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 | yes | yes: 1, no: 10 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: A4HKB2
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 12 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 10 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009056 | catabolic process | 2 | 10 |
GO:0009057 | macromolecule catabolic process | 4 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0016579 | protein deubiquitination | 6 | 12 |
GO:0019538 | protein metabolic process | 3 | 12 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 10 |
GO:0036211 | protein modification process | 4 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043412 | macromolecule modification | 4 | 12 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 10 |
GO:0044237 | cellular metabolic process | 2 | 10 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044248 | cellular catabolic process | 3 | 10 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 10 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 10 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 10 |
GO:0070646 | protein modification by small protein removal | 5 | 12 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 12 |
GO:1901575 | organic substance catabolic process | 3 | 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004843 | cysteine-type deubiquitinase activity | 5 | 12 |
GO:0008233 | peptidase activity | 3 | 12 |
GO:0008234 | cysteine-type peptidase activity | 4 | 12 |
GO:0016787 | hydrolase activity | 2 | 12 |
GO:0019783 | ubiquitin-like protein peptidase activity | 4 | 12 |
GO:0101005 | deubiquitinase activity | 5 | 12 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 155 | 159 | PF00656 | 0.223 |
CLV_C14_Caspase3-7 | 314 | 318 | PF00656 | 0.239 |
CLV_NRD_NRD_1 | 281 | 283 | PF00675 | 0.333 |
CLV_PCSK_KEX2_1 | 281 | 283 | PF00082 | 0.329 |
CLV_PCSK_KEX2_1 | 301 | 303 | PF00082 | 0.365 |
CLV_PCSK_PC1ET2_1 | 301 | 303 | PF00082 | 0.410 |
CLV_PCSK_SKI1_1 | 261 | 265 | PF00082 | 0.311 |
CLV_PCSK_SKI1_1 | 301 | 305 | PF00082 | 0.425 |
CLV_PCSK_SKI1_1 | 47 | 51 | PF00082 | 0.203 |
CLV_PCSK_SKI1_1 | 79 | 83 | PF00082 | 0.182 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.326 |
DEG_SCF_FBW7_1 | 141 | 147 | PF00400 | 0.182 |
DEG_SPOP_SBC_1 | 146 | 150 | PF00917 | 0.299 |
DOC_CKS1_1 | 141 | 146 | PF01111 | 0.182 |
DOC_CYCLIN_RxL_1 | 299 | 309 | PF00134 | 0.338 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 261 | 267 | PF00134 | 0.395 |
DOC_MAPK_DCC_7 | 268 | 277 | PF00069 | 0.319 |
DOC_MAPK_gen_1 | 177 | 184 | PF00069 | 0.338 |
DOC_MAPK_gen_1 | 212 | 221 | PF00069 | 0.326 |
DOC_MAPK_gen_1 | 261 | 269 | PF00069 | 0.350 |
DOC_MAPK_MEF2A_6 | 214 | 223 | PF00069 | 0.424 |
DOC_MAPK_MEF2A_6 | 225 | 233 | PF00069 | 0.389 |
DOC_MAPK_MEF2A_6 | 268 | 277 | PF00069 | 0.319 |
DOC_MAPK_RevD_3 | 267 | 282 | PF00069 | 0.389 |
DOC_PP2B_LxvP_1 | 304 | 307 | PF13499 | 0.304 |
DOC_USP7_MATH_1 | 134 | 138 | PF00917 | 0.329 |
DOC_USP7_MATH_1 | 144 | 148 | PF00917 | 0.360 |
DOC_USP7_MATH_1 | 385 | 389 | PF00917 | 0.244 |
DOC_USP7_UBL2_3 | 177 | 181 | PF12436 | 0.361 |
DOC_USP7_UBL2_3 | 261 | 265 | PF12436 | 0.308 |
DOC_USP7_UBL2_3 | 393 | 397 | PF12436 | 0.424 |
DOC_WW_Pin1_4 | 140 | 145 | PF00397 | 0.338 |
DOC_WW_Pin1_4 | 161 | 166 | PF00397 | 0.421 |
DOC_WW_Pin1_4 | 348 | 353 | PF00397 | 0.390 |
DOC_WW_Pin1_4 | 369 | 374 | PF00397 | 0.429 |
DOC_WW_Pin1_4 | 79 | 84 | PF00397 | 0.362 |
LIG_14-3-3_CanoR_1 | 218 | 222 | PF00244 | 0.383 |
LIG_14-3-3_CanoR_1 | 324 | 329 | PF00244 | 0.416 |
LIG_14-3-3_CanoR_1 | 59 | 65 | PF00244 | 0.328 |
LIG_BIR_III_4 | 158 | 162 | PF00653 | 0.182 |
LIG_BIR_III_4 | 189 | 193 | PF00653 | 0.356 |
LIG_BIR_III_4 | 334 | 338 | PF00653 | 0.182 |
LIG_Clathr_ClatBox_1 | 118 | 122 | PF01394 | 0.424 |
LIG_Clathr_ClatBox_1 | 291 | 295 | PF01394 | 0.338 |
LIG_FHA_1 | 249 | 255 | PF00498 | 0.363 |
LIG_FHA_1 | 264 | 270 | PF00498 | 0.313 |
LIG_FHA_1 | 320 | 326 | PF00498 | 0.235 |
LIG_FHA_1 | 341 | 347 | PF00498 | 0.341 |
LIG_FHA_1 | 349 | 355 | PF00498 | 0.328 |
LIG_FHA_1 | 376 | 382 | PF00498 | 0.401 |
LIG_Integrin_RGD_1 | 332 | 334 | PF01839 | 0.424 |
LIG_LIR_Apic_2 | 224 | 230 | PF02991 | 0.424 |
LIG_LIR_Gen_1 | 105 | 114 | PF02991 | 0.316 |
LIG_LIR_Gen_1 | 21 | 29 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 21 | 25 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 224 | 229 | PF02991 | 0.310 |
LIG_LIR_Nem_3 | 320 | 326 | PF02991 | 0.312 |
LIG_LIR_Nem_3 | 398 | 404 | PF02991 | 0.298 |
LIG_MYND_1 | 65 | 69 | PF01753 | 0.450 |
LIG_NRBOX | 106 | 112 | PF00104 | 0.361 |
LIG_Pex14_1 | 48 | 52 | PF04695 | 0.319 |
LIG_Pex14_1 | 53 | 57 | PF04695 | 0.319 |
LIG_Pex14_2 | 18 | 22 | PF04695 | 0.338 |
LIG_SH2_CRK | 227 | 231 | PF00017 | 0.450 |
LIG_SH2_CRK | 323 | 327 | PF00017 | 0.338 |
LIG_SH2_STAT5 | 208 | 211 | PF00017 | 0.182 |
LIG_SH2_STAT5 | 227 | 230 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 341 | 344 | PF00017 | 0.304 |
LIG_SH2_STAT5 | 401 | 404 | PF00017 | 0.304 |
LIG_SH3_3 | 138 | 144 | PF00018 | 0.182 |
LIG_SH3_3 | 66 | 72 | PF00018 | 0.450 |
LIG_SUMO_SIM_anti_2 | 217 | 224 | PF11976 | 0.393 |
LIG_SUMO_SIM_par_1 | 116 | 123 | PF11976 | 0.223 |
LIG_TRAF2_1 | 98 | 101 | PF00917 | 0.338 |
LIG_TYR_ITSM | 397 | 404 | PF00017 | 0.424 |
LIG_WRC_WIRS_1 | 19 | 24 | PF05994 | 0.409 |
LIG_WRC_WIRS_1 | 42 | 47 | PF05994 | 0.182 |
MOD_CK1_1 | 120 | 126 | PF00069 | 0.284 |
MOD_CK1_1 | 145 | 151 | PF00069 | 0.393 |
MOD_CK2_1 | 120 | 126 | PF00069 | 0.321 |
MOD_CK2_1 | 254 | 260 | PF00069 | 0.381 |
MOD_CK2_1 | 95 | 101 | PF00069 | 0.324 |
MOD_DYRK1A_RPxSP_1 | 140 | 144 | PF00069 | 0.182 |
MOD_GlcNHglycan | 136 | 139 | PF01048 | 0.320 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.381 |
MOD_GlcNHglycan | 165 | 168 | PF01048 | 0.250 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.190 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.405 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.411 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.328 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.390 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.448 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.416 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.349 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.233 |
MOD_N-GLC_1 | 161 | 166 | PF02516 | 0.318 |
MOD_N-GLC_1 | 385 | 390 | PF02516 | 0.428 |
MOD_N-GLC_2 | 5 | 7 | PF02516 | 0.319 |
MOD_NEK2_1 | 196 | 201 | PF00069 | 0.386 |
MOD_NEK2_1 | 245 | 250 | PF00069 | 0.304 |
MOD_NEK2_1 | 25 | 30 | PF00069 | 0.120 |
MOD_NEK2_1 | 263 | 268 | PF00069 | 0.319 |
MOD_NEK2_1 | 60 | 65 | PF00069 | 0.402 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.318 |
MOD_NEK2_1 | 95 | 100 | PF00069 | 0.330 |
MOD_PIKK_1 | 88 | 94 | PF00454 | 0.377 |
MOD_PK_1 | 324 | 330 | PF00069 | 0.450 |
MOD_PKA_2 | 139 | 145 | PF00069 | 0.328 |
MOD_PKA_2 | 217 | 223 | PF00069 | 0.450 |
MOD_Plk_1 | 237 | 243 | PF00069 | 0.319 |
MOD_Plk_1 | 245 | 251 | PF00069 | 0.193 |
MOD_Plk_1 | 312 | 318 | PF00069 | 0.298 |
MOD_Plk_1 | 319 | 325 | PF00069 | 0.300 |
MOD_Plk_1 | 385 | 391 | PF00069 | 0.424 |
MOD_Plk_2-3 | 117 | 123 | PF00069 | 0.335 |
MOD_Plk_4 | 120 | 126 | PF00069 | 0.182 |
MOD_Plk_4 | 196 | 202 | PF00069 | 0.397 |
MOD_Plk_4 | 204 | 210 | PF00069 | 0.359 |
MOD_Plk_4 | 217 | 223 | PF00069 | 0.307 |
MOD_Plk_4 | 324 | 330 | PF00069 | 0.362 |
MOD_Plk_4 | 340 | 346 | PF00069 | 0.335 |
MOD_Plk_4 | 375 | 381 | PF00069 | 0.389 |
MOD_Plk_4 | 396 | 402 | PF00069 | 0.424 |
MOD_Plk_4 | 8 | 14 | PF00069 | 0.416 |
MOD_ProDKin_1 | 140 | 146 | PF00069 | 0.338 |
MOD_ProDKin_1 | 161 | 167 | PF00069 | 0.421 |
MOD_ProDKin_1 | 348 | 354 | PF00069 | 0.390 |
MOD_ProDKin_1 | 369 | 375 | PF00069 | 0.429 |
MOD_ProDKin_1 | 79 | 85 | PF00069 | 0.362 |
TRG_DiLeu_BaEn_2 | 397 | 403 | PF01217 | 0.389 |
TRG_DiLeu_BaEn_4 | 116 | 122 | PF01217 | 0.450 |
TRG_DiLeu_BaLyEn_6 | 321 | 326 | PF01217 | 0.424 |
TRG_ENDOCYTIC_2 | 226 | 229 | PF00928 | 0.424 |
TRG_ENDOCYTIC_2 | 323 | 326 | PF00928 | 0.304 |
TRG_ENDOCYTIC_2 | 401 | 404 | PF00928 | 0.304 |
TRG_ER_diArg_1 | 280 | 282 | PF00400 | 0.350 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IMP3 | Leptomonas seymouri | 65% | 80% |
A0A0S4IXL6 | Bodo saltans | 32% | 75% |
A0A1X0NUI1 | Trypanosomatidae | 43% | 92% |
A0A3S7X5G6 | Leishmania donovani | 78% | 97% |
A0A422P1B8 | Trypanosoma rangeli | 41% | 93% |
A4I7U2 | Leishmania infantum | 78% | 76% |
D0AA02 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 93% |
E9B2Q0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 100% |
O94269 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 24% | 80% |
Q4Q5F7 | Leishmania major | 78% | 100% |
Q9FPS3 | Arabidopsis thaliana | 25% | 74% |
V5DHM6 | Trypanosoma cruzi | 40% | 100% |