Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 2 |
Forrest at al. (procyclic) | no | yes: 2 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 15 |
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: 6 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 12 |
GO:0043226 | organelle | 2 | 12 |
GO:0043227 | membrane-bounded organelle | 3 | 12 |
GO:0043229 | intracellular organelle | 3 | 12 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0000785 | chromatin | 2 | 1 |
Related structures:
AlphaFold database: A4HJF7
Term | Name | Level | Count |
---|---|---|---|
GO:0006325 | chromatin organization | 4 | 12 |
GO:0006334 | nucleosome assembly | 7 | 12 |
GO:0006338 | chromatin remodeling | 5 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016043 | cellular component organization | 3 | 12 |
GO:0022607 | cellular component assembly | 4 | 12 |
GO:0034728 | nucleosome organization | 6 | 12 |
GO:0043933 | protein-containing complex organization | 4 | 12 |
GO:0065003 | protein-containing complex assembly | 5 | 12 |
GO:0065004 | protein-DNA complex assembly | 6 | 12 |
GO:0071824 | protein-DNA complex subunit organization | 5 | 12 |
GO:0071840 | cellular component organization or biogenesis | 2 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003682 | chromatin binding | 2 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0005515 | protein binding | 2 | 1 |
GO:0042393 | histone binding | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 387 | 389 | PF00675 | 0.679 |
CLV_NRD_NRD_1 | 40 | 42 | PF00675 | 0.289 |
CLV_NRD_NRD_1 | 55 | 57 | PF00675 | 0.306 |
CLV_NRD_NRD_1 | 80 | 82 | PF00675 | 0.348 |
CLV_PCSK_KEX2_1 | 387 | 389 | PF00082 | 0.784 |
CLV_PCSK_KEX2_1 | 39 | 41 | PF00082 | 0.327 |
CLV_PCSK_KEX2_1 | 57 | 59 | PF00082 | 0.306 |
CLV_PCSK_PC1ET2_1 | 57 | 59 | PF00082 | 0.216 |
CLV_PCSK_SKI1_1 | 117 | 121 | PF00082 | 0.320 |
CLV_PCSK_SKI1_1 | 167 | 171 | PF00082 | 0.283 |
CLV_PCSK_SKI1_1 | 190 | 194 | PF00082 | 0.380 |
CLV_PCSK_SKI1_1 | 238 | 242 | PF00082 | 0.288 |
CLV_PCSK_SKI1_1 | 313 | 317 | PF00082 | 0.323 |
CLV_PCSK_SKI1_1 | 89 | 93 | PF00082 | 0.300 |
DEG_APCC_DBOX_1 | 166 | 174 | PF00400 | 0.492 |
DOC_MAPK_gen_1 | 165 | 173 | PF00069 | 0.502 |
DOC_MAPK_gen_1 | 234 | 244 | PF00069 | 0.519 |
DOC_MAPK_gen_1 | 250 | 259 | PF00069 | 0.409 |
DOC_MAPK_MEF2A_6 | 237 | 244 | PF00069 | 0.547 |
DOC_PP1_RVXF_1 | 188 | 194 | PF00149 | 0.523 |
DOC_PP1_RVXF_1 | 96 | 102 | PF00149 | 0.416 |
DOC_PP4_FxxP_1 | 272 | 275 | PF00568 | 0.484 |
DOC_USP7_MATH_1 | 138 | 142 | PF00917 | 0.552 |
DOC_USP7_MATH_1 | 265 | 269 | PF00917 | 0.576 |
DOC_USP7_MATH_1 | 367 | 371 | PF00917 | 0.738 |
DOC_USP7_UBL2_3 | 116 | 120 | PF12436 | 0.542 |
DOC_USP7_UBL2_3 | 234 | 238 | PF12436 | 0.499 |
DOC_USP7_UBL2_3 | 248 | 252 | PF12436 | 0.441 |
DOC_WW_Pin1_4 | 101 | 106 | PF00397 | 0.425 |
DOC_WW_Pin1_4 | 136 | 141 | PF00397 | 0.557 |
DOC_WW_Pin1_4 | 193 | 198 | PF00397 | 0.549 |
DOC_WW_Pin1_4 | 271 | 276 | PF00397 | 0.575 |
LIG_14-3-3_CanoR_1 | 222 | 227 | PF00244 | 0.533 |
LIG_14-3-3_CanoR_1 | 58 | 66 | PF00244 | 0.416 |
LIG_14-3-3_CanoR_1 | 98 | 108 | PF00244 | 0.603 |
LIG_BIR_III_2 | 111 | 115 | PF00653 | 0.579 |
LIG_CaM_IQ_9 | 42 | 58 | PF13499 | 0.575 |
LIG_eIF4E_1 | 43 | 49 | PF01652 | 0.492 |
LIG_FHA_1 | 222 | 228 | PF00498 | 0.567 |
LIG_FHA_1 | 239 | 245 | PF00498 | 0.396 |
LIG_FHA_1 | 305 | 311 | PF00498 | 0.567 |
LIG_FHA_2 | 161 | 167 | PF00498 | 0.482 |
LIG_FHA_2 | 210 | 216 | PF00498 | 0.529 |
LIG_FHA_2 | 285 | 291 | PF00498 | 0.524 |
LIG_FHA_2 | 324 | 330 | PF00498 | 0.598 |
LIG_FHA_2 | 33 | 39 | PF00498 | 0.502 |
LIG_FHA_2 | 342 | 348 | PF00498 | 0.775 |
LIG_FHA_2 | 90 | 96 | PF00498 | 0.491 |
LIG_LIR_Gen_1 | 267 | 278 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 267 | 273 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 370 | 375 | PF02991 | 0.715 |
LIG_LIR_Nem_3 | 51 | 55 | PF02991 | 0.506 |
LIG_NRBOX | 44 | 50 | PF00104 | 0.492 |
LIG_PCNA_PIPBox_1 | 46 | 55 | PF02747 | 0.579 |
LIG_PCNA_yPIPBox_3 | 39 | 53 | PF02747 | 0.464 |
LIG_Pex14_2 | 269 | 273 | PF04695 | 0.481 |
LIG_SH2_STAT3 | 43 | 46 | PF00017 | 0.575 |
LIG_SH2_STAT5 | 200 | 203 | PF00017 | 0.484 |
LIG_SH2_STAT5 | 318 | 321 | PF00017 | 0.492 |
LIG_SH3_2 | 105 | 110 | PF14604 | 0.579 |
LIG_SH3_3 | 102 | 108 | PF00018 | 0.595 |
LIG_SH3_3 | 272 | 278 | PF00018 | 0.577 |
LIG_SH3_4 | 398 | 405 | PF00018 | 0.560 |
LIG_SUMO_SIM_anti_2 | 26 | 33 | PF11976 | 0.588 |
LIG_TRAF2_1 | 400 | 403 | PF00917 | 0.784 |
LIG_TRAF2_1 | 92 | 95 | PF00917 | 0.506 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.732 |
MOD_CK2_1 | 150 | 156 | PF00069 | 0.556 |
MOD_CK2_1 | 18 | 24 | PF00069 | 0.681 |
MOD_CK2_1 | 193 | 199 | PF00069 | 0.555 |
MOD_CK2_1 | 32 | 38 | PF00069 | 0.384 |
MOD_CK2_1 | 323 | 329 | PF00069 | 0.559 |
MOD_CK2_1 | 89 | 95 | PF00069 | 0.491 |
MOD_Cter_Amidation | 385 | 388 | PF01082 | 0.689 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.370 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.722 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.606 |
MOD_N-GLC_1 | 202 | 207 | PF02516 | 0.346 |
MOD_N-GLC_1 | 238 | 243 | PF02516 | 0.292 |
MOD_N-GLC_2 | 68 | 70 | PF02516 | 0.379 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.481 |
MOD_NEK2_1 | 240 | 245 | PF00069 | 0.579 |
MOD_NEK2_1 | 32 | 37 | PF00069 | 0.366 |
MOD_NEK2_2 | 265 | 270 | PF00069 | 0.575 |
MOD_PIKK_1 | 304 | 310 | PF00454 | 0.579 |
MOD_PKA_2 | 221 | 227 | PF00069 | 0.590 |
MOD_PKB_1 | 56 | 64 | PF00069 | 0.416 |
MOD_Plk_1 | 202 | 208 | PF00069 | 0.546 |
MOD_Plk_1 | 238 | 244 | PF00069 | 0.492 |
MOD_Plk_1 | 32 | 38 | PF00069 | 0.484 |
MOD_Plk_2-3 | 209 | 215 | PF00069 | 0.534 |
MOD_Plk_2-3 | 284 | 290 | PF00069 | 0.416 |
MOD_Plk_2-3 | 341 | 347 | PF00069 | 0.753 |
MOD_Plk_4 | 222 | 228 | PF00069 | 0.479 |
MOD_Plk_4 | 265 | 271 | PF00069 | 0.481 |
MOD_ProDKin_1 | 101 | 107 | PF00069 | 0.425 |
MOD_ProDKin_1 | 136 | 142 | PF00069 | 0.557 |
MOD_ProDKin_1 | 193 | 199 | PF00069 | 0.549 |
MOD_ProDKin_1 | 271 | 277 | PF00069 | 0.575 |
TRG_DiLeu_BaLyEn_6 | 187 | 192 | PF01217 | 0.479 |
TRG_ENDOCYTIC_2 | 52 | 55 | PF00928 | 0.492 |
TRG_ER_diArg_1 | 376 | 379 | PF00400 | 0.714 |
TRG_ER_diArg_1 | 39 | 41 | PF00400 | 0.417 |
TRG_ER_diArg_1 | 55 | 58 | PF00400 | 0.575 |
TRG_ER_FFAT_2 | 267 | 277 | PF00635 | 0.461 |
TRG_NES_CRM1_1 | 26 | 38 | PF08389 | 0.478 |
TRG_NLS_Bipartite_1 | 237 | 251 | PF00514 | 0.575 |
TRG_NLS_Bipartite_1 | 39 | 61 | PF00514 | 0.357 |
TRG_NLS_MonoExtC_3 | 55 | 60 | PF00514 | 0.416 |
TRG_NLS_MonoExtN_4 | 245 | 251 | PF00514 | 0.481 |
TRG_NLS_MonoExtN_4 | 56 | 61 | PF00514 | 0.416 |
TRG_Pf-PMV_PEXEL_1 | 328 | 332 | PF00026 | 0.580 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1J2 | Leptomonas seymouri | 31% | 100% |
A0A0N1IJI7 | Leptomonas seymouri | 68% | 100% |
A0A0S4J1L1 | Bodo saltans | 41% | 99% |
A0A1X0NTY9 | Trypanosomatidae | 42% | 94% |
A0A1X0P6J1 | Trypanosomatidae | 29% | 97% |
A0A3Q8IA70 | Leishmania donovani | 32% | 100% |
A0A3R7KHX6 | Trypanosoma rangeli | 41% | 94% |
A0A3R7KRI5 | Trypanosoma rangeli | 29% | 100% |
A0A3S7X4M4 | Leishmania donovani | 84% | 100% |
A4HA02 | Leishmania braziliensis | 32% | 100% |
A4HY66 | Leishmania infantum | 31% | 100% |
A4I6V2 | Leishmania infantum | 84% | 100% |
A6H767 | Bos taurus | 34% | 100% |
B8AW64 | Oryza sativa subsp. indica | 33% | 100% |
B8B2R4 | Oryza sativa subsp. indica | 33% | 100% |
B9FU45 | Oryza sativa subsp. japonica | 29% | 100% |
C9ZXT4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 97% |
D0A0I6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
E9ARZ6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
E9B1X5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
O59797 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 34% | 100% |
P25293 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 32% | 98% |
P28656 | Mus musculus | 33% | 100% |
P55209 | Homo sapiens | 34% | 100% |
P78920 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 33% | 100% |
Q28EB4 | Xenopus tropicalis | 34% | 100% |
Q2TA40 | Bos taurus | 32% | 100% |
Q4Q687 | Leishmania major | 83% | 100% |
Q4QDH7 | Leishmania major | 33% | 100% |
Q4U0Y4 | Xenopus laevis | 32% | 100% |
Q53WK4 | Oryza sativa subsp. japonica | 33% | 100% |
Q55ED1 | Dictyostelium discoideum | 30% | 100% |
Q5AAI8 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 31% | 94% |
Q5R4D4 | Pongo abelii | 34% | 100% |
Q5U2Z3 | Rattus norvegicus | 32% | 100% |
Q5VND6 | Oryza sativa subsp. japonica | 33% | 100% |
Q70Z17 | Nicotiana tabacum | 33% | 100% |
Q70Z18 | Nicotiana tabacum | 34% | 100% |
Q70Z19 | Nicotiana tabacum | 31% | 100% |
Q78ZA7 | Mus musculus | 33% | 100% |
Q7ZY81 | Xenopus laevis | 34% | 100% |
Q94K07 | Arabidopsis thaliana | 35% | 100% |
Q99733 | Homo sapiens | 33% | 100% |
Q9SZI2 | Arabidopsis thaliana | 34% | 100% |
Q9Z2G8 | Rattus norvegicus | 33% | 100% |
Q9ZUP3 | Arabidopsis thaliana | 34% | 100% |
V5BUC1 | Trypanosoma cruzi | 42% | 90% |
V5BX23 | Trypanosoma cruzi | 26% | 100% |