | 610 | 613 | PF13499 | 0.483 |
DOC_PP4_FxxP_1 | 1087 | 1090 | PF00568 | 0.630 |
DOC_USP7_MATH_1 | 1029 | 1033 | PF00917 | 0.827 |
DOC_USP7_MATH_1 | 1104 | 1108 | PF00917 | 0.832 |
DOC_USP7_MATH_1 | 215 | 219 | PF00917 | 0.476 |
DOC_USP7_MATH_1 | 263 | 267 | PF00917 | 0.306 |
DOC_USP7_MATH_1 | 28 | 32 | PF00917 | 0.498 |
DOC_USP7_MATH_1 | 451 | 455 | PF00917 | 0.437 |
DOC_USP7_MATH_1 | 474 | 478 | PF00917 | 0.445 |
DOC_USP7_MATH_1 | 730 | 734 | PF00917 | 0.568 |
DOC_USP7_MATH_1 | 984 | 988 | PF00917 | 0.714 |
DOC_WW_Pin1_4 | 475 | 480 | PF00397 | 0.407 |
DOC_WW_Pin1_4 | 520 | 525 | PF00397 | 0.365 |
DOC_WW_Pin1_4 | 540 | 545 | PF00397 | 0.259 |
DOC_WW_Pin1_4 | 56 | 61 | PF00397 | 0.461 |
DOC_WW_Pin1_4 | 612 | 617 | PF00397 | 0.367 |
DOC_WW_Pin1_4 | 627 | 632 | PF00397 | 0.531 |
DOC_WW_Pin1_4 | 820 | 825 | PF00397 | 0.548 |
LIG_14-3-3_CanoR_1 | 162 | 170 | PF00244 | 0.403 |
LIG_14-3-3_CanoR_1 | 22 | 28 | PF00244 | 0.446 |
LIG_14-3-3_CanoR_1 | 287 | 292 | PF00244 | 0.343 |
LIG_14-3-3_CanoR_1 | 29 | 36 | PF00244 | 0.444 |
LIG_14-3-3_CanoR_1 | 298 | 305 | PF00244 | 0.293 |
LIG_14-3-3_CanoR_1 | 371 | 380 | PF00244 | 0.472 |
LIG_14-3-3_CanoR_1 | 401 | 407 | PF00244 | 0.383 |
LIG_14-3-3_CanoR_1 | 485 | 490 | PF00244 | 0.438 |
LIG_14-3-3_CanoR_1 | 623 | 631 | PF00244 | 0.548 |
LIG_14-3-3_CanoR_1 | 782 | 788 | PF00244 | 0.635 |
LIG_14-3-3_CanoR_1 | 964 | 972 | PF00244 | 0.689 |
LIG_14-3-3_CanoR_1 | 982 | 987 | PF00244 | 0.671 |
LIG_Actin_WH2_2 | 356 | 373 | PF00022 | 0.245 |
LIG_APCC_ABBA_1 | 458 | 463 | PF00400 | 0.321 |
LIG_APCC_ABBA_1 | 46 | 51 | PF00400 | 0.332 |
LIG_BIR_III_2 | 666 | 670 | PF00653 | 0.638 |
LIG_BIR_III_2 | 880 | 884 | PF00653 | 0.587 |
LIG_BRCT_BRCA1_1 | 1048 | 1052 | PF00533 | 0.811 |
LIG_BRCT_BRCA1_1 | 171 | 175 | PF00533 | 0.401 |
LIG_Clathr_ClatBox_1 | 534 | 538 | PF01394 | 0.282 |
LIG_eIF4E_1 | 337 | 343 | PF01652 | 0.267 |
LIG_eIF4E_1 | 503 | 509 | PF01652 | 0.269 |
LIG_eIF4E_1 | 522 | 528 | PF01652 | 0.211 |
LIG_FHA_1 | 144 | 150 | PF00498 | 0.399 |
LIG_FHA_1 | 284 | 290 | PF00498 | 0.406 |
LIG_FHA_1 | 311 | 317 | PF00498 | 0.371 |
LIG_FHA_1 | 394 | 400 | PF00498 | 0.360 |
LIG_FHA_1 | 417 | 423 | PF00498 | 0.413 |
LIG_FHA_1 | 467 | 473 | PF00498 | 0.410 |
LIG_FHA_1 | 530 | 536 | PF00498 | 0.305 |
LIG_FHA_1 | 613 | 619 | PF00498 | 0.339 |
LIG_FHA_1 | 744 | 750 | PF00498 | 0.566 |
LIG_FHA_1 | 753 | 759 | PF00498 | 0.500 |
LIG_FHA_1 | 77 | 83 | PF00498 | 0.387 |
LIG_FHA_1 | 778 | 784 | PF00498 | 0.513 |
LIG_FHA_1 | 828 | 834 | PF00498 | 0.510 |
LIG_FHA_1 | 94 | 100 | PF00498 | 0.516 |
LIG_FHA_2 | 225 | 231 | PF00498 | 0.385 |
LIG_FHA_2 | 436 | 442 | PF00498 | 0.375 |
LIG_FHA_2 | 57 | 63 | PF00498 | 0.459 |
LIG_FHA_2 | 628 | 634 | PF00498 | 0.490 |
LIG_FHA_2 | 679 | 685 | PF00498 | 0.505 |
LIG_FHA_2 | 720 | 726 | PF00498 | 0.509 |
LIG_FHA_2 | 890 | 896 | PF00498 | 0.782 |
LIG_FHA_2 | 900 | 906 | PF00498 | 0.823 |
LIG_FXI_DFP_1 | 503 | 507 | PF00024 | 0.452 |
LIG_GBD_Chelix_1 | 17 | 25 | PF00786 | 0.538 |
LIG_GBD_Chelix_1 | 317 | 325 | PF00786 | 0.653 |
LIG_GBD_Chelix_1 | 740 | 748 | PF00786 | 0.409 |
LIG_KLC1_Yacidic_2 | 500 | 505 | PF13176 | 0.254 |
LIG_LIR_Apic_2 | 190 | 194 | PF02991 | 0.451 |
LIG_LIR_Apic_2 | 328 | 333 | PF02991 | 0.378 |
LIG_LIR_Apic_2 | 405 | 411 | PF02991 | 0.466 |
LIG_LIR_Apic_2 | 773 | 779 | PF02991 | 0.489 |
LIG_LIR_Gen_1 | 172 | 182 | PF02991 | 0.290 |
LIG_LIR_Gen_1 | 19 | 28 | PF02991 | 0.438 |
LIG_LIR_Gen_1 | 222 | 233 | PF02991 | 0.490 |
LIG_LIR_Gen_1 | 290 | 301 | PF02991 | 0.401 |
LIG_LIR_Gen_1 | 488 | 494 | PF02991 | 0.350 |
LIG_LIR_Gen_1 | 500 | 511 | PF02991 | 0.424 |
LIG_LIR_Gen_1 | 677 | 688 | PF02991 | 0.506 |
LIG_LIR_Gen_1 | 785 | 795 | PF02991 | 0.563 |
LIG_LIR_Gen_1 | 807 | 817 | PF02991 | 0.604 |
LIG_LIR_Nem_3 | 19 | 23 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 2 | 6 | PF02991 | 0.338 |
LIG_LIR_Nem_3 | 222 | 228 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 230 | 236 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 290 | 296 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 488 | 492 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 500 | 506 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 677 | 683 | PF02991 | 0.506 |
LIG_LIR_Nem_3 | 687 | 693 | PF02991 | 0.609 |
LIG_LIR_Nem_3 | 752 | 756 | PF02991 | 0.527 |
LIG_LIR_Nem_3 | 759 | 765 | PF02991 | 0.507 |
LIG_LIR_Nem_3 | 785 | 791 | PF02991 | 0.506 |
LIG_LIR_Nem_3 | 807 | 813 | PF02991 | 0.523 |
LIG_LIR_Nem_3 | 814 | 820 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 843 | 849 | PF02991 | 0.520 |
LIG_LIR_Nem_3 | 933 | 939 | PF02991 | 0.695 |
LIG_LIR_Nem_3 | 969 | 975 | PF02991 | 0.614 |
LIG_LYPXL_yS_3 | 3 | 6 | PF13949 | 0.291 |
LIG_MAD2 | 280 | 288 | PF02301 | 0.287 |
LIG_MYND_3 | 353 | 357 | PF01753 | 0.444 |
LIG_PCNA_yPIPBox_3 | 142 | 152 | PF02747 | 0.481 |
LIG_PCNA_yPIPBox_3 | 634 | 642 | PF02747 | 0.260 |
LIG_PTB_Apo_2 | 345 | 352 | PF02174 | 0.477 |
LIG_PTB_Phospho_1 | 345 | 351 | PF10480 | 0.481 |
LIG_SH2_CRK | 191 | 195 | PF00017 | 0.452 |
LIG_SH2_CRK | 408 | 412 | PF00017 | 0.484 |
LIG_SH2_CRK | 468 | 472 | PF00017 | 0.469 |
LIG_SH2_GRB2like | 293 | 296 | PF00017 | 0.250 |
LIG_SH2_GRB2like | 364 | 367 | PF00017 | 0.403 |
LIG_SH2_NCK_1 | 408 | 412 | PF00017 | 0.320 |
LIG_SH2_NCK_1 | 810 | 814 | PF00017 | 0.597 |
LIG_SH2_PTP2 | 349 | 352 | PF00017 | 0.444 |
LIG_SH2_PTP2 | 776 | 779 | PF00017 | 0.538 |
LIG_SH2_SRC | 180 | 183 | PF00017 | 0.472 |
LIG_SH2_SRC | 293 | 296 | PF00017 | 0.324 |
LIG_SH2_SRC | 776 | 779 | PF00017 | 0.551 |
LIG_SH2_SRC | 810 | 813 | PF00017 | 0.597 |
LIG_SH2_STAP1 | 312 | 316 | PF00017 | 0.391 |
LIG_SH2_STAP1 | 364 | 368 | PF00017 | 0.458 |
LIG_SH2_STAP1 | 468 | 472 | PF00017 | 0.295 |
LIG_SH2_STAP1 | 50 | 54 | PF00017 | 0.465 |
LIG_SH2_STAP1 | 514 | 518 | PF00017 | 0.254 |
LIG_SH2_STAP1 | 788 | 792 | PF00017 | 0.564 |
LIG_SH2_STAT3 | 207 | 210 | PF00017 | 0.514 |
LIG_SH2_STAT3 | 589 | 592 | PF00017 | 0.347 |
LIG_SH2_STAT3 | 92 | 95 | PF00017 | 0.292 |
LIG_SH2_STAT5 | 180 | 183 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 186 | 189 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 207 | 210 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 235 | 238 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 293 | 296 | PF00017 | 0.401 |
LIG_SH2_STAT5 | 312 | 315 | PF00017 | 0.479 |
LIG_SH2_STAT5 | 330 | 333 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 34 | 37 | PF00017 | 0.346 |
LIG_SH2_STAT5 | 349 | 352 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 468 | 471 | PF00017 | 0.363 |
LIG_SH2_STAT5 | 503 | 506 | PF00017 | 0.421 |
LIG_SH2_STAT5 | 522 | 525 | PF00017 | 0.338 |
LIG_SH2_STAT5 | 657 | 660 | PF00017 | 0.666 |
LIG_SH2_STAT5 | 776 | 779 | PF00017 | 0.485 |
LIG_SH3_1 | 191 | 197 | PF00018 | 0.345 |
LIG_SH3_3 | 1112 | 1118 | PF00018 | 0.758 |
LIG_SH3_3 | 1121 | 1127 | PF00018 | 0.833 |
LIG_SH3_3 | 191 | 197 | PF00018 | 0.345 |
LIG_SH3_3 | 329 | 335 | PF00018 | 0.378 |
LIG_SH3_3 | 411 | 417 | PF00018 | 0.376 |
LIG_SH3_3 | 602 | 608 | PF00018 | 0.376 |
LIG_SH3_3 | 610 | 616 | PF00018 | 0.357 |
LIG_SH3_3 | 954 | 960 | PF00018 | 0.640 |
LIG_SUMO_SIM_anti_2 | 1109 | 1116 | PF11976 | 0.775 |
LIG_SUMO_SIM_anti_2 | 454 | 460 | PF11976 | 0.356 |
LIG_SUMO_SIM_anti_2 | 673 | 682 | PF11976 | 0.508 |
LIG_SUMO_SIM_par_1 | 412 | 419 | PF11976 | 0.297 |
LIG_SUMO_SIM_par_1 | 433 | 438 | PF11976 | 0.406 |
LIG_SUMO_SIM_par_1 | 456 | 463 | PF11976 | 0.409 |
LIG_SUMO_SIM_par_1 | 532 | 538 | PF11976 | 0.287 |
LIG_SUMO_SIM_par_1 | 593 | 598 | PF11976 | 0.330 |
LIG_SUMO_SIM_par_1 | 642 | 648 | PF11976 | 0.450 |
LIG_SUMO_SIM_par_1 | 754 | 759 | PF11976 | 0.413 |
LIG_SxIP_EBH_1 | 75 | 86 | PF03271 | 0.293 |
LIG_TRAF2_1 | 1095 | 1098 | PF00917 | 0.815 |
LIG_TRAF2_1 | 227 | 230 | PF00917 | 0.297 |
LIG_TRAF2_1 | 784 | 787 | PF00917 | 0.629 |
LIG_TRAF2_1 | 850 | 853 | PF00917 | 0.538 |
LIG_TYR_ITIM | 362 | 367 | PF00017 | 0.456 |
LIG_TYR_ITIM | 466 | 471 | PF00017 | 0.422 |
LIG_TYR_ITIM | 808 | 813 | PF00017 | 0.483 |
LIG_WRC_WIRS_1 | 486 | 491 | PF05994 | 0.560 |
LIG_WW_3 | 1036 | 1040 | PF00397 | 0.859 |
LIG_WW_3 | 959 | 963 | PF00397 | 0.699 |
MOD_CDK_SPxxK_3 | 627 | 634 | PF00069 | 0.538 |
MOD_CK1_1 | 1032 | 1038 | PF00069 | 0.792 |
MOD_CK1_1 | 1074 | 1080 | PF00069 | 0.601 |
MOD_CK1_1 | 123 | 129 | PF00069 | 0.677 |
MOD_CK1_1 | 166 | 172 | PF00069 | 0.425 |
MOD_CK1_1 | 242 | 248 | PF00069 | 0.528 |
MOD_CK1_1 | 375 | 381 | PF00069 | 0.447 |
MOD_CK1_1 | 393 | 399 | PF00069 | 0.394 |
MOD_CK1_1 | 402 | 408 | PF00069 | 0.417 |
MOD_CK1_1 | 418 | 424 | PF00069 | 0.530 |
MOD_CK1_1 | 496 | 502 | PF00069 | 0.541 |
MOD_CK1_1 | 520 | 526 | PF00069 | 0.414 |
MOD_CK1_1 | 627 | 633 | PF00069 | 0.562 |
MOD_CK1_1 | 67 | 73 | PF00069 | 0.650 |
MOD_CK1_1 | 733 | 739 | PF00069 | 0.507 |
MOD_CK1_1 | 917 | 923 | PF00069 | 0.577 |
MOD_CK2_1 | 1065 | 1071 | PF00069 | 0.777 |
MOD_CK2_1 | 224 | 230 | PF00069 | 0.392 |
MOD_CK2_1 | 627 | 633 | PF00069 | 0.657 |
MOD_CK2_1 | 678 | 684 | PF00069 | 0.354 |
MOD_CK2_1 | 781 | 787 | PF00069 | 0.530 |
MOD_CK2_1 | 847 | 853 | PF00069 | 0.363 |
MOD_CK2_1 | 889 | 895 | PF00069 | 0.708 |
MOD_CK2_1 | 899 | 905 | PF00069 | 0.718 |
MOD_Cter_Amidation | 883 | 886 | PF01082 | 0.546 |
MOD_GlcNHglycan | 1031 | 1034 | PF01048 | 0.821 |
MOD_GlcNHglycan | 1041 | 1046 | PF01048 | 0.755 |
MOD_GlcNHglycan | 1073 | 1076 | PF01048 | 0.585 |
MOD_GlcNHglycan | 1104 | 1107 | PF01048 | 0.813 |
MOD_GlcNHglycan | 1133 | 1136 | PF01048 | 0.839 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.681 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.321 |
MOD_GlcNHglycan | 221 | 224 | PF01048 | 0.529 |
MOD_GlcNHglycan | 229 | 233 | PF01048 | 0.584 |
MOD_GlcNHglycan | 31 | 34 | PF01048 | 0.549 |
MOD_GlcNHglycan | 377 | 380 | PF01048 | 0.489 |
MOD_GlcNHglycan | 401 | 404 | PF01048 | 0.505 |
MOD_GlcNHglycan | 423 | 426 | PF01048 | 0.471 |
MOD_GlcNHglycan | 452 | 456 | PF01048 | 0.384 |
MOD_GlcNHglycan | 547 | 550 | PF01048 | 0.581 |
MOD_GlcNHglycan | 579 | 582 | PF01048 | 0.515 |
MOD_GlcNHglycan | 626 | 629 | PF01048 | 0.546 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.651 |
MOD_GlcNHglycan | 732 | 735 | PF01048 | 0.448 |
MOD_GlcNHglycan | 908 | 911 | PF01048 | 0.656 |
MOD_GlcNHglycan | 921 | 924 | PF01048 | 0.458 |
MOD_GSK3_1 | 1037 | 1044 | PF00069 | 0.824 |
MOD_GSK3_1 | 1065 | 1072 | PF00069 | 0.813 |
MOD_GSK3_1 | 1085 | 1092 | PF00069 | 0.840 |
MOD_GSK3_1 | 1102 | 1109 | PF00069 | 0.689 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.425 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.586 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.428 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.524 |
MOD_GSK3_1 | 239 | 246 | PF00069 | 0.560 |
MOD_GSK3_1 | 252 | 259 | PF00069 | 0.430 |
MOD_GSK3_1 | 283 | 290 | PF00069 | 0.479 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.478 |
MOD_GSK3_1 | 466 | 473 | PF00069 | 0.538 |
MOD_GSK3_1 | 474 | 481 | PF00069 | 0.530 |
MOD_GSK3_1 | 623 | 630 | PF00069 | 0.568 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.617 |
MOD_GSK3_1 | 674 | 681 | PF00069 | 0.371 |
MOD_GSK3_1 | 719 | 726 | PF00069 | 0.362 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.608 |
MOD_GSK3_1 | 777 | 784 | PF00069 | 0.511 |
MOD_GSK3_1 | 899 | 906 | PF00069 | 0.643 |
MOD_GSK3_1 | 913 | 920 | PF00069 | 0.666 |
MOD_GSK3_1 | 960 | 967 | PF00069 | 0.686 |
MOD_N-GLC_1 | 310 | 315 | PF02516 | 0.545 |
MOD_N-GLC_1 | 520 | 525 | PF02516 | 0.454 |
MOD_N-GLC_1 | 77 | 82 | PF02516 | 0.446 |
MOD_NEK2_1 | 1046 | 1051 | PF00069 | 0.633 |
MOD_NEK2_1 | 143 | 148 | PF00069 | 0.457 |
MOD_NEK2_1 | 164 | 169 | PF00069 | 0.351 |
MOD_NEK2_1 | 264 | 269 | PF00069 | 0.400 |
MOD_NEK2_1 | 289 | 294 | PF00069 | 0.414 |
MOD_NEK2_1 | 399 | 404 | PF00069 | 0.390 |
MOD_NEK2_1 | 435 | 440 | PF00069 | 0.505 |
MOD_NEK2_1 | 466 | 471 | PF00069 | 0.385 |
MOD_NEK2_1 | 65 | 70 | PF00069 | 0.401 |
MOD_NEK2_1 | 914 | 919 | PF00069 | 0.601 |
MOD_NEK2_1 | 93 | 98 | PF00069 | 0.601 |
MOD_NEK2_1 | 930 | 935 | PF00069 | 0.398 |
MOD_NEK2_2 | 34 | 39 | PF00069 | 0.339 |
MOD_PIKK_1 | 72 | 78 | PF00454 | 0.489 |
MOD_PIKK_1 | 984 | 990 | PF00454 | 0.687 |
MOD_PK_1 | 372 | 378 | PF00069 | 0.560 |
MOD_PKA_1 | 1069 | 1075 | PF00069 | 0.830 |
MOD_PKA_1 | 1093 | 1099 | PF00069 | 0.619 |
MOD_PKA_1 | 1102 | 1108 | PF00069 | 0.560 |
MOD_PKA_1 | 371 | 377 | PF00069 | 0.548 |
MOD_PKA_2 | 1029 | 1035 | PF00069 | 0.832 |
MOD_PKA_2 | 1046 | 1052 | PF00069 | 0.687 |
MOD_PKA_2 | 1093 | 1099 | PF00069 | 0.862 |
MOD_PKA_2 | 1102 | 1108 | PF00069 | 0.811 |
MOD_PKA_2 | 28 | 34 | PF00069 | 0.557 |
MOD_PKA_2 | 297 | 303 | PF00069 | 0.507 |
MOD_PKA_2 | 371 | 377 | PF00069 | 0.529 |
MOD_PKA_2 | 781 | 787 | PF00069 | 0.533 |
MOD_PKB_1 | 621 | 629 | PF00069 | 0.464 |
MOD_PKB_1 | 962 | 970 | PF00069 | 0.735 |
MOD_Plk_1 | 390 | 396 | PF00069 | 0.423 |
MOD_Plk_1 | 451 | 457 | PF00069 | 0.510 |
MOD_Plk_1 | 77 | 83 | PF00069 | 0.511 |
MOD_Plk_1 | 99 | 105 | PF00069 | 0.501 |
MOD_Plk_2-3 | 719 | 725 | PF00069 | 0.352 |
MOD_Plk_4 | 154 | 160 | PF00069 | 0.584 |
MOD_Plk_4 | 252 | 258 | PF00069 | 0.437 |
MOD_Plk_4 | 409 | 415 | PF00069 | 0.308 |
MOD_Plk_4 | 523 | 529 | PF00069 | 0.365 |
MOD_Plk_4 | 590 | 596 | PF00069 | 0.394 |
MOD_Plk_4 | 614 | 620 | PF00069 | 0.436 |
MOD_Plk_4 | 674 | 680 | PF00069 | 0.352 |
MOD_Plk_4 | 723 | 729 | PF00069 | 0.366 |
MOD_Plk_4 | 99 | 105 | PF00069 | 0.602 |
MOD_ProDKin_1 | 475 | 481 | PF00069 | 0.497 |
MOD_ProDKin_1 | 520 | 526 | PF00069 | 0.432 |
MOD_ProDKin_1 | 540 | 546 | PF00069 | 0.282 |
MOD_ProDKin_1 | 56 | 62 | PF00069 | 0.574 |
MOD_ProDKin_1 | 612 | 618 | PF00069 | 0.434 |
MOD_ProDKin_1 | 627 | 633 | PF00069 | 0.663 |
MOD_ProDKin_1 | 820 | 826 | PF00069 | 0.413 |
MOD_SUMO_rev_2 | 102 | 111 | PF00179 | 0.624 |
TRG_DiLeu_BaEn_1 | 674 | 679 | PF01217 | 0.484 |
TRG_DiLeu_BaEn_2 | 356 | 362 | PF01217 | 0.363 |
TRG_DiLeu_LyEn_5 | 947 | 952 | PF01217 | 0.545 |
TRG_ENDOCYTIC_2 | 293 | 296 | PF00928 | 0.357 |
TRG_ENDOCYTIC_2 | 3 | 6 | PF00928 | 0.616 |
TRG_ENDOCYTIC_2 | 349 | 352 | PF00928 | 0.552 |
TRG_ENDOCYTIC_2 | 364 | 367 | PF00928 | 0.500 |
TRG_ENDOCYTIC_2 | 468 | 471 | PF00928 | 0.426 |
TRG_ENDOCYTIC_2 | 49 | 52 | PF00928 | 0.525 |
TRG_ENDOCYTIC_2 | 503 | 506 | PF00928 | 0.594 |
TRG_ENDOCYTIC_2 | 657 | 660 | PF00928 | 0.649 |
TRG_ENDOCYTIC_2 | 762 | 765 | PF00928 | 0.360 |
TRG_ENDOCYTIC_2 | 788 | 791 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 810 | 813 | PF00928 | 0.481 |
TRG_ER_diArg_1 | 1052 | 1054 | PF00400 | 0.829 |
TRG_ER_diArg_1 | 130 | 132 | PF00400 | 0.386 |
TRG_ER_diArg_1 | 370 | 372 | PF00400 | 0.296 |
TRG_ER_diArg_1 | 427 | 429 | PF00400 | 0.617 |
TRG_ER_diArg_1 | 620 | 623 | PF00400 | 0.525 |
TRG_ER_diArg_1 | 795 | 798 | PF00400 | 0.354 |
TRG_ER_diArg_1 | 961 | 964 | PF00400 | 0.703 |
TRG_ER_diArg_1 | 990 | 993 | PF00400 | 0.685 |
TRG_Pf-PMV_PEXEL_1 | 706 | 710 | PF00026 | 0.428 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P457 | Leptomonas seymouri | 30% | 86% |
A0A1X0P171 | Trypanosomatidae | 34% | 89% |
A0A3Q8IJB0 | Leishmania donovani | 68% | 86% |
A0A3R7M6J4 | Trypanosoma rangeli | 38% | 100% |
A0A3R7R8G4 | Trypanosoma rangeli | 32% | 100% |
A0A3S5H6Z8 | Leishmania donovani | 68% | 86% |
A0A3S7WU91 | Leishmania donovani | 60% | 81% |
A0A3S7WU94 | Leishmania donovani | 52% | 83% |
A0A3S7WU95 | Leishmania donovani | 67% | 82% |
A0A3S7XB85 | Leishmania donovani | 31% | 81% |
A4H8U6 | Leishmania braziliensis | 65% | 100% |
A4H8V5 | Leishmania braziliensis | 69% | 100% |
A4H8V8 | Leishmania braziliensis | 91% | 81% |
A4HPI4 | Leishmania braziliensis | 30% | 81% |
A4HX84 | Leishmania infantum | 53% | 83% |
A4HX85 | Leishmania infantum | 67% | 82% |
A4HX87 | Leishmania infantum | 60% | 87% |
A4HX88 | Leishmania infantum | 62% | 100% |
A4IDA6 | Leishmania infantum | 31% | 82% |
C9ZM79 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 92% |
C9ZM80 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 92% |
C9ZM81 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 92% |
C9ZM82 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 92% |
C9ZM83 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 89% |
C9ZM86 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 93% |
C9ZN26 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 90% |
C9ZN41 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 93% |
C9ZN43 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 95% |
C9ZN44 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 93% |
C9ZN45 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 93% |
C9ZN46 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 93% |
C9ZNA5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 93% |
C9ZNA6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 95% |
C9ZNH3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 89% |
C9ZNT1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 92% |
C9ZPZ6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 92% |
C9ZQ51 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 92% |
C9ZQ89 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 90% |
C9ZQ90 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
C9ZQ92 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 94% |
C9ZTS4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 90% |
C9ZTS5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 90% |
C9ZTS6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 95% |
C9ZUE6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 95% |
C9ZWQ5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 90% |
C9ZWU2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 94% |
C9ZWU3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
C9ZWY7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 92% |
C9ZZQ4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 92% |
D0A0U3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 93% |
D0A0W7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 91% |
D0A0X5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 90% |
D0A1S1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 92% |
D0A5D2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 95% |
D0A5D5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 92% |
D0A5U0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 92% |
D0A5U1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 92% |
D0A7A0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 92% |
D0A9R3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 94% |
D0AAV3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 91% |
E8NHJ6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 49% | 100% |
E9AQY0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 60% | 81% |
E9AQY1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 54% | 82% |
E9AQY2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 66% | 82% |
E9AQY4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 67% | 86% |
E9ARD7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 54% | 83% |
E9AT96 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 81% |
Q25263 | Leishmania donovani | 68% | 86% |
Q26721 | Trypanosoma brucei brucei | 35% | 93% |
Q27675 | Leishmania donovani | 52% | 83% |
Q4Q1A1 | Leishmania major | 31% | 82% |
Q4QEH9 | Leishmania major | 67% | 100% |
Q4QEI0 | Leishmania major | 67% | 100% |
Q4QEI1 | Leishmania major | 69% | 100% |
Q4QEI2 | Leishmania major | 60% | 100% |
Q4QEI3 | Leishmania major | 52% | 100% |
Q99279 | Trypanosoma brucei brucei | 31% | 92% |
Q99280 | Trypanosoma brucei brucei | 34% | 93% |
V5AYH7 | Trypanosoma cruzi | 36% | 89% |
V5B1C8 | Trypanosoma cruzi | 39% | 100% |