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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005654 | nucleoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4H9A9
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 10 |
GO:0003723 | RNA binding | 4 | 10 |
GO:0005488 | binding | 1 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_PCSK_SKI1_1 | 146 | 150 | PF00082 | 0.461 |
CLV_PCSK_SKI1_1 | 217 | 221 | PF00082 | 0.713 |
CLV_PCSK_SKI1_1 | 271 | 275 | PF00082 | 0.551 |
CLV_PCSK_SKI1_1 | 315 | 319 | PF00082 | 0.571 |
CLV_PCSK_SKI1_1 | 340 | 344 | PF00082 | 0.566 |
CLV_PCSK_SKI1_1 | 55 | 59 | PF00082 | 0.205 |
DEG_APCC_KENBOX_2 | 294 | 298 | PF00400 | 0.520 |
DEG_SPOP_SBC_1 | 100 | 104 | PF00917 | 0.662 |
DEG_SPOP_SBC_1 | 317 | 321 | PF00917 | 0.446 |
DOC_CYCLIN_RxL_1 | 268 | 278 | PF00134 | 0.304 |
DOC_CYCLIN_yCln2_LP_2 | 126 | 129 | PF00134 | 0.644 |
DOC_MAPK_gen_1 | 163 | 171 | PF00069 | 0.342 |
DOC_MAPK_gen_1 | 71 | 79 | PF00069 | 0.482 |
DOC_PP1_RVXF_1 | 36 | 42 | PF00149 | 0.586 |
DOC_PP2B_LxvP_1 | 126 | 129 | PF13499 | 0.644 |
DOC_USP7_MATH_1 | 316 | 320 | PF00917 | 0.568 |
DOC_WW_Pin1_4 | 207 | 212 | PF00397 | 0.690 |
DOC_WW_Pin1_4 | 236 | 241 | PF00397 | 0.581 |
DOC_WW_Pin1_4 | 78 | 83 | PF00397 | 0.501 |
LIG_14-3-3_CanoR_1 | 109 | 114 | PF00244 | 0.518 |
LIG_14-3-3_CanoR_1 | 188 | 195 | PF00244 | 0.407 |
LIG_14-3-3_CanoR_1 | 217 | 222 | PF00244 | 0.689 |
LIG_14-3-3_CanoR_1 | 315 | 323 | PF00244 | 0.591 |
LIG_14-3-3_CanoR_1 | 55 | 64 | PF00244 | 0.463 |
LIG_APCC_ABBA_1 | 169 | 174 | PF00400 | 0.605 |
LIG_APCC_ABBA_1 | 8 | 13 | PF00400 | 0.355 |
LIG_Clathr_ClatBox_1 | 326 | 330 | PF01394 | 0.720 |
LIG_FHA_1 | 116 | 122 | PF00498 | 0.646 |
LIG_FHA_1 | 177 | 183 | PF00498 | 0.518 |
LIG_FHA_1 | 216 | 222 | PF00498 | 0.663 |
LIG_FHA_2 | 84 | 90 | PF00498 | 0.488 |
LIG_LIR_Gen_1 | 120 | 131 | PF02991 | 0.603 |
LIG_LIR_Gen_1 | 156 | 164 | PF02991 | 0.543 |
LIG_LIR_Gen_1 | 170 | 177 | PF02991 | 0.543 |
LIG_LIR_Gen_1 | 26 | 35 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 120 | 126 | PF02991 | 0.602 |
LIG_LIR_Nem_3 | 156 | 161 | PF02991 | 0.494 |
LIG_LIR_Nem_3 | 170 | 175 | PF02991 | 0.534 |
LIG_LIR_Nem_3 | 248 | 254 | PF02991 | 0.539 |
LIG_LIR_Nem_3 | 26 | 30 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 304 | 308 | PF02991 | 0.627 |
LIG_MYND_3 | 141 | 145 | PF01753 | 0.546 |
LIG_NRBOX | 188 | 194 | PF00104 | 0.551 |
LIG_PCNA_yPIPBox_3 | 163 | 172 | PF02747 | 0.457 |
LIG_PCNA_yPIPBox_3 | 334 | 343 | PF02747 | 0.615 |
LIG_PDZ_Class_2 | 339 | 344 | PF00595 | 0.645 |
LIG_SH2_NCK_1 | 84 | 88 | PF00017 | 0.522 |
LIG_SH2_PTP2 | 9 | 12 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 51 | 54 | PF00017 | 0.570 |
LIG_SH2_STAT5 | 66 | 69 | PF00017 | 0.430 |
LIG_SH2_STAT5 | 9 | 12 | PF00017 | 0.447 |
LIG_SH3_3 | 91 | 97 | PF00018 | 0.746 |
LIG_SUMO_SIM_par_1 | 241 | 248 | PF11976 | 0.568 |
LIG_SUMO_SIM_par_1 | 252 | 259 | PF11976 | 0.366 |
LIG_SUMO_SIM_par_1 | 327 | 332 | PF11976 | 0.452 |
LIG_SUMO_SIM_par_1 | 75 | 81 | PF11976 | 0.623 |
LIG_TRAF2_1 | 276 | 279 | PF00917 | 0.448 |
LIG_TYR_ITIM | 7 | 12 | PF00017 | 0.493 |
MOD_CDK_SPxK_1 | 236 | 242 | PF00069 | 0.612 |
MOD_CK1_1 | 102 | 108 | PF00069 | 0.703 |
MOD_CK1_1 | 255 | 261 | PF00069 | 0.542 |
MOD_CK2_1 | 113 | 119 | PF00069 | 0.578 |
MOD_CK2_1 | 83 | 89 | PF00069 | 0.523 |
MOD_GlcNHglycan | 104 | 107 | PF01048 | 0.696 |
MOD_GlcNHglycan | 199 | 202 | PF01048 | 0.553 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.240 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.234 |
MOD_GSK3_1 | 109 | 116 | PF00069 | 0.712 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.644 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.475 |
MOD_GSK3_1 | 283 | 290 | PF00069 | 0.607 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.512 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.654 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.557 |
MOD_NEK2_1 | 202 | 207 | PF00069 | 0.635 |
MOD_NEK2_1 | 83 | 88 | PF00069 | 0.571 |
MOD_PIKK_1 | 259 | 265 | PF00454 | 0.560 |
MOD_PKA_2 | 187 | 193 | PF00069 | 0.468 |
MOD_Plk_1 | 144 | 150 | PF00069 | 0.456 |
MOD_Plk_2-3 | 113 | 119 | PF00069 | 0.455 |
MOD_Plk_4 | 202 | 208 | PF00069 | 0.674 |
MOD_Plk_4 | 304 | 310 | PF00069 | 0.544 |
MOD_ProDKin_1 | 207 | 213 | PF00069 | 0.690 |
MOD_ProDKin_1 | 236 | 242 | PF00069 | 0.579 |
MOD_ProDKin_1 | 78 | 84 | PF00069 | 0.502 |
MOD_SUMO_rev_2 | 33 | 39 | PF00179 | 0.484 |
TRG_ENDOCYTIC_2 | 172 | 175 | PF00928 | 0.515 |
TRG_ENDOCYTIC_2 | 51 | 54 | PF00928 | 0.570 |
TRG_ENDOCYTIC_2 | 9 | 12 | PF00928 | 0.447 |
TRG_NES_CRM1_1 | 167 | 180 | PF08389 | 0.606 |
TRG_NES_CRM1_1 | 26 | 40 | PF08389 | 0.562 |
TRG_Pf-PMV_PEXEL_1 | 166 | 170 | PF00026 | 0.519 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IJR6 | Leptomonas seymouri | 43% | 99% |
A0A3S7WUR3 | Leishmania donovani | 66% | 100% |
A0A422NWM0 | Trypanosoma rangeli | 30% | 96% |
A4HXM9 | Leishmania infantum | 66% | 100% |
C9ZZY5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
D0A069 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
E9ARE0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 67% | 100% |
Q4QE39 | Leishmania major | 65% | 100% |
V5B9X5 | Trypanosoma cruzi | 30% | 99% |