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: A4HM56
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 45 | 47 | PF00675 | 0.412 |
CLV_NRD_NRD_1 | 72 | 74 | PF00675 | 0.501 |
CLV_PCSK_KEX2_1 | 18 | 20 | PF00082 | 0.584 |
CLV_PCSK_KEX2_1 | 85 | 87 | PF00082 | 0.416 |
CLV_PCSK_PC1ET2_1 | 18 | 20 | PF00082 | 0.504 |
CLV_PCSK_PC1ET2_1 | 85 | 87 | PF00082 | 0.416 |
CLV_PCSK_SKI1_1 | 134 | 138 | PF00082 | 0.547 |
CLV_PCSK_SKI1_1 | 15 | 19 | PF00082 | 0.381 |
CLV_PCSK_SKI1_1 | 174 | 178 | PF00082 | 0.588 |
CLV_PCSK_SKI1_1 | 288 | 292 | PF00082 | 0.380 |
CLV_PCSK_SKI1_1 | 61 | 65 | PF00082 | 0.385 |
DOC_CDC14_PxL_1 | 298 | 306 | PF14671 | 0.367 |
DOC_CYCLIN_RxL_1 | 131 | 138 | PF00134 | 0.487 |
DOC_CYCLIN_RxL_1 | 275 | 289 | PF00134 | 0.343 |
DOC_MAPK_gen_1 | 243 | 253 | PF00069 | 0.367 |
DOC_PP1_RVXF_1 | 45 | 52 | PF00149 | 0.474 |
DOC_PP2B_LxvP_1 | 321 | 324 | PF13499 | 0.561 |
DOC_USP7_MATH_1 | 297 | 301 | PF00917 | 0.358 |
LIG_14-3-3_CanoR_1 | 215 | 219 | PF00244 | 0.452 |
LIG_14-3-3_CanoR_1 | 224 | 230 | PF00244 | 0.415 |
LIG_14-3-3_CanoR_1 | 98 | 108 | PF00244 | 0.417 |
LIG_Actin_WH2_2 | 171 | 188 | PF00022 | 0.464 |
LIG_Actin_WH2_2 | 278 | 294 | PF00022 | 0.406 |
LIG_Actin_WH2_2 | 84 | 102 | PF00022 | 0.374 |
LIG_BRCT_BRCA1_1 | 219 | 223 | PF00533 | 0.366 |
LIG_eIF4E_1 | 245 | 251 | PF01652 | 0.365 |
LIG_FHA_1 | 161 | 167 | PF00498 | 0.711 |
LIG_FHA_1 | 203 | 209 | PF00498 | 0.414 |
LIG_FHA_2 | 112 | 118 | PF00498 | 0.509 |
LIG_FHA_2 | 188 | 194 | PF00498 | 0.442 |
LIG_FHA_2 | 39 | 45 | PF00498 | 0.412 |
LIG_FHA_2 | 78 | 84 | PF00498 | 0.360 |
LIG_MLH1_MIPbox_1 | 219 | 223 | PF16413 | 0.366 |
LIG_NRBOX | 229 | 235 | PF00104 | 0.407 |
LIG_NRBOX | 65 | 71 | PF00104 | 0.362 |
LIG_NRP_CendR_1 | 336 | 339 | PF00754 | 0.530 |
LIG_PCNA_PIPBox_1 | 216 | 225 | PF02747 | 0.415 |
LIG_PCNA_yPIPBox_3 | 212 | 223 | PF02747 | 0.376 |
LIG_PCNA_yPIPBox_3 | 36 | 49 | PF02747 | 0.483 |
LIG_REV1ctd_RIR_1 | 220 | 228 | PF16727 | 0.423 |
LIG_SH2_GRB2like | 229 | 232 | PF00017 | 0.355 |
LIG_SH2_SRC | 229 | 232 | PF00017 | 0.355 |
LIG_SH2_STAP1 | 154 | 158 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 189 | 192 | PF00017 | 0.497 |
LIG_SH2_STAT5 | 20 | 23 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 229 | 232 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 48 | 51 | PF00017 | 0.473 |
LIG_SUMO_SIM_par_1 | 309 | 315 | PF11976 | 0.483 |
LIG_WRC_WIRS_1 | 219 | 224 | PF05994 | 0.505 |
MOD_CK1_1 | 144 | 150 | PF00069 | 0.552 |
MOD_CK1_1 | 217 | 223 | PF00069 | 0.369 |
MOD_CK1_1 | 326 | 332 | PF00069 | 0.591 |
MOD_CK2_1 | 111 | 117 | PF00069 | 0.511 |
MOD_CK2_1 | 191 | 197 | PF00069 | 0.438 |
MOD_CK2_1 | 38 | 44 | PF00069 | 0.412 |
MOD_GlcNHglycan | 225 | 228 | PF01048 | 0.387 |
MOD_GSK3_1 | 187 | 194 | PF00069 | 0.482 |
MOD_GSK3_1 | 214 | 221 | PF00069 | 0.559 |
MOD_N-GLC_1 | 144 | 149 | PF02516 | 0.501 |
MOD_N-GLC_1 | 326 | 331 | PF02516 | 0.494 |
MOD_N-GLC_2 | 330 | 332 | PF02516 | 0.517 |
MOD_NEK2_1 | 130 | 135 | PF00069 | 0.468 |
MOD_NEK2_1 | 141 | 146 | PF00069 | 0.418 |
MOD_NEK2_1 | 158 | 163 | PF00069 | 0.432 |
MOD_NEK2_1 | 185 | 190 | PF00069 | 0.598 |
MOD_NEK2_1 | 218 | 223 | PF00069 | 0.636 |
MOD_NEK2_1 | 256 | 261 | PF00069 | 0.460 |
MOD_PKA_2 | 214 | 220 | PF00069 | 0.511 |
MOD_PKA_2 | 223 | 229 | PF00069 | 0.460 |
MOD_PKA_2 | 239 | 245 | PF00069 | 0.422 |
MOD_PKA_2 | 99 | 105 | PF00069 | 0.366 |
MOD_Plk_1 | 144 | 150 | PF00069 | 0.534 |
MOD_Plk_1 | 158 | 164 | PF00069 | 0.549 |
MOD_Plk_1 | 77 | 83 | PF00069 | 0.384 |
MOD_Plk_4 | 191 | 197 | PF00069 | 0.438 |
MOD_Plk_4 | 214 | 220 | PF00069 | 0.444 |
MOD_Plk_4 | 225 | 231 | PF00069 | 0.357 |
MOD_Plk_4 | 286 | 292 | PF00069 | 0.357 |
MOD_Plk_4 | 77 | 83 | PF00069 | 0.403 |
MOD_SUMO_rev_2 | 53 | 63 | PF00179 | 0.407 |
TRG_DiLeu_BaEn_1 | 12 | 17 | PF01217 | 0.495 |
TRG_DiLeu_BaEn_1 | 214 | 219 | PF01217 | 0.521 |
TRG_DiLeu_BaLyEn_6 | 65 | 70 | PF01217 | 0.386 |
TRG_ENDOCYTIC_2 | 48 | 51 | PF00928 | 0.473 |
TRG_ER_diArg_1 | 98 | 101 | PF00400 | 0.448 |
TRG_NES_CRM1_1 | 257 | 271 | PF08389 | 0.527 |
TRG_NES_CRM1_1 | 89 | 103 | PF08389 | 0.387 |
TRG_Pf-PMV_PEXEL_1 | 134 | 138 | PF00026 | 0.509 |
TRG_Pf-PMV_PEXEL_1 | 281 | 286 | PF00026 | 0.356 |
TRG_Pf-PMV_PEXEL_1 | 29 | 33 | PF00026 | 0.519 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5M0 | Leptomonas seymouri | 34% | 99% |
A0A3Q8INY6 | Leishmania donovani | 60% | 99% |
A4IAR8 | Leishmania infantum | 60% | 99% |
E9AEJ4 | Leishmania major | 61% | 100% |
E9B5Q5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 61% | 100% |