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: E9AX76
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_PCSK_SKI1_1 | 138 | 142 | PF00082 | 0.703 |
CLV_PCSK_SKI1_1 | 169 | 173 | PF00082 | 0.633 |
DEG_APCC_DBOX_1 | 137 | 145 | PF00400 | 0.695 |
DEG_APCC_DBOX_1 | 168 | 176 | PF00400 | 0.691 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.782 |
DOC_MIT_MIM_1 | 97 | 105 | PF04212 | 0.624 |
DOC_USP7_MATH_1 | 143 | 147 | PF00917 | 0.574 |
DOC_USP7_MATH_1 | 20 | 24 | PF00917 | 0.732 |
DOC_USP7_MATH_1 | 215 | 219 | PF00917 | 0.403 |
DOC_USP7_MATH_1 | 25 | 29 | PF00917 | 0.664 |
DOC_USP7_MATH_1 | 49 | 53 | PF00917 | 0.706 |
DOC_USP7_MATH_1 | 66 | 70 | PF00917 | 0.491 |
DOC_USP7_UBL2_3 | 107 | 111 | PF12436 | 0.702 |
LIG_14-3-3_CanoR_1 | 101 | 106 | PF00244 | 0.614 |
LIG_14-3-3_CanoR_1 | 160 | 165 | PF00244 | 0.423 |
LIG_14-3-3_CanoR_1 | 211 | 219 | PF00244 | 0.640 |
LIG_Actin_WH2_2 | 141 | 157 | PF00022 | 0.673 |
LIG_Actin_WH2_2 | 56 | 74 | PF00022 | 0.690 |
LIG_BRCT_BRCA1_1 | 51 | 55 | PF00533 | 0.437 |
LIG_Clathr_ClatBox_1 | 102 | 106 | PF01394 | 0.397 |
LIG_Clathr_ClatBox_1 | 123 | 127 | PF01394 | 0.662 |
LIG_DLG_GKlike_1 | 101 | 109 | PF00625 | 0.615 |
LIG_FHA_1 | 149 | 155 | PF00498 | 0.532 |
LIG_FHA_1 | 229 | 235 | PF00498 | 0.449 |
LIG_FHA_2 | 117 | 123 | PF00498 | 0.671 |
LIG_FHA_2 | 154 | 160 | PF00498 | 0.432 |
LIG_FHA_2 | 199 | 205 | PF00498 | 0.478 |
LIG_LIR_Gen_1 | 146 | 154 | PF02991 | 0.572 |
LIG_LIR_Gen_1 | 2 | 11 | PF02991 | 0.711 |
LIG_LIR_Gen_1 | 218 | 227 | PF02991 | 0.496 |
LIG_LIR_Nem_3 | 146 | 150 | PF02991 | 0.572 |
LIG_LIR_Nem_3 | 2 | 7 | PF02991 | 0.696 |
LIG_LIR_Nem_3 | 218 | 223 | PF02991 | 0.464 |
LIG_NRBOX | 108 | 114 | PF00104 | 0.577 |
LIG_SH2_GRB2like | 33 | 36 | PF00017 | 0.714 |
LIG_SH2_NCK_1 | 33 | 37 | PF00017 | 0.634 |
LIG_SH2_NCK_1 | 4 | 8 | PF00017 | 0.688 |
LIG_SH2_NCK_1 | 48 | 52 | PF00017 | 0.456 |
LIG_SH2_SRC | 33 | 36 | PF00017 | 0.714 |
LIG_SH2_STAP1 | 33 | 37 | PF00017 | 0.604 |
LIG_SH2_STAP1 | 4 | 8 | PF00017 | 0.766 |
LIG_SH2_STAT5 | 39 | 42 | PF00017 | 0.655 |
LIG_SUMO_SIM_par_1 | 100 | 106 | PF11976 | 0.403 |
LIG_SUMO_SIM_par_1 | 121 | 127 | PF11976 | 0.668 |
LIG_TRAF2_1 | 119 | 122 | PF00917 | 0.653 |
LIG_TRAF2_1 | 201 | 204 | PF00917 | 0.506 |
LIG_UBA3_1 | 98 | 107 | PF00899 | 0.406 |
LIG_WRC_WIRS_1 | 144 | 149 | PF05994 | 0.587 |
MOD_CK1_1 | 131 | 137 | PF00069 | 0.570 |
MOD_CK1_1 | 146 | 152 | PF00069 | 0.449 |
MOD_CK1_1 | 27 | 33 | PF00069 | 0.611 |
MOD_CK1_1 | 92 | 98 | PF00069 | 0.704 |
MOD_CK2_1 | 116 | 122 | PF00069 | 0.705 |
MOD_CK2_1 | 153 | 159 | PF00069 | 0.373 |
MOD_CK2_1 | 197 | 203 | PF00069 | 0.543 |
MOD_CK2_1 | 215 | 221 | PF00069 | 0.361 |
MOD_GlcNHglycan | 113 | 116 | PF01048 | 0.391 |
MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.698 |
MOD_GlcNHglycan | 138 | 141 | PF01048 | 0.621 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.555 |
MOD_GlcNHglycan | 22 | 25 | PF01048 | 0.685 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.674 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.605 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.742 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.616 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.714 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.591 |
MOD_N-GLC_1 | 128 | 133 | PF02516 | 0.728 |
MOD_NEK2_1 | 13 | 18 | PF00069 | 0.677 |
MOD_NEK2_1 | 153 | 158 | PF00069 | 0.539 |
MOD_NEK2_1 | 187 | 192 | PF00069 | 0.478 |
MOD_NEK2_1 | 209 | 214 | PF00069 | 0.658 |
MOD_NEK2_2 | 215 | 220 | PF00069 | 0.519 |
MOD_PK_1 | 3 | 9 | PF00069 | 0.689 |
MOD_PKA_1 | 197 | 203 | PF00069 | 0.364 |
MOD_PKA_2 | 20 | 26 | PF00069 | 0.660 |
MOD_PKA_2 | 210 | 216 | PF00069 | 0.647 |
MOD_Plk_1 | 105 | 111 | PF00069 | 0.694 |
MOD_Plk_1 | 128 | 134 | PF00069 | 0.640 |
MOD_Plk_1 | 66 | 72 | PF00069 | 0.642 |
MOD_Plk_2-3 | 122 | 128 | PF00069 | 0.662 |
MOD_Plk_4 | 143 | 149 | PF00069 | 0.593 |
MOD_Plk_4 | 215 | 221 | PF00069 | 0.416 |
MOD_Plk_4 | 66 | 72 | PF00069 | 0.713 |
MOD_SUMO_rev_2 | 190 | 200 | PF00179 | 0.635 |
TRG_DiLeu_BaEn_4 | 121 | 127 | PF01217 | 0.661 |
TRG_ENDOCYTIC_2 | 4 | 7 | PF00928 | 0.756 |
TRG_ER_diArg_1 | 80 | 83 | PF00400 | 0.586 |
TRG_Pf-PMV_PEXEL_1 | 155 | 159 | PF00026 | 0.450 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3C0 | Leptomonas seymouri | 26% | 100% |
A0A3S7WYM3 | Leishmania donovani | 82% | 100% |
A4HDU1 | Leishmania braziliensis | 62% | 100% |
A4I138 | Leishmania infantum | 81% | 100% |
Q4QAA0 | Leishmania major | 82% | 100% |