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: Q4QAA0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_PCSK_SKI1_1 | 138 | 142 | PF00082 | 0.736 |
CLV_PCSK_SKI1_1 | 169 | 173 | PF00082 | 0.715 |
CLV_PCSK_SKI1_1 | 232 | 236 | PF00082 | 0.546 |
DEG_APCC_DBOX_1 | 137 | 145 | PF00400 | 0.730 |
DEG_APCC_DBOX_1 | 168 | 176 | PF00400 | 0.711 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.808 |
DOC_MIT_MIM_1 | 97 | 105 | PF04212 | 0.631 |
DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.550 |
DOC_USP7_MATH_1 | 143 | 147 | PF00917 | 0.561 |
DOC_USP7_MATH_1 | 20 | 24 | PF00917 | 0.622 |
DOC_USP7_MATH_1 | 49 | 53 | PF00917 | 0.712 |
DOC_USP7_MATH_1 | 85 | 89 | PF00917 | 0.555 |
DOC_USP7_UBL2_3 | 107 | 111 | PF12436 | 0.714 |
LIG_14-3-3_CanoR_1 | 101 | 106 | PF00244 | 0.621 |
LIG_14-3-3_CanoR_1 | 138 | 148 | PF00244 | 0.607 |
LIG_14-3-3_CanoR_1 | 200 | 206 | PF00244 | 0.499 |
LIG_14-3-3_CterR_2 | 232 | 236 | PF00244 | 0.546 |
LIG_Actin_WH2_2 | 141 | 157 | PF00022 | 0.706 |
LIG_Actin_WH2_2 | 185 | 202 | PF00022 | 0.449 |
LIG_Actin_WH2_2 | 56 | 74 | PF00022 | 0.701 |
LIG_Clathr_ClatBox_1 | 123 | 127 | PF01394 | 0.651 |
LIG_DLG_GKlike_1 | 101 | 109 | PF00625 | 0.624 |
LIG_FHA_1 | 200 | 206 | PF00498 | 0.483 |
LIG_FHA_2 | 117 | 123 | PF00498 | 0.692 |
LIG_FHA_2 | 192 | 198 | PF00498 | 0.604 |
LIG_IRF3_LxIS_1 | 144 | 151 | PF10401 | 0.476 |
LIG_LIR_Gen_1 | 146 | 154 | PF02991 | 0.701 |
LIG_LIR_Gen_1 | 2 | 11 | PF02991 | 0.793 |
LIG_LIR_Gen_1 | 58 | 68 | PF02991 | 0.603 |
LIG_LIR_Nem_3 | 146 | 150 | PF02991 | 0.707 |
LIG_LIR_Nem_3 | 2 | 7 | PF02991 | 0.719 |
LIG_LIR_Nem_3 | 58 | 63 | PF02991 | 0.610 |
LIG_NRBOX | 108 | 114 | PF00104 | 0.626 |
LIG_SH2_GRB2like | 33 | 36 | PF00017 | 0.744 |
LIG_SH2_NCK_1 | 33 | 37 | PF00017 | 0.662 |
LIG_SH2_NCK_1 | 4 | 8 | PF00017 | 0.713 |
LIG_SH2_NCK_1 | 48 | 52 | PF00017 | 0.462 |
LIG_SH2_SRC | 33 | 36 | PF00017 | 0.744 |
LIG_SH2_STAP1 | 33 | 37 | PF00017 | 0.701 |
LIG_SH2_STAP1 | 4 | 8 | PF00017 | 0.791 |
LIG_SH2_STAT5 | 39 | 42 | PF00017 | 0.744 |
LIG_SUMO_SIM_par_1 | 121 | 127 | PF11976 | 0.656 |
LIG_SUMO_SIM_par_1 | 54 | 61 | PF11976 | 0.602 |
LIG_TRAF2_1 | 119 | 122 | PF00917 | 0.657 |
LIG_TRAF2_1 | 194 | 197 | PF00917 | 0.537 |
LIG_UBA3_1 | 153 | 160 | PF00899 | 0.461 |
LIG_WRC_WIRS_1 | 144 | 149 | PF05994 | 0.718 |
MOD_CK1_1 | 131 | 137 | PF00069 | 0.739 |
MOD_CK1_1 | 139 | 145 | PF00069 | 0.591 |
MOD_CK1_1 | 146 | 152 | PF00069 | 0.453 |
MOD_CK1_1 | 213 | 219 | PF00069 | 0.680 |
MOD_CK1_1 | 23 | 29 | PF00069 | 0.766 |
MOD_CK1_1 | 88 | 94 | PF00069 | 0.703 |
MOD_CK2_1 | 116 | 122 | PF00069 | 0.646 |
MOD_CK2_1 | 191 | 197 | PF00069 | 0.635 |
MOD_CK2_1 | 3 | 9 | PF00069 | 0.636 |
MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.569 |
MOD_GlcNHglycan | 150 | 153 | PF01048 | 0.407 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.721 |
MOD_GlcNHglycan | 22 | 25 | PF01048 | 0.759 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.706 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.627 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.617 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.775 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.682 |
MOD_GSK3_1 | 228 | 235 | PF00069 | 0.593 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.661 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.751 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.538 |
MOD_N-GLC_1 | 128 | 133 | PF02516 | 0.765 |
MOD_NEK2_1 | 13 | 18 | PF00069 | 0.797 |
MOD_NEK2_1 | 148 | 153 | PF00069 | 0.682 |
MOD_NEK2_1 | 209 | 214 | PF00069 | 0.723 |
MOD_PIKK_1 | 13 | 19 | PF00454 | 0.565 |
MOD_PK_1 | 3 | 9 | PF00069 | 0.713 |
MOD_PKA_2 | 199 | 205 | PF00069 | 0.500 |
MOD_PKA_2 | 20 | 26 | PF00069 | 0.691 |
MOD_Plk_1 | 105 | 111 | PF00069 | 0.704 |
MOD_Plk_1 | 128 | 134 | PF00069 | 0.759 |
MOD_Plk_1 | 66 | 72 | PF00069 | 0.647 |
MOD_Plk_2-3 | 122 | 128 | PF00069 | 0.657 |
MOD_Plk_4 | 143 | 149 | PF00069 | 0.713 |
MOD_Plk_4 | 66 | 72 | PF00069 | 0.724 |
MOD_SUMO_rev_2 | 193 | 199 | PF00179 | 0.550 |
TRG_DiLeu_BaEn_4 | 121 | 127 | PF01217 | 0.656 |
TRG_DiLeu_BaLyEn_6 | 79 | 84 | PF01217 | 0.513 |
TRG_ENDOCYTIC_2 | 4 | 7 | PF00928 | 0.797 |
TRG_ER_diArg_1 | 80 | 83 | PF00400 | 0.569 |
TRG_Pf-PMV_PEXEL_1 | 111 | 115 | PF00026 | 0.542 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WYM3 | Leishmania donovani | 86% | 100% |
A4HDU1 | Leishmania braziliensis | 62% | 100% |
A4I138 | Leishmania infantum | 86% | 100% |
E9AX76 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |