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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: A4I6A7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 18 | 20 | PF00675 | 0.440 |
CLV_NRD_NRD_1 | 185 | 187 | PF00675 | 0.547 |
CLV_NRD_NRD_1 | 258 | 260 | PF00675 | 0.532 |
CLV_NRD_NRD_1 | 282 | 284 | PF00675 | 0.380 |
CLV_NRD_NRD_1 | 292 | 294 | PF00675 | 0.388 |
CLV_NRD_NRD_1 | 61 | 63 | PF00675 | 0.426 |
CLV_PCSK_KEX2_1 | 18 | 20 | PF00082 | 0.448 |
CLV_PCSK_KEX2_1 | 185 | 187 | PF00082 | 0.517 |
CLV_PCSK_KEX2_1 | 257 | 259 | PF00082 | 0.545 |
CLV_PCSK_KEX2_1 | 292 | 294 | PF00082 | 0.440 |
CLV_PCSK_KEX2_1 | 61 | 63 | PF00082 | 0.501 |
CLV_PCSK_PC7_1 | 14 | 20 | PF00082 | 0.526 |
CLV_PCSK_PC7_1 | 57 | 63 | PF00082 | 0.536 |
CLV_PCSK_SKI1_1 | 172 | 176 | PF00082 | 0.506 |
CLV_PCSK_SKI1_1 | 18 | 22 | PF00082 | 0.429 |
CLV_PCSK_SKI1_1 | 186 | 190 | PF00082 | 0.421 |
CLV_PCSK_SKI1_1 | 307 | 311 | PF00082 | 0.532 |
CLV_PCSK_SKI1_1 | 315 | 319 | PF00082 | 0.499 |
DEG_APCC_DBOX_1 | 17 | 25 | PF00400 | 0.442 |
DEG_APCC_DBOX_1 | 291 | 299 | PF00400 | 0.517 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.706 |
DOC_AGCK_PIF_1 | 248 | 253 | PF00069 | 0.496 |
DOC_CKS1_1 | 67 | 72 | PF01111 | 0.555 |
DOC_CYCLIN_RxL_1 | 14 | 25 | PF00134 | 0.560 |
DOC_CYCLIN_RxL_1 | 310 | 322 | PF00134 | 0.315 |
DOC_MAPK_gen_1 | 18 | 26 | PF00069 | 0.459 |
DOC_MAPK_gen_1 | 314 | 320 | PF00069 | 0.467 |
DOC_PP1_RVXF_1 | 313 | 320 | PF00149 | 0.524 |
DOC_PP4_FxxP_1 | 64 | 67 | PF00568 | 0.561 |
DOC_USP7_MATH_1 | 112 | 116 | PF00917 | 0.385 |
DOC_USP7_MATH_1 | 302 | 306 | PF00917 | 0.463 |
DOC_USP7_MATH_1 | 83 | 87 | PF00917 | 0.437 |
DOC_USP7_UBL2_3 | 310 | 314 | PF12436 | 0.420 |
DOC_WW_Pin1_4 | 242 | 247 | PF00397 | 0.546 |
DOC_WW_Pin1_4 | 298 | 303 | PF00397 | 0.483 |
DOC_WW_Pin1_4 | 66 | 71 | PF00397 | 0.527 |
LIG_14-3-3_CanoR_1 | 141 | 146 | PF00244 | 0.503 |
LIG_14-3-3_CanoR_1 | 202 | 211 | PF00244 | 0.298 |
LIG_14-3-3_CanoR_1 | 263 | 273 | PF00244 | 0.508 |
LIG_14-3-3_CanoR_1 | 283 | 287 | PF00244 | 0.453 |
LIG_14-3-3_CanoR_1 | 34 | 44 | PF00244 | 0.570 |
LIG_14-3-3_CanoR_1 | 61 | 65 | PF00244 | 0.533 |
LIG_Actin_WH2_2 | 41 | 59 | PF00022 | 0.573 |
LIG_Actin_WH2_2 | 9 | 24 | PF00022 | 0.495 |
LIG_BRCT_BRCA1_1 | 244 | 248 | PF00533 | 0.498 |
LIG_deltaCOP1_diTrp_1 | 269 | 278 | PF00928 | 0.568 |
LIG_DLG_GKlike_1 | 141 | 149 | PF00625 | 0.306 |
LIG_eIF4E_1 | 108 | 114 | PF01652 | 0.499 |
LIG_FHA_1 | 212 | 218 | PF00498 | 0.447 |
LIG_FHA_1 | 30 | 36 | PF00498 | 0.577 |
LIG_FHA_1 | 7 | 13 | PF00498 | 0.605 |
LIG_LIR_Apic_2 | 46 | 52 | PF02991 | 0.517 |
LIG_LIR_Apic_2 | 63 | 67 | PF02991 | 0.428 |
LIG_LIR_Gen_1 | 191 | 199 | PF02991 | 0.383 |
LIG_LIR_Gen_1 | 232 | 240 | PF02991 | 0.494 |
LIG_LIR_Gen_1 | 275 | 286 | PF02991 | 0.431 |
LIG_LIR_Gen_1 | 38 | 48 | PF02991 | 0.479 |
LIG_LIR_Gen_1 | 95 | 103 | PF02991 | 0.539 |
LIG_LIR_Nem_3 | 103 | 108 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 15 | 20 | PF02991 | 0.427 |
LIG_LIR_Nem_3 | 191 | 196 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 230 | 236 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 270 | 276 | PF02991 | 0.541 |
LIG_LIR_Nem_3 | 38 | 43 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 95 | 99 | PF02991 | 0.509 |
LIG_NRBOX | 194 | 200 | PF00104 | 0.437 |
LIG_NRBOX | 316 | 322 | PF00104 | 0.314 |
LIG_PCNA_yPIPBox_3 | 136 | 146 | PF02747 | 0.485 |
LIG_SH2_CRK | 17 | 21 | PF00017 | 0.487 |
LIG_SH2_CRK | 273 | 277 | PF00017 | 0.584 |
LIG_SH2_NCK_1 | 68 | 72 | PF00017 | 0.549 |
LIG_SH2_STAT5 | 145 | 148 | PF00017 | 0.489 |
LIG_SH2_STAT5 | 207 | 210 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 68 | 71 | PF00017 | 0.556 |
LIG_SH3_3 | 296 | 302 | PF00018 | 0.561 |
LIG_SH3_3 | 64 | 70 | PF00018 | 0.560 |
LIG_SUMO_SIM_anti_2 | 194 | 200 | PF11976 | 0.412 |
LIG_SUMO_SIM_par_1 | 22 | 28 | PF11976 | 0.502 |
LIG_TRAF2_1 | 152 | 155 | PF00917 | 0.548 |
LIG_WRC_WIRS_1 | 212 | 217 | PF05994 | 0.404 |
MOD_CK1_1 | 130 | 136 | PF00069 | 0.519 |
MOD_CK1_1 | 194 | 200 | PF00069 | 0.432 |
MOD_CK1_1 | 301 | 307 | PF00069 | 0.485 |
MOD_CK1_1 | 86 | 92 | PF00069 | 0.485 |
MOD_CK2_1 | 149 | 155 | PF00069 | 0.551 |
MOD_CK2_1 | 178 | 184 | PF00069 | 0.481 |
MOD_CK2_1 | 22 | 28 | PF00069 | 0.519 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.328 |
MOD_GlcNHglycan | 179 | 183 | PF01048 | 0.470 |
MOD_GlcNHglycan | 303 | 307 | PF01048 | 0.518 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.469 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.484 |
MOD_N-GLC_1 | 242 | 247 | PF02516 | 0.540 |
MOD_N-GLC_2 | 201 | 203 | PF02516 | 0.452 |
MOD_NEK2_1 | 12 | 17 | PF00069 | 0.463 |
MOD_NEK2_2 | 229 | 234 | PF00069 | 0.512 |
MOD_NEK2_2 | 83 | 88 | PF00069 | 0.469 |
MOD_PIKK_1 | 29 | 35 | PF00454 | 0.600 |
MOD_PK_1 | 22 | 28 | PF00069 | 0.459 |
MOD_PKA_2 | 282 | 288 | PF00069 | 0.476 |
MOD_PKA_2 | 60 | 66 | PF00069 | 0.538 |
MOD_Plk_1 | 178 | 184 | PF00069 | 0.487 |
MOD_Plk_1 | 191 | 197 | PF00069 | 0.409 |
MOD_Plk_1 | 229 | 235 | PF00069 | 0.537 |
MOD_Plk_2-3 | 158 | 164 | PF00069 | 0.548 |
MOD_Plk_4 | 194 | 200 | PF00069 | 0.389 |
MOD_Plk_4 | 211 | 217 | PF00069 | 0.360 |
MOD_Plk_4 | 222 | 228 | PF00069 | 0.375 |
MOD_Plk_4 | 282 | 288 | PF00069 | 0.476 |
MOD_Plk_4 | 83 | 89 | PF00069 | 0.447 |
MOD_ProDKin_1 | 242 | 248 | PF00069 | 0.536 |
MOD_ProDKin_1 | 298 | 304 | PF00069 | 0.488 |
MOD_ProDKin_1 | 66 | 72 | PF00069 | 0.523 |
MOD_SUMO_for_1 | 188 | 191 | PF00179 | 0.472 |
MOD_SUMO_rev_2 | 181 | 190 | PF00179 | 0.561 |
TRG_DiLeu_BaEn_1 | 191 | 196 | PF01217 | 0.464 |
TRG_DiLeu_BaEn_1 | 260 | 265 | PF01217 | 0.548 |
TRG_DiLeu_LyEn_5 | 260 | 265 | PF01217 | 0.481 |
TRG_ENDOCYTIC_2 | 108 | 111 | PF00928 | 0.507 |
TRG_ENDOCYTIC_2 | 17 | 20 | PF00928 | 0.435 |
TRG_ENDOCYTIC_2 | 253 | 256 | PF00928 | 0.476 |
TRG_ENDOCYTIC_2 | 273 | 276 | PF00928 | 0.578 |
TRG_ER_diArg_1 | 140 | 143 | PF00400 | 0.509 |
TRG_ER_diArg_1 | 17 | 19 | PF00400 | 0.467 |
TRG_ER_diArg_1 | 256 | 259 | PF00400 | 0.532 |
TRG_ER_diArg_1 | 291 | 293 | PF00400 | 0.507 |
TRG_ER_diArg_1 | 60 | 62 | PF00400 | 0.496 |
TRG_Pf-PMV_PEXEL_1 | 91 | 95 | PF00026 | 0.484 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1X3 | Leptomonas seymouri | 55% | 100% |
A0A1X0NJP2 | Trypanosomatidae | 27% | 100% |
A0A3S5H7P2 | Leishmania donovani | 99% | 100% |
A0A422N5I6 | Trypanosoma rangeli | 29% | 99% |
A4HIX9 | Leishmania braziliensis | 76% | 100% |
C9ZN34 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
E9B1G3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q4Q6P9 | Leishmania major | 92% | 100% |
V5DEV4 | Trypanosoma cruzi | 30% | 100% |