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. | yes | yes: 20 |
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. | yes | yes: 16 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | yes | yes: 9, no: 1 |
NetGPI | no | yes: 0, no: 10 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pescher et al. (upgregulation) | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Lahav et al. - mRNA
- Protein
|
Related structures:
AlphaFold database: A0A3S7X8Z2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 118 | 122 | PF00656 | 0.428 |
CLV_C14_Caspase3-7 | 184 | 188 | PF00656 | 0.516 |
CLV_C14_Caspase3-7 | 211 | 215 | PF00656 | 0.565 |
CLV_NRD_NRD_1 | 129 | 131 | PF00675 | 0.455 |
CLV_NRD_NRD_1 | 99 | 101 | PF00675 | 0.515 |
CLV_PCSK_KEX2_1 | 129 | 131 | PF00082 | 0.432 |
CLV_PCSK_KEX2_1 | 73 | 75 | PF00082 | 0.474 |
CLV_PCSK_KEX2_1 | 98 | 100 | PF00082 | 0.488 |
CLV_PCSK_PC1ET2_1 | 73 | 75 | PF00082 | 0.474 |
CLV_PCSK_SKI1_1 | 2 | 6 | PF00082 | 0.637 |
CLV_PCSK_SKI1_1 | 28 | 32 | PF00082 | 0.465 |
CLV_PCSK_SKI1_1 | 36 | 40 | PF00082 | 0.446 |
DEG_MDM2_SWIB_1 | 81 | 88 | PF02201 | 0.383 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.675 |
DOC_PP1_RVXF_1 | 146 | 153 | PF00149 | 0.477 |
DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.469 |
DOC_USP7_MATH_1 | 175 | 179 | PF00917 | 0.485 |
DOC_USP7_MATH_1 | 67 | 71 | PF00917 | 0.581 |
DOC_USP7_UBL2_3 | 144 | 148 | PF12436 | 0.364 |
DOC_USP7_UBL2_3 | 29 | 33 | PF12436 | 0.264 |
DOC_WW_Pin1_4 | 135 | 140 | PF00397 | 0.548 |
DOC_WW_Pin1_4 | 166 | 171 | PF00397 | 0.441 |
LIG_14-3-3_CanoR_1 | 195 | 203 | PF00244 | 0.409 |
LIG_Actin_WH2_2 | 128 | 146 | PF00022 | 0.509 |
LIG_BRCT_BRCA1_1 | 155 | 159 | PF00533 | 0.441 |
LIG_FHA_1 | 196 | 202 | PF00498 | 0.444 |
LIG_FHA_1 | 63 | 69 | PF00498 | 0.474 |
LIG_FHA_2 | 109 | 115 | PF00498 | 0.388 |
LIG_FHA_2 | 136 | 142 | PF00498 | 0.422 |
LIG_FHA_2 | 159 | 165 | PF00498 | 0.355 |
LIG_FHA_2 | 21 | 27 | PF00498 | 0.438 |
LIG_LIR_Gen_1 | 106 | 116 | PF02991 | 0.550 |
LIG_LIR_Gen_1 | 156 | 167 | PF02991 | 0.452 |
LIG_LIR_Gen_1 | 53 | 60 | PF02991 | 0.289 |
LIG_LIR_Nem_3 | 106 | 112 | PF02991 | 0.512 |
LIG_LIR_Nem_3 | 145 | 150 | PF02991 | 0.406 |
LIG_LIR_Nem_3 | 156 | 162 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 83 | 88 | PF02991 | 0.375 |
LIG_PDZ_Class_3 | 214 | 219 | PF00595 | 0.505 |
LIG_Pex14_2 | 81 | 85 | PF04695 | 0.358 |
LIG_PTB_Apo_2 | 204 | 211 | PF02174 | 0.453 |
LIG_PTB_Apo_2 | 75 | 82 | PF02174 | 0.503 |
LIG_PTB_Phospho_1 | 204 | 210 | PF10480 | 0.450 |
LIG_SH2_NCK_1 | 210 | 214 | PF00017 | 0.584 |
LIG_SH2_SRC | 210 | 213 | PF00017 | 0.576 |
LIG_SH2_STAT3 | 123 | 126 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 123 | 126 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 151 | 154 | PF00017 | 0.464 |
LIG_SH2_STAT5 | 165 | 168 | PF00017 | 0.404 |
MOD_CK1_1 | 178 | 184 | PF00069 | 0.383 |
MOD_CMANNOS | 82 | 85 | PF00535 | 0.342 |
MOD_Cter_Amidation | 127 | 130 | PF01082 | 0.403 |
MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.413 |
MOD_GlcNHglycan | 18 | 21 | PF01048 | 0.636 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.488 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.533 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.634 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.429 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.364 |
MOD_GSK3_1 | 16 | 23 | PF00069 | 0.617 |
MOD_N-GLC_2 | 91 | 93 | PF02516 | 0.383 |
MOD_NEK2_1 | 13 | 18 | PF00069 | 0.492 |
MOD_NEK2_1 | 142 | 147 | PF00069 | 0.353 |
MOD_NEK2_1 | 158 | 163 | PF00069 | 0.408 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.531 |
MOD_PKA_2 | 62 | 68 | PF00069 | 0.459 |
MOD_Plk_4 | 119 | 125 | PF00069 | 0.393 |
MOD_Plk_4 | 13 | 19 | PF00069 | 0.512 |
MOD_Plk_4 | 178 | 184 | PF00069 | 0.440 |
MOD_ProDKin_1 | 135 | 141 | PF00069 | 0.544 |
MOD_ProDKin_1 | 166 | 172 | PF00069 | 0.440 |
MOD_SUMO_for_1 | 72 | 75 | PF00179 | 0.498 |
MOD_SUMO_for_1 | 89 | 92 | PF00179 | 0.301 |
MOD_SUMO_rev_2 | 24 | 30 | PF00179 | 0.308 |
TRG_DiLeu_BaEn_2 | 50 | 56 | PF01217 | 0.284 |
TRG_ENDOCYTIC_2 | 210 | 213 | PF00928 | 0.462 |
TRG_ER_diArg_1 | 129 | 131 | PF00400 | 0.478 |
TRG_ER_diArg_1 | 97 | 100 | PF00400 | 0.443 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HYS8 | Leptomonas seymouri | 74% | 100% |
A0A0S4IZ22 | Bodo saltans | 38% | 100% |
A0A1X0NHR2 | Trypanosomatidae | 56% | 97% |
A0A422N9T4 | Trypanosoma rangeli | 50% | 95% |
A4HME3 | Leishmania braziliensis | 81% | 100% |
A4IB15 | Leishmania infantum | 100% | 100% |
C9ZNP7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 50% | 96% |
E9AEU4 | Leishmania major | 98% | 100% |
E9B600 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 98% | 100% |