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 | 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:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9APL0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 12 | 14 | PF00675 | 0.485 |
CLV_NRD_NRD_1 | 165 | 167 | PF00675 | 0.716 |
CLV_NRD_NRD_1 | 168 | 170 | PF00675 | 0.718 |
CLV_PCSK_FUR_1 | 166 | 170 | PF00082 | 0.678 |
CLV_PCSK_KEX2_1 | 12 | 14 | PF00082 | 0.485 |
CLV_PCSK_KEX2_1 | 168 | 170 | PF00082 | 0.634 |
CLV_PCSK_KEX2_1 | 190 | 192 | PF00082 | 0.699 |
CLV_PCSK_KEX2_1 | 38 | 40 | PF00082 | 0.602 |
CLV_PCSK_KEX2_1 | 78 | 80 | PF00082 | 0.629 |
CLV_PCSK_KEX2_1 | 95 | 97 | PF00082 | 0.579 |
CLV_PCSK_PC1ET2_1 | 168 | 170 | PF00082 | 0.667 |
CLV_PCSK_PC1ET2_1 | 190 | 192 | PF00082 | 0.683 |
CLV_PCSK_PC1ET2_1 | 38 | 40 | PF00082 | 0.602 |
CLV_PCSK_PC1ET2_1 | 78 | 80 | PF00082 | 0.650 |
CLV_PCSK_PC1ET2_1 | 95 | 97 | PF00082 | 0.579 |
CLV_PCSK_SKI1_1 | 170 | 174 | PF00082 | 0.671 |
CLV_PCSK_SKI1_1 | 341 | 345 | PF00082 | 0.526 |
CLV_PCSK_SKI1_1 | 7 | 11 | PF00082 | 0.308 |
CLV_PCSK_SKI1_1 | 75 | 79 | PF00082 | 0.728 |
DEG_SCF_FBW7_2 | 318 | 324 | PF00400 | 0.624 |
DEG_SPOP_SBC_1 | 87 | 91 | PF00917 | 0.592 |
DOC_CDC14_PxL_1 | 180 | 188 | PF14671 | 0.682 |
DOC_CDC14_PxL_1 | 243 | 251 | PF14671 | 0.608 |
DOC_CKS1_1 | 318 | 323 | PF01111 | 0.624 |
DOC_MAPK_MEF2A_6 | 331 | 339 | PF00069 | 0.457 |
DOC_MAPK_MEF2A_6 | 341 | 349 | PF00069 | 0.373 |
DOC_PP1_RVXF_1 | 339 | 345 | PF00149 | 0.536 |
DOC_PP2B_LxvP_1 | 119 | 122 | PF13499 | 0.707 |
DOC_PP4_FxxP_1 | 257 | 260 | PF00568 | 0.685 |
DOC_USP7_MATH_1 | 172 | 176 | PF00917 | 0.703 |
DOC_USP7_MATH_1 | 234 | 238 | PF00917 | 0.426 |
DOC_WW_Pin1_4 | 208 | 213 | PF00397 | 0.563 |
DOC_WW_Pin1_4 | 280 | 285 | PF00397 | 0.596 |
DOC_WW_Pin1_4 | 308 | 313 | PF00397 | 0.630 |
DOC_WW_Pin1_4 | 317 | 322 | PF00397 | 0.633 |
DOC_WW_Pin1_4 | 98 | 103 | PF00397 | 0.779 |
LIG_14-3-3_CanoR_1 | 169 | 179 | PF00244 | 0.665 |
LIG_14-3-3_CanoR_1 | 236 | 243 | PF00244 | 0.504 |
LIG_14-3-3_CanoR_1 | 276 | 280 | PF00244 | 0.609 |
LIG_14-3-3_CanoR_1 | 331 | 336 | PF00244 | 0.479 |
LIG_14-3-3_CanoR_1 | 96 | 101 | PF00244 | 0.769 |
LIG_APCC_ABBA_1 | 294 | 299 | PF00400 | 0.680 |
LIG_BIR_III_4 | 130 | 134 | PF00653 | 0.574 |
LIG_BRCT_BRCA1_1 | 282 | 286 | PF00533 | 0.686 |
LIG_deltaCOP1_diTrp_1 | 66 | 73 | PF00928 | 0.680 |
LIG_FHA_1 | 174 | 180 | PF00498 | 0.689 |
LIG_FHA_1 | 320 | 326 | PF00498 | 0.681 |
LIG_FHA_1 | 352 | 358 | PF00498 | 0.535 |
LIG_FHA_2 | 3 | 9 | PF00498 | 0.615 |
LIG_FHA_2 | 59 | 65 | PF00498 | 0.581 |
LIG_FHA_2 | 87 | 93 | PF00498 | 0.748 |
LIG_LIR_Nem_3 | 338 | 343 | PF02991 | 0.479 |
LIG_NRBOX | 113 | 119 | PF00104 | 0.639 |
LIG_Pex14_2 | 213 | 217 | PF04695 | 0.707 |
LIG_Pex14_2 | 340 | 344 | PF04695 | 0.533 |
LIG_SH2_PTP2 | 305 | 308 | PF00017 | 0.566 |
LIG_SH2_STAP1 | 23 | 27 | PF00017 | 0.439 |
LIG_SH2_STAT3 | 107 | 110 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 107 | 110 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 305 | 308 | PF00017 | 0.440 |
LIG_SH2_STAT5 | 351 | 354 | PF00017 | 0.538 |
LIG_SH2_STAT5 | 4 | 7 | PF00017 | 0.579 |
LIG_SH3_3 | 209 | 215 | PF00018 | 0.712 |
LIG_SH3_3 | 312 | 318 | PF00018 | 0.600 |
LIG_SH3_3 | 339 | 345 | PF00018 | 0.568 |
LIG_SUMO_SIM_anti_2 | 109 | 115 | PF11976 | 0.671 |
LIG_SUMO_SIM_par_1 | 142 | 148 | PF11976 | 0.599 |
LIG_SUMO_SIM_par_1 | 259 | 264 | PF11976 | 0.669 |
LIG_TRAF2_1 | 289 | 292 | PF00917 | 0.606 |
LIG_TRAF2_1 | 61 | 64 | PF00917 | 0.590 |
LIG_WW_3 | 120 | 124 | PF00397 | 0.622 |
MOD_CK2_1 | 2 | 8 | PF00069 | 0.609 |
MOD_CK2_1 | 58 | 64 | PF00069 | 0.594 |
MOD_CK2_1 | 86 | 92 | PF00069 | 0.763 |
MOD_DYRK1A_RPxSP_1 | 98 | 102 | PF00069 | 0.742 |
MOD_GlcNHglycan | 153 | 158 | PF01048 | 0.592 |
MOD_GlcNHglycan | 252 | 255 | PF01048 | 0.544 |
MOD_GlcNHglycan | 287 | 290 | PF01048 | 0.661 |
MOD_GSK3_1 | 168 | 175 | PF00069 | 0.722 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.539 |
MOD_GSK3_1 | 331 | 338 | PF00069 | 0.458 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.745 |
MOD_LATS_1 | 239 | 245 | PF00433 | 0.575 |
MOD_LATS_1 | 329 | 335 | PF00433 | 0.582 |
MOD_N-GLC_1 | 159 | 164 | PF02516 | 0.743 |
MOD_NEK2_1 | 159 | 164 | PF00069 | 0.729 |
MOD_NEK2_1 | 250 | 255 | PF00069 | 0.559 |
MOD_NEK2_1 | 275 | 280 | PF00069 | 0.583 |
MOD_NEK2_1 | 285 | 290 | PF00069 | 0.532 |
MOD_NEK2_1 | 353 | 358 | PF00069 | 0.517 |
MOD_NEK2_1 | 86 | 91 | PF00069 | 0.740 |
MOD_PK_1 | 241 | 247 | PF00069 | 0.586 |
MOD_PK_1 | 96 | 102 | PF00069 | 0.767 |
MOD_PKA_1 | 168 | 174 | PF00069 | 0.648 |
MOD_PKA_2 | 168 | 174 | PF00069 | 0.704 |
MOD_PKA_2 | 235 | 241 | PF00069 | 0.555 |
MOD_PKA_2 | 275 | 281 | PF00069 | 0.617 |
MOD_Plk_1 | 153 | 159 | PF00069 | 0.629 |
MOD_Plk_1 | 32 | 38 | PF00069 | 0.511 |
MOD_Plk_4 | 139 | 145 | PF00069 | 0.586 |
MOD_Plk_4 | 196 | 202 | PF00069 | 0.580 |
MOD_Plk_4 | 335 | 341 | PF00069 | 0.427 |
MOD_Plk_4 | 353 | 359 | PF00069 | 0.497 |
MOD_ProDKin_1 | 208 | 214 | PF00069 | 0.564 |
MOD_ProDKin_1 | 280 | 286 | PF00069 | 0.597 |
MOD_ProDKin_1 | 308 | 314 | PF00069 | 0.637 |
MOD_ProDKin_1 | 317 | 323 | PF00069 | 0.635 |
MOD_ProDKin_1 | 98 | 104 | PF00069 | 0.776 |
MOD_SUMO_for_1 | 25 | 28 | PF00179 | 0.486 |
TRG_DiLeu_BaEn_1 | 140 | 145 | PF01217 | 0.615 |
TRG_DiLeu_BaEn_3 | 138 | 144 | PF01217 | 0.713 |
TRG_DiLeu_BaEn_3 | 153 | 159 | PF01217 | 0.459 |
TRG_ER_diArg_1 | 12 | 14 | PF00400 | 0.485 |
TRG_NLS_Bipartite_1 | 78 | 99 | PF00514 | 0.773 |
TRG_NLS_MonoCore_2 | 165 | 170 | PF00514 | 0.607 |
TRG_NLS_MonoExtC_3 | 165 | 170 | PF00514 | 0.721 |
TRG_NLS_MonoExtN_4 | 166 | 172 | PF00514 | 0.644 |
TRG_NLS_MonoExtN_4 | 93 | 99 | PF00514 | 0.770 |
TRG_Pf-PMV_PEXEL_1 | 12 | 16 | PF00026 | 0.581 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I624 | Leptomonas seymouri | 54% | 92% |
A0A1X0NPE6 | Trypanosomatidae | 29% | 100% |
A0A3Q8ID14 | Leishmania donovani | 92% | 100% |
A0A422NX90 | Trypanosoma rangeli | 31% | 100% |
A4H7H7 | Leishmania braziliensis | 82% | 100% |
A4HVV8 | Leishmania infantum | 92% | 100% |
C9ZT68 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
Q4QFW9 | Leishmania major | 89% | 98% |
V5BM97 | Trypanosoma cruzi | 30% | 100% |