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. | 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 |
Related structures:
AlphaFold database: Q4Q0D4
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 | 17 | 19 | PF00675 | 0.361 |
CLV_NRD_NRD_1 | 252 | 254 | PF00675 | 0.439 |
CLV_NRD_NRD_1 | 355 | 357 | PF00675 | 0.520 |
CLV_PCSK_KEX2_1 | 17 | 19 | PF00082 | 0.439 |
CLV_PCSK_KEX2_1 | 355 | 357 | PF00082 | 0.491 |
CLV_PCSK_PC7_1 | 351 | 357 | PF00082 | 0.433 |
CLV_PCSK_SKI1_1 | 101 | 105 | PF00082 | 0.446 |
CLV_PCSK_SKI1_1 | 175 | 179 | PF00082 | 0.398 |
CLV_PCSK_SKI1_1 | 196 | 200 | PF00082 | 0.444 |
CLV_PCSK_SKI1_1 | 378 | 382 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 394 | 398 | PF00082 | 0.397 |
CLV_Separin_Metazoa | 14 | 18 | PF03568 | 0.236 |
DEG_APCC_DBOX_1 | 315 | 323 | PF00400 | 0.290 |
DEG_SPOP_SBC_1 | 399 | 403 | PF00917 | 0.420 |
DOC_CKS1_1 | 117 | 122 | PF01111 | 0.290 |
DOC_CKS1_1 | 232 | 237 | PF01111 | 0.386 |
DOC_CKS1_1 | 370 | 375 | PF01111 | 0.427 |
DOC_CYCLIN_RxL_1 | 172 | 180 | PF00134 | 0.391 |
DOC_CYCLIN_RxL_1 | 391 | 401 | PF00134 | 0.630 |
DOC_CYCLIN_yCln2_LP_2 | 347 | 350 | PF00134 | 0.387 |
DOC_MAPK_gen_1 | 304 | 311 | PF00069 | 0.355 |
DOC_PP2B_LxvP_1 | 347 | 350 | PF13499 | 0.387 |
DOC_PP2B_LxvP_1 | 388 | 391 | PF13499 | 0.382 |
DOC_PP2B_LxvP_1 | 408 | 411 | PF13499 | 0.333 |
DOC_USP7_MATH_1 | 399 | 403 | PF00917 | 0.420 |
DOC_USP7_MATH_1 | 61 | 65 | PF00917 | 0.325 |
DOC_WW_Pin1_4 | 116 | 121 | PF00397 | 0.290 |
DOC_WW_Pin1_4 | 166 | 171 | PF00397 | 0.474 |
DOC_WW_Pin1_4 | 231 | 236 | PF00397 | 0.380 |
DOC_WW_Pin1_4 | 369 | 374 | PF00397 | 0.427 |
DOC_WW_Pin1_4 | 64 | 69 | PF00397 | 0.481 |
LIG_14-3-3_CanoR_1 | 131 | 140 | PF00244 | 0.277 |
LIG_14-3-3_CanoR_1 | 163 | 167 | PF00244 | 0.481 |
LIG_14-3-3_CanoR_1 | 21 | 26 | PF00244 | 0.440 |
LIG_14-3-3_CanoR_1 | 364 | 373 | PF00244 | 0.669 |
LIG_14-3-3_CanoR_1 | 398 | 408 | PF00244 | 0.402 |
LIG_Actin_WH2_2 | 45 | 62 | PF00022 | 0.322 |
LIG_BRCT_BRCA1_1 | 225 | 229 | PF00533 | 0.315 |
LIG_BRCT_BRCA1_1 | 417 | 421 | PF00533 | 0.420 |
LIG_CaM_NSCaTE_8 | 361 | 368 | PF13499 | 0.403 |
LIG_Clathr_ClatBox_1 | 49 | 53 | PF01394 | 0.290 |
LIG_CSL_BTD_1 | 41 | 44 | PF09270 | 0.382 |
LIG_deltaCOP1_diTrp_1 | 136 | 142 | PF00928 | 0.410 |
LIG_deltaCOP1_diTrp_1 | 324 | 332 | PF00928 | 0.355 |
LIG_FHA_1 | 172 | 178 | PF00498 | 0.469 |
LIG_FHA_1 | 212 | 218 | PF00498 | 0.447 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.364 |
LIG_FHA_1 | 342 | 348 | PF00498 | 0.321 |
LIG_FHA_1 | 370 | 376 | PF00498 | 0.596 |
LIG_FHA_1 | 399 | 405 | PF00498 | 0.590 |
LIG_FHA_2 | 178 | 184 | PF00498 | 0.427 |
LIG_FHA_2 | 264 | 270 | PF00498 | 0.264 |
LIG_FHA_2 | 43 | 49 | PF00498 | 0.391 |
LIG_GBD_Chelix_1 | 7 | 15 | PF00786 | 0.200 |
LIG_LIR_Apic_2 | 165 | 170 | PF02991 | 0.472 |
LIG_LIR_Apic_2 | 231 | 235 | PF02991 | 0.355 |
LIG_LIR_Gen_1 | 67 | 75 | PF02991 | 0.457 |
LIG_LIR_Gen_1 | 86 | 97 | PF02991 | 0.244 |
LIG_LIR_Nem_3 | 226 | 232 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 418 | 422 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 67 | 72 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 86 | 92 | PF02991 | 0.201 |
LIG_NRBOX | 11 | 17 | PF00104 | 0.351 |
LIG_Pex14_1 | 327 | 331 | PF04695 | 0.433 |
LIG_REV1ctd_RIR_1 | 419 | 427 | PF16727 | 0.440 |
LIG_SH2_CRK | 69 | 73 | PF00017 | 0.508 |
LIG_SH2_NCK_1 | 147 | 151 | PF00017 | 0.290 |
LIG_SH2_SRC | 147 | 150 | PF00017 | 0.290 |
LIG_SH2_SRC | 89 | 92 | PF00017 | 0.419 |
LIG_SH2_STAP1 | 173 | 177 | PF00017 | 0.497 |
LIG_SH2_STAP1 | 273 | 277 | PF00017 | 0.390 |
LIG_SH2_STAP1 | 69 | 73 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 173 | 176 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 232 | 235 | PF00017 | 0.403 |
LIG_SH2_STAT5 | 263 | 266 | PF00017 | 0.386 |
LIG_SH2_STAT5 | 338 | 341 | PF00017 | 0.355 |
LIG_SH3_2 | 373 | 378 | PF14604 | 0.426 |
LIG_SH3_3 | 292 | 298 | PF00018 | 0.264 |
LIG_SH3_3 | 330 | 336 | PF00018 | 0.454 |
LIG_SH3_3 | 346 | 352 | PF00018 | 0.492 |
LIG_SH3_3 | 370 | 376 | PF00018 | 0.426 |
LIG_SUMO_SIM_par_1 | 48 | 53 | PF11976 | 0.290 |
LIG_TRAF2_1 | 45 | 48 | PF00917 | 0.351 |
LIG_TYR_ITSM | 85 | 92 | PF00017 | 0.200 |
LIG_UBA3_1 | 11 | 19 | PF00899 | 0.200 |
LIG_WRC_WIRS_1 | 416 | 421 | PF05994 | 0.416 |
LIG_WW_3 | 348 | 352 | PF00397 | 0.413 |
MOD_CDK_SPxxK_3 | 116 | 123 | PF00069 | 0.290 |
MOD_CDK_SPxxK_3 | 231 | 238 | PF00069 | 0.264 |
MOD_CK1_1 | 363 | 369 | PF00069 | 0.435 |
MOD_CK1_1 | 415 | 421 | PF00069 | 0.412 |
MOD_CK1_1 | 64 | 70 | PF00069 | 0.376 |
MOD_CK2_1 | 110 | 116 | PF00069 | 0.364 |
MOD_CK2_1 | 177 | 183 | PF00069 | 0.486 |
MOD_CK2_1 | 42 | 48 | PF00069 | 0.384 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.420 |
MOD_GlcNHglycan | 225 | 228 | PF01048 | 0.276 |
MOD_GlcNHglycan | 366 | 369 | PF01048 | 0.545 |
MOD_GlcNHglycan | 63 | 66 | PF01048 | 0.318 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.290 |
MOD_GSK3_1 | 162 | 169 | PF00069 | 0.458 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.473 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.441 |
MOD_GSK3_1 | 360 | 367 | PF00069 | 0.429 |
MOD_GSK3_1 | 400 | 407 | PF00069 | 0.395 |
MOD_GSK3_1 | 411 | 418 | PF00069 | 0.368 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.447 |
MOD_N-GLC_1 | 171 | 176 | PF02516 | 0.470 |
MOD_NEK2_1 | 177 | 182 | PF00069 | 0.365 |
MOD_NEK2_1 | 404 | 409 | PF00069 | 0.371 |
MOD_NEK2_1 | 412 | 417 | PF00069 | 0.368 |
MOD_PIKK_1 | 211 | 217 | PF00454 | 0.431 |
MOD_PIKK_1 | 341 | 347 | PF00454 | 0.200 |
MOD_PIKK_1 | 6 | 12 | PF00454 | 0.509 |
MOD_PKA_2 | 162 | 168 | PF00069 | 0.346 |
MOD_PKA_2 | 20 | 26 | PF00069 | 0.439 |
MOD_PKA_2 | 363 | 369 | PF00069 | 0.429 |
MOD_PKB_1 | 58 | 66 | PF00069 | 0.417 |
MOD_Plk_1 | 110 | 116 | PF00069 | 0.285 |
MOD_Plk_4 | 162 | 168 | PF00069 | 0.447 |
MOD_Plk_4 | 213 | 219 | PF00069 | 0.326 |
MOD_Plk_4 | 259 | 265 | PF00069 | 0.417 |
MOD_Plk_4 | 84 | 90 | PF00069 | 0.362 |
MOD_ProDKin_1 | 116 | 122 | PF00069 | 0.290 |
MOD_ProDKin_1 | 166 | 172 | PF00069 | 0.474 |
MOD_ProDKin_1 | 231 | 237 | PF00069 | 0.380 |
MOD_ProDKin_1 | 369 | 375 | PF00069 | 0.426 |
MOD_ProDKin_1 | 64 | 70 | PF00069 | 0.481 |
MOD_SUMO_for_1 | 187 | 190 | PF00179 | 0.276 |
MOD_SUMO_rev_2 | 86 | 94 | PF00179 | 0.398 |
TRG_DiLeu_BaEn_1 | 213 | 218 | PF01217 | 0.290 |
TRG_DiLeu_BaLyEn_6 | 232 | 237 | PF01217 | 0.391 |
TRG_ENDOCYTIC_2 | 100 | 103 | PF00928 | 0.436 |
TRG_ENDOCYTIC_2 | 69 | 72 | PF00928 | 0.347 |
TRG_ENDOCYTIC_2 | 89 | 92 | PF00928 | 0.483 |
TRG_ER_diArg_1 | 16 | 18 | PF00400 | 0.438 |
TRG_NES_CRM1_1 | 231 | 244 | PF08389 | 0.290 |
TRG_NLS_MonoExtN_4 | 17 | 22 | PF00514 | 0.245 |
TRG_Pf-PMV_PEXEL_1 | 131 | 136 | PF00026 | 0.340 |
TRG_Pf-PMV_PEXEL_1 | 196 | 201 | PF00026 | 0.315 |
TRG_Pf-PMV_PEXEL_1 | 253 | 257 | PF00026 | 0.451 |
TRG_Pf-PMV_PEXEL_1 | 265 | 269 | PF00026 | 0.441 |
TRG_Pf-PMV_PEXEL_1 | 285 | 289 | PF00026 | 0.340 |
TRG_PTS2 | 1 | 29 | PF00400 | 0.213 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4IZ28 | Bodo saltans | 45% | 95% |
A0A1X0NY67 | Trypanosomatidae | 51% | 84% |
A0A1X0P441 | Trypanosomatidae | 52% | 85% |
A0A1X0P598 | Trypanosomatidae | 55% | 85% |
A0A3Q8IBW2 | Leishmania donovani | 93% | 85% |
A0A3Q8IJY8 | Leishmania donovani | 89% | 94% |
A0A3Q8IU74 | Leishmania donovani | 51% | 86% |
A0A3S7WSA3 | Leishmania donovani | 51% | 85% |
A0A422P042 | Trypanosoma rangeli | 49% | 85% |
A0A422P4R1 | Trypanosoma rangeli | 52% | 85% |
A4H716 | Leishmania braziliensis | 49% | 85% |
A4HLW4 | Leishmania braziliensis | 48% | 86% |
A4HVE5 | Leishmania infantum | 51% | 85% |
A4HVW0 | Leishmania infantum | 93% | 85% |
A4I993 | Leishmania infantum | 51% | 86% |
A4IC85 | Leishmania infantum | 88% | 100% |
D0A656 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 54% | 85% |
E9AP43 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 51% | 85% |
E9B493 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 50% | 86% |
P42663 | Thermus aquaticus | 33% | 84% |
P50848 | Bacillus subtilis (strain 168) | 34% | 85% |
Q4Q3T3 | Leishmania major | 50% | 86% |
Q4QFW7 | Leishmania major | 96% | 85% |
Q4QGE5 | Leishmania major | 51% | 85% |
Q5SLM3 | Thermus thermophilus (strain ATCC 27634 / DSM 579 / HB8) | 33% | 84% |
Q8U3L0 | Pyrococcus furiosus (strain ATCC 43587 / DSM 3638 / JCM 8422 / Vc1) | 31% | 86% |
V5DQA0 | Trypanosoma cruzi | 52% | 85% |