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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: E9ALN2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 222 | 226 | PF00656 | 0.682 |
CLV_NRD_NRD_1 | 158 | 160 | PF00675 | 0.706 |
CLV_NRD_NRD_1 | 163 | 165 | PF00675 | 0.592 |
CLV_NRD_NRD_1 | 248 | 250 | PF00675 | 0.604 |
CLV_PCSK_FUR_1 | 246 | 250 | PF00082 | 0.718 |
CLV_PCSK_KEX2_1 | 158 | 160 | PF00082 | 0.658 |
CLV_PCSK_KEX2_1 | 163 | 165 | PF00082 | 0.643 |
CLV_PCSK_KEX2_1 | 246 | 248 | PF00082 | 0.629 |
CLV_PCSK_KEX2_1 | 270 | 272 | PF00082 | 0.609 |
CLV_PCSK_PC1ET2_1 | 270 | 272 | PF00082 | 0.666 |
CLV_PCSK_PC7_1 | 159 | 165 | PF00082 | 0.588 |
CLV_PCSK_PC7_1 | 242 | 248 | PF00082 | 0.500 |
CLV_PCSK_SKI1_1 | 175 | 179 | PF00082 | 0.674 |
CLV_PCSK_SKI1_1 | 249 | 253 | PF00082 | 0.605 |
DEG_SPOP_SBC_1 | 99 | 103 | PF00917 | 0.707 |
DOC_CKS1_1 | 69 | 74 | PF01111 | 0.650 |
DOC_CYCLIN_yCln2_LP_2 | 252 | 255 | PF00134 | 0.731 |
DOC_MAPK_DCC_7 | 8 | 18 | PF00069 | 0.585 |
DOC_MAPK_gen_1 | 129 | 138 | PF00069 | 0.600 |
DOC_MAPK_gen_1 | 172 | 181 | PF00069 | 0.699 |
DOC_MAPK_gen_1 | 246 | 253 | PF00069 | 0.612 |
DOC_MAPK_MEF2A_6 | 172 | 181 | PF00069 | 0.697 |
DOC_MAPK_MEF2A_6 | 260 | 269 | PF00069 | 0.698 |
DOC_PP1_RVXF_1 | 173 | 179 | PF00149 | 0.608 |
DOC_PP2B_LxvP_1 | 252 | 255 | PF13499 | 0.731 |
DOC_PP4_FxxP_1 | 113 | 116 | PF00568 | 0.644 |
DOC_USP7_MATH_1 | 120 | 124 | PF00917 | 0.644 |
DOC_USP7_MATH_1 | 188 | 192 | PF00917 | 0.663 |
DOC_USP7_MATH_1 | 211 | 215 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 219 | 223 | PF00917 | 0.666 |
DOC_USP7_MATH_1 | 7 | 11 | PF00917 | 0.555 |
DOC_USP7_MATH_1 | 99 | 103 | PF00917 | 0.702 |
DOC_USP7_UBL2_3 | 224 | 228 | PF12436 | 0.726 |
DOC_WW_Pin1_4 | 102 | 107 | PF00397 | 0.802 |
DOC_WW_Pin1_4 | 182 | 187 | PF00397 | 0.600 |
DOC_WW_Pin1_4 | 68 | 73 | PF00397 | 0.650 |
LIG_14-3-3_CanoR_1 | 121 | 125 | PF00244 | 0.675 |
LIG_14-3-3_CanoR_1 | 158 | 166 | PF00244 | 0.682 |
LIG_14-3-3_CanoR_1 | 189 | 193 | PF00244 | 0.664 |
LIG_14-3-3_CanoR_1 | 209 | 218 | PF00244 | 0.429 |
LIG_Actin_WH2_2 | 177 | 195 | PF00022 | 0.691 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.726 |
LIG_FHA_1 | 195 | 201 | PF00498 | 0.604 |
LIG_FHA_1 | 259 | 265 | PF00498 | 0.558 |
LIG_FHA_1 | 52 | 58 | PF00498 | 0.678 |
LIG_FHA_1 | 78 | 84 | PF00498 | 0.657 |
LIG_LIR_Apic_2 | 111 | 116 | PF02991 | 0.594 |
LIG_LIR_Apic_2 | 123 | 127 | PF02991 | 0.704 |
LIG_LIR_Gen_1 | 261 | 269 | PF02991 | 0.601 |
LIG_LIR_Nem_3 | 261 | 265 | PF02991 | 0.574 |
LIG_SH2_CRK | 124 | 128 | PF00017 | 0.706 |
LIG_SH2_STAP1 | 118 | 122 | PF00017 | 0.642 |
LIG_SH2_STAT5 | 207 | 210 | PF00017 | 0.704 |
LIG_SH3_3 | 136 | 142 | PF00018 | 0.612 |
LIG_SH3_3 | 25 | 31 | PF00018 | 0.742 |
MOD_CDK_SPxxK_3 | 182 | 189 | PF00069 | 0.604 |
MOD_CK1_1 | 201 | 207 | PF00069 | 0.689 |
MOD_CK1_1 | 212 | 218 | PF00069 | 0.664 |
MOD_CK1_1 | 220 | 226 | PF00069 | 0.563 |
MOD_CK1_1 | 98 | 104 | PF00069 | 0.818 |
MOD_CK2_1 | 193 | 199 | PF00069 | 0.706 |
MOD_GlcNHglycan | 106 | 109 | PF01048 | 0.598 |
MOD_GlcNHglycan | 167 | 171 | PF01048 | 0.795 |
MOD_GlcNHglycan | 211 | 214 | PF01048 | 0.656 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.655 |
MOD_GlcNHglycan | 96 | 100 | PF01048 | 0.786 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.592 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.500 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.691 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.658 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.681 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.775 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.703 |
MOD_NEK2_1 | 192 | 197 | PF00069 | 0.613 |
MOD_NEK2_2 | 108 | 113 | PF00069 | 0.499 |
MOD_NEK2_2 | 188 | 193 | PF00069 | 0.690 |
MOD_PIKK_1 | 240 | 246 | PF00454 | 0.775 |
MOD_PKA_1 | 158 | 164 | PF00069 | 0.727 |
MOD_PKA_2 | 120 | 126 | PF00069 | 0.693 |
MOD_PKA_2 | 158 | 164 | PF00069 | 0.811 |
MOD_PKA_2 | 188 | 194 | PF00069 | 0.666 |
MOD_PKA_2 | 87 | 93 | PF00069 | 0.520 |
MOD_Plk_1 | 198 | 204 | PF00069 | 0.610 |
MOD_Plk_1 | 47 | 53 | PF00069 | 0.790 |
MOD_Plk_4 | 108 | 114 | PF00069 | 0.499 |
MOD_ProDKin_1 | 102 | 108 | PF00069 | 0.797 |
MOD_ProDKin_1 | 182 | 188 | PF00069 | 0.602 |
MOD_ProDKin_1 | 68 | 74 | PF00069 | 0.649 |
TRG_ER_diArg_1 | 246 | 249 | PF00400 | 0.630 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZ42 | Leptomonas seymouri | 37% | 100% |
A0A3Q8IBJ9 | Leishmania donovani | 87% | 100% |
A4HHJ2 | Leishmania braziliensis | 69% | 100% |
A4I4Q0 | Leishmania infantum | 88% | 100% |
E9AE53 | Leishmania major | 87% | 100% |