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: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: A4HHZ0
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 3 |
GO:0016787 | hydrolase activity | 2 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 148 | 152 | PF00656 | 0.362 |
CLV_C14_Caspase3-7 | 231 | 235 | PF00656 | 0.379 |
CLV_C14_Caspase3-7 | 3 | 7 | PF00656 | 0.589 |
CLV_NRD_NRD_1 | 218 | 220 | PF00675 | 0.384 |
CLV_NRD_NRD_1 | 224 | 226 | PF00675 | 0.396 |
CLV_NRD_NRD_1 | 310 | 312 | PF00675 | 0.554 |
CLV_PCSK_KEX2_1 | 220 | 222 | PF00082 | 0.344 |
CLV_PCSK_KEX2_1 | 224 | 226 | PF00082 | 0.360 |
CLV_PCSK_KEX2_1 | 310 | 312 | PF00082 | 0.690 |
CLV_PCSK_PC1ET2_1 | 220 | 222 | PF00082 | 0.344 |
CLV_PCSK_SKI1_1 | 225 | 229 | PF00082 | 0.382 |
CLV_PCSK_SKI1_1 | 237 | 241 | PF00082 | 0.370 |
CLV_PCSK_SKI1_1 | 266 | 270 | PF00082 | 0.487 |
CLV_PCSK_SKI1_1 | 330 | 334 | PF00082 | 0.584 |
CLV_PCSK_SKI1_1 | 5 | 9 | PF00082 | 0.405 |
DEG_APCC_DBOX_1 | 132 | 140 | PF00400 | 0.269 |
DEG_APCC_DBOX_1 | 4 | 12 | PF00400 | 0.371 |
DEG_COP1_1 | 333 | 342 | PF00400 | 0.509 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.537 |
DEG_SPOP_SBC_1 | 375 | 379 | PF00917 | 0.691 |
DOC_CKS1_1 | 276 | 281 | PF01111 | 0.527 |
DOC_CYCLIN_RxL_1 | 310 | 324 | PF00134 | 0.603 |
DOC_MAPK_DCC_7 | 240 | 249 | PF00069 | 0.453 |
DOC_MAPK_gen_1 | 201 | 211 | PF00069 | 0.436 |
DOC_MAPK_MEF2A_6 | 240 | 249 | PF00069 | 0.453 |
DOC_PP1_RVXF_1 | 62 | 69 | PF00149 | 0.463 |
DOC_PP4_FxxP_1 | 256 | 259 | PF00568 | 0.350 |
DOC_PP4_FxxP_1 | 269 | 272 | PF00568 | 0.383 |
DOC_USP7_MATH_1 | 144 | 148 | PF00917 | 0.394 |
DOC_USP7_MATH_1 | 183 | 187 | PF00917 | 0.413 |
DOC_USP7_MATH_1 | 259 | 263 | PF00917 | 0.263 |
DOC_USP7_MATH_1 | 321 | 325 | PF00917 | 0.549 |
DOC_USP7_MATH_1 | 331 | 335 | PF00917 | 0.605 |
DOC_USP7_MATH_1 | 375 | 379 | PF00917 | 0.712 |
DOC_WW_Pin1_4 | 179 | 184 | PF00397 | 0.284 |
DOC_WW_Pin1_4 | 255 | 260 | PF00397 | 0.543 |
DOC_WW_Pin1_4 | 275 | 280 | PF00397 | 0.233 |
DOC_WW_Pin1_4 | 309 | 314 | PF00397 | 0.435 |
DOC_WW_Pin1_4 | 362 | 367 | PF00397 | 0.775 |
DOC_WW_Pin1_4 | 371 | 376 | PF00397 | 0.753 |
LIG_14-3-3_CanoR_1 | 105 | 111 | PF00244 | 0.249 |
LIG_14-3-3_CanoR_1 | 27 | 35 | PF00244 | 0.536 |
LIG_14-3-3_CanoR_1 | 286 | 294 | PF00244 | 0.270 |
LIG_14-3-3_CanoR_1 | 67 | 73 | PF00244 | 0.362 |
LIG_BIR_III_2 | 267 | 271 | PF00653 | 0.420 |
LIG_BIR_III_2 | 357 | 361 | PF00653 | 0.512 |
LIG_BRCT_BRCA1_1 | 126 | 130 | PF00533 | 0.273 |
LIG_Clathr_ClatBox_1 | 110 | 114 | PF01394 | 0.284 |
LIG_eIF4E_1 | 131 | 137 | PF01652 | 0.337 |
LIG_FHA_1 | 200 | 206 | PF00498 | 0.337 |
LIG_FHA_1 | 310 | 316 | PF00498 | 0.656 |
LIG_FHA_2 | 258 | 264 | PF00498 | 0.359 |
LIG_LIR_Apic_2 | 253 | 259 | PF02991 | 0.363 |
LIG_LIR_Apic_2 | 267 | 272 | PF02991 | 0.376 |
LIG_LIR_Apic_2 | 71 | 75 | PF02991 | 0.267 |
LIG_LIR_Gen_1 | 122 | 131 | PF02991 | 0.223 |
LIG_LIR_Gen_1 | 141 | 150 | PF02991 | 0.413 |
LIG_LIR_Gen_1 | 181 | 191 | PF02991 | 0.269 |
LIG_LIR_Gen_1 | 295 | 303 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 122 | 128 | PF02991 | 0.230 |
LIG_LIR_Nem_3 | 141 | 145 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 181 | 187 | PF02991 | 0.278 |
LIG_LIR_Nem_3 | 295 | 300 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 71 | 76 | PF02991 | 0.354 |
LIG_PCNA_PIPBox_1 | 291 | 300 | PF02747 | 0.328 |
LIG_PCNA_yPIPBox_3 | 286 | 298 | PF02747 | 0.341 |
LIG_Pex14_1 | 72 | 76 | PF04695 | 0.442 |
LIG_Pex14_2 | 111 | 115 | PF04695 | 0.413 |
LIG_Pex14_2 | 68 | 72 | PF04695 | 0.429 |
LIG_SH2_PTP2 | 125 | 128 | PF00017 | 0.328 |
LIG_SH2_STAT3 | 131 | 134 | PF00017 | 0.269 |
LIG_SH2_STAT5 | 125 | 128 | PF00017 | 0.331 |
LIG_SH2_STAT5 | 301 | 304 | PF00017 | 0.349 |
LIG_SH2_STAT5 | 86 | 89 | PF00017 | 0.295 |
LIG_SH3_3 | 333 | 339 | PF00018 | 0.745 |
LIG_SUMO_SIM_anti_2 | 135 | 141 | PF11976 | 0.337 |
LIG_SUMO_SIM_par_1 | 135 | 141 | PF11976 | 0.337 |
LIG_SUMO_SIM_par_1 | 346 | 352 | PF11976 | 0.514 |
LIG_WRPW_2 | 73 | 76 | PF00400 | 0.302 |
LIG_WW_3 | 27 | 31 | PF00397 | 0.432 |
MOD_CDK_SPxxK_3 | 309 | 316 | PF00069 | 0.428 |
MOD_CK1_1 | 118 | 124 | PF00069 | 0.277 |
MOD_CK1_1 | 334 | 340 | PF00069 | 0.606 |
MOD_CK1_1 | 349 | 355 | PF00069 | 0.593 |
MOD_CK1_1 | 374 | 380 | PF00069 | 0.642 |
MOD_CK2_1 | 118 | 124 | PF00069 | 0.269 |
MOD_CK2_1 | 257 | 263 | PF00069 | 0.346 |
MOD_CK2_1 | 28 | 34 | PF00069 | 0.416 |
MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.275 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.507 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.517 |
MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.494 |
MOD_GlcNHglycan | 333 | 336 | PF01048 | 0.657 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.318 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.302 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.557 |
MOD_GSK3_1 | 330 | 337 | PF00069 | 0.615 |
MOD_GSK3_1 | 348 | 355 | PF00069 | 0.715 |
MOD_GSK3_1 | 362 | 369 | PF00069 | 0.653 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.685 |
MOD_N-GLC_1 | 321 | 326 | PF02516 | 0.483 |
MOD_N-GLC_2 | 20 | 22 | PF02516 | 0.285 |
MOD_NEK2_1 | 115 | 120 | PF00069 | 0.312 |
MOD_NEK2_1 | 68 | 73 | PF00069 | 0.365 |
MOD_NEK2_1 | 9 | 14 | PF00069 | 0.530 |
MOD_NEK2_2 | 183 | 188 | PF00069 | 0.284 |
MOD_PKA_2 | 285 | 291 | PF00069 | 0.413 |
MOD_PKA_2 | 29 | 35 | PF00069 | 0.494 |
MOD_Plk_4 | 68 | 74 | PF00069 | 0.286 |
MOD_ProDKin_1 | 179 | 185 | PF00069 | 0.284 |
MOD_ProDKin_1 | 255 | 261 | PF00069 | 0.537 |
MOD_ProDKin_1 | 275 | 281 | PF00069 | 0.231 |
MOD_ProDKin_1 | 309 | 315 | PF00069 | 0.442 |
MOD_ProDKin_1 | 362 | 368 | PF00069 | 0.776 |
MOD_ProDKin_1 | 371 | 377 | PF00069 | 0.752 |
TRG_DiLeu_BaEn_1 | 132 | 137 | PF01217 | 0.337 |
TRG_DiLeu_BaLyEn_6 | 185 | 190 | PF01217 | 0.303 |
TRG_ENDOCYTIC_2 | 125 | 128 | PF00928 | 0.356 |
TRG_ENDOCYTIC_2 | 95 | 98 | PF00928 | 0.303 |
TRG_ER_diArg_1 | 218 | 221 | PF00400 | 0.337 |
TRG_ER_diArg_1 | 223 | 225 | PF00400 | 0.360 |
TRG_NES_CRM1_1 | 134 | 149 | PF08389 | 0.413 |
TRG_NES_CRM1_1 | 289 | 304 | PF08389 | 0.426 |
TRG_NES_CRM1_1 | 99 | 114 | PF08389 | 0.284 |
TRG_NLS_MonoExtN_4 | 217 | 223 | PF00514 | 0.340 |
TRG_Pf-PMV_PEXEL_1 | 188 | 192 | PF00026 | 0.274 |
TRG_Pf-PMV_PEXEL_1 | 212 | 216 | PF00026 | 0.294 |
TRG_Pf-PMV_PEXEL_1 | 64 | 69 | PF00026 | 0.391 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HRJ3 | Leptomonas seymouri | 70% | 100% |
A0A0S4JBE5 | Bodo saltans | 50% | 88% |
A0A1X0P2B9 | Trypanosomatidae | 55% | 93% |
A0A3S5H7M3 | Leishmania donovani | 80% | 77% |
A0A422NMM6 | Trypanosoma rangeli | 58% | 96% |
A4I567 | Leishmania infantum | 86% | 77% |
C9ZQJ3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 52% | 93% |
E9B0G4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 80% |
Q4Q7R9 | Leishmania major | 78% | 100% |
V5BCE0 | Trypanosoma cruzi | 53% | 95% |