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: 18 |
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 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0005635 | nuclear envelope | 4 | 1 |
GO:0005783 | endoplasmic reticulum | 5 | 1 |
GO:0005794 | Golgi apparatus | 5 | 1 |
GO:0031967 | organelle envelope | 3 | 1 |
GO:0031975 | envelope | 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: A4H5P5
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 | 12 |
GO:0016409 | palmitoyltransferase activity | 5 | 12 |
GO:0016417 | S-acyltransferase activity | 5 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016746 | acyltransferase activity | 3 | 12 |
GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 12 |
GO:0019706 | protein-cysteine S-palmitoyltransferase activity | 4 | 12 |
GO:0019707 | protein-cysteine S-acyltransferase activity | 3 | 12 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 150 | 152 | PF00675 | 0.368 |
CLV_NRD_NRD_1 | 167 | 169 | PF00675 | 0.362 |
CLV_NRD_NRD_1 | 269 | 271 | PF00675 | 0.231 |
CLV_NRD_NRD_1 | 409 | 411 | PF00675 | 0.423 |
CLV_NRD_NRD_1 | 421 | 423 | PF00675 | 0.260 |
CLV_NRD_NRD_1 | 452 | 454 | PF00675 | 0.314 |
CLV_NRD_NRD_1 | 63 | 65 | PF00675 | 0.338 |
CLV_PCSK_KEX2_1 | 150 | 152 | PF00082 | 0.349 |
CLV_PCSK_KEX2_1 | 163 | 165 | PF00082 | 0.450 |
CLV_PCSK_KEX2_1 | 172 | 174 | PF00082 | 0.469 |
CLV_PCSK_KEX2_1 | 269 | 271 | PF00082 | 0.231 |
CLV_PCSK_KEX2_1 | 454 | 456 | PF00082 | 0.408 |
CLV_PCSK_PC1ET2_1 | 163 | 165 | PF00082 | 0.460 |
CLV_PCSK_PC1ET2_1 | 172 | 174 | PF00082 | 0.469 |
CLV_PCSK_PC1ET2_1 | 454 | 456 | PF00082 | 0.408 |
CLV_PCSK_PC7_1 | 168 | 174 | PF00082 | 0.486 |
CLV_PCSK_SKI1_1 | 156 | 160 | PF00082 | 0.437 |
CLV_PCSK_SKI1_1 | 163 | 167 | PF00082 | 0.460 |
CLV_PCSK_SKI1_1 | 169 | 173 | PF00082 | 0.492 |
CLV_PCSK_SKI1_1 | 191 | 195 | PF00082 | 0.351 |
CLV_PCSK_SKI1_1 | 288 | 292 | PF00082 | 0.249 |
CLV_PCSK_SKI1_1 | 313 | 317 | PF00082 | 0.456 |
CLV_PCSK_SKI1_1 | 41 | 45 | PF00082 | 0.535 |
CLV_PCSK_SKI1_1 | 425 | 429 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 454 | 458 | PF00082 | 0.340 |
CLV_PCSK_SKI1_1 | 72 | 76 | PF00082 | 0.317 |
DEG_APCC_DBOX_1 | 287 | 295 | PF00400 | 0.431 |
DEG_APCC_DBOX_1 | 412 | 420 | PF00400 | 0.539 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.675 |
DOC_ANK_TNKS_1 | 205 | 212 | PF00023 | 0.558 |
DOC_CDC14_PxL_1 | 102 | 110 | PF14671 | 0.355 |
DOC_CYCLIN_RxL_1 | 422 | 432 | PF00134 | 0.562 |
DOC_MAPK_gen_1 | 168 | 177 | PF00069 | 0.589 |
DOC_MAPK_gen_1 | 38 | 48 | PF00069 | 0.335 |
DOC_MAPK_gen_1 | 422 | 430 | PF00069 | 0.657 |
DOC_MAPK_MEF2A_6 | 41 | 50 | PF00069 | 0.335 |
DOC_PP1_RVXF_1 | 113 | 120 | PF00149 | 0.298 |
DOC_PP4_FxxP_1 | 134 | 137 | PF00568 | 0.498 |
DOC_USP7_MATH_1 | 158 | 162 | PF00917 | 0.699 |
DOC_USP7_MATH_1 | 253 | 257 | PF00917 | 0.448 |
DOC_USP7_UBL2_3 | 454 | 458 | PF12436 | 0.586 |
DOC_WW_Pin1_4 | 180 | 185 | PF00397 | 0.719 |
DOC_WW_Pin1_4 | 193 | 198 | PF00397 | 0.472 |
DOC_WW_Pin1_4 | 231 | 236 | PF00397 | 0.648 |
LIG_14-3-3_CanoR_1 | 156 | 165 | PF00244 | 0.715 |
LIG_14-3-3_CanoR_1 | 41 | 47 | PF00244 | 0.335 |
LIG_Actin_WH2_2 | 371 | 389 | PF00022 | 0.411 |
LIG_Actin_WH2_2 | 472 | 489 | PF00022 | 0.571 |
LIG_Actin_WH2_2 | 95 | 111 | PF00022 | 0.414 |
LIG_BRCT_BRCA1_1 | 55 | 59 | PF00533 | 0.349 |
LIG_deltaCOP1_diTrp_1 | 126 | 134 | PF00928 | 0.411 |
LIG_deltaCOP1_diTrp_1 | 80 | 88 | PF00928 | 0.474 |
LIG_EH1_1 | 206 | 214 | PF00400 | 0.540 |
LIG_FHA_1 | 180 | 186 | PF00498 | 0.608 |
LIG_FHA_1 | 247 | 253 | PF00498 | 0.431 |
LIG_FHA_1 | 331 | 337 | PF00498 | 0.311 |
LIG_FHA_1 | 399 | 405 | PF00498 | 0.597 |
LIG_FHA_2 | 131 | 137 | PF00498 | 0.398 |
LIG_FHA_2 | 380 | 386 | PF00498 | 0.442 |
LIG_FHA_2 | 75 | 81 | PF00498 | 0.545 |
LIG_GBD_Chelix_1 | 35 | 43 | PF00786 | 0.529 |
LIG_LIR_Apic_2 | 133 | 137 | PF02991 | 0.383 |
LIG_LIR_Apic_2 | 231 | 235 | PF02991 | 0.684 |
LIG_LIR_Gen_1 | 18 | 27 | PF02991 | 0.378 |
LIG_LIR_Gen_1 | 300 | 309 | PF02991 | 0.312 |
LIG_LIR_Gen_1 | 339 | 348 | PF02991 | 0.262 |
LIG_LIR_Gen_1 | 97 | 108 | PF02991 | 0.276 |
LIG_LIR_Nem_3 | 116 | 122 | PF02991 | 0.173 |
LIG_LIR_Nem_3 | 18 | 24 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 300 | 306 | PF02991 | 0.257 |
LIG_LIR_Nem_3 | 307 | 312 | PF02991 | 0.256 |
LIG_LIR_Nem_3 | 339 | 344 | PF02991 | 0.262 |
LIG_LIR_Nem_3 | 80 | 86 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 97 | 103 | PF02991 | 0.215 |
LIG_NRBOX | 123 | 129 | PF00104 | 0.189 |
LIG_NRBOX | 290 | 296 | PF00104 | 0.411 |
LIG_NRBOX | 38 | 44 | PF00104 | 0.396 |
LIG_Pex14_1 | 324 | 328 | PF04695 | 0.278 |
LIG_Pex14_2 | 357 | 361 | PF04695 | 0.364 |
LIG_Pex14_2 | 84 | 88 | PF04695 | 0.318 |
LIG_PTAP_UEV_1 | 481 | 486 | PF05743 | 0.553 |
LIG_PTB_Apo_2 | 201 | 208 | PF02174 | 0.538 |
LIG_PTB_Phospho_1 | 201 | 207 | PF10480 | 0.534 |
LIG_Rb_pABgroove_1 | 462 | 470 | PF01858 | 0.492 |
LIG_SH2_CRK | 341 | 345 | PF00017 | 0.279 |
LIG_SH2_NCK_1 | 214 | 218 | PF00017 | 0.654 |
LIG_SH2_PTP2 | 21 | 24 | PF00017 | 0.289 |
LIG_SH2_PTP2 | 232 | 235 | PF00017 | 0.513 |
LIG_SH2_PTP2 | 89 | 92 | PF00017 | 0.266 |
LIG_SH2_SRC | 21 | 24 | PF00017 | 0.381 |
LIG_SH2_SRC | 271 | 274 | PF00017 | 0.474 |
LIG_SH2_SRC | 442 | 445 | PF00017 | 0.645 |
LIG_SH2_STAP1 | 341 | 345 | PF00017 | 0.289 |
LIG_SH2_STAT5 | 100 | 103 | PF00017 | 0.274 |
LIG_SH2_STAT5 | 207 | 210 | PF00017 | 0.516 |
LIG_SH2_STAT5 | 21 | 24 | PF00017 | 0.289 |
LIG_SH2_STAT5 | 232 | 235 | PF00017 | 0.634 |
LIG_SH2_STAT5 | 89 | 92 | PF00017 | 0.279 |
LIG_SH3_2 | 482 | 487 | PF14604 | 0.567 |
LIG_SH3_3 | 100 | 106 | PF00018 | 0.349 |
LIG_SH3_3 | 172 | 178 | PF00018 | 0.603 |
LIG_SH3_3 | 181 | 187 | PF00018 | 0.582 |
LIG_SH3_3 | 234 | 240 | PF00018 | 0.616 |
LIG_SH3_3 | 249 | 255 | PF00018 | 0.404 |
LIG_SH3_3 | 394 | 400 | PF00018 | 0.547 |
LIG_SH3_3 | 430 | 436 | PF00018 | 0.644 |
LIG_SH3_3 | 479 | 485 | PF00018 | 0.528 |
LIG_SUMO_SIM_anti_2 | 401 | 406 | PF11976 | 0.605 |
LIG_SUMO_SIM_par_1 | 120 | 126 | PF11976 | 0.309 |
LIG_SUMO_SIM_par_1 | 332 | 337 | PF11976 | 0.307 |
LIG_SUMO_SIM_par_1 | 394 | 401 | PF11976 | 0.548 |
LIG_SUMO_SIM_par_1 | 426 | 432 | PF11976 | 0.566 |
LIG_TRAF2_1 | 197 | 200 | PF00917 | 0.606 |
LIG_TYR_ITIM | 19 | 24 | PF00017 | 0.240 |
LIG_TYR_ITIM | 87 | 92 | PF00017 | 0.281 |
LIG_UBA3_1 | 101 | 109 | PF00899 | 0.381 |
MOD_CK1_1 | 111 | 117 | PF00069 | 0.386 |
MOD_CK2_1 | 193 | 199 | PF00069 | 0.370 |
MOD_CK2_1 | 74 | 80 | PF00069 | 0.427 |
MOD_GlcNHglycan | 482 | 485 | PF01048 | 0.526 |
MOD_GlcNHglycan | 488 | 491 | PF01048 | 0.603 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.375 |
MOD_GSK3_1 | 132 | 139 | PF00069 | 0.467 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.523 |
MOD_GSK3_1 | 219 | 226 | PF00069 | 0.578 |
MOD_GSK3_1 | 330 | 337 | PF00069 | 0.413 |
MOD_N-GLC_1 | 379 | 384 | PF02516 | 0.266 |
MOD_N-GLC_2 | 49 | 51 | PF02516 | 0.189 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.379 |
MOD_NEK2_1 | 108 | 113 | PF00069 | 0.339 |
MOD_NEK2_1 | 15 | 20 | PF00069 | 0.378 |
MOD_NEK2_1 | 336 | 341 | PF00069 | 0.396 |
MOD_NEK2_1 | 395 | 400 | PF00069 | 0.472 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.405 |
MOD_NEK2_1 | 486 | 491 | PF00069 | 0.618 |
MOD_NEK2_1 | 53 | 58 | PF00069 | 0.252 |
MOD_NEK2_1 | 68 | 73 | PF00069 | 0.441 |
MOD_NEK2_2 | 283 | 288 | PF00069 | 0.295 |
MOD_OFUCOSY | 296 | 301 | PF10250 | 0.360 |
MOD_OFUCOSY | 51 | 57 | PF10250 | 0.361 |
MOD_PIKK_1 | 336 | 342 | PF00454 | 0.331 |
MOD_PKA_2 | 253 | 259 | PF00069 | 0.266 |
MOD_PKA_2 | 486 | 492 | PF00069 | 0.621 |
MOD_Plk_1 | 283 | 289 | PF00069 | 0.232 |
MOD_Plk_1 | 379 | 385 | PF00069 | 0.300 |
MOD_Plk_1 | 389 | 395 | PF00069 | 0.358 |
MOD_Plk_4 | 108 | 114 | PF00069 | 0.356 |
MOD_Plk_4 | 15 | 21 | PF00069 | 0.306 |
MOD_ProDKin_1 | 180 | 186 | PF00069 | 0.664 |
MOD_ProDKin_1 | 193 | 199 | PF00069 | 0.325 |
MOD_ProDKin_1 | 231 | 237 | PF00069 | 0.566 |
MOD_SUMO_for_1 | 436 | 439 | PF00179 | 0.571 |
MOD_SUMO_rev_2 | 417 | 424 | PF00179 | 0.587 |
MOD_SUMO_rev_2 | 462 | 467 | PF00179 | 0.382 |
TRG_DiLeu_BaEn_1 | 97 | 102 | PF01217 | 0.360 |
TRG_DiLeu_BaEn_2 | 79 | 85 | PF01217 | 0.404 |
TRG_DiLeu_BaLyEn_6 | 161 | 166 | PF01217 | 0.560 |
TRG_DiLeu_BaLyEn_6 | 38 | 43 | PF01217 | 0.496 |
TRG_ENDOCYTIC_2 | 100 | 103 | PF00928 | 0.266 |
TRG_ENDOCYTIC_2 | 21 | 24 | PF00928 | 0.288 |
TRG_ENDOCYTIC_2 | 341 | 344 | PF00928 | 0.300 |
TRG_ENDOCYTIC_2 | 89 | 92 | PF00928 | 0.266 |
TRG_ER_diArg_1 | 268 | 270 | PF00400 | 0.266 |
TRG_ER_diArg_1 | 452 | 455 | PF00400 | 0.505 |
TRG_NES_CRM1_1 | 373 | 385 | PF08389 | 0.301 |
TRG_NLS_Bipartite_1 | 150 | 166 | PF00514 | 0.423 |
TRG_NLS_MonoExtC_3 | 452 | 457 | PF00514 | 0.502 |
TRG_NLS_MonoExtN_4 | 453 | 458 | PF00514 | 0.472 |
TRG_Pf-PMV_PEXEL_1 | 310 | 314 | PF00026 | 0.381 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PD29 | Leptomonas seymouri | 65% | 98% |
A0A0S4JKC0 | Bodo saltans | 36% | 100% |
A0A1X0NN08 | Trypanosomatidae | 49% | 100% |
A0A3Q8I8F6 | Leishmania donovani | 82% | 100% |
A0A3R7L7T0 | Trypanosoma rangeli | 49% | 100% |
A4HTY5 | Leishmania infantum | 82% | 100% |
D0A9E1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
E9AMR5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
Q4QHW0 | Leishmania major | 81% | 100% |
V5BSN7 | Trypanosoma cruzi | 48% | 97% |