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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005730 | nucleolus | 5 | 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 |
Related structures:
AlphaFold database: A0A3Q8I7S8
Term | Name | Level | Count |
---|---|---|---|
GO:0000463 | maturation of LSU-rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA) | 10 | 1 |
GO:0000470 | maturation of LSU-rRNA | 9 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006364 | rRNA processing | 8 | 1 |
GO:0006396 | RNA processing | 6 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0016072 | rRNA metabolic process | 7 | 1 |
GO:0034470 | ncRNA processing | 7 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0034660 | ncRNA metabolic process | 6 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 8 |
GO:0003723 | RNA binding | 4 | 8 |
GO:0005488 | binding | 1 | 8 |
GO:0097159 | organic cyclic compound binding | 2 | 8 |
GO:1901363 | heterocyclic compound binding | 2 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 298 | 302 | PF00656 | 0.370 |
CLV_NRD_NRD_1 | 18 | 20 | PF00675 | 0.623 |
CLV_NRD_NRD_1 | 253 | 255 | PF00675 | 0.483 |
CLV_NRD_NRD_1 | 264 | 266 | PF00675 | 0.399 |
CLV_NRD_NRD_1 | 284 | 286 | PF00675 | 0.663 |
CLV_NRD_NRD_1 | 374 | 376 | PF00675 | 0.671 |
CLV_NRD_NRD_1 | 59 | 61 | PF00675 | 0.752 |
CLV_PCSK_FUR_1 | 206 | 210 | PF00082 | 0.263 |
CLV_PCSK_KEX2_1 | 18 | 20 | PF00082 | 0.691 |
CLV_PCSK_KEX2_1 | 208 | 210 | PF00082 | 0.263 |
CLV_PCSK_KEX2_1 | 252 | 254 | PF00082 | 0.544 |
CLV_PCSK_KEX2_1 | 263 | 265 | PF00082 | 0.385 |
CLV_PCSK_KEX2_1 | 284 | 286 | PF00082 | 0.657 |
CLV_PCSK_KEX2_1 | 333 | 335 | PF00082 | 0.565 |
CLV_PCSK_KEX2_1 | 370 | 372 | PF00082 | 0.650 |
CLV_PCSK_KEX2_1 | 374 | 376 | PF00082 | 0.633 |
CLV_PCSK_KEX2_1 | 59 | 61 | PF00082 | 0.667 |
CLV_PCSK_KEX2_1 | 85 | 87 | PF00082 | 0.689 |
CLV_PCSK_KEX2_1 | 93 | 95 | PF00082 | 0.661 |
CLV_PCSK_PC1ET2_1 | 18 | 20 | PF00082 | 0.640 |
CLV_PCSK_PC1ET2_1 | 208 | 210 | PF00082 | 0.306 |
CLV_PCSK_PC1ET2_1 | 333 | 335 | PF00082 | 0.565 |
CLV_PCSK_PC1ET2_1 | 370 | 372 | PF00082 | 0.639 |
CLV_PCSK_PC1ET2_1 | 85 | 87 | PF00082 | 0.678 |
CLV_PCSK_PC1ET2_1 | 93 | 95 | PF00082 | 0.590 |
CLV_PCSK_SKI1_1 | 247 | 251 | PF00082 | 0.506 |
CLV_PCSK_SKI1_1 | 264 | 268 | PF00082 | 0.491 |
CLV_PCSK_SKI1_1 | 370 | 374 | PF00082 | 0.664 |
CLV_PCSK_SKI1_1 | 79 | 83 | PF00082 | 0.649 |
DEG_SPOP_SBC_1 | 70 | 74 | PF00917 | 0.647 |
DOC_CYCLIN_RxL_1 | 17 | 28 | PF00134 | 0.580 |
DOC_MAPK_gen_1 | 18 | 24 | PF00069 | 0.597 |
DOC_MAPK_gen_1 | 212 | 221 | PF00069 | 0.506 |
DOC_MAPK_gen_1 | 284 | 293 | PF00069 | 0.497 |
DOC_MAPK_MEF2A_6 | 223 | 231 | PF00069 | 0.506 |
DOC_MAPK_MEF2A_6 | 284 | 293 | PF00069 | 0.535 |
DOC_PP1_RVXF_1 | 173 | 179 | PF00149 | 0.300 |
DOC_PP1_RVXF_1 | 18 | 25 | PF00149 | 0.591 |
DOC_PP4_FxxP_1 | 178 | 181 | PF00568 | 0.460 |
DOC_PP4_FxxP_1 | 183 | 186 | PF00568 | 0.468 |
DOC_USP7_MATH_1 | 103 | 107 | PF00917 | 0.653 |
DOC_USP7_MATH_1 | 124 | 128 | PF00917 | 0.731 |
DOC_USP7_MATH_1 | 154 | 158 | PF00917 | 0.806 |
DOC_USP7_UBL2_3 | 352 | 356 | PF12436 | 0.704 |
DOC_USP7_UBL2_3 | 366 | 370 | PF12436 | 0.632 |
DOC_USP7_UBL2_3 | 4 | 8 | PF12436 | 0.675 |
DOC_USP7_UBL2_3 | 46 | 50 | PF12436 | 0.582 |
DOC_WW_Pin1_4 | 365 | 370 | PF00397 | 0.684 |
LIG_14-3-3_CanoR_1 | 175 | 179 | PF00244 | 0.359 |
LIG_14-3-3_CanoR_1 | 19 | 25 | PF00244 | 0.601 |
LIG_14-3-3_CanoR_1 | 206 | 216 | PF00244 | 0.484 |
LIG_14-3-3_CanoR_1 | 247 | 252 | PF00244 | 0.516 |
LIG_14-3-3_CanoR_1 | 336 | 345 | PF00244 | 0.704 |
LIG_FHA_1 | 355 | 361 | PF00498 | 0.739 |
LIG_FHA_1 | 36 | 42 | PF00498 | 0.574 |
LIG_FHA_2 | 296 | 302 | PF00498 | 0.420 |
LIG_FHA_2 | 93 | 99 | PF00498 | 0.562 |
LIG_LIR_Apic_2 | 177 | 181 | PF02991 | 0.468 |
LIG_LIR_Apic_2 | 182 | 186 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 169 | 174 | PF02991 | 0.433 |
LIG_Pex14_2 | 191 | 195 | PF04695 | 0.463 |
LIG_Pex14_2 | 313 | 317 | PF04695 | 0.436 |
LIG_SH2_CRK | 171 | 175 | PF00017 | 0.459 |
LIG_SH2_CRK | 189 | 193 | PF00017 | 0.506 |
LIG_SH2_SRC | 305 | 308 | PF00017 | 0.427 |
LIG_SH2_STAT3 | 271 | 274 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 218 | 221 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 305 | 308 | PF00017 | 0.489 |
LIG_SH3_3 | 38 | 44 | PF00018 | 0.690 |
LIG_SH3_3 | 96 | 102 | PF00018 | 0.775 |
LIG_SUMO_SIM_par_1 | 227 | 233 | PF11976 | 0.506 |
LIG_TRAF2_1 | 106 | 109 | PF00917 | 0.695 |
LIG_TRAF2_1 | 95 | 98 | PF00917 | 0.646 |
MOD_CDC14_SPxK_1 | 368 | 371 | PF00782 | 0.625 |
MOD_CDK_SPK_2 | 365 | 370 | PF00069 | 0.625 |
MOD_CDK_SPxK_1 | 365 | 371 | PF00069 | 0.715 |
MOD_CK1_1 | 156 | 162 | PF00069 | 0.630 |
MOD_CK1_1 | 164 | 170 | PF00069 | 0.571 |
MOD_CK1_1 | 207 | 213 | PF00069 | 0.463 |
MOD_CK1_1 | 337 | 343 | PF00069 | 0.605 |
MOD_CK2_1 | 103 | 109 | PF00069 | 0.671 |
MOD_CK2_1 | 138 | 144 | PF00069 | 0.604 |
MOD_CK2_1 | 20 | 26 | PF00069 | 0.534 |
MOD_CK2_1 | 92 | 98 | PF00069 | 0.558 |
MOD_Cter_Amidation | 16 | 19 | PF01082 | 0.629 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.598 |
MOD_GlcNHglycan | 156 | 159 | PF01048 | 0.631 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.289 |
MOD_GlcNHglycan | 362 | 365 | PF01048 | 0.555 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.747 |
MOD_GlcNHglycan | 86 | 89 | PF01048 | 0.557 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.644 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.563 |
MOD_GSK3_1 | 317 | 324 | PF00069 | 0.591 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.712 |
MOD_GSK3_1 | 355 | 362 | PF00069 | 0.638 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.726 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.661 |
MOD_N-GLC_1 | 109 | 114 | PF02516 | 0.655 |
MOD_N-GLC_1 | 164 | 169 | PF02516 | 0.563 |
MOD_N-GLC_1 | 341 | 346 | PF02516 | 0.553 |
MOD_N-GLC_1 | 70 | 75 | PF02516 | 0.626 |
MOD_NEK2_1 | 195 | 200 | PF00069 | 0.506 |
MOD_NEK2_1 | 24 | 29 | PF00069 | 0.550 |
MOD_NEK2_1 | 317 | 322 | PF00069 | 0.478 |
MOD_NEK2_1 | 84 | 89 | PF00069 | 0.642 |
MOD_NEK2_2 | 25 | 30 | PF00069 | 0.549 |
MOD_NEK2_2 | 3 | 8 | PF00069 | 0.587 |
MOD_PIKK_1 | 270 | 276 | PF00454 | 0.375 |
MOD_PIKK_1 | 317 | 323 | PF00454 | 0.525 |
MOD_PKA_1 | 20 | 26 | PF00069 | 0.594 |
MOD_PKA_1 | 332 | 338 | PF00069 | 0.668 |
MOD_PKA_1 | 370 | 376 | PF00069 | 0.636 |
MOD_PKA_1 | 66 | 72 | PF00069 | 0.658 |
MOD_PKA_2 | 161 | 167 | PF00069 | 0.601 |
MOD_PKA_2 | 174 | 180 | PF00069 | 0.260 |
MOD_PKA_2 | 370 | 376 | PF00069 | 0.682 |
MOD_PKB_1 | 245 | 253 | PF00069 | 0.495 |
MOD_Plk_1 | 25 | 31 | PF00069 | 0.522 |
MOD_Plk_1 | 341 | 347 | PF00069 | 0.530 |
MOD_Plk_2-3 | 109 | 115 | PF00069 | 0.622 |
MOD_Plk_4 | 174 | 180 | PF00069 | 0.360 |
MOD_Plk_4 | 195 | 201 | PF00069 | 0.517 |
MOD_ProDKin_1 | 365 | 371 | PF00069 | 0.689 |
MOD_SUMO_rev_2 | 307 | 315 | PF00179 | 0.381 |
TRG_ENDOCYTIC_2 | 171 | 174 | PF00928 | 0.398 |
TRG_ENDOCYTIC_2 | 189 | 192 | PF00928 | 0.463 |
TRG_ENDOCYTIC_2 | 218 | 221 | PF00928 | 0.463 |
TRG_ER_diArg_1 | 244 | 247 | PF00400 | 0.468 |
TRG_ER_diArg_1 | 251 | 254 | PF00400 | 0.528 |
TRG_ER_diArg_1 | 263 | 265 | PF00400 | 0.421 |
TRG_ER_diArg_1 | 283 | 285 | PF00400 | 0.386 |
TRG_ER_diArg_1 | 58 | 60 | PF00400 | 0.656 |
TRG_NLS_Bipartite_1 | 8 | 23 | PF00514 | 0.646 |
TRG_NLS_MonoCore_2 | 17 | 22 | PF00514 | 0.613 |
TRG_NLS_MonoCore_2 | 330 | 335 | PF00514 | 0.609 |
TRG_NLS_MonoExtC_3 | 331 | 336 | PF00514 | 0.618 |
TRG_NLS_MonoExtN_4 | 18 | 23 | PF00514 | 0.598 |
TRG_NLS_MonoExtN_4 | 331 | 337 | PF00514 | 0.623 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1P9B0 | Leptomonas seymouri | 59% | 92% |
A0A3R7KMG8 | Trypanosoma rangeli | 47% | 91% |
A4H691 | Leishmania braziliensis | 73% | 100% |
A4HUL4 | Leishmania infantum | 99% | 100% |
E9ANB3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
Q4QHB1 | Leishmania major | 90% | 99% |