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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 10 |
GO:0043226 | organelle | 2 | 10 |
GO:0043227 | membrane-bounded organelle | 3 | 10 |
GO:0043229 | intracellular organelle | 3 | 10 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
Related structures:
AlphaFold database: Q4QCE7
Term | Name | Level | Count |
---|---|---|---|
GO:0006325 | chromatin organization | 4 | 10 |
GO:0006355 | regulation of DNA-templated transcription | 6 | 2 |
GO:0006357 | regulation of transcription by RNA polymerase II | 7 | 2 |
GO:0006476 | protein deacetylation | 6 | 10 |
GO:0006807 | nitrogen compound metabolic process | 2 | 10 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0009889 | regulation of biosynthetic process | 4 | 2 |
GO:0009987 | cellular process | 1 | 10 |
GO:0010468 | regulation of gene expression | 5 | 2 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 2 |
GO:0016043 | cellular component organization | 3 | 10 |
GO:0016570 | histone modification | 5 | 10 |
GO:0016575 | histone deacetylation | 6 | 10 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 2 |
GO:0019222 | regulation of metabolic process | 3 | 2 |
GO:0019538 | protein metabolic process | 3 | 10 |
GO:0031323 | regulation of cellular metabolic process | 4 | 2 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 2 |
GO:0035601 | protein deacylation | 5 | 10 |
GO:0036211 | protein modification process | 4 | 10 |
GO:0043170 | macromolecule metabolic process | 3 | 10 |
GO:0043412 | macromolecule modification | 4 | 10 |
GO:0044238 | primary metabolic process | 2 | 10 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0050794 | regulation of cellular process | 3 | 2 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 2 |
GO:0051252 | regulation of RNA metabolic process | 5 | 2 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 10 |
GO:0071840 | cellular component organization or biogenesis | 2 | 10 |
GO:0080090 | regulation of primary metabolic process | 4 | 2 |
GO:0098732 | macromolecule deacylation | 5 | 10 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 10 |
GO:1903506 | regulation of nucleic acid-templated transcription | 7 | 2 |
GO:2001141 | regulation of RNA biosynthetic process | 6 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 10 |
GO:0004407 | histone deacetylase activity | 4 | 10 |
GO:0005488 | binding | 1 | 9 |
GO:0016787 | hydrolase activity | 2 | 10 |
GO:0016810 | hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds | 3 | 10 |
GO:0016811 | hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amides | 4 | 10 |
GO:0019213 | deacetylase activity | 3 | 10 |
GO:0033558 | protein lysine deacetylase activity | 3 | 10 |
GO:0043167 | ion binding | 2 | 9 |
GO:0043169 | cation binding | 3 | 9 |
GO:0046872 | metal ion binding | 4 | 9 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 265 | 267 | PF00675 | 0.265 |
CLV_PCSK_KEX2_1 | 265 | 267 | PF00082 | 0.302 |
CLV_PCSK_SKI1_1 | 107 | 111 | PF00082 | 0.265 |
CLV_PCSK_SKI1_1 | 206 | 210 | PF00082 | 0.219 |
CLV_PCSK_SKI1_1 | 21 | 25 | PF00082 | 0.377 |
CLV_PCSK_SKI1_1 | 405 | 409 | PF00082 | 0.399 |
CLV_PCSK_SKI1_1 | 58 | 62 | PF00082 | 0.299 |
CLV_Separin_Metazoa | 55 | 59 | PF03568 | 0.495 |
DEG_APCC_DBOX_1 | 284 | 292 | PF00400 | 0.502 |
DOC_CYCLIN_yCln2_LP_2 | 306 | 312 | PF00134 | 0.435 |
DOC_MAPK_DCC_7 | 304 | 313 | PF00069 | 0.418 |
DOC_MAPK_DCC_7 | 67 | 76 | PF00069 | 0.418 |
DOC_MAPK_gen_1 | 233 | 241 | PF00069 | 0.502 |
DOC_MAPK_gen_1 | 46 | 56 | PF00069 | 0.418 |
DOC_MAPK_MEF2A_6 | 183 | 191 | PF00069 | 0.418 |
DOC_MAPK_MEF2A_6 | 235 | 243 | PF00069 | 0.418 |
DOC_MAPK_MEF2A_6 | 304 | 313 | PF00069 | 0.418 |
DOC_MAPK_MEF2A_6 | 67 | 76 | PF00069 | 0.418 |
DOC_PP1_RVXF_1 | 105 | 111 | PF00149 | 0.435 |
DOC_PP2B_LxvP_1 | 306 | 309 | PF13499 | 0.418 |
DOC_USP7_MATH_1 | 103 | 107 | PF00917 | 0.465 |
DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.464 |
DOC_USP7_MATH_1 | 259 | 263 | PF00917 | 0.435 |
DOC_WW_Pin1_4 | 265 | 270 | PF00397 | 0.465 |
DOC_WW_Pin1_4 | 357 | 362 | PF00397 | 0.386 |
LIG_14-3-3_CanoR_1 | 206 | 211 | PF00244 | 0.419 |
LIG_14-3-3_CanoR_1 | 235 | 240 | PF00244 | 0.435 |
LIG_APCC_Cbox_2 | 391 | 397 | PF00515 | 0.430 |
LIG_BRCT_BRCA1_1 | 105 | 109 | PF00533 | 0.465 |
LIG_Clathr_ClatBox_1 | 73 | 77 | PF01394 | 0.435 |
LIG_DLG_GKlike_1 | 235 | 243 | PF00625 | 0.502 |
LIG_FHA_1 | 103 | 109 | PF00498 | 0.465 |
LIG_FHA_1 | 207 | 213 | PF00498 | 0.418 |
LIG_FHA_1 | 329 | 335 | PF00498 | 0.441 |
LIG_FHA_1 | 385 | 391 | PF00498 | 0.383 |
LIG_FHA_1 | 419 | 425 | PF00498 | 0.548 |
LIG_FHA_2 | 406 | 412 | PF00498 | 0.420 |
LIG_FHA_2 | 420 | 426 | PF00498 | 0.649 |
LIG_GBD_Chelix_1 | 170 | 178 | PF00786 | 0.218 |
LIG_LIR_Gen_1 | 162 | 172 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 162 | 167 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 248 | 253 | PF02991 | 0.444 |
LIG_Pex14_2 | 215 | 219 | PF04695 | 0.418 |
LIG_SH2_CRK | 48 | 52 | PF00017 | 0.418 |
LIG_SH2_GRB2like | 166 | 169 | PF00017 | 0.418 |
LIG_SH2_PTP2 | 186 | 189 | PF00017 | 0.418 |
LIG_SH2_SRC | 186 | 189 | PF00017 | 0.502 |
LIG_SH2_STAP1 | 237 | 241 | PF00017 | 0.453 |
LIG_SH2_STAP1 | 30 | 34 | PF00017 | 0.486 |
LIG_SH2_STAP1 | 329 | 333 | PF00017 | 0.418 |
LIG_SH2_STAT5 | 166 | 169 | PF00017 | 0.418 |
LIG_SH2_STAT5 | 186 | 189 | PF00017 | 0.332 |
LIG_SH2_STAT5 | 252 | 255 | PF00017 | 0.479 |
LIG_SH2_STAT5 | 318 | 321 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 87 | 90 | PF00017 | 0.418 |
LIG_SH3_3 | 335 | 341 | PF00018 | 0.442 |
LIG_SH3_3 | 66 | 72 | PF00018 | 0.418 |
LIG_SUMO_SIM_anti_2 | 359 | 366 | PF11976 | 0.392 |
LIG_TYR_ITIM | 184 | 189 | PF00017 | 0.418 |
LIG_UBA3_1 | 174 | 179 | PF00899 | 0.418 |
LIG_WRC_WIRS_1 | 291 | 296 | PF05994 | 0.502 |
MOD_CK1_1 | 124 | 130 | PF00069 | 0.487 |
MOD_CK1_1 | 332 | 338 | PF00069 | 0.516 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.438 |
MOD_CK2_1 | 11 | 17 | PF00069 | 0.469 |
MOD_CK2_1 | 405 | 411 | PF00069 | 0.422 |
MOD_CK2_1 | 419 | 425 | PF00069 | 0.652 |
MOD_GlcNHglycan | 110 | 113 | PF01048 | 0.218 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.218 |
MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.228 |
MOD_GlcNHglycan | 160 | 164 | PF01048 | 0.220 |
MOD_GlcNHglycan | 26 | 30 | PF01048 | 0.366 |
MOD_GlcNHglycan | 352 | 355 | PF01048 | 0.323 |
MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.367 |
MOD_GSK3_1 | 11 | 18 | PF00069 | 0.576 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.435 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.299 |
MOD_GSK3_1 | 328 | 335 | PF00069 | 0.502 |
MOD_N-GLC_1 | 289 | 294 | PF02516 | 0.218 |
MOD_N-GLC_1 | 34 | 39 | PF02516 | 0.424 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.449 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.369 |
MOD_NEK2_1 | 153 | 158 | PF00069 | 0.502 |
MOD_NEK2_1 | 208 | 213 | PF00069 | 0.436 |
MOD_NEK2_1 | 215 | 220 | PF00069 | 0.450 |
MOD_NEK2_1 | 24 | 29 | PF00069 | 0.324 |
MOD_NEK2_1 | 289 | 294 | PF00069 | 0.418 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.364 |
MOD_NEK2_2 | 316 | 321 | PF00069 | 0.435 |
MOD_NEK2_2 | 92 | 97 | PF00069 | 0.502 |
MOD_PKB_1 | 233 | 241 | PF00069 | 0.465 |
MOD_Plk_1 | 121 | 127 | PF00069 | 0.433 |
MOD_Plk_1 | 289 | 295 | PF00069 | 0.429 |
MOD_Plk_1 | 329 | 335 | PF00069 | 0.418 |
MOD_Plk_1 | 34 | 40 | PF00069 | 0.415 |
MOD_Plk_4 | 128 | 134 | PF00069 | 0.418 |
MOD_Plk_4 | 215 | 221 | PF00069 | 0.427 |
MOD_Plk_4 | 259 | 265 | PF00069 | 0.494 |
MOD_Plk_4 | 329 | 335 | PF00069 | 0.418 |
MOD_Plk_4 | 340 | 346 | PF00069 | 0.352 |
MOD_Plk_4 | 83 | 89 | PF00069 | 0.502 |
MOD_ProDKin_1 | 265 | 271 | PF00069 | 0.465 |
MOD_ProDKin_1 | 357 | 363 | PF00069 | 0.378 |
MOD_SUMO_for_1 | 74 | 77 | PF00179 | 0.502 |
TRG_DiLeu_BaLyEn_6 | 358 | 363 | PF01217 | 0.452 |
TRG_ENDOCYTIC_2 | 186 | 189 | PF00928 | 0.421 |
TRG_ENDOCYTIC_2 | 236 | 239 | PF00928 | 0.461 |
TRG_ENDOCYTIC_2 | 252 | 255 | PF00928 | 0.418 |
TRG_ENDOCYTIC_2 | 383 | 386 | PF00928 | 0.461 |
TRG_ENDOCYTIC_2 | 48 | 51 | PF00928 | 0.418 |
TRG_ER_diArg_1 | 19 | 22 | PF00400 | 0.467 |
TRG_ER_diArg_1 | 233 | 236 | PF00400 | 0.493 |
TRG_ER_diArg_1 | 264 | 266 | PF00400 | 0.465 |
TRG_NES_CRM1_1 | 245 | 257 | PF08389 | 0.476 |
TRG_Pf-PMV_PEXEL_1 | 183 | 188 | PF00026 | 0.218 |
TRG_Pf-PMV_PEXEL_1 | 58 | 63 | PF00026 | 0.235 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCD3 | Leptomonas seymouri | 38% | 80% |
A0A0N1PFX6 | Leptomonas seymouri | 84% | 100% |
A0A1X0NVQ2 | Trypanosomatidae | 40% | 94% |
A0A1X0NXU7 | Trypanosomatidae | 69% | 100% |
A0A3Q8IC47 | Leishmania donovani | 39% | 80% |
A0A3R7L005 | Trypanosoma rangeli | 72% | 100% |
A0A3S7WWE6 | Leishmania donovani | 98% | 100% |
A0A422N1V5 | Trypanosoma rangeli | 39% | 95% |
A4HBR4 | Leishmania braziliensis | 92% | 99% |
A4HDK5 | Leishmania braziliensis | 40% | 99% |
A4HZ67 | Leishmania infantum | 98% | 100% |
A4I0X6 | Leishmania infantum | 39% | 80% |
B1H369 | Xenopus tropicalis | 42% | 100% |
B1WC68 | Rattus norvegicus | 42% | 100% |
D0A1H7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 71% | 100% |
E9AV34 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 97% | 94% |
E9AWY0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 39% | 79% |
O09106 | Mus musculus | 46% | 89% |
O13298 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 44% | 99% |
O15379 | Homo sapiens | 42% | 100% |
O17695 | Caenorhabditis elegans | 41% | 93% |
O22446 | Arabidopsis thaliana | 49% | 85% |
O27262 | Methanothermobacter thermautotrophicus (strain ATCC 29096 / DSM 1053 / JCM 10044 / NBRC 100330 / Delta H) | 23% | 100% |
O30107 | Archaeoglobus fulgidus (strain ATCC 49558 / DSM 4304 / JCM 9628 / NBRC 100126 / VC-16) | 27% | 100% |
O42227 | Xenopus laevis | 45% | 89% |
O59702 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 39% | 100% |
O88895 | Mus musculus | 42% | 100% |
P32561 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 40% | 99% |
P39067 | Bacillus subtilis (strain 168) | 32% | 100% |
P53096 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 43% | 95% |
P56517 | Gallus gallus | 41% | 89% |
P56518 | Strongylocentrotus purpuratus | 45% | 74% |
P56519 | Gallus gallus | 40% | 88% |
P56520 | Gallus gallus | 42% | 100% |
P56521 | Zea mays | 45% | 83% |
P64375 | Staphylococcus aureus (strain Mu50 / ATCC 700699) | 28% | 100% |
P64376 | Staphylococcus aureus (strain N315) | 28% | 100% |
P70288 | Mus musculus | 41% | 88% |
Q09440 | Caenorhabditis elegans | 45% | 84% |
Q0VCB2 | Bos taurus | 41% | 100% |
Q13547 | Homo sapiens | 46% | 89% |
Q28DV3 | Xenopus tropicalis | 42% | 100% |
Q32PJ8 | Bos taurus | 46% | 89% |
Q4QAJ4 | Leishmania major | 39% | 80% |
Q4QQW4 | Rattus norvegicus | 46% | 89% |
Q4SFA0 | Tetraodon nigroviridis | 41% | 100% |
Q55BW2 | Dictyostelium discoideum | 43% | 100% |
Q55FN5 | Dictyostelium discoideum | 44% | 86% |
Q56195 | Staphylococcus xylosus | 29% | 100% |
Q57955 | Methanocaldococcus jannaschii (strain ATCC 43067 / DSM 2661 / JAL-1 / JCM 10045 / NBRC 100440) | 26% | 100% |
Q5HF39 | Staphylococcus aureus (strain COL) | 28% | 100% |
Q5RAG0 | Pongo abelii | 46% | 89% |
Q5RB76 | Pongo abelii | 44% | 100% |
Q6G8J2 | Staphylococcus aureus (strain MSSA476) | 28% | 100% |
Q6GFX3 | Staphylococcus aureus (strain MRSA252) | 28% | 100% |
Q6IRL9 | Xenopus laevis | 44% | 100% |
Q6P6W3 | Rattus norvegicus | 42% | 100% |
Q6YV04 | Oryza sativa subsp. japonica | 48% | 84% |
Q7SXM0 | Danio rerio | 40% | 100% |
Q7Y0Y6 | Oryza sativa subsp. japonica | 42% | 84% |
Q7Y0Y8 | Oryza sativa subsp. japonica | 49% | 83% |
Q803C3 | Danio rerio | 43% | 100% |
Q8H0W2 | Arabidopsis thaliana | 40% | 100% |
Q8NW34 | Staphylococcus aureus (strain MW2) | 28% | 100% |
Q8VH37 | Mus musculus | 42% | 100% |
Q91695 | Xenopus laevis | 45% | 89% |
Q92769 | Homo sapiens | 42% | 88% |
Q944K3 | Arabidopsis thaliana | 27% | 100% |
Q94517 | Drosophila melanogaster | 46% | 82% |
Q94EJ2 | Arabidopsis thaliana | 29% | 100% |
Q9BY41 | Homo sapiens | 41% | 100% |
Q9FH09 | Arabidopsis thaliana | 38% | 100% |
Q9FML2 | Arabidopsis thaliana | 47% | 91% |
V5B3T3 | Trypanosoma cruzi | 34% | 96% |