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: Q4Q8P1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 183 | 187 | PF00656 | 0.611 |
CLV_C14_Caspase3-7 | 72 | 76 | PF00656 | 0.699 |
CLV_NRD_NRD_1 | 164 | 166 | PF00675 | 0.673 |
CLV_NRD_NRD_1 | 2 | 4 | PF00675 | 0.697 |
CLV_NRD_NRD_1 | 212 | 214 | PF00675 | 0.611 |
CLV_NRD_NRD_1 | 60 | 62 | PF00675 | 0.524 |
CLV_PCSK_KEX2_1 | 138 | 140 | PF00082 | 0.568 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.697 |
CLV_PCSK_KEX2_1 | 60 | 62 | PF00082 | 0.524 |
CLV_PCSK_PC1ET2_1 | 138 | 140 | PF00082 | 0.568 |
CLV_PCSK_PC1ET2_1 | 2 | 4 | PF00082 | 0.697 |
CLV_PCSK_SKI1_1 | 49 | 53 | PF00082 | 0.614 |
CLV_PCSK_SKI1_1 | 61 | 65 | PF00082 | 0.454 |
DEG_COP1_1 | 152 | 162 | PF00400 | 0.568 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.699 |
DOC_CKS1_1 | 198 | 203 | PF01111 | 0.550 |
DOC_MAPK_gen_1 | 165 | 172 | PF00069 | 0.640 |
DOC_USP7_MATH_1 | 181 | 185 | PF00917 | 0.667 |
DOC_USP7_MATH_1 | 28 | 32 | PF00917 | 0.541 |
DOC_USP7_MATH_1 | 42 | 46 | PF00917 | 0.497 |
DOC_USP7_MATH_1 | 63 | 67 | PF00917 | 0.462 |
DOC_WW_Pin1_4 | 116 | 121 | PF00397 | 0.642 |
DOC_WW_Pin1_4 | 144 | 149 | PF00397 | 0.649 |
DOC_WW_Pin1_4 | 174 | 179 | PF00397 | 0.658 |
DOC_WW_Pin1_4 | 185 | 190 | PF00397 | 0.581 |
DOC_WW_Pin1_4 | 197 | 202 | PF00397 | 0.431 |
LIG_14-3-3_CanoR_1 | 165 | 171 | PF00244 | 0.627 |
LIG_Actin_WH2_2 | 125 | 143 | PF00022 | 0.404 |
LIG_APCC_ABBA_1 | 109 | 114 | PF00400 | 0.692 |
LIG_BIR_III_2 | 117 | 121 | PF00653 | 0.717 |
LIG_BIR_III_4 | 95 | 99 | PF00653 | 0.689 |
LIG_CtBP_PxDLS_1 | 21 | 25 | PF00389 | 0.538 |
LIG_eIF4E_1 | 198 | 204 | PF01652 | 0.520 |
LIG_FHA_1 | 198 | 204 | PF00498 | 0.520 |
LIG_FHA_1 | 32 | 38 | PF00498 | 0.506 |
LIG_FHA_2 | 28 | 34 | PF00498 | 0.647 |
LIG_FHA_2 | 70 | 76 | PF00498 | 0.682 |
LIG_LIR_Nem_3 | 108 | 112 | PF02991 | 0.727 |
LIG_LIR_Nem_3 | 188 | 194 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 238 | 244 | PF02991 | 0.623 |
LIG_LYPXL_S_1 | 190 | 194 | PF13949 | 0.500 |
LIG_LYPXL_yS_3 | 191 | 194 | PF13949 | 0.493 |
LIG_PDZ_Class_1 | 247 | 252 | PF00595 | 0.490 |
LIG_SH3_3 | 169 | 175 | PF00018 | 0.624 |
LIG_SH3_3 | 186 | 192 | PF00018 | 0.506 |
LIG_SH3_3 | 225 | 231 | PF00018 | 0.558 |
LIG_SH3_3 | 8 | 14 | PF00018 | 0.759 |
LIG_SUMO_SIM_anti_2 | 79 | 85 | PF11976 | 0.593 |
LIG_SUMO_SIM_par_1 | 230 | 236 | PF11976 | 0.661 |
LIG_WRC_WIRS_1 | 106 | 111 | PF05994 | 0.722 |
MOD_CDC14_SPxK_1 | 147 | 150 | PF00782 | 0.687 |
MOD_CDK_SPxK_1 | 144 | 150 | PF00069 | 0.657 |
MOD_CK1_1 | 233 | 239 | PF00069 | 0.563 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.516 |
MOD_CK1_1 | 71 | 77 | PF00069 | 0.692 |
MOD_CK2_1 | 116 | 122 | PF00069 | 0.642 |
MOD_CK2_1 | 221 | 227 | PF00069 | 0.615 |
MOD_CK2_1 | 27 | 33 | PF00069 | 0.641 |
MOD_CK2_1 | 63 | 69 | PF00069 | 0.583 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.495 |
MOD_GlcNHglycan | 222 | 226 | PF01048 | 0.718 |
MOD_GlcNHglycan | 235 | 238 | PF01048 | 0.593 |
MOD_GlcNHglycan | 30 | 33 | PF01048 | 0.564 |
MOD_GlcNHglycan | 44 | 47 | PF01048 | 0.504 |
MOD_GSK3_1 | 181 | 188 | PF00069 | 0.541 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.564 |
MOD_PK_1 | 166 | 172 | PF00069 | 0.517 |
MOD_PKA_2 | 152 | 158 | PF00069 | 0.665 |
MOD_Plk_1 | 68 | 74 | PF00069 | 0.698 |
MOD_Plk_1 | 79 | 85 | PF00069 | 0.572 |
MOD_Plk_2-3 | 69 | 75 | PF00069 | 0.679 |
MOD_Plk_4 | 102 | 108 | PF00069 | 0.678 |
MOD_Plk_4 | 127 | 133 | PF00069 | 0.620 |
MOD_Plk_4 | 166 | 172 | PF00069 | 0.741 |
MOD_Plk_4 | 244 | 250 | PF00069 | 0.651 |
MOD_Plk_4 | 31 | 37 | PF00069 | 0.516 |
MOD_ProDKin_1 | 116 | 122 | PF00069 | 0.642 |
MOD_ProDKin_1 | 144 | 150 | PF00069 | 0.657 |
MOD_ProDKin_1 | 174 | 180 | PF00069 | 0.653 |
MOD_ProDKin_1 | 185 | 191 | PF00069 | 0.573 |
MOD_ProDKin_1 | 197 | 203 | PF00069 | 0.426 |
MOD_SUMO_rev_2 | 161 | 168 | PF00179 | 0.676 |
TRG_DiLeu_BaEn_1 | 22 | 27 | PF01217 | 0.521 |
TRG_DiLeu_BaLyEn_6 | 239 | 244 | PF01217 | 0.642 |
TRG_ENDOCYTIC_2 | 191 | 194 | PF00928 | 0.493 |
TRG_ER_diArg_1 | 59 | 61 | PF00400 | 0.507 |
TRG_NLS_MonoExtC_3 | 212 | 218 | PF00514 | 0.595 |
TRG_Pf-PMV_PEXEL_1 | 49 | 53 | PF00026 | 0.550 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7G9 | Leptomonas seymouri | 46% | 96% |
A0A3S7X157 | Leishmania donovani | 89% | 100% |
A4HG70 | Leishmania braziliensis | 73% | 100% |
A4I3B3 | Leishmania infantum | 90% | 100% |
E9AZJ0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |