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: E9AXP3
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:0008374 | O-acyltransferase activity | 5 | 9 |
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 |
GO:0004144 | diacylglycerol O-acyltransferase activity | 7 | 4 |
GO:0016411 | acylglycerol O-acyltransferase activity | 6 | 4 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 403 | 407 | PF00656 | 0.463 |
CLV_NRD_NRD_1 | 153 | 155 | PF00675 | 0.287 |
CLV_NRD_NRD_1 | 290 | 292 | PF00675 | 0.283 |
CLV_NRD_NRD_1 | 374 | 376 | PF00675 | 0.286 |
CLV_NRD_NRD_1 | 447 | 449 | PF00675 | 0.222 |
CLV_NRD_NRD_1 | 483 | 485 | PF00675 | 0.218 |
CLV_NRD_NRD_1 | 54 | 56 | PF00675 | 0.466 |
CLV_NRD_NRD_1 | 555 | 557 | PF00675 | 0.441 |
CLV_NRD_NRD_1 | 590 | 592 | PF00675 | 0.463 |
CLV_PCSK_KEX2_1 | 153 | 155 | PF00082 | 0.336 |
CLV_PCSK_KEX2_1 | 241 | 243 | PF00082 | 0.436 |
CLV_PCSK_KEX2_1 | 290 | 292 | PF00082 | 0.283 |
CLV_PCSK_KEX2_1 | 373 | 375 | PF00082 | 0.284 |
CLV_PCSK_KEX2_1 | 483 | 485 | PF00082 | 0.227 |
CLV_PCSK_KEX2_1 | 54 | 56 | PF00082 | 0.470 |
CLV_PCSK_KEX2_1 | 555 | 557 | PF00082 | 0.441 |
CLV_PCSK_PC1ET2_1 | 241 | 243 | PF00082 | 0.478 |
CLV_PCSK_PC1ET2_1 | 483 | 485 | PF00082 | 0.255 |
CLV_PCSK_SKI1_1 | 153 | 157 | PF00082 | 0.316 |
CLV_PCSK_SKI1_1 | 226 | 230 | PF00082 | 0.354 |
CLV_PCSK_SKI1_1 | 489 | 493 | PF00082 | 0.217 |
CLV_PCSK_SKI1_1 | 542 | 546 | PF00082 | 0.320 |
CLV_Separin_Metazoa | 567 | 571 | PF03568 | 0.152 |
DEG_APCC_DBOX_1 | 153 | 161 | PF00400 | 0.559 |
DEG_COP1_1 | 180 | 188 | PF00400 | 0.570 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.725 |
DOC_CKS1_1 | 191 | 196 | PF01111 | 0.707 |
DOC_CKS1_1 | 21 | 26 | PF01111 | 0.610 |
DOC_CKS1_1 | 215 | 220 | PF01111 | 0.622 |
DOC_CKS1_1 | 284 | 289 | PF01111 | 0.601 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 422 | 429 | PF00134 | 0.432 |
DOC_MAPK_gen_1 | 226 | 234 | PF00069 | 0.552 |
DOC_MAPK_gen_1 | 290 | 297 | PF00069 | 0.515 |
DOC_MAPK_gen_1 | 356 | 366 | PF00069 | 0.360 |
DOC_MAPK_gen_1 | 473 | 482 | PF00069 | 0.433 |
DOC_MAPK_gen_1 | 483 | 492 | PF00069 | 0.405 |
DOC_MAPK_gen_1 | 555 | 562 | PF00069 | 0.241 |
DOC_MAPK_HePTP_8 | 480 | 492 | PF00069 | 0.484 |
DOC_MAPK_MEF2A_6 | 290 | 299 | PF00069 | 0.464 |
DOC_MAPK_MEF2A_6 | 359 | 368 | PF00069 | 0.377 |
DOC_MAPK_MEF2A_6 | 409 | 418 | PF00069 | 0.458 |
DOC_MAPK_MEF2A_6 | 422 | 429 | PF00069 | 0.427 |
DOC_MAPK_MEF2A_6 | 483 | 492 | PF00069 | 0.419 |
DOC_MAPK_MEF2A_6 | 555 | 562 | PF00069 | 0.217 |
DOC_PP2B_LxvP_1 | 183 | 186 | PF13499 | 0.652 |
DOC_PP2B_LxvP_1 | 35 | 38 | PF13499 | 0.570 |
DOC_PP2B_LxvP_1 | 366 | 369 | PF13499 | 0.417 |
DOC_PP2B_LxvP_1 | 425 | 428 | PF13499 | 0.484 |
DOC_PP2B_LxvP_1 | 566 | 569 | PF13499 | 0.284 |
DOC_PP4_FxxP_1 | 336 | 339 | PF00568 | 0.345 |
DOC_PP4_FxxP_1 | 534 | 537 | PF00568 | 0.252 |
DOC_USP7_MATH_1 | 172 | 176 | PF00917 | 0.669 |
DOC_USP7_MATH_1 | 208 | 212 | PF00917 | 0.697 |
DOC_USP7_MATH_1 | 31 | 35 | PF00917 | 0.662 |
DOC_USP7_MATH_1 | 442 | 446 | PF00917 | 0.441 |
DOC_USP7_MATH_1 | 455 | 459 | PF00917 | 0.412 |
DOC_USP7_MATH_1 | 466 | 470 | PF00917 | 0.399 |
DOC_USP7_MATH_2 | 195 | 201 | PF00917 | 0.595 |
DOC_USP7_UBL2_3 | 485 | 489 | PF12436 | 0.484 |
DOC_WW_Pin1_4 | 190 | 195 | PF00397 | 0.754 |
DOC_WW_Pin1_4 | 20 | 25 | PF00397 | 0.717 |
DOC_WW_Pin1_4 | 214 | 219 | PF00397 | 0.626 |
DOC_WW_Pin1_4 | 242 | 247 | PF00397 | 0.615 |
DOC_WW_Pin1_4 | 26 | 31 | PF00397 | 0.719 |
DOC_WW_Pin1_4 | 283 | 288 | PF00397 | 0.606 |
DOC_WW_Pin1_4 | 493 | 498 | PF00397 | 0.441 |
LIG_14-3-3_CanoR_1 | 142 | 152 | PF00244 | 0.560 |
LIG_14-3-3_CanoR_1 | 15 | 22 | PF00244 | 0.685 |
LIG_14-3-3_CanoR_1 | 266 | 272 | PF00244 | 0.539 |
LIG_14-3-3_CanoR_1 | 290 | 296 | PF00244 | 0.489 |
LIG_14-3-3_CanoR_1 | 320 | 324 | PF00244 | 0.284 |
LIG_14-3-3_CanoR_1 | 448 | 452 | PF00244 | 0.441 |
LIG_14-3-3_CanoR_1 | 94 | 101 | PF00244 | 0.596 |
LIG_ActinCP_TwfCPI_2 | 336 | 345 | PF01115 | 0.345 |
LIG_APCC_Cbox_2 | 141 | 147 | PF00515 | 0.435 |
LIG_BIR_III_4 | 272 | 276 | PF00653 | 0.502 |
LIG_BRCT_BRCA1_1 | 267 | 271 | PF00533 | 0.602 |
LIG_BRCT_BRCA1_1 | 66 | 70 | PF00533 | 0.637 |
LIG_DLG_GKlike_1 | 291 | 299 | PF00625 | 0.484 |
LIG_eIF4E_1 | 361 | 367 | PF01652 | 0.417 |
LIG_FHA_1 | 311 | 317 | PF00498 | 0.362 |
LIG_FHA_1 | 413 | 419 | PF00498 | 0.457 |
LIG_FHA_1 | 494 | 500 | PF00498 | 0.441 |
LIG_FHA_1 | 61 | 67 | PF00498 | 0.639 |
LIG_FHA_2 | 205 | 211 | PF00498 | 0.578 |
LIG_FHA_2 | 267 | 273 | PF00498 | 0.541 |
LIG_FHA_2 | 44 | 50 | PF00498 | 0.652 |
LIG_FHA_2 | 573 | 579 | PF00498 | 0.217 |
LIG_LIR_Apic_2 | 210 | 215 | PF02991 | 0.663 |
LIG_LIR_Apic_2 | 319 | 324 | PF02991 | 0.273 |
LIG_LIR_Apic_2 | 335 | 339 | PF02991 | 0.204 |
LIG_LIR_Gen_1 | 298 | 308 | PF02991 | 0.258 |
LIG_LIR_Gen_1 | 322 | 333 | PF02991 | 0.323 |
LIG_LIR_Gen_1 | 67 | 77 | PF02991 | 0.642 |
LIG_LIR_LC3C_4 | 458 | 463 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 279 | 283 | PF02991 | 0.572 |
LIG_LIR_Nem_3 | 298 | 303 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 360 | 364 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 379 | 385 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 393 | 397 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 518 | 523 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 67 | 73 | PF02991 | 0.625 |
LIG_NRBOX | 311 | 317 | PF00104 | 0.191 |
LIG_Pex14_1 | 332 | 336 | PF04695 | 0.345 |
LIG_Pex14_1 | 582 | 586 | PF04695 | 0.217 |
LIG_Pex14_2 | 330 | 334 | PF04695 | 0.202 |
LIG_Pex14_2 | 349 | 353 | PF04695 | 0.526 |
LIG_PTB_Apo_2 | 543 | 550 | PF02174 | 0.345 |
LIG_PTB_Phospho_1 | 543 | 549 | PF10480 | 0.345 |
LIG_SH2_CRK | 321 | 325 | PF00017 | 0.337 |
LIG_SH2_CRK | 549 | 553 | PF00017 | 0.284 |
LIG_SH2_NCK_1 | 321 | 325 | PF00017 | 0.273 |
LIG_SH2_NCK_1 | 510 | 514 | PF00017 | 0.468 |
LIG_SH2_PTP2 | 426 | 429 | PF00017 | 0.463 |
LIG_SH2_SRC | 129 | 132 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 143 | 146 | PF00017 | 0.562 |
LIG_SH2_STAT5 | 261 | 264 | PF00017 | 0.520 |
LIG_SH2_STAT5 | 321 | 324 | PF00017 | 0.323 |
LIG_SH2_STAT5 | 329 | 332 | PF00017 | 0.224 |
LIG_SH2_STAT5 | 361 | 364 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 382 | 385 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 426 | 429 | PF00017 | 0.484 |
LIG_SH2_STAT5 | 523 | 526 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 531 | 534 | PF00017 | 0.244 |
LIG_SH2_STAT5 | 586 | 589 | PF00017 | 0.217 |
LIG_SH3_3 | 16 | 22 | PF00018 | 0.694 |
LIG_SH3_3 | 183 | 189 | PF00018 | 0.721 |
LIG_SH3_3 | 212 | 218 | PF00018 | 0.666 |
LIG_SH3_3 | 27 | 33 | PF00018 | 0.600 |
LIG_SH3_3 | 336 | 342 | PF00018 | 0.253 |
LIG_SH3_3 | 382 | 388 | PF00018 | 0.559 |
LIG_SH3_3 | 494 | 500 | PF00018 | 0.441 |
LIG_SH3_3 | 559 | 565 | PF00018 | 0.224 |
LIG_SH3_3 | 566 | 572 | PF00018 | 0.208 |
LIG_SUMO_SIM_anti_2 | 313 | 319 | PF11976 | 0.260 |
LIG_SUMO_SIM_anti_2 | 458 | 463 | PF11976 | 0.419 |
LIG_SUMO_SIM_par_1 | 294 | 301 | PF11976 | 0.290 |
LIG_SUMO_SIM_par_1 | 313 | 319 | PF11976 | 0.140 |
LIG_SUMO_SIM_par_1 | 558 | 564 | PF11976 | 0.241 |
LIG_TRAF2_1 | 116 | 119 | PF00917 | 0.571 |
LIG_TRAF2_1 | 491 | 494 | PF00917 | 0.417 |
LIG_TRFH_1 | 549 | 553 | PF08558 | 0.268 |
LIG_UBA3_1 | 524 | 529 | PF00899 | 0.477 |
LIG_WRC_WIRS_1 | 299 | 304 | PF05994 | 0.359 |
LIG_WRC_WIRS_1 | 333 | 338 | PF05994 | 0.328 |
LIG_WRC_WIRS_1 | 391 | 396 | PF05994 | 0.441 |
LIG_WW_3 | 23 | 27 | PF00397 | 0.627 |
MOD_CDK_SPK_2 | 242 | 247 | PF00069 | 0.615 |
MOD_CDK_SPxK_1 | 190 | 196 | PF00069 | 0.706 |
MOD_CDK_SPxK_1 | 20 | 26 | PF00069 | 0.667 |
MOD_CDK_SPxxK_3 | 283 | 290 | PF00069 | 0.594 |
MOD_CK1_1 | 177 | 183 | PF00069 | 0.655 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.667 |
MOD_CK1_1 | 267 | 273 | PF00069 | 0.689 |
MOD_CK1_1 | 279 | 285 | PF00069 | 0.510 |
MOD_CK1_1 | 298 | 304 | PF00069 | 0.445 |
MOD_CK1_1 | 319 | 325 | PF00069 | 0.263 |
MOD_CK1_1 | 64 | 70 | PF00069 | 0.661 |
MOD_CK1_1 | 78 | 84 | PF00069 | 0.565 |
MOD_CK2_1 | 112 | 118 | PF00069 | 0.583 |
MOD_CK2_1 | 204 | 210 | PF00069 | 0.576 |
MOD_CK2_1 | 508 | 514 | PF00069 | 0.460 |
MOD_Cter_Amidation | 239 | 242 | PF01082 | 0.461 |
MOD_DYRK1A_RPxSP_1 | 20 | 24 | PF00069 | 0.718 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.442 |
MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.441 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.446 |
MOD_GlcNHglycan | 223 | 226 | PF01048 | 0.401 |
MOD_GlcNHglycan | 441 | 445 | PF01048 | 0.227 |
MOD_GlcNHglycan | 452 | 455 | PF01048 | 0.254 |
MOD_GlcNHglycan | 76 | 80 | PF01048 | 0.461 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.624 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.797 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.726 |
MOD_GSK3_1 | 279 | 286 | PF00069 | 0.587 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.383 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.653 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.733 |
MOD_LATS_1 | 110 | 116 | PF00433 | 0.699 |
MOD_N-GLC_1 | 264 | 269 | PF02516 | 0.265 |
MOD_NEK2_1 | 295 | 300 | PF00069 | 0.252 |
MOD_NEK2_1 | 310 | 315 | PF00069 | 0.345 |
MOD_NEK2_1 | 316 | 321 | PF00069 | 0.451 |
MOD_NEK2_1 | 603 | 608 | PF00069 | 0.284 |
MOD_NEK2_1 | 62 | 67 | PF00069 | 0.584 |
MOD_OFUCOSY | 439 | 446 | PF10250 | 0.284 |
MOD_PIKK_1 | 14 | 20 | PF00454 | 0.677 |
MOD_PIKK_1 | 81 | 87 | PF00454 | 0.785 |
MOD_PKA_1 | 54 | 60 | PF00069 | 0.612 |
MOD_PKA_2 | 14 | 20 | PF00069 | 0.630 |
MOD_PKA_2 | 166 | 172 | PF00069 | 0.508 |
MOD_PKA_2 | 235 | 241 | PF00069 | 0.637 |
MOD_PKA_2 | 265 | 271 | PF00069 | 0.524 |
MOD_PKA_2 | 319 | 325 | PF00069 | 0.284 |
MOD_PKA_2 | 337 | 343 | PF00069 | 0.484 |
MOD_PKA_2 | 447 | 453 | PF00069 | 0.417 |
MOD_PKA_2 | 54 | 60 | PF00069 | 0.659 |
MOD_PKA_2 | 89 | 95 | PF00069 | 0.655 |
MOD_Plk_1 | 196 | 202 | PF00069 | 0.718 |
MOD_Plk_1 | 405 | 411 | PF00069 | 0.376 |
MOD_Plk_1 | 466 | 472 | PF00069 | 0.484 |
MOD_Plk_4 | 291 | 297 | PF00069 | 0.400 |
MOD_Plk_4 | 455 | 461 | PF00069 | 0.429 |
MOD_Plk_4 | 466 | 472 | PF00069 | 0.399 |
MOD_Plk_4 | 54 | 60 | PF00069 | 0.542 |
MOD_ProDKin_1 | 190 | 196 | PF00069 | 0.755 |
MOD_ProDKin_1 | 20 | 26 | PF00069 | 0.719 |
MOD_ProDKin_1 | 214 | 220 | PF00069 | 0.622 |
MOD_ProDKin_1 | 242 | 248 | PF00069 | 0.604 |
MOD_ProDKin_1 | 283 | 289 | PF00069 | 0.602 |
MOD_ProDKin_1 | 493 | 499 | PF00069 | 0.441 |
MOD_SUMO_rev_2 | 146 | 152 | PF00179 | 0.577 |
TRG_DiLeu_BaLyEn_6 | 250 | 255 | PF01217 | 0.542 |
TRG_ENDOCYTIC_2 | 361 | 364 | PF00928 | 0.404 |
TRG_ENDOCYTIC_2 | 382 | 385 | PF00928 | 0.417 |
TRG_ENDOCYTIC_2 | 426 | 429 | PF00928 | 0.484 |
TRG_ENDOCYTIC_2 | 523 | 526 | PF00928 | 0.456 |
TRG_ENDOCYTIC_2 | 531 | 534 | PF00928 | 0.228 |
TRG_ENDOCYTIC_2 | 549 | 552 | PF00928 | 0.309 |
TRG_ER_diArg_1 | 152 | 154 | PF00400 | 0.502 |
TRG_ER_diArg_1 | 290 | 292 | PF00400 | 0.483 |
TRG_ER_diArg_1 | 372 | 375 | PF00400 | 0.484 |
TRG_ER_diArg_1 | 539 | 542 | PF00400 | 0.398 |
TRG_ER_diArg_1 | 54 | 56 | PF00400 | 0.625 |
TRG_ER_diArg_1 | 555 | 557 | PF00400 | 0.190 |
TRG_Pf-PMV_PEXEL_1 | 591 | 596 | PF00026 | 0.463 |
TRG_Pf-PMV_PEXEL_1 | 598 | 602 | PF00026 | 0.417 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PE36 | Leptomonas seymouri | 58% | 94% |
A0A3R7NQK7 | Trypanosoma rangeli | 45% | 100% |
A0A3S7WZ82 | Leishmania donovani | 90% | 100% |
A4HEI1 | Leishmania braziliensis | 77% | 99% |
A4I1K9 | Leishmania infantum | 89% | 100% |
C9ZK51 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
Q08650 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 31% | 100% |
Q4Q9S8 | Leishmania major | 88% | 100% |