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: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: E9AMR1
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0019538 | protein metabolic process | 3 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0008233 | peptidase activity | 3 | 12 |
GO:0008236 | serine-type peptidase activity | 4 | 12 |
GO:0016787 | hydrolase activity | 2 | 12 |
GO:0017171 | serine hydrolase activity | 3 | 12 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 283 | 287 | PF00656 | 0.404 |
CLV_C14_Caspase3-7 | 84 | 88 | PF00656 | 0.384 |
CLV_NRD_NRD_1 | 112 | 114 | PF00675 | 0.234 |
CLV_NRD_NRD_1 | 219 | 221 | PF00675 | 0.301 |
CLV_PCSK_KEX2_1 | 112 | 114 | PF00082 | 0.223 |
CLV_PCSK_KEX2_1 | 163 | 165 | PF00082 | 0.233 |
CLV_PCSK_KEX2_1 | 219 | 221 | PF00082 | 0.261 |
CLV_PCSK_KEX2_1 | 229 | 231 | PF00082 | 0.213 |
CLV_PCSK_PC1ET2_1 | 163 | 165 | PF00082 | 0.233 |
CLV_PCSK_PC1ET2_1 | 229 | 231 | PF00082 | 0.234 |
CLV_PCSK_SKI1_1 | 164 | 168 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 226 | 230 | PF00082 | 0.229 |
DEG_SPOP_SBC_1 | 325 | 329 | PF00917 | 0.491 |
DOC_CKS1_1 | 34 | 39 | PF01111 | 0.528 |
DOC_CYCLIN_yCln2_LP_2 | 304 | 310 | PF00134 | 0.390 |
DOC_MAPK_DCC_7 | 68 | 77 | PF00069 | 0.528 |
DOC_MAPK_gen_1 | 163 | 171 | PF00069 | 0.433 |
DOC_PP4_FxxP_1 | 21 | 24 | PF00568 | 0.460 |
DOC_USP7_MATH_1 | 134 | 138 | PF00917 | 0.441 |
DOC_USP7_MATH_1 | 325 | 329 | PF00917 | 0.581 |
DOC_WW_Pin1_4 | 263 | 268 | PF00397 | 0.571 |
DOC_WW_Pin1_4 | 33 | 38 | PF00397 | 0.507 |
LIG_14-3-3_CanoR_1 | 263 | 267 | PF00244 | 0.572 |
LIG_14-3-3_CanoR_1 | 68 | 73 | PF00244 | 0.452 |
LIG_AP2alpha_2 | 314 | 316 | PF02296 | 0.399 |
LIG_APCC_ABBA_1 | 206 | 211 | PF00400 | 0.434 |
LIG_FHA_1 | 253 | 259 | PF00498 | 0.276 |
LIG_FHA_1 | 271 | 277 | PF00498 | 0.581 |
LIG_FHA_1 | 295 | 301 | PF00498 | 0.490 |
LIG_FHA_1 | 37 | 43 | PF00498 | 0.445 |
LIG_FHA_1 | 49 | 55 | PF00498 | 0.505 |
LIG_FHA_1 | 60 | 66 | PF00498 | 0.530 |
LIG_FHA_2 | 178 | 184 | PF00498 | 0.563 |
LIG_FHA_2 | 264 | 270 | PF00498 | 0.584 |
LIG_FHA_2 | 82 | 88 | PF00498 | 0.380 |
LIG_FHA_2 | 93 | 99 | PF00498 | 0.524 |
LIG_LIR_Apic_2 | 156 | 160 | PF02991 | 0.475 |
LIG_LIR_Apic_2 | 19 | 24 | PF02991 | 0.433 |
LIG_LIR_Gen_1 | 188 | 199 | PF02991 | 0.427 |
LIG_LIR_Gen_1 | 221 | 232 | PF02991 | 0.451 |
LIG_LIR_Gen_1 | 240 | 247 | PF02991 | 0.442 |
LIG_LIR_Gen_1 | 314 | 322 | PF02991 | 0.531 |
LIG_LIR_Nem_3 | 188 | 194 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 240 | 245 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 314 | 319 | PF02991 | 0.405 |
LIG_NRBOX | 118 | 124 | PF00104 | 0.528 |
LIG_NRBOX | 299 | 305 | PF00104 | 0.422 |
LIG_SH2_NCK_1 | 253 | 257 | PF00017 | 0.390 |
LIG_SH2_NCK_1 | 52 | 56 | PF00017 | 0.464 |
LIG_SH2_PTP2 | 193 | 196 | PF00017 | 0.434 |
LIG_SH2_STAP1 | 253 | 257 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 157 | 160 | PF00017 | 0.528 |
LIG_SH2_STAT5 | 193 | 196 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 46 | 49 | PF00017 | 0.423 |
LIG_SH3_3 | 304 | 310 | PF00018 | 0.436 |
LIG_SH3_3 | 31 | 37 | PF00018 | 0.528 |
LIG_SUMO_SIM_anti_2 | 98 | 103 | PF11976 | 0.490 |
LIG_SUMO_SIM_par_1 | 280 | 286 | PF11976 | 0.470 |
LIG_SUMO_SIM_par_1 | 309 | 314 | PF11976 | 0.348 |
LIG_SUMO_SIM_par_1 | 98 | 103 | PF11976 | 0.434 |
LIG_TRAF2_2 | 74 | 79 | PF00917 | 0.460 |
LIG_UBA3_1 | 244 | 248 | PF00899 | 0.497 |
LIG_UBA3_1 | 30 | 38 | PF00899 | 0.493 |
MOD_CDK_SPK_2 | 33 | 38 | PF00069 | 0.528 |
MOD_CK1_1 | 146 | 152 | PF00069 | 0.464 |
MOD_CK1_1 | 328 | 334 | PF00069 | 0.643 |
MOD_CK2_1 | 175 | 181 | PF00069 | 0.517 |
MOD_CK2_1 | 54 | 60 | PF00069 | 0.473 |
MOD_DYRK1A_RPxSP_1 | 263 | 267 | PF00069 | 0.483 |
MOD_GlcNHglycan | 102 | 105 | PF01048 | 0.238 |
MOD_GlcNHglycan | 136 | 139 | PF01048 | 0.233 |
MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.226 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.221 |
MOD_GlcNHglycan | 150 | 153 | PF01048 | 0.207 |
MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.627 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.434 |
MOD_GSK3_1 | 142 | 149 | PF00069 | 0.447 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.500 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.530 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.613 |
MOD_GSK3_1 | 268 | 275 | PF00069 | 0.586 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.512 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.546 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.505 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.455 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.376 |
MOD_N-GLC_1 | 85 | 90 | PF02516 | 0.192 |
MOD_NEK2_1 | 13 | 18 | PF00069 | 0.295 |
MOD_NEK2_1 | 187 | 192 | PF00069 | 0.528 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.489 |
MOD_NEK2_1 | 54 | 59 | PF00069 | 0.433 |
MOD_NEK2_1 | 92 | 97 | PF00069 | 0.433 |
MOD_NEK2_2 | 104 | 109 | PF00069 | 0.434 |
MOD_PIKK_1 | 210 | 216 | PF00454 | 0.498 |
MOD_PIKK_1 | 54 | 60 | PF00454 | 0.533 |
MOD_PKA_2 | 262 | 268 | PF00069 | 0.509 |
MOD_Plk_1 | 59 | 65 | PF00069 | 0.460 |
MOD_Plk_2-3 | 23 | 29 | PF00069 | 0.528 |
MOD_Plk_4 | 104 | 110 | PF00069 | 0.423 |
MOD_Plk_4 | 153 | 159 | PF00069 | 0.528 |
MOD_Plk_4 | 29 | 35 | PF00069 | 0.507 |
MOD_Plk_4 | 328 | 334 | PF00069 | 0.638 |
MOD_Plk_4 | 60 | 66 | PF00069 | 0.503 |
MOD_ProDKin_1 | 263 | 269 | PF00069 | 0.578 |
MOD_ProDKin_1 | 33 | 39 | PF00069 | 0.507 |
TRG_DiLeu_BaEn_1 | 60 | 65 | PF01217 | 0.460 |
TRG_ENDOCYTIC_2 | 193 | 196 | PF00928 | 0.423 |
TRG_ER_diArg_1 | 111 | 113 | PF00400 | 0.434 |
TRG_ER_diArg_1 | 218 | 220 | PF00400 | 0.490 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I426 | Leptomonas seymouri | 72% | 100% |
A0A0S4KJ65 | Bodo saltans | 40% | 93% |
A0A1X0NMP2 | Trypanosomatidae | 47% | 99% |
A0A3S7WQM7 | Leishmania donovani | 92% | 100% |
A0A422NV72 | Trypanosoma rangeli | 50% | 99% |
A4H5P2 | Leishmania braziliensis | 84% | 100% |
A4HTY1 | Leishmania infantum | 92% | 100% |
D0A9D7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
P41179 | Trypanosoma brucei brucei | 33% | 100% |
Q4QHW4 | Leishmania major | 93% | 100% |
V5BII1 | Trypanosoma cruzi | 49% | 95% |