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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: E9AVF4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 92 | 96 | PF00656 | 0.503 |
CLV_NRD_NRD_1 | 129 | 131 | PF00675 | 0.540 |
CLV_NRD_NRD_1 | 220 | 222 | PF00675 | 0.505 |
CLV_PCSK_KEX2_1 | 168 | 170 | PF00082 | 0.492 |
CLV_PCSK_KEX2_1 | 244 | 246 | PF00082 | 0.506 |
CLV_PCSK_PC1ET2_1 | 168 | 170 | PF00082 | 0.492 |
CLV_PCSK_PC1ET2_1 | 244 | 246 | PF00082 | 0.506 |
CLV_PCSK_SKI1_1 | 122 | 126 | PF00082 | 0.525 |
CLV_PCSK_SKI1_1 | 43 | 47 | PF00082 | 0.531 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.635 |
DEG_SCF_FBW7_1 | 231 | 237 | PF00400 | 0.464 |
DOC_CKS1_1 | 231 | 236 | PF01111 | 0.623 |
DOC_CYCLIN_RxL_1 | 130 | 143 | PF00134 | 0.432 |
DOC_CYCLIN_yCln2_LP_2 | 228 | 234 | PF00134 | 0.528 |
DOC_MAPK_gen_1 | 130 | 140 | PF00069 | 0.497 |
DOC_MAPK_gen_1 | 17 | 25 | PF00069 | 0.625 |
DOC_MAPK_JIP1_4 | 9 | 15 | PF00069 | 0.476 |
DOC_PP4_FxxP_1 | 7 | 10 | PF00568 | 0.469 |
DOC_SPAK_OSR1_1 | 193 | 197 | PF12202 | 0.437 |
DOC_USP7_MATH_1 | 30 | 34 | PF00917 | 0.472 |
DOC_USP7_UBL2_3 | 147 | 151 | PF12436 | 0.491 |
DOC_USP7_UBL2_3 | 36 | 40 | PF12436 | 0.515 |
DOC_USP7_UBL2_3 | 43 | 47 | PF12436 | 0.430 |
DOC_WW_Pin1_4 | 230 | 235 | PF00397 | 0.638 |
DOC_WW_Pin1_4 | 24 | 29 | PF00397 | 0.560 |
LIG_14-3-3_CanoR_1 | 139 | 148 | PF00244 | 0.334 |
LIG_14-3-3_CanoR_1 | 211 | 220 | PF00244 | 0.488 |
LIG_Actin_WH2_2 | 110 | 127 | PF00022 | 0.500 |
LIG_AP2alpha_1 | 183 | 187 | PF02296 | 0.463 |
LIG_APCC_ABBA_1 | 196 | 201 | PF00400 | 0.442 |
LIG_BRCT_BRCA1_1 | 110 | 114 | PF00533 | 0.482 |
LIG_FHA_1 | 10 | 16 | PF00498 | 0.492 |
LIG_FHA_1 | 135 | 141 | PF00498 | 0.595 |
LIG_FHA_1 | 55 | 61 | PF00498 | 0.483 |
LIG_FHA_2 | 14 | 20 | PF00498 | 0.517 |
LIG_LIR_Apic_2 | 5 | 10 | PF02991 | 0.462 |
LIG_LIR_Gen_1 | 184 | 194 | PF02991 | 0.557 |
LIG_LIR_Nem_3 | 111 | 117 | PF02991 | 0.493 |
LIG_LIR_Nem_3 | 184 | 190 | PF02991 | 0.558 |
LIG_LIR_Nem_3 | 191 | 197 | PF02991 | 0.481 |
LIG_NRP_CendR_1 | 244 | 247 | PF00754 | 0.511 |
LIG_PCNA_PIPBox_1 | 202 | 211 | PF02747 | 0.386 |
LIG_Pex14_2 | 183 | 187 | PF04695 | 0.527 |
LIG_Pex14_2 | 190 | 194 | PF04695 | 0.508 |
LIG_SH2_STAT5 | 162 | 165 | PF00017 | 0.604 |
LIG_SH3_2 | 231 | 236 | PF14604 | 0.459 |
LIG_SH3_3 | 12 | 18 | PF00018 | 0.483 |
LIG_SH3_3 | 228 | 234 | PF00018 | 0.583 |
LIG_SH3_3 | 235 | 241 | PF00018 | 0.572 |
LIG_SUMO_SIM_par_1 | 11 | 16 | PF11976 | 0.477 |
LIG_SUMO_SIM_par_1 | 76 | 83 | PF11976 | 0.496 |
MOD_CDK_SPK_2 | 234 | 239 | PF00069 | 0.571 |
MOD_CDK_SPxK_1 | 230 | 236 | PF00069 | 0.450 |
MOD_CK1_1 | 109 | 115 | PF00069 | 0.438 |
MOD_CK1_1 | 214 | 220 | PF00069 | 0.477 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.309 |
MOD_CK2_1 | 129 | 135 | PF00069 | 0.499 |
MOD_CK2_1 | 13 | 19 | PF00069 | 0.585 |
MOD_CK2_1 | 85 | 91 | PF00069 | 0.423 |
MOD_GlcNHglycan | 213 | 216 | PF01048 | 0.476 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.481 |
MOD_GlcNHglycan | 82 | 85 | PF01048 | 0.475 |
MOD_GlcNHglycan | 87 | 90 | PF01048 | 0.412 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.456 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.393 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.549 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.679 |
MOD_NEK2_1 | 106 | 111 | PF00069 | 0.428 |
MOD_NEK2_1 | 13 | 18 | PF00069 | 0.659 |
MOD_NEK2_1 | 140 | 145 | PF00069 | 0.428 |
MOD_NEK2_1 | 163 | 168 | PF00069 | 0.483 |
MOD_NEK2_2 | 134 | 139 | PF00069 | 0.320 |
MOD_PIKK_1 | 140 | 146 | PF00454 | 0.490 |
MOD_PIKK_1 | 163 | 169 | PF00454 | 0.498 |
MOD_PKA_2 | 129 | 135 | PF00069 | 0.499 |
MOD_PKA_2 | 54 | 60 | PF00069 | 0.439 |
MOD_Plk_1 | 106 | 112 | PF00069 | 0.473 |
MOD_Plk_1 | 134 | 140 | PF00069 | 0.488 |
MOD_Plk_1 | 174 | 180 | PF00069 | 0.489 |
MOD_Plk_1 | 28 | 34 | PF00069 | 0.505 |
MOD_Plk_4 | 82 | 88 | PF00069 | 0.309 |
MOD_ProDKin_1 | 230 | 236 | PF00069 | 0.647 |
MOD_ProDKin_1 | 24 | 30 | PF00069 | 0.553 |
MOD_SUMO_rev_2 | 119 | 127 | PF00179 | 0.507 |
MOD_SUMO_rev_2 | 153 | 158 | PF00179 | 0.548 |
MOD_SUMO_rev_2 | 200 | 205 | PF00179 | 0.474 |
TRG_DiLeu_BaLyEn_6 | 136 | 141 | PF01217 | 0.328 |
TRG_ENDOCYTIC_2 | 199 | 202 | PF00928 | 0.634 |
TRG_Pf-PMV_PEXEL_1 | 122 | 126 | PF00026 | 0.525 |
TRG_Pf-PMV_PEXEL_1 | 139 | 144 | PF00026 | 0.338 |
TRG_Pf-PMV_PEXEL_1 | 203 | 207 | PF00026 | 0.421 |
TRG_Pf-PMV_PEXEL_1 | 44 | 48 | PF00026 | 0.497 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WWW7 | Leishmania donovani | 92% | 100% |
A4HC21 | Leishmania braziliensis | 75% | 100% |
A4HZG4 | Leishmania infantum | 91% | 100% |
Q4QC25 | Leishmania major | 88% | 100% |