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: 2 |
NetGPI | no | yes: 0, no: 2 |
Related structures:
AlphaFold database: A4I0B2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 20 | 24 | PF00656 | 0.416 |
CLV_PCSK_KEX2_1 | 161 | 163 | PF00082 | 0.438 |
CLV_PCSK_PC1ET2_1 | 161 | 163 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 158 | 162 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 62 | 66 | PF00082 | 0.394 |
CLV_PCSK_SKI1_1 | 72 | 76 | PF00082 | 0.354 |
CLV_PCSK_SKI1_1 | 78 | 82 | PF00082 | 0.318 |
DEG_SPOP_SBC_1 | 262 | 266 | PF00917 | 0.601 |
DOC_CYCLIN_RxL_1 | 158 | 168 | PF00134 | 0.444 |
DOC_CYCLIN_RxL_1 | 69 | 79 | PF00134 | 0.417 |
DOC_MAPK_gen_1 | 245 | 253 | PF00069 | 0.554 |
DOC_MAPK_MEF2A_6 | 12 | 21 | PF00069 | 0.377 |
DOC_PP1_RVXF_1 | 70 | 76 | PF00149 | 0.415 |
DOC_PP2B_LxvP_1 | 251 | 254 | PF13499 | 0.602 |
DOC_PP2B_LxvP_1 | 33 | 36 | PF13499 | 0.536 |
DOC_PP2B_LxvP_1 | 74 | 77 | PF13499 | 0.444 |
DOC_USP7_MATH_1 | 137 | 141 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 145 | 149 | PF00917 | 0.532 |
DOC_USP7_MATH_1 | 205 | 209 | PF00917 | 0.726 |
DOC_USP7_MATH_1 | 260 | 264 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 46 | 50 | PF00917 | 0.564 |
DOC_WW_Pin1_4 | 215 | 220 | PF00397 | 0.689 |
DOC_WW_Pin1_4 | 269 | 274 | PF00397 | 0.671 |
LIG_14-3-3_CanoR_1 | 121 | 130 | PF00244 | 0.451 |
LIG_APCC_ABBA_1 | 15 | 20 | PF00400 | 0.368 |
LIG_DCNL_PONY_1 | 1 | 4 | PF03556 | 0.503 |
LIG_FHA_1 | 152 | 158 | PF00498 | 0.526 |
LIG_FHA_1 | 23 | 29 | PF00498 | 0.627 |
LIG_FHA_1 | 77 | 83 | PF00498 | 0.416 |
LIG_FHA_2 | 187 | 193 | PF00498 | 0.653 |
LIG_FHA_2 | 54 | 60 | PF00498 | 0.435 |
LIG_GBD_Chelix_1 | 156 | 164 | PF00786 | 0.432 |
LIG_LIR_Nem_3 | 151 | 156 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 83 | 87 | PF02991 | 0.368 |
LIG_NRBOX | 159 | 165 | PF00104 | 0.436 |
LIG_PCNA_PIPBox_1 | 1 | 10 | PF02747 | 0.475 |
LIG_PCNA_yPIPBox_3 | 232 | 245 | PF02747 | 0.490 |
LIG_PCNA_yPIPBox_3 | 5 | 18 | PF02747 | 0.420 |
LIG_PTB_Apo_2 | 190 | 197 | PF02174 | 0.607 |
LIG_SH2_CRK | 153 | 157 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 153 | 156 | PF00017 | 0.565 |
LIG_SH2_STAT5 | 198 | 201 | PF00017 | 0.624 |
LIG_SH2_STAT5 | 87 | 90 | PF00017 | 0.400 |
LIG_SH3_3 | 28 | 34 | PF00018 | 0.497 |
LIG_SUMO_SIM_anti_2 | 187 | 192 | PF11976 | 0.594 |
LIG_SUMO_SIM_anti_2 | 56 | 63 | PF11976 | 0.412 |
LIG_SUMO_SIM_par_1 | 249 | 256 | PF11976 | 0.595 |
LIG_TYR_ITSM | 149 | 156 | PF00017 | 0.469 |
LIG_WRC_WIRS_1 | 81 | 86 | PF05994 | 0.374 |
MOD_CDC14_SPxK_1 | 218 | 221 | PF00782 | 0.664 |
MOD_CDK_SPxK_1 | 215 | 221 | PF00069 | 0.665 |
MOD_CK1_1 | 140 | 146 | PF00069 | 0.607 |
MOD_CK1_1 | 148 | 154 | PF00069 | 0.453 |
MOD_CK1_1 | 263 | 269 | PF00069 | 0.707 |
MOD_CK2_1 | 186 | 192 | PF00069 | 0.765 |
MOD_GlcNHglycan | 108 | 112 | PF01048 | 0.479 |
MOD_GlcNHglycan | 142 | 145 | PF01048 | 0.611 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.624 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.744 |
MOD_GlcNHglycan | 267 | 270 | PF01048 | 0.660 |
MOD_GlcNHglycan | 37 | 40 | PF01048 | 0.550 |
MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.500 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.601 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.604 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.724 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.709 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.439 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.753 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.560 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.414 |
MOD_N-GLC_1 | 137 | 142 | PF02516 | 0.595 |
MOD_N-GLC_1 | 192 | 197 | PF02516 | 0.611 |
MOD_N-GLC_2 | 139 | 141 | PF02516 | 0.604 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.614 |
MOD_NEK2_1 | 191 | 196 | PF00069 | 0.555 |
MOD_NEK2_2 | 22 | 27 | PF00069 | 0.428 |
MOD_NEK2_2 | 80 | 85 | PF00069 | 0.388 |
MOD_PK_1 | 184 | 190 | PF00069 | 0.502 |
MOD_Plk_1 | 107 | 113 | PF00069 | 0.537 |
MOD_Plk_1 | 191 | 197 | PF00069 | 0.608 |
MOD_Plk_1 | 22 | 28 | PF00069 | 0.434 |
MOD_Plk_4 | 148 | 154 | PF00069 | 0.594 |
MOD_Plk_4 | 186 | 192 | PF00069 | 0.589 |
MOD_ProDKin_1 | 215 | 221 | PF00069 | 0.691 |
MOD_ProDKin_1 | 269 | 275 | PF00069 | 0.669 |
TRG_DiLeu_BaLyEn_6 | 159 | 164 | PF01217 | 0.429 |
TRG_ENDOCYTIC_2 | 153 | 156 | PF00928 | 0.503 |
TRG_ER_diArg_1 | 244 | 247 | PF00400 | 0.489 |
TRG_Pf-PMV_PEXEL_1 | 161 | 165 | PF00026 | 0.449 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WXL8 | Leishmania donovani | 100% | 100% |