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: E9ANB5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 204 | 206 | PF00675 | 0.561 |
CLV_NRD_NRD_1 | 227 | 229 | PF00675 | 0.419 |
CLV_NRD_NRD_1 | 32 | 34 | PF00675 | 0.395 |
CLV_PCSK_KEX2_1 | 204 | 206 | PF00082 | 0.559 |
CLV_PCSK_KEX2_1 | 227 | 229 | PF00082 | 0.392 |
CLV_PCSK_KEX2_1 | 34 | 36 | PF00082 | 0.292 |
CLV_PCSK_PC1ET2_1 | 34 | 36 | PF00082 | 0.317 |
CLV_PCSK_SKI1_1 | 126 | 130 | PF00082 | 0.656 |
CLV_PCSK_SKI1_1 | 245 | 249 | PF00082 | 0.580 |
CLV_PCSK_SKI1_1 | 53 | 57 | PF00082 | 0.410 |
CLV_PCSK_SKI1_1 | 70 | 74 | PF00082 | 0.521 |
DEG_APCC_KENBOX_2 | 171 | 175 | PF00400 | 0.489 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.539 |
DOC_ANK_TNKS_1 | 8 | 15 | PF00023 | 0.416 |
DOC_CYCLIN_RxL_1 | 67 | 74 | PF00134 | 0.306 |
DOC_MAPK_gen_1 | 147 | 155 | PF00069 | 0.422 |
DOC_MAPK_gen_1 | 33 | 39 | PF00069 | 0.311 |
DOC_MAPK_MEF2A_6 | 147 | 155 | PF00069 | 0.455 |
DOC_MIT_MIM_1 | 31 | 39 | PF04212 | 0.391 |
DOC_PP1_RVXF_1 | 16 | 23 | PF00149 | 0.496 |
DOC_PP4_FxxP_1 | 116 | 119 | PF00568 | 0.529 |
DOC_PP4_FxxP_1 | 128 | 131 | PF00568 | 0.604 |
DOC_PP4_FxxP_1 | 22 | 25 | PF00568 | 0.416 |
DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.664 |
DOC_USP7_MATH_1 | 151 | 155 | PF00917 | 0.558 |
DOC_USP7_MATH_1 | 87 | 91 | PF00917 | 0.787 |
DOC_USP7_MATH_1 | 92 | 96 | PF00917 | 0.721 |
LIG_14-3-3_CanoR_1 | 126 | 131 | PF00244 | 0.620 |
LIG_14-3-3_CanoR_1 | 134 | 141 | PF00244 | 0.583 |
LIG_deltaCOP1_diTrp_1 | 106 | 116 | PF00928 | 0.633 |
LIG_LIR_Apic_2 | 115 | 119 | PF02991 | 0.549 |
LIG_LIR_Gen_1 | 106 | 116 | PF02991 | 0.577 |
LIG_LIR_Gen_1 | 154 | 162 | PF02991 | 0.463 |
LIG_LIR_Gen_1 | 192 | 202 | PF02991 | 0.592 |
LIG_LIR_Gen_1 | 63 | 73 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 106 | 112 | PF02991 | 0.634 |
LIG_LIR_Nem_3 | 154 | 158 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 192 | 197 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 239 | 244 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 63 | 69 | PF02991 | 0.311 |
LIG_NRBOX | 68 | 74 | PF00104 | 0.357 |
LIG_Pex14_2 | 128 | 132 | PF04695 | 0.608 |
LIG_SH2_CRK | 66 | 70 | PF00017 | 0.279 |
LIG_SH2_PTP2 | 246 | 249 | PF00017 | 0.471 |
LIG_SH2_STAP1 | 161 | 165 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 193 | 196 | PF00017 | 0.526 |
LIG_SH2_STAT5 | 246 | 249 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 66 | 69 | PF00017 | 0.355 |
LIG_TYR_ITIM | 244 | 249 | PF00017 | 0.471 |
MOD_CK1_1 | 121 | 127 | PF00069 | 0.641 |
MOD_CK1_1 | 139 | 145 | PF00069 | 0.539 |
MOD_CK2_1 | 139 | 145 | PF00069 | 0.587 |
MOD_Cter_Amidation | 225 | 228 | PF01082 | 0.423 |
MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.518 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.667 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.670 |
MOD_GSK3_1 | 132 | 139 | PF00069 | 0.639 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.487 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.607 |
MOD_GSK3_1 | 236 | 243 | PF00069 | 0.493 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.415 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.618 |
MOD_N-GLC_1 | 151 | 156 | PF02516 | 0.517 |
MOD_N-GLC_1 | 183 | 188 | PF02516 | 0.385 |
MOD_NEK2_2 | 193 | 198 | PF00069 | 0.346 |
MOD_NEK2_2 | 240 | 245 | PF00069 | 0.501 |
MOD_PKA_1 | 204 | 210 | PF00069 | 0.679 |
MOD_PKA_2 | 133 | 139 | PF00069 | 0.638 |
MOD_PKA_2 | 168 | 174 | PF00069 | 0.571 |
MOD_PKA_2 | 204 | 210 | PF00069 | 0.679 |
MOD_PKA_2 | 87 | 93 | PF00069 | 0.755 |
MOD_Plk_1 | 151 | 157 | PF00069 | 0.425 |
MOD_Plk_4 | 136 | 142 | PF00069 | 0.556 |
MOD_SUMO_rev_2 | 139 | 148 | PF00179 | 0.506 |
MOD_SUMO_rev_2 | 46 | 55 | PF00179 | 0.282 |
TRG_DiLeu_BaLyEn_6 | 15 | 20 | PF01217 | 0.251 |
TRG_ENDOCYTIC_2 | 246 | 249 | PF00928 | 0.427 |
TRG_ENDOCYTIC_2 | 66 | 69 | PF00928 | 0.279 |
TRG_ER_diArg_1 | 227 | 230 | PF00400 | 0.444 |
TRG_ER_diArg_1 | 32 | 35 | PF00400 | 0.399 |
TRG_Pf-PMV_PEXEL_1 | 163 | 168 | PF00026 | 0.524 |
TRG_Pf-PMV_PEXEL_1 | 18 | 23 | PF00026 | 0.528 |
TRG_Pf-PMV_PEXEL_1 | 70 | 74 | PF00026 | 0.470 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HRV7 | Leptomonas seymouri | 59% | 100% |
A0A0S4JQU3 | Bodo saltans | 31% | 99% |
A0A1X0NRW0 | Trypanosomatidae | 36% | 100% |
A0A3Q8IB40 | Leishmania donovani | 90% | 91% |
A0A3R7ND09 | Trypanosoma rangeli | 33% | 100% |
A4H693 | Leishmania braziliensis | 78% | 100% |
A4HUL6 | Leishmania infantum | 90% | 91% |
C9ZVP3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
Q4QHA9 | Leishmania major | 90% | 100% |