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: A4HMB7
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 | 110 | 114 | PF00656 | 0.468 |
CLV_C14_Caspase3-7 | 139 | 143 | PF00656 | 0.736 |
CLV_C14_Caspase3-7 | 150 | 154 | PF00656 | 0.704 |
CLV_C14_Caspase3-7 | 216 | 220 | PF00656 | 0.783 |
CLV_C14_Caspase3-7 | 286 | 290 | PF00656 | 0.682 |
CLV_C14_Caspase3-7 | 4 | 8 | PF00656 | 0.760 |
CLV_NRD_NRD_1 | 151 | 153 | PF00675 | 0.700 |
CLV_NRD_NRD_1 | 275 | 277 | PF00675 | 0.563 |
CLV_NRD_NRD_1 | 315 | 317 | PF00675 | 0.642 |
CLV_NRD_NRD_1 | 386 | 388 | PF00675 | 0.490 |
CLV_PCSK_FUR_1 | 313 | 317 | PF00082 | 0.720 |
CLV_PCSK_KEX2_1 | 123 | 125 | PF00082 | 0.749 |
CLV_PCSK_KEX2_1 | 151 | 153 | PF00082 | 0.669 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.761 |
CLV_PCSK_KEX2_1 | 315 | 317 | PF00082 | 0.642 |
CLV_PCSK_KEX2_1 | 386 | 388 | PF00082 | 0.507 |
CLV_PCSK_PC1ET2_1 | 123 | 125 | PF00082 | 0.777 |
CLV_PCSK_PC1ET2_1 | 2 | 4 | PF00082 | 0.761 |
CLV_PCSK_PC7_1 | 147 | 153 | PF00082 | 0.689 |
CLV_PCSK_SKI1_1 | 19 | 23 | PF00082 | 0.652 |
CLV_PCSK_SKI1_1 | 248 | 252 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 276 | 280 | PF00082 | 0.536 |
CLV_PCSK_SKI1_1 | 386 | 390 | PF00082 | 0.641 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.741 |
DEG_SCF_FBW7_1 | 70 | 75 | PF00400 | 0.513 |
DEG_SPOP_SBC_1 | 212 | 216 | PF00917 | 0.763 |
DOC_MAPK_DCC_7 | 252 | 262 | PF00069 | 0.302 |
DOC_MAPK_gen_1 | 14 | 22 | PF00069 | 0.601 |
DOC_MAPK_gen_1 | 276 | 283 | PF00069 | 0.567 |
DOC_MAPK_gen_1 | 313 | 323 | PF00069 | 0.582 |
DOC_MAPK_gen_1 | 41 | 50 | PF00069 | 0.504 |
DOC_MAPK_MEF2A_6 | 170 | 177 | PF00069 | 0.440 |
DOC_MAPK_MEF2A_6 | 276 | 283 | PF00069 | 0.534 |
DOC_MAPK_MEF2A_6 | 297 | 306 | PF00069 | 0.706 |
DOC_MAPK_MEF2A_6 | 316 | 325 | PF00069 | 0.484 |
DOC_MAPK_NFAT4_5 | 170 | 178 | PF00069 | 0.554 |
DOC_MAPK_NFAT4_5 | 276 | 284 | PF00069 | 0.542 |
DOC_MAPK_RevD_3 | 323 | 337 | PF00069 | 0.565 |
DOC_PP1_RVXF_1 | 295 | 301 | PF00149 | 0.568 |
DOC_PP2B_LxvP_1 | 175 | 178 | PF13499 | 0.545 |
DOC_PP2B_LxvP_1 | 302 | 305 | PF13499 | 0.467 |
DOC_SPAK_OSR1_1 | 352 | 356 | PF12202 | 0.446 |
DOC_USP7_MATH_1 | 107 | 111 | PF00917 | 0.511 |
DOC_USP7_MATH_1 | 122 | 126 | PF00917 | 0.691 |
DOC_USP7_MATH_1 | 145 | 149 | PF00917 | 0.761 |
DOC_USP7_MATH_1 | 206 | 210 | PF00917 | 0.739 |
DOC_USP7_MATH_1 | 211 | 215 | PF00917 | 0.751 |
DOC_USP7_MATH_1 | 230 | 234 | PF00917 | 0.348 |
DOC_USP7_MATH_1 | 305 | 309 | PF00917 | 0.718 |
DOC_USP7_MATH_1 | 339 | 343 | PF00917 | 0.593 |
DOC_USP7_MATH_1 | 357 | 361 | PF00917 | 0.418 |
DOC_USP7_MATH_1 | 94 | 98 | PF00917 | 0.547 |
DOC_USP7_UBL2_3 | 62 | 66 | PF12436 | 0.526 |
DOC_WW_Pin1_4 | 132 | 137 | PF00397 | 0.790 |
DOC_WW_Pin1_4 | 219 | 224 | PF00397 | 0.603 |
DOC_WW_Pin1_4 | 68 | 73 | PF00397 | 0.626 |
DOC_WW_Pin1_4 | 87 | 92 | PF00397 | 0.642 |
LIG_14-3-3_CanoR_1 | 234 | 240 | PF00244 | 0.588 |
LIG_14-3-3_CanoR_1 | 313 | 319 | PF00244 | 0.594 |
LIG_14-3-3_CanoR_1 | 364 | 368 | PF00244 | 0.430 |
LIG_14-3-3_CanoR_1 | 386 | 394 | PF00244 | 0.602 |
LIG_14-3-3_CanoR_1 | 81 | 87 | PF00244 | 0.730 |
LIG_BRCT_BRCA1_1 | 158 | 162 | PF00533 | 0.672 |
LIG_Clathr_ClatBox_1 | 257 | 261 | PF01394 | 0.278 |
LIG_CtBP_PxDLS_1 | 259 | 263 | PF00389 | 0.283 |
LIG_FHA_1 | 223 | 229 | PF00498 | 0.552 |
LIG_FHA_1 | 234 | 240 | PF00498 | 0.502 |
LIG_FHA_1 | 318 | 324 | PF00498 | 0.582 |
LIG_FHA_1 | 343 | 349 | PF00498 | 0.495 |
LIG_FHA_1 | 368 | 374 | PF00498 | 0.488 |
LIG_FHA_1 | 405 | 411 | PF00498 | 0.591 |
LIG_FHA_1 | 52 | 58 | PF00498 | 0.610 |
LIG_FHA_2 | 125 | 131 | PF00498 | 0.666 |
LIG_FHA_2 | 195 | 201 | PF00498 | 0.657 |
LIG_FHA_2 | 214 | 220 | PF00498 | 0.777 |
LIG_FHA_2 | 265 | 271 | PF00498 | 0.475 |
LIG_FHA_2 | 329 | 335 | PF00498 | 0.494 |
LIG_LIR_Apic_2 | 159 | 164 | PF02991 | 0.662 |
LIG_LIR_Gen_1 | 237 | 247 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 159 | 165 | PF02991 | 0.650 |
LIG_LIR_Nem_3 | 237 | 243 | PF02991 | 0.441 |
LIG_NRBOX | 274 | 280 | PF00104 | 0.485 |
LIG_NRBOX | 97 | 103 | PF00104 | 0.732 |
LIG_PALB2_WD40_1 | 157 | 165 | PF16756 | 0.670 |
LIG_Pex14_2 | 251 | 255 | PF04695 | 0.509 |
LIG_SH2_STAP1 | 365 | 369 | PF00017 | 0.333 |
LIG_SH2_STAT5 | 172 | 175 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 365 | 368 | PF00017 | 0.347 |
LIG_SH2_STAT5 | 49 | 52 | PF00017 | 0.504 |
LIG_SH3_3 | 181 | 187 | PF00018 | 0.577 |
LIG_SH3_3 | 224 | 230 | PF00018 | 0.527 |
LIG_SH3_3 | 263 | 269 | PF00018 | 0.416 |
LIG_SH3_3 | 88 | 94 | PF00018 | 0.745 |
LIG_SUMO_SIM_par_1 | 258 | 263 | PF11976 | 0.284 |
LIG_TRAF2_1 | 36 | 39 | PF00917 | 0.539 |
LIG_TRFH_1 | 255 | 259 | PF08558 | 0.407 |
MOD_CK1_1 | 233 | 239 | PF00069 | 0.549 |
MOD_CK1_1 | 342 | 348 | PF00069 | 0.497 |
MOD_CK1_1 | 360 | 366 | PF00069 | 0.458 |
MOD_CK1_1 | 51 | 57 | PF00069 | 0.617 |
MOD_CK1_1 | 68 | 74 | PF00069 | 0.746 |
MOD_CK1_1 | 92 | 98 | PF00069 | 0.648 |
MOD_CK2_1 | 122 | 128 | PF00069 | 0.600 |
MOD_CK2_1 | 194 | 200 | PF00069 | 0.741 |
MOD_CK2_1 | 211 | 217 | PF00069 | 0.710 |
MOD_CK2_1 | 264 | 270 | PF00069 | 0.479 |
MOD_CK2_1 | 328 | 334 | PF00069 | 0.488 |
MOD_CK2_1 | 52 | 58 | PF00069 | 0.596 |
MOD_GlcNHglycan | 341 | 344 | PF01048 | 0.505 |
MOD_GlcNHglycan | 407 | 410 | PF01048 | 0.552 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.764 |
MOD_GSK3_1 | 176 | 183 | PF00069 | 0.550 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.454 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.648 |
MOD_GSK3_1 | 363 | 370 | PF00069 | 0.584 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.619 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.703 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.675 |
MOD_N-GLC_1 | 180 | 185 | PF02516 | 0.649 |
MOD_N-GLC_1 | 328 | 333 | PF02516 | 0.469 |
MOD_N-GLC_1 | 87 | 92 | PF02516 | 0.684 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.768 |
MOD_NEK2_1 | 30 | 35 | PF00069 | 0.484 |
MOD_NEK2_1 | 323 | 328 | PF00069 | 0.522 |
MOD_NEK2_1 | 404 | 409 | PF00069 | 0.601 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.525 |
MOD_NEK2_2 | 314 | 319 | PF00069 | 0.683 |
MOD_PIKK_1 | 108 | 114 | PF00454 | 0.464 |
MOD_PIKK_1 | 357 | 363 | PF00454 | 0.416 |
MOD_PKA_1 | 386 | 392 | PF00069 | 0.586 |
MOD_PKA_2 | 156 | 162 | PF00069 | 0.695 |
MOD_PKA_2 | 206 | 212 | PF00069 | 0.765 |
MOD_PKA_2 | 233 | 239 | PF00069 | 0.591 |
MOD_PKA_2 | 314 | 320 | PF00069 | 0.580 |
MOD_PKA_2 | 363 | 369 | PF00069 | 0.354 |
MOD_PKA_2 | 386 | 392 | PF00069 | 0.586 |
MOD_PKA_2 | 80 | 86 | PF00069 | 0.797 |
MOD_Plk_1 | 180 | 186 | PF00069 | 0.622 |
MOD_Plk_1 | 288 | 294 | PF00069 | 0.730 |
MOD_Plk_1 | 328 | 334 | PF00069 | 0.613 |
MOD_Plk_1 | 367 | 373 | PF00069 | 0.463 |
MOD_Plk_4 | 222 | 228 | PF00069 | 0.509 |
MOD_Plk_4 | 97 | 103 | PF00069 | 0.572 |
MOD_ProDKin_1 | 132 | 138 | PF00069 | 0.792 |
MOD_ProDKin_1 | 219 | 225 | PF00069 | 0.589 |
MOD_ProDKin_1 | 68 | 74 | PF00069 | 0.630 |
MOD_ProDKin_1 | 87 | 93 | PF00069 | 0.641 |
MOD_SUMO_rev_2 | 138 | 145 | PF00179 | 0.563 |
MOD_SUMO_rev_2 | 4 | 10 | PF00179 | 0.748 |
TRG_ENDOCYTIC_2 | 172 | 175 | PF00928 | 0.481 |
TRG_ER_diArg_1 | 116 | 119 | PF00400 | 0.664 |
TRG_ER_diArg_1 | 313 | 316 | PF00400 | 0.664 |
TRG_NLS_MonoExtC_3 | 122 | 128 | PF00514 | 0.772 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IGK4 | Leptomonas seymouri | 65% | 99% |
A0A0S4J2S0 | Bodo saltans | 29% | 100% |
A0A1X0NJH1 | Trypanosomatidae | 37% | 100% |
A0A3Q8IHS0 | Leishmania donovani | 80% | 99% |
A0A3R7NE95 | Trypanosoma rangeli | 42% | 100% |
A4IAY3 | Leishmania infantum | 80% | 99% |
D0A272 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
E9AER1 | Leishmania major | 79% | 100% |
E9B5W6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 99% |