Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 8 |
GO:0110165 | cellular anatomical entity | 1 | 8 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005789 | endoplasmic reticulum membrane | 4 | 3 |
GO:0031090 | organelle membrane | 3 | 3 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 1 |
GO:0097014 | ciliary plasm | 5 | 1 |
GO:0099568 | cytoplasmic region | 3 | 1 |
Related structures:
AlphaFold database: A4HEI1
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 1 |
GO:0006638 | neutral lipid metabolic process | 4 | 1 |
GO:0006639 | acylglycerol metabolic process | 5 | 1 |
GO:0006641 | triglyceride metabolic process | 6 | 1 |
GO:0006643 | membrane lipid metabolic process | 4 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0008610 | lipid biosynthetic process | 4 | 1 |
GO:0009058 | biosynthetic process | 2 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0019432 | triglyceride biosynthetic process | 6 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044249 | cellular biosynthetic process | 3 | 1 |
GO:0044255 | cellular lipid metabolic process | 3 | 1 |
GO:0045017 | glycerolipid biosynthetic process | 4 | 1 |
GO:0046460 | neutral lipid biosynthetic process | 4 | 1 |
GO:0046463 | acylglycerol biosynthetic process | 5 | 1 |
GO:0046467 | membrane lipid biosynthetic process | 4 | 1 |
GO:0046486 | glycerolipid metabolic process | 4 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901576 | organic substance biosynthetic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 9 |
GO:0004144 | diacylglycerol O-acyltransferase activity | 7 | 5 |
GO:0008374 | O-acyltransferase activity | 5 | 9 |
GO:0016411 | acylglycerol O-acyltransferase activity | 6 | 5 |
GO:0016740 | transferase activity | 2 | 9 |
GO:0016746 | acyltransferase activity | 3 | 9 |
GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 399 | 403 | PF00656 | 0.598 |
CLV_NRD_NRD_1 | 149 | 151 | PF00675 | 0.361 |
CLV_NRD_NRD_1 | 286 | 288 | PF00675 | 0.366 |
CLV_NRD_NRD_1 | 369 | 371 | PF00675 | 0.339 |
CLV_NRD_NRD_1 | 443 | 445 | PF00675 | 0.306 |
CLV_NRD_NRD_1 | 479 | 481 | PF00675 | 0.302 |
CLV_NRD_NRD_1 | 51 | 53 | PF00675 | 0.577 |
CLV_NRD_NRD_1 | 551 | 553 | PF00675 | 0.525 |
CLV_NRD_NRD_1 | 586 | 588 | PF00675 | 0.591 |
CLV_NRD_NRD_1 | 92 | 94 | PF00675 | 0.528 |
CLV_PCSK_KEX2_1 | 149 | 151 | PF00082 | 0.405 |
CLV_PCSK_KEX2_1 | 237 | 239 | PF00082 | 0.510 |
CLV_PCSK_KEX2_1 | 286 | 288 | PF00082 | 0.366 |
CLV_PCSK_KEX2_1 | 369 | 371 | PF00082 | 0.341 |
CLV_PCSK_KEX2_1 | 479 | 481 | PF00082 | 0.311 |
CLV_PCSK_KEX2_1 | 50 | 52 | PF00082 | 0.580 |
CLV_PCSK_KEX2_1 | 551 | 553 | PF00082 | 0.515 |
CLV_PCSK_PC1ET2_1 | 237 | 239 | PF00082 | 0.543 |
CLV_PCSK_PC1ET2_1 | 479 | 481 | PF00082 | 0.337 |
CLV_PCSK_SKI1_1 | 149 | 153 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 347 | 351 | PF00082 | 0.257 |
CLV_PCSK_SKI1_1 | 369 | 373 | PF00082 | 0.217 |
CLV_PCSK_SKI1_1 | 485 | 489 | PF00082 | 0.301 |
CLV_PCSK_SKI1_1 | 538 | 542 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 71 | 75 | PF00082 | 0.416 |
DEG_APCC_DBOX_1 | 149 | 157 | PF00400 | 0.627 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.807 |
DEG_SCF_FBW7_1 | 258 | 265 | PF00400 | 0.578 |
DEG_SPOP_SBC_1 | 174 | 178 | PF00917 | 0.678 |
DEG_SPOP_SBC_1 | 262 | 266 | PF00917 | 0.643 |
DOC_ANK_TNKS_1 | 112 | 119 | PF00023 | 0.538 |
DOC_CKS1_1 | 187 | 192 | PF01111 | 0.839 |
DOC_CKS1_1 | 21 | 26 | PF01111 | 0.679 |
DOC_CKS1_1 | 280 | 285 | PF01111 | 0.667 |
DOC_CYCLIN_RxL_1 | 366 | 375 | PF00134 | 0.418 |
DOC_MAPK_gen_1 | 286 | 293 | PF00069 | 0.597 |
DOC_MAPK_gen_1 | 469 | 478 | PF00069 | 0.503 |
DOC_MAPK_gen_1 | 479 | 488 | PF00069 | 0.486 |
DOC_MAPK_gen_1 | 551 | 558 | PF00069 | 0.325 |
DOC_MAPK_HePTP_8 | 476 | 488 | PF00069 | 0.560 |
DOC_MAPK_MEF2A_6 | 286 | 295 | PF00069 | 0.544 |
DOC_MAPK_MEF2A_6 | 341 | 350 | PF00069 | 0.472 |
DOC_MAPK_MEF2A_6 | 405 | 414 | PF00069 | 0.537 |
DOC_MAPK_MEF2A_6 | 479 | 488 | PF00069 | 0.503 |
DOC_MAPK_MEF2A_6 | 551 | 558 | PF00069 | 0.301 |
DOC_MAPK_RevD_3 | 36 | 51 | PF00069 | 0.598 |
DOC_PP1_RVXF_1 | 345 | 351 | PF00149 | 0.418 |
DOC_PP2B_LxvP_1 | 362 | 365 | PF13499 | 0.501 |
DOC_PP2B_LxvP_1 | 421 | 424 | PF13499 | 0.560 |
DOC_PP2B_LxvP_1 | 562 | 565 | PF13499 | 0.350 |
DOC_PP4_FxxP_1 | 332 | 335 | PF00568 | 0.438 |
DOC_PP4_FxxP_1 | 530 | 533 | PF00568 | 0.357 |
DOC_USP7_MATH_1 | 438 | 442 | PF00917 | 0.525 |
DOC_USP7_MATH_1 | 451 | 455 | PF00917 | 0.501 |
DOC_USP7_MATH_1 | 462 | 466 | PF00917 | 0.471 |
DOC_USP7_MATH_1 | 75 | 79 | PF00917 | 0.637 |
DOC_USP7_UBL2_3 | 481 | 485 | PF12436 | 0.560 |
DOC_WW_Pin1_4 | 186 | 191 | PF00397 | 0.818 |
DOC_WW_Pin1_4 | 20 | 25 | PF00397 | 0.795 |
DOC_WW_Pin1_4 | 238 | 243 | PF00397 | 0.689 |
DOC_WW_Pin1_4 | 258 | 263 | PF00397 | 0.459 |
DOC_WW_Pin1_4 | 27 | 32 | PF00397 | 0.793 |
DOC_WW_Pin1_4 | 279 | 284 | PF00397 | 0.668 |
DOC_WW_Pin1_4 | 339 | 344 | PF00397 | 0.490 |
DOC_WW_Pin1_4 | 489 | 494 | PF00397 | 0.525 |
DOC_WW_Pin1_4 | 93 | 98 | PF00397 | 0.706 |
LIG_14-3-3_CanoR_1 | 138 | 148 | PF00244 | 0.633 |
LIG_14-3-3_CanoR_1 | 286 | 292 | PF00244 | 0.575 |
LIG_14-3-3_CanoR_1 | 316 | 320 | PF00244 | 0.360 |
LIG_14-3-3_CanoR_1 | 444 | 448 | PF00244 | 0.525 |
LIG_14-3-3_CanoR_1 | 50 | 55 | PF00244 | 0.748 |
LIG_ActinCP_TwfCPI_2 | 332 | 341 | PF01115 | 0.438 |
LIG_BRCT_BRCA1_1 | 263 | 267 | PF00533 | 0.667 |
LIG_BRCT_BRCA1_1 | 341 | 345 | PF00533 | 0.480 |
LIG_BRCT_BRCA1_1 | 62 | 66 | PF00533 | 0.770 |
LIG_DLG_GKlike_1 | 287 | 295 | PF00625 | 0.560 |
LIG_EH1_1 | 357 | 365 | PF00400 | 0.418 |
LIG_eIF4E_1 | 357 | 363 | PF01652 | 0.501 |
LIG_FHA_1 | 290 | 296 | PF00498 | 0.310 |
LIG_FHA_1 | 307 | 313 | PF00498 | 0.450 |
LIG_FHA_1 | 316 | 322 | PF00498 | 0.305 |
LIG_FHA_1 | 409 | 415 | PF00498 | 0.533 |
LIG_FHA_1 | 490 | 496 | PF00498 | 0.525 |
LIG_FHA_1 | 57 | 63 | PF00498 | 0.770 |
LIG_FHA_1 | 570 | 576 | PF00498 | 0.398 |
LIG_FHA_2 | 243 | 249 | PF00498 | 0.548 |
LIG_FHA_2 | 263 | 269 | PF00498 | 0.614 |
LIG_FHA_2 | 280 | 286 | PF00498 | 0.579 |
LIG_FHA_2 | 569 | 575 | PF00498 | 0.301 |
LIG_LIR_Apic_2 | 315 | 320 | PF02991 | 0.352 |
LIG_LIR_Apic_2 | 331 | 335 | PF02991 | 0.193 |
LIG_LIR_Gen_1 | 294 | 304 | PF02991 | 0.364 |
LIG_LIR_Gen_1 | 342 | 350 | PF02991 | 0.512 |
LIG_LIR_Gen_1 | 63 | 74 | PF02991 | 0.783 |
LIG_LIR_LC3C_4 | 454 | 459 | PF02991 | 0.525 |
LIG_LIR_LC3C_4 | 560 | 564 | PF02991 | 0.217 |
LIG_LIR_Nem_3 | 273 | 279 | PF02991 | 0.627 |
LIG_LIR_Nem_3 | 294 | 299 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 342 | 348 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 356 | 360 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 375 | 381 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 389 | 393 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 513 | 519 | PF02991 | 0.527 |
LIG_LIR_Nem_3 | 522 | 527 | PF02991 | 0.523 |
LIG_LIR_Nem_3 | 63 | 69 | PF02991 | 0.749 |
LIG_Pex14_1 | 328 | 332 | PF04695 | 0.438 |
LIG_Pex14_1 | 578 | 582 | PF04695 | 0.301 |
LIG_Pex14_2 | 326 | 330 | PF04695 | 0.279 |
LIG_Pex14_2 | 345 | 349 | PF04695 | 0.580 |
LIG_PTB_Apo_2 | 539 | 546 | PF02174 | 0.438 |
LIG_PTB_Phospho_1 | 539 | 545 | PF10480 | 0.438 |
LIG_Rb_pABgroove_1 | 366 | 374 | PF01858 | 0.418 |
LIG_REV1ctd_RIR_1 | 347 | 356 | PF16727 | 0.418 |
LIG_SH2_CRK | 317 | 321 | PF00017 | 0.433 |
LIG_SH2_CRK | 340 | 344 | PF00017 | 0.418 |
LIG_SH2_CRK | 506 | 510 | PF00017 | 0.439 |
LIG_SH2_CRK | 545 | 549 | PF00017 | 0.360 |
LIG_SH2_PTP2 | 422 | 425 | PF00017 | 0.598 |
LIG_SH2_SRC | 125 | 128 | PF00017 | 0.512 |
LIG_SH2_SRC | 162 | 165 | PF00017 | 0.558 |
LIG_SH2_STAT5 | 139 | 142 | PF00017 | 0.634 |
LIG_SH2_STAT5 | 257 | 260 | PF00017 | 0.607 |
LIG_SH2_STAT5 | 317 | 320 | PF00017 | 0.422 |
LIG_SH2_STAT5 | 325 | 328 | PF00017 | 0.325 |
LIG_SH2_STAT5 | 354 | 357 | PF00017 | 0.519 |
LIG_SH2_STAT5 | 378 | 381 | PF00017 | 0.501 |
LIG_SH2_STAT5 | 422 | 425 | PF00017 | 0.527 |
LIG_SH2_STAT5 | 519 | 522 | PF00017 | 0.552 |
LIG_SH2_STAT5 | 582 | 585 | PF00017 | 0.284 |
LIG_SH3_3 | 179 | 185 | PF00018 | 0.789 |
LIG_SH3_3 | 18 | 24 | PF00018 | 0.773 |
LIG_SH3_3 | 332 | 338 | PF00018 | 0.357 |
LIG_SH3_3 | 378 | 384 | PF00018 | 0.560 |
LIG_SH3_3 | 490 | 496 | PF00018 | 0.523 |
LIG_SH3_3 | 555 | 561 | PF00018 | 0.301 |
LIG_SH3_3 | 562 | 568 | PF00018 | 0.291 |
LIG_SH3_3 | 96 | 102 | PF00018 | 0.715 |
LIG_SUMO_SIM_anti_2 | 309 | 315 | PF11976 | 0.366 |
LIG_SUMO_SIM_anti_2 | 454 | 459 | PF11976 | 0.507 |
LIG_SUMO_SIM_par_1 | 290 | 297 | PF11976 | 0.395 |
LIG_SUMO_SIM_par_1 | 309 | 315 | PF11976 | 0.178 |
LIG_SUMO_SIM_par_1 | 554 | 560 | PF11976 | 0.325 |
LIG_TRAF2_1 | 112 | 115 | PF00917 | 0.647 |
LIG_TRAF2_1 | 487 | 490 | PF00917 | 0.501 |
LIG_TRAF2_2 | 10 | 15 | PF00917 | 0.656 |
LIG_UBA3_1 | 520 | 525 | PF00899 | 0.431 |
LIG_WRC_WIRS_1 | 295 | 300 | PF05994 | 0.448 |
LIG_WRC_WIRS_1 | 329 | 334 | PF05994 | 0.422 |
LIG_WRC_WIRS_1 | 387 | 392 | PF05994 | 0.391 |
LIG_WW_2 | 182 | 185 | PF00397 | 0.562 |
MOD_CDK_SPK_2 | 238 | 243 | PF00069 | 0.619 |
MOD_CDK_SPK_2 | 93 | 98 | PF00069 | 0.585 |
MOD_CDK_SPxK_1 | 186 | 192 | PF00069 | 0.830 |
MOD_CDK_SPxxK_3 | 279 | 286 | PF00069 | 0.576 |
MOD_CK1_1 | 176 | 182 | PF00069 | 0.704 |
MOD_CK1_1 | 263 | 269 | PF00069 | 0.659 |
MOD_CK1_1 | 270 | 276 | PF00069 | 0.652 |
MOD_CK1_1 | 294 | 300 | PF00069 | 0.496 |
MOD_CK1_1 | 315 | 321 | PF00069 | 0.492 |
MOD_CK1_1 | 60 | 66 | PF00069 | 0.682 |
MOD_CK2_1 | 109 | 115 | PF00069 | 0.572 |
MOD_CK2_1 | 279 | 285 | PF00069 | 0.475 |
MOD_Cter_Amidation | 235 | 238 | PF01082 | 0.766 |
MOD_DYRK1A_RPxSP_1 | 20 | 24 | PF00069 | 0.769 |
MOD_GlcNHglycan | 268 | 272 | PF01048 | 0.433 |
MOD_GlcNHglycan | 437 | 441 | PF01048 | 0.342 |
MOD_GlcNHglycan | 448 | 451 | PF01048 | 0.312 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.673 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.656 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.766 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.506 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.300 |
MOD_GSK3_1 | 275 | 282 | PF00069 | 0.559 |
MOD_GSK3_1 | 287 | 294 | PF00069 | 0.297 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.674 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.754 |
MOD_N-GLC_2 | 89 | 91 | PF02516 | 0.579 |
MOD_NEK2_1 | 267 | 272 | PF00069 | 0.503 |
MOD_NEK2_1 | 291 | 296 | PF00069 | 0.357 |
MOD_NEK2_1 | 312 | 317 | PF00069 | 0.500 |
MOD_NEK2_1 | 599 | 604 | PF00069 | 0.430 |
MOD_OFUCOSY | 435 | 442 | PF10250 | 0.438 |
MOD_PKA_1 | 50 | 56 | PF00069 | 0.630 |
MOD_PKA_2 | 315 | 321 | PF00069 | 0.438 |
MOD_PKA_2 | 333 | 339 | PF00069 | 0.434 |
MOD_PKA_2 | 443 | 449 | PF00069 | 0.357 |
MOD_PKA_2 | 50 | 56 | PF00069 | 0.747 |
MOD_PKA_2 | 75 | 81 | PF00069 | 0.741 |
MOD_Plk_1 | 34 | 40 | PF00069 | 0.517 |
MOD_Plk_1 | 462 | 468 | PF00069 | 0.438 |
MOD_Plk_4 | 275 | 281 | PF00069 | 0.583 |
MOD_Plk_4 | 291 | 297 | PF00069 | 0.306 |
MOD_Plk_4 | 341 | 347 | PF00069 | 0.403 |
MOD_Plk_4 | 451 | 457 | PF00069 | 0.378 |
MOD_Plk_4 | 462 | 468 | PF00069 | 0.315 |
MOD_ProDKin_1 | 186 | 192 | PF00069 | 0.801 |
MOD_ProDKin_1 | 20 | 26 | PF00069 | 0.770 |
MOD_ProDKin_1 | 238 | 244 | PF00069 | 0.604 |
MOD_ProDKin_1 | 258 | 264 | PF00069 | 0.295 |
MOD_ProDKin_1 | 27 | 33 | PF00069 | 0.761 |
MOD_ProDKin_1 | 279 | 285 | PF00069 | 0.587 |
MOD_ProDKin_1 | 339 | 345 | PF00069 | 0.341 |
MOD_ProDKin_1 | 489 | 495 | PF00069 | 0.391 |
MOD_ProDKin_1 | 93 | 99 | PF00069 | 0.641 |
MOD_SUMO_rev_2 | 142 | 148 | PF00179 | 0.558 |
TRG_DiLeu_BaLyEn_6 | 246 | 251 | PF01217 | 0.513 |
TRG_DiLeu_BaLyEn_6 | 358 | 363 | PF01217 | 0.240 |
TRG_ENDOCYTIC_2 | 357 | 360 | PF00928 | 0.335 |
TRG_ENDOCYTIC_2 | 378 | 381 | PF00928 | 0.357 |
TRG_ENDOCYTIC_2 | 422 | 425 | PF00928 | 0.397 |
TRG_ENDOCYTIC_2 | 545 | 548 | PF00928 | 0.438 |
TRG_ER_diArg_1 | 136 | 139 | PF00400 | 0.577 |
TRG_ER_diArg_1 | 148 | 150 | PF00400 | 0.460 |
TRG_ER_diArg_1 | 286 | 288 | PF00400 | 0.448 |
TRG_ER_diArg_1 | 368 | 370 | PF00400 | 0.412 |
TRG_ER_diArg_1 | 50 | 52 | PF00400 | 0.637 |
TRG_ER_diArg_1 | 551 | 553 | PF00400 | 0.391 |
TRG_Pf-PMV_PEXEL_1 | 369 | 373 | PF00026 | 0.240 |
TRG_Pf-PMV_PEXEL_1 | 518 | 522 | PF00026 | 0.240 |
TRG_Pf-PMV_PEXEL_1 | 52 | 57 | PF00026 | 0.705 |
TRG_Pf-PMV_PEXEL_1 | 587 | 592 | PF00026 | 0.492 |
TRG_Pf-PMV_PEXEL_1 | 594 | 598 | PF00026 | 0.377 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PE36 | Leptomonas seymouri | 57% | 93% |
A0A3R7NQK7 | Trypanosoma rangeli | 44% | 100% |
A0A3S7WZ82 | Leishmania donovani | 78% | 100% |
A4I1K9 | Leishmania infantum | 77% | 100% |
C9ZK51 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
E9AXP3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 77% | 99% |
Q4Q9S8 | Leishmania major | 76% | 100% |