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 | yes | yes: 1, no: 8 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: A4HLI3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 182 | 184 | PF00675 | 0.581 |
CLV_NRD_NRD_1 | 187 | 189 | PF00675 | 0.588 |
CLV_NRD_NRD_1 | 191 | 193 | PF00675 | 0.594 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.619 |
CLV_PCSK_FUR_1 | 257 | 261 | PF00082 | 0.435 |
CLV_PCSK_KEX2_1 | 186 | 188 | PF00082 | 0.586 |
CLV_PCSK_KEX2_1 | 191 | 193 | PF00082 | 0.588 |
CLV_PCSK_KEX2_1 | 259 | 261 | PF00082 | 0.432 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.583 |
CLV_PCSK_PC1ET2_1 | 259 | 261 | PF00082 | 0.432 |
CLV_PCSK_PC7_1 | 183 | 189 | PF00082 | 0.575 |
CLV_PCSK_SKI1_1 | 129 | 133 | PF00082 | 0.561 |
CLV_PCSK_SKI1_1 | 191 | 195 | PF00082 | 0.684 |
CLV_Separin_Metazoa | 116 | 120 | PF03568 | 0.343 |
DOC_ANK_TNKS_1 | 118 | 125 | PF00023 | 0.314 |
DOC_CYCLIN_yCln2_LP_2 | 16 | 22 | PF00134 | 0.534 |
DOC_MAPK_DCC_7 | 4 | 14 | PF00069 | 0.442 |
DOC_MAPK_gen_1 | 231 | 241 | PF00069 | 0.549 |
DOC_MAPK_gen_1 | 249 | 258 | PF00069 | 0.645 |
DOC_MAPK_MEF2A_6 | 249 | 258 | PF00069 | 0.633 |
DOC_PP2B_LxvP_1 | 16 | 19 | PF13499 | 0.466 |
DOC_PP4_FxxP_1 | 297 | 300 | PF00568 | 0.608 |
DOC_SPAK_OSR1_1 | 31 | 35 | PF12202 | 0.370 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.664 |
DOC_USP7_MATH_1 | 280 | 284 | PF00917 | 0.594 |
DOC_USP7_UBL2_3 | 180 | 184 | PF12436 | 0.384 |
DOC_WW_Pin1_4 | 197 | 202 | PF00397 | 0.388 |
DOC_WW_Pin1_4 | 276 | 281 | PF00397 | 0.634 |
LIG_14-3-3_CanoR_1 | 24 | 30 | PF00244 | 0.554 |
LIG_14-3-3_CanoR_1 | 260 | 266 | PF00244 | 0.608 |
LIG_14-3-3_CanoR_1 | 284 | 292 | PF00244 | 0.681 |
LIG_14-3-3_CanoR_1 | 3 | 9 | PF00244 | 0.625 |
LIG_14-3-3_CanoR_1 | 31 | 39 | PF00244 | 0.430 |
LIG_14-3-3_CanoR_1 | 46 | 51 | PF00244 | 0.439 |
LIG_14-3-3_CanoR_1 | 72 | 81 | PF00244 | 0.347 |
LIG_Actin_WH2_2 | 114 | 131 | PF00022 | 0.368 |
LIG_AP2alpha_2 | 253 | 255 | PF02296 | 0.606 |
LIG_deltaCOP1_diTrp_1 | 253 | 261 | PF00928 | 0.606 |
LIG_eIF4E_1 | 212 | 218 | PF01652 | 0.403 |
LIG_FHA_1 | 134 | 140 | PF00498 | 0.338 |
LIG_FHA_1 | 209 | 215 | PF00498 | 0.376 |
LIG_FHA_1 | 34 | 40 | PF00498 | 0.442 |
LIG_FHA_1 | 74 | 80 | PF00498 | 0.385 |
LIG_FHA_2 | 130 | 136 | PF00498 | 0.359 |
LIG_FHA_2 | 171 | 177 | PF00498 | 0.404 |
LIG_FHA_2 | 180 | 186 | PF00498 | 0.370 |
LIG_FHA_2 | 243 | 249 | PF00498 | 0.607 |
LIG_FHA_2 | 88 | 94 | PF00498 | 0.386 |
LIG_LIR_Apic_2 | 294 | 300 | PF02991 | 0.612 |
LIG_LIR_Gen_1 | 252 | 261 | PF02991 | 0.610 |
LIG_LIR_Nem_3 | 132 | 137 | PF02991 | 0.363 |
LIG_LIR_Nem_3 | 252 | 258 | PF02991 | 0.610 |
LIG_LIR_Nem_3 | 304 | 310 | PF02991 | 0.535 |
LIG_NRBOX | 11 | 17 | PF00104 | 0.448 |
LIG_PCNA_yPIPBox_3 | 110 | 121 | PF02747 | 0.352 |
LIG_SH2_GRB2like | 204 | 207 | PF00017 | 0.442 |
LIG_SH2_GRB2like | 80 | 83 | PF00017 | 0.256 |
LIG_SH2_SRC | 204 | 207 | PF00017 | 0.442 |
LIG_SH2_SRC | 80 | 83 | PF00017 | 0.371 |
LIG_SH2_STAT5 | 107 | 110 | PF00017 | 0.305 |
LIG_SH2_STAT5 | 127 | 130 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 171 | 174 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 204 | 207 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 80 | 83 | PF00017 | 0.314 |
LIG_SH3_3 | 65 | 71 | PF00018 | 0.419 |
LIG_SUMO_SIM_anti_2 | 93 | 101 | PF11976 | 0.274 |
LIG_SxIP_EBH_1 | 62 | 75 | PF03271 | 0.361 |
LIG_TRAF2_1 | 245 | 248 | PF00917 | 0.602 |
LIG_WW_3 | 69 | 73 | PF00397 | 0.443 |
MOD_CDC14_SPxK_1 | 200 | 203 | PF00782 | 0.381 |
MOD_CDK_SPxK_1 | 197 | 203 | PF00069 | 0.387 |
MOD_CK1_1 | 179 | 185 | PF00069 | 0.436 |
MOD_CK1_1 | 283 | 289 | PF00069 | 0.611 |
MOD_CK1_1 | 295 | 301 | PF00069 | 0.634 |
MOD_CK1_1 | 35 | 41 | PF00069 | 0.517 |
MOD_CK1_1 | 48 | 54 | PF00069 | 0.425 |
MOD_CK1_1 | 56 | 62 | PF00069 | 0.489 |
MOD_CK2_1 | 129 | 135 | PF00069 | 0.357 |
MOD_CK2_1 | 170 | 176 | PF00069 | 0.395 |
MOD_CK2_1 | 242 | 248 | PF00069 | 0.612 |
MOD_CK2_1 | 87 | 93 | PF00069 | 0.411 |
MOD_GlcNHglycan | 286 | 289 | PF01048 | 0.436 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.708 |
MOD_GlcNHglycan | 50 | 53 | PF01048 | 0.621 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.593 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.362 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.387 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.565 |
MOD_GSK3_1 | 276 | 283 | PF00069 | 0.624 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.459 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.401 |
MOD_N-GLC_1 | 129 | 134 | PF02516 | 0.579 |
MOD_N-GLC_1 | 205 | 210 | PF02516 | 0.618 |
MOD_N-GLC_1 | 81 | 86 | PF02516 | 0.509 |
MOD_NEK2_1 | 170 | 175 | PF00069 | 0.375 |
MOD_NEK2_1 | 20 | 25 | PF00069 | 0.508 |
MOD_NEK2_1 | 205 | 210 | PF00069 | 0.441 |
MOD_NEK2_1 | 273 | 278 | PF00069 | 0.665 |
MOD_NEK2_1 | 32 | 37 | PF00069 | 0.494 |
MOD_NEK2_1 | 44 | 49 | PF00069 | 0.490 |
MOD_NEK2_1 | 81 | 86 | PF00069 | 0.420 |
MOD_NEK2_2 | 226 | 231 | PF00069 | 0.524 |
MOD_PK_1 | 4 | 10 | PF00069 | 0.438 |
MOD_PK_1 | 46 | 52 | PF00069 | 0.367 |
MOD_PKA_1 | 259 | 265 | PF00069 | 0.633 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.584 |
MOD_PKA_2 | 259 | 265 | PF00069 | 0.607 |
MOD_PKA_2 | 283 | 289 | PF00069 | 0.618 |
MOD_PKA_2 | 292 | 298 | PF00069 | 0.603 |
MOD_PKA_2 | 45 | 51 | PF00069 | 0.440 |
MOD_Plk_1 | 205 | 211 | PF00069 | 0.325 |
MOD_Plk_1 | 271 | 277 | PF00069 | 0.659 |
MOD_Plk_1 | 94 | 100 | PF00069 | 0.319 |
MOD_Plk_4 | 25 | 31 | PF00069 | 0.487 |
MOD_Plk_4 | 273 | 279 | PF00069 | 0.657 |
MOD_Plk_4 | 38 | 44 | PF00069 | 0.484 |
MOD_Plk_4 | 4 | 10 | PF00069 | 0.584 |
MOD_Plk_4 | 74 | 80 | PF00069 | 0.360 |
MOD_Plk_4 | 94 | 100 | PF00069 | 0.301 |
MOD_ProDKin_1 | 197 | 203 | PF00069 | 0.387 |
MOD_ProDKin_1 | 276 | 282 | PF00069 | 0.633 |
MOD_SUMO_rev_2 | 97 | 106 | PF00179 | 0.329 |
TRG_DiLeu_BaLyEn_6 | 16 | 21 | PF01217 | 0.603 |
TRG_ER_diArg_1 | 186 | 188 | PF00400 | 0.394 |
TRG_ER_diArg_1 | 191 | 193 | PF00400 | 0.378 |
TRG_ER_diArg_1 | 2 | 4 | PF00400 | 0.518 |
TRG_ER_diArg_1 | 99 | 102 | PF00400 | 0.316 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4F7 | Leptomonas seymouri | 82% | 100% |
A0A0S4JAA8 | Bodo saltans | 58% | 100% |
A0A1X0P101 | Trypanosomatidae | 74% | 98% |
A0A3Q8IHR6 | Leishmania donovani | 89% | 98% |
A4I8Z3 | Leishmania infantum | 89% | 98% |
D0A4Z1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 65% | 100% |
E9B3W2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 98% |
Q4Q462 | Leishmania major | 89% | 100% |