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: 4 |
NetGPI | no | yes: 0, no: 4 |
Related structures:
AlphaFold database: A4IE24
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 162 | 164 | PF00675 | 0.654 |
CLV_NRD_NRD_1 | 232 | 234 | PF00675 | 0.782 |
CLV_NRD_NRD_1 | 307 | 309 | PF00675 | 0.651 |
CLV_NRD_NRD_1 | 4 | 6 | PF00675 | 0.729 |
CLV_PCSK_KEX2_1 | 162 | 164 | PF00082 | 0.654 |
CLV_PCSK_KEX2_1 | 27 | 29 | PF00082 | 0.785 |
CLV_PCSK_KEX2_1 | 4 | 6 | PF00082 | 0.792 |
CLV_PCSK_PC1ET2_1 | 27 | 29 | PF00082 | 0.785 |
CLV_PCSK_SKI1_1 | 127 | 131 | PF00082 | 0.566 |
DEG_COP1_1 | 53 | 63 | PF00400 | 0.803 |
DEG_SCF_FBW7_1 | 29 | 34 | PF00400 | 0.767 |
DOC_CKS1_1 | 7 | 12 | PF01111 | 0.660 |
DOC_MAPK_gen_1 | 308 | 315 | PF00069 | 0.721 |
DOC_MAPK_MEF2A_6 | 308 | 315 | PF00069 | 0.601 |
DOC_MAPK_RevD_3 | 218 | 234 | PF00069 | 0.767 |
DOC_PP1_RVXF_1 | 314 | 321 | PF00149 | 0.625 |
DOC_PP4_FxxP_1 | 252 | 255 | PF00568 | 0.648 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.782 |
DOC_USP7_MATH_1 | 19 | 23 | PF00917 | 0.683 |
DOC_USP7_MATH_1 | 221 | 225 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 241 | 245 | PF00917 | 0.533 |
DOC_USP7_MATH_1 | 271 | 275 | PF00917 | 0.723 |
DOC_USP7_MATH_1 | 83 | 87 | PF00917 | 0.728 |
DOC_WW_Pin1_4 | 27 | 32 | PF00397 | 0.779 |
DOC_WW_Pin1_4 | 6 | 11 | PF00397 | 0.723 |
LIG_14-3-3_CanoR_1 | 127 | 132 | PF00244 | 0.652 |
LIG_14-3-3_CanoR_1 | 142 | 150 | PF00244 | 0.423 |
LIG_14-3-3_CanoR_1 | 201 | 209 | PF00244 | 0.611 |
LIG_14-3-3_CanoR_1 | 88 | 97 | PF00244 | 0.552 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.802 |
LIG_BIR_III_4 | 69 | 73 | PF00653 | 0.730 |
LIG_CaM_IQ_9 | 101 | 116 | PF13499 | 0.640 |
LIG_FHA_1 | 28 | 34 | PF00498 | 0.771 |
LIG_FHA_1 | 310 | 316 | PF00498 | 0.736 |
LIG_FHA_1 | 76 | 82 | PF00498 | 0.590 |
LIG_GBD_Chelix_1 | 178 | 186 | PF00786 | 0.581 |
LIG_Integrin_isoDGR_2 | 189 | 191 | PF01839 | 0.609 |
LIG_LIR_Gen_1 | 206 | 216 | PF02991 | 0.612 |
LIG_LIR_Nem_3 | 206 | 212 | PF02991 | 0.614 |
LIG_NRBOX | 114 | 120 | PF00104 | 0.638 |
LIG_PCNA_PIPBox_1 | 169 | 178 | PF02747 | 0.623 |
LIG_PCNA_yPIPBox_3 | 106 | 119 | PF02747 | 0.638 |
LIG_PCNA_yPIPBox_3 | 162 | 176 | PF02747 | 0.628 |
LIG_Pex14_2 | 248 | 252 | PF04695 | 0.656 |
LIG_PTAP_UEV_1 | 254 | 259 | PF05743 | 0.702 |
LIG_SH2_NCK_1 | 209 | 213 | PF00017 | 0.726 |
LIG_SH2_STAP1 | 209 | 213 | PF00017 | 0.726 |
LIG_SH2_STAP1 | 283 | 287 | PF00017 | 0.719 |
LIG_SH2_STAT5 | 283 | 286 | PF00017 | 0.651 |
LIG_SH3_1 | 234 | 240 | PF00018 | 0.649 |
LIG_SH3_3 | 217 | 223 | PF00018 | 0.749 |
LIG_SH3_3 | 234 | 240 | PF00018 | 0.506 |
LIG_SH3_3 | 252 | 258 | PF00018 | 0.597 |
LIG_SUMO_SIM_par_1 | 8 | 15 | PF11976 | 0.660 |
LIG_TRAF2_1 | 167 | 170 | PF00917 | 0.630 |
LIG_WRC_WIRS_1 | 212 | 217 | PF05994 | 0.724 |
LIG_WRC_WIRS_1 | 33 | 38 | PF05994 | 0.764 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.787 |
MOD_CK1_1 | 200 | 206 | PF00069 | 0.614 |
MOD_CK1_1 | 22 | 28 | PF00069 | 0.683 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.583 |
MOD_CK1_1 | 256 | 262 | PF00069 | 0.742 |
MOD_CK1_1 | 43 | 49 | PF00069 | 0.728 |
MOD_CK1_1 | 86 | 92 | PF00069 | 0.702 |
MOD_GlcNHglycan | 115 | 118 | PF01048 | 0.634 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.784 |
MOD_GlcNHglycan | 204 | 208 | PF01048 | 0.715 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.613 |
MOD_GlcNHglycan | 245 | 248 | PF01048 | 0.640 |
MOD_GlcNHglycan | 255 | 258 | PF01048 | 0.581 |
MOD_GlcNHglycan | 259 | 262 | PF01048 | 0.537 |
MOD_GlcNHglycan | 267 | 270 | PF01048 | 0.629 |
MOD_GlcNHglycan | 273 | 276 | PF01048 | 0.543 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.698 |
MOD_GSK3_1 | 11 | 18 | PF00069 | 0.772 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.653 |
MOD_GSK3_1 | 203 | 210 | PF00069 | 0.734 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.698 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.506 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.557 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.642 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.527 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.644 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.505 |
MOD_NEK2_1 | 168 | 173 | PF00069 | 0.618 |
MOD_NEK2_1 | 197 | 202 | PF00069 | 0.752 |
MOD_NEK2_1 | 40 | 45 | PF00069 | 0.652 |
MOD_NEK2_1 | 97 | 102 | PF00069 | 0.650 |
MOD_NEK2_2 | 83 | 88 | PF00069 | 0.602 |
MOD_PIKK_1 | 142 | 148 | PF00454 | 0.659 |
MOD_PIKK_1 | 71 | 77 | PF00454 | 0.776 |
MOD_PIKK_1 | 92 | 98 | PF00454 | 0.666 |
MOD_PIKK_1 | 99 | 105 | PF00454 | 0.534 |
MOD_PKA_1 | 309 | 315 | PF00069 | 0.729 |
MOD_PKA_2 | 200 | 206 | PF00069 | 0.614 |
MOD_PKA_2 | 253 | 259 | PF00069 | 0.704 |
MOD_PKA_2 | 295 | 301 | PF00069 | 0.738 |
MOD_PKA_2 | 40 | 46 | PF00069 | 0.711 |
MOD_Plk_1 | 203 | 209 | PF00069 | 0.734 |
MOD_Plk_4 | 211 | 217 | PF00069 | 0.725 |
MOD_Plk_4 | 221 | 227 | PF00069 | 0.602 |
MOD_Plk_4 | 309 | 315 | PF00069 | 0.729 |
MOD_ProDKin_1 | 27 | 33 | PF00069 | 0.778 |
MOD_ProDKin_1 | 6 | 12 | PF00069 | 0.721 |
TRG_DiLeu_BaLyEn_6 | 234 | 239 | PF01217 | 0.649 |
TRG_ENDOCYTIC_2 | 136 | 139 | PF00928 | 0.652 |
TRG_ENDOCYTIC_2 | 209 | 212 | PF00928 | 0.726 |
TRG_ER_diArg_1 | 161 | 163 | PF00400 | 0.656 |
TRG_ER_diArg_1 | 38 | 41 | PF00400 | 0.764 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IK47 | Leishmania donovani | 100% | 100% |
E9AU48 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 99% |
Q4Q0E7 | Leishmania major | 86% | 99% |