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: E9B2P0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 89 | 93 | PF00656 | 0.353 |
CLV_NRD_NRD_1 | 151 | 153 | PF00675 | 0.314 |
DEG_SPOP_SBC_1 | 87 | 91 | PF00917 | 0.491 |
DOC_MAPK_gen_1 | 74 | 81 | PF00069 | 0.423 |
DOC_MAPK_RevD_3 | 234 | 249 | PF00069 | 0.492 |
DOC_PP1_RVXF_1 | 159 | 165 | PF00149 | 0.414 |
DOC_PP1_RVXF_1 | 240 | 247 | PF00149 | 0.406 |
DOC_USP7_MATH_1 | 238 | 242 | PF00917 | 0.448 |
DOC_USP7_MATH_1 | 87 | 91 | PF00917 | 0.512 |
DOC_USP7_MATH_2 | 124 | 130 | PF00917 | 0.419 |
LIG_14-3-3_CanoR_1 | 14 | 21 | PF00244 | 0.506 |
LIG_14-3-3_CanoR_1 | 147 | 154 | PF00244 | 0.289 |
LIG_14-3-3_CanoR_1 | 52 | 61 | PF00244 | 0.431 |
LIG_Actin_WH2_2 | 244 | 260 | PF00022 | 0.441 |
LIG_APCC_ABBA_1 | 65 | 70 | PF00400 | 0.377 |
LIG_BRCT_BRCA1_1 | 129 | 133 | PF00533 | 0.396 |
LIG_Clathr_ClatBox_1 | 285 | 289 | PF01394 | 0.494 |
LIG_deltaCOP1_diTrp_1 | 225 | 234 | PF00928 | 0.492 |
LIG_FHA_1 | 154 | 160 | PF00498 | 0.321 |
LIG_FHA_1 | 231 | 237 | PF00498 | 0.370 |
LIG_FHA_2 | 204 | 210 | PF00498 | 0.679 |
LIG_FHA_2 | 220 | 226 | PF00498 | 0.675 |
LIG_FHA_2 | 258 | 264 | PF00498 | 0.563 |
LIG_FHA_2 | 285 | 291 | PF00498 | 0.566 |
LIG_FHA_2 | 31 | 37 | PF00498 | 0.466 |
LIG_FHA_2 | 52 | 58 | PF00498 | 0.519 |
LIG_FHA_2 | 89 | 95 | PF00498 | 0.554 |
LIG_GBD_Chelix_1 | 104 | 112 | PF00786 | 0.458 |
LIG_LIR_Gen_1 | 102 | 109 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 102 | 106 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 225 | 231 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 253 | 257 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 73 | 79 | PF02991 | 0.336 |
LIG_MYND_1 | 142 | 146 | PF01753 | 0.518 |
LIG_PDZ_Class_1 | 299 | 304 | PF00595 | 0.534 |
LIG_Pex14_2 | 133 | 137 | PF04695 | 0.373 |
LIG_SH2_CRK | 21 | 25 | PF00017 | 0.397 |
LIG_SH2_CRK | 26 | 30 | PF00017 | 0.433 |
LIG_SH2_STAP1 | 26 | 30 | PF00017 | 0.396 |
LIG_SH2_STAT5 | 78 | 81 | PF00017 | 0.419 |
LIG_SH3_1 | 249 | 255 | PF00018 | 0.509 |
LIG_SH3_3 | 249 | 255 | PF00018 | 0.509 |
LIG_TRAF2_1 | 287 | 290 | PF00917 | 0.341 |
LIG_TRAF2_1 | 33 | 36 | PF00917 | 0.257 |
LIG_TYR_ITIM | 24 | 29 | PF00017 | 0.284 |
LIG_WRC_WIRS_1 | 154 | 159 | PF05994 | 0.327 |
LIG_WRC_WIRS_1 | 231 | 236 | PF05994 | 0.430 |
LIG_WRC_WIRS_1 | 78 | 83 | PF05994 | 0.387 |
MOD_CK1_1 | 189 | 195 | PF00069 | 0.630 |
MOD_CK1_1 | 205 | 211 | PF00069 | 0.690 |
MOD_CK1_1 | 44 | 50 | PF00069 | 0.437 |
MOD_CK2_1 | 203 | 209 | PF00069 | 0.750 |
MOD_CK2_1 | 219 | 225 | PF00069 | 0.540 |
MOD_CK2_1 | 237 | 243 | PF00069 | 0.277 |
MOD_CK2_1 | 284 | 290 | PF00069 | 0.515 |
MOD_CK2_1 | 30 | 36 | PF00069 | 0.306 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.462 |
MOD_GlcNHglycan | 188 | 191 | PF01048 | 0.683 |
MOD_GlcNHglycan | 301 | 304 | PF01048 | 0.666 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.494 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.423 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.739 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.629 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.615 |
MOD_NEK2_1 | 12 | 17 | PF00069 | 0.591 |
MOD_NEK2_1 | 257 | 262 | PF00069 | 0.576 |
MOD_NEK2_1 | 277 | 282 | PF00069 | 0.351 |
MOD_NEK2_1 | 30 | 35 | PF00069 | 0.415 |
MOD_NEK2_2 | 77 | 82 | PF00069 | 0.382 |
MOD_PIKK_1 | 107 | 113 | PF00454 | 0.473 |
MOD_PKA_2 | 13 | 19 | PF00069 | 0.492 |
MOD_PKA_2 | 146 | 152 | PF00069 | 0.418 |
MOD_PKA_2 | 257 | 263 | PF00069 | 0.415 |
MOD_PKA_2 | 51 | 57 | PF00069 | 0.490 |
MOD_Plk_1 | 278 | 284 | PF00069 | 0.423 |
MOD_Plk_1 | 296 | 302 | PF00069 | 0.417 |
MOD_Plk_1 | 30 | 36 | PF00069 | 0.453 |
MOD_Plk_2-3 | 198 | 204 | PF00069 | 0.737 |
MOD_Plk_4 | 153 | 159 | PF00069 | 0.397 |
MOD_Plk_4 | 6 | 12 | PF00069 | 0.580 |
MOD_Plk_4 | 77 | 83 | PF00069 | 0.360 |
MOD_SUMO_rev_2 | 145 | 154 | PF00179 | 0.400 |
MOD_SUMO_rev_2 | 265 | 275 | PF00179 | 0.489 |
MOD_SUMO_rev_2 | 70 | 76 | PF00179 | 0.412 |
TRG_DiLeu_BaLyEn_6 | 139 | 144 | PF01217 | 0.505 |
TRG_ENDOCYTIC_2 | 21 | 24 | PF00928 | 0.397 |
TRG_ENDOCYTIC_2 | 26 | 29 | PF00928 | 0.428 |
TRG_ENDOCYTIC_2 | 78 | 81 | PF00928 | 0.456 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I9E0 | Leptomonas seymouri | 52% | 100% |
A0A0S4J915 | Bodo saltans | 31% | 100% |
A0A1X0NV05 | Trypanosomatidae | 36% | 100% |
A0A3R7N1Z4 | Trypanosoma rangeli | 36% | 100% |
A0A3S7X5F5 | Leishmania donovani | 83% | 100% |
A4HKA2 | Leishmania braziliensis | 68% | 100% |
A4I7T2 | Leishmania infantum | 83% | 100% |
D0A9Z3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
Q4Q5G7 | Leishmania major | 84% | 100% |
V5BGN1 | Trypanosoma cruzi | 40% | 100% |