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: A0A3S7WYM3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 21 | 23 | PF00675 | 0.557 |
CLV_PCSK_KEX2_1 | 21 | 23 | PF00082 | 0.649 |
CLV_PCSK_PC7_1 | 17 | 23 | PF00082 | 0.561 |
CLV_PCSK_SKI1_1 | 138 | 142 | PF00082 | 0.708 |
CLV_PCSK_SKI1_1 | 169 | 173 | PF00082 | 0.707 |
DEG_APCC_DBOX_1 | 137 | 145 | PF00400 | 0.698 |
DEG_APCC_DBOX_1 | 168 | 176 | PF00400 | 0.703 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.781 |
DOC_MIT_MIM_1 | 97 | 105 | PF04212 | 0.619 |
DOC_USP7_MATH_1 | 143 | 147 | PF00917 | 0.578 |
DOC_USP7_MATH_1 | 20 | 24 | PF00917 | 0.703 |
DOC_USP7_MATH_1 | 25 | 29 | PF00917 | 0.543 |
DOC_USP7_MATH_1 | 49 | 53 | PF00917 | 0.690 |
DOC_USP7_MATH_1 | 66 | 70 | PF00917 | 0.487 |
DOC_USP7_UBL2_3 | 107 | 111 | PF12436 | 0.688 |
LIG_14-3-3_CanoR_1 | 101 | 106 | PF00244 | 0.613 |
LIG_14-3-3_CanoR_1 | 138 | 148 | PF00244 | 0.578 |
LIG_14-3-3_CanoR_1 | 211 | 219 | PF00244 | 0.559 |
LIG_Actin_WH2_2 | 141 | 157 | PF00022 | 0.683 |
LIG_Actin_WH2_2 | 56 | 74 | PF00022 | 0.684 |
LIG_Clathr_ClatBox_1 | 123 | 127 | PF01394 | 0.641 |
LIG_DLG_GKlike_1 | 101 | 109 | PF00625 | 0.609 |
LIG_FHA_1 | 149 | 155 | PF00498 | 0.546 |
LIG_FHA_1 | 93 | 99 | PF00498 | 0.422 |
LIG_FHA_2 | 117 | 123 | PF00498 | 0.726 |
LIG_LIR_Gen_1 | 146 | 154 | PF02991 | 0.680 |
LIG_LIR_Gen_1 | 2 | 11 | PF02991 | 0.658 |
LIG_LIR_Gen_1 | 58 | 68 | PF02991 | 0.589 |
LIG_LIR_Gen_1 | 78 | 86 | PF02991 | 0.354 |
LIG_LIR_Nem_3 | 146 | 150 | PF02991 | 0.677 |
LIG_LIR_Nem_3 | 2 | 7 | PF02991 | 0.643 |
LIG_LIR_Nem_3 | 58 | 63 | PF02991 | 0.594 |
LIG_LIR_Nem_3 | 78 | 83 | PF02991 | 0.352 |
LIG_NRBOX | 108 | 114 | PF00104 | 0.564 |
LIG_SH2_GRB2like | 33 | 36 | PF00017 | 0.725 |
LIG_SH2_NCK_1 | 227 | 231 | PF00017 | 0.439 |
LIG_SH2_NCK_1 | 33 | 37 | PF00017 | 0.644 |
LIG_SH2_NCK_1 | 4 | 8 | PF00017 | 0.683 |
LIG_SH2_SRC | 227 | 230 | PF00017 | 0.440 |
LIG_SH2_SRC | 33 | 36 | PF00017 | 0.725 |
LIG_SH2_STAP1 | 33 | 37 | PF00017 | 0.683 |
LIG_SH2_STAP1 | 4 | 8 | PF00017 | 0.761 |
LIG_SH2_STAT5 | 39 | 42 | PF00017 | 0.721 |
LIG_SUMO_SIM_par_1 | 121 | 127 | PF11976 | 0.642 |
LIG_SUMO_SIM_par_1 | 52 | 61 | PF11976 | 0.583 |
LIG_TRAF2_1 | 119 | 122 | PF00917 | 0.681 |
LIG_TYR_ITIM | 225 | 230 | PF00017 | 0.440 |
LIG_WRC_WIRS_1 | 144 | 149 | PF05994 | 0.689 |
MOD_CK1_1 | 131 | 137 | PF00069 | 0.683 |
MOD_CK1_1 | 139 | 145 | PF00069 | 0.592 |
MOD_CK1_1 | 146 | 152 | PF00069 | 0.539 |
MOD_CK1_1 | 153 | 159 | PF00069 | 0.567 |
MOD_CK1_1 | 213 | 219 | PF00069 | 0.647 |
MOD_CK1_1 | 23 | 29 | PF00069 | 0.717 |
MOD_CK1_1 | 92 | 98 | PF00069 | 0.696 |
MOD_CK2_1 | 116 | 122 | PF00069 | 0.727 |
MOD_CK2_1 | 197 | 203 | PF00069 | 0.593 |
MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.652 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.695 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.568 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.683 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.603 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.631 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.748 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.668 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.637 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.690 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.526 |
MOD_N-GLC_1 | 128 | 133 | PF02516 | 0.718 |
MOD_N-GLC_1 | 179 | 184 | PF02516 | 0.550 |
MOD_NEK2_1 | 13 | 18 | PF00069 | 0.770 |
MOD_NEK2_1 | 148 | 153 | PF00069 | 0.664 |
MOD_NEK2_1 | 209 | 214 | PF00069 | 0.646 |
MOD_PK_1 | 3 | 9 | PF00069 | 0.685 |
MOD_PKA_2 | 20 | 26 | PF00069 | 0.666 |
MOD_PKA_2 | 210 | 216 | PF00069 | 0.641 |
MOD_Plk_1 | 105 | 111 | PF00069 | 0.684 |
MOD_Plk_1 | 128 | 134 | PF00069 | 0.713 |
MOD_Plk_1 | 66 | 72 | PF00069 | 0.636 |
MOD_Plk_2-3 | 122 | 128 | PF00069 | 0.643 |
MOD_Plk_4 | 143 | 149 | PF00069 | 0.683 |
MOD_Plk_4 | 66 | 72 | PF00069 | 0.707 |
MOD_SUMO_rev_2 | 193 | 200 | PF00179 | 0.685 |
TRG_DiLeu_BaEn_4 | 121 | 127 | PF01217 | 0.642 |
TRG_ENDOCYTIC_2 | 227 | 230 | PF00928 | 0.464 |
TRG_ENDOCYTIC_2 | 4 | 7 | PF00928 | 0.662 |
TRG_ER_diArg_1 | 15 | 18 | PF00400 | 0.563 |
TRG_ER_diArg_1 | 20 | 22 | PF00400 | 0.489 |
TRG_Pf-PMV_PEXEL_1 | 111 | 115 | PF00026 | 0.655 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3C0 | Leptomonas seymouri | 26% | 100% |
A4HDU1 | Leishmania braziliensis | 60% | 100% |
A4I138 | Leishmania infantum | 99% | 100% |
E9AX76 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
Q4QAA0 | Leishmania major | 86% | 100% |