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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
GO:0005783 | endoplasmic reticulum | 5 | 1 |
GO:0012505 | endomembrane system | 2 | 1 |
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 |
Related structures:
AlphaFold database: E9AR64
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 1 |
GO:0006644 | phospholipid metabolic process | 4 | 1 |
GO:0006650 | glycerophospholipid metabolic process | 5 | 1 |
GO:0006793 | phosphorus metabolic process | 3 | 1 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0019637 | organophosphate metabolic process | 3 | 1 |
GO:0036149 | phosphatidylinositol acyl-chain remodeling | 7 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044255 | cellular lipid metabolic process | 3 | 1 |
GO:0046486 | glycerolipid metabolic process | 4 | 1 |
GO:0046488 | phosphatidylinositol metabolic process | 6 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016746 | acyltransferase activity | 3 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 82 | 86 | PF00656 | 0.544 |
CLV_NRD_NRD_1 | 387 | 389 | PF00675 | 0.392 |
CLV_NRD_NRD_1 | 462 | 464 | PF00675 | 0.378 |
CLV_NRD_NRD_1 | 470 | 472 | PF00675 | 0.433 |
CLV_PCSK_FUR_1 | 460 | 464 | PF00082 | 0.364 |
CLV_PCSK_FUR_1 | 468 | 472 | PF00082 | 0.412 |
CLV_PCSK_KEX2_1 | 194 | 196 | PF00082 | 0.264 |
CLV_PCSK_KEX2_1 | 333 | 335 | PF00082 | 0.161 |
CLV_PCSK_KEX2_1 | 387 | 389 | PF00082 | 0.358 |
CLV_PCSK_KEX2_1 | 462 | 464 | PF00082 | 0.383 |
CLV_PCSK_KEX2_1 | 468 | 470 | PF00082 | 0.425 |
CLV_PCSK_PC1ET2_1 | 194 | 196 | PF00082 | 0.139 |
CLV_PCSK_PC1ET2_1 | 333 | 335 | PF00082 | 0.161 |
CLV_PCSK_PC7_1 | 383 | 389 | PF00082 | 0.369 |
CLV_PCSK_SKI1_1 | 178 | 182 | PF00082 | 0.236 |
CLV_PCSK_SKI1_1 | 2 | 6 | PF00082 | 0.299 |
CLV_PCSK_SKI1_1 | 338 | 342 | PF00082 | 0.276 |
CLV_PCSK_SKI1_1 | 359 | 363 | PF00082 | 0.296 |
CLV_PCSK_SKI1_1 | 37 | 41 | PF00082 | 0.530 |
CLV_PCSK_SKI1_1 | 434 | 438 | PF00082 | 0.414 |
CLV_PCSK_SKI1_1 | 462 | 466 | PF00082 | 0.377 |
CLV_Separin_Metazoa | 175 | 179 | PF03568 | 0.339 |
DEG_APCC_DBOX_1 | 416 | 424 | PF00400 | 0.322 |
DEG_APCC_DBOX_1 | 60 | 68 | PF00400 | 0.310 |
DEG_MDM2_SWIB_1 | 415 | 423 | PF02201 | 0.324 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.616 |
DOC_CDC14_PxL_1 | 164 | 172 | PF14671 | 0.510 |
DOC_CKS1_1 | 274 | 279 | PF01111 | 0.437 |
DOC_CYCLIN_RxL_1 | 175 | 183 | PF00134 | 0.477 |
DOC_CYCLIN_RxL_1 | 332 | 343 | PF00134 | 0.522 |
DOC_MAPK_gen_1 | 122 | 130 | PF00069 | 0.395 |
DOC_MAPK_gen_1 | 293 | 299 | PF00069 | 0.562 |
DOC_MAPK_gen_1 | 387 | 395 | PF00069 | 0.515 |
DOC_MAPK_MEF2A_6 | 122 | 130 | PF00069 | 0.379 |
DOC_PP1_RVXF_1 | 134 | 140 | PF00149 | 0.437 |
DOC_PP1_RVXF_1 | 193 | 200 | PF00149 | 0.522 |
DOC_PP2B_LxvP_1 | 117 | 120 | PF13499 | 0.573 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.561 |
DOC_USP7_UBL2_3 | 190 | 194 | PF12436 | 0.408 |
DOC_WW_Pin1_4 | 203 | 208 | PF00397 | 0.522 |
DOC_WW_Pin1_4 | 216 | 221 | PF00397 | 0.522 |
DOC_WW_Pin1_4 | 273 | 278 | PF00397 | 0.580 |
DOC_WW_Pin1_4 | 405 | 410 | PF00397 | 0.285 |
LIG_14-3-3_CanoR_1 | 150 | 160 | PF00244 | 0.555 |
LIG_14-3-3_CanoR_1 | 417 | 426 | PF00244 | 0.312 |
LIG_14-3-3_CanoR_1 | 78 | 84 | PF00244 | 0.484 |
LIG_Actin_RPEL_3 | 410 | 429 | PF02755 | 0.244 |
LIG_Actin_WH2_2 | 435 | 451 | PF00022 | 0.459 |
LIG_APCC_ABBA_1 | 209 | 214 | PF00400 | 0.443 |
LIG_BIR_III_4 | 85 | 89 | PF00653 | 0.376 |
LIG_BRCT_BRCA1_1 | 342 | 346 | PF00533 | 0.374 |
LIG_CaM_IQ_9 | 455 | 471 | PF13499 | 0.595 |
LIG_deltaCOP1_diTrp_1 | 138 | 146 | PF00928 | 0.426 |
LIG_eIF4E_1 | 390 | 396 | PF01652 | 0.399 |
LIG_FHA_1 | 147 | 153 | PF00498 | 0.453 |
LIG_FHA_1 | 204 | 210 | PF00498 | 0.459 |
LIG_FHA_1 | 245 | 251 | PF00498 | 0.439 |
LIG_FHA_1 | 34 | 40 | PF00498 | 0.292 |
LIG_FHA_1 | 346 | 352 | PF00498 | 0.545 |
LIG_FHA_2 | 274 | 280 | PF00498 | 0.456 |
LIG_FHA_2 | 80 | 86 | PF00498 | 0.543 |
LIG_GBD_Chelix_1 | 425 | 433 | PF00786 | 0.249 |
LIG_LIR_Apic_2 | 273 | 277 | PF02991 | 0.595 |
LIG_LIR_Gen_1 | 138 | 147 | PF02991 | 0.426 |
LIG_LIR_Gen_1 | 445 | 455 | PF02991 | 0.548 |
LIG_LIR_Nem_3 | 108 | 113 | PF02991 | 0.567 |
LIG_LIR_Nem_3 | 142 | 146 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 408 | 414 | PF02991 | 0.367 |
LIG_LIR_Nem_3 | 445 | 450 | PF02991 | 0.537 |
LIG_LYPXL_yS_3 | 110 | 113 | PF13949 | 0.385 |
LIG_MAD2 | 115 | 123 | PF02301 | 0.573 |
LIG_MLH1_MIPbox_1 | 342 | 346 | PF16413 | 0.374 |
LIG_PCNA_PIPBox_1 | 193 | 202 | PF02747 | 0.477 |
LIG_Pex14_1 | 139 | 143 | PF04695 | 0.451 |
LIG_Pex14_1 | 385 | 389 | PF04695 | 0.567 |
LIG_Pex14_2 | 414 | 418 | PF04695 | 0.368 |
LIG_Pex14_2 | 432 | 436 | PF04695 | 0.435 |
LIG_REV1ctd_RIR_1 | 412 | 421 | PF16727 | 0.387 |
LIG_SH2_CRK | 274 | 278 | PF00017 | 0.613 |
LIG_SH2_CRK | 390 | 394 | PF00017 | 0.572 |
LIG_SH2_NCK_1 | 81 | 85 | PF00017 | 0.489 |
LIG_SH2_STAP1 | 141 | 145 | PF00017 | 0.510 |
LIG_SH2_STAP1 | 229 | 233 | PF00017 | 0.524 |
LIG_SH2_STAT3 | 389 | 392 | PF00017 | 0.551 |
LIG_SH2_STAT5 | 141 | 144 | PF00017 | 0.510 |
LIG_SH2_STAT5 | 145 | 148 | PF00017 | 0.471 |
LIG_SH2_STAT5 | 158 | 161 | PF00017 | 0.346 |
LIG_SH2_STAT5 | 179 | 182 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 272 | 275 | PF00017 | 0.493 |
LIG_SH2_STAT5 | 34 | 37 | PF00017 | 0.371 |
LIG_SH2_STAT5 | 38 | 41 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 447 | 450 | PF00017 | 0.565 |
LIG_SH2_STAT5 | 63 | 66 | PF00017 | 0.371 |
LIG_SH2_STAT5 | 81 | 84 | PF00017 | 0.393 |
LIG_SH3_2 | 120 | 125 | PF14604 | 0.533 |
LIG_SH3_3 | 113 | 119 | PF00018 | 0.511 |
LIG_SH3_3 | 230 | 236 | PF00018 | 0.466 |
LIG_SH3_3 | 238 | 244 | PF00018 | 0.415 |
LIG_SH3_3 | 378 | 384 | PF00018 | 0.596 |
LIG_SH3_3 | 396 | 402 | PF00018 | 0.330 |
LIG_SH3_3 | 447 | 453 | PF00018 | 0.590 |
LIG_SUMO_SIM_anti_2 | 249 | 254 | PF11976 | 0.385 |
LIG_SUMO_SIM_par_1 | 263 | 269 | PF11976 | 0.389 |
LIG_TRAF2_1 | 261 | 264 | PF00917 | 0.339 |
LIG_TRAF2_1 | 321 | 324 | PF00917 | 0.575 |
LIG_TYR_ITIM | 177 | 182 | PF00017 | 0.339 |
LIG_TYR_ITIM | 79 | 84 | PF00017 | 0.469 |
LIG_UBA3_1 | 152 | 161 | PF00899 | 0.547 |
LIG_UBA3_1 | 327 | 333 | PF00899 | 0.371 |
LIG_WRC_WIRS_1 | 140 | 145 | PF05994 | 0.510 |
LIG_WRC_WIRS_1 | 22 | 27 | PF05994 | 0.148 |
MOD_CDK_SPK_2 | 216 | 221 | PF00069 | 0.339 |
MOD_CDK_SPxxK_3 | 273 | 280 | PF00069 | 0.431 |
MOD_CK2_1 | 20 | 26 | PF00069 | 0.387 |
MOD_CK2_1 | 258 | 264 | PF00069 | 0.339 |
MOD_CK2_1 | 273 | 279 | PF00069 | 0.430 |
MOD_Cter_Amidation | 466 | 469 | PF01082 | 0.284 |
MOD_GlcNHglycan | 420 | 423 | PF01048 | 0.395 |
MOD_GSK3_1 | 266 | 273 | PF00069 | 0.426 |
MOD_N-GLC_1 | 200 | 205 | PF02516 | 0.185 |
MOD_NEK2_1 | 146 | 151 | PF00069 | 0.532 |
MOD_NEK2_1 | 15 | 20 | PF00069 | 0.272 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.475 |
MOD_NEK2_1 | 284 | 289 | PF00069 | 0.630 |
MOD_NEK2_1 | 298 | 303 | PF00069 | 0.561 |
MOD_NEK2_1 | 33 | 38 | PF00069 | 0.371 |
MOD_NEK2_1 | 340 | 345 | PF00069 | 0.479 |
MOD_NEK2_1 | 395 | 400 | PF00069 | 0.296 |
MOD_NEK2_1 | 5 | 10 | PF00069 | 0.525 |
MOD_NEK2_1 | 59 | 64 | PF00069 | 0.336 |
MOD_NEK2_2 | 96 | 101 | PF00069 | 0.580 |
MOD_PIKK_1 | 223 | 229 | PF00454 | 0.522 |
MOD_PKA_2 | 244 | 250 | PF00069 | 0.441 |
MOD_PKA_2 | 49 | 55 | PF00069 | 0.364 |
MOD_PKA_2 | 5 | 11 | PF00069 | 0.339 |
MOD_Plk_1 | 266 | 272 | PF00069 | 0.406 |
MOD_Plk_1 | 282 | 288 | PF00069 | 0.601 |
MOD_Plk_1 | 374 | 380 | PF00069 | 0.522 |
MOD_Plk_1 | 453 | 459 | PF00069 | 0.583 |
MOD_Plk_4 | 139 | 145 | PF00069 | 0.510 |
MOD_Plk_4 | 395 | 401 | PF00069 | 0.324 |
MOD_Plk_4 | 44 | 50 | PF00069 | 0.223 |
MOD_Plk_4 | 442 | 448 | PF00069 | 0.524 |
MOD_Plk_4 | 453 | 459 | PF00069 | 0.523 |
MOD_Plk_4 | 79 | 85 | PF00069 | 0.474 |
MOD_ProDKin_1 | 203 | 209 | PF00069 | 0.522 |
MOD_ProDKin_1 | 216 | 222 | PF00069 | 0.522 |
MOD_ProDKin_1 | 273 | 279 | PF00069 | 0.579 |
MOD_ProDKin_1 | 405 | 411 | PF00069 | 0.285 |
TRG_DiLeu_BaEn_1 | 323 | 328 | PF01217 | 0.392 |
TRG_DiLeu_BaEn_1 | 337 | 342 | PF01217 | 0.541 |
TRG_DiLeu_BaEn_4 | 263 | 269 | PF01217 | 0.476 |
TRG_ENDOCYTIC_2 | 110 | 113 | PF00928 | 0.595 |
TRG_ENDOCYTIC_2 | 141 | 144 | PF00928 | 0.522 |
TRG_ENDOCYTIC_2 | 179 | 182 | PF00928 | 0.437 |
TRG_ENDOCYTIC_2 | 390 | 393 | PF00928 | 0.572 |
TRG_ENDOCYTIC_2 | 411 | 414 | PF00928 | 0.287 |
TRG_ENDOCYTIC_2 | 447 | 450 | PF00928 | 0.575 |
TRG_ENDOCYTIC_2 | 81 | 84 | PF00928 | 0.484 |
TRG_ER_diArg_1 | 386 | 388 | PF00400 | 0.571 |
TRG_ER_diArg_1 | 460 | 463 | PF00400 | 0.604 |
TRG_ER_diArg_1 | 468 | 471 | PF00400 | 0.649 |
TRG_ER_diLys_1 | 472 | 477 | PF00400 | 0.686 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IKC7 | Leptomonas seymouri | 57% | 100% |
A0A0S4J7G6 | Bodo saltans | 30% | 100% |
A0A1X0NU94 | Trypanosomatidae | 38% | 100% |
A0A3Q8IE09 | Leishmania donovani | 83% | 100% |
A0A422NH08 | Trypanosoma rangeli | 42% | 100% |
A4H937 | Leishmania braziliensis | 75% | 100% |
A4HXG9 | Leishmania infantum | 83% | 100% |
C9ZP55 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
Q4QE99 | Leishmania major | 82% | 100% |
Q5F3X0 | Gallus gallus | 28% | 100% |
V5BF39 | Trypanosoma cruzi | 39% | 100% |