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: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: E9B742
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 276 | 280 | PF00656 | 0.462 |
CLV_NRD_NRD_1 | 301 | 303 | PF00675 | 0.505 |
CLV_PCSK_KEX2_1 | 293 | 295 | PF00082 | 0.387 |
CLV_PCSK_KEX2_1 | 301 | 303 | PF00082 | 0.410 |
CLV_PCSK_PC1ET2_1 | 293 | 295 | PF00082 | 0.387 |
CLV_PCSK_SKI1_1 | 24 | 28 | PF00082 | 0.344 |
CLV_Separin_Metazoa | 131 | 135 | PF03568 | 0.456 |
DEG_APCC_DBOX_1 | 23 | 31 | PF00400 | 0.328 |
DEG_Nend_UBRbox_4 | 1 | 3 | PF02207 | 0.337 |
DOC_CYCLIN_RxL_1 | 18 | 28 | PF00134 | 0.457 |
DOC_MAPK_DCC_7 | 261 | 271 | PF00069 | 0.482 |
DOC_MAPK_gen_1 | 177 | 187 | PF00069 | 0.467 |
DOC_MAPK_gen_1 | 261 | 271 | PF00069 | 0.366 |
DOC_MAPK_MEF2A_6 | 264 | 271 | PF00069 | 0.428 |
DOC_MAPK_MEF2A_6 | 4 | 12 | PF00069 | 0.380 |
DOC_MAPK_MEF2A_6 | 96 | 103 | PF00069 | 0.336 |
DOC_MAPK_RevD_3 | 281 | 294 | PF00069 | 0.352 |
DOC_PP1_RVXF_1 | 27 | 34 | PF00149 | 0.329 |
DOC_PP2B_PxIxI_1 | 266 | 272 | PF00149 | 0.239 |
DOC_PP4_FxxP_1 | 200 | 203 | PF00568 | 0.474 |
DOC_USP7_MATH_1 | 204 | 208 | PF00917 | 0.260 |
DOC_WW_Pin1_4 | 150 | 155 | PF00397 | 0.612 |
LIG_14-3-3_CanoR_1 | 108 | 118 | PF00244 | 0.468 |
LIG_14-3-3_CanoR_1 | 248 | 252 | PF00244 | 0.426 |
LIG_14-3-3_CanoR_1 | 273 | 278 | PF00244 | 0.541 |
LIG_14-3-3_CanoR_1 | 43 | 47 | PF00244 | 0.474 |
LIG_14-3-3_CanoR_1 | 57 | 65 | PF00244 | 0.543 |
LIG_14-3-3_CanoR_1 | 70 | 74 | PF00244 | 0.287 |
LIG_FHA_1 | 207 | 213 | PF00498 | 0.416 |
LIG_FHA_1 | 244 | 250 | PF00498 | 0.483 |
LIG_FHA_1 | 266 | 272 | PF00498 | 0.467 |
LIG_FHA_2 | 274 | 280 | PF00498 | 0.479 |
LIG_FHA_2 | 59 | 65 | PF00498 | 0.471 |
LIG_GBD_Chelix_1 | 291 | 299 | PF00786 | 0.396 |
LIG_LIR_Gen_1 | 195 | 205 | PF02991 | 0.401 |
LIG_LIR_Gen_1 | 3 | 12 | PF02991 | 0.353 |
LIG_LIR_Nem_3 | 16 | 22 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 193 | 197 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 3 | 8 | PF02991 | 0.369 |
LIG_MYND_1 | 238 | 242 | PF01753 | 0.440 |
LIG_NRBOX | 113 | 119 | PF00104 | 0.432 |
LIG_PCNA_yPIPBox_3 | 57 | 69 | PF02747 | 0.426 |
LIG_SH2_CRK | 5 | 9 | PF00017 | 0.368 |
LIG_SH2_STAT5 | 20 | 23 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 233 | 236 | PF00017 | 0.578 |
LIG_SH2_STAT5 | 270 | 273 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 68 | 71 | PF00017 | 0.474 |
LIG_TYR_ITIM | 17 | 22 | PF00017 | 0.426 |
LIG_WRC_WIRS_1 | 144 | 149 | PF05994 | 0.499 |
MOD_CK1_1 | 143 | 149 | PF00069 | 0.635 |
MOD_CK1_1 | 87 | 93 | PF00069 | 0.523 |
MOD_CK2_1 | 136 | 142 | PF00069 | 0.379 |
MOD_CK2_1 | 58 | 64 | PF00069 | 0.390 |
MOD_GlcNHglycan | 135 | 139 | PF01048 | 0.545 |
MOD_GlcNHglycan | 166 | 170 | PF01048 | 0.461 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.593 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.532 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.429 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.557 |
MOD_N-GLC_1 | 122 | 127 | PF02516 | 0.458 |
MOD_N-GLC_1 | 190 | 195 | PF02516 | 0.473 |
MOD_N-GLC_2 | 280 | 282 | PF02516 | 0.379 |
MOD_NEK2_1 | 192 | 197 | PF00069 | 0.300 |
MOD_NEK2_1 | 205 | 210 | PF00069 | 0.461 |
MOD_NEK2_1 | 25 | 30 | PF00069 | 0.347 |
MOD_PIKK_1 | 58 | 64 | PF00454 | 0.390 |
MOD_PIKK_1 | 87 | 93 | PF00454 | 0.445 |
MOD_PKA_2 | 247 | 253 | PF00069 | 0.435 |
MOD_PKA_2 | 272 | 278 | PF00069 | 0.509 |
MOD_PKA_2 | 42 | 48 | PF00069 | 0.452 |
MOD_PKA_2 | 56 | 62 | PF00069 | 0.488 |
MOD_PKA_2 | 69 | 75 | PF00069 | 0.284 |
MOD_Plk_1 | 122 | 128 | PF00069 | 0.456 |
MOD_Plk_1 | 140 | 146 | PF00069 | 0.597 |
MOD_Plk_1 | 190 | 196 | PF00069 | 0.528 |
MOD_Plk_1 | 37 | 43 | PF00069 | 0.425 |
MOD_Plk_1 | 55 | 61 | PF00069 | 0.250 |
MOD_Plk_4 | 123 | 129 | PF00069 | 0.419 |
MOD_Plk_4 | 247 | 253 | PF00069 | 0.557 |
MOD_Plk_4 | 265 | 271 | PF00069 | 0.474 |
MOD_Plk_4 | 281 | 287 | PF00069 | 0.449 |
MOD_Plk_4 | 69 | 75 | PF00069 | 0.419 |
MOD_ProDKin_1 | 150 | 156 | PF00069 | 0.611 |
TRG_DiLeu_LyEn_5 | 95 | 100 | PF01217 | 0.375 |
TRG_ENDOCYTIC_2 | 19 | 22 | PF00928 | 0.339 |
TRG_ENDOCYTIC_2 | 5 | 8 | PF00928 | 0.392 |
TRG_ER_diArg_1 | 301 | 304 | PF00400 | 0.398 |
TRG_Pf-PMV_PEXEL_1 | 294 | 298 | PF00026 | 0.422 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P619 | Leptomonas seymouri | 54% | 94% |
A0A3S7XA31 | Leishmania donovani | 91% | 100% |
A0A422P2U5 | Trypanosoma rangeli | 38% | 77% |
A4HNH8 | Leishmania braziliensis | 76% | 100% |
A4IC34 | Leishmania infantum | 91% | 100% |
C9ZZ55 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 74% |
E9AFY9 | Leishmania major | 89% | 100% |
V5BTH5 | Trypanosoma cruzi | 37% | 76% |