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:0031390 | Ctf18 RFC-like complex | 3 | 12 |
GO:0032991 | protein-containing complex | 1 | 12 |
GO:0140513 | nuclear protein-containing complex | 2 | 12 |
GO:0000775 | chromosome, centromeric region | 3 | 1 |
GO:0000785 | chromatin | 2 | 1 |
GO:0005634 | nucleus | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0098687 | chromosomal region | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AVJ9
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006259 | DNA metabolic process | 4 | 12 |
GO:0006260 | DNA replication | 5 | 12 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0006996 | organelle organization | 4 | 11 |
GO:0007062 | sister chromatid cohesion | 3 | 11 |
GO:0007064 | mitotic sister chromatid cohesion | 4 | 11 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016043 | cellular component organization | 3 | 11 |
GO:0022402 | cell cycle process | 2 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0051276 | chromosome organization | 5 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0071840 | cellular component organization or biogenesis | 2 | 11 |
GO:0090304 | nucleic acid metabolic process | 4 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
GO:1903047 | mitotic cell cycle process | 3 | 12 |
GO:0034086 | maintenance of sister chromatid cohesion | 3 | 1 |
GO:0034088 | maintenance of mitotic sister chromatid cohesion | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 181 | 185 | PF00656 | 0.492 |
CLV_C14_Caspase3-7 | 249 | 253 | PF00656 | 0.184 |
CLV_NRD_NRD_1 | 100 | 102 | PF00675 | 0.330 |
CLV_NRD_NRD_1 | 57 | 59 | PF00675 | 0.367 |
CLV_NRD_NRD_1 | 87 | 89 | PF00675 | 0.329 |
CLV_PCSK_KEX2_1 | 100 | 102 | PF00082 | 0.305 |
CLV_PCSK_KEX2_1 | 47 | 49 | PF00082 | 0.453 |
CLV_PCSK_KEX2_1 | 59 | 61 | PF00082 | 0.438 |
CLV_PCSK_KEX2_1 | 87 | 89 | PF00082 | 0.338 |
CLV_PCSK_PC1ET2_1 | 47 | 49 | PF00082 | 0.453 |
CLV_PCSK_PC1ET2_1 | 59 | 61 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 27 | 31 | PF00082 | 0.372 |
CLV_PCSK_SKI1_1 | 421 | 425 | PF00082 | 0.355 |
DEG_MDM2_SWIB_1 | 349 | 357 | PF02201 | 0.328 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.671 |
DEG_SCF_FBW7_1 | 129 | 136 | PF00400 | 0.184 |
DOC_CYCLIN_RxL_1 | 418 | 425 | PF00134 | 0.347 |
DOC_CYCLIN_yCln2_LP_2 | 443 | 446 | PF00134 | 0.571 |
DOC_MAPK_gen_1 | 382 | 389 | PF00069 | 0.398 |
DOC_MAPK_gen_1 | 58 | 67 | PF00069 | 0.335 |
DOC_MAPK_MEF2A_6 | 409 | 416 | PF00069 | 0.398 |
DOC_MAPK_MEF2A_6 | 58 | 67 | PF00069 | 0.411 |
DOC_PP2B_LxvP_1 | 310 | 313 | PF13499 | 0.409 |
DOC_PP2B_LxvP_1 | 443 | 446 | PF13499 | 0.545 |
DOC_USP7_MATH_1 | 105 | 109 | PF00917 | 0.384 |
DOC_USP7_MATH_1 | 193 | 197 | PF00917 | 0.413 |
DOC_USP7_MATH_1 | 240 | 244 | PF00917 | 0.449 |
DOC_USP7_MATH_1 | 356 | 360 | PF00917 | 0.469 |
DOC_USP7_MATH_1 | 408 | 412 | PF00917 | 0.491 |
DOC_USP7_MATH_1 | 446 | 450 | PF00917 | 0.580 |
DOC_USP7_MATH_1 | 49 | 53 | PF00917 | 0.466 |
DOC_USP7_MATH_2 | 408 | 414 | PF00917 | 0.475 |
DOC_WW_Pin1_4 | 129 | 134 | PF00397 | 0.445 |
DOC_WW_Pin1_4 | 209 | 214 | PF00397 | 0.399 |
DOC_WW_Pin1_4 | 35 | 40 | PF00397 | 0.420 |
DOC_WW_Pin1_4 | 50 | 55 | PF00397 | 0.370 |
LIG_14-3-3_CanoR_1 | 17 | 22 | PF00244 | 0.482 |
LIG_14-3-3_CanoR_1 | 198 | 203 | PF00244 | 0.387 |
LIG_14-3-3_CanoR_1 | 207 | 213 | PF00244 | 0.338 |
LIG_14-3-3_CanoR_1 | 333 | 340 | PF00244 | 0.302 |
LIG_14-3-3_CanoR_1 | 48 | 54 | PF00244 | 0.453 |
LIG_14-3-3_CanoR_1 | 58 | 67 | PF00244 | 0.440 |
LIG_APCC_ABBA_1 | 324 | 329 | PF00400 | 0.184 |
LIG_BIR_III_2 | 355 | 359 | PF00653 | 0.475 |
LIG_BRCT_BRCA1_1 | 151 | 155 | PF00533 | 0.413 |
LIG_BRCT_BRCA1_1 | 358 | 362 | PF00533 | 0.396 |
LIG_BRCT_BRCA1_1 | 392 | 396 | PF00533 | 0.398 |
LIG_BRCT_BRCA1_1 | 412 | 416 | PF00533 | 0.475 |
LIG_Clathr_ClatBox_1 | 18 | 22 | PF01394 | 0.363 |
LIG_CSL_BTD_1 | 405 | 408 | PF09270 | 0.449 |
LIG_eIF4E_1 | 91 | 97 | PF01652 | 0.363 |
LIG_FHA_1 | 124 | 130 | PF00498 | 0.372 |
LIG_FHA_1 | 134 | 140 | PF00498 | 0.329 |
LIG_FHA_1 | 141 | 147 | PF00498 | 0.281 |
LIG_FHA_1 | 243 | 249 | PF00498 | 0.393 |
LIG_FHA_1 | 335 | 341 | PF00498 | 0.413 |
LIG_FHA_1 | 81 | 87 | PF00498 | 0.355 |
LIG_FHA_1 | 92 | 98 | PF00498 | 0.302 |
LIG_FHA_2 | 174 | 180 | PF00498 | 0.328 |
LIG_FHA_2 | 247 | 253 | PF00498 | 0.428 |
LIG_FHA_2 | 293 | 299 | PF00498 | 0.262 |
LIG_LIR_Apic_2 | 282 | 288 | PF02991 | 0.359 |
LIG_LIR_Apic_2 | 402 | 408 | PF02991 | 0.461 |
LIG_LIR_Apic_2 | 458 | 464 | PF02991 | 0.464 |
LIG_LIR_Gen_1 | 172 | 180 | PF02991 | 0.402 |
LIG_LIR_Gen_1 | 201 | 209 | PF02991 | 0.397 |
LIG_LIR_Gen_1 | 447 | 455 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 15 | 19 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 172 | 177 | PF02991 | 0.384 |
LIG_LIR_Nem_3 | 201 | 205 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 271 | 276 | PF02991 | 0.384 |
LIG_LIR_Nem_3 | 447 | 453 | PF02991 | 0.484 |
LIG_LYPXL_L_2 | 272 | 281 | PF13949 | 0.413 |
LIG_LYPXL_S_1 | 272 | 276 | PF13949 | 0.363 |
LIG_LYPXL_yS_3 | 273 | 276 | PF13949 | 0.363 |
LIG_NRBOX | 215 | 221 | PF00104 | 0.449 |
LIG_NRBOX | 230 | 236 | PF00104 | 0.449 |
LIG_PCNA_PIPBox_1 | 433 | 442 | PF02747 | 0.262 |
LIG_PCNA_yPIPBox_3 | 427 | 440 | PF02747 | 0.433 |
LIG_Pex14_2 | 257 | 261 | PF04695 | 0.184 |
LIG_Pex14_2 | 349 | 353 | PF04695 | 0.328 |
LIG_Rb_pABgroove_1 | 149 | 157 | PF01858 | 0.449 |
LIG_SH2_CRK | 16 | 20 | PF00017 | 0.363 |
LIG_SH2_CRK | 285 | 289 | PF00017 | 0.411 |
LIG_SH2_CRK | 461 | 465 | PF00017 | 0.502 |
LIG_SH2_CRK | 470 | 474 | PF00017 | 0.442 |
LIG_SH2_GRB2like | 142 | 145 | PF00017 | 0.475 |
LIG_SH2_GRB2like | 91 | 94 | PF00017 | 0.344 |
LIG_SH2_PTP2 | 386 | 389 | PF00017 | 0.475 |
LIG_SH2_STAP1 | 142 | 146 | PF00017 | 0.475 |
LIG_SH2_STAP1 | 91 | 95 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 142 | 145 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 174 | 177 | PF00017 | 0.407 |
LIG_SH2_STAT5 | 200 | 203 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 386 | 389 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 439 | 442 | PF00017 | 0.426 |
LIG_SH3_1 | 461 | 467 | PF00018 | 0.554 |
LIG_SH3_3 | 301 | 307 | PF00018 | 0.475 |
LIG_SH3_3 | 461 | 467 | PF00018 | 0.485 |
LIG_SUMO_SIM_anti_2 | 297 | 305 | PF11976 | 0.376 |
LIG_SUMO_SIM_anti_2 | 61 | 67 | PF11976 | 0.437 |
LIG_SUMO_SIM_par_1 | 17 | 23 | PF11976 | 0.328 |
LIG_TRAF2_1 | 176 | 179 | PF00917 | 0.385 |
LIG_TRFH_1 | 424 | 428 | PF08558 | 0.413 |
LIG_TYR_ITIM | 468 | 473 | PF00017 | 0.438 |
LIG_WRC_WIRS_1 | 247 | 252 | PF05994 | 0.359 |
LIG_WRC_WIRS_1 | 346 | 351 | PF05994 | 0.413 |
MOD_CK1_1 | 173 | 179 | PF00069 | 0.374 |
MOD_CK1_1 | 187 | 193 | PF00069 | 0.482 |
MOD_CK1_1 | 292 | 298 | PF00069 | 0.345 |
MOD_CK1_1 | 53 | 59 | PF00069 | 0.455 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.449 |
MOD_CK2_1 | 173 | 179 | PF00069 | 0.330 |
MOD_CK2_1 | 209 | 215 | PF00069 | 0.346 |
MOD_CK2_1 | 333 | 339 | PF00069 | 0.239 |
MOD_DYRK1A_RPxSP_1 | 50 | 54 | PF00069 | 0.475 |
MOD_GlcNHglycan | 107 | 110 | PF01048 | 0.459 |
MOD_GlcNHglycan | 166 | 169 | PF01048 | 0.469 |
MOD_GlcNHglycan | 187 | 190 | PF01048 | 0.429 |
MOD_GlcNHglycan | 195 | 198 | PF01048 | 0.322 |
MOD_GlcNHglycan | 392 | 395 | PF01048 | 0.440 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.457 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.446 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.423 |
MOD_GSK3_1 | 242 | 249 | PF00069 | 0.339 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.424 |
MOD_N-GLC_1 | 164 | 169 | PF02516 | 0.439 |
MOD_NEK2_1 | 154 | 159 | PF00069 | 0.395 |
MOD_NEK2_1 | 170 | 175 | PF00069 | 0.385 |
MOD_NEK2_1 | 208 | 213 | PF00069 | 0.370 |
MOD_NEK2_1 | 219 | 224 | PF00069 | 0.383 |
MOD_NEK2_1 | 257 | 262 | PF00069 | 0.410 |
MOD_NEK2_1 | 400 | 405 | PF00069 | 0.227 |
MOD_PK_1 | 17 | 23 | PF00069 | 0.413 |
MOD_PKA_1 | 58 | 64 | PF00069 | 0.184 |
MOD_PKA_2 | 115 | 121 | PF00069 | 0.398 |
MOD_PKA_2 | 455 | 461 | PF00069 | 0.576 |
MOD_PKA_2 | 49 | 55 | PF00069 | 0.492 |
MOD_PKB_1 | 138 | 146 | PF00069 | 0.398 |
MOD_Plk_1 | 164 | 170 | PF00069 | 0.398 |
MOD_Plk_1 | 257 | 263 | PF00069 | 0.407 |
MOD_Plk_1 | 297 | 303 | PF00069 | 0.475 |
MOD_Plk_1 | 446 | 452 | PF00069 | 0.563 |
MOD_Plk_2-3 | 410 | 416 | PF00069 | 0.398 |
MOD_Plk_4 | 170 | 176 | PF00069 | 0.449 |
MOD_Plk_4 | 246 | 252 | PF00069 | 0.356 |
MOD_Plk_4 | 268 | 274 | PF00069 | 0.358 |
MOD_Plk_4 | 357 | 363 | PF00069 | 0.327 |
MOD_Plk_4 | 400 | 406 | PF00069 | 0.364 |
MOD_Plk_4 | 439 | 445 | PF00069 | 0.469 |
MOD_Plk_4 | 91 | 97 | PF00069 | 0.357 |
MOD_ProDKin_1 | 129 | 135 | PF00069 | 0.445 |
MOD_ProDKin_1 | 209 | 215 | PF00069 | 0.399 |
MOD_ProDKin_1 | 35 | 41 | PF00069 | 0.420 |
MOD_ProDKin_1 | 50 | 56 | PF00069 | 0.370 |
TRG_DiLeu_BaEn_1 | 215 | 220 | PF01217 | 0.449 |
TRG_DiLeu_BaLyEn_6 | 14 | 19 | PF01217 | 0.202 |
TRG_DiLeu_BaLyEn_6 | 230 | 235 | PF01217 | 0.328 |
TRG_ENDOCYTIC_2 | 16 | 19 | PF00928 | 0.417 |
TRG_ENDOCYTIC_2 | 174 | 177 | PF00928 | 0.392 |
TRG_ENDOCYTIC_2 | 273 | 276 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 386 | 389 | PF00928 | 0.417 |
TRG_ENDOCYTIC_2 | 470 | 473 | PF00928 | 0.439 |
TRG_ER_diArg_1 | 100 | 102 | PF00400 | 0.317 |
TRG_ER_diArg_1 | 86 | 88 | PF00400 | 0.345 |
TRG_Pf-PMV_PEXEL_1 | 27 | 31 | PF00026 | 0.390 |
TRG_Pf-PMV_PEXEL_1 | 377 | 381 | PF00026 | 0.475 |
TRG_Pf-PMV_PEXEL_1 | 421 | 425 | PF00026 | 0.395 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PC72 | Leptomonas seymouri | 56% | 98% |
A0A0S4JIP1 | Bodo saltans | 22% | 100% |
A0A1X0NTK3 | Trypanosomatidae | 32% | 97% |
A0A3S7WWY5 | Leishmania donovani | 92% | 100% |
A0A422NSK5 | Trypanosoma rangeli | 35% | 100% |
A4HC68 | Leishmania braziliensis | 79% | 100% |
A4HZP3 | Leishmania infantum | 92% | 100% |
C9ZSD4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
Q4QBY0 | Leishmania major | 91% | 100% |
V5BFR5 | Trypanosoma cruzi | 34% | 100% |