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: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 13 |
GO:0110165 | cellular anatomical entity | 1 | 13 |
GO:0005783 | endoplasmic reticulum | 5 | 2 |
GO:0005794 | Golgi apparatus | 5 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
Related structures:
AlphaFold database: E9AVW7
Term | Name | Level | Count |
---|---|---|---|
GO:0006497 | protein lipidation | 5 | 2 |
GO:0006605 | protein targeting | 5 | 2 |
GO:0006612 | protein targeting to membrane | 5 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0006810 | transport | 3 | 2 |
GO:0006886 | intracellular protein transport | 4 | 2 |
GO:0006897 | endocytosis | 5 | 2 |
GO:0008104 | protein localization | 4 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0015031 | protein transport | 4 | 2 |
GO:0016192 | vesicle-mediated transport | 4 | 2 |
GO:0018193 | peptidyl-amino acid modification | 5 | 2 |
GO:0018198 | peptidyl-cysteine modification | 6 | 2 |
GO:0018230 | peptidyl-L-cysteine S-palmitoylation | 7 | 2 |
GO:0018231 | peptidyl-S-diacylglycerol-L-cysteine biosynthetic process from peptidyl-cysteine | 7 | 2 |
GO:0018345 | protein palmitoylation | 6 | 2 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0033036 | macromolecule localization | 2 | 2 |
GO:0036211 | protein modification process | 4 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043412 | macromolecule modification | 4 | 2 |
GO:0043543 | protein acylation | 5 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0045184 | establishment of protein localization | 3 | 2 |
GO:0046907 | intracellular transport | 3 | 2 |
GO:0051179 | localization | 1 | 2 |
GO:0051234 | establishment of localization | 2 | 2 |
GO:0051641 | cellular localization | 2 | 2 |
GO:0051649 | establishment of localization in cell | 3 | 2 |
GO:0051668 | localization within membrane | 3 | 2 |
GO:0070727 | cellular macromolecule localization | 3 | 2 |
GO:0071702 | organic substance transport | 4 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0071705 | nitrogen compound transport | 4 | 2 |
GO:0072657 | protein localization to membrane | 4 | 2 |
GO:0090150 | establishment of protein localization to membrane | 4 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 13 |
GO:0016409 | palmitoyltransferase activity | 5 | 13 |
GO:0016417 | S-acyltransferase activity | 5 | 13 |
GO:0016740 | transferase activity | 2 | 13 |
GO:0016746 | acyltransferase activity | 3 | 13 |
GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 13 |
GO:0019706 | protein-cysteine S-palmitoyltransferase activity | 4 | 13 |
GO:0019707 | protein-cysteine S-acyltransferase activity | 3 | 13 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 13 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 125 | 127 | PF00675 | 0.257 |
CLV_NRD_NRD_1 | 198 | 200 | PF00675 | 0.391 |
CLV_NRD_NRD_1 | 257 | 259 | PF00675 | 0.382 |
CLV_NRD_NRD_1 | 26 | 28 | PF00675 | 0.316 |
CLV_NRD_NRD_1 | 285 | 287 | PF00675 | 0.428 |
CLV_NRD_NRD_1 | 288 | 290 | PF00675 | 0.405 |
CLV_NRD_NRD_1 | 352 | 354 | PF00675 | 0.577 |
CLV_NRD_NRD_1 | 362 | 364 | PF00675 | 0.542 |
CLV_PCSK_FUR_1 | 24 | 28 | PF00082 | 0.323 |
CLV_PCSK_FUR_1 | 286 | 290 | PF00082 | 0.438 |
CLV_PCSK_KEX2_1 | 125 | 127 | PF00082 | 0.258 |
CLV_PCSK_KEX2_1 | 197 | 199 | PF00082 | 0.492 |
CLV_PCSK_KEX2_1 | 256 | 258 | PF00082 | 0.372 |
CLV_PCSK_KEX2_1 | 26 | 28 | PF00082 | 0.316 |
CLV_PCSK_KEX2_1 | 261 | 263 | PF00082 | 0.380 |
CLV_PCSK_KEX2_1 | 287 | 289 | PF00082 | 0.410 |
CLV_PCSK_KEX2_1 | 292 | 294 | PF00082 | 0.430 |
CLV_PCSK_KEX2_1 | 354 | 356 | PF00082 | 0.563 |
CLV_PCSK_KEX2_1 | 362 | 364 | PF00082 | 0.541 |
CLV_PCSK_PC1ET2_1 | 197 | 199 | PF00082 | 0.537 |
CLV_PCSK_PC1ET2_1 | 256 | 258 | PF00082 | 0.367 |
CLV_PCSK_PC1ET2_1 | 261 | 263 | PF00082 | 0.371 |
CLV_PCSK_PC1ET2_1 | 287 | 289 | PF00082 | 0.418 |
CLV_PCSK_PC1ET2_1 | 292 | 294 | PF00082 | 0.443 |
CLV_PCSK_PC1ET2_1 | 354 | 356 | PF00082 | 0.362 |
CLV_PCSK_PC7_1 | 257 | 263 | PF00082 | 0.442 |
CLV_PCSK_PC7_1 | 288 | 294 | PF00082 | 0.452 |
CLV_PCSK_SKI1_1 | 261 | 265 | PF00082 | 0.421 |
CLV_PCSK_SKI1_1 | 289 | 293 | PF00082 | 0.480 |
CLV_PCSK_SKI1_1 | 83 | 87 | PF00082 | 0.322 |
DEG_APCC_DBOX_1 | 97 | 105 | PF00400 | 0.549 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.681 |
DOC_MAPK_gen_1 | 362 | 369 | PF00069 | 0.579 |
DOC_PP1_RVXF_1 | 233 | 240 | PF00149 | 0.373 |
DOC_USP7_MATH_1 | 114 | 118 | PF00917 | 0.611 |
DOC_USP7_MATH_1 | 25 | 29 | PF00917 | 0.534 |
DOC_USP7_MATH_1 | 315 | 319 | PF00917 | 0.776 |
DOC_USP7_MATH_1 | 357 | 361 | PF00917 | 0.772 |
DOC_USP7_UBL2_3 | 256 | 260 | PF12436 | 0.529 |
DOC_WW_Pin1_4 | 204 | 209 | PF00397 | 0.314 |
LIG_14-3-3_CanoR_1 | 162 | 168 | PF00244 | 0.514 |
LIG_14-3-3_CanoR_1 | 198 | 208 | PF00244 | 0.267 |
LIG_14-3-3_CanoR_1 | 7 | 15 | PF00244 | 0.642 |
LIG_APCC_ABBA_1 | 239 | 244 | PF00400 | 0.514 |
LIG_BRCT_BRCA1_1 | 386 | 390 | PF00533 | 0.707 |
LIG_BRCT_BRCA1_1 | 77 | 81 | PF00533 | 0.406 |
LIG_BRCT_BRCA1_2 | 77 | 83 | PF00533 | 0.246 |
LIG_CaM_IQ_9 | 183 | 199 | PF13499 | 0.418 |
LIG_EH1_1 | 183 | 191 | PF00400 | 0.386 |
LIG_EH1_1 | 63 | 71 | PF00400 | 0.162 |
LIG_eIF4E_1 | 64 | 70 | PF01652 | 0.162 |
LIG_FHA_1 | 183 | 189 | PF00498 | 0.460 |
LIG_FHA_1 | 52 | 58 | PF00498 | 0.171 |
LIG_FHA_1 | 75 | 81 | PF00498 | 0.281 |
LIG_IRF3_LxIS_1 | 33 | 40 | PF10401 | 0.520 |
LIG_IRF3_LxIS_1 | 65 | 72 | PF10401 | 0.461 |
LIG_LIR_Apic_2 | 17 | 22 | PF02991 | 0.545 |
LIG_LIR_Apic_2 | 202 | 208 | PF02991 | 0.314 |
LIG_LIR_Apic_2 | 28 | 33 | PF02991 | 0.501 |
LIG_LIR_Gen_1 | 249 | 255 | PF02991 | 0.462 |
LIG_LIR_Gen_1 | 40 | 49 | PF02991 | 0.435 |
LIG_LIR_Gen_1 | 78 | 89 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 12 | 18 | PF02991 | 0.566 |
LIG_LIR_Nem_3 | 166 | 170 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 249 | 254 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 387 | 393 | PF02991 | 0.809 |
LIG_LIR_Nem_3 | 40 | 45 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 78 | 84 | PF02991 | 0.322 |
LIG_Pex14_1 | 15 | 19 | PF04695 | 0.547 |
LIG_Pex14_2 | 123 | 127 | PF04695 | 0.450 |
LIG_SH2_CRK | 205 | 209 | PF00017 | 0.314 |
LIG_SH2_CRK | 358 | 362 | PF00017 | 0.613 |
LIG_SH2_CRK | 366 | 370 | PF00017 | 0.597 |
LIG_SH2_SRC | 242 | 245 | PF00017 | 0.542 |
LIG_SH2_SRC | 251 | 254 | PF00017 | 0.490 |
LIG_SH2_SRC | 30 | 33 | PF00017 | 0.582 |
LIG_SH2_SRC | 64 | 67 | PF00017 | 0.162 |
LIG_SH2_STAP1 | 184 | 188 | PF00017 | 0.378 |
LIG_SH2_STAP1 | 251 | 255 | PF00017 | 0.481 |
LIG_SH2_STAT3 | 184 | 187 | PF00017 | 0.418 |
LIG_SH2_STAT3 | 267 | 270 | PF00017 | 0.644 |
LIG_SH2_STAT3 | 89 | 92 | PF00017 | 0.554 |
LIG_SH2_STAT5 | 184 | 187 | PF00017 | 0.301 |
LIG_SH2_STAT5 | 242 | 245 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 64 | 67 | PF00017 | 0.408 |
LIG_SH3_1 | 19 | 25 | PF00018 | 0.536 |
LIG_SH3_2 | 22 | 27 | PF14604 | 0.517 |
LIG_SH3_2 | 322 | 327 | PF14604 | 0.655 |
LIG_SH3_3 | 19 | 25 | PF00018 | 0.532 |
LIG_SH3_3 | 316 | 322 | PF00018 | 0.806 |
LIG_SH3_3 | 52 | 58 | PF00018 | 0.305 |
LIG_SUMO_SIM_par_1 | 67 | 73 | PF11976 | 0.329 |
LIG_WRC_WIRS_1 | 164 | 169 | PF05994 | 0.397 |
MOD_CK1_1 | 182 | 188 | PF00069 | 0.412 |
MOD_CK1_1 | 331 | 337 | PF00069 | 0.799 |
MOD_CK1_1 | 341 | 347 | PF00069 | 0.799 |
MOD_CK2_1 | 246 | 252 | PF00069 | 0.505 |
MOD_CK2_1 | 25 | 31 | PF00069 | 0.499 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.434 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.332 |
MOD_GlcNHglycan | 331 | 334 | PF01048 | 0.582 |
MOD_GlcNHglycan | 344 | 347 | PF01048 | 0.546 |
MOD_GlcNHglycan | 377 | 380 | PF01048 | 0.517 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.340 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.329 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.674 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.450 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.766 |
MOD_GSK3_1 | 375 | 382 | PF00069 | 0.789 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.282 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.320 |
MOD_N-GLC_2 | 153 | 155 | PF02516 | 0.265 |
MOD_NEK2_1 | 163 | 168 | PF00069 | 0.330 |
MOD_NEK2_1 | 243 | 248 | PF00069 | 0.462 |
MOD_NEK2_1 | 37 | 42 | PF00069 | 0.524 |
MOD_NEK2_1 | 51 | 56 | PF00069 | 0.249 |
MOD_NEK2_1 | 69 | 74 | PF00069 | 0.361 |
MOD_NEK2_1 | 75 | 80 | PF00069 | 0.303 |
MOD_NEK2_2 | 357 | 362 | PF00069 | 0.562 |
MOD_OFUCOSY | 149 | 155 | PF10250 | 0.264 |
MOD_PIKK_1 | 199 | 205 | PF00454 | 0.274 |
MOD_PIKK_1 | 266 | 272 | PF00454 | 0.604 |
MOD_PIKK_1 | 338 | 344 | PF00454 | 0.748 |
MOD_PK_1 | 133 | 139 | PF00069 | 0.505 |
MOD_PKA_2 | 25 | 31 | PF00069 | 0.499 |
MOD_Plk_1 | 315 | 321 | PF00069 | 0.713 |
MOD_Plk_4 | 163 | 169 | PF00069 | 0.428 |
MOD_Plk_4 | 179 | 185 | PF00069 | 0.440 |
MOD_Plk_4 | 70 | 76 | PF00069 | 0.388 |
MOD_ProDKin_1 | 204 | 210 | PF00069 | 0.314 |
MOD_SUMO_rev_2 | 10 | 18 | PF00179 | 0.638 |
MOD_SUMO_rev_2 | 269 | 279 | PF00179 | 0.658 |
TRG_DiLeu_BaEn_1 | 61 | 66 | PF01217 | 0.154 |
TRG_ENDOCYTIC_2 | 161 | 164 | PF00928 | 0.465 |
TRG_ENDOCYTIC_2 | 242 | 245 | PF00928 | 0.500 |
TRG_ENDOCYTIC_2 | 251 | 254 | PF00928 | 0.431 |
TRG_ENDOCYTIC_2 | 358 | 361 | PF00928 | 0.719 |
TRG_ENDOCYTIC_2 | 366 | 369 | PF00928 | 0.734 |
TRG_ER_diArg_1 | 125 | 127 | PF00400 | 0.465 |
TRG_ER_diArg_1 | 198 | 200 | PF00400 | 0.191 |
TRG_ER_diArg_1 | 23 | 26 | PF00400 | 0.521 |
TRG_ER_diArg_1 | 285 | 288 | PF00400 | 0.622 |
TRG_ER_diArg_1 | 352 | 355 | PF00400 | 0.773 |
TRG_ER_diArg_1 | 361 | 363 | PF00400 | 0.733 |
TRG_NLS_MonoCore_2 | 285 | 290 | PF00514 | 0.708 |
TRG_NLS_MonoExtN_4 | 286 | 291 | PF00514 | 0.685 |
TRG_Pf-PMV_PEXEL_1 | 262 | 266 | PF00026 | 0.463 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3T7 | Leptomonas seymouri | 72% | 98% |
A0A1X0NUX2 | Trypanosomatidae | 50% | 100% |
A0A3Q8IIC8 | Leishmania donovani | 24% | 100% |
A0A3R7RC91 | Trypanosoma rangeli | 44% | 100% |
A0A3S5H6J6 | Leishmania donovani | 30% | 100% |
A0A3S7WX91 | Leishmania donovani | 89% | 100% |
A4HCH5 | Leishmania braziliensis | 74% | 100% |
A4IBG8 | Leishmania infantum | 25% | 100% |
B3DN87 | Arabidopsis thaliana | 24% | 100% |
C9ZSP6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
E7EZI4 | Danio rerio | 28% | 92% |
E7F4Z4 | Danio rerio | 27% | 69% |
E9AF82 | Leishmania major | 26% | 100% |
E9AH03 | Leishmania infantum | 89% | 100% |
E9AWG2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9B6D8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
P0C7U3 | Homo sapiens | 26% | 100% |
Q14AK4 | Mus musculus | 28% | 100% |
Q4QB09 | Leishmania major | 25% | 100% |
Q4QBL2 | Leishmania major | 88% | 99% |
Q4QGX1 | Leishmania major | 28% | 100% |
Q8WTX9 | Homo sapiens | 27% | 82% |
Q9H8X9 | Homo sapiens | 27% | 96% |
V5B8P9 | Trypanosoma cruzi | 47% | 100% |
V5BWI0 | Trypanosoma cruzi | 27% | 100% |