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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: E9B3M4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 179 | 183 | PF00656 | 0.576 |
CLV_C14_Caspase3-7 | 190 | 194 | PF00656 | 0.616 |
CLV_NRD_NRD_1 | 138 | 140 | PF00675 | 0.592 |
CLV_NRD_NRD_1 | 248 | 250 | PF00675 | 0.505 |
CLV_NRD_NRD_1 | 53 | 55 | PF00675 | 0.688 |
CLV_PCSK_KEX2_1 | 137 | 139 | PF00082 | 0.602 |
CLV_PCSK_KEX2_1 | 148 | 150 | PF00082 | 0.410 |
CLV_PCSK_KEX2_1 | 248 | 250 | PF00082 | 0.505 |
CLV_PCSK_KEX2_1 | 53 | 55 | PF00082 | 0.646 |
CLV_PCSK_PC1ET2_1 | 148 | 150 | PF00082 | 0.497 |
CLV_PCSK_PC7_1 | 134 | 140 | PF00082 | 0.554 |
CLV_PCSK_SKI1_1 | 199 | 203 | PF00082 | 0.516 |
DEG_SPOP_SBC_1 | 185 | 189 | PF00917 | 0.559 |
DOC_CYCLIN_yCln2_LP_2 | 80 | 86 | PF00134 | 0.634 |
DOC_MAPK_gen_1 | 145 | 154 | PF00069 | 0.359 |
DOC_MAPK_gen_1 | 234 | 243 | PF00069 | 0.420 |
DOC_MAPK_MEF2A_6 | 145 | 154 | PF00069 | 0.403 |
DOC_PP1_RVXF_1 | 240 | 246 | PF00149 | 0.339 |
DOC_PP1_RVXF_1 | 265 | 272 | PF00149 | 0.471 |
DOC_PP2B_LxvP_1 | 112 | 115 | PF13499 | 0.545 |
DOC_PP2B_LxvP_1 | 80 | 83 | PF13499 | 0.637 |
DOC_USP7_MATH_1 | 178 | 182 | PF00917 | 0.614 |
DOC_USP7_MATH_1 | 197 | 201 | PF00917 | 0.555 |
DOC_USP7_UBL2_3 | 96 | 100 | PF12436 | 0.365 |
DOC_WW_Pin1_4 | 203 | 208 | PF00397 | 0.637 |
LIG_14-3-3_CanoR_1 | 274 | 283 | PF00244 | 0.542 |
LIG_14-3-3_CanoR_1 | 53 | 62 | PF00244 | 0.662 |
LIG_Actin_WH2_2 | 228 | 244 | PF00022 | 0.354 |
LIG_APCC_ABBAyCdc20_2 | 272 | 278 | PF00400 | 0.484 |
LIG_FHA_1 | 186 | 192 | PF00498 | 0.711 |
LIG_FHA_1 | 69 | 75 | PF00498 | 0.663 |
LIG_FHA_2 | 127 | 133 | PF00498 | 0.459 |
LIG_FHA_2 | 185 | 191 | PF00498 | 0.625 |
LIG_FHA_2 | 223 | 229 | PF00498 | 0.390 |
LIG_FHA_2 | 73 | 79 | PF00498 | 0.489 |
LIG_LIR_Gen_1 | 37 | 48 | PF02991 | 0.490 |
LIG_LIR_Gen_1 | 6 | 14 | PF02991 | 0.590 |
LIG_LIR_Nem_3 | 37 | 43 | PF02991 | 0.489 |
LIG_LIR_Nem_3 | 6 | 10 | PF02991 | 0.645 |
LIG_PCNA_PIPBox_1 | 150 | 159 | PF02747 | 0.346 |
LIG_PDZ_Class_3 | 283 | 288 | PF00595 | 0.609 |
LIG_SH2_STAT5 | 119 | 122 | PF00017 | 0.457 |
LIG_SH2_STAT5 | 156 | 159 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 222 | 225 | PF00017 | 0.433 |
LIG_SH2_STAT5 | 9 | 12 | PF00017 | 0.659 |
LIG_SH3_1 | 29 | 35 | PF00018 | 0.633 |
LIG_SH3_3 | 204 | 210 | PF00018 | 0.624 |
LIG_SH3_3 | 29 | 35 | PF00018 | 0.633 |
LIG_SUMO_SIM_par_1 | 69 | 75 | PF11976 | 0.619 |
LIG_TRAF2_1 | 225 | 228 | PF00917 | 0.482 |
LIG_TRAF2_1 | 230 | 233 | PF00917 | 0.509 |
LIG_WRC_WIRS_1 | 4 | 9 | PF05994 | 0.645 |
MOD_CDK_SPK_2 | 208 | 213 | PF00069 | 0.588 |
MOD_CDK_SPxxK_3 | 208 | 215 | PF00069 | 0.578 |
MOD_CK1_1 | 200 | 206 | PF00069 | 0.666 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.503 |
MOD_CK2_1 | 126 | 132 | PF00069 | 0.446 |
MOD_CK2_1 | 222 | 228 | PF00069 | 0.388 |
MOD_CK2_1 | 54 | 60 | PF00069 | 0.579 |
MOD_GlcNHglycan | 178 | 181 | PF01048 | 0.586 |
MOD_GlcNHglycan | 193 | 196 | PF01048 | 0.617 |
MOD_GlcNHglycan | 198 | 202 | PF01048 | 0.592 |
MOD_GlcNHglycan | 56 | 59 | PF01048 | 0.546 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.532 |
MOD_GSK3_1 | 256 | 263 | PF00069 | 0.464 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.657 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.485 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.506 |
MOD_PKA_1 | 53 | 59 | PF00069 | 0.685 |
MOD_PKA_2 | 191 | 197 | PF00069 | 0.534 |
MOD_PKA_2 | 260 | 266 | PF00069 | 0.481 |
MOD_PKA_2 | 53 | 59 | PF00069 | 0.639 |
MOD_PKB_1 | 272 | 280 | PF00069 | 0.492 |
MOD_Plk_1 | 256 | 262 | PF00069 | 0.580 |
MOD_Plk_1 | 68 | 74 | PF00069 | 0.601 |
MOD_Plk_1 | 76 | 82 | PF00069 | 0.566 |
MOD_Plk_4 | 39 | 45 | PF00069 | 0.494 |
MOD_ProDKin_1 | 203 | 209 | PF00069 | 0.631 |
TRG_DiLeu_BaEn_1 | 163 | 168 | PF01217 | 0.366 |
TRG_ER_diArg_1 | 137 | 139 | PF00400 | 0.611 |
TRG_ER_diArg_1 | 212 | 215 | PF00400 | 0.564 |
TRG_ER_diArg_1 | 248 | 250 | PF00400 | 0.503 |
TRG_NES_CRM1_1 | 78 | 93 | PF08389 | 0.523 |
TRG_Pf-PMV_PEXEL_1 | 138 | 142 | PF00026 | 0.610 |
TRG_Pf-PMV_PEXEL_1 | 215 | 219 | PF00026 | 0.542 |
TRG_Pf-PMV_PEXEL_1 | 248 | 252 | PF00026 | 0.366 |
TRG_Pf-PMV_PEXEL_1 | 29 | 34 | PF00026 | 0.635 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IHC5 | Leishmania donovani | 84% | 100% |
A4HL81 | Leishmania braziliensis | 65% | 100% |
A4I8Q9 | Leishmania infantum | 84% | 100% |
Q4Q4G3 | Leishmania major | 85% | 100% |