Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 4 |
Forrest at al. (procyclic) | no | yes: 4 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 12 |
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: 10 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HI17
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 13 |
GO:0007165 | signal transduction | 2 | 13 |
GO:0008152 | metabolic process | 1 | 13 |
GO:0009987 | cellular process | 1 | 13 |
GO:0035556 | intracellular signal transduction | 3 | 13 |
GO:0044238 | primary metabolic process | 2 | 13 |
GO:0050789 | regulation of biological process | 2 | 13 |
GO:0050794 | regulation of cellular process | 3 | 13 |
GO:0065007 | biological regulation | 1 | 13 |
GO:0071704 | organic substance metabolic process | 2 | 13 |
GO:0048015 | phosphatidylinositol-mediated signaling | 5 | 1 |
GO:0048017 | inositol lipid-mediated signaling | 4 | 1 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0016042 | lipid catabolic process | 4 | 1 |
GO:1901575 | organic substance catabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 13 |
GO:0008081 | phosphoric diester hydrolase activity | 5 | 13 |
GO:0016787 | hydrolase activity | 2 | 13 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 13 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 13 |
GO:0004435 | phosphatidylinositol phospholipase C activity | 7 | 2 |
GO:0004620 | phospholipase activity | 5 | 2 |
GO:0004629 | phospholipase C activity | 6 | 2 |
GO:0016298 | lipase activity | 4 | 2 |
GO:0005488 | binding | 1 | 1 |
GO:0005509 | calcium ion binding | 5 | 1 |
GO:0043167 | ion binding | 2 | 1 |
GO:0043169 | cation binding | 3 | 1 |
GO:0046872 | metal ion binding | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 576 | 580 | PF00656 | 0.606 |
CLV_C14_Caspase3-7 | 61 | 65 | PF00656 | 0.442 |
CLV_C14_Caspase3-7 | 90 | 94 | PF00656 | 0.356 |
CLV_NRD_NRD_1 | 413 | 415 | PF00675 | 0.240 |
CLV_NRD_NRD_1 | 496 | 498 | PF00675 | 0.476 |
CLV_NRD_NRD_1 | 555 | 557 | PF00675 | 0.484 |
CLV_PCSK_KEX2_1 | 28 | 30 | PF00082 | 0.775 |
CLV_PCSK_KEX2_1 | 314 | 316 | PF00082 | 0.473 |
CLV_PCSK_KEX2_1 | 496 | 498 | PF00082 | 0.511 |
CLV_PCSK_PC1ET2_1 | 28 | 30 | PF00082 | 0.775 |
CLV_PCSK_PC1ET2_1 | 314 | 316 | PF00082 | 0.473 |
CLV_PCSK_SKI1_1 | 133 | 137 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 158 | 162 | PF00082 | 0.490 |
CLV_PCSK_SKI1_1 | 213 | 217 | PF00082 | 0.422 |
CLV_PCSK_SKI1_1 | 249 | 253 | PF00082 | 0.549 |
CLV_PCSK_SKI1_1 | 314 | 318 | PF00082 | 0.410 |
CLV_PCSK_SKI1_1 | 36 | 40 | PF00082 | 0.758 |
CLV_PCSK_SKI1_1 | 415 | 419 | PF00082 | 0.239 |
CLV_PCSK_SKI1_1 | 557 | 561 | PF00082 | 0.569 |
CLV_PCSK_SKI1_1 | 690 | 694 | PF00082 | 0.494 |
CLV_PCSK_SKI1_1 | 78 | 82 | PF00082 | 0.365 |
DEG_APCC_DBOX_1 | 117 | 125 | PF00400 | 0.504 |
DEG_APCC_DBOX_1 | 480 | 488 | PF00400 | 0.367 |
DEG_APCC_DBOX_1 | 496 | 504 | PF00400 | 0.503 |
DOC_ANK_TNKS_1 | 314 | 321 | PF00023 | 0.455 |
DOC_CKS1_1 | 368 | 373 | PF01111 | 0.360 |
DOC_CYCLIN_RxL_1 | 130 | 141 | PF00134 | 0.467 |
DOC_CYCLIN_RxL_1 | 155 | 165 | PF00134 | 0.493 |
DOC_CYCLIN_RxL_1 | 72 | 82 | PF00134 | 0.384 |
DOC_MAPK_gen_1 | 114 | 123 | PF00069 | 0.422 |
DOC_MAPK_gen_1 | 425 | 432 | PF00069 | 0.487 |
DOC_MAPK_MEF2A_6 | 114 | 123 | PF00069 | 0.438 |
DOC_MAPK_MEF2A_6 | 425 | 432 | PF00069 | 0.463 |
DOC_MAPK_MEF2A_6 | 439 | 446 | PF00069 | 0.246 |
DOC_MAPK_MEF2A_6 | 98 | 105 | PF00069 | 0.406 |
DOC_MAPK_NFAT4_5 | 116 | 124 | PF00069 | 0.561 |
DOC_MAPK_NFAT4_5 | 98 | 106 | PF00069 | 0.486 |
DOC_PP1_RVXF_1 | 192 | 199 | PF00149 | 0.495 |
DOC_PP1_RVXF_1 | 597 | 604 | PF00149 | 0.393 |
DOC_PP1_RVXF_1 | 73 | 80 | PF00149 | 0.286 |
DOC_PP2B_LxvP_1 | 135 | 138 | PF13499 | 0.525 |
DOC_USP7_MATH_1 | 17 | 21 | PF00917 | 0.611 |
DOC_USP7_MATH_1 | 284 | 288 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 518 | 522 | PF00917 | 0.473 |
DOC_USP7_MATH_1 | 545 | 549 | PF00917 | 0.530 |
DOC_USP7_MATH_1 | 645 | 649 | PF00917 | 0.561 |
DOC_USP7_MATH_1 | 707 | 711 | PF00917 | 0.484 |
DOC_USP7_UBL2_3 | 116 | 120 | PF12436 | 0.476 |
DOC_WW_Pin1_4 | 11 | 16 | PF00397 | 0.651 |
DOC_WW_Pin1_4 | 364 | 369 | PF00397 | 0.385 |
DOC_WW_Pin1_4 | 406 | 411 | PF00397 | 0.330 |
DOC_WW_Pin1_4 | 450 | 455 | PF00397 | 0.309 |
DOC_WW_Pin1_4 | 624 | 629 | PF00397 | 0.503 |
DOC_WW_Pin1_4 | 641 | 646 | PF00397 | 0.564 |
LIG_14-3-3_CanoR_1 | 207 | 212 | PF00244 | 0.410 |
LIG_14-3-3_CanoR_1 | 221 | 229 | PF00244 | 0.444 |
LIG_14-3-3_CanoR_1 | 285 | 293 | PF00244 | 0.514 |
LIG_14-3-3_CanoR_1 | 599 | 604 | PF00244 | 0.390 |
LIG_14-3-3_CanoR_1 | 690 | 700 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 86 | 92 | PF00244 | 0.387 |
LIG_Actin_WH2_2 | 298 | 316 | PF00022 | 0.317 |
LIG_Actin_WH2_2 | 465 | 483 | PF00022 | 0.360 |
LIG_BIR_III_4 | 579 | 583 | PF00653 | 0.419 |
LIG_BRCT_BRCA1_1 | 523 | 527 | PF00533 | 0.523 |
LIG_deltaCOP1_diTrp_1 | 288 | 297 | PF00928 | 0.444 |
LIG_deltaCOP1_diTrp_1 | 47 | 52 | PF00928 | 0.527 |
LIG_FHA_1 | 123 | 129 | PF00498 | 0.420 |
LIG_FHA_1 | 183 | 189 | PF00498 | 0.488 |
LIG_FHA_1 | 284 | 290 | PF00498 | 0.435 |
LIG_FHA_1 | 357 | 363 | PF00498 | 0.396 |
LIG_FHA_1 | 539 | 545 | PF00498 | 0.469 |
LIG_FHA_1 | 549 | 555 | PF00498 | 0.428 |
LIG_FHA_1 | 673 | 679 | PF00498 | 0.387 |
LIG_FHA_2 | 307 | 313 | PF00498 | 0.516 |
LIG_FHA_2 | 343 | 349 | PF00498 | 0.367 |
LIG_FHA_2 | 42 | 48 | PF00498 | 0.524 |
LIG_FHA_2 | 553 | 559 | PF00498 | 0.526 |
LIG_FHA_2 | 571 | 577 | PF00498 | 0.603 |
LIG_FHA_2 | 618 | 624 | PF00498 | 0.606 |
LIG_FHA_2 | 667 | 673 | PF00498 | 0.449 |
LIG_GBD_Chelix_1 | 380 | 388 | PF00786 | 0.342 |
LIG_Integrin_isoDGR_2 | 611 | 613 | PF01839 | 0.461 |
LIG_LIR_Gen_1 | 153 | 164 | PF02991 | 0.375 |
LIG_LIR_Gen_1 | 169 | 178 | PF02991 | 0.349 |
LIG_LIR_Gen_1 | 197 | 206 | PF02991 | 0.374 |
LIG_LIR_Gen_1 | 216 | 224 | PF02991 | 0.531 |
LIG_LIR_Gen_1 | 287 | 297 | PF02991 | 0.435 |
LIG_LIR_Gen_1 | 74 | 84 | PF02991 | 0.377 |
LIG_LIR_Gen_1 | 85 | 96 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 153 | 159 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 185 | 190 | PF02991 | 0.552 |
LIG_LIR_Nem_3 | 197 | 201 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 216 | 222 | PF02991 | 0.528 |
LIG_LIR_Nem_3 | 294 | 300 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 357 | 363 | PF02991 | 0.349 |
LIG_LIR_Nem_3 | 524 | 530 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 629 | 635 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 74 | 79 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 85 | 91 | PF02991 | 0.551 |
LIG_LYPXL_yS_3 | 360 | 363 | PF13949 | 0.330 |
LIG_PCNA_PIPBox_1 | 180 | 189 | PF02747 | 0.527 |
LIG_PCNA_yPIPBox_3 | 180 | 194 | PF02747 | 0.561 |
LIG_Pex14_1 | 48 | 52 | PF04695 | 0.527 |
LIG_Pex14_2 | 255 | 259 | PF04695 | 0.419 |
LIG_Pex14_2 | 692 | 696 | PF04695 | 0.343 |
LIG_PTB_Apo_2 | 164 | 171 | PF02174 | 0.518 |
LIG_PTB_Apo_2 | 181 | 188 | PF02174 | 0.525 |
LIG_PTB_Phospho_1 | 164 | 170 | PF10480 | 0.411 |
LIG_PTB_Phospho_1 | 181 | 187 | PF10480 | 0.610 |
LIG_SH2_CRK | 266 | 270 | PF00017 | 0.498 |
LIG_SH2_CRK | 705 | 709 | PF00017 | 0.364 |
LIG_SH2_CRK | 727 | 731 | PF00017 | 0.385 |
LIG_SH2_GRB2like | 530 | 533 | PF00017 | 0.344 |
LIG_SH2_STAP1 | 170 | 174 | PF00017 | 0.403 |
LIG_SH2_STAT3 | 22 | 25 | PF00017 | 0.618 |
LIG_SH2_STAT5 | 187 | 190 | PF00017 | 0.550 |
LIG_SH2_STAT5 | 616 | 619 | PF00017 | 0.384 |
LIG_SH2_STAT5 | 727 | 730 | PF00017 | 0.382 |
LIG_SH3_3 | 365 | 371 | PF00018 | 0.402 |
LIG_SUMO_SIM_anti_2 | 674 | 680 | PF11976 | 0.383 |
LIG_SUMO_SIM_par_1 | 99 | 104 | PF11976 | 0.402 |
LIG_TRAF2_1 | 713 | 716 | PF00917 | 0.468 |
LIG_UBA3_1 | 127 | 136 | PF00899 | 0.392 |
MOD_CAAXbox | 728 | 731 | PF01239 | 0.385 |
MOD_CDK_SPxxK_3 | 450 | 457 | PF00069 | 0.309 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.628 |
MOD_CK1_1 | 244 | 250 | PF00069 | 0.449 |
MOD_CK1_1 | 274 | 280 | PF00069 | 0.423 |
MOD_CK1_1 | 367 | 373 | PF00069 | 0.517 |
MOD_CK1_1 | 521 | 527 | PF00069 | 0.544 |
MOD_CK1_1 | 531 | 537 | PF00069 | 0.546 |
MOD_CK1_1 | 548 | 554 | PF00069 | 0.509 |
MOD_CK1_1 | 570 | 576 | PF00069 | 0.419 |
MOD_CK1_1 | 644 | 650 | PF00069 | 0.483 |
MOD_CK1_1 | 664 | 670 | PF00069 | 0.476 |
MOD_CK1_1 | 710 | 716 | PF00069 | 0.498 |
MOD_CK2_1 | 105 | 111 | PF00069 | 0.400 |
MOD_CK2_1 | 342 | 348 | PF00069 | 0.342 |
MOD_CK2_1 | 41 | 47 | PF00069 | 0.521 |
MOD_CK2_1 | 5 | 11 | PF00069 | 0.688 |
MOD_CK2_1 | 710 | 716 | PF00069 | 0.448 |
MOD_GlcNHglycan | 19 | 22 | PF01048 | 0.586 |
MOD_GlcNHglycan | 389 | 392 | PF01048 | 0.354 |
MOD_GlcNHglycan | 518 | 521 | PF01048 | 0.424 |
MOD_GlcNHglycan | 693 | 696 | PF01048 | 0.400 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.579 |
MOD_GlcNHglycan | 71 | 74 | PF01048 | 0.602 |
MOD_GlcNHglycan | 712 | 715 | PF01048 | 0.435 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.421 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.469 |
MOD_GSK3_1 | 162 | 169 | PF00069 | 0.442 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.730 |
MOD_GSK3_1 | 267 | 274 | PF00069 | 0.412 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.410 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.491 |
MOD_GSK3_1 | 514 | 521 | PF00069 | 0.444 |
MOD_GSK3_1 | 544 | 551 | PF00069 | 0.477 |
MOD_GSK3_1 | 567 | 574 | PF00069 | 0.467 |
MOD_GSK3_1 | 617 | 624 | PF00069 | 0.487 |
MOD_GSK3_1 | 641 | 648 | PF00069 | 0.535 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.362 |
MOD_N-GLC_1 | 271 | 276 | PF02516 | 0.533 |
MOD_N-GLC_1 | 384 | 389 | PF02516 | 0.237 |
MOD_N-GLC_1 | 528 | 533 | PF02516 | 0.508 |
MOD_N-GLC_1 | 641 | 646 | PF02516 | 0.564 |
MOD_N-GLC_1 | 649 | 654 | PF02516 | 0.555 |
MOD_N-GLC_1 | 661 | 666 | PF02516 | 0.414 |
MOD_N-GLC_2 | 107 | 109 | PF02516 | 0.362 |
MOD_N-GLC_2 | 193 | 195 | PF02516 | 0.321 |
MOD_NEK2_1 | 103 | 108 | PF00069 | 0.325 |
MOD_NEK2_1 | 127 | 132 | PF00069 | 0.430 |
MOD_NEK2_1 | 293 | 298 | PF00069 | 0.503 |
MOD_NEK2_1 | 480 | 485 | PF00069 | 0.386 |
MOD_NEK2_1 | 528 | 533 | PF00069 | 0.429 |
MOD_NEK2_1 | 549 | 554 | PF00069 | 0.554 |
MOD_NEK2_1 | 649 | 654 | PF00069 | 0.583 |
MOD_NEK2_1 | 661 | 666 | PF00069 | 0.447 |
MOD_NEK2_1 | 688 | 693 | PF00069 | 0.338 |
MOD_NEK2_1 | 87 | 92 | PF00069 | 0.456 |
MOD_NEK2_2 | 628 | 633 | PF00069 | 0.329 |
MOD_NMyristoyl | 1 | 7 | PF02799 | 0.648 |
MOD_PIKK_1 | 21 | 27 | PF00454 | 0.849 |
MOD_PIKK_1 | 291 | 297 | PF00454 | 0.380 |
MOD_PIKK_1 | 549 | 555 | PF00454 | 0.440 |
MOD_PIKK_1 | 661 | 667 | PF00454 | 0.508 |
MOD_PIKK_1 | 91 | 97 | PF00454 | 0.476 |
MOD_PK_1 | 207 | 213 | PF00069 | 0.418 |
MOD_PKA_1 | 314 | 320 | PF00069 | 0.552 |
MOD_PKA_2 | 220 | 226 | PF00069 | 0.438 |
MOD_PKA_2 | 284 | 290 | PF00069 | 0.440 |
MOD_PKA_2 | 314 | 320 | PF00069 | 0.552 |
MOD_PKA_2 | 444 | 450 | PF00069 | 0.313 |
MOD_PKA_2 | 480 | 486 | PF00069 | 0.360 |
MOD_PKA_2 | 606 | 612 | PF00069 | 0.494 |
MOD_PKA_2 | 716 | 722 | PF00069 | 0.566 |
MOD_Plk_1 | 140 | 146 | PF00069 | 0.528 |
MOD_Plk_1 | 384 | 390 | PF00069 | 0.317 |
MOD_Plk_1 | 491 | 497 | PF00069 | 0.324 |
MOD_Plk_1 | 570 | 576 | PF00069 | 0.558 |
MOD_Plk_1 | 628 | 634 | PF00069 | 0.452 |
MOD_Plk_1 | 649 | 655 | PF00069 | 0.597 |
MOD_Plk_1 | 671 | 677 | PF00069 | 0.292 |
MOD_Plk_1 | 688 | 694 | PF00069 | 0.466 |
MOD_Plk_2-3 | 342 | 348 | PF00069 | 0.456 |
MOD_Plk_2-3 | 571 | 577 | PF00069 | 0.384 |
MOD_Plk_4 | 182 | 188 | PF00069 | 0.509 |
MOD_Plk_4 | 271 | 277 | PF00069 | 0.381 |
MOD_Plk_4 | 342 | 348 | PF00069 | 0.369 |
MOD_Plk_4 | 545 | 551 | PF00069 | 0.547 |
MOD_Plk_4 | 707 | 713 | PF00069 | 0.309 |
MOD_ProDKin_1 | 11 | 17 | PF00069 | 0.653 |
MOD_ProDKin_1 | 364 | 370 | PF00069 | 0.385 |
MOD_ProDKin_1 | 406 | 412 | PF00069 | 0.330 |
MOD_ProDKin_1 | 450 | 456 | PF00069 | 0.309 |
MOD_ProDKin_1 | 624 | 630 | PF00069 | 0.490 |
MOD_ProDKin_1 | 641 | 647 | PF00069 | 0.563 |
MOD_SPalmitoyl_4 | 1 | 7 | PF01529 | 0.699 |
MOD_SUMO_rev_2 | 130 | 138 | PF00179 | 0.401 |
MOD_SUMO_rev_2 | 308 | 316 | PF00179 | 0.485 |
MOD_SUMO_rev_2 | 498 | 506 | PF00179 | 0.462 |
MOD_SUMO_rev_2 | 531 | 538 | PF00179 | 0.583 |
TRG_AP2beta_CARGO_1 | 217 | 226 | PF09066 | 0.439 |
TRG_DiLeu_BaLyEn_6 | 135 | 140 | PF01217 | 0.537 |
TRG_DiLeu_BaLyEn_6 | 636 | 641 | PF01217 | 0.497 |
TRG_ENDOCYTIC_2 | 170 | 173 | PF00928 | 0.523 |
TRG_ENDOCYTIC_2 | 266 | 269 | PF00928 | 0.490 |
TRG_ENDOCYTIC_2 | 360 | 363 | PF00928 | 0.330 |
TRG_ENDOCYTIC_2 | 705 | 708 | PF00928 | 0.349 |
TRG_ENDOCYTIC_2 | 727 | 730 | PF00928 | 0.365 |
TRG_ER_diArg_1 | 495 | 497 | PF00400 | 0.456 |
TRG_ER_diArg_1 | 605 | 608 | PF00400 | 0.501 |
TRG_NES_CRM1_1 | 424 | 436 | PF08389 | 0.315 |
TRG_Pf-PMV_PEXEL_1 | 78 | 82 | PF00026 | 0.493 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7S8 | Leptomonas seymouri | 71% | 99% |
A0A0S4KHF2 | Bodo saltans | 42% | 100% |
A0A1X0P2U3 | Trypanosomatidae | 45% | 100% |
A0A3Q8IES3 | Leishmania donovani | 86% | 100% |
A0A3R7MG69 | Trypanosoma rangeli | 44% | 96% |
A4I027 | Leishmania infantum | 24% | 93% |
A4I594 | Leishmania infantum | 86% | 100% |
C9ZQM5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
E9B0J1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 99% |
Q4Q7P2 | Leishmania major | 86% | 100% |
V5AS75 | Trypanosoma cruzi | 47% | 100% |