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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: E9AXE9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 204 | 208 | PF00656 | 0.436 |
CLV_NRD_NRD_1 | 209 | 211 | PF00675 | 0.503 |
CLV_NRD_NRD_1 | 217 | 219 | PF00675 | 0.636 |
CLV_PCSK_KEX2_1 | 209 | 211 | PF00082 | 0.503 |
CLV_PCSK_PC1ET2_1 | 209 | 211 | PF00082 | 0.503 |
CLV_PCSK_SKI1_1 | 261 | 265 | PF00082 | 0.706 |
CLV_PCSK_SKI1_1 | 273 | 277 | PF00082 | 0.649 |
DOC_ANK_TNKS_1 | 181 | 188 | PF00023 | 0.621 |
DOC_CKS1_1 | 143 | 148 | PF01111 | 0.573 |
DOC_CYCLIN_yCln2_LP_2 | 166 | 172 | PF00134 | 0.592 |
DOC_MAPK_MEF2A_6 | 157 | 166 | PF00069 | 0.500 |
DOC_PP2B_LxvP_1 | 166 | 169 | PF13499 | 0.475 |
DOC_USP7_MATH_1 | 221 | 225 | PF00917 | 0.586 |
DOC_USP7_MATH_1 | 255 | 259 | PF00917 | 0.459 |
DOC_USP7_UBL2_3 | 232 | 236 | PF12436 | 0.502 |
DOC_USP7_UBL2_3 | 261 | 265 | PF12436 | 0.634 |
DOC_USP7_UBL2_3 | 270 | 274 | PF12436 | 0.682 |
DOC_WW_Pin1_4 | 142 | 147 | PF00397 | 0.666 |
LIG_14-3-3_CanoR_1 | 256 | 260 | PF00244 | 0.714 |
LIG_BRCT_BRCA1_1 | 13 | 17 | PF00533 | 0.489 |
LIG_FHA_1 | 196 | 202 | PF00498 | 0.621 |
LIG_FHA_2 | 150 | 156 | PF00498 | 0.722 |
LIG_FHA_2 | 202 | 208 | PF00498 | 0.567 |
LIG_LIR_Apic_2 | 224 | 228 | PF02991 | 0.664 |
LIG_LIR_Gen_1 | 110 | 119 | PF02991 | 0.480 |
LIG_LIR_Gen_1 | 14 | 25 | PF02991 | 0.649 |
LIG_LIR_Gen_1 | 186 | 194 | PF02991 | 0.556 |
LIG_LIR_Gen_1 | 73 | 83 | PF02991 | 0.523 |
LIG_LIR_Nem_3 | 110 | 115 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 186 | 192 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 73 | 79 | PF02991 | 0.515 |
LIG_PTB_Apo_2 | 188 | 195 | PF02174 | 0.650 |
LIG_PTB_Phospho_1 | 188 | 194 | PF10480 | 0.647 |
LIG_SH2_CRK | 189 | 193 | PF00017 | 0.522 |
LIG_SH2_CRK | 225 | 229 | PF00017 | 0.605 |
LIG_SH2_CRK | 76 | 80 | PF00017 | 0.538 |
LIG_SH2_GRB2like | 189 | 192 | PF00017 | 0.543 |
LIG_SH2_PTP2 | 159 | 162 | PF00017 | 0.613 |
LIG_SH2_SRC | 159 | 162 | PF00017 | 0.613 |
LIG_SH2_STAT5 | 118 | 121 | PF00017 | 0.468 |
LIG_SH2_STAT5 | 159 | 162 | PF00017 | 0.613 |
LIG_SH2_STAT5 | 229 | 232 | PF00017 | 0.573 |
LIG_SH3_1 | 159 | 165 | PF00018 | 0.612 |
LIG_SH3_2 | 146 | 151 | PF14604 | 0.573 |
LIG_SH3_3 | 143 | 149 | PF00018 | 0.665 |
LIG_SH3_3 | 159 | 165 | PF00018 | 0.425 |
LIG_SH3_3 | 197 | 203 | PF00018 | 0.460 |
LIG_SH3_3 | 227 | 233 | PF00018 | 0.594 |
LIG_SH3_3 | 23 | 29 | PF00018 | 0.545 |
LIG_SH3_3 | 249 | 255 | PF00018 | 0.642 |
LIG_SH3_4 | 232 | 239 | PF00018 | 0.493 |
LIG_SH3_4 | 261 | 268 | PF00018 | 0.690 |
LIG_TRAF2_1 | 152 | 155 | PF00917 | 0.644 |
LIG_TRAF2_1 | 19 | 22 | PF00917 | 0.726 |
LIG_TRAF2_1 | 39 | 42 | PF00917 | 0.760 |
LIG_WW_3 | 148 | 152 | PF00397 | 0.559 |
MOD_CK1_1 | 110 | 116 | PF00069 | 0.568 |
MOD_CK1_1 | 117 | 123 | PF00069 | 0.522 |
MOD_CK1_1 | 84 | 90 | PF00069 | 0.446 |
MOD_CK2_1 | 149 | 155 | PF00069 | 0.614 |
MOD_CK2_1 | 245 | 251 | PF00069 | 0.648 |
MOD_CK2_1 | 43 | 49 | PF00069 | 0.712 |
MOD_GlcNHglycan | 170 | 173 | PF01048 | 0.633 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.626 |
MOD_GlcNHglycan | 33 | 36 | PF01048 | 0.692 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.580 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.527 |
MOD_N-GLC_1 | 120 | 125 | PF02516 | 0.443 |
MOD_NEK2_1 | 107 | 112 | PF00069 | 0.564 |
MOD_PIKK_1 | 195 | 201 | PF00454 | 0.704 |
MOD_PIKK_1 | 268 | 274 | PF00454 | 0.607 |
MOD_PKA_2 | 255 | 261 | PF00069 | 0.595 |
MOD_Plk_1 | 107 | 113 | PF00069 | 0.579 |
MOD_Plk_1 | 120 | 126 | PF00069 | 0.465 |
MOD_Plk_4 | 107 | 113 | PF00069 | 0.539 |
MOD_Plk_4 | 114 | 120 | PF00069 | 0.509 |
MOD_Plk_4 | 75 | 81 | PF00069 | 0.543 |
MOD_ProDKin_1 | 142 | 148 | PF00069 | 0.659 |
MOD_SUMO_for_1 | 175 | 178 | PF00179 | 0.527 |
MOD_SUMO_for_1 | 263 | 266 | PF00179 | 0.653 |
TRG_ENDOCYTIC_2 | 189 | 192 | PF00928 | 0.473 |
TRG_ENDOCYTIC_2 | 76 | 79 | PF00928 | 0.539 |
TRG_NLS_MonoExtC_3 | 208 | 214 | PF00514 | 0.627 |
TRG_Pf-PMV_PEXEL_1 | 182 | 186 | PF00026 | 0.525 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P685 | Leptomonas seymouri | 57% | 94% |
A0A1X0P5H5 | Trypanosomatidae | 33% | 100% |
A0A3Q8IC96 | Leishmania donovani | 88% | 100% |
A0A422NX50 | Trypanosoma rangeli | 35% | 100% |
A4HE03 | Leishmania braziliensis | 69% | 98% |
A4I1B3 | Leishmania infantum | 88% | 100% |
D0A5K5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
Q4QA23 | Leishmania major | 87% | 100% |
V5BN56 | Trypanosoma cruzi | 31% | 100% |