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: A0A3S7X1X0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 101 | 105 | PF00656 | 0.749 |
CLV_C14_Caspase3-7 | 129 | 133 | PF00656 | 0.797 |
CLV_NRD_NRD_1 | 10 | 12 | PF00675 | 0.610 |
CLV_PCSK_KEX2_1 | 10 | 12 | PF00082 | 0.610 |
CLV_PCSK_KEX2_1 | 125 | 127 | PF00082 | 0.741 |
CLV_PCSK_KEX2_1 | 93 | 95 | PF00082 | 0.770 |
CLV_PCSK_PC1ET2_1 | 125 | 127 | PF00082 | 0.802 |
CLV_PCSK_PC1ET2_1 | 93 | 95 | PF00082 | 0.770 |
CLV_Separin_Metazoa | 117 | 121 | PF03568 | 0.573 |
CLV_Separin_Metazoa | 205 | 209 | PF03568 | 0.555 |
DEG_SCF_FBW7_1 | 182 | 187 | PF00400 | 0.517 |
DEG_SCF_SKP2-CKS1_1 | 70 | 77 | PF00560 | 0.787 |
DEG_SPOP_SBC_1 | 36 | 40 | PF00917 | 0.584 |
DOC_CYCLIN_RxL_1 | 50 | 62 | PF00134 | 0.615 |
DOC_MAPK_MEF2A_6 | 208 | 216 | PF00069 | 0.549 |
DOC_USP7_MATH_1 | 137 | 141 | PF00917 | 0.797 |
DOC_USP7_MATH_1 | 147 | 151 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 173 | 177 | PF00917 | 0.676 |
DOC_USP7_MATH_1 | 184 | 188 | PF00917 | 0.630 |
DOC_WW_Pin1_4 | 112 | 117 | PF00397 | 0.740 |
DOC_WW_Pin1_4 | 140 | 145 | PF00397 | 0.720 |
DOC_WW_Pin1_4 | 180 | 185 | PF00397 | 0.549 |
DOC_WW_Pin1_4 | 22 | 27 | PF00397 | 0.752 |
DOC_WW_Pin1_4 | 71 | 76 | PF00397 | 0.726 |
LIG_14-3-3_CanoR_1 | 126 | 134 | PF00244 | 0.626 |
LIG_14-3-3_CanoR_1 | 160 | 164 | PF00244 | 0.702 |
LIG_14-3-3_CanoR_1 | 27 | 33 | PF00244 | 0.658 |
LIG_14-3-3_CanoR_1 | 37 | 44 | PF00244 | 0.660 |
LIG_14-3-3_CanoR_1 | 50 | 57 | PF00244 | 0.523 |
LIG_FHA_1 | 129 | 135 | PF00498 | 0.585 |
LIG_FHA_1 | 183 | 189 | PF00498 | 0.628 |
LIG_FHA_1 | 199 | 205 | PF00498 | 0.385 |
LIG_FHA_1 | 23 | 29 | PF00498 | 0.732 |
LIG_FHA_1 | 49 | 55 | PF00498 | 0.654 |
LIG_FHA_2 | 67 | 73 | PF00498 | 0.764 |
LIG_LIR_Gen_1 | 187 | 197 | PF02991 | 0.666 |
LIG_LIR_Nem_3 | 187 | 192 | PF02991 | 0.573 |
LIG_PDZ_Class_2 | 221 | 226 | PF00595 | 0.671 |
LIG_PDZ_Wminus1_1 | 224 | 226 | PF00595 | 0.690 |
LIG_REV1ctd_RIR_1 | 6 | 15 | PF16727 | 0.629 |
LIG_SH2_CRK | 12 | 16 | PF00017 | 0.557 |
LIG_SH2_NCK_1 | 12 | 16 | PF00017 | 0.557 |
LIG_SH2_PTP2 | 189 | 192 | PF00017 | 0.534 |
LIG_SH2_STAP1 | 12 | 16 | PF00017 | 0.616 |
LIG_SH2_STAP1 | 194 | 198 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 12 | 15 | PF00017 | 0.637 |
LIG_SH2_STAT5 | 189 | 192 | PF00017 | 0.512 |
LIG_SH2_STAT5 | 218 | 221 | PF00017 | 0.536 |
LIG_SH3_3 | 113 | 119 | PF00018 | 0.664 |
LIG_SH3_3 | 131 | 137 | PF00018 | 0.587 |
LIG_SH3_3 | 206 | 212 | PF00018 | 0.577 |
LIG_UBA3_1 | 56 | 63 | PF00899 | 0.597 |
LIG_WW_3 | 117 | 121 | PF00397 | 0.573 |
MOD_CDK_SPK_2 | 22 | 27 | PF00069 | 0.752 |
MOD_CDK_SPxK_1 | 71 | 77 | PF00069 | 0.789 |
MOD_CK1_1 | 112 | 118 | PF00069 | 0.718 |
MOD_CK1_1 | 140 | 146 | PF00069 | 0.641 |
MOD_CK1_1 | 176 | 182 | PF00069 | 0.616 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.709 |
MOD_CK1_1 | 43 | 49 | PF00069 | 0.566 |
MOD_CK1_1 | 66 | 72 | PF00069 | 0.767 |
MOD_CK1_1 | 84 | 90 | PF00069 | 0.499 |
MOD_CK2_1 | 103 | 109 | PF00069 | 0.629 |
MOD_CK2_1 | 70 | 76 | PF00069 | 0.785 |
MOD_GlcNHglycan | 104 | 108 | PF01048 | 0.791 |
MOD_GlcNHglycan | 134 | 137 | PF01048 | 0.734 |
MOD_GlcNHglycan | 139 | 143 | PF01048 | 0.690 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.628 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.655 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.632 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.576 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.742 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.722 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.669 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.624 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.613 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.576 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.424 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.611 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.550 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.644 |
MOD_GSK3_1 | 99 | 106 | PF00069 | 0.576 |
MOD_NEK2_1 | 108 | 113 | PF00069 | 0.601 |
MOD_NEK2_1 | 220 | 225 | PF00069 | 0.563 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.595 |
MOD_NEK2_2 | 184 | 189 | PF00069 | 0.612 |
MOD_PIKK_1 | 63 | 69 | PF00454 | 0.552 |
MOD_PKA_1 | 10 | 16 | PF00069 | 0.615 |
MOD_PKA_2 | 10 | 16 | PF00069 | 0.615 |
MOD_PKA_2 | 159 | 165 | PF00069 | 0.702 |
MOD_PKA_2 | 36 | 42 | PF00069 | 0.619 |
MOD_PKA_2 | 49 | 55 | PF00069 | 0.626 |
MOD_PKB_1 | 126 | 134 | PF00069 | 0.684 |
MOD_Plk_1 | 103 | 109 | PF00069 | 0.574 |
MOD_Plk_4 | 184 | 190 | PF00069 | 0.694 |
MOD_Plk_4 | 220 | 226 | PF00069 | 0.538 |
MOD_ProDKin_1 | 112 | 118 | PF00069 | 0.730 |
MOD_ProDKin_1 | 140 | 146 | PF00069 | 0.723 |
MOD_ProDKin_1 | 180 | 186 | PF00069 | 0.548 |
MOD_ProDKin_1 | 22 | 28 | PF00069 | 0.752 |
MOD_ProDKin_1 | 71 | 77 | PF00069 | 0.728 |
MOD_SUMO_for_1 | 153 | 156 | PF00179 | 0.710 |
MOD_SUMO_rev_2 | 117 | 127 | PF00179 | 0.723 |
TRG_ENDOCYTIC_2 | 12 | 15 | PF00928 | 0.554 |
TRG_ENDOCYTIC_2 | 189 | 192 | PF00928 | 0.484 |
TRG_ER_diArg_1 | 9 | 11 | PF00400 | 0.610 |
TRG_NLS_MonoExtC_3 | 124 | 130 | PF00514 | 0.727 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P417 | Leptomonas seymouri | 44% | 100% |
A4HGW0 | Leishmania braziliensis | 70% | 100% |
A4I3Z0 | Leishmania infantum | 99% | 100% |
E9B080 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4Q805 | Leishmania major | 90% | 100% |