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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: Q4QBD9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 133 | 137 | PF00656 | 0.382 |
CLV_NRD_NRD_1 | 138 | 140 | PF00675 | 0.482 |
CLV_NRD_NRD_1 | 23 | 25 | PF00675 | 0.718 |
CLV_NRD_NRD_1 | 270 | 272 | PF00675 | 0.592 |
CLV_PCSK_KEX2_1 | 138 | 140 | PF00082 | 0.524 |
CLV_PCSK_KEX2_1 | 154 | 156 | PF00082 | 0.399 |
CLV_PCSK_KEX2_1 | 205 | 207 | PF00082 | 0.580 |
CLV_PCSK_KEX2_1 | 22 | 24 | PF00082 | 0.724 |
CLV_PCSK_PC1ET2_1 | 138 | 140 | PF00082 | 0.539 |
CLV_PCSK_PC1ET2_1 | 154 | 156 | PF00082 | 0.563 |
CLV_PCSK_PC1ET2_1 | 205 | 207 | PF00082 | 0.645 |
CLV_PCSK_PC7_1 | 134 | 140 | PF00082 | 0.514 |
CLV_PCSK_PC7_1 | 19 | 25 | PF00082 | 0.605 |
CLV_PCSK_SKI1_1 | 142 | 146 | PF00082 | 0.564 |
CLV_PCSK_SKI1_1 | 171 | 175 | PF00082 | 0.621 |
CLV_PCSK_SKI1_1 | 176 | 180 | PF00082 | 0.587 |
CLV_PCSK_SKI1_1 | 247 | 251 | PF00082 | 0.624 |
CLV_PCSK_SKI1_1 | 57 | 61 | PF00082 | 0.528 |
DEG_SPOP_SBC_1 | 58 | 62 | PF00917 | 0.463 |
DOC_AGCK_PIF_2 | 289 | 294 | PF00069 | 0.470 |
DOC_MAPK_gen_1 | 138 | 146 | PF00069 | 0.517 |
DOC_MAPK_gen_1 | 201 | 210 | PF00069 | 0.554 |
DOC_MAPK_MEF2A_6 | 204 | 212 | PF00069 | 0.600 |
DOC_PP1_RVXF_1 | 169 | 175 | PF00149 | 0.514 |
DOC_PP4_FxxP_1 | 72 | 75 | PF00568 | 0.411 |
DOC_USP7_UBL2_3 | 138 | 142 | PF12436 | 0.551 |
DOC_USP7_UBL2_3 | 201 | 205 | PF12436 | 0.623 |
DOC_USP7_UBL2_3 | 272 | 276 | PF12436 | 0.548 |
DOC_WW_Pin1_4 | 212 | 217 | PF00397 | 0.605 |
DOC_WW_Pin1_4 | 218 | 223 | PF00397 | 0.554 |
LIG_14-3-3_CanoR_1 | 57 | 66 | PF00244 | 0.603 |
LIG_BRCT_BRCA1_1 | 60 | 64 | PF00533 | 0.535 |
LIG_CAP-Gly_1 | 288 | 294 | PF01302 | 0.471 |
LIG_FHA_1 | 58 | 64 | PF00498 | 0.515 |
LIG_FHA_2 | 131 | 137 | PF00498 | 0.487 |
LIG_FHA_2 | 182 | 188 | PF00498 | 0.547 |
LIG_FHA_2 | 192 | 198 | PF00498 | 0.467 |
LIG_FHA_2 | 256 | 262 | PF00498 | 0.557 |
LIG_LIR_Apic_2 | 123 | 129 | PF02991 | 0.541 |
LIG_LIR_Apic_2 | 48 | 54 | PF02991 | 0.632 |
LIG_LIR_Gen_1 | 280 | 289 | PF02991 | 0.574 |
LIG_LIR_Nem_3 | 148 | 152 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 280 | 286 | PF02991 | 0.606 |
LIG_LIR_Nem_3 | 287 | 292 | PF02991 | 0.550 |
LIG_Pex14_1 | 141 | 145 | PF04695 | 0.447 |
LIG_SH2_GRB2like | 105 | 108 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 126 | 129 | PF00017 | 0.585 |
LIG_SH2_STAT5 | 152 | 155 | PF00017 | 0.501 |
LIG_SH2_STAT5 | 257 | 260 | PF00017 | 0.635 |
LIG_SH3_3 | 217 | 223 | PF00018 | 0.712 |
LIG_TRAF2_1 | 194 | 197 | PF00917 | 0.536 |
LIG_WW_3 | 19 | 23 | PF00397 | 0.520 |
MOD_CK1_1 | 253 | 259 | PF00069 | 0.429 |
MOD_CK1_1 | 38 | 44 | PF00069 | 0.591 |
MOD_CK2_1 | 181 | 187 | PF00069 | 0.536 |
MOD_CK2_1 | 191 | 197 | PF00069 | 0.481 |
MOD_CK2_1 | 228 | 234 | PF00069 | 0.511 |
MOD_Cter_Amidation | 136 | 139 | PF01082 | 0.455 |
MOD_Cter_Amidation | 14 | 17 | PF01082 | 0.634 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.558 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.592 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.678 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.459 |
MOD_LATS_1 | 275 | 281 | PF00433 | 0.600 |
MOD_NEK2_1 | 59 | 64 | PF00069 | 0.520 |
MOD_NEK2_1 | 92 | 97 | PF00069 | 0.452 |
MOD_PIKK_1 | 36 | 42 | PF00454 | 0.613 |
MOD_PKA_1 | 250 | 256 | PF00069 | 0.645 |
MOD_PKA_2 | 281 | 287 | PF00069 | 0.706 |
MOD_PKA_2 | 82 | 88 | PF00069 | 0.468 |
MOD_Plk_1 | 191 | 197 | PF00069 | 0.559 |
MOD_Plk_4 | 127 | 133 | PF00069 | 0.625 |
MOD_Plk_4 | 59 | 65 | PF00069 | 0.532 |
MOD_ProDKin_1 | 212 | 218 | PF00069 | 0.605 |
MOD_SUMO_rev_2 | 117 | 127 | PF00179 | 0.568 |
TRG_DiLeu_BaLyEn_6 | 87 | 92 | PF01217 | 0.564 |
TRG_ER_diArg_1 | 21 | 24 | PF00400 | 0.541 |
TRG_NLS_Bipartite_1 | 124 | 143 | PF00514 | 0.480 |
TRG_NLS_MonoExtC_3 | 137 | 142 | PF00514 | 0.476 |
TRG_NLS_MonoExtC_3 | 15 | 20 | PF00514 | 0.613 |
TRG_NLS_MonoExtC_3 | 203 | 209 | PF00514 | 0.623 |
TRG_NLS_MonoExtN_4 | 13 | 20 | PF00514 | 0.613 |
TRG_NLS_MonoExtN_4 | 138 | 143 | PF00514 | 0.649 |
TRG_NLS_MonoExtN_4 | 201 | 208 | PF00514 | 0.634 |
TRG_Pf-PMV_PEXEL_1 | 90 | 94 | PF00026 | 0.578 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P555 | Leptomonas seymouri | 60% | 84% |
A0A0S4IRA8 | Bodo saltans | 25% | 93% |
A0A1X0NX54 | Trypanosomatidae | 37% | 100% |
A0A3Q8IAW9 | Leishmania donovani | 94% | 100% |
A0A422NW66 | Trypanosoma rangeli | 38% | 100% |
A4HCP9 | Leishmania braziliensis | 71% | 98% |
A4I075 | Leishmania infantum | 93% | 100% |
C9ZUZ1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
E9AW38 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |