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: E9AVI9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 136 | 140 | PF00656 | 0.365 |
CLV_C14_Caspase3-7 | 178 | 182 | PF00656 | 0.451 |
CLV_C14_Caspase3-7 | 37 | 41 | PF00656 | 0.405 |
CLV_NRD_NRD_1 | 222 | 224 | PF00675 | 0.324 |
CLV_PCSK_KEX2_1 | 222 | 224 | PF00082 | 0.324 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.382 |
DOC_CDC14_PxL_1 | 44 | 52 | PF14671 | 0.442 |
DOC_MAPK_FxFP_2 | 255 | 258 | PF00069 | 0.482 |
DOC_MAPK_gen_1 | 222 | 229 | PF00069 | 0.482 |
DOC_MAPK_MEF2A_6 | 155 | 162 | PF00069 | 0.464 |
DOC_PP1_RVXF_1 | 270 | 276 | PF00149 | 0.463 |
DOC_PP4_FxxP_1 | 186 | 189 | PF00568 | 0.462 |
DOC_PP4_FxxP_1 | 255 | 258 | PF00568 | 0.482 |
DOC_PP4_FxxP_1 | 281 | 284 | PF00568 | 0.452 |
DOC_USP7_MATH_1 | 140 | 144 | PF00917 | 0.451 |
DOC_USP7_MATH_1 | 171 | 175 | PF00917 | 0.495 |
DOC_WW_Pin1_4 | 101 | 106 | PF00397 | 0.536 |
DOC_WW_Pin1_4 | 51 | 56 | PF00397 | 0.337 |
DOC_WW_Pin1_4 | 58 | 63 | PF00397 | 0.329 |
LIG_14-3-3_CanoR_1 | 72 | 77 | PF00244 | 0.413 |
LIG_14-3-3_CanoR_1 | 82 | 86 | PF00244 | 0.338 |
LIG_APCC_ABBA_1 | 207 | 212 | PF00400 | 0.499 |
LIG_CaM_NSCaTE_8 | 63 | 70 | PF13499 | 0.397 |
LIG_FHA_1 | 122 | 128 | PF00498 | 0.396 |
LIG_FHA_1 | 212 | 218 | PF00498 | 0.521 |
LIG_FHA_1 | 244 | 250 | PF00498 | 0.486 |
LIG_FHA_1 | 71 | 77 | PF00498 | 0.489 |
LIG_FHA_2 | 134 | 140 | PF00498 | 0.412 |
LIG_FHA_2 | 35 | 41 | PF00498 | 0.413 |
LIG_FHA_2 | 73 | 79 | PF00498 | 0.423 |
LIG_LIR_Apic_2 | 183 | 189 | PF02991 | 0.479 |
LIG_LIR_Apic_2 | 253 | 258 | PF02991 | 0.482 |
LIG_LIR_Gen_1 | 92 | 102 | PF02991 | 0.314 |
LIG_LIR_LC3C_4 | 143 | 146 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 254 | 260 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 277 | 282 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 92 | 98 | PF02991 | 0.375 |
LIG_LYPXL_yS_3 | 257 | 260 | PF13949 | 0.451 |
LIG_MYND_1 | 189 | 193 | PF01753 | 0.449 |
LIG_PCNA_TLS_4 | 103 | 110 | PF02747 | 0.513 |
LIG_PDZ_Class_3 | 282 | 287 | PF00595 | 0.428 |
LIG_Pex14_1 | 275 | 279 | PF04695 | 0.313 |
LIG_SH2_CRK | 19 | 23 | PF00017 | 0.406 |
LIG_SH2_PTP2 | 259 | 262 | PF00017 | 0.578 |
LIG_SH2_SRC | 19 | 22 | PF00017 | 0.397 |
LIG_SH2_SRC | 259 | 262 | PF00017 | 0.409 |
LIG_SH2_STAP1 | 269 | 273 | PF00017 | 0.478 |
LIG_SH2_STAP1 | 85 | 89 | PF00017 | 0.474 |
LIG_SH2_STAT3 | 109 | 112 | PF00017 | 0.584 |
LIG_SH2_STAT5 | 109 | 112 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 21 | 24 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 259 | 262 | PF00017 | 0.464 |
LIG_SH2_STAT5 | 49 | 52 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 74 | 77 | PF00017 | 0.418 |
LIG_SH3_3 | 174 | 180 | PF00018 | 0.453 |
LIG_SH3_3 | 99 | 105 | PF00018 | 0.513 |
LIG_SUMO_SIM_anti_2 | 42 | 48 | PF11976 | 0.430 |
LIG_TRAF2_1 | 105 | 108 | PF00917 | 0.365 |
LIG_TRAF2_1 | 75 | 78 | PF00917 | 0.491 |
LIG_TYR_ITIM | 17 | 22 | PF00017 | 0.385 |
LIG_UBA3_1 | 229 | 235 | PF00899 | 0.482 |
MOD_CK2_1 | 101 | 107 | PF00069 | 0.531 |
MOD_CK2_1 | 72 | 78 | PF00069 | 0.485 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.375 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.412 |
MOD_GSK3_1 | 89 | 96 | PF00069 | 0.363 |
MOD_N-GLC_1 | 205 | 210 | PF02516 | 0.302 |
MOD_NEK2_1 | 211 | 216 | PF00069 | 0.488 |
MOD_NEK2_1 | 268 | 273 | PF00069 | 0.371 |
MOD_NEK2_2 | 205 | 210 | PF00069 | 0.493 |
MOD_NEK2_2 | 34 | 39 | PF00069 | 0.369 |
MOD_NEK2_2 | 90 | 95 | PF00069 | 0.351 |
MOD_PKA_1 | 222 | 228 | PF00069 | 0.539 |
MOD_PKA_2 | 222 | 228 | PF00069 | 0.470 |
MOD_PKA_2 | 243 | 249 | PF00069 | 0.492 |
MOD_PKA_2 | 81 | 87 | PF00069 | 0.504 |
MOD_Plk_1 | 151 | 157 | PF00069 | 0.493 |
MOD_Plk_1 | 205 | 211 | PF00069 | 0.517 |
MOD_Plk_1 | 253 | 259 | PF00069 | 0.531 |
MOD_Plk_4 | 140 | 146 | PF00069 | 0.477 |
MOD_Plk_4 | 187 | 193 | PF00069 | 0.531 |
MOD_Plk_4 | 205 | 211 | PF00069 | 0.418 |
MOD_Plk_4 | 90 | 96 | PF00069 | 0.293 |
MOD_ProDKin_1 | 101 | 107 | PF00069 | 0.536 |
MOD_ProDKin_1 | 51 | 57 | PF00069 | 0.339 |
MOD_ProDKin_1 | 58 | 64 | PF00069 | 0.322 |
TRG_DiLeu_BaEn_1 | 42 | 47 | PF01217 | 0.315 |
TRG_DiLeu_BaLyEn_6 | 216 | 221 | PF01217 | 0.531 |
TRG_ENDOCYTIC_2 | 19 | 22 | PF00928 | 0.459 |
TRG_ENDOCYTIC_2 | 257 | 260 | PF00928 | 0.445 |
TRG_ER_diArg_1 | 221 | 223 | PF00400 | 0.524 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZC8 | Leptomonas seymouri | 65% | 82% |
A0A1X0NT21 | Trypanosomatidae | 41% | 100% |
A0A3R7M657 | Trypanosoma rangeli | 40% | 100% |
A0A3S7WWX4 | Leishmania donovani | 95% | 100% |
A4HC56 | Leishmania braziliensis | 85% | 100% |
C9ZSB9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
E9AGY4 | Leishmania infantum | 96% | 100% |
Q4QBZ0 | Leishmania major | 94% | 100% |
V5BB74 | Trypanosoma cruzi | 39% | 99% |