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. | yes | yes: 5 |
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 | yes | yes: 4, no: 1 |
NetGPI | no | yes: 0, no: 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
Related structures:
AlphaFold database: A4HJI0
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 6 |
GO:0006807 | nitrogen compound metabolic process | 2 | 6 |
GO:0007155 | cell adhesion | 2 | 6 |
GO:0008152 | metabolic process | 1 | 6 |
GO:0009987 | cellular process | 1 | 6 |
GO:0019538 | protein metabolic process | 3 | 6 |
GO:0043170 | macromolecule metabolic process | 3 | 6 |
GO:0044238 | primary metabolic process | 2 | 6 |
GO:0071704 | organic substance metabolic process | 2 | 6 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 6 |
GO:0004175 | endopeptidase activity | 4 | 6 |
GO:0004222 | metalloendopeptidase activity | 5 | 6 |
GO:0005488 | binding | 1 | 6 |
GO:0008233 | peptidase activity | 3 | 6 |
GO:0008237 | metallopeptidase activity | 4 | 6 |
GO:0016787 | hydrolase activity | 2 | 6 |
GO:0043167 | ion binding | 2 | 6 |
GO:0043169 | cation binding | 3 | 6 |
GO:0046872 | metal ion binding | 4 | 6 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 6 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 107 | 111 | PF00656 | 0.310 |
CLV_NRD_NRD_1 | 68 | 70 | PF00675 | 0.590 |
CLV_PCSK_KEX2_1 | 161 | 163 | PF00082 | 0.386 |
CLV_PCSK_KEX2_1 | 68 | 70 | PF00082 | 0.590 |
CLV_PCSK_KEX2_1 | 83 | 85 | PF00082 | 0.486 |
CLV_PCSK_PC1ET2_1 | 161 | 163 | PF00082 | 0.386 |
CLV_PCSK_PC1ET2_1 | 83 | 85 | PF00082 | 0.446 |
DEG_SCF_FBW7_2 | 120 | 126 | PF00400 | 0.186 |
DOC_CKS1_1 | 120 | 125 | PF01111 | 0.186 |
DOC_MAPK_MEF2A_6 | 10 | 19 | PF00069 | 0.417 |
DOC_MAPK_MEF2A_6 | 75 | 82 | PF00069 | 0.444 |
DOC_MAPK_NFAT4_5 | 10 | 18 | PF00069 | 0.354 |
DOC_PP4_FxxP_1 | 204 | 207 | PF00568 | 0.189 |
DOC_USP7_MATH_1 | 140 | 144 | PF00917 | 0.186 |
DOC_USP7_MATH_1 | 28 | 32 | PF00917 | 0.624 |
DOC_USP7_MATH_1 | 5 | 9 | PF00917 | 0.428 |
DOC_WW_Pin1_4 | 119 | 124 | PF00397 | 0.186 |
DOC_WW_Pin1_4 | 228 | 233 | PF00397 | 0.186 |
DOC_WW_Pin1_4 | 43 | 48 | PF00397 | 0.448 |
LIG_14-3-3_CanoR_1 | 148 | 153 | PF00244 | 0.186 |
LIG_14-3-3_CanoR_1 | 162 | 170 | PF00244 | 0.221 |
LIG_14-3-3_CanoR_1 | 99 | 105 | PF00244 | 0.186 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.410 |
LIG_FHA_1 | 120 | 126 | PF00498 | 0.198 |
LIG_FHA_1 | 187 | 193 | PF00498 | 0.210 |
LIG_FHA_1 | 210 | 216 | PF00498 | 0.190 |
LIG_FHA_1 | 24 | 30 | PF00498 | 0.577 |
LIG_FHA_1 | 246 | 252 | PF00498 | 0.201 |
LIG_LIR_Apic_2 | 203 | 207 | PF02991 | 0.198 |
LIG_LIR_Nem_3 | 110 | 116 | PF02991 | 0.186 |
LIG_LIR_Nem_3 | 217 | 223 | PF02991 | 0.190 |
LIG_LIR_Nem_3 | 63 | 67 | PF02991 | 0.463 |
LIG_PTB_Apo_2 | 260 | 267 | PF02174 | 0.221 |
LIG_PTB_Phospho_1 | 260 | 266 | PF10480 | 0.221 |
LIG_SH2_GRB2like | 261 | 264 | PF00017 | 0.186 |
LIG_SH2_PTP2 | 64 | 67 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 131 | 134 | PF00017 | 0.221 |
LIG_SH2_STAT5 | 21 | 24 | PF00017 | 0.377 |
LIG_SH2_STAT5 | 223 | 226 | PF00017 | 0.189 |
LIG_SH2_STAT5 | 261 | 264 | PF00017 | 0.199 |
LIG_SH2_STAT5 | 266 | 269 | PF00017 | 0.245 |
LIG_SH2_STAT5 | 64 | 67 | PF00017 | 0.461 |
LIG_SH3_3 | 117 | 123 | PF00018 | 0.186 |
LIG_SH3_3 | 179 | 185 | PF00018 | 0.248 |
LIG_SH3_3 | 210 | 216 | PF00018 | 0.186 |
LIG_SUMO_SIM_par_1 | 188 | 195 | PF11976 | 0.186 |
LIG_TYR_ITIM | 62 | 67 | PF00017 | 0.455 |
MOD_CDK_SPK_2 | 228 | 233 | PF00069 | 0.192 |
MOD_CK1_1 | 105 | 111 | PF00069 | 0.182 |
MOD_CK1_1 | 142 | 148 | PF00069 | 0.192 |
MOD_CK1_1 | 55 | 61 | PF00069 | 0.409 |
MOD_CK1_1 | 88 | 94 | PF00069 | 0.654 |
MOD_GlcNHglycan | 110 | 113 | PF01048 | 0.241 |
MOD_GlcNHglycan | 141 | 145 | PF01048 | 0.192 |
MOD_GlcNHglycan | 31 | 34 | PF01048 | 0.418 |
MOD_GlcNHglycan | 87 | 90 | PF01048 | 0.520 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.192 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.289 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.318 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.247 |
MOD_GSK3_1 | 245 | 252 | PF00069 | 0.172 |
MOD_N-GLC_1 | 85 | 90 | PF02516 | 0.447 |
MOD_NEK2_1 | 164 | 169 | PF00069 | 0.281 |
MOD_NEK2_1 | 85 | 90 | PF00069 | 0.447 |
MOD_PK_1 | 148 | 154 | PF00069 | 0.192 |
MOD_PKA_1 | 160 | 166 | PF00069 | 0.192 |
MOD_PKA_1 | 68 | 74 | PF00069 | 0.445 |
MOD_PKA_2 | 147 | 153 | PF00069 | 0.192 |
MOD_PKA_2 | 68 | 74 | PF00069 | 0.445 |
MOD_Plk_1 | 187 | 193 | PF00069 | 0.192 |
MOD_Plk_4 | 142 | 148 | PF00069 | 0.255 |
MOD_Plk_4 | 164 | 170 | PF00069 | 0.488 |
MOD_Plk_4 | 187 | 193 | PF00069 | 0.215 |
MOD_Plk_4 | 60 | 66 | PF00069 | 0.449 |
MOD_ProDKin_1 | 119 | 125 | PF00069 | 0.192 |
MOD_ProDKin_1 | 228 | 234 | PF00069 | 0.192 |
MOD_ProDKin_1 | 43 | 49 | PF00069 | 0.442 |
TRG_ENDOCYTIC_2 | 21 | 24 | PF00928 | 0.358 |
TRG_ENDOCYTIC_2 | 64 | 67 | PF00928 | 0.461 |
TRG_ER_diArg_1 | 67 | 69 | PF00400 | 0.595 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A1X0NDC6 | Trypanosomatidae | 25% | 72% |
A0A1X0NFI2 | Trypanosomatidae | 27% | 78% |
A0A1X0P868 | Trypanosomatidae | 26% | 86% |
A0A422MNW0 | Trypanosoma rangeli | 34% | 67% |