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: A0A3S7X9A9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 240 | 244 | PF00656 | 0.508 |
CLV_NRD_NRD_1 | 120 | 122 | PF00675 | 0.702 |
CLV_NRD_NRD_1 | 253 | 255 | PF00675 | 0.515 |
CLV_NRD_NRD_1 | 296 | 298 | PF00675 | 0.617 |
CLV_NRD_NRD_1 | 299 | 301 | PF00675 | 0.643 |
CLV_NRD_NRD_1 | 314 | 316 | PF00675 | 0.583 |
CLV_NRD_NRD_1 | 327 | 329 | PF00675 | 0.440 |
CLV_NRD_NRD_1 | 331 | 333 | PF00675 | 0.411 |
CLV_PCSK_FUR_1 | 297 | 301 | PF00082 | 0.579 |
CLV_PCSK_KEX2_1 | 120 | 122 | PF00082 | 0.739 |
CLV_PCSK_KEX2_1 | 253 | 255 | PF00082 | 0.535 |
CLV_PCSK_KEX2_1 | 298 | 300 | PF00082 | 0.589 |
CLV_PCSK_KEX2_1 | 326 | 328 | PF00082 | 0.466 |
CLV_PCSK_KEX2_1 | 333 | 335 | PF00082 | 0.491 |
CLV_PCSK_PC1ET2_1 | 298 | 300 | PF00082 | 0.589 |
CLV_PCSK_PC1ET2_1 | 333 | 335 | PF00082 | 0.544 |
CLV_PCSK_SKI1_1 | 175 | 179 | PF00082 | 0.534 |
DEG_APCC_DBOX_1 | 252 | 260 | PF00400 | 0.411 |
DEG_SPOP_SBC_1 | 185 | 189 | PF00917 | 0.520 |
DOC_CYCLIN_yCln2_LP_2 | 205 | 208 | PF00134 | 0.515 |
DOC_MAPK_FxFP_2 | 231 | 234 | PF00069 | 0.427 |
DOC_MAPK_gen_1 | 253 | 263 | PF00069 | 0.413 |
DOC_MAPK_MEF2A_6 | 253 | 260 | PF00069 | 0.407 |
DOC_MAPK_MEF2A_6 | 265 | 272 | PF00069 | 0.413 |
DOC_MAPK_NFAT4_5 | 253 | 261 | PF00069 | 0.519 |
DOC_PP2B_LxvP_1 | 205 | 208 | PF13499 | 0.417 |
DOC_PP4_FxxP_1 | 166 | 169 | PF00568 | 0.425 |
DOC_PP4_FxxP_1 | 231 | 234 | PF00568 | 0.427 |
DOC_PP4_FxxP_1 | 264 | 267 | PF00568 | 0.512 |
DOC_USP7_MATH_1 | 218 | 222 | PF00917 | 0.596 |
DOC_USP7_MATH_1 | 64 | 68 | PF00917 | 0.701 |
DOC_USP7_MATH_2 | 169 | 175 | PF00917 | 0.356 |
DOC_WW_Pin1_4 | 301 | 306 | PF00397 | 0.675 |
DOC_WW_Pin1_4 | 35 | 40 | PF00397 | 0.555 |
DOC_WW_Pin1_4 | 66 | 71 | PF00397 | 0.635 |
DOC_WW_Pin1_4 | 95 | 100 | PF00397 | 0.583 |
LIG_14-3-3_CanoR_1 | 186 | 191 | PF00244 | 0.553 |
LIG_14-3-3_CanoR_1 | 278 | 288 | PF00244 | 0.477 |
LIG_14-3-3_CanoR_1 | 49 | 53 | PF00244 | 0.565 |
LIG_APCC_ABBA_1 | 261 | 266 | PF00400 | 0.462 |
LIG_deltaCOP1_diTrp_1 | 243 | 250 | PF00928 | 0.548 |
LIG_FHA_1 | 159 | 165 | PF00498 | 0.406 |
LIG_FHA_1 | 201 | 207 | PF00498 | 0.492 |
LIG_FHA_1 | 282 | 288 | PF00498 | 0.462 |
LIG_FHA_1 | 289 | 295 | PF00498 | 0.466 |
LIG_FHA_2 | 128 | 134 | PF00498 | 0.649 |
LIG_FHA_2 | 154 | 160 | PF00498 | 0.493 |
LIG_FHA_2 | 187 | 193 | PF00498 | 0.652 |
LIG_FHA_2 | 40 | 46 | PF00498 | 0.648 |
LIG_LIR_Apic_2 | 163 | 169 | PF02991 | 0.416 |
LIG_LIR_Gen_1 | 136 | 143 | PF02991 | 0.554 |
LIG_LIR_Nem_3 | 136 | 142 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 178 | 183 | PF02991 | 0.563 |
LIG_LIR_Nem_3 | 312 | 317 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 7 | 12 | PF02991 | 0.567 |
LIG_Pex14_1 | 246 | 250 | PF04695 | 0.539 |
LIG_Pex14_1 | 276 | 280 | PF04695 | 0.383 |
LIG_Pex14_2 | 166 | 170 | PF04695 | 0.531 |
LIG_Pex14_2 | 314 | 318 | PF04695 | 0.517 |
LIG_SH2_STAP1 | 139 | 143 | PF00017 | 0.584 |
LIG_SH3_5 | 2 | 6 | PF00018 | 0.631 |
LIG_SUMO_SIM_anti_2 | 201 | 206 | PF11976 | 0.459 |
LIG_SUMO_SIM_par_1 | 158 | 165 | PF11976 | 0.493 |
LIG_TRAF2_1 | 321 | 324 | PF00917 | 0.477 |
LIG_TYR_ITIM | 137 | 142 | PF00017 | 0.591 |
MOD_CDK_SPxxK_3 | 301 | 308 | PF00069 | 0.667 |
MOD_CK1_1 | 111 | 117 | PF00069 | 0.772 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.630 |
MOD_CK1_1 | 35 | 41 | PF00069 | 0.655 |
MOD_CK1_1 | 48 | 54 | PF00069 | 0.519 |
MOD_CK2_1 | 153 | 159 | PF00069 | 0.528 |
MOD_CK2_1 | 16 | 22 | PF00069 | 0.666 |
MOD_CK2_1 | 173 | 179 | PF00069 | 0.544 |
MOD_CK2_1 | 186 | 192 | PF00069 | 0.604 |
MOD_CK2_1 | 39 | 45 | PF00069 | 0.676 |
MOD_CK2_1 | 95 | 101 | PF00069 | 0.793 |
MOD_Cter_Amidation | 118 | 121 | PF01082 | 0.696 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.659 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.286 |
MOD_GlcNHglycan | 18 | 21 | PF01048 | 0.657 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.666 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.647 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.731 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.688 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.679 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.376 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.469 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.533 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.590 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.617 |
MOD_GSK3_1 | 279 | 286 | PF00069 | 0.417 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.683 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.676 |
MOD_N-GLC_1 | 111 | 116 | PF02516 | 0.770 |
MOD_N-GLC_1 | 82 | 87 | PF02516 | 0.680 |
MOD_NEK2_1 | 12 | 17 | PF00069 | 0.691 |
MOD_NEK2_1 | 138 | 143 | PF00069 | 0.507 |
MOD_NEK2_1 | 200 | 205 | PF00069 | 0.476 |
MOD_NEK2_1 | 212 | 217 | PF00069 | 0.424 |
MOD_NEK2_1 | 270 | 275 | PF00069 | 0.504 |
MOD_PIKK_1 | 153 | 159 | PF00454 | 0.419 |
MOD_PIKK_1 | 288 | 294 | PF00454 | 0.584 |
MOD_PK_1 | 173 | 179 | PF00069 | 0.565 |
MOD_PKA_2 | 185 | 191 | PF00069 | 0.535 |
MOD_PKA_2 | 48 | 54 | PF00069 | 0.587 |
MOD_Plk_1 | 158 | 164 | PF00069 | 0.533 |
MOD_Plk_1 | 200 | 206 | PF00069 | 0.478 |
MOD_Plk_1 | 282 | 288 | PF00069 | 0.442 |
MOD_Plk_4 | 162 | 168 | PF00069 | 0.409 |
MOD_Plk_4 | 270 | 276 | PF00069 | 0.452 |
MOD_Plk_4 | 283 | 289 | PF00069 | 0.500 |
MOD_ProDKin_1 | 301 | 307 | PF00069 | 0.667 |
MOD_ProDKin_1 | 35 | 41 | PF00069 | 0.556 |
MOD_ProDKin_1 | 66 | 72 | PF00069 | 0.636 |
MOD_ProDKin_1 | 95 | 101 | PF00069 | 0.584 |
MOD_SUMO_for_1 | 93 | 96 | PF00179 | 0.710 |
MOD_SUMO_rev_2 | 165 | 174 | PF00179 | 0.343 |
TRG_DiLeu_BaEn_1 | 201 | 206 | PF01217 | 0.459 |
TRG_DiLeu_BaLyEn_6 | 254 | 259 | PF01217 | 0.408 |
TRG_ENDOCYTIC_2 | 139 | 142 | PF00928 | 0.480 |
TRG_ER_diArg_1 | 252 | 254 | PF00400 | 0.440 |
TRG_ER_diArg_1 | 297 | 300 | PF00400 | 0.579 |
TRG_ER_diArg_1 | 325 | 328 | PF00400 | 0.508 |
TRG_Pf-PMV_PEXEL_1 | 257 | 262 | PF00026 | 0.379 |
TRG_Pf-PMV_PEXEL_1 | 334 | 338 | PF00026 | 0.606 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PE56 | Leptomonas seymouri | 51% | 100% |
A0A0S4KNN3 | Bodo saltans | 31% | 100% |
A0A1X0P6G0 | Trypanosomatidae | 40% | 100% |
A0A3R7NBC1 | Trypanosoma rangeli | 42% | 100% |
A4HMS4 | Leishmania braziliensis | 73% | 100% |
A4IBG2 | Leishmania infantum | 99% | 100% |
C9ZZA2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
E9AF76 | Leishmania major | 89% | 100% |
E9B6D2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
V5BJ90 | Trypanosoma cruzi | 37% | 100% |