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. | yes | 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: A0A3S7WZ82
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 | 402 | 406 | PF00656 | 0.509 |
CLV_NRD_NRD_1 | 152 | 154 | PF00675 | 0.318 |
CLV_NRD_NRD_1 | 289 | 291 | PF00675 | 0.316 |
CLV_NRD_NRD_1 | 373 | 375 | PF00675 | 0.323 |
CLV_NRD_NRD_1 | 446 | 448 | PF00675 | 0.260 |
CLV_NRD_NRD_1 | 482 | 484 | PF00675 | 0.255 |
CLV_NRD_NRD_1 | 54 | 56 | PF00675 | 0.485 |
CLV_NRD_NRD_1 | 554 | 556 | PF00675 | 0.479 |
CLV_NRD_NRD_1 | 589 | 591 | PF00675 | 0.509 |
CLV_PCSK_KEX2_1 | 152 | 154 | PF00082 | 0.367 |
CLV_PCSK_KEX2_1 | 240 | 242 | PF00082 | 0.485 |
CLV_PCSK_KEX2_1 | 289 | 291 | PF00082 | 0.316 |
CLV_PCSK_KEX2_1 | 372 | 374 | PF00082 | 0.321 |
CLV_PCSK_KEX2_1 | 482 | 484 | PF00082 | 0.264 |
CLV_PCSK_KEX2_1 | 54 | 56 | PF00082 | 0.482 |
CLV_PCSK_KEX2_1 | 554 | 556 | PF00082 | 0.479 |
CLV_PCSK_PC1ET2_1 | 240 | 242 | PF00082 | 0.507 |
CLV_PCSK_PC1ET2_1 | 482 | 484 | PF00082 | 0.293 |
CLV_PCSK_PC7_1 | 369 | 375 | PF00082 | 0.213 |
CLV_PCSK_SKI1_1 | 152 | 156 | PF00082 | 0.378 |
CLV_PCSK_SKI1_1 | 488 | 492 | PF00082 | 0.254 |
CLV_PCSK_SKI1_1 | 541 | 545 | PF00082 | 0.360 |
DEG_APCC_DBOX_1 | 152 | 160 | PF00400 | 0.589 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.767 |
DEG_SPOP_SBC_1 | 265 | 269 | PF00917 | 0.622 |
DOC_CKS1_1 | 190 | 195 | PF01111 | 0.725 |
DOC_CKS1_1 | 214 | 219 | PF01111 | 0.654 |
DOC_CKS1_1 | 283 | 288 | PF01111 | 0.634 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 421 | 428 | PF00134 | 0.474 |
DOC_MAPK_gen_1 | 289 | 296 | PF00069 | 0.550 |
DOC_MAPK_gen_1 | 472 | 481 | PF00069 | 0.471 |
DOC_MAPK_gen_1 | 482 | 491 | PF00069 | 0.441 |
DOC_MAPK_gen_1 | 554 | 561 | PF00069 | 0.279 |
DOC_MAPK_HePTP_8 | 479 | 491 | PF00069 | 0.521 |
DOC_MAPK_MEF2A_6 | 289 | 298 | PF00069 | 0.501 |
DOC_MAPK_MEF2A_6 | 408 | 417 | PF00069 | 0.493 |
DOC_MAPK_MEF2A_6 | 421 | 428 | PF00069 | 0.467 |
DOC_MAPK_MEF2A_6 | 482 | 491 | PF00069 | 0.456 |
DOC_MAPK_MEF2A_6 | 554 | 561 | PF00069 | 0.254 |
DOC_PP2B_LxvP_1 | 182 | 185 | PF13499 | 0.680 |
DOC_PP2B_LxvP_1 | 365 | 368 | PF13499 | 0.454 |
DOC_PP2B_LxvP_1 | 424 | 427 | PF13499 | 0.521 |
DOC_PP2B_LxvP_1 | 565 | 568 | PF13499 | 0.321 |
DOC_PP4_FxxP_1 | 335 | 338 | PF00568 | 0.385 |
DOC_PP4_FxxP_1 | 533 | 536 | PF00568 | 0.291 |
DOC_USP7_MATH_1 | 171 | 175 | PF00917 | 0.694 |
DOC_USP7_MATH_1 | 207 | 211 | PF00917 | 0.724 |
DOC_USP7_MATH_1 | 30 | 34 | PF00917 | 0.720 |
DOC_USP7_MATH_1 | 441 | 445 | PF00917 | 0.479 |
DOC_USP7_MATH_1 | 454 | 458 | PF00917 | 0.449 |
DOC_USP7_MATH_1 | 465 | 469 | PF00917 | 0.436 |
DOC_USP7_UBL2_3 | 484 | 488 | PF12436 | 0.521 |
DOC_WW_Pin1_4 | 189 | 194 | PF00397 | 0.762 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.766 |
DOC_WW_Pin1_4 | 213 | 218 | PF00397 | 0.657 |
DOC_WW_Pin1_4 | 241 | 246 | PF00397 | 0.647 |
DOC_WW_Pin1_4 | 25 | 30 | PF00397 | 0.779 |
DOC_WW_Pin1_4 | 282 | 287 | PF00397 | 0.635 |
DOC_WW_Pin1_4 | 492 | 497 | PF00397 | 0.479 |
LIG_14-3-3_CanoR_1 | 141 | 151 | PF00244 | 0.612 |
LIG_14-3-3_CanoR_1 | 289 | 295 | PF00244 | 0.523 |
LIG_14-3-3_CanoR_1 | 319 | 323 | PF00244 | 0.321 |
LIG_14-3-3_CanoR_1 | 447 | 451 | PF00244 | 0.479 |
LIG_14-3-3_CanoR_1 | 54 | 58 | PF00244 | 0.664 |
LIG_ActinCP_TwfCPI_2 | 335 | 344 | PF01115 | 0.385 |
LIG_BRCT_BRCA1_1 | 266 | 270 | PF00533 | 0.655 |
LIG_BRCT_BRCA1_1 | 65 | 69 | PF00533 | 0.670 |
LIG_DLG_GKlike_1 | 290 | 298 | PF00625 | 0.521 |
LIG_eIF4E_1 | 360 | 366 | PF01652 | 0.454 |
LIG_FHA_1 | 310 | 316 | PF00498 | 0.401 |
LIG_FHA_1 | 412 | 418 | PF00498 | 0.491 |
LIG_FHA_1 | 493 | 499 | PF00498 | 0.479 |
LIG_FHA_1 | 60 | 66 | PF00498 | 0.743 |
LIG_FHA_2 | 39 | 45 | PF00498 | 0.659 |
LIG_FHA_2 | 572 | 578 | PF00498 | 0.254 |
LIG_Integrin_isoDGR_2 | 92 | 94 | PF01839 | 0.462 |
LIG_LIR_Apic_2 | 210 | 214 | PF02991 | 0.702 |
LIG_LIR_Apic_2 | 318 | 323 | PF02991 | 0.310 |
LIG_LIR_Apic_2 | 334 | 338 | PF02991 | 0.241 |
LIG_LIR_Gen_1 | 297 | 307 | PF02991 | 0.297 |
LIG_LIR_Gen_1 | 321 | 332 | PF02991 | 0.363 |
LIG_LIR_Gen_1 | 66 | 76 | PF02991 | 0.759 |
LIG_LIR_LC3C_4 | 457 | 462 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 278 | 282 | PF02991 | 0.592 |
LIG_LIR_Nem_3 | 297 | 302 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 359 | 363 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 378 | 384 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 392 | 396 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 516 | 522 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 66 | 72 | PF02991 | 0.740 |
LIG_Pex14_1 | 331 | 335 | PF04695 | 0.385 |
LIG_Pex14_1 | 581 | 585 | PF04695 | 0.254 |
LIG_Pex14_2 | 348 | 352 | PF04695 | 0.532 |
LIG_PTB_Apo_2 | 542 | 549 | PF02174 | 0.385 |
LIG_PTB_Phospho_1 | 542 | 548 | PF10480 | 0.385 |
LIG_SH2_CRK | 320 | 324 | PF00017 | 0.377 |
LIG_SH2_CRK | 548 | 552 | PF00017 | 0.321 |
LIG_SH2_NCK_1 | 320 | 324 | PF00017 | 0.319 |
LIG_SH2_NCK_1 | 509 | 513 | PF00017 | 0.505 |
LIG_SH2_PTP2 | 425 | 428 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 142 | 145 | PF00017 | 0.604 |
LIG_SH2_STAT5 | 260 | 263 | PF00017 | 0.562 |
LIG_SH2_STAT5 | 320 | 323 | PF00017 | 0.363 |
LIG_SH2_STAT5 | 328 | 331 | PF00017 | 0.263 |
LIG_SH2_STAT5 | 357 | 360 | PF00017 | 0.472 |
LIG_SH2_STAT5 | 381 | 384 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 425 | 428 | PF00017 | 0.521 |
LIG_SH2_STAT5 | 522 | 525 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 530 | 533 | PF00017 | 0.283 |
LIG_SH2_STAT5 | 585 | 588 | PF00017 | 0.254 |
LIG_SH3_3 | 15 | 21 | PF00018 | 0.732 |
LIG_SH3_3 | 182 | 188 | PF00018 | 0.751 |
LIG_SH3_3 | 211 | 217 | PF00018 | 0.700 |
LIG_SH3_3 | 335 | 341 | PF00018 | 0.291 |
LIG_SH3_3 | 381 | 387 | PF00018 | 0.592 |
LIG_SH3_3 | 493 | 499 | PF00018 | 0.479 |
LIG_SH3_3 | 558 | 564 | PF00018 | 0.262 |
LIG_SH3_3 | 565 | 571 | PF00018 | 0.245 |
LIG_SH3_3 | 99 | 105 | PF00018 | 0.664 |
LIG_SUMO_SIM_anti_2 | 312 | 318 | PF11976 | 0.300 |
LIG_SUMO_SIM_anti_2 | 457 | 462 | PF11976 | 0.456 |
LIG_SUMO_SIM_par_1 | 293 | 300 | PF11976 | 0.330 |
LIG_SUMO_SIM_par_1 | 312 | 318 | PF11976 | 0.172 |
LIG_SUMO_SIM_par_1 | 557 | 563 | PF11976 | 0.279 |
LIG_TRAF2_1 | 115 | 118 | PF00917 | 0.602 |
LIG_TRAF2_1 | 490 | 493 | PF00917 | 0.454 |
LIG_TRFH_1 | 548 | 552 | PF08558 | 0.305 |
LIG_TYR_ITIM | 520 | 525 | PF00017 | 0.414 |
LIG_UBA3_1 | 523 | 528 | PF00899 | 0.514 |
LIG_WRC_WIRS_1 | 298 | 303 | PF05994 | 0.398 |
LIG_WRC_WIRS_1 | 332 | 337 | PF05994 | 0.367 |
LIG_WRC_WIRS_1 | 390 | 395 | PF05994 | 0.479 |
LIG_WW_3 | 22 | 26 | PF00397 | 0.671 |
MOD_CDK_SPK_2 | 241 | 246 | PF00069 | 0.647 |
MOD_CDK_SPxK_1 | 189 | 195 | PF00069 | 0.723 |
MOD_CDK_SPxK_1 | 19 | 25 | PF00069 | 0.714 |
MOD_CDK_SPxxK_3 | 282 | 289 | PF00069 | 0.624 |
MOD_CK1_1 | 176 | 182 | PF00069 | 0.699 |
MOD_CK1_1 | 234 | 240 | PF00069 | 0.704 |
MOD_CK1_1 | 266 | 272 | PF00069 | 0.739 |
MOD_CK1_1 | 278 | 284 | PF00069 | 0.530 |
MOD_CK1_1 | 297 | 303 | PF00069 | 0.479 |
MOD_CK1_1 | 318 | 324 | PF00069 | 0.308 |
MOD_CK1_1 | 63 | 69 | PF00069 | 0.685 |
MOD_CK1_1 | 77 | 83 | PF00069 | 0.683 |
MOD_CK2_1 | 112 | 118 | PF00069 | 0.632 |
MOD_CK2_1 | 507 | 513 | PF00069 | 0.497 |
MOD_Cter_Amidation | 238 | 241 | PF01082 | 0.497 |
MOD_Cter_Amidation | 52 | 55 | PF01082 | 0.388 |
MOD_DYRK1A_RPxSP_1 | 19 | 23 | PF00069 | 0.760 |
MOD_GlcNHglycan | 173 | 176 | PF01048 | 0.451 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.475 |
MOD_GlcNHglycan | 217 | 220 | PF01048 | 0.482 |
MOD_GlcNHglycan | 222 | 225 | PF01048 | 0.444 |
MOD_GlcNHglycan | 440 | 444 | PF01048 | 0.254 |
MOD_GlcNHglycan | 451 | 454 | PF01048 | 0.254 |
MOD_GlcNHglycan | 75 | 79 | PF01048 | 0.512 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.668 |
MOD_GSK3_1 | 203 | 210 | PF00069 | 0.747 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.673 |
MOD_GSK3_1 | 278 | 285 | PF00069 | 0.612 |
MOD_GSK3_1 | 290 | 297 | PF00069 | 0.419 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.598 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.692 |
MOD_GSK3_1 | 83 | 90 | PF00069 | 0.764 |
MOD_NEK2_1 | 194 | 199 | PF00069 | 0.636 |
MOD_NEK2_1 | 294 | 299 | PF00069 | 0.291 |
MOD_NEK2_1 | 309 | 314 | PF00069 | 0.291 |
MOD_NEK2_1 | 315 | 320 | PF00069 | 0.441 |
MOD_NEK2_1 | 602 | 607 | PF00069 | 0.321 |
MOD_NEK2_1 | 61 | 66 | PF00069 | 0.593 |
MOD_NEK2_2 | 406 | 411 | PF00069 | 0.449 |
MOD_OFUCOSY | 438 | 445 | PF10250 | 0.321 |
MOD_PIKK_1 | 13 | 19 | PF00454 | 0.719 |
MOD_PIKK_1 | 80 | 86 | PF00454 | 0.814 |
MOD_PKA_2 | 234 | 240 | PF00069 | 0.677 |
MOD_PKA_2 | 318 | 324 | PF00069 | 0.321 |
MOD_PKA_2 | 446 | 452 | PF00069 | 0.454 |
MOD_PKA_2 | 53 | 59 | PF00069 | 0.682 |
MOD_Plk_1 | 465 | 471 | PF00069 | 0.521 |
MOD_Plk_2-3 | 38 | 44 | PF00069 | 0.615 |
MOD_Plk_4 | 290 | 296 | PF00069 | 0.437 |
MOD_Plk_4 | 454 | 460 | PF00069 | 0.466 |
MOD_Plk_4 | 465 | 471 | PF00069 | 0.436 |
MOD_ProDKin_1 | 189 | 195 | PF00069 | 0.763 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.767 |
MOD_ProDKin_1 | 213 | 219 | PF00069 | 0.654 |
MOD_ProDKin_1 | 241 | 247 | PF00069 | 0.636 |
MOD_ProDKin_1 | 282 | 288 | PF00069 | 0.632 |
MOD_ProDKin_1 | 492 | 498 | PF00069 | 0.479 |
MOD_SUMO_rev_2 | 145 | 151 | PF00179 | 0.611 |
MOD_SUMO_rev_2 | 44 | 50 | PF00179 | 0.600 |
TRG_DiLeu_BaLyEn_6 | 249 | 254 | PF01217 | 0.575 |
TRG_ENDOCYTIC_2 | 360 | 363 | PF00928 | 0.440 |
TRG_ENDOCYTIC_2 | 381 | 384 | PF00928 | 0.454 |
TRG_ENDOCYTIC_2 | 425 | 428 | PF00928 | 0.521 |
TRG_ENDOCYTIC_2 | 522 | 525 | PF00928 | 0.494 |
TRG_ENDOCYTIC_2 | 530 | 533 | PF00928 | 0.266 |
TRG_ENDOCYTIC_2 | 548 | 551 | PF00928 | 0.345 |
TRG_ER_diArg_1 | 139 | 142 | PF00400 | 0.630 |
TRG_ER_diArg_1 | 151 | 153 | PF00400 | 0.550 |
TRG_ER_diArg_1 | 289 | 291 | PF00400 | 0.517 |
TRG_ER_diArg_1 | 371 | 374 | PF00400 | 0.521 |
TRG_ER_diArg_1 | 538 | 541 | PF00400 | 0.435 |
TRG_ER_diArg_1 | 554 | 556 | PF00400 | 0.225 |
TRG_Pf-PMV_PEXEL_1 | 55 | 60 | PF00026 | 0.461 |
TRG_Pf-PMV_PEXEL_1 | 590 | 595 | PF00026 | 0.509 |
TRG_Pf-PMV_PEXEL_1 | 597 | 601 | PF00026 | 0.457 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PE36 | Leptomonas seymouri | 56% | 94% |
A0A3R7NQK7 | Trypanosoma rangeli | 45% | 100% |
A4HEI1 | Leishmania braziliensis | 78% | 99% |
A4I1K9 | Leishmania infantum | 100% | 100% |
C9ZK51 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
E9AXP3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4Q9S8 | Leishmania major | 90% | 100% |