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: A4HC68
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 | 183 | 187 | PF00656 | 0.447 |
CLV_NRD_NRD_1 | 101 | 103 | PF00675 | 0.276 |
CLV_NRD_NRD_1 | 13 | 15 | PF00675 | 0.325 |
CLV_NRD_NRD_1 | 88 | 90 | PF00675 | 0.275 |
CLV_PCSK_FUR_1 | 45 | 49 | PF00082 | 0.360 |
CLV_PCSK_KEX2_1 | 101 | 103 | PF00082 | 0.253 |
CLV_PCSK_KEX2_1 | 13 | 15 | PF00082 | 0.325 |
CLV_PCSK_KEX2_1 | 47 | 49 | PF00082 | 0.432 |
CLV_PCSK_KEX2_1 | 88 | 90 | PF00082 | 0.284 |
CLV_PCSK_PC1ET2_1 | 47 | 49 | PF00082 | 0.424 |
CLV_PCSK_SKI1_1 | 372 | 376 | PF00082 | 0.312 |
CLV_PCSK_SKI1_1 | 423 | 427 | PF00082 | 0.362 |
DEG_MDM2_SWIB_1 | 351 | 359 | PF02201 | 0.274 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.536 |
DEG_SPOP_SBC_1 | 128 | 132 | PF00917 | 0.193 |
DOC_CYCLIN_RxL_1 | 341 | 350 | PF00134 | 0.193 |
DOC_CYCLIN_RxL_1 | 420 | 427 | PF00134 | 0.352 |
DOC_CYCLIN_yCln2_LP_2 | 306 | 312 | PF00134 | 0.193 |
DOC_CYCLIN_yCln2_LP_2 | 445 | 448 | PF00134 | 0.425 |
DOC_MAPK_gen_1 | 13 | 21 | PF00069 | 0.193 |
DOC_PP2B_LxvP_1 | 306 | 309 | PF13499 | 0.377 |
DOC_PP2B_LxvP_1 | 445 | 448 | PF13499 | 0.492 |
DOC_USP7_MATH_1 | 115 | 119 | PF00917 | 0.369 |
DOC_USP7_MATH_1 | 35 | 39 | PF00917 | 0.410 |
DOC_USP7_MATH_1 | 448 | 452 | PF00917 | 0.441 |
DOC_USP7_MATH_1 | 49 | 53 | PF00917 | 0.476 |
DOC_USP7_MATH_2 | 410 | 416 | PF00917 | 0.350 |
DOC_WW_Pin1_4 | 111 | 116 | PF00397 | 0.381 |
DOC_WW_Pin1_4 | 194 | 199 | PF00397 | 0.378 |
DOC_WW_Pin1_4 | 211 | 216 | PF00397 | 0.402 |
DOC_WW_Pin1_4 | 358 | 363 | PF00397 | 0.223 |
DOC_WW_Pin1_4 | 50 | 55 | PF00397 | 0.437 |
LIG_14-3-3_CanoR_1 | 105 | 115 | PF00244 | 0.193 |
LIG_14-3-3_CanoR_1 | 17 | 22 | PF00244 | 0.473 |
LIG_14-3-3_CanoR_1 | 200 | 205 | PF00244 | 0.371 |
LIG_14-3-3_CanoR_1 | 209 | 215 | PF00244 | 0.306 |
LIG_14-3-3_CanoR_1 | 48 | 54 | PF00244 | 0.432 |
LIG_BIR_III_2 | 357 | 361 | PF00653 | 0.350 |
LIG_BRCT_BRCA1_1 | 153 | 157 | PF00533 | 0.368 |
LIG_BRCT_BRCA1_1 | 360 | 364 | PF00533 | 0.346 |
LIG_BRCT_BRCA1_1 | 414 | 418 | PF00533 | 0.350 |
LIG_BRCT_BRCA1_1 | 64 | 68 | PF00533 | 0.381 |
LIG_Clathr_ClatBox_1 | 18 | 22 | PF01394 | 0.308 |
LIG_CSL_BTD_1 | 407 | 410 | PF09270 | 0.417 |
LIG_eIF4E_1 | 92 | 98 | PF01652 | 0.308 |
LIG_FHA_1 | 129 | 135 | PF00498 | 0.234 |
LIG_FHA_1 | 143 | 149 | PF00498 | 0.393 |
LIG_FHA_1 | 245 | 251 | PF00498 | 0.343 |
LIG_FHA_1 | 337 | 343 | PF00498 | 0.368 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.323 |
LIG_FHA_1 | 93 | 99 | PF00498 | 0.279 |
LIG_FHA_2 | 176 | 182 | PF00498 | 0.274 |
LIG_FHA_2 | 249 | 255 | PF00498 | 0.388 |
LIG_FHA_2 | 295 | 301 | PF00498 | 0.217 |
LIG_FHA_2 | 348 | 354 | PF00498 | 0.247 |
LIG_FHA_2 | 378 | 384 | PF00498 | 0.487 |
LIG_FHA_2 | 399 | 405 | PF00498 | 0.193 |
LIG_LIR_Apic_2 | 284 | 290 | PF02991 | 0.278 |
LIG_LIR_Apic_2 | 404 | 410 | PF02991 | 0.437 |
LIG_LIR_Apic_2 | 460 | 466 | PF02991 | 0.398 |
LIG_LIR_Gen_1 | 174 | 182 | PF02991 | 0.353 |
LIG_LIR_Gen_1 | 203 | 211 | PF02991 | 0.348 |
LIG_LIR_Gen_1 | 440 | 448 | PF02991 | 0.420 |
LIG_LIR_Gen_1 | 449 | 459 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 15 | 19 | PF02991 | 0.300 |
LIG_LIR_Nem_3 | 174 | 179 | PF02991 | 0.334 |
LIG_LIR_Nem_3 | 203 | 207 | PF02991 | 0.280 |
LIG_LIR_Nem_3 | 273 | 278 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 449 | 455 | PF02991 | 0.423 |
LIG_LYPXL_L_2 | 274 | 283 | PF13949 | 0.368 |
LIG_LYPXL_S_1 | 274 | 278 | PF13949 | 0.308 |
LIG_LYPXL_yS_3 | 275 | 278 | PF13949 | 0.308 |
LIG_NRBOX | 217 | 223 | PF00104 | 0.417 |
LIG_NRBOX | 232 | 238 | PF00104 | 0.417 |
LIG_PCNA_PIPBox_1 | 435 | 444 | PF02747 | 0.217 |
LIG_PCNA_yPIPBox_3 | 429 | 442 | PF02747 | 0.394 |
LIG_Pex14_2 | 351 | 355 | PF04695 | 0.274 |
LIG_Rb_pABgroove_1 | 151 | 159 | PF01858 | 0.417 |
LIG_SH2_CRK | 16 | 20 | PF00017 | 0.308 |
LIG_SH2_CRK | 287 | 291 | PF00017 | 0.368 |
LIG_SH2_CRK | 463 | 467 | PF00017 | 0.434 |
LIG_SH2_CRK | 472 | 476 | PF00017 | 0.375 |
LIG_SH2_GRB2like | 144 | 147 | PF00017 | 0.350 |
LIG_SH2_GRB2like | 92 | 95 | PF00017 | 0.289 |
LIG_SH2_PTP2 | 388 | 391 | PF00017 | 0.350 |
LIG_SH2_STAP1 | 144 | 148 | PF00017 | 0.350 |
LIG_SH2_STAP1 | 459 | 463 | PF00017 | 0.286 |
LIG_SH2_STAP1 | 92 | 96 | PF00017 | 0.289 |
LIG_SH2_STAT5 | 144 | 147 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 176 | 179 | PF00017 | 0.371 |
LIG_SH2_STAT5 | 202 | 205 | PF00017 | 0.289 |
LIG_SH2_STAT5 | 388 | 391 | PF00017 | 0.350 |
LIG_SH2_STAT5 | 441 | 444 | PF00017 | 0.362 |
LIG_SH2_STAT5 | 459 | 462 | PF00017 | 0.391 |
LIG_SH3_1 | 463 | 469 | PF00018 | 0.496 |
LIG_SH3_3 | 258 | 264 | PF00018 | 0.193 |
LIG_SH3_3 | 463 | 469 | PF00018 | 0.417 |
LIG_SUMO_SIM_par_1 | 17 | 23 | PF11976 | 0.288 |
LIG_TRAF2_1 | 178 | 181 | PF00917 | 0.334 |
LIG_TRFH_1 | 426 | 430 | PF08558 | 0.368 |
LIG_TYR_ITIM | 470 | 475 | PF00017 | 0.367 |
LIG_WRC_WIRS_1 | 249 | 254 | PF05994 | 0.278 |
LIG_WRC_WIRS_1 | 348 | 353 | PF05994 | 0.368 |
MOD_CDC14_SPxK_1 | 114 | 117 | PF00782 | 0.193 |
MOD_CDK_SPxK_1 | 111 | 117 | PF00069 | 0.193 |
MOD_CDK_SPxK_1 | 194 | 200 | PF00069 | 0.193 |
MOD_CK1_1 | 111 | 117 | PF00069 | 0.391 |
MOD_CK1_1 | 175 | 181 | PF00069 | 0.340 |
MOD_CK1_1 | 189 | 195 | PF00069 | 0.281 |
MOD_CK1_1 | 213 | 219 | PF00069 | 0.300 |
MOD_CK1_1 | 294 | 300 | PF00069 | 0.320 |
MOD_CK1_1 | 393 | 399 | PF00069 | 0.463 |
MOD_CK1_1 | 53 | 59 | PF00069 | 0.370 |
MOD_CK1_1 | 83 | 89 | PF00069 | 0.417 |
MOD_CK2_1 | 17 | 23 | PF00069 | 0.348 |
MOD_CK2_1 | 175 | 181 | PF00069 | 0.310 |
MOD_CK2_1 | 211 | 217 | PF00069 | 0.293 |
MOD_CK2_1 | 294 | 300 | PF00069 | 0.193 |
MOD_CK2_1 | 347 | 353 | PF00069 | 0.303 |
MOD_CK2_1 | 377 | 383 | PF00069 | 0.386 |
MOD_DYRK1A_RPxSP_1 | 50 | 54 | PF00069 | 0.350 |
MOD_GlcNHglycan | 108 | 111 | PF01048 | 0.433 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.375 |
MOD_GlcNHglycan | 37 | 40 | PF01048 | 0.383 |
MOD_GlcNHglycan | 395 | 398 | PF01048 | 0.403 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.403 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.349 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.383 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.256 |
MOD_GSK3_1 | 358 | 365 | PF00069 | 0.214 |
MOD_GSK3_1 | 398 | 405 | PF00069 | 0.386 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.402 |
MOD_N-GLC_1 | 62 | 67 | PF02516 | 0.227 |
MOD_N-GLC_2 | 167 | 169 | PF02516 | 0.355 |
MOD_NEK2_1 | 127 | 132 | PF00069 | 0.208 |
MOD_NEK2_1 | 156 | 161 | PF00069 | 0.370 |
MOD_NEK2_1 | 172 | 177 | PF00069 | 0.349 |
MOD_NEK2_1 | 221 | 226 | PF00069 | 0.330 |
MOD_NEK2_1 | 377 | 382 | PF00069 | 0.269 |
MOD_NEK2_1 | 97 | 102 | PF00069 | 0.378 |
MOD_NEK2_2 | 248 | 253 | PF00069 | 0.193 |
MOD_PK_1 | 17 | 23 | PF00069 | 0.370 |
MOD_PKA_2 | 393 | 399 | PF00069 | 0.193 |
MOD_PKA_2 | 457 | 463 | PF00069 | 0.444 |
MOD_PKA_2 | 49 | 55 | PF00069 | 0.350 |
MOD_Plk_1 | 259 | 265 | PF00069 | 0.360 |
MOD_Plk_1 | 299 | 305 | PF00069 | 0.350 |
MOD_Plk_1 | 448 | 454 | PF00069 | 0.524 |
MOD_Plk_1 | 62 | 68 | PF00069 | 0.203 |
MOD_Plk_4 | 172 | 178 | PF00069 | 0.417 |
MOD_Plk_4 | 237 | 243 | PF00069 | 0.209 |
MOD_Plk_4 | 248 | 254 | PF00069 | 0.361 |
MOD_Plk_4 | 270 | 276 | PF00069 | 0.289 |
MOD_Plk_4 | 377 | 383 | PF00069 | 0.371 |
MOD_Plk_4 | 92 | 98 | PF00069 | 0.323 |
MOD_ProDKin_1 | 111 | 117 | PF00069 | 0.381 |
MOD_ProDKin_1 | 194 | 200 | PF00069 | 0.378 |
MOD_ProDKin_1 | 211 | 217 | PF00069 | 0.402 |
MOD_ProDKin_1 | 358 | 364 | PF00069 | 0.223 |
MOD_ProDKin_1 | 50 | 56 | PF00069 | 0.437 |
TRG_DiLeu_BaEn_1 | 217 | 222 | PF01217 | 0.417 |
TRG_DiLeu_BaLyEn_6 | 232 | 237 | PF01217 | 0.274 |
TRG_ENDOCYTIC_2 | 16 | 19 | PF00928 | 0.372 |
TRG_ENDOCYTIC_2 | 176 | 179 | PF00928 | 0.340 |
TRG_ENDOCYTIC_2 | 275 | 278 | PF00928 | 0.289 |
TRG_ENDOCYTIC_2 | 388 | 391 | PF00928 | 0.372 |
TRG_ENDOCYTIC_2 | 441 | 444 | PF00928 | 0.356 |
TRG_ENDOCYTIC_2 | 472 | 475 | PF00928 | 0.369 |
TRG_ER_diArg_1 | 101 | 103 | PF00400 | 0.264 |
TRG_ER_diArg_1 | 87 | 89 | PF00400 | 0.290 |
TRG_NES_CRM1_1 | 427 | 440 | PF08389 | 0.457 |
TRG_NLS_MonoExtN_4 | 45 | 51 | PF00514 | 0.416 |
TRG_Pf-PMV_PEXEL_1 | 27 | 31 | PF00026 | 0.394 |
TRG_Pf-PMV_PEXEL_1 | 344 | 349 | PF00026 | 0.303 |
TRG_Pf-PMV_PEXEL_1 | 379 | 383 | PF00026 | 0.350 |
TRG_Pf-PMV_PEXEL_1 | 423 | 427 | PF00026 | 0.344 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PC72 | Leptomonas seymouri | 54% | 98% |
A0A0S4JIP1 | Bodo saltans | 24% | 100% |
A0A1X0NTK3 | Trypanosomatidae | 32% | 97% |
A0A3S7WWY5 | Leishmania donovani | 79% | 100% |
A0A422NSK5 | Trypanosoma rangeli | 33% | 100% |
A4HZP3 | Leishmania infantum | 79% | 100% |
C9ZSD4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
E9AVJ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 100% |
Q4QBY0 | Leishmania major | 80% | 100% |
V5BFR5 | Trypanosoma cruzi | 31% | 100% |