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: A4H5P2
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 | 274 | 278 | PF00656 | 0.427 |
CLV_C14_Caspase3-7 | 291 | 295 | PF00656 | 0.405 |
CLV_NRD_NRD_1 | 120 | 122 | PF00675 | 0.235 |
CLV_NRD_NRD_1 | 227 | 229 | PF00675 | 0.303 |
CLV_NRD_NRD_1 | 300 | 302 | PF00675 | 0.547 |
CLV_PCSK_KEX2_1 | 120 | 122 | PF00082 | 0.225 |
CLV_PCSK_KEX2_1 | 227 | 229 | PF00082 | 0.263 |
CLV_PCSK_KEX2_1 | 237 | 239 | PF00082 | 0.215 |
CLV_PCSK_KEX2_1 | 299 | 301 | PF00082 | 0.448 |
CLV_PCSK_PC1ET2_1 | 237 | 239 | PF00082 | 0.235 |
CLV_PCSK_SKI1_1 | 171 | 175 | PF00082 | 0.330 |
DEG_COP1_1 | 309 | 318 | PF00400 | 0.285 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.454 |
DOC_CKS1_1 | 42 | 47 | PF01111 | 0.530 |
DOC_MAPK_DCC_7 | 76 | 85 | PF00069 | 0.530 |
DOC_MAPK_RevD_3 | 285 | 301 | PF00069 | 0.362 |
DOC_PP2B_LxvP_1 | 312 | 315 | PF13499 | 0.342 |
DOC_PP4_FxxP_1 | 29 | 32 | PF00568 | 0.377 |
DOC_USP7_MATH_1 | 142 | 146 | PF00917 | 0.474 |
DOC_USP7_MATH_1 | 260 | 264 | PF00917 | 0.516 |
DOC_USP7_MATH_1 | 267 | 271 | PF00917 | 0.466 |
DOC_USP7_MATH_1 | 318 | 322 | PF00917 | 0.303 |
DOC_USP7_MATH_1 | 333 | 337 | PF00917 | 0.574 |
DOC_USP7_MATH_1 | 89 | 93 | PF00917 | 0.391 |
DOC_WW_Pin1_4 | 41 | 46 | PF00397 | 0.521 |
LIG_14-3-3_CanoR_1 | 76 | 81 | PF00244 | 0.448 |
LIG_Actin_WH2_2 | 163 | 178 | PF00022 | 0.373 |
LIG_AP2alpha_2 | 322 | 324 | PF02296 | 0.399 |
LIG_APCC_ABBA_1 | 214 | 219 | PF00400 | 0.435 |
LIG_BRCT_BRCA1_1 | 320 | 324 | PF00533 | 0.391 |
LIG_CaM_IQ_9 | 163 | 178 | PF13499 | 0.373 |
LIG_FHA_1 | 102 | 108 | PF00498 | 0.373 |
LIG_FHA_1 | 231 | 237 | PF00498 | 0.508 |
LIG_FHA_1 | 279 | 285 | PF00498 | 0.503 |
LIG_FHA_1 | 302 | 308 | PF00498 | 0.498 |
LIG_FHA_1 | 314 | 320 | PF00498 | 0.444 |
LIG_FHA_1 | 45 | 51 | PF00498 | 0.469 |
LIG_FHA_1 | 57 | 63 | PF00498 | 0.379 |
LIG_FHA_1 | 68 | 74 | PF00498 | 0.491 |
LIG_FHA_2 | 1 | 7 | PF00498 | 0.422 |
LIG_FHA_2 | 184 | 190 | PF00498 | 0.556 |
LIG_FHA_2 | 272 | 278 | PF00498 | 0.500 |
LIG_LIR_Gen_1 | 196 | 207 | PF02991 | 0.451 |
LIG_LIR_Gen_1 | 229 | 240 | PF02991 | 0.456 |
LIG_LIR_Gen_1 | 248 | 255 | PF02991 | 0.512 |
LIG_LIR_Gen_1 | 258 | 267 | PF02991 | 0.505 |
LIG_LIR_Gen_1 | 321 | 330 | PF02991 | 0.531 |
LIG_LIR_Nem_3 | 196 | 202 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 24 | 29 | PF02991 | 0.285 |
LIG_LIR_Nem_3 | 248 | 253 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 258 | 264 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 321 | 327 | PF02991 | 0.406 |
LIG_NRBOX | 126 | 132 | PF00104 | 0.530 |
LIG_NRBOX | 209 | 215 | PF00104 | 0.373 |
LIG_NRBOX | 307 | 313 | PF00104 | 0.407 |
LIG_SH2_NCK_1 | 261 | 265 | PF00017 | 0.374 |
LIG_SH2_NCK_1 | 60 | 64 | PF00017 | 0.492 |
LIG_SH2_PTP2 | 201 | 204 | PF00017 | 0.456 |
LIG_SH2_STAP1 | 261 | 265 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 165 | 168 | PF00017 | 0.537 |
LIG_SH2_STAT5 | 201 | 204 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 54 | 57 | PF00017 | 0.425 |
LIG_SH3_3 | 261 | 267 | PF00018 | 0.495 |
LIG_SH3_3 | 312 | 318 | PF00018 | 0.416 |
LIG_SH3_3 | 39 | 45 | PF00018 | 0.530 |
LIG_SH3_3 | 82 | 88 | PF00018 | 0.441 |
LIG_SUMO_SIM_anti_2 | 106 | 111 | PF11976 | 0.491 |
LIG_SUMO_SIM_par_1 | 106 | 111 | PF11976 | 0.435 |
LIG_SUMO_SIM_par_1 | 288 | 294 | PF11976 | 0.463 |
LIG_TRAF2_1 | 3 | 6 | PF00917 | 0.350 |
LIG_TRAF2_2 | 82 | 87 | PF00917 | 0.463 |
LIG_UBA3_1 | 252 | 256 | PF00899 | 0.463 |
LIG_UBA3_1 | 38 | 46 | PF00899 | 0.494 |
MOD_CDK_SPK_2 | 41 | 46 | PF00069 | 0.530 |
MOD_CK1_1 | 154 | 160 | PF00069 | 0.479 |
MOD_CK2_1 | 183 | 189 | PF00069 | 0.524 |
MOD_GlcNHglycan | 110 | 113 | PF01048 | 0.239 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.258 |
MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.248 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.224 |
MOD_GlcNHglycan | 23 | 26 | PF01048 | 0.303 |
MOD_GlcNHglycan | 274 | 277 | PF01048 | 0.403 |
MOD_GlcNHglycan | 336 | 339 | PF01048 | 0.621 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.456 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.488 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.521 |
MOD_GSK3_1 | 267 | 274 | PF00069 | 0.575 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.551 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.381 |
MOD_NEK2_1 | 166 | 171 | PF00069 | 0.532 |
MOD_NEK2_1 | 195 | 200 | PF00069 | 0.552 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.339 |
MOD_NEK2_1 | 218 | 223 | PF00069 | 0.506 |
MOD_NEK2_2 | 112 | 117 | PF00069 | 0.435 |
MOD_PIKK_1 | 218 | 224 | PF00454 | 0.491 |
MOD_PKB_1 | 299 | 307 | PF00069 | 0.468 |
MOD_Plk_1 | 67 | 73 | PF00069 | 0.463 |
MOD_Plk_2-3 | 31 | 37 | PF00069 | 0.461 |
MOD_Plk_4 | 112 | 118 | PF00069 | 0.425 |
MOD_Plk_4 | 161 | 167 | PF00069 | 0.530 |
MOD_Plk_4 | 68 | 74 | PF00069 | 0.505 |
MOD_ProDKin_1 | 41 | 47 | PF00069 | 0.521 |
TRG_DiLeu_BaEn_1 | 68 | 73 | PF01217 | 0.463 |
TRG_ENDOCYTIC_2 | 201 | 204 | PF00928 | 0.453 |
TRG_ENDOCYTIC_2 | 26 | 29 | PF00928 | 0.336 |
TRG_ENDOCYTIC_2 | 261 | 264 | PF00928 | 0.233 |
TRG_ER_diArg_1 | 119 | 121 | PF00400 | 0.435 |
TRG_ER_diArg_1 | 226 | 228 | PF00400 | 0.491 |
TRG_ER_diArg_1 | 299 | 301 | PF00400 | 0.433 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I426 | Leptomonas seymouri | 74% | 100% |
A0A0S4KJ65 | Bodo saltans | 40% | 95% |
A0A1X0NMP2 | Trypanosomatidae | 48% | 100% |
A0A3S7WQM7 | Leishmania donovani | 85% | 100% |
A0A422NV72 | Trypanosoma rangeli | 51% | 100% |
A4HTY1 | Leishmania infantum | 85% | 100% |
D0A9D7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
E9AMR1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
P41179 | Trypanosoma brucei brucei | 34% | 100% |
Q4QHW4 | Leishmania major | 84% | 100% |
V5BII1 | Trypanosoma cruzi | 48% | 97% |