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: E9B008
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_MEL_PAP_1 | 126 | 132 | PF00089 | 0.274 |
CLV_NRD_NRD_1 | 102 | 104 | PF00675 | 0.471 |
CLV_NRD_NRD_1 | 159 | 161 | PF00675 | 0.314 |
CLV_NRD_NRD_1 | 279 | 281 | PF00675 | 0.248 |
CLV_NRD_NRD_1 | 321 | 323 | PF00675 | 0.252 |
CLV_NRD_NRD_1 | 424 | 426 | PF00675 | 0.422 |
CLV_PCSK_KEX2_1 | 102 | 104 | PF00082 | 0.484 |
CLV_PCSK_KEX2_1 | 161 | 163 | PF00082 | 0.427 |
CLV_PCSK_KEX2_1 | 320 | 322 | PF00082 | 0.263 |
CLV_PCSK_KEX2_1 | 405 | 407 | PF00082 | 0.372 |
CLV_PCSK_KEX2_1 | 424 | 426 | PF00082 | 0.449 |
CLV_PCSK_KEX2_1 | 437 | 439 | PF00082 | 0.376 |
CLV_PCSK_PC1ET2_1 | 102 | 104 | PF00082 | 0.492 |
CLV_PCSK_PC1ET2_1 | 161 | 163 | PF00082 | 0.396 |
CLV_PCSK_PC1ET2_1 | 405 | 407 | PF00082 | 0.407 |
CLV_PCSK_PC1ET2_1 | 437 | 439 | PF00082 | 0.388 |
CLV_PCSK_PC7_1 | 157 | 163 | PF00082 | 0.375 |
CLV_PCSK_SKI1_1 | 115 | 119 | PF00082 | 0.432 |
CLV_PCSK_SKI1_1 | 411 | 415 | PF00082 | 0.338 |
CLV_PCSK_SKI1_1 | 438 | 442 | PF00082 | 0.369 |
CLV_PCSK_SKI1_1 | 7 | 11 | PF00082 | 0.410 |
DEG_SPOP_SBC_1 | 174 | 178 | PF00917 | 0.541 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 415 | 421 | PF00134 | 0.518 |
DOC_MAPK_FxFP_2 | 132 | 135 | PF00069 | 0.474 |
DOC_MAPK_gen_1 | 157 | 165 | PF00069 | 0.616 |
DOC_MAPK_gen_1 | 424 | 430 | PF00069 | 0.480 |
DOC_MAPK_gen_1 | 437 | 443 | PF00069 | 0.544 |
DOC_PP4_FxxP_1 | 132 | 135 | PF00568 | 0.469 |
DOC_PP4_FxxP_1 | 190 | 193 | PF00568 | 0.251 |
DOC_USP7_UBL2_3 | 148 | 152 | PF12436 | 0.562 |
LIG_14-3-3_CanoR_1 | 129 | 133 | PF00244 | 0.555 |
LIG_14-3-3_CanoR_1 | 226 | 232 | PF00244 | 0.506 |
LIG_14-3-3_CanoR_1 | 280 | 288 | PF00244 | 0.457 |
LIG_14-3-3_CanoR_1 | 425 | 431 | PF00244 | 0.603 |
LIG_AP2alpha_1 | 431 | 435 | PF02296 | 0.541 |
LIG_APCC_ABBA_1 | 428 | 433 | PF00400 | 0.440 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.650 |
LIG_BRCT_BRCA1_1 | 130 | 134 | PF00533 | 0.590 |
LIG_deltaCOP1_diTrp_1 | 202 | 208 | PF00928 | 0.262 |
LIG_deltaCOP1_diTrp_1 | 213 | 220 | PF00928 | 0.196 |
LIG_FHA_1 | 11 | 17 | PF00498 | 0.558 |
LIG_FHA_1 | 135 | 141 | PF00498 | 0.573 |
LIG_FHA_1 | 339 | 345 | PF00498 | 0.342 |
LIG_FHA_1 | 354 | 360 | PF00498 | 0.286 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.622 |
LIG_FHA_2 | 255 | 261 | PF00498 | 0.596 |
LIG_FHA_2 | 348 | 354 | PF00498 | 0.330 |
LIG_FHA_2 | 52 | 58 | PF00498 | 0.602 |
LIG_GBD_Chelix_1 | 362 | 370 | PF00786 | 0.312 |
LIG_IBAR_NPY_1 | 407 | 409 | PF08397 | 0.554 |
LIG_LIR_Apic_2 | 131 | 135 | PF02991 | 0.473 |
LIG_LIR_Apic_2 | 177 | 183 | PF02991 | 0.344 |
LIG_LIR_Apic_2 | 187 | 193 | PF02991 | 0.344 |
LIG_LIR_Apic_2 | 231 | 237 | PF02991 | 0.486 |
LIG_LIR_Gen_1 | 141 | 150 | PF02991 | 0.576 |
LIG_LIR_Gen_1 | 185 | 194 | PF02991 | 0.397 |
LIG_LIR_Gen_1 | 213 | 222 | PF02991 | 0.325 |
LIG_LIR_Gen_1 | 267 | 278 | PF02991 | 0.536 |
LIG_LIR_Gen_1 | 324 | 333 | PF02991 | 0.504 |
LIG_LIR_Gen_1 | 350 | 360 | PF02991 | 0.392 |
LIG_LIR_Gen_1 | 382 | 392 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 13 | 17 | PF02991 | 0.561 |
LIG_LIR_Nem_3 | 131 | 136 | PF02991 | 0.578 |
LIG_LIR_Nem_3 | 141 | 145 | PF02991 | 0.552 |
LIG_LIR_Nem_3 | 185 | 189 | PF02991 | 0.376 |
LIG_LIR_Nem_3 | 213 | 217 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 267 | 273 | PF02991 | 0.547 |
LIG_LIR_Nem_3 | 324 | 329 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 350 | 355 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 382 | 388 | PF02991 | 0.493 |
LIG_MLH1_MIPbox_1 | 130 | 134 | PF16413 | 0.627 |
LIG_PCNA_PIPBox_1 | 342 | 351 | PF02747 | 0.312 |
LIG_PDZ_Class_1 | 452 | 457 | PF00595 | 0.692 |
LIG_Pex14_1 | 196 | 200 | PF04695 | 0.468 |
LIG_Pex14_1 | 205 | 209 | PF04695 | 0.327 |
LIG_Pex14_2 | 130 | 134 | PF04695 | 0.615 |
LIG_Pex14_2 | 186 | 190 | PF04695 | 0.251 |
LIG_Pex14_2 | 431 | 435 | PF04695 | 0.541 |
LIG_PTB_Apo_2 | 413 | 420 | PF02174 | 0.578 |
LIG_PTB_Phospho_1 | 413 | 419 | PF10480 | 0.581 |
LIG_REV1ctd_RIR_1 | 411 | 419 | PF16727 | 0.518 |
LIG_SH2_CRK | 14 | 18 | PF00017 | 0.498 |
LIG_SH2_CRK | 150 | 154 | PF00017 | 0.624 |
LIG_SH2_CRK | 166 | 170 | PF00017 | 0.633 |
LIG_SH2_CRK | 180 | 184 | PF00017 | 0.308 |
LIG_SH2_CRK | 419 | 423 | PF00017 | 0.560 |
LIG_SH2_GRB2like | 168 | 171 | PF00017 | 0.618 |
LIG_SH2_NCK_1 | 150 | 154 | PF00017 | 0.624 |
LIG_SH2_NCK_1 | 229 | 233 | PF00017 | 0.478 |
LIG_SH2_PTP2 | 168 | 171 | PF00017 | 0.623 |
LIG_SH2_PTP2 | 221 | 224 | PF00017 | 0.346 |
LIG_SH2_PTP2 | 234 | 237 | PF00017 | 0.565 |
LIG_SH2_SRC | 168 | 171 | PF00017 | 0.623 |
LIG_SH2_STAP1 | 75 | 79 | PF00017 | 0.602 |
LIG_SH2_STAT5 | 142 | 145 | PF00017 | 0.544 |
LIG_SH2_STAT5 | 168 | 171 | PF00017 | 0.561 |
LIG_SH2_STAT5 | 200 | 203 | PF00017 | 0.276 |
LIG_SH2_STAT5 | 221 | 224 | PF00017 | 0.311 |
LIG_SH2_STAT5 | 234 | 237 | PF00017 | 0.471 |
LIG_SH2_STAT5 | 298 | 301 | PF00017 | 0.462 |
LIG_SH3_3 | 13 | 19 | PF00018 | 0.503 |
LIG_SH3_3 | 34 | 40 | PF00018 | 0.509 |
LIG_SH3_4 | 148 | 155 | PF00018 | 0.553 |
LIG_SUMO_SIM_par_1 | 341 | 346 | PF11976 | 0.336 |
LIG_TRAF2_1 | 252 | 255 | PF00917 | 0.714 |
LIG_TYR_ITIM | 12 | 17 | PF00017 | 0.544 |
LIG_TYR_ITIM | 219 | 224 | PF00017 | 0.360 |
LIG_TYR_ITIM | 417 | 422 | PF00017 | 0.553 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.660 |
MOD_CK1_1 | 331 | 337 | PF00069 | 0.495 |
MOD_CK2_1 | 265 | 271 | PF00069 | 0.563 |
MOD_CK2_1 | 347 | 353 | PF00069 | 0.400 |
MOD_CK2_1 | 390 | 396 | PF00069 | 0.447 |
MOD_CMANNOS | 205 | 208 | PF00535 | 0.372 |
MOD_CMANNOS | 349 | 352 | PF00535 | 0.467 |
MOD_Cter_Amidation | 145 | 148 | PF01082 | 0.361 |
MOD_Cter_Amidation | 318 | 321 | PF01082 | 0.249 |
MOD_GlcNHglycan | 118 | 121 | PF01048 | 0.361 |
MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.420 |
MOD_GlcNHglycan | 345 | 348 | PF01048 | 0.179 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.374 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.417 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.450 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.493 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.241 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.390 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.341 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.685 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.568 |
MOD_N-GLC_2 | 170 | 172 | PF02516 | 0.375 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.679 |
MOD_NEK2_1 | 355 | 360 | PF00069 | 0.189 |
MOD_NEK2_1 | 377 | 382 | PF00069 | 0.356 |
MOD_NEK2_1 | 384 | 389 | PF00069 | 0.491 |
MOD_NEK2_1 | 85 | 90 | PF00069 | 0.643 |
MOD_PIKK_1 | 386 | 392 | PF00454 | 0.467 |
MOD_PIKK_1 | 64 | 70 | PF00454 | 0.611 |
MOD_PKA_2 | 128 | 134 | PF00069 | 0.485 |
MOD_PKA_2 | 265 | 271 | PF00069 | 0.586 |
MOD_Plk_1 | 254 | 260 | PF00069 | 0.641 |
MOD_Plk_2-3 | 254 | 260 | PF00069 | 0.643 |
MOD_Plk_4 | 105 | 111 | PF00069 | 0.627 |
MOD_Plk_4 | 265 | 271 | PF00069 | 0.641 |
MOD_Plk_4 | 331 | 337 | PF00069 | 0.309 |
MOD_Plk_4 | 338 | 344 | PF00069 | 0.284 |
MOD_Plk_4 | 355 | 361 | PF00069 | 0.347 |
MOD_Plk_4 | 371 | 377 | PF00069 | 0.368 |
MOD_Plk_4 | 380 | 386 | PF00069 | 0.372 |
MOD_Plk_4 | 426 | 432 | PF00069 | 0.514 |
TRG_ENDOCYTIC_2 | 14 | 17 | PF00928 | 0.501 |
TRG_ENDOCYTIC_2 | 142 | 145 | PF00928 | 0.565 |
TRG_ENDOCYTIC_2 | 150 | 153 | PF00928 | 0.578 |
TRG_ENDOCYTIC_2 | 166 | 169 | PF00928 | 0.606 |
TRG_ENDOCYTIC_2 | 200 | 203 | PF00928 | 0.312 |
TRG_ENDOCYTIC_2 | 221 | 224 | PF00928 | 0.362 |
TRG_ENDOCYTIC_2 | 418 | 421 | PF00928 | 0.580 |
TRG_ER_diArg_1 | 159 | 162 | PF00400 | 0.618 |
TRG_ER_diArg_1 | 320 | 322 | PF00400 | 0.529 |
TRG_ER_diArg_1 | 424 | 426 | PF00400 | 0.588 |
TRG_NES_CRM1_1 | 267 | 279 | PF08389 | 0.608 |
TRG_NLS_Bipartite_1 | 147 | 164 | PF00514 | 0.550 |
TRG_NLS_MonoExtC_3 | 159 | 164 | PF00514 | 0.622 |
TRG_NLS_MonoExtN_4 | 157 | 164 | PF00514 | 0.610 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P832 | Leptomonas seymouri | 64% | 99% |
A0A1X0NSC8 | Trypanosomatidae | 40% | 92% |
A0A3S5ISD2 | Trypanosoma rangeli | 41% | 100% |
A0A3S7X1Q3 | Leishmania donovani | 95% | 100% |
A4HGP2 | Leishmania braziliensis | 76% | 100% |
A4I3R5 | Leishmania infantum | 95% | 100% |
D0A893 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 97% |
Q4Q877 | Leishmania major | 92% | 100% |