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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
GO:0005783 | endoplasmic reticulum | 5 | 1 |
GO:0005794 | Golgi apparatus | 5 | 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: A4HGP2
Term | Name | Level | Count |
---|---|---|---|
GO:0006497 | protein lipidation | 5 | 1 |
GO:0006605 | protein targeting | 5 | 1 |
GO:0006612 | protein targeting to membrane | 5 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0006810 | transport | 3 | 1 |
GO:0006886 | intracellular protein transport | 4 | 1 |
GO:0006897 | endocytosis | 5 | 1 |
GO:0008104 | protein localization | 4 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0015031 | protein transport | 4 | 1 |
GO:0016192 | vesicle-mediated transport | 4 | 1 |
GO:0018193 | peptidyl-amino acid modification | 5 | 1 |
GO:0018198 | peptidyl-cysteine modification | 6 | 1 |
GO:0018230 | peptidyl-L-cysteine S-palmitoylation | 7 | 1 |
GO:0018231 | peptidyl-S-diacylglycerol-L-cysteine biosynthetic process from peptidyl-cysteine | 7 | 1 |
GO:0018345 | protein palmitoylation | 6 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0033036 | macromolecule localization | 2 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0043543 | protein acylation | 5 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0045184 | establishment of protein localization | 3 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
GO:0051668 | localization within membrane | 3 | 1 |
GO:0070727 | cellular macromolecule localization | 3 | 1 |
GO:0071702 | organic substance transport | 4 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0071705 | nitrogen compound transport | 4 | 1 |
GO:0072657 | protein localization to membrane | 4 | 1 |
GO:0090150 | establishment of protein localization to membrane | 4 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 10 |
GO:0016409 | palmitoyltransferase activity | 5 | 10 |
GO:0016417 | S-acyltransferase activity | 5 | 10 |
GO:0016740 | transferase activity | 2 | 10 |
GO:0016746 | acyltransferase activity | 3 | 10 |
GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 10 |
GO:0019706 | protein-cysteine S-palmitoyltransferase activity | 4 | 10 |
GO:0019707 | protein-cysteine S-acyltransferase activity | 3 | 10 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 243 | 247 | PF00656 | 0.622 |
CLV_NRD_NRD_1 | 159 | 161 | PF00675 | 0.281 |
CLV_NRD_NRD_1 | 278 | 280 | PF00675 | 0.248 |
CLV_NRD_NRD_1 | 320 | 322 | PF00675 | 0.252 |
CLV_NRD_NRD_1 | 424 | 426 | PF00675 | 0.405 |
CLV_PCSK_KEX2_1 | 102 | 104 | PF00082 | 0.490 |
CLV_PCSK_KEX2_1 | 161 | 163 | PF00082 | 0.410 |
CLV_PCSK_KEX2_1 | 320 | 322 | PF00082 | 0.266 |
CLV_PCSK_KEX2_1 | 405 | 407 | PF00082 | 0.374 |
CLV_PCSK_KEX2_1 | 424 | 426 | PF00082 | 0.432 |
CLV_PCSK_KEX2_1 | 437 | 439 | PF00082 | 0.352 |
CLV_PCSK_PC1ET2_1 | 102 | 104 | PF00082 | 0.498 |
CLV_PCSK_PC1ET2_1 | 161 | 163 | PF00082 | 0.379 |
CLV_PCSK_PC1ET2_1 | 405 | 407 | PF00082 | 0.409 |
CLV_PCSK_PC1ET2_1 | 437 | 439 | PF00082 | 0.364 |
CLV_PCSK_PC7_1 | 157 | 163 | PF00082 | 0.353 |
CLV_PCSK_SKI1_1 | 102 | 106 | PF00082 | 0.507 |
CLV_PCSK_SKI1_1 | 115 | 119 | PF00082 | 0.424 |
CLV_PCSK_SKI1_1 | 411 | 415 | PF00082 | 0.332 |
CLV_PCSK_SKI1_1 | 428 | 432 | PF00082 | 0.283 |
CLV_PCSK_SKI1_1 | 438 | 442 | PF00082 | 0.355 |
CLV_PCSK_SKI1_1 | 7 | 11 | PF00082 | 0.436 |
DEG_APCC_DBOX_1 | 410 | 418 | PF00400 | 0.469 |
DOC_CKS1_1 | 354 | 359 | PF01111 | 0.189 |
DOC_CYCLIN_RxL_1 | 424 | 434 | PF00134 | 0.567 |
DOC_CYCLIN_yCln2_LP_2 | 132 | 138 | PF00134 | 0.572 |
DOC_MAPK_gen_1 | 157 | 165 | PF00069 | 0.592 |
DOC_MAPK_gen_1 | 320 | 328 | PF00069 | 0.443 |
DOC_MAPK_MEF2A_6 | 320 | 328 | PF00069 | 0.450 |
DOC_PP2B_LxvP_1 | 367 | 370 | PF13499 | 0.203 |
DOC_WW_Pin1_4 | 353 | 358 | PF00397 | 0.244 |
LIG_14-3-3_CanoR_1 | 103 | 107 | PF00244 | 0.563 |
LIG_14-3-3_CanoR_1 | 175 | 181 | PF00244 | 0.428 |
LIG_14-3-3_CanoR_1 | 226 | 232 | PF00244 | 0.354 |
LIG_14-3-3_CanoR_1 | 279 | 287 | PF00244 | 0.457 |
LIG_AP2alpha_1 | 431 | 435 | PF02296 | 0.519 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.657 |
LIG_BIR_III_2 | 66 | 70 | PF00653 | 0.544 |
LIG_BRCT_BRCA1_1 | 126 | 130 | PF00533 | 0.584 |
LIG_BRCT_BRCA1_1 | 431 | 435 | PF00533 | 0.444 |
LIG_BRCT_BRCA1_2 | 431 | 437 | PF00533 | 0.445 |
LIG_eIF4E_1 | 211 | 217 | PF01652 | 0.331 |
LIG_FHA_1 | 11 | 17 | PF00498 | 0.580 |
LIG_FHA_1 | 135 | 141 | PF00498 | 0.573 |
LIG_FHA_1 | 183 | 189 | PF00498 | 0.241 |
LIG_FHA_1 | 338 | 344 | PF00498 | 0.342 |
LIG_FHA_2 | 254 | 260 | PF00498 | 0.571 |
LIG_FHA_2 | 347 | 353 | PF00498 | 0.330 |
LIG_FHA_2 | 391 | 397 | PF00498 | 0.385 |
LIG_FHA_2 | 52 | 58 | PF00498 | 0.663 |
LIG_IBAR_NPY_1 | 407 | 409 | PF08397 | 0.554 |
LIG_LIR_Apic_2 | 177 | 183 | PF02991 | 0.344 |
LIG_LIR_Apic_2 | 231 | 237 | PF02991 | 0.476 |
LIG_LIR_Gen_1 | 127 | 138 | PF02991 | 0.550 |
LIG_LIR_Gen_1 | 141 | 150 | PF02991 | 0.564 |
LIG_LIR_Gen_1 | 218 | 229 | PF02991 | 0.319 |
LIG_LIR_Gen_1 | 26 | 35 | PF02991 | 0.570 |
LIG_LIR_Gen_1 | 266 | 277 | PF02991 | 0.527 |
LIG_LIR_Gen_1 | 323 | 333 | PF02991 | 0.504 |
LIG_LIR_Gen_1 | 355 | 366 | PF02991 | 0.189 |
LIG_LIR_Nem_3 | 127 | 133 | PF02991 | 0.573 |
LIG_LIR_Nem_3 | 13 | 17 | PF02991 | 0.583 |
LIG_LIR_Nem_3 | 141 | 145 | PF02991 | 0.550 |
LIG_LIR_Nem_3 | 148 | 153 | PF02991 | 0.528 |
LIG_LIR_Nem_3 | 218 | 224 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 26 | 30 | PF02991 | 0.537 |
LIG_LIR_Nem_3 | 266 | 272 | PF02991 | 0.537 |
LIG_LIR_Nem_3 | 323 | 328 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 355 | 361 | PF02991 | 0.189 |
LIG_LYPXL_SIV_4 | 208 | 216 | PF13949 | 0.203 |
LIG_MLH1_MIPbox_1 | 130 | 134 | PF16413 | 0.629 |
LIG_PDZ_Class_1 | 452 | 457 | PF00595 | 0.701 |
LIG_Pex14_1 | 205 | 209 | PF04695 | 0.327 |
LIG_Pex14_2 | 126 | 130 | PF04695 | 0.606 |
LIG_Pex14_2 | 431 | 435 | PF04695 | 0.519 |
LIG_PTB_Apo_2 | 413 | 420 | PF02174 | 0.574 |
LIG_PTB_Phospho_1 | 413 | 419 | PF10480 | 0.577 |
LIG_REV1ctd_RIR_1 | 116 | 126 | PF16727 | 0.491 |
LIG_SH2_CRK | 14 | 18 | PF00017 | 0.521 |
LIG_SH2_CRK | 150 | 154 | PF00017 | 0.596 |
LIG_SH2_CRK | 166 | 170 | PF00017 | 0.601 |
LIG_SH2_CRK | 180 | 184 | PF00017 | 0.308 |
LIG_SH2_CRK | 221 | 225 | PF00017 | 0.454 |
LIG_SH2_CRK | 419 | 423 | PF00017 | 0.559 |
LIG_SH2_GRB2like | 168 | 171 | PF00017 | 0.583 |
LIG_SH2_GRB2like | 63 | 66 | PF00017 | 0.541 |
LIG_SH2_NCK_1 | 150 | 154 | PF00017 | 0.596 |
LIG_SH2_NCK_1 | 180 | 184 | PF00017 | 0.279 |
LIG_SH2_NCK_1 | 229 | 233 | PF00017 | 0.468 |
LIG_SH2_PTP2 | 168 | 171 | PF00017 | 0.588 |
LIG_SH2_PTP2 | 211 | 214 | PF00017 | 0.302 |
LIG_SH2_PTP2 | 234 | 237 | PF00017 | 0.555 |
LIG_SH2_SRC | 168 | 171 | PF00017 | 0.588 |
LIG_SH2_STAP1 | 221 | 225 | PF00017 | 0.336 |
LIG_SH2_STAP1 | 63 | 67 | PF00017 | 0.543 |
LIG_SH2_STAP1 | 75 | 79 | PF00017 | 0.647 |
LIG_SH2_STAT5 | 138 | 141 | PF00017 | 0.538 |
LIG_SH2_STAT5 | 142 | 145 | PF00017 | 0.543 |
LIG_SH2_STAT5 | 168 | 171 | PF00017 | 0.526 |
LIG_SH2_STAT5 | 211 | 214 | PF00017 | 0.401 |
LIG_SH2_STAT5 | 221 | 224 | PF00017 | 0.311 |
LIG_SH2_STAT5 | 234 | 237 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 297 | 300 | PF00017 | 0.462 |
LIG_SH3_3 | 13 | 19 | PF00018 | 0.526 |
LIG_SUMO_SIM_anti_2 | 213 | 218 | PF11976 | 0.388 |
LIG_SUMO_SIM_anti_2 | 327 | 333 | PF11976 | 0.203 |
LIG_SUMO_SIM_par_1 | 339 | 344 | PF11976 | 0.331 |
LIG_TYR_ITIM | 12 | 17 | PF00017 | 0.565 |
LIG_TYR_ITIM | 219 | 224 | PF00017 | 0.360 |
LIG_TYR_ITIM | 417 | 422 | PF00017 | 0.554 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.683 |
MOD_CK1_1 | 429 | 435 | PF00069 | 0.439 |
MOD_CK2_1 | 264 | 270 | PF00069 | 0.547 |
MOD_CK2_1 | 346 | 352 | PF00069 | 0.400 |
MOD_CK2_1 | 390 | 396 | PF00069 | 0.447 |
MOD_GlcNHglycan | 246 | 249 | PF01048 | 0.504 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.419 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.426 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.545 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.363 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.287 |
MOD_GSK3_1 | 348 | 355 | PF00069 | 0.237 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.390 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.341 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.589 |
MOD_N-GLC_2 | 170 | 172 | PF02516 | 0.341 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.692 |
MOD_NEK2_1 | 176 | 181 | PF00069 | 0.476 |
MOD_NEK2_1 | 219 | 224 | PF00069 | 0.371 |
MOD_NEK2_1 | 324 | 329 | PF00069 | 0.454 |
MOD_NEK2_1 | 377 | 382 | PF00069 | 0.356 |
MOD_NEK2_1 | 384 | 389 | PF00069 | 0.491 |
MOD_NEK2_1 | 85 | 90 | PF00069 | 0.653 |
MOD_PIKK_1 | 105 | 111 | PF00454 | 0.631 |
MOD_PIKK_1 | 440 | 446 | PF00454 | 0.564 |
MOD_PKA_1 | 102 | 108 | PF00069 | 0.560 |
MOD_PKA_2 | 102 | 108 | PF00069 | 0.560 |
MOD_PKA_2 | 174 | 180 | PF00069 | 0.428 |
MOD_PKA_2 | 264 | 270 | PF00069 | 0.570 |
MOD_Plk_1 | 212 | 218 | PF00069 | 0.203 |
MOD_Plk_1 | 426 | 432 | PF00069 | 0.450 |
MOD_Plk_2-3 | 253 | 259 | PF00069 | 0.616 |
MOD_Plk_4 | 134 | 140 | PF00069 | 0.547 |
MOD_Plk_4 | 212 | 218 | PF00069 | 0.414 |
MOD_Plk_4 | 219 | 225 | PF00069 | 0.373 |
MOD_Plk_4 | 264 | 270 | PF00069 | 0.625 |
MOD_Plk_4 | 324 | 330 | PF00069 | 0.520 |
MOD_Plk_4 | 337 | 343 | PF00069 | 0.284 |
MOD_Plk_4 | 371 | 377 | PF00069 | 0.368 |
MOD_Plk_4 | 426 | 432 | PF00069 | 0.508 |
MOD_ProDKin_1 | 353 | 359 | PF00069 | 0.244 |
TRG_ENDOCYTIC_2 | 14 | 17 | PF00928 | 0.525 |
TRG_ENDOCYTIC_2 | 142 | 145 | PF00928 | 0.565 |
TRG_ENDOCYTIC_2 | 150 | 153 | PF00928 | 0.548 |
TRG_ENDOCYTIC_2 | 166 | 169 | PF00928 | 0.579 |
TRG_ENDOCYTIC_2 | 209 | 212 | PF00928 | 0.430 |
TRG_ENDOCYTIC_2 | 221 | 224 | PF00928 | 0.362 |
TRG_ENDOCYTIC_2 | 418 | 421 | PF00928 | 0.583 |
TRG_ER_diArg_1 | 159 | 162 | PF00400 | 0.587 |
TRG_ER_diArg_1 | 320 | 322 | PF00400 | 0.532 |
TRG_ER_diArg_1 | 424 | 426 | PF00400 | 0.571 |
TRG_NES_CRM1_1 | 266 | 278 | PF08389 | 0.600 |
TRG_NLS_MonoExtC_3 | 159 | 164 | PF00514 | 0.596 |
TRG_NLS_MonoExtN_4 | 157 | 164 | PF00514 | 0.587 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P832 | Leptomonas seymouri | 64% | 99% |
A0A1X0NSC8 | Trypanosomatidae | 39% | 92% |
A0A3S5ISD2 | Trypanosoma rangeli | 41% | 100% |
A0A3S7X1Q3 | Leishmania donovani | 77% | 100% |
A4I3R5 | Leishmania infantum | 77% | 100% |
D0A893 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 97% |
E9B008 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 76% | 100% |
Q4Q877 | Leishmania major | 76% | 100% |