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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 12 |
GO:0032299 | ribonuclease H2 complex | 3 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0140535 | intracellular protein-containing complex | 2 | 2 |
GO:1902494 | catalytic complex | 2 | 2 |
Related structures:
AlphaFold database: Q8WSZ0
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 2 |
GO:0006259 | DNA metabolic process | 4 | 2 |
GO:0006281 | DNA repair | 5 | 2 |
GO:0006298 | mismatch repair | 6 | 2 |
GO:0006401 | RNA catabolic process | 5 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0006950 | response to stress | 2 | 2 |
GO:0006974 | DNA damage response | 4 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009056 | catabolic process | 2 | 2 |
GO:0009057 | macromolecule catabolic process | 4 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016070 | RNA metabolic process | 5 | 2 |
GO:0019439 | aromatic compound catabolic process | 4 | 2 |
GO:0033554 | cellular response to stress | 3 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 2 |
GO:0034655 | nucleobase-containing compound catabolic process | 4 | 2 |
GO:0043137 | DNA replication, removal of RNA primer | 6 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044248 | cellular catabolic process | 3 | 2 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 2 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 2 |
GO:0044270 | cellular nitrogen compound catabolic process | 4 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 2 |
GO:0046700 | heterocycle catabolic process | 4 | 2 |
GO:0050896 | response to stimulus | 1 | 2 |
GO:0051716 | cellular response to stimulus | 2 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0090304 | nucleic acid metabolic process | 4 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 2 |
GO:1901361 | organic cyclic compound catabolic process | 4 | 2 |
GO:1901575 | organic substance catabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003723 | RNA binding | 4 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004518 | nuclease activity | 4 | 12 |
GO:0004519 | endonuclease activity | 5 | 12 |
GO:0004521 | RNA endonuclease activity | 5 | 12 |
GO:0004523 | RNA-DNA hybrid ribonuclease activity | 7 | 12 |
GO:0004540 | RNA nuclease activity | 4 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0016787 | hydrolase activity | 2 | 12 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 12 |
GO:0016891 | RNA endonuclease activity, producing 5'-phosphomonoesters | 6 | 12 |
GO:0016893 | endonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 5'-phosphomonoesters | 6 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043169 | cation binding | 3 | 12 |
GO:0046872 | metal ion binding | 4 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 12 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 104 | 106 | PF00675 | 0.585 |
CLV_NRD_NRD_1 | 126 | 128 | PF00675 | 0.634 |
CLV_NRD_NRD_1 | 456 | 458 | PF00675 | 0.277 |
CLV_NRD_NRD_1 | 472 | 474 | PF00675 | 0.523 |
CLV_PCSK_FUR_1 | 124 | 128 | PF00082 | 0.691 |
CLV_PCSK_FUR_1 | 29 | 33 | PF00082 | 0.775 |
CLV_PCSK_KEX2_1 | 104 | 106 | PF00082 | 0.634 |
CLV_PCSK_KEX2_1 | 119 | 121 | PF00082 | 0.531 |
CLV_PCSK_KEX2_1 | 126 | 128 | PF00082 | 0.523 |
CLV_PCSK_KEX2_1 | 31 | 33 | PF00082 | 0.710 |
CLV_PCSK_KEX2_1 | 340 | 342 | PF00082 | 0.573 |
CLV_PCSK_KEX2_1 | 400 | 402 | PF00082 | 0.287 |
CLV_PCSK_PC1ET2_1 | 119 | 121 | PF00082 | 0.643 |
CLV_PCSK_PC1ET2_1 | 31 | 33 | PF00082 | 0.772 |
CLV_PCSK_PC1ET2_1 | 340 | 342 | PF00082 | 0.581 |
CLV_PCSK_PC1ET2_1 | 400 | 402 | PF00082 | 0.287 |
CLV_PCSK_SKI1_1 | 127 | 131 | PF00082 | 0.584 |
CLV_PCSK_SKI1_1 | 244 | 248 | PF00082 | 0.395 |
CLV_PCSK_SKI1_1 | 352 | 356 | PF00082 | 0.449 |
CLV_PCSK_SKI1_1 | 464 | 468 | PF00082 | 0.542 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.659 |
DEG_SPOP_SBC_1 | 11 | 15 | PF00917 | 0.663 |
DEG_SPOP_SBC_1 | 317 | 321 | PF00917 | 0.650 |
DOC_CKS1_1 | 249 | 254 | PF01111 | 0.410 |
DOC_CYCLIN_RxL_1 | 240 | 251 | PF00134 | 0.432 |
DOC_MAPK_gen_1 | 104 | 115 | PF00069 | 0.622 |
DOC_MAPK_gen_1 | 119 | 125 | PF00069 | 0.502 |
DOC_MAPK_gen_1 | 126 | 136 | PF00069 | 0.528 |
DOC_MAPK_gen_1 | 230 | 238 | PF00069 | 0.602 |
DOC_MAPK_RevD_3 | 113 | 127 | PF00069 | 0.686 |
DOC_PP1_RVXF_1 | 188 | 195 | PF00149 | 0.462 |
DOC_PP2B_LxvP_1 | 91 | 94 | PF13499 | 0.700 |
DOC_PP4_FxxP_1 | 38 | 41 | PF00568 | 0.727 |
DOC_USP7_MATH_1 | 153 | 157 | PF00917 | 0.426 |
DOC_USP7_MATH_1 | 159 | 163 | PF00917 | 0.456 |
DOC_USP7_MATH_1 | 16 | 20 | PF00917 | 0.723 |
DOC_USP7_MATH_1 | 317 | 321 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 376 | 380 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 406 | 410 | PF00917 | 0.473 |
DOC_USP7_MATH_1 | 94 | 98 | PF00917 | 0.649 |
DOC_USP7_UBL2_3 | 240 | 244 | PF12436 | 0.480 |
DOC_USP7_UBL2_3 | 445 | 449 | PF12436 | 0.562 |
DOC_WW_Pin1_4 | 248 | 253 | PF00397 | 0.420 |
DOC_WW_Pin1_4 | 33 | 38 | PF00397 | 0.704 |
LIG_14-3-3_CanoR_1 | 12 | 21 | PF00244 | 0.696 |
LIG_14-3-3_CanoR_1 | 157 | 167 | PF00244 | 0.502 |
LIG_14-3-3_CanoR_1 | 308 | 315 | PF00244 | 0.548 |
LIG_14-3-3_CanoR_1 | 316 | 326 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 457 | 461 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 55 | 62 | PF00244 | 0.639 |
LIG_Clathr_ClatBox_1 | 367 | 371 | PF01394 | 0.476 |
LIG_FHA_1 | 12 | 18 | PF00498 | 0.710 |
LIG_FHA_1 | 196 | 202 | PF00498 | 0.492 |
LIG_FHA_1 | 249 | 255 | PF00498 | 0.392 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.599 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.651 |
LIG_FHA_1 | 94 | 100 | PF00498 | 0.633 |
LIG_FHA_2 | 276 | 282 | PF00498 | 0.422 |
LIG_FHA_2 | 413 | 419 | PF00498 | 0.537 |
LIG_FHA_2 | 463 | 469 | PF00498 | 0.543 |
LIG_LIR_Apic_2 | 168 | 174 | PF02991 | 0.654 |
LIG_LIR_Apic_2 | 339 | 345 | PF02991 | 0.685 |
LIG_LIR_Apic_2 | 36 | 41 | PF02991 | 0.715 |
LIG_LIR_Gen_1 | 166 | 174 | PF02991 | 0.593 |
LIG_LIR_Gen_1 | 175 | 185 | PF02991 | 0.454 |
LIG_LIR_Gen_1 | 191 | 201 | PF02991 | 0.371 |
LIG_LIR_Gen_1 | 299 | 309 | PF02991 | 0.579 |
LIG_LIR_Gen_1 | 379 | 388 | PF02991 | 0.525 |
LIG_LIR_Gen_1 | 43 | 52 | PF02991 | 0.708 |
LIG_LIR_Nem_3 | 166 | 170 | PF02991 | 0.590 |
LIG_LIR_Nem_3 | 175 | 180 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 191 | 197 | PF02991 | 0.353 |
LIG_LIR_Nem_3 | 202 | 206 | PF02991 | 0.329 |
LIG_LIR_Nem_3 | 256 | 260 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 281 | 286 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 299 | 304 | PF02991 | 0.329 |
LIG_LIR_Nem_3 | 355 | 360 | PF02991 | 0.560 |
LIG_LIR_Nem_3 | 379 | 383 | PF02991 | 0.509 |
LIG_LIR_Nem_3 | 424 | 430 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 43 | 47 | PF02991 | 0.720 |
LIG_Pex14_2 | 163 | 167 | PF04695 | 0.637 |
LIG_PTB_Apo_2 | 273 | 280 | PF02174 | 0.372 |
LIG_PTB_Phospho_1 | 273 | 279 | PF10480 | 0.372 |
LIG_SH2_CRK | 342 | 346 | PF00017 | 0.637 |
LIG_SH2_NCK_1 | 171 | 175 | PF00017 | 0.650 |
LIG_SH2_NCK_1 | 260 | 264 | PF00017 | 0.555 |
LIG_SH2_SRC | 422 | 425 | PF00017 | 0.524 |
LIG_SH2_STAT5 | 253 | 256 | PF00017 | 0.379 |
LIG_SH2_STAT5 | 266 | 269 | PF00017 | 0.402 |
LIG_SH2_STAT5 | 279 | 282 | PF00017 | 0.353 |
LIG_SH2_STAT5 | 325 | 328 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 357 | 360 | PF00017 | 0.549 |
LIG_SH2_STAT5 | 382 | 385 | PF00017 | 0.562 |
LIG_SH2_STAT5 | 422 | 425 | PF00017 | 0.487 |
LIG_SH2_STAT5 | 446 | 449 | PF00017 | 0.562 |
LIG_SH3_3 | 34 | 40 | PF00018 | 0.724 |
LIG_SH3_3 | 359 | 365 | PF00018 | 0.476 |
LIG_SH3_3 | 372 | 378 | PF00018 | 0.474 |
LIG_SH3_5 | 378 | 382 | PF00018 | 0.562 |
LIG_SUMO_SIM_anti_2 | 67 | 72 | PF11976 | 0.615 |
LIG_SUMO_SIM_par_1 | 365 | 371 | PF11976 | 0.476 |
LIG_WRC_WIRS_1 | 160 | 165 | PF05994 | 0.547 |
MOD_CDC14_SPxK_1 | 36 | 39 | PF00782 | 0.718 |
MOD_CDK_SPxK_1 | 33 | 39 | PF00069 | 0.767 |
MOD_CK1_1 | 248 | 254 | PF00069 | 0.416 |
MOD_CK1_1 | 289 | 295 | PF00069 | 0.374 |
MOD_CK1_1 | 296 | 302 | PF00069 | 0.399 |
MOD_CK1_1 | 97 | 103 | PF00069 | 0.662 |
MOD_CK2_1 | 125 | 131 | PF00069 | 0.570 |
MOD_CK2_1 | 181 | 187 | PF00069 | 0.476 |
MOD_CK2_1 | 412 | 418 | PF00069 | 0.519 |
MOD_CK2_1 | 462 | 468 | PF00069 | 0.537 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.740 |
MOD_GlcNHglycan | 18 | 21 | PF01048 | 0.730 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.525 |
MOD_GlcNHglycan | 295 | 298 | PF01048 | 0.426 |
MOD_GlcNHglycan | 95 | 99 | PF01048 | 0.707 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.734 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.550 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.494 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.717 |
MOD_GSK3_1 | 289 | 296 | PF00069 | 0.403 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.646 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.620 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.646 |
MOD_N-GLC_1 | 275 | 280 | PF02516 | 0.426 |
MOD_N-GLC_1 | 286 | 291 | PF02516 | 0.443 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.660 |
MOD_NEK2_1 | 125 | 130 | PF00069 | 0.600 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.696 |
MOD_NEK2_1 | 293 | 298 | PF00069 | 0.402 |
MOD_NEK2_1 | 87 | 92 | PF00069 | 0.720 |
MOD_NEK2_2 | 382 | 387 | PF00069 | 0.525 |
MOD_PK_1 | 318 | 324 | PF00069 | 0.569 |
MOD_PK_1 | 401 | 407 | PF00069 | 0.537 |
MOD_PKA_2 | 11 | 17 | PF00069 | 0.707 |
MOD_PKA_2 | 125 | 131 | PF00069 | 0.570 |
MOD_PKA_2 | 22 | 28 | PF00069 | 0.604 |
MOD_PKA_2 | 307 | 313 | PF00069 | 0.545 |
MOD_PKA_2 | 317 | 323 | PF00069 | 0.528 |
MOD_PKA_2 | 456 | 462 | PF00069 | 0.466 |
MOD_PKA_2 | 54 | 60 | PF00069 | 0.687 |
MOD_PKB_1 | 316 | 324 | PF00069 | 0.653 |
MOD_Plk_1 | 220 | 226 | PF00069 | 0.731 |
MOD_Plk_1 | 275 | 281 | PF00069 | 0.410 |
MOD_Plk_1 | 286 | 292 | PF00069 | 0.439 |
MOD_Plk_2-3 | 181 | 187 | PF00069 | 0.482 |
MOD_Plk_4 | 275 | 281 | PF00069 | 0.410 |
MOD_Plk_4 | 296 | 302 | PF00069 | 0.519 |
MOD_ProDKin_1 | 248 | 254 | PF00069 | 0.414 |
MOD_ProDKin_1 | 33 | 39 | PF00069 | 0.704 |
MOD_SUMO_rev_2 | 175 | 185 | PF00179 | 0.496 |
TRG_ENDOCYTIC_2 | 266 | 269 | PF00928 | 0.418 |
TRG_ENDOCYTIC_2 | 35 | 38 | PF00928 | 0.739 |
TRG_ENDOCYTIC_2 | 357 | 360 | PF00928 | 0.581 |
TRG_ENDOCYTIC_2 | 380 | 383 | PF00928 | 0.540 |
TRG_ER_diArg_1 | 123 | 126 | PF00400 | 0.631 |
TRG_ER_diArg_1 | 315 | 318 | PF00400 | 0.663 |
TRG_Pf-PMV_PEXEL_1 | 105 | 110 | PF00026 | 0.641 |
TRG_Pf-PMV_PEXEL_1 | 127 | 131 | PF00026 | 0.626 |
TRG_Pf-PMV_PEXEL_1 | 26 | 30 | PF00026 | 0.764 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1ILG3 | Leptomonas seymouri | 81% | 100% |
A0A0S4JMV0 | Bodo saltans | 35% | 82% |
A0A1X0P978 | Trypanosomatidae | 57% | 100% |
A0A3Q8IFS0 | Leishmania donovani | 99% | 100% |
A0A3R7P2T0 | Trypanosoma rangeli | 61% | 99% |
A4HNP1 | Leishmania braziliensis | 90% | 100% |
A4ICV4 | Leishmania infantum | 99% | 100% |
D0A2J6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 57% | 99% |
E9ASF0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 97% | 100% |
V5BQJ3 | Trypanosoma cruzi | 60% | 99% |