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: E9AVA4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 97 | 101 | PF00656 | 0.528 |
CLV_NRD_NRD_1 | 147 | 149 | PF00675 | 0.629 |
CLV_NRD_NRD_1 | 165 | 167 | PF00675 | 0.424 |
CLV_NRD_NRD_1 | 226 | 228 | PF00675 | 0.430 |
CLV_NRD_NRD_1 | 281 | 283 | PF00675 | 0.508 |
CLV_PCSK_FUR_1 | 145 | 149 | PF00082 | 0.600 |
CLV_PCSK_KEX2_1 | 147 | 149 | PF00082 | 0.592 |
CLV_PCSK_KEX2_1 | 165 | 167 | PF00082 | 0.405 |
CLV_PCSK_KEX2_1 | 226 | 228 | PF00082 | 0.430 |
CLV_PCSK_KEX2_1 | 281 | 283 | PF00082 | 0.508 |
CLV_PCSK_KEX2_1 | 63 | 65 | PF00082 | 0.632 |
CLV_PCSK_PC1ET2_1 | 63 | 65 | PF00082 | 0.632 |
CLV_PCSK_SKI1_1 | 166 | 170 | PF00082 | 0.479 |
CLV_PCSK_SKI1_1 | 226 | 230 | PF00082 | 0.446 |
CLV_PCSK_SKI1_1 | 46 | 50 | PF00082 | 0.469 |
DEG_APCC_DBOX_1 | 15 | 23 | PF00400 | 0.590 |
DEG_COP1_1 | 263 | 272 | PF00400 | 0.448 |
DEG_SPOP_SBC_1 | 108 | 112 | PF00917 | 0.517 |
DEG_SPOP_SBC_1 | 151 | 155 | PF00917 | 0.417 |
DEG_SPOP_SBC_1 | 93 | 97 | PF00917 | 0.623 |
DOC_CYCLIN_RxL_1 | 163 | 171 | PF00134 | 0.492 |
DOC_CYCLIN_RxL_1 | 41 | 53 | PF00134 | 0.459 |
DOC_MAPK_gen_1 | 226 | 233 | PF00069 | 0.442 |
DOC_MAPK_MEF2A_6 | 226 | 233 | PF00069 | 0.442 |
DOC_MAPK_RevD_3 | 47 | 62 | PF00069 | 0.530 |
DOC_PP4_FxxP_1 | 288 | 291 | PF00568 | 0.459 |
DOC_USP7_MATH_1 | 106 | 110 | PF00917 | 0.569 |
DOC_USP7_MATH_1 | 146 | 150 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 283 | 287 | PF00917 | 0.544 |
DOC_WW_Pin1_4 | 115 | 120 | PF00397 | 0.552 |
DOC_WW_Pin1_4 | 132 | 137 | PF00397 | 0.584 |
DOC_WW_Pin1_4 | 76 | 81 | PF00397 | 0.525 |
LIG_14-3-3_CanoR_1 | 11 | 16 | PF00244 | 0.544 |
LIG_14-3-3_CanoR_1 | 145 | 151 | PF00244 | 0.639 |
LIG_14-3-3_CanoR_1 | 282 | 291 | PF00244 | 0.437 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.587 |
LIG_BRCT_BRCA1_1 | 34 | 38 | PF00533 | 0.711 |
LIG_FHA_1 | 228 | 234 | PF00498 | 0.454 |
LIG_FHA_1 | 257 | 263 | PF00498 | 0.637 |
LIG_FHA_1 | 32 | 38 | PF00498 | 0.568 |
LIG_FHA_1 | 52 | 58 | PF00498 | 0.779 |
LIG_FHA_1 | 94 | 100 | PF00498 | 0.593 |
LIG_FHA_2 | 232 | 238 | PF00498 | 0.444 |
LIG_LIR_Apic_2 | 286 | 291 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 179 | 185 | PF02991 | 0.445 |
LIG_NRBOX | 224 | 230 | PF00104 | 0.503 |
LIG_SH2_CRK | 182 | 186 | PF00017 | 0.445 |
LIG_SH2_STAT3 | 250 | 253 | PF00017 | 0.457 |
LIG_SH2_STAT5 | 209 | 212 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 250 | 253 | PF00017 | 0.468 |
LIG_SH3_3 | 12 | 18 | PF00018 | 0.528 |
LIG_SH3_3 | 264 | 270 | PF00018 | 0.605 |
LIG_SUMO_SIM_par_1 | 47 | 54 | PF11976 | 0.582 |
LIG_SUMO_SIM_par_1 | 90 | 97 | PF11976 | 0.478 |
LIG_TRAF2_1 | 234 | 237 | PF00917 | 0.514 |
LIG_WRC_WIRS_1 | 285 | 290 | PF05994 | 0.447 |
MOD_CK1_1 | 109 | 115 | PF00069 | 0.740 |
MOD_CK1_1 | 27 | 33 | PF00069 | 0.628 |
MOD_CK1_1 | 50 | 56 | PF00069 | 0.745 |
MOD_CK1_1 | 66 | 72 | PF00069 | 0.693 |
MOD_CK2_1 | 231 | 237 | PF00069 | 0.446 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.387 |
MOD_GlcNHglycan | 26 | 29 | PF01048 | 0.560 |
MOD_GlcNHglycan | 262 | 265 | PF01048 | 0.446 |
MOD_GlcNHglycan | 87 | 90 | PF01048 | 0.602 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.665 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.600 |
MOD_GSK3_1 | 203 | 210 | PF00069 | 0.429 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.453 |
MOD_GSK3_1 | 256 | 263 | PF00069 | 0.433 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.523 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.728 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.581 |
MOD_LATS_1 | 9 | 15 | PF00433 | 0.475 |
MOD_NEK2_1 | 168 | 173 | PF00069 | 0.473 |
MOD_NEK2_1 | 202 | 207 | PF00069 | 0.448 |
MOD_NEK2_1 | 49 | 54 | PF00069 | 0.613 |
MOD_NEK2_1 | 83 | 88 | PF00069 | 0.595 |
MOD_PK_1 | 11 | 17 | PF00069 | 0.476 |
MOD_PKA_1 | 63 | 69 | PF00069 | 0.612 |
MOD_PKA_2 | 10 | 16 | PF00069 | 0.552 |
MOD_PKA_2 | 146 | 152 | PF00069 | 0.583 |
MOD_PKA_2 | 207 | 213 | PF00069 | 0.429 |
MOD_PKA_2 | 63 | 69 | PF00069 | 0.612 |
MOD_Plk_1 | 178 | 184 | PF00069 | 0.440 |
MOD_ProDKin_1 | 115 | 121 | PF00069 | 0.550 |
MOD_ProDKin_1 | 132 | 138 | PF00069 | 0.585 |
MOD_ProDKin_1 | 76 | 82 | PF00069 | 0.521 |
MOD_SUMO_for_1 | 176 | 179 | PF00179 | 0.498 |
TRG_DiLeu_BaEn_1 | 224 | 229 | PF01217 | 0.436 |
TRG_DiLeu_BaLyEn_6 | 53 | 58 | PF01217 | 0.528 |
TRG_DiLeu_LyEn_5 | 224 | 229 | PF01217 | 0.500 |
TRG_ENDOCYTIC_2 | 182 | 185 | PF00928 | 0.435 |
TRG_ENDOCYTIC_2 | 186 | 189 | PF00928 | 0.414 |
TRG_ENDOCYTIC_2 | 209 | 212 | PF00928 | 0.424 |
TRG_ER_diArg_1 | 145 | 148 | PF00400 | 0.605 |
TRG_ER_diArg_1 | 164 | 166 | PF00400 | 0.366 |
TRG_ER_diArg_1 | 225 | 227 | PF00400 | 0.439 |
TRG_NLS_MonoCore_2 | 60 | 65 | PF00514 | 0.571 |
TRG_NLS_MonoExtN_4 | 61 | 66 | PF00514 | 0.572 |
TRG_Pf-PMV_PEXEL_1 | 166 | 170 | PF00026 | 0.494 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P384 | Leptomonas seymouri | 45% | 100% |
A0A3S7WWL4 | Leishmania donovani | 88% | 100% |
A4HBX6 | Leishmania braziliensis | 75% | 99% |
A4HZ96 | Leishmania infantum | 88% | 100% |
Q4QC76 | Leishmania major | 87% | 100% |