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:0005737 | cytoplasm | 2 | 2 |
GO:0005789 | endoplasmic reticulum membrane | 4 | 4 |
GO:0016020 | membrane | 2 | 8 |
GO:0031090 | organelle membrane | 3 | 4 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 2 |
GO:0097014 | ciliary plasm | 5 | 2 |
GO:0099568 | cytoplasmic region | 3 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 8 |
Related structures:
AlphaFold database: Q4Q9S8
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 2 |
GO:0006638 | neutral lipid metabolic process | 4 | 2 |
GO:0006639 | acylglycerol metabolic process | 5 | 2 |
GO:0006641 | triglyceride metabolic process | 6 | 2 |
GO:0006643 | membrane lipid metabolic process | 4 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0008610 | lipid biosynthetic process | 4 | 2 |
GO:0009058 | biosynthetic process | 2 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0019432 | triglyceride biosynthetic process | 6 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044249 | cellular biosynthetic process | 3 | 2 |
GO:0044255 | cellular lipid metabolic process | 3 | 2 |
GO:0045017 | glycerolipid biosynthetic process | 4 | 2 |
GO:0046460 | neutral lipid biosynthetic process | 4 | 2 |
GO:0046463 | acylglycerol biosynthetic process | 5 | 2 |
GO:0046467 | membrane lipid biosynthetic process | 4 | 2 |
GO:0046486 | glycerolipid metabolic process | 4 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:1901576 | organic substance biosynthetic process | 3 | 2 |
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 | 402 | 406 | PF00656 | 0.566 |
CLV_NRD_NRD_1 | 152 | 154 | PF00675 | 0.317 |
CLV_NRD_NRD_1 | 289 | 291 | PF00675 | 0.328 |
CLV_NRD_NRD_1 | 373 | 375 | PF00675 | 0.329 |
CLV_NRD_NRD_1 | 446 | 448 | PF00675 | 0.275 |
CLV_NRD_NRD_1 | 482 | 484 | PF00675 | 0.270 |
CLV_NRD_NRD_1 | 54 | 56 | PF00675 | 0.535 |
CLV_NRD_NRD_1 | 554 | 556 | PF00675 | 0.493 |
CLV_NRD_NRD_1 | 589 | 591 | PF00675 | 0.566 |
CLV_NRD_NRD_1 | 93 | 95 | PF00675 | 0.525 |
CLV_PCSK_KEX2_1 | 152 | 154 | PF00082 | 0.367 |
CLV_PCSK_KEX2_1 | 240 | 242 | PF00082 | 0.475 |
CLV_PCSK_KEX2_1 | 289 | 291 | PF00082 | 0.328 |
CLV_PCSK_KEX2_1 | 372 | 374 | PF00082 | 0.328 |
CLV_PCSK_KEX2_1 | 482 | 484 | PF00082 | 0.279 |
CLV_PCSK_KEX2_1 | 53 | 55 | PF00082 | 0.541 |
CLV_PCSK_KEX2_1 | 554 | 556 | PF00082 | 0.493 |
CLV_PCSK_KEX2_1 | 93 | 95 | PF00082 | 0.510 |
CLV_PCSK_PC1ET2_1 | 240 | 242 | PF00082 | 0.509 |
CLV_PCSK_PC1ET2_1 | 482 | 484 | PF00082 | 0.306 |
CLV_PCSK_SKI1_1 | 152 | 156 | PF00082 | 0.353 |
CLV_PCSK_SKI1_1 | 488 | 492 | PF00082 | 0.269 |
CLV_PCSK_SKI1_1 | 541 | 545 | PF00082 | 0.388 |
DEG_APCC_DBOX_1 | 152 | 160 | PF00400 | 0.588 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.735 |
DOC_CKS1_1 | 190 | 195 | PF01111 | 0.792 |
DOC_CKS1_1 | 283 | 288 | PF01111 | 0.631 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 421 | 428 | PF00134 | 0.511 |
DOC_MAPK_gen_1 | 289 | 296 | PF00069 | 0.568 |
DOC_MAPK_gen_1 | 482 | 491 | PF00069 | 0.455 |
DOC_MAPK_gen_1 | 554 | 561 | PF00069 | 0.293 |
DOC_MAPK_HePTP_8 | 479 | 491 | PF00069 | 0.528 |
DOC_MAPK_MEF2A_6 | 289 | 298 | PF00069 | 0.512 |
DOC_MAPK_MEF2A_6 | 421 | 428 | PF00069 | 0.483 |
DOC_MAPK_MEF2A_6 | 482 | 491 | PF00069 | 0.471 |
DOC_MAPK_MEF2A_6 | 554 | 561 | PF00069 | 0.269 |
DOC_PP2B_LxvP_1 | 182 | 185 | PF13499 | 0.664 |
DOC_PP2B_LxvP_1 | 365 | 368 | PF13499 | 0.469 |
DOC_PP2B_LxvP_1 | 424 | 427 | PF13499 | 0.528 |
DOC_PP2B_LxvP_1 | 565 | 568 | PF13499 | 0.328 |
DOC_PP4_FxxP_1 | 335 | 338 | PF00568 | 0.407 |
DOC_PP4_FxxP_1 | 533 | 536 | PF00568 | 0.325 |
DOC_USP7_MATH_1 | 171 | 175 | PF00917 | 0.704 |
DOC_USP7_MATH_1 | 207 | 211 | PF00917 | 0.722 |
DOC_USP7_MATH_1 | 30 | 34 | PF00917 | 0.725 |
DOC_USP7_MATH_1 | 441 | 445 | PF00917 | 0.493 |
DOC_USP7_MATH_1 | 454 | 458 | PF00917 | 0.464 |
DOC_USP7_MATH_1 | 465 | 469 | PF00917 | 0.448 |
DOC_USP7_UBL2_3 | 484 | 488 | PF12436 | 0.528 |
DOC_WW_Pin1_4 | 189 | 194 | PF00397 | 0.725 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.761 |
DOC_WW_Pin1_4 | 241 | 246 | PF00397 | 0.653 |
DOC_WW_Pin1_4 | 25 | 30 | PF00397 | 0.760 |
DOC_WW_Pin1_4 | 282 | 287 | PF00397 | 0.632 |
DOC_WW_Pin1_4 | 492 | 497 | PF00397 | 0.493 |
LIG_14-3-3_CanoR_1 | 14 | 21 | PF00244 | 0.718 |
LIG_14-3-3_CanoR_1 | 141 | 151 | PF00244 | 0.593 |
LIG_14-3-3_CanoR_1 | 289 | 295 | PF00244 | 0.514 |
LIG_14-3-3_CanoR_1 | 319 | 323 | PF00244 | 0.328 |
LIG_14-3-3_CanoR_1 | 447 | 451 | PF00244 | 0.493 |
LIG_14-3-3_CanoR_1 | 53 | 58 | PF00244 | 0.706 |
LIG_ActinCP_TwfCPI_2 | 335 | 344 | PF01115 | 0.407 |
LIG_BRCT_BRCA1_1 | 266 | 270 | PF00533 | 0.629 |
LIG_BRCT_BRCA1_1 | 65 | 69 | PF00533 | 0.728 |
LIG_DLG_GKlike_1 | 290 | 298 | PF00625 | 0.528 |
LIG_eIF4E_1 | 360 | 366 | PF01652 | 0.469 |
LIG_FHA_1 | 195 | 201 | PF00498 | 0.703 |
LIG_FHA_1 | 310 | 316 | PF00498 | 0.418 |
LIG_FHA_1 | 412 | 418 | PF00498 | 0.504 |
LIG_FHA_1 | 493 | 499 | PF00498 | 0.493 |
LIG_FHA_1 | 60 | 66 | PF00498 | 0.729 |
LIG_FHA_2 | 43 | 49 | PF00498 | 0.734 |
LIG_FHA_2 | 572 | 578 | PF00498 | 0.269 |
LIG_LIR_Apic_2 | 210 | 214 | PF02991 | 0.718 |
LIG_LIR_Apic_2 | 318 | 323 | PF02991 | 0.320 |
LIG_LIR_Apic_2 | 332 | 338 | PF02991 | 0.300 |
LIG_LIR_Gen_1 | 278 | 286 | PF02991 | 0.674 |
LIG_LIR_Gen_1 | 297 | 307 | PF02991 | 0.332 |
LIG_LIR_Gen_1 | 321 | 330 | PF02991 | 0.390 |
LIG_LIR_Gen_1 | 343 | 353 | PF02991 | 0.485 |
LIG_LIR_Gen_1 | 66 | 76 | PF02991 | 0.736 |
LIG_LIR_LC3C_4 | 457 | 462 | PF02991 | 0.493 |
LIG_LIR_Nem_3 | 278 | 282 | PF02991 | 0.569 |
LIG_LIR_Nem_3 | 297 | 302 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 343 | 348 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 359 | 363 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 378 | 384 | PF02991 | 0.528 |
LIG_LIR_Nem_3 | 392 | 396 | PF02991 | 0.493 |
LIG_LIR_Nem_3 | 517 | 522 | PF02991 | 0.492 |
LIG_LIR_Nem_3 | 66 | 72 | PF02991 | 0.707 |
LIG_NRBOX | 290 | 296 | PF00104 | 0.399 |
LIG_Pex14_1 | 331 | 335 | PF04695 | 0.407 |
LIG_Pex14_1 | 581 | 585 | PF04695 | 0.269 |
LIG_Pex14_2 | 348 | 352 | PF04695 | 0.535 |
LIG_PTB_Apo_2 | 542 | 549 | PF02174 | 0.407 |
LIG_PTB_Phospho_1 | 542 | 548 | PF10480 | 0.407 |
LIG_SH2_CRK | 320 | 324 | PF00017 | 0.401 |
LIG_SH2_CRK | 548 | 552 | PF00017 | 0.328 |
LIG_SH2_NCK_1 | 320 | 324 | PF00017 | 0.383 |
LIG_SH2_NCK_1 | 509 | 513 | PF00017 | 0.516 |
LIG_SH2_PTP2 | 425 | 428 | PF00017 | 0.566 |
LIG_SH2_STAT5 | 142 | 145 | PF00017 | 0.567 |
LIG_SH2_STAT5 | 260 | 263 | PF00017 | 0.569 |
LIG_SH2_STAT5 | 320 | 323 | PF00017 | 0.390 |
LIG_SH2_STAT5 | 328 | 331 | PF00017 | 0.293 |
LIG_SH2_STAT5 | 357 | 360 | PF00017 | 0.487 |
LIG_SH2_STAT5 | 381 | 384 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 425 | 428 | PF00017 | 0.528 |
LIG_SH2_STAT5 | 522 | 525 | PF00017 | 0.520 |
LIG_SH2_STAT5 | 530 | 533 | PF00017 | 0.316 |
LIG_SH2_STAT5 | 585 | 588 | PF00017 | 0.269 |
LIG_SH3_3 | 15 | 21 | PF00018 | 0.770 |
LIG_SH3_3 | 182 | 188 | PF00018 | 0.663 |
LIG_SH3_3 | 197 | 203 | PF00018 | 0.725 |
LIG_SH3_3 | 210 | 216 | PF00018 | 0.713 |
LIG_SH3_3 | 26 | 32 | PF00018 | 0.623 |
LIG_SH3_3 | 335 | 341 | PF00018 | 0.325 |
LIG_SH3_3 | 381 | 387 | PF00018 | 0.570 |
LIG_SH3_3 | 493 | 499 | PF00018 | 0.493 |
LIG_SH3_3 | 558 | 564 | PF00018 | 0.277 |
LIG_SH3_3 | 565 | 571 | PF00018 | 0.259 |
LIG_SUMO_SIM_anti_2 | 312 | 318 | PF11976 | 0.334 |
LIG_SUMO_SIM_anti_2 | 457 | 462 | PF11976 | 0.471 |
LIG_SUMO_SIM_par_1 | 293 | 300 | PF11976 | 0.363 |
LIG_SUMO_SIM_par_1 | 312 | 318 | PF11976 | 0.147 |
LIG_SUMO_SIM_par_1 | 557 | 563 | PF11976 | 0.293 |
LIG_TRAF2_1 | 115 | 118 | PF00917 | 0.613 |
LIG_TRAF2_1 | 490 | 493 | PF00917 | 0.469 |
LIG_TRAF2_1 | 95 | 98 | PF00917 | 0.706 |
LIG_TRFH_1 | 548 | 552 | PF08558 | 0.316 |
LIG_UBA3_1 | 523 | 528 | PF00899 | 0.522 |
LIG_WRC_WIRS_1 | 298 | 303 | PF05994 | 0.416 |
LIG_WRC_WIRS_1 | 345 | 350 | PF05994 | 0.543 |
LIG_WRC_WIRS_1 | 390 | 395 | PF05994 | 0.493 |
MOD_CDK_SPK_2 | 241 | 246 | PF00069 | 0.653 |
MOD_CDK_SPxK_1 | 189 | 195 | PF00069 | 0.788 |
MOD_CDK_SPxK_1 | 19 | 25 | PF00069 | 0.746 |
MOD_CDK_SPxxK_3 | 282 | 289 | PF00069 | 0.621 |
MOD_CK1_1 | 176 | 182 | PF00069 | 0.686 |
MOD_CK1_1 | 234 | 240 | PF00069 | 0.704 |
MOD_CK1_1 | 266 | 272 | PF00069 | 0.674 |
MOD_CK1_1 | 278 | 284 | PF00069 | 0.636 |
MOD_CK1_1 | 297 | 303 | PF00069 | 0.464 |
MOD_CK1_1 | 318 | 324 | PF00069 | 0.366 |
MOD_CK1_1 | 56 | 62 | PF00069 | 0.692 |
MOD_CK1_1 | 63 | 69 | PF00069 | 0.691 |
MOD_CK1_1 | 77 | 83 | PF00069 | 0.560 |
MOD_CK2_1 | 112 | 118 | PF00069 | 0.615 |
MOD_Cter_Amidation | 238 | 241 | PF01082 | 0.555 |
MOD_DYRK1A_RPxSP_1 | 19 | 23 | PF00069 | 0.759 |
MOD_GlcNHglycan | 175 | 178 | PF01048 | 0.484 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.462 |
MOD_GlcNHglycan | 440 | 444 | PF01048 | 0.269 |
MOD_GlcNHglycan | 451 | 454 | PF01048 | 0.269 |
MOD_GlcNHglycan | 75 | 79 | PF01048 | 0.502 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.670 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.797 |
MOD_GSK3_1 | 203 | 210 | PF00069 | 0.742 |
MOD_GSK3_1 | 278 | 285 | PF00069 | 0.615 |
MOD_GSK3_1 | 290 | 297 | PF00069 | 0.427 |
MOD_GSK3_1 | 336 | 343 | PF00069 | 0.372 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.710 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.686 |
MOD_GSK3_1 | 83 | 90 | PF00069 | 0.772 |
MOD_NEK2_1 | 265 | 270 | PF00069 | 0.549 |
MOD_NEK2_1 | 294 | 299 | PF00069 | 0.325 |
MOD_NEK2_1 | 315 | 320 | PF00069 | 0.467 |
MOD_NEK2_1 | 329 | 334 | PF00069 | 0.285 |
MOD_NEK2_1 | 49 | 54 | PF00069 | 0.613 |
MOD_NEK2_1 | 602 | 607 | PF00069 | 0.328 |
MOD_NEK2_1 | 61 | 66 | PF00069 | 0.631 |
MOD_OFUCOSY | 438 | 445 | PF10250 | 0.328 |
MOD_PIKK_1 | 13 | 19 | PF00454 | 0.729 |
MOD_PIKK_1 | 56 | 62 | PF00454 | 0.566 |
MOD_PIKK_1 | 80 | 86 | PF00454 | 0.739 |
MOD_PKA_1 | 53 | 59 | PF00069 | 0.653 |
MOD_PKA_2 | 13 | 19 | PF00069 | 0.645 |
MOD_PKA_2 | 234 | 240 | PF00069 | 0.712 |
MOD_PKA_2 | 318 | 324 | PF00069 | 0.328 |
MOD_PKA_2 | 336 | 342 | PF00069 | 0.528 |
MOD_PKA_2 | 446 | 452 | PF00069 | 0.469 |
MOD_PKA_2 | 53 | 59 | PF00069 | 0.737 |
MOD_Plk_1 | 465 | 471 | PF00069 | 0.528 |
MOD_Plk_4 | 278 | 284 | PF00069 | 0.632 |
MOD_Plk_4 | 290 | 296 | PF00069 | 0.450 |
MOD_Plk_4 | 454 | 460 | PF00069 | 0.482 |
MOD_Plk_4 | 465 | 471 | PF00069 | 0.448 |
MOD_ProDKin_1 | 189 | 195 | PF00069 | 0.728 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.763 |
MOD_ProDKin_1 | 241 | 247 | PF00069 | 0.642 |
MOD_ProDKin_1 | 282 | 288 | PF00069 | 0.629 |
MOD_ProDKin_1 | 492 | 498 | PF00069 | 0.493 |
TRG_DiLeu_BaLyEn_6 | 102 | 107 | PF01217 | 0.607 |
TRG_DiLeu_BaLyEn_6 | 249 | 254 | PF01217 | 0.580 |
TRG_ENDOCYTIC_2 | 345 | 348 | PF00928 | 0.506 |
TRG_ENDOCYTIC_2 | 360 | 363 | PF00928 | 0.454 |
TRG_ENDOCYTIC_2 | 381 | 384 | PF00928 | 0.469 |
TRG_ENDOCYTIC_2 | 425 | 428 | PF00928 | 0.528 |
TRG_ENDOCYTIC_2 | 522 | 525 | PF00928 | 0.507 |
TRG_ENDOCYTIC_2 | 530 | 533 | PF00928 | 0.297 |
TRG_ENDOCYTIC_2 | 548 | 551 | PF00928 | 0.344 |
TRG_ER_diArg_1 | 139 | 142 | PF00400 | 0.583 |
TRG_ER_diArg_1 | 151 | 153 | PF00400 | 0.555 |
TRG_ER_diArg_1 | 289 | 291 | PF00400 | 0.528 |
TRG_ER_diArg_1 | 371 | 374 | PF00400 | 0.528 |
TRG_ER_diArg_1 | 53 | 55 | PF00400 | 0.662 |
TRG_ER_diArg_1 | 538 | 541 | PF00400 | 0.439 |
TRG_ER_diArg_1 | 554 | 556 | PF00400 | 0.236 |
TRG_Pf-PMV_PEXEL_1 | 55 | 60 | PF00026 | 0.505 |
TRG_Pf-PMV_PEXEL_1 | 590 | 595 | PF00026 | 0.566 |
TRG_Pf-PMV_PEXEL_1 | 597 | 601 | PF00026 | 0.483 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PE36 | Leptomonas seymouri | 56% | 94% |
A0A3R7NQK7 | Trypanosoma rangeli | 44% | 100% |
A0A3S7WZ82 | Leishmania donovani | 90% | 100% |
A4HEI1 | Leishmania braziliensis | 76% | 100% |
A4I1K9 | Leishmania infantum | 90% | 100% |
C9ZK51 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
E9AXP3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q08650 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 32% | 100% |