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:0005634 | nucleus | 5 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4QFW9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 12 | 14 | PF00675 | 0.463 |
CLV_NRD_NRD_1 | 156 | 158 | PF00675 | 0.664 |
CLV_NRD_NRD_1 | 93 | 95 | PF00675 | 0.636 |
CLV_PCSK_FUR_1 | 93 | 97 | PF00082 | 0.591 |
CLV_PCSK_KEX2_1 | 12 | 14 | PF00082 | 0.463 |
CLV_PCSK_KEX2_1 | 181 | 183 | PF00082 | 0.548 |
CLV_PCSK_KEX2_1 | 38 | 40 | PF00082 | 0.596 |
CLV_PCSK_KEX2_1 | 74 | 76 | PF00082 | 0.560 |
CLV_PCSK_KEX2_1 | 78 | 80 | PF00082 | 0.567 |
CLV_PCSK_KEX2_1 | 93 | 95 | PF00082 | 0.510 |
CLV_PCSK_PC1ET2_1 | 181 | 183 | PF00082 | 0.543 |
CLV_PCSK_PC1ET2_1 | 38 | 40 | PF00082 | 0.475 |
CLV_PCSK_PC1ET2_1 | 74 | 76 | PF00082 | 0.586 |
CLV_PCSK_PC1ET2_1 | 78 | 80 | PF00082 | 0.590 |
CLV_PCSK_PC1ET2_1 | 95 | 97 | PF00082 | 0.546 |
CLV_PCSK_SKI1_1 | 161 | 165 | PF00082 | 0.538 |
CLV_PCSK_SKI1_1 | 332 | 336 | PF00082 | 0.487 |
CLV_PCSK_SKI1_1 | 75 | 79 | PF00082 | 0.707 |
DEG_SPOP_SBC_1 | 87 | 91 | PF00917 | 0.527 |
DOC_CDC14_PxL_1 | 171 | 179 | PF14671 | 0.630 |
DOC_CDC14_PxL_1 | 234 | 242 | PF14671 | 0.461 |
DOC_MAPK_MEF2A_6 | 218 | 225 | PF00069 | 0.417 |
DOC_MAPK_MEF2A_6 | 322 | 330 | PF00069 | 0.404 |
DOC_MAPK_MEF2A_6 | 332 | 340 | PF00069 | 0.312 |
DOC_MAPK_NFAT4_5 | 218 | 226 | PF00069 | 0.416 |
DOC_PP1_RVXF_1 | 330 | 336 | PF00149 | 0.498 |
DOC_PP2B_LxvP_1 | 119 | 122 | PF13499 | 0.673 |
DOC_PP4_FxxP_1 | 248 | 251 | PF00568 | 0.628 |
DOC_USP7_MATH_1 | 163 | 167 | PF00917 | 0.618 |
DOC_USP7_UBL2_3 | 74 | 78 | PF12436 | 0.536 |
DOC_WW_Pin1_4 | 199 | 204 | PF00397 | 0.490 |
DOC_WW_Pin1_4 | 271 | 276 | PF00397 | 0.580 |
DOC_WW_Pin1_4 | 299 | 304 | PF00397 | 0.597 |
DOC_WW_Pin1_4 | 308 | 313 | PF00397 | 0.586 |
DOC_WW_Pin1_4 | 98 | 103 | PF00397 | 0.790 |
LIG_14-3-3_CanoR_1 | 161 | 166 | PF00244 | 0.531 |
LIG_14-3-3_CanoR_1 | 227 | 234 | PF00244 | 0.517 |
LIG_14-3-3_CanoR_1 | 267 | 271 | PF00244 | 0.556 |
LIG_14-3-3_CanoR_1 | 322 | 327 | PF00244 | 0.419 |
LIG_14-3-3_CanoR_1 | 96 | 101 | PF00244 | 0.662 |
LIG_APCC_ABBA_1 | 285 | 290 | PF00400 | 0.546 |
LIG_BIR_III_2 | 82 | 86 | PF00653 | 0.640 |
LIG_BRCT_BRCA1_1 | 273 | 277 | PF00533 | 0.559 |
LIG_deltaCOP1_diTrp_1 | 66 | 73 | PF00928 | 0.552 |
LIG_FHA_1 | 160 | 166 | PF00498 | 0.656 |
LIG_FHA_1 | 311 | 317 | PF00498 | 0.642 |
LIG_FHA_1 | 343 | 349 | PF00498 | 0.457 |
LIG_FHA_2 | 3 | 9 | PF00498 | 0.473 |
LIG_FHA_2 | 303 | 309 | PF00498 | 0.498 |
LIG_FHA_2 | 59 | 65 | PF00498 | 0.534 |
LIG_FHA_2 | 87 | 93 | PF00498 | 0.767 |
LIG_LIR_Nem_3 | 180 | 186 | PF02991 | 0.406 |
LIG_LIR_Nem_3 | 2 | 6 | PF02991 | 0.353 |
LIG_LIR_Nem_3 | 329 | 334 | PF02991 | 0.422 |
LIG_NRBOX | 113 | 119 | PF00104 | 0.615 |
LIG_Pex14_2 | 204 | 208 | PF04695 | 0.561 |
LIG_Pex14_2 | 331 | 335 | PF04695 | 0.495 |
LIG_SH2_PTP2 | 296 | 299 | PF00017 | 0.440 |
LIG_SH2_SRC | 296 | 299 | PF00017 | 0.416 |
LIG_SH2_STAP1 | 23 | 27 | PF00017 | 0.386 |
LIG_SH2_STAT5 | 296 | 299 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 342 | 345 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 4 | 7 | PF00017 | 0.530 |
LIG_SH3_3 | 200 | 206 | PF00018 | 0.564 |
LIG_SH3_3 | 330 | 336 | PF00018 | 0.443 |
LIG_SUMO_SIM_anti_2 | 109 | 115 | PF11976 | 0.661 |
LIG_SUMO_SIM_par_1 | 133 | 139 | PF11976 | 0.544 |
LIG_SUMO_SIM_par_1 | 250 | 255 | PF11976 | 0.584 |
LIG_TRAF2_1 | 128 | 131 | PF00917 | 0.712 |
LIG_TRAF2_1 | 280 | 283 | PF00917 | 0.546 |
LIG_TRAF2_1 | 5 | 8 | PF00917 | 0.395 |
LIG_TRAF2_1 | 61 | 64 | PF00917 | 0.543 |
MOD_CK2_1 | 2 | 8 | PF00069 | 0.574 |
MOD_CK2_1 | 58 | 64 | PF00069 | 0.561 |
MOD_CK2_1 | 86 | 92 | PF00069 | 0.603 |
MOD_DYRK1A_RPxSP_1 | 98 | 102 | PF00069 | 0.724 |
MOD_GlcNHglycan | 144 | 149 | PF01048 | 0.560 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.528 |
MOD_GlcNHglycan | 278 | 281 | PF01048 | 0.637 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.667 |
MOD_GSK3_1 | 187 | 194 | PF00069 | 0.480 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.477 |
MOD_GSK3_1 | 322 | 329 | PF00069 | 0.397 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.725 |
MOD_LATS_1 | 230 | 236 | PF00433 | 0.432 |
MOD_LATS_1 | 320 | 326 | PF00433 | 0.450 |
MOD_N-GLC_1 | 150 | 155 | PF02516 | 0.580 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.671 |
MOD_NEK2_1 | 241 | 246 | PF00069 | 0.531 |
MOD_NEK2_1 | 266 | 271 | PF00069 | 0.557 |
MOD_NEK2_1 | 276 | 281 | PF00069 | 0.467 |
MOD_NEK2_1 | 344 | 349 | PF00069 | 0.431 |
MOD_NEK2_1 | 86 | 91 | PF00069 | 0.694 |
MOD_PK_1 | 232 | 238 | PF00069 | 0.554 |
MOD_PK_1 | 96 | 102 | PF00069 | 0.658 |
MOD_PKA_1 | 94 | 100 | PF00069 | 0.640 |
MOD_PKA_2 | 226 | 232 | PF00069 | 0.509 |
MOD_PKA_2 | 266 | 272 | PF00069 | 0.587 |
MOD_PKB_1 | 94 | 102 | PF00069 | 0.707 |
MOD_Plk_1 | 144 | 150 | PF00069 | 0.559 |
MOD_Plk_1 | 32 | 38 | PF00069 | 0.499 |
MOD_Plk_4 | 130 | 136 | PF00069 | 0.526 |
MOD_Plk_4 | 187 | 193 | PF00069 | 0.514 |
MOD_Plk_4 | 326 | 332 | PF00069 | 0.364 |
MOD_Plk_4 | 344 | 350 | PF00069 | 0.478 |
MOD_ProDKin_1 | 199 | 205 | PF00069 | 0.492 |
MOD_ProDKin_1 | 271 | 277 | PF00069 | 0.580 |
MOD_ProDKin_1 | 299 | 305 | PF00069 | 0.603 |
MOD_ProDKin_1 | 308 | 314 | PF00069 | 0.588 |
MOD_ProDKin_1 | 98 | 104 | PF00069 | 0.787 |
MOD_SUMO_for_1 | 25 | 28 | PF00179 | 0.390 |
TRG_DiLeu_BaEn_1 | 131 | 136 | PF01217 | 0.553 |
TRG_DiLeu_BaEn_3 | 129 | 135 | PF01217 | 0.585 |
TRG_DiLeu_BaEn_3 | 144 | 150 | PF01217 | 0.398 |
TRG_ENDOCYTIC_2 | 3 | 6 | PF00928 | 0.389 |
TRG_ER_diArg_1 | 12 | 14 | PF00400 | 0.461 |
TRG_ER_diArg_1 | 93 | 96 | PF00400 | 0.636 |
TRG_NLS_Bipartite_1 | 78 | 99 | PF00514 | 0.645 |
TRG_NLS_MonoExtC_3 | 156 | 161 | PF00514 | 0.664 |
TRG_NLS_MonoExtC_3 | 93 | 98 | PF00514 | 0.641 |
TRG_NLS_MonoExtN_4 | 157 | 162 | PF00514 | 0.562 |
TRG_NLS_MonoExtN_4 | 93 | 99 | PF00514 | 0.659 |
TRG_Pf-PMV_PEXEL_1 | 12 | 16 | PF00026 | 0.541 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I624 | Leptomonas seymouri | 52% | 90% |
A0A1X0NPE6 | Trypanosomatidae | 29% | 100% |
A0A3Q8ID14 | Leishmania donovani | 91% | 98% |
A0A422NX90 | Trypanosoma rangeli | 31% | 100% |
A4H7H7 | Leishmania braziliensis | 80% | 98% |
A4HVV8 | Leishmania infantum | 91% | 98% |
C9ZT68 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
E9APL0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 98% |
V5BM97 | Trypanosoma cruzi | 29% | 100% |