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 |
Related structures:
AlphaFold database: A4H3H5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 45 | 49 | PF00656 | 0.634 |
CLV_NRD_NRD_1 | 208 | 210 | PF00675 | 0.502 |
CLV_NRD_NRD_1 | 236 | 238 | PF00675 | 0.536 |
CLV_NRD_NRD_1 | 92 | 94 | PF00675 | 0.605 |
CLV_PCSK_FUR_1 | 92 | 96 | PF00082 | 0.508 |
CLV_PCSK_KEX2_1 | 208 | 210 | PF00082 | 0.487 |
CLV_PCSK_KEX2_1 | 236 | 238 | PF00082 | 0.557 |
CLV_PCSK_KEX2_1 | 34 | 36 | PF00082 | 0.596 |
CLV_PCSK_KEX2_1 | 92 | 94 | PF00082 | 0.583 |
CLV_PCSK_PC1ET2_1 | 34 | 36 | PF00082 | 0.665 |
CLV_PCSK_PC1ET2_1 | 94 | 96 | PF00082 | 0.595 |
CLV_PCSK_SKI1_1 | 208 | 212 | PF00082 | 0.478 |
CLV_PCSK_SKI1_1 | 215 | 219 | PF00082 | 0.296 |
DEG_APCC_DBOX_1 | 198 | 206 | PF00400 | 0.522 |
DOC_MAPK_DCC_7 | 8 | 17 | PF00069 | 0.513 |
DOC_MAPK_gen_1 | 240 | 249 | PF00069 | 0.593 |
DOC_MAPK_gen_1 | 8 | 14 | PF00069 | 0.518 |
DOC_MAPK_MEF2A_6 | 8 | 17 | PF00069 | 0.502 |
DOC_PP2B_LxvP_1 | 56 | 59 | PF13499 | 0.713 |
DOC_PP4_FxxP_1 | 211 | 214 | PF00568 | 0.467 |
DOC_USP7_MATH_1 | 170 | 174 | PF00917 | 0.527 |
DOC_USP7_MATH_1 | 256 | 260 | PF00917 | 0.468 |
DOC_USP7_UBL2_3 | 154 | 158 | PF12436 | 0.532 |
DOC_WW_Pin1_4 | 190 | 195 | PF00397 | 0.477 |
DOC_WW_Pin1_4 | 238 | 243 | PF00397 | 0.552 |
LIG_14-3-3_CanoR_1 | 95 | 100 | PF00244 | 0.649 |
LIG_BRCT_BRCA1_1 | 128 | 132 | PF00533 | 0.590 |
LIG_deltaCOP1_diTrp_1 | 203 | 211 | PF00928 | 0.481 |
LIG_eIF4E_1 | 131 | 137 | PF01652 | 0.534 |
LIG_FHA_1 | 151 | 157 | PF00498 | 0.464 |
LIG_FHA_1 | 170 | 176 | PF00498 | 0.384 |
LIG_FHA_1 | 187 | 193 | PF00498 | 0.378 |
LIG_LIR_Gen_1 | 133 | 141 | PF02991 | 0.424 |
LIG_LIR_Gen_1 | 16 | 21 | PF02991 | 0.470 |
LIG_LIR_Gen_1 | 203 | 211 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 128 | 134 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 16 | 20 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 203 | 207 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 241 | 247 | PF02991 | 0.594 |
LIG_MLH1_MIPbox_1 | 128 | 132 | PF16413 | 0.590 |
LIG_MYND_3 | 12 | 16 | PF01753 | 0.583 |
LIG_PDZ_Class_3 | 263 | 268 | PF00595 | 0.644 |
LIG_SH2_PTP2 | 167 | 170 | PF00017 | 0.502 |
LIG_SH2_STAT5 | 131 | 134 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 167 | 170 | PF00017 | 0.375 |
LIG_SUMO_SIM_anti_2 | 116 | 121 | PF11976 | 0.418 |
LIG_SUMO_SIM_anti_2 | 147 | 153 | PF11976 | 0.368 |
LIG_SUMO_SIM_par_1 | 179 | 184 | PF11976 | 0.466 |
LIG_SUMO_SIM_par_1 | 187 | 193 | PF11976 | 0.470 |
LIG_TRAF2_1 | 264 | 267 | PF00917 | 0.613 |
LIG_TRAF2_1 | 88 | 91 | PF00917 | 0.547 |
MOD_CDC14_SPxK_1 | 193 | 196 | PF00782 | 0.507 |
MOD_CDK_SPK_2 | 238 | 243 | PF00069 | 0.596 |
MOD_CDK_SPxK_1 | 190 | 196 | PF00069 | 0.489 |
MOD_CK1_1 | 147 | 153 | PF00069 | 0.457 |
MOD_CK1_1 | 184 | 190 | PF00069 | 0.515 |
MOD_CK1_1 | 22 | 28 | PF00069 | 0.430 |
MOD_CK1_1 | 258 | 264 | PF00069 | 0.636 |
MOD_CK1_1 | 44 | 50 | PF00069 | 0.582 |
MOD_CK1_1 | 76 | 82 | PF00069 | 0.678 |
MOD_CK2_1 | 22 | 28 | PF00069 | 0.515 |
MOD_CK2_1 | 254 | 260 | PF00069 | 0.557 |
MOD_CK2_1 | 261 | 267 | PF00069 | 0.575 |
MOD_CK2_1 | 85 | 91 | PF00069 | 0.763 |
MOD_CK2_1 | 95 | 101 | PF00069 | 0.724 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.384 |
MOD_GlcNHglycan | 251 | 254 | PF01048 | 0.610 |
MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.732 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.722 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.554 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.461 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.328 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.627 |
MOD_GSK3_1 | 254 | 261 | PF00069 | 0.488 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.560 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.748 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.649 |
MOD_NEK2_1 | 132 | 137 | PF00069 | 0.509 |
MOD_NEK2_1 | 85 | 90 | PF00069 | 0.491 |
MOD_PIKK_1 | 37 | 43 | PF00454 | 0.603 |
MOD_PIKK_1 | 86 | 92 | PF00454 | 0.645 |
MOD_PK_1 | 95 | 101 | PF00069 | 0.537 |
MOD_PKA_1 | 93 | 99 | PF00069 | 0.650 |
MOD_PKA_2 | 73 | 79 | PF00069 | 0.533 |
MOD_PKB_1 | 93 | 101 | PF00069 | 0.620 |
MOD_Plk_1 | 132 | 138 | PF00069 | 0.524 |
MOD_Plk_1 | 181 | 187 | PF00069 | 0.532 |
MOD_Plk_1 | 259 | 265 | PF00069 | 0.596 |
MOD_Plk_1 | 64 | 70 | PF00069 | 0.510 |
MOD_Plk_4 | 102 | 108 | PF00069 | 0.579 |
MOD_Plk_4 | 147 | 153 | PF00069 | 0.444 |
MOD_Plk_4 | 170 | 176 | PF00069 | 0.446 |
MOD_Plk_4 | 186 | 192 | PF00069 | 0.458 |
MOD_ProDKin_1 | 190 | 196 | PF00069 | 0.491 |
MOD_ProDKin_1 | 238 | 244 | PF00069 | 0.548 |
TRG_DiLeu_BaEn_1 | 7 | 12 | PF01217 | 0.550 |
TRG_DiLeu_BaLyEn_6 | 10 | 15 | PF01217 | 0.539 |
TRG_ENDOCYTIC_2 | 131 | 134 | PF00928 | 0.456 |
TRG_ER_diArg_1 | 207 | 209 | PF00400 | 0.521 |
TRG_ER_diArg_1 | 92 | 95 | PF00400 | 0.596 |
TRG_ER_KDEL_1 | 265 | 268 | PF00810 | 0.496 |
TRG_NLS_MonoExtC_3 | 92 | 97 | PF00514 | 0.708 |
TRG_NLS_MonoExtN_4 | 92 | 98 | PF00514 | 0.656 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1P9W5 | Leptomonas seymouri | 45% | 100% |
A0A1X0P8M5 | Trypanosomatidae | 30% | 100% |
A0A3R7KU56 | Trypanosoma rangeli | 29% | 100% |
A0A3S5H519 | Leishmania donovani | 73% | 100% |
E9ACF0 | Leishmania major | 74% | 100% |
E9AG22 | Leishmania infantum | 73% | 100% |
E9AJN8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 72% | 100% |
V5ANT9 | Trypanosoma cruzi | 30% | 100% |