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: Q4QCV5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 139 | 143 | PF00656 | 0.605 |
CLV_C14_Caspase3-7 | 259 | 263 | PF00656 | 0.681 |
CLV_NRD_NRD_1 | 75 | 77 | PF00675 | 0.472 |
CLV_PCSK_KEX2_1 | 103 | 105 | PF00082 | 0.451 |
CLV_PCSK_KEX2_1 | 75 | 77 | PF00082 | 0.472 |
CLV_PCSK_KEX2_1 | 84 | 86 | PF00082 | 0.422 |
CLV_PCSK_PC1ET2_1 | 103 | 105 | PF00082 | 0.365 |
CLV_PCSK_PC1ET2_1 | 84 | 86 | PF00082 | 0.488 |
CLV_PCSK_SKI1_1 | 81 | 85 | PF00082 | 0.469 |
DEG_APCC_DBOX_1 | 84 | 92 | PF00400 | 0.427 |
DEG_SPOP_SBC_1 | 179 | 183 | PF00917 | 0.692 |
DEG_SPOP_SBC_1 | 256 | 260 | PF00917 | 0.646 |
DOC_ANK_TNKS_1 | 198 | 205 | PF00023 | 0.573 |
DOC_MAPK_MEF2A_6 | 55 | 62 | PF00069 | 0.500 |
DOC_USP7_MATH_1 | 137 | 141 | PF00917 | 0.660 |
DOC_USP7_MATH_1 | 155 | 159 | PF00917 | 0.482 |
DOC_USP7_MATH_1 | 179 | 183 | PF00917 | 0.685 |
DOC_USP7_MATH_1 | 192 | 196 | PF00917 | 0.569 |
DOC_USP7_MATH_1 | 256 | 260 | PF00917 | 0.651 |
DOC_USP7_UBL2_3 | 235 | 239 | PF12436 | 0.558 |
DOC_WW_Pin1_4 | 107 | 112 | PF00397 | 0.528 |
DOC_WW_Pin1_4 | 181 | 186 | PF00397 | 0.636 |
DOC_WW_Pin1_4 | 252 | 257 | PF00397 | 0.678 |
LIG_14-3-3_CanoR_1 | 177 | 185 | PF00244 | 0.621 |
LIG_14-3-3_CanoR_1 | 31 | 40 | PF00244 | 0.539 |
LIG_FHA_1 | 111 | 117 | PF00498 | 0.526 |
LIG_FHA_1 | 267 | 273 | PF00498 | 0.659 |
LIG_LIR_Gen_1 | 26 | 34 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 26 | 30 | PF02991 | 0.465 |
LIG_SH2_CRK | 80 | 84 | PF00017 | 0.458 |
LIG_SH2_STAT3 | 109 | 112 | PF00017 | 0.494 |
LIG_SH2_STAT3 | 69 | 72 | PF00017 | 0.440 |
LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 78 | 81 | PF00017 | 0.455 |
LIG_SH3_3 | 159 | 165 | PF00018 | 0.606 |
LIG_SH3_3 | 182 | 188 | PF00018 | 0.661 |
LIG_SUMO_SIM_par_1 | 58 | 65 | PF11976 | 0.483 |
LIG_WRC_WIRS_1 | 24 | 29 | PF05994 | 0.460 |
MOD_CDC14_SPxK_1 | 184 | 187 | PF00782 | 0.639 |
MOD_CDK_SPxK_1 | 181 | 187 | PF00069 | 0.639 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.620 |
MOD_CK1_1 | 178 | 184 | PF00069 | 0.685 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.610 |
MOD_CK1_1 | 255 | 261 | PF00069 | 0.700 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.512 |
MOD_CK1_1 | 61 | 67 | PF00069 | 0.491 |
MOD_CK2_1 | 141 | 147 | PF00069 | 0.729 |
MOD_CK2_1 | 192 | 198 | PF00069 | 0.633 |
MOD_CK2_1 | 7 | 13 | PF00069 | 0.491 |
MOD_GlcNHglycan | 132 | 136 | PF01048 | 0.643 |
MOD_GlcNHglycan | 173 | 176 | PF01048 | 0.679 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.685 |
MOD_GlcNHglycan | 194 | 197 | PF01048 | 0.524 |
MOD_GlcNHglycan | 269 | 272 | PF01048 | 0.750 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.622 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.564 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.635 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.675 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.630 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.639 |
MOD_GSK3_1 | 252 | 259 | PF00069 | 0.634 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.588 |
MOD_N-GLC_1 | 116 | 121 | PF02516 | 0.474 |
MOD_N-GLC_1 | 175 | 180 | PF02516 | 0.679 |
MOD_N-GLC_2 | 154 | 156 | PF02516 | 0.533 |
MOD_NEK2_1 | 116 | 121 | PF00069 | 0.553 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.646 |
MOD_NEK2_1 | 25 | 30 | PF00069 | 0.523 |
MOD_PIKK_1 | 225 | 231 | PF00454 | 0.642 |
MOD_PIKK_1 | 238 | 244 | PF00454 | 0.545 |
MOD_PIKK_1 | 68 | 74 | PF00454 | 0.468 |
MOD_PKA_2 | 121 | 127 | PF00069 | 0.576 |
MOD_Plk_1 | 116 | 122 | PF00069 | 0.512 |
MOD_Plk_1 | 40 | 46 | PF00069 | 0.444 |
MOD_Plk_4 | 116 | 122 | PF00069 | 0.530 |
MOD_Plk_4 | 58 | 64 | PF00069 | 0.478 |
MOD_ProDKin_1 | 107 | 113 | PF00069 | 0.529 |
MOD_ProDKin_1 | 181 | 187 | PF00069 | 0.639 |
MOD_ProDKin_1 | 252 | 258 | PF00069 | 0.679 |
MOD_SUMO_for_1 | 272 | 275 | PF00179 | 0.530 |
MOD_SUMO_for_1 | 83 | 86 | PF00179 | 0.477 |
TRG_DiLeu_BaLyEn_6 | 17 | 22 | PF01217 | 0.458 |
TRG_DiLeu_BaLyEn_6 | 55 | 60 | PF01217 | 0.511 |
TRG_ENDOCYTIC_2 | 24 | 27 | PF00928 | 0.446 |
TRG_ENDOCYTIC_2 | 80 | 83 | PF00928 | 0.515 |
TRG_ER_diArg_1 | 29 | 32 | PF00400 | 0.466 |
TRG_ER_diArg_1 | 75 | 77 | PF00400 | 0.472 |
TRG_ER_diArg_1 | 94 | 97 | PF00400 | 0.311 |
TRG_NLS_MonoExtN_4 | 100 | 107 | PF00514 | 0.485 |
TRG_Pf-PMV_PEXEL_1 | 97 | 101 | PF00026 | 0.489 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IBK6 | Leishmania donovani | 87% | 100% |
A4HYT3 | Leishmania infantum | 87% | 100% |
E9AIE2 | Leishmania braziliensis | 66% | 100% |
E9AUM9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 77% | 100% |