Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 1 |
Forrest at al. (metacyclic) | no | yes: 3 |
Forrest at al. (procyclic) | no | yes: 3 |
Silverman et al. | no | yes: 2 |
Pissara et al. | no | yes: 12 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 6 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 25 |
NetGPI | no | yes: 0, no: 25 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005829 | cytosol | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3Q8IJY8
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 26 |
GO:0006807 | nitrogen compound metabolic process | 2 | 26 |
GO:0008152 | metabolic process | 1 | 26 |
GO:0019538 | protein metabolic process | 3 | 26 |
GO:0043170 | macromolecule metabolic process | 3 | 26 |
GO:0044238 | primary metabolic process | 2 | 26 |
GO:0071704 | organic substance metabolic process | 2 | 26 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 26 |
GO:0006518 | peptide metabolic process | 4 | 1 |
GO:0043603 | amide metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 26 |
GO:0004180 | carboxypeptidase activity | 5 | 26 |
GO:0004181 | metallocarboxypeptidase activity | 6 | 26 |
GO:0008233 | peptidase activity | 3 | 26 |
GO:0008235 | metalloexopeptidase activity | 5 | 26 |
GO:0008237 | metallopeptidase activity | 4 | 26 |
GO:0008238 | exopeptidase activity | 4 | 26 |
GO:0016787 | hydrolase activity | 2 | 26 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 26 |
GO:0016853 | isomerase activity | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 102 | 104 | PF00675 | 0.320 |
CLV_NRD_NRD_1 | 11 | 13 | PF00675 | 0.180 |
CLV_NRD_NRD_1 | 190 | 192 | PF00675 | 0.180 |
CLV_NRD_NRD_1 | 336 | 338 | PF00675 | 0.412 |
CLV_NRD_NRD_1 | 348 | 350 | PF00675 | 0.380 |
CLV_NRD_NRD_1 | 441 | 443 | PF00675 | 0.494 |
CLV_PCSK_KEX2_1 | 101 | 103 | PF00082 | 0.412 |
CLV_PCSK_KEX2_1 | 441 | 443 | PF00082 | 0.491 |
CLV_PCSK_PC7_1 | 437 | 443 | PF00082 | 0.401 |
CLV_PCSK_SKI1_1 | 18 | 22 | PF00082 | 0.310 |
CLV_PCSK_SKI1_1 | 185 | 189 | PF00082 | 0.393 |
CLV_PCSK_SKI1_1 | 259 | 263 | PF00082 | 0.373 |
CLV_PCSK_SKI1_1 | 280 | 284 | PF00082 | 0.369 |
CLV_PCSK_SKI1_1 | 35 | 39 | PF00082 | 0.375 |
CLV_PCSK_SKI1_1 | 59 | 63 | PF00082 | 0.398 |
CLV_PCSK_SKI1_1 | 65 | 69 | PF00082 | 0.374 |
CLV_Separin_Metazoa | 84 | 88 | PF03568 | 0.225 |
CLV_Separin_Metazoa | 98 | 102 | PF03568 | 0.203 |
DEG_APCC_DBOX_1 | 102 | 110 | PF00400 | 0.180 |
DEG_APCC_DBOX_1 | 401 | 409 | PF00400 | 0.256 |
DEG_APCC_DBOX_1 | 78 | 86 | PF00400 | 0.299 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.535 |
DOC_CKS1_1 | 201 | 206 | PF01111 | 0.256 |
DOC_CYCLIN_RxL_1 | 256 | 264 | PF00134 | 0.358 |
DOC_CYCLIN_yCln2_LP_2 | 433 | 436 | PF00134 | 0.375 |
DOC_MAPK_gen_1 | 15 | 23 | PF00069 | 0.286 |
DOC_MAPK_gen_1 | 390 | 397 | PF00069 | 0.332 |
DOC_PP1_RVXF_1 | 407 | 414 | PF00149 | 0.161 |
DOC_PP2B_LxvP_1 | 433 | 436 | PF13499 | 0.375 |
DOC_USP7_MATH_1 | 145 | 149 | PF00917 | 0.301 |
DOC_USP7_UBL2_3 | 334 | 338 | PF12436 | 0.161 |
DOC_WW_Pin1_4 | 148 | 153 | PF00397 | 0.438 |
DOC_WW_Pin1_4 | 200 | 205 | PF00397 | 0.256 |
DOC_WW_Pin1_4 | 250 | 255 | PF00397 | 0.443 |
DOC_WW_Pin1_4 | 30 | 35 | PF00397 | 0.142 |
LIG_14-3-3_CanoR_1 | 103 | 113 | PF00244 | 0.363 |
LIG_14-3-3_CanoR_1 | 12 | 18 | PF00244 | 0.277 |
LIG_14-3-3_CanoR_1 | 215 | 224 | PF00244 | 0.400 |
LIG_14-3-3_CanoR_1 | 247 | 251 | PF00244 | 0.451 |
LIG_14-3-3_CanoR_1 | 40 | 45 | PF00244 | 0.470 |
LIG_14-3-3_CanoR_1 | 450 | 455 | PF00244 | 0.653 |
LIG_14-3-3_CanoR_1 | 52 | 58 | PF00244 | 0.390 |
LIG_Actin_WH2_2 | 129 | 146 | PF00022 | 0.298 |
LIG_Actin_WH2_2 | 393 | 411 | PF00022 | 0.161 |
LIG_BRCT_BRCA1_1 | 309 | 313 | PF00533 | 0.291 |
LIG_Clathr_ClatBox_1 | 133 | 137 | PF01394 | 0.256 |
LIG_CSL_BTD_1 | 125 | 128 | PF09270 | 0.357 |
LIG_deltaCOP1_diTrp_1 | 220 | 226 | PF00928 | 0.384 |
LIG_FHA_1 | 256 | 262 | PF00498 | 0.441 |
LIG_FHA_1 | 296 | 302 | PF00498 | 0.454 |
LIG_FHA_2 | 127 | 133 | PF00498 | 0.366 |
LIG_FHA_2 | 262 | 268 | PF00498 | 0.377 |
LIG_FHA_2 | 41 | 47 | PF00498 | 0.351 |
LIG_GBD_Chelix_1 | 60 | 68 | PF00786 | 0.375 |
LIG_HP1_1 | 58 | 62 | PF01393 | 0.212 |
LIG_LIR_Apic_2 | 249 | 254 | PF02991 | 0.250 |
LIG_LIR_Apic_2 | 315 | 319 | PF02991 | 0.332 |
LIG_LIR_Gen_1 | 170 | 181 | PF02991 | 0.204 |
LIG_LIR_Gen_1 | 244 | 251 | PF02991 | 0.167 |
LIG_LIR_Nem_3 | 151 | 156 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 170 | 176 | PF02991 | 0.167 |
LIG_LIR_Nem_3 | 310 | 316 | PF02991 | 0.309 |
LIG_LIR_Nem_3 | 393 | 397 | PF02991 | 0.305 |
LIG_NRBOX | 16 | 22 | PF00104 | 0.407 |
LIG_PDZ_Class_1 | 450 | 455 | PF00595 | 0.388 |
LIG_Pex14_1 | 413 | 417 | PF04695 | 0.407 |
LIG_SH2_CRK | 153 | 157 | PF00017 | 0.256 |
LIG_SH2_NCK_1 | 231 | 235 | PF00017 | 0.256 |
LIG_SH2_SRC | 173 | 176 | PF00017 | 0.346 |
LIG_SH2_SRC | 231 | 234 | PF00017 | 0.256 |
LIG_SH2_STAP1 | 257 | 261 | PF00017 | 0.466 |
LIG_SH2_STAP1 | 357 | 361 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 245 | 248 | PF00017 | 0.361 |
LIG_SH2_STAT5 | 257 | 260 | PF00017 | 0.398 |
LIG_SH2_STAT5 | 316 | 319 | PF00017 | 0.378 |
LIG_SH2_STAT5 | 424 | 427 | PF00017 | 0.341 |
LIG_SH3_3 | 432 | 438 | PF00018 | 0.351 |
LIG_SUMO_SIM_par_1 | 132 | 137 | PF11976 | 0.256 |
LIG_SUMO_SIM_par_1 | 19 | 25 | PF11976 | 0.331 |
LIG_TRAF2_1 | 129 | 132 | PF00917 | 0.449 |
LIG_TRAF2_1 | 3 | 6 | PF00917 | 0.279 |
LIG_WW_3 | 434 | 438 | PF00397 | 0.389 |
MOD_CDK_SPK_2 | 30 | 35 | PF00069 | 0.142 |
MOD_CDK_SPxxK_3 | 200 | 207 | PF00069 | 0.256 |
MOD_CK1_1 | 148 | 154 | PF00069 | 0.343 |
MOD_CK1_1 | 449 | 455 | PF00069 | 0.418 |
MOD_CK2_1 | 126 | 132 | PF00069 | 0.360 |
MOD_CK2_1 | 194 | 200 | PF00069 | 0.340 |
MOD_CK2_1 | 261 | 267 | PF00069 | 0.446 |
MOD_CK2_1 | 40 | 46 | PF00069 | 0.393 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.298 |
MOD_GlcNHglycan | 291 | 294 | PF01048 | 0.424 |
MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.237 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.304 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.256 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.256 |
MOD_GSK3_1 | 246 | 253 | PF00069 | 0.413 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.436 |
MOD_GSK3_1 | 446 | 453 | PF00069 | 0.411 |
MOD_LATS_1 | 11 | 17 | PF00433 | 0.250 |
MOD_N-GLC_1 | 255 | 260 | PF02516 | 0.380 |
MOD_NEK2_1 | 261 | 266 | PF00069 | 0.348 |
MOD_NEK2_2 | 329 | 334 | PF00069 | 0.283 |
MOD_NEK2_2 | 357 | 362 | PF00069 | 0.161 |
MOD_PIKK_1 | 295 | 301 | PF00454 | 0.391 |
MOD_PIKK_1 | 90 | 96 | PF00454 | 0.477 |
MOD_PKA_1 | 101 | 107 | PF00069 | 0.353 |
MOD_PKA_2 | 101 | 107 | PF00069 | 0.366 |
MOD_PKA_2 | 246 | 252 | PF00069 | 0.311 |
MOD_PKA_2 | 449 | 455 | PF00069 | 0.411 |
MOD_PKB_1 | 103 | 111 | PF00069 | 0.180 |
MOD_Plk_4 | 175 | 181 | PF00069 | 0.322 |
MOD_Plk_4 | 246 | 252 | PF00069 | 0.348 |
MOD_Plk_4 | 27 | 33 | PF00069 | 0.314 |
MOD_Plk_4 | 297 | 303 | PF00069 | 0.283 |
MOD_ProDKin_1 | 148 | 154 | PF00069 | 0.438 |
MOD_ProDKin_1 | 200 | 206 | PF00069 | 0.256 |
MOD_ProDKin_1 | 250 | 256 | PF00069 | 0.443 |
MOD_ProDKin_1 | 30 | 36 | PF00069 | 0.142 |
MOD_SUMO_for_1 | 271 | 274 | PF00179 | 0.251 |
MOD_SUMO_for_1 | 70 | 73 | PF00179 | 0.469 |
MOD_SUMO_rev_2 | 170 | 178 | PF00179 | 0.373 |
MOD_SUMO_rev_2 | 5 | 10 | PF00179 | 0.223 |
TRG_DiLeu_BaEn_1 | 297 | 302 | PF01217 | 0.256 |
TRG_DiLeu_BaEn_4 | 5 | 11 | PF01217 | 0.212 |
TRG_DiLeu_BaLyEn_6 | 316 | 321 | PF01217 | 0.358 |
TRG_ENDOCYTIC_2 | 153 | 156 | PF00928 | 0.323 |
TRG_ENDOCYTIC_2 | 173 | 176 | PF00928 | 0.136 |
TRG_ENDOCYTIC_2 | 184 | 187 | PF00928 | 0.236 |
TRG_ENDOCYTIC_2 | 245 | 248 | PF00928 | 0.450 |
TRG_ENDOCYTIC_2 | 394 | 397 | PF00928 | 0.326 |
TRG_ENDOCYTIC_2 | 4 | 7 | PF00928 | 0.364 |
TRG_ER_diArg_1 | 100 | 103 | PF00400 | 0.411 |
TRG_NES_CRM1_1 | 315 | 328 | PF08389 | 0.437 |
TRG_Pf-PMV_PEXEL_1 | 215 | 220 | PF00026 | 0.307 |
TRG_Pf-PMV_PEXEL_1 | 280 | 285 | PF00026 | 0.282 |
TRG_Pf-PMV_PEXEL_1 | 337 | 341 | PF00026 | 0.423 |
TRG_Pf-PMV_PEXEL_1 | 349 | 353 | PF00026 | 0.414 |
TRG_Pf-PMV_PEXEL_1 | 371 | 375 | PF00026 | 0.316 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IMA5 | Leptomonas seymouri | 43% | 100% |
A0A0S4IZ28 | Bodo saltans | 44% | 100% |
A0A1X0NY67 | Trypanosomatidae | 48% | 90% |
A0A1X0P441 | Trypanosomatidae | 51% | 90% |
A0A1X0P598 | Trypanosomatidae | 51% | 90% |
A0A3Q8IBW2 | Leishmania donovani | 89% | 100% |
A0A3Q8IU74 | Leishmania donovani | 46% | 91% |
A0A3S7WSA3 | Leishmania donovani | 49% | 90% |
A0A422P042 | Trypanosoma rangeli | 47% | 90% |
A0A422P4R1 | Trypanosoma rangeli | 47% | 91% |
A4H716 | Leishmania braziliensis | 49% | 100% |
A4HLW4 | Leishmania braziliensis | 46% | 100% |
A4HVE5 | Leishmania infantum | 49% | 100% |
A4HVW0 | Leishmania infantum | 89% | 100% |
A4I993 | Leishmania infantum | 46% | 100% |
A4IC85 | Leishmania infantum | 98% | 100% |
D0A656 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 90% |
E9AP43 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 49% | 100% |
E9B493 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 45% | 100% |
P42663 | Thermus aquaticus | 32% | 89% |
P50848 | Bacillus subtilis (strain 168) | 30% | 91% |
Q4Q0D4 | Leishmania major | 89% | 100% |
Q4Q3T3 | Leishmania major | 45% | 100% |
Q4QFW7 | Leishmania major | 87% | 100% |
Q4QGE5 | Leishmania major | 47% | 100% |
Q5SLM3 | Thermus thermophilus (strain ATCC 27634 / DSM 579 / HB8) | 31% | 89% |
Q8U3L0 | Pyrococcus furiosus (strain ATCC 43587 / DSM 3638 / JCM 8422 / Vc1) | 28% | 91% |
V5DQA0 | Trypanosoma cruzi | 50% | 90% |