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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 8 |
GO:0110165 | cellular anatomical entity | 1 | 8 |
Related structures:
AlphaFold database: Q4Q5E1
Term | Name | Level | Count |
---|---|---|---|
GO:0006082 | organic acid metabolic process | 3 | 10 |
GO:0006520 | amino acid metabolic process | 3 | 10 |
GO:0006568 | tryptophan metabolic process | 5 | 10 |
GO:0006569 | tryptophan catabolic process | 5 | 10 |
GO:0006576 | biogenic amine metabolic process | 5 | 10 |
GO:0006586 | indolalkylamine metabolic process | 5 | 10 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 10 |
GO:0006807 | nitrogen compound metabolic process | 2 | 10 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0009056 | catabolic process | 2 | 10 |
GO:0009063 | amino acid catabolic process | 4 | 10 |
GO:0009072 | aromatic amino acid metabolic process | 4 | 10 |
GO:0009074 | aromatic amino acid family catabolic process | 5 | 10 |
GO:0009308 | amine metabolic process | 4 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0016054 | organic acid catabolic process | 4 | 10 |
GO:0019439 | aromatic compound catabolic process | 4 | 10 |
GO:0019441 | tryptophan catabolic process to kynurenine | 5 | 10 |
GO:0019752 | carboxylic acid metabolic process | 5 | 10 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 10 |
GO:0042180 | cellular ketone metabolic process | 3 | 10 |
GO:0042430 | indole-containing compound metabolic process | 4 | 10 |
GO:0042436 | indole-containing compound catabolic process | 5 | 10 |
GO:0042537 | benzene-containing compound metabolic process | 4 | 10 |
GO:0043436 | oxoacid metabolic process | 4 | 10 |
GO:0044237 | cellular metabolic process | 2 | 10 |
GO:0044238 | primary metabolic process | 2 | 10 |
GO:0044248 | cellular catabolic process | 3 | 10 |
GO:0044270 | cellular nitrogen compound catabolic process | 4 | 10 |
GO:0044281 | small molecule metabolic process | 2 | 10 |
GO:0044282 | small molecule catabolic process | 3 | 10 |
GO:0046395 | carboxylic acid catabolic process | 5 | 10 |
GO:0046483 | heterocycle metabolic process | 3 | 10 |
GO:0046700 | heterocycle catabolic process | 4 | 10 |
GO:0070189 | kynurenine metabolic process | 4 | 10 |
GO:0071704 | organic substance metabolic process | 2 | 10 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 10 |
GO:1901361 | organic cyclic compound catabolic process | 4 | 10 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 10 |
GO:1901565 | organonitrogen compound catabolic process | 4 | 10 |
GO:1901575 | organic substance catabolic process | 3 | 10 |
GO:1901605 | alpha-amino acid metabolic process | 4 | 10 |
GO:1901606 | alpha-amino acid catabolic process | 5 | 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 10 |
GO:0004061 | arylformamidase activity | 5 | 10 |
GO:0016787 | hydrolase activity | 2 | 10 |
GO:0016810 | hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds | 3 | 10 |
GO:0016811 | hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amides | 4 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 146 | 150 | PF00656 | 0.229 |
CLV_C14_Caspase3-7 | 168 | 172 | PF00656 | 0.361 |
CLV_NRD_NRD_1 | 105 | 107 | PF00675 | 0.475 |
CLV_NRD_NRD_1 | 12 | 14 | PF00675 | 0.564 |
CLV_PCSK_KEX2_1 | 105 | 107 | PF00082 | 0.469 |
CLV_PCSK_KEX2_1 | 19 | 21 | PF00082 | 0.607 |
CLV_PCSK_PC1ET2_1 | 19 | 21 | PF00082 | 0.621 |
CLV_PCSK_SKI1_1 | 157 | 161 | PF00082 | 0.546 |
CLV_PCSK_SKI1_1 | 20 | 24 | PF00082 | 0.657 |
CLV_PCSK_SKI1_1 | 243 | 247 | PF00082 | 0.490 |
CLV_PCSK_SKI1_1 | 270 | 274 | PF00082 | 0.594 |
CLV_PCSK_SKI1_1 | 321 | 325 | PF00082 | 0.550 |
DEG_APCC_DBOX_1 | 320 | 328 | PF00400 | 0.350 |
DEG_MDM2_SWIB_1 | 103 | 111 | PF02201 | 0.595 |
DOC_CYCLIN_RxL_1 | 239 | 248 | PF00134 | 0.294 |
DOC_MAPK_FxFP_2 | 306 | 309 | PF00069 | 0.350 |
DOC_MAPK_gen_1 | 19 | 30 | PF00069 | 0.482 |
DOC_MAPK_MEF2A_6 | 317 | 324 | PF00069 | 0.316 |
DOC_PP1_RVXF_1 | 268 | 274 | PF00149 | 0.258 |
DOC_PP4_FxxP_1 | 306 | 309 | PF00568 | 0.343 |
DOC_USP7_MATH_1 | 118 | 122 | PF00917 | 0.501 |
DOC_USP7_MATH_1 | 212 | 216 | PF00917 | 0.229 |
DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.490 |
DOC_USP7_MATH_1 | 297 | 301 | PF00917 | 0.341 |
DOC_USP7_MATH_1 | 75 | 79 | PF00917 | 0.443 |
DOC_USP7_MATH_1 | 90 | 94 | PF00917 | 0.672 |
DOC_USP7_UBL2_3 | 19 | 23 | PF12436 | 0.466 |
DOC_USP7_UBL2_3 | 225 | 229 | PF12436 | 0.390 |
DOC_WW_Pin1_4 | 144 | 149 | PF00397 | 0.463 |
DOC_WW_Pin1_4 | 252 | 257 | PF00397 | 0.333 |
DOC_WW_Pin1_4 | 276 | 281 | PF00397 | 0.258 |
DOC_WW_Pin1_4 | 326 | 331 | PF00397 | 0.327 |
DOC_WW_Pin1_4 | 362 | 367 | PF00397 | 0.407 |
DOC_WW_Pin1_4 | 48 | 53 | PF00397 | 0.466 |
DOC_WW_Pin1_4 | 93 | 98 | PF00397 | 0.683 |
LIG_14-3-3_CanoR_1 | 105 | 114 | PF00244 | 0.679 |
LIG_14-3-3_CanoR_1 | 137 | 144 | PF00244 | 0.514 |
LIG_14-3-3_CanoR_1 | 157 | 162 | PF00244 | 0.308 |
LIG_14-3-3_CanoR_1 | 178 | 185 | PF00244 | 0.334 |
LIG_14-3-3_CanoR_1 | 249 | 256 | PF00244 | 0.301 |
LIG_14-3-3_CanoR_1 | 398 | 403 | PF00244 | 0.402 |
LIG_14-3-3_CanoR_1 | 57 | 65 | PF00244 | 0.498 |
LIG_Actin_WH2_2 | 346 | 362 | PF00022 | 0.424 |
LIG_BIR_III_4 | 396 | 400 | PF00653 | 0.401 |
LIG_BRCT_BRCA1_1 | 120 | 124 | PF00533 | 0.484 |
LIG_BRCT_BRCA1_1 | 400 | 404 | PF00533 | 0.375 |
LIG_BRCT_BRCA1_1 | 77 | 81 | PF00533 | 0.400 |
LIG_Clathr_ClatBox_1 | 324 | 328 | PF01394 | 0.361 |
LIG_CtBP_PxDLS_1 | 27 | 31 | PF00389 | 0.519 |
LIG_EVH1_2 | 268 | 272 | PF00568 | 0.363 |
LIG_FHA_1 | 106 | 112 | PF00498 | 0.609 |
LIG_FHA_1 | 217 | 223 | PF00498 | 0.290 |
LIG_FHA_1 | 260 | 266 | PF00498 | 0.375 |
LIG_FHA_1 | 283 | 289 | PF00498 | 0.261 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.452 |
LIG_FHA_1 | 56 | 62 | PF00498 | 0.420 |
LIG_FHA_1 | 84 | 90 | PF00498 | 0.369 |
LIG_FHA_2 | 144 | 150 | PF00498 | 0.229 |
LIG_FHA_2 | 166 | 172 | PF00498 | 0.308 |
LIG_FHA_2 | 293 | 299 | PF00498 | 0.317 |
LIG_FHA_2 | 4 | 10 | PF00498 | 0.461 |
LIG_GBD_Chelix_1 | 195 | 203 | PF00786 | 0.550 |
LIG_GBD_Chelix_1 | 30 | 38 | PF00786 | 0.604 |
LIG_LIR_Gen_1 | 121 | 132 | PF02991 | 0.443 |
LIG_LIR_Gen_1 | 139 | 148 | PF02991 | 0.337 |
LIG_LIR_Gen_1 | 2 | 11 | PF02991 | 0.496 |
LIG_LIR_Gen_1 | 301 | 312 | PF02991 | 0.333 |
LIG_LIR_Gen_1 | 51 | 61 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 121 | 127 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 139 | 144 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 2 | 8 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 301 | 307 | PF02991 | 0.327 |
LIG_LIR_Nem_3 | 51 | 56 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 78 | 84 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 93 | 98 | PF02991 | 0.593 |
LIG_LYPXL_yS_3 | 132 | 135 | PF13949 | 0.468 |
LIG_MAD2 | 44 | 52 | PF02301 | 0.357 |
LIG_MYND_1 | 48 | 52 | PF01753 | 0.463 |
LIG_NRBOX | 83 | 89 | PF00104 | 0.428 |
LIG_PDZ_Class_3 | 405 | 410 | PF00595 | 0.453 |
LIG_Pex14_2 | 103 | 107 | PF04695 | 0.644 |
LIG_PTB_Apo_2 | 355 | 362 | PF02174 | 0.358 |
LIG_PTB_Phospho_1 | 355 | 361 | PF10480 | 0.412 |
LIG_SH2_CRK | 304 | 308 | PF00017 | 0.331 |
LIG_SH2_CRK | 361 | 365 | PF00017 | 0.448 |
LIG_SH2_GRB2like | 141 | 144 | PF00017 | 0.469 |
LIG_SH2_SRC | 185 | 188 | PF00017 | 0.361 |
LIG_SH2_SRC | 394 | 397 | PF00017 | 0.386 |
LIG_SH2_STAP1 | 304 | 308 | PF00017 | 0.331 |
LIG_SH2_STAT5 | 314 | 317 | PF00017 | 0.287 |
LIG_SH2_STAT5 | 361 | 364 | PF00017 | 0.437 |
LIG_SH3_3 | 145 | 151 | PF00018 | 0.307 |
LIG_SH3_3 | 225 | 231 | PF00018 | 0.366 |
LIG_SH3_3 | 268 | 274 | PF00018 | 0.391 |
LIG_SH3_3 | 329 | 335 | PF00018 | 0.330 |
LIG_SH3_3 | 43 | 49 | PF00018 | 0.442 |
LIG_SH3_3 | 63 | 69 | PF00018 | 0.420 |
LIG_SUMO_SIM_anti_2 | 219 | 224 | PF11976 | 0.339 |
LIG_SUMO_SIM_par_1 | 195 | 202 | PF11976 | 0.274 |
LIG_SUMO_SIM_par_1 | 218 | 224 | PF11976 | 0.355 |
LIG_SUMO_SIM_par_1 | 243 | 248 | PF11976 | 0.308 |
LIG_SUMO_SIM_par_1 | 273 | 279 | PF11976 | 0.273 |
LIG_SUMO_SIM_par_1 | 85 | 91 | PF11976 | 0.422 |
LIG_TYR_ITIM | 359 | 364 | PF00017 | 0.438 |
LIG_WW_3 | 267 | 271 | PF00397 | 0.252 |
MOD_CK1_1 | 251 | 257 | PF00069 | 0.383 |
MOD_CK1_1 | 383 | 389 | PF00069 | 0.386 |
MOD_CK1_1 | 70 | 76 | PF00069 | 0.359 |
MOD_CK1_1 | 93 | 99 | PF00069 | 0.687 |
MOD_CK2_1 | 136 | 142 | PF00069 | 0.509 |
MOD_CK2_1 | 257 | 263 | PF00069 | 0.348 |
MOD_CK2_1 | 292 | 298 | PF00069 | 0.317 |
MOD_GlcNHglycan | 190 | 193 | PF01048 | 0.533 |
MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.643 |
MOD_GlcNHglycan | 257 | 260 | PF01048 | 0.555 |
MOD_GlcNHglycan | 380 | 383 | PF01048 | 0.588 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.443 |
MOD_GSK3_1 | 114 | 121 | PF00069 | 0.487 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.309 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.301 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.469 |
MOD_GSK3_1 | 245 | 252 | PF00069 | 0.342 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.292 |
MOD_GSK3_1 | 278 | 285 | PF00069 | 0.359 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.438 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.258 |
MOD_N-GLC_1 | 142 | 147 | PF02516 | 0.661 |
MOD_N-GLC_1 | 388 | 393 | PF02516 | 0.653 |
MOD_NEK2_1 | 159 | 164 | PF00069 | 0.323 |
MOD_NEK2_1 | 176 | 181 | PF00069 | 0.290 |
MOD_NEK2_1 | 245 | 250 | PF00069 | 0.284 |
MOD_NEK2_1 | 359 | 364 | PF00069 | 0.383 |
MOD_NEK2_1 | 388 | 393 | PF00069 | 0.410 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.557 |
MOD_PIKK_1 | 136 | 142 | PF00454 | 0.497 |
MOD_PIKK_1 | 161 | 167 | PF00454 | 0.334 |
MOD_PIKK_1 | 278 | 284 | PF00454 | 0.258 |
MOD_PIKK_1 | 388 | 394 | PF00454 | 0.383 |
MOD_PIKK_1 | 60 | 66 | PF00454 | 0.455 |
MOD_PK_1 | 398 | 404 | PF00069 | 0.404 |
MOD_PKA_1 | 105 | 111 | PF00069 | 0.677 |
MOD_PKA_2 | 105 | 111 | PF00069 | 0.661 |
MOD_PKA_2 | 136 | 142 | PF00069 | 0.525 |
MOD_PKA_2 | 248 | 254 | PF00069 | 0.328 |
MOD_PKA_2 | 359 | 365 | PF00069 | 0.387 |
MOD_PKA_2 | 56 | 62 | PF00069 | 0.495 |
MOD_PKB_1 | 129 | 137 | PF00069 | 0.499 |
MOD_Plk_1 | 212 | 218 | PF00069 | 0.229 |
MOD_Plk_1 | 34 | 40 | PF00069 | 0.337 |
MOD_Plk_2-3 | 328 | 334 | PF00069 | 0.308 |
MOD_Plk_4 | 118 | 124 | PF00069 | 0.449 |
MOD_Plk_4 | 380 | 386 | PF00069 | 0.351 |
MOD_Plk_4 | 398 | 404 | PF00069 | 0.343 |
MOD_Plk_4 | 83 | 89 | PF00069 | 0.380 |
MOD_ProDKin_1 | 144 | 150 | PF00069 | 0.330 |
MOD_ProDKin_1 | 252 | 258 | PF00069 | 0.333 |
MOD_ProDKin_1 | 276 | 282 | PF00069 | 0.258 |
MOD_ProDKin_1 | 326 | 332 | PF00069 | 0.327 |
MOD_ProDKin_1 | 362 | 368 | PF00069 | 0.403 |
MOD_ProDKin_1 | 48 | 54 | PF00069 | 0.464 |
MOD_ProDKin_1 | 93 | 99 | PF00069 | 0.683 |
MOD_SUMO_rev_2 | 17 | 25 | PF00179 | 0.450 |
TRG_DiLeu_BaLyEn_6 | 107 | 112 | PF01217 | 0.670 |
TRG_DiLeu_BaLyEn_6 | 240 | 245 | PF01217 | 0.308 |
TRG_DiLeu_BaLyEn_6 | 363 | 368 | PF01217 | 0.402 |
TRG_ENDOCYTIC_2 | 132 | 135 | PF00928 | 0.432 |
TRG_ENDOCYTIC_2 | 141 | 144 | PF00928 | 0.486 |
TRG_ENDOCYTIC_2 | 304 | 307 | PF00928 | 0.363 |
TRG_ENDOCYTIC_2 | 361 | 364 | PF00928 | 0.446 |
TRG_ER_diArg_1 | 104 | 106 | PF00400 | 0.691 |
TRG_ER_diArg_1 | 128 | 131 | PF00400 | 0.372 |
TRG_Pf-PMV_PEXEL_1 | 126 | 130 | PF00026 | 0.559 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I9C3 | Leptomonas seymouri | 53% | 100% |
A0A0S4J7K0 | Bodo saltans | 29% | 100% |
A0A1X0NW41 | Trypanosomatidae | 37% | 100% |
A0A3S7X5K2 | Leishmania donovani | 90% | 100% |
A0A422NIA6 | Trypanosoma rangeli | 31% | 100% |
A4HKC9 | Leishmania braziliensis | 73% | 100% |
A4I7V8 | Leishmania infantum | 90% | 100% |
E9B2R6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |