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: 9 |
NetGPI | no | yes: 0, no: 9 |
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: A0A3Q8IG17
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 12 | 16 | PF00656 | 0.236 |
CLV_NRD_NRD_1 | 134 | 136 | PF00675 | 0.500 |
CLV_NRD_NRD_1 | 164 | 166 | PF00675 | 0.348 |
CLV_PCSK_KEX2_1 | 134 | 136 | PF00082 | 0.426 |
CLV_PCSK_SKI1_1 | 223 | 227 | PF00082 | 0.446 |
DOC_CDC14_PxL_1 | 338 | 346 | PF14671 | 0.392 |
DOC_MAPK_gen_1 | 134 | 142 | PF00069 | 0.450 |
DOC_MAPK_gen_1 | 165 | 172 | PF00069 | 0.293 |
DOC_MAPK_gen_1 | 221 | 229 | PF00069 | 0.390 |
DOC_MAPK_MEF2A_6 | 4 | 11 | PF00069 | 0.351 |
DOC_PP2B_LxvP_1 | 208 | 211 | PF13499 | 0.453 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.488 |
DOC_USP7_MATH_1 | 276 | 280 | PF00917 | 0.594 |
DOC_WW_Pin1_4 | 184 | 189 | PF00397 | 0.563 |
DOC_WW_Pin1_4 | 193 | 198 | PF00397 | 0.617 |
DOC_WW_Pin1_4 | 200 | 205 | PF00397 | 0.621 |
DOC_WW_Pin1_4 | 255 | 260 | PF00397 | 0.383 |
LIG_14-3-3_CanoR_1 | 102 | 111 | PF00244 | 0.523 |
LIG_14-3-3_CanoR_1 | 245 | 254 | PF00244 | 0.591 |
LIG_14-3-3_CanoR_1 | 29 | 33 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 4 | 10 | PF00244 | 0.381 |
LIG_CaM_IQ_9 | 158 | 173 | PF13499 | 0.353 |
LIG_FHA_1 | 19 | 25 | PF00498 | 0.486 |
LIG_FHA_1 | 321 | 327 | PF00498 | 0.477 |
LIG_FHA_1 | 49 | 55 | PF00498 | 0.339 |
LIG_FHA_1 | 96 | 102 | PF00498 | 0.389 |
LIG_FHA_2 | 107 | 113 | PF00498 | 0.347 |
LIG_FHA_2 | 87 | 93 | PF00498 | 0.557 |
LIG_Integrin_RGD_1 | 349 | 351 | PF01839 | 0.461 |
LIG_LIR_Apic_2 | 251 | 257 | PF02991 | 0.467 |
LIG_LIR_Gen_1 | 137 | 145 | PF02991 | 0.428 |
LIG_LIR_Gen_1 | 30 | 37 | PF02991 | 0.452 |
LIG_LIR_Gen_1 | 8 | 18 | PF02991 | 0.331 |
LIG_LIR_Gen_1 | 95 | 105 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 137 | 142 | PF02991 | 0.406 |
LIG_LIR_Nem_3 | 30 | 35 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 323 | 327 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 8 | 14 | PF02991 | 0.320 |
LIG_LIR_Nem_3 | 95 | 100 | PF02991 | 0.410 |
LIG_PDZ_Class_1 | 350 | 355 | PF00595 | 0.593 |
LIG_SH2_CRK | 254 | 258 | PF00017 | 0.457 |
LIG_SH2_NCK_1 | 105 | 109 | PF00017 | 0.510 |
LIG_SH2_NCK_1 | 254 | 258 | PF00017 | 0.548 |
LIG_SH2_STAP1 | 32 | 36 | PF00017 | 0.400 |
LIG_SH2_STAT5 | 105 | 108 | PF00017 | 0.367 |
LIG_SH2_STAT5 | 139 | 142 | PF00017 | 0.470 |
LIG_SH3_3 | 191 | 197 | PF00018 | 0.711 |
LIG_SUMO_SIM_anti_2 | 190 | 196 | PF11976 | 0.451 |
LIG_SUMO_SIM_par_1 | 5 | 10 | PF11976 | 0.348 |
LIG_TRAF2_1 | 89 | 92 | PF00917 | 0.517 |
LIG_WRC_WIRS_1 | 32 | 37 | PF05994 | 0.418 |
LIG_WRC_WIRS_1 | 93 | 98 | PF05994 | 0.493 |
MOD_CK1_1 | 196 | 202 | PF00069 | 0.606 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.372 |
MOD_CK1_1 | 340 | 346 | PF00069 | 0.608 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.434 |
MOD_CK2_1 | 86 | 92 | PF00069 | 0.523 |
MOD_GlcNHglycan | 175 | 179 | PF01048 | 0.696 |
MOD_GlcNHglycan | 247 | 250 | PF01048 | 0.360 |
MOD_GlcNHglycan | 278 | 281 | PF01048 | 0.507 |
MOD_GlcNHglycan | 339 | 342 | PF01048 | 0.625 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.547 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.552 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.591 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.545 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.404 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.445 |
MOD_N-GLC_1 | 48 | 53 | PF02516 | 0.482 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.474 |
MOD_NEK2_1 | 145 | 150 | PF00069 | 0.487 |
MOD_NEK2_1 | 213 | 218 | PF00069 | 0.464 |
MOD_NEK2_1 | 326 | 331 | PF00069 | 0.447 |
MOD_NEK2_1 | 337 | 342 | PF00069 | 0.532 |
MOD_NEK2_1 | 43 | 48 | PF00069 | 0.487 |
MOD_OFUCOSY | 47 | 52 | PF10250 | 0.468 |
MOD_PKA_2 | 101 | 107 | PF00069 | 0.377 |
MOD_PKA_2 | 249 | 255 | PF00069 | 0.461 |
MOD_PKA_2 | 28 | 34 | PF00069 | 0.499 |
MOD_Plk_1 | 174 | 180 | PF00069 | 0.501 |
MOD_Plk_4 | 106 | 112 | PF00069 | 0.379 |
MOD_Plk_4 | 13 | 19 | PF00069 | 0.346 |
MOD_Plk_4 | 149 | 155 | PF00069 | 0.423 |
MOD_Plk_4 | 31 | 37 | PF00069 | 0.253 |
MOD_ProDKin_1 | 184 | 190 | PF00069 | 0.564 |
MOD_ProDKin_1 | 193 | 199 | PF00069 | 0.614 |
MOD_ProDKin_1 | 200 | 206 | PF00069 | 0.606 |
MOD_ProDKin_1 | 255 | 261 | PF00069 | 0.376 |
TRG_DiLeu_BaLyEn_6 | 238 | 243 | PF01217 | 0.484 |
TRG_ENDOCYTIC_2 | 139 | 142 | PF00928 | 0.417 |
TRG_ENDOCYTIC_2 | 32 | 35 | PF00928 | 0.371 |
TRG_ER_diArg_1 | 133 | 135 | PF00400 | 0.495 |
TRG_ER_diArg_1 | 220 | 223 | PF00400 | 0.490 |
TRG_Pf-PMV_PEXEL_1 | 22 | 27 | PF00026 | 0.431 |
TRG_Pf-PMV_PEXEL_1 | 99 | 103 | PF00026 | 0.526 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5N9 | Leptomonas seymouri | 53% | 100% |
A0A1X0NS57 | Trypanosomatidae | 29% | 100% |
A0A422N888 | Trypanosoma rangeli | 29% | 100% |
A4HKN1 | Leishmania braziliensis | 77% | 100% |
D0AAC8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
E9B319 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
Q4Q535 | Leishmania major | 91% | 100% |
V5BCW8 | Trypanosoma cruzi | 28% | 100% |