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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005789 | endoplasmic reticulum membrane | 4 | 12 |
GO:0016020 | membrane | 2 | 12 |
GO:0031090 | organelle membrane | 3 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
Related structures:
AlphaFold database: Q4QFL4
Term | Name | Level | Count |
---|---|---|---|
GO:0006575 | cellular modified amino acid metabolic process | 3 | 12 |
GO:0006629 | lipid metabolic process | 3 | 12 |
GO:0006644 | phospholipid metabolic process | 4 | 12 |
GO:0006650 | glycerophospholipid metabolic process | 5 | 12 |
GO:0006658 | phosphatidylserine metabolic process | 4 | 12 |
GO:0006659 | phosphatidylserine biosynthetic process | 5 | 12 |
GO:0006793 | phosphorus metabolic process | 3 | 12 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0008610 | lipid biosynthetic process | 4 | 12 |
GO:0008654 | phospholipid biosynthetic process | 5 | 12 |
GO:0009058 | biosynthetic process | 2 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0019637 | organophosphate metabolic process | 3 | 12 |
GO:0042398 | cellular modified amino acid biosynthetic process | 4 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044249 | cellular biosynthetic process | 3 | 12 |
GO:0044255 | cellular lipid metabolic process | 3 | 12 |
GO:0045017 | glycerolipid biosynthetic process | 4 | 12 |
GO:0046474 | glycerophospholipid biosynthetic process | 5 | 12 |
GO:0046486 | glycerolipid metabolic process | 4 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0090407 | organophosphate biosynthetic process | 4 | 12 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 12 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 12 |
GO:1901576 | organic substance biosynthetic process | 3 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0003882 | CDP-diacylglycerol-serine O-phosphatidyltransferase activity | 6 | 5 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 12 |
GO:0016780 | phosphotransferase activity, for other substituted phosphate groups | 4 | 12 |
GO:0017169 | CDP-alcohol phosphatidyltransferase activity | 5 | 5 |
GO:0106245 | L-serine-phosphatidylethanolamine phosphatidyltransferase activity | 5 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 15 | 17 | PF00675 | 0.571 |
CLV_NRD_NRD_1 | 2 | 4 | PF00675 | 0.419 |
CLV_NRD_NRD_1 | 48 | 50 | PF00675 | 0.489 |
CLV_NRD_NRD_1 | 480 | 482 | PF00675 | 0.349 |
CLV_NRD_NRD_1 | 55 | 57 | PF00675 | 0.437 |
CLV_PCSK_FUR_1 | 409 | 413 | PF00082 | 0.294 |
CLV_PCSK_FUR_1 | 477 | 481 | PF00082 | 0.398 |
CLV_PCSK_KEX2_1 | 15 | 17 | PF00082 | 0.548 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.593 |
CLV_PCSK_KEX2_1 | 325 | 327 | PF00082 | 0.284 |
CLV_PCSK_KEX2_1 | 37 | 39 | PF00082 | 0.532 |
CLV_PCSK_KEX2_1 | 411 | 413 | PF00082 | 0.270 |
CLV_PCSK_KEX2_1 | 479 | 481 | PF00082 | 0.340 |
CLV_PCSK_KEX2_1 | 55 | 57 | PF00082 | 0.494 |
CLV_PCSK_PC1ET2_1 | 325 | 327 | PF00082 | 0.305 |
CLV_PCSK_PC1ET2_1 | 37 | 39 | PF00082 | 0.532 |
CLV_PCSK_PC1ET2_1 | 411 | 413 | PF00082 | 0.270 |
CLV_PCSK_SKI1_1 | 165 | 169 | PF00082 | 0.297 |
CLV_PCSK_SKI1_1 | 251 | 255 | PF00082 | 0.313 |
CLV_PCSK_SKI1_1 | 325 | 329 | PF00082 | 0.278 |
CLV_PCSK_SKI1_1 | 371 | 375 | PF00082 | 0.445 |
CLV_PCSK_SKI1_1 | 386 | 390 | PF00082 | 0.297 |
CLV_PCSK_SKI1_1 | 514 | 518 | PF00082 | 0.530 |
CLV_PCSK_SKI1_1 | 526 | 530 | PF00082 | 0.493 |
CLV_PCSK_SKI1_1 | 80 | 84 | PF00082 | 0.526 |
DEG_APCC_DBOX_1 | 385 | 393 | PF00400 | 0.354 |
DEG_MDM2_SWIB_1 | 274 | 282 | PF02201 | 0.245 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.621 |
DOC_CDC14_PxL_1 | 504 | 512 | PF14671 | 0.433 |
DOC_CYCLIN_RxL_1 | 240 | 249 | PF00134 | 0.354 |
DOC_CYCLIN_yCln2_LP_2 | 81 | 87 | PF00134 | 0.669 |
DOC_MAPK_gen_1 | 248 | 258 | PF00069 | 0.445 |
DOC_MAPK_gen_1 | 479 | 488 | PF00069 | 0.593 |
DOC_MAPK_gen_1 | 55 | 62 | PF00069 | 0.716 |
DOC_MAPK_MEF2A_6 | 165 | 172 | PF00069 | 0.313 |
DOC_MAPK_MEF2A_6 | 251 | 260 | PF00069 | 0.297 |
DOC_MAPK_MEF2A_6 | 481 | 490 | PF00069 | 0.550 |
DOC_MAPK_MEF2A_6 | 55 | 64 | PF00069 | 0.698 |
DOC_MAPK_NFAT4_5 | 165 | 173 | PF00069 | 0.364 |
DOC_PP1_RVXF_1 | 384 | 391 | PF00149 | 0.251 |
DOC_PP1_RVXF_1 | 524 | 531 | PF00149 | 0.263 |
DOC_PP1_RVXF_1 | 88 | 95 | PF00149 | 0.633 |
DOC_PP4_FxxP_1 | 344 | 347 | PF00568 | 0.456 |
DOC_USP7_MATH_1 | 516 | 520 | PF00917 | 0.392 |
DOC_USP7_MATH_1 | 68 | 72 | PF00917 | 0.665 |
DOC_USP7_MATH_2 | 68 | 74 | PF00917 | 0.674 |
DOC_WW_Pin1_4 | 26 | 31 | PF00397 | 0.704 |
DOC_WW_Pin1_4 | 343 | 348 | PF00397 | 0.499 |
DOC_WW_Pin1_4 | 83 | 88 | PF00397 | 0.637 |
DOC_WW_Pin1_4 | 97 | 102 | PF00397 | 0.546 |
LIG_14-3-3_CanoR_1 | 214 | 223 | PF00244 | 0.245 |
LIG_14-3-3_CanoR_1 | 251 | 260 | PF00244 | 0.297 |
LIG_14-3-3_CanoR_1 | 412 | 422 | PF00244 | 0.470 |
LIG_14-3-3_CanoR_1 | 55 | 64 | PF00244 | 0.694 |
LIG_AP2alpha_2 | 220 | 222 | PF02296 | 0.331 |
LIG_APCC_ABBA_1 | 180 | 185 | PF00400 | 0.417 |
LIG_BRCT_BRCA1_1 | 112 | 116 | PF00533 | 0.348 |
LIG_BRCT_BRCA1_1 | 256 | 260 | PF00533 | 0.297 |
LIG_deltaCOP1_diTrp_1 | 218 | 229 | PF00928 | 0.332 |
LIG_EH1_1 | 239 | 247 | PF00400 | 0.332 |
LIG_EH1_1 | 350 | 358 | PF00400 | 0.384 |
LIG_EH1_1 | 367 | 375 | PF00400 | 0.198 |
LIG_eIF4E_1 | 195 | 201 | PF01652 | 0.328 |
LIG_eIF4E_1 | 240 | 246 | PF01652 | 0.354 |
LIG_eIF4E_1 | 485 | 491 | PF01652 | 0.363 |
LIG_FHA_1 | 101 | 107 | PF00498 | 0.458 |
LIG_FHA_1 | 177 | 183 | PF00498 | 0.417 |
LIG_FHA_1 | 352 | 358 | PF00498 | 0.392 |
LIG_FHA_1 | 377 | 383 | PF00498 | 0.275 |
LIG_FHA_1 | 393 | 399 | PF00498 | 0.259 |
LIG_FHA_1 | 414 | 420 | PF00498 | 0.321 |
LIG_FHA_1 | 426 | 432 | PF00498 | 0.288 |
LIG_FHA_1 | 52 | 58 | PF00498 | 0.714 |
LIG_FHA_2 | 215 | 221 | PF00498 | 0.256 |
LIG_FHA_2 | 225 | 231 | PF00498 | 0.227 |
LIG_FHA_2 | 46 | 52 | PF00498 | 0.636 |
LIG_GBD_Chelix_1 | 496 | 504 | PF00786 | 0.210 |
LIG_LIR_Gen_1 | 103 | 112 | PF02991 | 0.395 |
LIG_LIR_Gen_1 | 179 | 186 | PF02991 | 0.299 |
LIG_LIR_Gen_1 | 227 | 235 | PF02991 | 0.270 |
LIG_LIR_Gen_1 | 257 | 267 | PF02991 | 0.297 |
LIG_LIR_Gen_1 | 276 | 287 | PF02991 | 0.245 |
LIG_LIR_Gen_1 | 400 | 410 | PF02991 | 0.466 |
LIG_LIR_Gen_1 | 415 | 426 | PF02991 | 0.212 |
LIG_LIR_Nem_3 | 103 | 108 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 179 | 183 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 219 | 225 | PF02991 | 0.240 |
LIG_LIR_Nem_3 | 227 | 232 | PF02991 | 0.239 |
LIG_LIR_Nem_3 | 249 | 253 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 257 | 263 | PF02991 | 0.265 |
LIG_LIR_Nem_3 | 264 | 270 | PF02991 | 0.235 |
LIG_LIR_Nem_3 | 276 | 282 | PF02991 | 0.245 |
LIG_LIR_Nem_3 | 335 | 339 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 348 | 353 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 415 | 421 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 525 | 530 | PF02991 | 0.358 |
LIG_LYPXL_yS_3 | 123 | 126 | PF13949 | 0.351 |
LIG_NRBOX | 357 | 363 | PF00104 | 0.362 |
LIG_NRBOX | 388 | 394 | PF00104 | 0.417 |
LIG_Pex14_1 | 464 | 468 | PF04695 | 0.297 |
LIG_Pex14_2 | 274 | 278 | PF04695 | 0.245 |
LIG_PTB_Apo_2 | 486 | 493 | PF02174 | 0.332 |
LIG_REV1ctd_RIR_1 | 527 | 532 | PF16727 | 0.362 |
LIG_SH2_CRK | 121 | 125 | PF00017 | 0.257 |
LIG_SH2_CRK | 493 | 497 | PF00017 | 0.257 |
LIG_SH2_SRC | 121 | 124 | PF00017 | 0.254 |
LIG_SH2_STAP1 | 196 | 200 | PF00017 | 0.322 |
LIG_SH2_STAP1 | 493 | 497 | PF00017 | 0.417 |
LIG_SH2_STAP1 | 524 | 528 | PF00017 | 0.323 |
LIG_SH2_STAT5 | 240 | 243 | PF00017 | 0.349 |
LIG_SH2_STAT5 | 440 | 443 | PF00017 | 0.320 |
LIG_SH2_STAT5 | 468 | 471 | PF00017 | 0.377 |
LIG_SH2_STAT5 | 485 | 488 | PF00017 | 0.213 |
LIG_SH2_STAT5 | 527 | 530 | PF00017 | 0.352 |
LIG_SH2_STAT5 | 99 | 102 | PF00017 | 0.541 |
LIG_SH3_3 | 146 | 152 | PF00018 | 0.417 |
LIG_SH3_3 | 447 | 453 | PF00018 | 0.322 |
LIG_SH3_3 | 81 | 87 | PF00018 | 0.683 |
LIG_SUMO_SIM_anti_2 | 354 | 360 | PF11976 | 0.418 |
LIG_SUMO_SIM_par_1 | 243 | 249 | PF11976 | 0.297 |
LIG_SUMO_SIM_par_1 | 261 | 266 | PF11976 | 0.297 |
LIG_SUMO_SIM_par_1 | 358 | 364 | PF11976 | 0.268 |
LIG_SUMO_SIM_par_1 | 470 | 475 | PF11976 | 0.530 |
LIG_TRAF2_1 | 216 | 219 | PF00917 | 0.324 |
LIG_TYR_ITIM | 466 | 471 | PF00017 | 0.382 |
LIG_UBA3_1 | 182 | 191 | PF00899 | 0.397 |
LIG_UBA3_1 | 300 | 307 | PF00899 | 0.382 |
LIG_WRC_WIRS_1 | 177 | 182 | PF05994 | 0.299 |
MOD_CDC14_SPxK_1 | 346 | 349 | PF00782 | 0.505 |
MOD_CDK_SPxK_1 | 343 | 349 | PF00069 | 0.505 |
MOD_CDK_SPxxK_3 | 83 | 90 | PF00069 | 0.652 |
MOD_CK1_1 | 45 | 51 | PF00069 | 0.755 |
MOD_CK1_1 | 71 | 77 | PF00069 | 0.708 |
MOD_CK2_1 | 213 | 219 | PF00069 | 0.281 |
MOD_CK2_1 | 30 | 36 | PF00069 | 0.762 |
MOD_CK2_1 | 45 | 51 | PF00069 | 0.563 |
MOD_GlcNHglycan | 136 | 139 | PF01048 | 0.338 |
MOD_GlcNHglycan | 518 | 521 | PF01048 | 0.597 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.415 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.743 |
MOD_GSK3_1 | 425 | 432 | PF00069 | 0.384 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.711 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.621 |
MOD_NEK2_1 | 224 | 229 | PF00069 | 0.245 |
MOD_NEK2_1 | 234 | 239 | PF00069 | 0.297 |
MOD_NEK2_1 | 351 | 356 | PF00069 | 0.350 |
MOD_NEK2_1 | 392 | 397 | PF00069 | 0.408 |
MOD_PIKK_1 | 55 | 61 | PF00454 | 0.724 |
MOD_PKA_1 | 55 | 61 | PF00069 | 0.690 |
MOD_PKA_2 | 213 | 219 | PF00069 | 0.264 |
MOD_PKA_2 | 55 | 61 | PF00069 | 0.602 |
MOD_Plk_1 | 196 | 202 | PF00069 | 0.317 |
MOD_Plk_1 | 205 | 211 | PF00069 | 0.298 |
MOD_Plk_1 | 263 | 269 | PF00069 | 0.297 |
MOD_Plk_4 | 100 | 106 | PF00069 | 0.475 |
MOD_Plk_4 | 110 | 116 | PF00069 | 0.278 |
MOD_Plk_4 | 151 | 157 | PF00069 | 0.521 |
MOD_Plk_4 | 176 | 182 | PF00069 | 0.347 |
MOD_Plk_4 | 196 | 202 | PF00069 | 0.114 |
MOD_Plk_4 | 425 | 431 | PF00069 | 0.313 |
MOD_ProDKin_1 | 26 | 32 | PF00069 | 0.705 |
MOD_ProDKin_1 | 343 | 349 | PF00069 | 0.499 |
MOD_ProDKin_1 | 83 | 89 | PF00069 | 0.631 |
MOD_ProDKin_1 | 97 | 103 | PF00069 | 0.541 |
TRG_DiLeu_BaLyEn_6 | 323 | 328 | PF01217 | 0.531 |
TRG_DiLeu_BaLyEn_6 | 77 | 82 | PF01217 | 0.675 |
TRG_ENDOCYTIC_2 | 123 | 126 | PF00928 | 0.324 |
TRG_ENDOCYTIC_2 | 174 | 177 | PF00928 | 0.297 |
TRG_ENDOCYTIC_2 | 309 | 312 | PF00928 | 0.463 |
TRG_ENDOCYTIC_2 | 402 | 405 | PF00928 | 0.445 |
TRG_ENDOCYTIC_2 | 468 | 471 | PF00928 | 0.377 |
TRG_ENDOCYTIC_2 | 485 | 488 | PF00928 | 0.382 |
TRG_ENDOCYTIC_2 | 493 | 496 | PF00928 | 0.417 |
TRG_ENDOCYTIC_2 | 527 | 530 | PF00928 | 0.359 |
TRG_ER_diArg_1 | 1 | 3 | PF00400 | 0.622 |
TRG_ER_diArg_1 | 477 | 480 | PF00400 | 0.537 |
TRG_ER_diArg_1 | 55 | 57 | PF00400 | 0.607 |
TRG_Pf-PMV_PEXEL_1 | 326 | 330 | PF00026 | 0.243 |
TRG_Pf-PMV_PEXEL_1 | 399 | 403 | PF00026 | 0.331 |
TRG_Pf-PMV_PEXEL_1 | 55 | 59 | PF00026 | 0.403 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IIC0 | Leptomonas seymouri | 72% | 100% |
A0A0S4ILR0 | Bodo saltans | 49% | 100% |
A0A1X0NNG6 | Trypanosomatidae | 57% | 100% |
A0A3R7N202 | Trypanosoma rangeli | 52% | 100% |
A0A3S7WT59 | Leishmania donovani | 94% | 100% |
A4H7U0 | Leishmania braziliensis | 86% | 100% |
A4HW66 | Leishmania infantum | 94% | 100% |
B2GV22 | Rattus norvegicus | 34% | 100% |
C9ZSV8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
E1BYA3 | Gallus gallus | 34% | 100% |
E7EY42 | Danio rerio | 34% | 100% |
E9APW7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
O08888 | Cricetulus griseus | 34% | 100% |
P48651 | Homo sapiens | 32% | 100% |
Q00576 | Cricetulus griseus | 32% | 100% |
Q08D11 | Xenopus tropicalis | 35% | 100% |
Q0JR55 | Oryza sativa subsp. japonica | 33% | 100% |
Q2KHY9 | Bos taurus | 32% | 100% |
Q5PQL5 | Rattus norvegicus | 32% | 100% |
Q5ZM65 | Gallus gallus | 32% | 100% |
Q6I628 | Oryza sativa subsp. japonica | 34% | 100% |
Q803C9 | Danio rerio | 32% | 100% |
Q99LH2 | Mus musculus | 32% | 100% |
Q9VPD3 | Drosophila melanogaster | 31% | 100% |
Q9Z1X2 | Mus musculus | 34% | 100% |
V5DC50 | Trypanosoma cruzi | 50% | 100% |