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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4I070
Term | Name | Level | Count |
---|---|---|---|
GO:0006082 | organic acid metabolic process | 3 | 12 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006399 | tRNA metabolic process | 7 | 12 |
GO:0006418 | tRNA aminoacylation for protein translation | 6 | 12 |
GO:0006436 | tryptophanyl-tRNA aminoacylation | 7 | 12 |
GO:0006520 | amino acid metabolic process | 3 | 12 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016070 | RNA metabolic process | 5 | 12 |
GO:0019752 | carboxylic acid metabolic process | 5 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0034660 | ncRNA metabolic process | 6 | 12 |
GO:0043038 | amino acid activation | 4 | 12 |
GO:0043039 | tRNA aminoacylation | 5 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043436 | oxoacid metabolic process | 4 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044281 | small molecule metabolic process | 2 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0090304 | nucleic acid metabolic process | 4 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004812 | aminoacyl-tRNA ligase activity | 4 | 12 |
GO:0004830 | tryptophan-tRNA ligase activity | 5 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0016874 | ligase activity | 2 | 12 |
GO:0016875 | ligase activity, forming carbon-oxygen bonds | 3 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0030554 | adenyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 12 |
GO:0140101 | catalytic activity, acting on a tRNA | 4 | 12 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 212 | 216 | PF00656 | 0.456 |
CLV_NRD_NRD_1 | 16 | 18 | PF00675 | 0.561 |
CLV_NRD_NRD_1 | 236 | 238 | PF00675 | 0.280 |
CLV_NRD_NRD_1 | 312 | 314 | PF00675 | 0.237 |
CLV_NRD_NRD_1 | 317 | 319 | PF00675 | 0.223 |
CLV_NRD_NRD_1 | 389 | 391 | PF00675 | 0.290 |
CLV_NRD_NRD_1 | 392 | 394 | PF00675 | 0.297 |
CLV_PCSK_FUR_1 | 16 | 20 | PF00082 | 0.350 |
CLV_PCSK_FUR_1 | 390 | 394 | PF00082 | 0.450 |
CLV_PCSK_KEX2_1 | 15 | 17 | PF00082 | 0.549 |
CLV_PCSK_KEX2_1 | 18 | 20 | PF00082 | 0.557 |
CLV_PCSK_KEX2_1 | 236 | 238 | PF00082 | 0.280 |
CLV_PCSK_KEX2_1 | 317 | 319 | PF00082 | 0.274 |
CLV_PCSK_KEX2_1 | 391 | 393 | PF00082 | 0.299 |
CLV_PCSK_PC1ET2_1 | 15 | 17 | PF00082 | 0.416 |
CLV_PCSK_PC1ET2_1 | 18 | 20 | PF00082 | 0.441 |
CLV_PCSK_PC1ET2_1 | 391 | 393 | PF00082 | 0.313 |
CLV_PCSK_PC7_1 | 313 | 319 | PF00082 | 0.256 |
CLV_PCSK_SKI1_1 | 143 | 147 | PF00082 | 0.231 |
CLV_PCSK_SKI1_1 | 19 | 23 | PF00082 | 0.446 |
CLV_PCSK_SKI1_1 | 198 | 202 | PF00082 | 0.207 |
CLV_PCSK_SKI1_1 | 219 | 223 | PF00082 | 0.229 |
CLV_PCSK_SKI1_1 | 236 | 240 | PF00082 | 0.177 |
CLV_PCSK_SKI1_1 | 317 | 321 | PF00082 | 0.228 |
CLV_PCSK_SKI1_1 | 383 | 387 | PF00082 | 0.359 |
CLV_PCSK_SKI1_1 | 392 | 396 | PF00082 | 0.344 |
CLV_PCSK_SKI1_1 | 408 | 412 | PF00082 | 0.283 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.390 |
DEG_SCF_FBW7_1 | 32 | 38 | PF00400 | 0.504 |
DEG_SPOP_SBC_1 | 20 | 24 | PF00917 | 0.374 |
DOC_CKS1_1 | 32 | 37 | PF01111 | 0.596 |
DOC_MAPK_DCC_7 | 58 | 66 | PF00069 | 0.485 |
DOC_MAPK_MEF2A_6 | 58 | 66 | PF00069 | 0.485 |
DOC_PP1_RVXF_1 | 217 | 223 | PF00149 | 0.495 |
DOC_PP1_RVXF_1 | 70 | 77 | PF00149 | 0.311 |
DOC_PP4_FxxP_1 | 130 | 133 | PF00568 | 0.449 |
DOC_PP4_FxxP_1 | 348 | 351 | PF00568 | 0.455 |
DOC_USP7_MATH_1 | 367 | 371 | PF00917 | 0.354 |
DOC_USP7_UBL2_3 | 310 | 314 | PF12436 | 0.506 |
DOC_WW_Pin1_4 | 21 | 26 | PF00397 | 0.628 |
DOC_WW_Pin1_4 | 31 | 36 | PF00397 | 0.687 |
DOC_WW_Pin1_4 | 43 | 48 | PF00397 | 0.486 |
DOC_WW_Pin1_4 | 49 | 54 | PF00397 | 0.454 |
LIG_14-3-3_CanoR_1 | 175 | 179 | PF00244 | 0.436 |
LIG_14-3-3_CanoR_1 | 181 | 189 | PF00244 | 0.419 |
LIG_14-3-3_CanoR_1 | 19 | 25 | PF00244 | 0.607 |
LIG_14-3-3_CanoR_1 | 392 | 397 | PF00244 | 0.324 |
LIG_AP2alpha_2 | 257 | 259 | PF02296 | 0.431 |
LIG_BIR_III_2 | 44 | 48 | PF00653 | 0.539 |
LIG_BRCT_BRCA1_1 | 231 | 235 | PF00533 | 0.417 |
LIG_Clathr_ClatBox_1 | 85 | 89 | PF01394 | 0.321 |
LIG_FHA_1 | 109 | 115 | PF00498 | 0.451 |
LIG_FHA_1 | 121 | 127 | PF00498 | 0.370 |
LIG_FHA_1 | 206 | 212 | PF00498 | 0.452 |
LIG_FHA_1 | 278 | 284 | PF00498 | 0.514 |
LIG_FHA_1 | 32 | 38 | PF00498 | 0.561 |
LIG_FHA_2 | 137 | 143 | PF00498 | 0.427 |
LIG_FHA_2 | 210 | 216 | PF00498 | 0.456 |
LIG_FHA_2 | 302 | 308 | PF00498 | 0.420 |
LIG_FHA_2 | 393 | 399 | PF00498 | 0.315 |
LIG_LIR_Apic_2 | 128 | 133 | PF02991 | 0.449 |
LIG_LIR_Gen_1 | 340 | 351 | PF02991 | 0.431 |
LIG_LIR_Gen_1 | 353 | 363 | PF02991 | 0.431 |
LIG_LIR_Gen_1 | 403 | 412 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 188 | 193 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 232 | 238 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 257 | 262 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 340 | 346 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 353 | 359 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 403 | 407 | PF02991 | 0.328 |
LIG_LYPXL_S_1 | 189 | 193 | PF13949 | 0.274 |
LIG_LYPXL_yS_3 | 190 | 193 | PF13949 | 0.474 |
LIG_MAD2 | 237 | 245 | PF02301 | 0.510 |
LIG_PDZ_Class_2 | 407 | 412 | PF00595 | 0.326 |
LIG_Pex14_2 | 231 | 235 | PF04695 | 0.407 |
LIG_PTB_Apo_2 | 179 | 186 | PF02174 | 0.423 |
LIG_PTB_Phospho_1 | 179 | 185 | PF10480 | 0.423 |
LIG_REV1ctd_RIR_1 | 67 | 76 | PF16727 | 0.323 |
LIG_SH2_CRK | 343 | 347 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 102 | 105 | PF00017 | 0.412 |
LIG_SH2_STAT5 | 125 | 128 | PF00017 | 0.471 |
LIG_SH2_STAT5 | 345 | 348 | PF00017 | 0.517 |
LIG_SH3_3 | 29 | 35 | PF00018 | 0.554 |
LIG_SUMO_SIM_anti_2 | 36 | 42 | PF11976 | 0.451 |
LIG_SUMO_SIM_par_1 | 301 | 309 | PF11976 | 0.431 |
LIG_SUMO_SIM_par_1 | 84 | 89 | PF11976 | 0.371 |
LIG_TRAF2_1 | 296 | 299 | PF00917 | 0.540 |
LIG_TYR_ITIM | 341 | 346 | PF00017 | 0.431 |
MOD_CK1_1 | 108 | 114 | PF00069 | 0.383 |
MOD_CK1_1 | 91 | 97 | PF00069 | 0.355 |
MOD_CK2_1 | 136 | 142 | PF00069 | 0.427 |
MOD_CK2_1 | 292 | 298 | PF00069 | 0.451 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.668 |
MOD_GlcNHglycan | 295 | 298 | PF01048 | 0.247 |
MOD_GlcNHglycan | 320 | 323 | PF01048 | 0.207 |
MOD_GlcNHglycan | 364 | 367 | PF01048 | 0.264 |
MOD_GlcNHglycan | 369 | 372 | PF01048 | 0.280 |
MOD_GlcNHglycan | 41 | 44 | PF01048 | 0.683 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.522 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.512 |
MOD_GSK3_1 | 301 | 308 | PF00069 | 0.438 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.482 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.478 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.453 |
MOD_NEK2_1 | 100 | 105 | PF00069 | 0.359 |
MOD_NEK2_1 | 120 | 125 | PF00069 | 0.412 |
MOD_NEK2_1 | 159 | 164 | PF00069 | 0.419 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.416 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.460 |
MOD_NEK2_1 | 277 | 282 | PF00069 | 0.437 |
MOD_NEK2_2 | 301 | 306 | PF00069 | 0.449 |
MOD_NEK2_2 | 351 | 356 | PF00069 | 0.419 |
MOD_NEK2_2 | 95 | 100 | PF00069 | 0.332 |
MOD_PIKK_1 | 222 | 228 | PF00454 | 0.474 |
MOD_PIKK_1 | 357 | 363 | PF00454 | 0.456 |
MOD_PKA_1 | 392 | 398 | PF00069 | 0.445 |
MOD_PKA_2 | 174 | 180 | PF00069 | 0.436 |
MOD_PKA_2 | 392 | 398 | PF00069 | 0.449 |
MOD_PKB_1 | 17 | 25 | PF00069 | 0.463 |
MOD_PKB_1 | 390 | 398 | PF00069 | 0.341 |
MOD_Plk_1 | 35 | 41 | PF00069 | 0.594 |
MOD_Plk_1 | 351 | 357 | PF00069 | 0.419 |
MOD_Plk_1 | 88 | 94 | PF00069 | 0.504 |
MOD_Plk_1 | 95 | 101 | PF00069 | 0.389 |
MOD_Plk_4 | 174 | 180 | PF00069 | 0.425 |
MOD_Plk_4 | 189 | 195 | PF00069 | 0.459 |
MOD_Plk_4 | 35 | 41 | PF00069 | 0.450 |
MOD_Plk_4 | 351 | 357 | PF00069 | 0.480 |
MOD_Plk_4 | 95 | 101 | PF00069 | 0.424 |
MOD_ProDKin_1 | 21 | 27 | PF00069 | 0.635 |
MOD_ProDKin_1 | 31 | 37 | PF00069 | 0.688 |
MOD_ProDKin_1 | 43 | 49 | PF00069 | 0.488 |
MOD_SUMO_rev_2 | 140 | 145 | PF00179 | 0.407 |
MOD_SUMO_rev_2 | 294 | 302 | PF00179 | 0.401 |
MOD_SUMO_rev_2 | 370 | 376 | PF00179 | 0.480 |
TRG_ENDOCYTIC_2 | 190 | 193 | PF00928 | 0.445 |
TRG_ENDOCYTIC_2 | 343 | 346 | PF00928 | 0.431 |
TRG_ER_diArg_1 | 16 | 19 | PF00400 | 0.476 |
TRG_ER_diArg_1 | 235 | 237 | PF00400 | 0.480 |
TRG_ER_diArg_1 | 316 | 318 | PF00400 | 0.474 |
TRG_ER_diArg_1 | 389 | 392 | PF00400 | 0.360 |
TRG_NLS_MonoCore_2 | 14 | 19 | PF00514 | 0.345 |
TRG_NLS_MonoCore_2 | 389 | 394 | PF00514 | 0.244 |
TRG_NLS_MonoExtC_3 | 14 | 19 | PF00514 | 0.345 |
TRG_NLS_MonoExtC_3 | 312 | 317 | PF00514 | 0.433 |
TRG_NLS_MonoExtN_4 | 15 | 21 | PF00514 | 0.440 |
TRG_NLS_MonoExtN_4 | 310 | 317 | PF00514 | 0.509 |
TRG_NLS_MonoExtN_4 | 390 | 395 | PF00514 | 0.257 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3G3 | Leptomonas seymouri | 44% | 100% |
A0A0N1HXL2 | Leptomonas seymouri | 71% | 88% |
A0A0S4IN16 | Bodo saltans | 46% | 100% |
A0A0S4JC70 | Bodo saltans | 59% | 91% |
A0A1X0NGJ6 | Trypanosomatidae | 62% | 89% |
A0A1X0NZB4 | Trypanosomatidae | 47% | 100% |
A0A3R7MPN7 | Trypanosoma rangeli | 47% | 100% |
A0A3S7WXL2 | Leishmania donovani | 100% | 100% |
A0A3S7X238 | Leishmania donovani | 42% | 100% |
A0A422NW64 | Trypanosoma rangeli | 62% | 92% |
A2BLD4 | Hyperthermus butylicus (strain DSM 5456 / JCM 9403 / PLM1-5) | 27% | 100% |
A3MX72 | Pyrobaculum calidifontis (strain DSM 21063 / JCM 11548 / VA1) | 37% | 100% |
A4HCP4 | Leishmania braziliensis | 80% | 100% |
A4HH14 | Leishmania braziliensis | 44% | 100% |
A4I443 | Leishmania infantum | 42% | 100% |
A4WL99 | Pyrobaculum arsenaticum (strain DSM 13514 / JCM 11321 / PZ6) | 36% | 100% |
B6YUH1 | Thermococcus onnurineus (strain NA1) | 39% | 100% |
C6A032 | Thermococcus sibiricus (strain DSM 12597 / MM 739) | 38% | 100% |
C9ZKR9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 100% |
E9ADK8 | Leishmania major | 45% | 100% |
E9AM73 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 44% | 100% |
E9AW33 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
O26352 | Methanothermobacter thermautotrophicus (strain ATCC 29096 / DSM 1053 / JCM 10044 / NBRC 100330 / Delta H) | 28% | 100% |
O59584 | Pyrococcus horikoshii (strain ATCC 700860 / DSM 12428 / JCM 9974 / NBRC 100139 / OT-3) | 39% | 100% |
O96771 | Encephalitozoon cuniculi (strain GB-M1) | 41% | 100% |
P17248 | Bos taurus | 45% | 87% |
P23381 | Homo sapiens | 45% | 87% |
P23612 | Oryctolagus cuniculus | 45% | 87% |
P32921 | Mus musculus | 46% | 86% |
Q09692 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 47% | 100% |
Q12109 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 46% | 95% |
Q4JBG7 | Sulfolobus acidocaldarius (strain ATCC 33909 / DSM 639 / JCM 8929 / NBRC 15157 / NCIMB 11770) | 42% | 100% |
Q4QBE4 | Leishmania major | 94% | 100% |
Q55DZ8 | Dictyostelium discoideum | 45% | 100% |
Q58810 | Methanocaldococcus jannaschii (strain ATCC 43067 / DSM 2661 / JAL-1 / JCM 10045 / NBRC 100440) | 32% | 100% |
Q5JEP3 | Thermococcus kodakarensis (strain ATCC BAA-918 / JCM 12380 / KOD1) | 40% | 100% |
Q5R4J1 | Pongo abelii | 45% | 87% |
Q6P7B0 | Rattus norvegicus | 45% | 86% |
Q8TYF7 | Methanopyrus kandleri (strain AV19 / DSM 6324 / JCM 9639 / NBRC 100938) | 28% | 100% |
Q8U453 | Pyrococcus furiosus (strain ATCC 43587 / DSM 3638 / JCM 8422 / Vc1) | 41% | 100% |
Q8ZTU5 | Pyrobaculum aerophilum (strain ATCC 51768 / DSM 7523 / JCM 9630 / CIP 104966 / NBRC 100827 / IM2) | 38% | 100% |
Q976M1 | Sulfurisphaera tokodaii (strain DSM 16993 / JCM 10545 / NBRC 100140 / 7) | 42% | 100% |
Q97ZX0 | Saccharolobus solfataricus (strain ATCC 35092 / DSM 1617 / JCM 11322 / P2) | 40% | 100% |
Q9HN66 | Halobacterium salinarum (strain ATCC 700922 / JCM 11081 / NRC-1) | 38% | 100% |
Q9SR15 | Arabidopsis thaliana | 42% | 100% |
Q9UY11 | Pyrococcus abyssi (strain GE5 / Orsay) | 40% | 100% |
Q9Y924 | Aeropyrum pernix (strain ATCC 700893 / DSM 11879 / JCM 9820 / NBRC 100138 / K1) | 30% | 100% |
V5B4S5 | Trypanosoma cruzi | 46% | 100% |