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: A4HN94
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 109 | 113 | PF00656 | 0.535 |
CLV_NRD_NRD_1 | 274 | 276 | PF00675 | 0.405 |
CLV_PCSK_KEX2_1 | 274 | 276 | PF00082 | 0.405 |
CLV_PCSK_SKI1_1 | 133 | 137 | PF00082 | 0.373 |
CLV_PCSK_SKI1_1 | 146 | 150 | PF00082 | 0.551 |
CLV_PCSK_SKI1_1 | 177 | 181 | PF00082 | 0.630 |
CLV_PCSK_SKI1_1 | 286 | 290 | PF00082 | 0.462 |
CLV_Separin_Metazoa | 245 | 249 | PF03568 | 0.445 |
DEG_APCC_DBOX_1 | 132 | 140 | PF00400 | 0.369 |
DEG_APCC_DBOX_1 | 230 | 238 | PF00400 | 0.288 |
DEG_SCF_FBW7_2 | 238 | 245 | PF00400 | 0.416 |
DEG_SPOP_SBC_1 | 172 | 176 | PF00917 | 0.450 |
DEG_SPOP_SBC_1 | 6 | 10 | PF00917 | 0.484 |
DOC_CKS1_1 | 239 | 244 | PF01111 | 0.409 |
DOC_CYCLIN_RxL_1 | 283 | 292 | PF00134 | 0.498 |
DOC_CYCLIN_yCln2_LP_2 | 114 | 120 | PF00134 | 0.508 |
DOC_CYCLIN_yCln2_LP_2 | 217 | 223 | PF00134 | 0.297 |
DOC_MAPK_gen_1 | 231 | 239 | PF00069 | 0.506 |
DOC_PP2B_LxvP_1 | 217 | 220 | PF13499 | 0.375 |
DOC_USP7_MATH_1 | 208 | 212 | PF00917 | 0.630 |
DOC_USP7_MATH_1 | 6 | 10 | PF00917 | 0.628 |
DOC_WW_Pin1_4 | 238 | 243 | PF00397 | 0.333 |
LIG_14-3-3_CanoR_1 | 146 | 155 | PF00244 | 0.606 |
LIG_14-3-3_CanoR_1 | 231 | 239 | PF00244 | 0.414 |
LIG_14-3-3_CanoR_1 | 36 | 40 | PF00244 | 0.415 |
LIG_14-3-3_CanoR_1 | 7 | 16 | PF00244 | 0.582 |
LIG_Actin_WH2_2 | 132 | 148 | PF00022 | 0.329 |
LIG_APCC_ABBA_1 | 221 | 226 | PF00400 | 0.242 |
LIG_BRCT_BRCA1_1 | 8 | 12 | PF00533 | 0.427 |
LIG_deltaCOP1_diTrp_1 | 40 | 46 | PF00928 | 0.436 |
LIG_FHA_1 | 149 | 155 | PF00498 | 0.638 |
LIG_FHA_1 | 214 | 220 | PF00498 | 0.388 |
LIG_FHA_1 | 73 | 79 | PF00498 | 0.374 |
LIG_FHA_1 | 83 | 89 | PF00498 | 0.383 |
LIG_FHA_2 | 247 | 253 | PF00498 | 0.441 |
LIG_Integrin_RGD_1 | 110 | 112 | PF01839 | 0.427 |
LIG_LIR_Gen_1 | 89 | 99 | PF02991 | 0.302 |
LIG_LIR_Gen_1 | 9 | 20 | PF02991 | 0.619 |
LIG_LIR_LC3C_4 | 216 | 219 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 124 | 129 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 19 | 23 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 40 | 46 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 89 | 95 | PF02991 | 0.302 |
LIG_LIR_Nem_3 | 9 | 15 | PF02991 | 0.619 |
LIG_LIR_Nem_3 | 97 | 102 | PF02991 | 0.313 |
LIG_PCNA_yPIPBox_3 | 28 | 41 | PF02747 | 0.290 |
LIG_Rb_LxCxE_1 | 249 | 265 | PF01857 | 0.410 |
LIG_SH2_SRC | 224 | 227 | PF00017 | 0.478 |
LIG_SH2_STAT5 | 123 | 126 | PF00017 | 0.385 |
LIG_SH2_STAT5 | 127 | 130 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 224 | 227 | PF00017 | 0.478 |
LIG_SUMO_SIM_par_1 | 287 | 292 | PF11976 | 0.495 |
LIG_TRAF2_1 | 256 | 259 | PF00917 | 0.264 |
MOD_CK1_1 | 10 | 16 | PF00069 | 0.620 |
MOD_CK1_1 | 141 | 147 | PF00069 | 0.555 |
MOD_CK2_1 | 18 | 24 | PF00069 | 0.533 |
MOD_CK2_1 | 246 | 252 | PF00069 | 0.542 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.656 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.424 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.651 |
MOD_GlcNHglycan | 96 | 99 | PF01048 | 0.380 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.529 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.628 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.476 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.548 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.683 |
MOD_N-GLC_1 | 121 | 126 | PF02516 | 0.478 |
MOD_N-GLC_1 | 208 | 213 | PF02516 | 0.417 |
MOD_N-GLC_1 | 294 | 299 | PF02516 | 0.527 |
MOD_NEK2_1 | 129 | 134 | PF00069 | 0.358 |
MOD_NEK2_1 | 246 | 251 | PF00069 | 0.503 |
MOD_NEK2_1 | 269 | 274 | PF00069 | 0.374 |
MOD_NEK2_1 | 289 | 294 | PF00069 | 0.485 |
MOD_NEK2_1 | 5 | 10 | PF00069 | 0.638 |
MOD_NEK2_1 | 82 | 87 | PF00069 | 0.464 |
MOD_NEK2_1 | 91 | 96 | PF00069 | 0.324 |
MOD_OFUCOSY | 69 | 76 | PF10250 | 0.439 |
MOD_PIKK_1 | 24 | 30 | PF00454 | 0.460 |
MOD_PIKK_1 | 44 | 50 | PF00454 | 0.559 |
MOD_PKA_2 | 232 | 238 | PF00069 | 0.442 |
MOD_PKA_2 | 35 | 41 | PF00069 | 0.466 |
MOD_PKA_2 | 6 | 12 | PF00069 | 0.539 |
MOD_Plk_1 | 163 | 169 | PF00069 | 0.462 |
MOD_Plk_1 | 294 | 300 | PF00069 | 0.409 |
MOD_Plk_4 | 149 | 155 | PF00069 | 0.698 |
MOD_Plk_4 | 213 | 219 | PF00069 | 0.476 |
MOD_Plk_4 | 284 | 290 | PF00069 | 0.423 |
MOD_Plk_4 | 294 | 300 | PF00069 | 0.462 |
MOD_Plk_4 | 91 | 97 | PF00069 | 0.440 |
MOD_ProDKin_1 | 238 | 244 | PF00069 | 0.333 |
MOD_SUMO_for_1 | 278 | 281 | PF00179 | 0.509 |
TRG_ENDOCYTIC_2 | 126 | 129 | PF00928 | 0.470 |
TRG_ENDOCYTIC_2 | 20 | 23 | PF00928 | 0.536 |
TRG_ER_diArg_1 | 231 | 234 | PF00400 | 0.579 |
TRG_ER_diArg_1 | 247 | 250 | PF00400 | 0.408 |
TRG_ER_diArg_1 | 273 | 275 | PF00400 | 0.388 |
TRG_Pf-PMV_PEXEL_1 | 86 | 90 | PF00026 | 0.390 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HY73 | Leptomonas seymouri | 48% | 100% |
A0A0S4JF57 | Bodo saltans | 35% | 100% |
A0A1X0P581 | Trypanosomatidae | 34% | 100% |
A0A3R7NNI3 | Trypanosoma rangeli | 38% | 100% |
A0A3S7X9V8 | Leishmania donovani | 72% | 100% |
A4IBW4 | Leishmania infantum | 72% | 100% |
C9ZYP7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
E9AFQ1 | Leishmania major | 71% | 98% |
E9B6V4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 72% | 100% |
V5BCR5 | Trypanosoma cruzi | 33% | 100% |