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: 5 |
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: 2 |
NetGPI | no | yes: 0, no: 2 |
Related structures:
AlphaFold database: A0A3Q8IEB6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 161 | 165 | PF00656 | 0.633 |
CLV_C14_Caspase3-7 | 260 | 264 | PF00656 | 0.523 |
CLV_MEL_PAP_1 | 49 | 55 | PF00089 | 0.441 |
CLV_NRD_NRD_1 | 177 | 179 | PF00675 | 0.427 |
CLV_NRD_NRD_1 | 257 | 259 | PF00675 | 0.433 |
CLV_PCSK_KEX2_1 | 257 | 259 | PF00082 | 0.433 |
CLV_PCSK_SKI1_1 | 148 | 152 | PF00082 | 0.437 |
CLV_PCSK_SKI1_1 | 158 | 162 | PF00082 | 0.316 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.443 |
DOC_CDC14_PxL_1 | 20 | 28 | PF14671 | 0.427 |
DOC_CKS1_1 | 6 | 11 | PF01111 | 0.434 |
DOC_MAPK_gen_1 | 173 | 182 | PF00069 | 0.633 |
DOC_MAPK_MEF2A_6 | 44 | 53 | PF00069 | 0.450 |
DOC_PP1_RVXF_1 | 176 | 183 | PF00149 | 0.633 |
DOC_PP2B_LxvP_1 | 21 | 24 | PF13499 | 0.593 |
DOC_PP2B_LxvP_1 | 26 | 29 | PF13499 | 0.408 |
DOC_PP4_FxxP_1 | 87 | 90 | PF00568 | 0.409 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.616 |
DOC_USP7_MATH_1 | 213 | 217 | PF00917 | 0.516 |
DOC_USP7_MATH_1 | 45 | 49 | PF00917 | 0.465 |
DOC_USP7_MATH_1 | 67 | 71 | PF00917 | 0.437 |
DOC_USP7_MATH_1 | 9 | 13 | PF00917 | 0.437 |
DOC_USP7_UBL2_3 | 154 | 158 | PF12436 | 0.633 |
DOC_USP7_UBL2_3 | 171 | 175 | PF12436 | 0.434 |
DOC_WW_Pin1_4 | 107 | 112 | PF00397 | 0.422 |
DOC_WW_Pin1_4 | 197 | 202 | PF00397 | 0.633 |
DOC_WW_Pin1_4 | 5 | 10 | PF00397 | 0.428 |
DOC_WW_Pin1_4 | 51 | 56 | PF00397 | 0.438 |
DOC_WW_Pin1_4 | 80 | 85 | PF00397 | 0.476 |
DOC_WW_Pin1_4 | 86 | 91 | PF00397 | 0.406 |
LIG_14-3-3_CanoR_1 | 103 | 109 | PF00244 | 0.418 |
LIG_14-3-3_CanoR_1 | 178 | 183 | PF00244 | 0.633 |
LIG_14-3-3_CanoR_1 | 265 | 272 | PF00244 | 0.755 |
LIG_14-3-3_CanoR_1 | 68 | 72 | PF00244 | 0.446 |
LIG_14-3-3_CanoR_1 | 95 | 99 | PF00244 | 0.431 |
LIG_FHA_1 | 94 | 100 | PF00498 | 0.433 |
LIG_FHA_2 | 159 | 165 | PF00498 | 0.633 |
LIG_FHA_2 | 198 | 204 | PF00498 | 0.633 |
LIG_FHA_2 | 216 | 222 | PF00498 | 0.423 |
LIG_FHA_2 | 240 | 246 | PF00498 | 0.633 |
LIG_LIR_Apic_2 | 4 | 9 | PF02991 | 0.424 |
LIG_LIR_Gen_1 | 126 | 133 | PF02991 | 0.608 |
LIG_LIR_Gen_1 | 144 | 150 | PF02991 | 0.483 |
LIG_LIR_Gen_1 | 166 | 177 | PF02991 | 0.633 |
LIG_LIR_Gen_1 | 181 | 190 | PF02991 | 0.458 |
LIG_LIR_Gen_1 | 8 | 17 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 126 | 130 | PF02991 | 0.583 |
LIG_LIR_Nem_3 | 166 | 172 | PF02991 | 0.633 |
LIG_LIR_Nem_3 | 181 | 185 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 69 | 75 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 8 | 13 | PF02991 | 0.435 |
LIG_MYND_1 | 114 | 118 | PF01753 | 0.426 |
LIG_Pex14_1 | 6 | 10 | PF04695 | 0.430 |
LIG_Pex14_2 | 123 | 127 | PF04695 | 0.433 |
LIG_Pex14_2 | 71 | 75 | PF04695 | 0.443 |
LIG_Pex14_2 | 94 | 98 | PF04695 | 0.436 |
LIG_PTB_Apo_2 | 140 | 147 | PF02174 | 0.616 |
LIG_SH2_STAT5 | 106 | 109 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 232 | 235 | PF00017 | 0.575 |
LIG_SH2_STAT5 | 86 | 89 | PF00017 | 0.569 |
LIG_SH3_3 | 108 | 114 | PF00018 | 0.424 |
LIG_SH3_3 | 32 | 38 | PF00018 | 0.449 |
LIG_SH3_3 | 78 | 84 | PF00018 | 0.589 |
LIG_WRC_WIRS_1 | 130 | 135 | PF05994 | 0.616 |
MOD_CK1_1 | 109 | 115 | PF00069 | 0.422 |
MOD_CK1_1 | 12 | 18 | PF00069 | 0.432 |
MOD_CK1_1 | 132 | 138 | PF00069 | 0.623 |
MOD_CK1_1 | 144 | 150 | PF00069 | 0.503 |
MOD_CK1_1 | 159 | 165 | PF00069 | 0.458 |
MOD_CK1_1 | 19 | 25 | PF00069 | 0.415 |
MOD_CK1_1 | 215 | 221 | PF00069 | 0.605 |
MOD_CK1_1 | 230 | 236 | PF00069 | 0.446 |
MOD_CK2_1 | 178 | 184 | PF00069 | 0.633 |
MOD_GlcNHglycan | 100 | 103 | PF01048 | 0.430 |
MOD_GlcNHglycan | 134 | 137 | PF01048 | 0.316 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.316 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.427 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.434 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.418 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.633 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.516 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.433 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.434 |
MOD_NEK2_1 | 104 | 109 | PF00069 | 0.480 |
MOD_NEK2_1 | 141 | 146 | PF00069 | 0.557 |
MOD_NEK2_1 | 167 | 172 | PF00069 | 0.625 |
MOD_NEK2_1 | 94 | 99 | PF00069 | 0.481 |
MOD_NEK2_2 | 67 | 72 | PF00069 | 0.440 |
MOD_OFUCOSY | 11 | 16 | PF10250 | 0.433 |
MOD_PKA_1 | 178 | 184 | PF00069 | 0.633 |
MOD_PKA_2 | 264 | 270 | PF00069 | 0.566 |
MOD_PKA_2 | 67 | 73 | PF00069 | 0.436 |
MOD_PKA_2 | 94 | 100 | PF00069 | 0.433 |
MOD_Plk_1 | 141 | 147 | PF00069 | 0.633 |
MOD_Plk_1 | 227 | 233 | PF00069 | 0.633 |
MOD_Plk_4 | 16 | 22 | PF00069 | 0.549 |
MOD_Plk_4 | 53 | 59 | PF00069 | 0.435 |
MOD_Plk_4 | 67 | 73 | PF00069 | 0.436 |
MOD_Plk_4 | 94 | 100 | PF00069 | 0.433 |
MOD_ProDKin_1 | 107 | 113 | PF00069 | 0.425 |
MOD_ProDKin_1 | 197 | 203 | PF00069 | 0.633 |
MOD_ProDKin_1 | 5 | 11 | PF00069 | 0.432 |
MOD_ProDKin_1 | 51 | 57 | PF00069 | 0.438 |
MOD_ProDKin_1 | 80 | 86 | PF00069 | 0.479 |
MOD_SUMO_rev_2 | 147 | 156 | PF00179 | 0.633 |
MOD_SUMO_rev_2 | 221 | 231 | PF00179 | 0.562 |
TRG_DiLeu_BaLyEn_6 | 21 | 26 | PF01217 | 0.423 |
TRG_Pf-PMV_PEXEL_1 | 148 | 152 | PF00026 | 0.433 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A4H7S1 | Leishmania braziliensis | 76% | 100% |