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. | yes | yes: 20 |
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: 8 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | yes | yes: 5, no: 5 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: Q4QGX6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 84 | 86 | PF00675 | 0.408 |
CLV_PCSK_KEX2_1 | 84 | 86 | PF00082 | 0.408 |
CLV_PCSK_SKI1_1 | 119 | 123 | PF00082 | 0.559 |
CLV_PCSK_SKI1_1 | 129 | 133 | PF00082 | 0.452 |
CLV_PCSK_SKI1_1 | 141 | 145 | PF00082 | 0.319 |
CLV_PCSK_SKI1_1 | 79 | 83 | PF00082 | 0.364 |
CLV_PCSK_SKI1_1 | 93 | 97 | PF00082 | 0.386 |
DOC_MAPK_gen_1 | 129 | 138 | PF00069 | 0.460 |
DOC_MAPK_gen_1 | 84 | 92 | PF00069 | 0.422 |
DOC_MAPK_MEF2A_6 | 132 | 140 | PF00069 | 0.500 |
DOC_MAPK_RevD_3 | 71 | 85 | PF00069 | 0.386 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.390 |
DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.425 |
DOC_USP7_UBL2_3 | 141 | 145 | PF12436 | 0.448 |
DOC_WW_Pin1_4 | 257 | 262 | PF00397 | 0.591 |
LIG_14-3-3_CanoR_1 | 135 | 139 | PF00244 | 0.441 |
LIG_14-3-3_CanoR_1 | 148 | 153 | PF00244 | 0.513 |
LIG_APCC_ABBA_1 | 180 | 185 | PF00400 | 0.440 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.451 |
LIG_FHA_1 | 156 | 162 | PF00498 | 0.459 |
LIG_FHA_1 | 175 | 181 | PF00498 | 0.453 |
LIG_FHA_1 | 73 | 79 | PF00498 | 0.404 |
LIG_FHA_1 | 87 | 93 | PF00498 | 0.555 |
LIG_FHA_2 | 142 | 148 | PF00498 | 0.501 |
LIG_GBD_Chelix_1 | 233 | 241 | PF00786 | 0.490 |
LIG_LIR_Gen_1 | 144 | 153 | PF02991 | 0.559 |
LIG_LIR_Nem_3 | 144 | 149 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 229 | 233 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 67 | 73 | PF02991 | 0.501 |
LIG_SH2_CRK | 230 | 234 | PF00017 | 0.508 |
LIG_SH2_CRK | 56 | 60 | PF00017 | 0.469 |
LIG_SH2_CRK | 70 | 74 | PF00017 | 0.338 |
LIG_SH2_NCK_1 | 217 | 221 | PF00017 | 0.556 |
LIG_SH2_NCK_1 | 56 | 60 | PF00017 | 0.567 |
LIG_SH2_STAP1 | 56 | 60 | PF00017 | 0.495 |
LIG_SH2_STAT5 | 217 | 220 | PF00017 | 0.501 |
LIG_SH3_3 | 136 | 142 | PF00018 | 0.507 |
LIG_SH3_3 | 56 | 62 | PF00018 | 0.452 |
LIG_SH3_4 | 141 | 148 | PF00018 | 0.555 |
LIG_SUMO_SIM_anti_2 | 134 | 140 | PF11976 | 0.444 |
LIG_SUMO_SIM_anti_2 | 4 | 9 | PF11976 | 0.440 |
LIG_SUMO_SIM_par_1 | 188 | 195 | PF11976 | 0.381 |
LIG_WRC_WIRS_1 | 114 | 119 | PF05994 | 0.319 |
MOD_CDK_SPK_2 | 257 | 262 | PF00069 | 0.521 |
MOD_CK1_1 | 102 | 108 | PF00069 | 0.553 |
MOD_CK1_1 | 167 | 173 | PF00069 | 0.542 |
MOD_CK1_1 | 229 | 235 | PF00069 | 0.411 |
MOD_CK1_1 | 25 | 31 | PF00069 | 0.453 |
MOD_CK1_1 | 39 | 45 | PF00069 | 0.409 |
MOD_CK1_1 | 64 | 70 | PF00069 | 0.537 |
MOD_CK2_1 | 141 | 147 | PF00069 | 0.498 |
MOD_GlcNHglycan | 101 | 104 | PF01048 | 0.542 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.455 |
MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.514 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.494 |
MOD_GSK3_1 | 153 | 160 | PF00069 | 0.525 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.346 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.436 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.446 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.566 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.504 |
MOD_NEK2_1 | 131 | 136 | PF00069 | 0.529 |
MOD_NEK2_1 | 153 | 158 | PF00069 | 0.473 |
MOD_NEK2_1 | 35 | 40 | PF00069 | 0.594 |
MOD_NEK2_2 | 220 | 225 | PF00069 | 0.434 |
MOD_PKA_2 | 134 | 140 | PF00069 | 0.448 |
MOD_PKA_2 | 153 | 159 | PF00069 | 0.420 |
MOD_Plk_4 | 134 | 140 | PF00069 | 0.455 |
MOD_Plk_4 | 148 | 154 | PF00069 | 0.468 |
MOD_Plk_4 | 176 | 182 | PF00069 | 0.549 |
MOD_Plk_4 | 185 | 191 | PF00069 | 0.548 |
MOD_Plk_4 | 212 | 218 | PF00069 | 0.493 |
MOD_Plk_4 | 72 | 78 | PF00069 | 0.438 |
MOD_ProDKin_1 | 257 | 263 | PF00069 | 0.592 |
MOD_SUMO_for_1 | 246 | 249 | PF00179 | 0.545 |
MOD_SUMO_for_1 | 251 | 254 | PF00179 | 0.550 |
MOD_SUMO_rev_2 | 239 | 244 | PF00179 | 0.514 |
TRG_DiLeu_BaEn_4 | 239 | 245 | PF01217 | 0.468 |
TRG_ENDOCYTIC_2 | 146 | 149 | PF00928 | 0.442 |
TRG_ENDOCYTIC_2 | 230 | 233 | PF00928 | 0.513 |
TRG_ENDOCYTIC_2 | 56 | 59 | PF00928 | 0.469 |
TRG_ENDOCYTIC_2 | 70 | 73 | PF00928 | 0.334 |
TRG_ER_diArg_1 | 83 | 85 | PF00400 | 0.526 |
TRG_Pf-PMV_PEXEL_1 | 93 | 97 | PF00026 | 0.499 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1X8 | Leptomonas seymouri | 74% | 100% |
A0A0S4IPH5 | Bodo saltans | 46% | 100% |
A0A1X0NV63 | Trypanosomatidae | 51% | 100% |
A0A3Q8I815 | Leishmania donovani | 96% | 100% |
A0A3R7NL41 | Trypanosoma rangeli | 51% | 100% |
A4H6M9 | Leishmania braziliensis | 89% | 100% |
A4HV12 | Leishmania infantum | 96% | 100% |
D0A7D6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 49% | 100% |
E9ANP7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |