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: E9AFY9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 153 | 157 | PF00656 | 0.555 |
CLV_C14_Caspase3-7 | 276 | 280 | PF00656 | 0.467 |
CLV_NRD_NRD_1 | 301 | 303 | PF00675 | 0.503 |
CLV_PCSK_KEX2_1 | 293 | 295 | PF00082 | 0.400 |
CLV_PCSK_KEX2_1 | 300 | 302 | PF00082 | 0.400 |
CLV_PCSK_PC1ET2_1 | 293 | 295 | PF00082 | 0.400 |
CLV_PCSK_PC1ET2_1 | 300 | 302 | PF00082 | 0.400 |
CLV_PCSK_SKI1_1 | 24 | 28 | PF00082 | 0.347 |
CLV_Separin_Metazoa | 131 | 135 | PF03568 | 0.460 |
DEG_APCC_DBOX_1 | 23 | 31 | PF00400 | 0.335 |
DEG_SPOP_SBC_1 | 150 | 154 | PF00917 | 0.494 |
DOC_CYCLIN_RxL_1 | 18 | 28 | PF00134 | 0.463 |
DOC_MAPK_DCC_7 | 261 | 271 | PF00069 | 0.491 |
DOC_MAPK_gen_1 | 177 | 187 | PF00069 | 0.497 |
DOC_MAPK_gen_1 | 261 | 271 | PF00069 | 0.371 |
DOC_MAPK_MEF2A_6 | 264 | 271 | PF00069 | 0.431 |
DOC_MAPK_MEF2A_6 | 4 | 12 | PF00069 | 0.360 |
DOC_MAPK_MEF2A_6 | 96 | 103 | PF00069 | 0.344 |
DOC_MAPK_RevD_3 | 281 | 294 | PF00069 | 0.360 |
DOC_PP1_RVXF_1 | 27 | 34 | PF00149 | 0.339 |
DOC_PP4_FxxP_1 | 147 | 150 | PF00568 | 0.479 |
DOC_PP4_FxxP_1 | 200 | 203 | PF00568 | 0.470 |
DOC_USP7_MATH_1 | 150 | 154 | PF00917 | 0.630 |
DOC_USP7_MATH_1 | 165 | 169 | PF00917 | 0.439 |
DOC_WW_Pin1_4 | 151 | 156 | PF00397 | 0.703 |
LIG_14-3-3_CanoR_1 | 108 | 118 | PF00244 | 0.503 |
LIG_14-3-3_CanoR_1 | 248 | 252 | PF00244 | 0.480 |
LIG_14-3-3_CanoR_1 | 273 | 278 | PF00244 | 0.547 |
LIG_14-3-3_CanoR_1 | 43 | 47 | PF00244 | 0.460 |
LIG_14-3-3_CanoR_1 | 57 | 65 | PF00244 | 0.486 |
LIG_14-3-3_CanoR_1 | 70 | 74 | PF00244 | 0.291 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.434 |
LIG_FHA_1 | 207 | 213 | PF00498 | 0.369 |
LIG_FHA_1 | 244 | 250 | PF00498 | 0.509 |
LIG_FHA_1 | 266 | 272 | PF00498 | 0.448 |
LIG_FHA_2 | 274 | 280 | PF00498 | 0.485 |
LIG_FHA_2 | 59 | 65 | PF00498 | 0.480 |
LIG_GBD_Chelix_1 | 291 | 299 | PF00786 | 0.407 |
LIG_LIR_Gen_1 | 2 | 12 | PF02991 | 0.372 |
LIG_LIR_Nem_3 | 16 | 22 | PF02991 | 0.367 |
LIG_LIR_Nem_3 | 193 | 197 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 2 | 8 | PF02991 | 0.392 |
LIG_MYND_1 | 238 | 242 | PF01753 | 0.453 |
LIG_NRBOX | 113 | 119 | PF00104 | 0.439 |
LIG_PCNA_yPIPBox_3 | 57 | 69 | PF02747 | 0.439 |
LIG_RPA_C_Insects | 289 | 304 | PF08784 | 0.354 |
LIG_SH2_CRK | 274 | 278 | PF00017 | 0.316 |
LIG_SH2_CRK | 5 | 9 | PF00017 | 0.377 |
LIG_SH2_NCK_1 | 274 | 278 | PF00017 | 0.316 |
LIG_SH2_STAP1 | 274 | 278 | PF00017 | 0.316 |
LIG_SH2_STAT5 | 20 | 23 | PF00017 | 0.339 |
LIG_SH2_STAT5 | 233 | 236 | PF00017 | 0.614 |
LIG_SH2_STAT5 | 270 | 273 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 274 | 277 | PF00017 | 0.494 |
LIG_SH2_STAT5 | 68 | 71 | PF00017 | 0.462 |
LIG_SUMO_SIM_anti_2 | 245 | 253 | PF11976 | 0.302 |
LIG_TYR_ITIM | 17 | 22 | PF00017 | 0.436 |
LIG_UBA3_1 | 295 | 300 | PF00899 | 0.333 |
MOD_CK1_1 | 154 | 160 | PF00069 | 0.645 |
MOD_CK1_1 | 87 | 93 | PF00069 | 0.533 |
MOD_CK2_1 | 58 | 64 | PF00069 | 0.399 |
MOD_GlcNHglycan | 135 | 139 | PF01048 | 0.552 |
MOD_GlcNHglycan | 166 | 170 | PF01048 | 0.468 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.540 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.608 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.490 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.435 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.536 |
MOD_N-GLC_1 | 122 | 127 | PF02516 | 0.472 |
MOD_N-GLC_1 | 190 | 195 | PF02516 | 0.473 |
MOD_N-GLC_2 | 280 | 282 | PF02516 | 0.384 |
MOD_NEK2_1 | 205 | 210 | PF00069 | 0.433 |
MOD_NEK2_1 | 25 | 30 | PF00069 | 0.337 |
MOD_PIKK_1 | 58 | 64 | PF00454 | 0.399 |
MOD_PIKK_1 | 87 | 93 | PF00454 | 0.456 |
MOD_PKA_2 | 247 | 253 | PF00069 | 0.440 |
MOD_PKA_2 | 272 | 278 | PF00069 | 0.514 |
MOD_PKA_2 | 42 | 48 | PF00069 | 0.458 |
MOD_PKA_2 | 56 | 62 | PF00069 | 0.503 |
MOD_PKA_2 | 69 | 75 | PF00069 | 0.377 |
MOD_Plk_1 | 122 | 128 | PF00069 | 0.467 |
MOD_Plk_1 | 140 | 146 | PF00069 | 0.599 |
MOD_Plk_1 | 165 | 171 | PF00069 | 0.335 |
MOD_Plk_1 | 190 | 196 | PF00069 | 0.524 |
MOD_Plk_1 | 37 | 43 | PF00069 | 0.567 |
MOD_Plk_1 | 55 | 61 | PF00069 | 0.304 |
MOD_Plk_4 | 123 | 129 | PF00069 | 0.440 |
MOD_Plk_4 | 157 | 163 | PF00069 | 0.540 |
MOD_Plk_4 | 247 | 253 | PF00069 | 0.551 |
MOD_Plk_4 | 265 | 271 | PF00069 | 0.476 |
MOD_Plk_4 | 281 | 287 | PF00069 | 0.454 |
MOD_Plk_4 | 69 | 75 | PF00069 | 0.452 |
MOD_ProDKin_1 | 151 | 157 | PF00069 | 0.700 |
TRG_ENDOCYTIC_2 | 19 | 22 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 274 | 277 | PF00928 | 0.308 |
TRG_ENDOCYTIC_2 | 5 | 8 | PF00928 | 0.375 |
TRG_ER_diArg_1 | 301 | 304 | PF00400 | 0.404 |
TRG_NLS_MonoExtC_3 | 299 | 304 | PF00514 | 0.383 |
TRG_Pf-PMV_PEXEL_1 | 294 | 298 | PF00026 | 0.429 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P619 | Leptomonas seymouri | 57% | 94% |
A0A3S7XA31 | Leishmania donovani | 93% | 100% |
A0A422P2U5 | Trypanosoma rangeli | 38% | 77% |
A4HNH8 | Leishmania braziliensis | 77% | 100% |
A4IC34 | Leishmania infantum | 93% | 100% |
C9ZZ55 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 74% |
E9B742 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
V5BTH5 | Trypanosoma cruzi | 38% | 76% |