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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0032991 | protein-containing complex | 1 | 11 |
GO:0061695 | transferase complex, transferring phosphorus-containing groups | 4 | 11 |
GO:0090730 | Las1 complex | 4 | 11 |
GO:0140535 | intracellular protein-containing complex | 2 | 11 |
GO:1902494 | catalytic complex | 2 | 11 |
GO:1902555 | endoribonuclease complex | 4 | 11 |
GO:1902911 | protein kinase complex | 5 | 11 |
GO:1905348 | endonuclease complex | 3 | 11 |
GO:1905354 | exoribonuclease complex | 3 | 11 |
GO:1990234 | transferase complex | 3 | 11 |
GO:0005730 | nucleolus | 5 | 1 |
GO:0030684 | preribosome | 3 | 1 |
GO:0030687 | preribosome, large subunit precursor | 4 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:1990904 | ribonucleoprotein complex | 2 | 1 |
Related structures:
AlphaFold database: E9AQH6
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 11 |
GO:0006364 | rRNA processing | 8 | 11 |
GO:0006396 | RNA processing | 6 | 11 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016070 | RNA metabolic process | 5 | 11 |
GO:0016072 | rRNA metabolic process | 7 | 11 |
GO:0034470 | ncRNA processing | 7 | 11 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 11 |
GO:0034660 | ncRNA metabolic process | 6 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0046483 | heterocycle metabolic process | 3 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:0090304 | nucleic acid metabolic process | 4 | 11 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 11 |
GO:0000460 | maturation of 5.8S rRNA | 9 | 1 |
GO:0000470 | maturation of LSU-rRNA | 9 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004518 | nuclease activity | 4 | 11 |
GO:0004519 | endonuclease activity | 5 | 11 |
GO:0016787 | hydrolase activity | 2 | 11 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 298 | 302 | PF00656 | 0.719 |
CLV_C14_Caspase3-7 | 33 | 37 | PF00656 | 0.499 |
CLV_NRD_NRD_1 | 11 | 13 | PF00675 | 0.528 |
CLV_NRD_NRD_1 | 121 | 123 | PF00675 | 0.377 |
CLV_NRD_NRD_1 | 18 | 20 | PF00675 | 0.484 |
CLV_NRD_NRD_1 | 181 | 183 | PF00675 | 0.307 |
CLV_NRD_NRD_1 | 2 | 4 | PF00675 | 0.599 |
CLV_NRD_NRD_1 | 252 | 254 | PF00675 | 0.735 |
CLV_NRD_NRD_1 | 26 | 28 | PF00675 | 0.475 |
CLV_NRD_NRD_1 | 353 | 355 | PF00675 | 0.506 |
CLV_NRD_NRD_1 | 40 | 42 | PF00675 | 0.670 |
CLV_NRD_NRD_1 | 43 | 45 | PF00675 | 0.671 |
CLV_PCSK_FUR_1 | 24 | 28 | PF00082 | 0.553 |
CLV_PCSK_KEX2_1 | 107 | 109 | PF00082 | 0.150 |
CLV_PCSK_KEX2_1 | 11 | 13 | PF00082 | 0.506 |
CLV_PCSK_KEX2_1 | 18 | 20 | PF00082 | 0.500 |
CLV_PCSK_KEX2_1 | 183 | 185 | PF00082 | 0.307 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.554 |
CLV_PCSK_KEX2_1 | 26 | 28 | PF00082 | 0.456 |
CLV_PCSK_KEX2_1 | 353 | 355 | PF00082 | 0.506 |
CLV_PCSK_KEX2_1 | 40 | 42 | PF00082 | 0.604 |
CLV_PCSK_KEX2_1 | 94 | 96 | PF00082 | 0.373 |
CLV_PCSK_PC1ET2_1 | 107 | 109 | PF00082 | 0.150 |
CLV_PCSK_PC1ET2_1 | 183 | 185 | PF00082 | 0.307 |
CLV_PCSK_PC1ET2_1 | 40 | 42 | PF00082 | 0.714 |
CLV_PCSK_PC1ET2_1 | 94 | 96 | PF00082 | 0.373 |
CLV_PCSK_SKI1_1 | 108 | 112 | PF00082 | 0.290 |
CLV_PCSK_SKI1_1 | 12 | 16 | PF00082 | 0.635 |
CLV_PCSK_SKI1_1 | 290 | 294 | PF00082 | 0.538 |
CLV_PCSK_SKI1_1 | 94 | 98 | PF00082 | 0.316 |
DEG_APCC_DBOX_1 | 107 | 115 | PF00400 | 0.307 |
DEG_APCC_DBOX_1 | 25 | 33 | PF00400 | 0.651 |
DEG_APCC_DBOX_1 | 289 | 297 | PF00400 | 0.483 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.597 |
DEG_SPOP_SBC_1 | 263 | 267 | PF00917 | 0.694 |
DOC_CYCLIN_RxL_1 | 92 | 99 | PF00134 | 0.305 |
DOC_MAPK_gen_1 | 182 | 190 | PF00069 | 0.307 |
DOC_MAPK_MEF2A_6 | 213 | 222 | PF00069 | 0.307 |
DOC_PP1_RVXF_1 | 92 | 99 | PF00149 | 0.321 |
DOC_PP2B_LxvP_1 | 279 | 282 | PF13499 | 0.658 |
DOC_PP2B_LxvP_1 | 35 | 38 | PF13499 | 0.686 |
DOC_USP7_MATH_1 | 106 | 110 | PF00917 | 0.311 |
DOC_USP7_MATH_1 | 174 | 178 | PF00917 | 0.379 |
DOC_USP7_MATH_1 | 207 | 211 | PF00917 | 0.377 |
DOC_USP7_MATH_1 | 261 | 265 | PF00917 | 0.720 |
DOC_USP7_MATH_2 | 268 | 274 | PF00917 | 0.489 |
DOC_WW_Pin1_4 | 264 | 269 | PF00397 | 0.760 |
DOC_WW_Pin1_4 | 317 | 322 | PF00397 | 0.692 |
DOC_WW_Pin1_4 | 46 | 51 | PF00397 | 0.622 |
DOC_WW_Pin1_4 | 72 | 77 | PF00397 | 0.567 |
LIG_14-3-3_CanoR_1 | 182 | 191 | PF00244 | 0.432 |
LIG_14-3-3_CanoR_1 | 262 | 268 | PF00244 | 0.669 |
LIG_14-3-3_CanoR_1 | 53 | 60 | PF00244 | 0.683 |
LIG_14-3-3_CterR_2 | 353 | 356 | PF00244 | 0.710 |
LIG_Actin_WH2_2 | 134 | 152 | PF00022 | 0.378 |
LIG_BRCT_BRCA1_1 | 79 | 83 | PF00533 | 0.527 |
LIG_deltaCOP1_diTrp_1 | 85 | 90 | PF00928 | 0.366 |
LIG_FHA_1 | 111 | 117 | PF00498 | 0.399 |
LIG_FHA_1 | 132 | 138 | PF00498 | 0.288 |
LIG_FHA_1 | 207 | 213 | PF00498 | 0.387 |
LIG_FHA_1 | 317 | 323 | PF00498 | 0.477 |
LIG_FHA_1 | 73 | 79 | PF00498 | 0.677 |
LIG_FHA_2 | 265 | 271 | PF00498 | 0.695 |
LIG_FHA_2 | 283 | 289 | PF00498 | 0.535 |
LIG_Integrin_RGD_1 | 315 | 317 | PF01839 | 0.545 |
LIG_LIR_Gen_1 | 89 | 98 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 89 | 93 | PF02991 | 0.291 |
LIG_Pex14_2 | 224 | 228 | PF04695 | 0.288 |
LIG_Pex14_2 | 79 | 83 | PF04695 | 0.416 |
LIG_SH2_SRC | 130 | 133 | PF00017 | 0.288 |
LIG_SH2_STAT5 | 130 | 133 | PF00017 | 0.307 |
LIG_SH2_STAT5 | 236 | 239 | PF00017 | 0.530 |
LIG_SUMO_SIM_par_1 | 317 | 326 | PF11976 | 0.609 |
LIG_TRAF2_1 | 268 | 271 | PF00917 | 0.622 |
MOD_CDK_SPxxK_3 | 46 | 53 | PF00069 | 0.523 |
MOD_CK1_1 | 172 | 178 | PF00069 | 0.417 |
MOD_CK1_1 | 244 | 250 | PF00069 | 0.592 |
MOD_CK1_1 | 264 | 270 | PF00069 | 0.655 |
MOD_CK1_1 | 275 | 281 | PF00069 | 0.557 |
MOD_CK1_1 | 343 | 349 | PF00069 | 0.678 |
MOD_CK2_1 | 106 | 112 | PF00069 | 0.459 |
MOD_CK2_1 | 264 | 270 | PF00069 | 0.607 |
MOD_CK2_1 | 299 | 305 | PF00069 | 0.675 |
MOD_CK2_1 | 46 | 52 | PF00069 | 0.546 |
MOD_CMANNOS | 87 | 90 | PF00535 | 0.288 |
MOD_Cter_Amidation | 351 | 354 | PF01082 | 0.470 |
MOD_GlcNHglycan | 108 | 111 | PF01048 | 0.363 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.411 |
MOD_GlcNHglycan | 246 | 249 | PF01048 | 0.679 |
MOD_GlcNHglycan | 259 | 262 | PF01048 | 0.679 |
MOD_GlcNHglycan | 274 | 277 | PF01048 | 0.678 |
MOD_GlcNHglycan | 297 | 300 | PF01048 | 0.656 |
MOD_GlcNHglycan | 325 | 328 | PF01048 | 0.756 |
MOD_GlcNHglycan | 342 | 345 | PF01048 | 0.620 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.570 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.446 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.797 |
MOD_GSK3_1 | 295 | 302 | PF00069 | 0.575 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.538 |
MOD_GSK3_1 | 339 | 346 | PF00069 | 0.687 |
MOD_GSK3_1 | 61 | 68 | PF00069 | 0.638 |
MOD_N-GLC_1 | 100 | 105 | PF02516 | 0.407 |
MOD_N-GLC_1 | 66 | 71 | PF02516 | 0.454 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.644 |
MOD_NEK2_1 | 100 | 105 | PF00069 | 0.373 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.403 |
MOD_NEK2_1 | 222 | 227 | PF00069 | 0.468 |
MOD_NEK2_2 | 110 | 115 | PF00069 | 0.324 |
MOD_PIKK_1 | 222 | 228 | PF00454 | 0.378 |
MOD_PIKK_1 | 6 | 12 | PF00454 | 0.454 |
MOD_PKA_1 | 183 | 189 | PF00069 | 0.378 |
MOD_PKA_2 | 1 | 7 | PF00069 | 0.605 |
MOD_PKA_2 | 183 | 189 | PF00069 | 0.479 |
MOD_PKA_2 | 257 | 263 | PF00069 | 0.596 |
MOD_PKA_2 | 338 | 344 | PF00069 | 0.639 |
MOD_PKA_2 | 52 | 58 | PF00069 | 0.770 |
MOD_Plk_1 | 269 | 275 | PF00069 | 0.670 |
MOD_Plk_4 | 78 | 84 | PF00069 | 0.407 |
MOD_ProDKin_1 | 264 | 270 | PF00069 | 0.762 |
MOD_ProDKin_1 | 317 | 323 | PF00069 | 0.694 |
MOD_ProDKin_1 | 46 | 52 | PF00069 | 0.622 |
MOD_ProDKin_1 | 72 | 78 | PF00069 | 0.564 |
MOD_SUMO_rev_2 | 86 | 96 | PF00179 | 0.329 |
TRG_DiLeu_BaEn_4 | 30 | 36 | PF01217 | 0.573 |
TRG_ER_diArg_1 | 1 | 3 | PF00400 | 0.656 |
TRG_ER_diArg_1 | 117 | 120 | PF00400 | 0.424 |
TRG_ER_diArg_1 | 18 | 20 | PF00400 | 0.512 |
TRG_ER_diArg_1 | 181 | 184 | PF00400 | 0.288 |
TRG_ER_diArg_1 | 197 | 200 | PF00400 | 0.288 |
TRG_ER_diArg_1 | 24 | 27 | PF00400 | 0.566 |
TRG_ER_diArg_1 | 255 | 258 | PF00400 | 0.710 |
TRG_ER_diArg_1 | 353 | 355 | PF00400 | 0.469 |
TRG_NES_CRM1_1 | 211 | 221 | PF08389 | 0.288 |
TRG_NLS_MonoCore_2 | 252 | 257 | PF00514 | 0.610 |
TRG_NLS_MonoExtC_3 | 181 | 187 | PF00514 | 0.332 |
TRG_Pf-PMV_PEXEL_1 | 27 | 31 | PF00026 | 0.542 |
TRG_Pf-PMV_PEXEL_1 | 290 | 295 | PF00026 | 0.477 |
TRG_Pf-PMV_PEXEL_1 | 95 | 99 | PF00026 | 0.393 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IAG6 | Leptomonas seymouri | 56% | 100% |
A0A0S4JJ56 | Bodo saltans | 35% | 100% |
A0A1X0NFY0 | Trypanosomatidae | 43% | 100% |
A0A3Q8IA87 | Leishmania donovani | 86% | 100% |
A0A3R7K8F7 | Trypanosoma rangeli | 45% | 100% |
A4H8E5 | Leishmania braziliensis | 75% | 98% |
A4HWR8 | Leishmania infantum | 86% | 100% |
C9ZW55 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 94% |
Q4QF01 | Leishmania major | 86% | 100% |