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: A0A3S7WWY5
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 | 182 | 186 | PF00656 | 0.468 |
CLV_NRD_NRD_1 | 101 | 103 | PF00675 | 0.330 |
CLV_NRD_NRD_1 | 289 | 291 | PF00675 | 0.393 |
CLV_NRD_NRD_1 | 88 | 90 | PF00675 | 0.329 |
CLV_PCSK_FUR_1 | 45 | 49 | PF00082 | 0.437 |
CLV_PCSK_KEX2_1 | 101 | 103 | PF00082 | 0.305 |
CLV_PCSK_KEX2_1 | 289 | 291 | PF00082 | 0.358 |
CLV_PCSK_KEX2_1 | 47 | 49 | PF00082 | 0.453 |
CLV_PCSK_KEX2_1 | 88 | 90 | PF00082 | 0.338 |
CLV_PCSK_PC1ET2_1 | 47 | 49 | PF00082 | 0.453 |
CLV_PCSK_SKI1_1 | 27 | 31 | PF00082 | 0.372 |
CLV_PCSK_SKI1_1 | 422 | 426 | PF00082 | 0.376 |
DEG_MDM2_SWIB_1 | 350 | 358 | PF02201 | 0.328 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.662 |
DOC_CYCLIN_RxL_1 | 419 | 426 | PF00134 | 0.366 |
DOC_CYCLIN_yCln2_LP_2 | 444 | 447 | PF00134 | 0.572 |
DOC_MAPK_gen_1 | 383 | 390 | PF00069 | 0.398 |
DOC_MAPK_MEF2A_6 | 410 | 417 | PF00069 | 0.398 |
DOC_PP2B_LxvP_1 | 311 | 314 | PF13499 | 0.409 |
DOC_PP2B_LxvP_1 | 444 | 447 | PF13499 | 0.545 |
DOC_USP7_MATH_1 | 106 | 110 | PF00917 | 0.400 |
DOC_USP7_MATH_1 | 194 | 198 | PF00917 | 0.435 |
DOC_USP7_MATH_1 | 241 | 245 | PF00917 | 0.398 |
DOC_USP7_MATH_1 | 35 | 39 | PF00917 | 0.445 |
DOC_USP7_MATH_1 | 357 | 361 | PF00917 | 0.428 |
DOC_USP7_MATH_1 | 409 | 413 | PF00917 | 0.491 |
DOC_USP7_MATH_1 | 43 | 47 | PF00917 | 0.448 |
DOC_USP7_MATH_1 | 447 | 451 | PF00917 | 0.579 |
DOC_USP7_MATH_2 | 409 | 415 | PF00917 | 0.475 |
DOC_WW_Pin1_4 | 130 | 135 | PF00397 | 0.491 |
DOC_WW_Pin1_4 | 210 | 215 | PF00397 | 0.439 |
DOC_WW_Pin1_4 | 33 | 38 | PF00397 | 0.432 |
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 | 199 | 204 | PF00244 | 0.387 |
LIG_14-3-3_CanoR_1 | 208 | 214 | PF00244 | 0.338 |
LIG_14-3-3_CanoR_1 | 48 | 54 | PF00244 | 0.453 |
LIG_BIR_III_2 | 356 | 360 | PF00653 | 0.475 |
LIG_BRCT_BRCA1_1 | 152 | 156 | PF00533 | 0.413 |
LIG_BRCT_BRCA1_1 | 359 | 363 | PF00533 | 0.396 |
LIG_BRCT_BRCA1_1 | 393 | 397 | PF00533 | 0.398 |
LIG_BRCT_BRCA1_1 | 413 | 417 | PF00533 | 0.475 |
LIG_Clathr_ClatBox_1 | 18 | 22 | PF01394 | 0.363 |
LIG_CSL_BTD_1 | 406 | 409 | PF09270 | 0.449 |
LIG_eIF4E_1 | 92 | 98 | PF01652 | 0.363 |
LIG_FHA_1 | 125 | 131 | PF00498 | 0.484 |
LIG_FHA_1 | 142 | 148 | PF00498 | 0.281 |
LIG_FHA_1 | 336 | 342 | PF00498 | 0.413 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.363 |
LIG_FHA_1 | 93 | 99 | PF00498 | 0.328 |
LIG_FHA_2 | 175 | 181 | PF00498 | 0.315 |
LIG_FHA_2 | 377 | 383 | PF00498 | 0.489 |
LIG_LIR_Apic_2 | 31 | 37 | PF02991 | 0.359 |
LIG_LIR_Apic_2 | 403 | 409 | PF02991 | 0.461 |
LIG_LIR_Apic_2 | 459 | 465 | PF02991 | 0.461 |
LIG_LIR_Gen_1 | 173 | 181 | PF02991 | 0.409 |
LIG_LIR_Gen_1 | 202 | 210 | PF02991 | 0.397 |
LIG_LIR_Gen_1 | 448 | 456 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 15 | 19 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 173 | 178 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 202 | 206 | PF02991 | 0.330 |
LIG_LIR_Nem_3 | 272 | 277 | PF02991 | 0.384 |
LIG_LIR_Nem_3 | 448 | 454 | PF02991 | 0.486 |
LIG_LYPXL_L_2 | 273 | 282 | PF13949 | 0.413 |
LIG_LYPXL_S_1 | 273 | 277 | PF13949 | 0.363 |
LIG_LYPXL_yS_3 | 274 | 277 | PF13949 | 0.363 |
LIG_NRBOX | 216 | 222 | PF00104 | 0.449 |
LIG_NRBOX | 231 | 237 | PF00104 | 0.475 |
LIG_PCNA_yPIPBox_3 | 428 | 441 | PF02747 | 0.433 |
LIG_Pex14_2 | 350 | 354 | PF04695 | 0.328 |
LIG_Rb_pABgroove_1 | 150 | 158 | PF01858 | 0.449 |
LIG_SH2_CRK | 16 | 20 | PF00017 | 0.363 |
LIG_SH2_CRK | 462 | 466 | PF00017 | 0.498 |
LIG_SH2_CRK | 471 | 475 | PF00017 | 0.430 |
LIG_SH2_GRB2like | 143 | 146 | PF00017 | 0.475 |
LIG_SH2_GRB2like | 92 | 95 | PF00017 | 0.344 |
LIG_SH2_PTP2 | 387 | 390 | PF00017 | 0.475 |
LIG_SH2_STAP1 | 143 | 147 | PF00017 | 0.475 |
LIG_SH2_STAP1 | 92 | 96 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 143 | 146 | PF00017 | 0.423 |
LIG_SH2_STAT5 | 175 | 178 | PF00017 | 0.407 |
LIG_SH2_STAT5 | 201 | 204 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 387 | 390 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 440 | 443 | PF00017 | 0.434 |
LIG_SH3_1 | 462 | 468 | PF00018 | 0.549 |
LIG_SH3_3 | 190 | 196 | PF00018 | 0.449 |
LIG_SH3_3 | 302 | 308 | PF00018 | 0.475 |
LIG_SH3_3 | 386 | 392 | PF00018 | 0.390 |
LIG_SH3_3 | 462 | 468 | PF00018 | 0.480 |
LIG_SUMO_SIM_anti_2 | 300 | 306 | PF11976 | 0.394 |
LIG_SUMO_SIM_anti_2 | 63 | 68 | PF11976 | 0.435 |
LIG_SUMO_SIM_par_1 | 17 | 23 | PF11976 | 0.328 |
LIG_TRAF2_1 | 177 | 180 | PF00917 | 0.378 |
LIG_TRFH_1 | 425 | 429 | PF08558 | 0.413 |
LIG_TYR_ITIM | 469 | 474 | PF00017 | 0.425 |
LIG_WRC_WIRS_1 | 347 | 352 | PF05994 | 0.413 |
MOD_CK1_1 | 174 | 180 | PF00069 | 0.370 |
MOD_CK1_1 | 188 | 194 | PF00069 | 0.301 |
MOD_CK1_1 | 46 | 52 | PF00069 | 0.385 |
MOD_CK1_1 | 53 | 59 | PF00069 | 0.455 |
MOD_CK1_1 | 83 | 89 | PF00069 | 0.449 |
MOD_CK2_1 | 174 | 180 | PF00069 | 0.317 |
MOD_CK2_1 | 210 | 216 | PF00069 | 0.346 |
MOD_CK2_1 | 376 | 382 | PF00069 | 0.437 |
MOD_DYRK1A_RPxSP_1 | 50 | 54 | PF00069 | 0.475 |
MOD_GlcNHglycan | 108 | 111 | PF01048 | 0.459 |
MOD_GlcNHglycan | 167 | 170 | PF01048 | 0.485 |
MOD_GlcNHglycan | 188 | 191 | PF01048 | 0.391 |
MOD_GlcNHglycan | 196 | 199 | PF01048 | 0.341 |
MOD_GlcNHglycan | 37 | 40 | PF01048 | 0.409 |
MOD_GlcNHglycan | 393 | 396 | PF01048 | 0.440 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.457 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.434 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.421 |
MOD_GSK3_1 | 181 | 188 | PF00069 | 0.404 |
MOD_GSK3_1 | 397 | 404 | PF00069 | 0.427 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.449 |
MOD_N-GLC_1 | 165 | 170 | PF02516 | 0.398 |
MOD_N-GLC_1 | 298 | 303 | PF02516 | 0.461 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.415 |
MOD_NEK2_1 | 171 | 176 | PF00069 | 0.449 |
MOD_NEK2_1 | 209 | 214 | PF00069 | 0.370 |
MOD_NEK2_1 | 220 | 225 | PF00069 | 0.383 |
MOD_NEK2_1 | 397 | 402 | PF00069 | 0.469 |
MOD_NEK2_1 | 97 | 102 | PF00069 | 0.399 |
MOD_PK_1 | 17 | 23 | PF00069 | 0.413 |
MOD_PKA_2 | 116 | 122 | PF00069 | 0.398 |
MOD_PKA_2 | 456 | 462 | PF00069 | 0.575 |
MOD_PKA_2 | 49 | 55 | PF00069 | 0.475 |
MOD_PKB_1 | 139 | 147 | PF00069 | 0.398 |
MOD_Plk_1 | 165 | 171 | PF00069 | 0.398 |
MOD_Plk_1 | 258 | 264 | PF00069 | 0.407 |
MOD_Plk_1 | 298 | 304 | PF00069 | 0.475 |
MOD_Plk_1 | 447 | 453 | PF00069 | 0.564 |
MOD_Plk_2-3 | 411 | 417 | PF00069 | 0.398 |
MOD_Plk_4 | 171 | 177 | PF00069 | 0.449 |
MOD_Plk_4 | 269 | 275 | PF00069 | 0.358 |
MOD_Plk_4 | 298 | 304 | PF00069 | 0.359 |
MOD_Plk_4 | 358 | 364 | PF00069 | 0.314 |
MOD_Plk_4 | 376 | 382 | PF00069 | 0.389 |
MOD_Plk_4 | 401 | 407 | PF00069 | 0.364 |
MOD_Plk_4 | 440 | 446 | PF00069 | 0.474 |
MOD_Plk_4 | 92 | 98 | PF00069 | 0.361 |
MOD_ProDKin_1 | 130 | 136 | PF00069 | 0.491 |
MOD_ProDKin_1 | 210 | 216 | PF00069 | 0.439 |
MOD_ProDKin_1 | 33 | 39 | PF00069 | 0.432 |
MOD_ProDKin_1 | 50 | 56 | PF00069 | 0.370 |
TRG_DiLeu_BaEn_1 | 216 | 221 | PF01217 | 0.449 |
TRG_DiLeu_BaLyEn_6 | 231 | 236 | PF01217 | 0.328 |
TRG_ENDOCYTIC_2 | 16 | 19 | PF00928 | 0.417 |
TRG_ENDOCYTIC_2 | 175 | 178 | PF00928 | 0.409 |
TRG_ENDOCYTIC_2 | 274 | 277 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 387 | 390 | PF00928 | 0.417 |
TRG_ENDOCYTIC_2 | 471 | 474 | PF00928 | 0.425 |
TRG_ER_diArg_1 | 101 | 103 | PF00400 | 0.317 |
TRG_ER_diArg_1 | 87 | 89 | PF00400 | 0.345 |
TRG_NES_CRM1_1 | 426 | 439 | PF08389 | 0.474 |
TRG_NLS_MonoExtN_4 | 45 | 51 | PF00514 | 0.448 |
TRG_Pf-PMV_PEXEL_1 | 27 | 31 | PF00026 | 0.390 |
TRG_Pf-PMV_PEXEL_1 | 378 | 382 | PF00026 | 0.475 |
TRG_Pf-PMV_PEXEL_1 | 422 | 426 | PF00026 | 0.395 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PC72 | Leptomonas seymouri | 56% | 98% |
A0A0S4JIP1 | Bodo saltans | 23% | 100% |
A0A1X0NTK3 | Trypanosomatidae | 34% | 97% |
A0A422NSK5 | Trypanosoma rangeli | 35% | 100% |
A4HC68 | Leishmania braziliensis | 79% | 100% |
A4HZP3 | Leishmania infantum | 100% | 100% |
C9ZSD4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
E9AVJ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
Q4QBY0 | Leishmania major | 94% | 100% |
V5BFR5 | Trypanosoma cruzi | 34% | 100% |