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: A4HKA2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 211 | 215 | PF00656 | 0.665 |
CLV_C14_Caspase3-7 | 89 | 93 | PF00656 | 0.363 |
CLV_NRD_NRD_1 | 139 | 141 | PF00675 | 0.520 |
CLV_NRD_NRD_1 | 193 | 195 | PF00675 | 0.686 |
CLV_PCSK_KEX2_1 | 138 | 140 | PF00082 | 0.536 |
CLV_PCSK_KEX2_1 | 193 | 195 | PF00082 | 0.692 |
CLV_PCSK_KEX2_1 | 293 | 295 | PF00082 | 0.442 |
CLV_PCSK_PC1ET2_1 | 293 | 295 | PF00082 | 0.442 |
CLV_PCSK_SKI1_1 | 186 | 190 | PF00082 | 0.457 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.509 |
DEG_SCF_FBW7_1 | 283 | 288 | PF00400 | 0.296 |
DEG_SCF_TRCP1_1 | 214 | 219 | PF00400 | 0.522 |
DOC_MAPK_gen_1 | 74 | 81 | PF00069 | 0.469 |
DOC_MAPK_RevD_3 | 235 | 250 | PF00069 | 0.512 |
DOC_PP1_RVXF_1 | 160 | 166 | PF00149 | 0.451 |
DOC_PP1_RVXF_1 | 241 | 248 | PF00149 | 0.442 |
DOC_PP4_FxxP_1 | 30 | 33 | PF00568 | 0.509 |
DOC_USP7_MATH_1 | 239 | 243 | PF00917 | 0.481 |
DOC_USP7_MATH_1 | 299 | 303 | PF00917 | 0.635 |
DOC_USP7_MATH_2 | 124 | 130 | PF00917 | 0.465 |
DOC_WW_Pin1_4 | 253 | 258 | PF00397 | 0.585 |
DOC_WW_Pin1_4 | 281 | 286 | PF00397 | 0.434 |
LIG_APCC_ABBA_1 | 65 | 70 | PF00400 | 0.408 |
LIG_BRCT_BRCA1_1 | 129 | 133 | PF00533 | 0.432 |
LIG_Clathr_ClatBox_1 | 286 | 290 | PF01394 | 0.551 |
LIG_deltaCOP1_diTrp_1 | 225 | 235 | PF00928 | 0.526 |
LIG_FHA_1 | 155 | 161 | PF00498 | 0.351 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.523 |
LIG_FHA_2 | 187 | 193 | PF00498 | 0.672 |
LIG_FHA_2 | 205 | 211 | PF00498 | 0.686 |
LIG_FHA_2 | 221 | 227 | PF00498 | 0.612 |
LIG_FHA_2 | 259 | 265 | PF00498 | 0.611 |
LIG_FHA_2 | 266 | 272 | PF00498 | 0.533 |
LIG_FHA_2 | 89 | 95 | PF00498 | 0.553 |
LIG_GBD_Chelix_1 | 104 | 112 | PF00786 | 0.521 |
LIG_LIR_Apic_2 | 27 | 33 | PF02991 | 0.488 |
LIG_LIR_Gen_1 | 102 | 109 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 102 | 106 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 226 | 232 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 254 | 258 | PF02991 | 0.547 |
LIG_LIR_Nem_3 | 73 | 79 | PF02991 | 0.368 |
LIG_MYND_1 | 142 | 146 | PF01753 | 0.535 |
LIG_Pex14_2 | 133 | 137 | PF04695 | 0.424 |
LIG_REV1ctd_RIR_1 | 79 | 88 | PF16727 | 0.487 |
LIG_SH2_CRK | 21 | 25 | PF00017 | 0.421 |
LIG_SH2_STAT5 | 78 | 81 | PF00017 | 0.440 |
LIG_SH2_STAT5 | 95 | 98 | PF00017 | 0.276 |
LIG_SH3_3 | 12 | 18 | PF00018 | 0.517 |
LIG_SH3_3 | 146 | 152 | PF00018 | 0.328 |
LIG_SUMO_SIM_par_1 | 256 | 261 | PF11976 | 0.396 |
LIG_WRC_WIRS_1 | 134 | 139 | PF05994 | 0.305 |
LIG_WRC_WIRS_1 | 155 | 160 | PF05994 | 0.357 |
LIG_WRC_WIRS_1 | 232 | 237 | PF05994 | 0.457 |
LIG_WRC_WIRS_1 | 252 | 257 | PF05994 | 0.254 |
LIG_WRC_WIRS_1 | 78 | 83 | PF05994 | 0.411 |
MOD_CK1_1 | 129 | 135 | PF00069 | 0.432 |
MOD_CK2_1 | 170 | 176 | PF00069 | 0.494 |
MOD_CK2_1 | 204 | 210 | PF00069 | 0.747 |
MOD_CK2_1 | 220 | 226 | PF00069 | 0.553 |
MOD_CK2_1 | 238 | 244 | PF00069 | 0.304 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.630 |
MOD_GlcNHglycan | 2 | 6 | PF01048 | 0.483 |
MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.754 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.730 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.416 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.393 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.341 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.753 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.764 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.571 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.421 |
MOD_N-GLC_1 | 170 | 175 | PF02516 | 0.574 |
MOD_N-GLC_1 | 265 | 270 | PF02516 | 0.508 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.743 |
MOD_NEK2_1 | 112 | 117 | PF00069 | 0.364 |
MOD_NEK2_1 | 133 | 138 | PF00069 | 0.407 |
MOD_NEK2_1 | 158 | 163 | PF00069 | 0.358 |
MOD_NEK2_1 | 258 | 263 | PF00069 | 0.617 |
MOD_NEK2_1 | 279 | 284 | PF00069 | 0.465 |
MOD_NEK2_2 | 77 | 82 | PF00069 | 0.408 |
MOD_PIKK_1 | 107 | 113 | PF00454 | 0.488 |
MOD_PIKK_1 | 119 | 125 | PF00454 | 0.460 |
MOD_PKA_1 | 193 | 199 | PF00069 | 0.718 |
MOD_PKA_2 | 193 | 199 | PF00069 | 0.733 |
MOD_Plk_1 | 170 | 176 | PF00069 | 0.549 |
MOD_Plk_1 | 279 | 285 | PF00069 | 0.437 |
MOD_Plk_4 | 129 | 135 | PF00069 | 0.396 |
MOD_Plk_4 | 154 | 160 | PF00069 | 0.444 |
MOD_Plk_4 | 77 | 83 | PF00069 | 0.386 |
MOD_ProDKin_1 | 253 | 259 | PF00069 | 0.593 |
MOD_ProDKin_1 | 281 | 287 | PF00069 | 0.429 |
MOD_SUMO_for_1 | 153 | 156 | PF00179 | 0.263 |
MOD_SUMO_for_1 | 292 | 295 | PF00179 | 0.444 |
MOD_SUMO_rev_2 | 271 | 276 | PF00179 | 0.531 |
MOD_SUMO_rev_2 | 70 | 76 | PF00179 | 0.443 |
TRG_DiLeu_BaLyEn_6 | 139 | 144 | PF01217 | 0.532 |
TRG_DiLeu_BaLyEn_6 | 254 | 259 | PF01217 | 0.486 |
TRG_ENDOCYTIC_2 | 21 | 24 | PF00928 | 0.421 |
TRG_ENDOCYTIC_2 | 78 | 81 | PF00928 | 0.470 |
TRG_ER_diArg_1 | 137 | 140 | PF00400 | 0.518 |
TRG_ER_diArg_1 | 162 | 165 | PF00400 | 0.546 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I9E0 | Leptomonas seymouri | 51% | 100% |
A0A0S4J915 | Bodo saltans | 29% | 100% |
A0A1X0NV05 | Trypanosomatidae | 34% | 100% |
A0A3R7N1Z4 | Trypanosoma rangeli | 36% | 100% |
A0A3S7X5F5 | Leishmania donovani | 68% | 100% |
A4I7T2 | Leishmania infantum | 68% | 100% |
D0A9Z3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
E9B2P0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 68% | 100% |
Q4Q5G7 | Leishmania major | 69% | 100% |
V5BGN1 | Trypanosoma cruzi | 38% | 100% |