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: A4H7Z4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 129 | 131 | PF00675 | 0.478 |
CLV_NRD_NRD_1 | 232 | 234 | PF00675 | 0.671 |
CLV_NRD_NRD_1 | 63 | 65 | PF00675 | 0.759 |
CLV_PCSK_KEX2_1 | 234 | 236 | PF00082 | 0.683 |
CLV_PCSK_PC1ET2_1 | 234 | 236 | PF00082 | 0.708 |
CLV_PCSK_SKI1_1 | 175 | 179 | PF00082 | 0.440 |
CLV_PCSK_SKI1_1 | 68 | 72 | PF00082 | 0.522 |
DOC_CDC14_PxL_1 | 77 | 85 | PF14671 | 0.471 |
DOC_CYCLIN_yCln2_LP_2 | 103 | 109 | PF00134 | 0.514 |
DOC_MAPK_DCC_7 | 144 | 154 | PF00069 | 0.633 |
DOC_MAPK_MEF2A_6 | 144 | 152 | PF00069 | 0.545 |
DOC_MAPK_MEF2A_6 | 46 | 54 | PF00069 | 0.481 |
DOC_MAPK_RevD_3 | 50 | 65 | PF00069 | 0.480 |
DOC_PP2B_LxvP_1 | 103 | 106 | PF13499 | 0.489 |
DOC_PP4_FxxP_1 | 160 | 163 | PF00568 | 0.633 |
DOC_PP4_FxxP_1 | 36 | 39 | PF00568 | 0.480 |
DOC_PP4_FxxP_1 | 84 | 87 | PF00568 | 0.298 |
DOC_USP7_MATH_1 | 124 | 128 | PF00917 | 0.595 |
DOC_USP7_MATH_1 | 212 | 216 | PF00917 | 0.555 |
DOC_USP7_MATH_1 | 26 | 30 | PF00917 | 0.471 |
DOC_WW_Pin1_4 | 214 | 219 | PF00397 | 0.489 |
DOC_WW_Pin1_4 | 235 | 240 | PF00397 | 0.578 |
DOC_WW_Pin1_4 | 46 | 51 | PF00397 | 0.484 |
LIG_14-3-3_CanoR_1 | 64 | 68 | PF00244 | 0.676 |
LIG_Actin_WH2_2 | 31 | 48 | PF00022 | 0.480 |
LIG_Actin_WH2_2 | 79 | 97 | PF00022 | 0.616 |
LIG_BRCT_BRCA1_1 | 117 | 121 | PF00533 | 0.468 |
LIG_BRCT_BRCA1_1 | 23 | 27 | PF00533 | 0.466 |
LIG_CtBP_PxDLS_1 | 39 | 43 | PF00389 | 0.481 |
LIG_FHA_1 | 153 | 159 | PF00498 | 0.376 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.479 |
LIG_LIR_Apic_2 | 157 | 163 | PF02991 | 0.652 |
LIG_LIR_Gen_1 | 12 | 21 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 219 | 224 | PF02991 | 0.617 |
LIG_LIR_Nem_3 | 256 | 262 | PF02991 | 0.601 |
LIG_MYND_2 | 254 | 258 | PF01753 | 0.486 |
LIG_SH2_CRK | 259 | 263 | PF00017 | 0.655 |
LIG_SH2_NCK_1 | 259 | 263 | PF00017 | 0.644 |
LIG_SH2_SRC | 259 | 262 | PF00017 | 0.599 |
LIG_SH2_STAT5 | 133 | 136 | PF00017 | 0.281 |
LIG_SH2_STAT5 | 203 | 206 | PF00017 | 0.584 |
LIG_SH3_3 | 103 | 109 | PF00018 | 0.615 |
LIG_SH3_3 | 145 | 151 | PF00018 | 0.548 |
LIG_SUMO_SIM_anti_2 | 29 | 35 | PF11976 | 0.471 |
LIG_SUMO_SIM_par_1 | 150 | 155 | PF11976 | 0.518 |
LIG_TYR_ITIM | 257 | 262 | PF00017 | 0.651 |
LIG_UBA3_1 | 52 | 58 | PF00899 | 0.483 |
MOD_CK1_1 | 206 | 212 | PF00069 | 0.601 |
MOD_CK1_1 | 214 | 220 | PF00069 | 0.588 |
MOD_CK1_1 | 227 | 233 | PF00069 | 0.542 |
MOD_CK1_1 | 29 | 35 | PF00069 | 0.471 |
MOD_CK1_1 | 66 | 72 | PF00069 | 0.608 |
MOD_CK2_1 | 247 | 253 | PF00069 | 0.503 |
MOD_CK2_1 | 66 | 72 | PF00069 | 0.650 |
MOD_DYRK1A_RPxSP_1 | 235 | 239 | PF00069 | 0.577 |
MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.413 |
MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.342 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.547 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.512 |
MOD_GlcNHglycan | 229 | 232 | PF01048 | 0.690 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.484 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.587 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.523 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.649 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.565 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.478 |
MOD_GSK3_1 | 89 | 96 | PF00069 | 0.499 |
MOD_N-GLC_1 | 21 | 26 | PF02516 | 0.455 |
MOD_N-GLC_1 | 29 | 34 | PF02516 | 0.446 |
MOD_NEK2_1 | 152 | 157 | PF00069 | 0.354 |
MOD_NEK2_1 | 178 | 183 | PF00069 | 0.314 |
MOD_NEK2_1 | 229 | 234 | PF00069 | 0.519 |
MOD_NEK2_1 | 45 | 50 | PF00069 | 0.567 |
MOD_NEK2_1 | 63 | 68 | PF00069 | 0.592 |
MOD_NEK2_1 | 82 | 87 | PF00069 | 0.467 |
MOD_NEK2_1 | 94 | 99 | PF00069 | 0.378 |
MOD_PKA_1 | 233 | 239 | PF00069 | 0.751 |
MOD_PKA_2 | 224 | 230 | PF00069 | 0.512 |
MOD_PKA_2 | 45 | 51 | PF00069 | 0.502 |
MOD_PKA_2 | 63 | 69 | PF00069 | 0.658 |
MOD_Plk_1 | 114 | 120 | PF00069 | 0.466 |
MOD_Plk_1 | 225 | 231 | PF00069 | 0.493 |
MOD_Plk_1 | 29 | 35 | PF00069 | 0.471 |
MOD_Plk_4 | 253 | 259 | PF00069 | 0.554 |
MOD_Plk_4 | 29 | 35 | PF00069 | 0.471 |
MOD_ProDKin_1 | 214 | 220 | PF00069 | 0.481 |
MOD_ProDKin_1 | 235 | 241 | PF00069 | 0.575 |
MOD_ProDKin_1 | 46 | 52 | PF00069 | 0.486 |
MOD_SUMO_rev_2 | 140 | 146 | PF00179 | 0.625 |
TRG_DiLeu_BaEn_1 | 253 | 258 | PF01217 | 0.634 |
TRG_DiLeu_BaEn_2 | 218 | 224 | PF01217 | 0.342 |
TRG_DiLeu_BaLyEn_6 | 78 | 83 | PF01217 | 0.369 |
TRG_ENDOCYTIC_2 | 133 | 136 | PF00928 | 0.281 |
TRG_ENDOCYTIC_2 | 259 | 262 | PF00928 | 0.610 |
TRG_ER_diArg_1 | 173 | 176 | PF00400 | 0.544 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCF0 | Leptomonas seymouri | 46% | 100% |
A0A3Q8IA55 | Leishmania donovani | 70% | 100% |
A4HWC2 | Leishmania infantum | 70% | 100% |
E9AQ22 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 71% | 100% |
Q4QFF9 | Leishmania major | 71% | 100% |