Proteases, carboxypeptidase
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 1 |
Forrest at al. (metacyclic) | yes | yes: 3 |
Forrest at al. (procyclic) | yes | yes: 3 |
Silverman et al. | no | yes: 2 |
Pissara et al. | yes | 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: 24 |
NetGPI | no | yes: 0, no: 24 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005829 | cytosol | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pescher et al. (upgregulation) | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Lahav et al. - mRNA
- Protein
|
Related structures:
AlphaFold database: A4HVW0
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 25 |
GO:0006807 | nitrogen compound metabolic process | 2 | 25 |
GO:0008152 | metabolic process | 1 | 25 |
GO:0019538 | protein metabolic process | 3 | 25 |
GO:0043170 | macromolecule metabolic process | 3 | 25 |
GO:0044238 | primary metabolic process | 2 | 25 |
GO:0071704 | organic substance metabolic process | 2 | 25 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 25 |
GO:0006518 | peptide metabolic process | 4 | 1 |
GO:0043603 | amide metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 25 |
GO:0004180 | carboxypeptidase activity | 5 | 25 |
GO:0004181 | metallocarboxypeptidase activity | 6 | 25 |
GO:0008233 | peptidase activity | 3 | 25 |
GO:0008235 | metalloexopeptidase activity | 5 | 25 |
GO:0008237 | metallopeptidase activity | 4 | 25 |
GO:0008238 | exopeptidase activity | 4 | 25 |
GO:0016787 | hydrolase activity | 2 | 25 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 25 |
GO:0016853 | isomerase activity | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 102 | 104 | PF00675 | 0.323 |
CLV_NRD_NRD_1 | 11 | 13 | PF00675 | 0.187 |
CLV_NRD_NRD_1 | 190 | 192 | PF00675 | 0.191 |
CLV_NRD_NRD_1 | 336 | 338 | PF00675 | 0.400 |
CLV_NRD_NRD_1 | 497 | 499 | PF00675 | 0.270 |
CLV_PCSK_KEX2_1 | 101 | 103 | PF00082 | 0.426 |
CLV_PCSK_KEX2_1 | 497 | 499 | PF00082 | 0.270 |
CLV_PCSK_SKI1_1 | 18 | 22 | PF00082 | 0.289 |
CLV_PCSK_SKI1_1 | 185 | 189 | PF00082 | 0.423 |
CLV_PCSK_SKI1_1 | 259 | 263 | PF00082 | 0.376 |
CLV_PCSK_SKI1_1 | 280 | 284 | PF00082 | 0.412 |
CLV_PCSK_SKI1_1 | 35 | 39 | PF00082 | 0.405 |
CLV_PCSK_SKI1_1 | 59 | 63 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 65 | 69 | PF00082 | 0.356 |
CLV_Separin_Metazoa | 84 | 88 | PF03568 | 0.221 |
CLV_Separin_Metazoa | 98 | 102 | PF03568 | 0.200 |
DEG_APCC_DBOX_1 | 102 | 110 | PF00400 | 0.187 |
DEG_APCC_DBOX_1 | 399 | 407 | PF00400 | 0.259 |
DEG_APCC_DBOX_1 | 78 | 86 | PF00400 | 0.279 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.526 |
DEG_SCF_FBW7_2 | 317 | 322 | PF00400 | 0.176 |
DOC_CKS1_1 | 201 | 206 | PF01111 | 0.304 |
DOC_CKS1_1 | 316 | 321 | PF01111 | 0.342 |
DOC_CYCLIN_RxL_1 | 256 | 264 | PF00134 | 0.336 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 13 | 21 | PF00134 | 0.223 |
DOC_MAPK_gen_1 | 388 | 395 | PF00069 | 0.326 |
DOC_PP4_MxPP_1 | 31 | 34 | PF00568 | 0.258 |
DOC_USP7_MATH_1 | 145 | 149 | PF00917 | 0.293 |
DOC_WW_Pin1_4 | 148 | 153 | PF00397 | 0.336 |
DOC_WW_Pin1_4 | 200 | 205 | PF00397 | 0.303 |
DOC_WW_Pin1_4 | 250 | 255 | PF00397 | 0.258 |
DOC_WW_Pin1_4 | 315 | 320 | PF00397 | 0.319 |
LIG_14-3-3_CanoR_1 | 103 | 113 | PF00244 | 0.392 |
LIG_14-3-3_CanoR_1 | 215 | 224 | PF00244 | 0.240 |
LIG_14-3-3_CanoR_1 | 247 | 251 | PF00244 | 0.450 |
LIG_Actin_WH2_2 | 129 | 146 | PF00022 | 0.278 |
LIG_BRCT_BRCA1_1 | 309 | 313 | PF00533 | 0.271 |
LIG_Clathr_ClatBox_1 | 133 | 137 | PF01394 | 0.251 |
LIG_CSL_BTD_1 | 125 | 128 | PF09270 | 0.373 |
LIG_deltaCOP1_diTrp_1 | 220 | 226 | PF00928 | 0.367 |
LIG_deltaCOP1_diTrp_1 | 408 | 416 | PF00928 | 0.311 |
LIG_FHA_1 | 256 | 262 | PF00498 | 0.437 |
LIG_FHA_1 | 296 | 302 | PF00498 | 0.375 |
LIG_FHA_1 | 316 | 322 | PF00498 | 0.379 |
LIG_FHA_1 | 444 | 450 | PF00498 | 0.253 |
LIG_FHA_1 | 472 | 478 | PF00498 | 0.301 |
LIG_FHA_2 | 127 | 133 | PF00498 | 0.354 |
LIG_FHA_2 | 262 | 268 | PF00498 | 0.376 |
LIG_FHA_2 | 348 | 354 | PF00498 | 0.230 |
LIG_GBD_Chelix_1 | 60 | 68 | PF00786 | 0.357 |
LIG_HP1_1 | 58 | 62 | PF01393 | 0.213 |
LIG_LIR_Apic_2 | 249 | 254 | PF02991 | 0.245 |
LIG_LIR_Apic_2 | 315 | 319 | PF02991 | 0.311 |
LIG_LIR_Gen_1 | 151 | 159 | PF02991 | 0.421 |
LIG_LIR_Gen_1 | 170 | 181 | PF02991 | 0.214 |
LIG_LIR_Nem_3 | 151 | 156 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 170 | 176 | PF02991 | 0.186 |
LIG_LIR_Nem_3 | 310 | 316 | PF02991 | 0.278 |
LIG_LIR_Nem_3 | 391 | 395 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 418 | 422 | PF02991 | 0.176 |
LIG_NRBOX | 16 | 22 | PF00104 | 0.251 |
LIG_NRBOX | 467 | 473 | PF00104 | 0.351 |
LIG_Pex14_1 | 411 | 415 | PF04695 | 0.394 |
LIG_SH2_CRK | 153 | 157 | PF00017 | 0.251 |
LIG_SH2_NCK_1 | 231 | 235 | PF00017 | 0.251 |
LIG_SH2_SRC | 173 | 176 | PF00017 | 0.337 |
LIG_SH2_SRC | 231 | 234 | PF00017 | 0.251 |
LIG_SH2_STAP1 | 153 | 157 | PF00017 | 0.295 |
LIG_SH2_STAP1 | 257 | 261 | PF00017 | 0.472 |
LIG_SH2_STAP1 | 357 | 361 | PF00017 | 0.346 |
LIG_SH2_STAT5 | 257 | 260 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 316 | 319 | PF00017 | 0.360 |
LIG_SH2_STAT5 | 347 | 350 | PF00017 | 0.342 |
LIG_SH2_STAT5 | 422 | 425 | PF00017 | 0.320 |
LIG_SH2_STAT5 | 499 | 502 | PF00017 | 0.535 |
LIG_SH3_3 | 376 | 382 | PF00018 | 0.230 |
LIG_SH3_3 | 482 | 488 | PF00018 | 0.276 |
LIG_SUMO_SIM_par_1 | 132 | 137 | PF11976 | 0.251 |
LIG_SUMO_SIM_par_1 | 19 | 25 | PF11976 | 0.311 |
LIG_TRAF2_1 | 129 | 132 | PF00917 | 0.302 |
LIG_TRAF2_1 | 3 | 6 | PF00917 | 0.285 |
MOD_CDK_SPxxK_3 | 200 | 207 | PF00069 | 0.256 |
MOD_CK1_1 | 148 | 154 | PF00069 | 0.333 |
MOD_CK2_1 | 126 | 132 | PF00069 | 0.366 |
MOD_CK2_1 | 194 | 200 | PF00069 | 0.319 |
MOD_CK2_1 | 261 | 267 | PF00069 | 0.444 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.279 |
MOD_GlcNHglycan | 291 | 294 | PF01048 | 0.240 |
MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.280 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.309 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.259 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.289 |
MOD_GSK3_1 | 246 | 253 | PF00069 | 0.443 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.462 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.403 |
MOD_N-GLC_1 | 255 | 260 | PF02516 | 0.414 |
MOD_NEK2_1 | 194 | 199 | PF00069 | 0.188 |
MOD_NEK2_1 | 261 | 266 | PF00069 | 0.328 |
MOD_PIKK_1 | 295 | 301 | PF00454 | 0.363 |
MOD_PIKK_1 | 443 | 449 | PF00454 | 0.203 |
MOD_PIKK_1 | 90 | 96 | PF00454 | 0.314 |
MOD_PKA_1 | 101 | 107 | PF00069 | 0.332 |
MOD_PKA_2 | 101 | 107 | PF00069 | 0.401 |
MOD_PKA_2 | 246 | 252 | PF00069 | 0.301 |
MOD_PKB_1 | 103 | 111 | PF00069 | 0.187 |
MOD_PKB_1 | 142 | 150 | PF00069 | 0.376 |
MOD_Plk_4 | 175 | 181 | PF00069 | 0.315 |
MOD_Plk_4 | 246 | 252 | PF00069 | 0.346 |
MOD_Plk_4 | 27 | 33 | PF00069 | 0.313 |
MOD_Plk_4 | 297 | 303 | PF00069 | 0.291 |
MOD_Plk_4 | 343 | 349 | PF00069 | 0.376 |
MOD_ProDKin_1 | 148 | 154 | PF00069 | 0.336 |
MOD_ProDKin_1 | 200 | 206 | PF00069 | 0.303 |
MOD_ProDKin_1 | 250 | 256 | PF00069 | 0.258 |
MOD_ProDKin_1 | 315 | 321 | PF00069 | 0.319 |
MOD_SUMO_for_1 | 271 | 274 | PF00179 | 0.237 |
MOD_SUMO_for_1 | 70 | 73 | PF00179 | 0.476 |
MOD_SUMO_rev_2 | 170 | 178 | PF00179 | 0.355 |
MOD_SUMO_rev_2 | 380 | 389 | PF00179 | 0.280 |
MOD_SUMO_rev_2 | 5 | 10 | PF00179 | 0.223 |
TRG_DiLeu_BaEn_1 | 297 | 302 | PF01217 | 0.251 |
TRG_DiLeu_BaEn_1 | 473 | 478 | PF01217 | 0.288 |
TRG_DiLeu_BaEn_4 | 5 | 11 | PF01217 | 0.213 |
TRG_DiLeu_BaLyEn_6 | 316 | 321 | PF01217 | 0.336 |
TRG_ENDOCYTIC_2 | 153 | 156 | PF00928 | 0.302 |
TRG_ENDOCYTIC_2 | 173 | 176 | PF00928 | 0.150 |
TRG_ENDOCYTIC_2 | 184 | 187 | PF00928 | 0.215 |
TRG_ENDOCYTIC_2 | 392 | 395 | PF00928 | 0.305 |
TRG_ENDOCYTIC_2 | 4 | 7 | PF00928 | 0.359 |
TRG_ER_diArg_1 | 100 | 103 | PF00400 | 0.426 |
TRG_ER_diArg_1 | 497 | 499 | PF00400 | 0.270 |
TRG_NES_CRM1_1 | 315 | 328 | PF08389 | 0.251 |
TRG_Pf-PMV_PEXEL_1 | 215 | 220 | PF00026 | 0.293 |
TRG_Pf-PMV_PEXEL_1 | 280 | 285 | PF00026 | 0.272 |
TRG_Pf-PMV_PEXEL_1 | 337 | 341 | PF00026 | 0.414 |
TRG_Pf-PMV_PEXEL_1 | 349 | 353 | PF00026 | 0.402 |
TRG_Pf-PMV_PEXEL_1 | 369 | 373 | PF00026 | 0.295 |
TRG_Pf-PMV_PEXEL_1 | 489 | 493 | PF00026 | 0.222 |
TRG_Pf-PMV_PEXEL_1 | 498 | 503 | PF00026 | 0.518 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4IZ28 | Bodo saltans | 46% | 100% |
A0A1X0NY67 | Trypanosomatidae | 52% | 100% |
A0A1X0P441 | Trypanosomatidae | 56% | 100% |
A0A1X0P598 | Trypanosomatidae | 57% | 100% |
A0A3Q8IBW2 | Leishmania donovani | 99% | 100% |
A0A3Q8IJY8 | Leishmania donovani | 89% | 100% |
A0A3Q8IU74 | Leishmania donovani | 52% | 100% |
A0A3S7WSA3 | Leishmania donovani | 53% | 100% |
A0A422P042 | Trypanosoma rangeli | 52% | 100% |
A0A422P4R1 | Trypanosoma rangeli | 52% | 100% |
A4H716 | Leishmania braziliensis | 54% | 100% |
A4HLW4 | Leishmania braziliensis | 52% | 99% |
A4HVE5 | Leishmania infantum | 53% | 100% |
A4I993 | Leishmania infantum | 52% | 100% |
A4IC85 | Leishmania infantum | 87% | 100% |
D0A656 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 53% | 100% |
E9AP43 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 53% | 100% |
E9B493 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 51% | 100% |
P42663 | Thermus aquaticus | 32% | 99% |
P50848 | Bacillus subtilis (strain 168) | 31% | 100% |
Q4Q0D4 | Leishmania major | 93% | 100% |
Q4Q3T3 | Leishmania major | 51% | 100% |
Q4QFW7 | Leishmania major | 96% | 100% |
Q4QGE5 | Leishmania major | 53% | 100% |
Q5SLM3 | Thermus thermophilus (strain ATCC 27634 / DSM 579 / HB8) | 32% | 99% |
Q8U3L0 | Pyrococcus furiosus (strain ATCC 43587 / DSM 3638 / JCM 8422 / Vc1) | 30% | 100% |
V5DQA0 | Trypanosoma cruzi | 54% | 100% |