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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: A0A3Q8I8Y2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 151 | 157 | PF00089 | 0.430 |
CLV_NRD_NRD_1 | 105 | 107 | PF00675 | 0.471 |
CLV_NRD_NRD_1 | 167 | 169 | PF00675 | 0.419 |
CLV_NRD_NRD_1 | 310 | 312 | PF00675 | 0.577 |
CLV_PCSK_KEX2_1 | 105 | 107 | PF00082 | 0.452 |
CLV_PCSK_KEX2_1 | 167 | 169 | PF00082 | 0.419 |
CLV_PCSK_KEX2_1 | 310 | 312 | PF00082 | 0.577 |
CLV_PCSK_PC7_1 | 163 | 169 | PF00082 | 0.390 |
CLV_PCSK_SKI1_1 | 125 | 129 | PF00082 | 0.439 |
CLV_PCSK_SKI1_1 | 247 | 251 | PF00082 | 0.543 |
CLV_PCSK_SKI1_1 | 84 | 88 | PF00082 | 0.377 |
CLV_PCSK_SKI1_1 | 99 | 103 | PF00082 | 0.359 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.469 |
DOC_CYCLIN_RxL_1 | 78 | 91 | PF00134 | 0.381 |
DOC_CYCLIN_RxL_1 | 96 | 104 | PF00134 | 0.315 |
DOC_CYCLIN_yCln2_LP_2 | 86 | 92 | PF00134 | 0.498 |
DOC_MAPK_gen_1 | 53 | 61 | PF00069 | 0.442 |
DOC_PP1_RVXF_1 | 176 | 183 | PF00149 | 0.432 |
DOC_PP4_FxxP_1 | 155 | 158 | PF00568 | 0.466 |
DOC_PP4_FxxP_1 | 278 | 281 | PF00568 | 0.593 |
DOC_SPAK_OSR1_1 | 154 | 158 | PF12202 | 0.433 |
DOC_USP7_MATH_1 | 172 | 176 | PF00917 | 0.419 |
DOC_WW_Pin1_4 | 277 | 282 | PF00397 | 0.612 |
LIG_14-3-3_CanoR_1 | 154 | 158 | PF00244 | 0.434 |
LIG_14-3-3_CanoR_1 | 167 | 173 | PF00244 | 0.381 |
LIG_14-3-3_CanoR_1 | 24 | 32 | PF00244 | 0.353 |
LIG_14-3-3_CanoR_1 | 274 | 279 | PF00244 | 0.562 |
LIG_14-3-3_CanoR_1 | 82 | 87 | PF00244 | 0.363 |
LIG_FHA_1 | 102 | 108 | PF00498 | 0.408 |
LIG_FHA_2 | 217 | 223 | PF00498 | 0.631 |
LIG_FHA_2 | 83 | 89 | PF00498 | 0.434 |
LIG_LIR_Apic_2 | 276 | 281 | PF02991 | 0.588 |
LIG_LIR_Gen_1 | 38 | 48 | PF02991 | 0.365 |
LIG_LIR_Gen_1 | 58 | 69 | PF02991 | 0.322 |
LIG_LIR_Nem_3 | 161 | 165 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 22 | 26 | PF02991 | 0.373 |
LIG_LIR_Nem_3 | 38 | 43 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 58 | 64 | PF02991 | 0.306 |
LIG_LIR_Nem_3 | 85 | 90 | PF02991 | 0.537 |
LIG_NRBOX | 123 | 129 | PF00104 | 0.433 |
LIG_NRBOX | 97 | 103 | PF00104 | 0.501 |
LIG_SH2_STAP1 | 297 | 301 | PF00017 | 0.468 |
LIG_SH3_3 | 126 | 132 | PF00018 | 0.410 |
LIG_SH3_3 | 154 | 160 | PF00018 | 0.473 |
LIG_SH3_3 | 200 | 206 | PF00018 | 0.609 |
LIG_SH3_3 | 284 | 290 | PF00018 | 0.623 |
LIG_SUMO_SIM_anti_2 | 88 | 94 | PF11976 | 0.402 |
LIG_SUMO_SIM_par_1 | 130 | 136 | PF11976 | 0.427 |
LIG_WRC_WIRS_1 | 159 | 164 | PF05994 | 0.378 |
LIG_WRC_WIRS_1 | 275 | 280 | PF05994 | 0.552 |
MOD_CK1_1 | 216 | 222 | PF00069 | 0.702 |
MOD_CK1_1 | 273 | 279 | PF00069 | 0.594 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.430 |
MOD_CK1_1 | 280 | 286 | PF00069 | 0.585 |
MOD_CK2_1 | 110 | 116 | PF00069 | 0.382 |
MOD_CK2_1 | 216 | 222 | PF00069 | 0.573 |
MOD_CK2_1 | 235 | 241 | PF00069 | 0.410 |
MOD_CK2_1 | 82 | 88 | PF00069 | 0.403 |
MOD_GlcNHglycan | 168 | 171 | PF01048 | 0.459 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.368 |
MOD_GlcNHglycan | 231 | 235 | PF01048 | 0.537 |
MOD_GlcNHglycan | 237 | 240 | PF01048 | 0.484 |
MOD_GlcNHglycan | 282 | 285 | PF01048 | 0.659 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.525 |
MOD_GSK3_1 | 172 | 179 | PF00069 | 0.321 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.362 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.569 |
MOD_N-GLC_1 | 110 | 115 | PF02516 | 0.419 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.398 |
MOD_NEK2_1 | 26 | 31 | PF00069 | 0.398 |
MOD_PKA_2 | 153 | 159 | PF00069 | 0.437 |
MOD_PKA_2 | 166 | 172 | PF00069 | 0.382 |
MOD_PKA_2 | 273 | 279 | PF00069 | 0.558 |
MOD_Plk_1 | 110 | 116 | PF00069 | 0.390 |
MOD_Plk_1 | 38 | 44 | PF00069 | 0.402 |
MOD_Plk_4 | 251 | 257 | PF00069 | 0.523 |
MOD_ProDKin_1 | 277 | 283 | PF00069 | 0.614 |
MOD_SUMO_rev_2 | 179 | 186 | PF00179 | 0.342 |
TRG_AP2beta_CARGO_1 | 58 | 68 | PF09066 | 0.392 |
TRG_DiLeu_BaEn_2 | 37 | 43 | PF01217 | 0.404 |
TRG_DiLeu_BaEn_4 | 38 | 44 | PF01217 | 0.376 |
TRG_ER_diArg_1 | 105 | 107 | PF00400 | 0.471 |
TRG_ER_diArg_1 | 166 | 168 | PF00400 | 0.408 |
TRG_ER_diArg_1 | 52 | 55 | PF00400 | 0.423 |
TRG_Pf-PMV_PEXEL_1 | 125 | 130 | PF00026 | 0.404 |
TRG_Pf-PMV_PEXEL_1 | 178 | 183 | PF00026 | 0.439 |
TRG_Pf-PMV_PEXEL_1 | 188 | 192 | PF00026 | 0.455 |
TRG_Pf-PMV_PEXEL_1 | 84 | 88 | PF00026 | 0.439 |
TRG_Pf-PMV_PEXEL_1 | 99 | 103 | PF00026 | 0.284 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3Q5 | Leptomonas seymouri | 43% | 76% |
A4H7V8 | Leishmania braziliensis | 69% | 100% |
A4HW84 | Leishmania infantum | 99% | 100% |
E9APY6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
Q4QFJ6 | Leishmania major | 90% | 100% |