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: 3 |
NetGPI | no | yes: 0, no: 3 |
Related structures:
AlphaFold database: A4I5M9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 195 | 199 | PF00656 | 0.714 |
CLV_NRD_NRD_1 | 302 | 304 | PF00675 | 0.745 |
CLV_NRD_NRD_1 | 335 | 337 | PF00675 | 0.672 |
CLV_PCSK_FUR_1 | 333 | 337 | PF00082 | 0.622 |
CLV_PCSK_KEX2_1 | 304 | 306 | PF00082 | 0.744 |
CLV_PCSK_KEX2_1 | 333 | 335 | PF00082 | 0.691 |
CLV_PCSK_PC1ET2_1 | 304 | 306 | PF00082 | 0.744 |
CLV_PCSK_PC7_1 | 329 | 335 | PF00082 | 0.702 |
DEG_SCF_FBW7_1 | 24 | 30 | PF00400 | 0.596 |
DEG_SPOP_SBC_1 | 64 | 68 | PF00917 | 0.615 |
DOC_CKS1_1 | 24 | 29 | PF01111 | 0.687 |
DOC_PP2B_LxvP_1 | 113 | 116 | PF13499 | 0.691 |
DOC_PP2B_LxvP_1 | 96 | 99 | PF13499 | 0.715 |
DOC_PP4_FxxP_1 | 187 | 190 | PF00568 | 0.621 |
DOC_USP7_MATH_1 | 135 | 139 | PF00917 | 0.670 |
DOC_USP7_MATH_1 | 142 | 146 | PF00917 | 0.739 |
DOC_USP7_MATH_1 | 181 | 185 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 65 | 69 | PF00917 | 0.678 |
DOC_WW_Pin1_4 | 145 | 150 | PF00397 | 0.714 |
DOC_WW_Pin1_4 | 177 | 182 | PF00397 | 0.607 |
DOC_WW_Pin1_4 | 186 | 191 | PF00397 | 0.627 |
DOC_WW_Pin1_4 | 196 | 201 | PF00397 | 0.621 |
DOC_WW_Pin1_4 | 23 | 28 | PF00397 | 0.687 |
DOC_WW_Pin1_4 | 233 | 238 | PF00397 | 0.686 |
DOC_WW_Pin1_4 | 242 | 247 | PF00397 | 0.599 |
LIG_14-3-3_CanoR_1 | 164 | 169 | PF00244 | 0.761 |
LIG_14-3-3_CanoR_1 | 241 | 246 | PF00244 | 0.612 |
LIG_14-3-3_CanoR_1 | 63 | 71 | PF00244 | 0.617 |
LIG_BRCT_BRCA1_1 | 183 | 187 | PF00533 | 0.601 |
LIG_eIF4E_1 | 225 | 231 | PF01652 | 0.591 |
LIG_FHA_1 | 225 | 231 | PF00498 | 0.691 |
LIG_FHA_1 | 253 | 259 | PF00498 | 0.705 |
LIG_FHA_1 | 313 | 319 | PF00498 | 0.638 |
LIG_FHA_2 | 191 | 197 | PF00498 | 0.724 |
LIG_FHA_2 | 259 | 265 | PF00498 | 0.807 |
LIG_FHA_2 | 65 | 71 | PF00498 | 0.662 |
LIG_LIR_Apic_2 | 184 | 190 | PF02991 | 0.610 |
LIG_LIR_Nem_3 | 221 | 225 | PF02991 | 0.602 |
LIG_SH2_CRK | 86 | 90 | PF00017 | 0.689 |
LIG_SH2_SRC | 288 | 291 | PF00017 | 0.720 |
LIG_SH2_STAT3 | 108 | 111 | PF00017 | 0.597 |
LIG_SH2_STAT3 | 225 | 228 | PF00017 | 0.593 |
LIG_SH3_3 | 231 | 237 | PF00018 | 0.688 |
LIG_SH3_3 | 320 | 326 | PF00018 | 0.604 |
LIG_SH3_3 | 54 | 60 | PF00018 | 0.606 |
LIG_SH3_CIN85_PxpxPR_1 | 58 | 63 | PF14604 | 0.603 |
LIG_SUMO_SIM_anti_2 | 315 | 321 | PF11976 | 0.589 |
LIG_SUMO_SIM_par_1 | 20 | 26 | PF11976 | 0.601 |
LIG_TRAF2_1 | 261 | 264 | PF00917 | 0.730 |
MOD_CK1_1 | 138 | 144 | PF00069 | 0.632 |
MOD_CK1_1 | 145 | 151 | PF00069 | 0.806 |
MOD_CK1_1 | 159 | 165 | PF00069 | 0.614 |
MOD_CK1_1 | 251 | 257 | PF00069 | 0.727 |
MOD_CK2_1 | 190 | 196 | PF00069 | 0.724 |
MOD_CK2_1 | 258 | 264 | PF00069 | 0.726 |
MOD_CK2_1 | 41 | 47 | PF00069 | 0.607 |
MOD_CK2_1 | 64 | 70 | PF00069 | 0.661 |
MOD_CK2_1 | 97 | 103 | PF00069 | 0.613 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.694 |
MOD_GlcNHglycan | 118 | 121 | PF01048 | 0.502 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.753 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.807 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.733 |
MOD_GlcNHglycan | 43 | 46 | PF01048 | 0.602 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.618 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.728 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.807 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.652 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.652 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.677 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.680 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.719 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.624 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.719 |
MOD_NEK2_1 | 248 | 253 | PF00069 | 0.642 |
MOD_PIKK_1 | 15 | 21 | PF00454 | 0.605 |
MOD_PIKK_1 | 224 | 230 | PF00454 | 0.695 |
MOD_PKA_2 | 76 | 82 | PF00069 | 0.597 |
MOD_Plk_1 | 162 | 168 | PF00069 | 0.705 |
MOD_Plk_1 | 276 | 282 | PF00069 | 0.674 |
MOD_Plk_1 | 284 | 290 | PF00069 | 0.677 |
MOD_Plk_2-3 | 259 | 265 | PF00069 | 0.627 |
MOD_Plk_2-3 | 284 | 290 | PF00069 | 0.717 |
MOD_Plk_4 | 164 | 170 | PF00069 | 0.798 |
MOD_Plk_4 | 248 | 254 | PF00069 | 0.591 |
MOD_Plk_4 | 97 | 103 | PF00069 | 0.613 |
MOD_ProDKin_1 | 145 | 151 | PF00069 | 0.716 |
MOD_ProDKin_1 | 177 | 183 | PF00069 | 0.603 |
MOD_ProDKin_1 | 186 | 192 | PF00069 | 0.627 |
MOD_ProDKin_1 | 196 | 202 | PF00069 | 0.621 |
MOD_ProDKin_1 | 23 | 29 | PF00069 | 0.686 |
MOD_ProDKin_1 | 233 | 239 | PF00069 | 0.686 |
MOD_ProDKin_1 | 242 | 248 | PF00069 | 0.601 |
MOD_SUMO_rev_2 | 259 | 269 | PF00179 | 0.727 |
TRG_DiLeu_BaEn_1 | 8 | 13 | PF01217 | 0.569 |
TRG_ENDOCYTIC_2 | 86 | 89 | PF00928 | 0.689 |
TRG_ER_diArg_1 | 302 | 305 | PF00400 | 0.747 |
TRG_ER_diArg_1 | 332 | 335 | PF00400 | 0.694 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IEZ3 | Leishmania donovani | 100% | 100% |
Q4Q792 | Leishmania major | 78% | 78% |