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:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9B5W6
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 11 |
GO:0006396 | RNA processing | 6 | 11 |
GO:0006399 | tRNA metabolic process | 7 | 11 |
GO:0006400 | tRNA modification | 6 | 11 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0008033 | tRNA processing | 8 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009451 | RNA modification | 5 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016070 | RNA metabolic process | 5 | 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:0043412 | macromolecule modification | 4 | 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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 11 |
GO:0003723 | RNA binding | 4 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
GO:0003824 | catalytic activity | 1 | 3 |
GO:0009055 | electron transfer activity | 3 | 3 |
GO:0016491 | oxidoreductase activity | 2 | 3 |
GO:0020037 | heme binding | 4 | 3 |
GO:0043167 | ion binding | 2 | 2 |
GO:0043169 | cation binding | 3 | 2 |
GO:0046872 | metal ion binding | 4 | 2 |
GO:0046906 | tetrapyrrole binding | 3 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 140 | 144 | PF00656 | 0.727 |
CLV_C14_Caspase3-7 | 218 | 222 | PF00656 | 0.793 |
CLV_C14_Caspase3-7 | 4 | 8 | PF00656 | 0.767 |
CLV_C14_Caspase3-7 | 74 | 78 | PF00656 | 0.727 |
CLV_C14_Caspase3-7 | 85 | 89 | PF00656 | 0.562 |
CLV_NRD_NRD_1 | 153 | 155 | PF00675 | 0.683 |
CLV_NRD_NRD_1 | 159 | 161 | PF00675 | 0.703 |
CLV_NRD_NRD_1 | 277 | 279 | PF00675 | 0.671 |
CLV_NRD_NRD_1 | 317 | 319 | PF00675 | 0.671 |
CLV_NRD_NRD_1 | 388 | 390 | PF00675 | 0.588 |
CLV_NRD_NRD_1 | 393 | 395 | PF00675 | 0.554 |
CLV_PCSK_FUR_1 | 150 | 154 | PF00082 | 0.761 |
CLV_PCSK_FUR_1 | 315 | 319 | PF00082 | 0.748 |
CLV_PCSK_KEX2_1 | 123 | 125 | PF00082 | 0.757 |
CLV_PCSK_KEX2_1 | 150 | 152 | PF00082 | 0.669 |
CLV_PCSK_KEX2_1 | 153 | 155 | PF00082 | 0.651 |
CLV_PCSK_KEX2_1 | 159 | 161 | PF00082 | 0.703 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.770 |
CLV_PCSK_KEX2_1 | 317 | 319 | PF00082 | 0.671 |
CLV_PCSK_KEX2_1 | 388 | 390 | PF00082 | 0.605 |
CLV_PCSK_KEX2_1 | 393 | 395 | PF00082 | 0.577 |
CLV_PCSK_PC1ET2_1 | 123 | 125 | PF00082 | 0.785 |
CLV_PCSK_PC1ET2_1 | 2 | 4 | PF00082 | 0.770 |
CLV_PCSK_PC7_1 | 389 | 395 | PF00082 | 0.514 |
CLV_PCSK_SKI1_1 | 19 | 23 | PF00082 | 0.708 |
CLV_PCSK_SKI1_1 | 250 | 254 | PF00082 | 0.520 |
CLV_PCSK_SKI1_1 | 278 | 282 | PF00082 | 0.629 |
CLV_PCSK_SKI1_1 | 388 | 392 | PF00082 | 0.714 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.749 |
DEG_SCF_FBW7_2 | 53 | 58 | PF00400 | 0.369 |
DEG_SPOP_SBC_1 | 214 | 218 | PF00917 | 0.760 |
DOC_CYCLIN_RxL_1 | 13 | 25 | PF00134 | 0.462 |
DOC_CYCLIN_RxL_1 | 275 | 282 | PF00134 | 0.578 |
DOC_MAPK_gen_1 | 14 | 22 | PF00069 | 0.636 |
DOC_MAPK_gen_1 | 278 | 285 | PF00069 | 0.672 |
DOC_MAPK_gen_1 | 315 | 325 | PF00069 | 0.673 |
DOC_MAPK_gen_1 | 41 | 50 | PF00069 | 0.523 |
DOC_MAPK_MEF2A_6 | 172 | 179 | PF00069 | 0.470 |
DOC_MAPK_MEF2A_6 | 278 | 285 | PF00069 | 0.639 |
DOC_MAPK_MEF2A_6 | 318 | 327 | PF00069 | 0.599 |
DOC_MAPK_NFAT4_5 | 172 | 180 | PF00069 | 0.584 |
DOC_MAPK_NFAT4_5 | 278 | 286 | PF00069 | 0.641 |
DOC_PP2B_LxvP_1 | 177 | 180 | PF13499 | 0.574 |
DOC_SPAK_OSR1_1 | 354 | 358 | PF12202 | 0.549 |
DOC_USP7_MATH_1 | 107 | 111 | PF00917 | 0.513 |
DOC_USP7_MATH_1 | 213 | 217 | PF00917 | 0.750 |
DOC_USP7_MATH_1 | 232 | 236 | PF00917 | 0.366 |
DOC_USP7_MATH_1 | 307 | 311 | PF00917 | 0.764 |
DOC_USP7_MATH_1 | 316 | 320 | PF00917 | 0.721 |
DOC_USP7_MATH_1 | 341 | 345 | PF00917 | 0.665 |
DOC_USP7_MATH_1 | 359 | 363 | PF00917 | 0.448 |
DOC_USP7_MATH_1 | 79 | 83 | PF00917 | 0.762 |
DOC_USP7_MATH_1 | 92 | 96 | PF00917 | 0.578 |
DOC_WW_Pin1_4 | 133 | 138 | PF00397 | 0.817 |
DOC_WW_Pin1_4 | 153 | 158 | PF00397 | 0.739 |
DOC_WW_Pin1_4 | 412 | 417 | PF00397 | 0.682 |
DOC_WW_Pin1_4 | 51 | 56 | PF00397 | 0.411 |
LIG_14-3-3_CanoR_1 | 118 | 125 | PF00244 | 0.732 |
LIG_14-3-3_CanoR_1 | 159 | 167 | PF00244 | 0.647 |
LIG_14-3-3_CanoR_1 | 236 | 242 | PF00244 | 0.618 |
LIG_14-3-3_CanoR_1 | 278 | 284 | PF00244 | 0.590 |
LIG_14-3-3_CanoR_1 | 315 | 321 | PF00244 | 0.649 |
LIG_14-3-3_CanoR_1 | 388 | 396 | PF00244 | 0.676 |
LIG_BIR_III_2 | 221 | 225 | PF00653 | 0.666 |
LIG_BIR_III_4 | 77 | 81 | PF00653 | 0.736 |
LIG_BRCT_BRCA1_1 | 160 | 164 | PF00533 | 0.663 |
LIG_BRCT_BRCA1_1 | 281 | 285 | PF00533 | 0.605 |
LIG_FHA_1 | 225 | 231 | PF00498 | 0.614 |
LIG_FHA_1 | 236 | 242 | PF00498 | 0.532 |
LIG_FHA_1 | 320 | 326 | PF00498 | 0.722 |
LIG_FHA_1 | 345 | 351 | PF00498 | 0.579 |
LIG_FHA_1 | 370 | 376 | PF00498 | 0.623 |
LIG_FHA_1 | 52 | 58 | PF00498 | 0.627 |
LIG_FHA_2 | 197 | 203 | PF00498 | 0.638 |
LIG_FHA_2 | 216 | 222 | PF00498 | 0.784 |
LIG_FHA_2 | 267 | 273 | PF00498 | 0.580 |
LIG_FHA_2 | 331 | 337 | PF00498 | 0.580 |
LIG_LIR_Apic_2 | 161 | 166 | PF02991 | 0.645 |
LIG_LIR_Gen_1 | 239 | 249 | PF02991 | 0.526 |
LIG_LIR_Nem_3 | 161 | 167 | PF02991 | 0.635 |
LIG_LIR_Nem_3 | 239 | 245 | PF02991 | 0.478 |
LIG_NRBOX | 276 | 282 | PF00104 | 0.585 |
LIG_NRBOX | 97 | 103 | PF00104 | 0.686 |
LIG_PALB2_WD40_1 | 159 | 167 | PF16756 | 0.660 |
LIG_Pex14_2 | 253 | 257 | PF04695 | 0.562 |
LIG_PTB_Apo_2 | 6 | 13 | PF02174 | 0.490 |
LIG_SH2_STAT5 | 174 | 177 | PF00017 | 0.500 |
LIG_SH2_STAT5 | 49 | 52 | PF00017 | 0.522 |
LIG_SH3_3 | 183 | 189 | PF00018 | 0.604 |
LIG_SH3_3 | 226 | 232 | PF00018 | 0.584 |
LIG_SH3_3 | 265 | 271 | PF00018 | 0.524 |
LIG_SH3_3 | 355 | 361 | PF00018 | 0.546 |
LIG_SH3_3 | 88 | 94 | PF00018 | 0.757 |
LIG_TRAF2_1 | 36 | 39 | PF00917 | 0.556 |
LIG_TRFH_1 | 257 | 261 | PF08558 | 0.488 |
MOD_CDK_SPK_2 | 412 | 417 | PF00069 | 0.682 |
MOD_CDK_SPxK_1 | 153 | 159 | PF00069 | 0.738 |
MOD_CDK_SPxxK_3 | 153 | 160 | PF00069 | 0.734 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.578 |
MOD_CK1_1 | 319 | 325 | PF00069 | 0.680 |
MOD_CK1_1 | 344 | 350 | PF00069 | 0.578 |
MOD_CK1_1 | 362 | 368 | PF00069 | 0.509 |
MOD_CK1_1 | 415 | 421 | PF00069 | 0.592 |
MOD_CK1_1 | 51 | 57 | PF00069 | 0.631 |
MOD_CK1_1 | 67 | 73 | PF00069 | 0.736 |
MOD_CK1_1 | 97 | 103 | PF00069 | 0.558 |
MOD_CK2_1 | 196 | 202 | PF00069 | 0.719 |
MOD_CK2_1 | 213 | 219 | PF00069 | 0.710 |
MOD_CK2_1 | 266 | 272 | PF00069 | 0.587 |
MOD_CK2_1 | 330 | 336 | PF00069 | 0.585 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.704 |
MOD_GlcNHglycan | 343 | 346 | PF01048 | 0.578 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.805 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.749 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.597 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.781 |
MOD_GSK3_1 | 178 | 185 | PF00069 | 0.566 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.559 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.561 |
MOD_GSK3_1 | 365 | 372 | PF00069 | 0.684 |
MOD_GSK3_1 | 388 | 395 | PF00069 | 0.633 |
MOD_GSK3_1 | 415 | 422 | PF00069 | 0.579 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.500 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.657 |
MOD_N-GLC_1 | 119 | 124 | PF02516 | 0.733 |
MOD_N-GLC_1 | 182 | 187 | PF02516 | 0.663 |
MOD_N-GLC_1 | 290 | 295 | PF02516 | 0.428 |
MOD_N-GLC_1 | 330 | 335 | PF02516 | 0.566 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.776 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.785 |
MOD_NEK2_1 | 205 | 210 | PF00069 | 0.755 |
MOD_NEK2_1 | 289 | 294 | PF00069 | 0.523 |
MOD_NEK2_1 | 30 | 35 | PF00069 | 0.529 |
MOD_NEK2_1 | 325 | 330 | PF00069 | 0.646 |
MOD_NEK2_1 | 406 | 411 | PF00069 | 0.653 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.544 |
MOD_NEK2_1 | 64 | 69 | PF00069 | 0.593 |
MOD_NEK2_2 | 316 | 321 | PF00069 | 0.744 |
MOD_PKA_1 | 388 | 394 | PF00069 | 0.654 |
MOD_PKA_2 | 158 | 164 | PF00069 | 0.687 |
MOD_PKA_2 | 235 | 241 | PF00069 | 0.619 |
MOD_PKA_2 | 316 | 322 | PF00069 | 0.656 |
MOD_PKA_2 | 388 | 394 | PF00069 | 0.654 |
MOD_PKA_2 | 68 | 74 | PF00069 | 0.472 |
MOD_PKA_2 | 80 | 86 | PF00069 | 0.803 |
MOD_Plk_1 | 182 | 188 | PF00069 | 0.643 |
MOD_Plk_1 | 290 | 296 | PF00069 | 0.723 |
MOD_Plk_1 | 330 | 336 | PF00069 | 0.710 |
MOD_Plk_1 | 369 | 375 | PF00069 | 0.592 |
MOD_Plk_1 | 87 | 93 | PF00069 | 0.747 |
MOD_Plk_4 | 224 | 230 | PF00069 | 0.571 |
MOD_Plk_4 | 97 | 103 | PF00069 | 0.526 |
MOD_ProDKin_1 | 133 | 139 | PF00069 | 0.817 |
MOD_ProDKin_1 | 153 | 159 | PF00069 | 0.738 |
MOD_ProDKin_1 | 412 | 418 | PF00069 | 0.679 |
MOD_ProDKin_1 | 51 | 57 | PF00069 | 0.406 |
MOD_SUMO_for_1 | 416 | 419 | PF00179 | 0.680 |
TRG_ENDOCYTIC_2 | 174 | 177 | PF00928 | 0.511 |
TRG_ER_diArg_1 | 150 | 153 | PF00400 | 0.664 |
TRG_ER_diArg_1 | 315 | 318 | PF00400 | 0.687 |
TRG_ER_diArg_1 | 388 | 390 | PF00400 | 0.597 |
TRG_NLS_MonoCore_2 | 122 | 127 | PF00514 | 0.769 |
TRG_NLS_MonoExtC_3 | 122 | 128 | PF00514 | 0.779 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IGK4 | Leptomonas seymouri | 67% | 100% |
A0A0S4J2S0 | Bodo saltans | 27% | 100% |
A0A1X0NJH1 | Trypanosomatidae | 37% | 100% |
A0A3Q8IHS0 | Leishmania donovani | 91% | 100% |
A0A3R7NE95 | Trypanosoma rangeli | 42% | 100% |
A4HMB7 | Leishmania braziliensis | 78% | 99% |
A4IAY3 | Leishmania infantum | 91% | 100% |
D0A272 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
E9AER1 | Leishmania major | 92% | 100% |