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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: E9AHA7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 260 | 264 | PF00656 | 0.433 |
CLV_NRD_NRD_1 | 183 | 185 | PF00675 | 0.496 |
CLV_NRD_NRD_1 | 190 | 192 | PF00675 | 0.549 |
CLV_NRD_NRD_1 | 225 | 227 | PF00675 | 0.408 |
CLV_PCSK_KEX2_1 | 227 | 229 | PF00082 | 0.442 |
CLV_PCSK_PC1ET2_1 | 227 | 229 | PF00082 | 0.478 |
CLV_PCSK_SKI1_1 | 123 | 127 | PF00082 | 0.459 |
CLV_PCSK_SKI1_1 | 70 | 74 | PF00082 | 0.416 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.541 |
DEG_SPOP_SBC_1 | 101 | 105 | PF00917 | 0.416 |
DOC_CKS1_1 | 136 | 141 | PF01111 | 0.454 |
DOC_MAPK_MEF2A_6 | 14 | 21 | PF00069 | 0.403 |
DOC_MAPK_MEF2A_6 | 250 | 257 | PF00069 | 0.396 |
DOC_MAPK_NFAT4_5 | 250 | 258 | PF00069 | 0.389 |
DOC_PP1_RVXF_1 | 175 | 182 | PF00149 | 0.462 |
DOC_PP2B_LxvP_1 | 47 | 50 | PF13499 | 0.509 |
DOC_PP4_FxxP_1 | 136 | 139 | PF00568 | 0.450 |
DOC_USP7_MATH_1 | 197 | 201 | PF00917 | 0.674 |
DOC_WW_Pin1_4 | 135 | 140 | PF00397 | 0.353 |
LIG_14-3-3_CanoR_1 | 14 | 20 | PF00244 | 0.405 |
LIG_14-3-3_CanoR_1 | 70 | 80 | PF00244 | 0.345 |
LIG_deltaCOP1_diTrp_1 | 150 | 159 | PF00928 | 0.371 |
LIG_FHA_1 | 102 | 108 | PF00498 | 0.500 |
LIG_FHA_1 | 135 | 141 | PF00498 | 0.361 |
LIG_FHA_1 | 234 | 240 | PF00498 | 0.364 |
LIG_FHA_1 | 66 | 72 | PF00498 | 0.432 |
LIG_FHA_1 | 73 | 79 | PF00498 | 0.388 |
LIG_FHA_2 | 207 | 213 | PF00498 | 0.506 |
LIG_FHA_2 | 41 | 47 | PF00498 | 0.485 |
LIG_GBD_Chelix_1 | 253 | 261 | PF00786 | 0.426 |
LIG_LIR_Apic_2 | 81 | 87 | PF02991 | 0.476 |
LIG_LIR_Gen_1 | 158 | 167 | PF02991 | 0.429 |
LIG_LIR_Gen_1 | 212 | 223 | PF02991 | 0.461 |
LIG_LIR_LC3C_4 | 124 | 128 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 150 | 156 | PF02991 | 0.595 |
LIG_LIR_Nem_3 | 158 | 162 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 168 | 174 | PF02991 | 0.297 |
LIG_LIR_Nem_3 | 212 | 218 | PF02991 | 0.493 |
LIG_NRBOX | 57 | 63 | PF00104 | 0.473 |
LIG_PDZ_Wminus1_1 | 267 | 269 | PF00595 | 0.412 |
LIG_Rb_LxCxE_1 | 206 | 219 | PF01857 | 0.446 |
LIG_SH2_CRK | 90 | 94 | PF00017 | 0.453 |
LIG_SH2_STAP1 | 90 | 94 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 90 | 93 | PF00017 | 0.392 |
LIG_SH3_3 | 159 | 165 | PF00018 | 0.596 |
LIG_SH3_3 | 241 | 247 | PF00018 | 0.476 |
LIG_SUMO_SIM_anti_2 | 73 | 81 | PF11976 | 0.380 |
LIG_SUMO_SIM_par_1 | 73 | 81 | PF11976 | 0.404 |
LIG_TYR_ITIM | 88 | 93 | PF00017 | 0.474 |
LIG_UBA3_1 | 178 | 185 | PF00899 | 0.376 |
LIG_WRC_WIRS_1 | 156 | 161 | PF05994 | 0.424 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.385 |
MOD_CK1_1 | 195 | 201 | PF00069 | 0.624 |
MOD_CK2_1 | 144 | 150 | PF00069 | 0.458 |
MOD_CK2_1 | 20 | 26 | PF00069 | 0.447 |
MOD_CK2_1 | 206 | 212 | PF00069 | 0.487 |
MOD_CK2_1 | 40 | 46 | PF00069 | 0.303 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.514 |
MOD_GlcNHglycan | 199 | 202 | PF01048 | 0.602 |
MOD_GlcNHglycan | 23 | 26 | PF01048 | 0.620 |
MOD_GlcNHglycan | 257 | 260 | PF01048 | 0.499 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.423 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.417 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.398 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.468 |
MOD_NEK2_1 | 12 | 17 | PF00069 | 0.407 |
MOD_NEK2_1 | 255 | 260 | PF00069 | 0.403 |
MOD_NEK2_1 | 64 | 69 | PF00069 | 0.385 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.410 |
MOD_NEK2_1 | 80 | 85 | PF00069 | 0.362 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.469 |
MOD_PIKK_1 | 105 | 111 | PF00454 | 0.454 |
MOD_PIKK_1 | 72 | 78 | PF00454 | 0.409 |
MOD_PKA_2 | 52 | 58 | PF00069 | 0.494 |
MOD_Plk_4 | 148 | 154 | PF00069 | 0.501 |
MOD_Plk_4 | 155 | 161 | PF00069 | 0.507 |
MOD_Plk_4 | 203 | 209 | PF00069 | 0.598 |
MOD_Plk_4 | 233 | 239 | PF00069 | 0.373 |
MOD_Plk_4 | 261 | 267 | PF00069 | 0.443 |
MOD_Plk_4 | 88 | 94 | PF00069 | 0.468 |
MOD_ProDKin_1 | 135 | 141 | PF00069 | 0.359 |
TRG_DiLeu_BaEn_1 | 248 | 253 | PF01217 | 0.345 |
TRG_DiLeu_BaLyEn_6 | 174 | 179 | PF01217 | 0.545 |
TRG_DiLeu_BaLyEn_6 | 57 | 62 | PF01217 | 0.382 |
TRG_ENDOCYTIC_2 | 90 | 93 | PF00928 | 0.371 |
TRG_NES_CRM1_1 | 229 | 243 | PF08389 | 0.438 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2Y9 | Leptomonas seymouri | 33% | 95% |
A0A3Q8IDH0 | Leishmania donovani | 100% | 100% |
E9ACT2 | Leishmania major | 90% | 100% |
E9AIR8 | Leishmania braziliensis | 65% | 100% |
E9AXZ0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |