Phospholipid biosynthesis, Inositol phosphosphingolipid phospholipase C-Like ISCL
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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005739 | mitochondrion | 5 | 1 |
GO:0005783 | endoplasmic reticulum | 5 | 1 |
GO:0016020 | membrane | 2 | 5 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0071944 | cell periphery | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pescher et al. (upgregulation) | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Lahav et al. - mRNA
- Protein
|
Related structures:
AlphaFold database: A4HTH1
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 1 |
GO:0006643 | membrane lipid metabolic process | 4 | 1 |
GO:0006644 | phospholipid metabolic process | 4 | 1 |
GO:0006665 | sphingolipid metabolic process | 4 | 1 |
GO:0006672 | ceramide metabolic process | 4 | 1 |
GO:0006684 | sphingomyelin metabolic process | 4 | 1 |
GO:0006685 | sphingomyelin catabolic process | 5 | 1 |
GO:0006793 | phosphorus metabolic process | 3 | 1 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0008610 | lipid biosynthetic process | 4 | 1 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009058 | biosynthetic process | 2 | 1 |
GO:0009268 | response to pH | 3 | 1 |
GO:0009395 | phospholipid catabolic process | 5 | 1 |
GO:0009628 | response to abiotic stimulus | 2 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010447 | response to acidic pH | 4 | 1 |
GO:0016042 | lipid catabolic process | 4 | 1 |
GO:0019637 | organophosphate metabolic process | 3 | 1 |
GO:0030148 | sphingolipid biosynthetic process | 5 | 1 |
GO:0030149 | sphingolipid catabolic process | 5 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0043603 | amide metabolic process | 3 | 1 |
GO:0043604 | amide biosynthetic process | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044242 | cellular lipid catabolic process | 4 | 1 |
GO:0044248 | cellular catabolic process | 3 | 1 |
GO:0044249 | cellular biosynthetic process | 3 | 1 |
GO:0044255 | cellular lipid metabolic process | 3 | 1 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 1 |
GO:0046434 | organophosphate catabolic process | 4 | 1 |
GO:0046466 | membrane lipid catabolic process | 5 | 1 |
GO:0046467 | membrane lipid biosynthetic process | 4 | 1 |
GO:0046513 | ceramide biosynthetic process | 5 | 1 |
GO:0050896 | response to stimulus | 1 | 1 |
GO:0051716 | cellular response to stimulus | 2 | 1 |
GO:0071214 | cellular response to abiotic stimulus | 3 | 1 |
GO:0071467 | cellular response to pH | 4 | 1 |
GO:0071468 | cellular response to acidic pH | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0104004 | cellular response to environmental stimulus | 3 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
GO:1901565 | organonitrogen compound catabolic process | 4 | 1 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 1 |
GO:1901575 | organic substance catabolic process | 3 | 1 |
GO:1901576 | organic substance biosynthetic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004620 | phospholipase activity | 5 | 11 |
GO:0004767 | sphingomyelin phosphodiesterase activity | 6 | 11 |
GO:0008081 | phosphoric diester hydrolase activity | 5 | 11 |
GO:0016298 | lipase activity | 4 | 11 |
GO:0016787 | hydrolase activity | 2 | 11 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 11 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 11 |
GO:0003676 | nucleic acid binding | 3 | 3 |
GO:0003743 | translation initiation factor activity | 4 | 3 |
GO:0005488 | binding | 1 | 3 |
GO:0008135 | translation factor activity, RNA binding | 3 | 3 |
GO:0045182 | translation regulator activity | 1 | 3 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 3 |
GO:0097159 | organic cyclic compound binding | 2 | 3 |
GO:1901363 | heterocyclic compound binding | 2 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 252 | 256 | PF00656 | 0.206 |
CLV_C14_Caspase3-7 | 300 | 304 | PF00656 | 0.356 |
CLV_NRD_NRD_1 | 360 | 362 | PF00675 | 0.671 |
CLV_NRD_NRD_1 | 467 | 469 | PF00675 | 0.449 |
CLV_NRD_NRD_1 | 76 | 78 | PF00675 | 0.505 |
CLV_PCSK_KEX2_1 | 166 | 168 | PF00082 | 0.467 |
CLV_PCSK_KEX2_1 | 218 | 220 | PF00082 | 0.540 |
CLV_PCSK_KEX2_1 | 344 | 346 | PF00082 | 0.685 |
CLV_PCSK_KEX2_1 | 467 | 469 | PF00082 | 0.449 |
CLV_PCSK_KEX2_1 | 579 | 581 | PF00082 | 0.531 |
CLV_PCSK_KEX2_1 | 76 | 78 | PF00082 | 0.474 |
CLV_PCSK_PC1ET2_1 | 166 | 168 | PF00082 | 0.421 |
CLV_PCSK_PC1ET2_1 | 218 | 220 | PF00082 | 0.526 |
CLV_PCSK_PC1ET2_1 | 344 | 346 | PF00082 | 0.685 |
CLV_PCSK_PC1ET2_1 | 579 | 581 | PF00082 | 0.531 |
CLV_PCSK_SKI1_1 | 15 | 19 | PF00082 | 0.521 |
CLV_PCSK_SKI1_1 | 249 | 253 | PF00082 | 0.577 |
CLV_PCSK_SKI1_1 | 268 | 272 | PF00082 | 0.393 |
CLV_PCSK_SKI1_1 | 287 | 291 | PF00082 | 0.524 |
CLV_PCSK_SKI1_1 | 579 | 583 | PF00082 | 0.526 |
DEG_SPOP_SBC_1 | 398 | 402 | PF00917 | 0.421 |
DOC_CYCLIN_RxL_1 | 166 | 176 | PF00134 | 0.267 |
DOC_CYCLIN_RxL_1 | 263 | 275 | PF00134 | 0.336 |
DOC_MAPK_gen_1 | 166 | 173 | PF00069 | 0.309 |
DOC_MAPK_gen_1 | 28 | 36 | PF00069 | 0.286 |
DOC_MAPK_MEF2A_6 | 121 | 130 | PF00069 | 0.244 |
DOC_PP1_RVXF_1 | 13 | 20 | PF00149 | 0.349 |
DOC_PP2B_LxvP_1 | 228 | 231 | PF13499 | 0.327 |
DOC_PP4_FxxP_1 | 285 | 288 | PF00568 | 0.337 |
DOC_USP7_MATH_1 | 548 | 552 | PF00917 | 0.766 |
DOC_USP7_MATH_1 | 559 | 563 | PF00917 | 0.800 |
DOC_USP7_MATH_1 | 611 | 615 | PF00917 | 0.565 |
DOC_USP7_UBL2_3 | 358 | 362 | PF12436 | 0.576 |
DOC_WW_Pin1_4 | 405 | 410 | PF00397 | 0.502 |
DOC_WW_Pin1_4 | 417 | 422 | PF00397 | 0.423 |
DOC_WW_Pin1_4 | 534 | 539 | PF00397 | 0.662 |
DOC_WW_Pin1_4 | 544 | 549 | PF00397 | 0.674 |
DOC_WW_Pin1_4 | 581 | 586 | PF00397 | 0.703 |
DOC_WW_Pin1_4 | 63 | 68 | PF00397 | 0.267 |
LIG_14-3-3_CanoR_1 | 15 | 20 | PF00244 | 0.340 |
LIG_14-3-3_CanoR_1 | 174 | 181 | PF00244 | 0.244 |
LIG_14-3-3_CanoR_1 | 249 | 254 | PF00244 | 0.259 |
LIG_14-3-3_CanoR_1 | 425 | 431 | PF00244 | 0.410 |
LIG_14-3-3_CanoR_1 | 580 | 585 | PF00244 | 0.799 |
LIG_14-3-3_CanoR_1 | 71 | 76 | PF00244 | 0.355 |
LIG_14-3-3_CanoR_1 | 77 | 83 | PF00244 | 0.343 |
LIG_14-3-3_CanoR_1 | 92 | 100 | PF00244 | 0.324 |
LIG_Actin_WH2_2 | 220 | 237 | PF00022 | 0.267 |
LIG_ActinCP_TwfCPI_2 | 285 | 293 | PF01115 | 0.221 |
LIG_APCC_ABBA_1 | 111 | 116 | PF00400 | 0.324 |
LIG_APCC_Cbox_1 | 168 | 174 | PF00515 | 0.324 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.455 |
LIG_BRCT_BRCA1_1 | 255 | 259 | PF00533 | 0.203 |
LIG_BRCT_BRCA1_1 | 381 | 385 | PF00533 | 0.332 |
LIG_BRCT_BRCA1_1 | 613 | 617 | PF00533 | 0.433 |
LIG_BRCT_BRCA1_1 | 95 | 99 | PF00533 | 0.256 |
LIG_Clathr_ClatBox_1 | 269 | 273 | PF01394 | 0.337 |
LIG_EH1_1 | 384 | 392 | PF00400 | 0.358 |
LIG_FHA_1 | 100 | 106 | PF00498 | 0.228 |
LIG_FHA_1 | 147 | 153 | PF00498 | 0.248 |
LIG_FHA_1 | 16 | 22 | PF00498 | 0.252 |
LIG_FHA_1 | 190 | 196 | PF00498 | 0.259 |
LIG_FHA_1 | 351 | 357 | PF00498 | 0.558 |
LIG_FHA_1 | 400 | 406 | PF00498 | 0.512 |
LIG_FHA_1 | 412 | 418 | PF00498 | 0.339 |
LIG_FHA_1 | 493 | 499 | PF00498 | 0.718 |
LIG_FHA_1 | 524 | 530 | PF00498 | 0.626 |
LIG_FHA_1 | 618 | 624 | PF00498 | 0.411 |
LIG_FHA_2 | 131 | 137 | PF00498 | 0.267 |
LIG_FHA_2 | 250 | 256 | PF00498 | 0.233 |
LIG_FHA_2 | 318 | 324 | PF00498 | 0.370 |
LIG_FHA_2 | 37 | 43 | PF00498 | 0.304 |
LIG_FHA_2 | 418 | 424 | PF00498 | 0.336 |
LIG_FHA_2 | 427 | 433 | PF00498 | 0.275 |
LIG_FHA_2 | 489 | 495 | PF00498 | 0.544 |
LIG_LIR_Gen_1 | 180 | 186 | PF02991 | 0.287 |
LIG_LIR_Gen_1 | 256 | 267 | PF02991 | 0.334 |
LIG_LIR_Gen_1 | 335 | 341 | PF02991 | 0.446 |
LIG_LIR_Gen_1 | 42 | 49 | PF02991 | 0.324 |
LIG_LIR_Gen_1 | 447 | 458 | PF02991 | 0.341 |
LIG_LIR_Gen_1 | 56 | 65 | PF02991 | 0.256 |
LIG_LIR_Nem_3 | 168 | 173 | PF02991 | 0.242 |
LIG_LIR_Nem_3 | 180 | 184 | PF02991 | 0.298 |
LIG_LIR_Nem_3 | 264 | 270 | PF02991 | 0.330 |
LIG_LIR_Nem_3 | 335 | 340 | PF02991 | 0.466 |
LIG_LIR_Nem_3 | 42 | 47 | PF02991 | 0.324 |
LIG_LIR_Nem_3 | 447 | 453 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 56 | 61 | PF02991 | 0.256 |
LIG_LIR_Nem_3 | 594 | 598 | PF02991 | 0.567 |
LIG_LIR_Nem_3 | 72 | 78 | PF02991 | 0.199 |
LIG_LYPXL_yS_3 | 108 | 111 | PF13949 | 0.319 |
LIG_Pex14_2 | 58 | 62 | PF04695 | 0.378 |
LIG_Pex14_2 | 78 | 82 | PF04695 | 0.188 |
LIG_Pex14_2 | 99 | 103 | PF04695 | 0.304 |
LIG_REV1ctd_RIR_1 | 115 | 125 | PF16727 | 0.337 |
LIG_REV1ctd_RIR_1 | 282 | 287 | PF16727 | 0.267 |
LIG_SH2_CRK | 44 | 48 | PF00017 | 0.244 |
LIG_SH2_CRK | 450 | 454 | PF00017 | 0.367 |
LIG_SH2_NCK_1 | 156 | 160 | PF00017 | 0.267 |
LIG_SH2_NCK_1 | 485 | 489 | PF00017 | 0.554 |
LIG_SH2_STAP1 | 148 | 152 | PF00017 | 0.253 |
LIG_SH2_STAP1 | 44 | 48 | PF00017 | 0.244 |
LIG_SH2_STAP1 | 485 | 489 | PF00017 | 0.591 |
LIG_SH2_STAP1 | 608 | 612 | PF00017 | 0.658 |
LIG_SH2_STAT5 | 148 | 151 | PF00017 | 0.300 |
LIG_SH2_STAT5 | 170 | 173 | PF00017 | 0.228 |
LIG_SH2_STAT5 | 266 | 269 | PF00017 | 0.373 |
LIG_SH2_STAT5 | 437 | 440 | PF00017 | 0.342 |
LIG_SH2_STAT5 | 73 | 76 | PF00017 | 0.254 |
LIG_SH3_3 | 125 | 131 | PF00018 | 0.308 |
LIG_SH3_3 | 224 | 230 | PF00018 | 0.263 |
LIG_SH3_3 | 321 | 327 | PF00018 | 0.343 |
LIG_SH3_3 | 495 | 501 | PF00018 | 0.702 |
LIG_SH3_3 | 555 | 561 | PF00018 | 0.786 |
LIG_SH3_4 | 358 | 365 | PF00018 | 0.405 |
LIG_Sin3_3 | 454 | 461 | PF02671 | 0.225 |
LIG_SUMO_SIM_anti_2 | 45 | 51 | PF11976 | 0.244 |
LIG_SUMO_SIM_anti_2 | 455 | 460 | PF11976 | 0.434 |
LIG_SUMO_SIM_par_1 | 149 | 157 | PF11976 | 0.323 |
LIG_SUMO_SIM_par_1 | 45 | 51 | PF11976 | 0.244 |
LIG_TRAF2_1 | 240 | 243 | PF00917 | 0.249 |
LIG_TRAF2_1 | 471 | 474 | PF00917 | 0.598 |
LIG_TYR_ITSM | 446 | 453 | PF00017 | 0.319 |
LIG_UBA3_1 | 212 | 218 | PF00899 | 0.301 |
LIG_UBA3_1 | 390 | 397 | PF00899 | 0.306 |
LIG_WRC_WIRS_1 | 16 | 21 | PF05994 | 0.259 |
LIG_WW_3 | 229 | 233 | PF00397 | 0.324 |
MOD_CK1_1 | 160 | 166 | PF00069 | 0.324 |
MOD_CK1_1 | 189 | 195 | PF00069 | 0.263 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.429 |
MOD_CK1_1 | 204 | 210 | PF00069 | 0.314 |
MOD_CK1_1 | 261 | 267 | PF00069 | 0.369 |
MOD_CK1_1 | 408 | 414 | PF00069 | 0.506 |
MOD_CK1_1 | 531 | 537 | PF00069 | 0.662 |
MOD_CK2_1 | 317 | 323 | PF00069 | 0.406 |
MOD_CK2_1 | 36 | 42 | PF00069 | 0.332 |
MOD_CK2_1 | 362 | 368 | PF00069 | 0.488 |
MOD_CK2_1 | 404 | 410 | PF00069 | 0.495 |
MOD_CK2_1 | 417 | 423 | PF00069 | 0.338 |
MOD_CK2_1 | 467 | 473 | PF00069 | 0.631 |
MOD_CK2_1 | 580 | 586 | PF00069 | 0.692 |
MOD_Cter_Amidation | 342 | 345 | PF01082 | 0.680 |
MOD_Cter_Amidation | 359 | 362 | PF01082 | 0.569 |
MOD_GlcNHglycan | 135 | 140 | PF01048 | 0.511 |
MOD_GlcNHglycan | 329 | 332 | PF01048 | 0.734 |
MOD_GlcNHglycan | 370 | 373 | PF01048 | 0.747 |
MOD_GlcNHglycan | 469 | 472 | PF01048 | 0.480 |
MOD_GlcNHglycan | 476 | 479 | PF01048 | 0.464 |
MOD_GlcNHglycan | 609 | 612 | PF01048 | 0.414 |
MOD_GlcNHglycan | 614 | 617 | PF01048 | 0.331 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.444 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.291 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.239 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.260 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.268 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.263 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.297 |
MOD_GSK3_1 | 360 | 367 | PF00069 | 0.498 |
MOD_GSK3_1 | 404 | 411 | PF00069 | 0.530 |
MOD_GSK3_1 | 440 | 447 | PF00069 | 0.396 |
MOD_GSK3_1 | 488 | 495 | PF00069 | 0.589 |
MOD_GSK3_1 | 544 | 551 | PF00069 | 0.726 |
MOD_GSK3_1 | 565 | 572 | PF00069 | 0.752 |
MOD_GSK3_1 | 607 | 614 | PF00069 | 0.628 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.344 |
MOD_N-GLC_1 | 201 | 206 | PF02516 | 0.457 |
MOD_N-GLC_1 | 350 | 355 | PF02516 | 0.757 |
MOD_N-GLC_1 | 617 | 622 | PF02516 | 0.315 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.267 |
MOD_NEK2_1 | 173 | 178 | PF00069 | 0.324 |
MOD_NEK2_1 | 184 | 189 | PF00069 | 0.299 |
MOD_NEK2_1 | 201 | 206 | PF00069 | 0.257 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.311 |
MOD_NEK2_1 | 404 | 409 | PF00069 | 0.483 |
MOD_NEK2_1 | 607 | 612 | PF00069 | 0.657 |
MOD_NEK2_1 | 617 | 622 | PF00069 | 0.423 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.314 |
MOD_NEK2_1 | 99 | 104 | PF00069 | 0.304 |
MOD_NEK2_2 | 504 | 509 | PF00069 | 0.623 |
MOD_NEK2_2 | 523 | 528 | PF00069 | 0.496 |
MOD_PIKK_1 | 157 | 163 | PF00454 | 0.300 |
MOD_PIKK_1 | 173 | 179 | PF00454 | 0.244 |
MOD_PIKK_1 | 201 | 207 | PF00454 | 0.257 |
MOD_PIKK_1 | 275 | 281 | PF00454 | 0.324 |
MOD_PIKK_1 | 440 | 446 | PF00454 | 0.389 |
MOD_PIKK_1 | 93 | 99 | PF00454 | 0.249 |
MOD_PKA_1 | 467 | 473 | PF00069 | 0.580 |
MOD_PKA_1 | 579 | 585 | PF00069 | 0.728 |
MOD_PKA_2 | 173 | 179 | PF00069 | 0.244 |
MOD_PKA_2 | 189 | 195 | PF00069 | 0.337 |
MOD_PKA_2 | 360 | 366 | PF00069 | 0.524 |
MOD_PKA_2 | 467 | 473 | PF00069 | 0.582 |
MOD_PKA_2 | 492 | 498 | PF00069 | 0.663 |
MOD_PKA_2 | 579 | 585 | PF00069 | 0.728 |
MOD_Plk_1 | 143 | 149 | PF00069 | 0.273 |
MOD_Plk_2-3 | 51 | 57 | PF00069 | 0.248 |
MOD_Plk_4 | 143 | 149 | PF00069 | 0.300 |
MOD_Plk_4 | 223 | 229 | PF00069 | 0.284 |
MOD_Plk_4 | 262 | 268 | PF00069 | 0.331 |
MOD_Plk_4 | 426 | 432 | PF00069 | 0.352 |
MOD_Plk_4 | 78 | 84 | PF00069 | 0.346 |
MOD_ProDKin_1 | 405 | 411 | PF00069 | 0.502 |
MOD_ProDKin_1 | 417 | 423 | PF00069 | 0.416 |
MOD_ProDKin_1 | 534 | 540 | PF00069 | 0.666 |
MOD_ProDKin_1 | 544 | 550 | PF00069 | 0.672 |
MOD_ProDKin_1 | 581 | 587 | PF00069 | 0.703 |
MOD_ProDKin_1 | 63 | 69 | PF00069 | 0.267 |
MOD_SUMO_for_1 | 270 | 273 | PF00179 | 0.324 |
MOD_SUMO_for_1 | 471 | 474 | PF00179 | 0.630 |
TRG_DiLeu_BaEn_1 | 56 | 61 | PF01217 | 0.337 |
TRG_ENDOCYTIC_2 | 108 | 111 | PF00928 | 0.319 |
TRG_ENDOCYTIC_2 | 156 | 159 | PF00928 | 0.313 |
TRG_ENDOCYTIC_2 | 170 | 173 | PF00928 | 0.241 |
TRG_ENDOCYTIC_2 | 266 | 269 | PF00928 | 0.317 |
TRG_ENDOCYTIC_2 | 378 | 381 | PF00928 | 0.360 |
TRG_ENDOCYTIC_2 | 44 | 47 | PF00928 | 0.244 |
TRG_ENDOCYTIC_2 | 450 | 453 | PF00928 | 0.355 |
TRG_ER_diArg_1 | 466 | 468 | PF00400 | 0.567 |
TRG_ER_diArg_1 | 75 | 77 | PF00400 | 0.322 |
TRG_Pf-PMV_PEXEL_1 | 206 | 211 | PF00026 | 0.457 |
TRG_Pf-PMV_PEXEL_1 | 232 | 236 | PF00026 | 0.537 |
TRG_Pf-PMV_PEXEL_1 | 334 | 339 | PF00026 | 0.527 |
TRG_Pf-PMV_PEXEL_1 | 596 | 600 | PF00026 | 0.467 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P935 | Leptomonas seymouri | 57% | 100% |
A0A1X0NNY2 | Trypanosomatidae | 40% | 100% |
A0A3S5H634 | Leishmania donovani | 100% | 100% |
A0A422NTR5 | Trypanosoma rangeli | 44% | 100% |
A4H587 | Leishmania braziliensis | 73% | 100% |
C9ZPP9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
E9AM99 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 98% |
Q4QIE9 | Leishmania major | 94% | 100% |
V5BLM5 | Trypanosoma cruzi | 38% | 100% |