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: A0A3S7WNR8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 133 | 137 | PF00656 | 0.558 |
CLV_C14_Caspase3-7 | 156 | 160 | PF00656 | 0.611 |
CLV_NRD_NRD_1 | 115 | 117 | PF00675 | 0.669 |
CLV_NRD_NRD_1 | 94 | 96 | PF00675 | 0.694 |
CLV_PCSK_FUR_1 | 113 | 117 | PF00082 | 0.562 |
CLV_PCSK_KEX2_1 | 112 | 114 | PF00082 | 0.681 |
CLV_PCSK_KEX2_1 | 115 | 117 | PF00082 | 0.640 |
CLV_PCSK_KEX2_1 | 94 | 96 | PF00082 | 0.692 |
CLV_PCSK_PC1ET2_1 | 112 | 114 | PF00082 | 0.558 |
CLV_PCSK_SKI1_1 | 116 | 120 | PF00082 | 0.573 |
DEG_SPOP_SBC_1 | 147 | 151 | PF00917 | 0.688 |
DOC_CDC14_PxL_1 | 46 | 54 | PF14671 | 0.638 |
DOC_CKS1_1 | 19 | 24 | PF01111 | 0.618 |
DOC_USP7_MATH_1 | 147 | 151 | PF00917 | 0.746 |
DOC_USP7_MATH_1 | 152 | 156 | PF00917 | 0.686 |
DOC_USP7_UBL2_3 | 119 | 123 | PF12436 | 0.689 |
DOC_WW_Pin1_4 | 18 | 23 | PF00397 | 0.616 |
LIG_14-3-3_CanoR_1 | 41 | 47 | PF00244 | 0.595 |
LIG_Actin_WH2_2 | 39 | 55 | PF00022 | 0.745 |
LIG_APCC_ABBAyCdc20_2 | 94 | 100 | PF00400 | 0.520 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.792 |
LIG_CaM_IQ_9 | 105 | 121 | PF13499 | 0.521 |
LIG_FHA_2 | 101 | 107 | PF00498 | 0.436 |
LIG_FHA_2 | 19 | 25 | PF00498 | 0.615 |
LIG_MYND_1 | 18 | 22 | PF01753 | 0.627 |
LIG_PDZ_Class_3 | 162 | 167 | PF00595 | 0.650 |
LIG_SH2_STAT5 | 39 | 42 | PF00017 | 0.633 |
LIG_TRAF2_1 | 21 | 24 | PF00917 | 0.720 |
MOD_CDK_SPxxK_3 | 18 | 25 | PF00069 | 0.620 |
MOD_CK1_1 | 139 | 145 | PF00069 | 0.740 |
MOD_CK1_1 | 146 | 152 | PF00069 | 0.718 |
MOD_CK1_1 | 153 | 159 | PF00069 | 0.625 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.807 |
MOD_CK1_1 | 42 | 48 | PF00069 | 0.469 |
MOD_CK2_1 | 100 | 106 | PF00069 | 0.423 |
MOD_CK2_1 | 18 | 24 | PF00069 | 0.623 |
MOD_GlcNHglycan | 144 | 148 | PF01048 | 0.740 |
MOD_GlcNHglycan | 150 | 153 | PF01048 | 0.646 |
MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.756 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.424 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.633 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.716 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.600 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.441 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.616 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.790 |
MOD_NEK2_1 | 148 | 153 | PF00069 | 0.611 |
MOD_NEK2_1 | 52 | 57 | PF00069 | 0.670 |
MOD_PK_1 | 104 | 110 | PF00069 | 0.516 |
MOD_PKA_1 | 111 | 117 | PF00069 | 0.478 |
MOD_PKA_2 | 157 | 163 | PF00069 | 0.615 |
MOD_PKA_2 | 52 | 58 | PF00069 | 0.670 |
MOD_PKB_1 | 132 | 140 | PF00069 | 0.547 |
MOD_Plk_4 | 35 | 41 | PF00069 | 0.565 |
MOD_ProDKin_1 | 18 | 24 | PF00069 | 0.611 |
TRG_DiLeu_BaLyEn_6 | 15 | 20 | PF01217 | 0.490 |
TRG_ER_diArg_1 | 113 | 116 | PF00400 | 0.675 |
TRG_ER_diArg_1 | 131 | 134 | PF00400 | 0.392 |
TRG_ER_diArg_1 | 50 | 53 | PF00400 | 0.651 |
TRG_NLS_Bipartite_1 | 94 | 116 | PF00514 | 0.555 |
TRG_NLS_MonoExtC_3 | 110 | 115 | PF00514 | 0.560 |
TRG_NLS_MonoExtC_3 | 118 | 123 | PF00514 | 0.487 |
TRG_NLS_MonoExtN_4 | 111 | 116 | PF00514 | 0.564 |
TRG_NLS_MonoExtN_4 | 119 | 126 | PF00514 | 0.478 |