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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 100 | 104 | PF00656 | 0.459 |
CLV_C14_Caspase3-7 | 262 | 266 | PF00656 | 0.515 |
CLV_NRD_NRD_1 | 259 | 261 | PF00675 | 0.371 |
CLV_NRD_NRD_1 | 29 | 31 | PF00675 | 0.372 |
CLV_PCSK_KEX2_1 | 191 | 193 | PF00082 | 0.553 |
CLV_PCSK_KEX2_1 | 259 | 261 | PF00082 | 0.371 |
CLV_PCSK_KEX2_1 | 29 | 31 | PF00082 | 0.355 |
CLV_PCSK_PC1ET2_1 | 191 | 193 | PF00082 | 0.394 |
CLV_PCSK_PC7_1 | 255 | 261 | PF00082 | 0.354 |
CLV_PCSK_SKI1_1 | 213 | 217 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 62 | 66 | PF00082 | 0.459 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.503 |
DEG_SCF_FBW7_1 | 83 | 90 | PF00400 | 0.449 |
DEG_SPOP_SBC_1 | 88 | 92 | PF00917 | 0.459 |
DOC_CYCLIN_yCln2_LP_2 | 38 | 44 | PF00134 | 0.442 |
DOC_MAPK_gen_1 | 11 | 19 | PF00069 | 0.365 |
DOC_MAPK_gen_1 | 26 | 34 | PF00069 | 0.262 |
DOC_MAPK_MEF2A_6 | 110 | 118 | PF00069 | 0.425 |
DOC_PP4_FxxP_1 | 286 | 289 | PF00568 | 0.376 |
DOC_USP7_MATH_1 | 175 | 179 | PF00917 | 0.554 |
DOC_USP7_MATH_1 | 269 | 273 | PF00917 | 0.409 |
DOC_USP7_MATH_1 | 88 | 92 | PF00917 | 0.699 |
DOC_USP7_MATH_1 | 99 | 103 | PF00917 | 0.470 |
DOC_WW_Pin1_4 | 199 | 204 | PF00397 | 0.347 |
DOC_WW_Pin1_4 | 273 | 278 | PF00397 | 0.369 |
DOC_WW_Pin1_4 | 83 | 88 | PF00397 | 0.641 |
LIG_14-3-3_CanoR_1 | 207 | 216 | PF00244 | 0.284 |
LIG_14-3-3_CanoR_1 | 241 | 249 | PF00244 | 0.328 |
LIG_FHA_1 | 2 | 8 | PF00498 | 0.427 |
LIG_FHA_1 | 225 | 231 | PF00498 | 0.353 |
LIG_FHA_1 | 43 | 49 | PF00498 | 0.337 |
LIG_FHA_1 | 59 | 65 | PF00498 | 0.342 |
LIG_FHA_1 | 84 | 90 | PF00498 | 0.729 |
LIG_LIR_Apic_2 | 283 | 289 | PF02991 | 0.393 |
LIG_LIR_Apic_2 | 71 | 77 | PF02991 | 0.363 |
LIG_LIR_Gen_1 | 159 | 169 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 159 | 164 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 16 | 21 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 227 | 232 | PF02991 | 0.524 |
LIG_LRP6_Inhibitor_1 | 104 | 110 | PF00058 | 0.389 |
LIG_PTB_Apo_2 | 125 | 132 | PF02174 | 0.289 |
LIG_SH2_CRK | 171 | 175 | PF00017 | 0.378 |
LIG_SH2_CRK | 74 | 78 | PF00017 | 0.443 |
LIG_SH2_NCK_1 | 74 | 78 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 117 | 120 | PF00017 | 0.311 |
LIG_SH2_STAT5 | 18 | 21 | PF00017 | 0.309 |
LIG_SH2_STAT5 | 248 | 251 | PF00017 | 0.340 |
LIG_SH3_3 | 123 | 129 | PF00018 | 0.303 |
LIG_SH3_3 | 200 | 206 | PF00018 | 0.343 |
LIG_SH3_3 | 38 | 44 | PF00018 | 0.454 |
LIG_TYR_ITIM | 169 | 174 | PF00017 | 0.358 |
MOD_CK1_1 | 243 | 249 | PF00069 | 0.417 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.514 |
MOD_CK2_1 | 139 | 145 | PF00069 | 0.490 |
MOD_CK2_1 | 175 | 181 | PF00069 | 0.508 |
MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.371 |
MOD_GlcNHglycan | 235 | 238 | PF01048 | 0.360 |
MOD_GSK3_1 | 269 | 276 | PF00069 | 0.356 |
MOD_GSK3_1 | 58 | 65 | PF00069 | 0.413 |
MOD_GSK3_1 | 83 | 90 | PF00069 | 0.496 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.489 |
MOD_NEK2_1 | 116 | 121 | PF00069 | 0.313 |
MOD_NEK2_1 | 139 | 144 | PF00069 | 0.575 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.417 |
MOD_NEK2_1 | 89 | 94 | PF00069 | 0.463 |
MOD_NEK2_2 | 254 | 259 | PF00069 | 0.346 |
MOD_PIKK_1 | 137 | 143 | PF00454 | 0.518 |
MOD_PIKK_1 | 235 | 241 | PF00454 | 0.360 |
MOD_PKA_2 | 240 | 246 | PF00069 | 0.334 |
MOD_PKA_2 | 254 | 260 | PF00069 | 0.360 |
MOD_PKA_2 | 28 | 34 | PF00069 | 0.378 |
MOD_PKA_2 | 81 | 87 | PF00069 | 0.616 |
MOD_Plk_1 | 282 | 288 | PF00069 | 0.477 |
MOD_Plk_4 | 13 | 19 | PF00069 | 0.479 |
MOD_Plk_4 | 156 | 162 | PF00069 | 0.349 |
MOD_Plk_4 | 43 | 49 | PF00069 | 0.295 |
MOD_ProDKin_1 | 199 | 205 | PF00069 | 0.345 |
MOD_ProDKin_1 | 273 | 279 | PF00069 | 0.365 |
MOD_ProDKin_1 | 83 | 89 | PF00069 | 0.642 |
MOD_SUMO_for_1 | 97 | 100 | PF00179 | 0.457 |
MOD_SUMO_rev_2 | 16 | 24 | PF00179 | 0.297 |
TRG_DiLeu_BaLyEn_6 | 38 | 43 | PF01217 | 0.435 |
TRG_DiLeu_BaLyEn_6 | 59 | 64 | PF01217 | 0.473 |
TRG_ENDOCYTIC_2 | 161 | 164 | PF00928 | 0.381 |
TRG_ENDOCYTIC_2 | 171 | 174 | PF00928 | 0.336 |
TRG_ENDOCYTIC_2 | 21 | 24 | PF00928 | 0.335 |
TRG_ENDOCYTIC_2 | 214 | 217 | PF00928 | 0.367 |
TRG_ER_diArg_1 | 258 | 260 | PF00400 | 0.360 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P378 | Leptomonas seymouri | 81% | 100% |
A0A0S4JD50 | Bodo saltans | 58% | 100% |
A0A1X0P6P5 | Trypanosomatidae | 70% | 100% |
A0A3S7X993 | Leishmania donovani | 92% | 100% |
A0A422MYC0 | Trypanosoma rangeli | 67% | 100% |
A4IBB5 | Leishmania infantum | 92% | 100% |
C9ZZD8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 66% | 99% |
E9AF47 | Leishmania major | 91% | 100% |
E9B6A3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
V5BTH8 | Trypanosoma cruzi | 69% | 100% |