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: E9AP43
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 | 138 | 140 | PF00675 | 0.445 |
CLV_NRD_NRD_1 | 496 | 498 | PF00675 | 0.391 |
CLV_NRD_NRD_1 | 86 | 88 | PF00675 | 0.351 |
CLV_PCSK_KEX2_1 | 138 | 140 | PF00082 | 0.445 |
CLV_PCSK_KEX2_1 | 496 | 498 | PF00082 | 0.363 |
CLV_PCSK_KEX2_1 | 86 | 88 | PF00082 | 0.357 |
CLV_PCSK_SKI1_1 | 171 | 175 | PF00082 | 0.503 |
CLV_PCSK_SKI1_1 | 258 | 262 | PF00082 | 0.412 |
CLV_PCSK_SKI1_1 | 290 | 294 | PF00082 | 0.491 |
CLV_PCSK_SKI1_1 | 61 | 65 | PF00082 | 0.409 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.561 |
DOC_CYCLIN_RxL_1 | 168 | 178 | PF00134 | 0.265 |
DOC_CYCLIN_RxL_1 | 255 | 263 | PF00134 | 0.405 |
DOC_MAPK_gen_1 | 13 | 23 | PF00069 | 0.333 |
DOC_MAPK_gen_1 | 387 | 394 | PF00069 | 0.369 |
DOC_PP4_FxxP_1 | 315 | 318 | PF00568 | 0.303 |
DOC_USP7_UBL2_3 | 459 | 463 | PF12436 | 0.342 |
DOC_USP7_UBL2_3 | 9 | 13 | PF12436 | 0.414 |
DOC_WW_Pin1_4 | 107 | 112 | PF00397 | 0.259 |
DOC_WW_Pin1_4 | 54 | 59 | PF00397 | 0.356 |
LIG_14-3-3_CanoR_1 | 144 | 152 | PF00244 | 0.227 |
LIG_14-3-3_CanoR_1 | 246 | 253 | PF00244 | 0.480 |
LIG_14-3-3_CanoR_1 | 86 | 96 | PF00244 | 0.402 |
LIG_BRCT_BRCA1_1 | 308 | 312 | PF00533 | 0.320 |
LIG_CtBP_PxDLS_1 | 278 | 282 | PF00389 | 0.397 |
LIG_deltaCOP1_diTrp_1 | 407 | 415 | PF00928 | 0.369 |
LIG_eIF4E_1 | 15 | 21 | PF01652 | 0.286 |
LIG_eIF4E_1 | 356 | 362 | PF01652 | 0.284 |
LIG_eIF4E_1 | 471 | 477 | PF01652 | 0.476 |
LIG_FHA_1 | 107 | 113 | PF00498 | 0.284 |
LIG_FHA_1 | 255 | 261 | PF00498 | 0.484 |
LIG_FHA_1 | 327 | 333 | PF00498 | 0.245 |
LIG_FHA_1 | 418 | 424 | PF00498 | 0.326 |
LIG_FHA_1 | 471 | 477 | PF00498 | 0.359 |
LIG_FHA_1 | 58 | 64 | PF00498 | 0.436 |
LIG_FHA_2 | 247 | 253 | PF00498 | 0.394 |
LIG_FHA_2 | 261 | 267 | PF00498 | 0.419 |
LIG_FHA_2 | 291 | 297 | PF00498 | 0.259 |
LIG_FHA_2 | 60 | 66 | PF00498 | 0.356 |
LIG_LIR_Apic_2 | 314 | 318 | PF02991 | 0.369 |
LIG_LIR_Gen_1 | 122 | 130 | PF02991 | 0.465 |
LIG_LIR_Gen_1 | 299 | 306 | PF02991 | 0.346 |
LIG_LIR_Gen_1 | 309 | 320 | PF02991 | 0.311 |
LIG_LIR_Gen_1 | 97 | 106 | PF02991 | 0.251 |
LIG_LIR_Nem_3 | 122 | 126 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 154 | 160 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 299 | 304 | PF02991 | 0.425 |
LIG_LIR_Nem_3 | 309 | 315 | PF02991 | 0.353 |
LIG_LIR_Nem_3 | 46 | 51 | PF02991 | 0.313 |
LIG_LIR_Nem_3 | 97 | 102 | PF02991 | 0.251 |
LIG_NRBOX | 16 | 22 | PF00104 | 0.303 |
LIG_PCNA_PIPBox_1 | 210 | 219 | PF02747 | 0.381 |
LIG_PCNA_yPIPBox_3 | 382 | 392 | PF02747 | 0.364 |
LIG_Pex14_1 | 221 | 225 | PF04695 | 0.269 |
LIG_SH2_CRK | 48 | 52 | PF00017 | 0.227 |
LIG_SH2_STAP1 | 153 | 157 | PF00017 | 0.354 |
LIG_SH2_STAP1 | 89 | 93 | PF00017 | 0.284 |
LIG_SH2_STAT3 | 251 | 254 | PF00017 | 0.414 |
LIG_SH2_STAT3 | 498 | 501 | PF00017 | 0.354 |
LIG_SH2_STAT3 | 89 | 92 | PF00017 | 0.284 |
LIG_SH2_STAT5 | 323 | 326 | PF00017 | 0.293 |
LIG_SH2_STAT5 | 391 | 394 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 417 | 420 | PF00017 | 0.363 |
LIG_SH2_STAT5 | 493 | 496 | PF00017 | 0.481 |
LIG_SH2_STAT5 | 498 | 501 | PF00017 | 0.355 |
LIG_SH2_STAT5 | 89 | 92 | PF00017 | 0.518 |
LIG_SH3_3 | 198 | 204 | PF00018 | 0.262 |
LIG_SH3_3 | 351 | 357 | PF00018 | 0.361 |
LIG_SUMO_SIM_par_1 | 172 | 178 | PF11976 | 0.431 |
LIG_SUMO_SIM_par_1 | 328 | 333 | PF11976 | 0.195 |
LIG_UBA3_1 | 183 | 192 | PF00899 | 0.323 |
LIG_UBA3_1 | 431 | 437 | PF00899 | 0.476 |
LIG_WRC_WIRS_1 | 123 | 128 | PF05994 | 0.400 |
MOD_CDK_SPxxK_3 | 54 | 61 | PF00069 | 0.259 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.379 |
MOD_CK1_1 | 145 | 151 | PF00069 | 0.387 |
MOD_CK1_1 | 162 | 168 | PF00069 | 0.242 |
MOD_CK1_1 | 245 | 251 | PF00069 | 0.284 |
MOD_CK1_1 | 422 | 428 | PF00069 | 0.517 |
MOD_CK1_1 | 57 | 63 | PF00069 | 0.282 |
MOD_CK2_1 | 2 | 8 | PF00069 | 0.470 |
MOD_CK2_1 | 260 | 266 | PF00069 | 0.489 |
MOD_CK2_1 | 267 | 273 | PF00069 | 0.523 |
MOD_CK2_1 | 290 | 296 | PF00069 | 0.259 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.379 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.337 |
MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.293 |
MOD_GSK3_1 | 242 | 249 | PF00069 | 0.492 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.503 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.439 |
MOD_GSK3_1 | 290 | 297 | PF00069 | 0.370 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.359 |
MOD_LATS_1 | 269 | 275 | PF00433 | 0.284 |
MOD_N-GLC_1 | 338 | 343 | PF02516 | 0.436 |
MOD_NEK2_1 | 106 | 111 | PF00069 | 0.436 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.386 |
MOD_NEK2_1 | 338 | 343 | PF00069 | 0.457 |
MOD_NEK2_1 | 431 | 436 | PF00069 | 0.289 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.386 |
MOD_PIKK_1 | 2 | 8 | PF00454 | 0.519 |
MOD_PIKK_1 | 294 | 300 | PF00454 | 0.419 |
MOD_PIKK_1 | 463 | 469 | PF00454 | 0.473 |
MOD_PIKK_1 | 88 | 94 | PF00454 | 0.371 |
MOD_PKA_2 | 143 | 149 | PF00069 | 0.227 |
MOD_PKA_2 | 245 | 251 | PF00069 | 0.359 |
MOD_Plk_1 | 242 | 248 | PF00069 | 0.467 |
MOD_Plk_1 | 338 | 344 | PF00069 | 0.410 |
MOD_Plk_1 | 440 | 446 | PF00069 | 0.284 |
MOD_Plk_1 | 72 | 78 | PF00069 | 0.486 |
MOD_Plk_1 | 97 | 103 | PF00069 | 0.253 |
MOD_Plk_4 | 122 | 128 | PF00069 | 0.465 |
MOD_Plk_4 | 175 | 181 | PF00069 | 0.372 |
MOD_Plk_4 | 27 | 33 | PF00069 | 0.383 |
MOD_Plk_4 | 422 | 428 | PF00069 | 0.361 |
MOD_Plk_4 | 59 | 65 | PF00069 | 0.381 |
MOD_ProDKin_1 | 107 | 113 | PF00069 | 0.259 |
MOD_ProDKin_1 | 54 | 60 | PF00069 | 0.356 |
MOD_SUMO_for_1 | 435 | 438 | PF00179 | 0.284 |
MOD_SUMO_for_1 | 70 | 73 | PF00179 | 0.361 |
MOD_SUMO_rev_2 | 170 | 178 | PF00179 | 0.412 |
MOD_SUMO_rev_2 | 22 | 31 | PF00179 | 0.259 |
TRG_DiLeu_BaEn_1 | 333 | 338 | PF01217 | 0.284 |
TRG_DiLeu_BaEn_1 | 46 | 51 | PF01217 | 0.436 |
TRG_DiLeu_BaLyEn_6 | 108 | 113 | PF01217 | 0.284 |
TRG_DiLeu_BaLyEn_6 | 315 | 320 | PF01217 | 0.405 |
TRG_ENDOCYTIC_2 | 153 | 156 | PF00928 | 0.361 |
TRG_ENDOCYTIC_2 | 391 | 394 | PF00928 | 0.364 |
TRG_ENDOCYTIC_2 | 4 | 7 | PF00928 | 0.385 |
TRG_ENDOCYTIC_2 | 48 | 51 | PF00928 | 0.227 |
TRG_ER_diArg_1 | 347 | 350 | PF00400 | 0.386 |
TRG_ER_diArg_1 | 496 | 498 | PF00400 | 0.363 |
TRG_ER_diArg_1 | 85 | 87 | PF00400 | 0.351 |
TRG_Pf-PMV_PEXEL_1 | 150 | 154 | PF00026 | 0.423 |
TRG_Pf-PMV_PEXEL_1 | 368 | 372 | PF00026 | 0.354 |
TRG_Pf-PMV_PEXEL_1 | 437 | 441 | PF00026 | 0.232 |
TRG_Pf-PMV_PEXEL_1 | 497 | 501 | PF00026 | 0.524 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4IZ28 | Bodo saltans | 45% | 100% |
A0A1X0NY67 | Trypanosomatidae | 52% | 99% |
A0A1X0P441 | Trypanosomatidae | 55% | 100% |
A0A1X0P598 | Trypanosomatidae | 56% | 100% |
A0A3Q8IBW2 | Leishmania donovani | 53% | 100% |
A0A3Q8IJY8 | Leishmania donovani | 49% | 100% |
A0A3Q8IU74 | Leishmania donovani | 54% | 100% |
A0A3S7WSA3 | Leishmania donovani | 96% | 100% |
A0A422P042 | Trypanosoma rangeli | 54% | 100% |
A0A422P4R1 | Trypanosoma rangeli | 53% | 100% |
A4H716 | Leishmania braziliensis | 81% | 100% |
A4HLW4 | Leishmania braziliensis | 55% | 100% |
A4HVE5 | Leishmania infantum | 96% | 100% |
A4HVW0 | Leishmania infantum | 53% | 100% |
A4I993 | Leishmania infantum | 54% | 100% |
A4IC85 | Leishmania infantum | 49% | 100% |
D0A656 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 54% | 100% |
E9B493 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 54% | 100% |
P42663 | Thermus aquaticus | 36% | 98% |
P50848 | Bacillus subtilis (strain 168) | 34% | 100% |
Q4Q0D4 | Leishmania major | 51% | 100% |
Q4Q3T3 | Leishmania major | 54% | 100% |
Q4QFW7 | Leishmania major | 53% | 100% |
Q4QGE5 | Leishmania major | 93% | 100% |
Q5SLM3 | Thermus thermophilus (strain ATCC 27634 / DSM 579 / HB8) | 35% | 99% |
Q8U3L0 | Pyrococcus furiosus (strain ATCC 43587 / DSM 3638 / JCM 8422 / Vc1) | 35% | 100% |
V5DQA0 | Trypanosoma cruzi | 54% | 100% |