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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: E9B4D4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 100 | 102 | PF00675 | 0.706 |
CLV_NRD_NRD_1 | 176 | 178 | PF00675 | 0.589 |
CLV_NRD_NRD_1 | 201 | 203 | PF00675 | 0.570 |
CLV_NRD_NRD_1 | 206 | 208 | PF00675 | 0.588 |
CLV_NRD_NRD_1 | 223 | 225 | PF00675 | 0.734 |
CLV_PCSK_KEX2_1 | 176 | 178 | PF00082 | 0.594 |
CLV_PCSK_KEX2_1 | 201 | 203 | PF00082 | 0.598 |
CLV_PCSK_KEX2_1 | 206 | 208 | PF00082 | 0.634 |
CLV_PCSK_KEX2_1 | 223 | 225 | PF00082 | 0.592 |
CLV_PCSK_PC1ET2_1 | 223 | 225 | PF00082 | 0.601 |
CLV_PCSK_PC7_1 | 172 | 178 | PF00082 | 0.604 |
CLV_PCSK_PC7_1 | 202 | 208 | PF00082 | 0.584 |
CLV_PCSK_SKI1_1 | 201 | 205 | PF00082 | 0.638 |
CLV_PCSK_SKI1_1 | 212 | 216 | PF00082 | 0.638 |
CLV_PCSK_SKI1_1 | 90 | 94 | PF00082 | 0.635 |
DOC_ANK_TNKS_1 | 205 | 212 | PF00023 | 0.596 |
DOC_CKS1_1 | 268 | 273 | PF01111 | 0.458 |
DOC_MAPK_gen_1 | 135 | 143 | PF00069 | 0.625 |
DOC_PP4_FxxP_1 | 92 | 95 | PF00568 | 0.556 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.741 |
DOC_USP7_MATH_1 | 170 | 174 | PF00917 | 0.474 |
DOC_USP7_MATH_1 | 183 | 187 | PF00917 | 0.617 |
DOC_USP7_MATH_1 | 263 | 267 | PF00917 | 0.595 |
DOC_USP7_MATH_1 | 85 | 89 | PF00917 | 0.727 |
DOC_WW_Pin1_4 | 267 | 272 | PF00397 | 0.551 |
LIG_14-3-3_CanoR_1 | 101 | 107 | PF00244 | 0.588 |
LIG_14-3-3_CanoR_1 | 146 | 152 | PF00244 | 0.608 |
LIG_14-3-3_CanoR_1 | 249 | 254 | PF00244 | 0.681 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.586 |
LIG_BRCT_BRCA1_1 | 128 | 132 | PF00533 | 0.602 |
LIG_BRCT_BRCA1_1 | 295 | 299 | PF00533 | 0.618 |
LIG_BRCT_BRCA1_1 | 88 | 92 | PF00533 | 0.643 |
LIG_FHA_1 | 268 | 274 | PF00498 | 0.503 |
LIG_IBAR_NPY_1 | 44 | 46 | PF08397 | 0.555 |
LIG_Integrin_RGD_1 | 188 | 190 | PF01839 | 0.608 |
LIG_LIR_Apic_2 | 266 | 271 | PF02991 | 0.737 |
LIG_LIR_Apic_2 | 89 | 95 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 2 | 6 | PF02991 | 0.586 |
LIG_LIR_Nem_3 | 215 | 220 | PF02991 | 0.604 |
LIG_LIR_Nem_3 | 232 | 237 | PF02991 | 0.623 |
LIG_LIR_Nem_3 | 291 | 295 | PF02991 | 0.588 |
LIG_MLH1_MIPbox_1 | 128 | 132 | PF16413 | 0.584 |
LIG_PTB_Apo_2 | 59 | 66 | PF02174 | 0.466 |
LIG_PTB_Phospho_1 | 59 | 65 | PF10480 | 0.466 |
LIG_REV1ctd_RIR_1 | 129 | 139 | PF16727 | 0.587 |
LIG_SH2_CRK | 217 | 221 | PF00017 | 0.546 |
LIG_SH2_CRK | 268 | 272 | PF00017 | 0.625 |
LIG_SH2_CRK | 292 | 296 | PF00017 | 0.592 |
LIG_SH2_CRK | 73 | 77 | PF00017 | 0.548 |
LIG_SH2_NCK_1 | 73 | 77 | PF00017 | 0.524 |
LIG_SH2_STAT3 | 27 | 30 | PF00017 | 0.633 |
LIG_SH2_STAT3 | 52 | 55 | PF00017 | 0.608 |
LIG_SH2_STAT5 | 27 | 30 | PF00017 | 0.735 |
LIG_SH2_STAT5 | 73 | 76 | PF00017 | 0.577 |
LIG_SH3_3 | 194 | 200 | PF00018 | 0.565 |
LIG_SH3_3 | 250 | 256 | PF00018 | 0.599 |
LIG_SH3_3 | 275 | 281 | PF00018 | 0.568 |
LIG_SH3_3 | 48 | 54 | PF00018 | 0.779 |
LIG_SH3_4 | 255 | 262 | PF00018 | 0.476 |
LIG_SUMO_SIM_par_1 | 270 | 276 | PF11976 | 0.452 |
LIG_TYR_ITSM | 213 | 220 | PF00017 | 0.607 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.628 |
MOD_CK1_1 | 111 | 117 | PF00069 | 0.569 |
MOD_CK1_1 | 119 | 125 | PF00069 | 0.546 |
MOD_CK1_1 | 88 | 94 | PF00069 | 0.568 |
MOD_CK2_1 | 295 | 301 | PF00069 | 0.585 |
MOD_GlcNHglycan | 118 | 121 | PF01048 | 0.528 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.675 |
MOD_GlcNHglycan | 57 | 60 | PF01048 | 0.640 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.614 |
MOD_GlcNHglycan | 95 | 98 | PF01048 | 0.542 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.628 |
MOD_GSK3_1 | 263 | 270 | PF00069 | 0.569 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.557 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.642 |
MOD_N-GLC_1 | 293 | 298 | PF02516 | 0.611 |
MOD_NEK2_1 | 86 | 91 | PF00069 | 0.656 |
MOD_NEK2_2 | 147 | 152 | PF00069 | 0.631 |
MOD_PIKK_1 | 136 | 142 | PF00454 | 0.625 |
MOD_PIKK_1 | 71 | 77 | PF00454 | 0.605 |
MOD_PK_1 | 102 | 108 | PF00069 | 0.622 |
MOD_PK_1 | 126 | 132 | PF00069 | 0.627 |
MOD_PK_1 | 249 | 255 | PF00069 | 0.489 |
MOD_PKA_1 | 101 | 107 | PF00069 | 0.678 |
MOD_PKA_1 | 201 | 207 | PF00069 | 0.646 |
MOD_PKA_2 | 114 | 120 | PF00069 | 0.604 |
MOD_PKA_2 | 136 | 142 | PF00069 | 0.634 |
MOD_PKA_2 | 201 | 207 | PF00069 | 0.641 |
MOD_Plk_1 | 25 | 31 | PF00069 | 0.597 |
MOD_Plk_2-3 | 156 | 162 | PF00069 | 0.453 |
MOD_Plk_2-3 | 297 | 303 | PF00069 | 0.633 |
MOD_Plk_4 | 126 | 132 | PF00069 | 0.625 |
MOD_Plk_4 | 263 | 269 | PF00069 | 0.596 |
MOD_ProDKin_1 | 267 | 273 | PF00069 | 0.550 |
MOD_SUMO_rev_2 | 155 | 165 | PF00179 | 0.476 |
MOD_SUMO_rev_2 | 96 | 104 | PF00179 | 0.592 |
TRG_DiLeu_BaEn_4 | 157 | 163 | PF01217 | 0.527 |
TRG_ENDOCYTIC_2 | 166 | 169 | PF00928 | 0.494 |
TRG_ENDOCYTIC_2 | 217 | 220 | PF00928 | 0.545 |
TRG_ENDOCYTIC_2 | 292 | 295 | PF00928 | 0.615 |
TRG_ENDOCYTIC_2 | 46 | 49 | PF00928 | 0.627 |
TRG_ER_diArg_1 | 176 | 178 | PF00400 | 0.606 |
TRG_ER_diArg_1 | 200 | 202 | PF00400 | 0.582 |
TRG_NLS_Bipartite_1 | 206 | 227 | PF00514 | 0.628 |
TRG_Pf-PMV_PEXEL_1 | 152 | 156 | PF00026 | 0.618 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HYS4 | Leptomonas seymouri | 54% | 100% |
A0A1X0NRB6 | Trypanosomatidae | 35% | 100% |
A0A3S7X783 | Leishmania donovani | 90% | 100% |
A4HM03 | Leishmania braziliensis | 67% | 100% |
A4I9D4 | Leishmania infantum | 90% | 100% |
Q4Q3P3 | Leishmania major | 87% | 100% |