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: 8 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: A4HDK5
Term | Name | Level | Count |
---|---|---|---|
GO:0006325 | chromatin organization | 4 | 9 |
GO:0006476 | protein deacetylation | 6 | 9 |
GO:0006807 | nitrogen compound metabolic process | 2 | 9 |
GO:0008152 | metabolic process | 1 | 9 |
GO:0009987 | cellular process | 1 | 9 |
GO:0016043 | cellular component organization | 3 | 9 |
GO:0016570 | histone modification | 5 | 9 |
GO:0016575 | histone deacetylation | 6 | 9 |
GO:0019538 | protein metabolic process | 3 | 9 |
GO:0035601 | protein deacylation | 5 | 9 |
GO:0036211 | protein modification process | 4 | 9 |
GO:0043170 | macromolecule metabolic process | 3 | 9 |
GO:0043412 | macromolecule modification | 4 | 9 |
GO:0044238 | primary metabolic process | 2 | 9 |
GO:0071704 | organic substance metabolic process | 2 | 9 |
GO:0071840 | cellular component organization or biogenesis | 2 | 9 |
GO:0098732 | macromolecule deacylation | 5 | 9 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 9 |
GO:0006355 | regulation of DNA-templated transcription | 6 | 1 |
GO:0006357 | regulation of transcription by RNA polymerase II | 7 | 1 |
GO:0009889 | regulation of biosynthetic process | 4 | 1 |
GO:0010468 | regulation of gene expression | 5 | 1 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 1 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0051252 | regulation of RNA metabolic process | 5 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:1903506 | regulation of nucleic acid-templated transcription | 7 | 1 |
GO:2001141 | regulation of RNA biosynthetic process | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 9 |
GO:0004407 | histone deacetylase activity | 4 | 9 |
GO:0016787 | hydrolase activity | 2 | 9 |
GO:0016810 | hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds | 3 | 9 |
GO:0016811 | hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amides | 4 | 9 |
GO:0019213 | deacetylase activity | 3 | 9 |
GO:0033558 | protein lysine deacetylase activity | 3 | 9 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 198 | 202 | PF00656 | 0.536 |
CLV_NRD_NRD_1 | 143 | 145 | PF00675 | 0.287 |
CLV_NRD_NRD_1 | 385 | 387 | PF00675 | 0.509 |
CLV_PCSK_FUR_1 | 383 | 387 | PF00082 | 0.582 |
CLV_PCSK_KEX2_1 | 143 | 145 | PF00082 | 0.287 |
CLV_PCSK_KEX2_1 | 329 | 331 | PF00082 | 0.416 |
CLV_PCSK_KEX2_1 | 385 | 387 | PF00082 | 0.466 |
CLV_PCSK_KEX2_1 | 410 | 412 | PF00082 | 0.692 |
CLV_PCSK_PC1ET2_1 | 329 | 331 | PF00082 | 0.563 |
CLV_PCSK_PC1ET2_1 | 410 | 412 | PF00082 | 0.700 |
CLV_PCSK_SKI1_1 | 143 | 147 | PF00082 | 0.336 |
CLV_PCSK_SKI1_1 | 174 | 178 | PF00082 | 0.263 |
CLV_PCSK_SKI1_1 | 223 | 227 | PF00082 | 0.278 |
CLV_PCSK_SKI1_1 | 30 | 34 | PF00082 | 0.302 |
CLV_PCSK_SKI1_1 | 386 | 390 | PF00082 | 0.510 |
DEG_APCC_DBOX_1 | 222 | 230 | PF00400 | 0.502 |
DOC_CYCLIN_RxL_1 | 352 | 360 | PF00134 | 0.349 |
DOC_MAPK_gen_1 | 329 | 337 | PF00069 | 0.555 |
DOC_MAPK_MEF2A_6 | 151 | 159 | PF00069 | 0.484 |
DOC_MAPK_MEF2A_6 | 303 | 312 | PF00069 | 0.508 |
DOC_MAPK_MEF2A_6 | 329 | 337 | PF00069 | 0.424 |
DOC_PP2B_LxvP_1 | 310 | 313 | PF13499 | 0.480 |
DOC_PP4_FxxP_1 | 272 | 275 | PF00568 | 0.394 |
DOC_PP4_FxxP_1 | 336 | 339 | PF00568 | 0.539 |
DOC_PP4_FxxP_1 | 71 | 74 | PF00568 | 0.478 |
DOC_USP7_MATH_1 | 127 | 131 | PF00917 | 0.481 |
DOC_USP7_MATH_1 | 225 | 229 | PF00917 | 0.536 |
DOC_USP7_MATH_1 | 74 | 78 | PF00917 | 0.536 |
DOC_USP7_MATH_1 | 96 | 100 | PF00917 | 0.462 |
DOC_WW_Pin1_4 | 324 | 329 | PF00397 | 0.594 |
LIG_14-3-3_CanoR_1 | 174 | 179 | PF00244 | 0.478 |
LIG_14-3-3_CanoR_1 | 223 | 233 | PF00244 | 0.502 |
LIG_14-3-3_CanoR_1 | 30 | 37 | PF00244 | 0.478 |
LIG_14-3-3_CterR_2 | 429 | 433 | PF00244 | 0.710 |
LIG_APCC_ABBA_1 | 333 | 338 | PF00400 | 0.420 |
LIG_BRCT_BRCA1_1 | 349 | 353 | PF00533 | 0.538 |
LIG_BRCT_BRCA1_1 | 63 | 67 | PF00533 | 0.536 |
LIG_BRCT_BRCA1_2 | 63 | 69 | PF00533 | 0.536 |
LIG_CaM_IQ_9 | 358 | 374 | PF13499 | 0.474 |
LIG_FHA_1 | 175 | 181 | PF00498 | 0.478 |
LIG_FHA_1 | 261 | 267 | PF00498 | 0.503 |
LIG_FHA_1 | 274 | 280 | PF00498 | 0.429 |
LIG_FHA_1 | 330 | 336 | PF00498 | 0.410 |
LIG_FHA_1 | 365 | 371 | PF00498 | 0.461 |
LIG_FHA_1 | 376 | 382 | PF00498 | 0.495 |
LIG_FHA_2 | 31 | 37 | PF00498 | 0.480 |
LIG_GBD_Chelix_1 | 138 | 146 | PF00786 | 0.278 |
LIG_GBD_Chelix_1 | 247 | 255 | PF00786 | 0.278 |
LIG_Integrin_RGD_1 | 108 | 110 | PF01839 | 0.336 |
LIG_LIR_Apic_2 | 271 | 275 | PF02991 | 0.394 |
LIG_LIR_Apic_2 | 70 | 74 | PF02991 | 0.502 |
LIG_LIR_Gen_1 | 130 | 140 | PF02991 | 0.478 |
LIG_LIR_Gen_1 | 87 | 96 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 130 | 135 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 316 | 322 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 87 | 92 | PF02991 | 0.478 |
LIG_Pex14_2 | 183 | 187 | PF04695 | 0.466 |
LIG_Pex14_2 | 67 | 71 | PF04695 | 0.528 |
LIG_Pex14_2 | 85 | 89 | PF04695 | 0.377 |
LIG_PTB_Apo_2 | 182 | 189 | PF02174 | 0.478 |
LIG_Rb_LxCxE_1 | 99 | 112 | PF01857 | 0.478 |
LIG_SH2_CRK | 149 | 153 | PF00017 | 0.536 |
LIG_SH2_PTP2 | 154 | 157 | PF00017 | 0.536 |
LIG_SH2_STAT5 | 154 | 157 | PF00017 | 0.478 |
LIG_SH2_STAT5 | 218 | 221 | PF00017 | 0.478 |
LIG_SH2_STAT5 | 311 | 314 | PF00017 | 0.382 |
LIG_SH2_STAT5 | 45 | 48 | PF00017 | 0.478 |
LIG_SH3_3 | 204 | 210 | PF00018 | 0.482 |
LIG_SH3_3 | 325 | 331 | PF00018 | 0.444 |
LIG_SH3_3 | 338 | 344 | PF00018 | 0.406 |
LIG_SH3_3 | 403 | 409 | PF00018 | 0.758 |
LIG_SH3_3 | 80 | 86 | PF00018 | 0.478 |
LIG_TRAF2_1 | 33 | 36 | PF00917 | 0.478 |
LIG_TRAF2_1 | 394 | 397 | PF00917 | 0.578 |
LIG_TRAF2_1 | 421 | 424 | PF00917 | 0.522 |
LIG_TRAF2_1 | 76 | 79 | PF00917 | 0.552 |
LIG_TYR_ITIM | 152 | 157 | PF00017 | 0.478 |
LIG_WRC_WIRS_1 | 219 | 224 | PF05994 | 0.575 |
LIG_WRC_WIRS_1 | 269 | 274 | PF05994 | 0.394 |
LIG_WRC_WIRS_1 | 37 | 42 | PF05994 | 0.394 |
MOD_CDK_SPK_2 | 324 | 329 | PF00069 | 0.594 |
MOD_CDK_SPxK_1 | 324 | 330 | PF00069 | 0.592 |
MOD_CK1_1 | 221 | 227 | PF00069 | 0.575 |
MOD_CK1_1 | 414 | 420 | PF00069 | 0.732 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.479 |
MOD_CK2_1 | 30 | 36 | PF00069 | 0.462 |
MOD_CK2_1 | 418 | 424 | PF00069 | 0.635 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.278 |
MOD_GlcNHglycan | 401 | 404 | PF01048 | 0.678 |
MOD_GlcNHglycan | 406 | 409 | PF01048 | 0.698 |
MOD_GlcNHglycan | 413 | 416 | PF01048 | 0.673 |
MOD_GlcNHglycan | 419 | 423 | PF01048 | 0.549 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.519 |
MOD_GSK3_1 | 256 | 263 | PF00069 | 0.536 |
MOD_GSK3_1 | 411 | 418 | PF00069 | 0.797 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.438 |
MOD_LATS_1 | 28 | 34 | PF00433 | 0.536 |
MOD_NEK2_1 | 12 | 17 | PF00069 | 0.478 |
MOD_NEK2_1 | 176 | 181 | PF00069 | 0.478 |
MOD_NEK2_1 | 255 | 260 | PF00069 | 0.471 |
MOD_NEK2_1 | 301 | 306 | PF00069 | 0.563 |
MOD_NEK2_1 | 347 | 352 | PF00069 | 0.432 |
MOD_NEK2_1 | 357 | 362 | PF00069 | 0.333 |
MOD_NEK2_1 | 375 | 380 | PF00069 | 0.449 |
MOD_NEK2_1 | 91 | 96 | PF00069 | 0.478 |
MOD_NEK2_2 | 218 | 223 | PF00069 | 0.575 |
MOD_PIKK_1 | 260 | 266 | PF00454 | 0.536 |
MOD_PIKK_1 | 392 | 398 | PF00454 | 0.615 |
MOD_PIKK_1 | 74 | 80 | PF00454 | 0.562 |
MOD_PIKK_1 | 91 | 97 | PF00454 | 0.378 |
MOD_PKA_1 | 329 | 335 | PF00069 | 0.547 |
MOD_PKA_2 | 1 | 7 | PF00069 | 0.466 |
MOD_PKA_2 | 196 | 202 | PF00069 | 0.536 |
MOD_PKA_2 | 273 | 279 | PF00069 | 0.575 |
MOD_PKA_2 | 329 | 335 | PF00069 | 0.411 |
MOD_Plk_1 | 109 | 115 | PF00069 | 0.575 |
MOD_Plk_1 | 61 | 67 | PF00069 | 0.516 |
MOD_Plk_4 | 225 | 231 | PF00069 | 0.501 |
MOD_Plk_4 | 243 | 249 | PF00069 | 0.397 |
MOD_Plk_4 | 273 | 279 | PF00069 | 0.478 |
MOD_Plk_4 | 347 | 353 | PF00069 | 0.327 |
MOD_ProDKin_1 | 324 | 330 | PF00069 | 0.592 |
TRG_DiLeu_BaEn_1 | 87 | 92 | PF01217 | 0.502 |
TRG_DiLeu_BaLyEn_6 | 141 | 146 | PF01217 | 0.478 |
TRG_ENDOCYTIC_2 | 149 | 152 | PF00928 | 0.489 |
TRG_ENDOCYTIC_2 | 154 | 157 | PF00928 | 0.465 |
TRG_ENDOCYTIC_2 | 284 | 287 | PF00928 | 0.478 |
TRG_ER_diArg_1 | 142 | 144 | PF00400 | 0.487 |
TRG_ER_diArg_1 | 383 | 386 | PF00400 | 0.574 |
TRG_NLS_MonoCore_2 | 409 | 414 | PF00514 | 0.763 |
TRG_NLS_MonoExtN_4 | 409 | 414 | PF00514 | 0.684 |
TRG_Pf-PMV_PEXEL_1 | 151 | 156 | PF00026 | 0.278 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCD3 | Leptomonas seymouri | 84% | 81% |
A0A0N1PD56 | Leptomonas seymouri | 22% | 100% |
A0A0N1PFX6 | Leptomonas seymouri | 37% | 100% |
A0A1X0NVQ2 | Trypanosomatidae | 71% | 95% |
A0A1X0NXU7 | Trypanosomatidae | 38% | 100% |
A0A3Q8IC47 | Leishmania donovani | 93% | 81% |
A0A3R7L005 | Trypanosoma rangeli | 39% | 100% |
A0A3S7WWE6 | Leishmania donovani | 40% | 100% |
A0A422N1V5 | Trypanosoma rangeli | 70% | 96% |
A4HBR4 | Leishmania braziliensis | 36% | 100% |
A4HZ67 | Leishmania infantum | 40% | 100% |
A4I0X6 | Leishmania infantum | 94% | 81% |
B1H369 | Xenopus tropicalis | 40% | 100% |
B1WC68 | Rattus norvegicus | 37% | 100% |
D0A1H7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
E9AV34 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 95% |
E9AWY0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 79% |
O09106 | Mus musculus | 41% | 90% |
O13298 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 39% | 100% |
O15379 | Homo sapiens | 37% | 100% |
O17695 | Caenorhabditis elegans | 40% | 94% |
O22446 | Arabidopsis thaliana | 41% | 86% |
O42227 | Xenopus laevis | 40% | 90% |
O59702 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 41% | 100% |
O88895 | Mus musculus | 37% | 100% |
P32561 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 42% | 100% |
P39067 | Bacillus subtilis (strain 168) | 32% | 100% |
P53096 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 38% | 96% |
P56517 | Gallus gallus | 42% | 90% |
P56518 | Strongylocentrotus purpuratus | 40% | 75% |
P56519 | Gallus gallus | 41% | 89% |
P56520 | Gallus gallus | 37% | 100% |
P56521 | Zea mays | 42% | 84% |
P64375 | Staphylococcus aureus (strain Mu50 / ATCC 700699) | 29% | 100% |
P64376 | Staphylococcus aureus (strain N315) | 29% | 100% |
P70288 | Mus musculus | 41% | 89% |
Q09440 | Caenorhabditis elegans | 39% | 85% |
Q0VCB2 | Bos taurus | 36% | 100% |
Q13547 | Homo sapiens | 41% | 90% |
Q28DV3 | Xenopus tropicalis | 37% | 100% |
Q32PJ8 | Bos taurus | 41% | 90% |
Q4QAJ4 | Leishmania major | 93% | 100% |
Q4QCE7 | Leishmania major | 40% | 100% |
Q4QQW4 | Rattus norvegicus | 41% | 90% |
Q4SFA0 | Tetraodon nigroviridis | 38% | 100% |
Q55BW2 | Dictyostelium discoideum | 40% | 100% |
Q55FN5 | Dictyostelium discoideum | 38% | 87% |
Q56195 | Staphylococcus xylosus | 29% | 100% |
Q569C4 | Rattus norvegicus | 29% | 74% |
Q5HF39 | Staphylococcus aureus (strain COL) | 29% | 100% |
Q5RAG0 | Pongo abelii | 41% | 90% |
Q5RB76 | Pongo abelii | 34% | 100% |
Q6G8J2 | Staphylococcus aureus (strain MSSA476) | 29% | 100% |
Q6GFX3 | Staphylococcus aureus (strain MRSA252) | 29% | 100% |
Q6GPA7 | Xenopus laevis | 41% | 100% |
Q6IRL9 | Xenopus laevis | 38% | 100% |
Q6P6W3 | Rattus norvegicus | 37% | 100% |
Q6YV04 | Oryza sativa subsp. japonica | 43% | 85% |
Q7SXM0 | Danio rerio | 41% | 100% |
Q7Y0Y6 | Oryza sativa subsp. japonica | 42% | 85% |
Q7Y0Y8 | Oryza sativa subsp. japonica | 43% | 84% |
Q803C3 | Danio rerio | 34% | 100% |
Q8H0W2 | Arabidopsis thaliana | 40% | 100% |
Q8NW34 | Staphylococcus aureus (strain MW2) | 29% | 100% |
Q8VH37 | Mus musculus | 37% | 100% |
Q91695 | Xenopus laevis | 40% | 90% |
Q91WA3 | Mus musculus | 26% | 100% |
Q92769 | Homo sapiens | 41% | 89% |
Q941D6 | Arabidopsis thaliana | 26% | 100% |
Q94517 | Drosophila melanogaster | 41% | 83% |
Q9BY41 | Homo sapiens | 37% | 100% |
Q9FH09 | Arabidopsis thaliana | 35% | 100% |
Q9FML2 | Arabidopsis thaliana | 39% | 92% |
Q9I3T5 | Pseudomonas aeruginosa (strain ATCC 15692 / DSM 22644 / CIP 104116 / JCM 14847 / LMG 12228 / 1C / PRS 101 / PAO1) | 23% | 100% |
Q9I6H0 | Pseudomonas aeruginosa (strain ATCC 15692 / DSM 22644 / CIP 104116 / JCM 14847 / LMG 12228 / 1C / PRS 101 / PAO1) | 24% | 100% |