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:0000785 | chromatin | 2 | 2 |
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 |
Related structures:
AlphaFold database: Q4Q687
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 | 2 |
GO:0005488 | binding | 1 | 2 |
GO:0005515 | protein binding | 2 | 2 |
GO:0042393 | histone binding | 3 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 13 | 17 | PF00656 | 0.745 |
CLV_C14_Caspase3-7 | 350 | 354 | PF00656 | 0.775 |
CLV_NRD_NRD_1 | 40 | 42 | PF00675 | 0.280 |
CLV_NRD_NRD_1 | 80 | 82 | PF00675 | 0.336 |
CLV_PCSK_KEX2_1 | 39 | 41 | PF00082 | 0.333 |
CLV_PCSK_SKI1_1 | 119 | 123 | PF00082 | 0.318 |
CLV_PCSK_SKI1_1 | 169 | 173 | PF00082 | 0.283 |
CLV_PCSK_SKI1_1 | 192 | 196 | PF00082 | 0.398 |
CLV_PCSK_SKI1_1 | 240 | 244 | PF00082 | 0.277 |
CLV_PCSK_SKI1_1 | 315 | 319 | PF00082 | 0.322 |
CLV_PCSK_SKI1_1 | 89 | 93 | PF00082 | 0.297 |
DEG_APCC_DBOX_1 | 168 | 176 | PF00400 | 0.492 |
DOC_ANK_TNKS_1 | 179 | 186 | PF00023 | 0.530 |
DOC_MAPK_gen_1 | 236 | 246 | PF00069 | 0.511 |
DOC_MAPK_gen_1 | 252 | 261 | PF00069 | 0.404 |
DOC_MAPK_gen_1 | 58 | 66 | PF00069 | 0.480 |
DOC_MAPK_MEF2A_6 | 239 | 246 | PF00069 | 0.543 |
DOC_PP1_RVXF_1 | 117 | 124 | PF00149 | 0.530 |
DOC_PP1_RVXF_1 | 190 | 196 | PF00149 | 0.522 |
DOC_PP4_FxxP_1 | 123 | 126 | PF00568 | 0.530 |
DOC_PP4_FxxP_1 | 274 | 277 | PF00568 | 0.483 |
DOC_USP7_MATH_1 | 140 | 144 | PF00917 | 0.542 |
DOC_USP7_MATH_1 | 159 | 163 | PF00917 | 0.567 |
DOC_USP7_MATH_1 | 20 | 24 | PF00917 | 0.730 |
DOC_USP7_MATH_1 | 267 | 271 | PF00917 | 0.567 |
DOC_USP7_UBL2_3 | 118 | 122 | PF12436 | 0.538 |
DOC_USP7_UBL2_3 | 236 | 240 | PF12436 | 0.497 |
DOC_USP7_UBL2_3 | 250 | 254 | PF12436 | 0.445 |
DOC_WW_Pin1_4 | 138 | 143 | PF00397 | 0.551 |
DOC_WW_Pin1_4 | 195 | 200 | PF00397 | 0.542 |
DOC_WW_Pin1_4 | 273 | 278 | PF00397 | 0.567 |
DOC_WW_Pin1_4 | 382 | 387 | PF00397 | 0.726 |
LIG_14-3-3_CanoR_1 | 173 | 182 | PF00244 | 0.434 |
LIG_14-3-3_CanoR_1 | 98 | 108 | PF00244 | 0.558 |
LIG_BIR_III_2 | 113 | 117 | PF00653 | 0.586 |
LIG_CaM_IQ_9 | 42 | 58 | PF13499 | 0.567 |
LIG_eIF4E_1 | 43 | 49 | PF01652 | 0.492 |
LIG_FHA_1 | 224 | 230 | PF00498 | 0.577 |
LIG_FHA_1 | 241 | 247 | PF00498 | 0.480 |
LIG_FHA_1 | 307 | 313 | PF00498 | 0.560 |
LIG_FHA_2 | 104 | 110 | PF00498 | 0.481 |
LIG_FHA_2 | 11 | 17 | PF00498 | 0.688 |
LIG_FHA_2 | 163 | 169 | PF00498 | 0.482 |
LIG_FHA_2 | 174 | 180 | PF00498 | 0.483 |
LIG_FHA_2 | 212 | 218 | PF00498 | 0.527 |
LIG_FHA_2 | 326 | 332 | PF00498 | 0.610 |
LIG_FHA_2 | 33 | 39 | PF00498 | 0.501 |
LIG_FHA_2 | 90 | 96 | PF00498 | 0.490 |
LIG_LIR_Gen_1 | 269 | 280 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 269 | 275 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 51 | 55 | PF02991 | 0.506 |
LIG_NRBOX | 44 | 50 | PF00104 | 0.492 |
LIG_PCNA_PIPBox_1 | 46 | 55 | PF02747 | 0.586 |
LIG_PCNA_yPIPBox_3 | 39 | 53 | PF02747 | 0.480 |
LIG_Pex14_2 | 271 | 275 | PF04695 | 0.481 |
LIG_SH2_STAT3 | 43 | 46 | PF00017 | 0.567 |
LIG_SH2_STAT5 | 202 | 205 | PF00017 | 0.549 |
LIG_SH2_STAT5 | 320 | 323 | PF00017 | 0.492 |
LIG_SH3_2 | 105 | 110 | PF14604 | 0.586 |
LIG_SH3_3 | 102 | 108 | PF00018 | 0.586 |
LIG_SH3_3 | 274 | 280 | PF00018 | 0.568 |
LIG_SUMO_SIM_anti_2 | 26 | 33 | PF11976 | 0.581 |
LIG_SUMO_SIM_par_1 | 26 | 33 | PF11976 | 0.552 |
LIG_TRAF2_1 | 354 | 357 | PF00917 | 0.712 |
LIG_TRAF2_1 | 401 | 404 | PF00917 | 0.785 |
LIG_TRAF2_1 | 92 | 95 | PF00917 | 0.506 |
MOD_CDK_SPxxK_3 | 382 | 389 | PF00069 | 0.732 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.734 |
MOD_CK1_1 | 162 | 168 | PF00069 | 0.475 |
MOD_CK2_1 | 152 | 158 | PF00069 | 0.560 |
MOD_CK2_1 | 173 | 179 | PF00069 | 0.530 |
MOD_CK2_1 | 18 | 24 | PF00069 | 0.686 |
MOD_CK2_1 | 195 | 201 | PF00069 | 0.550 |
MOD_CK2_1 | 32 | 38 | PF00069 | 0.387 |
MOD_CK2_1 | 325 | 331 | PF00069 | 0.574 |
MOD_CK2_1 | 351 | 357 | PF00069 | 0.724 |
MOD_CK2_1 | 89 | 95 | PF00069 | 0.502 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.351 |
MOD_GlcNHglycan | 142 | 145 | PF01048 | 0.320 |
MOD_GlcNHglycan | 255 | 258 | PF01048 | 0.273 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.724 |
MOD_GSK3_1 | 99 | 106 | PF00069 | 0.481 |
MOD_N-GLC_1 | 204 | 209 | PF02516 | 0.339 |
MOD_N-GLC_1 | 240 | 245 | PF02516 | 0.292 |
MOD_N-GLC_2 | 68 | 70 | PF02516 | 0.386 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.565 |
MOD_NEK2_1 | 149 | 154 | PF00069 | 0.481 |
MOD_NEK2_1 | 242 | 247 | PF00069 | 0.573 |
MOD_NEK2_2 | 267 | 272 | PF00069 | 0.567 |
MOD_PIKK_1 | 306 | 312 | PF00454 | 0.586 |
MOD_PIKK_1 | 394 | 400 | PF00454 | 0.780 |
MOD_PKA_2 | 223 | 229 | PF00069 | 0.579 |
MOD_Plk_1 | 204 | 210 | PF00069 | 0.539 |
MOD_Plk_1 | 240 | 246 | PF00069 | 0.485 |
MOD_Plk_1 | 32 | 38 | PF00069 | 0.474 |
MOD_Plk_2-3 | 349 | 355 | PF00069 | 0.740 |
MOD_Plk_4 | 159 | 165 | PF00069 | 0.484 |
MOD_Plk_4 | 267 | 273 | PF00069 | 0.478 |
MOD_ProDKin_1 | 138 | 144 | PF00069 | 0.551 |
MOD_ProDKin_1 | 195 | 201 | PF00069 | 0.542 |
MOD_ProDKin_1 | 273 | 279 | PF00069 | 0.567 |
MOD_ProDKin_1 | 382 | 388 | PF00069 | 0.728 |
TRG_DiLeu_BaLyEn_6 | 189 | 194 | PF01217 | 0.475 |
TRG_ENDOCYTIC_2 | 52 | 55 | PF00928 | 0.485 |
TRG_ER_diArg_1 | 377 | 380 | PF00400 | 0.751 |
TRG_ER_diArg_1 | 39 | 41 | PF00400 | 0.412 |
TRG_ER_diArg_1 | 55 | 58 | PF00400 | 0.471 |
TRG_NES_CRM1_1 | 26 | 38 | PF08389 | 0.482 |
TRG_NLS_Bipartite_1 | 239 | 253 | PF00514 | 0.567 |
TRG_NLS_MonoExtN_4 | 247 | 253 | PF00514 | 0.481 |
TRG_Pf-PMV_PEXEL_1 | 173 | 177 | PF00026 | 0.219 |
TRG_Pf-PMV_PEXEL_1 | 330 | 334 | PF00026 | 0.591 |
TRG_Pf-PMV_PEXEL_1 | 89 | 93 | PF00026 | 0.294 |
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 | 30% | 97% |
A0A3Q8IA70 | Leishmania donovani | 32% | 100% |
A0A3R7KHX6 | Trypanosoma rangeli | 42% | 94% |
A0A3R7KRI5 | Trypanosoma rangeli | 30% | 100% |
A0A3S7X4M4 | Leishmania donovani | 93% | 100% |
A4HA02 | Leishmania braziliensis | 33% | 100% |
A4HJF7 | Leishmania braziliensis | 83% | 100% |
A4HY66 | Leishmania infantum | 31% | 100% |
A4I6V2 | Leishmania infantum | 93% | 100% |
A6H767 | Bos taurus | 34% | 100% |
B8B2R4 | Oryza sativa subsp. indica | 34% | 100% |
C9ZXT4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 97% |
D0A0I6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
E9ARZ6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
E9B1X5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
O59797 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 35% | 100% |
P25293 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 31% | 98% |
P28656 | Mus musculus | 34% | 100% |
P55209 | Homo sapiens | 34% | 100% |
P78920 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 33% | 100% |
Q28EB4 | Xenopus tropicalis | 33% | 100% |
Q2TA40 | Bos taurus | 33% | 100% |
Q4QDH7 | Leishmania major | 31% | 100% |
Q4U0Y4 | Xenopus laevis | 32% | 100% |
Q55ED1 | Dictyostelium discoideum | 28% | 100% |
Q5AAI8 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 30% | 94% |
Q5R4D4 | Pongo abelii | 34% | 100% |
Q5U2Z3 | Rattus norvegicus | 34% | 100% |
Q70Z17 | Nicotiana tabacum | 33% | 100% |
Q70Z18 | Nicotiana tabacum | 34% | 100% |
Q70Z19 | Nicotiana tabacum | 32% | 100% |
Q78ZA7 | Mus musculus | 34% | 100% |
Q7ZY81 | Xenopus laevis | 33% | 100% |
Q94K07 | Arabidopsis thaliana | 34% | 100% |
Q99733 | Homo sapiens | 33% | 100% |
Q9SZI2 | Arabidopsis thaliana | 34% | 100% |
Q9Z2G8 | Rattus norvegicus | 34% | 100% |
Q9ZUP3 | Arabidopsis thaliana | 33% | 100% |
V5BUC1 | Trypanosoma cruzi | 42% | 90% |
V5BX23 | Trypanosoma cruzi | 25% | 100% |