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: 5 |
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: 5, no: 4 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: A0A3Q8IHV2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 220 | 222 | PF00675 | 0.702 |
CLV_NRD_NRD_1 | 84 | 86 | PF00675 | 0.648 |
CLV_PCSK_KEX2_1 | 84 | 86 | PF00082 | 0.635 |
CLV_PCSK_SKI1_1 | 37 | 41 | PF00082 | 0.486 |
DOC_CKS1_1 | 42 | 47 | PF01111 | 0.556 |
DOC_PP4_FxxP_1 | 165 | 168 | PF00568 | 0.587 |
DOC_PP4_FxxP_1 | 210 | 213 | PF00568 | 0.419 |
DOC_PP4_FxxP_1 | 260 | 263 | PF00568 | 0.532 |
DOC_PP4_FxxP_1 | 42 | 45 | PF00568 | 0.529 |
DOC_PP4_FxxP_1 | 80 | 83 | PF00568 | 0.465 |
DOC_WW_Pin1_4 | 109 | 114 | PF00397 | 0.630 |
DOC_WW_Pin1_4 | 41 | 46 | PF00397 | 0.530 |
LIG_14-3-3_CanoR_1 | 23 | 31 | PF00244 | 0.564 |
LIG_14-3-3_CanoR_1 | 241 | 251 | PF00244 | 0.708 |
LIG_14-3-3_CanoR_1 | 85 | 95 | PF00244 | 0.612 |
LIG_Actin_WH2_2 | 205 | 223 | PF00022 | 0.522 |
LIG_Clathr_ClatBox_1 | 192 | 196 | PF01394 | 0.533 |
LIG_eIF4E_1 | 109 | 115 | PF01652 | 0.595 |
LIG_FHA_1 | 110 | 116 | PF00498 | 0.593 |
LIG_FHA_1 | 215 | 221 | PF00498 | 0.586 |
LIG_FHA_1 | 246 | 252 | PF00498 | 0.698 |
LIG_FHA_1 | 25 | 31 | PF00498 | 0.497 |
LIG_FHA_1 | 254 | 260 | PF00498 | 0.509 |
LIG_FHA_1 | 72 | 78 | PF00498 | 0.502 |
LIG_FHA_2 | 175 | 181 | PF00498 | 0.617 |
LIG_LIR_Apic_2 | 154 | 160 | PF02991 | 0.712 |
LIG_LIR_Apic_2 | 208 | 213 | PF02991 | 0.444 |
LIG_LIR_Apic_2 | 258 | 263 | PF02991 | 0.544 |
LIG_LIR_Nem_3 | 116 | 122 | PF02991 | 0.485 |
LIG_LIR_Nem_3 | 194 | 200 | PF02991 | 0.423 |
LIG_PCNA_PIPBox_1 | 1 | 10 | PF02747 | 0.602 |
LIG_Pex14_1 | 186 | 190 | PF04695 | 0.629 |
LIG_Pex14_2 | 260 | 264 | PF04695 | 0.591 |
LIG_SH2_CRK | 190 | 194 | PF00017 | 0.494 |
LIG_SH2_NCK_1 | 157 | 161 | PF00017 | 0.679 |
LIG_SH2_SRC | 157 | 160 | PF00017 | 0.609 |
LIG_SH2_STAT3 | 22 | 25 | PF00017 | 0.579 |
LIG_SH2_STAT5 | 120 | 123 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 72 | 75 | PF00017 | 0.579 |
LIG_SH2_STAT5 | 8 | 11 | PF00017 | 0.458 |
LIG_SH2_STAT5 | 86 | 89 | PF00017 | 0.539 |
LIG_SUMO_SIM_par_1 | 191 | 196 | PF11976 | 0.411 |
LIG_SUMO_SIM_par_1 | 248 | 256 | PF11976 | 0.612 |
LIG_TRAF2_1 | 177 | 180 | PF00917 | 0.671 |
LIG_TRAF2_1 | 230 | 233 | PF00917 | 0.652 |
MOD_CK1_1 | 142 | 148 | PF00069 | 0.582 |
MOD_CK1_1 | 150 | 156 | PF00069 | 0.622 |
MOD_CK1_1 | 225 | 231 | PF00069 | 0.704 |
MOD_CK1_1 | 245 | 251 | PF00069 | 0.607 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.562 |
MOD_CK2_1 | 101 | 107 | PF00069 | 0.464 |
MOD_CK2_1 | 142 | 148 | PF00069 | 0.593 |
MOD_CK2_1 | 174 | 180 | PF00069 | 0.625 |
MOD_CK2_1 | 86 | 92 | PF00069 | 0.615 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.577 |
MOD_GlcNHglycan | 140 | 144 | PF01048 | 0.557 |
MOD_GlcNHglycan | 227 | 230 | PF01048 | 0.656 |
MOD_GlcNHglycan | 232 | 237 | PF01048 | 0.690 |
MOD_GlcNHglycan | 244 | 247 | PF01048 | 0.644 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.690 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.663 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.679 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.746 |
MOD_GSK3_1 | 86 | 93 | PF00069 | 0.616 |
MOD_N-GLC_1 | 122 | 127 | PF02516 | 0.484 |
MOD_N-GLC_1 | 268 | 273 | PF02516 | 0.648 |
MOD_NEK2_1 | 139 | 144 | PF00069 | 0.552 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.684 |
MOD_NEK2_1 | 173 | 178 | PF00069 | 0.622 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.470 |
MOD_PKA_1 | 221 | 227 | PF00069 | 0.633 |
MOD_PKA_1 | 84 | 90 | PF00069 | 0.644 |
MOD_PKA_2 | 101 | 107 | PF00069 | 0.329 |
MOD_PKA_2 | 25 | 31 | PF00069 | 0.535 |
MOD_PKA_2 | 84 | 90 | PF00069 | 0.638 |
MOD_PKB_1 | 239 | 247 | PF00069 | 0.642 |
MOD_Plk_1 | 115 | 121 | PF00069 | 0.460 |
MOD_Plk_1 | 153 | 159 | PF00069 | 0.666 |
MOD_Plk_1 | 232 | 238 | PF00069 | 0.589 |
MOD_Plk_1 | 268 | 274 | PF00069 | 0.515 |
MOD_Plk_2-3 | 191 | 197 | PF00069 | 0.525 |
MOD_Plk_2-3 | 253 | 259 | PF00069 | 0.562 |
MOD_Plk_4 | 115 | 121 | PF00069 | 0.525 |
MOD_Plk_4 | 25 | 31 | PF00069 | 0.430 |
MOD_Plk_4 | 90 | 96 | PF00069 | 0.502 |
MOD_ProDKin_1 | 109 | 115 | PF00069 | 0.620 |
MOD_ProDKin_1 | 41 | 47 | PF00069 | 0.540 |
TRG_DiLeu_BaEn_4 | 232 | 238 | PF01217 | 0.589 |
TRG_DiLeu_BaLyEn_6 | 247 | 252 | PF01217 | 0.630 |
TRG_ENDOCYTIC_2 | 190 | 193 | PF00928 | 0.582 |
TRG_ER_diArg_1 | 64 | 67 | PF00400 | 0.639 |
TRG_ER_diArg_1 | 83 | 85 | PF00400 | 0.544 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I5Y1 | Leptomonas seymouri | 52% | 78% |
A0A0S4JB49 | Bodo saltans | 28% | 93% |
A0A1X0P5P8 | Trypanosomatidae | 30% | 93% |
A0A3R7LR32 | Trypanosoma rangeli | 33% | 93% |
A4HMH1 | Leishmania braziliensis | 74% | 100% |
A4IB51 | Leishmania infantum | 100% | 100% |
C9ZZF6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 90% |
E9B628 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |