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 |
Related structures:
AlphaFold database: E9AM99
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 | 402 | 406 | PF00656 | 0.369 |
CLV_NRD_NRD_1 | 76 | 78 | PF00675 | 0.507 |
CLV_PCSK_KEX2_1 | 165 | 167 | PF00082 | 0.470 |
CLV_PCSK_KEX2_1 | 217 | 219 | PF00082 | 0.543 |
CLV_PCSK_KEX2_1 | 343 | 345 | PF00082 | 0.714 |
CLV_PCSK_KEX2_1 | 567 | 569 | PF00082 | 0.538 |
CLV_PCSK_KEX2_1 | 76 | 78 | PF00082 | 0.476 |
CLV_PCSK_PC1ET2_1 | 165 | 167 | PF00082 | 0.424 |
CLV_PCSK_PC1ET2_1 | 217 | 219 | PF00082 | 0.528 |
CLV_PCSK_PC1ET2_1 | 343 | 345 | PF00082 | 0.714 |
CLV_PCSK_PC1ET2_1 | 567 | 569 | PF00082 | 0.538 |
CLV_PCSK_SKI1_1 | 248 | 252 | PF00082 | 0.580 |
CLV_PCSK_SKI1_1 | 255 | 259 | PF00082 | 0.527 |
CLV_PCSK_SKI1_1 | 267 | 271 | PF00082 | 0.395 |
CLV_PCSK_SKI1_1 | 286 | 290 | PF00082 | 0.526 |
CLV_PCSK_SKI1_1 | 361 | 365 | PF00082 | 0.564 |
CLV_PCSK_SKI1_1 | 564 | 568 | PF00082 | 0.520 |
DOC_CYCLIN_RxL_1 | 165 | 175 | PF00134 | 0.270 |
DOC_CYCLIN_RxL_1 | 262 | 274 | PF00134 | 0.338 |
DOC_MAPK_gen_1 | 165 | 172 | PF00069 | 0.311 |
DOC_MAPK_gen_1 | 438 | 448 | PF00069 | 0.195 |
DOC_MAPK_MEF2A_6 | 121 | 130 | PF00069 | 0.246 |
DOC_MAPK_MEF2A_6 | 441 | 450 | PF00069 | 0.194 |
DOC_PP1_RVXF_1 | 13 | 20 | PF00149 | 0.352 |
DOC_PP2B_LxvP_1 | 227 | 230 | PF13499 | 0.329 |
DOC_PP4_FxxP_1 | 284 | 287 | PF00568 | 0.339 |
DOC_USP7_MATH_1 | 257 | 261 | PF00917 | 0.333 |
DOC_USP7_MATH_1 | 410 | 414 | PF00917 | 0.291 |
DOC_USP7_MATH_1 | 536 | 540 | PF00917 | 0.764 |
DOC_USP7_MATH_1 | 547 | 551 | PF00917 | 0.811 |
DOC_USP7_UBL2_3 | 357 | 361 | PF12436 | 0.568 |
DOC_WW_Pin1_4 | 532 | 537 | PF00397 | 0.665 |
DOC_WW_Pin1_4 | 569 | 574 | PF00397 | 0.695 |
DOC_WW_Pin1_4 | 63 | 68 | PF00397 | 0.270 |
LIG_14-3-3_CanoR_1 | 15 | 20 | PF00244 | 0.343 |
LIG_14-3-3_CanoR_1 | 173 | 180 | PF00244 | 0.246 |
LIG_14-3-3_CanoR_1 | 248 | 253 | PF00244 | 0.262 |
LIG_14-3-3_CanoR_1 | 417 | 423 | PF00244 | 0.412 |
LIG_14-3-3_CanoR_1 | 459 | 467 | PF00244 | 0.481 |
LIG_14-3-3_CanoR_1 | 568 | 573 | PF00244 | 0.793 |
LIG_14-3-3_CanoR_1 | 71 | 76 | PF00244 | 0.358 |
LIG_14-3-3_CanoR_1 | 77 | 83 | PF00244 | 0.346 |
LIG_Actin_WH2_2 | 219 | 236 | PF00022 | 0.270 |
LIG_ActinCP_TwfCPI_2 | 284 | 292 | PF01115 | 0.223 |
LIG_APCC_ABBA_1 | 111 | 116 | PF00400 | 0.326 |
LIG_APCC_Cbox_1 | 167 | 173 | PF00515 | 0.326 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.456 |
LIG_BRCT_BRCA1_1 | 380 | 384 | PF00533 | 0.340 |
LIG_BRCT_BRCA1_1 | 605 | 609 | PF00533 | 0.436 |
LIG_Clathr_ClatBox_1 | 268 | 272 | PF01394 | 0.339 |
LIG_EH1_1 | 383 | 391 | PF00400 | 0.359 |
LIG_FHA_1 | 100 | 106 | PF00498 | 0.231 |
LIG_FHA_1 | 146 | 152 | PF00498 | 0.251 |
LIG_FHA_1 | 189 | 195 | PF00498 | 0.261 |
LIG_FHA_1 | 350 | 356 | PF00498 | 0.560 |
LIG_FHA_1 | 485 | 491 | PF00498 | 0.724 |
LIG_FHA_1 | 516 | 522 | PF00498 | 0.664 |
LIG_FHA_1 | 610 | 616 | PF00498 | 0.414 |
LIG_FHA_2 | 131 | 137 | PF00498 | 0.270 |
LIG_FHA_2 | 249 | 255 | PF00498 | 0.235 |
LIG_FHA_2 | 317 | 323 | PF00498 | 0.366 |
LIG_FHA_2 | 37 | 43 | PF00498 | 0.307 |
LIG_FHA_2 | 410 | 416 | PF00498 | 0.337 |
LIG_FHA_2 | 419 | 425 | PF00498 | 0.275 |
LIG_FHA_2 | 481 | 487 | PF00498 | 0.562 |
LIG_FHA_2 | 569 | 575 | PF00498 | 0.625 |
LIG_HCF-1_HBM_1 | 474 | 477 | PF13415 | 0.471 |
LIG_LIR_Apic_2 | 321 | 327 | PF02991 | 0.247 |
LIG_LIR_Gen_1 | 179 | 185 | PF02991 | 0.289 |
LIG_LIR_Gen_1 | 334 | 342 | PF02991 | 0.478 |
LIG_LIR_Gen_1 | 42 | 49 | PF02991 | 0.326 |
LIG_LIR_Gen_1 | 439 | 450 | PF02991 | 0.344 |
LIG_LIR_Gen_1 | 56 | 65 | PF02991 | 0.259 |
LIG_LIR_Nem_3 | 167 | 172 | PF02991 | 0.244 |
LIG_LIR_Nem_3 | 179 | 183 | PF02991 | 0.301 |
LIG_LIR_Nem_3 | 263 | 269 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 329 | 335 | PF02991 | 0.512 |
LIG_LIR_Nem_3 | 42 | 47 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 439 | 445 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 56 | 61 | PF02991 | 0.259 |
LIG_LIR_Nem_3 | 586 | 590 | PF02991 | 0.568 |
LIG_LIR_Nem_3 | 72 | 78 | PF02991 | 0.202 |
LIG_NRBOX | 445 | 451 | PF00104 | 0.175 |
LIG_Pex14_2 | 58 | 62 | PF04695 | 0.380 |
LIG_Pex14_2 | 78 | 82 | PF04695 | 0.190 |
LIG_Pex14_2 | 99 | 103 | PF04695 | 0.307 |
LIG_Rb_pABgroove_1 | 471 | 479 | PF01858 | 0.469 |
LIG_REV1ctd_RIR_1 | 115 | 125 | PF16727 | 0.339 |
LIG_REV1ctd_RIR_1 | 281 | 286 | PF16727 | 0.270 |
LIG_SH2_CRK | 44 | 48 | PF00017 | 0.246 |
LIG_SH2_CRK | 442 | 446 | PF00017 | 0.370 |
LIG_SH2_NCK_1 | 155 | 159 | PF00017 | 0.270 |
LIG_SH2_NCK_1 | 477 | 481 | PF00017 | 0.569 |
LIG_SH2_PTP2 | 324 | 327 | PF00017 | 0.292 |
LIG_SH2_SRC | 324 | 327 | PF00017 | 0.296 |
LIG_SH2_STAP1 | 147 | 151 | PF00017 | 0.255 |
LIG_SH2_STAP1 | 44 | 48 | PF00017 | 0.246 |
LIG_SH2_STAP1 | 477 | 481 | PF00017 | 0.606 |
LIG_SH2_STAP1 | 600 | 604 | PF00017 | 0.658 |
LIG_SH2_STAT5 | 147 | 150 | PF00017 | 0.302 |
LIG_SH2_STAT5 | 169 | 172 | PF00017 | 0.231 |
LIG_SH2_STAT5 | 265 | 268 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 324 | 327 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 429 | 432 | PF00017 | 0.346 |
LIG_SH2_STAT5 | 73 | 76 | PF00017 | 0.257 |
LIG_SH3_3 | 125 | 131 | PF00018 | 0.311 |
LIG_SH3_3 | 223 | 229 | PF00018 | 0.266 |
LIG_SH3_3 | 320 | 326 | PF00018 | 0.338 |
LIG_SH3_3 | 543 | 549 | PF00018 | 0.795 |
LIG_SUMO_SIM_anti_2 | 447 | 452 | PF11976 | 0.436 |
LIG_SUMO_SIM_anti_2 | 45 | 51 | PF11976 | 0.246 |
LIG_SUMO_SIM_par_1 | 148 | 156 | PF11976 | 0.325 |
LIG_SUMO_SIM_par_1 | 45 | 51 | PF11976 | 0.246 |
LIG_TRAF2_1 | 365 | 368 | PF00917 | 0.356 |
LIG_TRAF2_1 | 463 | 466 | PF00917 | 0.603 |
LIG_TYR_ITSM | 438 | 445 | PF00017 | 0.329 |
LIG_UBA3_1 | 211 | 217 | PF00899 | 0.304 |
LIG_WRC_WIRS_1 | 16 | 21 | PF05994 | 0.262 |
LIG_WRC_WIRS_1 | 4 | 9 | PF05994 | 0.416 |
LIG_WW_3 | 228 | 232 | PF00397 | 0.326 |
MOD_CK1_1 | 159 | 165 | PF00069 | 0.326 |
MOD_CK1_1 | 188 | 194 | PF00069 | 0.266 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.432 |
MOD_CK1_1 | 203 | 209 | PF00069 | 0.317 |
MOD_CK1_1 | 260 | 266 | PF00069 | 0.371 |
MOD_CK1_1 | 400 | 406 | PF00069 | 0.503 |
MOD_CK2_1 | 316 | 322 | PF00069 | 0.402 |
MOD_CK2_1 | 36 | 42 | PF00069 | 0.335 |
MOD_CK2_1 | 362 | 368 | PF00069 | 0.456 |
MOD_CK2_1 | 396 | 402 | PF00069 | 0.442 |
MOD_CK2_1 | 409 | 415 | PF00069 | 0.338 |
MOD_CK2_1 | 459 | 465 | PF00069 | 0.633 |
MOD_CK2_1 | 568 | 574 | PF00069 | 0.685 |
MOD_GlcNHglycan | 135 | 140 | PF01048 | 0.513 |
MOD_GlcNHglycan | 357 | 360 | PF01048 | 0.799 |
MOD_GlcNHglycan | 367 | 372 | PF01048 | 0.703 |
MOD_GlcNHglycan | 399 | 402 | PF01048 | 0.717 |
MOD_GlcNHglycan | 461 | 464 | PF01048 | 0.482 |
MOD_GlcNHglycan | 468 | 471 | PF01048 | 0.472 |
MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.588 |
MOD_GlcNHglycan | 606 | 609 | PF01048 | 0.334 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.446 |
MOD_GSK3_1 | 142 | 149 | PF00069 | 0.295 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.241 |
MOD_GSK3_1 | 172 | 179 | PF00069 | 0.263 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.270 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.299 |
MOD_GSK3_1 | 327 | 334 | PF00069 | 0.351 |
MOD_GSK3_1 | 355 | 362 | PF00069 | 0.477 |
MOD_GSK3_1 | 363 | 370 | PF00069 | 0.470 |
MOD_GSK3_1 | 393 | 400 | PF00069 | 0.444 |
MOD_GSK3_1 | 432 | 439 | PF00069 | 0.400 |
MOD_GSK3_1 | 480 | 487 | PF00069 | 0.609 |
MOD_GSK3_1 | 532 | 539 | PF00069 | 0.719 |
MOD_GSK3_1 | 553 | 560 | PF00069 | 0.759 |
MOD_GSK3_1 | 599 | 606 | PF00069 | 0.629 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.347 |
MOD_N-GLC_1 | 200 | 205 | PF02516 | 0.459 |
MOD_N-GLC_1 | 349 | 354 | PF02516 | 0.758 |
MOD_N-GLC_1 | 609 | 614 | PF02516 | 0.318 |
MOD_NEK2_1 | 146 | 151 | PF00069 | 0.269 |
MOD_NEK2_1 | 172 | 177 | PF00069 | 0.326 |
MOD_NEK2_1 | 183 | 188 | PF00069 | 0.302 |
MOD_NEK2_1 | 200 | 205 | PF00069 | 0.259 |
MOD_NEK2_1 | 261 | 266 | PF00069 | 0.313 |
MOD_NEK2_1 | 355 | 360 | PF00069 | 0.476 |
MOD_NEK2_1 | 599 | 604 | PF00069 | 0.656 |
MOD_NEK2_1 | 609 | 614 | PF00069 | 0.425 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.316 |
MOD_NEK2_1 | 99 | 104 | PF00069 | 0.306 |
MOD_NEK2_2 | 142 | 147 | PF00069 | 0.168 |
MOD_NEK2_2 | 257 | 262 | PF00069 | 0.168 |
MOD_NEK2_2 | 496 | 501 | PF00069 | 0.622 |
MOD_NEK2_2 | 515 | 520 | PF00069 | 0.535 |
MOD_PIKK_1 | 156 | 162 | PF00454 | 0.302 |
MOD_PIKK_1 | 172 | 178 | PF00454 | 0.246 |
MOD_PIKK_1 | 200 | 206 | PF00454 | 0.260 |
MOD_PIKK_1 | 274 | 280 | PF00454 | 0.326 |
MOD_PIKK_1 | 432 | 438 | PF00454 | 0.394 |
MOD_PKA_1 | 567 | 573 | PF00069 | 0.726 |
MOD_PKA_2 | 172 | 178 | PF00069 | 0.246 |
MOD_PKA_2 | 188 | 194 | PF00069 | 0.339 |
MOD_PKA_2 | 484 | 490 | PF00069 | 0.674 |
MOD_PKA_2 | 567 | 573 | PF00069 | 0.726 |
MOD_Plk_4 | 142 | 148 | PF00069 | 0.304 |
MOD_Plk_4 | 222 | 228 | PF00069 | 0.286 |
MOD_Plk_4 | 261 | 267 | PF00069 | 0.334 |
MOD_Plk_4 | 327 | 333 | PF00069 | 0.489 |
MOD_Plk_4 | 418 | 424 | PF00069 | 0.352 |
MOD_Plk_4 | 444 | 450 | PF00069 | 0.307 |
MOD_Plk_4 | 600 | 606 | PF00069 | 0.570 |
MOD_Plk_4 | 78 | 84 | PF00069 | 0.348 |
MOD_ProDKin_1 | 532 | 538 | PF00069 | 0.665 |
MOD_ProDKin_1 | 569 | 575 | PF00069 | 0.694 |
MOD_ProDKin_1 | 63 | 69 | PF00069 | 0.270 |
MOD_SUMO_for_1 | 269 | 272 | PF00179 | 0.326 |
MOD_SUMO_for_1 | 463 | 466 | PF00179 | 0.635 |
TRG_DiLeu_BaEn_1 | 56 | 61 | PF01217 | 0.339 |
TRG_ENDOCYTIC_2 | 155 | 158 | PF00928 | 0.315 |
TRG_ENDOCYTIC_2 | 169 | 172 | PF00928 | 0.243 |
TRG_ENDOCYTIC_2 | 265 | 268 | PF00928 | 0.320 |
TRG_ENDOCYTIC_2 | 332 | 335 | PF00928 | 0.423 |
TRG_ENDOCYTIC_2 | 377 | 380 | PF00928 | 0.370 |
TRG_ENDOCYTIC_2 | 44 | 47 | PF00928 | 0.246 |
TRG_ENDOCYTIC_2 | 442 | 445 | PF00928 | 0.357 |
TRG_ER_diArg_1 | 75 | 77 | PF00400 | 0.324 |
TRG_Pf-PMV_PEXEL_1 | 205 | 210 | PF00026 | 0.459 |
TRG_Pf-PMV_PEXEL_1 | 231 | 235 | PF00026 | 0.539 |
TRG_Pf-PMV_PEXEL_1 | 588 | 592 | PF00026 | 0.475 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P935 | Leptomonas seymouri | 57% | 100% |
A0A1X0NNY2 | Trypanosomatidae | 35% | 100% |
A0A3S5H634 | Leishmania donovani | 89% | 99% |
A0A422NTR5 | Trypanosoma rangeli | 36% | 100% |
A4H587 | Leishmania braziliensis | 71% | 100% |
A4HTH1 | Leishmania infantum | 89% | 99% |
C9ZPP9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
Q4QIE9 | Leishmania major | 86% | 99% |
V5BLM5 | Trypanosoma cruzi | 37% | 100% |