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: A4HL61
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 2 |
GO:0006396 | RNA processing | 6 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016070 | RNA metabolic process | 5 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0090304 | nucleic acid metabolic process | 4 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 2 |
GO:0003723 | RNA binding | 4 | 2 |
GO:0003824 | catalytic activity | 1 | 2 |
GO:0004000 | adenosine deaminase activity | 4 | 2 |
GO:0005488 | binding | 1 | 2 |
GO:0016787 | hydrolase activity | 2 | 2 |
GO:0016810 | hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds | 3 | 2 |
GO:0016814 | hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in cyclic amidines | 4 | 2 |
GO:0019239 | deaminase activity | 3 | 2 |
GO:0097159 | organic cyclic compound binding | 2 | 2 |
GO:1901363 | heterocyclic compound binding | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 260 | 264 | PF00656 | 0.808 |
CLV_NRD_NRD_1 | 124 | 126 | PF00675 | 0.830 |
CLV_NRD_NRD_1 | 177 | 179 | PF00675 | 0.769 |
CLV_NRD_NRD_1 | 19 | 21 | PF00675 | 0.449 |
CLV_NRD_NRD_1 | 62 | 64 | PF00675 | 0.723 |
CLV_PCSK_FUR_1 | 60 | 64 | PF00082 | 0.699 |
CLV_PCSK_KEX2_1 | 126 | 128 | PF00082 | 0.829 |
CLV_PCSK_KEX2_1 | 177 | 179 | PF00082 | 0.769 |
CLV_PCSK_KEX2_1 | 18 | 20 | PF00082 | 0.449 |
CLV_PCSK_KEX2_1 | 62 | 64 | PF00082 | 0.723 |
CLV_PCSK_PC1ET2_1 | 126 | 128 | PF00082 | 0.829 |
CLV_PCSK_PC7_1 | 173 | 179 | PF00082 | 0.772 |
CLV_PCSK_SKI1_1 | 92 | 96 | PF00082 | 0.820 |
DEG_APCC_DBOX_1 | 19 | 27 | PF00400 | 0.650 |
DEG_SCF_TRCP1_1 | 107 | 113 | PF00400 | 0.798 |
DOC_MAPK_DCC_7 | 18 | 28 | PF00069 | 0.650 |
DOC_MAPK_gen_1 | 6 | 15 | PF00069 | 0.650 |
DOC_MAPK_MEF2A_6 | 200 | 207 | PF00069 | 0.756 |
DOC_MAPK_NFAT4_5 | 200 | 208 | PF00069 | 0.756 |
DOC_PP1_RVXF_1 | 266 | 272 | PF00149 | 0.742 |
DOC_PP4_FxxP_1 | 24 | 27 | PF00568 | 0.650 |
DOC_USP7_MATH_1 | 133 | 137 | PF00917 | 0.830 |
DOC_USP7_MATH_1 | 223 | 227 | PF00917 | 0.815 |
DOC_USP7_MATH_1 | 96 | 100 | PF00917 | 0.839 |
LIG_14-3-3_CanoR_1 | 177 | 183 | PF00244 | 0.776 |
LIG_14-3-3_CanoR_1 | 18 | 24 | PF00244 | 0.650 |
LIG_14-3-3_CanoR_1 | 62 | 72 | PF00244 | 0.755 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.650 |
LIG_Clathr_ClatBox_1 | 275 | 279 | PF01394 | 0.762 |
LIG_deltaCOP1_diTrp_1 | 5 | 10 | PF00928 | 0.650 |
LIG_EH1_1 | 198 | 206 | PF00400 | 0.752 |
LIG_FHA_1 | 2 | 8 | PF00498 | 0.650 |
LIG_FHA_1 | 209 | 215 | PF00498 | 0.801 |
LIG_FHA_2 | 148 | 154 | PF00498 | 0.790 |
LIG_FHA_2 | 179 | 185 | PF00498 | 0.768 |
LIG_FHA_2 | 237 | 243 | PF00498 | 0.808 |
LIG_FHA_2 | 260 | 266 | PF00498 | 0.806 |
LIG_LIR_Apic_2 | 142 | 148 | PF02991 | 0.770 |
LIG_LIR_Apic_2 | 22 | 27 | PF02991 | 0.650 |
LIG_LIR_Gen_1 | 113 | 122 | PF02991 | 0.772 |
LIG_LIR_Gen_1 | 38 | 46 | PF02991 | 0.650 |
LIG_LIR_Gen_1 | 77 | 88 | PF02991 | 0.707 |
LIG_LIR_Nem_3 | 113 | 118 | PF02991 | 0.750 |
LIG_LIR_Nem_3 | 136 | 141 | PF02991 | 0.811 |
LIG_LIR_Nem_3 | 234 | 240 | PF02991 | 0.818 |
LIG_LIR_Nem_3 | 38 | 43 | PF02991 | 0.650 |
LIG_LIR_Nem_3 | 77 | 83 | PF02991 | 0.681 |
LIG_SH2_NCK_1 | 227 | 231 | PF00017 | 0.818 |
LIG_SH2_SRC | 227 | 230 | PF00017 | 0.819 |
LIG_SH2_STAP1 | 233 | 237 | PF00017 | 0.823 |
LIG_SH2_STAT3 | 255 | 258 | PF00017 | 0.816 |
LIG_SH3_3 | 69 | 75 | PF00018 | 0.752 |
LIG_SxIP_EBH_1 | 177 | 191 | PF03271 | 0.759 |
LIG_UBA3_1 | 203 | 209 | PF00899 | 0.763 |
MOD_CK1_1 | 105 | 111 | PF00069 | 0.811 |
MOD_CK1_1 | 180 | 186 | PF00069 | 0.766 |
MOD_CK1_1 | 217 | 223 | PF00069 | 0.813 |
MOD_CK1_1 | 236 | 242 | PF00069 | 0.481 |
MOD_CK1_1 | 81 | 87 | PF00069 | 0.719 |
MOD_CK2_1 | 125 | 131 | PF00069 | 0.834 |
MOD_CK2_1 | 178 | 184 | PF00069 | 0.771 |
MOD_CK2_1 | 228 | 234 | PF00069 | 0.817 |
MOD_CK2_1 | 63 | 69 | PF00069 | 0.748 |
MOD_CK2_1 | 81 | 87 | PF00069 | 0.403 |
MOD_Cter_Amidation | 16 | 19 | PF01082 | 0.449 |
MOD_GlcNHglycan | 107 | 110 | PF01048 | 0.806 |
MOD_GlcNHglycan | 134 | 138 | PF01048 | 0.831 |
MOD_GlcNHglycan | 223 | 226 | PF01048 | 0.813 |
MOD_GlcNHglycan | 259 | 262 | PF01048 | 0.817 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.722 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.823 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.813 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.810 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.793 |
MOD_N-GLC_1 | 105 | 110 | PF02516 | 0.813 |
MOD_NEK2_1 | 116 | 121 | PF00069 | 0.773 |
MOD_NEK2_1 | 246 | 251 | PF00069 | 0.784 |
MOD_NEK2_1 | 257 | 262 | PF00069 | 0.628 |
MOD_NEK2_1 | 270 | 275 | PF00069 | 0.496 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.650 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.780 |
MOD_NEK2_2 | 78 | 83 | PF00069 | 0.680 |
MOD_PIKK_1 | 246 | 252 | PF00454 | 0.784 |
MOD_PK_1 | 29 | 35 | PF00069 | 0.650 |
MOD_PKA_1 | 125 | 131 | PF00069 | 0.834 |
MOD_PKA_1 | 177 | 183 | PF00069 | 0.776 |
MOD_PKA_1 | 19 | 25 | PF00069 | 0.650 |
MOD_PKA_2 | 177 | 183 | PF00069 | 0.776 |
MOD_PKA_2 | 19 | 25 | PF00069 | 0.650 |
MOD_Plk_1 | 133 | 139 | PF00069 | 0.827 |
MOD_Plk_1 | 233 | 239 | PF00069 | 0.819 |
MOD_Plk_1 | 244 | 250 | PF00069 | 0.597 |
MOD_Plk_4 | 117 | 123 | PF00069 | 0.787 |
MOD_Plk_4 | 154 | 160 | PF00069 | 0.739 |
MOD_Plk_4 | 19 | 25 | PF00069 | 0.650 |
MOD_Plk_4 | 228 | 234 | PF00069 | 0.817 |
MOD_Plk_4 | 271 | 277 | PF00069 | 0.733 |
MOD_SUMO_rev_2 | 119 | 128 | PF00179 | 0.817 |
MOD_SUMO_rev_2 | 71 | 81 | PF00179 | 0.712 |
TRG_DiLeu_BaLyEn_6 | 265 | 270 | PF01217 | 0.764 |
TRG_ER_diArg_1 | 112 | 115 | PF00400 | 0.770 |
TRG_ER_diArg_1 | 176 | 178 | PF00400 | 0.785 |
TRG_ER_diArg_1 | 18 | 20 | PF00400 | 0.650 |
TRG_ER_diArg_1 | 59 | 62 | PF00400 | 0.691 |