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:0032991 | protein-containing complex | 1 | 10 |
GO:0061695 | transferase complex, transferring phosphorus-containing groups | 4 | 10 |
GO:0090730 | Las1 complex | 4 | 10 |
GO:0140535 | intracellular protein-containing complex | 2 | 10 |
GO:1902494 | catalytic complex | 2 | 10 |
GO:1902555 | endoribonuclease complex | 4 | 10 |
GO:1902911 | protein kinase complex | 5 | 10 |
GO:1905348 | endonuclease complex | 3 | 10 |
GO:1905354 | exoribonuclease complex | 3 | 10 |
GO:1990234 | transferase complex | 3 | 10 |
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: A0A3Q8IA87
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 10 |
GO:0006364 | rRNA processing | 8 | 10 |
GO:0006396 | RNA processing | 6 | 10 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 10 |
GO:0006807 | nitrogen compound metabolic process | 2 | 10 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0016070 | RNA metabolic process | 5 | 10 |
GO:0016072 | rRNA metabolic process | 7 | 10 |
GO:0034470 | ncRNA processing | 7 | 10 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 10 |
GO:0034660 | ncRNA metabolic process | 6 | 10 |
GO:0043170 | macromolecule metabolic process | 3 | 10 |
GO:0044237 | cellular metabolic process | 2 | 10 |
GO:0044238 | primary metabolic process | 2 | 10 |
GO:0046483 | heterocycle metabolic process | 3 | 10 |
GO:0071704 | organic substance metabolic process | 2 | 10 |
GO:0090304 | nucleic acid metabolic process | 4 | 10 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 10 |
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 | 10 |
GO:0004518 | nuclease activity | 4 | 10 |
GO:0004519 | endonuclease activity | 5 | 10 |
GO:0016787 | hydrolase activity | 2 | 10 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 295 | 299 | PF00656 | 0.718 |
CLV_NRD_NRD_1 | 11 | 13 | PF00675 | 0.567 |
CLV_NRD_NRD_1 | 118 | 120 | PF00675 | 0.420 |
CLV_NRD_NRD_1 | 178 | 180 | PF00675 | 0.347 |
CLV_NRD_NRD_1 | 18 | 20 | PF00675 | 0.524 |
CLV_NRD_NRD_1 | 249 | 251 | PF00675 | 0.713 |
CLV_NRD_NRD_1 | 26 | 28 | PF00675 | 0.525 |
CLV_NRD_NRD_1 | 335 | 337 | PF00675 | 0.767 |
CLV_NRD_NRD_1 | 40 | 42 | PF00675 | 0.709 |
CLV_PCSK_FUR_1 | 24 | 28 | PF00082 | 0.646 |
CLV_PCSK_KEX2_1 | 104 | 106 | PF00082 | 0.155 |
CLV_PCSK_KEX2_1 | 11 | 13 | PF00082 | 0.565 |
CLV_PCSK_KEX2_1 | 18 | 20 | PF00082 | 0.553 |
CLV_PCSK_KEX2_1 | 180 | 182 | PF00082 | 0.349 |
CLV_PCSK_KEX2_1 | 26 | 28 | PF00082 | 0.523 |
CLV_PCSK_KEX2_1 | 335 | 337 | PF00082 | 0.770 |
CLV_PCSK_KEX2_1 | 40 | 42 | PF00082 | 0.658 |
CLV_PCSK_KEX2_1 | 91 | 93 | PF00082 | 0.406 |
CLV_PCSK_PC1ET2_1 | 104 | 106 | PF00082 | 0.155 |
CLV_PCSK_PC1ET2_1 | 180 | 182 | PF00082 | 0.345 |
CLV_PCSK_PC1ET2_1 | 40 | 42 | PF00082 | 0.762 |
CLV_PCSK_PC1ET2_1 | 91 | 93 | PF00082 | 0.406 |
CLV_PCSK_SKI1_1 | 105 | 109 | PF00082 | 0.357 |
CLV_PCSK_SKI1_1 | 12 | 16 | PF00082 | 0.684 |
CLV_PCSK_SKI1_1 | 287 | 291 | PF00082 | 0.589 |
CLV_PCSK_SKI1_1 | 315 | 319 | PF00082 | 0.574 |
CLV_PCSK_SKI1_1 | 91 | 95 | PF00082 | 0.376 |
DEG_APCC_DBOX_1 | 104 | 112 | PF00400 | 0.369 |
DEG_APCC_DBOX_1 | 25 | 33 | PF00400 | 0.688 |
DOC_CYCLIN_RxL_1 | 89 | 96 | PF00134 | 0.342 |
DOC_MAPK_gen_1 | 179 | 187 | PF00069 | 0.344 |
DOC_MAPK_gen_1 | 312 | 321 | PF00069 | 0.570 |
DOC_MAPK_MEF2A_6 | 210 | 219 | PF00069 | 0.369 |
DOC_PP1_RVXF_1 | 89 | 96 | PF00149 | 0.358 |
DOC_PP2B_LxvP_1 | 276 | 279 | PF13499 | 0.684 |
DOC_PP2B_LxvP_1 | 35 | 38 | PF13499 | 0.723 |
DOC_USP7_MATH_1 | 103 | 107 | PF00917 | 0.388 |
DOC_USP7_MATH_1 | 204 | 208 | PF00917 | 0.418 |
DOC_USP7_MATH_1 | 258 | 262 | PF00917 | 0.753 |
DOC_USP7_MATH_1 | 272 | 276 | PF00917 | 0.620 |
DOC_WW_Pin1_4 | 240 | 245 | PF00397 | 0.537 |
DOC_WW_Pin1_4 | 261 | 266 | PF00397 | 0.778 |
DOC_WW_Pin1_4 | 319 | 324 | PF00397 | 0.713 |
DOC_WW_Pin1_4 | 69 | 74 | PF00397 | 0.656 |
LIG_14-3-3_CanoR_1 | 179 | 188 | PF00244 | 0.418 |
LIG_14-3-3_CanoR_1 | 239 | 244 | PF00244 | 0.690 |
LIG_14-3-3_CanoR_1 | 259 | 267 | PF00244 | 0.757 |
LIG_14-3-3_CanoR_1 | 50 | 57 | PF00244 | 0.785 |
LIG_14-3-3_CterR_2 | 351 | 353 | PF00244 | 0.649 |
LIG_Actin_WH2_2 | 131 | 149 | PF00022 | 0.485 |
LIG_BIR_III_4 | 296 | 300 | PF00653 | 0.645 |
LIG_BRCT_BRCA1_1 | 76 | 80 | PF00533 | 0.547 |
LIG_deltaCOP1_diTrp_1 | 83 | 87 | PF00928 | 0.401 |
LIG_FHA_1 | 108 | 114 | PF00498 | 0.429 |
LIG_FHA_1 | 129 | 135 | PF00498 | 0.344 |
LIG_FHA_1 | 262 | 268 | PF00498 | 0.754 |
LIG_FHA_1 | 59 | 65 | PF00498 | 0.763 |
LIG_FHA_1 | 70 | 76 | PF00498 | 0.599 |
LIG_FHA_2 | 280 | 286 | PF00498 | 0.584 |
LIG_FHA_2 | 54 | 60 | PF00498 | 0.728 |
LIG_LIR_Gen_1 | 86 | 95 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 86 | 90 | PF02991 | 0.348 |
LIG_Pex14_2 | 221 | 225 | PF04695 | 0.344 |
LIG_Pex14_2 | 76 | 80 | PF04695 | 0.467 |
LIG_SH2_SRC | 127 | 130 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 127 | 130 | PF00017 | 0.369 |
LIG_SH3_3 | 266 | 272 | PF00018 | 0.631 |
LIG_SUMO_SIM_anti_2 | 313 | 320 | PF11976 | 0.570 |
LIG_SUMO_SIM_par_1 | 317 | 322 | PF11976 | 0.705 |
MOD_CDK_SPxxK_3 | 319 | 326 | PF00069 | 0.684 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.444 |
MOD_CK1_1 | 261 | 267 | PF00069 | 0.595 |
MOD_CK1_1 | 340 | 346 | PF00069 | 0.741 |
MOD_CK1_1 | 58 | 64 | PF00069 | 0.703 |
MOD_CK2_1 | 103 | 109 | PF00069 | 0.476 |
MOD_CMANNOS | 84 | 87 | PF00535 | 0.344 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.421 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.439 |
MOD_GlcNHglycan | 339 | 342 | PF01048 | 0.761 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.466 |
MOD_GSK3_1 | 336 | 343 | PF00069 | 0.781 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.713 |
MOD_GSK3_1 | 58 | 65 | PF00069 | 0.634 |
MOD_N-GLC_1 | 97 | 102 | PF02516 | 0.435 |
MOD_NEK2_1 | 166 | 171 | PF00069 | 0.392 |
MOD_NEK2_1 | 219 | 224 | PF00069 | 0.485 |
MOD_NEK2_1 | 97 | 102 | PF00069 | 0.478 |
MOD_NEK2_2 | 107 | 112 | PF00069 | 0.408 |
MOD_PIKK_1 | 219 | 225 | PF00454 | 0.485 |
MOD_PKA_1 | 180 | 186 | PF00069 | 0.449 |
MOD_PKA_1 | 335 | 341 | PF00069 | 0.673 |
MOD_PKA_2 | 180 | 186 | PF00069 | 0.449 |
MOD_PKA_2 | 238 | 244 | PF00069 | 0.548 |
MOD_PKA_2 | 258 | 264 | PF00069 | 0.651 |
MOD_PKA_2 | 335 | 341 | PF00069 | 0.712 |
MOD_PKA_2 | 49 | 55 | PF00069 | 0.786 |
MOD_Plk_2-3 | 292 | 298 | PF00069 | 0.697 |
MOD_Plk_4 | 75 | 81 | PF00069 | 0.456 |
MOD_ProDKin_1 | 240 | 246 | PF00069 | 0.540 |
MOD_ProDKin_1 | 261 | 267 | PF00069 | 0.777 |
MOD_ProDKin_1 | 319 | 325 | PF00069 | 0.714 |
MOD_ProDKin_1 | 69 | 75 | PF00069 | 0.652 |
MOD_SUMO_rev_2 | 280 | 289 | PF00179 | 0.607 |
MOD_SUMO_rev_2 | 83 | 93 | PF00179 | 0.394 |
TRG_DiLeu_BaEn_4 | 30 | 36 | PF01217 | 0.664 |
TRG_ER_diArg_1 | 114 | 117 | PF00400 | 0.449 |
TRG_ER_diArg_1 | 178 | 181 | PF00400 | 0.327 |
TRG_ER_diArg_1 | 18 | 20 | PF00400 | 0.553 |
TRG_ER_diArg_1 | 194 | 197 | PF00400 | 0.334 |
TRG_ER_diArg_1 | 24 | 27 | PF00400 | 0.615 |
TRG_ER_diArg_1 | 252 | 255 | PF00400 | 0.708 |
TRG_NES_CRM1_1 | 208 | 218 | PF08389 | 0.344 |
TRG_NLS_MonoCore_2 | 249 | 254 | PF00514 | 0.718 |
TRG_NLS_MonoExtC_3 | 178 | 184 | PF00514 | 0.344 |
TRG_Pf-PMV_PEXEL_1 | 27 | 31 | PF00026 | 0.632 |
TRG_Pf-PMV_PEXEL_1 | 92 | 96 | PF00026 | 0.424 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IAG6 | Leptomonas seymouri | 55% | 100% |
A0A0S4JJ56 | Bodo saltans | 35% | 100% |
A0A1X0NFY0 | Trypanosomatidae | 44% | 100% |
A0A3R7K8F7 | Trypanosoma rangeli | 45% | 100% |
A4H8E5 | Leishmania braziliensis | 72% | 98% |
A4HWR8 | Leishmania infantum | 100% | 100% |
E9AQH6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
Q4QF01 | Leishmania major | 86% | 100% |