Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 2 |
Forrest at al. (procyclic) | no | yes: 2 |
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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4H6V4
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 1 |
GO:0006913 | nucleocytoplasmic transport | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0051169 | nuclear transport | 4 | 1 |
GO:0051170 | import into nucleus | 6 | 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 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 122 | 126 | PF00656 | 0.668 |
CLV_C14_Caspase3-7 | 152 | 156 | PF00656 | 0.395 |
CLV_C14_Caspase3-7 | 209 | 213 | PF00656 | 0.417 |
CLV_C14_Caspase3-7 | 57 | 61 | PF00656 | 0.499 |
CLV_NRD_NRD_1 | 152 | 154 | PF00675 | 0.407 |
CLV_NRD_NRD_1 | 294 | 296 | PF00675 | 0.508 |
CLV_NRD_NRD_1 | 299 | 301 | PF00675 | 0.536 |
CLV_NRD_NRD_1 | 368 | 370 | PF00675 | 0.623 |
CLV_NRD_NRD_1 | 67 | 69 | PF00675 | 0.579 |
CLV_PCSK_KEX2_1 | 108 | 110 | PF00082 | 0.479 |
CLV_PCSK_KEX2_1 | 294 | 296 | PF00082 | 0.508 |
CLV_PCSK_KEX2_1 | 299 | 301 | PF00082 | 0.536 |
CLV_PCSK_PC1ET2_1 | 108 | 110 | PF00082 | 0.617 |
CLV_PCSK_PC7_1 | 295 | 301 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 136 | 140 | PF00082 | 0.431 |
CLV_PCSK_SKI1_1 | 283 | 287 | PF00082 | 0.422 |
CLV_PCSK_SKI1_1 | 303 | 307 | PF00082 | 0.613 |
CLV_PCSK_SKI1_1 | 92 | 96 | PF00082 | 0.446 |
DEG_SPOP_SBC_1 | 243 | 247 | PF00917 | 0.468 |
DOC_CYCLIN_yCln2_LP_2 | 373 | 379 | PF00134 | 0.533 |
DOC_MAPK_DCC_7 | 306 | 314 | PF00069 | 0.350 |
DOC_MAPK_gen_1 | 299 | 309 | PF00069 | 0.425 |
DOC_MAPK_RevD_3 | 282 | 295 | PF00069 | 0.288 |
DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.666 |
DOC_USP7_MATH_1 | 225 | 229 | PF00917 | 0.489 |
DOC_USP7_MATH_1 | 243 | 247 | PF00917 | 0.481 |
DOC_USP7_MATH_1 | 258 | 262 | PF00917 | 0.473 |
DOC_USP7_MATH_1 | 320 | 324 | PF00917 | 0.360 |
DOC_USP7_MATH_1 | 54 | 58 | PF00917 | 0.704 |
DOC_WW_Pin1_4 | 184 | 189 | PF00397 | 0.469 |
DOC_WW_Pin1_4 | 277 | 282 | PF00397 | 0.470 |
DOC_WW_Pin1_4 | 307 | 312 | PF00397 | 0.370 |
DOC_WW_Pin1_4 | 325 | 330 | PF00397 | 0.459 |
DOC_WW_Pin1_4 | 73 | 78 | PF00397 | 0.723 |
DOC_WW_Pin1_4 | 81 | 86 | PF00397 | 0.558 |
LIG_14-3-3_CanoR_1 | 35 | 44 | PF00244 | 0.444 |
LIG_14-3-3_CterR_2 | 411 | 414 | PF00244 | 0.505 |
LIG_Actin_WH2_2 | 23 | 39 | PF00022 | 0.473 |
LIG_BRCT_BRCA1_1 | 245 | 249 | PF00533 | 0.573 |
LIG_deltaCOP1_diTrp_1 | 97 | 105 | PF00928 | 0.354 |
LIG_FHA_1 | 172 | 178 | PF00498 | 0.431 |
LIG_FHA_1 | 229 | 235 | PF00498 | 0.509 |
LIG_FHA_1 | 252 | 258 | PF00498 | 0.407 |
LIG_FHA_1 | 78 | 84 | PF00498 | 0.353 |
LIG_FHA_1 | 8 | 14 | PF00498 | 0.364 |
LIG_FHA_2 | 150 | 156 | PF00498 | 0.392 |
LIG_FHA_2 | 50 | 56 | PF00498 | 0.394 |
LIG_FHA_2 | 82 | 88 | PF00498 | 0.513 |
LIG_LIR_Apic_2 | 179 | 183 | PF02991 | 0.305 |
LIG_LIR_Gen_1 | 143 | 149 | PF02991 | 0.392 |
LIG_LIR_Gen_1 | 166 | 173 | PF02991 | 0.307 |
LIG_LIR_Gen_1 | 246 | 257 | PF02991 | 0.412 |
LIG_LIR_Gen_1 | 26 | 36 | PF02991 | 0.278 |
LIG_LIR_Gen_1 | 42 | 51 | PF02991 | 0.500 |
LIG_LIR_Gen_1 | 95 | 106 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 133 | 138 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 166 | 170 | PF02991 | 0.310 |
LIG_LIR_Nem_3 | 245 | 251 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 26 | 31 | PF02991 | 0.272 |
LIG_LIR_Nem_3 | 392 | 397 | PF02991 | 0.329 |
LIG_LIR_Nem_3 | 42 | 47 | PF02991 | 0.515 |
LIG_LIR_Nem_3 | 95 | 101 | PF02991 | 0.352 |
LIG_PCNA_yPIPBox_3 | 24 | 37 | PF02747 | 0.495 |
LIG_PDZ_Class_2 | 409 | 414 | PF00595 | 0.488 |
LIG_Pex14_2 | 101 | 105 | PF04695 | 0.349 |
LIG_SH2_CRK | 135 | 139 | PF00017 | 0.426 |
LIG_SH2_CRK | 167 | 171 | PF00017 | 0.372 |
LIG_SH2_CRK | 180 | 184 | PF00017 | 0.390 |
LIG_SH2_CRK | 28 | 32 | PF00017 | 0.261 |
LIG_SH2_NCK_1 | 180 | 184 | PF00017 | 0.446 |
LIG_SH2_NCK_1 | 349 | 353 | PF00017 | 0.457 |
LIG_SH2_SRC | 167 | 170 | PF00017 | 0.312 |
LIG_SH2_SRC | 349 | 352 | PF00017 | 0.454 |
LIG_SH2_STAP1 | 44 | 48 | PF00017 | 0.494 |
LIG_SH2_STAT5 | 169 | 172 | PF00017 | 0.306 |
LIG_SH2_STAT5 | 251 | 254 | PF00017 | 0.274 |
LIG_SH3_2 | 376 | 381 | PF14604 | 0.360 |
LIG_SH3_3 | 331 | 337 | PF00018 | 0.572 |
LIG_SH3_3 | 373 | 379 | PF00018 | 0.444 |
LIG_SUMO_SIM_par_1 | 29 | 34 | PF11976 | 0.322 |
LIG_SUMO_SIM_par_1 | 79 | 84 | PF11976 | 0.452 |
LIG_SUMO_SIM_par_1 | 92 | 97 | PF11976 | 0.279 |
LIG_TRAF2_1 | 84 | 87 | PF00917 | 0.421 |
LIG_UBA3_1 | 284 | 288 | PF00899 | 0.242 |
MOD_CDC14_SPxK_1 | 280 | 283 | PF00782 | 0.272 |
MOD_CDK_SPxK_1 | 277 | 283 | PF00069 | 0.310 |
MOD_CK1_1 | 137 | 143 | PF00069 | 0.308 |
MOD_CK1_1 | 187 | 193 | PF00069 | 0.378 |
MOD_CK1_1 | 210 | 216 | PF00069 | 0.673 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.512 |
MOD_CK1_1 | 239 | 245 | PF00069 | 0.406 |
MOD_CK2_1 | 258 | 264 | PF00069 | 0.437 |
MOD_CK2_1 | 39 | 45 | PF00069 | 0.601 |
MOD_CK2_1 | 49 | 55 | PF00069 | 0.411 |
MOD_CK2_1 | 81 | 87 | PF00069 | 0.522 |
MOD_GlcNHglycan | 110 | 113 | PF01048 | 0.549 |
MOD_GlcNHglycan | 120 | 124 | PF01048 | 0.557 |
MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.367 |
MOD_GlcNHglycan | 157 | 160 | PF01048 | 0.512 |
MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.363 |
MOD_GlcNHglycan | 228 | 231 | PF01048 | 0.428 |
MOD_GlcNHglycan | 238 | 241 | PF01048 | 0.312 |
MOD_GlcNHglycan | 275 | 278 | PF01048 | 0.477 |
MOD_GlcNHglycan | 322 | 325 | PF01048 | 0.404 |
MOD_GlcNHglycan | 340 | 343 | PF01048 | 0.616 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.679 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.542 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.476 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.374 |
MOD_GSK3_1 | 69 | 76 | PF00069 | 0.648 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.597 |
MOD_LATS_1 | 269 | 275 | PF00433 | 0.478 |
MOD_NEK2_1 | 149 | 154 | PF00069 | 0.388 |
MOD_NEK2_1 | 178 | 183 | PF00069 | 0.373 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.447 |
MOD_PIKK_1 | 99 | 105 | PF00454 | 0.555 |
MOD_PKA_1 | 108 | 114 | PF00069 | 0.492 |
MOD_PKA_2 | 108 | 114 | PF00069 | 0.614 |
MOD_Plk_1 | 258 | 264 | PF00069 | 0.430 |
MOD_Plk_1 | 99 | 105 | PF00069 | 0.428 |
MOD_Plk_2-3 | 259 | 265 | PF00069 | 0.487 |
MOD_Plk_4 | 23 | 29 | PF00069 | 0.286 |
MOD_Plk_4 | 244 | 250 | PF00069 | 0.399 |
MOD_Plk_4 | 43 | 49 | PF00069 | 0.402 |
MOD_ProDKin_1 | 184 | 190 | PF00069 | 0.479 |
MOD_ProDKin_1 | 277 | 283 | PF00069 | 0.461 |
MOD_ProDKin_1 | 307 | 313 | PF00069 | 0.356 |
MOD_ProDKin_1 | 325 | 331 | PF00069 | 0.475 |
MOD_ProDKin_1 | 73 | 79 | PF00069 | 0.712 |
MOD_ProDKin_1 | 81 | 87 | PF00069 | 0.552 |
TRG_DiLeu_BaEn_4 | 99 | 105 | PF01217 | 0.428 |
TRG_ENDOCYTIC_2 | 135 | 138 | PF00928 | 0.363 |
TRG_ENDOCYTIC_2 | 144 | 147 | PF00928 | 0.312 |
TRG_ENDOCYTIC_2 | 167 | 170 | PF00928 | 0.312 |
TRG_ENDOCYTIC_2 | 28 | 31 | PF00928 | 0.266 |
TRG_ENDOCYTIC_2 | 44 | 47 | PF00928 | 0.503 |
TRG_ER_diArg_1 | 299 | 301 | PF00400 | 0.549 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6D9 | Leptomonas seymouri | 50% | 100% |
A0A1X0NR33 | Trypanosomatidae | 33% | 100% |
A0A3S7WRX1 | Leishmania donovani | 73% | 100% |
A0A422NA30 | Trypanosoma rangeli | 37% | 100% |
C9ZUI6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
E9AGC6 | Leishmania infantum | 72% | 100% |
E9ANW6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 72% | 100% |
Q4QGQ4 | Leishmania major | 72% | 100% |
V5BTJ4 | Trypanosoma cruzi | 36% | 100% |