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: A4I396
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 250 | 252 | PF00675 | 0.754 |
CLV_PCSK_KEX2_1 | 249 | 251 | PF00082 | 0.757 |
CLV_PCSK_KEX2_1 | 301 | 303 | PF00082 | 0.610 |
CLV_PCSK_PC1ET2_1 | 301 | 303 | PF00082 | 0.610 |
CLV_Separin_Metazoa | 246 | 250 | PF03568 | 0.580 |
DOC_CKS1_1 | 15 | 20 | PF01111 | 0.778 |
DOC_USP7_MATH_1 | 174 | 178 | PF00917 | 0.666 |
DOC_USP7_MATH_1 | 199 | 203 | PF00917 | 0.720 |
DOC_USP7_MATH_1 | 97 | 101 | PF00917 | 0.828 |
DOC_WW_Pin1_4 | 100 | 105 | PF00397 | 0.742 |
DOC_WW_Pin1_4 | 137 | 142 | PF00397 | 0.720 |
DOC_WW_Pin1_4 | 14 | 19 | PF00397 | 0.807 |
DOC_WW_Pin1_4 | 28 | 33 | PF00397 | 0.672 |
LIG_14-3-3_CanoR_1 | 175 | 183 | PF00244 | 0.640 |
LIG_14-3-3_CanoR_1 | 215 | 220 | PF00244 | 0.820 |
LIG_14-3-3_CanoR_1 | 262 | 269 | PF00244 | 0.571 |
LIG_14-3-3_CanoR_1 | 69 | 79 | PF00244 | 0.762 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.780 |
LIG_BIR_III_4 | 121 | 125 | PF00653 | 0.611 |
LIG_BRCT_BRCA1_1 | 309 | 313 | PF00533 | 0.704 |
LIG_FHA_1 | 153 | 159 | PF00498 | 0.716 |
LIG_FHA_1 | 216 | 222 | PF00498 | 0.704 |
LIG_FHA_1 | 243 | 249 | PF00498 | 0.763 |
LIG_FHA_1 | 29 | 35 | PF00498 | 0.855 |
LIG_FHA_1 | 41 | 47 | PF00498 | 0.713 |
LIG_FHA_1 | 56 | 62 | PF00498 | 0.714 |
LIG_FHA_2 | 131 | 137 | PF00498 | 0.725 |
LIG_FHA_2 | 6 | 12 | PF00498 | 0.789 |
LIG_FXI_DFP_1 | 321 | 325 | PF00024 | 0.695 |
LIG_LIR_Gen_1 | 146 | 154 | PF02991 | 0.641 |
LIG_LIR_Gen_1 | 76 | 84 | PF02991 | 0.847 |
LIG_LIR_Nem_3 | 146 | 152 | PF02991 | 0.645 |
LIG_LIR_Nem_3 | 291 | 296 | PF02991 | 0.606 |
LIG_LIR_Nem_3 | 76 | 81 | PF02991 | 0.848 |
LIG_PDZ_Class_2 | 323 | 328 | PF00595 | 0.777 |
LIG_Pex14_2 | 276 | 280 | PF04695 | 0.501 |
LIG_Pex14_2 | 320 | 324 | PF04695 | 0.766 |
LIG_SH2_CRK | 149 | 153 | PF00017 | 0.722 |
LIG_SH2_STAT5 | 149 | 152 | PF00017 | 0.724 |
LIG_SH3_3 | 105 | 111 | PF00018 | 0.834 |
LIG_SH3_3 | 136 | 142 | PF00018 | 0.718 |
LIG_SUMO_SIM_par_1 | 224 | 232 | PF11976 | 0.692 |
LIG_TRAF2_1 | 133 | 136 | PF00917 | 0.839 |
LIG_TRAF2_1 | 143 | 146 | PF00917 | 0.675 |
LIG_TRAF2_1 | 154 | 157 | PF00917 | 0.609 |
LIG_TRAF2_1 | 268 | 271 | PF00917 | 0.714 |
LIG_TRAF2_1 | 60 | 63 | PF00917 | 0.644 |
MOD_CDK_SPxxK_3 | 14 | 21 | PF00069 | 0.780 |
MOD_CDK_SPxxK_3 | 28 | 35 | PF00069 | 0.601 |
MOD_CK1_1 | 100 | 106 | PF00069 | 0.766 |
MOD_CK1_1 | 193 | 199 | PF00069 | 0.806 |
MOD_CK1_1 | 225 | 231 | PF00069 | 0.814 |
MOD_CK1_1 | 71 | 77 | PF00069 | 0.698 |
MOD_CK2_1 | 130 | 136 | PF00069 | 0.693 |
MOD_CK2_1 | 174 | 180 | PF00069 | 0.676 |
MOD_CK2_1 | 225 | 231 | PF00069 | 0.739 |
MOD_CK2_1 | 5 | 11 | PF00069 | 0.788 |
MOD_CK2_1 | 57 | 63 | PF00069 | 0.749 |
MOD_CK2_1 | 70 | 76 | PF00069 | 0.693 |
MOD_CK2_1 | 87 | 93 | PF00069 | 0.780 |
MOD_GlcNHglycan | 159 | 163 | PF01048 | 0.814 |
MOD_GlcNHglycan | 288 | 291 | PF01048 | 0.663 |
MOD_GlcNHglycan | 44 | 49 | PF01048 | 0.733 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.718 |
MOD_GlcNHglycan | 98 | 102 | PF01048 | 0.806 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.645 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.684 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.745 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.724 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.768 |
MOD_N-GLC_1 | 55 | 60 | PF02516 | 0.760 |
MOD_NEK2_1 | 307 | 312 | PF00069 | 0.630 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.832 |
MOD_PIKK_1 | 130 | 136 | PF00454 | 0.715 |
MOD_PIKK_1 | 147 | 153 | PF00454 | 0.691 |
MOD_PIKK_1 | 210 | 216 | PF00454 | 0.801 |
MOD_PIKK_1 | 68 | 74 | PF00454 | 0.763 |
MOD_PKA_2 | 174 | 180 | PF00069 | 0.676 |
MOD_PKA_2 | 261 | 267 | PF00069 | 0.590 |
MOD_PKA_2 | 68 | 74 | PF00069 | 0.763 |
MOD_PKB_1 | 35 | 43 | PF00069 | 0.777 |
MOD_Plk_1 | 124 | 130 | PF00069 | 0.803 |
MOD_Plk_1 | 158 | 164 | PF00069 | 0.737 |
MOD_Plk_1 | 37 | 43 | PF00069 | 0.851 |
MOD_Plk_4 | 190 | 196 | PF00069 | 0.636 |
MOD_Plk_4 | 204 | 210 | PF00069 | 0.573 |
MOD_Plk_4 | 222 | 228 | PF00069 | 0.509 |
MOD_Plk_4 | 37 | 43 | PF00069 | 0.777 |
MOD_Plk_4 | 46 | 52 | PF00069 | 0.667 |
MOD_Plk_4 | 74 | 80 | PF00069 | 0.685 |
MOD_ProDKin_1 | 100 | 106 | PF00069 | 0.739 |
MOD_ProDKin_1 | 137 | 143 | PF00069 | 0.719 |
MOD_ProDKin_1 | 14 | 20 | PF00069 | 0.804 |
MOD_ProDKin_1 | 28 | 34 | PF00069 | 0.672 |
TRG_DiLeu_BaEn_1 | 159 | 164 | PF01217 | 0.649 |
TRG_DiLeu_BaLyEn_6 | 162 | 167 | PF01217 | 0.781 |
TRG_ENDOCYTIC_2 | 149 | 152 | PF00928 | 0.646 |
TRG_ER_diArg_1 | 248 | 251 | PF00400 | 0.748 |
TRG_ER_diArg_1 | 34 | 37 | PF00400 | 0.741 |
TRG_Pf-PMV_PEXEL_1 | 251 | 255 | PF00026 | 0.749 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IHW6 | Leishmania donovani | 99% | 100% |
A4HG64 | Leishmania braziliensis | 55% | 100% |
E9AZI4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
Q4Q8P7 | Leishmania major | 88% | 100% |