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: Q4Q5G7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_PCSK_SKI1_1 | 218 | 222 | PF00082 | 0.621 |
DEG_SPOP_SBC_1 | 87 | 91 | PF00917 | 0.432 |
DOC_MAPK_gen_1 | 74 | 81 | PF00069 | 0.405 |
DOC_MAPK_RevD_3 | 235 | 250 | PF00069 | 0.472 |
DOC_PP1_RVXF_1 | 160 | 166 | PF00149 | 0.388 |
DOC_PP1_RVXF_1 | 241 | 248 | PF00149 | 0.378 |
DOC_PP4_FxxP_1 | 30 | 33 | PF00568 | 0.440 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.696 |
DOC_USP7_MATH_1 | 87 | 91 | PF00917 | 0.522 |
DOC_USP7_MATH_2 | 124 | 130 | PF00917 | 0.390 |
DOC_WW_Pin1_4 | 238 | 243 | PF00397 | 0.481 |
LIG_14-3-3_CanoR_1 | 14 | 21 | PF00244 | 0.473 |
LIG_14-3-3_CanoR_1 | 52 | 61 | PF00244 | 0.375 |
LIG_Actin_WH2_2 | 245 | 261 | PF00022 | 0.385 |
LIG_APCC_ABBA_1 | 65 | 70 | PF00400 | 0.349 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.594 |
LIG_BIR_III_1 | 1 | 5 | PF00653 | 0.463 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.463 |
LIG_BRCT_BRCA1_1 | 129 | 133 | PF00533 | 0.359 |
LIG_Clathr_ClatBox_1 | 286 | 290 | PF01394 | 0.413 |
LIG_deltaCOP1_diTrp_1 | 226 | 235 | PF00928 | 0.458 |
LIG_FHA_1 | 150 | 156 | PF00498 | 0.361 |
LIG_FHA_1 | 219 | 225 | PF00498 | 0.543 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.307 |
LIG_FHA_2 | 194 | 200 | PF00498 | 0.663 |
LIG_FHA_2 | 205 | 211 | PF00498 | 0.692 |
LIG_FHA_2 | 221 | 227 | PF00498 | 0.360 |
LIG_FHA_2 | 286 | 292 | PF00498 | 0.566 |
LIG_FHA_2 | 52 | 58 | PF00498 | 0.493 |
LIG_FHA_2 | 89 | 95 | PF00498 | 0.534 |
LIG_GBD_Chelix_1 | 104 | 112 | PF00786 | 0.393 |
LIG_LIR_Apic_2 | 27 | 33 | PF02991 | 0.504 |
LIG_LIR_Gen_1 | 102 | 109 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 102 | 106 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 226 | 232 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 254 | 258 | PF02991 | 0.499 |
LIG_LIR_Nem_3 | 73 | 79 | PF02991 | 0.352 |
LIG_MYND_1 | 142 | 146 | PF01753 | 0.491 |
LIG_PDZ_Class_1 | 300 | 305 | PF00595 | 0.486 |
LIG_Pex14_2 | 133 | 137 | PF04695 | 0.322 |
LIG_REV1ctd_RIR_1 | 79 | 86 | PF16727 | 0.425 |
LIG_SH2_CRK | 21 | 25 | PF00017 | 0.403 |
LIG_SH2_CRK | 26 | 30 | PF00017 | 0.452 |
LIG_SH2_STAP1 | 26 | 30 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 269 | 272 | PF00017 | 0.301 |
LIG_SH2_STAT5 | 78 | 81 | PF00017 | 0.425 |
LIG_SH3_1 | 250 | 256 | PF00018 | 0.484 |
LIG_SH3_3 | 250 | 256 | PF00018 | 0.496 |
LIG_TYR_ITIM | 24 | 29 | PF00017 | 0.255 |
LIG_UBA3_1 | 236 | 243 | PF00899 | 0.263 |
LIG_WRC_WIRS_1 | 155 | 160 | PF05994 | 0.302 |
LIG_WRC_WIRS_1 | 232 | 237 | PF05994 | 0.402 |
LIG_WRC_WIRS_1 | 78 | 83 | PF05994 | 0.362 |
MOD_CDK_SPK_2 | 238 | 243 | PF00069 | 0.452 |
MOD_CK1_1 | 187 | 193 | PF00069 | 0.580 |
MOD_CK2_1 | 193 | 199 | PF00069 | 0.660 |
MOD_CK2_1 | 204 | 210 | PF00069 | 0.741 |
MOD_CK2_1 | 220 | 226 | PF00069 | 0.374 |
MOD_CK2_1 | 238 | 244 | PF00069 | 0.428 |
MOD_CK2_1 | 285 | 291 | PF00069 | 0.538 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.602 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.580 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.501 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.388 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.309 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.725 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.568 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.652 |
MOD_N-GLC_1 | 170 | 175 | PF02516 | 0.528 |
MOD_NEK2_1 | 12 | 17 | PF00069 | 0.532 |
MOD_NEK2_1 | 158 | 163 | PF00069 | 0.321 |
MOD_NEK2_1 | 236 | 241 | PF00069 | 0.265 |
MOD_NEK2_1 | 278 | 283 | PF00069 | 0.343 |
MOD_NEK2_2 | 220 | 225 | PF00069 | 0.669 |
MOD_NEK2_2 | 77 | 82 | PF00069 | 0.361 |
MOD_PIKK_1 | 107 | 113 | PF00454 | 0.459 |
MOD_PKA_2 | 13 | 19 | PF00069 | 0.421 |
MOD_PKA_2 | 51 | 57 | PF00069 | 0.384 |
MOD_Plk_1 | 170 | 176 | PF00069 | 0.488 |
MOD_Plk_1 | 279 | 285 | PF00069 | 0.393 |
MOD_Plk_2-3 | 199 | 205 | PF00069 | 0.707 |
MOD_Plk_4 | 154 | 160 | PF00069 | 0.370 |
MOD_Plk_4 | 231 | 237 | PF00069 | 0.251 |
MOD_Plk_4 | 6 | 12 | PF00069 | 0.522 |
MOD_Plk_4 | 77 | 83 | PF00069 | 0.334 |
MOD_ProDKin_1 | 238 | 244 | PF00069 | 0.477 |
MOD_SUMO_rev_2 | 145 | 155 | PF00179 | 0.352 |
MOD_SUMO_rev_2 | 183 | 188 | PF00179 | 0.400 |
MOD_SUMO_rev_2 | 266 | 276 | PF00179 | 0.411 |
MOD_SUMO_rev_2 | 70 | 76 | PF00179 | 0.385 |
TRG_DiLeu_BaLyEn_6 | 139 | 144 | PF01217 | 0.481 |
TRG_ENDOCYTIC_2 | 21 | 24 | PF00928 | 0.403 |
TRG_ENDOCYTIC_2 | 26 | 29 | PF00928 | 0.447 |
TRG_ENDOCYTIC_2 | 78 | 81 | PF00928 | 0.440 |
TRG_ER_diArg_1 | 162 | 165 | PF00400 | 0.539 |
TRG_Pf-PMV_PEXEL_1 | 222 | 226 | PF00026 | 0.483 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I9E0 | Leptomonas seymouri | 55% | 100% |
A0A0S4J915 | Bodo saltans | 31% | 100% |
A0A1X0NV05 | Trypanosomatidae | 36% | 100% |
A0A3R7N1Z4 | Trypanosoma rangeli | 37% | 100% |
A0A3S7X5F5 | Leishmania donovani | 87% | 100% |
A4HKA2 | Leishmania braziliensis | 69% | 100% |
A4I7T2 | Leishmania infantum | 88% | 100% |
D0A9Z3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
E9B2P0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
V5BGN1 | Trypanosoma cruzi | 40% | 100% |