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: O97195
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 278 | 282 | PF00656 | 0.607 |
CLV_C14_Caspase3-7 | 3 | 7 | PF00656 | 0.567 |
CLV_NRD_NRD_1 | 193 | 195 | PF00675 | 0.615 |
CLV_NRD_NRD_1 | 32 | 34 | PF00675 | 0.726 |
CLV_PCSK_KEX2_1 | 14 | 16 | PF00082 | 0.631 |
CLV_PCSK_KEX2_1 | 193 | 195 | PF00082 | 0.607 |
CLV_PCSK_PC1ET2_1 | 14 | 16 | PF00082 | 0.782 |
CLV_PCSK_SKI1_1 | 168 | 172 | PF00082 | 0.616 |
CLV_PCSK_SKI1_1 | 181 | 185 | PF00082 | 0.462 |
CLV_PCSK_SKI1_1 | 194 | 198 | PF00082 | 0.481 |
DOC_PP2B_LxvP_1 | 116 | 119 | PF13499 | 0.588 |
DOC_USP7_MATH_1 | 125 | 129 | PF00917 | 0.754 |
DOC_USP7_MATH_1 | 141 | 145 | PF00917 | 0.710 |
DOC_USP7_MATH_1 | 218 | 222 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 232 | 236 | PF00917 | 0.742 |
DOC_USP7_MATH_1 | 238 | 242 | PF00917 | 0.716 |
DOC_USP7_MATH_1 | 272 | 276 | PF00917 | 0.742 |
DOC_USP7_MATH_1 | 67 | 71 | PF00917 | 0.759 |
DOC_USP7_MATH_1 | 72 | 76 | PF00917 | 0.805 |
DOC_USP7_UBL2_3 | 34 | 38 | PF12436 | 0.709 |
DOC_WW_Pin1_4 | 1 | 6 | PF00397 | 0.696 |
DOC_WW_Pin1_4 | 102 | 107 | PF00397 | 0.721 |
DOC_WW_Pin1_4 | 268 | 273 | PF00397 | 0.814 |
LIG_14-3-3_CanoR_1 | 193 | 199 | PF00244 | 0.618 |
LIG_14-3-3_CanoR_1 | 94 | 98 | PF00244 | 0.768 |
LIG_14-3-3_CanoR_1 | 99 | 106 | PF00244 | 0.800 |
LIG_AP2alpha_2 | 55 | 57 | PF02296 | 0.656 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.706 |
LIG_CtBP_PxDLS_1 | 213 | 217 | PF00389 | 0.546 |
LIG_deltaCOP1_diTrp_1 | 55 | 60 | PF00928 | 0.691 |
LIG_FHA_1 | 290 | 296 | PF00498 | 0.701 |
LIG_FXI_DFP_1 | 57 | 61 | PF00024 | 0.669 |
LIG_HCF-1_HBM_1 | 149 | 152 | PF13415 | 0.552 |
LIG_LIR_Gen_1 | 55 | 62 | PF02991 | 0.779 |
LIG_LIR_Nem_3 | 148 | 154 | PF02991 | 0.705 |
LIG_LIR_Nem_3 | 55 | 60 | PF02991 | 0.684 |
LIG_PTAP_UEV_1 | 254 | 259 | PF05743 | 0.714 |
LIG_SH2_STAT5 | 152 | 155 | PF00017 | 0.708 |
LIG_SH2_STAT5 | 21 | 24 | PF00017 | 0.574 |
LIG_SH3_1 | 252 | 258 | PF00018 | 0.754 |
LIG_SH3_3 | 2 | 8 | PF00018 | 0.724 |
LIG_SH3_3 | 252 | 258 | PF00018 | 0.824 |
LIG_SH3_3 | 266 | 272 | PF00018 | 0.731 |
LIG_SH3_3 | 50 | 56 | PF00018 | 0.672 |
LIG_SH3_4 | 34 | 41 | PF00018 | 0.689 |
LIG_TRAF2_1 | 217 | 220 | PF00917 | 0.696 |
LIG_WW_1 | 18 | 21 | PF00397 | 0.592 |
LIG_WW_3 | 51 | 55 | PF00397 | 0.770 |
MOD_CDK_SPK_2 | 268 | 273 | PF00069 | 0.742 |
MOD_CDK_SPxxK_3 | 102 | 109 | PF00069 | 0.781 |
MOD_CK1_1 | 105 | 111 | PF00069 | 0.767 |
MOD_CK1_1 | 282 | 288 | PF00069 | 0.696 |
MOD_CK1_1 | 98 | 104 | PF00069 | 0.745 |
MOD_CK2_1 | 141 | 147 | PF00069 | 0.734 |
MOD_CK2_1 | 159 | 165 | PF00069 | 0.566 |
MOD_GlcNHglycan | 113 | 116 | PF01048 | 0.655 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.622 |
MOD_GlcNHglycan | 219 | 223 | PF01048 | 0.674 |
MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.794 |
MOD_GlcNHglycan | 255 | 258 | PF01048 | 0.743 |
MOD_GlcNHglycan | 70 | 73 | PF01048 | 0.709 |
MOD_GlcNHglycan | 74 | 77 | PF01048 | 0.696 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.796 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.579 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.682 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.656 |
MOD_GSK3_1 | 268 | 275 | PF00069 | 0.807 |
MOD_GSK3_1 | 279 | 286 | PF00069 | 0.635 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.756 |
MOD_GSK3_1 | 89 | 96 | PF00069 | 0.790 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.717 |
MOD_LATS_1 | 107 | 113 | PF00433 | 0.747 |
MOD_LATS_1 | 27 | 33 | PF00433 | 0.753 |
MOD_NEK2_1 | 279 | 284 | PF00069 | 0.700 |
MOD_PIKK_1 | 125 | 131 | PF00454 | 0.599 |
MOD_PIKK_1 | 184 | 190 | PF00454 | 0.640 |
MOD_PIKK_1 | 74 | 80 | PF00454 | 0.841 |
MOD_PK_1 | 109 | 115 | PF00069 | 0.749 |
MOD_PKA_2 | 243 | 249 | PF00069 | 0.711 |
MOD_PKA_2 | 272 | 278 | PF00069 | 0.724 |
MOD_PKA_2 | 93 | 99 | PF00069 | 0.766 |
MOD_Plk_1 | 238 | 244 | PF00069 | 0.745 |
MOD_Plk_4 | 194 | 200 | PF00069 | 0.610 |
MOD_ProDKin_1 | 1 | 7 | PF00069 | 0.690 |
MOD_ProDKin_1 | 102 | 108 | PF00069 | 0.721 |
MOD_ProDKin_1 | 268 | 274 | PF00069 | 0.816 |
TRG_ENDOCYTIC_2 | 151 | 154 | PF00928 | 0.706 |
TRG_ER_diArg_1 | 193 | 195 | PF00400 | 0.622 |
TRG_ER_diArg_1 | 199 | 202 | PF00400 | 0.599 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IIT4 | Leptomonas seymouri | 37% | 93% |
A0A3S5H5F0 | Leishmania donovani | 90% | 100% |
A4H428 | Leishmania braziliensis | 58% | 99% |
A4HSB2 | Leishmania infantum | 90% | 100% |
E9AK95 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 84% |