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: 14 |
NetGPI | no | yes: 0, no: 14 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005741 | mitochondrial outer membrane | 5 | 1 |
GO:0019867 | outer membrane | 3 | 1 |
GO:0031090 | organelle membrane | 3 | 1 |
GO:0031966 | mitochondrial membrane | 4 | 1 |
GO:0031968 | organelle outer membrane | 4 | 1 |
GO:0098588 | bounding membrane of organelle | 4 | 1 |
Related structures:
AlphaFold database: E9AX07
Term | Name | Level | Count |
---|---|---|---|
GO:0006605 | protein targeting | 5 | 1 |
GO:0006626 | protein targeting to mitochondrion | 5 | 1 |
GO:0006810 | transport | 3 | 1 |
GO:0006839 | mitochondrial transport | 4 | 1 |
GO:0006886 | intracellular protein transport | 4 | 1 |
GO:0008104 | protein localization | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0015031 | protein transport | 4 | 1 |
GO:0033036 | macromolecule localization | 2 | 1 |
GO:0033365 | protein localization to organelle | 5 | 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:0070585 | protein localization to mitochondrion | 6 | 1 |
GO:0070727 | cellular macromolecule localization | 3 | 1 |
GO:0071702 | organic substance transport | 4 | 1 |
GO:0071705 | nitrogen compound transport | 4 | 1 |
GO:0072594 | establishment of protein localization to organelle | 4 | 1 |
GO:0072655 | establishment of protein localization to mitochondrion | 5 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 188 | 190 | PF00675 | 0.449 |
CLV_NRD_NRD_1 | 24 | 26 | PF00675 | 0.394 |
CLV_NRD_NRD_1 | 51 | 53 | PF00675 | 0.426 |
CLV_NRD_NRD_1 | 80 | 82 | PF00675 | 0.519 |
CLV_PCSK_KEX2_1 | 150 | 152 | PF00082 | 0.468 |
CLV_PCSK_KEX2_1 | 188 | 190 | PF00082 | 0.436 |
CLV_PCSK_KEX2_1 | 239 | 241 | PF00082 | 0.561 |
CLV_PCSK_KEX2_1 | 272 | 274 | PF00082 | 0.542 |
CLV_PCSK_KEX2_1 | 380 | 382 | PF00082 | 0.540 |
CLV_PCSK_KEX2_1 | 51 | 53 | PF00082 | 0.418 |
CLV_PCSK_KEX2_1 | 79 | 81 | PF00082 | 0.526 |
CLV_PCSK_PC1ET2_1 | 150 | 152 | PF00082 | 0.468 |
CLV_PCSK_PC1ET2_1 | 239 | 241 | PF00082 | 0.518 |
CLV_PCSK_PC1ET2_1 | 272 | 274 | PF00082 | 0.542 |
CLV_PCSK_SKI1_1 | 201 | 205 | PF00082 | 0.489 |
CLV_PCSK_SKI1_1 | 26 | 30 | PF00082 | 0.461 |
CLV_PCSK_SKI1_1 | 273 | 277 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 72 | 76 | PF00082 | 0.595 |
DEG_APCC_DBOX_1 | 13 | 21 | PF00400 | 0.583 |
DEG_APCC_DBOX_1 | 79 | 87 | PF00400 | 0.295 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.676 |
DOC_ANK_TNKS_1 | 50 | 57 | PF00023 | 0.429 |
DOC_CYCLIN_RxL_1 | 270 | 279 | PF00134 | 0.268 |
DOC_CYCLIN_yCln2_LP_2 | 291 | 297 | PF00134 | 0.328 |
DOC_MAPK_gen_1 | 236 | 243 | PF00069 | 0.328 |
DOC_MAPK_gen_1 | 79 | 85 | PF00069 | 0.330 |
DOC_MAPK_MEF2A_6 | 92 | 100 | PF00069 | 0.370 |
DOC_MAPK_RevD_3 | 226 | 239 | PF00069 | 0.419 |
DOC_PP1_RVXF_1 | 199 | 205 | PF00149 | 0.268 |
DOC_PP2B_LxvP_1 | 137 | 140 | PF13499 | 0.229 |
DOC_PP2B_LxvP_1 | 291 | 294 | PF13499 | 0.292 |
DOC_PP4_FxxP_1 | 99 | 102 | PF00568 | 0.271 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.715 |
DOC_USP7_MATH_1 | 171 | 175 | PF00917 | 0.237 |
DOC_USP7_MATH_1 | 245 | 249 | PF00917 | 0.405 |
DOC_USP7_MATH_1 | 30 | 34 | PF00917 | 0.563 |
DOC_USP7_MATH_1 | 339 | 343 | PF00917 | 0.348 |
DOC_USP7_UBL2_3 | 365 | 369 | PF12436 | 0.345 |
DOC_WW_Pin1_4 | 101 | 106 | PF00397 | 0.329 |
DOC_WW_Pin1_4 | 44 | 49 | PF00397 | 0.592 |
LIG_14-3-3_CanoR_1 | 14 | 18 | PF00244 | 0.678 |
LIG_14-3-3_CanoR_1 | 188 | 192 | PF00244 | 0.311 |
LIG_14-3-3_CanoR_1 | 240 | 250 | PF00244 | 0.382 |
LIG_14-3-3_CanoR_1 | 273 | 281 | PF00244 | 0.313 |
LIG_14-3-3_CanoR_1 | 323 | 329 | PF00244 | 0.292 |
LIG_14-3-3_CanoR_1 | 340 | 344 | PF00244 | 0.463 |
LIG_14-3-3_CanoR_1 | 72 | 77 | PF00244 | 0.436 |
LIG_APCC_ABBAyCdc20_2 | 272 | 278 | PF00400 | 0.268 |
LIG_BRCT_BRCA1_1 | 332 | 336 | PF00533 | 0.264 |
LIG_BRCT_BRCA1_1 | 70 | 74 | PF00533 | 0.419 |
LIG_EH1_1 | 192 | 200 | PF00400 | 0.237 |
LIG_eIF4E_1 | 193 | 199 | PF01652 | 0.237 |
LIG_FHA_1 | 214 | 220 | PF00498 | 0.384 |
LIG_FHA_1 | 365 | 371 | PF00498 | 0.346 |
LIG_FHA_2 | 113 | 119 | PF00498 | 0.332 |
LIG_FHA_2 | 280 | 286 | PF00498 | 0.231 |
LIG_FHA_2 | 353 | 359 | PF00498 | 0.560 |
LIG_FHA_2 | 73 | 79 | PF00498 | 0.397 |
LIG_IRF3_LxIS_1 | 215 | 222 | PF10401 | 0.399 |
LIG_LIR_Gen_1 | 305 | 316 | PF02991 | 0.324 |
LIG_LIR_Gen_1 | 326 | 336 | PF02991 | 0.308 |
LIG_LIR_Gen_1 | 71 | 78 | PF02991 | 0.380 |
LIG_LIR_Gen_1 | 94 | 105 | PF02991 | 0.296 |
LIG_LIR_Nem_3 | 143 | 149 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 244 | 249 | PF02991 | 0.351 |
LIG_LIR_Nem_3 | 305 | 311 | PF02991 | 0.291 |
LIG_LIR_Nem_3 | 326 | 332 | PF02991 | 0.235 |
LIG_LIR_Nem_3 | 71 | 77 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 94 | 100 | PF02991 | 0.389 |
LIG_MYND_1 | 108 | 112 | PF01753 | 0.311 |
LIG_NRP_CendR_1 | 380 | 382 | PF00754 | 0.540 |
LIG_Pex14_2 | 6 | 10 | PF04695 | 0.603 |
LIG_SH2_CRK | 200 | 204 | PF00017 | 0.268 |
LIG_SH2_CRK | 246 | 250 | PF00017 | 0.315 |
LIG_SH2_CRK | 289 | 293 | PF00017 | 0.257 |
LIG_SH2_CRK | 308 | 312 | PF00017 | 0.257 |
LIG_SH2_GRB2like | 320 | 323 | PF00017 | 0.331 |
LIG_SH2_NCK_1 | 308 | 312 | PF00017 | 0.337 |
LIG_SH2_STAP1 | 233 | 237 | PF00017 | 0.332 |
LIG_SH2_STAP1 | 284 | 288 | PF00017 | 0.222 |
LIG_SH2_STAP1 | 289 | 293 | PF00017 | 0.222 |
LIG_SH2_STAP1 | 308 | 312 | PF00017 | 0.289 |
LIG_SH2_STAT3 | 149 | 152 | PF00017 | 0.268 |
LIG_SH2_STAT5 | 274 | 277 | PF00017 | 0.311 |
LIG_SH2_STAT5 | 320 | 323 | PF00017 | 0.263 |
LIG_SH2_STAT5 | 5 | 8 | PF00017 | 0.571 |
LIG_SH3_3 | 99 | 105 | PF00018 | 0.348 |
LIG_TYR_ITIM | 126 | 131 | PF00017 | 0.425 |
LIG_TYR_ITIM | 198 | 203 | PF00017 | 0.277 |
LIG_WRC_WIRS_1 | 117 | 122 | PF05994 | 0.250 |
MOD_CDK_SPxxK_3 | 44 | 51 | PF00069 | 0.494 |
MOD_CK1_1 | 174 | 180 | PF00069 | 0.340 |
MOD_CK1_1 | 248 | 254 | PF00069 | 0.473 |
MOD_CK1_1 | 300 | 306 | PF00069 | 0.212 |
MOD_CK1_1 | 330 | 336 | PF00069 | 0.376 |
MOD_CK1_1 | 375 | 381 | PF00069 | 0.719 |
MOD_CK1_1 | 44 | 50 | PF00069 | 0.605 |
MOD_CK2_1 | 112 | 118 | PF00069 | 0.425 |
MOD_CK2_1 | 29 | 35 | PF00069 | 0.643 |
MOD_CK2_1 | 352 | 358 | PF00069 | 0.727 |
MOD_CK2_1 | 72 | 78 | PF00069 | 0.469 |
MOD_GlcNHglycan | 304 | 307 | PF01048 | 0.419 |
MOD_GlcNHglycan | 308 | 311 | PF01048 | 0.387 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.334 |
MOD_GlcNHglycan | 333 | 336 | PF01048 | 0.467 |
MOD_GlcNHglycan | 374 | 377 | PF01048 | 0.737 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.375 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.406 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.455 |
MOD_GSK3_1 | 276 | 283 | PF00069 | 0.285 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.406 |
MOD_GSK3_1 | 327 | 334 | PF00069 | 0.486 |
MOD_GSK3_1 | 339 | 346 | PF00069 | 0.515 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.416 |
MOD_N-GLC_1 | 279 | 284 | PF02516 | 0.266 |
MOD_NEK2_1 | 172 | 177 | PF00069 | 0.350 |
MOD_NEK2_1 | 219 | 224 | PF00069 | 0.552 |
MOD_NEK2_1 | 241 | 246 | PF00069 | 0.497 |
MOD_NEK2_1 | 276 | 281 | PF00069 | 0.307 |
MOD_NEK2_1 | 338 | 343 | PF00069 | 0.597 |
MOD_PKA_2 | 13 | 19 | PF00069 | 0.644 |
MOD_PKA_2 | 187 | 193 | PF00069 | 0.393 |
MOD_PKA_2 | 322 | 328 | PF00069 | 0.328 |
MOD_PKA_2 | 339 | 345 | PF00069 | 0.473 |
MOD_PKA_2 | 91 | 97 | PF00069 | 0.441 |
MOD_Plk_1 | 172 | 178 | PF00069 | 0.470 |
MOD_Plk_1 | 191 | 197 | PF00069 | 0.213 |
MOD_Plk_1 | 279 | 285 | PF00069 | 0.308 |
MOD_Plk_1 | 352 | 358 | PF00069 | 0.702 |
MOD_Plk_2-3 | 353 | 359 | PF00069 | 0.443 |
MOD_Plk_4 | 116 | 122 | PF00069 | 0.234 |
MOD_Plk_4 | 245 | 251 | PF00069 | 0.508 |
MOD_ProDKin_1 | 101 | 107 | PF00069 | 0.404 |
MOD_ProDKin_1 | 44 | 50 | PF00069 | 0.489 |
TRG_DiLeu_BaEn_1 | 143 | 148 | PF01217 | 0.321 |
TRG_DiLeu_BaEn_2 | 92 | 98 | PF01217 | 0.378 |
TRG_DiLeu_BaLyEn_6 | 194 | 199 | PF01217 | 0.277 |
TRG_ENDOCYTIC_2 | 128 | 131 | PF00928 | 0.402 |
TRG_ENDOCYTIC_2 | 200 | 203 | PF00928 | 0.443 |
TRG_ENDOCYTIC_2 | 246 | 249 | PF00928 | 0.371 |
TRG_ENDOCYTIC_2 | 289 | 292 | PF00928 | 0.256 |
TRG_ENDOCYTIC_2 | 308 | 311 | PF00928 | 0.256 |
TRG_ER_diArg_1 | 151 | 154 | PF00400 | 0.321 |
TRG_ER_diArg_1 | 187 | 189 | PF00400 | 0.297 |
TRG_ER_diArg_1 | 224 | 227 | PF00400 | 0.420 |
TRG_ER_diArg_1 | 379 | 382 | PF00400 | 0.422 |
TRG_ER_diArg_1 | 51 | 53 | PF00400 | 0.563 |
TRG_ER_diArg_1 | 79 | 81 | PF00400 | 0.415 |
TRG_NLS_MonoExtC_3 | 149 | 155 | PF00514 | 0.321 |
TRG_NLS_MonoExtN_4 | 236 | 242 | PF00514 | 0.346 |
TRG_Pf-PMV_PEXEL_1 | 273 | 278 | PF00026 | 0.321 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IM13 | Leptomonas seymouri | 63% | 87% |
A0A0N1PD54 | Leptomonas seymouri | 30% | 100% |
A0A0S4JQS8 | Bodo saltans | 30% | 100% |
A0A1X0NVQ5 | Trypanosomatidae | 26% | 100% |
A0A1X0NVT0 | Trypanosomatidae | 27% | 82% |
A0A3S5H7D4 | Leishmania donovani | 91% | 100% |
A0A422N8G9 | Trypanosoma rangeli | 29% | 100% |
A0A422N8I7 | Trypanosoma rangeli | 32% | 95% |
A4HDM2 | Leishmania braziliensis | 76% | 100% |
E9AH69 | Leishmania infantum | 91% | 100% |
Q4QAG9 | Leishmania major | 86% | 100% |
V5BK31 | Trypanosoma cruzi | 29% | 100% |
V5DBK9 | Trypanosoma cruzi | 32% | 93% |