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: 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 | no | yes: 46, no: 29 |
NetGPI | no | yes: 0, no: 75 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 70 |
GO:0110165 | cellular anatomical entity | 1 | 76 |
Related structures:
AlphaFold database: A4H8V5
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 76 |
GO:0006163 | purine nucleotide metabolic process | 5 | 76 |
GO:0006164 | purine nucleotide biosynthetic process | 6 | 76 |
GO:0006171 | cAMP biosynthetic process | 8 | 76 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 76 |
GO:0006753 | nucleoside phosphate metabolic process | 4 | 76 |
GO:0006793 | phosphorus metabolic process | 3 | 76 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 76 |
GO:0006807 | nitrogen compound metabolic process | 2 | 76 |
GO:0007165 | signal transduction | 2 | 76 |
GO:0008152 | metabolic process | 1 | 76 |
GO:0009058 | biosynthetic process | 2 | 76 |
GO:0009117 | nucleotide metabolic process | 5 | 76 |
GO:0009150 | purine ribonucleotide metabolic process | 6 | 76 |
GO:0009152 | purine ribonucleotide biosynthetic process | 7 | 76 |
GO:0009165 | nucleotide biosynthetic process | 6 | 76 |
GO:0009187 | cyclic nucleotide metabolic process | 6 | 76 |
GO:0009190 | cyclic nucleotide biosynthetic process | 7 | 76 |
GO:0009259 | ribonucleotide metabolic process | 5 | 76 |
GO:0009260 | ribonucleotide biosynthetic process | 6 | 76 |
GO:0009987 | cellular process | 1 | 76 |
GO:0018130 | heterocycle biosynthetic process | 4 | 76 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 76 |
GO:0019637 | organophosphate metabolic process | 3 | 76 |
GO:0019693 | ribose phosphate metabolic process | 4 | 76 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 76 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 76 |
GO:0035556 | intracellular signal transduction | 3 | 76 |
GO:0044237 | cellular metabolic process | 2 | 76 |
GO:0044238 | primary metabolic process | 2 | 76 |
GO:0044249 | cellular biosynthetic process | 3 | 76 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 76 |
GO:0044281 | small molecule metabolic process | 2 | 76 |
GO:0046058 | cAMP metabolic process | 7 | 76 |
GO:0046390 | ribose phosphate biosynthetic process | 5 | 76 |
GO:0046483 | heterocycle metabolic process | 3 | 76 |
GO:0050789 | regulation of biological process | 2 | 76 |
GO:0050794 | regulation of cellular process | 3 | 76 |
GO:0052652 | cyclic purine nucleotide metabolic process | 6 | 76 |
GO:0055086 | nucleobase-containing small molecule metabolic process | 3 | 76 |
GO:0065007 | biological regulation | 1 | 76 |
GO:0071704 | organic substance metabolic process | 2 | 76 |
GO:0072521 | purine-containing compound metabolic process | 4 | 76 |
GO:0072522 | purine-containing compound biosynthetic process | 5 | 76 |
GO:0090407 | organophosphate biosynthetic process | 4 | 76 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 76 |
GO:1901137 | carbohydrate derivative biosynthetic process | 4 | 76 |
GO:1901293 | nucleoside phosphate biosynthetic process | 5 | 76 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 76 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 76 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 76 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 76 |
GO:1901576 | organic substance biosynthetic process | 3 | 76 |
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 | 1010 | 1014 | PF00656 | 0.811 |
CLV_C14_Caspase3-7 | 609 | 613 | PF00656 | 0.663 |
CLV_C14_Caspase3-7 | 670 | 674 | PF00656 | 0.505 |
CLV_MEL_PAP_1 | 743 | 749 | PF00089 | 0.296 |
CLV_NRD_NRD_1 | 1018 | 1020 | PF00675 | 0.419 |
CLV_NRD_NRD_1 | 114 | 116 | PF00675 | 0.535 |
CLV_NRD_NRD_1 | 78 | 80 | PF00675 | 0.714 |
CLV_NRD_NRD_1 | 833 | 835 | PF00675 | 0.426 |
CLV_PCSK_KEX2_1 | 1018 | 1020 | PF00082 | 0.416 |
CLV_PCSK_KEX2_1 | 114 | 116 | PF00082 | 0.487 |
CLV_PCSK_KEX2_1 | 78 | 80 | PF00082 | 0.515 |
CLV_PCSK_KEX2_1 | 833 | 835 | PF00082 | 0.426 |
CLV_PCSK_SKI1_1 | 177 | 181 | PF00082 | 0.567 |
CLV_PCSK_SKI1_1 | 254 | 258 | PF00082 | 0.520 |
CLV_PCSK_SKI1_1 | 340 | 344 | PF00082 | 0.545 |
CLV_PCSK_SKI1_1 | 457 | 461 | PF00082 | 0.659 |
CLV_PCSK_SKI1_1 | 475 | 479 | PF00082 | 0.594 |
CLV_PCSK_SKI1_1 | 78 | 82 | PF00082 | 0.634 |
CLV_PCSK_SKI1_1 | 926 | 930 | PF00082 | 0.444 |
DEG_APCC_DBOX_1 | 811 | 819 | PF00400 | 0.412 |
DEG_ODPH_VHL_1 | 373 | 384 | PF01847 | 0.241 |
DEG_SPOP_SBC_1 | 494 | 498 | PF00917 | 0.524 |
DOC_CKS1_1 | 141 | 146 | PF01111 | 0.279 |
DOC_CKS1_1 | 561 | 566 | PF01111 | 0.408 |
DOC_CYCLIN_yCln2_LP_2 | 105 | 111 | PF00134 | 0.272 |
DOC_CYCLIN_yCln2_LP_2 | 558 | 564 | PF00134 | 0.411 |
DOC_MAPK_MEF2A_6 | 196 | 205 | PF00069 | 0.454 |
DOC_MAPK_MEF2A_6 | 475 | 482 | PF00069 | 0.340 |
DOC_MAPK_RevD_3 | 820 | 834 | PF00069 | 0.620 |
DOC_PP1_RVXF_1 | 375 | 381 | PF00149 | 0.266 |
DOC_PP2B_LxvP_1 | 1062 | 1065 | PF13499 | 0.762 |
DOC_PP2B_LxvP_1 | 558 | 561 | PF13499 | 0.486 |
DOC_PP4_FxxP_1 | 284 | 287 | PF00568 | 0.311 |
DOC_PP4_FxxP_1 | 298 | 301 | PF00568 | 0.386 |
DOC_PP4_FxxP_1 | 353 | 356 | PF00568 | 0.478 |
DOC_PP4_FxxP_1 | 463 | 466 | PF00568 | 0.325 |
DOC_USP7_MATH_1 | 1007 | 1011 | PF00917 | 0.760 |
DOC_USP7_MATH_1 | 1038 | 1042 | PF00917 | 0.695 |
DOC_USP7_MATH_1 | 1046 | 1050 | PF00917 | 0.695 |
DOC_USP7_MATH_1 | 319 | 323 | PF00917 | 0.462 |
DOC_USP7_MATH_1 | 356 | 360 | PF00917 | 0.459 |
DOC_USP7_MATH_1 | 365 | 369 | PF00917 | 0.462 |
DOC_USP7_MATH_1 | 398 | 402 | PF00917 | 0.425 |
DOC_USP7_MATH_1 | 678 | 682 | PF00917 | 0.573 |
DOC_USP7_MATH_1 | 932 | 936 | PF00917 | 0.711 |
DOC_USP7_MATH_1 | 977 | 981 | PF00917 | 0.829 |
DOC_WW_Pin1_4 | 140 | 145 | PF00397 | 0.462 |
DOC_WW_Pin1_4 | 278 | 283 | PF00397 | 0.349 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.543 |
DOC_WW_Pin1_4 | 361 | 366 | PF00397 | 0.357 |
DOC_WW_Pin1_4 | 450 | 455 | PF00397 | 0.437 |
DOC_WW_Pin1_4 | 467 | 472 | PF00397 | 0.361 |
DOC_WW_Pin1_4 | 560 | 565 | PF00397 | 0.373 |
DOC_WW_Pin1_4 | 575 | 580 | PF00397 | 0.444 |
LIG_14-3-3_CanoR_1 | 1018 | 1024 | PF00244 | 0.614 |
LIG_14-3-3_CanoR_1 | 126 | 135 | PF00244 | 0.374 |
LIG_14-3-3_CanoR_1 | 217 | 222 | PF00244 | 0.311 |
LIG_14-3-3_CanoR_1 | 432 | 437 | PF00244 | 0.440 |
LIG_14-3-3_CanoR_1 | 457 | 466 | PF00244 | 0.460 |
LIG_14-3-3_CanoR_1 | 502 | 509 | PF00244 | 0.364 |
LIG_14-3-3_CanoR_1 | 571 | 579 | PF00244 | 0.546 |
LIG_14-3-3_CanoR_1 | 730 | 736 | PF00244 | 0.532 |
LIG_14-3-3_CanoR_1 | 912 | 920 | PF00244 | 0.680 |
LIG_14-3-3_CanoR_1 | 930 | 935 | PF00244 | 0.672 |
LIG_Actin_WH2_2 | 1005 | 1020 | PF00022 | 0.587 |
LIG_Actin_WH2_2 | 257 | 272 | PF00022 | 0.260 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.385 |
LIG_BIR_III_2 | 614 | 618 | PF00653 | 0.644 |
LIG_BIR_III_2 | 828 | 832 | PF00653 | 0.587 |
LIG_BRCT_BRCA1_1 | 170 | 174 | PF00533 | 0.463 |
LIG_BRCT_BRCA1_1 | 280 | 284 | PF00533 | 0.245 |
LIG_BRCT_BRCA1_1 | 478 | 482 | PF00533 | 0.416 |
LIG_DLG_GKlike_1 | 432 | 439 | PF00625 | 0.269 |
LIG_FHA_1 | 1055 | 1061 | PF00498 | 0.710 |
LIG_FHA_1 | 16 | 22 | PF00498 | 0.376 |
LIG_FHA_1 | 258 | 264 | PF00498 | 0.383 |
LIG_FHA_1 | 275 | 281 | PF00498 | 0.242 |
LIG_FHA_1 | 350 | 356 | PF00498 | 0.368 |
LIG_FHA_1 | 358 | 364 | PF00498 | 0.356 |
LIG_FHA_1 | 41 | 47 | PF00498 | 0.515 |
LIG_FHA_1 | 468 | 474 | PF00498 | 0.378 |
LIG_FHA_1 | 561 | 567 | PF00498 | 0.342 |
LIG_FHA_1 | 692 | 698 | PF00498 | 0.570 |
LIG_FHA_1 | 701 | 707 | PF00498 | 0.505 |
LIG_FHA_1 | 726 | 732 | PF00498 | 0.513 |
LIG_FHA_1 | 776 | 782 | PF00498 | 0.510 |
LIG_FHA_2 | 383 | 389 | PF00498 | 0.375 |
LIG_FHA_2 | 4 | 10 | PF00498 | 0.540 |
LIG_FHA_2 | 576 | 582 | PF00498 | 0.511 |
LIG_FHA_2 | 627 | 633 | PF00498 | 0.507 |
LIG_FHA_2 | 668 | 674 | PF00498 | 0.509 |
LIG_FHA_2 | 838 | 844 | PF00498 | 0.750 |
LIG_FHA_2 | 848 | 854 | PF00498 | 0.801 |
LIG_FXI_DFP_1 | 205 | 209 | PF00024 | 0.577 |
LIG_GBD_Chelix_1 | 688 | 696 | PF00786 | 0.416 |
LIG_IRF3_LxIS_1 | 274 | 281 | PF10401 | 0.256 |
LIG_LIR_Apic_2 | 137 | 141 | PF02991 | 0.410 |
LIG_LIR_Apic_2 | 281 | 287 | PF02991 | 0.367 |
LIG_LIR_Apic_2 | 352 | 356 | PF02991 | 0.479 |
LIG_LIR_Apic_2 | 460 | 466 | PF02991 | 0.455 |
LIG_LIR_Apic_2 | 721 | 727 | PF02991 | 0.492 |
LIG_LIR_Gen_1 | 22 | 31 | PF02991 | 0.312 |
LIG_LIR_Gen_1 | 232 | 241 | PF02991 | 0.418 |
LIG_LIR_Gen_1 | 294 | 303 | PF02991 | 0.434 |
LIG_LIR_Gen_1 | 407 | 415 | PF02991 | 0.299 |
LIG_LIR_Gen_1 | 435 | 441 | PF02991 | 0.357 |
LIG_LIR_Gen_1 | 625 | 636 | PF02991 | 0.507 |
LIG_LIR_Gen_1 | 733 | 743 | PF02991 | 0.560 |
LIG_LIR_Gen_1 | 755 | 765 | PF02991 | 0.604 |
LIG_LIR_Gen_1 | 996 | 1004 | PF02991 | 0.759 |
LIG_LIR_Nem_3 | 206 | 211 | PF02991 | 0.384 |
LIG_LIR_Nem_3 | 22 | 26 | PF02991 | 0.333 |
LIG_LIR_Nem_3 | 232 | 236 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 294 | 299 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 306 | 311 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 407 | 411 | PF02991 | 0.329 |
LIG_LIR_Nem_3 | 414 | 418 | PF02991 | 0.345 |
LIG_LIR_Nem_3 | 435 | 439 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 531 | 537 | PF02991 | 0.492 |
LIG_LIR_Nem_3 | 625 | 631 | PF02991 | 0.507 |
LIG_LIR_Nem_3 | 635 | 641 | PF02991 | 0.609 |
LIG_LIR_Nem_3 | 700 | 704 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 707 | 713 | PF02991 | 0.507 |
LIG_LIR_Nem_3 | 733 | 739 | PF02991 | 0.507 |
LIG_LIR_Nem_3 | 755 | 761 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 762 | 768 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 791 | 797 | PF02991 | 0.516 |
LIG_LIR_Nem_3 | 881 | 887 | PF02991 | 0.691 |
LIG_LIR_Nem_3 | 917 | 923 | PF02991 | 0.607 |
LIG_LIR_Nem_3 | 996 | 1000 | PF02991 | 0.835 |
LIG_MYND_3 | 300 | 304 | PF01753 | 0.446 |
LIG_PCNA_yPIPBox_3 | 582 | 590 | PF02747 | 0.261 |
LIG_Pex14_2 | 459 | 463 | PF04695 | 0.301 |
LIG_Rb_pABgroove_1 | 116 | 124 | PF01858 | 0.329 |
LIG_RPA_C_Fungi | 308 | 320 | PF08784 | 0.255 |
LIG_SH2_CRK | 138 | 142 | PF00017 | 0.503 |
LIG_SH2_CRK | 23 | 27 | PF00017 | 0.366 |
LIG_SH2_CRK | 415 | 419 | PF00017 | 0.581 |
LIG_SH2_GRB2like | 23 | 26 | PF00017 | 0.654 |
LIG_SH2_GRB2like | 534 | 537 | PF00017 | 0.368 |
LIG_SH2_NCK_1 | 23 | 27 | PF00017 | 0.460 |
LIG_SH2_NCK_1 | 334 | 338 | PF00017 | 0.609 |
LIG_SH2_NCK_1 | 758 | 762 | PF00017 | 0.481 |
LIG_SH2_PTP2 | 724 | 727 | PF00017 | 0.395 |
LIG_SH2_SRC | 127 | 130 | PF00017 | 0.548 |
LIG_SH2_SRC | 23 | 26 | PF00017 | 0.594 |
LIG_SH2_SRC | 724 | 727 | PF00017 | 0.414 |
LIG_SH2_SRC | 758 | 761 | PF00017 | 0.481 |
LIG_SH2_STAP1 | 182 | 186 | PF00017 | 0.521 |
LIG_SH2_STAP1 | 259 | 263 | PF00017 | 0.468 |
LIG_SH2_STAP1 | 311 | 315 | PF00017 | 0.270 |
LIG_SH2_STAP1 | 415 | 419 | PF00017 | 0.331 |
LIG_SH2_STAP1 | 736 | 740 | PF00017 | 0.432 |
LIG_SH2_STAT3 | 154 | 157 | PF00017 | 0.613 |
LIG_SH2_STAT3 | 39 | 42 | PF00017 | 0.336 |
LIG_SH2_STAT3 | 537 | 540 | PF00017 | 0.399 |
LIG_SH2_STAT5 | 117 | 120 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 127 | 130 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 133 | 136 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 154 | 157 | PF00017 | 0.558 |
LIG_SH2_STAT5 | 188 | 191 | PF00017 | 0.523 |
LIG_SH2_STAT5 | 259 | 262 | PF00017 | 0.596 |
LIG_SH2_STAT5 | 296 | 299 | PF00017 | 0.487 |
LIG_SH2_STAT5 | 308 | 311 | PF00017 | 0.336 |
LIG_SH2_STAT5 | 504 | 507 | PF00017 | 0.492 |
LIG_SH2_STAT5 | 605 | 608 | PF00017 | 0.567 |
LIG_SH2_STAT5 | 724 | 727 | PF00017 | 0.321 |
LIG_SH3_1 | 138 | 144 | PF00018 | 0.358 |
LIG_SH3_3 | 138 | 144 | PF00018 | 0.358 |
LIG_SH3_3 | 191 | 197 | PF00018 | 0.417 |
LIG_SH3_3 | 276 | 282 | PF00018 | 0.425 |
LIG_SH3_3 | 394 | 400 | PF00018 | 0.313 |
LIG_SH3_3 | 550 | 556 | PF00018 | 0.468 |
LIG_SH3_3 | 558 | 564 | PF00018 | 0.435 |
LIG_SH3_3 | 902 | 908 | PF00018 | 0.534 |
LIG_SUMO_SIM_anti_2 | 260 | 265 | PF11976 | 0.576 |
LIG_SUMO_SIM_anti_2 | 401 | 407 | PF11976 | 0.474 |
LIG_SUMO_SIM_anti_2 | 621 | 630 | PF11976 | 0.359 |
LIG_SUMO_SIM_par_1 | 259 | 265 | PF11976 | 0.314 |
LIG_SUMO_SIM_par_1 | 276 | 281 | PF11976 | 0.327 |
LIG_SUMO_SIM_par_1 | 541 | 546 | PF11976 | 0.387 |
LIG_SUMO_SIM_par_1 | 590 | 596 | PF11976 | 0.452 |
LIG_SUMO_SIM_par_1 | 702 | 707 | PF11976 | 0.223 |
LIG_TRAF2_1 | 1074 | 1077 | PF00917 | 0.488 |
LIG_TRAF2_1 | 498 | 501 | PF00917 | 0.467 |
LIG_TRAF2_1 | 732 | 735 | PF00917 | 0.419 |
LIG_TRAF2_1 | 798 | 801 | PF00917 | 0.401 |
LIG_TYR_ITIM | 21 | 26 | PF00017 | 0.600 |
LIG_TYR_ITIM | 756 | 761 | PF00017 | 0.484 |
LIG_UBA3_1 | 163 | 169 | PF00899 | 0.623 |
LIG_WRC_WIRS_1 | 392 | 397 | PF05994 | 0.495 |
LIG_WRC_WIRS_1 | 405 | 410 | PF05994 | 0.355 |
LIG_WRC_WIRS_1 | 433 | 438 | PF05994 | 0.563 |
LIG_WW_3 | 907 | 911 | PF00397 | 0.692 |
LIG_WW_3 | 984 | 988 | PF00397 | 0.833 |
MOD_CDK_SPxxK_3 | 450 | 457 | PF00069 | 0.561 |
MOD_CDK_SPxxK_3 | 575 | 582 | PF00069 | 0.536 |
MOD_CK1_1 | 1022 | 1028 | PF00069 | 0.580 |
MOD_CK1_1 | 1037 | 1043 | PF00069 | 0.824 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.686 |
MOD_CK1_1 | 175 | 181 | PF00069 | 0.551 |
MOD_CK1_1 | 335 | 341 | PF00069 | 0.464 |
MOD_CK1_1 | 368 | 374 | PF00069 | 0.537 |
MOD_CK1_1 | 414 | 420 | PF00069 | 0.415 |
MOD_CK1_1 | 435 | 441 | PF00069 | 0.485 |
MOD_CK1_1 | 443 | 449 | PF00069 | 0.564 |
MOD_CK1_1 | 522 | 528 | PF00069 | 0.510 |
MOD_CK1_1 | 575 | 581 | PF00069 | 0.634 |
MOD_CK1_1 | 681 | 687 | PF00069 | 0.502 |
MOD_CK1_1 | 70 | 76 | PF00069 | 0.701 |
MOD_CK1_1 | 865 | 871 | PF00069 | 0.615 |
MOD_CK1_1 | 980 | 986 | PF00069 | 0.812 |
MOD_CK2_1 | 1041 | 1047 | PF00069 | 0.837 |
MOD_CK2_1 | 445 | 451 | PF00069 | 0.393 |
MOD_CK2_1 | 495 | 501 | PF00069 | 0.519 |
MOD_CK2_1 | 575 | 581 | PF00069 | 0.694 |
MOD_CK2_1 | 626 | 632 | PF00069 | 0.357 |
MOD_CK2_1 | 729 | 735 | PF00069 | 0.419 |
MOD_CK2_1 | 795 | 801 | PF00069 | 0.364 |
MOD_CK2_1 | 837 | 843 | PF00069 | 0.681 |
MOD_CK2_1 | 847 | 853 | PF00069 | 0.705 |
MOD_Cter_Amidation | 831 | 834 | PF01082 | 0.551 |
MOD_GlcNHglycan | 1036 | 1039 | PF01048 | 0.824 |
MOD_GlcNHglycan | 1040 | 1043 | PF01048 | 0.830 |
MOD_GlcNHglycan | 1047 | 1051 | PF01048 | 0.811 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.713 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.574 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.267 |
MOD_GlcNHglycan | 227 | 231 | PF01048 | 0.506 |
MOD_GlcNHglycan | 323 | 326 | PF01048 | 0.471 |
MOD_GlcNHglycan | 335 | 338 | PF01048 | 0.495 |
MOD_GlcNHglycan | 400 | 403 | PF01048 | 0.389 |
MOD_GlcNHglycan | 447 | 450 | PF01048 | 0.459 |
MOD_GlcNHglycan | 527 | 530 | PF01048 | 0.538 |
MOD_GlcNHglycan | 574 | 577 | PF01048 | 0.675 |
MOD_GlcNHglycan | 680 | 683 | PF01048 | 0.450 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.706 |
MOD_GlcNHglycan | 856 | 859 | PF01048 | 0.686 |
MOD_GlcNHglycan | 869 | 872 | PF01048 | 0.454 |
MOD_GlcNHglycan | 979 | 982 | PF01048 | 0.800 |
MOD_GlcNHglycan | 989 | 994 | PF01048 | 0.735 |
MOD_GSK3_1 | 1007 | 1014 | PF00069 | 0.776 |
MOD_GSK3_1 | 1018 | 1025 | PF00069 | 0.810 |
MOD_GSK3_1 | 1034 | 1041 | PF00069 | 0.824 |
MOD_GSK3_1 | 1042 | 1049 | PF00069 | 0.817 |
MOD_GSK3_1 | 1054 | 1061 | PF00069 | 0.758 |
MOD_GSK3_1 | 11 | 18 | PF00069 | 0.701 |
MOD_GSK3_1 | 168 | 175 | PF00069 | 0.585 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.526 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.355 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.458 |
MOD_GSK3_1 | 357 | 364 | PF00069 | 0.489 |
MOD_GSK3_1 | 365 | 372 | PF00069 | 0.528 |
MOD_GSK3_1 | 420 | 427 | PF00069 | 0.534 |
MOD_GSK3_1 | 465 | 472 | PF00069 | 0.474 |
MOD_GSK3_1 | 519 | 526 | PF00069 | 0.567 |
MOD_GSK3_1 | 556 | 563 | PF00069 | 0.483 |
MOD_GSK3_1 | 571 | 578 | PF00069 | 0.567 |
MOD_GSK3_1 | 622 | 629 | PF00069 | 0.374 |
MOD_GSK3_1 | 667 | 674 | PF00069 | 0.363 |
MOD_GSK3_1 | 725 | 732 | PF00069 | 0.515 |
MOD_GSK3_1 | 847 | 854 | PF00069 | 0.625 |
MOD_GSK3_1 | 861 | 868 | PF00069 | 0.679 |
MOD_GSK3_1 | 908 | 915 | PF00069 | 0.662 |
MOD_GSK3_1 | 985 | 992 | PF00069 | 0.789 |
MOD_N-GLC_1 | 203 | 208 | PF02516 | 0.512 |
MOD_N-GLC_1 | 241 | 246 | PF02516 | 0.437 |
MOD_N-GLC_1 | 257 | 262 | PF02516 | 0.615 |
MOD_N-GLC_1 | 274 | 279 | PF02516 | 0.295 |
MOD_N-GLC_1 | 494 | 499 | PF02516 | 0.538 |
MOD_NEK2_1 | 1011 | 1016 | PF00069 | 0.584 |
MOD_NEK2_1 | 1029 | 1034 | PF00069 | 0.496 |
MOD_NEK2_1 | 12 | 17 | PF00069 | 0.492 |
MOD_NEK2_1 | 241 | 246 | PF00069 | 0.430 |
MOD_NEK2_1 | 40 | 45 | PF00069 | 0.608 |
MOD_NEK2_1 | 434 | 439 | PF00069 | 0.308 |
MOD_NEK2_1 | 458 | 463 | PF00069 | 0.530 |
MOD_NEK2_1 | 519 | 524 | PF00069 | 0.505 |
MOD_NEK2_1 | 862 | 867 | PF00069 | 0.589 |
MOD_NEK2_1 | 878 | 883 | PF00069 | 0.390 |
MOD_PIKK_1 | 241 | 247 | PF00454 | 0.470 |
MOD_PIKK_1 | 85 | 91 | PF00454 | 0.541 |
MOD_PIKK_1 | 932 | 938 | PF00454 | 0.681 |
MOD_PK_1 | 1019 | 1025 | PF00069 | 0.486 |
MOD_PKA_1 | 1018 | 1024 | PF00069 | 0.513 |
MOD_PKA_2 | 1018 | 1024 | PF00069 | 0.538 |
MOD_PKA_2 | 285 | 291 | PF00069 | 0.401 |
MOD_PKA_2 | 729 | 735 | PF00069 | 0.391 |
MOD_PKA_2 | 977 | 983 | PF00069 | 0.841 |
MOD_PKB_1 | 569 | 577 | PF00069 | 0.464 |
MOD_PKB_1 | 910 | 918 | PF00069 | 0.717 |
MOD_Plk_1 | 257 | 263 | PF00069 | 0.547 |
MOD_Plk_1 | 340 | 346 | PF00069 | 0.452 |
MOD_Plk_1 | 46 | 52 | PF00069 | 0.496 |
MOD_Plk_1 | 494 | 500 | PF00069 | 0.509 |
MOD_Plk_2-3 | 1072 | 1078 | PF00069 | 0.519 |
MOD_Plk_2-3 | 667 | 673 | PF00069 | 0.353 |
MOD_Plk_4 | 1007 | 1013 | PF00069 | 0.783 |
MOD_Plk_4 | 1029 | 1035 | PF00069 | 0.481 |
MOD_Plk_4 | 274 | 280 | PF00069 | 0.345 |
MOD_Plk_4 | 285 | 291 | PF00069 | 0.429 |
MOD_Plk_4 | 391 | 397 | PF00069 | 0.524 |
MOD_Plk_4 | 414 | 420 | PF00069 | 0.460 |
MOD_Plk_4 | 458 | 464 | PF00069 | 0.481 |
MOD_Plk_4 | 46 | 52 | PF00069 | 0.603 |
MOD_Plk_4 | 469 | 475 | PF00069 | 0.376 |
MOD_Plk_4 | 538 | 544 | PF00069 | 0.413 |
MOD_Plk_4 | 562 | 568 | PF00069 | 0.445 |
MOD_Plk_4 | 622 | 628 | PF00069 | 0.355 |
MOD_Plk_4 | 671 | 677 | PF00069 | 0.367 |
MOD_ProDKin_1 | 140 | 146 | PF00069 | 0.570 |
MOD_ProDKin_1 | 278 | 284 | PF00069 | 0.415 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.684 |
MOD_ProDKin_1 | 361 | 367 | PF00069 | 0.425 |
MOD_ProDKin_1 | 450 | 456 | PF00069 | 0.531 |
MOD_ProDKin_1 | 467 | 473 | PF00069 | 0.428 |
MOD_ProDKin_1 | 560 | 566 | PF00069 | 0.441 |
MOD_ProDKin_1 | 575 | 581 | PF00069 | 0.543 |
MOD_SUMO_rev_2 | 49 | 58 | PF00179 | 0.638 |
TRG_DiLeu_BaEn_1 | 622 | 627 | PF01217 | 0.485 |
TRG_DiLeu_BaLyEn_6 | 264 | 269 | PF01217 | 0.536 |
TRG_DiLeu_LyEn_5 | 895 | 900 | PF01217 | 0.549 |
TRG_ENDOCYTIC_2 | 23 | 26 | PF00928 | 0.415 |
TRG_ENDOCYTIC_2 | 296 | 299 | PF00928 | 0.545 |
TRG_ENDOCYTIC_2 | 311 | 314 | PF00928 | 0.553 |
TRG_ENDOCYTIC_2 | 415 | 418 | PF00928 | 0.421 |
TRG_ENDOCYTIC_2 | 605 | 608 | PF00928 | 0.642 |
TRG_ENDOCYTIC_2 | 710 | 713 | PF00928 | 0.361 |
TRG_ENDOCYTIC_2 | 736 | 739 | PF00928 | 0.345 |
TRG_ENDOCYTIC_2 | 758 | 761 | PF00928 | 0.478 |
TRG_ER_diArg_1 | 1017 | 1019 | PF00400 | 0.507 |
TRG_ER_diArg_1 | 568 | 571 | PF00400 | 0.532 |
TRG_ER_diArg_1 | 743 | 746 | PF00400 | 0.353 |
TRG_ER_diArg_1 | 77 | 79 | PF00400 | 0.400 |
TRG_ER_diArg_1 | 909 | 912 | PF00400 | 0.685 |
TRG_ER_diArg_1 | 938 | 941 | PF00400 | 0.713 |
TRG_Pf-PMV_PEXEL_1 | 654 | 658 | PF00026 | 0.430 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P457 | Leptomonas seymouri | 30% | 81% |
A0A0S4J2K5 | Bodo saltans | 27% | 81% |
A0A1X0P171 | Trypanosomatidae | 36% | 84% |
A0A3Q8IJB0 | Leishmania donovani | 62% | 81% |
A0A3R7M6J4 | Trypanosoma rangeli | 38% | 100% |
A0A3S5H6Z8 | Leishmania donovani | 62% | 81% |
A0A3S7WU91 | Leishmania donovani | 68% | 76% |
A0A3S7WU94 | Leishmania donovani | 57% | 78% |
A0A3S7WU95 | Leishmania donovani | 60% | 77% |
A0A3S7XB85 | Leishmania donovani | 30% | 77% |
A4H8U6 | Leishmania braziliensis | 68% | 100% |
A4H8V7 | Leishmania braziliensis | 69% | 94% |
A4H8V8 | Leishmania braziliensis | 70% | 77% |
A4HPI4 | Leishmania braziliensis | 29% | 77% |
A4HX84 | Leishmania infantum | 57% | 78% |
A4HX85 | Leishmania infantum | 60% | 77% |
A4HX87 | Leishmania infantum | 68% | 82% |
A4IDA6 | Leishmania infantum | 30% | 77% |
C9ZM79 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 87% |
C9ZM80 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 87% |
C9ZM81 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 86% |
C9ZM82 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 87% |
C9ZM83 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 84% |
C9ZM86 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 88% |
C9ZN26 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 85% |
C9ZN41 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 88% |
C9ZN43 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 90% |
C9ZN44 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 88% |
C9ZN45 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 88% |
C9ZN46 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 88% |
C9ZNA5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 87% |
C9ZNA6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 89% |
C9ZNH3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 84% |
C9ZNT1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 86% |
C9ZPZ6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 87% |
C9ZQ51 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 87% |
C9ZQ89 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 85% |
C9ZQ90 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
C9ZQ92 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 89% |
C9ZTS4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 85% |
C9ZTS5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 85% |
C9ZTS6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 90% |
C9ZUE6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 90% |
C9ZWQ5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 85% |
C9ZWU1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 80% |
C9ZWU2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 89% |
C9ZWU3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 98% |
C9ZWY7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 87% |
C9ZZQ4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 87% |
D0A0U3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 87% |
D0A0W7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 86% |
D0A0X5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 85% |
D0A1S1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 87% |
D0A5D2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 89% |
D0A5D5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 87% |
D0A5U0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 87% |
D0A5U1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 87% |
D0A7A0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 87% |
D0A9R3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 89% |
D0AAV3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 86% |
E9AQY0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 67% | 77% |
E9AQY1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 56% | 78% |
E9AQY2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 59% | 77% |
E9AQY4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 62% | 81% |
E9ARD7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 55% | 79% |
E9AT96 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 77% |
Q25263 | Leishmania donovani | 63% | 81% |
Q26721 | Trypanosoma brucei brucei | 39% | 87% |
Q27675 | Leishmania donovani | 56% | 78% |
Q4Q1A1 | Leishmania major | 29% | 77% |
Q4QEH9 | Leishmania major | 62% | 100% |
Q4QEI0 | Leishmania major | 62% | 100% |
Q4QEI1 | Leishmania major | 62% | 100% |
Q4QEI2 | Leishmania major | 68% | 100% |
Q4QEI3 | Leishmania major | 56% | 100% |
Q99279 | Trypanosoma brucei brucei | 33% | 87% |
Q99280 | Trypanosoma brucei brucei | 36% | 88% |
V5AYH7 | Trypanosoma cruzi | 34% | 84% |
V5B1C8 | Trypanosoma cruzi | 39% | 100% |