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: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005783 | endoplasmic reticulum | 5 | 10 |
GO:0016020 | membrane | 2 | 10 |
GO:0043226 | organelle | 2 | 10 |
GO:0043227 | membrane-bounded organelle | 3 | 10 |
GO:0043229 | intracellular organelle | 3 | 10 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
Related structures:
AlphaFold database: A0A3Q8IJJ2
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 11 |
GO:0006644 | phospholipid metabolic process | 4 | 11 |
GO:0006793 | phosphorus metabolic process | 3 | 11 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0008610 | lipid biosynthetic process | 4 | 11 |
GO:0008654 | phospholipid biosynthetic process | 5 | 11 |
GO:0009058 | biosynthetic process | 2 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016310 | phosphorylation | 5 | 9 |
GO:0019637 | organophosphate metabolic process | 3 | 11 |
GO:0043048 | dolichyl monophosphate biosynthetic process | 6 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0044255 | cellular lipid metabolic process | 3 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:0090407 | organophosphate biosynthetic process | 4 | 11 |
GO:1901576 | organic substance biosynthetic process | 3 | 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004168 | dolichol kinase activity | 5 | 11 |
GO:0016301 | kinase activity | 4 | 11 |
GO:0016740 | transferase activity | 2 | 11 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 11 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 348 | 352 | PF00656 | 0.626 |
CLV_C14_Caspase3-7 | 490 | 494 | PF00656 | 0.343 |
CLV_NRD_NRD_1 | 207 | 209 | PF00675 | 0.443 |
CLV_NRD_NRD_1 | 210 | 212 | PF00675 | 0.412 |
CLV_NRD_NRD_1 | 285 | 287 | PF00675 | 0.325 |
CLV_NRD_NRD_1 | 418 | 420 | PF00675 | 0.402 |
CLV_NRD_NRD_1 | 66 | 68 | PF00675 | 0.427 |
CLV_PCSK_KEX2_1 | 206 | 208 | PF00082 | 0.471 |
CLV_PCSK_KEX2_1 | 212 | 214 | PF00082 | 0.408 |
CLV_PCSK_KEX2_1 | 285 | 287 | PF00082 | 0.327 |
CLV_PCSK_KEX2_1 | 418 | 420 | PF00082 | 0.402 |
CLV_PCSK_KEX2_1 | 66 | 68 | PF00082 | 0.425 |
CLV_PCSK_PC1ET2_1 | 212 | 214 | PF00082 | 0.408 |
CLV_PCSK_PC7_1 | 208 | 214 | PF00082 | 0.385 |
CLV_PCSK_PC7_1 | 281 | 287 | PF00082 | 0.358 |
CLV_PCSK_SKI1_1 | 243 | 247 | PF00082 | 0.588 |
CLV_PCSK_SKI1_1 | 286 | 290 | PF00082 | 0.282 |
CLV_PCSK_SKI1_1 | 423 | 427 | PF00082 | 0.438 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.452 |
DOC_CYCLIN_yCln2_LP_2 | 23 | 29 | PF00134 | 0.363 |
DOC_CYCLIN_yCln2_LP_2 | 495 | 501 | PF00134 | 0.282 |
DOC_MAPK_gen_1 | 206 | 218 | PF00069 | 0.612 |
DOC_MAPK_gen_1 | 285 | 294 | PF00069 | 0.474 |
DOC_MAPK_MEF2A_6 | 211 | 218 | PF00069 | 0.537 |
DOC_MAPK_MEF2A_6 | 22 | 30 | PF00069 | 0.325 |
DOC_MAPK_MEF2A_6 | 355 | 364 | PF00069 | 0.447 |
DOC_MAPK_NFAT4_5 | 22 | 30 | PF00069 | 0.364 |
DOC_MAPK_NFAT4_5 | 355 | 363 | PF00069 | 0.434 |
DOC_PP2B_LxvP_1 | 159 | 162 | PF13499 | 0.446 |
DOC_PP2B_LxvP_1 | 23 | 26 | PF13499 | 0.348 |
DOC_PP2B_LxvP_1 | 495 | 498 | PF13499 | 0.304 |
DOC_PP2B_LxvP_1 | 511 | 514 | PF13499 | 0.447 |
DOC_PP4_FxxP_1 | 546 | 549 | PF00568 | 0.714 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.451 |
DOC_USP7_MATH_1 | 434 | 438 | PF00917 | 0.595 |
DOC_USP7_MATH_1 | 542 | 546 | PF00917 | 0.731 |
DOC_WW_Pin1_4 | 295 | 300 | PF00397 | 0.335 |
DOC_WW_Pin1_4 | 41 | 46 | PF00397 | 0.353 |
DOC_WW_Pin1_4 | 538 | 543 | PF00397 | 0.745 |
DOC_WW_Pin1_4 | 545 | 550 | PF00397 | 0.729 |
DOC_WW_Pin1_4 | 67 | 72 | PF00397 | 0.676 |
LIG_14-3-3_CanoR_1 | 165 | 169 | PF00244 | 0.377 |
LIG_14-3-3_CanoR_1 | 255 | 260 | PF00244 | 0.344 |
LIG_14-3-3_CanoR_1 | 418 | 422 | PF00244 | 0.651 |
LIG_14-3-3_CanoR_1 | 98 | 103 | PF00244 | 0.330 |
LIG_Actin_WH2_2 | 265 | 283 | PF00022 | 0.468 |
LIG_APCC_ABBAyCdc20_2 | 426 | 432 | PF00400 | 0.713 |
LIG_BRCT_BRCA1_1 | 214 | 218 | PF00533 | 0.490 |
LIG_BRCT_BRCA1_1 | 233 | 237 | PF00533 | 0.386 |
LIG_BRCT_BRCA1_1 | 250 | 254 | PF00533 | 0.396 |
LIG_BRCT_BRCA1_1 | 410 | 414 | PF00533 | 0.447 |
LIG_Clathr_ClatBox_1 | 512 | 516 | PF01394 | 0.402 |
LIG_EH1_1 | 363 | 371 | PF00400 | 0.383 |
LIG_eIF4E_1 | 424 | 430 | PF01652 | 0.710 |
LIG_FHA_1 | 442 | 448 | PF00498 | 0.488 |
LIG_FHA_1 | 9 | 15 | PF00498 | 0.387 |
LIG_FHA_2 | 299 | 305 | PF00498 | 0.480 |
LIG_FHA_2 | 481 | 487 | PF00498 | 0.392 |
LIG_GBD_Chelix_1 | 272 | 280 | PF00786 | 0.526 |
LIG_HP1_1 | 498 | 502 | PF01393 | 0.447 |
LIG_LIR_Apic_2 | 516 | 522 | PF02991 | 0.667 |
LIG_LIR_Apic_2 | 545 | 549 | PF02991 | 0.590 |
LIG_LIR_Gen_1 | 110 | 120 | PF02991 | 0.408 |
LIG_LIR_Gen_1 | 166 | 176 | PF02991 | 0.354 |
LIG_LIR_Gen_1 | 191 | 197 | PF02991 | 0.598 |
LIG_LIR_Gen_1 | 304 | 315 | PF02991 | 0.282 |
LIG_LIR_Gen_1 | 356 | 366 | PF02991 | 0.447 |
LIG_LIR_Gen_1 | 475 | 484 | PF02991 | 0.333 |
LIG_LIR_Gen_1 | 55 | 64 | PF02991 | 0.343 |
LIG_LIR_Gen_1 | 80 | 91 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 110 | 115 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 166 | 171 | PF02991 | 0.375 |
LIG_LIR_Nem_3 | 191 | 196 | PF02991 | 0.571 |
LIG_LIR_Nem_3 | 304 | 310 | PF02991 | 0.287 |
LIG_LIR_Nem_3 | 356 | 362 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 475 | 479 | PF02991 | 0.315 |
LIG_LIR_Nem_3 | 540 | 546 | PF02991 | 0.722 |
LIG_LIR_Nem_3 | 55 | 59 | PF02991 | 0.343 |
LIG_LIR_Nem_3 | 80 | 86 | PF02991 | 0.487 |
LIG_NRBOX | 507 | 513 | PF00104 | 0.447 |
LIG_PALB2_WD40_1 | 258 | 266 | PF16756 | 0.402 |
LIG_PCNA_TLS_4 | 418 | 426 | PF02747 | 0.678 |
LIG_Pex14_1 | 244 | 248 | PF04695 | 0.330 |
LIG_PTB_Apo_2 | 424 | 431 | PF02174 | 0.607 |
LIG_REV1ctd_RIR_1 | 112 | 119 | PF16727 | 0.410 |
LIG_SH2_CRK | 83 | 87 | PF00017 | 0.441 |
LIG_SH2_GRB2like | 327 | 330 | PF00017 | 0.621 |
LIG_SH2_NCK_1 | 168 | 172 | PF00017 | 0.374 |
LIG_SH2_NCK_1 | 83 | 87 | PF00017 | 0.441 |
LIG_SH2_PTP2 | 182 | 185 | PF00017 | 0.441 |
LIG_SH2_STAP1 | 168 | 172 | PF00017 | 0.374 |
LIG_SH2_STAP1 | 474 | 478 | PF00017 | 0.404 |
LIG_SH2_STAP1 | 49 | 53 | PF00017 | 0.347 |
LIG_SH2_STAT5 | 107 | 110 | PF00017 | 0.364 |
LIG_SH2_STAT5 | 112 | 115 | PF00017 | 0.349 |
LIG_SH2_STAT5 | 137 | 140 | PF00017 | 0.408 |
LIG_SH2_STAT5 | 168 | 171 | PF00017 | 0.351 |
LIG_SH2_STAT5 | 182 | 185 | PF00017 | 0.396 |
LIG_SH2_STAT5 | 248 | 251 | PF00017 | 0.336 |
LIG_SH2_STAT5 | 271 | 274 | PF00017 | 0.408 |
LIG_SH2_STAT5 | 359 | 362 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 424 | 427 | PF00017 | 0.613 |
LIG_SH2_STAT5 | 56 | 59 | PF00017 | 0.355 |
LIG_SH3_3 | 377 | 383 | PF00018 | 0.453 |
LIG_SUMO_SIM_anti_2 | 5 | 11 | PF11976 | 0.390 |
LIG_SUMO_SIM_anti_2 | 55 | 61 | PF11976 | 0.355 |
LIG_SUMO_SIM_par_1 | 182 | 188 | PF11976 | 0.411 |
LIG_SUMO_SIM_par_1 | 271 | 277 | PF11976 | 0.432 |
LIG_SUMO_SIM_par_1 | 384 | 389 | PF11976 | 0.382 |
LIG_SUMO_SIM_par_1 | 459 | 465 | PF11976 | 0.403 |
LIG_SUMO_SIM_par_1 | 477 | 483 | PF11976 | 0.223 |
LIG_SUMO_SIM_par_1 | 5 | 11 | PF11976 | 0.383 |
LIG_TRFH_1 | 263 | 267 | PF08558 | 0.402 |
LIG_TYR_ITIM | 54 | 59 | PF00017 | 0.355 |
LIG_TYR_ITIM | 81 | 86 | PF00017 | 0.441 |
LIG_TYR_ITSM | 164 | 171 | PF00017 | 0.404 |
LIG_UBA3_1 | 113 | 117 | PF00899 | 0.402 |
LIG_WRC_WIRS_1 | 473 | 478 | PF05994 | 0.379 |
MOD_CDC14_SPxK_1 | 541 | 544 | PF00782 | 0.710 |
MOD_CDK_SPK_2 | 67 | 72 | PF00069 | 0.676 |
MOD_CDK_SPxK_1 | 538 | 544 | PF00069 | 0.706 |
MOD_CDK_SPxxK_3 | 67 | 74 | PF00069 | 0.675 |
MOD_CK1_1 | 155 | 161 | PF00069 | 0.511 |
MOD_CK1_1 | 188 | 194 | PF00069 | 0.553 |
MOD_CK1_1 | 202 | 208 | PF00069 | 0.592 |
MOD_CK1_1 | 417 | 423 | PF00069 | 0.666 |
MOD_CK1_1 | 545 | 551 | PF00069 | 0.730 |
MOD_CK1_1 | 55 | 61 | PF00069 | 0.349 |
MOD_CK2_1 | 480 | 486 | PF00069 | 0.350 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.447 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.352 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.621 |
MOD_GSK3_1 | 310 | 317 | PF00069 | 0.358 |
MOD_GSK3_1 | 330 | 337 | PF00069 | 0.596 |
MOD_GSK3_1 | 409 | 416 | PF00069 | 0.335 |
MOD_GSK3_1 | 436 | 443 | PF00069 | 0.587 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.341 |
MOD_GSK3_1 | 527 | 534 | PF00069 | 0.734 |
MOD_GSK3_1 | 538 | 545 | PF00069 | 0.735 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.395 |
MOD_N-GLC_1 | 145 | 150 | PF02516 | 0.624 |
MOD_N-GLC_1 | 434 | 439 | PF02516 | 0.393 |
MOD_NEK2_1 | 129 | 134 | PF00069 | 0.349 |
MOD_NEK2_1 | 218 | 223 | PF00069 | 0.338 |
MOD_NEK2_1 | 231 | 236 | PF00069 | 0.412 |
MOD_NEK2_1 | 249 | 254 | PF00069 | 0.421 |
MOD_NEK2_1 | 310 | 315 | PF00069 | 0.346 |
MOD_NEK2_1 | 364 | 369 | PF00069 | 0.322 |
MOD_NEK2_1 | 413 | 418 | PF00069 | 0.504 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.347 |
MOD_PIKK_1 | 522 | 528 | PF00454 | 0.538 |
MOD_PK_1 | 212 | 218 | PF00069 | 0.501 |
MOD_PK_1 | 373 | 379 | PF00069 | 0.474 |
MOD_PKA_1 | 207 | 213 | PF00069 | 0.637 |
MOD_PKA_2 | 152 | 158 | PF00069 | 0.504 |
MOD_PKA_2 | 164 | 170 | PF00069 | 0.242 |
MOD_PKA_2 | 207 | 213 | PF00069 | 0.578 |
MOD_PKA_2 | 280 | 286 | PF00069 | 0.569 |
MOD_PKA_2 | 417 | 423 | PF00069 | 0.660 |
MOD_PKB_1 | 253 | 261 | PF00069 | 0.328 |
MOD_PKB_1 | 371 | 379 | PF00069 | 0.463 |
MOD_Plk_1 | 145 | 151 | PF00069 | 0.428 |
MOD_Plk_1 | 386 | 392 | PF00069 | 0.346 |
MOD_Plk_1 | 434 | 440 | PF00069 | 0.597 |
MOD_Plk_4 | 129 | 135 | PF00069 | 0.378 |
MOD_Plk_4 | 152 | 158 | PF00069 | 0.481 |
MOD_Plk_4 | 185 | 191 | PF00069 | 0.381 |
MOD_Plk_4 | 2 | 8 | PF00069 | 0.364 |
MOD_Plk_4 | 298 | 304 | PF00069 | 0.394 |
MOD_Plk_4 | 409 | 415 | PF00069 | 0.335 |
MOD_Plk_4 | 49 | 55 | PF00069 | 0.335 |
MOD_Plk_4 | 77 | 83 | PF00069 | 0.402 |
MOD_ProDKin_1 | 295 | 301 | PF00069 | 0.335 |
MOD_ProDKin_1 | 41 | 47 | PF00069 | 0.349 |
MOD_ProDKin_1 | 538 | 544 | PF00069 | 0.747 |
MOD_ProDKin_1 | 545 | 551 | PF00069 | 0.730 |
MOD_ProDKin_1 | 67 | 73 | PF00069 | 0.674 |
MOD_SUMO_for_1 | 62 | 65 | PF00179 | 0.666 |
TRG_DiLeu_BaEn_1 | 20 | 25 | PF01217 | 0.337 |
TRG_DiLeu_BaLyEn_6 | 19 | 24 | PF01217 | 0.368 |
TRG_ENDOCYTIC_2 | 112 | 115 | PF00928 | 0.365 |
TRG_ENDOCYTIC_2 | 168 | 171 | PF00928 | 0.378 |
TRG_ENDOCYTIC_2 | 182 | 185 | PF00928 | 0.348 |
TRG_ENDOCYTIC_2 | 327 | 330 | PF00928 | 0.580 |
TRG_ENDOCYTIC_2 | 359 | 362 | PF00928 | 0.417 |
TRG_ENDOCYTIC_2 | 56 | 59 | PF00928 | 0.355 |
TRG_ENDOCYTIC_2 | 83 | 86 | PF00928 | 0.399 |
TRG_ER_diArg_1 | 206 | 208 | PF00400 | 0.677 |
TRG_ER_diArg_1 | 211 | 214 | PF00400 | 0.602 |
TRG_ER_diArg_1 | 284 | 286 | PF00400 | 0.560 |
TRG_ER_diArg_1 | 370 | 373 | PF00400 | 0.389 |
TRG_NLS_MonoExtN_4 | 208 | 215 | PF00514 | 0.638 |
TRG_Pf-PMV_PEXEL_1 | 342 | 346 | PF00026 | 0.437 |
TRG_Pf-PMV_PEXEL_1 | 373 | 378 | PF00026 | 0.651 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IJ90 | Leptomonas seymouri | 76% | 91% |
A0A1X0P5F5 | Trypanosomatidae | 50% | 100% |
A0A3R7KY54 | Trypanosoma rangeli | 50% | 100% |
A4HMW0 | Leishmania braziliensis | 88% | 100% |
A4IBI1 | Leishmania infantum | 100% | 100% |
C9ZZ59 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 99% |
E9AFB7 | Leishmania major | 95% | 100% |
E9B6H2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
V5BTH9 | Trypanosoma cruzi | 51% | 100% |