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: 1 |
NetGPI | no | yes: 0, no: 1 |
Related structures:
AlphaFold database: A4HE04
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 135 | 137 | PF00675 | 0.807 |
CLV_NRD_NRD_1 | 174 | 176 | PF00675 | 0.686 |
CLV_PCSK_KEX2_1 | 135 | 137 | PF00082 | 0.807 |
CLV_PCSK_KEX2_1 | 144 | 146 | PF00082 | 0.539 |
CLV_PCSK_KEX2_1 | 164 | 166 | PF00082 | 0.312 |
CLV_PCSK_KEX2_1 | 174 | 176 | PF00082 | 0.511 |
CLV_PCSK_PC1ET2_1 | 144 | 146 | PF00082 | 0.697 |
CLV_PCSK_PC1ET2_1 | 164 | 166 | PF00082 | 0.312 |
CLV_PCSK_PC1ET2_1 | 174 | 176 | PF00082 | 0.511 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.870 |
DEG_SCF_FBW7_1 | 28 | 35 | PF00400 | 0.840 |
DOC_CKS1_1 | 29 | 34 | PF01111 | 0.839 |
DOC_USP7_MATH_1 | 32 | 36 | PF00917 | 0.842 |
DOC_USP7_MATH_1 | 59 | 63 | PF00917 | 0.833 |
DOC_USP7_MATH_2 | 75 | 81 | PF00917 | 0.754 |
DOC_USP7_UBL2_3 | 176 | 180 | PF12436 | 0.682 |
DOC_WW_Pin1_4 | 112 | 117 | PF00397 | 0.814 |
DOC_WW_Pin1_4 | 28 | 33 | PF00397 | 0.838 |
LIG_14-3-3_CanoR_1 | 191 | 200 | PF00244 | 0.764 |
LIG_14-3-3_CanoR_1 | 46 | 56 | PF00244 | 0.859 |
LIG_14-3-3_CanoR_1 | 6 | 15 | PF00244 | 0.816 |
LIG_AP2alpha_1 | 14 | 18 | PF02296 | 0.812 |
LIG_APCC_ABBA_1 | 217 | 222 | PF00400 | 0.699 |
LIG_FHA_1 | 108 | 114 | PF00498 | 0.814 |
LIG_FHA_1 | 115 | 121 | PF00498 | 0.699 |
LIG_FHA_2 | 156 | 162 | PF00498 | 0.659 |
LIG_FHA_2 | 76 | 82 | PF00498 | 0.744 |
LIG_LIR_Nem_3 | 204 | 210 | PF02991 | 0.735 |
LIG_MYND_1 | 197 | 201 | PF01753 | 0.758 |
LIG_NRP_CendR_1 | 224 | 226 | PF00754 | 0.755 |
LIG_Pex14_2 | 14 | 18 | PF04695 | 0.812 |
LIG_SH2_SRC | 159 | 162 | PF00017 | 0.656 |
LIG_SH2_STAT3 | 210 | 213 | PF00017 | 0.723 |
LIG_SH2_STAT5 | 159 | 162 | PF00017 | 0.656 |
LIG_SH2_STAT5 | 211 | 214 | PF00017 | 0.723 |
LIG_SH3_3 | 110 | 116 | PF00018 | 0.809 |
LIG_SxIP_EBH_1 | 189 | 202 | PF03271 | 0.761 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.550 |
MOD_CK1_1 | 114 | 120 | PF00069 | 0.700 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.857 |
MOD_CK1_1 | 92 | 98 | PF00069 | 0.747 |
MOD_CK2_1 | 155 | 161 | PF00069 | 0.661 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.857 |
MOD_GlcNHglycan | 66 | 72 | PF01048 | 0.545 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.821 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.811 |
MOD_GSK3_1 | 187 | 194 | PF00069 | 0.763 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.835 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.493 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.832 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.860 |
MOD_LATS_1 | 128 | 134 | PF00433 | 0.806 |
MOD_LATS_1 | 162 | 168 | PF00433 | 0.661 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.849 |
MOD_NEK2_1 | 103 | 108 | PF00069 | 0.810 |
MOD_NEK2_1 | 18 | 23 | PF00069 | 0.521 |
MOD_NEK2_2 | 32 | 37 | PF00069 | 0.843 |
MOD_PK_1 | 164 | 170 | PF00069 | 0.664 |
MOD_PKA_1 | 164 | 170 | PF00069 | 0.664 |
MOD_PKA_2 | 164 | 170 | PF00069 | 0.664 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.837 |
MOD_PKA_2 | 75 | 81 | PF00069 | 0.754 |
MOD_PKA_2 | 92 | 98 | PF00069 | 0.449 |
MOD_PKB_1 | 189 | 197 | PF00069 | 0.766 |
MOD_Plk_2-3 | 155 | 161 | PF00069 | 0.661 |
MOD_Plk_2-3 | 77 | 83 | PF00069 | 0.725 |
MOD_Plk_4 | 155 | 161 | PF00069 | 0.661 |
MOD_ProDKin_1 | 112 | 118 | PF00069 | 0.816 |
MOD_ProDKin_1 | 28 | 34 | PF00069 | 0.839 |
TRG_DiLeu_BaEn_1 | 86 | 91 | PF01217 | 0.700 |
TRG_ER_diArg_1 | 189 | 192 | PF00400 | 0.767 |
TRG_ER_diArg_1 | 223 | 226 | PF00400 | 0.747 |
TRG_NLS_Bipartite_1 | 163 | 178 | PF00514 | 0.671 |
TRG_NLS_MonoExtC_3 | 173 | 178 | PF00514 | 0.684 |