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: 3 |
NetGPI | no | yes: 0, no: 3 |
Related structures:
AlphaFold database: A0A3Q8ISD3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 112 | 114 | PF00675 | 0.743 |
CLV_NRD_NRD_1 | 132 | 134 | PF00675 | 0.474 |
CLV_NRD_NRD_1 | 137 | 139 | PF00675 | 0.668 |
CLV_NRD_NRD_1 | 148 | 150 | PF00675 | 0.494 |
CLV_PCSK_FUR_1 | 135 | 139 | PF00082 | 0.720 |
CLV_PCSK_KEX2_1 | 112 | 114 | PF00082 | 0.743 |
CLV_PCSK_KEX2_1 | 132 | 134 | PF00082 | 0.474 |
CLV_PCSK_KEX2_1 | 137 | 139 | PF00082 | 0.668 |
CLV_PCSK_KEX2_1 | 147 | 149 | PF00082 | 0.508 |
CLV_PCSK_PC7_1 | 133 | 139 | PF00082 | 0.717 |
CLV_PCSK_SKI1_1 | 148 | 152 | PF00082 | 0.681 |
DEG_APCC_DBOX_1 | 111 | 119 | PF00400 | 0.741 |
DOC_CYCLIN_RxL_1 | 146 | 157 | PF00134 | 0.678 |
DOC_CYCLIN_yCln2_LP_2 | 117 | 120 | PF00134 | 0.668 |
DOC_MAPK_gen_1 | 147 | 153 | PF00069 | 0.681 |
DOC_PP1_RVXF_1 | 146 | 153 | PF00149 | 0.681 |
DOC_PP2B_LxvP_1 | 117 | 120 | PF13499 | 0.742 |
DOC_USP7_UBL2_3 | 33 | 37 | PF12436 | 0.602 |
LIG_14-3-3_CanoR_1 | 112 | 116 | PF00244 | 0.744 |
LIG_14-3-3_CanoR_1 | 137 | 143 | PF00244 | 0.721 |
LIG_14-3-3_CanoR_1 | 69 | 79 | PF00244 | 0.663 |
LIG_APCC_ABBA_1 | 5 | 10 | PF00400 | 0.629 |
LIG_BRCT_BRCA1_1 | 19 | 23 | PF00533 | 0.653 |
LIG_DCNL_PONY_1 | 1 | 4 | PF03556 | 0.668 |
LIG_LIR_Apic_2 | 141 | 145 | PF02991 | 0.703 |
LIG_LIR_Gen_1 | 10 | 17 | PF02991 | 0.526 |
LIG_LIR_Gen_1 | 96 | 105 | PF02991 | 0.664 |
LIG_LIR_Nem_3 | 10 | 14 | PF02991 | 0.532 |
LIG_LIR_Nem_3 | 96 | 101 | PF02991 | 0.675 |
LIG_MYND_1 | 3 | 7 | PF01753 | 0.648 |
LIG_MYND_3 | 2 | 6 | PF01753 | 0.657 |
LIG_SH2_PTP2 | 142 | 145 | PF00017 | 0.697 |
LIG_SH2_STAT5 | 142 | 145 | PF00017 | 0.697 |
LIG_SH3_3 | 140 | 146 | PF00018 | 0.702 |
LIG_SUMO_SIM_anti_2 | 12 | 18 | PF11976 | 0.599 |
LIG_WRC_WIRS_1 | 51 | 56 | PF05994 | 0.714 |
LIG_WW_3 | 118 | 122 | PF00397 | 0.679 |
LIG_WW_3 | 144 | 148 | PF00397 | 0.683 |
MOD_CK1_1 | 111 | 117 | PF00069 | 0.741 |
MOD_CK1_1 | 70 | 76 | PF00069 | 0.575 |
MOD_CK2_1 | 81 | 87 | PF00069 | 0.656 |
MOD_GlcNHglycan | 159 | 162 | PF01048 | 0.663 |
MOD_GlcNHglycan | 19 | 22 | PF01048 | 0.696 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.688 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.535 |
MOD_GlcNHglycan | 95 | 98 | PF01048 | 0.520 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.677 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.618 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.622 |
MOD_NEK2_1 | 24 | 29 | PF00069 | 0.532 |
MOD_NEK2_1 | 67 | 72 | PF00069 | 0.679 |
MOD_NEK2_1 | 77 | 82 | PF00069 | 0.522 |
MOD_OFUCOSY | 35 | 41 | PF10250 | 0.566 |
MOD_PKA_2 | 111 | 117 | PF00069 | 0.741 |
MOD_PKA_2 | 157 | 163 | PF00069 | 0.669 |
MOD_PKA_2 | 17 | 23 | PF00069 | 0.575 |
MOD_Plk_1 | 9 | 15 | PF00069 | 0.610 |
MOD_SUMO_for_1 | 36 | 39 | PF00179 | 0.616 |
TRG_DiLeu_BaLyEn_6 | 113 | 118 | PF01217 | 0.586 |
TRG_DiLeu_BaLyEn_6 | 146 | 151 | PF01217 | 0.681 |
TRG_ER_diArg_1 | 132 | 135 | PF00400 | 0.711 |
TRG_ER_diArg_1 | 137 | 140 | PF00400 | 0.667 |
TRG_ER_diArg_1 | 146 | 149 | PF00400 | 0.519 |